JP2018051557A - Rare earth removal of hydrated and hydroxyl species - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a method to remove a target substance in the form of a hydroxide, carbonate, hydrate, or oxyhydroxyl, from aqueous liquid media, and also provide additives containing rare-earth elements.SOLUTION: A target substance or target substance-containing species is removed and/or detoxified by forming a target substance-laden rare earth-containing composition comprising the target substance, target substance-containing species, or a derivative thereof.SELECTED DRAWING: Figure 1

Description

  The present invention relates generally to hydration and removal of rare earth elements of chemical species containing hydroxyl groups, and more particularly to hydration and / or rare earth elements of chemical species containing hydroxyl groups containing metals and metalloids. Regarding removal.

(Cross-reference of related applications)
This application is a continuation-in-part of US Provisional Patent Application No. 13 / 356,581, filed January 23, 2012 and entitled “Removal of Chemical Species Containing Hydration and Hydroxyl Group by Rare Earth Elements”. And claims the benefit of the following US provisional patent application: 61 / 474,902, filed April 13, 2011, entitled “Method of treating water using rare earth metals and water handling system”, “Reduction / oxidation and soluble and insoluble rare earths” No. 61 / 475,155, filed April 13, 2011, entitled “Method and apparatus for removing oxyanions using elements”, “Rare earth elements and / or additives containing rare earth elements” No. 61 / 539,780, filed September 27, 2011, entitled “Method of using and removing water from a fluid stream”, “Method of treating water using rare earth metals and water No. 61 / 553,809, filed October 31, 2011, entitled “Handling System”, “Oxygenated Hydrated Chemical Species Using Rare Earth Elements No. 61 / 546,803, filed Oct. 13, 2011, entitled “Removing Rare Earth Elements from Chemical Species Containing Hydrated Hydroxy”, entitled “Method of Removal from Sex Stream” No. 61 / 614,427, filed March 22, 2012, entitled “Method and Water Handling System for Treating Water Using Rare Earth Metals”, filed April 18, 2011 No. 61 / 476,667, No. 61 / 553,809, filed October 31, 2011, named “Method of treating water using rare earth metals and water handling system” No. 61 / 558,887, filed November 11, 2011, entitled “Method of treating water using rare earth metals and water handling system”, filed in 2011 61 / 564,132, January 28, entitled “Removal of Phosphorus-Containing Materials with Rare Earth Elements”, 61 / 614,418, filed March 22, 2012, “Phosphorus Containing No. 61 / 613,883, filed March 21, 2012, entitled “Removal of materials by rare earth elements”, “Removal of non-metal-containing oxyanions from water using rare earth elements” No. 61 / 613,857, filed March 21, 2012, entitled “Removal of contaminants by rare earth elements in pools, hot tubs and hot springs”, filed on September 23, 2011 No. 61 / 538,634. Note that each of these is incorporated herein by reference in its entirety.

  The name of the invention filed on September 23, 2011 is “Water treatment method and water handling system for removing scale and reducing the tendency of scale adhesion”, and the agent reference number is 6062-89-3. A cross reference is made to US patent application Ser. No. 13 / 244,092. The entirety of which is incorporated herein by reference.

  The name of the invention filed on September 23, 2011 is "particulate cerium dioxide and method for producing and using it in situ" and the agent serial number is 6062-89-4. Cross reference is made to US patent application Ser. No. 13 / 244,117. The entirety of which is incorporated herein by reference.

US patent application filed on Mar. 2, 2012 with the title "Removal of contaminants from water using rare earth elements" and agent serial number 6062-89-1. Cross reference is made to 13 / 410,081. The entirety of which is incorporated herein by reference.

  US Patent Application No. 13 / filed on Jan. 23, 2012, whose title is “Removal of Phosphorus Containing Substances by Rare Earth Elements” and whose Attorney Docket No. 6062-89-5 Cross references are made for 356,574. The entirety of which is incorporated herein by reference.

  US patent filed on Mar. 28, 2012, entitled "Removal of non-metal-containing oxyanions using rare earth elements from water" and agent serial number 6062-89-2 Cross references are made to the application. The entirety of which is incorporated herein by reference.

  A cross-reference was made to a US patent application filed on March 28, 2012, with the title of the invention "removal of rare earth elements in phosphorus-containing materials" and agent serial number 6062-89-5-CIP. The The entirety of which is incorporated herein by reference.

As fresh water resources become increasingly scarce, water quality is rapidly becoming a major and global concern. In addition to higher pollution from industrial and local water resources and intrusion of saltwater into freshwater aquifers, disinfectants commonly used in drinking water, especially (HOCl / OCl ⁻ Free chlorine and monochloramine (NH ₂ Cl) (in the form of) react with metals and metalloids to give soluble products. For example, monochloramine is believed to react with lead to produce a soluble lead (II) product that leads to higher lead levels in drinking water.

  Various techniques have been used to remove contaminants from urban, industrial and recreational waters. Examples of such techniques include adsorption on high surface area materials such as alumina and activated carbon, ion exchange with anion exchange resins, simultaneous precipitation and electrodialysis. However, most techniques for removing contaminants are hampered by the difficulty of removing problematic contaminants, and more particularly the difficulty of removing metallic and non-metallic contaminant species. It is done.

  These and other needs are addressed by the various embodiments and configurations of this disclosure. The present disclosure is directed to the removal of various contaminants, including metal and metalloid target materials, using compositions comprising rare earth elements.

  In one embodiment, the composition has the following chemical formula:

In the above formula, 0 ≦ X ≦ 8, MS is one of the following:
M (H ₂ O) ₆ ⁿ , M (H ₂ O) ₅ OH ^(n-1) , M (OH) ^(n-1) M (H ₂ O
) ₄ (OH) ₂ ^(n-2) , M (OH) ₂ ^(n-2) , M (H ₂ O) ₃ (OH) ₃ ^(n-3) , M (OH) ₃ ^{(n-3) _{, M (H 2 O) 2}} (OH) 4 (n-4), M (OH) 4 (n-4), M (H 2 O) (OH) 5 (n-5), M (OH) 5 ^(N-5) , M (OH) ₆ ^(n-6) , M (H ₂ O) ₅ O ^(n-2) , M (H ₂ O) ₄ (O) ₂ ^(n-4) , M ( ^{_{H 2 O) 3 (O)}} 3 (n-6), M (H 2 O) 2 (O) 4 (n-8), M (H 2 O) (O) 5 (n-10), M ( ^{_{H 2 O) 5 CO 3 (}} n-2), MCO 3 (n-2), M (H 2 O) 4 (CO 3) 2 (n-4), M (CO 3) 2 (n-4) , M (H ₂ O) ₃ (CO ₃ ) ₃ ^(n-6) , M (CO ₃ ) ₃ ^(n-6) _{, M (H 2 O) 2} (CO 3) 4 (n-8), M (CO 3) 4 (n-8), M (H 2 O) (CO 3) 5 (n-10), M ( ^{_{CO 3) 5 (n-10}} ), M (CO 3) 6 (n-12), M (H 2 O) 4 n, M (H 2 O) 3 OH (n-1), M (H 2 O ) ₂ (OH) ₂ ^(n-2) , M (H ₂ O) (OH) ₃ ^(n-3) , M (H ₂ O) ₃ O ^(n-2) , M (H ₂ O) ₂ ( ^{_{O) 2 (n-4)}} , and ^{_{M (H 2 O) (O}} ) 3 (n-6). M is a metal or metalloid having an atomic number selected from the group consisting of 5, 13, 22-33, 40-52, 56, 72-84 and 88-94. The symbol n is a real number of 8 or less and represents the charge or oxidation state of M.

In one application, the composition is in a liquid medium, and the medium has a pH and Eh sufficient to favor MS as the main species of M.
In one application, M is one or more of boron, vanadium, chromium, cadmium, antimony, lead and bismuth.

  In one embodiment, the method contacts an additive containing a rare earth element with a metal or metalloid target material in a medium to remove the target material. The target substance is in the form of a hydroxide, carbonate, hydrate or oxyhydroxide as the main chemical species.

  In one embodiment, an additive containing a rare earth element is added in a medium to a metal or metalloid hydroxide, carbonate, to remove metal or metalloid hydroxide, carbonate and / or hydrate. Methods are provided for contacting with one or more of salts and hydrates.

The additive containing the rare earth element can be water-soluble or water-insoluble.
In one application, the target substance has an atomic number selected from the group consisting of 5, 13, 22-33, 40-52, 56, 72-84 and 88-94.

In one application, the contacting step comprises
(A) using as a medium an oxidizing agent that oxidizes the chemical species containing the target substance to one or more major chemical species of metal or metalloid hydroxides, carbonates, oxyhydroxyls and hydrates A sub-step wherein the chemical species containing the target substance is different from the metal or metalloid hydroxide, carbonate, oxyhydroxyl and / or hydrate;
(B) Thereafter, an additive containing a rare earth element is brought into contact with the metal or metalloid hydroxide, carbonate, oxyhydroxyl and / or hydrate in the medium, thereby bringing the metal or metalloid water into contact. Substeps for removing oxides, carbonates, oxyhydroxyls and / or hydrates.

In one application, the contacting step comprises
(A) a medium for reducing a target substance-containing species comprising a metal or metalloid to a major species in the form of a hydroxide, carbonate, oxyhydroxyl and / or hydrate of said metal or metalloid A sub-step in which the reducing agent is different from the metal or metalloid hydroxide, carbonate, oxyhydroxyl and / or hydrate;
(B) Thereafter, an additive containing a rare earth element is brought into contact with a metal or metalloid hydroxide, carbonate, oxyhydroxyl and / or hydrate in the medium, and the metal or metalloid hydroxide is contacted. Product, carbonate, oxyhydroxyl and / or hydrate.

In one application, the contacting step comprises
(A) A base and / or base equivalent is introduced into a medium, and a target substance-containing species including a metal or a metalloid is converted into a metal or metalloid hydroxide, carbonate, oxyhydroxyl and / or hydrated. A sub-step in which the target substance-containing species is different from the metal or metalloid hydroxide, carbonate, oxyhydroxyl and / or hydrate, and (b) Thereafter, in the medium, a rare earth element-containing additive is brought into contact with the metal or metalloid hydroxide, carbonate and / or hydrate so that the metal or metalloid hydroxide, carbonate, and And / or a sub-step of removing hydrate.

In one application, the contacting step comprises
(A) introducing an acid and / or an acid equivalent into a medium to convert a metal or metalloid-containing target species into a metal or metalloid hydroxide, carbonate, oxyhydroxyl and / or hydrated A sub-step in which the target substance-containing species is different from the metal or metalloid hydroxide, carbonate, oxyhydroxyl and / or hydrate,
(B) Thereafter, in the medium, the rare earth element-containing additive is brought into contact with a metal or metalloid hydroxide, carbonate, oxyhydroxyl and / or hydrate to form the metal or metalloid hydroxide, carbonic acid. Substeps for removing salts, oxyhydroxyls and / or hydrates.

  The present disclosure can have many advantages. For example, a rare earth element-containing composition can effectively remove a large number of target substances regardless of the form of a dissolved or undissolved chemical species. Illustratively, the composition can remove various forms of lead and lead species, including colloids, hydrates, carbonates, hydroxides and oxyhydroxyls. The pH and / or Eh can be adjusted to produce the selected main target species, which is more effective by the rare earth composition compared to the rare earth removal of other target species. Removed. Therefore, high-level removal of the selected target substance can be realized.

These and other advantages are apparent from this disclosure.
As used herein, the term “a” or “an” entity refers to one or more of the entities. As such, the terms “a” (or “an”), “one or more” and “at least one” are used interchangeably herein. It should be noted that the terms “comprising”, “including” and “having” can be used interchangeably.

“Absorption” refers to the penetration of one substance into the internal structure of another substance and is distinct from adsorption.
“Adsorption” refers to the attachment of atoms, ions, molecules, polyatomic ions or other materials to the surface of other materials called adsorbents. Typically, the attractive force for adsorption is a bond such as a covalent bond, metal bond, coordination bond, ionic bond, hydrogen bond, electrostatic force (eg, van der Waals force and / or London force), and the like. And / or in the form of force.

“At least one”, “one or more” and “and / or” are open expressions of both connected and disconnected in use. For example, “at least one A, B and C”, “at least one A, B or C”, “one or more of A, B and C”, “one or more of A, B or C” and Each expression “A, B, and / or C” means A only, B only, C only, A and B together, A and C together, B and C together, or A, B and C means together. The term “water” refers to any aqueous stream. The water can originate from any aqueous stream, and the aqueous stream can come from any natural and / or industrial water source. Non-limiting examples of such aqueous streams and / or water include drinking water, drinking water, recreational water, water from production processes, sewage, pool water, hot spring water, cooling water, boiler water, treated water, Local water, sewage, agricultural water, surface water, power plant water, improvement water, mixed water, and combinations thereof.

The terms “agglomerate” and “aggregate” refer to a composition formed by the collection of one or more substances into a mass.
“Binder” generally refers to one or more substances that bind together the aggregated substances. The binder is typically a solid, semi-solid or liquid. Non-limiting examples of binders are polymeric substances, tar, pitch, asphalt, wax, cement water, solution, dispersion, powder, silicate, gels, oil, alcohol, clay, starch, silicate, Acid, molasses, lime, lignosulfonate oil, hydrocarbon, glycerin, stearate, or combinations thereof. The binder can or cannot react chemically with the substance that aggregates. Non-limiting examples of chemical reactions include hydration / dehydration, metal ion reactions, precipitation / gelation reactions and surface charge modification.

“Carbonate” generally refers to a chemical that contains a carbonate radical or ion (CO ₃ ⁻² ). The most common carbonates are salts formed by reacting an inorganic base (eg, a metal hydroxide) with carbonic acid (H ₂ CO ₃ ). Normal carbonate is formed when equal amounts of acid and base react, bicarbonate is also called acidic carbonate or bicarbonate and is formed when acid is present in excess. Examples of carbonates include sodium carbonate (Na ₂ CO ₃ ), sodium bicarbonate (NaHCO ₃ ) and potassium carbonate (K ₂ CO ₃ ).

The term “clarification” or “clarification” refers to the removal of suspended or colloidal solids by gravity subsidence techniques.
The term “coagulation” refers to destabilizing a colloid by neutralizing the ability to keep the colloidal material in suspension. Cationic coagulants impart a positive charge and reduce the negative charge (zeta potential) of the colloid. The colloid thereby forms larger particles (known as agglomerated particles).

  The term “composition” refers to one or more chemical units comprising one or more atoms, such as molecules, polyatomic ions, chemicals, coordination complexes, coordination compounds, and the like. As is apparent, the composition can be of various types of bonds such as covalent bonds, metal bonds, coordination bonds, ionic bonds, hydrogen bonds, electrostatic forces (eg van der Waals and London forces), and the like. And / or can be held together by force.

“Chemical species” or “species” are atoms, elements, molecules, molecular fragments, ions, compounds and other chemical structures.
“Chemical conversion” refers to a process in which at least a portion of a substance converts its chemical composition through a chemical reaction. “Chemical transformation” is different from “physical transformation”. Physical transformation refers to a process in which a chemical composition is not chemically transformed, but a physical property such as size or shape is transformed.

The term “contained within the water” generally refers to a substance that is suspended and / or dissolved within the water. Water is typically a solvent for soluble materials and water soluble materials. Furthermore, water is typically not a solvent for insoluble materials and water-insoluble materials. Suspended materials are substantially insoluble in water, and dissolved materials are substantially soluble in water. The suspended material has a certain particle size.

  “Detoxify” or “detoxify” includes making a target substance, such as a chemical and / or biological target substance, nontoxic or harmful to an organism such as a human or other animal. The target substance can be made non-toxic by converting the target substance into a non-toxic or harmful form or chemical species.

  The term “digest” or “digestion” refers to the use of microorganisms, particularly bacteria, to digest a target substance. This is generally established by forcibly mixing contaminated water with bacteria and molecular oxygen.

  The terms “disinfect” or “disinfect” refer to the use of antimicrobial substances to kill or inhibit the growth of microorganisms such as bacteria, fungi, protozoa and viruses. Common antibacterial substances include oxidizing agents, reducing agents, alcohols, aldehydes, halogens, phenolic resins, quaternary ammonium compounds, silver, copper, ultraviolet light and other substances.

  The term “agglomeration” refers to the process of using a flocculant, typically a polymer, to form crosslinks between the agglomerated particles and bind the particles to large agglomerates or agglomerates. Crosslinking occurs when portions of the polymer chain adsorb to different particles to help the particles aggregate.

The term “fluid” refers to a liquid, a gas, or both.
“Halogen” is a nonmetallic element of Group 17 (formerly Group VII, VIIA) of the IUPAC format in the periodic table, and includes fluorine (F), chlorine (Cl), bromine (Br), iodine (I) And astatine (At). The artificially created element 117, called ununseptium, tentatively by systematic name, can also be a halogen.

A “halide compound” is a compound that has at least one halogen atom as part of the compound and the other part is an element or free radical that is less negatively charged (or more positively charged) than halogen. It is. The halide compound is typically a fluoride, chloride, bromide, iodide or asteride compound. Many salts are halides having a halide anion. A halide anion is a halogen atom that supports a negative charge. Halide anions are fluoride (F ⁻ ), chloride (Cl ⁻ ), bromide (Br ⁻ ), iodide (I ⁻ ), and asteride (At ⁻ ).

“Hydroxyl” generally refers to a chemical functional group that accommodates an attached oxygen atom by a covalent bond to a hydrogen atom. When it appears in a chemical species, the hydroxyl group imparts some reactive and interactive properties to water (ionizability, hydrogen bonding, etc.). Chemical species that contain one or more hydroxyl groups are typically referred to as “hydroxyl species”. The neutral form of the hydroxyl group is the hydroxyl radical. The form of the anion of the hydroxyl group (OH ⁻ ) is called “hydroxide” or “hydroxide anion”.

Whether it occurs as a solid or fluid component, and whether it occurs as a compound or charged species, the type of compound or any other chemical species that is chemically contained by water The term “hydrated species” is generally referred to. In some hydrates, such as sodium carbonate, Na ₂ CO ₃ · 10H ₂ O, water is held loose and easily lost by heating, but sulfuric acid, SO ₃ · H ₂ O or H ₂ In other cases, such as SO ₄ , the water is strongly retained as compound water.

The term “inorganic” generally refers to a chemical or other species that is not organic.
The term “insoluble” refers to a substance that is intended to be solid and / or remain as a solid in water. Insoluble materials can be retained in an apparatus such as a column or can be easily recovered from the batch reaction using physical means such as filtration. Insoluble materials can be soaked in water for many weeks or months, with little loss of mass. Typically, a small loss of mass refers to a loss of mass of less than about 5% after long-term immersion of an insoluble material.

“Ion” generally refers to a charged atom or group of atoms. The charge on the ions can be negative or positive.
"Organic carbon" or "organic matter" is generally a binary element such as carbon oxide, carbide, carbon disulfide, etc., ternary compounds such as metal cyanide, metal carbonyl, phosgene, carbonyl sulfide, etc. And any carbon compound except metal carbonates such as alkali and alkaline earth metal carbonates.

  The term “oxidant” generally refers to one or both of chemical and physical processes that communicate and / or assist in the removal of one or more electrons from a substance. The material from which one or more electrons have been removed is oxidized. With respect to physical processes, physical processes can be removed and / or supported in the removal of one or more electrons from the material being oxidized. For example, a material to be oxidized can be oxidized by electromagnetic energy when the interaction of electromagnetic energy with the material being oxidized is sufficient to substantially remove one or more electrons from the material. On the other hand, when the interaction of electromagnetic energy with the material to be oxidized is not sufficient to remove one or more electrons, but may be sufficient to excite the electrons to a higher energy state, Excited electrons can be more easily removed by chemicals, thermal energy, or one or more of such.

The terms “oxyanion” and / or “oxoanion” generally refer to an anionic chemical having a negative charge of the general formula A _x xO _y ^z- . (Here, A represents a chemical element other than oxygen, “O” represents oxygen as an element, and x, y, and z represent real numbers). In embodiments that include an oxyanion as a contaminating chemical, “A” refers to a metal, metalloid and / or non-metal element. Examples of metal-based oxyanions include chromate, wolframate, molybdate, aluminate, zirconate, and others. Examples of metalloid based oxyanions include arsenate, arsenite, antimonate, germanate, silicate, and others. Examples of non-metal based oxyanions include phosphate, selenate, sulfate, etc. Preferably, the oxyanion is 7, 13-17, 22-26, 31-35, 40-42, 44, 45, 49-53, 72-75, 77, 78, 82, 8385, 88, and 92. Including oxyanions of elements of the number of atoms. These elements include nitrogen, aluminum, silicon, phosphorus, sulfur, chlorine, titanium, vanadium, chromium, manganese, barium, arsenic, selenium, bromine, gallium, germanium, zirconium, niobium, molybdenum, ruthenium, rhodium, indium, Includes tin, iodine, antimony, tellurium, hafnium, tantalum, tungsten, rhenium, iridium, platinum, lead, bismuth astatine, radium and uranium.

The terms “oxy species” and / or “oxo species” generally refer to chemicals of the general formula A _x O _y that are cationic, anionic, or neutral (where , A represents a chemical element other than oxygen, O represents oxygen as an element, and x and y represent real numbers). In embodiments where the contaminating chemical is an oxyanion, “A” refers to a metal, metalloid and / or non-metal element. Oxy anions or oxo anions are one type of oxy species or oxo species.

The term “scouring” refers to any treatment, such as filtration, to remove small (usually microscopic) particulate material or a very small collection of dissolved target material from water.
The terms “pore volume” and “pore size” refer to the determination of pore volume and pore size made by any combination of measurement methods, respectively. Preferably, the pore size and pore volume are determined by any suitable BJH method (Barret-Joyner-Halenda method) for determining pore size and volume. Further, it is understood herein that the pore sizes and pore diameters used herein can be used interchangeably.

  “Precipitation” generally refers to the removal of dissolved target material in the form of a rare earth element composition loaded with insoluble target material. The composition of the rare earth element bearing the target substance includes a cerium (IV) composition bearing the target, a rare earth element-containing additive composition bearing the target, and a composition containing rare earth elements other than the cerium (IV) bearing the target. Product, or a combination thereof. As a typical example, the rare earth element composition with a target substance includes a rare earth element composition with an insoluble target substance. For example, “precipitation” includes processes such as adsorption and absorption of a target material by one or more of a cerium (IV) composition, a rare earth-containing additive, or a rare earth element other than cerium (IV). The composition bearing the target substance may comprise a rare earth element with an oxidation number of +3, such as cerium (III), lanthanum (III), or other lanthanoids with an oxidation state of +3.

  “Major species” generally refers to the major species in which a cation is present under a particular combination of conditions. Although usually applied to cations, the term “main species” also applies to those that are negatively charged or uncharged.

  A “radical” generally refers to an atom or group of atoms that are connected together in several specific spatial structures and that are typically involved in chemical reactions as a single unit. A radical is more generally an atom, molecule or ion with one or more unpaired electrons (the atomic group is also probably ok). The radicals can have a net positive or negative charge, or can be neutral.

  “Rare earth element” refers to one or more of yttrium, scandium, lanthanum, cerium, praseodymium, neodymium, samarium, europium, gadolinium, terbium, dysprosium, holmium erbium, thulium, ytterbium and lutetium. As is apparent, lanthanum, cerium, praseodymium, neodymium, samarium, europium, gadolinium, terbium, dysprosium, holmium erbium, thulium, ytterbium and lutetium are known as lanthanoids.

The terms “rare earth element”, “rare earth element-containing composition”, “rare earth element-containing additive” and “rare earth element-containing particles” refer to both the singular and plural forms of the term. By way of example, the term “rare earth element” refers to a single rare earth element and / or a combination and / or mixture of rare earth elements, and the term “rare earth element-containing composition” includes a single rare earth element. It refers to a single composition and / or a mixture of different rare earth-containing compositions containing one or more rare earth elements and / or a single composition containing one or more rare earth elements. The terms “rare earth element-containing additive” and “rare earth element-containing particles” refer to a single composition comprising a single rare earth element, and / or different rare earth element-containing compositions containing one or more rare earth elements. And / or an additive or particle comprising a single composition containing one or more rare earth elements. The term “treated rare earth composition” does not only refer to any composition comprising rare earth elements other than rare earth-containing minerals that are not compositionally altered. In other words, as used herein, “treated rare earth-containing composition” excludes ground naturally occurring rare earth-containing minerals. However, as used herein, a “treated rare earth-containing composition” includes a rare earth-containing mineral in which one or both of the chemical composition and chemical structure of the mineral-containing portion of the mineral is changed. More particularly, ground naturally occurring bust nesite is not considered a treated rare earth-containing composition and / or treated rare earth-containing additive. However, a rare earth element-containing composition prepared by chemical conversion of synthetically prepared bust nesitet or naturally occurring bust nesitet is treated with a treated rare earth element-containing composition and / or treated rare earth element. It is considered an element-containing additive. Treated rare earth elements and / or rare earth-containing compositions and / or additives are, in one application, synthetically produced, but not naturally occurring minerals. Exemplary naturally occurring rare earth-containing minerals include bastonite (carbonic fluoride mineral) and monazite. Other naturally occurring rare earth-containing minerals include esinite, cassiterite, apatite, britlite, badger stone, celite, fluorite, fluorite, gadolinite, parisite, stilwellite, scintillite, titanium Stone, xenotime, zircon and zirconolite are included. Exemplary uranium minerals include sphalerite (UO ₂ ), pitch blends (mixed oxides, usually U ₃ O ₈ ), branelite (complex oxides of uranium, rare earths, iron and titanium), coffinite (uranium silicate) Acid salt), carnotite, phosphide uranium, davidite, rubber stone, copper uranium ore and uranophene. In one formulation, the rare earth-containing composition contains one or more elements from groups 1, 2, 4-15 or 17 of the periodic table, radioactive species such as uranium, sulfur, selenium, tellurium and polonium. It does not contain substantially.

  The terms “reducing agent”, “reducing agent” or “reducer” generally refer to an element or compound that provides one or more electrons to another chemical species or agent to be reduced. In the reduction process, reducing agents are oxidized and other species that accept one or more electrons are reduced.

  The terms “removal”, “removing” or “removing” refer to the sorption, precipitation, conversion, detoxification, inactivation and / or deactivation of target substances contained in water and / or water handling systems. Refers to a combination.

  The term “soluble” refers to a material that readily dissolves in a fluid, such as water or other solvent. For the purposes of this disclosure, what is expected is that dissolution of soluble material necessarily occurs on a time scale of minutes rather than days. For substances considered to be soluble, the substance / composition has a significant solubility in fluid, such that at least about 5 g of the substance dissolves in about 1 liter of fluid and is stable in fluid. Must have.

The term “sorption” refers to adsorption, absorption or both adsorption and absorption.
The term “suspension” refers to a heterogeneous mixture of solids dispersed in a liquid, typically in the form of particulates. In suspension, the solid particulates are in the form of a dispersed phase dispersed in a continuous liquid phase. The term “colloid” refers to a suspension containing solid particulates that typically do not settle out of a continuous liquid phase due to attractive forces. “Colloid” typically refers to a system having microparticles dispersed in a continuous medium ranging in size from about 10 to 10,000 angstroms. As used herein below, the term “suspension”, “colloid” or “slurry” refers to one or more substances dispersed and / or suspended in a continuous liquid phase. Used interchangeably for.

  The term “surface area” refers to the surface area of a material and / or substance as determined by any suitable surface area measurement method. Preferably, the surface area is determined by any suitable BET (Brunauer-Emmett-Teller) analytical technique that determines the specific area of the material and / or substance.

  The term “water handling system” means containing, transporting, operating, physically converting, chemically treating, mechanically treating, purifying, producing a water-soluble composition and / or Refers to a system that forms, processes the water-soluble composition, and mixes and / or mixes with one or more other waters and any combination thereof.

  “Components of the water handling system” refers to one or more operating units and / or parts (sewage tanks, reactors, purifiers, processing vessels or units, stirring tanks or units) of the apparatus that processes and / or processes water. Element, washing circuit, precipitation vessel, separation vessel or unit, precipitation tank or vessel, reservoir, pump, aerator, cooling tower, heat exchanger, valve, boiler, filtration device, solid-liquid and / or gas-liquid separator, nozzle , Charcoal turbines, etc.), conduits (piping, hoses, channels, aqua ducts, grooves, etc.) interconnecting operating units and / or devices, and water carried by the conduits. The water handling system components and conduits are in fluid communication.

  The terms “water” and “water handling system” are used interchangeably. That is, the term “water” can be used to refer to the term “water handling system” and the term “water handling system” can be used to refer to the term “water”.

  The above is a simplified summary of the disclosure in order to provide an understanding of some aspects of the disclosure. This summary is not an extensive or exhaustive overview of the disclosure and its various embodiments. It is not intended to identify the key or critical elements of this disclosure or to delineate the scope of this disclosure in detail, but as an introduction to the more detailed description presented below. It is intended to illustrate selected concepts of this disclosure in a simplified form. As will be apparent, an atomic number selected from the group consisting of one or more of the features described above or detailed below, 5, 13, 22-33, 40-52, 72-84 and 89-94. Other embodiments of this disclosure are possible using metals or metalloids alone or in combination.

  The accompanying drawings, which are incorporated in and constitute a part of this specification, illustrate embodiments of this disclosure and, together with the general description of this disclosure and the following detailed description, described above, It serves to explain the principle.

The flowchart which shows the water handling system and method of one Embodiment. FIG. 2 is a pool diagram of the prior art under specific conditions of major boron species. FIG. 2 is a pool diagram of the prior art under specific conditions of major boron species. FIG. 2 is a pool diagram of the prior art under specific conditions of major boron species. FIG. 2 is a pool diagram of the prior art under specific conditions of major boron species. FIG. 2 is a pool diagram of the prior art under specific conditions of major boron species. A pool diagram of the prior art under specific conditions of the main species of aluminum. A pool diagram of the prior art under specific conditions of the main species of aluminum. A pool diagram of the prior art under specific conditions of the main species of aluminum. A pool diagram of the prior art under specific conditions of the main species of aluminum. A pool diagram of the prior art under specific conditions of the main species of aluminum. Pool diagram of the prior art under specific conditions of the main species of thallium. Pool diagram of the prior art under specific conditions of the main species of thallium. Pool diagram of the prior art under specific conditions of the main species of thallium. Pool diagram of the prior art under specific conditions of the main species of thallium. A prior art pool diagram under specific conditions of the main species of vanadium. A prior art pool diagram under specific conditions of the main species of vanadium. A prior art pool diagram under specific conditions of the main species of vanadium. A prior art pool diagram under specific conditions of the main species of vanadium. A prior art pool diagram under specific conditions of the main species of vanadium. A pool diagram of the prior art under specific conditions of the main species of chromium. A pool diagram of the prior art under specific conditions of the main species of chromium. A pool diagram of the prior art under specific conditions of the main species of chromium. A pool diagram of the prior art under specific conditions of the main species of chromium. A pool diagram of the prior art under specific conditions of the main species of chromium. A pool diagram of the prior art under certain conditions of the main chemical species of manganese. A pool diagram of the prior art under certain conditions of the main chemical species of manganese. A pool diagram of the prior art under certain conditions of the main chemical species of manganese. A pool diagram of the prior art under certain conditions of the main chemical species of manganese. A pool diagram of the prior art under certain conditions of the main chemical species of manganese. A pool diagram of the prior art under certain conditions of the main chemical species of manganese. A pool diagram of the prior art under specific conditions of the main chemical species of iron. A pool diagram of the prior art under specific conditions of the main chemical species of iron. A pool diagram of the prior art under specific conditions of the main chemical species of iron. A pool diagram of the prior art under specific conditions of the main chemical species of iron. A pool diagram of the prior art under specific conditions of the main chemical species of iron. A pool diagram of the prior art under specific conditions of the main chemical species of iron. A pool diagram of the prior art under specific conditions of the main species of cobalt. A pool diagram of the prior art under specific conditions of the main species of cobalt. A pool diagram of the prior art under specific conditions of the main species of cobalt. A pool diagram of the prior art under specific conditions of the main species of cobalt. A pool diagram of the prior art under specific conditions of the main species of cobalt. A pool diagram of the prior art under specific conditions of the main species of nickel. A pool diagram of the prior art under specific conditions of the main species of nickel. A pool diagram of the prior art under specific conditions of the main species of nickel. A pool diagram of the prior art under specific conditions of the main species of nickel. A pool diagram of the prior art under specific conditions of the main species of nickel. A pool diagram of the prior art under specific conditions of the main chemical species of copper. A pool diagram of the prior art under specific conditions of the main chemical species of copper. A pool diagram of the prior art under specific conditions of the main chemical species of copper. A pool diagram of the prior art under specific conditions of the main chemical species of copper. A pool diagram of the prior art under specific conditions of the main chemical species of copper. A pool diagram of the prior art under specific conditions of the main chemical species of zinc. A pool diagram of the prior art under specific conditions of the main chemical species of zinc. A pool diagram of the prior art under specific conditions of the main chemical species of zinc. A pool diagram of the prior art under specific conditions of the main chemical species of zinc. A pool diagram of the prior art under specific conditions of the main chemical species of gallium. A pool diagram of the prior art under specific conditions of the main chemical species of gallium. FIG. 2 is a pool chart of the prior art under a specific state of the main chemical species of germanium. FIG. 2 shows a prior art pool diagram under specific conditions for the main species of arsenic. FIG. 2 shows a prior art pool diagram under specific conditions for the main species of arsenic. FIG. 2 shows a prior art pool diagram under specific conditions for the main species of arsenic. FIG. 2 shows a prior art pool diagram under specific conditions for the main species of arsenic. FIG. 2 is a pool diagram of the prior art under specific conditions of the main chemical species of zirconium. FIG. 2 is a pool diagram of the prior art under specific conditions of the main chemical species of zirconium. FIG. 2 is a pool diagram of the prior art under specific conditions of the main chemical species of zirconium. FIG. 2 is a pool diagram of the prior art under specific conditions of the main chemical species of zirconium. Prior art pool chart under specific conditions of the major species of niobium. Prior art pool chart under specific conditions of the major species of niobium. Prior art pool chart under specific conditions of the major species of niobium. Prior art pool chart under specific conditions of the major species of niobium. A pool diagram of the prior art under specific conditions of the main species of molybdenum. A pool diagram of the prior art under specific conditions of the main species of molybdenum. A pool diagram of the prior art under specific conditions of the main species of molybdenum. A pool diagram of the prior art under specific conditions of the main chemical species of technetium. A pool diagram of the prior art under specific conditions of the main chemical species of technetium. A pool diagram of the prior art under specific conditions of the main chemical species of technetium. A pool diagram of the prior art under specific conditions of the main chemical species of technetium. A pool diagram of the prior art under specific conditions of the main chemical species of technetium. A pool diagram of the prior art under specific conditions of the main chemical species of technetium. A pool diagram of the prior art under specific conditions of the main ruthenium species. A pool diagram of the prior art under specific conditions of the main ruthenium species. A pool diagram of the prior art under specific conditions of the main ruthenium species. A pool diagram of the prior art under specific conditions of the main ruthenium species. A pool diagram of the prior art under specific conditions of the main chemical species of rhodium. A pool diagram of the prior art under specific conditions of the main chemical species of rhodium. FIG. 5 is a pool diagram of the prior art under specific conditions of the main species of palladium. FIG. 5 is a pool diagram of the prior art under specific conditions of the main species of palladium. FIG. 5 is a pool diagram of the prior art under specific conditions of the main species of palladium. A pool diagram of the prior art under specific conditions of major silver species. A pool diagram of the prior art under specific conditions of major silver species. A pool diagram of the prior art under specific conditions of major silver species. A pool diagram of the prior art under specific conditions of major silver species. A pool diagram of the prior art under specific conditions of major silver species. A prior art pool diagram under specific conditions of the main species of cadmium. A prior art pool diagram under specific conditions of the main species of cadmium. A prior art pool diagram under specific conditions of the main species of cadmium. FIG. 2 is a pool of prior art under specific conditions of the main species of indium. FIG. 2 is a pool of prior art under specific conditions of the main species of indium. Pool diagram of the prior art under specific conditions of the main chemical species of tin. Pool diagram of the prior art under specific conditions of the main chemical species of tin. Pool diagram of the prior art under specific conditions of the main chemical species of tin. Pool diagram of the prior art under specific conditions of the main chemical species of tin. Pool diagram of the prior art under specific conditions of the main chemical species of tin. A pool of prior art under specific conditions of the main species of antimony. A pool of prior art under specific conditions of the main species of antimony. A pool of prior art under specific conditions of the main species of antimony. A pool of prior art under specific conditions of the main species of antimony. Prior art pool diagram under specific conditions of tellurium main species. A pool diagram of the prior art under specific conditions of the main chemical species of hafnium. A pool diagram of the prior art under specific conditions of the main chemical species of lead. A pool diagram of the prior art under specific conditions of the main chemical species of tungsten. A pool diagram of the prior art under specific conditions of the main chemical species of tungsten. A pool diagram of the prior art under specific conditions of the main species of rhenium. A pool diagram of the prior art under specific conditions of the main species of rhenium. A prior art pool diagram under specific conditions of the major species of osmium. A pool diagram of the prior art under specific conditions of the main species of uranium. A pool diagram of the prior art under specific conditions of the main chemical species of platinum. A pool diagram of the prior art under specific conditions of the main chemical species of platinum. A pool diagram of the prior art under specific conditions of the main species of gold. A pool diagram of the prior art under specific conditions of the main species of gold. A pool diagram of the prior art under specific conditions of the main species of gold. A pool diagram of the prior art under specific conditions of major mercury species. A pool diagram of the prior art under specific conditions of major mercury species. A pool diagram of the prior art under specific conditions of major mercury species. A pool diagram of the prior art under specific conditions of major mercury species. A pool diagram of the prior art under specific conditions of the main chemical species of lead. A pool diagram of the prior art under specific conditions of the main chemical species of lead. A pool diagram of the prior art under specific conditions of the main chemical species of lead. A pool diagram of the prior art under specific conditions of the main chemical species of lead. A pool diagram of the prior art under specific conditions of the main chemical species of lead. A pool diagram of the prior art under specific conditions of the main chemical species of lead. A pool diagram of the prior art under specific conditions of the main chemical species of bismuth. A pool diagram of the prior art under specific conditions of the main chemical species of bismuth. A pool diagram of the prior art under specific conditions of the main chemical species of bismuth. A pool diagram of the prior art under specific conditions of the main polonium species. A pool diagram of the prior art under specific conditions of the main polonium species. FIG. 2 is a pool of prior art under specific conditions of the main species of actinium. FIG. 2 is a pool of prior art under specific conditions of the main species of actinium. A pool diagram of the prior art under specific conditions of the main species of thorium. A pool diagram of the prior art under specific conditions of the main species of thorium. A pool diagram of the prior art under specific conditions of the main species of thorium. A pool diagram of the prior art under specific conditions of the main species of thorium. A pool diagram of the prior art under specific conditions of the main species of thorium. FIG. 5 is a prior art Pourbaille diagram under specific conditions of the main species of protoactinium. FIG. 5 is a prior art Pourbaille diagram under specific conditions of the main species of protoactinium. A pool diagram of the prior art under specific conditions of the main species of uranium. A pool diagram of the prior art under specific conditions of the main species of uranium. A pool diagram of the prior art under specific conditions of the main species of uranium. A pool diagram of the prior art under specific conditions of the main species of uranium. A pool diagram of the prior art under specific conditions of the main species of uranium. A pool diagram of the prior art under specific conditions of the main species of uranium. A pool diagram of the prior art under specific conditions of the main species of uranium. FIG. 2 is a prior art pool chart under specific conditions of major species of neptunium. FIG. 2 is a prior art pool chart under specific conditions of major species of neptunium. FIG. 2 is a prior art pool chart under specific conditions of major species of neptunium. FIG. 2 is a prior art pool chart under specific conditions of major species of neptunium. FIG. 2 is a prior art pool chart under specific conditions of major species of neptunium. A pool diagram of the prior art under specific conditions of the main species of plutonium. A pool diagram of the prior art under specific conditions of the main species of plutonium. A pool diagram of the prior art under specific conditions of the main species of plutonium. A pool diagram of the prior art under specific conditions of the main species of plutonium. A pool diagram of the prior art under specific conditions of the main species of plutonium. A pool diagram of the prior art under specific conditions of the main species of plutonium. The graph which shows a load capacity (mg / g) (vertical axis) and an arsenic concentration (gram / liter) (horizontal axis). A graph showing final arsenic concentration (mg / L) (vertical axis) and cerium: arsenic molar ratio (horizontal axis). Graph showing final arsenic concentration (mg / L) (vertical axis) and molar ratio of cerium to arsenic (horizontal axis). A series of XRD patterns of precipitates formed by adding a cerium (III) or cerium (IV) solution to a sulfide arsenite solution and a sulfate arsenate solution. A graph showing trapped arsenic (micromolar) (vertical axis) and added cerium (micromolar) (horizontal axis). A series of XRD patterns showing structural differences between gas pearlite (CeAsO ₄ ) and the novel trigonal phase CeAsO _4. (H ₂ O) _X. Structure between trigonal CeAsO ₄ · (H ₂ O) _X (experiment), trigonal CeAsO ₄ · (H ₂ O) _X (simulation) and trigonal BiPO ₄ · (H ₂ O) _0.67 (simulation) A series of XRD patterns showing typical differences. Graph showing arsenic capacity (mg arsenic / g cerium oxide) and various solution compositions. Graph showing arsenic (V) concentration (ppb) and total volume processed. The graph which shows the state (horizontal axis) of mg arsenic / g cerium oxide (vertical axis) and a test solution. A pool diagram of the prior art under specific conditions of the main chemical species of bismuth. A pool diagram of the prior art under specific conditions of the main chemical species of bismuth. A pool diagram of the prior art under specific conditions of the main chemical species of bismuth. A pool diagram of the prior art under specific conditions of the main chemical species of bismuth. A pool diagram of the prior art under specific conditions of the main species of aluminum. A pool diagram of the prior art under specific conditions of the main species of aluminum. A pool diagram of the prior art under specific conditions of the main species of aluminum. A pool diagram of the prior art under specific conditions of the main species of aluminum. A pool diagram of the prior art under specific conditions of the main species of aluminum. A pool diagram of the prior art under specific conditions of the main species of cobalt. A pool diagram of the prior art under specific conditions of the main species of cobalt. A pool diagram of the prior art under specific conditions of the main species of cobalt. A pool diagram of the prior art under specific conditions of the main species of cobalt. A pool diagram of the prior art under specific conditions of the main species of cobalt. A pool diagram of the prior art under specific conditions of the main species of chromium. A pool diagram of the prior art under specific conditions of the main species of chromium. A pool diagram of the prior art under specific conditions of the main species of chromium. A pool diagram of the prior art under specific conditions of the main species of chromium. A pool diagram of the prior art under specific conditions of the main species of chromium. A pool diagram of the prior art under certain conditions of the main chemical species of manganese. A pool diagram of the prior art under certain conditions of the main chemical species of manganese. A pool diagram of the prior art under certain conditions of the main chemical species of manganese. A pool diagram of the prior art under certain conditions of the main chemical species of manganese. A pool diagram of the prior art under certain conditions of the main chemical species of manganese. A pool diagram of the prior art under specific conditions of the main chemical species of copper. A pool diagram of the prior art under specific conditions of the main chemical species of copper. A pool diagram of the prior art under specific conditions of the main chemical species of copper. A pool diagram of the prior art under specific conditions of the main chemical species of copper. A pool diagram of the prior art under specific conditions of the main chemical species of copper. FIG. 2 is a pool diagram of the prior art under specific conditions of the main chemical species of zirconium. FIG. 2 is a pool diagram of the prior art under specific conditions of the main chemical species of zirconium. FIG. 2 is a pool diagram of the prior art under specific conditions of the main chemical species of zirconium. FIG. 2 is a pool diagram of the prior art under specific conditions of the main chemical species of zirconium. FIG. 2 is a pool diagram of the prior art under specific conditions of the main chemical species of zirconium. A pool diagram of the prior art under specific conditions of the main chemical species of zinc. A pool diagram of the prior art under specific conditions of the main chemical species of zinc. A pool diagram of the prior art under specific conditions of the main chemical species of zinc. A pool diagram of the prior art under specific conditions of the main chemical species of zinc. A pool diagram of the prior art under specific conditions of the main chemical species of zinc. A pool diagram of the prior art under specific conditions of the main species of barium. A pool diagram of the prior art under specific conditions of the main species of barium. A pool diagram of the prior art under specific conditions of the main species of barium. A pool diagram of the prior art under specific conditions of the main species of barium. A pool diagram of the prior art under specific conditions of the main species of barium. A pool diagram of the prior art under specific conditions of the main species of radium. A pool diagram of the prior art under specific conditions of the main species of radium. A pool diagram of the prior art under specific conditions of the main species of radium. A pool diagram of the prior art under specific conditions of the main species of radium. A pool diagram of the prior art under specific conditions of the main species of radium.

  As shown in FIG. 1, the present disclosure provides for the removal and / or removal of a target substance, such as a contamination or contaminant, or a chemical species containing the target substance from water with a rare earth element-containing composition, additive, or particle. It is directed to water detoxification, water handling systems, or water-soluble media or other water-soluble media. Preferably, the rare earth element-containing composition, additive or particle is a treated rare earth element-containing composition, additive or particle. In some embodiments, the target substance or target substance-containing species is removed by forming a composition containing a rare earth element bearing the target substance, including the target substance, target substance-containing species or derivatives thereof. And / or detoxified. The target substance is one or more of inorganic oxy species (other than oxyanions), hydroxyl species including hydroxide ions or hydroxyl radicals, hydrated species, or combinations thereof. The rare earth element-containing composition can be soluble or insoluble and is generally cerium, a cerium-containing compound, lanthanum, a lanthanum-containing compound, or a mixture thereof. More common rare earth-containing compositions include cerium (IV) oxide, cerium (III) oxide, cerium (IV) salt, cerium (III) salt, lanthanum oxide (III), lanthanum (III) salt, or mixtures thereof It is. The rare earth element composition bearing the target material includes the target material and / or chemical species thereof, or a part of the target material and / or one or more of the chemical species.

Rare earth element-containing additives Rare earth element containing compositions, additives and / or particles are water soluble, water insoluble, water soluble and / or water insoluble rare earth element containing compositions, additives and / or particles, partially water soluble Rare earth-containing compositions, additives and / or particles, and / or combinations of partially water-insoluble rare earth-containing compositions, additives and / or particles.

  In general, the rare earth-containing composition, additive and / or particles comprise cerium, cerium-containing compound form and / or cerium, lanthanum separated ion form, lanthanum-containing compound form and / or lanthanum In the form of separated ions, or a mixture thereof. More common rare earth-containing compositions, additives and particles include cerium (IV) oxide, cerium (III) oxide, cerium (IV) salts, cerium (III) salts, lanthanum (III) oxide, lanthanum ( III) Salts, or mixtures and / or combinations thereof.

  The rare earth-containing composition, additive and / or particles can contain one or more rare earth elements and can be in any suitable form, such as free-flowing powders, liquid formulations, or other forms can do. Examples of additives and particles of rare earth element-containing compositions include cerium (III) oxide, cerium (IV) oxide, cerium (IV) salts (cerium chloride, cerium bromide, cerium iodide, cerium sulfate, cerium Nitrates, cerium chlorates and cerium oxalates), cerium (III) salts (cerium chloride, cerium bromide, cerium iodide, cerium sulfate, cerium nitrate, cerium chlorate, cerium chloride and cerium oxalate, etc.) Lanthanum (III) oxides, lanthanum (III) salts (such as lanthanum chloride, lanthanum bromide, lanthanum iodide, lanthanum chlorate, lanthanum sulfate, lanthanum succinate and lanthanum nitrate), and mixtures thereof are included.

  The rare earth element and / or the rare earth element-containing composition in the rare earth element-containing additive can be in the form of rare earth elements, ions, or composite forms. The rare earth element and / or the rare earth element-containing composition is contained in a fluid such as water, or is in the form of nanoparticles, particles larger than nanoparticles, aggregates, or aggregates, or combinations and / or mixtures thereof. Can do. The rare earth element and / or the rare earth element-containing composition can be supported or unsupported. The rare earth element and / or the rare earth element-containing composition may include one or more rare earth elements. The rare earth elements can have the same or different valences and / or oxidation states and / or oxidation numbers. The rare earth element can be a mixture of different rare earth elements, such as two or more of two or more of yttrium, scandium, cerium, lanthanum, praseodymium and neodymium.

  The rare earth element and / or rare earth element-containing composition, in one application, is a treated rare earth element-containing composition that is free or substantially free of naturally occurring and / or derived minerals. In one formulation, the rare earth element or rare earth element-containing composition is substantially free of one or more elements from Groups 1, 2, 4-15, or Group 17 of the Periodic Table, and contains uranium, sulfur, It is substantially free of radioactive species such as selenium, tellurium and polonium.

  In some formulations, the rare earth-containing composition includes one or more rare earth elements. While not wishing to be limited by example, the rare earth-containing composition can include a first rare earth element and a second rare earth element. The first and second rare earth elements can have the same or different atomic numbers. In some formulations, the first rare earth element comprises cerium (III) and the second rare earth element includes a rare earth element other than cerium (III). The rare earth element other than cerium (III) can be one or more of trivalent rare earth elements, cerium (IV), or other rare earth elements other than trivalent cerium. For example, the mixture of rare earth-containing compositions can be composed of a first rare earth element in the +3 oxidation state and a second rare earth element in the +4 oxidation state. In some embodiments, the first and second rare earth elements are the same and include cerium. More specifically, the first rare earth element is composed of cerium (III), and the second rare earth element includes cerium (IV). Preferably, the cerium is predominantly in the form of water-soluble cerium (III) salts and the remaining cerium is present as cerium oxide, which is a substantially water-insoluble cerium composition.

  In one formulation, cerium is primarily in the form of cerium (IV) oxide, while the remaining cerium exists as isolated cerium (III) salts. In compositions containing rare earth elements in a mixture of +3 and +4 oxidation states, typically at least some of the rare earth elements are in the +4 oxidation state, and more commonly at least most of the rare earth elements are in the +4 oxidation state. More generally, at least about 75% by weight of the rare earth element is in the +4 oxidation state, and even more typically at least about 90% by weight of the rare earth element is in the +4 oxidation state, and even more Generally, at least about 98% by weight of the rare earth element is in the +4 oxidation state. The rare earth-containing composition typically comprises at least about 1 ppm, more typically at least about 10 ppm, and even more typically at least about 100 ppm cerium (III) salts. In some embodiments, the rare earth-containing composition comprises at least about 0.0001 wt% cerium (III) salts, preferably at least 0.001 wt% cerium (III) salts, calculated as cerium oxide, and More preferably, it contains at least 0.01% by weight of cerium (III) salts. Further, in some embodiments, the rare earth-containing composition is generally at least about 20,000 ppm cerium (IV), more typically at least about 100,000 ppm cerium (IV), and even more Generally it contains at least about 250,000 ppm cerium (IV).

In some formulations, the molar ratio of cerium (IV) to cerium (III) is from about 1 to about 1 × 10 ⁻⁶ , more typically from about 1 to about 1 × 10 ⁻⁵ , and even more typically. Is about 1 to about 1 × 10 ⁻⁴ , yet more typically about 1 to about 1 × 10 ⁻³ , even more typically about 1 to about 1 × 10 ⁻² , and even more typically Is from about 1 to about 1 × 10 ⁻¹ , even more typically from about 1 to about 1. Moreover, the molar ratio of cerium (III) to cerium (IV) in some formulations is from about 1 to about 1 × 10 ⁻⁶ , more typically from about 1 to about 1 × 10 ⁻⁵ , even more common. About 1 to about 1 × 10 ⁻⁴ , yet more typically about 1 to about 1 × 10 ⁻³ , even more typically about 1 to about 1 × 10 ⁻² , still more More typically from about 1 to about 1 × 10 ⁻¹ , yet still more typically from about 1 to about 1. Furthermore, these molar ratios apply to any combination of soluble and insoluble forms of Ce (III) and soluble and insoluble forms of Ce (IV).

  In one formulation, cerium is predominantly in the form of separated cerium (III) salts and the remaining cerium is present as cerium (IV) oxide. In a rare earth-containing composition comprising a mixture of +3 and +4 oxidation states, typically at least some of the rare earth elements are in the +3 oxidation state, and more commonly at least most of the rare earth elements are in the +3 oxidation state. More typically at least about 75% by weight of the rare earth element is in the +3 oxidation state, and even more typically at least about 90% by weight of the rare earth element is in the +3 oxidation state, and Even more generally, at least about 98% by weight of the rare earth element is in the +3 oxidation state. Rare earth-containing compositions typically include at least about 1 ppm, more typically at least about 10 ppm, and even more typically at least about 100 ppm cerium (IV) oxide. In some embodiments, the rare earth-containing composition is at least about 0.0001 wt% cerium (IV), preferably at least 0.001 wt% cerium (IV), calculated as cerium oxide, and more preferably Contains at least 0.01% by weight of cerium (IV). Further, in some embodiments, the rare earth-containing composition is typically at least about 20,000 ppm cerium (III), more typically at least about 100,000 ppm cerium (III), and further More typically it has at least about 250,000 ppm cerium (III).

In some formulations, the molar ratio of cerium (III) to cerium (IV) is from about 1 to about 1 × 10 ⁻⁶ , more typically from about 1 to about 1 × 10 ⁻⁵ , even more typically. About 1 × 10 ⁻⁴ , even more typically about 1 to about 1 × 10 ⁻³ , still more typically about 1 to about 1 × 10 ⁻² , even more common Is about 1 to about 1 × 10 ⁻¹ , and more typically about 1 to about 1. Moreover, in some formulations, the molar ratio of cerium (IV) to cerium (III) is about 1 to about 1 × 10 ⁻⁶ , more typically about 1 to about 1 × 10 ⁻⁵ , and even more common. About 1 to about 1 × 10 ⁻⁴ , more typically about 1 to about 1 × 10 ⁻³ , more typically about 1 to about 1 × 10 ⁻² , and above Typically from about 1 to about 1 × 10 ⁻¹ , or even more typically from about 1 to about 1. Furthermore, these molar ratios apply to any combination of soluble and insoluble forms of Ce (III) and soluble and insoluble forms of Ce (IV).

The form of a preferably separated cerium (III) salt and cerium (IV) composition having a mixture of +3 and +4 cerium may be advantageous. Suitable, non-limiting example cerium (IV) compositions include cerium (IV) dioxide, cerium (IV) oxide, cerium (IV) oxyhydroxide, cerium (IV) hydroxide, and water. It is a cerium (IV) oxide containing. For example, isolated cerium (III) provides an opportunity to take advantage of sorption and / or precipitation chemistry of cerium (III) solutions, such as the formation of insoluble cerium oxyanion compositions. Furthermore, the presence of the cerium (IV) composition contains cerium (IV) sorption and oxidation / reduction chemistries, such as cerium (IV), metal and / or metalloid target substances. Gives you the opportunity to take advantage of strong interactions with other chemical species and other compositions. In general, cerium (IV) is also referred to as cerium (+4) and / or cerium.

In one formulation, the rare earth composition comprises a water soluble rare earth composition in the +3 oxidation state. Non-limiting examples of suitable water-soluble rare earth element compositions include rare earth chlorides, rare earth bromides, rare earth iodides, rare earth asterides, rare earth nitrates, rare earth sulfates, rare earth oxalates, rare earth elements Including perchlorates, rare earth carbonates and mixtures thereof. In one formulation, the rare earth-containing additive comprises a water soluble cerium (III) and lanthanum (III) composition. For some applications, the water-soluble cerium composition comprises cerium (III) chloride (CeCl ₃ ). In general, cerium (III) is called cerium (+3) and / or cerium.

  Preferably, the rare earth element composition comprises a water soluble cerium + 3 composition. Non-limiting examples of suitable water-soluble cerium + 3 compositions are cerium (III) chloride, cerium (III) nitrate, cerium (III) sulfate, cerium (III) succinate and mixtures thereof.

  In some formulations, the water soluble cerium (III) composition can include one or more other water soluble rare earth elements in addition to cerium. Rare earth elements other than cerium include yttrium, scandium, lanthanum, praseodymium, neodymium, samarium, europium, gadolinium, terbium, dysprosium, holmium, erbium, thulium, ytterbium and lutetium. Other rare earth elements can be water-soluble or water-insoluble.

  In some formulations, a water soluble cerium-containing additive (such as but not limited to one or more of lanthanum, neodymium, praseodymium and samarium) and water soluble cerium (III) and one or more other Contains water-soluble and trivalent rare earth elements. The molar ratio of cerium (III) to other trivalent rare earth elements is generally at least about 1: 1, more typically at least about 10: 1, more typically at least about 15: 1, and more. Generally at least about 20: 1, more typically at least about 25: 1, more usually at least about 30: 1, more usually at least about 35: 1, more usually at least about 45: 1, and more typically at least about 50: 1.

In some formulations, the water soluble cerium-containing additive comprises one or more of cerium (III) and water soluble lanthanum, neodymium, praseodymium and samarium. The water-soluble rare earth-containing additive generally comprises at least about 0.01% by weight of one or more of lanthanum, neodymium, praseodymium and samarium. Water-soluble rare earth-containing additives are typically about 10 wt% or less lanthanum on a dry basis, more typically about 9 wt% or less, and even more typically about 8 wt% or less. Lanthanum, even more typically up to about 7% by weight lanthanum, even more typically up to about 6% by weight lanthanum, even more typically up to about 5% by weight lanthanum, and even more typically Up to about 4% by weight of lanthanum, even more typically up to about 3% by weight of lanthanum, even more typically up to about 2% by weight of lanthanum, even more typically up to about 1% by weight of lanthanum, Even more typically it contains no more than about 0.5% by weight lanthanum, and even more typically no more than about 0.1% by weight lanthanum. Water-soluble rare earth-containing additives are typically less than about 8 wt.% Neodymium on a dry basis, more typically less than about 7 wt.% Neodymium, and even more typically less than about 6 wt.%. Neodymium, even more typically less than about 5% by weight neodymium, even more typically less than about 4% by weight neodymium, even more typically less than about 3% by weight neodymium, and even more typically Up to about 2 wt% neodymium, even more typically up to about 1 wt% neodymium, even more typically up to about 0.5 wt% neodymium, and even more typically up to about 0.1 wt%. Contains neodymium up to wt%. Water-soluble rare earth-containing additives are typically about 5 wt.% Or less praseodymium on a dry basis, more typically about 4 wt.% Or less praseodymium, and even more typically about 3 wt. Even more typically up to about 2.5% by weight of praseodymium, even more typically up to about 2.0% by weight of praseodymium, even more typically up to about 1.5% by weight of praseodymium, More generally less than about 1.0 wt.% Praseodymium, even more typically less than about 0.5 wt.% Praseodymium, even more typically less than about 0.4 wt.% Praseodymium, even more common Typically about 0.3 wt.% Or less praseodymium, even more typically about 0.2 wt.% Or less praseodymium, and even more typically about 0.1 wt.% Or less praseodymium. The water-soluble rare earth-containing additive generally has no more than about 3 wt.% Samarium, more usually no more than about 2.5 wt.% Samarium, even more typically about 2 wt.% On such dry basis. 0.0% by weight or less of samarium, even more typically about 1.5% by weight or less of samarium, even more typically about 1.0% by weight or less of samarium, even more typically about 0.5% by weight. % By weight samarium, even more typically less than about 0.4% by weight samarium, even more typically less than about 0.3% by weight samarium, and even more typically about 0.2% by weight The following samariums, even more typically up to about 0.1% by weight samarium, even more typically up to about 0.05% by weight samarium, and even more typically up to about 0.01% by weight The summer Including the Umm,
In some formulations, the water-soluble cerium-containing additive is water-soluble cerium (III) and one or more other water-soluble, trivalent (such as one or more of lanthanum, neodymium, praseodymium and samarium). Of rare earth elements. The molar ratio of cerium (III) to other trivalent rare earth elements is generally at least about 1: 1, more typically at least about 10: 1, more typically at least about 15: 1, and more. Generally at least about 20: 1, more typically at least about 25: 1, more usually at least about 30: 1, more usually at least about 35: 1, more usually at least about 40: 1, more typically at least about 45: 1, and more typically at least about 50: 1.

  In one formulation, the rare earth-containing additive is cerium (III) chloride, cerium (III) bromide, cerium (III) iodide, cerium (III) asteride, cerium perhalide, cerium (III) carbonate, Water-soluble cerium (III) salts such as cerium (III) nitrate, cerium (III) sulfate, cerium (III) oxalate and mixtures thereof are essentially included. The rare earth elements in this formulation are typically predominantly cerium (III), more typically at least about 75 mole percent of the rare earth element content in the rare earth-containing additive is cerium (III); About 25 mol% or less of the rare earth element content of the rare earth element-containing additive contains rare earth elements other than cerium (III). Even more commonly, the rare earth elements of this formulation are typically predominantly at least about 80 mole percent cerium (III), even more typically at least about 85 mole percent cerium (III), and even more common. Typically at least about 90 mole percent cerium (III), and even more typically at least about 95 mole percent cerium (III).

The rare earth element composition may comprise a water insoluble composition such as a water insoluble rare earth oxide, oxyhydroxide and / or hydrated oxide. The insoluble rare earth element composition can be in the form of a dispersion, suspension or slurry of rare earth element fine particles. The rare earth element microparticles may have an average particle size ranging from submicron to micron or greater than micron. The insoluble rare earth element composition can have a surface area of at least about 1 m ² / g. Generally, the insoluble rare earth element has a surface area of at least about 70 m ² / g. In other formulations, the insoluble rare earth composition can have a surface area of from about 25 m ² / g to about 500 m ² / g.

  In some formulations, the rare earth element composition can agglomerate. In general, the rare earth composition can be in the form of an aggregate, which includes a polymer binder and a rare earth-containing composition.

  In one formulation, the rare earth-containing additive comprises a rare earth-containing composition containing a rare earth element and / or at least some water-insoluble cerium (IV) and water-soluble cerium (III) and / or lanthanum (III). Including. The rare earth element and / or rare earth-containing composition typically includes at least some water soluble cerium (III) in the form of water soluble cerium (III) salts. Generally, the rare earth-containing additive is greater than about 1 wt% water soluble cerium (III) composition, more typically greater than about 5 wt% water soluble cerium (III) composition, and even more generally Typically more than about 10% by weight of a water-soluble cerium (III) composition, still more typically more than about 20% by weight of a water-soluble cerium (III) composition, still more typically about 30% by weight More than about 40% by weight of the water-soluble cerium (III) composition, or even more typically more than about 40% by weight.

  According to some formulations, the rare earth-containing additive typically includes greater than about 50% by weight of the water soluble cerium (III) composition, and more typically the rare earth element-containing additive is greater than about 60% by weight. A water-soluble cerium (III) composition, and even more typically the rare earth-containing additive comprises greater than about 65% by weight of the water-soluble cerium (III) composition, and even more typically the rare earth element. The additive containing comprises a water soluble cerium (III) composition of greater than about 70% by weight, yet still more typically the rare earth element containing additive comprises a water soluble cerium (III) composition of greater than about 75% by weight. And still more typically, the rare earth-containing additive comprises greater than about 80% by weight of the water-soluble cerium (III) composition, yet still more typically rare. The elemental-containing additive comprises greater than about 85% by weight of the water-soluble cerium (III) composition, yet still more typically the rare earth element-containing additive is greater than about 90% by weight of the water-soluble cerium (III). And still more typically the rare earth-containing additive comprises greater than about 95% by weight of the water-soluble cerium (III) composition, yet still more typically the rare earth-containing additive. The product comprises greater than about 98% by weight of the water soluble cerium (III) composition, yet still more typically the rare earth-containing additive comprises greater than about 99% by weight of the water soluble cerium (III) composition. Or even more typically comprises about 100% by weight of a water soluble cerium (III) composition.

  In some formulations, the rare earth-containing additive includes one or more nitrogen-containing materials. The one or more nitrogen-containing materials are typically ammonia, ammonium-containing compositions, primary amines, secondary amines, tertiary amines, amides, cyclic amines, cyclic amides, polycyclic amines, It includes one or more of polycyclic amides and combinations thereof. The nitrogen-containing material is typically less than about 1 ppm, less than about 5 ppm, less than about 10 ppm, less than about 25 ppm, less than about 50 ppm, less than about 100 ppm, less than about 200 ppm, less than about 500 ppm of a water soluble rare earth-containing additive, Less than about 750 ppm or less than about 1000 ppm. In general, the rare earth-containing additive comprises a water-soluble cerium (III) and / or lanthanum (III) composition. More generally, the rare earth-containing additive includes cerium (III) chloride. The rare earth-containing additive typically dissolves in the liquid. The liquid in which the rare earth element-containing additive dissolves is preferably water.

In some formulations, the rare earth-containing additive is in one or more of the following forms: a substantially separate, dissolved form of the rare earth element and / or an aqueous solution containing the rare earth element-containing composition. Free-flowing granules, powders, particles and / or fine particles, rare earth elements and / or bonds of a rare earth-containing composition containing an aqueous solution, rare earth elements and / or at least some water-soluble cerium (III) Free-flowing agglomerated granules, powders, particles and / or fine particles, binders and rare earth elements and rare earth element-containing compositions containing at least some water-soluble cerium (III) substantially free of agents At least some water-soluble cerium (III) in one or both of aggregated and non-aggregated forms Free flowing agglomerated granules, powders, particles, and / or fine particles, including rare earth element-containing compositions, containing at least a rare earth element and / or some water-soluble cerium (III) and supported on a substrate Rare earth element-containing compositions, and combinations thereof.

  For particulate forms of rare earth-containing compositions, the particles can have a particle size ranging from about 1 nanometer to about 1000 nanometers in one formulation. In other embodiments, the particles can have a particle size of less than about 1 nanometer. In yet another embodiment, the particles can have a particle size ranging from about 1 micrometer to about 1,000 micrometers.

  For rare earth elements and / or rare earth-containing compositions supported on a substrate, a suitable substrate can comprise a porous and fluid permeable solid having a desired shape and physical dimensions. . This substrate can be, for example, sintered ceramic, sintered metal, microporous carbon, glass fiber, cellulosic fiber, alumina, gamma alumina, activated alumina, acidified alumina, metal oxide containing unstable anions, Crystalline aluminosilicates such as zeolite, amorphous silica alumina, ion exchange resin, clay, ferric sulfate, porous ceramic, and the like can be used. Such substrates can be in the form of meshes, such as screens, tubes, honeycomb structures, monoliths, blocks of various shapes including cylinders and rings. The structure of the substrate varies depending on the application. Suitable structural forms of the substrate include woven substrates, non-woven substrates, porous membranes, filters, fabrics, fabrics or other fluid permeable structures. The rare earth-containing additive can be incorporated into or coated on a monolith for use as a filter, such as a filter block or a cross-flow type filter. The rare earth element and / or the rare earth element-containing additive can be in the form of particles coated or incorporated onto the substrate. In some configurations, the rare earth element and / or the rare earth element-containing additive can ion exchange with the cations of the substrate. Typically, the rare earth-coated substrate is at least about 0.1 wt%, more typically 1 wt%, more typically at least about 5 wt%, more typically at least about 10 wt%. %, More typically at least about 15%, more typically at least about 20%, more typically at least about 25%, more typically at least about 30%, more typically Containing at least about 35 wt%, more typically at least about 40 wt%, more typically at least about 45 wt%, and more typically at least about 50 wt% rare earth elements and / or rare earth elements Including a composition. Typically, the rare earth-coated substrate is about 95 wt% or less, more typically about 90 wt% or less, more typically about 85 wt% or less, more typically about 80 wt%. %, More typically about 75% or less, more typically about 70% or less, even more typically about 65% or less of rare earth elements and / or rare earth-containing compositions.

  In some formulations, the rare earth-containing additive comprises a rare earth-containing composition supported, coated, or incorporated into the substrate, preferably the rare earth-containing composition is particulate. It is a form. The fine particles containing a rare earth element can be supported or coated on a substrate, for example, with or without a binder. The binder can be any suitable binder, such as those described herein.

Furthermore, for formulations containing rare earth-containing additives, including granules, powders, particles, and / or fine particles aggregated and / or coagulated together with or without a binder containing rare earth elements. Formulations generally have an average value of at least about 1 micrometer, more typically at least about 5 micrometers, more typically at least about 10 micrometers, and even more typically at least about 25 micrometers, It has a median or _P90 particle size. In some formulations, aggregates or aggregates containing rare earth elements have an average value of about 100 to about 5,000 microns, a median or P ₉₀ particle size distribution, an average value of about 200 to about 2,500 microns. , Median or P ₉₀ particle size distribution, average value of about 250 to about 2500 microns, median or P ₉₀ particle size distribution, or average value of about 300 to about 500 microns, median value, or P ₉₀ particle size Have a distribution. In other formulations, the agglomerates or aggregates are at least about 100 nanometers, specifically at least about 250 nanometers, more specifically at least about 500 nanometers, and even more specifically at least about 1 micrometer. , the average value of the yet still more specifically at least about 0.5 nanometers, can have a median or P ₉₀ particle size distribution, the average value of the aggregates and / or aggregate, the median or P ₉₀ The particle size distribution can be up to about 1 micrometer or greater. In addition, the rare earth-containing microparticles can have a surface area of at least about 5 m ² / g, in some cases, individually and / or in the form of aggregates and / or aggregates, and in other cases Is at least about 10 m ² / g, in other cases at least about 70 m ² / g, in still other cases at least about 85 m ² / g, yet in other cases above it, at least about 100 m ² / g, yet In other cases above it, at least about 115 m ² / g, yet in other cases above it, at least about 125 m ² / g, in still other cases above it, at least about 150 m ² / g, still above In other cases, it may have a surface area of at least 300 m ² / g, and still in other cases above it at least about 400 m ² / g. In some configurations, the rare earth-containing microparticles are individually and / or in the form of aggregates or aggregates, generally from about 50 to about 500 m ² / g, more typically from about 110 to It may have a surface area of about 250 m ² / g. Generally, aggregates containing rare earth elements are greater than 10.01 wt%, more typically greater than about 85 wt%, even more typically greater than about 90 wt%, and even more It typically contains more than about 92% by weight and even more typically from about 95 to about 96.5% by weight of rare earth-containing particulates, with the balance being primarily binders. In other words, the binder is less than about 15% by weight of the aggregate, in some cases less than about 10%, in other cases less than about 8%, and in other cases about 5% by weight. And in still other cases it may be less than about 3.5% by weight. In some formulations, the rare earth-containing microparticles were in the form of a powder and agglomerated nanocrystalline regions. The binder can include one or more polymers selected from the group consisting of thermosetting polymers, thermoplastic polymers, elastomeric polymers, cellulose polymers, and glass. Preferably, the binder comprises a fluorocarbon containing polymer and / or an acrylic polymer.

In one embodiment, the rare earth-containing composition is in the form of a particulate colloid, suspension or slurry. The microparticles typically have an average, median and / or _P90 particle size of less than about 1 nanometer, more typically an average, median and / or P1 particle size of about 1 nanometer to about 1,000 nanometers. Or P ₉₀ particle size, even more typically an average, median and / or P ₉₀ particle size of about 1 micron to about 1,000 microns, or even more typically at least about 1, It can have an average, median and / or P ₉₀ particle size of 000 microns. Preferably, the microparticles have an average, median and / or _P90 particle size of about 0.1 to about 1,000 nanometers, preferably about 0.1 to about 500 nanometers. More preferably, the cerium (IV) microparticles have an average, median and / or _P90 particle size of about 0.2 to about 100 nanometers.

In some embodiments, the microparticles have an average and / or median surface area of at least about 1 m ² / g, preferably an average and / or median surface area of at least about 70 m ² / g. Can do. In another embodiment, the microparticles preferably, from about ^{25 m} 2 / g to an average value and / or the surface area of the median of about 500 meters ² / g, and preferably an average value and / or from about 100 to about 250 meters ² / g It can have a median surface area. In some embodiments, the microparticles can be in the form of one or more of granules, crystals, microcrystals and particles.

In one application, the microparticles include cerium (IV), typically cerium (IV) oxide. A weight percent (wt.%) Cerium (IV) content based on the overall rare earth content of the cerium (IV) particulates is typically at least about 50 wt% cerium (IV), more typically At least about 60 wt% cerium (IV), even more typically at least about 70 wt% cerium (IV), and more typically at least about 75 wt% cerium (IV), yet Even more typically at least about 80% by weight of cerium (IV), yet still more typically at least about 85% by weight of cerium (IV), yet still more typically at least about 90%. % By weight of cerium (IV), yet still more typically at least about 95% by weight of cerium (IV), and even more typically less Both about 99 wt% of cerium (IV). Preferably, the cerium (IV) fine particles are substantially free of rare earth elements other than cerium (IV). More preferably, the cerium (IV) particulate has an overall rare earth content based weight percent (wt%) cerium (IV) content of about 100 wt% cerium (IV) and cerium (IV) Oxide, cerium (IV) hydroxide, cerium (IV) oxyhydroxyl, cerium (IV) hydrated oxide, cerium (IV) hydrated oxyhydroxyl, cerium oxide, and / or Ce (IV) (O) _{w (OH) x (OH) y} zH 2 O, consists of one or more of, in the above formula, w, x, y can be zero or a positive real number.

Medium (or medium) 104
The medium (or medium) 104 can be any fluid flow. The fluid stream can be derived from any source that contains one or more target substances. In general, the medium (or medium) 104 is derived from any aqueous source that contains one or more target substances.

  Non-limiting examples of suitable media (or media) 104 include recreational water, municipal water (such as sewage, wastewater, agricultural or ground water), industrial (such as cooling, boiler or process water) Water, sewage, well water, septic water, drinking water, naturally occurring water (such as lakes, ponds, reservoirs, rivers or streams) and / or other water and / or aqueous process streams. Non-limiting examples of recreational water are swimming pool water, saltwater pool water, treatment pool water, diving pool water, sauna water, hot spring water and hot tub water. Non-limiting examples of city water include drinking water, water for irrigation, well water, water for agricultural use, water for architectural use, reflective pool water, fountain water, water cooling wall water Water that is not suitable for beverages, for use, urban use, and city water that is not suitable for other beverages. Non-limiting sewage includes urban and / or agricultural drainage, perishable water, water formed and / or generated during industrial and / or production processes, formed by medical equipment and / or Or water generated, mining, mineral production, water associated with recovery or treatment (including petroleum), evaporative pond water, and treated water not suitable for beverages. Well water includes water produced from subsurface wells for human consumption, agricultural use (including consumption by animals, crop irrigation or domesticated livestock), mineral-containing water, mining And water associated with oil production is included without limitation. Non-limiting examples of naturally occurring water include those associated with rain, storms, streams, rivers, lakes, aquifers, estuaries, small swamps, and others.

The medium (or medium) 104 is typically obtained from one or more of the water sources described above and is processed, transported and / or manipulated by a water handling system. The medium (or medium) can be primarily water from a water handling system.

  The components and configuration of the water handling system can vary depending on the treatment process, water and water source. While not wishing to be limited by example, a system that handles local and / or sewage is typically one or more of the following process units: cleaning, disinfection, coagulation, aeration, filtration , Solid and liquid separation, digestion and polishing. The number and order of process units can be changed. Furthermore, some process units can occur two or more times within the water handling system. It will be understood that one or more process units are in fluid communication.

  The water handling system may or may not have a clarification device. Some water handling systems can have more than one clarification device, such as a first and final clarification device. Clarification devices typically reduce clouding of water by removing raw materials (such as bacteria and / or algae), suspended and / or dispersed chemicals, and / or particulates from the water. Generally, the clarification process occurs before and / or after filtration.

  The water handling system may or may not include a filtration process. Typically, a water handling system includes at least one filtration process. Non-limiting examples of common filtration processes include screen filtration, water filtration, particle filtration, sand filtration, macrofiltration, microfiltration, ultrafiltration, nanofiltration, reverse osmosis, carbon / activated carbon filtration, dual media filtration Including, without limitation, gravity filtration and combinations thereof. Generally, the filtration process occurs before and / or after the disinfection process. For example, a filtration process that removes solid foreign matter such as solid organic matter and sand from water typically precedes the disinfection process. In some embodiments, a filtration process such as activated carbon filtration or sand filtration follows the disinfection process. Post-disinfection filtration methods remove at least some of the chemical disinfectant remaining in the treated water.

The water handling system may or may not include a disinfection process. Disinfection processes include fluorine, fluorination, chlorine, chlorination, bromine, bromination, iodine, iodination, ozone, ozone oxidation, electromagnetic irradiation, ultraviolet light, gamma light, electrolysis, chlorine dioxide, hypochlorite ion, heat , Ultrasound, trichloroisocyanuric acid, soap / detergent, alcohol, bromine chloride (BrCl), cupric ion (Cu ²⁺ ), silver, silver ion (Ag ⁺ ), permanganate, phenol and combinations thereof Treating the aqueous stream and / or water with one or more of the following can be included without limitation. Preferably, the water handling system includes a single disinfection process. Preferably, the water handling system includes two or more disinfection processes. A disinfection process is typically provided to at least remove, kill and / or detoxify pathogenic substances contained in water. As a typical example, pathogenic substances include biological contaminants, in particular biological contaminants include target substances. In some embodiments, the disinfection process converts the chemical species of the target material into a chemical species that can be removed and / or detoxified by the rare earth-containing composition, additives, and / or particles or particulates.

The water handling system may or may not include coagulation. The water handling system can include one or more agglomeration processes. Typically, the flocculation process involves adding a flocculant to the water of the water handling system. Typical flocculants include aluminum sulfate, polyelectrolytes, polymers, lime and ferric chloride. The aggregating agent aggregates powder particles suspended and / or dispersed in water, and the aggregated powder particles form aggregates. The setting process may or may not involve separating the set from the liquid phase. In some embodiments, the condensation constitutes part or all of the overall clarification process. In other embodiments, the condensing process is separate and different from the clarification process. Typically, the agglomeration process occurs before the disinfection process.

  The water handling system may or may not include aeration. Within the water handling system, aeration involves passing a stream of air and / or molecular oxygen through the water contained in the water handling system. The aeration process promotes the oxidation of contaminants contained in the water treated by the water handling system, preferably the aeration promotes the oxidation of biological contaminants such as target substances. In some embodiments, the aeration process converts the target material species into a species that can be removed and / or detoxified by a rare earth-containing composition, additive, and / or particles or particulates. The water handling system can include one or more aeration processes. Typically, the disinfection process occurs after the aeration process.

  The water handling system may or may not have one or more heaters, coolers and heat exchangers for heating and / or cooling the water being processed by the water handling system. The heater can be any method suitable for heating water. Non-limiting examples of suitable heating processes include solar heating systems, electromagnetic heating systems (such as induction heating, microwave heating and infrared), immersion heaters, and heat transfer (such as combustion, flow, hot oil, etc.) A heating system, where the thermal source has a higher temperature than water and transfers heat to the water to increase the temperature of the water. A heat exchanger can be any process that transfers thermal energy to or from water. The heat exchanger can remove thermal energy from the water to cool and / or reduce the temperature of the water. Alternatively, the heat exchanger can transfer thermal energy to heat and / or increase the temperature of the water. The cooler can be any method suitable for cooling water. Non-limiting examples of suitable cooling processes include refrigeration processes, evaporative coolers, and (heat (cooling) sources have a lower temperature than water to remove heat from the water and lower the temperature of the water A heat transfer cooling system (such as a cooling device). Any of clarification, disinfection, agglomeration, aeration, filtration, sludge treatment, digestion, nutrient control, solid / liquid separation and / or polisher process, before, after and / or during one or more heating and cooling processes Both can be included. It is understood that a heat exchanger typically includes at least one heating and cooling process.

  The water handling system may or may not include a digestion process. Typically, the digestion process is one of an anaerobic or aerobic digestion process. In some configurations, the digestion process can include one of an anaerobic or aerobic digestion process, followed by the other of the anaerobic or aerobic digestion process. For example, one such configuration is an aerobic digestion process, followed by an anaerobic digestion process. Generally, the digestion process involves microorganisms that destroy biodegradable substances contained in water. In some embodiments, the biodegradable substance includes a target substance. Furthermore, the digestion process converts the target chemical species into chemical species that can be removed and / or detoxified by the composition, additives and / or particles or particulates containing the rare earth elements. Anaerobic digestion of biodegradable substances proceeds in the absence of oxygen, while aerobic digestion of biodegradable substances proceeds in the presence of oxygen. In some water handling systems, this digestion process is typically referred to as a biological stage / digestion tank or a biological treatment stage / digestion tank. Moreover, in some systems, the disinfection process includes a digestion process.

The water handling system may or may not include a nutrient control process. Furthermore, the water handling system can include one or more nutrient control processes. The nutrient control process typically includes nitrogen and / or phosphorus control. In addition, nitrogen control generally can include nitrifying bacteria. Typically, phosphorus control refers to biological phosphorus control, preferably controlling phosphorus that can be used as a nutrient for algae.
Nutrient control typically includes processes associated with controlling oxygen demand substances, including pathogens and inorganic and synthetic organic compositions in addition to nutrients. The nutrient control process can occur before or after the disinfection process. In some embodiments, the nutrient control process converts the target chemical species into chemical species that can be removed and / or detoxified by the rare earth-containing composition, additives, and / or particles or particulates. To do.

  The water handling system may or may not include a solid / liquid separation process. Preferably, the water handling system includes one or more solid / liquid separation processes. The solid / liquid separation process can include any process that separates the solid phase from a liquid phase, such as water. Non-limiting examples of suitable solid-liquid separation processes include clarification (including sprinkling filtration), filtration (as described above), vacuum or pressure filtration, cyclone (including liquid cyclone), flotation separation, sedimentation separation. (Including gravitational settling separation), flocculation (as described above), precipitation (including but not limited to sand basins), and combinations thereof.

  The water handling system may or may not include a polisher. The polishing process can include one or more of removing fine particulates from the water, an ion exchange process that softens the water, adjusting the pH value of the water, or a combination thereof. Typically, the polishing process is after the disinfection step.

  While water handling systems typically include one or more of clarification, disinfection, flocculation, aeration, filtration, solid and liquid separation, digestion, and polishing processes, the water handling system further includes additional processing equipment. be able to. Additional processing equipment includes sewage tanks, reactors, purifiers, processing vessels or units, stirring vessels or elements, washing circuits, precipitation vessels, separation vessels or units, sedimentation tanks or vessels, reservoirs, pumps, cooling towers, Heat exchangers, valves, boilers, gas-liquid separators, nozzles, charcoal turbines, etc. are included without limitation. Furthermore, the water handling system includes conduits interconnecting the operating units and / or additional treatment devices. Conduits include, without limitation, piping, hoses, channels, aqua ducts, grooves, and the like. The water is carried by / to the working unit and / or the additional processing device. Further, each actuation unit and / or additional processing device is in fluid communication with other actuation units and / or additional processing devices by conduits.

Target Material The aqueous medium treated with the rare earth element-containing composition, additives and / or particles can include one or more target materials. Chemical species containing one or more target substances can include various forms of metals (other than scandium, yttrium and lanthanoids), metalloids, and / or radioisotopes. In some aqueous media, the species containing the target substance may be hydrated metals (but not limited to alkali metals, alkaline earth metals, actinides, transitions other than scandium, yttrium and lanthanoids) Metals and post-transition metals), metalloids, and / or radioisotopes, hydrated metals, metalloids, or anions, cations, or radioisotope oxyspecies in a form having no net charge (eg, M _a O _x ^{n +} or MaO _x ⁰ , where 0 <a ≦ 4, 0 <x ≦ 4 and 0 <n ≦ 6), positively charged, negatively charged or uncharged metal , Metalloids, or radioisotope carbonates (eg, M _c (CO ₃ ) _y , 0 <c ≦ 4 and 0 <y ≦ 4), or positively charged, negatively charged, or Or uncharged metal, metalloid, or radioisotope hydroxyl species (especially metal or metalloid hydroxides (eg M (OH) _z , 0 <z ≦ 8), positively charged) Including, but not limited to, negatively charged or uncharged metals, metalloids, or radioisotope oxyhydroxyl species, and mixtures thereof Target substance-containing species include solid, dissolved species Alternatively, it can be in the form of a suspension.

In some embodiments, the composition comprising the rare earth element removes the anion, cation, oxygen, hydroxy group, hydration, or combination thereof species of the target substance, wherein the target substance M Has an atomic number of 5, 13, 22-33, 40-52, 72-84 and 89-94. Examples of hydrated hydroxyl groups and hydrated oxygen compounds (anionic, neutral, or cationic, indicated below by the symbol MS) include M (H ₂ O) ₆ ⁿ , M (H ₂ O) ₅ OH ^(n-1) , M (OH) ^(n-1) M (H ₂ O) ₄ (OH) ₂ ^(n-2) , M (OH) ₂ ^(n-2) , M ( ^{_{H 2 O) 3 (OH)}} 3 (n-3), M (OH) 3 (n-3), M (H 2 O) 2 (OH) 4 (n-4), M (OH) 4 (n ^{_{-4), M (H 2 O}} ) (OH) 5 (n-5), M (OH) 5 (n-5), M (OH) 6 (n-6), M (H 2 O) 5 O ^(N-2) , M (H ₂ O) ₄ (O) ₂ ^(n-4) , M (H ₂ O) ₃ (O) ₃ ^(n-6) , M (H ₂ O) ₂ (O) ^{_{4 (n-8), M}} (H 2 O) (O) 5 (n-10) ^{_{M (H 2 O) 5 CO}} 3 (n-2), MCO 3 (n-2), M (H 2 O) 4 (CO 3) 2 (n-4), M (CO 3) 2 (n- ⁴⁾ , M (H ₂ O) ₃ (CO ₃ ) ₃ ^(n-6) , M (CO ₃ ) ₃ ^(n-6) , M (H ₂ O) ₂ (CO ₃ ) ₄ ^(n-8) , M (CO ₃ ) ₄ ^(n-8) , M (H ₂ O) (CO ₃ ) ₅ ^(n-10) , M (CO ₃ ) ₅ ^(n-10) , M (CO ₃ ) ₆ ^{(n _{-12), M (H 2 O}} ) 4 n, M (H 2 O) 3 OH (n-1), M (H 2 O) 2 (OH) 2 (n-2), M (H 2 O) ^{_{(OH) 3 (n-3}} ), M (H 2 O) 3 O (n-2), M (H 2 O) 2 (O) 2 (n-4), M (H 2 O) (O) ₃ ^(n-6), and ^{_{M (O) 4 (n-}} 8) but are To these it is not limited. In the above chemical formula, n is a real number of 8 or less and represents the charge or oxidation state of the metal or metalloid M (for example, when M is lead (II), n is 2 and M is lead (IV ), N is 4. In general, M has a positive charge n not greater than about 8.

Pool diagrams for each of the metals, metalloids and radioisotopes are shown in FIGS. 2 to 47 show the main chemical species of the target substance under different thermodynamic conditions of the aqueous solution. Referring to FIG. 39, lead as a target substance is Pb (H ₂ O) ₆ ²⁺ , Pb (H ₂ O) ₅ CO ₃ , Pb (H ₂ O) ₄ (CO ₃ ) ₂ ²⁺ , Pb (H ₂ O) ₅ (OH) ₂ , Pb (H ₂ O) ₂ (OH) ₄ ²⁻ , and Pb (H ₂ O) (O) ₃ ²⁻ . The state of the lead compound (whether it is solid _(s) or aqueous _(aq) ) is shown in the lead pool diagram. Typically, lead includes lead in the +2 oxidation state. Referring to FIG. 27, antimony as a target substance is Sb (H ₂ O) ₂ (OH) ₄ ¹⁻ , Sb (H ₂ O) ₄ (OH) ₂ ¹⁺ , Sb (H ₂ O) ₃ (OH). ₃ , Sb (H ₂ O) (OH) ₅ , and Sb (OH) ₆ ^1- species. Typically, antimony includes one of +5 or +3 oxidation states. Referring to FIG. 40, bismuth as target substances are Bi (H ₂ O) ₆ ³⁺ , Bi (H ₂ O) ₅ (OH) ²⁺ , Bi (H ₂ O) ₄ (OH) ₂ ¹⁺ , Bi (H ₂ O) ₃ (OH) ₃ , and Bi (H ₂ O) ₂ (OH) ₄ ^1- . Typically, bismuth includes one bismuth in the +5 or +3 oxidation state.

  There are many possible mechanisms for removing the target material. The exact mechanism is the specific form and / or properties of the rare earth-containing composition, additives and / or particles or microparticles, the specific form and / or properties of the target substance, the pH of the medium 104, the Eh of the medium 104 May depend on a number of variables, including the temperature of the media 104, the components of the media 104, and other parameters known to those skilled in the art.

Although not wishing to be bound by any theory, the anion form of the target material can be determined by sorption, precipitation, complex, ionic bond, inter-valence complex with rare earth-containing compositions. shell complexed) (any one or more hybridized or uncrossed s, p, d or f orbitals), one or more of covalent bonds or combinations thereof. Anionic forms include target substance oxyanions, hydroxyl, hydration, or combinations thereof having a net negative charge. While not wishing to be bound by any theory, the target material can selectively interact with the surface or edge of the particulates of the composition containing the rare earth element. Other theories do not wish to be constrained by it, but anionic target substances form substantially insoluble products with rare earth elements. The rare earth element is in the form of a salt containing a substantially water-soluble rare earth element or in the form of a substantially water insoluble substance that strongly sorbs, binds and chemically reacts with the anionic target substance. It can be.

  While not wishing to be bound by any theory, there are many mechanisms for removing target materials in the form of cations. Cationic forms include target substance complexes having a net positive charge, hydroxyl, hydration, or combinations thereof. While not wishing to be bound by any theory, the cation form of the target material can be determined by sorption, precipitation, complex, ionic bond, valence-intershell complex with rare earth-containing compositions. shell complexed) (any one or more hybridized or uncrossed s, p, d or f orbitals), one or more of covalent bonds or combinations thereof. While not wishing to be bound by any theory, the target material can selectively interact with the surface or edge of the particulates of the composition containing the rare earth element. Other theories do not wish to be constrained thereby, but the cationic target material forms a substantially insoluble and / or stable product with the rare earth cation.

  While not wishing to be bound by any theory, other possible mechanisms for removing anionic, cationic, or uncharged species containing the target substance are water Chemical species such as Japanese water, hydroxyl-containing radicals, hydroxide ions, or carbonate species that are mixed, chelated, or otherwise attached to the target substance adhere to the rare earth element or the rare earth element-containing composition. It acts as a chemical entity that sorbs and / or chemically binds. Without wishing to be limited by theory and / or by way of illustration, a possible cationic metal or metalloid adsorption process is as shown in formula (2):

The rare earth element is a substantially water-soluble rare earth element that strongly sorbs, binds, chemically reacts, or otherwise adheres to the cationic target material, as shown in chemical formula (3). It can be in the form of a contained salt or a substantially water-insoluble substance.

Where M is generally 5, 13, 22-33, 40-52, 72-84 and 89-94, more typically 5, 13, 22-33, 40-52, 56, 72, 80. One of the number of -84, 88, and 90-94. The number of hydrated water of ceria oxide is shown as “4”, but what is understood here is that there is more or less hydrated water depending on the application.

  Without wishing to be limited by theory, and by way of further illustration, a possible cationic lead adsorption process can be as shown in formula (4).

The cation of the rare earth element strongly sorbs, binds and chemically reacts with the cationic target substance as shown in the chemical formula (5). In the form of a water-insoluble substance.

While not wishing to be bound by any theory, another possible mechanism is that a rare earth-containing additive such as cerium (IV) oxide can oxidize the target substance and / or the target substance-containing species. is there. The contact between the oxidizing agent containing the rare earth element and the target substance-containing chemical species is either or both of the following. a) chemical interaction with the target substance-containing species, and b) formation of reduced rare earth elements and / or rare earth element-containing oxidants and oxidized target substances and / or target substance-containing species. Illustratively, a cerium (IV) oxidant is obtained by contacting a first cerium-containing composition having cerium in the +3 oxidation state with an oxidant (listed below) to provide a second cerium in the +4 oxidation state. Of the cerium-containing composition (or cerium (IV) oxidant). Generally, the second cerium-containing composition comprises cerium oxide particles. The cerium (IV) oxidant then oxidizes the target substance or target substance-containing species that forms the first (reduced) cerium (III) -containing composition.

  Regardless of the exact mechanism, contact of the rare earth-containing additive with the target substance-containing species forms a product containing the rare earth element and the target substance. The product containing the rare earth element and the target substance can be in the form of a substance dissolved in water, a solid substance contained in water or a solid substance phase separated from water. The product containing the solid rare earth element and the target material can be a precipitate, solid particles suspended in water, agglomerated solid particles, and combinations thereof.

  As can be seen from the prior art pool diagrams of FIGS. 2 to 47, the major species of metal or metalloid in solution is determined by pH and Eh. These values are generally selected so that water is electrochemically stable and the target substance is a dissolved (non-solid) species. The cation form of lead, for example, is typically but not necessarily present as a major species in an aqueous medium with a pH value of less than about pH 7 and a potential of less than about + 1V. As described below, the form of the metal or metalloid present in the solution, and thus precipitation or sorption of the metal or metalloid by treatment with the composition, additives and / or particles or fine particles containing rare earth elements, Alternatively, the effectiveness of otherwise removing from an aqueous medium and / or detoxifying can be substantially increased by adjusting one or both of the pH and Eh of the medium. What can be understood here is that the effectiveness of precipitation, sorption or removal of the target substance has been illustrated for various pH and Eh values, but the concept of adjusting one or both of pH and Eh includes targets that contain interfering substances. It can be applied to effectively remove components other than metals and / or metalloids containing substances and / or detoxify aqueous solutions.

  According to some embodiments, the target material is removed from an aqueous medium having a selected pH value. In general, the selected pH value of the aqueous medium can be about pH 0 to about pH 14, more typically the pH of the aqueous medium can be about pH 1 to about pH 13, and even more common In particular, the pH of the aqueous medium can be about pH 2 to about pH 12, and even more typically the pH of the aqueous medium can be about pH 3 to about pH 11, and even more typically aqueous. The pH of the medium can be from about pH 4 to about pH 10, and even more typically the pH of the aqueous medium can be from about pH 5 to about pH 9, or still more common. In this case, the pH of the aqueous medium can be about pH 6 to about pH 8.

In one embodiment, the aqueous medium typically has a selected pH value of about pH 6 to about pH 9, and more typically the aqueous medium has a pH value of about pH 6.5 to about pH 8.5. .
In general, in other embodiments, the aqueous medium has a selected pH of about pH 0, more typically a selected pH of about pH 1, and even more typically a selection of about pH 2. Still having a selected pH of about pH 3 and even more generally still having a selected pH of about pH 4 and being substantially acidic. obtain. In other embodiments, even more generally, the aqueous medium has a selected pH of about pH 5, more typically a selected pH of about pH 6, and even more typically about having a selected pH of pH 7, still more typically having a selected pH of about pH 8, or still more typically having a selected pH of about pH 9, Can be neutral. In other embodiments, typically, the aqueous medium has a selected pH of about pH 10, more typically a selected pH of about pH 11, and even more typically about pH 12 Has a selected pH of about pH 13, or even more typically has a selected pH of about pH 14, and even more typically has a selected pH of about pH 14, May be alkaline.

According to some embodiments, target material is removed from an aqueous medium having an Eh value selected with respect to a standardized reference electrode, such as a standard hydrogen electrode (SHE). Generally, the selected Eh of the aqueous medium is at least about -0.5V, more typically at least about -0.4V, more typically at least about -0.3V, more typically At least about −0.2V, more typically at least about −0.1V, more usually at least about 0V, more usually at least about 0.1V, more usually at least about 0.2V, More typically at least about 0.3V, more typically at least about 0.4V, and more typically at least about 0.5V. Generally, the selected Eh of the aqueous medium is below a level where the water is not electrochemically stable, more typically less than about 1.7V, more typically less than about 1.6V, and more Generally less than about 1.5V, more typically less than about 1.4V, more usually less than about 1.3V, more usually less than about 1.2V, more usually less than about 1V. .1V or less, more typically about 1.0V or less, more typically about 0.9V or less, more typically about 0.8V or less, and more typically about 0.7V or less. .

  The ratio of the rare earth element to the target substance of the product containing the insoluble rare earth element and the target substance also varies depending on the pH and / or Eh value of the solution. In other words, a rare earth element with a rare earth element ratio of less than 1 to the target material has a larger molar removal capacity of the target substance than a rare earth element with a rare earth element ratio of 1 or greater than 1. . In some embodiments, the higher the pH value, the greater the ratio of rare earth element to target material. In other embodiments, the ratio of the rare earth element to the target material decreases as the pH increases. In yet other embodiments, the ratio of the rare earth element to the target material is substantially unchanged above the pH value range. In some embodiments, at pH values below about pH-2, at pH values above about pH-1, at pH values above about pH 0, at pH values above about pH 1 and above pH values above about pH 2. In pH values above about pH 3, at pH values above about pH 4, at pH values above about pH 5, at pH values above about pH 6, at pH values above about pH 7, at pH values above about pH 8, Target at pH values above about pH 9, at pH values above about pH 10, at pH values above about pH 11, at pH values above about pH 12, at pH values above about pH 13, or at pH values above about pH 14. The ratio of the rare earth element to the substance is about 0.1 or less, and the rare earth element to the target substance The ratio of the rare earth element to the target substance is about 0.3 or less, the ratio of the rare earth element to the target substance is about 0.4 or less, and the ratio of the rare earth element to the target substance Is about 0.5 or less, the ratio of the rare earth element to the target substance is about 0.6 or less, the ratio of the rare earth element to the target substance is about 0.7 or less, and the ratio of the rare earth element to the target substance is about The ratio of the rare earth element to the target substance is about 0.9 or less, the ratio of the rare earth element to the target substance is about 1.0 or less, and the ratio of the rare earth element to the target substance is about 1. 1 or less, the ratio of the rare earth element to the target substance is about 1.2 or less, the ratio of the rare earth element to the target substance is about 1.3 or less, and the ratio of the rare earth element to the target substance is about 1.4. The ratio of the rare earth element to the target substance is about 1.5 or less, the ratio of the rare earth element to the target substance is about 1.6 or less, and the ratio of the rare earth element to the target substance is about 1.7 or less. And the ratio of the rare earth element to the target substance is about 1.8 or less, the ratio of the rare earth element to the target substance is about 1.9 or less, and the ratio of the rare earth element to the target substance is about 1.9 or less, Alternatively, the ratio of the rare earth element to the target substance is about 2.0 or less.

In some embodiments, when the pH value of water is about −2 or less, when the pH value of water is greater than about −1, when the pH value of water is greater than about 0, the pH value of water is about 1. If the pH value of the water exceeds about 2, the pH value of the water exceeds about 3, the pH value of the water exceeds about 4, the pH value of the water exceeds about 5, the pH of the water When the value exceeds about 6, when the pH value of water exceeds about 7, when the pH value of water exceeds about 8, when the pH value of water exceeds about 9, the pH value of water exceeds about 10. And when the pH value of water exceeds about 11, the pH value of water exceeds about 12, the pH value of water exceeds about 13, or the pH value of water exceeds about 14, The ratio of the target substance is about 0.1 or less, the ratio of the rare earth element to the target substance is about 0.2 or less, and the ratio of the rare earth element to the target substance is about 0.00. Below, the ratio of rare earth element to target substance is about 0.4 or less, the ratio of rare earth element to target substance is about 0.5 or less, the ratio of rare earth element to target substance is about 0.6 or less, The ratio is about 0.7 or less, the ratio of the rare earth element to the target substance is about 0.8 or less, the ratio of the rare earth element to the target substance is about 0.9 or less, the ratio of the rare earth element to the target substance is about 1.0 or less, The ratio of the rare earth element to the target substance is about 1.1 or less, the ratio of the rare earth element to the target substance is about 1.2 or less, the ratio of the rare earth element to the target substance is about 1.3 or less, and the ratio of the rare earth element to the target substance is About 1.4 or less, ratio of rare earth element to target substance is about 1.5 or less, ratio of rare earth element to target substance is about 1.6 or less, ratio of rare earth element to target substance is about 1.7 or less, rare earth element The ratio between the target substance and the target substance is about 1.8 or less, and the ratio between the rare earth element and the target substance is 1.9, the ratio of the rare earth element and the target substance is about 1.9 or less, or the ratio of the rare earth element and the target substance is about 2.0 or less.

CeO ₂ as a composition, additive, and / or particle or particulate material containing rare earth elements may have a removal capacity of about 0.1 mg target material / gREO (eg, CeO ₂ ) or less. In this case, the ratio between the rare earth element and the target substance can be significantly greater than 2. For example, since 0.1 mg is 0.0001 g, 1 g of CeO ₂ /0.0001 g of target substance = 10,000. In such embodiments, when the pH value of water is about pH-2 or less, when the pH value of water exceeds about pH-1, when the pH value of water exceeds about pH 0, the pH value of water is about When the pH value exceeds 1, the pH value of water exceeds about pH 2, the pH value of water exceeds about pH 3, the pH value of water exceeds about pH 4, the pH value of water exceeds about pH 5, When the pH value of water exceeds about pH 6, when the pH value of water exceeds about pH 7, when the pH value of water exceeds about pH 8, when the pH value of water exceeds about pH 9, the pH value of water is about pH 10 , When the pH value of water exceeds about pH 11, when the pH value of water exceeds about pH 12, when the pH value of water exceeds about pH 13, or when the pH value of water exceeds about pH 14, The ratio of element to target substance is usually about 50,000 The ratio of the rare earth element to the target substance is usually about 47,500 or less, the ratio of the rare earth element to the target substance is usually about 45,000 or less, the ratio of the rare earth element to the target substance is usually about 42,500 or less, The ratio of the target substance is usually about 40,000 or less, the ratio of the rare earth element to the target substance is usually about 37,500 or less, the ratio of the rare earth element to the target substance is usually about 35,000 or less, and the ratio of the rare earth element to the target substance is Usually about 35,000 or less, the ratio of the rare earth element to the target substance is usually about 32,500 or less, the ratio of the rare earth element to the target substance is usually about 30,000 or less, and the ratio of the rare earth element to the target substance is usually about 37,500. Hereinafter, the ratio of the rare earth element to the target substance is usually about 35,000 or less, the ratio of the rare earth element to the target substance is usually about 32,500 or less, and the ratio of the rare earth element to the target substance is usually about 3 The ratio between the rare earth element and the target substance is usually about 27,500 or less, the ratio between the rare earth element and the target substance is usually about 25,000 or less, and the ratio between the rare earth element and the target substance is usually about 22,500 or less, or The ratio between the rare earth element and the target substance is usually about 20,000 or less.

  The concentration of the target substance and the target substance-containing species can vary depending on a myriad of factors. For example, one or both of these concentrations are typically at least about 5 ppm, usually at least about 50 ppm, usually at least about 100 ppm, usually at least about 500 ppm, usually at least about 1,000 ppm, usually at least about 5,000 ppm, usually at least about 10, 000 ppm, and usually at least about 100,000 ppm.

In a media pretreatment step 108, the media 104 is optionally pretreated to produce the selected main species of the target substance. Generally selected main chemical species are more effectively removed by the rare earth element-containing composition, additives, and / or particulate matter rather than the main chemical species in the medium 104. For example, one or more of the Eh or pH values may change due to more effective removal and / or detoxification of the target substance. For example, when Eh is less than about −0.3 (more negative potential), the main species of lead is the element (Pb _S ). By increasing the Eh of the aqueous solution and changing the pH, the main chemical species of lead are Pb (H ₂ O) ₆ ²⁺ , Pb (H ₂ O) ₅ CO ₃ , Pb (H ₂ O) ₄ (CO ₃ ) _2. ^It can be one or more of ²⁺ , Pb (H ₂ O) ₅ (OH) ₂ , or Pb (H ₂ O) ₂ (OH) ₄ ²⁻ . As is apparent, pH is a measure of hydrogen ion activity, while Eh is a measure of electrochemical (oxidation / reduction) potential.

The type of pretreatment used can vary depending on the application.
In one application, an acid, acid equivalent, base, or base equivalent is added to adjust the pH to the desired pH value. Examples of acids or acid equivalents include monobasic and polybasic acids such as mineral acids, sulfonic acids, carboxylic acids, vinylogs of carboxylic acids, nucleic acids, and mixtures thereof. Examples of bases or base equivalents include strong bases (potassium hydroxide, barium hydroxide, cesium hydroxide, sodium hydroxide, strontium hydroxide, calcium hydroxide, magnesium hydroxide, lithium hydroxide, rubidium hydroxide, etc.) , Super strong bases, carbonates, ammonia, hydroxides, metal oxides (especially alkoxides) and weak acid counter anions.

  In one application, a redox reaction can be used to adjust the Eh value. Eh is a measure of the oxidation potential or reduction potential of the medium 104. The oxidation potential or reduction potential is usually called electromotive force or EMF. EMF is generally measured against a standard reference electrode. Some non-limiting examples of standard reference electrodes include a hydrogen electrode (usually called SHE), a copper / copper sulfate electrode, and a silver / silver chloride electrode.

  In one variation, the target substance or target substance-containing species oxidizes the target substance or target substance-containing species by contacting with the oxidizing agent. The oxidant may include a chemical oxidant, an oxidation process, or a combination thereof.

  A chemical oxidant comprises a chemical composition in elemental or compound form. The chemical oxidant receives electrons from the target substance or the target substance-containing species. Upon receiving electrons, the oxidant is reduced to form a reduced form of the oxidant. Non-limiting examples of preferred chemical oxidants are chlorine, chloroamine, chlorine dioxide, hypochlorite, trihalomethane, haloacetic acid, ozone, hydrogen peroxide, peroxy compounds, hypobromite, bromoamine, hypobromine Acid salt, hypochlorous acid, isocyanurate, trichloro-s-triazinetrione, hydantoin, bromochloro-dimethylhydantoin, 1-bromo-3-chloro-5,5-dimethylhydantoin, 1,3-dichloro-5,5- Dimethylhydantoin, sulfur dioxide, bisulfate, and combinations thereof. In some configurations, one or more of the following chemical compositions: bromine, bromine monochloride, permanganate phenol, alcohol, oxyanion, arsenite, chromate, trichloroisocyanuric acid, and surfactant Is further thought to oxidize target substances or target substance-containing species. Chemical oxidants may be further referred to as “oxidants” or “oxidizing substances”.

  The oxidation process comprises a physical process, alone or in combination with a chemical oxidant. The oxidation process removes electrons from the target substance or target substance-containing species, or helps to remove electrons, or a combination thereof. Non-limiting examples of oxidation processes are electromagnetic energy, ultraviolet light, thermal energy, ultrasonic energy, and gamma rays.

  In another variation, the target substance or target substance-containing species reduces the target substance or target substance-containing species by contacting with the reducing agent. The oxidant may include a chemical oxidant, an oxidation process, or a combination thereof.

A chemical reducing agent has a chemical composition in elemental or compound form. The chemical reducing agent donates electrons to the target substance or the target substance-containing species. When donating electrons, the reducing agent is oxidized to form an oxidized form of the oxidizing agent. Non-limiting examples of preferred chemical reducing agents include lithium aluminum hydride, nascent (atomic) hydrogen, sodium amalgam, sodium borohydride, compounds containing divalent tin ions, sulfites, hydrazine, zinc- Mercury amalgam, diisobutylaluminum hydride, Lindlar catalyst, oxalic acid, formic acid, ascorbic acid, phosphite, hypophosphite, phosphorous acid, dithiothreitol, and compounds containing divalent iron ions. A chemical reducing agent may be further referred to as a “reduced form” or “reducing agent”.

  The oxidation-reduction process is a physical process alone or in combination with a chemical oxidant, and transfers electrons to a target substance or a target substance-containing species. Non-limiting examples of oxidation processes are electromagnetic energy, ultraviolet light, thermal energy, ultrasonic energy, gamma radiation, and biological processes.

  In one variation, the medium is contacted with a halogenated species such as chlorine, bromine, iodine, or acids, bases or salts thereof. As is apparent, the halogen affects the Eh of the medium. In some configurations, the halogen can affect the pH value of the aqueous medium.

  Other types of pre-treatments may be used to remove target species or target species-containing species and / or chemical species from the media that may impair the pH and / or Eh adjustment of the media.

  The pretreatment process may comprise one or more of clarification, disinfection, coagulation, aeration, filtration, solid-liquid separation, digestion, and finishing processes. More specifically, the pretreatment process typically comprises one of the following processes: clarification, disinfection, coagulation, aeration, filtration, solid-liquid separation, digestion, and finishing, and clarification, disinfection, coagulation, aeration, Typically, any two of filtration, solid-liquid separation, digestion, and finishing processes are usually provided in random order, and also among clarification, disinfection, coagulation, aeration, filtration, solid-liquid separation, digestion, and finishing processes. Any three of these are usually provided in random order, and any four of the clarification, disinfection, coagulation, aeration, filtration, solid-liquid separation, digestion, and finishing processes are usually provided in random order, and It is usually equipped with any five of randomization, disinfection, coagulation, aeration, filtration, solid-liquid separation, digestion, and finishing processes in random order, and further clarification, disinfection, coagulation, aeration, filtration, solid-liquid separation, Digestion and finishing process Any six of the above are usually provided in random order, and any seven of the clarification, disinfection, coagulation, aeration, filtration, solid-liquid separation, digestion, and finishing processes are usually provided in random order, and further It is usually equipped with any 8 of randomization, disinfection, coagulation, aeration, filtration, solid-liquid separation, digestion, and finishing processes in random order, and further, clarification, disinfection, coagulation, aeration, filtration, solid-liquid separation, Any nine of the digestion and finishing processes are typically provided in random order, and any ten of the clarification, disinfection, coagulation, aeration, filtration, solid-liquid separation, digestion, and finishing processes are in random order. In addition to any one of the clarification, disinfection, coagulation, aeration, filtration, solid-liquid separation, digestion, and finishing processes, usually in random order, and further clarification, disinfection, coagulation, aeration, Filtration, solid-liquid separation, disinfection , And it may include normal random order to each of the finishing process. In some configurations, the pretreatment may comprise or further comprise a step of treatment by one or more of the additional water treatment system process equipment.

In the contacting step 112 of the medium with the rare earth-containing additive, the optionally pretreated medium is contacted with the rare earth-containing composition, additive, or particle or particulate material to provide the rare earth element and the target material. A product containing is formed. As described above, the rare earth-containing composition, additive, or particle or particulate material, or a combination thereof, reacts chemically and / or physically to the target material or target material-containing species. Adsorb, precipitate, chemically convert, or otherwise inactivate or bind to. In one configuration, the rare earth-containing additive is at least about 25%, usually at least about 50%, usually greater than about 50%, usually at least about 75%, and more usually at least about 95%. React, adsorb, precipitate, chemically convert, or otherwise inactivate or bind to a target substance or target substance-containing species. The product containing the rare earth element and the target substance may comprise one or more other constituents of the rare earth element-containing composition and / or target substance-containing species, depending on the rare earth element, the target substance, and the contained substance Contains chemical components. While not wishing to be bound by any theory, in some processes, the binding mechanism is a hydrated water, hydroxyl radical, hydroxide ion, compounded, compounded, or otherwise attached to the target material, Or it is believed to be due to carbonate species. This acts as a chemical that attaches, adsorbs, and / or chemically bonds to the rare earth element or the rare earth-containing composition.

  The temperature of the medium 104 can change during the contacting step. In general, the temperature of the aqueous solution can change during the contacting step. For example, the temperature of the aqueous solution can vary depending on the water. Usually, the temperature of the aqueous solution is the ambient temperature. Generally, the solution temperature is from about -5 degrees Celsius to about 50 degrees Celsius, usually from about 0 degrees Celsius to about 45 degrees Celsius, more usually from about 5 degrees Celsius to about 40 degrees Celsius, and more usually, The range is from about 10 degrees Celsius to about 35 degrees Celsius. Each of the waters comprising the clarification, disinfection, coagulation, aeration, filtration, solid-liquid separation, digestion, and finishing processes can be heated and / or cooled with one or more of the respective waters. It will be appreciated that any process unit and / or operation to be performed may be included. In some configurations, each water is heated to a temperature typically at least about 20 degrees Celsius, more typically at least about 25 degrees Celsius, and more typically at least about 30 degrees Celsius, In addition, more typically at least about 35 degrees Celsius, more typically at least about 40 degrees Celsius, even more typically at least about 45 degrees Celsius, and more typically at least about 50 degrees Celsius. Degrees, more typically at least about 60 degrees Celsius, more typically at least about 70 degrees Celsius, even more typically at least about 80 degrees Celsius, and more typically at least about Celsius. About 90 degrees, more typically at least about 100 degrees Celsius, even more typically at least about 110 degrees Celsius, and more typically at least about Celsius. 120 degrees, further more typically at least Celsius about 140 degrees, further more typically at least Celsius about 150 degrees, or in addition, more typically may be at least Celsius about 200 degrees. In some configurations, each water comprising each of the clarification, disinfection, coagulation, aeration, filtration, solid-liquid separation, digestion, and finishing processes is cooled to a temperature typically about 110 degrees Celsius. Less than, more typically less than about 100 degrees Celsius, even more typically less than about 90 degrees Celsius, even more typically less than about 80 degrees Celsius, even more typically less than about 70 degrees Celsius, Even more typically less than about 60 degrees Celsius, even more typically less than about 50 degrees Celsius, even more typically less than about 45 degrees Celsius, even more typically less than about 40 degrees Celsius, even more Typically less than about 35 degrees Celsius, even more typically less than about 30 degrees Celsius, even more typically less than about 25 degrees Celsius, even more typically less than about 20 degrees Celsius, even more typical In about 15 degrees Celsius or less, More typically below about 10 degrees Celsius, even more typically below about 5 degrees Celsius, and even more typically may be below about 0 degrees Celsius.

Separation of Rare Earth Elements and Target Substance-Containing Products from the Medium In an optional step 116, the product is removed from the medium 104 to form a treatment medium 124. In one configuration, at least about 25%, typically at least about 50%, usually greater than about 50%, usually at least about 75%, and more usually at least about 95% rare earth and target material-containing products. Is removed from the medium. In such cases, it can be seen that the product contains insoluble material.

  Solid rare earth elements and target substance-containing products may be removed by suitable techniques such as solid-liquid separation systems. Non-limiting examples of solid-liquid separation systems are filtration, flotation sorting, sedimentation, cyclone classification, and centrifugation. Alternatively, the rare earth-containing additive is in the form of a porous and permeable supported matrix through which the medium passes, such as a particle layer or a filter.

Alternatively, the rare earth element and target substance-containing product dissolved in water may remain in an inactivated form in water. Non-limiting examples of deactivated rare earth elements and target substance-containing products that may remain dissolved include environmentally stable coordination compounds of target substance-containing species and rare earth element-containing compositions. It is.

According to some embodiments, the content of at least one target substance in the processing medium 124 is less than the target substance-containing medium 104. Typically, the content of the processing medium 124 is at least about 0.9 of the target substance-containing medium 104, more usually the content of the processing medium 124 is at least about 0.8 of the target substance-containing medium 104, and In general, the content of the processing medium 124 is at least about 0.7 of the target substance-containing medium 104, and moreover, usually, the content of the processing medium 124 is at least about 0.6 of the target substance-containing medium 104 Further, typically, the content of the processing medium 124 is at least about 0.5 of the target substance-containing medium 104, and more usually, the content of the processing medium 124 is at least about 0.4 of the target substance-containing medium 104. In addition, usually, the content of the processing medium 124 is at least about 0.3 of the target substance-containing medium 104, and moreover, usually, the content of the processing medium 124 is equal to the target substance. The content of the containing medium 104 is at least about 0.2, and the content of the treatment medium 124 is usually at least about 0.1 of the target substance-containing medium 104, and the content of the treated water medium 124 is usually , At least about 0.05 of the target substance-containing medium 104, and usually the content of the processing medium 124 is at least about 0.01 of the target substance-containing medium 104, and usually contains the processing medium 124 The amount is at least about 0.005 of the target substance-containing medium 104, and moreover, typically, the content of the processing medium 124 is at least about 0.001 of the target substance-containing medium 104, and more usually, the processing medium 124. Is at least about 0.5 of the target substance-containing medium 104, and moreover, the content of the processing medium 124 is usually less than that of the target substance-containing medium 104. In addition, the content of the processing medium 124 is usually at least about 0.0001 of the target substance-containing medium 104, and the content of the processing medium 124 is usually equal to the target substance-containing medium 104 104 is at least about 5 × 10 ⁻⁵ , and usually the content of the processing medium 124 is at least about 1 × 10 ⁻⁵ of the target substance-containing medium 104, and more usually the content of the processing medium 124. Is at least about 5 × 10 ⁻⁶ of the target substance-containing medium 104, and moreover, typically, the content of the processing medium 124 is at least about 1 × 10 ⁻⁶ of the target substance-containing medium 104. Usually, the content of the target substance in the content of the processing medium 124 is about 100,000 ppm or less, and more usually, the content of the target substance in the content of the processing medium 124 is about 10,000 ppm or less. Further, the content of the target substance in the content of the processing medium 124 is usually about 1,000 ppm or less, and the content of the target substance in the content of the processing medium 124 is usually about 100 ppm or less. Further, the content of the target substance in the content of the processing medium 124 is usually about 10 ppm or less, and the content of the target substance in the content of the processing medium 124 is usually about 1 ppm or less. Furthermore, the content of the target substance in the content of the processing medium 124 is usually about 100 ppb or less, and the content of the target substance in the content of the processing medium 124 is usually about The content of the target substance in the content of the processing medium 124 is usually about 1 ppb or less, and more usually the content of the target substance in the content of the processing medium 124 is about 0.1 ppb or less.

Step 116 may include any processing steps.
The treatment process may comprise one or more of clarification, disinfection, coagulation, aeration, filtration, solid-liquid separation, digestion, and finishing processes. More specifically, the treatment process typically comprises one of clarification, disinfection, coagulation, aeration, filtration, solid-liquid separation, digestion, and finishing, and clarification, disinfection, coagulation, aeration, filtration, solidification. Any two of liquid separation, digestion, and finishing are usually provided in random order, and any three of clarification, disinfection, coagulation, aeration, filtration, solid-liquid separation, digestion, and finishing are in random order It is usually equipped with any four of clarification, disinfection, coagulation, aeration, filtration, solid-liquid separation, digestion, and finishing in random order, and further clarification, disinfection, coagulation, aeration, filtration , Solid-liquid separation, digestion, and finishing are usually provided in random order, and any six of clarification, disinfection, coagulation, aeration, filtration, solid-liquid separation, digestion, and finishing are included. Usually in random order, further clarification, disinfection, coagulation, It is usually provided in random order with any 7 of gas, filtration, solid-liquid separation, digestion, and finishing, plus any of clarification, disinfection, coagulation, aeration, filtration, solid-liquid separation, digestion, and finishing Are usually provided in random order, and any nine of clarification, disinfection, coagulation, aeration, filtration, solid-liquid separation, digestion, and finishing are usually provided in random order, and clarification, disinfection, Any 10 of coagulation, aeration, filtration, solid-liquid separation, digestion, and finishing are usually provided in random order, and further of clarification, disinfection, coagulation, aeration, filtration, solid-liquid separation, digestion, and finishing Arbitrary 11 are usually provided in random order, and each of clarification, disinfection, coagulation, aeration, filtration, solid-liquid separation, digestion, and finishing can be normally provided in random order.

Regeneration of rare earth elements in rare earth elements and target substance-containing products for reuse Elements may be reused in step 112. The regeneration process includes, for example, desorption, oxidation, reduction, thermal process, irradiation and the like.

  As used herein, cerium (III) refers to cerium (+3) and cerium (+3) refers to cerium (III). As used herein, cerium (IV) refers to cerium (+4) and cerium (+4) refers to cerium (IV).

  The following examples are provided to illustrate specific embodiments and should not be construed as limiting the examples described in the appended claims. Unless otherwise noted, all parts and percentages are by weight.

Example 1
To reduce the arsenic concentration to less than 50 ppm, a series of tests were conducted to measure the maximum arsenic adsorption capacity of soluble cerium (III) chloride CeCl ₃ in arsenic-containing streams. As shown in Table 1, the arsenic-containing stream tested (hereinafter alkaline leaching solution) had the following composition:

The initial pH of the seven alkaline leaching solutions was about pH 11, the temperature of the solution was about 70 to 80 ° C., and the reaction time was about 30 minutes.

Seven alkaline leaching solutions were prepared at various arsenic (V) concentrations, as can be seen from Table 1 above. Each solution contained the same amount of sodium carbonate (20 g / L) and sodium sulfate (17.75 g / L). In the first series of tests, 3.44 mL of cerium chloride (CeCl ₃ ) is added for all isotherm tests, which is equal to 0.918 g CeO ₂ (about 0.05 mol Ce). . In the second series of tests, 6.88 mL of cerium chloride is added to all tests, which is equal to 1.836 g CeO ₂ (about 0.1 mol Ce). The following are guidelines on how each isotherm test was performed.

  In the first step, 200 mL of the solution was weighed out and transferred to a 400 mL Pyrex® beaker. The beaker was then placed on a hot / stir plate and heated to 70-80 ° C. with stirring.

In the second step, 3.44 mL of cerium chloride was weighed out and poured into a mixed beaker of hot alkaline leaching solution. A white precipitate formed instantly with the addition of cerium chloride. Step 3 was performed to confirm that the white precipitate was not cerium carbonate [Ce ₂ (CO ₃ ) ₃ .xH ₂ O].

  In the third step, 4.8 mL concentrated HCl was slowly added dropwise. Foaming was observed with the sound of a shoe. The solution was mixed continuously for 30 minutes and then allowed to cool for 4 hours before sampling.

  The results are shown in Table 2 "Analysis using ICP-AES".

FIG. 48 shows that the adsorption capacity starts to level off at 436 mg / g, which is the theoretical capacity when cerium arsenate (CeAsO ₄ ) is formed, and it is considered that cerium arsenate was formed. . FIG. 49 shows that the molar ratio of cerium to arsenic required to reduce the arsenic concentration below 50 ppm is somewhere between 1 molar ratio and 2 molar ratio. However, an adsorption capacity of 217 was obtained at a molar ratio of 2. FIG. 50 shows very similar results (essentially 2 times the addition of CeCl ₃ ), and at a molar ratio between 1 and 2, the dissolved arsenic concentration can be below 50 ppm. This capacity can be improved by lower molar ratios and tighter pH control.

Example 2
In this example, the cerium and arsenic product was shown to contain more arsenic than could be predicted based on the stoichiometry of gas pearlite, the expected product of cerium and arsenic. Furthermore, the X-ray diffraction pattern suggests that the product is amorphous or nanocrystalline and is ceria or possibly consistent with gas perlite. The amorphous or nanocrystalline phase not only allows for reuse of process water after arsenic capture, but also allows for a much greater arsenic removal capability than is observed from other types of cerium addition, Reduce processing costs and limit environmental hazards.

  Eight 50 mL centrifuge tubes were each filled with 25 ml arsenate / sulfate / NaOH complete oxidation solution, and another eight 50 mL centrifuge tubes were each 25 ml arsenite with oxygen molecules sparged for 2 hours. A fully reduced solution of / sulphide / NaOH was filled. Both solutions contained 24 g / L arsenic, 25 g / L NaOH, and 80 g / L sulfide equivalents. Each sample was then treated with either cerium (IV) nitrate or cerium (III) chloride. Cerium salt solution was added at a dose of 1, 2, 3, or 5 mL. No pH adjustment was made, and no attempt was made to adjust the temperature from an ambient temperature of 22 ° C.

  Fifteen of the 16 test samples showed rapid precipitate formation and occupied a volume from the total volume to 25 ml. The reaction between the two concentrated solutions occurred almost immediately and filled the entire solution volume with a gel-like precipitate. Sixteen samples containing 5 mL of cerium (IV) remained bright yellow, but an additional 5 mL of 50% NaOH formed a purple solid at that time.

  The solid formed from the reaction of cerium and arsenic was deposited for 1 hour, but little clarification was observed. The sample was then centrifuged at 50% speed for 5 minutes. At this point, the total volume of the solution and the volume of precipitated solids were recorded and a 5 mL sample was collected for analysis. Because a slightly higher supernatant solution was available (meaning that the arsenic concentration was 24 g / L and the cerium concentration was also significantly increased), the sample was filtered using 0.45 micron filter paper. Four samples with 5 mL of cerium salt added were not filtered. The supernatant solution was collected and the volume was recorded.

  The reaction-derived filter cake was left in a plastic weighing boat above the drying chamber over the weekend. After 72 hours, the contents of each boat were weighed and found that the pellets were still very wet (there was more mass than was added to the sample as a dissolved solid). A sample semi-dry solid with 2 mL of cerium salt solution was transferred to a 130 ° C. drying chamber and analyzed by XRD after 1 hour.

The XRD result is shown in FIG. XRD results are shown for gas pearlite (predicted product) and various systems present during the experiment, with “ceria” corresponding to cerium dioxide. As can be seen from FIG. 51, XRD analysis did not detect any crystal peaks or phases of arsenic and cerium solids in various systems. The only crystalline material present was identified as either NaCl, NaNO ₃ (introduced in the rare earth solution) or Na ₂ SO ₄ present in samples prepared from Na ₂ SO ₄ . However, broad diffraction peaks near 29, 49, and 57 degrees 2-θ can indicate very small particle ceria or, in some cases, gas pearlite.

  The arsenic content of the supernatant solution was measured using ICP-AES. It was confirmed that both cerium (IV) and cerium (III) effectively removed arsenic from the system to approximately the same extent. As can be seen from Table 3 below and FIG. 52, a large difference in arsenic removal was observed between the fully oxidized system and the system that was completely reduced before oxygen molecule sparging. FIG. 52 shows arsenic micromoles removed in an “oxidation” system starting from arsenate and subsequently in an “oxygen molecular sparging” system starting from arsenite that is subsequently oxidized to arsenate by sparging of oxygen molecules. A plot is shown.

FIG. 52 shows the amount of arsenic consumed by the formation of precipitated solids plotted as a function of the amount of added cerium. The soluble arsenic concentration obtained from this experiment is divided into two groups: samples containing fully oxidized arsenate and sulfate, and samples containing arsenite and sulfite in which oxygen molecules are sparged Is possible. Both the Ce (III) and Ce (IV) data fit the single regression line of each test solution, as the oxidation state of cerium used as a soluble fixative had a much lower impact on process effectiveness. . In the case of a fully oxidized solution, arsenic capture by the solid increases the molar ratio of arsenic to cerium to 1: 3, which may constitute a stoichiometric product of Ce ₃ As ₄ .

Example 3
A series of experiments was conducted. The experiment was carried out from a highly concentrated waste stream with a pH below pH 2 by adding soluble cerium salt in the Ce (III) state followed by titration with sodium hydroxide (NaOH) solution to a pH range of 6 to 10. The arsenic precipitation in the As (V) state is embodied.

In the first test, 400 mL of a solution containing 33.5 mL of 0.07125 mol / L NaH ₂ AsO ₄ solution was stirred in a beaker at room temperature. The pH was roughly adjusted to pH 1.5 by adding 4.0 mol / L HNO ₃ . Followed by the addition of _{Ce (NO 3) 3 · 6H} 2 O in 1.05 g. No change in color tone due to the addition of cerium (III) salt or any precipitate was observed. NaOH (1.0 mol / L) was added dropwise to the stirred solution to bring the pH to 10.1. The pH was maintained at pH 10.2 ± 0.2 for 1.5 hours under magnetic stirring. After the reaction, the solution was removed from the stir plate and allowed to settle gently for 12 to 18 hours. The supernatant was removed by decantation and reserved for Ce and As ICP-MS analysis. The solid was filtered through a 0.4 μm cellulose membrane and washed thoroughly with 500 to 800 mL of deionized water. The solid was air dried and analyzed by X-ray diffraction.

In the second test, the simulated waste stream solution is composed of the following components: As (1,200 ppm), F (650 ppm), Fe (120 ppm), S (80 ppm), Si (50 ppm), Ca (35 ppm), Mg ( 25 ppm), Zn (10 ppm), and less than 10 ppm Al, K, and Cu. The pH of the solution was titrated with concentrated HCl (12.1 mol / L) to pH 0.4 and the solution was heated to 70 ° C. A solution of CeCl ₃ (6.3 mL, 1.194 mol / L) is added to the hot solution and the pH is gradually increased to pH 7.5 by dropwise addition of NaOH (20 wt.%, 6.2 mol / L). I let you. The solution was then aged at 70 ° C. for 1.5 hours under magnetic stirring to maintain the solution at pH 7.5 ± 0.2. The solution was then removed from the heat source and allowed to settle gently for 12 to 18 hours. The supernatant was removed by decantation and reserved for Ce and As ICP-MS analysis. The precipitated solid was centrifuged, washed twice, filtered through a 0.4 μm cellulose membrane, and thoroughly washed with 500 to 800 mL of deionized water. The solid was air dried and analyzed by X-ray diffraction.

  In a third test, a new Ce-As compound solid powder was tested for stability in a low pH leaching test. 0.5 g of the new Ce-As compound was added to 10 mL of acetic acid solution at either pH 2.9 or pH 5.0. The vessel was sealed and rotated at 30 ± 2 revolutions per minute for 18 ± 2 hours at ambient temperatures in the range of 22 ± 5 ° C. After the required spin time, the solution was filtered through a 0.2 micron filter and analyzed by ICP-MS for Ce and As that may have been leached from the solid. Less than 1 ppm As was detected by ICP-MS.

FIG. 53 shows X-ray diffraction (“XRD”) of a new Ce—As compound (shown as trigonal CeAsO _4. (H ₂ O) _x (both experimental and simulated)) and gas pearlite (both experimental and simulated). ]) Comparison of results. FIG. 9 compares XRD results for trigonal CeAsO _4. (H ₂ O) _x (both experimental and simulated) and trigonal BiPO _4. (H ₂ O) _0.67 (simulated). XRD results are structurally different from gas pearlite (CeAsO ₄ ) in which the precipitated crystalline compound crystallizes in a monoclinic space group with a monazite structure, and is trigonal BiPO _4. (H ₂ O) _0.67 Is very similar.

Experiments on Ce and As in different oxidation states demonstrate that the new Ce-As compounds require cerium in the Ce (III) state and arsenic in the As (V) state. It appears that pH titration with a strong base such as sodium hydroxide is necessary. PH titration with sodium carbonate produces either gas pearlite, a known naturally occurring compound or a combination of gas pearlite and trigonal CeAsO _4. (H ₂ O) _x . The use of cerium chloride and cerium nitrate both successfully demonstrated the successful synthesis of new compounds. The presence of other metal species such as magnesium, aluminum, silicon, calcium, iron, copper, and zinc has not been shown to inhibit the synthesis of new compounds. The fluoride present will compete with arsenic removal and produce an insoluble CeF ₃ precipitate. A solution containing only arsenic and cerium is preferred to have a 1: 1 atomic ratio of Ce: As for the formation of the new compound, and a solution containing excess cerium may be added to the new compound in addition to cerium oxide (CeO ₂ ). It shows that a precipitate was formed. In addition, the new compounds appear to be extremely stable when considering leaching tests that require arsenic dissolution in solutions at pH 2.9 and pH 5.0 to be less than 1 ppm.

Example 4
In this example, a reagent solution containing 1.0 ppmw chromium calculated as Cr was prepared by dissolving reagent grade potassium dichromate in distilled water. This solution contained Cr ⁺⁶ in the form of oxyanions and no other metal oxyanions. A mixture of 0.5 grams of lanthanum oxide (La ₂ O ₃ ) and 0.5 grams of cerium dioxide (CeO ₂ ) was slurried with 100 mL of test solution in a glass container. The resulting slurry was stirred with a Teflon-coated magnetic stir bar for 15 minutes. After stirring, water and solids were separated by filtration through Whatman # 41 filter paper and analyzed for chromium using an inductively coupled plasma atomic emission spectrophotometer. This procedure was repeated twice, but instead of slurrying a mixture of lanthanum oxide and cerium dioxide with 100 mL of test solution, 1.0 g of each was used. The results of these three tests 1-3 are listed in Table 4 below.

As can be seen from the above, lanthanum oxide, cerium dioxide, and their equivalents were effective in removing over 98% of the chromium from the test solution.

Test 4-6
The procedures of Tests 1 to 3 were repeated. However, a test solution containing 1.0 ppmw of antimony calculated as Sb was used instead of the chromium test solution. The antimony test solution contains 100 ppmw of antimony, As, Be, Ca, Cd, Co, Cr, Fe, Li, Mg, Mn, Mo, Ni, Pb, Se, Sr, Ti, Tl, V, and Zn, respectively. A certified standard solution containing 100 ppmw was prepared by diluting with distilled water. These test results are also listed in Table 4, indicating that the two rare earth compounds were effective in removing over 90% of antimony from the test solution, either alone or as a mixture. .

Tests 7-9
The procedures of Tests 1 to 3 were repeated. However, instead of the chromium test solution, a test solution containing 1.0 ppmw of molybdenum calculated as Mo was used. Molybdenum test solution contains 100 ppmw molybdenum, As, Be, Ca, Cd, Co, Cr, Fe, Li, Mg, Mn, Ni, Pb, Sb, Se, Sr, Ti, Tl, V, and Zn, respectively. A certified standard solution containing 100 ppmw was prepared by diluting with distilled water. These test results are also listed in Table 4, indicating that lanthanum oxide, cerium dioxide, and equal weight mixtures thereof were effective in removing over 99% of the molybdenum from the test solution.

Test 10-12
The procedures of Tests 1 to 3 were repeated. However, instead of the chromium test solution, a test solution containing 1.0 ppmw vanadium calculated as V was used. The vanadium test solution contains 100 ppmw vanadium, As, Be, Ca, Cd, Co, Cr, Fe, Li, Mg, Mn, Mo, Ni, Pb, Sb, Se, Sr, Ti, Tl, and Zn, respectively. A certified standard solution containing 100 ppmw was prepared by diluting with distilled water. These test results are also listed in Table 4, where lanthanum oxide and an equal weight mixture of lanthanum oxide and cerium dioxide were effective in removing more than 98% of vanadium from the test solution. Indicates that about 88% of the vanadium has been removed.

Test 13-15
The procedures of Tests 1 to 3 were repeated. However, instead of the chromium test solution, a test solution containing 2.0 ppmw uranium calculated as U was used. The uranium test solution was prepared by diluting a certified standard solution containing 1,000 ppmw uranium with distilled water. This solution did not contain other metals. The test results are listed in Table 4 and, as in Tests 10-12, lanthanum oxide and an equal weight mixture of lanthanum oxide and cerium dioxide remove most of the uranium from the test solution. It shows that it was effective. However, as in those examples, cerium dioxide was only effective to remove about 75% of the uranium.

Test 16-18
The procedures of Tests 1 to 3 were repeated. However, a test solution containing 1.0 ppmw of tungsten calculated as W was used instead of the chromium test solution. The tungsten test solution was prepared by diluting a certified standard solution containing 1,000 ppmw tungsten with distilled water. The solution contained no other metals. The test results are listed in Table 4, and lanthanum oxide, cerium dioxide, and an equal weight mixture of lanthanum oxide and cerium dioxide were equally effective in removing over 95% tungsten from the test solution. It is shown that.

Example 5
This example shows the affinity of halogen for rare earth metals. A series of tests were conducted to determine whether certain halogens, especially fluoride (and other halogens), would compete with arsenic binding to cerium chloride. Arsenic is known to bind strongly to cerium chloride in an aqueous medium when using water-soluble cerium chloride (CeCl ₃ ). This halogen binding affinity was determined by conducting a comparative test between a storage solution containing fluoride and a storage solution not containing fluoride. The materials used were CeCl ₃ (1.194 M Ce or 205.43 g / L rare earth oxide or REO) and 400 ml stock solution. Table 5 and Table 6 show the components of the stock solution according to NSF P231 “General Test Water 2” (“NSF”).

The initial pH of the stock solution was about 0 to 1. The temperature of the stock solution was raised to 70 ° C. The reaction or residence time was about 90 minutes.

The operation of precipitating cerium arsenate in the presence and absence of fluoride is as follows.
Step 1:
Two 3.5 L synthetic stock solutions were prepared. Here, one does not contain fluorine and the other contains fluorine. Both solutions contained the components listed in Table 5.

Step 2:
400 mL of the synthetic stock solution was measured gravimetrically (402.41 g) and transferred to a 600 mL Pyrex® beaker. The beaker was then placed on a hot / stir plate and heated to 70 ° C. with stirring.

Step 3:
Sufficient cerium chloride was added to the stock solution to meet the predetermined molar ratio of cerium and arsenic. For example, to obtain a molar ratio of 1 ceria mole and 1 mole of arsenic, 5.68 ml of cerium chloride was measured gravimetrically (7.17 g) and added to the stirred solution. With the addition of cerium chloride, a yellow / white precipitate formed instantly and the normality of the cerium chloride solution was 0.22, thus lowering the pH. The pH was adjusted to about 7 by using 20% sodium hydroxide.

Step 4:
Cerium chloride was added to the 70 ° C. solution and allowed to react for 90 minutes before sampling.
Step 5:
Repeat steps 2 through 4 for all desired molar ratios of fluoride-containing and non-fluoride-containing solutions.

The results are shown in Table 7 and FIGS. 55 and 56.
Table 7. Residual arsenic concentration in the supernatant solution after precipitation with cerium chloride solution.

By comparing the adsorption capacities of fluoride-containing or non-fluoride-containing solutions, the strong affinity of halogens and halogen compounds has been shown. FIG. 55 shows the affinity of cerium III for fluoride in the presence of arsenic. FIG. 56 shows that the adsorption capacity of the fluoride-free solution (defined as mg of As per gram of CeO ₂ ) at a low molar ratio of cerium to arsenic is quite high. The capture of fluorinated organic compounds, especially fluorinated pharmaceutical compounds, using rare earth metals, especially cerium, was clearly demonstrated.

In solution the molar ratio of about 1.4: 1 more cerium to arsenic, F ^- containing solution and F ^- the difference in adsorption capacity between the solution containing no was negligible. This would require an extra 40% cerium to capture F ⁻ and then the remaining cerium could react with arsenic.

These results confirm that the presence of fluoride is effectively competing with the capture of arsenic and other target substances. Interference from competing reaction to form CeF _3. This reaction has a much preferred Ksp. In view of these results, fluoride and other halogens should be removed prior to adding the rare earth element-containing additive.

Example 6
This example demonstrates the successful removal of sulfate-containing compounds, halogen compounds, carbonate-containing compounds, and phosphate-containing compounds using cerium dioxide powder. Cerium powder with arsenic removal capability of 400 ppb is contacted with various solutions containing arsenic (III) as arsenite and arsenic (V) as arsenate, and known binding affinity between arsenic and cerium Increased concentration of competing compounds. Competing organic compounds include sulfate ion, fluoride ion, chloride ion, carbonate ion, silicate ion, and phosphate ion, and the concentration of each ion is about 500% of the NSF concentration corresponding to each ion. Concentration. The cerium dioxide powder was further contacted with arsenic contaminated distilled water and NSF P231 “General Test Water 2” (“NSF”).

  Distilled water was used as the reference measurement value. The results are shown in FIG. As can be seen from FIG. 55, ions in NSF water have a reduced ability to remove cerium dioxide for both arsenite and arsenate relative to distilled water, and the binding of these compounds to rare earth metals was successful. It is shown that. In the presence of carbonate ions, the ability of cerium dioxide to remove arsenate was lower than arsenite. In the presence of silicate ions, the ability of cerium dioxide to remove both arsenite and arsenate was greatly reduced. Finally, phosphate ions have the most significant reduction in cerium dioxide removal performance for arsenite (10 times the NSF concentration) and arsenate (50 times the NSF concentration), and the ability to remove arsenite. The decline was the greatest.

Example 7
Several tests were performed to evaluate solution phase or soluble cerium ion precipitation.
Test 1:
A solution containing 250 ppm of Cr (VI) was corrected with a molar equivalent of cerium supplied as either Ce (III) chloride or Ce (IV) nitrate. Addition of Ce (III) to the chromate had no immediate visible effect on the solution, but after 24 hours a fine precipitate of dark solid appeared. In contrast, the addition of Ce (IV) immediately resulted in a large amount of solid formation.

  As in the previous example, an aliquot was filtered and the pH was adjusted to pH 3 for Ce (IV) and to pH 5 for Ce (III). Although the addition of Ce (III) had a negligible effect on Cr solubility, Ce (IV) removed almost 90% of the Cr from the solution at pH 3.

  Test 2: A solution containing 50 ppm molybdenum, possibly molybdate, of the Spex ICP standard was corrected with a molar equivalent of Ce (III) chloride. As with the previous sample, a solid was observed after the addition of cerium and an aliquot was filtered through a 0.45 micron syringe filter for ICP analysis. At pH 3, nearly 30 ppm of Mo remained in the solution. However, when the pH was raised to 5, the Mo concentration decreased to 20 ppm, and the Mo concentration was only 10 ppm at around pH 7.

Example 8
In these examples, adsorption and desorption of a series of non-arsenic anions was tested by using a method similar to that established for arsenic testing.

Permanganate:
Two examples were performed. In the first example, 40 g of ceria powder was added to 250 mL of 550 ppm KMnO ₄ solution. In a second example, 20 g of ceria powder was added to 250 mL of 500 ppm KMnO ₄ solution and the pH was lowered with 1.5 mL, 4N HCl. By reducing the slurry pH, Mn adsorption on ceria increased fourfold.

  In both examples, ceria was contacted with the permanganate for 18 hours and then filtered to retain the solid. The filtrate was analyzed for Mn using ICP-AES and the solid was washed with 250 mL DI water. The non-pH adjusted solid was washed twice.

  The filtered and washed Mn contact solids were weighed and divided into a series of three extraction tests and one control group. In these tests, the extent to which manganese can be recovered from the ceria surface when contacted with 1N NaOH, 10% oxalic acid, or 1M phosphate is compared to the results of DI water under the same conditions. It was.

  In the sample of permanganate adsorbed ceria powder contacted with water as a control group, the release of Mn was less than 5%. Like arsenate, NaOH effectively promoted desorption of permanganate from the ceria surface. This indicates that the basic pH level, or basification, behaves as an interferent for permanganate removal by ceria. In the case of the second example where the pH was lowered, the NaOH results were greater than in the first example where the permanganate adsorbed under higher pH conditions.

  Phosphate was much more effective at inducing permanganate desorption than at inducing arsenate desorption. Phosphate was the most effective desorption promoter that we tested with permanganate. In other words, the ability of ceria powder to remove permanganate in the presence of phosphoric acid appears to be relatively low because the ability of ceria powder to phosphoric acid is much higher than that to permanganate.

Oxalic acid significantly changed the color of the permanganate solution. This indicates that Mn (VII) has been reduced, possibly to Mn (II) or Mn (IV). Formation of MnO or MnO ₂ precipitates can prevent further detection of Mn, which is not known whether it can be removed from ceria. Thus, the reducing agent appears to be a ceria interference for Mn (VII) removal. In the non-pH adjusted sample, desorbed Mn was not detected. However, in samples prepared by slightly acidifying the slurry, a significant amount of Mn was recovered from the ceria surface.

Chromate A 250 mL solution was prepared using 0.6 g sodium dichromate and the solution was contacted with 20 g cerium powder for 18 hours without pH adjustment. After filtering the slurry and washing the solid with DI water, it was divided into 50 mL centrifuge tubes to test the ability of the three solutions to extract chromium from the ceria surface.

  The ability of ceria to chromate was significant, with> 20 mg Cr / g ceria adsorbed (pH of filtrate was about 8) without pH adjustment or system optimization. Similarly, the extraction of adsorbed chromate was easily accomplished. Increasing the pH of the slurry containing chromate-containing ceria with 1N NaOH was the most effective chromium desorption method tested. When phosphate was used, very little chromate was desorbed, and with oxalic acid, only a trace amount was desorbed. This indicates that phosphate and oxalic acid are not so strong interferents in chromate removal compared to permanganate removal. In the control test, only 5% chromate was recovered when the adsorbed solid was contacted with distilled water.

Antimony Since the solubility of antimony is somewhat low, these reactions were limited by the amount of antimony that could be dissolved. In this case, 100 mg of antimony (III) oxide was placed in 1 L of distilled water with 10 mL of concentrated HCl, allowed to equilibrate for several days, and filtered through a 0.8 micron polycarbonate membrane to remove insoluble antimony. One liter of antimony solution was contacted with 16 g of ceria powder to effectively remove antimony from the solution, but too little Sb (III) was available to adsorb to the surface in large quantities. For one thing, extraction tests showed that little Sb was recovered due to the low surface coverage and strong surface anion interactions. The use of hydrogen peroxide, which was expected to convert Sb (III) to Sb (V) species that are not easily adsorbed, did not result in significant amounts of Sb recovery.

Arsenic Tables 8-11 show test parameters and results.
Table 8: Adsorption amount of cerium oxide surface by arsenate and arsenite to clarify arsenic desorption technique

Example 9
NH ₄ a struvite particles comprising _{MgPO 4 · 6H 2 O, CeCl} 3 and _{NH 4} MgPO 4 · 6H ₂ such that the molar ratio of O is different, were mixed CeCl ₃ solution. Here, the molar ratio of CeCl ₃ and NH ₄ MgPO ₄ .6H ₂ O was about 0.8, 1.0, 1.2 and 1.5. In each case, the mass of the struvite was about 0.2 g, and the concentration of CeCl ₃ was about 0.5 mol / L. Furthermore, about 0.2 g of struvite in 0.1 L of deionized water was prepared as a control group. The pH value of each solution was adjusted to a pH of about pH 4.3 ± 0.2. Each sample solution was stirred using a magnetic stir bar. After stirring for at least about 16 hours, the solid was filtered from the solution. The filtered solid was analyzed by X-ray diffraction and the solution was analyzed by ICP-MS. The final solution pH value of the solution ranged from about pH 4.6 to about pH 8.0. The results are summarized in Table 12.

Example 10
The particles of struvite NH ₄ MgPO ₄ .6H ₂ O are about 0. 0 containing different rare earth chlorides.
Mixed in 1 L solution. The rare earth chloride solution was a solution of about 0.15 mol / L LaCl ₃ , CeCl ₃ , PrCl ₃ and NdCl ₃ . The mass of the struvite added to each rare earth chloride solution was about 0.2 g, and the molar ratio of the rare earth chloride to the struvite was about 1.0. The pH of each rare earth chloride solution was adjusted to a pH of about pH 4.3 ± 0.2. Each sample solution was stirred using a magnetic stir bar. After stirring for at least about 16 hours, the solid was filtered from the solution. The filtered solid was analyzed by X-ray diffraction and the solution was analyzed by ICP-MS. The final solution pH value of the solution ranged from about pH 4.6 to about pH 8.0. The results are summarized in Table 13.

Example 11
Example 11 is a control group in which about 0.2 g of struvite NH ₄ MgPO ₄ .6H ₂ O particles were mixed with about 0.1 L of a 0.15 mol / L acidic ferric chloride FeCl ₃ solution. It is. The molar ratio of ferric chloride to struvite was about 1.0, and the initial pH of the solution was about pH 2.5. The initial pH of the control solution was low enough to dissolve the struvite without the presence of ferric chloride. The control solution was stirred using a magnetic stir bar. After stirring for at least about 16 hours, the solid was filtered from the control solution. The filtered solid was analyzed by X-ray diffraction and the control solution was analyzed by ICP-MS. The final solution pH value of the solution was about pH 2.3. The results are summarized in Table 14.

Examples 9-11 show that sturbite can be more effectively removed with rare earth-containing compositions than other removal materials such as ferric chloride.

Example 12
Table 15 summarizes the ability of cerium dioxide to remove deposited material from deionized and NSF water.

Example 13
Experiments were conducted to remove metals and metalloids from deionized water and NSF standardized water (see Table 16) with cerium-containing compositions.

As can be seen from Table 16, the cerium-containing composition was effective in removing the target substance-containing species of Table 16.

Example 14
Experiments were performed to qualitatively determine the ability of cerium-containing additives to remove metals and metalloids from deionized and NSF standardized water (see Table 17).

As can be seen from Table 16, the cerium-containing composition was effective in removing the target substance-containing species of Table 17.

Example 15
Experiments were performed to qualitatively determine the removal of organic, metal, metalloid and non-metallic contaminants from deionized and NSF water (see Table 18 and Table 19).

CeO ₂ is in the form of a powder, and the aggregated CeO ₂ is aggregated with a polymer binder.

  The insoluble lead may be removed from the aqueous solution containing one or both of soluble lead and insoluble lead by the rare earth-containing composition. Insoluble lead may include, but is not limited to, for example, colloidal lead and / or particulate lead, such as lead oxide, lead hydroxide, or oxy (hydroxy lead). Good. The insoluble lead composition may be in the form of a hydrate with one or more waters of hydration.

The composition of NSF test water is defined in one or more of the following documents. Standard Developer NSF International, “NSF / ANSI 42-2007a NSF International Standard / American National”
Standard for Drinking Water Treatment Units Drinking Water Treatment Units Aesthetic Effects "American National Standards Commission, specified in the ANSI standard on August 28, 2009 the Standard Developer NSF International ed.," NSF / ANSI 53-2009e NSF International Standard / American National Standard “Drinking Water Treatment Units Health Effects”, and Standard Developer NSF International “NSF / ANS” specified in the ANSI standard on August 26, 2009 61-2009 NSF International Standard / American National Standard for Drinking Water Additives Drinking Water System Components Health Effects ".

Example 16
High surface area (“HAS”) ceria (surface area: 130 ± 10 with an adsorption capacity of about 20 mg
m ² / g) was contacted with an analyte that had about 0.5 mg / L of the reagent in question and was considered NSF53 water. The composition of NSF water is shown in Table 20 below.

The pH of the analyte was pH 12.25 ± 0.25 and the temperature was 20-25 ° C. or ambient temperature.

The analyte was contacted with HSF ceria for about 24 hours.
The reagents in question were bismuth, chromium, cobalt, manganese, zinc and zirconium species. Under the above conditions, the main species was considered to be in colloidal form.

The media was conditioned by measuring 20 mg of HSA ceria in a plastic weighing boat and moistening the HAS ceria media with deionized water for at least 30 minutes.
The analyte was prepared in a 2.0 L batch of NSF53 lead removal water without lead addition. A 1,000 mg / L SPEX nitrogen standard was obtained and used to adjust the influent of the reagent at 0.5 mg / L. This solution was mixed for 30 seconds with a high shear mixer (Ninja model number: BL500 30). The pH was adjusted to 12.25 ± 0.25 with 3M NaOH and mixed for an additional 60 seconds. Earlier tests at higher concentrations showed that particles were present at a pH of 12.25 ± 0.25.

  An isotherm test was prepared by pouring a 500 mL influent into four 500 mL bottles. Pre-moistened media was poured into each 500 mL sample bottle. The bottle was capped and sealed with insulating tape. Each bottle was then placed in a rolling container capable of holding up to 10 bottles. The container was sealed with duct tape and placed in a rolling device. Sample and control groups were rolled for 24 hours. After 24 hours, the rolling container was removed from the apparatus, and the bottle was collected from the container.

  A 5 mL sample was taken for each metal sample, diluted with 3 mL concentrated nitric acid and filtered through a 0.2 μm filter. Samples were acidified to confirm that all metals were soluble. Metal samples were analyzed by inductively coupled plasma mass spectrometry (ICP-MS). To confirm the presence of colloidal metal, the sample was first filtered to remove any particles and then acidified to confirm that all metal was soluble. All analyzes of these tests were below the detection limit of the analyzed metals. All isotherm tests were adjusted and tested in the same manner. For this reason, it was easily comparable.

  As shown in Table 21, colloidal bismuth, chromium, manganese, and zinc were all removed from NSF53 water containing HSA ceria. The ability to remove the reagent in question was based on the removal of at least 10% of the reagent in question from the influent.

In Table 22, the breakdown of cobalt and zirconium is shown.

Example 17
This example compares various test results and concludes that changes in temperature, surface area, speciation, and concentration affect arsenic adsorption capacity on ceria. The experimental procedure is described below.

material:
CeO ₂ : LOI-4.6%, SA-140 m ² / g;
CeO ₂ : LOI-6.3%, SA-210 m ² / g Amount used: 40 g
Test solution constituents (added to 20 L DI water):
NiSO ₄ · _6H 2 O of 2244.45g
119.37 g of CuSO ₄ .5H ₂ O
57.81 H ₃ BO ₃
406.11 NaCl
FeSO of 15.01 ₄ · 7H2O
CoSO of 4.79g ₄ · 7H2O
70 concentrated HCl
Test solution conditions:
pH: 1.63
Density: 1.08 mL / g
Column inflow:
pH: density ranged from 1.1 to 1.2 for all columns Temperature: 1.08 g / mL for all columns: Flow rate at which all columns were tested from room temperature to 21 ° C. or 70 ° C .: Flow rates ranged from 1 to 1.8 mL / min, or from 2.2% to 4.0% of the total volume. Approximate amount of flocculant used: 22% 22% column bed dimensions: 1% Nalco7871 8.5-9 cm x 2.54 cm ID for all columns
Medium:
150 g of ACS standard sodium chloride was added to a 1 L volume meter. The salt was then diluted to the 1 L mark with DI water. The salt was then transferred to a 2 L beaker and heated to boiling. Next, 15 mL of concentrated HCl was added to hot water while stirring using a magnetic stir bar. Immediately after the addition of HCl, 40.00 g of dry CeO ₂ was gradually added to the mixed acidic salt solution. The solution was allowed to stir for 5 minutes. Next, 22 drops of 1% Nalco7871 were added to clarify the solution and prevent separation when added into the column.

Packing the column:
Agglomerated CeO ₂ media is transferred into a 2.54 cm × 30 cm glass column. DI water is flowed through the bed at 12 mL / min, allowing the bed to settle down to 8.5 cm completely. The DI water on the floor was decanted and replaced with the influent solution, then capped and sealed tightly.

As can be seen from Table 23 and FIG. 57, the cerium (IV) oxide-containing arsenic species adsorption capacity is affected by changes in temperature, surface area, speciation, and arsenic species concentration.

Example 18
In this example, it is determined which colloidal metal can be removed from NSF 53 water by high surface area (“HSA”) cerium (IV) oxide. The test parameters are as follows.

Parameters:
Material: HSA ceria oxide (surface area: 130 ± 10 m ² / g)
Amount used: 20mg
Analyte concentration: 0.5 mg / L of NSF53 water as a reagent in question

pH: variable temperature: room temperature contact temperature of 20-25 ° C .: 24 hours Test metals: bismuth, chromium, cobalt, manganese, zinc, zirconium, aluminum, and copper Medium preparation:
20 mg of HSA ceria oxide was measured in a plastic weighing boat. The medium was moistened with DI water for at least 30 minutes.

Inflow water preparation:
The influent was prepared in a batch of 2.0 L NSF53 lead removal water without lead addition. A 1,000 mg / L SPEX nitrogen standard was obtained and used to adjust the influent of the reagent at 0.5 mg / L. This solution was first mixed with a high shear mixer (Ninja model number: BL500 30) for 30 seconds, then the pH was adjusted with 3M NaOH or concentrated HCl, and then the solution was mixed for another 30 seconds. The redox potential (“ORP”) value was then adjusted using solid sodium sulfite or 12.5% NaClO solution (see Table 25).

Test procedure:
Isotherm test preparation procedure:
Four 500 mL bottles were each filled with 500 g influent. Pre-moistened media was poured into each 500 mL sample bottle. The bottle was capped and sealed with insulating tape. Each bottle was then placed in a rolling container capable of holding up to 10 bottles. The container was then sealed with duct tape and placed in a rolling device. The sample was rolled for 24 hours. After 24 hours, the rolling container was removed from the apparatus, and the bottle was collected from the container.

Sample preparation procedure for analysis:
A 5 mL sample was taken for each metal sample, diluted by adding 5 mL of 10% nitric acid, and filtered through a 0.2 μm filter. Samples were acidified to confirm that all metals were soluble. Metal samples were analyzed by inductively coupled plasma mass spectrometry (ICP-MS). To confirm the presence of insoluble metal, the sample was first filtered through a 0.2 μm filter to remove any insoluble metal and then acidified to confirm that all samples were similar. All isotherm tests were prepared and tested in the same manner. For this reason, it was easily comparable.

result:
As shown in Table 26 and Table 27, Cr ₂ O ₃ (S), Mn ₃ O ₄ (S), Al ₂ O ₃ (H ₂ O) (S), Cu (OH) ₂ (S), and Cu ₂ O (S) was all removed from NSF53 water containing HSA ceria. The ability to remove the reagent in question was based on the removal of at least 10% of the reagent in question from the influent.

Conclusion:
Colloidal chromium, aluminum, and copper were all removed from NSF53 water containing HSA ceria. In some experiments, cobalt, zinc, and zirconium were also removed. The ability to remove HAS ceria against manganese was uncertain.

Example 19
In this example, it is determined whether the colloidal metal can be removed from NSF 53 water by high surface area (“HSA”) cerium (IV) oxide. The test parameters are as follows.

Parameters:
Material: HSA ceria oxide (surface area: 130 ± 10 m ² / g)
Amount used: 20mg
Analyte concentration: 0.5 mg / L of NSF53 water as reagent in question, see Table 34.

pH, ORP: variable. See Table 28.
Temperature: Room temperature from 20 to 25 ° C.
Contact time: 24 hours.
Test metals: bismuth, chromium, cobalt, manganese, zinc, zirconium, aluminum, and copper Medium preparation:
20 mg of HSA ceria was measured in a plastic weighing boat. The medium was moistened with DI water for at least 30 minutes.

Inflow water preparation:
The influent was prepared in a batch of 2.0 L NSF53 lead removal water without lead addition. A 1,000 mg / L SPEX nitrogen standard was obtained and used to prepare a 0.5 mg / L reagent influent. This solution was first mixed with a high shear mixer (Ninja model number: BL500 30) for 30 seconds, then the pH was adjusted with 3M NaOH or concentrated HCl, and then the solution was mixed for another 30 seconds. The ORP value was then adjusted using solid sodium sulfite or 12.5% NaClO solution.

procedure:
Isotherm test preparation procedure:
Four 500 mL bottles were each filled with 500 g influent. Pre-moistened media was poured into each 500 mL sample bottle. The bottle was capped and sealed with insulating tape. Each bottle was then placed in a rolling container capable of holding up to 10 bottles. The container was then sealed with duct tape and placed in a rolling device. The sample was rolled for 24 hours. After 24 hours, the rolling container was removed from the apparatus, and the bottle was collected from the container.

Sample preparation procedure for analysis:
A 5 mL sample was taken for each metal sample, diluted by adding 5 mL of 10% nitric acid, and filtered through a 0.2 μm filter. Samples were acidified to confirm that all metals were soluble. Metal samples were analyzed by inductively coupled plasma mass spectrometry (ICP-MS). To confirm the presence of insoluble metal, the sample was first filtered through a 0.2 μm filter to remove any insoluble metal and then acidified to confirm that all samples were similar. All isotherm tests were prepared and tested in the same manner. For this reason, it was easily comparable.

result:
The results are shown in Tables 29-30 below.

Conclusion All metal solutions were prepared with NSF53 arsenic test water without the addition of arsenic. All of these solutions were studied with HSA cerium oxide (CeO ₂ ). Bi (target substances BiOOH _(S) , BiO ⁺ ) was clearly removed. Cr (target material Cr ₂ O _{3 (S)} ), Mn (target material MnO _{2 (S)} , Mn ₂ O _{3 (S)} , and Mn ₃ O _{4 (S)} ), Zn (target material Z
_{n (OH) 2 (S)} ), Al ( target substance _{Al 2 O 3 (H 2 O} ) (S)), Cu ( target substance Cu _{(OH) 2 (S)} and _Cu 2 _{O (S)),} and Zr (target substance ZrO _{2 (S)} ) was clearly removed. In test 2AA, Co (target substance CoO _{2 (S)} ) was clearly removed. These results show that under controlled conditions, insoluble compounds of Al, Co, Cr, Cu, Mn, Zn, and Zr can be removed using HSA cerium oxide (CeO ₂ ).

58-65 show prior art pool diagrams of the above materials.
Example 20
In this example, it was determined whether or not the soluble metal selected by HAS cerium (IV) oxide could be removed from NSF53 water.

Parameters:
Substance: HSA ceria oxide (surface area: 130 ± 10 m ^s / g) Amount used: 20 mg
Analyte concentration: 0.5 mg / L of NSF53 water as a problem reagent, see Table 31.

pH, ORP: variable. See Table 32.
Temperature: Room temperature from 20 to 25 ° C.
Contact time: 24 hours.
Test metals: aluminum (Al ³⁺ ), barium (Ba ²⁺ ), cadmium (Cd ²⁺ ), chromium (Cr ³⁺ ), cobalt (Co ²⁺ ), copper (Cu ²⁺ ), iron (Fe ²⁺ ), manganese (Mn ²⁺ ) , And nickel (Ni ²⁺ )
Medium preparation:
20 mg of HSA ceria was measured in a plastic weighing boat. The medium was moistened with DI water for at least 30 minutes.

Inflow water preparation:
The influent was prepared in a batch of 2.0 L NSF53 lead removal water without arsenic addition. A 1,000 mg / L SPEX nitrogen standard was obtained and used to prepare a 0.5 mg / L reagent influent. After this solution was mixed on a stir plate, the pH was adjusted with 3M NaOH or concentrated HCl. The ORP value was then adjusted using solid sodium sulfite or 12.5% NaClO solution.

procedure:
Isotherm test preparation procedure:
Four 500 mL bottles were each filled with 500 g influent. Pre-moistened media was poured into each 500 mL sample bottle. The bottle was capped and sealed with insulating tape. Each bottle was then placed in a rolling container capable of holding up to 10 bottles. The container was then sealed with duct tape and placed in a rolling device. The sample was rolled for 24 hours. After 24 hours, the rolling container was removed from the apparatus, and the bottle was collected from the container.

Sample preparation procedure for analysis:
A 6 mL sample was taken for each metal sample, diluted with 0.667 mL concentrated nitric acid and filtered through a 0.2 μm filter. Samples were acidified to confirm that all metals were soluble. Metal samples were analyzed by ICP-MS. All isotherm tests were adjusted and tested in the same manner. For this reason, it was easily comparable.

result:
The results are shown in Table 32 and Table 33.

Conclusion:
Dissolved or soluble Al ³⁺ , Ba ²⁺ , Cd ²⁺ , Cr ³⁺ , Co ²⁺ , Cu ²⁺ , Fe ²⁺ , Mn ²⁺ , and Ni ²⁺ from NSF53 by HSA ceria were clearly removed.

  3A to 3E (aluminum), FIGS. 6A to 6E (chromium), FIGS. 7A to 7F (manganese), FIGS. 8A to 8F (iron), FIGS. 9A to 9E (cobalt), FIGS. 10A to 10E (Nickel), FIGS. 11A to 11E (Copper), FIGS. 24A to 24C (Cadmium), FIGS. 66A to 66E (Barium), and FIGS. 67A to 67E (Radium). It is.

  Several variations and modifications of the present disclosure can be used. One or more embodiments of the present disclosure can be used separately and in combination. That is, any single embodiment can be used, and all combinations and substitutions thereof can be used. It may be possible to provide several features without providing other features of the present disclosure.

  The disclosure in various embodiments, configurations, or aspects includes components substantially as shown and described herein, including various embodiments, configurations, aspects, subcombinations, and subsets thereof. , At least one of a method, process, system and / or apparatus. Those skilled in the art will understand how to make and use various embodiments, configurations, or aspects after understanding the present disclosure. This disclosure in various embodiments, configurations, and aspects is intended to be used in the present specification or various embodiments, configurations, or aspects thereof in the absence of elements that are neither shown and / or described in the description. And providing a process. This includes, for example, the absence of elements that can be used in previous devices or processes to improve performance, facilitate implementation and / or reduce implementation costs.

The foregoing description has been presented for purposes of illustration and description. The foregoing description is not intended to limit the present disclosure to the form disclosed herein. For example, in the foregoing detailed description, various features of the present disclosure are grouped together in one or more embodiments, configurations, or aspects in order to simplify the disclosure. Features of embodiments, configurations, or aspects of the present disclosure may be combined in other embodiments, configurations, or aspects other than those described above. This method of disclosure is not to be interpreted as expressing an intention that any claim and / or combination of claims requires more features than are expressly recited in each claim. Absent. Rather, as the following claims reflect, aspects of the invention reside in less than all features of the single disclosed embodiment, configuration, or aspect described above. Thus, the following claims are hereby incorporated into this detailed description, with each claim standing on its own as a separate preferred embodiment.

  Moreover, the description of the present disclosure has included one or more embodiments, configurations, or aspects and specific variations and modifications, for example, after understanding the present disclosure Other variations, combinations, and modifications as may be within the scope are within the scope of the present disclosure. It is intended to obtain the right to include other embodiments, configurations or aspects to the extent permitted. This includes interchangeable and / or equivalent structures, functions, ranges or steps other than those claimed, such alternative, replaceable and / or equivalent structures, functions, Regardless of whether the scope or steps are disclosed herein, it does not matter whether or not any patentable subject matter is not intended for public use.

Claims (39)

In a composition of the following form:

In the above formula, 0 ≦ X ≦ 8,
MS has the following chemical formula M (H ₂ O) ₆ ⁿ , M (H ₂ O) ₅ OH ^(n-1) , M (OH) ^(n-1) M (H ₂ O) ₄ (OH) ₂ ^{( n-2)} , M (OH) ₂ ^(n-2) , M (H ₂ O) ₃ (OH) ₃ ^(n-3) , M (OH) ₃ ^(n-3) , M (H ₂ O) ^{_{2 (OH) 4 (n-}} 4), M (OH) 4 (n-4), M (H 2 O) (OH) 5 (n-5), M (OH) 5 (n-5), M (OH) ₆ ^(n-6) , M (H ₂ O) ₅ O ^(n-2) , M (H ₂ O) ₄ (O) ₂ ^(n-4) , M (H 2 O) ₃ (O) ₃ ^(N-6) , M (H ₂ O) ₂ (O) ₄ ^(n-8) , M (H ₂ O) (O) ₅ ^(n-10) , M (H ₂ O) ₅ CO ₃ ^{(n -2)} , MCO ₃ ^(n-2) , M (H ₂ O) ₄ (CO ₃ ) ₂ ^{(n- 4)} , M (CO ₃ ) ₂ ^(n-4) , M (H ₂ O) ₃ (CO ₃ ) ₃ ^(n-6) , M (CO ₃ ) ₃ ^(n-6) , M (H ₂ O ) ₂ (CO ₃ ) ₄ ^(n-8) , M (CO ₃ ) ₄ ^(n-8) , M (H ₂ O) (CO ₃ ) ₅ ^(n-10) , M (CO ₃ ) ₅ ^{(n -10)} , M (CO ₃ ) ₆ ^(n-12) , M (H ₂ O) ₄ n, M (H ₂ O) ₃ OH ^(n-1) , M (H ₂ O) ₂ (OH) _{2 ^{(n-2), M (}} H 2 O) (OH) 3 (n-3), M (H 2 O) 3 O (n-2), M (H 2 O) 2 (O) 2 (n- ⁴⁾ and one of M (H ₂ O) (O) ₃ ^(n-6) ,
Wherein M is a metal or metalloid having an atomic number selected from the group consisting of atomic numbers 5, 13, 22-33, 40-52, 56, 72-84, and 88-94, n A composition wherein is a real number of 8 or less and n represents a charge or oxidation state of M.   The composition of claim 1, wherein the composition is present in an aqueous medium and the aqueous medium has a pH and Eh sufficient to favor MS as a major species of M.   The composition of claim 1, wherein the oxidation state of the cerium oxide is (IV), is in particulate form, and M is lead.   The composition of claim 1 wherein the MS is in the form of a hydroxide.   The composition of claim 1, wherein MS is in the form of an oxyhydroxyl compound.   The composition of claim 1 wherein the MS is in the form of a carbonate.   The composition of claim 1, wherein the MS is in the form of a metal or metalloid hydrate.   M is one or more of boron, vanadium, chromium, cadmium, antimony, lead, and bismuth, and MS is in the form of a hydroxide, carbonate, and metal or metalloid hydrate. The composition of claim 1, which is one or more of them. In order to remove one or more of the metal or metalloid hydroxides, carbonates, and hydrates in the liquid medium, the rare earth-containing additive is added to the metal or metalloid hydroxide,
Contacting the carbonate and one or more of the hydrates. The metal or metalloid has an atomic number selected from the group consisting of atomic numbers 5, 13, 22-33, 40-52, 56, 72-84, and 88-94; One or more of the hydroxides, carbonates, and hydrates may have the following chemical formulas M (H ₂ O) ₆ ⁿ , M (H ₂ O) ₅ OH ⁽ⁿ⁻¹⁾ , M (OH) ^{( _{n-1) M (H 2}} O) 4 (OH) 2 (n-2), M (OH) 2 (n-2), M (H 2 O) 3 (OH) 3 (n-3), M (OH) ₃ ^(n-3) , M (H ₂ O) ₂ (OH) ₄ ^(n-4) , M (OH) ₄ ^(n-4) , M (H ₂ O) (OH) ₅ ^{(n -5)} , M (OH) ₅ ^(n-5) , M (OH) ₆ ^(n-6) , M (H ₂ O) ₅ CO ₃ ^(n-2) , MCO ₃ ^(n-2) , M (H ₂ O) ₄ (CO ₃ ) ₂ ^(n-4) , M (CO ₃ ) ₂ ^(n-4) , M (H ₂ O) ₃ (CO ₃ ) ₃ ^(n-6) , M (CO ₃ ) ₃ ^{(n -6)} , M (H ₂ O) ₂ (CO ₃ ) ₄ ^(n-8) , M (CO ₃ ) ₄ ^(n-8) , M (H ₂ O) (CO ₃ ) ₅ ^(n-10) , M (CO ₃ ) ₅ ^(n-10) , M (CO ₃ ) ₆ ^(n-12) , M (H ₂ O) ₄ ⁿ , M (H ₂ O) ₃ OH ^(n-1) , M ( Having one or more chemical formulas of H ₂ O) ₂ (OH) ₂ ^(n-2) and M (H ₂ O) (OH) ₃ ^(n-3) ,
In the above formula, M is the metal or metalloid,
n is a real number of 8 or less,
The method of claim 9, wherein n represents the charge or oxidation state of M.   The liquid medium is an aqueous solution, Eh sufficient to bring one or more of the metal or metalloid hydroxides, carbonates, and hydrates into the main species of M and 11. A method according to claim 10 having a pH.   The method of claim 11, wherein the Eh and pH are determined using one or more of the pool diagrams of FIGS. 2 to 47 and 57 to 65.   The method according to claim 9, wherein the rare earth-containing additive is in the form of cerium (IV) and / or cerium (III), and M is lead.   10. A method according to claim 9, wherein the metal or metalloid is in the form of a hydroxide.   The method of claim 9, wherein the metal or metalloid is in the form of a carbonate.   10. The method of claim 9, wherein the metal or metalloid is in the form of a metal or metalloid hydrate.   The method of claim 9, wherein the metal or metalloid is one or more of boron, vanadium, chromium, cadmium, antimony, lead, and bismuth. The contacting step comprises:
In order to oxidize the target substance-containing species comprising the metal or metalloid in one or more forms of metal or metalloid hydroxides, carbonates, and hydrates to the main chemical species, the medium Introducing an oxidant, wherein the target substance-containing species is different from one or more of the metal or metalloid hydroxides, carbonates, and hydrates Substeps to
Thereafter, in order to remove one or more of the metal or metalloid hydroxide, carbonate, and hydrate in the medium, the rare earth element-containing additive is added to the metal or metalloid water. 10. The method of claim 9, comprising the step of contacting with one or more of oxides, carbonates, and hydrates. The contacting step comprises:
In order to reduce the target substance-containing species comprising the metal or metalloid in one or more forms of metal or metalloid hydroxides, carbonates, and hydrates to the main chemical species, the medium Introducing a reducing agent, wherein the target substance-containing species is different from one or more of the metal or metalloid hydroxides, carbonates and hydrates Substeps to
Thereafter, in order to remove one or more of the metal or metalloid hydroxide, carbonate, and hydrate in the medium, the rare earth element-containing additive is added to the metal or metalloid water. 10. The method of claim 9, comprising the step of contacting with one or more of oxides, carbonates, and hydrates. The contacting step comprises:
In order to convert the target substance-containing species comprising the metal or metalloid in one or more forms of metal or metalloid hydroxides, carbonates, and hydrates into the main chemical species, the medium A sub-step of introducing a base and / or base equivalent, wherein the target substance-containing species is different from one or more of the metal or metalloid hydroxides, carbonates and hydrates A sub-step for introducing a base and / or a base equivalent;
Thereafter, in order to remove one or more of the metal or metalloid hydroxide, carbonate, and hydrate in the medium, the rare earth element-containing additive is added to the metal or metalloid water. 10. The method of claim 9, comprising the step of contacting with one or more of oxides, carbonates, and hydrates. The contacting step comprises:
In order to convert the target substance-containing species comprising the metal or metalloid in one or more forms of metal or metalloid hydroxides, carbonates, and hydrates into the main chemical species, the medium A sub-step of introducing an acid and / or an acid equivalent, wherein the target substance-containing species is different from one or more of the metal or metalloid hydroxides, carbonates and hydrates A sub-step of introducing an acid and / or an acid equivalent; or
Thereafter, in order to remove one or more of the metal or metalloid hydroxide, carbonate, and hydrate in the medium, the rare earth element-containing additive is added to the metal or metalloid water. 10. The method of claim 9, comprising the step of contacting with one or more of oxides, carbonates, and hydrates.   The method according to claim 9, wherein the rare earth element-containing additive is water-soluble.   The method according to claim 9, wherein the rare earth element-containing additive is water-insoluble.   Contacting a rare earth element-containing additive with a metal or metalloid target material to remove the target material in a liquid medium, the target material as a main chemical species, hydroxide, carbonate, hydration Or a method in the form of an oxyhydroxyl group. The target substance has an atomic number selected from the group consisting of atomic numbers 5, 13, 22-33, 40-52, 56, 72-84, and 88-94, and the target substance has the following chemical formula M (H ₂ O) ₆ ⁿ , M (H ₂ O) ₅ OH ^(n-1) , M (OH) ^(n-1) M (H ₂ O) ₄ (OH) ₂ ^(n-2) , M ( OH) ₂ ^(n-2) , M (H ₂ O) ₃ (OH) ₃ ^(n-3) , M (OH) ₃ ^(n-3) , M (H ₂ O) ₂ (OH) ₄ ^{(n -4)} , M (OH) ₄ ^(n-4) , M (H ₂ O) (OH) ₅ ^(n-5) , M (OH) ₅ ^(n-5) , M (OH) ₆ ^{(n- 6)} , M (H ₂ O) ₅ O ^(n-2) , M (H ₂ O) ₄ (O) ₂ ^(n-4) , M (H ₂ O) ₃ (O) ₃ ^(n-6) _{, M (H 2 O) 2} (O) 4 (n- ^{_{), M (H 2 O)}} (O) 5 (n-10), M (H 2 O) 5 CO 3 (n-2), MCO 3 (n-2), M (H 2 O)
₄ (CO ₃ ) ₂ ^(n-4) , M (CO ₃ ) ₂ ^(n-4) , M (H ₂ O) ₃ (CO ₃ ) ₃ ^(n-6) , M (CO ₃ ) ₃ ^{(n -6)} , M (H ₂ O) ₂ (CO ₃ ) ₄ ^(n-8) , M (CO ₃ ) ₄ ^(n-8) , M (H ₂ O) (CO ₃ ) ₅ ^(n-10) , M (CO ₃ ) ₅ ^(n-10) , M (CO ₃ ) ₆ ^(n-12) , M (H ₂ O) ₄ ⁿ , M (H ₂ O) ₃ OH ^(n-1) , M ( ^{_{H 2 O) 2 (OH)}} 2 (n-2), M (H 2 O) (OH) 3 (n-3), M (H 2 O) 3 O (n-2), M (H 2 O ) ₂ (O) ₂ ^(n-4) and M (H ₂ O) (O) ₃ ^(n-6) ,
In the above formula, M is the metal or metalloid target substance,
n is a real number of 8 or less,
25. A method according to claim 24, wherein n represents the charge or oxidation state of M.   The liquid medium is an aqueous solution, and has a pH sufficient to bring one or more of the metal or metalloid hydroxides, carbonates, and hydrates into the main species of M; 26. The method of claim 25, having Eh.   27. The method of claim 26, wherein the Eh and pH are determined using one or more of the pool diagrams of FIGS. 2-47 and 57-65.   25. The method of claim 24, wherein the rare earth additive is in the form of cerium (IV) and / or cerium (III), and M is lead.   25. A method according to claim 24, wherein the target substance is in the form of a hydroxide.   The method according to claim 24, wherein the target substance is in the form of a carbonate.   25. The method of claim 24, wherein the target substance is in the form of a metal or metalloid hydrate.   The method according to claim 24, wherein the target substance is in the form of an oxyhydroxyl compound.   25. The method of claim 24, wherein the target substance is one or more of boron, vanadium, chromium, cadmium, antimony, lead, and bismuth. The contacting step comprises:
In order to oxidize the target substance-containing species to the main chemical species in one or more forms of metal or metalloid hydroxides, carbonates, oxyhydroxyl groups, and hydrates, an oxidizing agent is added to the medium. A sub-step of introducing an oxidant wherein the target substance-containing species is different from one or more of the metal or metalloid hydroxide, carbonate, oxyhydroxyl group, and hydrate Sub-steps to implement,
Thereafter, in order to remove one or more of the metal or metalloid hydroxide, carbonate, oxyhydroxyl group, and hydrate in the medium, the rare earth element-containing additive is added to the metal or metal 25. The method of claim 24, comprising the step of contacting with one or more of a metalloid hydroxide, carbonate, oxyhydroxyl group, and hydrate. The contacting step comprises:
In order to reduce a target substance-containing species containing the metal or metalloid in the form of one or more of a metal or metalloid hydroxide, carbonate, oxyhydroxyl group, and hydrate to a main chemical species A sub-step of introducing a reducing agent into the medium, wherein the target substance-containing species is one or more of the metal or metalloid hydroxide, carbonate, oxyhydroxyl group, and hydrate Different from the sub-step of introducing a reducing agent,
Thereafter, in order to remove one or more of the metal or metalloid hydroxide, carbonate, oxyhydroxyl group, and hydrate in the medium, the rare earth element-containing additive is added to the metal or metal 25. The method of claim 24, comprising the step of contacting with one or more of a metalloid hydroxide, carbonate, oxyhydroxyl group, and hydrate. The contacting step comprises:
To convert a target substance-containing species comprising one or more of metal or metalloid hydroxides, carbonates, oxyhydroxyl groups, and hydrates into the main chemical species containing the metal or metalloid A sub-step of introducing a base and / or base equivalent into the medium, wherein the target substance-containing species is selected from the metal or metalloid hydroxides, carbonates, oxyhydroxyl groups, and hydrates Substeps of introducing both bases and / or base equivalents different from one or more of:
Thereafter, in order to remove one or more of the metal or metalloid hydroxide, carbonate, oxyhydroxyl group, and hydrate in the medium, the rare earth element-containing additive is added to the metal or metal 25. The method of claim 24, comprising the step of contacting with one or more of a metalloid hydroxide, carbonate, oxyhydroxyl group, and hydrate. The contacting step comprises:
To convert a target substance-containing species comprising one or more of metal or metalloid hydroxides, carbonates, oxyhydroxyl groups, and hydrates into the main chemical species containing the metal or metalloid A sub-step of introducing an acid and / or an acid equivalent into the medium, wherein the target substance-containing species is selected from the group consisting of the metal or metalloid hydroxide, carbonate, oxyhydroxyl group, and hydrate A sub-step of introducing an acid and / or an acid equivalent different from one or more of
Thereafter, in order to remove one or more of the metal or metalloid hydroxide, carbonate, oxyhydroxyl group, and hydrate in the medium, the rare earth element-containing additive is added to the metal or metal 25. The method of claim 24, comprising the step of contacting with one or more of a metalloid hydroxide, carbonate, oxyhydroxyl group, and hydrate.   25. The method of claim 24, wherein the rare earth-containing additive is water soluble.   The method according to claim 24, wherein the rare earth-containing additive is water-insoluble.