Classifications

• • C—CHEMISTRY; METALLURGY
  • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
  • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
  • C04B7/00—Hydraulic cements
  • C04B7/24—Cements from oil shales, residues or waste other than slag
  • C04B7/26—Cements from oil shales, residues or waste other than slag from raw materials containing flue dust, i.e. fly ash
• • C—CHEMISTRY; METALLURGY
  • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
  • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
  • C04B20/00—Use of materials as fillers for mortars, concrete or artificial stone according to more than one of groups C04B14/00 - C04B18/00 and characterised by shape or grain distribution; Treatment of materials according to more than one of the groups C04B14/00 - C04B18/00 specially adapted to enhance their filling properties in mortars, concrete or artificial stone; Expanding or defibrillating materials
  • C04B20/02—Treatment
  • C04B20/023—Chemical treatment
• • C—CHEMISTRY; METALLURGY
  • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
  • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
  • C04B28/00—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
  • C04B28/02—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing hydraulic cements other than calcium sulfates
  • C04B28/04—Portland cements
• • C—CHEMISTRY; METALLURGY
  • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
  • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
  • C04B7/00—Hydraulic cements
  • C04B7/345—Hydraulic cements not provided for in one of the groups C04B7/02 - C04B7/34
• • C—CHEMISTRY; METALLURGY
  • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
  • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
  • C04B7/00—Hydraulic cements
  • C04B7/36—Manufacture of hydraulic cements in general
  • C04B7/43—Heat treatment, e.g. precalcining, burning, melting; Cooling
• • C—CHEMISTRY; METALLURGY
  • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
  • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
  • C04B7/00—Hydraulic cements
  • C04B7/36—Manufacture of hydraulic cements in general
  • C04B7/43—Heat treatment, e.g. precalcining, burning, melting; Cooling
  • C04B7/47—Cooling ; Waste heat management
• • C—CHEMISTRY; METALLURGY
  • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
  • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
  • C04B2103/00—Function or property of ingredients for mortars, concrete or artificial stone
  • C04B2103/0068—Ingredients with a function or property not provided for elsewhere in C04B2103/00
  • C04B2103/0088—Compounds chosen for their latent hydraulic characteristics, e.g. pozzuolanes
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
  • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
  • Y02P40/00—Technologies relating to the processing of minerals
  • Y02P40/10—Production of cement, e.g. improving or optimising the production methods; Cement grinding
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
  • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
  • Y02P40/00—Technologies relating to the processing of minerals
  • Y02P40/10—Production of cement, e.g. improving or optimising the production methods; Cement grinding
  • Y02P40/121—Energy efficiency measures, e.g. improving or optimising the production methods
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
  • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
  • Y02P40/00—Technologies relating to the processing of minerals
  • Y02P40/10—Production of cement, e.g. improving or optimising the production methods; Cement grinding
  • Y02P40/18—Carbon capture and storage [CCS]
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
  • Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
  • Y02W30/00—Technologies for solid waste management
  • Y02W30/50—Reuse, recycling or recovery technologies
  • Y02W30/91—Use of waste materials as fillers for mortars or concrete

Definitions

• the invention generally relates to a method for preparing a carbonatable clinker material by melting a raw mix, to carbonatable clinkers and carbonatable binders obtained thereof.
• Cements enable the manufacture of building materials such as mortar, concrete or stucco, in which they act as the 'glue' that gives strength to structures.
• Mortar is a mixture of cement and sand whereas concrete also includes coarse aggregates. These aggregates can be made out of lots of different materials, but the vast majority of aggregate is just sand, gravel, and rocks, which are cheap, plentiful, and easily obtained from nature.
• Cement on the other hand, is a man-made material that requires energy-intensive steps and causes large greenhouse gases emissions.
• Portland cement is the most common type of cement in general use around the world.
• the first step in the manufacture of Portland cement is to combine a variety of raw ingredients so that the resulting cement will have the desired chemical composition. These components are ground, blended, and then the resulting raw mix is fed into a cement kiln to produce clinker.
• the production of Portland cement requires temperatures of about 1450°C and is typically accomplished by using a rotary kiln.
• Rotary kilns comprise a long cylindrical kiln that slopes downward and rotates slowly. The raw mix enters at the upper end of the rotary kiln and slowly works its way downward over a period of 20-90 minutes, undergoing several different reactions.
• the final stage in the manufacturing process involves crushing and grinding the clinker into a fine powder.
• Portland cement In the case of Portland cement, a source of calcium sulphate such as gypsum is added. Also, other mineral components may be blended with cement, such as ground limestone, ground granulated blast furnace slag, fly ash, or pozzolans. Beyond Portland-type cements, there are also special cements to serve special construction need, such as calcium aluminate cements. These cements contain between about 40% to 80% per cent weight of Al 2 0 3 , which is much more than in Portland-type cements. These cements have unique properties such as rapid strength development, high temperature resistance or refractory performance which make them the material of choice in specialist applications where the performance of Portland cement is insufficient.
• Such cements are produced not by reactive sintering but by complete melting of adequate raw mixes in melting kilns at temperature of about 1450-1600°C, the resultant product being ground to a fine powder.
• the clinker for Ciment Fondu ® the world's first commercially manufactured calcium aluminate cement and still frequently encountered, is prepared in a production facility using a reverberatory furnace in which the raw materials are melted to form the clinker.
• the energy required to manufacture cement results in very high amounts of C0 2 released in the atmosphere.
• the overall carbon footprint of a typical Portland cement that does not contain other mineral components is about comprised between 800 and 900 kg of C0 2 per ton of cement produced.
• C0 2 greenhouse gas
• the clinker of such carbonatable materials is typically manufactured in rotary kilns from the same raw materials as Portland cement but formulated in different proportions.
• US20160031757 teaches preparation methods of carbonatable calcium silicate clinker.
• it describes the manufacturing of carbonatable clinker materials using a rotary kiln, wherein raw mixes are fired at temperatures ranging 1050°C to 1250°C ([0075] to [0079]).
• this document also describes the manufacturing of carbonatable materials using a melting furnace, in which raw mixes constituted of chemical grade Si0 2 , CaC0 3 and Al 2 0 3 are brought to 1600°C [0087]
• the fusion temperature of such raw mixes is high and therefore has the disadvantage of having a high C0 2 footprint.
• An aim of the present invention is to provide an optimized method for preparing a carbonatable clinker material in a melting kiln, wherein said method is carried out at temperatures below 1600°C.
• a clear advantage of this method is that it requires less energy, thereby lowering C0 2 emissions and decreasing operating costs of cement plants using melting kilns.
• the present invention facilitates the manufacture of carbonatable clinker material in areas where there are no plant cements with a standard rotary kiln.
• Another significant advantage of the method of the invention is its versatility as it can also be carried out in a standard cement plant, because the clinkerisation temperature of the method of the invention is in the range of the normal operating temperature of a cement rotary kiln.
• the raw mixes used in the method of the invention may contain higher content of MgO than the one used in standard carbonatable clinker manufacture.
• the associated advantage is that the method of the invention allows to use raw materials which are generally avoided in the Portland clinker production such as dolomite, and thus allows a better use of quarry resources as well as the use of alternative raw materials such as kiln dust.
• Another aim of the invention is to supply a novel carbonatable clinker material, and carbonatable binder, concrete or mortar obtained thereof.
• the chemical composition of either natural (e.g. raw mix) or synthetic (e.g. clinker) materials may be performed by a well-known method namely X-Ray Fluorescence spectroscopy (XRF).
• XRF X-Ray Fluorescence spectroscopy
• This technique allows to determine both major and minor elements.
• the material sample Prior to oxide analysis by XRF, the material sample is generally submitted to calcination (e.g. ignited at 950°C for 45 minutes) allowing volatile substances to escape, until its mass ceases to change.
• Loss on ignition (LOI) corresponding to sample mass prior to calcination m 0 minus the sample mass after calcination mi is then determined.
• the volatile materials lost usually consist of "combined water” (hydrates and labile hydroxy-compounds) and carbon dioxide from carbonates.
• LOI is reported as part of oxide composition without specifying its chemical nature.
• Na 2 0 equivalent (wt.%) Na 2 0 (wt.%) + (62.0/94.2) x K 2 0 (wt.%))
• alkali content of a clinker or cement can be expressed as "total soluble alkali" as detailed below.
• the chemical composition of the raw mix may be defined with its oxide composition, meaning that the raw mix chemical composition is defined by giving the oxide composition that the raw mix will comprise after calcination.
• the raw mix chemical composition is defined by giving the oxide composition that the raw mix will comprise after calcination.
• calcium carbonates and calcium and magnesium carbonates are respectively calcium oxide and magnesium oxide precursors as they are contained in the raw materials and are completely dissociated at temperatures between 500-900°C, as per following reactions:
• the amount of matter entering the process i.e. raw mix injected in the kiln in form of powder or slurry
• the amount of matter leaving the process i.e. clinker material and if so dusts, vapor and fumes released by the kiln.
• the oxide composition of the clinker material is a fair estimate of the calcined raw mix (i.e. raw mix after calcination) oxide composition.
• a person skilled in the art may easily, given the oxide composition of a calcined raw mix and the chemical composition of the different raw materials at his disposal, calculate the adequate composition of raw mixes allowing obtaining the desired clinker material.
• a first object of the invention is a carbonatable clinker material comprising at least 60 wt.% of amorphous phase, advantageously at least 80 wt.% of amorphous phase, more advantageously at least 99 wt.% of amorphous phase, more advantageously 100 wt.% of amorphous phase, compared to the total weight of the carbonatable clinker material, wherein said material has the following oxide composition:
• the total soluble alkali is measured using the following method: a) clinker material is ground until reaching a Blaine fineness of 5000 +/- 100 cm 2 /g- b) a 2.000 g sample of the ground carbonatable clinker of step a) is weighed in 100 mL of deionized water;
• step c) The mixture of step c) is filtered to remove all solid particles
• Soluble sodium oxide (Na 2 0) S oi_ and potassium oxide (K 2 0) S OL contents are measured by flame atomic absorption spectroscopy
• the oxides may be contained in the amorphous phase of the clinker, or in its crystalline phase, or distributed in both types of fractions.
• the molar amounts of CaO, MgO, Na 2 0, K 2 0, Si0 2 used to determine the (CaO + MgO + Na 2 0 + K 2 0)/Si0 2 molar ratio may be obtained using the chemical composition of the clinker material as measured by X-Ray Fluorescence.
• the carbonatable clinker material comprises from 35 to 50 wt.% of CaO, more advantageously 40 to 48 wt.% of CaO, relative to the total weight of clinker.
• the carbonatable clinker material comprises from 1 to 15 wt.% of MgO, more advantageously 1.5 to 10 wt.% of MgO, relative to the total weight of clinker.
• the carbonatable clinker material may for example comprise from 1 to 5 wt.% of MgO,
• the carbonatable clinker material comprises from 2 to 6 wt.% of MgO. These ranges are applicable to all the embodiments of the invention.
• the carbonatable clinker material comprises from 0.1 to 5.0 wt.% of Na 2 0, more advantageously 0.2 to 3.5 wt.% of Na 2 0, relative to the total weight of clinker.
• the carbonatable clinker material comprises from 0.1 to 5.0 wt.% of K 2 0, more advantageously 0.2 to 3.5 wt.% of K 2 0, relative to the total weight of clinker.
• the carbonatable clinker material comprises from 0.2 to 5.0 wt.% of Na 2 O eq ., more advantageously 0.5 to 4.0 wt.% of Na 2 O eq ., relative to the total weight of clinker.
• the carbonatable clinker material from 35 to 50 wt.% of silicon oxide Si0 2 , advantageously 37 to 48 wt.% of Si0 2 , relative to the total weight of clinker.
• the clinker material of the invention comprises at least at least 60 wt.%, advantageously at least 80 wt.%, more advantageously at least 99 wt.% of amorphous phase, more advantageously 100 wt.%, compared to the total weight of the carbonatable clinker material, wherein the clinker material comprises, relative to the total weight of clinker:
• the clinker material of the invention comprises at least at least 60 wt.%, advantageously at least 80 wt.%, more advantageously at least 99 wt.% of amorphous phase, more advantageously 100 wt.%, compared to the total weight of the carbonatable clinker material, wherein the clinker material comprises, relative to the total weight of clinker:
• calcium oxide content, magnesium oxide content, potassium oxide, sodium oxide content , and silicon dioxide content in the clinker are such that the molar ratio (CaO + MgO + Na 2 0 + K 2 0)/Si0 2 in the clinker ranges from 0.7 to 1.8, more preferentially from 0.9 to 1.6.
• the carbonatable clinker material is in the form of a powder, preferably a powder having a Blaine specific surface area of about 3000 to 7000 cm 2 /g, more preferentially of about 4000 to 6000 cm 2 /g.
• the clinker material is suitable for carbonation with C0 2 at a temperature of about 20°C to 90°C.
• the clinker material forms carbonates, preferably CaC0 3 , with a mass gain of about 20% or more.
• the mass gain reflects the net sequestration of C0 2 in the carbonated products.
• the clinker material is suitable for carbonation with C0 2 at a temperature of 20°C to 90°C (e.g.
• the ground clinker material has a low amount of soluble alkali.
• the Applicant believes that the alkali are mostly within the amorphous phases and are therefore insoluble, with the advantage of preventing their possible leaching from the binder and/or concretes of the invention.
• the clinker material as defined below may be used as a carbonatabie binder.
• the clinker may also comprise from 0.1 to 10 wt.% of minor and trace elements such as Fe 0 3 , AI O , Ti0 2 , F, Cl, P Os, B 0 3 , BaO, or S0 3 .
• a second object of the invention is a method for preparing a carbonatabie according to the first object of the invention comprising:
• T m sufficient for said raw mix to be completely in a molten state means that temperature T m must be sufficient or equal to the melting point T fm of said raw mix.
• step i) may be carried out at temperature T m equal or superior to 1250°C and strictly inferior to 1600°C.
• step i) may be carried out at temperature T m ranging from 1250°C to 1500°C, advantageously from 1300°C to 1500°C, more advantageously from 1350°C to
• the time required to completely melt the raw mix varies with the type and size of the kiln.
• the cooling down of step ii) comprises suddenly lowering the temperature of the molten mixture obtained at end of step i) at a temperature below the crystallization temperature.
• step ii) is carried out by air or water quenching the molten mixture, preferably is carried out by air quenching the molten mixture.
• the method may further comprise a step iii) after step ii), of grinding the clinker material obtained at the end of step ii) according to the invention.
• Step i) may be carried out in a melting furnace, preferably a melting furnace habitually used for melting a metal such as a crucible furnace, a cupola furnace, an induction furnace, shaft kiln, arc melting furnace or a reverberatory furnace.
• a melting furnace preferably a melting furnace habitually used for melting a metal such as a crucible furnace, a cupola furnace, an induction furnace, shaft kiln, arc melting furnace or a reverberatory furnace.
• step i) is carried out in a reverberatory furnace.
• a reverberatory furnace has for example a L-section, that is to say a vertical part and a horizontal part which communicate with each other.
• the vertical part may reach as high as several meters.
• raw materials are introduced into the melting furnace through an aperture located on the upper portion of the vertical part.
• These raw materials are loaded into the furnace so as to fully occupy the volume of this vertical part and they thus form, at a junction between horizontal part and vertical part, a slope-shaped pile of raw materials. The latter is then attacked by a flame located in the furnace horizontal part, in front of the slope-shaped pile.
• the solid material may be heated at a temperature above 1250°C, 1300°C, 1350°C, or even above 1450° C up to 1600°C. It thus brings the required thermal energy so as to make raw materials melt, thus forming a material liquid bath.
• the raw material temperature in the furnace typically reaches up to 1250°C, 1300°C, 1350°C, 1450°C.
• the materials, once melted, are discharged through a tap hole located in the horizontal part of the furnace. During the process, combustion gases develop and go a counter-current path as compared to the raw materials. They are then discharged through a gas stack located in the upper portion of the furnace vertical part.
• the firing of the raw materials sources of at least calcium, silicon, aluminium, magnesium, sodium and potassium alone or together, and iron oxides is effected at a temperature ranging preferably from 1250°C to 1500°C, advantageously from 1300°C to 1500°C, more advantageously from 1350°C to 1450°C, for a time period ranging preferably from 5 to 12 hours, in particular from 6 to 10 hours.
• a clinker material is thus obtained.
• this clinker is quenched immediately after the firing, so as to reduce the temperature of the clinker to a temperature below the crystallization temperature and to obtain an amorphous clinker.
• step i) may also be carried out in a rotary kiln, preferably a rotary kiln habitually used for manufacturing Portland cement.
• the method of the invention may further comprise a step i 0 ) before step i), of preparing a raw mix according to the invention, said raw mix being in the solid state (e.g. in the form of granular material).
• the step i 0 ) may be carried out by way of separately or simultaneously crushing or milling the source of oxides, and intermixing thereof in the case of separate grinding. Said grinding can be performed either in the presence of water (wet grinding) or without it (dry grinding).
• the raw mix of the invention comprises calcium, silicon, aluminium, iron sodium oxide, potassium oxide, and magnesium oxides or precursors thereof.
• the raw mix of the invention comprises a (CaO + MgO + Na 2 0 + K 2 0)/Si0 2 molar ratio ranging from 0.7 to 1.8, preferentially from 0.9 to 1.6.
• oxides may be provided in the raw mix by oxide precursors which are natural raw materials typical of the cement industry, such as limestone, marl, sand, dolomite, and clays.
• the oxides may also be provided by alternative suited raw materials selected from olivine, wollastonite, rankinite, monticellite, fosterite, serpentinite, talc, feldspar, anorthite, anorthosite, albite, microcline, sanidine, pyroxene, plagioclase, fluorspar and artificial ones which may include recycled concrete fines, asbestos fibres, cement clinker, cement kiln dust, recycled glass, blast furnace slag or steel slag.
• the raw mix of the invention advantageously comprises at least a raw material selected from the alternative raw materials defined above, preferably comprises cement kiln dust.
• a raw material that contains calcium oxide precursors may be selected among limestone, marl, calcite, aragonite, shale, or sea shells.
• a raw material that contains silicon dioxide precursors may be selected among clay, marl, sand, shale, fly ash, rice hull ash, slag, recycled glass or recycled concrete.
• a raw material that contains aluminium oxide precursors may be selected among clay, shale, fly ash, red mud or aluminium ore refuse.
• a raw material that contains iron oxide precursors may be selected among clay, iron ore, mill scale, shale, or blast furnace dust.
• a raw material that contains alkali oxide precursors may be selected among feldspar, albite, sanidine, microcline, plagioclase or recycled glass.
• Carbonatable binder composition, concrete, mortar, element for construction
• a third object of the invention is a carbonatable binder comprising a clinker material as defined in the second object of the invention.
• the carbonatable binder of the invention advantageously is in a powdery or granular form.
• the carbonatable binder advantageously comprise the clinker material of the invention in the form of a powder, preferably a powder having a Blaine specific surface area of about 3000 to 7000 cm 2 /g, more preferentially of about 4000 to 6000 cm 2 /g.
• the ground carbonatable clinker material may advantageously have a mean particle size from about 1 pm to about 100 pm.
• the carbonatable binder may also comprise additives such as set-retarding of hydration-controlling compounds of admixtures.
• the compounds that may be used are for example, lignosulfonates, hydroxycarboxylic acids and salts thereof, phosphonates, sugars, borates, phosphates, or mixtures thereof.
• Another object of the invention is a carbonatable composition comprising the carbonatable binder of the invention and sand and/or aggregates.
• the carbonatable composition of course comprises the clinker material of the invention.
• the carbonatable composition may optionally comprise sand.
• the sand is advantageously graded at (min/max) 0/4 mm, 0/2 mm, 0/8 mm, 2/4 mm or 2/8 mm.
• the sand is a siliceous sand such as quartz sand, a calcined or non- calcined bauxite sand, a silica-calcareous sand or mixtures thereof.
• the carbonatable composition may optionally comprise aggregates.
• Exemplary aggregates include inert materials such as trap rock, construction sand, pea- gravel.
• lightweight aggregates such as perlite or vermiculite may also be used as aggregates.
• Materials such as industrial waste materials (e.g., fly ash, slag, silica fume) may also be used as fine fillers.
• the plurality of aggregates may have any suitable mean particle size and size distribution.
• the plurality of aggregates is the mix of step a) advantageously has a mean particle size in the range from about 0.25 mm to about 25 mm, for example 5 mm to 20 mm, 5 mm to 18 mm, 5 mm to 15 mm, 5 mm to 12 mm, 7 mm to 20 mm, 10 mm to 20 mm.
• the carbonatable composition may advantageously comprise both sand and aggregates as defined hereinabove.
• a fourth object of the invention is a concrete or mortar comprising a carbonatable binder as defined in the third object of the invention.
• a fifth object of the invention is an element for construction or building comprising a carbonated concrete or mortar according to the fourth object of the invention.
• the element of the invention does not present efflorescence.
• a sixth object of the invention is a process for preparing a concrete or mortar according to the fourth object of the invention, said process comprising: a) providing a carbonatable clinker material as disclosed above or a carbonatable composition according to the invention;
• the carbonatable composition comprises the carbonatable clinker material according to the invention mixed with sand and/or aggregates as defined herein above.
• the carbonatable clinker material or composition is advantageously cured by reaction with carbon dioxide in any of its forms such as gaseous C0 2 in the presence of water, C0 2 in the form of carbonic acid, H 2 C0 3 , or in other forms that permit the reaction of C0 2 with the carbonatable clinker the invention.
• the curing process sequesters carbon dioxide gas within the cured material, thus providing obvious environmental benefits.
• the C0 2 curing regime is sufficient to cause the setting of the carbonatable clinker material or composition provided in step a).
• the setting of the carbonatable clinker material is only very minimally or not at all due to the hydration of the carbonatable clinker material.
• the development of the mechanic properties of concretes or mortars of the invention is primarily due to reaction with carbon dioxide, for example at least 50%, preferably at least 80%, even more preferably at least 90%, for example 95% or 99% of the development of the mechanic properties is due to reaction with carbon dioxide.
• the mass gain of the clinker material or composition between the end and the beginning of step b) advantageously reflects the net sequestration of C0 2 in the carbonated products and is of 10% or more (e.g. 15% or more, 20% or more, 25% or more, 30% or more).
• the carbonatable clinker material or composition is placed in a mold before being subjected to the C0 2 curing regime.
• the carbonatation may for example be carried via a controlled Hydrothermal Liquid Phase Sintering (HLPS) process.
• HLPS Hydrothermal Liquid Phase Sintering
• the carbonatable clinker material or composition is carbonated at a temperature of 20°C to 90°C (e.g. 40°C to 90°C, 50°C to 90°C, 60°C to 90°C, 30°C to 80°C; 30°C to 70°C, 20°C to 60°C, 20°C to 50°C).
• Carbonates are formed with a mass gain of 10% or more (e.g. 15% or more, 20% or more, 25% or more, 30% or more).
• Such carbonatation is advantageously carried out under a stirred C0 2 atmosphere partially saturated with water.
• XRF X-Ray Fluorescence spectroscopy
• the X-Ray Fluorescence spectroscopy analyses were performed using apparatus sold under the trade name FX Magix PRO, by the company PANanalyticalX.
• the X-Ray Diffraction analyses were performed using apparatus sold under the trade name Philips X'Pert Pro, by the company PANanalytical.
• the mixing of the raw mix was performed using apparatus under the trade name Turbula 2L type T2C, manufactured by the company Willy A. Bachofen (WAB).
• the melting of raw mixes was performed using apparatus sold under the trade name Thermoconcept HTL10/17, manufactured by the company CERADEL.
• Example 1 Preparation of carbonatable clinker material CM1, CM2, CM3, CM4,
• CM1, CM2, CM3, CM4, CM5, CM6 and CM7 emerged in form of a mass of solid glass.
• the clinker material is then ground with a laboratory closed ball mill capable of grinding up to 1 kg of material until reaching a Blaine fineness of 5000 +/- 100 cm 2 /g-
• Table 2 Chemical composition of the clinker materials (as measured by X-Ray Fluorescence)
• Table 2 shows the chemical composition of clinkers CM1, CM2, CM3, CM4, CM5, CM6 and CM7 according to the invention as determined by X-Ray Fluorescence spectroscopy.
• Table 3 Quantification of amorphous content in the clinker materials (as measured by X-Ray Diffraction).
• Table 3 lists X-Ray Diffraction (XRD) quantification of mineralogical phases present in ground clinker material CM1, CM2, CM3, CM4, CM5, CM6 and CM7.
• XRD X-Ray Diffraction
• CM1 comprise an amorphous phase as well as a crystalline merwinite phase
• CM2, CM3, CM4, CM5, CM6 and CM7 are exclusively amorphous.
• the total soluble alkalis (Na 2 O eq .)soL of the ground carbonatable clinker are expressed in weight percentage of the amount of clinker and are measured according the following laboratory protocol:
• Soluble sodium oxide (Na 2 0) S o L and potassium oxide (K 2 0) S OL contents are then measured by flame absorption spectroscopy in the solution obtained as described above.
• Total soluble alkalis (Na 2 O eq .)so L is then calculated according to the formula:
• Such mortar compositions were then subjected to a C0 2 curing regime in a custom- made reactor.
• the samples were carbonated at 60°C under a stirred C0 2 atmosphere partially saturated with water.

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• 2018
  • 2018-12-21 EP EP18306825.3A patent/EP3670467A1/de not_active Withdrawn
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