Classifications

• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
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  • B01J20/02—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
  • B01J20/0203—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising compounds of metals not provided for in B01J20/04
  • B01J20/0233—Compounds of Cu, Ag, Au
  • B01J20/0237—Compounds of Cu
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D15/00—Separating processes involving the treatment of liquids with solid sorbents; Apparatus therefor
  • B01D15/08—Selective adsorption, e.g. chromatography
  • B01D15/10—Selective adsorption, e.g. chromatography characterised by constructional or operational features
  • B01D15/20—Selective adsorption, e.g. chromatography characterised by constructional or operational features relating to the conditioning of the sorbent material
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
  • B01D53/02—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
  • B01D53/34—Chemical or biological purification of waste gases
  • B01D53/46—Removing components of defined structure
  • B01D53/64—Heavy metals or compounds thereof, e.g. mercury
• • B—PERFORMING OPERATIONS; TRANSPORTING
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  • B01J20/02—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
  • B01J20/0203—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising compounds of metals not provided for in B01J20/04
  • B01J20/0222—Compounds of Mn, Re
• • B—PERFORMING OPERATIONS; TRANSPORTING
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  • B01J20/02—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
  • B01J20/0203—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising compounds of metals not provided for in B01J20/04
  • B01J20/0225—Compounds of Fe, Ru, Os, Co, Rh, Ir, Ni, Pd, Pt
  • B01J20/0229—Compounds of Fe
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
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  • B01J20/02—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
  • B01J20/0203—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising compounds of metals not provided for in B01J20/04
  • B01J20/0262—Compounds of O, S, Se, Te
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
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  • B01J20/02—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
  • B01J20/0203—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising compounds of metals not provided for in B01J20/04
  • B01J20/0274—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising compounds of metals not provided for in B01J20/04 characterised by the type of anion
  • B01J20/0285—Sulfides of compounds other than those provided for in B01J20/045
• • B—PERFORMING OPERATIONS; TRANSPORTING
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  • B01J20/02—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
  • B01J20/06—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising oxides or hydroxides of metals not provided for in group B01J20/04
• • B—PERFORMING OPERATIONS; TRANSPORTING
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  • B01J20/06—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising oxides or hydroxides of metals not provided for in group B01J20/04
  • B01J20/08—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising oxides or hydroxides of metals not provided for in group B01J20/04 comprising aluminium oxide or hydroxide; comprising bauxite
• • B—PERFORMING OPERATIONS; TRANSPORTING
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  • B01J20/28—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof characterised by their form or physical properties
  • B01J20/28002—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof characterised by their form or physical properties characterised by their physical properties
  • B01J20/28004—Sorbent size or size distribution, e.g. particle size
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
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  • B01J20/28014—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof characterised by their form or physical properties characterised by their form
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
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  • B01J20/28—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof characterised by their form or physical properties
  • B01J20/28014—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof characterised by their form or physical properties characterised by their form
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• • B—PERFORMING OPERATIONS; TRANSPORTING
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  • B01J20/28045—Honeycomb or cellular structures; Solid foams or sponges
• • B—PERFORMING OPERATIONS; TRANSPORTING
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• • B—PERFORMING OPERATIONS; TRANSPORTING
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• • B—PERFORMING OPERATIONS; TRANSPORTING
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• • B—PERFORMING OPERATIONS; TRANSPORTING
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• • B—PERFORMING OPERATIONS; TRANSPORTING
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• • B—PERFORMING OPERATIONS; TRANSPORTING
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• • B—PERFORMING OPERATIONS; TRANSPORTING
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• • B—PERFORMING OPERATIONS; TRANSPORTING
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• • C—CHEMISTRY; METALLURGY
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  • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
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  • B01D2255/20761—Copper
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D2257/00—Components to be removed
  • B01D2257/60—Heavy metals or heavy metal compounds
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D2257/00—Components to be removed
  • B01D2257/60—Heavy metals or heavy metal compounds
  • B01D2257/602—Mercury or mercury compounds
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
  • B01J20/30—Processes for preparing, regenerating, or reactivating
  • B01J20/32—Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J2220/00—Aspects relating to sorbent materials
  • B01J2220/50—Aspects relating to the use of sorbent or filter aid materials
  • B01J2220/56—Use in the form of a bed
• • C—CHEMISTRY; METALLURGY
  • C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
  • C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
  • C02F2101/00—Nature of the contaminant
  • C02F2101/10—Inorganic compounds
  • C02F2101/20—Heavy metals or heavy metal compounds
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
  • C10L2290/00—Fuel preparation or upgrading, processes or apparatus therefore, comprising specific process steps or apparatus units
  • C10L2290/54—Specific separation steps for separating fractions, components or impurities during preparation or upgrading of a fuel
  • C10L2290/542—Adsorption of impurities during preparation or upgrading of a fuel

Definitions

• This invention relates to sorbents and in particular to metal sulphide absorbents suitable for capturing heavy metals, such as mercury, arsenic and antimony, from fluid streams.
• Mercury is found in small quantities in fluid streams such as hydrocarbon or other gas and liquid streams.
• Arsenic may also me found in small quantities in hydrocarbon streams.
• US 4094777 discloses the use of a pre-sulphided absorbent comprising copper sulphide for the absorption of mercury from a natural gas stream containing mercury.
• the sorbent is prepared by mixing a copper compound such as powdered copper hydroxycarbonate (also known as basic copper carbonate) with a support or dispersion material, for example a cement, and forming extrudates or granules.
• the sorbent is prepared by impregnation of a support, such as alumina spheres, with a solution of a soluble compound of copper such as copper nitrate.
• the copper compound in the granules, extrudates or support is sulphided using hydrogen sulphide or a solution of a sulphide in water or in an organic solvent.
• Impregnated materials such as copper-nitrate impregnated materials can require high sulphiding temperatures, or the addition of silver compounds in order to be fully sulphided, both of which are undesirable.
• the invention provides a method for preparing a sorbent composition, comprising the steps of:
• the method may further comprise the step of applying one or more sulphur compounds to effect sulphidation of the copper compound to form copper (II) sulphide, CuS.
• the invention further provides a sorbent composition obtainable by this method, comprising a sulphided copper compound in the form of a layer on the surface of a support material.
• the invention further provides a process for removing a heavy metal from a process fluid comprising contacting a heavy metal-containing -containing process fluid with the sulphided sorbent.
• sorbent we include adsorbent and absorbent.
• heavy metal used herein means mercury, arsenic, lead, cadmium and antimony, but the sorbent of the present invention is particularly useful for removing mercury and arsenic, especially mercury from fluid streams.
• the copper compound should be sulphidable, i.e. reactive with sulphur compounds to form copper (II) sulphide, CuS.
• Suitable copper compounds are one or more of copper
• copper compounds are copper carbonate compounds, such as basic copper carbonate. Copper nitrate and sulphate are less preferred due to the evolution of HNO 3 or H 2 SO 4 compounds during any subsequent sulphiding step.
• the copper content of the sorbent of the present invention is relatively low and is preferably in the range 0.5-20% by weight (expressed as copper present in the unsulphided material), more preferably 0.75-10% by weight, most preferably 0.75-5.0% by weight. Although this level is less than half and in some cases less than a third of the copper in granulated materials, the effectiveness has surprisingly been found to match these products in terms of mercury captured.
• the total sulphidable metal content of the sorbent, other than copper is preferably ⁇ 5% by weight. This is so that the corresponding water-soluble metal sulphates are formed in sufficiently low levels not to cause an increase in pressure drop and deactivation as a result of dissolution-re-deposition and agglomeration during use where the process fluids contain free water.
• the total metal sulphide content in the sulphided sorbent, other than copper is ⁇ 1 % wt, more preferably ⁇ 0.5% wt, especially ⁇ 0.1 % wt.
• the contaminant metal sulphide may be one or more of calcium sulphide, zinc sulphide, iron sulphide, nickel sulphide, chromium sulphide and manganese sulphide. They may be introduced by contamination of the copper compound or support material.
• the low contaminant metal sulphide level may be achieved by the selection of high purity copper compound and support, and by the exclusion of contaminant metal compounds from the composition.
• the copper compound is present as a layer on the surface of the support.
• the thickness of the layer in the dried material is in the range 1 to 200 ⁇ m (micrometres), but preferably is in the range 1-150 micrometres, more preferably 1-100 micrometres, particularly 1-50 micrometres. Thinner layers make more efficient use of the applied copper. Sulphiding will typically leave the layer thickness unchanged or slightly thinner depending on the copper compound.
• the copper compound layer in the sorbent of the present invention may be readily fully sulphided.
• the support material may be a ceramic or metal but preferably comprises an oxidic support such as an alumina, hydrated alumina, titania, zirconia, silica or aluminosilicate, or a mixture of two or more of these.
• the support has a relatively high surface area and porosity so that the surface area of the resulting layer may be maximised.
• the support has a BET surface area of 10-330 m 2 .g " ⁇ preferably 100-330 m 2 .g " ⁇ more preferably 130-330 m 2 .g ⁇ ⁇
• the pore volume is preferably 0.3-0.9 cm 3 .g "1 , more preferably 0.4-0.9 cm 3 .g "1 .
• the support may be macroporous, mesoporous or microporous but is preferably macroporous, i.e. it has an average pore diameter >50 nm, or mesoporous, i.e. is has an average pore diameter in the range 2-50 nm. In such materials preferably >50% of the pore volume arises from such pores. Macroporous materials are useful in the present invention because of their ability to hold copper compounds on their surface.
• the BET surface area may be conveniently measured using nitrogen physisorption. Pore volumes may also be determined using nitrogen physisorption, but in the present invention as the pore volumes are relatively large, mercury porosimetry may be more suitably used. Pore diameters may also be determined using these techniques.
• Preferred supports are aluminas such as gamma, theta and delta aluminas.
• the support is a gamma alumina.
• the copper compound is applied to the surface of the support. If the support is porous, some of the copper compound may enter pores at or near the surface of the support. However the thickness of the layer of copper compound in the dried coated support should remain in the range 1-200 ⁇ m.
• the support may be provided as a foam, monolith or honeycomb, or as a coating on a structured packing. Such supports offer a reduced pressure drop in sorbent vessels compared to spherical granulated sorbents.
• foam supports are described in EP-A-0260826.
• the support may be in the form of shaped particulate unit selected from the group consisting of spheres, rings (e.g. Rashig rings), trilobes, quadralobes, and cylinders, which may be lobed or fluted, having between 2 and 10 holes extending therethrough. Shaped supports that provide the combination of reduced pressure drop combined with high strength are preferred. 4-hole cylinders, and rings are particularly preferred.
• Particulate shaped units desirably have a minimum dimension, which may be the width, diameter or length, in the range 1-50 mm, and an aspect ratio (i.e. width or diameter/length) in the range 0.5-5. Units with a diameter or width in the range 3-10 mm are preferred for industrial scale sorbents, although 1-5 mm units may also be used.
• the layer of copper compounds may be formed on the support in a number of ways.
• a layer of copper carbonate is formed by applying a slurry, e.g. by dipping or spraying the support with a slurry, which may be aqueous or non aqueous, of an insoluble copper compound such as basic copper carbonate.
• the basic copper carbonate may be obtained commercially or prepared freshly by precipitating it from a copper salt solution using an alkaline carbonate precipitant, followed by washing to remove the corresponding alkaline metal salt.
• the basic copper carbonate is dispersed in a liquid medium, which is desirably aqueous.
• the solids content may conveniently be in the range 10- 30% wt.
• Binder materials such as alumina or hydrated alumina sols may be included in the layer and other conventional wash-coat preparation techniques may be applied, such as milling and mixing of the dispersion to achieve the desired particle size prior to coating the support.
• the support may be coated by dipping the support into the slurry dispersion or by spraying the slurry dispersion of the copper carbonate compounds onto the support. Multiple dipping and/or spraying may be applied.
• the slurry may be applied to supports at temperatures in the range 10-95 0 C or higher, preferably 10-50 0 C.
• the pH of the slurry can have an effect on the sulphur capacity and hence mercury capacity of the sorbent.
• the pH of the basic copper carbonate slurry is in the range 5-9.
• the layer of copper compound is formed by applying a solution of a copper ammine compound onto the support and simultaneously or subsequently heating the support to a temperature in the range 50-200°C.
• Copper ammine compounds may be formed by dissolving copper compounds such as basic copper carbonate, copper acetate or copper nitrate in aqueous ammonia solutions optionally in the presence of ammonium salts, using known methods.
• basic copper carbonate may be dissolved in a solution of ammonium carbonate and concentrated ammonia such that the Cu:NH 3 molar ratio is preferably at least 1 :4. Heating the solution causes the evolution of ammonia and the deposition of copper compounds on the surface of the support.
• the use of a heated support that destabilises the copper ammine compound on contact results in the formation of a layer of the copper compound on the surface of the support rather than permitting the copper to diffuse all the way through it.
• the heated support is preferably sprayed with a solution comprising copper ammine carbonate.
• the support may be dipped in the copper ammine compound solution and removed, with heating of the support before or after dipping, although this is less preferred. It is not preferred to form a slurry of the support in the solution of copper ammine compound as, upon heating, this could result in considerable amounts of unsupported copper compounds precipitating out of solution.
• the support is heated to a temperature in the range 50-200 0 C and a solution of copper ammine compound, preferably copper ammine carbonate, sprayed onto the heated support. This immediately forms a thin eggshell layer of copper compound on the surface of the support with evolution of ammonia.
• the coated support is dried prior to sulphiding to remove any solvents that may interfere with the sulphiding reaction, e.g. water.
• the drying temperature is preferably kept ⁇ 200°C, more preferably ⁇ 150°C to avoid bulk decomposition of the copper compounds.
• the coated supports may conveniently be dried at about 70-105°C in air for 1-16 hours.
• the un-dried or dried material may be calcined to convert the copper compounds to copper (II) oxide, e.g. by heating it to a temperature in the range 250-500°C in air or inert gas, this is not necessary, as we have found that the deposited copper compounds may be directly sulphided without this additional step.
• the sulphiding step which converts the copper compounds to copper (II) sulphide, CuS, may be carried out using conventional processes. Hence the sulphiding step may be performed by reacting the copper compound in the layer with a sulphur compound selected from hydrogen sulphide, alkali metal sulphide, ammonium sulphide, elemental sulphur or a polysulphide. Hydrogen sulphide is preferred. Using a hydrogen sulphide-containing gas mixture is considerably easier and faster than using alternatives such as solutions of sulphur or sulphur compounds such as polysulphides. The gas mixture may, if desired, contain other sulphur compounds such as carbonyl sulphide or volatile mercaptans.
• the sulphiding compounds are preferably used in a mixture with other gases. Inert gases such as nitrogen, helium or argon are a convenient means to control the process. Carbon dioxide may also be used.
• the sulphiding gas mixture is preferably free of reducing gases such as hydrogen and carbon monoxide, but these may be present where the sulphiding step is performed at temperatures below 15O 0 C, particularly below 100°C.
• Hydrogen sulphide is preferably provided to the copper carbonate layer in gas streams at concentrations of 0.1 to 5% by volume. Sulphiding temperatures in the range 1-100°C may be used.
• the sulphiding step may be performed on the dried sorbent precursor composition ex-situ in a sulphiding vessel through which a sulphiding agent is passed, or the sulphiding step may be performed in situ, in which case an absorbent precursor is installed and undergoes sulphidation in the vessel in which it is used to absorb heavy metals.
• In-situ sulphiding may be achieved using a sulphiding agent stream or where the stream containing heavy metal also contains sulphur compounds, the heavy metal-containing stream itself. Where such concomitant sulphiding and heavy metal absorption occurs, the amount of sulphur compound that is present depends on the type of sulphur compound and metal compound used. Usually, a
• concentration ratio as defined by the ratio of sulphur compound (expressed as hydrogen sulphide) concentration (v/v) to heavy metal concentration (v/v), of at least one, and preferably of at least 10 is used so that the precursor is sufficiently sulphided. Should the initial concentration of the sulphur compound in the feed stream be below the level necessary to establish the desired ratio of sulphur compound to heavy metal concentration then it is preferred that the concentration of the sulphur compound is increased by any suitable method.
• the sorbent according to the present invention is preferably pre-sulphided where the fluid to be treated contains free water. Pre-sulphiding also avoids problems caused by the change in volume and strength of the sorbent that can accompany the sulphiding step.
• the sulphided sorbents desirably have a BET surface area in the range 10 to 330 m 2 .g “1 , preferably 100 to 330 m 2 .g "1 , more preferably 130 to 330 m 2 .g “1 , and a pore volume of 0.3 to 0.8 cm 3 .g "1 , more preferably 0.4 to 0.7 cm 3 .g "1 .
• the present invention may be used to treat both liquid and gaseous fluids containing heavy metals, particularly mercury and arsenic, especially mercury.
• the fluid is a hydrocarbon stream.
• the hydrocarbon stream may be a refinery hydrocarbon stream such as naphtha (e.g. containing hydrocarbons having 5 or more carbon atoms and a final atmospheric pressure boiling point of up to 204 0 C), middle distillate or atmospheric gas oil (e.g. having an atmospheric pressure boiling point range of 177°C to 343°C), vacuum gas oil (e.g.
• Refinery hydrocarbon steams also include carrier streams such as "cycle oil” as used in FCC processes and hydrocarbons used in solvent extraction.
• the hydrocarbon stream may also be a crude oil stream, particularly when the crude oil is relatively light, or a synthetic crude stream as produced from tar oil or coal extraction for example.
• Gaseous hydrocarbons may be treated using the process of the invention, e.g. natural gas or refined paraffins or olefins, for example.
• Off-shore crude oil and off-shore natural gas streams in particular may be treated with the absorbent of the present invention.
• Contaminated fuels such as petrol or diesel may also be treated.
• the hydrocarbon may be a condensate such as natural gas liquid (NGL) or liquefied petroleum gas (LPG), a liquefied natural gas (LNG) or gases such as a coal bed methane, landfill gas or biogas.
• NNL natural gas liquid
• LPG liquefied petroleum gas
• LNG liquefied natural gas
• gases such as a coal bed methane, landfill gas or biogas.
• Non-hydrocarbon fluids which may be treated according to the invention include carbon dioxide, which may be used in carbonated drinks, enhanced oil recovery processes, in carbon capture and storage, solvents for decaffeination of coffee, flavour and fragrance extraction, solvent extraction of coal etc.
• Fluids such as alcohols (including glycols) and ethers used in wash processes or drying processes (e.g. triethylene glycol, monoethylene glycol, RectisolTM, PurisolTM and SelexolTM), may be treated by the inventive process.
• Mercury may also be removed from amine streams used in acid gas removal units.
• Natural oils and fats such as vegetable and fish oils may be treated by the process of the invention, optionally after further processing such as hydrogenation or transesterification e.g. to form biodiesel.
• Other fluid streams that may be treated include the regeneration gases from dehydration units, such as molecular sieve off-gases, or gases from the regeneration of glycol driers.
• Feed streams which are susceptible to being treated by the absorbents may also include those which inherently contain both heavy metal and a sulphur compound e.g. certain natural gas streams, or a mercury- and/or arsenic- containing stream to which a sulphur compound has been added to effect mercury and arsenic absorption.
• a sulphur compound e.g. certain natural gas streams, or a mercury- and/or arsenic- containing stream to which a sulphur compound has been added to effect mercury and arsenic absorption.
• the present invention is of particular utility where the fluid contains free water, preferably in low levels in the range 0.02 to 1 % vol. Higher levels up to 5% vol may be tolerated for short periods.
• the absorbents of the present invention may be regenerated simply after prolonged exposure to water simply by purging with a dry gas, preferably a dry inert gas such as nitrogen.
• the absorption of mercury is conducted at a temperature below 15O 0 C, preferably at or below 120 0 C in that at such temperatures the overall capacity for mercury absorption is increased. Temperatures as low as 4 0 C may be used to good effect in the present invention. A preferred temperature range is 10 to 60 0 C.
• the mercury may be in the form of elemental mercury, or organomercuric, or organomercurous compounds.
• the present invention is particularly effective in removing elemental mercury although other forms of mercury may be removed for short periods.
• concentration of mercury in a gaseous feed stream is from 0.01 to 1100 ⁇ g/Nm 3 , and more usually between 10 to 600 ⁇ g/Nm 3 .
• the sorbent material may be placed in a sorption vessel and the fluid stream containing heavy metal is passed through it. Desirably, the sorbent is placed in the vessel as one or more fixed beds according to known methods. More than one bed may be employed and the beds may be the same or different in composition.
• the gas hourly space velocity through the absorbent may be in the range normally employed.
• Example 1 Washcoat of basic copper carbonate
• Washcoat preparation Basic copper carbonate (81 g) and Sasol Disperal P3 [a high purity dispersible alumina binder] (9 g) were added to 210 g of demineralised water. The slurry was mixed on a high-speed mixerand milled to obtain the desired particle size. The pH was 5.9 after milling and the particle size (d90) was 4.4 microns.
• Spray Coating 100 g of gamma-, delta-theta-, or alpha-alumina spheres (1 mm diameter) were loaded into a foil-lined pan coater and sprayed with 12 g of washcoat. The support was maintained at 25 - 65°C throughout.
• the coated support was dried for 16 hours at 105 0 C.
• the copper contents of the dried materials were 2.53-3.66% wt.
• Example 2 Copper ammine carbonate [CU(NHJWCOJ)I
• Ammonium carbonate (46.18 g, 0.294 mol) was dissolved in ammonia solution (100 ml, 1.8 mol) under gentle heating. Copper hydroxycarbonate (20.22 g, 9.98 g Cu, 0.17 mol) was added to the ammonium carbonate/ammonia solution and stirred to dissolve. The resulting solution was determined to contain 93.1 g.L "1 copper.
• the coated support was dried for 16 hours at 105 0 C.
• the copper content of the dried materials was 0.98 - 1.46.% wt.
• the coated materials were sulphided using the method of Example 1.
• the copper layer thicknesses on the dried gamma-alumina supported material were measured by EPMA to be about 47 ⁇ m in each case.
• the dried delta-theta alumina support had a copper layer thickness of 41 ⁇ m and the dried alpha alumina support had a copper layer thickness of 28 ⁇ m.
• the experiment was repeated on the gamma alumina support at 12O 0 C but with subsequent calcination at 350 0 C for 2 hours to convert the copper carbonate layer to copper oxide prior to sulphidation using the method of Example 1.
• the copper content of the calcined material was 3.33% wt
• Ammonium acetate (22.64 g, 0.294 mols) was dissolved in ammonia solution (100 ml, 0.9 mol).
• the coated support was dried for 16 hours at 105°C and calcined at 350°C for 2 hours.
• the copper content of the calcined material was 0.78 % wt.
• Example 4 Mercury Static Testing
• Material 1 was analysed to assess porosity in comparison with commercially available granulated copper-zinc oxide/alumina mercury sorbent. The results were as follows;
• Example 5 Flowing Tests
• Material 1 shows superior mercury pickup to the commercially available product, on the inlet bed, at 4.5-5 wt% Hg.
• the profile is also sharp, with the majority of mercury removed by the inlet two beds and the remainder used to remove the mercury down to trace levels.
• Material 6 appears to be reaching saturation at ca. 2.5 wt% Hg, resulting in the different profile shape.
• Two sorbents were prepared according to the method of Example 1 by spray coating a slurry washcoat of basic copper carbonate onto 1 mm gamma alumina spheres.
• the copper contents of both were virtually identical at 3.6% wt.
• the only difference was in the pH of the basic copper carbonate slurry washcoat.
• the pH was 6.0-6.5.
• the pH was raised with tetramethylammonium hydroxide to 10.0 in order to thin the slurry for spray- coating.
• the pH 6-6.5 material proved superior to the material applied at pH 10.
• Washcoat preparation A basic copper carbonate washcoat slurry was prepared according to the method of Example 1.
• a macroporous alpha alumina support material in the form of rings with an outer diameter of 15 mm, surface area 0.4 m 2 /g and pore volume 0.09cm 3 /g was used. 3Og of the alumina support was dipped into the washcoat slurry for 10 minutes to coat the surface. The coated support was dried for 16 hours at 105 0 C. The coated rings were crushed to a particle size of 1-2 mm. The copper content of the dried material was 3.5% wt.
• Example 8 Gas phase testing
• a sulphided sorbent material was prepared according to the method of Example 1.
• the copper content of the sulphided sorbent was approximately 2% wt.
• the ability of the sorbent to capture mercury in the gas phase was determined as follows: 4ml of sorbent material was charged to a glass reactor of internal diameter 5mm. Nitrogen gas containing ⁇ 17ppb (w/v) of elemental mercury vapour was passed downwards over the sorbent material at atmosperic pressure and ambient temperature at a GHSV of 400hr "1 . The test was left under these conditions for 1173 hours. At the end of the test, the reactor was purged with clean nitrogen gas before discharging the sorbent material from the reactor. The sorbent was analysed for mercury content by acid digestion followed by ICP-OES analysis. The results show > 2% by weight mercury capture with a sharp profile through the bed.

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