WO1993002854A1 - Stabilizing inorganic substrates - Google Patents
Stabilizing inorganic substrates Download PDFInfo
- Publication number
- WO1993002854A1 WO1993002854A1 PCT/US1992/006068 US9206068W WO9302854A1 WO 1993002854 A1 WO1993002854 A1 WO 1993002854A1 US 9206068 W US9206068 W US 9206068W WO 9302854 A1 WO9302854 A1 WO 9302854A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- sulfur
- inorganic substrate
- ions
- substrate
- inorganic
- Prior art date
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- 239000000758 substrate Substances 0.000 title claims abstract description 52
- 230000000087 stabilizing effect Effects 0.000 title abstract description 6
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 62
- 239000011593 sulfur Substances 0.000 claims abstract description 55
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 55
- 238000000034 method Methods 0.000 claims abstract description 39
- 229910052751 metal Inorganic materials 0.000 claims abstract description 28
- 239000002184 metal Substances 0.000 claims abstract description 28
- 150000002739 metals Chemical class 0.000 claims abstract description 28
- 229910021645 metal ion Inorganic materials 0.000 claims abstract description 24
- 229910001410 inorganic ion Inorganic materials 0.000 claims abstract description 22
- 238000002844 melting Methods 0.000 claims abstract description 14
- 230000008018 melting Effects 0.000 claims abstract description 14
- 238000002386 leaching Methods 0.000 claims abstract description 12
- YQCIWBXEVYWRCW-UHFFFAOYSA-N methane;sulfane Chemical compound C.S YQCIWBXEVYWRCW-UHFFFAOYSA-N 0.000 claims abstract description 5
- 229920000642 polymer Polymers 0.000 claims abstract description 5
- 239000007787 solid Substances 0.000 claims abstract description 5
- 239000002689 soil Substances 0.000 claims description 31
- 239000004576 sand Substances 0.000 claims description 9
- 239000000126 substance Substances 0.000 claims description 9
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 claims description 6
- 239000004568 cement Substances 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 6
- 229910052785 arsenic Inorganic materials 0.000 claims description 5
- 229910052804 chromium Inorganic materials 0.000 claims description 5
- 239000011651 chromium Substances 0.000 claims description 5
- 239000000428 dust Substances 0.000 claims description 5
- 238000010438 heat treatment Methods 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims description 4
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 3
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 claims description 3
- 239000010881 fly ash Substances 0.000 claims description 3
- 230000008569 process Effects 0.000 abstract description 13
- 150000002894 organic compounds Chemical class 0.000 abstract description 2
- QGJOPFRUJISHPQ-UHFFFAOYSA-N Carbon disulfide Chemical compound S=C=S QGJOPFRUJISHPQ-UHFFFAOYSA-N 0.000 description 15
- 238000006243 chemical reaction Methods 0.000 description 9
- 239000007791 liquid phase Substances 0.000 description 9
- 239000012808 vapor phase Substances 0.000 description 9
- 239000000463 material Substances 0.000 description 8
- 230000006641 stabilisation Effects 0.000 description 8
- 238000011105 stabilization Methods 0.000 description 8
- 239000002699 waste material Substances 0.000 description 8
- 239000012633 leachable Substances 0.000 description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 3
- 229910052793 cadmium Inorganic materials 0.000 description 3
- 239000003518 caustics Substances 0.000 description 3
- 238000000605 extraction Methods 0.000 description 3
- 231100001261 hazardous Toxicity 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 238000009877 rendering Methods 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- -1 PO-i Chemical compound 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000002920 hazardous waste Substances 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- 229910052745 lead Inorganic materials 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229910052753 mercury Inorganic materials 0.000 description 2
- 150000003071 polychlorinated biphenyls Chemical class 0.000 description 2
- 125000005624 silicic acid group Chemical class 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Chemical class [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 description 2
- 229910052814 silicon oxide Inorganic materials 0.000 description 2
- 239000010802 sludge Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 231100000331 toxic Toxicity 0.000 description 2
- 230000002588 toxic effect Effects 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 229910052778 Plutonium Inorganic materials 0.000 description 1
- 238000000137 annealing Methods 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000010426 asphalt Substances 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
- 229910052790 beryllium Inorganic materials 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 150000001642 boronic acid derivatives Chemical class 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- 238000001354 calcination Methods 0.000 description 1
- VTYYLEPIZMXCLO-UHFFFAOYSA-L calcium carbonate Substances [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 239000012159 carrier gas Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000005341 cation exchange Methods 0.000 description 1
- 239000002894 chemical waste Substances 0.000 description 1
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical compound [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 230000009969 flowable effect Effects 0.000 description 1
- 229910052732 germanium Inorganic materials 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 230000003100 immobilizing effect Effects 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 229910052741 iridium Inorganic materials 0.000 description 1
- DCYOBGZUOMKFPA-UHFFFAOYSA-N iron(2+);iron(3+);octadecacyanide Chemical compound [Fe+2].[Fe+2].[Fe+2].[Fe+3].[Fe+3].[Fe+3].[Fe+3].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] DCYOBGZUOMKFPA-UHFFFAOYSA-N 0.000 description 1
- 229910052746 lanthanum Inorganic materials 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 150000002730 mercury Chemical class 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 229910052758 niobium Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 229910052762 osmium Inorganic materials 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 230000008439 repair process Effects 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 229910052706 scandium Inorganic materials 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- 239000002910 solid waste Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- QXKXDIKCIPXUPL-UHFFFAOYSA-N sulfanylidenemercury Chemical compound [Hg]=S QXKXDIKCIPXUPL-UHFFFAOYSA-N 0.000 description 1
- 229910052713 technetium Inorganic materials 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 238000001721 transfer moulding Methods 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229910052727 yttrium Inorganic materials 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A62—LIFE-SAVING; FIRE-FIGHTING
- A62D—CHEMICAL MEANS FOR EXTINGUISHING FIRES OR FOR COMBATING OR PROTECTING AGAINST HARMFUL CHEMICAL AGENTS; CHEMICAL MATERIALS FOR USE IN BREATHING APPARATUS
- A62D3/00—Processes for making harmful chemical substances harmless or less harmful, by effecting a chemical change in the substances
- A62D3/30—Processes for making harmful chemical substances harmless or less harmful, by effecting a chemical change in the substances by reacting with chemical agents
- A62D3/33—Processes for making harmful chemical substances harmless or less harmful, by effecting a chemical change in the substances by reacting with chemical agents by chemical fixing the harmful substance, e.g. by chelation or complexation
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B09—DISPOSAL OF SOLID WASTE; RECLAMATION OF CONTAMINATED SOIL
- B09C—RECLAMATION OF CONTAMINATED SOIL
- B09C1/00—Reclamation of contaminated soil
- B09C1/08—Reclamation of contaminated soil chemically
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F11/00—Treatment of sludge; Devices therefor
- C02F11/004—Sludge detoxification
-
- 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
- C04B28/36—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 sulfur, sulfides or selenium
-
- A—HUMAN NECESSITIES
- A62—LIFE-SAVING; FIRE-FIGHTING
- A62D—CHEMICAL MEANS FOR EXTINGUISHING FIRES OR FOR COMBATING OR PROTECTING AGAINST HARMFUL CHEMICAL AGENTS; CHEMICAL MATERIALS FOR USE IN BREATHING APPARATUS
- A62D2101/00—Harmful chemical substances made harmless, or less harmful, by effecting chemical change
- A62D2101/08—Toxic combustion residues, e.g. toxic substances contained in fly ash from waste incineration
-
- A—HUMAN NECESSITIES
- A62—LIFE-SAVING; FIRE-FIGHTING
- A62D—CHEMICAL MEANS FOR EXTINGUISHING FIRES OR FOR COMBATING OR PROTECTING AGAINST HARMFUL CHEMICAL AGENTS; CHEMICAL MATERIALS FOR USE IN BREATHING APPARATUS
- A62D2101/00—Harmful chemical substances made harmless, or less harmful, by effecting chemical change
- A62D2101/20—Organic substances
- A62D2101/22—Organic substances containing halogen
-
- A—HUMAN NECESSITIES
- A62—LIFE-SAVING; FIRE-FIGHTING
- A62D—CHEMICAL MEANS FOR EXTINGUISHING FIRES OR FOR COMBATING OR PROTECTING AGAINST HARMFUL CHEMICAL AGENTS; CHEMICAL MATERIALS FOR USE IN BREATHING APPARATUS
- A62D2101/00—Harmful chemical substances made harmless, or less harmful, by effecting chemical change
- A62D2101/20—Organic substances
- A62D2101/28—Organic substances containing oxygen, sulfur, selenium or tellurium, i.e. chalcogen
-
- A—HUMAN NECESSITIES
- A62—LIFE-SAVING; FIRE-FIGHTING
- A62D—CHEMICAL MEANS FOR EXTINGUISHING FIRES OR FOR COMBATING OR PROTECTING AGAINST HARMFUL CHEMICAL AGENTS; CHEMICAL MATERIALS FOR USE IN BREATHING APPARATUS
- A62D2101/00—Harmful chemical substances made harmless, or less harmful, by effecting chemical change
- A62D2101/40—Inorganic substances
-
- A—HUMAN NECESSITIES
- A62—LIFE-SAVING; FIRE-FIGHTING
- A62D—CHEMICAL MEANS FOR EXTINGUISHING FIRES OR FOR COMBATING OR PROTECTING AGAINST HARMFUL CHEMICAL AGENTS; CHEMICAL MATERIALS FOR USE IN BREATHING APPARATUS
- A62D2101/00—Harmful chemical substances made harmless, or less harmful, by effecting chemical change
- A62D2101/40—Inorganic substances
- A62D2101/43—Inorganic substances containing heavy metals, in the bonded or free state
-
- A—HUMAN NECESSITIES
- A62—LIFE-SAVING; FIRE-FIGHTING
- A62D—CHEMICAL MEANS FOR EXTINGUISHING FIRES OR FOR COMBATING OR PROTECTING AGAINST HARMFUL CHEMICAL AGENTS; CHEMICAL MATERIALS FOR USE IN BREATHING APPARATUS
- A62D2101/00—Harmful chemical substances made harmless, or less harmful, by effecting chemical change
- A62D2101/40—Inorganic substances
- A62D2101/45—Inorganic substances containing nitrogen or phosphorus
-
- 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
- C04B2111/00—Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
- C04B2111/00474—Uses not provided for elsewhere in C04B2111/00
- C04B2111/00732—Uses not provided for elsewhere in C04B2111/00 for soil stabilisation
-
- 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
- C04B2111/00—Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
- C04B2111/10—Compositions or ingredients thereof characterised by the absence or the very low content of a specific material
-
- 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
- This invention relates to the field of stabilization of inorganic substrates, the prevention of leaching therefrom, and particularly to the stabilization of metals, metal ions and other inorganic ions in soils which have been contaminated.
- Sanforth in United States Patent 4,889,640 describes a method for substantially reducing the leachability of lead and cadmium in foundry waste by treatment of the waste with calcium or magnesium carbonate.
- United States Patent 4,990,404 discloses that a carbon-sulfur polymer produced by the reaction of sulfur vapor with an organic material will bind any metals contained in the organic rendering them insoluble.
- einwurm, et al. in European Patent Application EP 313,016 describe a method for ins ⁇ lubilizing heavy metals in waste sludge by mixing with a plastic material, _. e-.g. a clay or shale, capable of immobilizing leachable metals, and heat ' treating to form a stable silicate complex. This procedure involved pyrolysis and' calcination in excess of 1000°C.
- Ader et al. in united States Patent No. 4,884,815 teach that certain sludges can be rendered non-leachable or stabilized by treatment with sulfur and cement kiln dust.
- the sludge is preferably treated with caustic prior to adding the cement kiln dust.
- the waste sludges contain 20-35% water, and the patent teaches that sulfur reacts with the caustic to produce S x ⁇ z which, in turn, reacts with mercury salts to form mercury sulfide.
- sulfur alone would render metals and, metal ions in soils or sands non-leachable.
- the object of this invention is to provide a process for stabilization of substantially inorganic substrates and a " useful product produced by this process. This process combines simplicity and reliability coupled with an inexpensive operation and economies resulting from sale of the useful product of the process.
- the process of this invention involves treating an inorganic substrate or substantially inorganic substrate "with elemental sulfur at a temperature above the melting point of ⁇ Mlfur thus converting the substrate into : . a solid, inert material.
- Soil is herein defined as the superficial, unconsolidated part of the mantle of the earth. Soil used for leaching experiments is USEPA Synthetic Soil Matrix
- Inorganic substrate is herein defined as a relatively free flowing material of intermediate to small particle size composed of chemical compounds which do not contain appreciable amounts of carbon to carbon bonds and containing at least 10% silicon oxides or silicic acids or salts thereof.
- Inorganic substrates include, but are not limited to soils, sandsy fly ashes, dredgings from waterways, sludges, slags, foundry wastes, mine wastes, chemical wastes, refining wastes, and the like.
- Substantially • inorganic substrate is defined as an inorganic substrate containing less than 10% organic compounds and at least i ⁇ % silicon oxides or silicic acids or salts thereof.
- Metals are herein defined as elements yielding positively charged ions in aqueous solution of their salts.
- Metals contemplated by this invention include, but are not limited to Be, Sc, V, Cr, Mn, Co, Ni, Ga, Ge, As, Se, Rb, Sr, Y, Zr, Nb, Mo, Tc, Ru, Rh, Cd, In, Sn, Sb, Te, Cs, Ba, La, Os, Ir, Hg, Pb, Bi, Po, Ra, U, Pu, and the like.
- Metals of special interest are those which are known to cause toxic effects when released into the environment; these include As, Cr, Pb, Hg, Cd, Se, Pu, and the like.
- Inorganic ions other than metal ions include CN, SCN, NCS, PO-i, NO3, halides, borates, metal oxide ions, and the like.
- Stabilize means to convert to a solid, hard, non-flowable mass which resists common solvents and retains the materials contained therein when subjected to leaching conditions.
- Non leachability as used herein is as defined by the United States Environmental Protection Agency (USEPA) in the Federal Register, 55., 26986-26998 (1990) which is incorporated herein by reference.
- This invention comprises a method of stabilizing a substantially inorganic substrate comprising treating said inorganic substrate with elemental sulfur in liquid or vapor phase at. a temperature above the melting point of sulfur; with the proviso that cement kiln dust is not added to said inorganic substrate.
- this invention comprises a method of stabilizing metals, metal ions and other inorganic ions, such as cyanide in soil comprising treating said soil with sulfur in liquid or vapor phase at a temperature above the melting point of sulfur.
- this invention involves treating a substantially inorganic substrate which is a hazardous waste containing metals, metal ions and other inorganic ions with sulfur in liquid or vapor phase at a temperature above the melting point of sulfur thereby converting said hazardous waste to a relatively inert material which is no longer hazardous as defined by the USEPA in the Federal Register, 5_5_, 11798 (1990) which is incorporated herein by reference.
- this invention involves treating a substantially inorganic substrate containing metals, metal ions and other inorganic ions and 10% or less organic chemicals with sulfur in liquid or vapor phase at a temperature above the melting point of sulfur thereby rendering the metals, metal ions and other inorganic ions non-leachable as defined by the USEPA and simultaneously converting said organic chemicals to an inert carbon-sulfur polymer.
- the above method is especially useful for treating soil, sand, dredgings from waterways and fly ash from waste-to-energy plants which contain metals, metal ions, other inorganic ions and toxic or hazardous organic chemicals such as polychlorinated biphenyls (PCB) or polychlorinated dibenzodioxine (PCDD).
- PCB polychlorinated biphenyls
- PCDD polychlorinated dibenzodioxine
- this invention involves treating soil which contains metals, metal ions or other inorganic ions with sulfur in liquid or vapor phase at a temperature above the melting point of sulfur thereby rendering the metals, metal ions and other inorganic ions nonleachable as de ined by the USEPA.
- this invention comprises the solid, inert product resulting from the treatment of a substantially inorganic substrate with sulfur in liquid or vapor phase.
- An inorganic or substantially inorganic substrate in a relatively finely divided form is mixed with elemental sulfur at ambient temperature.
- Particle size of the substrate and sul ur is not critical and may vary from submicron to five or ten mm; however, it is preferred that at least 10 to 20% of the substrate be composed of particles smaller than 2 mm.
- the amount of sulfur is not critical, but there must be sufficient sulfur to stabilize and render non-leachable any metals, metal ions, or other inorganic ions contained in the substrate.
- the ratio of sulfur to substrate is preferably in the range of 1/10 to 1/1 with a more preferred ratio being 1/3. This process will prevent the leaching of individual metals, metal ions and other inorganic ions alone or in combination.
- the amount of metals, metal ions and other inorganic ions is not critical and may range from the detectable limit to several percent in total.
- the resulting mixture of sulfur and inorganic substrate or substantially inorganic substrate is heated at a temperature above the melting point of sulfur, maintaining the sulfur in liquid or vapor phase for a period of time sufficient to effect the stabilization of the substrate.
- Stirring or shaking of the reactants may be used, but is not critical. Operable temperatures range from 115-1500° C; the preferred reaction conditions are with liquid sulfur at temperatures of about 350° C. Under these conditions, the reaction is complete in one hour or less. The worker of ordinary skill will be able to determine the optimum amount of sulfur and the temperature and time of his reaction with minimal experimentation.
- the inorganic or substantially inorganic substrate may be combined and reacted with sulfur liquid or sulfur vapor at a temperature above the melting point of sulfur.
- This invention also contemplates that the reaction may take place with sulfur in liquid or vapor phase in a continuous or batch process. If sulfur vapor is used, it may be desirable to use an inert carrier gas such as nitrogen or carbon dioxide. Alternatively, the reaction may be run at -a temperature above the boiling point of sulfur while containing the sulfur vapor within a pressure vessel.
- Excess sulfur may be removed from the product by extraction with a solvent such as carbon disulfide or by heating at an elevated temperature in a vacuum or in an inert gas stream to drive off any excess sulfur as a vapor.
- a solvent such as carbon disulfide
- the product produced by the process of this invention is a hard, chemically inert and biologically inert material which may be used as a building or industrial aggregate or a catalyst support, or as fillers in coatings, cement and asphalt.
- a variant of this process may be employed to mold the product into specific shapes using suitable transfer molding equipment.
- a quantity of inorganic substrate and powdered sulfur is mixed together and inserted into the cavity of the mold under pressures which compact the mixture which is held at a temperature above the melting point of sulfur until reaction is complete.
- Another application for the product of this invention is to fill holes and cracks in roadways and concrete or masonry structures.. As described above, a quantity of inorganic substrate mixed with sulfur is introduced into the cavity and heat is applied until the reaction is completed, thus effecting repair of the structure or roadway.
- a spiked soil sample containing 1000 mg kg each of As- 3 (as AszOa), Cr- 6 (as K ⁇ CrO * ), Pb- a (as PbSO * ), and complex cyanide as ferric ferrocyanide was prepared using the SSM soil from Example 1. Fifty grams of the above spiked soil was combined with 50g sulfur and the resulting mixture was heated at 350°C in a shaken autoclave. The product, which was very hard, was chiseled from the autoclave and extracted with carbon disulfide. The product was leached with acid; the acid leachate was surveyed with indicator papers and showed no lead or chromate in the leachate. Approximately 3% sulfur remained in the product after extraction with carbon disulfide.
- Example 2 Following the procedure of Example 2, 120 g of SSM soil was reacted with 40g sulfur. This sample was crushed, extracted with carbon disulfide and annealed at 500°C for one hour in.a tube swept with a nitrogen.stream; to remove free sulfur. The annealed product was found to contain 1.2% sulfur.
- Example 4 was repeated using sand in place of soil. The product was extremely hard and required a power drill to remove it from the reactor. Analysis showed that the product contained 1.45% sulfur after annealing. .
- Example 6
- Example 3 The product of Example 3 was analyzed for extractable metal ions and cyanide by the Wadsworth/Alert Laboratories, 450 William Pitt Way, Pittsburgh, PA 15238. The following methods,were employed:
- SW846 1311 6010 For arsenic, chromium and lead, SW846 1311 6010; for cyanide, SW846 9012 (SW846-Test Methods for Evaluating Solid Wastes, Physical/Chemical Methods, Third Edition, EPA, September, 1986, incorporated herein by reference).
- the leachate had no detectable arsenic, chromium, lead or cyanide at detection limits of 0.10, 0.01, 0.05 and 2.5 g/Kg respectively.
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Abstract
A process for stabilizing a substantially inorganic substrate comprises treating the substrate with sulfur at a temperature above the melting point of sulfur thus converting the substrate into a solid, inert product which resists the leaching of metals, metal ions, and other inorganic ions originally present in the substrate. Organic compounds contained in the substantially inorganic substrate are simultaneously converted to an inert carbon-sulfur polymer.
Description
STABILIZING INORGANIC SUBSTRATES Background of the Invention
1. Field of the Invention
This invention relates to the field of stabilization of inorganic substrates, the prevention of leaching therefrom, and particularly to the stabilization of metals, metal ions and other inorganic ions in soils which have been contaminated.
2. Description of the Prior Art Disposal of waste materials or materials inadvertently contaminated with metals, metal ions and other inorganic ions is extremely difficult and costly. There has been a long felt need for a safe and reliable process to stabilize inorganic substrates, especially soils to prevent leaching therefrom and to convert the inorganic substrate to a useful or at least, an innocuous material.
Sanforth in United States Patent 4,889,640 describes a method for substantially reducing the leachability of lead and cadmium in foundry waste by treatment of the waste with calcium or magnesium carbonate.
United States Patent 4,990,404 discloses that a carbon-sulfur polymer produced by the reaction of sulfur vapor with an organic material will bind any metals contained in the organic rendering them insoluble. einwurm, et al. in European Patent Application EP 313,016 (Chem. Abstr. Ill, 80889, 1989) describe a method for insόlubilizing heavy metals in waste sludge by mixing with a plastic material, _. e-.g. a clay or shale, capable of immobilizing leachable metals, and heat' treating to form a stable silicate complex. This procedure involved pyrolysis and' calcination in excess of 1000°C.
Ader et al. in united States Patent No. 4,884,815 teach that certain sludges can be rendered non-leachable or stabilized by treatment with sulfur and cement kiln dust. The sludge is preferably treated with caustic prior to adding the cement kiln dust. The waste sludges contain 20-35% water, and the patent teaches that sulfur reacts with the caustic to produce Sx ~z which, in turn, reacts with mercury salts to form mercury sulfide. There is no suggestion that sulfur alone would render metals and, metal
ions in soils or sands non-leachable.
Schwab, et al. in United States Patent No. 2,203,881 teach an apparatus for injecting molten sulfur into voids in soil thereby stabilizing the soil. This reference does not suggest that the sulfur mixes with the soil or that leaching of metals or metal ions from soils treated by this process would be prevented.
Summary of the Invention
The object of this invention is to provide a process for stabilization of substantially inorganic substrates and a" useful product produced by this process. This process combines simplicity and reliability coupled with an inexpensive operation and economies resulting from sale of the useful product of the process. The process of this invention involves treating an inorganic substrate or substantially inorganic substrate "with elemental sulfur at a temperature above the melting point of εMlfur thus converting the substrate into:. a solid, inert material.
The- leaching of metals, ntetal ions and other inorganic ions originally contained in the substrate is .thereby prevented. Caustic and cement kiln dust are not required in this process.
Detailed Description of the Invention
"Soil" is herein defined as the superficial, unconsolidated part of the mantle of the earth. Soil used for leaching experiments is USEPA Synthetic Soil Matrix
(SSM) available from USEPA Releases Control Branch, Risk
Reduction Engineering laboratory, Edison, NJ 08837.
"Inorganic substrate" is herein defined as a relatively free flowing material of intermediate to small particle size composed of chemical compounds which do not contain appreciable amounts of carbon to carbon bonds and containing at least 10% silicon oxides or silicic acids or salts thereof. Inorganic substrates include, but are not limited to soils, sandsy fly ashes, dredgings from waterways, sludges, slags, foundry wastes, mine wastes, chemical wastes, refining wastes, and the like.
"Substantially • inorganic substrate" is defined as an inorganic substrate containing less than 10% organic compounds and at least iθ% silicon oxides or silicic acids or salts thereof.
"Metals" are herein defined as elements yielding positively charged ions in aqueous solution of their salts. Metals contemplated by this invention include, but are not limited to Be, Sc, V, Cr, Mn, Co, Ni, Ga, Ge, As, Se, Rb, Sr, Y, Zr, Nb, Mo, Tc, Ru, Rh, Cd, In, Sn, Sb, Te, Cs, Ba, La, Os, Ir, Hg, Pb, Bi, Po, Ra, U, Pu, and the like. Metals of special interest are those which are known to cause toxic effects when released into the environment; these include As, Cr, Pb, Hg, Cd, Se, Pu, and the like.
"Inorganic ions" other than metal ions include CN, SCN, NCS, PO-i, NO3, halides, borates, metal oxide ions, and the like.
"Stabilize" means to convert to a solid, hard, non-flowable mass which resists common solvents and retains the materials contained therein when subjected to leaching conditions.
"Non leachability" as used herein is as defined by the United States Environmental Protection Agency (USEPA) in the Federal Register, 55., 26986-26998 (1990) which is incorporated herein by reference.
This invention - comprises a method of stabilizing a substantially inorganic substrate comprising treating said inorganic substrate with elemental sulfur in liquid or vapor phase at. a temperature above the melting point of sulfur; with the proviso that cement kiln dust is not added to said inorganic substrate.
In another aspect, this invention comprises a method of stabilizing metals, metal ions and other inorganic ions, such as cyanide in soil comprising treating said soil with sulfur in liquid or vapor phase at a temperature above the melting point of sulfur.
In another aspect, this invention involves treating a substantially inorganic substrate which is a hazardous waste containing metals, metal ions and other inorganic ions with sulfur in liquid or vapor phase at a temperature above the melting point of sulfur thereby converting said hazardous waste to a relatively inert material which is no longer hazardous as defined by the USEPA in the Federal Register, 5_5_, 11798 (1990) which is incorporated herein by reference.
In yet another aspect, this invention involves treating a substantially inorganic substrate containing metals, metal ions and other inorganic ions and 10% or less organic chemicals with sulfur in liquid or vapor phase at a temperature above the melting point of sulfur thereby rendering the metals, metal ions and other inorganic ions non-leachable as defined by the USEPA and simultaneously converting said organic chemicals to an inert carbon-sulfur polymer. The above method is especially useful for treating soil, sand, dredgings from waterways and fly ash from waste-to-energy plants which contain metals, metal ions, other inorganic ions and toxic or hazardous organic chemicals such as polychlorinated biphenyls (PCB) or polychlorinated dibenzodioxine (PCDD). Such substantially inorganic substrates are rendered non-leachable and non-hazardous by treatment with sulfur in the liquid or vapor phase, and any organic chemical contained therein is simultaneously converted to an inert carbon-sulfur polymer.
In yet another aspect, this invention involves treating soil which contains metals, metal ions or other inorganic ions with sulfur in liquid or vapor phase at a temperature above the melting point of sulfur thereby rendering the metals, metal ions and other inorganic ions nonleachable as de ined by the USEPA.
In yet another aspect, this invention comprises the solid, inert product resulting from the treatment of a substantially inorganic substrate with sulfur in liquid or vapor phase.
The process of this invention is easily carried out. An inorganic or substantially inorganic substrate in a relatively finely divided form is mixed with elemental sulfur at ambient temperature. Particle size of the substrate and sul ur is not critical and may vary from submicron to five or ten mm; however, it is preferred that at least 10 to 20% of the substrate be composed of particles smaller than 2 mm.
The amount of sulfur is not critical, but there must be sufficient sulfur to stabilize and render non-leachable any metals, metal ions, or other inorganic ions contained in the substrate. The ratio of sulfur to substrate is
preferably in the range of 1/10 to 1/1 with a more preferred ratio being 1/3. This process will prevent the leaching of individual metals, metal ions and other inorganic ions alone or in combination. The amount of metals, metal ions and other inorganic ions is not critical and may range from the detectable limit to several percent in total.
The resulting mixture of sulfur and inorganic substrate or substantially inorganic substrate is heated at a temperature above the melting point of sulfur, maintaining the sulfur in liquid or vapor phase for a period of time sufficient to effect the stabilization of the substrate. Stirring or shaking of the reactants may be used, but is not critical. Operable temperatures range from 115-1500° C; the preferred reaction conditions are with liquid sulfur at temperatures of about 350° C. Under these conditions, the reaction is complete in one hour or less. The worker of ordinary skill will be able to determine the optimum amount of sulfur and the temperature and time of his reaction with minimal experimentation.
Alternatively, the inorganic or substantially inorganic substrate may be combined and reacted with sulfur liquid or sulfur vapor at a temperature above the melting point of sulfur. This invention also contemplates that the reaction may take place with sulfur in liquid or vapor phase in a continuous or batch process. If sulfur vapor is used, it may be desirable to use an inert carrier gas such as nitrogen or carbon dioxide. Alternatively, the reaction may be run at -a temperature above the boiling point of sulfur while containing the sulfur vapor within a pressure vessel.
Excess sulfur may be removed from the product by extraction with a solvent such as carbon disulfide or by heating at an elevated temperature in a vacuum or in an inert gas stream to drive off any excess sulfur as a vapor.
In typical runs with soil and sand as substrates, the products contained 1.2-3% sulfur which could not be removed by extraction or vaporization. The exact molecular formulae of these products is not known at the present time, nor. is the mechanism of reaction known to be chemical or physical. When ground to powders, these
products are dark in color and have the appearance of "black sand".
The product produced by the process of this invention is a hard, chemically inert and biologically inert material which may be used as a building or industrial aggregate or a catalyst support, or as fillers in coatings, cement and asphalt. A variant of this process may be employed to mold the product into specific shapes using suitable transfer molding equipment. A quantity of inorganic substrate and powdered sulfur is mixed together and inserted into the cavity of the mold under pressures which compact the mixture which is held at a temperature above the melting point of sulfur until reaction is complete. Another application for the product of this invention is to fill holes and cracks in roadways and concrete or masonry structures.. As described above, a quantity of inorganic substrate mixed with sulfur is introduced into the cavity and heat is applied until the reaction is completed, thus effecting repair of the structure or roadway.
The following examples are provided solely for the purposes of illustration and do not limit the scope of the invention which is defined by the claims. Exam le 1
in SSM
This soil was found to have a cation exchange capacity of 30.0-34.5; a total organic content of 2.7-3.4 g/kg; and a pH of 8.0-8.2.
Example 2 Stabilization of SSM Soil
A spiked soil sample containing 1000 mg kg each of As-3 (as AszOa), Cr-6 (as K^CrO*), Pb-a (as PbSO*), and complex cyanide as ferric ferrocyanide was prepared using the SSM soil from Example 1. Fifty grams of the above spiked soil was combined with 50g sulfur and the resulting mixture was heated at 350°C in a shaken autoclave. The product, which was very hard, was chiseled from the autoclave and extracted with carbon disulfide. The product was leached with acid; the acid leachate was surveyed with indicator papers and showed no lead or chromate in the leachate. Approximately 3% sulfur remained in the product after extraction with carbon disulfide. Example 3
Stabilization of SSM Soil with 33% Sulfur
Following the procedure of Example 2, 120g of spiked soil was reacted with 40g sulfur. The sample was crushed and extracted with carbon disulfide; approximately 3% sulfur remained in the product.
Example 4 Stabilization of SSM Soil with Removal of Excess Sulfur
Following the procedure of Example 2, 120 g of SSM soil was reacted with 40g sulfur. This sample was crushed, extracted with carbon disulfide and annealed at 500°C for one hour in.a tube swept with a nitrogen.stream; to remove free sulfur. The annealed product was found to contain 1.2% sulfur.
Example 5 Stabilization of.Sand
Example 4 was repeated using sand in place of soil. The product was extremely hard and required a power drill to remove it from the reactor. Analysis showed that the product contained 1.45% sulfur after annealing. . Example 6
Analysis of Product for Extractable Metals
The product of Example 3 was analyzed for extractable metal ions and cyanide by the Wadsworth/Alert Laboratories, 450 William Pitt Way, Pittsburgh, PA 15238. The following methods,were employed:
For arsenic,, chromium and lead, SW846 1311 6010; for
cyanide, SW846 9012 (SW846-Test Methods for Evaluating Solid Wastes, Physical/Chemical Methods, Third Edition, EPA, September, 1986, incorporated herein by reference).
Analysis was performed in accordance with USEPA Toxicity Characteristic Leaching Procedure Method 13311 (55 FR 26986).
Under this procedure, the leachate had no detectable arsenic, chromium, lead or cyanide at detection limits of 0.10, 0.01, 0.05 and 2.5 g/Kg respectively. Although the invention has been described with regard to its preferred embodiments, which constitute the best mode presently known to the inventor,- it should be understood that various changes and modifications as would be obvious to one having ordinary skill in this art may be made without departing from the scope-of the invention which is defined by the claims.
Claims
1. A method of preventing the leaching of metals, metal ions and other inorganic ions from a substantially inorganic substrate containing metals, metal ions or other inorganic ions comprising mixing said substantially inorganic substrate with sulfur and heating the mixture at a temperature greater than the melting point of sulfur, with the proviso that cement kiln dust is not added to said substantially inorganic substrate.
2. The method of claim 1 wherein said substantially inorganic substrate is soil.
3. The method of claim 1 wherein said substantially inorganic substrate is sand.
4. The method of claim 1 wherein said temperature is approximately 300° to 350° C.
5. The method of claim 1 wherein said metal ions are arsenic, chromium, and lead; and said other inorganic ion is cyanide.
6. A solid, inert product produced by a) contacting a substantially inorganic substrate with sulfur at a temperature greater than _.the melting point of sulfur; b) removing unreacted sulfur from said product.
7. The product of claim 6 wherein said substantially inorganic substrate is soil.
8. The product of claim 6 wherein said substantially inorganic substrate is sand.
9. A method of preventing the leaching of metals, metal ions or other inorganic ions from soil or sand containing metals, metal ions or other inorganic ions comprising mixing said soil or sand with sulfur and heating said mixture at a temperature greater than the melting point of sulfur.
10. The method of claim 9 wherein said temperature is approximately 300° to 350° C.
11. A method of preventing the leaching of metals, metal ions and other inorganic ions from a substantially inorganic substrate containing metals, metal ions or other inorganic ions and simultaneously converting any organic chemical contained in said substantially inorganic substrate to an inert carbon-sulfur polymer comprising mixing said substantially inorganic substrate with sulfur and heating the mixture at a temperature greater than the melting point of sulfur.
12. The method of claim 11 wherein said substantially inorganic substrate is soil.
13. The method of claim 11 wherein said substantially inorganic substrate is fly ash.
14. The method of claim 11 wherein said substantially inorganic substrate is dredgings from waterways.
15. The method of claim 11 wherein said organic chemical is PCB.
16. The method of claim 11 wherein said organic chemical is PCDD.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US07/989,708 US5347072A (en) | 1991-08-01 | 1992-12-14 | Stabilizing inorganic substrates |
US08/453,797 US5562589A (en) | 1991-08-01 | 1995-05-30 | Stabilizing inorganic substrates |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US73886691A | 1991-08-01 | 1991-08-01 | |
US738,866 | 1991-08-01 |
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WO1993002854A1 true WO1993002854A1 (en) | 1993-02-18 |
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PCT/US1992/006068 WO1993002854A1 (en) | 1991-08-01 | 1992-07-22 | Stabilizing inorganic substrates |
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WO (1) | WO1993002854A1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0751924A1 (en) * | 1994-03-21 | 1997-01-08 | Sultech Inc. | Process for the destruction of explosives |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2203881A (en) * | 1937-12-02 | 1940-06-11 | Texas Gulf Sulphur Co | Solidification of sandy soils |
US4844815A (en) * | 1988-08-12 | 1989-07-04 | Chemical Waste Management, Inc. | Stabilization of mercury-containing waste |
-
1992
- 1992-07-22 CA CA002114646A patent/CA2114646A1/en not_active Abandoned
- 1992-07-22 WO PCT/US1992/006068 patent/WO1993002854A1/en active Application Filing
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2203881A (en) * | 1937-12-02 | 1940-06-11 | Texas Gulf Sulphur Co | Solidification of sandy soils |
US4844815A (en) * | 1988-08-12 | 1989-07-04 | Chemical Waste Management, Inc. | Stabilization of mercury-containing waste |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0751924A1 (en) * | 1994-03-21 | 1997-01-08 | Sultech Inc. | Process for the destruction of explosives |
EP0751924A4 (en) * | 1994-03-21 | 1997-08-20 | Sultech Inc | Process for the destruction of explosives |
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CA2114646A1 (en) | 1993-02-18 |
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