CN109628102A - A kind of repair materials and restorative procedure for organic material contaminated soil - Google Patents
A kind of repair materials and restorative procedure for organic material contaminated soil Download PDFInfo
- Publication number
- CN109628102A CN109628102A CN201811419646.8A CN201811419646A CN109628102A CN 109628102 A CN109628102 A CN 109628102A CN 201811419646 A CN201811419646 A CN 201811419646A CN 109628102 A CN109628102 A CN 109628102A
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- China
- Prior art keywords
- foam
- contaminated soil
- organic
- repair materials
- oxidant
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- 239000002689 soil Substances 0.000 title claims description 67
- 239000000463 material Substances 0.000 title claims description 60
- 238000000034 method Methods 0.000 title claims description 23
- 230000008439 repair process Effects 0.000 title description 46
- 239000011368 organic material Substances 0.000 title description 5
- 239000006260 foam Substances 0.000 claims description 96
- 239000012855 volatile organic compound Substances 0.000 claims description 28
- 239000007800 oxidant agent Substances 0.000 claims description 27
- 230000001590 oxidative effect Effects 0.000 claims description 27
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 claims description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 17
- BBEAQIROQSPTKN-UHFFFAOYSA-N pyrene Chemical compound C1=CC=C2C=CC3=CC=CC4=CC=C1C2=C43 BBEAQIROQSPTKN-UHFFFAOYSA-N 0.000 claims description 16
- 239000008367 deionised water Substances 0.000 claims description 14
- 229910021641 deionized water Inorganic materials 0.000 claims description 14
- 239000004088 foaming agent Substances 0.000 claims description 13
- 239000002562 thickening agent Substances 0.000 claims description 13
- 150000003839 salts Chemical class 0.000 claims description 12
- 229920002472 Starch Polymers 0.000 claims description 11
- 238000005067 remediation Methods 0.000 claims description 11
- 239000008107 starch Substances 0.000 claims description 11
- 235000019698 starch Nutrition 0.000 claims description 11
- FMMWHPNWAFZXNH-UHFFFAOYSA-N Benz[a]pyrene Chemical compound C1=C2C3=CC=CC=C3C=C(C=C3)C2=C2C3=CC=CC2=C1 FMMWHPNWAFZXNH-UHFFFAOYSA-N 0.000 claims description 10
- GVEPBJHOBDJJJI-UHFFFAOYSA-N fluoranthrene Natural products C1=CC(C2=CC=CC=C22)=C3C2=CC=CC3=C1 GVEPBJHOBDJJJI-UHFFFAOYSA-N 0.000 claims description 10
- 229910052708 sodium Inorganic materials 0.000 claims description 10
- 239000011734 sodium Substances 0.000 claims description 10
- -1 sodium alkyl sulfonate Chemical class 0.000 claims description 7
- 238000003756 stirring Methods 0.000 claims description 7
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 6
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims description 6
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 4
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 claims description 4
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims description 4
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 claims description 4
- YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 claims description 4
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 claims description 4
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 3
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 3
- 150000001336 alkenes Chemical class 0.000 claims description 3
- 239000001913 cellulose Substances 0.000 claims description 3
- 229920002678 cellulose Polymers 0.000 claims description 3
- 229910052751 metal Inorganic materials 0.000 claims description 3
- 239000002184 metal Substances 0.000 claims description 3
- 229920000945 Amylopectin Polymers 0.000 claims description 2
- 229920000856 Amylose Polymers 0.000 claims description 2
- TXVHTIQJNYSSKO-UHFFFAOYSA-N BeP Natural products C1=CC=C2C3=CC=CC=C3C3=CC=CC4=CC=C1C2=C34 TXVHTIQJNYSSKO-UHFFFAOYSA-N 0.000 claims description 2
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 claims description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
- 108010010803 Gelatin Proteins 0.000 claims description 2
- SXQBHARYMNFBPS-UHFFFAOYSA-N Indeno[1,2,3-cd]pyrene Chemical compound C=1C(C2=CC=CC=C22)=C3C2=CC=C(C=C2)C3=C3C2=CC=CC3=1 SXQBHARYMNFBPS-UHFFFAOYSA-N 0.000 claims description 2
- 229910002651 NO3 Inorganic materials 0.000 claims description 2
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 claims description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 claims description 2
- 239000000460 chlorine Substances 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims description 2
- 229920000159 gelatin Polymers 0.000 claims description 2
- 239000008273 gelatin Substances 0.000 claims description 2
- 235000019322 gelatine Nutrition 0.000 claims description 2
- 235000011852 gelatine desserts Nutrition 0.000 claims description 2
- RKZJFAONHOYOKU-UHFFFAOYSA-N indeno[1,2,3-cd]pyrene Natural products C1Cc2ccc3ccc4c5ccccc5c6cc(=C1)c2c3c46 RKZJFAONHOYOKU-UHFFFAOYSA-N 0.000 claims description 2
- 238000002156 mixing Methods 0.000 claims description 2
- 239000001814 pectin Substances 0.000 claims description 2
- 229920001277 pectin Polymers 0.000 claims description 2
- 235000010987 pectin Nutrition 0.000 claims description 2
- 150000002978 peroxides Chemical class 0.000 claims description 2
- JRKICGRDRMAZLK-UHFFFAOYSA-L peroxydisulfate Chemical compound [O-]S(=O)(=O)OOS([O-])(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 claims description 2
- 239000002994 raw material Substances 0.000 claims description 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims description 2
- 229910017053 inorganic salt Inorganic materials 0.000 claims 2
- RZXLPPRPEOUENN-UHFFFAOYSA-N Chlorfenson Chemical compound C1=CC(Cl)=CC=C1OS(=O)(=O)C1=CC=C(Cl)C=C1 RZXLPPRPEOUENN-UHFFFAOYSA-N 0.000 claims 1
- 239000000679 carrageenan Substances 0.000 claims 1
- 235000010418 carrageenan Nutrition 0.000 claims 1
- 229920001525 carrageenan Polymers 0.000 claims 1
- 229940113118 carrageenan Drugs 0.000 claims 1
- 235000010980 cellulose Nutrition 0.000 claims 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 claims 1
- 108090000623 proteins and genes Proteins 0.000 claims 1
- 102000004169 proteins and genes Human genes 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- 239000008096 xylene Substances 0.000 claims 1
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 claims 1
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 24
- 230000000694 effects Effects 0.000 description 21
- 125000005575 polycyclic aromatic hydrocarbon group Chemical group 0.000 description 16
- 239000003344 environmental pollutant Substances 0.000 description 13
- 231100000719 pollutant Toxicity 0.000 description 13
- 239000000243 solution Substances 0.000 description 13
- 239000011521 glass Substances 0.000 description 12
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
- 230000008878 coupling Effects 0.000 description 10
- 238000010168 coupling process Methods 0.000 description 10
- 238000005859 coupling reaction Methods 0.000 description 10
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 9
- 239000007789 gas Substances 0.000 description 9
- 230000004888 barrier function Effects 0.000 description 8
- 239000007788 liquid Substances 0.000 description 7
- 238000012544 monitoring process Methods 0.000 description 7
- 239000005416 organic matter Substances 0.000 description 7
- 230000000903 blocking effect Effects 0.000 description 6
- 239000000356 contaminant Substances 0.000 description 6
- 238000011156 evaluation Methods 0.000 description 6
- 238000004817 gas chromatography Methods 0.000 description 6
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 description 5
- 229950011008 tetrachloroethylene Drugs 0.000 description 5
- 230000015556 catabolic process Effects 0.000 description 4
- 238000010276 construction Methods 0.000 description 4
- 238000006731 degradation reaction Methods 0.000 description 4
- 239000000428 dust Substances 0.000 description 4
- 238000000944 Soxhlet extraction Methods 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000011161 development Methods 0.000 description 3
- DNJIEGIFACGWOD-UHFFFAOYSA-N ethanethiol Chemical compound CCS DNJIEGIFACGWOD-UHFFFAOYSA-N 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 238000000605 extraction Methods 0.000 description 3
- 238000005187 foaming Methods 0.000 description 3
- 231100000614 poison Toxicity 0.000 description 3
- 230000007096 poisonous effect Effects 0.000 description 3
- 230000035484 reaction time Effects 0.000 description 3
- 238000003900 soil pollution Methods 0.000 description 3
- 238000001179 sorption measurement Methods 0.000 description 3
- 238000005303 weighing Methods 0.000 description 3
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 2
- 229920000881 Modified starch Polymers 0.000 description 2
- 239000004368 Modified starch Substances 0.000 description 2
- 108010009736 Protein Hydrolysates Proteins 0.000 description 2
- 230000003213 activating effect Effects 0.000 description 2
- 239000006265 aqueous foam Substances 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 2
- 229910000359 iron(II) sulfate Inorganic materials 0.000 description 2
- 239000003595 mist Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 235000019426 modified starch Nutrition 0.000 description 2
- 239000002957 persistent organic pollutant Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000003531 protein hydrolysate Substances 0.000 description 2
- 238000005070 sampling Methods 0.000 description 2
- 230000007281 self degradation Effects 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 241001251371 Betula chinensis Species 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- 241000206575 Chondrus crispus Species 0.000 description 1
- RAASUWZPTOJQAY-UHFFFAOYSA-N Dibenz[a,c]anthracene Chemical compound C1=CC=C2C3=CC4=CC=CC=C4C=C3C3=CC=CC=C3C2=C1 RAASUWZPTOJQAY-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000000889 atomisation Methods 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 231100000481 chemical toxicant Toxicity 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- YDEXUEFDPVHGHE-GGMCWBHBSA-L disodium;(2r)-3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Na+].[Na+].COC1=CC=CC(C[C@H](CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O YDEXUEFDPVHGHE-GGMCWBHBSA-L 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000004134 energy conservation Methods 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 235000003891 ferrous sulphate Nutrition 0.000 description 1
- 239000011790 ferrous sulphate Substances 0.000 description 1
- 239000008394 flocculating agent Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 229940051250 hexylene glycol Drugs 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 230000005923 long-lasting effect Effects 0.000 description 1
- 229920005615 natural polymer Polymers 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 238000010525 oxidative degradation reaction Methods 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000000750 progressive effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000003440 toxic substance Substances 0.000 description 1
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
- 239000002435 venom Substances 0.000 description 1
- 231100000611 venom Toxicity 0.000 description 1
- 210000001048 venom Anatomy 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K17/00—Soil-conditioning materials or soil-stabilising materials
- C09K17/40—Soil-conditioning materials or soil-stabilising materials containing mixtures of inorganic and organic compounds
-
- 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
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K17/00—Soil-conditioning materials or soil-stabilising materials
- C09K17/52—Mulches
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B09—DISPOSAL OF SOLID WASTE; RECLAMATION OF CONTAMINATED SOIL
- B09C—RECLAMATION OF CONTAMINATED SOIL
- B09C2101/00—In situ
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Soil Sciences (AREA)
- Engineering & Computer Science (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Environmental & Geological Engineering (AREA)
- Processing Of Solid Wastes (AREA)
Abstract
The present invention relates to a kind of repair materials and restorative procedure for organic material contaminated soil, repair materials include the raw material of following mass percent: foaming agent 10%~20%;Inorganic salts 1%~5%;Oxidant 1%~5%;Starch 5%~15%;Thickener 1%~5%;Deionized water 60%~75%.The present invention is after 6 hours, and for the blocking rate of volatile organic matter after 80% or more, 24 small the reaction time, polycyclic aromatic hydrocarbon is 85% or more through the oxidant removal rate in foam.Compared with prior art, foam coupling oxidant repair materials of the invention and restorative procedure, it can effectively block and remove volatile organic matter, preparation process is simple, degradable green, it is without secondary pollution, energy conservation and environmental protection, contaminated site organic pollutant oxidation repair, peculiar smell block, hazardous chemical leakage in terms of have potential application prospect.
Description
Technical field
The present invention relates to environmental technology fields, and in particular to a kind of repair materials for organic material contaminated soil and repairs
Compound method.
Background technique
With being constantly progressive for China's development, the pollution situation of soil environment is further serious.The harm of soil pollution
It is numerous, cultivated land resource originally in short supply can be made deficienter, while bringing adverse effect to agricultural development;Pollution in soil
Object can migrate or be detained in the soil, to the environment of surrounding cause long lasting for influence;Soil pollution can be to economic construction
It makes a very bad impression, it is serious to hinder economic sustainable development;Soil pollution greatly threatens the body and health of the mankind, together
When also have complicated reciprocal effect with other pollutions.
For the peculiar smell and volatile contaminant generated during contaminated soil remediation, domestic general technology is to build to face
When peculiar smell warehousing storage or soil is covered using inflating green and steel construction greenhouse etc., above-mentioned construction, which exists, to be made
The disadvantages of tail gas needs processing that high price is expensive, can not move, collect easily causes secondary pollution.At home and abroad start to seek at present
Inhibit the evaporation of inflammable toxic chemical with foam.
Scott Metcalfe (Pollution Engineering, 2005 (2): 12-15) has reported 3 kinds and has inhibited gas processed
The method of factory's contaminated site peculiar smell and VOCs pollutant: interim storage is collected, film covering and aqueous foam cover.Aqueous bubble
Foam covering method have easy to use, long action time, effect is good, economy is high, does not delay construction speed, without secondary dirt
The advantages that dye.Its method is that aqueous foam is sprayed to Zhi Qi factory Polluted area, can effectively inhibit stench in 13-14 hours
And the release of VOCs pollutant.
Patent US7659316 (B2) (2007) is related to a kind of foam compositions, is suitable for the covering such as refuse landfill,
Forest fire protection, the fields such as escaping gas emission control.Foam by protein hydrolysate, ferrous sulfate, cationic modified starch and its
He is at being grouped as.Patent is related to influence of the different foam formula to foaming fluid viscosity, concrete application case, effect for foam
Fruit and evaluation method do not refer to.
A kind of method that patent CN201310431852.1 (2014) has invented foam pollution administration soil, foam component
Are as follows: protein hydrolysate, cationic modified starch GPC X201, FeSO4, hexylene glycol, chloro- 2 benzyl of 4- pour phenol, sodium lignin sulfonate,
Polysaccharide xanthan gum, polyacrylamide and water.Its administering method is foam coverage after foaming in contaminated soil surface layer, is utilized
Pollutant in the adsorption ability and the absorption of sterilization composition and resolution soil of foam, by 20 more than hour, will steep
Foam is sprayed after foam cleaning again, circulation is until soil is up to standard.The method only relates to foam and makees to the reparation degradation of contaminated soil
With, and do not refer to foam to the block function of peculiar smell stench.
Li Jianhuas etc. (fire prevention and product information, 2000,8:24-26) have rated fire foam to inflammable or have
Venom body lets out the effect that covering is implemented on beach, as a result, it has been found that MJPZ is best to the coverage effect of n-hexane, effective cover time can
Up to 120min.But it is fluorine-containing in MJPZ, secondary pollution may be caused to environment.
Mulligan C.N. (Engineering Geology, 2003,11:269-279) etc. has studied through surface-active
Repairing effect of the modified foam of agent to pentachlorophenol (PCP) contaminated soil.Its method is injected foam as leacheate
Into contaminated soil, as a result, it has been found that in the 1% removable soil of triton x-100 85% PCP is added in the foam.It is added to
The foam leacheate specific surface activating agent leacheate of surfactant can more effectively remove the PCP pollutant in soil.This research
Involved in foam injection into contaminated soil and by the method for pollutant elution removal, with this patent refer to by foam coverage
On contaminated site surface, thus the method for inhibiting and eliminating place peculiar smell and VOCs pollutant, the two application principle not phase
Together.
A kind of method that patent CN103230916A (2013) has invented foam inhibition dust, method is that foam is molten
Liquid is added in the water tank of dustproof spray nozzle, sprays to form mist through atomizer, forms a large amount of atomization bubbles through multiple nozzles
The foam area of coverage is adsorbed on the fugitive dust overwhelming majority in atomized foam overlay area on foam, and settles with water mist to reach
Ideal anti-dust effect.Foam main component is nonionic surfactant, anionic surfactant, hygroscopic inorganic salts
Flocculating agent, assistant for emulsifying agent.This patent only relates to application of the foam in terms of inhibiting dust, be not directed to foam inhibit peculiar smell and
The application of volatile contaminant.
Summary of the invention
It is dirty for organic matter that it is an object of the present invention to overcome the above-mentioned drawbacks of the prior art and provide one kind
Contaminate the repair materials and restorative procedure of soil.
The purpose of the present invention can be achieved through the following technical solutions: a kind of reparation for organic material contaminated soil
Material, the repair materials include the raw material of following mass percent:
Foaming agent is agitated in above-mentioned material forms froth bed, and the volatility for blocking contaminated site loss to go out is dirty
Contaminate object and peculiar smell;Half volatile pollutant in the soil of oxidizing pollution degradation place tentatively repairs contaminated site
It is multiple;Inorganic salts, starch and thickener play the role of foam stabilizing, and the stability for enhancing foaming structure increases the die-away time of foam, prolong
Blocking repair time of the long foam repair materials to contaminated site.The bubble cutoff repair materials green of this project application is without dirt
Dye, can natural degradation, block contaminated site in volatility and half volatile organic contaminant to atmosphere volatilize, reduce simultaneously
The effect of pollutant concentration.This application involves bubble cutoff repair materials have both to stench peculiar smell and VOCs pollutant loss
Barrier effect, and the oxidative degradation effect to the half volatiles pollutant such as polycyclic aromatic hydrocarbon.
Preferably, the foaming agent is selected from albumen, sodium alkyl sulfonate, alkene sulfonic acid sodium, sodium alkyl sulfate, olefinic sulphur
One or more of sour sodium, ester sodium sulphate or ester sodium sulfonate.Above-mentioned foaming agent metal surface activating agent class foaming agent, gas release
Greatly, green is without secondary pollution, can self-degradation.
Preferably, the inorganic salts are selected from one of sulfate, nitrate, borate or chlorine metal salt or a variety of.
Preferably, the oxidant is one or more of peroxide, persulfate, permanganate.
Preferably, the starch is selected from one or more of amylopectin or amylose.
Preferably, the thickener is selected from one or more of oxhide gelatin, carragheen, pectin or cellulose.It is above-mentioned
Thickener belongs to cellulose family and natural polymer subclass thickener, nontoxic to environment and human body, easy to dissolve in aqueous solution
Dispersion synthesizes conducive to the preparation of foam repair materials.
A kind of restorative procedure being used for organic material contaminated soil using repair materials as described above, comprising the following steps:
(1) foaming agent, inorganic salts, oxidant, starch, thickener and deionized water are proportionally mixed, stirring is equal
Even formation foam;
(2) foam coverage for obtaining step (1) the contaminated soil surface to be repaired containing volatile organic matter i.e.
It can.
The rate stirred in step (1) is 10~10000r/min, and mixing time is 0.5~20min.
Preferably, the repair materials are in soil surface to be repaired with a thickness of 0.1~50cm.Foam blanket exists
Soil surface needs to reach certain thickness, coating too it is thin not can guarantee froth bed to the blocking of organic pollutant in place and
Degradation effect;The coating too thick self-degradation time that will increase froth bed and rehabilitation cost.
Preferably, the volatile organic matter includes volatile organism and Semi-volatile organism, and described volatile have
Machine object includes carbon tetrachloride, methylene chloride, chloroform, tetrachloro-ethylene, dibromoethylene, trichloro ethylene, chloromethanes, normal heptane, positive fourth
One of alkane, pentane, n-hexane, toluene or dimethylbenzene;The semi-volatile organic matter includes naphthalene, anthracene, phenanthrene, pyrene, glimmering
One of anthracene, benzo (a) pyrene, dibenzanthracene or indeno [1,2,3-cd] pyrene.
The above-mentioned repair materials being prepared can be used for VOC release/gas-chromatography on-line monitoring evaluation method, real
When monitoring foam coupling oxidant repair materials barrier effect, can make an appraisal effect in time.Its monitoring temperature range is
20-60 DEG C, monitoring humidity range is 10%-60%.
Compared with prior art, the beneficial effects of the present invention are embodied in:
(1) repair materials of the invention can be blocked effectively and remove organic pollutant;
(2) repair materials preparation process of the invention is simple, and degradable green is without secondary pollution, energy conservation and environmental protection.
Detailed description of the invention
Fig. 1 is the schematic device in embodiment 1 for the evaluation of repair materials repairing effect.
Wherein, 1 is nitrogen cylinder, and 2 be pressure summary table, and 3 be pressure reducing valve table, and 4 be pressure maintaining valve, and 5 control for mass flow
Device, 6 be VOC release, and 7 be gas sampling mouth, and 8 be six-way valve, and 9 be gas-chromatography, and 10 be vacuum pump, and 11 be tail gas adsorption
Column.
Specific embodiment
Elaborate below to the embodiment of the present invention, the present embodiment under the premise of the technical scheme of the present invention into
Row is implemented, and the detailed implementation method and specific operation process are given, but protection scope of the present invention is not limited to following realities
Apply example.
Embodiment 1
The present embodiment is suitable for poisonous and harmful steam, volatile contaminant and the liquid beach of bubble cutoff contaminated site leakage,
The mass percent of foamed material each component are as follows: foaming agent 14.6%, starch 8.8%, inorganic salts 4.4%, oxidant 1.2%,
Thickener 1.6%, deionized water 69.4%.
The present embodiment foam couple oxidant repair materials application when the following steps are included:
Step (1): foam coupling oxidant repair materials are diluted using deionized water, expanding foam solution is made;
Step (2): being that expanding foam solution 3min is stirred under 1000 revs/min using mechanical agitator low whipping speed, is formed equal
The foam of even exquisiteness;
Step (3): being packed into a certain amount of tetrachloro-ethylene (PCE) in glass container, step (2) is formed uniform thin
Greasy foam uniform fold forms the foam blanket of about 5cm on PCE liquid level.
Step (4): the glass container that foam is covered in step (3) is put into the VOCs release in Fig. 1, temperature in cabin
Degree is adjusted to 40 DEG C, and humidity 30%, in Fig. 1, the connection of VOCs release is as follows:
1 quality of connection flow controller 5 of nitrogen cylinder, and in the gas outlet of nitrogen cylinder 1 setting pressure summary table 2 and subtract
Pressure maintaining valve 4 is arranged in pressure valve table 3 on the connecting line of nitrogen cylinder 1 and mass flow controller 5;
Pressure maintaining valve 4 is divided into multiply and connect with VOC release storehouse 6, drains for VOC to be discharged the air in storehouse 6, VOC release
Storehouse 6 is equipped with multiply nitrogen outlet;
VOC, which discharges, is equipped with gas sampling mouth 7 in storehouse 6, and is divided into two-way by six-way valve 8, connects gas-chromatography 9 all the way,
For measuring the volatile quantity of tetrachloro-ethylene;Another way connects tail gas adsorption column 11 by vacuum pump 10, prevents tetrachloro-ethylene from polluting
Air.
Step (5): passing through VOC release, and the evaluation method of gas-chromatography on-line monitoring is analyzed at interval of 15min and discharged
The concentration of PCE in cabin.
PCE concentration with the situation of change of cover time is shown in Table 1 in VOCs release after foam coverage PCE.
The barrier effect that 1 repair materials of table volatilize to PCE
From in upper table we can be found that: repair materials use 360min after be 80.7% to the blocking rate of PCE, repair
Material has excellent barrier effect to VOCs pollutant, blocks effective time long.
Embodiment 2
The present embodiment is suitable for foam coupling oxidant repair materials to semi-volatile organic matter polycyclic aromatic hydrocarbon soil
Removal, the mass percent of foamed material each component are as follows: foaming agent 14.6%, starch 8.8%, inorganic salts 4.4%, oxidant
1.2%, thickener 1.6%, deionized water 69.4%.
The present embodiment foam couple oxidant repair materials application when the following steps are included:
Step (1): foam coupling oxidant repair materials are diluted using deionized water, expanding foam solution is made;
Step (2): being that expanding foam solution 3min is stirred under 1500 revs/min using mechanical agitator low whipping speed, is formed equal
The foam of even exquisiteness;
Step (3): weighing soil in vial with cover, brush flat soil surface with brush, take a certain amount of BaP,
Anthracene, pyrene are dissolved in acetone, and obtained polycyclic aromatic hydrocarbon-acetone soln is added in soil, and stirs evenly rapidly, and brush flat soil table
Contaminated soil sample is made in face.
Step (4): step (3) contaminated soil (total polycyclic aromatic hydrocarbon content 361.2mg/ is packed into glass container with cover
Kg), the foam uniform fold of uniform and smooth step (2) formed forms the foam blanket of about 5cm on contaminated soil.
Step (5): the glass container with cover for covering foam in step (4) is put into draught cupboard, is terminated after 24 hours
Reaction.
Step (6): using the polycyclic aromatic hydrocarbon in soxhlet extraction extraction soil, polycyclic aromatic hydrocarbon removal rate is calculated.
Under identical experiment condition, when the reaction time is for 24 hours, foam couples oxidant repair materials to anthracene in soil
Removal rate be 88.8%, the removal rate of pyrene is 87.0%, and the removal rate of BaP is 73.5%, the removal of total polycyclic aromatic hydrocarbon
Rate is 87.1%.
Embodiment 3
The present embodiment is suitable for poisonous and harmful steam, volatile contaminant and the liquid beach of bubble cutoff contaminated site leakage,
The mass percent of foamed material each component are as follows: foaming agent 2.4%, starch 8%, inorganic salts 3.8%, oxidant 1%, thickening
Agent 1.6%, deionized water 73.2%.
The present embodiment foam couple oxidant repair materials application when the following steps are included:
Step (1): foam coupling oxidant repair materials are diluted using deionized water, expanding foam solution is made;
Step (2): being that expanding foam solution 3min is stirred under 1000 revs/min using mechanical agitator low whipping speed, is formed equal
The foam of even exquisiteness;
Step (3): being packed into a certain amount of tetrachloro-ethylene (PCE) in glass container, step (2) is formed uniform thin
Greasy foam uniform fold forms the foam blanket of about 5cm on PCE liquid level.
Step (4): the glass container that foam is covered in step (3) is put into the VOCs release in Fig. 1, temperature in cabin
Degree is adjusted to 40 DEG C, humidity 30%.
Step (5): pass through VOC release, the evaluation method of gas-chromatography on-line monitoring, interval 15min is analyzed in time to be released
Put the concentration of PC in cabin.
PCE concentration with the situation of change of cover time is shown in Table 2 in VOCs release after foam coverage PCE.
The barrier effect that 2 repair materials of table volatilize to PCE
From in upper table we can be found that: repair materials use 360min after be 83.6% to the blocking rate of PCE, repair
Material has excellent barrier effect to VOCs pollutant, blocks effective time long.
Embodiment 4
The present embodiment is suitable for foam coupling oxidant repair materials to semi-volatile organic matter polycyclic aromatic hydrocarbon soil
Removal, the mass percent of foamed material each component are as follows: foaming agent 2.4%, starch 8%, inorganic salts 3.8%, oxide 1%,
Thickener 1.6%, deionized water 73.2%.
The present embodiment foam couple oxidant repair materials application when the following steps are included:
Step (1): foam coupling oxidant repair materials are diluted using deionized water, expanding foam solution is made;
Step (2): being that expanding foam solution 3min is stirred under 1500 revs/min using mechanical agitator low whipping speed, is formed equal
The foam of even exquisiteness;
Step (3): weighing soil in vial with cover, brush flat soil surface with brush, take a certain amount of BaP,
Anthracene, pyrene are dissolved in acetone, and obtained polycyclic aromatic hydrocarbon-acetone soln is added in soil, and stirs evenly rapidly, and brush flat soil table
Contaminated soil sample is made in face.
Step (4): step (3) contaminated soil (total polycyclic aromatic hydrocarbon content 361.2mg/ is packed into glass container with cover
Kg), the foam uniform fold of uniform and smooth step (2) formed forms the foam blanket of about 5cm on contaminated soil.
Step (5): the glass container with cover for covering foam in step (4) is put into draught cupboard, is terminated after 24 hours
Reaction.
Step (6): using the polycyclic aromatic hydrocarbon in soxhlet extraction extraction soil, polycyclic aromatic hydrocarbon removal rate is calculated.
Under identical experiment condition, when the reaction time is for 24 hours, foam couples oxidant repair materials to anthracene in soil
Removal rate be 88.7%, the removal rate of pyrene is 87.6%, and the removal rate of BaP is 74.7%, the removal of total polycyclic aromatic hydrocarbon
Rate is 87.4%.
Embodiment 5
The present embodiment is suitable for poisonous and harmful steam, volatile contaminant and the liquid beach of bubble cutoff contaminated site leakage,
The mass percent of foamed material each component are as follows: foaming agent 14.6%, starch 8.8%, inorganic salts 2.8%, oxide 1.2%,
Thickener 3.2%, deionized water 69.4%.
The present embodiment foam couple oxidant repair materials application when the following steps are included:
Step (1): foam coupling oxidant repair materials are diluted using deionized water, expanding foam solution is made;
Step (2): being that expanding foam solution 3min is stirred under 1000 revs/min using mechanical agitator low whipping speed, is formed equal
The foam of even exquisiteness;
Step (3): being packed into a certain amount of tetrachloro-ethylene (PCE) in glass container, step (2) is formed uniform thin
Greasy foam uniform fold forms the foam blanket of about 5cm on PCE liquid level.
Step (4): the glass container that foam is covered in step (3) is put into the VOCs release in Fig. 1, temperature in cabin
Degree is adjusted to 40 DEG C, humidity 30%.
Step (5): pass through VOC release, the evaluation method of gas-chromatography on-line monitoring, interval 15min is analyzed in time to be released
Put the concentration of PC in cabin.
PCE concentration with the situation of change of cover time is shown in Table 3 in VOCs release after foam coverage PCE.
The barrier effect that 3 repair materials of table volatilize to PCE
From in upper table we can be found that: repair materials use 360min after be 80.8% to the blocking rate of PCE, repair
Material has excellent barrier effect to VOCs pollutant, blocks effective time long.
Embodiment 6
The present embodiment is suitable for foam coupling oxidant repair materials to semi-volatile organic matter polycyclic aromatic hydrocarbon soil
Removal, the mass percent of foamed material each component are as follows: foaming agent 14.6%, starch 8.8%, inorganic salts 2.8%, oxidant
1.2%, thickener 3.2%, deionized water 69.4%.
The present embodiment foam couple oxidant repair materials application when the following steps are included:
Step (1): foam coupling oxidant repair materials are diluted using deionized water, expanding foam solution is made;
Step (2): being that expanding foam solution 3min is stirred under 1500 revs/min using mechanical agitator low whipping speed, is formed equal
The foam of even exquisiteness;
Step (3): weighing soil in vial with cover, brush flat soil surface with brush, take a certain amount of BaP,
Anthracene, pyrene are dissolved in acetone, and obtained polycyclic aromatic hydrocarbon-acetone soln is added in soil, and stirs evenly rapidly, and brush flat soil table
Contaminated soil sample is made in face.
Step (4): step (3) contaminated soil (total polycyclic aromatic hydrocarbon content 361.2mg/ is packed into glass container with cover
Kg), the foam uniform fold of uniform and smooth step (2) formed forms the foam blanket of about 5cm on contaminated soil.
Step (5): the glass container with cover for covering foam in step (4) is put into draught cupboard, is terminated after 24 hours
Reaction.
Step (6): using the polycyclic aromatic hydrocarbon in soxhlet extraction extraction soil, polycyclic aromatic hydrocarbon removal rate is calculated.
Under identical experiment condition, when the reaction time is for 24 hours, foam couples oxidant repair materials to anthracene in soil
Removal rate be 87.8%, the removal rate of pyrene is 86.1%, and the removal rate of BaP is 72.8%, the removal of total polycyclic aromatic hydrocarbon
Rate is 86.2%.
Claims (10)
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CN111545558A (en) * | 2020-05-26 | 2020-08-18 | 上海化工研究院有限公司 | A kind of method for thermal desorption treatment of organic polluted soil |
CN111983094A (en) * | 2020-08-27 | 2020-11-24 | 上海化工研究院有限公司 | Method and system for testing and evaluating volatilization effect of foam barrier VOCs (volatile organic Compounds) |
CN112898837A (en) * | 2021-01-11 | 2021-06-04 | 中科鼎实环境工程有限公司 | Contaminated site odor control agent and preparation method thereof |
CN112898837B (en) * | 2021-01-11 | 2022-08-16 | 中科鼎实环境工程有限公司 | Contaminated site odor control agent and preparation method thereof |
CN112974508A (en) * | 2021-03-04 | 2021-06-18 | 华东理工大学 | Sustained-release adsorption foam and application thereof |
CN113856452A (en) * | 2021-09-03 | 2021-12-31 | 煜环环境科技有限公司 | A kind of odor inhibitor of polluted soil and preparation method and application thereof |
CN113856452B (en) * | 2021-09-03 | 2024-11-19 | 煜环环境科技有限公司 | An odor inhibitor for contaminated soil and its preparation method and application |
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