US20050229825A1 - Method of disposing of hazardous wastes connected with criminal activity - Google Patents
Method of disposing of hazardous wastes connected with criminal activity Download PDFInfo
- Publication number
- US20050229825A1 US20050229825A1 US11/128,968 US12896805A US2005229825A1 US 20050229825 A1 US20050229825 A1 US 20050229825A1 US 12896805 A US12896805 A US 12896805A US 2005229825 A1 US2005229825 A1 US 2005229825A1
- Authority
- US
- United States
- Prior art keywords
- incinerator
- waste materials
- site
- materials
- group
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 238000000034 method Methods 0.000 title claims abstract description 29
- 230000000694 effects Effects 0.000 title claims abstract description 17
- 239000002920 hazardous waste Substances 0.000 title claims abstract description 13
- 239000002699 waste material Substances 0.000 claims abstract description 43
- 231100000252 nontoxic Toxicity 0.000 claims abstract description 5
- 230000003000 nontoxic effect Effects 0.000 claims abstract description 5
- MYWUZJCMWCOHBA-VIFPVBQESA-N methamphetamine Chemical compound CN[C@@H](C)CC1=CC=CC=C1 MYWUZJCMWCOHBA-VIFPVBQESA-N 0.000 claims description 24
- 239000000463 material Substances 0.000 claims description 15
- 239000000446 fuel Substances 0.000 claims description 11
- 239000004615 ingredient Substances 0.000 claims description 11
- 238000002485 combustion reaction Methods 0.000 claims description 9
- 229910052751 metal Inorganic materials 0.000 claims description 9
- 239000002184 metal Substances 0.000 claims description 9
- 231100001244 hazardous air pollutant Toxicity 0.000 claims description 7
- 239000000203 mixture Substances 0.000 claims description 7
- 239000012530 fluid Substances 0.000 claims description 6
- -1 sodium metals Chemical class 0.000 claims description 6
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 5
- 239000002283 diesel fuel Substances 0.000 claims description 5
- 239000011521 glass Substances 0.000 claims description 5
- 229910052744 lithium Inorganic materials 0.000 claims description 5
- 239000010802 sludge Substances 0.000 claims description 5
- 229910052708 sodium Inorganic materials 0.000 claims description 5
- 239000011734 sodium Substances 0.000 claims description 5
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims description 4
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical class II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims description 4
- 239000007788 liquid Substances 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 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 3
- 239000013078 crystal Substances 0.000 claims description 3
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 claims description 3
- 229960001252 methamphetamine Drugs 0.000 claims description 3
- 239000011236 particulate material Substances 0.000 claims description 2
- 238000001816 cooling Methods 0.000 claims 3
- 238000010438 heat treatment Methods 0.000 claims 3
- 230000001954 sterilising effect Effects 0.000 claims 3
- 238000004659 sterilization and disinfection Methods 0.000 claims 3
- 238000000151 deposition Methods 0.000 claims 2
- 238000011835 investigation Methods 0.000 claims 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 11
- 239000000126 substance Substances 0.000 description 11
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- KWGRBVOPPLSCSI-WPRPVWTQSA-N (-)-ephedrine Chemical compound CN[C@@H](C)[C@H](O)C1=CC=CC=C1 KWGRBVOPPLSCSI-WPRPVWTQSA-N 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 4
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 4
- UBOXGVDOUJQMTN-UHFFFAOYSA-N 1,1,2-trichloroethane Chemical compound ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 description 3
- PBKONEOXTCPAFI-UHFFFAOYSA-N 1,2,4-trichlorobenzene Chemical compound ClC1=CC=C(Cl)C(Cl)=C1 PBKONEOXTCPAFI-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- QGJOPFRUJISHPQ-UHFFFAOYSA-N Carbon disulfide Chemical compound S=C=S QGJOPFRUJISHPQ-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 3
- KWGRBVOPPLSCSI-UHFFFAOYSA-N d-ephedrine Natural products CNC(C)C(O)C1=CC=CC=C1 KWGRBVOPPLSCSI-UHFFFAOYSA-N 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- KWGRBVOPPLSCSI-WCBMZHEXSA-N pseudoephedrine Chemical compound CN[C@@H](C)[C@@H](O)C1=CC=CC=C1 KWGRBVOPPLSCSI-WCBMZHEXSA-N 0.000 description 3
- 235000002639 sodium chloride Nutrition 0.000 description 3
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 2
- RHUYHJGZWVXEHW-UHFFFAOYSA-N 1,1-Dimethyhydrazine Chemical compound CN(C)N RHUYHJGZWVXEHW-UHFFFAOYSA-N 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 2
- HGUFODBRKLSHSI-UHFFFAOYSA-N 2,3,7,8-tetrachloro-dibenzo-p-dioxin Chemical compound O1C2=CC(Cl)=C(Cl)C=C2OC2=C1C=C(Cl)C(Cl)=C2 HGUFODBRKLSHSI-UHFFFAOYSA-N 0.000 description 2
- OZDGMOYKSFPLSE-UHFFFAOYSA-N 2-Methylaziridine Chemical compound CC1CN1 OZDGMOYKSFPLSE-UHFFFAOYSA-N 0.000 description 2
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 2
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 2
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 2
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 description 2
- ZNSMNVMLTJELDZ-UHFFFAOYSA-N Bis(2-chloroethyl)ether Chemical compound ClCCOCCCl ZNSMNVMLTJELDZ-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- NIQCNGHVCWTJSM-UHFFFAOYSA-N Dimethyl phthalate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OC NIQCNGHVCWTJSM-UHFFFAOYSA-N 0.000 description 2
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 2
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 2
- RWNKSTSCBHKHTB-UHFFFAOYSA-N Hexachloro-1,3-butadiene Chemical compound ClC(Cl)=C(Cl)C(Cl)=C(Cl)Cl RWNKSTSCBHKHTB-UHFFFAOYSA-N 0.000 description 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 2
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 2
- ZKXDGKXYMTYWTB-UHFFFAOYSA-N N-nitrosomorpholine Chemical compound O=NN1CCOCC1 ZKXDGKXYMTYWTB-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- NBBJYMSMWIIQGU-UHFFFAOYSA-N Propionic aldehyde Chemical compound CCC=O NBBJYMSMWIIQGU-UHFFFAOYSA-N 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- ISRUGXGCCGIOQO-UHFFFAOYSA-N Rhoden Chemical compound CNC(=O)OC1=CC=CC=C1OC(C)C ISRUGXGCCGIOQO-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 239000010425 asbestos Substances 0.000 description 2
- DMVOXQPQNTYEKQ-UHFFFAOYSA-N biphenyl-4-amine Chemical group C1=CC(N)=CC=C1C1=CC=CC=C1 DMVOXQPQNTYEKQ-UHFFFAOYSA-N 0.000 description 2
- DIKBFYAXUHHXCS-UHFFFAOYSA-N bromoform Chemical compound BrC(Br)Br DIKBFYAXUHHXCS-UHFFFAOYSA-N 0.000 description 2
- JJWKPURADFRFRB-UHFFFAOYSA-N carbonyl sulfide Chemical compound O=C=S JJWKPURADFRFRB-UHFFFAOYSA-N 0.000 description 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 229960002179 ephedrine Drugs 0.000 description 2
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000000383 hazardous chemical Substances 0.000 description 2
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
- 150000002611 lead compounds Chemical class 0.000 description 2
- RLSSMJSEOOYNOY-UHFFFAOYSA-N m-cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 239000002557 mineral fiber Substances 0.000 description 2
- UMFJAHHVKNCGLG-UHFFFAOYSA-N n-Nitrosodimethylamine Chemical compound CN(C)N=O UMFJAHHVKNCGLG-UHFFFAOYSA-N 0.000 description 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
- QWVGKYWNOKOFNN-UHFFFAOYSA-N o-cresol Chemical compound CC1=CC=CC=C1O QWVGKYWNOKOFNN-UHFFFAOYSA-N 0.000 description 2
- RNVCVTLRINQCPJ-UHFFFAOYSA-N o-toluidine Chemical compound CC1=CC=CC=C1N RNVCVTLRINQCPJ-UHFFFAOYSA-N 0.000 description 2
- IWDCLRJOBJJRNH-UHFFFAOYSA-N p-cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- LKPLKUMXSAEKID-UHFFFAOYSA-N pentachloronitrobenzene Chemical compound [O-][N+](=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl LKPLKUMXSAEKID-UHFFFAOYSA-N 0.000 description 2
- IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 229910052895 riebeckite Inorganic materials 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 229940089453 sudafed Drugs 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- 231100000331 toxic Toxicity 0.000 description 2
- 230000002588 toxic effect Effects 0.000 description 2
- 239000010891 toxic waste Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- LDVVMCZRFWMZSG-OLQVQODUSA-N (3ar,7as)-2-(trichloromethylsulfanyl)-3a,4,7,7a-tetrahydroisoindole-1,3-dione Chemical compound C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)Cl)C(=O)[C@H]21 LDVVMCZRFWMZSG-OLQVQODUSA-N 0.000 description 1
- UOORRWUZONOOLO-OWOJBTEDSA-N (E)-1,3-dichloropropene Chemical compound ClC\C=C\Cl UOORRWUZONOOLO-OWOJBTEDSA-N 0.000 description 1
- XEMRAKSQROQPBR-UHFFFAOYSA-N (trichloromethyl)benzene Chemical compound ClC(Cl)(Cl)C1=CC=CC=C1 XEMRAKSQROQPBR-UHFFFAOYSA-N 0.000 description 1
- IAKOZHOLGAGEJT-UHFFFAOYSA-N 1,1,1-trichloro-2,2-bis(p-methoxyphenyl)-Ethane Chemical compound C1=CC(OC)=CC=C1C(C(Cl)(Cl)Cl)C1=CC=C(OC)C=C1 IAKOZHOLGAGEJT-UHFFFAOYSA-N 0.000 description 1
- DQCMWCVJSOFDSA-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl.CC(Cl)(Cl)Cl DQCMWCVJSOFDSA-UHFFFAOYSA-N 0.000 description 1
- CYXCYBWHXJXHQX-UHFFFAOYSA-N 1,1-dibromoethane;1,2-dibromoethane Chemical compound CC(Br)Br.BrCCBr CYXCYBWHXJXHQX-UHFFFAOYSA-N 0.000 description 1
- WMIQCCDZARURRI-UHFFFAOYSA-N 1,1-dichloroethane Chemical compound CC(Cl)Cl.CC(Cl)Cl WMIQCCDZARURRI-UHFFFAOYSA-N 0.000 description 1
- YMOSUBJHLKNJIU-UHFFFAOYSA-N 1,1-dichloroethene Chemical compound ClC(Cl)=C.ClC(Cl)=C YMOSUBJHLKNJIU-UHFFFAOYSA-N 0.000 description 1
- WBEJYOJJBDISQU-UHFFFAOYSA-N 1,2-Dibromo-3-chloropropane Chemical compound ClCC(Br)CBr WBEJYOJJBDISQU-UHFFFAOYSA-N 0.000 description 1
- RBACIKXCRWGCBB-UHFFFAOYSA-N 1,2-Epoxybutane Chemical compound CCC1CO1 RBACIKXCRWGCBB-UHFFFAOYSA-N 0.000 description 1
- OGJCIAFFKGRGJC-UHFFFAOYSA-N 1,2-bis(chloranyl)ethane Chemical compound ClCCCl.ClCCCl OGJCIAFFKGRGJC-UHFFFAOYSA-N 0.000 description 1
- 229940100682 1,2-dibromo-3-chloropropane Drugs 0.000 description 1
- HWUQTXJBKRUEII-UHFFFAOYSA-N 1,2-dichloropropane Chemical compound CC(Cl)CCl.CC(Cl)CCl HWUQTXJBKRUEII-UHFFFAOYSA-N 0.000 description 1
- YBQZXXMEJHZYMB-UHFFFAOYSA-N 1,2-diphenylhydrazine Chemical compound C=1C=CC=CC=1NNC1=CC=CC=C1 YBQZXXMEJHZYMB-UHFFFAOYSA-N 0.000 description 1
- FSSPGSAQUIYDCN-UHFFFAOYSA-N 1,3-Propane sultone Chemical compound O=S1(=O)CCCO1 FSSPGSAQUIYDCN-UHFFFAOYSA-N 0.000 description 1
- OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 1
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 1
- CZIHNRWJTSTCEX-UHFFFAOYSA-N 2 Acetylaminofluorene Chemical compound C1=CC=C2C3=CC=C(NC(=O)C)C=C3CC2=C1 CZIHNRWJTSTCEX-UHFFFAOYSA-N 0.000 description 1
- USPMMJODHSTVIM-UHFFFAOYSA-N 2,3-dimethyl-6-phenyldiazenylaniline Chemical compound NC1=C(C)C(C)=CC=C1N=NC1=CC=CC=C1 USPMMJODHSTVIM-UHFFFAOYSA-N 0.000 description 1
- LHJGJYXLEPZJPM-UHFFFAOYSA-N 2,4,5-trichlorophenol Chemical compound OC1=CC(Cl)=C(Cl)C=C1Cl LHJGJYXLEPZJPM-UHFFFAOYSA-N 0.000 description 1
- LINPIYWFGCPVIE-UHFFFAOYSA-N 2,4,6-trichlorophenol Chemical compound OC1=C(Cl)C=C(Cl)C=C1Cl LINPIYWFGCPVIE-UHFFFAOYSA-N 0.000 description 1
- 239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 description 1
- VOZKAJLKRJDJLL-UHFFFAOYSA-N 2,4-diaminotoluene Chemical compound CC1=CC=C(N)C=C1N VOZKAJLKRJDJLL-UHFFFAOYSA-N 0.000 description 1
- UFBJCMHMOXMLKC-UHFFFAOYSA-N 2,4-dinitrophenol Chemical compound OC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O UFBJCMHMOXMLKC-UHFFFAOYSA-N 0.000 description 1
- RMBFBMJGBANMMK-UHFFFAOYSA-N 2,4-dinitrotoluene Chemical compound CC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O RMBFBMJGBANMMK-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- FGLBSLMDCBOPQK-UHFFFAOYSA-N 2-nitropropane Chemical compound CC(C)[N+]([O-])=O FGLBSLMDCBOPQK-UHFFFAOYSA-N 0.000 description 1
- JRBJSXQPQWSCCF-UHFFFAOYSA-N 3,3'-Dimethoxybenzidine Chemical compound C1=C(N)C(OC)=CC(C=2C=C(OC)C(N)=CC=2)=C1 JRBJSXQPQWSCCF-UHFFFAOYSA-N 0.000 description 1
- NUIURNJTPRWVAP-UHFFFAOYSA-N 3,3'-Dimethylbenzidine Chemical compound C1=C(N)C(C)=CC(C=2C=C(C)C(N)=CC=2)=C1 NUIURNJTPRWVAP-UHFFFAOYSA-N 0.000 description 1
- IBOFVQJTBBUKMU-UHFFFAOYSA-N 4,4'-methylene-bis-(2-chloroaniline) Chemical compound C1=C(Cl)C(N)=CC=C1CC1=CC=C(N)C(Cl)=C1 IBOFVQJTBBUKMU-UHFFFAOYSA-N 0.000 description 1
- ZXVONLUNISGICL-UHFFFAOYSA-N 4,6-dinitro-o-cresol Chemical compound CC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O ZXVONLUNISGICL-UHFFFAOYSA-N 0.000 description 1
- BAJQRLZAPXASRD-UHFFFAOYSA-N 4-Nitrobiphenyl Chemical group C1=CC([N+](=O)[O-])=CC=C1C1=CC=CC=C1 BAJQRLZAPXASRD-UHFFFAOYSA-N 0.000 description 1
- MVXMNHYVCLMLDD-UHFFFAOYSA-N 4-methoxynaphthalene-1-carbaldehyde Chemical compound C1=CC=C2C(OC)=CC=C(C=O)C2=C1 MVXMNHYVCLMLDD-UHFFFAOYSA-N 0.000 description 1
- BTJIUGUIPKRLHP-UHFFFAOYSA-N 4-nitrophenol Chemical compound OC1=CC=C([N+]([O-])=O)C=C1 BTJIUGUIPKRLHP-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- OSDWBNJEKMUWAV-UHFFFAOYSA-N Allyl chloride Chemical compound ClCC=C OSDWBNJEKMUWAV-UHFFFAOYSA-N 0.000 description 1
- 239000005745 Captan Substances 0.000 description 1
- HSSBORCLYSCBJR-UHFFFAOYSA-N Chloramben Chemical compound NC1=CC(Cl)=CC(C(O)=O)=C1Cl HSSBORCLYSCBJR-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- RAPBNVDSDCTNRC-UHFFFAOYSA-N Chlorobenzilate Chemical compound C=1C=C(Cl)C=CC=1C(O)(C(=O)OCC)C1=CC=C(Cl)C=C1 RAPBNVDSDCTNRC-UHFFFAOYSA-N 0.000 description 1
- XJUZRXYOEPSWMB-UHFFFAOYSA-N Chloromethyl methyl ether Chemical compound COCCl XJUZRXYOEPSWMB-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 208000032170 Congenital Abnormalities Diseases 0.000 description 1
- 206010010356 Congenital anomaly Diseases 0.000 description 1
- 239000004803 Di-2ethylhexylphthalate Substances 0.000 description 1
- YXHKONLOYHBTNS-UHFFFAOYSA-N Diazomethane Chemical compound C=[N+]=[N-] YXHKONLOYHBTNS-UHFFFAOYSA-N 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- YIIMEMSDCNDGTB-UHFFFAOYSA-N Dimethylcarbamoyl chloride Chemical compound CN(C)C(Cl)=O YIIMEMSDCNDGTB-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- PDQAZBWRQCGBEV-UHFFFAOYSA-N Ethylenethiourea Chemical compound S=C1NCCN1 PDQAZBWRQCGBEV-UHFFFAOYSA-N 0.000 description 1
- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- ZRKWMRDKSOPRRS-UHFFFAOYSA-N N-Methyl-N-nitrosourea Chemical compound O=NN(C)C(N)=O ZRKWMRDKSOPRRS-UHFFFAOYSA-N 0.000 description 1
- 206010028980 Neoplasm Diseases 0.000 description 1
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical compound ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 1
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 1
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- AWMVMTVKBNGEAK-UHFFFAOYSA-N Styrene oxide Chemical compound C1OC1C1=CC=CC=C1 AWMVMTVKBNGEAK-UHFFFAOYSA-N 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- CRPUJAZIXJMDBK-UHFFFAOYSA-N Toxaphene Natural products C1CC2C(=C)C(C)(C)C1C2 CRPUJAZIXJMDBK-UHFFFAOYSA-N 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- 229940058905 antimony compound for treatment of leishmaniasis and trypanosomiasis Drugs 0.000 description 1
- 150000001463 antimony compounds Chemical class 0.000 description 1
- RBFQJDQYXXHULB-UHFFFAOYSA-N arsane Chemical compound [AsH3] RBFQJDQYXXHULB-UHFFFAOYSA-N 0.000 description 1
- 229910052785 arsenic Inorganic materials 0.000 description 1
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 1
- 150000001495 arsenic compounds Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- HFACYLZERDEVSX-UHFFFAOYSA-N benzidine Chemical compound C1=CC(N)=CC=C1C1=CC=C(N)C=C1 HFACYLZERDEVSX-UHFFFAOYSA-N 0.000 description 1
- KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 description 1
- 229940073608 benzyl chloride Drugs 0.000 description 1
- 150000001573 beryllium compounds Chemical class 0.000 description 1
- VEZXCJBBBCKRPI-UHFFFAOYSA-N beta-propiolactone Chemical compound O=C1CCO1 VEZXCJBBBCKRPI-UHFFFAOYSA-N 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 230000007698 birth defect Effects 0.000 description 1
- HRQGCQVOJVTVLU-UHFFFAOYSA-N bis(chloromethyl) ether Chemical compound ClCOCCl HRQGCQVOJVTVLU-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- INLLPKCGLOXCIV-UHFFFAOYSA-N bromoethene Chemical compound BrC=C INLLPKCGLOXCIV-UHFFFAOYSA-N 0.000 description 1
- 229950005228 bromoform Drugs 0.000 description 1
- UQJPYTSEIDWJMP-UHFFFAOYSA-N bromomethane Chemical compound BrC.BrC UQJPYTSEIDWJMP-UHFFFAOYSA-N 0.000 description 1
- RFAZFSACZIVZDV-UHFFFAOYSA-N butan-2-one Chemical compound CCC(C)=O.CCC(C)=O RFAZFSACZIVZDV-UHFFFAOYSA-N 0.000 description 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N butyric aldehyde Natural products CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- 229940065285 cadmium compound Drugs 0.000 description 1
- 150000001662 cadmium compounds Chemical class 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 201000011510 cancer Diseases 0.000 description 1
- 229940117949 captan Drugs 0.000 description 1
- 229960005286 carbaryl Drugs 0.000 description 1
- CVXBEEMKQHEXEN-UHFFFAOYSA-N carbaryl Chemical compound C1=CC=C2C(OC(=O)NC)=CC=CC2=C1 CVXBEEMKQHEXEN-UHFFFAOYSA-N 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- BIWJNBZANLAXMG-YQELWRJZSA-N chloordaan Chemical compound ClC1=C(Cl)[C@@]2(Cl)C3CC(Cl)C(Cl)C3[C@]1(Cl)C2(Cl)Cl BIWJNBZANLAXMG-YQELWRJZSA-N 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 1
- 229940106681 chloroacetic acid Drugs 0.000 description 1
- HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 description 1
- RRQDOXSDGSRAFK-UHFFFAOYSA-N chloromethane Chemical compound ClC.ClC RRQDOXSDGSRAFK-UHFFFAOYSA-N 0.000 description 1
- 229940061627 chloromethyl methyl ether Drugs 0.000 description 1
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 150000001845 chromium compounds Chemical class 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 150000001869 cobalt compounds Chemical class 0.000 description 1
- 229940124579 cold medicine Drugs 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 150000001896 cresols Chemical class 0.000 description 1
- DEZRYPDIMOWBDS-UHFFFAOYSA-N dcm dichloromethane Chemical compound ClCCl.ClCCl DEZRYPDIMOWBDS-UHFFFAOYSA-N 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 150000004826 dibenzofurans Chemical class 0.000 description 1
- 229960002380 dibutyl phthalate Drugs 0.000 description 1
- OEBRKCOSUFCWJD-UHFFFAOYSA-N dichlorvos Chemical compound COP(=O)(OC)OC=C(Cl)Cl OEBRKCOSUFCWJD-UHFFFAOYSA-N 0.000 description 1
- 229950001327 dichlorvos Drugs 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- DENRZWYUOJLTMF-UHFFFAOYSA-N diethyl sulfate Chemical compound CCOS(=O)(=O)OCC DENRZWYUOJLTMF-UHFFFAOYSA-N 0.000 description 1
- 229940008406 diethyl sulfate Drugs 0.000 description 1
- FBSAITBEAPNWJG-UHFFFAOYSA-N dimethyl phthalate Natural products CC(=O)OC1=CC=CC=C1OC(C)=O FBSAITBEAPNWJG-UHFFFAOYSA-N 0.000 description 1
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 1
- 229960001826 dimethylphthalate Drugs 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- 238000005108 dry cleaning Methods 0.000 description 1
- 239000003344 environmental pollutant Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- JLYXXMFPNIAWKQ-GNIYUCBRSA-N gamma-hexachlorocyclohexane Chemical compound Cl[C@H]1[C@H](Cl)[C@@H](Cl)[C@@H](Cl)[C@H](Cl)[C@H]1Cl JLYXXMFPNIAWKQ-GNIYUCBRSA-N 0.000 description 1
- JLYXXMFPNIAWKQ-UHFFFAOYSA-N gamma-hexachlorocyclohexane Natural products ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl JLYXXMFPNIAWKQ-UHFFFAOYSA-N 0.000 description 1
- 239000003502 gasoline Substances 0.000 description 1
- 229940093920 gynecological arsenic compound Drugs 0.000 description 1
- 231100001261 hazardous Toxicity 0.000 description 1
- 230000008821 health effect Effects 0.000 description 1
- FRCCEHPWNOQAEU-UHFFFAOYSA-N heptachlor Chemical compound ClC1=C(Cl)C2(Cl)C3C=CC(Cl)C3C1(Cl)C2(Cl)Cl FRCCEHPWNOQAEU-UHFFFAOYSA-N 0.000 description 1
- CKAPSXZOOQJIBF-UHFFFAOYSA-N hexachlorobenzene Chemical compound ClC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl CKAPSXZOOQJIBF-UHFFFAOYSA-N 0.000 description 1
- VUNCWTMEJYMOOR-UHFFFAOYSA-N hexachlorocyclopentadiene Chemical compound ClC1=C(Cl)C(Cl)(Cl)C(Cl)=C1Cl VUNCWTMEJYMOOR-UHFFFAOYSA-N 0.000 description 1
- VHHHONWQHHHLTI-UHFFFAOYSA-N hexachloroethane Chemical compound ClC(Cl)(Cl)C(Cl)(Cl)Cl VHHHONWQHHHLTI-UHFFFAOYSA-N 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 description 1
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 1
- CUPFNGOKRMWUOO-UHFFFAOYSA-N hydron;difluoride Chemical compound F.F CUPFNGOKRMWUOO-UHFFFAOYSA-N 0.000 description 1
- 239000002117 illicit drug Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- AJOVJQYQEXKTQG-UHFFFAOYSA-N iodomethane Chemical compound IC.IC AJOVJQYQEXKTQG-UHFFFAOYSA-N 0.000 description 1
- 239000003041 laboratory chemical Substances 0.000 description 1
- 229960002809 lindane Drugs 0.000 description 1
- IVSZLXZYQVIEFR-UHFFFAOYSA-N m-xylene Chemical class CC1=CC=CC(C)=C1 IVSZLXZYQVIEFR-UHFFFAOYSA-N 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 150000002697 manganese compounds Chemical class 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 150000002731 mercury compounds Chemical class 0.000 description 1
- HAMGRBXTJNITHG-UHFFFAOYSA-N methyl isocyanate Chemical compound CN=C=O HAMGRBXTJNITHG-UHFFFAOYSA-N 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- HDZGCSFEDULWCS-UHFFFAOYSA-N monomethylhydrazine Chemical compound CNN HDZGCSFEDULWCS-UHFFFAOYSA-N 0.000 description 1
- CKYYXIOZPQZWSC-UHFFFAOYSA-N n,n-diethylaniline;n,n-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1.CCN(CC)C1=CC=CC=C1 CKYYXIOZPQZWSC-UHFFFAOYSA-N 0.000 description 1
- 150000002816 nickel compounds Chemical class 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- VMPITZXILSNTON-UHFFFAOYSA-N o-anisidine Chemical compound COC1=CC=CC=C1N VMPITZXILSNTON-UHFFFAOYSA-N 0.000 description 1
- 150000002884 o-xylenes Chemical class 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000005416 organic matter Substances 0.000 description 1
- 150000002938 p-xylenes Chemical class 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- LCCNCVORNKJIRZ-UHFFFAOYSA-N parathion Chemical compound CCOP(=S)(OCC)OC1=CC=C([N+]([O-])=O)C=C1 LCCNCVORNKJIRZ-UHFFFAOYSA-N 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- IMACFCSSMIZSPP-UHFFFAOYSA-N phenacyl chloride Chemical compound ClCC(=O)C1=CC=CC=C1 IMACFCSSMIZSPP-UHFFFAOYSA-N 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 1
- 231100000719 pollutant Toxicity 0.000 description 1
- 150000003071 polychlorinated biphenyls Chemical class 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 229960000380 propiolactone Drugs 0.000 description 1
- 229960003908 pseudoephedrine Drugs 0.000 description 1
- 230000005258 radioactive decay Effects 0.000 description 1
- 229910052704 radon Inorganic materials 0.000 description 1
- SYUHGPGVQRZVTB-UHFFFAOYSA-N radon atom Chemical compound [Rn] SYUHGPGVQRZVTB-UHFFFAOYSA-N 0.000 description 1
- 230000001850 reproductive effect Effects 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 229940065287 selenium compound Drugs 0.000 description 1
- 150000003343 selenium compounds Chemical class 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- UOORRWUZONOOLO-UHFFFAOYSA-N telone II Natural products ClCC=CCl UOORRWUZONOOLO-UHFFFAOYSA-N 0.000 description 1
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23G—CREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
- F23G5/00—Incineration of waste; Incinerator constructions; Details, accessories or control therefor
- F23G5/40—Portable or mobile incinerators
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23G—CREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
- F23G5/00—Incineration of waste; Incinerator constructions; Details, accessories or control therefor
- F23G5/02—Incineration of waste; Incinerator constructions; Details, accessories or control therefor with pretreatment
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23G—CREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
- F23G5/00—Incineration of waste; Incinerator constructions; Details, accessories or control therefor
- F23G5/08—Incineration of waste; Incinerator constructions; Details, accessories or control therefor having supplementary heating
- F23G5/14—Incineration of waste; Incinerator constructions; Details, accessories or control therefor having supplementary heating including secondary combustion
- F23G5/16—Incineration of waste; Incinerator constructions; Details, accessories or control therefor having supplementary heating including secondary combustion in a separate combustion chamber
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23G—CREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
- F23G7/00—Incinerators or other apparatus for consuming industrial waste, e.g. chemicals
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23G—CREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
- F23G2201/00—Pretreatment
- F23G2201/50—Devolatilising; from soil, objects
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23G—CREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
- F23G2201/00—Pretreatment
- F23G2201/60—Separating
- F23G2201/603—Separating recyclable material
Definitions
- methamphetamine (meth) lab problem is prevalent throughout the United States and the rest of the World. Meth labs used to make the illegal drug are discovered in houses, apartments, motel rooms, sheds, or even motor vehicles. In recent times, Federal, State and Local authorities were involved in the seizure of more than 500 labs in a single state, and the number of such labs seized by law enforcement agencies increases each year.
- the cost of loading, transporting, and burying waste materials from typical meth labs can run upwardly of $10,000 per meth lab, and sometimes substantially more.
- a further object of this invention is to provide a method of disposing of hazardous waste materials connected with criminal activity which is both safe and inexpensive.
- a method of disposing of hazardous wastes connected with criminal activity involves the steps of transporting a portable batch-type incinerator to a site where certain hazardous wastes are located connected to the criminal activity, such as a meth lab site.
- the next step is identifying the waste materials and sorting through them and selecting waste materials from a group which are combustible in the presence of heat without creating harmful emissions.
- the selected waste materials are then placed within the incinerator.
- the incinerator is then heated to a temperature of between 1600-1900° F. for a period of at least one hour and between one hour and two hours to create a particulate residue.
- the incinerator is then cooled to ambient temperatures, and the residue is collected from the incinerator and put into a portable container.
- the portable container is then moved from the site and deposited in a convenient local non-toxic landfill.
- the incinerator is thereupon removed from the site.
- ingredients and equipment that may be involved in typical meth lab activity include the following:
- the first step in cleaning up a meth site is to take an inventory of the material at the site and identify the same.
- a portable incinerator pulled behind a pickup truck or the like is brought directly to the site.
- An incinerator suitable for practicing the method is shown in U.S. Pat. No. 5,339,752, and the drawings and descriptive portion thereof are herein incorporated by reference. Any suitable number of wheels can be applied to the incinerator of U.S. Pat. No. 5,339,752 to enable it to be towed to the site.
- the incinerator has an after-burner through which emissions from the combusted material are channeled to permit particles in the emissions to be further combusted.
- hazardous air pollutants as described by the U.S. Environmental Protection Agency as “those pollutants that are known or suspected to cause cancer or other serious health effects, such as reproductive effects or birth defects, or adverse environmental effect”.
- hazardous air pollutants include benzene, which is found in gasoline; perchlorethlyene, which is emitted from some dry cleaning facilities; and methylene chloride, which is used as a solvent and paint stripper by a number of industries.
- hazardous air pollutants examples include dioxin, asbestos, toluene, and metals such as cadmium, mercury, chromium, and lead compounds.
- hazardous air pollutants mean the following chemicals: CAS Chemical Number Name 75070 Acetaldehyde 60355 Acetamide 75058 Acetonitrile 98862 Acetophenone 53963 2-Acetylaminofluorene 107028 Acrolein 79061 Acrylamide 79107 Acrylic acid 107131 Acrylonitrile 107051 Allyl chloride 92671 4-Aminobiphenyl 62533 Aniline 90040 o-Anisidine 1332214 Asbestos 71432 Benzene (including benzene from gasoline) 92875 Benzidine 98077 Benzotrichloride 100447 Benzyl chloride 92524 Biphenyl 117817 Bis(2-ethylhexyl) phthalate (DEHP) 542881 Bis(chloromethyl)
- Typical chemicals or utensils that can be subjected to heat would include, without limitation, completed supplies of meth itself which appear as hardened solid particles which are typically smoked. Sludge from the meth manufacturing containers is also collected as combustibles along with such meth ingredients as Sudafed® and Ephedrine.
- Equipment which can either be incinerated or at least sterilized would include laboratory glass ware, coffee filters, tubing, and the like. Such components are placed within the incinerator which is then ignited and heated to a temperature of preferably 1600-1900° F. for a period of at least an hour and preferably two hours. The temperature in the after-burner should be 1600° F. or higher.
- the present invention provides an incinerator having an interior of the incinerator lined with firebricks. More particularly, each sidewall, each end wall, bottom wall, and each lid includes a firebrick lining. Likewise, the present invention provides an incinerator having a combustion chamber lined with firebricks.
- a proper fuel is provided for thorough combustion.
- a primary burner of the incinerator preferably burns No. 2 diesel fuel, though other fuel may be utilized.
- the fuel may comprise a mixture such as (diesel fuel/either/Coleman® Fuel).
- Coleman® Fuel means a particular brand of the more generic product, white gas.
- iodine crystals, red phosphorous, Lithium, sodium crystals/metals, and lye can be stored in separately labeled Teflon® containers and kept dry for further disposal in accordance with Hazardous Laboratory Chemicals: Disposal Guide: Z28,182-4.
- Liquid brake fluid and brake cleaner can be absorbed by common floor dry and disposed in a landfill.
- drain cleaner such as Drano®
- acid mixes that have been neutralized by a neutralizer (e.g. baking soda) and which could be mixed with common floor dry to be disposed of in a local landfill.
- the metal or other containers placed in the incinerator and subjected to the foregoing conditions of heat will be thoroughly sterilized after the one hour period.
- the chemicals which have not been vaporized typically will form a fine particulate material which can be taken from the incinerator after it is cooled to ambient temperatures, placed in a suitable container, and transported to a local non-toxic landfill.
- the incinerator is thereupon towed from the site and is prepared to repeat the activity at the next discovered meth site.
- the method of this invention is also useful at other crime scenes where there is a residue of evidence after the law enforcement persons have removed whatever physical evidence is necessary.
- the incinerator can be brought to such a site and can be used for disposal purposes of residue material whether it be toxic waste or otherwise without having to introduce special toxic waste transporting equipment for transportation to far distant points.
- the method of this invention can be used at Courthouses and the like after meth or toxic ingredients have completed their function as evidence in a completed criminal case.
- the method of this invention will permit the swift disposal of many toxic ingredients at a meth lab site or other criminal scene in a very short time, under very safe conditions, and at a very low expense as compared to loading, transporting and then disposing of the same ingredients at a far distant point.
- Some of the selected wastes, such as meth, the meth sludge, are preferably combusted at a temperature of between 1100-1300° F. In that case, the incinerator is first heated to that temperature for about one hour, and then the heat is increased to 1600-1900° F. to deal with the remaining selected combustible ingredients.
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- General Engineering & Computer Science (AREA)
- Environmental & Geological Engineering (AREA)
- Processing Of Solid Wastes (AREA)
- Gasification And Melting Of Waste (AREA)
Abstract
A method of disposing of hazardous wastes connected with criminal activity comprising transporting a portable incinerator to the site of the criminal activity, sorting through waste materials at the site and selecting waste materials which are combustible and will not emit harmful emissions. The selected waste materials are placed within the incinerator and heated to a temperature of between 1600-1900° F. Non-combustible containers used to practice the illegal activity can be sterilized at the same time. The residue from the incinerator can then be collected and buried in a non-toxic landfill.
Description
- This application is a continuation-in-part of Ser. No. 10/100,325 filed Mar. 18, 2002.
- The methamphetamine (meth) lab problem is prevalent throughout the United States and the rest of the World. Meth labs used to make the illegal drug are discovered in houses, apartments, motel rooms, sheds, or even motor vehicles. In recent times, Federal, State and Local authorities were involved in the seizure of more than 500 labs in a single state, and the number of such labs seized by law enforcement agencies increases each year.
- After a lab is seized by law enforcement officials, professionals trained to handle hazardous materials are generally called in to remove lab wastes and any bulk materials. Some of the chemicals can be disposed of at the site by being mixed with water or other ingredients. However, there are certain chemicals and paraphernalia that must be carefully carried to a special truck or vehicle, and then transported to a far distance point where they are ultimately disposed of in a secluded landfill sometimes located hundreds and hundreds of miles from the site at which they were discovered. The long transportation of these hazardous wastes and materials invites a great problem in the event that any of them would be wrecked, thus creating a dangerous situation wherever such an accident might have taken place.
- The cost of loading, transporting, and burying waste materials from typical meth labs can run upwardly of $10,000 per meth lab, and sometimes substantially more.
- It is therefore a principal object of this invention to provide a method of disposing of hazardous wastes connected with criminal activity at the site of the activity.
- A further object of this invention is to provide a method of disposing of hazardous waste materials connected with criminal activity which is both safe and inexpensive.
- These and other objects will be apparent to those skilled in the art.
- A method of disposing of hazardous wastes connected with criminal activity involves the steps of transporting a portable batch-type incinerator to a site where certain hazardous wastes are located connected to the criminal activity, such as a meth lab site. The next step is identifying the waste materials and sorting through them and selecting waste materials from a group which are combustible in the presence of heat without creating harmful emissions. The selected waste materials are then placed within the incinerator. The incinerator is then heated to a temperature of between 1600-1900° F. for a period of at least one hour and between one hour and two hours to create a particulate residue. The incinerator is then cooled to ambient temperatures, and the residue is collected from the incinerator and put into a portable container. The portable container is then moved from the site and deposited in a convenient local non-toxic landfill. The incinerator is thereupon removed from the site.
- The ingredients and equipment that may be involved in typical meth lab activity include the following:
-
- Pool acid/Muratic acid
- Lye
- Acetone
- Brake Fluid
- Brake Cleaner
- Iodine Crystals
- Lithium Metal/Lithium Batteries
- Lighter Fluid
- Drain Cleaners (Drano or Liquid Fire)
- Cold Medicine Containing Pseudoephedrine (Sudafed)
- Ethyl Ether (Starting Fluid)
- Anhydrous Ammonia (stored in propane tanks or coolers)
- Sodium Metal
- Red Phosphorus
- Ephedrine
- Laboratory Glassware
- Coffee Filters
- Table Salt
- Two Quart Plastic Type Containers for anhydrous ammonia
- One gallon metal container or glass container of white gas.
- Sludge comprised of a mixture of all the chemicals located in various containers
- Various types of glassware used to mix the chemicals
- Plastic pop bottles, air tubing and the like
- The first step in cleaning up a meth site is to take an inventory of the material at the site and identify the same. At the same time, a portable incinerator pulled behind a pickup truck or the like is brought directly to the site. An incinerator suitable for practicing the method is shown in U.S. Pat. No. 5,339,752, and the drawings and descriptive portion thereof are herein incorporated by reference. Any suitable number of wheels can be applied to the incinerator of U.S. Pat. No. 5,339,752 to enable it to be towed to the site. The incinerator has an after-burner through which emissions from the combusted material are channeled to permit particles in the emissions to be further combusted.
- The professionals at the site should then sort through the waste materials and select waste materials from the total group of materials which are combustible in the presence of heat and which can be subjected to heat without creating harmful health emissions, defined herein as hazardous air pollutants as described by the U.S. Environmental Protection Agency as “those pollutants that are known or suspected to cause cancer or other serious health effects, such as reproductive effects or birth defects, or adverse environmental effect”. Examples of hazardous air pollutants include benzene, which is found in gasoline; perchlorethlyene, which is emitted from some dry cleaning facilities; and methylene chloride, which is used as a solvent and paint stripper by a number of industries. Examples of other listed hazardous air pollutants include dioxin, asbestos, toluene, and metals such as cadmium, mercury, chromium, and lead compounds. As defined by the EPA and as defined herein hazardous air pollutants mean the following chemicals:
CAS Chemical Number Name 75070 Acetaldehyde 60355 Acetamide 75058 Acetonitrile 98862 Acetophenone 53963 2-Acetylaminofluorene 107028 Acrolein 79061 Acrylamide 79107 Acrylic acid 107131 Acrylonitrile 107051 Allyl chloride 92671 4-Aminobiphenyl 62533 Aniline 90040 o-Anisidine 1332214 Asbestos 71432 Benzene (including benzene from gasoline) 92875 Benzidine 98077 Benzotrichloride 100447 Benzyl chloride 92524 Biphenyl 117817 Bis(2-ethylhexyl) phthalate (DEHP) 542881 Bis(chloromethyl) ether 75252 Bromoform 106990 1,3-Butadiene 156627 Calcium cyanamide 105602 Caprolactam(See Modification) 133062 Captan 63252 Carbaryl 75150 Carbon disulfide 56235 Carbon tetrachloride 463581 Carbonyl sulfide 120809 Catechol 133904 Chloramben 57749 Chlordane 7782505 Chlorine 79118 Chloroacetic acid 532274 2-Chloroacetophenone 108907 Chlorobenzene 510156 Chlorobenzilate 67663 Chloroform 107302 Chloromethyl methyl ether 126998 Chloroprene 1319773 Cresols/Cresylic acid (isomers and mixture) 95487 o-Cresol 108394 m-Cresol 106445 p-Cresol 98828 Cumene 94757 2,4-D, salts and esters 3547044 DDE 334883 Diazomethane 132649 Dibenzofurans 96128 1,2-Dibromo-3-chloropropane 84742 Dibutylphthalate 106467 1,4-Dichlorobenzene(p) 91941 3,3-Dichlorobenzidene 111444 Dichloroethyl ether (Bis(2- chloroethyl)ether) 542756 1,3-Dichloropropene 62737 Dichlorvos 111422 Diethanolamine 121697 N,N-Diethyl aniline (N,N- Dimethylaniline) 64675 Diethyl sulfate 119904 3,3-Dimethoxybenzidine 60117 Dimethyl aminoazobenzene 119937 3,3′-Dimethyl benzidine 79447 Dimethyl carbamoyl chloride 68122 Dimethyl formamide 57147 1,1-Dimethyl hydrazine 131113 Dimethyl phthalate 77781 Dimethyl sulfate 534521 4,6-Dinitro-o-cresol, and salts 51285 2,4-Dinitrophenol 121142 2,4-Dinitrotoluene 123911 1,4-Dioxane (1,4-Diethyleneoxide) 122667 1,2-Diphenylhydrazine 106898 Epichlorohydrin (1-Chloro-2,3- epoxypropane) 106887 1,2-Epoxybutane 140885 Ethyl acrylate 100414 Ethyl benzene 51796 Ethyl carbamate (Urethane) 75003 Ethyl chloride (Chloroethane) 106934 Ethylene dibromide (Dibromoethane) 107062 Ethylene dichloride (1,2- Dichloroethane) 107211 Ethylene glycol 151564 Ethylene imine (Aziridine) 75218 Ethylene oxide 96457 Ethylene thiourea 75343 Ethylidene dichloride (1,1- Dichloroethane) 50000 Formaldehyde 76448 Heptachlor 118741 Hexachlorobenzene 87683 Hexachlorobutadiene 77474 Hexachlorocyclopentadiene 67721 Hexachloroethane 822060 Hexamethylene-1,6-diisocyanate 680319 Hexamethylphosphoramide 110543 Hexane 302012 Hydrazine 7647010 Hydrochloric acid 7664393 Hydrogen fluoride (Hydrofluoric acid) 7783064 Hydrogen sulfide(See Modification) 123319 Hydroquinone 78591 Isophorone 58899 Lindane (all isomers) 108316 Maleic anhydride 67561 Methanol 72435 Methoxychlor 74839 Methyl bromide (Bromomethane) 74873 Methyl chloride (Chloromethane) 71556 Methyl chloroform (1,1,1- Trichloroethane) 78933 Methyl ethyl ketone (2-Butanone) 60344 Methyl hydrazine 74884 Methyl iodide (Iodomethane) 108101 Methyl isobutyl ketone (Hexone) 624839 Methyl isocyanate 80626 Methyl methacrylate 1634044 Methyl tert butyl ether 101144 4,4-Methylene bis(2-chloroaniline) 75092 Methylene chloride (Dichloromethane) 101688 Methylene diphenyl diisocyanate (MDI) 101779 4,4&&-Methylenedianiline 91203 Naphthalene 98953 Nitrobenzene 92933 4-Nitrobiphenyl 100027 4-Nitrophenol 79469 2-Nitropropane 684935 N-Nitroso-N-methylurea 62759 N-Nitrosodimethylamine 59892 N-Nitrosomorpholine 56382 Parathion 82688 Pentachloronitrobenzene (Quintobenzene) 87865 Pentachlorophenol 108952 Phenol 106503 p-Phenylenediamine 75445 Phosgene 7803512 Phosphine 7723140 Phosphorus 85449 Phthalic anhydride 1336363 Polychlorinated biphenyls (Aroclors) 1120714 1,3-Propane sultone 57578 beta-Propiolactone 123386 Propionaldehyde 114261 Propoxur (Baygon) 78875 Propylene dichloride (1,2- Dichloropropane) 75569 Propylene oxide 75558 1,2-Propylenimine (2-Methyl aziridine) 91225 Quinoline 106514 Quinone 100425 Styrene 96093 Styrene oxide 1746016 2,3,7,8-Tetrachlorodibenzo-p-dioxin 79345 1,1,2,2-Tetrachloroethane 127184 Tetrachloroethylene (Perchloroethylene) 7550450 Titanium tetrachloride 108883 Toluene 95807 2,4-Toluene diamine 584849 2,4-Toluene diisocyanate 95534 o-Toluidine 8001352 Toxaphene (chlorinated camphene) 120821 1,2,4-Trichlorobenzene 79005 1,1,2-Trichloroethane 79016 Trichloroethylene 95954 2,4,5-Trichlorophenol 88062 2,4,6-Trichlorophenol 121448 Triethylamine 1582098 Trifluralin 540841 2,2,4-Trimethylpentane 108054 Vinyl acetate 593602 Vinyl bromide 75014 Vinyl chloride 75354 Vinylidene chloride (1,1- Dichloroethylene) 1330207 Xylenes (isomers and mixture) 95476 o-Xylenes 108383 m-Xylenes 106423 p-Xylenes 0 Antimony Compounds 0 Arsenic Compounds (inorganic including arsine) 0 Beryllium Compounds 0 Cadmium Compounds 0 Chromium Compounds 0 Cobalt Compounds 0 Coke Oven Emissions 0 Cyanide Compounds (*1) 0 Glycol ethers (*2) 0 Lead Compounds 0 Manganese Compounds 0 Mercury Compounds 0 Fine mineral fibers (*3) 0 Nickel Compounds 0 Polycylic Organic Matter (*4) 0 Radionuclides (including radon) (*5) 0 Selenium Compounds
NOTE:
For all listings above which contain the word “compounds” and for glycol ethers, the following applies: Unless otherwise specified, these listings
# are defined as including any unique chemical substance that contains the named chemical (i.e., antimony, arsenic, etc.) as part of that chemical's infrastructure.
(*1) X′CN where X = H′ or any other group where a formal dissociation may occur. For example KCN or Ca (CN) 2.
(*2) Includes mono- and di-ethers of ethylene glycol, diethylene glycol, and triethylene glycol R-(OCH2CH2)n -OR′ where n = 1, 2, or 3; R = alkyl or
# aryl groups; R′ = R, H, or groups which, when removed, yield glycol ethers with the structure: R-(OCH2CH)n-OH. Polymers are excluded from the glycol category. (See Modification).
(*3) Includes mineral fiber emissions from facilities manufacturing or processing glass, rock, or slag fibers (or other mineral derived fibers) of average diameter 1 micrometer or less.
(*4) Includes organic compounds with more than one benzene ring, and which have a boiling point greater than or equal to 100° C.
(*5) A type of atom which spontaneously undergoes radioactive decay.
- Typical chemicals or utensils that can be subjected to heat would include, without limitation, completed supplies of meth itself which appear as hardened solid particles which are typically smoked. Sludge from the meth manufacturing containers is also collected as combustibles along with such meth ingredients as Sudafed® and Ephedrine. Equipment which can either be incinerated or at least sterilized would include laboratory glass ware, coffee filters, tubing, and the like. Such components are placed within the incinerator which is then ignited and heated to a temperature of preferably 1600-1900° F. for a period of at least an hour and preferably two hours. The temperature in the after-burner should be 1600° F. or higher.
- Due to the high temperatures, conventional incinerators having metal interiors or metal on metal drawers or other moving pieces may be subject to substantial warping and/or degradation during the incineration process. Accordingly, in one embodiment the present invention provides an incinerator having an interior of the incinerator lined with firebricks. More particularly, each sidewall, each end wall, bottom wall, and each lid includes a firebrick lining. Likewise, the present invention provides an incinerator having a combustion chamber lined with firebricks.
- A proper fuel is provided for thorough combustion. A primary burner of the incinerator preferably burns No. 2 diesel fuel, though other fuel may be utilized. For example, the fuel may comprise a mixture such as (diesel fuel/either/Coleman® Fuel). As used herein the term Coleman® Fuel means a particular brand of the more generic product, white gas.
- Other components could be the subject of incineration, but harmful emissions might result so they should not be incinerated. For example, iodine crystals, red phosphorous, Lithium, sodium crystals/metals, and lye can be stored in separately labeled Teflon® containers and kept dry for further disposal in accordance with Hazardous Laboratory Chemicals: Disposal Guide: Z28,182-4.
- Other harmful components such as anhydrous ammonia can be rendered harmless by being mixed with water under controlled conditions and disposed of at the site. Liquid brake fluid and brake cleaner, for example, can be absorbed by common floor dry and disposed in a landfill. The same would be true for drain cleaner (such as Drano®) or acid mixes that have been neutralized by a neutralizer (e.g. baking soda) and which could be mixed with common floor dry to be disposed of in a local landfill.
- The metal or other containers placed in the incinerator and subjected to the foregoing conditions of heat will be thoroughly sterilized after the one hour period. The chemicals which have not been vaporized typically will form a fine particulate material which can be taken from the incinerator after it is cooled to ambient temperatures, placed in a suitable container, and transported to a local non-toxic landfill. The incinerator is thereupon towed from the site and is prepared to repeat the activity at the next discovered meth site.
- The method of this invention is also useful at other crime scenes where there is a residue of evidence after the law enforcement persons have removed whatever physical evidence is necessary. The incinerator can be brought to such a site and can be used for disposal purposes of residue material whether it be toxic waste or otherwise without having to introduce special toxic waste transporting equipment for transportation to far distant points.
- Similarly, the method of this invention can be used at Courthouses and the like after meth or toxic ingredients have completed their function as evidence in a completed criminal case.
- It is therefore seen that the method of this invention will permit the swift disposal of many toxic ingredients at a meth lab site or other criminal scene in a very short time, under very safe conditions, and at a very low expense as compared to loading, transporting and then disposing of the same ingredients at a far distant point.
- Some of the selected wastes, such as meth, the meth sludge, are preferably combusted at a temperature of between 1100-1300° F. In that case, the incinerator is first heated to that temperature for about one hour, and then the heat is increased to 1600-1900° F. to deal with the remaining selected combustible ingredients.
- It is therefore seen that this invention will achieve at least all of its stated objectives.
Claims (19)
1. A method of disposing of hazardous wastes connected with criminal activity, comprising,
transporting a portable batch-type incinerator to a site where certain hazardous wastes are located connected to criminal activity,
sorting through the waste materials and selecting waste materials from a group which are combustible in the presence of heat without creating hazardous air pollutants,
placing the selected waste materials within the incinerator,
heating the incinerator to a temperature of between 1600-1900° F. for a period of at least one hour to create a particulate residue,
cooling the incinerator to ambient temperatures,
removing the residue from the incinerator into a portable container,
removing the portable container from the site and depositing the same in a non-toxic landfill, and
removing the portable incinerator from the site.
2. The method of claim 1 wherein the site is a criminal justice building, and the waste is comprised of materials gathered from a crime scene.
3. The method of claim 1 wherein the site is a crime scene and the waste is comprised of wastes not required as evidence for a subsequent investigation or judicial proceeding.
4. The method of claim 1 wherein the site is a meth lab site and the waste is comprised of ingredients and paraphernalia used in the creation of methamphetamine.
5. The method of claim 4 wherein non-combustible paraphernalia are gathered from the site and placed in the incinerator for sterilization purposes.
6. The method of claim 1 wherein the incinerator is heated to a temperature range of 1100° F.-1300° F. for a period of time before being heated to 1600°-1900° F. to properly combust certain wastes which are more easily combusted and destroyed at a temperature lower than 1600° F.-1900° F.
7. The method of claim 1 wherein the incinerator has an after-burner through which the emissions from combustion of the selected waste materials are channeled to further combust any particulate material in the emissions.
8. The method of claim 7 wherein the temperature in the after-burner exceeds 1600° F.
9. The method of claim 1 further comprising the step of providing an incinerator having an interior of the incinerator lined with firebricks.
10. The method of claim 1 further comprising the step of providing fuel to the incinerator, wherein the fuel comprises a mixture of diesel fuel, either, and white gas.
11. A method of disposing of hazardous wastes connected with criminal activity, comprising,
transporting a portable batch-type incinerator to a site where certain hazardous wastes are located connected to criminal activity,
sorting through the waste materials and selecting waste materials from a group which are combustible in the presence of heat and placing these selected waste materials within the incinerator,
sorting through the waste materials and selecting waste materials from a group which are non-combustible in the presence of heat and placing these non-combustible materials within the incinerator for sterilization,
sorting through the waste materials and selecting waste materials from a group which are treatable without combustion and excluding these treatable without combustion materials from the from the incinerator,
heating the incinerator to create a particulate residue,
cooling the incinerator to ambient temperatures, and
removing the residue from the incinerator.
12. The method of claim 11 wherein the selected waste materials are selected from the group consisting of completed supplies of meth, sludge from the meth manufacturing containers, and meth ingredients.
13. The method of claim 11 wherein the non-combustible materials are selected from the group consisting of laboratory glass ware, coffee filters, and tubing.
14. The method of claim 11 wherein the treatable without combustion materials are selected from the group consisting of iodine crystals, red phosphorous, lithium, sodium crystals, sodium metals, lye, anhydrous ammonia, liquid brake fluid, brake cleaner, drain cleaner, and acid mixes.
15. The method of claim 11 wherein the step of sorting through the waste materials includes sorting through the waste materials and selecting waste materials from a group which are combustible in the presence of heat without creating hazardous air pollutants.
16. The method of claim 11 further comprising the step of providing an incinerator having an interior of the incinerator lined with firebricks.
17. The method of claim 11 further comprising the step of providing fuel to the incinerator, wherein the fuel comprises a mixture of diesel fuel, either, and white gas.
18. The method of claim 11 wherein the incinerator is heated to a temperature range of 1100° F.-1300° F. for a period of time of about one hour before being heated to 1600°-1900° F. to properly combust certain wastes which are more easily combusted and destroyed at a temperature lower than 1600° F.-1900° F.
19. A method of disposing of hazardous wastes connected with criminal activity, comprising:
transporting a portable batch-type incinerator having an interior of the incinerator lined with firebricks to a site where certain hazardous wastes are located connected to criminal activity, and wherein the waste is comprised of ingredients and paraphernalia used in the creation of methamphetamine;
providing fuel to the incinerator, wherein the fuel comprises a mixture of diesel fuel, either, and white gas;
sorting through the waste materials and selecting waste materials from a group which are combustible in the presence of heat without creating hazardous air pollutants, placing these selected waste materials within the incinerator, and wherein the selected waste materials are selected from the group consisting of completed supplies of meth, sludge from the meth manufacturing containers, and meth ingredients;
sorting through the waste materials and selecting waste materials from a group which are non-combustible in the presence of heat and placing these non-combustible materials within the incinerator for sterilization, and wherein the non-combustible materials are selected from the group consisting of laboratory glass ware, coffee filters, and tubing;
sorting through the waste materials and selecting waste materials from a group which are treatable without combustion and excluding these treatable without combustion materials from the from the incinerator, and wherein the treatable without combustion materials are selected from the group consisting of iodine crystals, red phosphorous, lithium, sodium crystals, sodium metals, lye, anhydrous ammonia, liquid brake fluid, brake cleaner, drain cleaner, and acid mixes;
placing the selected waste materials within the incinerator;
heating the incinerator to a temperature range of 1100° F.-1300° F. for a period of time of about one hour before being heated to 1600°-1900° F. to properly combust certain wastes which are more easily combusted and destroyed at a temperature lower than 1600° F.-1900° F.;
cooling the incinerator to ambient temperatures;
removing the residue from the incinerator into a portable container;
removing the portable container from the site and depositing the same in a non-toxic landfill; and
removing the portable incinerator from the site.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11/128,968 US20050229825A1 (en) | 2002-03-18 | 2005-05-13 | Method of disposing of hazardous wastes connected with criminal activity |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/100,325 US20030176756A1 (en) | 2002-03-18 | 2002-03-18 | Method of disposing of hazardous wastes connected with criminal activity |
| US11/128,968 US20050229825A1 (en) | 2002-03-18 | 2005-05-13 | Method of disposing of hazardous wastes connected with criminal activity |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US10/100,325 Continuation-In-Part US20030176756A1 (en) | 2002-03-18 | 2002-03-18 | Method of disposing of hazardous wastes connected with criminal activity |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US20050229825A1 true US20050229825A1 (en) | 2005-10-20 |
Family
ID=46304562
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US11/128,968 Abandoned US20050229825A1 (en) | 2002-03-18 | 2005-05-13 | Method of disposing of hazardous wastes connected with criminal activity |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US20050229825A1 (en) |
Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4949652A (en) * | 1989-06-26 | 1990-08-21 | Hadley Henry H | Waste disposal system |
| US5339752A (en) * | 1993-07-19 | 1994-08-23 | Lewis Larry D | Livestock incinerator |
| US5401444A (en) * | 1989-06-09 | 1995-03-28 | Spintech Inc. | Apparatus and method for verifiably sterilizing, destroying and encapsulating regulated medical wastes |
| US5550311A (en) * | 1995-02-10 | 1996-08-27 | Hpr Corporation | Method and apparatus for thermal decomposition and separation of components within an aqueous stream |
| US5727481A (en) * | 1995-07-20 | 1998-03-17 | Voorhees; Randall Paul | Portable armored incinerator for dangerous substances |
| US5799591A (en) * | 1997-02-14 | 1998-09-01 | Anderson; Berris M. | Incinerator for medical waste |
| US6262405B1 (en) * | 1997-08-14 | 2001-07-17 | Westinghouse Savannah River Company | Medical waste treatment and decontamination system |
-
2005
- 2005-05-13 US US11/128,968 patent/US20050229825A1/en not_active Abandoned
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5401444A (en) * | 1989-06-09 | 1995-03-28 | Spintech Inc. | Apparatus and method for verifiably sterilizing, destroying and encapsulating regulated medical wastes |
| US4949652A (en) * | 1989-06-26 | 1990-08-21 | Hadley Henry H | Waste disposal system |
| US5339752A (en) * | 1993-07-19 | 1994-08-23 | Lewis Larry D | Livestock incinerator |
| US5550311A (en) * | 1995-02-10 | 1996-08-27 | Hpr Corporation | Method and apparatus for thermal decomposition and separation of components within an aqueous stream |
| US5727481A (en) * | 1995-07-20 | 1998-03-17 | Voorhees; Randall Paul | Portable armored incinerator for dangerous substances |
| US5799591A (en) * | 1997-02-14 | 1998-09-01 | Anderson; Berris M. | Incinerator for medical waste |
| US6262405B1 (en) * | 1997-08-14 | 2001-07-17 | Westinghouse Savannah River Company | Medical waste treatment and decontamination system |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Zacharia | Degradation pathways of persistent organic pollutants (POPs) in the environment | |
| Kao | Formation and removal reactions of hazardous air pollutants | |
| Qi et al. | Some technical issues in managing PCBs | |
| US5550311A (en) | Method and apparatus for thermal decomposition and separation of components within an aqueous stream | |
| US20050229825A1 (en) | Method of disposing of hazardous wastes connected with criminal activity | |
| Singh et al. | Hazardous waste characteristics and standard management approaches | |
| Spero et al. | Regulatory chemicals handbook | |
| National Research Council et al. | Recommendations for the disposal of chemical agents and munitions | |
| Costner et al. | Technical criteria for the destruction of stockpiled persistent organic pollutants | |
| Costner et al. | PVC: a primary contributor to the US dioxin burden | |
| RU2273625C2 (en) | Solid household waste disposal method | |
| RU93054955A (en) | METHOD FOR DEHALOGENING HALOGEN-CONTAINING ORGANIC AND ELEMENT ORGANIC COMPOUNDS | |
| Smukowski | Environmental regulation of surface engineering | |
| Lo | The development of guidelines for a hazardous materials safety program at the University of Hawaii | |
| Treger | Stockholm convention on persistent organic pollutants: The ways of its implementation in the Russian Federation | |
| USH2198H1 (en) | Multi-stage pyrolysis systems for treating chlorine contaminated wastes | |
| Brunner | Statutory Requirements | |
| Leonard | Toxic Air Pollutant Analysis | |
| Lee et al. | A comparision of regulated chemicals versus emitted PICs and PICs for risk analysis | |
| Bishop | Control strategies and technologies | |
| Olden et al. | Air toxics regulatory issues facing urban settings | |
| Pal et al. | Hazardous Waste Management | |
| Point | Air Pollutant Emission Factors | |
| Wong | Treatment of pesticide industry wastes | |
| Standard | List of Symbols |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| STCV | Information on status: appeal procedure |
Free format text: BOARD OF APPEALS DECISION RENDERED |