CA1116764A - Decontamination de sels quaternaires residuels - Google Patents
Decontamination de sels quaternaires residuelsInfo
- Publication number
- CA1116764A CA1116764A CA000322891A CA322891A CA1116764A CA 1116764 A CA1116764 A CA 1116764A CA 000322891 A CA000322891 A CA 000322891A CA 322891 A CA322891 A CA 322891A CA 1116764 A CA1116764 A CA 1116764A
- Authority
- CA
- Canada
- Prior art keywords
- sodium
- quaternary
- ppm
- dodecyl
- water
- 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.)
- Expired
Links
- 238000001784 detoxification Methods 0.000 title abstract 3
- 125000000129 anionic group Chemical group 0.000 claims abstract description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 8
- 239000000178 monomer Substances 0.000 claims abstract description 5
- 230000003472 neutralizing effect Effects 0.000 claims abstract description 4
- 150000003242 quaternary ammonium salts Chemical class 0.000 claims abstract description 4
- 238000000034 method Methods 0.000 claims description 7
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 claims description 6
- -1 dodecyl amino ethyl Chemical group 0.000 claims description 5
- 239000000126 substance Substances 0.000 claims description 5
- 235000019329 dioctyl sodium sulphosuccinate Nutrition 0.000 claims description 4
- YHAIUSTWZPMYGG-UHFFFAOYSA-L disodium;2,2-dioctyl-3-sulfobutanedioate Chemical compound [Na+].[Na+].CCCCCCCCC(C([O-])=O)(C(C([O-])=O)S(O)(=O)=O)CCCCCCCC YHAIUSTWZPMYGG-UHFFFAOYSA-L 0.000 claims description 4
- 239000002699 waste material Substances 0.000 claims description 4
- LNPHVNNRZGCOBK-UHFFFAOYSA-N 2-(dodecylazaniumyl)acetate Chemical compound CCCCCCCCCCCCNCC(O)=O LNPHVNNRZGCOBK-UHFFFAOYSA-N 0.000 claims description 3
- BCKXLBQYZLBQEK-KVVVOXFISA-M Sodium oleate Chemical compound [Na+].CCCCCCCC\C=C/CCCCCCCC([O-])=O BCKXLBQYZLBQEK-KVVVOXFISA-M 0.000 claims description 3
- 230000003115 biocidal effect Effects 0.000 claims description 3
- 231100000331 toxic Toxicity 0.000 claims description 3
- 230000002588 toxic effect Effects 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 229910052708 sodium Inorganic materials 0.000 claims description 2
- 239000011734 sodium Substances 0.000 claims description 2
- 229940045870 sodium palmitate Drugs 0.000 claims description 2
- WYPBVHPKMJYUEO-NBTZWHCOSA-M sodium;(9z,12z)-octadeca-9,12-dienoate Chemical compound [Na+].CCCCC\C=C/C\C=C/CCCCCCCC([O-])=O WYPBVHPKMJYUEO-NBTZWHCOSA-M 0.000 claims description 2
- GGXKEBACDBNFAF-UHFFFAOYSA-M sodium;hexadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCC([O-])=O GGXKEBACDBNFAF-UHFFFAOYSA-M 0.000 claims description 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Natural products NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 claims 1
- 239000004471 Glycine Substances 0.000 claims 1
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 claims 1
- 239000003139 biocide Substances 0.000 abstract description 3
- 150000003839 salts Chemical class 0.000 description 8
- 239000007864 aqueous solution Substances 0.000 description 3
- 230000001580 bacterial effect Effects 0.000 description 3
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
- 241000406799 Deto Species 0.000 description 2
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 231100000252 nontoxic Toxicity 0.000 description 2
- 230000003000 nontoxic effect Effects 0.000 description 2
- QDQHWKZZJJDBND-UHFFFAOYSA-M 4-ethyl-4-hexadecylmorpholin-4-ium;ethyl sulfate Chemical compound CCOS([O-])(=O)=O.CCCCCCCCCCCCCCCC[N+]1(CC)CCOCC1 QDQHWKZZJJDBND-UHFFFAOYSA-M 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- 239000002028 Biomass Substances 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 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 description 1
- 108091006629 SLC13A2 Proteins 0.000 description 1
- HHGFKQNULJGSQZ-UHFFFAOYSA-K [Cl-].C(CCCCCCC)[N+](C)(C)CCCCCCCC.[Cl-].C(CCCCCCCCCCCCCCC)[N+]1=CC=CC=C1.[Br-].C(CCCCCCCCCCCCCCC)[N+](C)(C)C Chemical compound [Cl-].C(CCCCCCC)[N+](C)(C)CCCCCCCC.[Cl-].C(CCCCCCCCCCCCCCC)[N+]1=CC=CC=C1.[Br-].C(CCCCCCCCCCCCCCC)[N+](C)(C)C HHGFKQNULJGSQZ-UHFFFAOYSA-K 0.000 description 1
- FWGYKDKINNGPSG-UHFFFAOYSA-N [Cl-].Cl[NH+](CC1=CC=CC=C1)Cl Chemical compound [Cl-].Cl[NH+](CC1=CC=CC=C1)Cl FWGYKDKINNGPSG-UHFFFAOYSA-N 0.000 description 1
- 229910052925 anhydrite Inorganic materials 0.000 description 1
- IUHDTQIYNQQIBP-UHFFFAOYSA-M benzyl-ethyl-dimethylazanium;chloride Chemical compound [Cl-].CC[N+](C)(C)CC1=CC=CC=C1 IUHDTQIYNQQIBP-UHFFFAOYSA-M 0.000 description 1
- UDSAIICHUKSCKT-UHFFFAOYSA-N bromophenol blue Chemical compound C1=C(Br)C(O)=C(Br)C=C1C1(C=2C=C(Br)C(O)=C(Br)C=2)C2=CC=CC=C2S(=O)(=O)O1 UDSAIICHUKSCKT-UHFFFAOYSA-N 0.000 description 1
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 1
- 238000004737 colorimetric analysis Methods 0.000 description 1
- 229940000425 combination drug Drugs 0.000 description 1
- 239000000498 cooling water Substances 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 229940049918 linoleate Drugs 0.000 description 1
- 230000002906 microbiologic effect Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000005064 octadecenyl group Chemical group C(=CCCCCCCCCCCCCCCCC)* 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F3/00—Biological treatment of water, waste water, or sewage
- C02F3/34—Biological treatment of water, waste water, or sewage characterised by the microorganisms used
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Microbiology (AREA)
- Biodiversity & Conservation Biology (AREA)
- Hydrology & Water Resources (AREA)
- Engineering & Computer Science (AREA)
- Environmental & Geological Engineering (AREA)
- Water Supply & Treatment (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Removal Of Specific Substances (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US92998178A | 1978-08-01 | 1978-08-01 | |
| US929,981 | 1978-08-01 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1116764A true CA1116764A (fr) | 1982-01-19 |
Family
ID=25458786
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000322891A Expired CA1116764A (fr) | 1978-08-01 | 1979-03-07 | Decontamination de sels quaternaires residuels |
Country Status (3)
| Country | Link |
|---|---|
| JP (1) | JPS5610390A (fr) |
| CA (1) | CA1116764A (fr) |
| GB (1) | GB2027003B (fr) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0394087A (ja) * | 1989-09-04 | 1991-04-18 | Eagle Ind Co Ltd | ステンレス合金粉末の製造方法 |
| NZ286510A (en) * | 1995-05-15 | 1998-06-26 | Rohm & Haas | Method of detoxifying biocide in waste water using a water soluble thio compound |
| US6849664B2 (en) * | 2001-10-18 | 2005-02-01 | Chevron U.S.A. Inc. | Process for disposing biocide-containing cooling water |
| US20070170404A1 (en) * | 2006-01-20 | 2007-07-26 | No-Burn Investments, Llc | Fire retardant with mold inhibitor and insecticide |
| CN104230073B (zh) * | 2013-06-07 | 2015-11-18 | 欣兴电子股份有限公司 | 含氨废水的处理方法 |
| CN119385158A (zh) * | 2016-08-11 | 2025-02-07 | 埃科莱布美国股份有限公司 | 抗微生物季化合物与阴离子聚合物或螯合剂的相互作用 |
| CN117756242B (zh) * | 2023-12-28 | 2025-10-21 | 北京工业大学 | 利用季铵盐对污水生物处理中全氟辛酸胁迫的解毒方法 |
-
1979
- 1979-03-07 CA CA000322891A patent/CA1116764A/fr not_active Expired
- 1979-06-27 GB GB7922358A patent/GB2027003B/en not_active Expired
- 1979-07-30 JP JP9618479A patent/JPS5610390A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5610390A (en) | 1981-02-02 |
| GB2027003A (en) | 1980-02-13 |
| GB2027003B (en) | 1982-09-15 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MKEX | Expiry |