ES2828363T3 - Composición de acetales sinergizados y método para la eliminación de sulfuros y mercaptanos - Google Patents
Composición de acetales sinergizados y método para la eliminación de sulfuros y mercaptanos Download PDFInfo
- Publication number
- ES2828363T3 ES2828363T3 ES19176651T ES19176651T ES2828363T3 ES 2828363 T3 ES2828363 T3 ES 2828363T3 ES 19176651 T ES19176651 T ES 19176651T ES 19176651 T ES19176651 T ES 19176651T ES 2828363 T3 ES2828363 T3 ES 2828363T3
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- group
- alkyl
- aldehyde
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- 239000000203 mixture Substances 0.000 title claims abstract description 129
- 150000001241 acetals Chemical class 0.000 title claims abstract description 29
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 title claims description 23
- 238000000034 method Methods 0.000 title claims description 18
- 150000003568 thioethers Chemical class 0.000 title 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 56
- 150000001299 aldehydes Chemical class 0.000 claims abstract description 46
- 239000007795 chemical reaction product Substances 0.000 claims abstract description 44
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims abstract description 33
- 150000002576 ketones Chemical class 0.000 claims abstract description 32
- 150000005846 sugar alcohols Polymers 0.000 claims abstract description 26
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims abstract description 24
- 150000002373 hemiacetals Chemical class 0.000 claims abstract description 23
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims abstract description 21
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims abstract description 18
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- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N butyric aldehyde Natural products CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 claims abstract description 12
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 claims abstract description 8
- BBMCTIGTTCKYKF-UHFFFAOYSA-N 1-heptanol Chemical compound CCCCCCCO BBMCTIGTTCKYKF-UHFFFAOYSA-N 0.000 claims abstract description 8
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 claims abstract description 8
- NBBJYMSMWIIQGU-UHFFFAOYSA-N Propionic aldehyde Chemical compound CCC=O NBBJYMSMWIIQGU-UHFFFAOYSA-N 0.000 claims abstract description 8
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 claims abstract description 8
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 claims abstract description 8
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 claims abstract description 8
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 claims abstract description 8
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims abstract description 7
- SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 claims abstract description 6
- 229930040373 Paraformaldehyde Natural products 0.000 claims abstract description 6
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 claims abstract description 6
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 claims abstract description 5
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 claims abstract description 5
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 claims abstract description 5
- 229920002866 paraformaldehyde Polymers 0.000 claims abstract description 5
- IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 claims abstract description 4
- 229940015043 glyoxal Drugs 0.000 claims abstract description 4
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims abstract description 4
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- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 65
- 150000001875 compounds Chemical class 0.000 claims description 55
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- 125000003277 amino group Chemical group 0.000 claims description 10
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- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 3
- 150000003973 alkyl amines Chemical class 0.000 claims description 3
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 3
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- 125000000524 functional group Chemical group 0.000 claims description 3
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
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- 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 claims 1
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- 150000001298 alcohols Chemical class 0.000 description 11
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- C10G29/24—Aldehydes or ketones
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- C—CHEMISTRY; METALLURGY
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- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2208/00—Aspects relating to compositions of drilling or well treatment fluids
- C09K2208/20—Hydrogen sulfide elimination
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- 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
- C09K2208/00—Aspects relating to compositions of drilling or well treatment fluids
- C09K2208/26—Gel breakers other than bacteria or enzymes
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- 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
- C09K2208/00—Aspects relating to compositions of drilling or well treatment fluids
- C09K2208/32—Anticorrosion additives
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/20—Characteristics of the feedstock or the products
- C10G2300/201—Impurities
- C10G2300/202—Heteroatoms content, i.e. S, N, O, P
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/20—Characteristics of the feedstock or the products
- C10G2300/201—Impurities
- C10G2300/207—Acid gases, e.g. H2S, COS, SO2, HCN
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- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Inorganic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Lubricants (AREA)
- Preventing Corrosion Or Incrustation Of Metals (AREA)
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Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PL3686181T3 (pl) | 2013-01-30 | 2024-11-04 | Ecolab Usa Inc. | Zmiatacze siarkowodoru |
| BR112017021486B1 (pt) | 2015-04-22 | 2022-03-22 | Championx Usa Inc | Método para tratar sulfeto de hidrogênio em uma corrente |
| CA2997416C (en) * | 2015-09-08 | 2023-06-27 | Ecolab Usa Inc. | Hydrogen sulfide scavengers |
| MY190322A (en) | 2016-07-01 | 2022-04-13 | Clariant Int Ltd | Synergized acetals composition and method for scavenging sulfides and mercaptans |
| CA3031535C (en) | 2016-07-29 | 2025-07-08 | Ecolab Usa Inc. | ANTI-FOULING AND HYDROGEN SULFIDE TRAPPING COMPOSITIONS |
| EP3652274A1 (en) | 2017-07-13 | 2020-05-20 | Ecolab USA, Inc. | Method of removing a sulfur containing compound by adding a composition |
| US11555140B2 (en) | 2017-12-22 | 2023-01-17 | Clariant International Ltd | Synergized hemiacetals composition and method for scavenging sulfides and mercaptans |
| US20190194551A1 (en) | 2017-12-22 | 2019-06-27 | Clariant International, Ltd. | Synergized acetals composition and method for scavenging sulfides and mercaptans |
| EP3891262B1 (en) | 2018-12-04 | 2024-07-31 | TotalEnergies OneTech | Hydrogen sulphide and mercaptans scavenging compositions |
| US11499108B2 (en) | 2019-01-23 | 2022-11-15 | Championx Usa Inc. | Complete removal of solids during hydrogen sulfide scavenging operations using a scavenger and a Michael acceptor |
| EP3918036A1 (en) * | 2019-01-31 | 2021-12-08 | Ecolab Usa Inc. | Alcohol-based hemi-formyls for hydrogen sulfide scavenging |
| WO2020256920A1 (en) | 2019-06-19 | 2020-12-24 | Bl Technologies, Inc. | Stabilized concentrated formaldehyde solutions and methods of use thereof |
| CN110467952B (zh) * | 2019-08-07 | 2021-04-13 | 蚌埠知博自动化技术开发有限公司 | 一种液化石油气氧化脱硫剂的制备方法 |
| CN110846018A (zh) * | 2019-11-06 | 2020-02-28 | 中国石油集团渤海钻探工程有限公司 | 一种小分子阳离子表面活性剂型防膨剂及其制备方法 |
| DE102020120287A1 (de) | 2020-07-31 | 2022-02-03 | Vink Chemicals Gmbh & Co. Kg | Zusammensetzungen und verfahren zur entfernung von schwefelverbindungen aus prozessströmen |
| CN112480893B (zh) * | 2020-10-30 | 2022-07-29 | 中海油(天津)油田化工有限公司 | 一种油田脱硫缓蚀剂及其制备方法 |
| EP4259757B1 (en) * | 2020-12-11 | 2025-02-05 | Totalenergies Onetech | Hydrogen sulphide and mercaptans scavenging compositions |
| US11802246B2 (en) | 2021-03-11 | 2023-10-31 | Baker Hughes Oilfield Operations Llc | Synergistic effects among mercaptan scavengers |
| GB2639425A (en) * | 2022-10-31 | 2025-09-24 | Cameron Tech Ltd | Mercaptan scavenger additives |
| JP2025539417A (ja) | 2022-11-30 | 2025-12-05 | ニッサン ケミカル アメリカ コーポレーション | 液体ストリームまたはガスストリーム中のｈ２ｓを低減するためのシリカナノ粒子の導入方法 |
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Family Cites Families (49)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FI93031B (fi) * | 1993-06-17 | 1994-10-31 | Cellkem Service Oy | Glutaarialdehydin käyttö peroksidin hajoamisen estämiseksi uusiomassan ja muun kuitumassan valmistuksessa |
| US2956963A (en) | 1954-08-02 | 1960-10-18 | Nat Sugar Refining Company | Saccharide-monohydroxy aldehyde reaction product and method of preparing same |
| GB1092657A (en) | 1963-12-28 | 1967-11-29 | Koei Chemical Company Ltd Koei | Improvements relating to the stabilization of aqueous formaldehyde solutions |
| US3928211A (en) | 1970-10-21 | 1975-12-23 | Milchem Inc | Process for scavenging hydrogen sulfide in aqueous drilling fluids and method of preventing metallic corrosion of subterranean well drilling apparatuses |
| US3880754A (en) * | 1971-03-12 | 1975-04-29 | Bayer Ag | Filtering with polyacrylonitrile or polyamide fibers as filter aid |
| US3880784A (en) * | 1973-12-21 | 1975-04-29 | Bayer Ag | Solutions of diisocyanate polyaddition products which contain free semiacetals and which are stable in storage |
| DE2721186C2 (de) | 1977-05-11 | 1986-04-24 | Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung eines Gemisches von niedermolekularen Polyhydroxylverbindungen |
| US4680127A (en) | 1985-12-13 | 1987-07-14 | Betz Laboratories, Inc. | Method of scavenging hydrogen sulfide |
| US4978512B1 (en) | 1988-12-23 | 1993-06-15 | Composition and method for sweetening hydrocarbons | |
| ZA904844B (en) | 1989-06-26 | 1991-04-24 | Henkel Corp | Masking composition and method |
| GB8917092D0 (en) | 1989-07-26 | 1989-09-13 | Bp Chem Int Ltd | Production of hydroxy ketones |
| US5486605A (en) | 1991-07-11 | 1996-01-23 | Gatlin; Larry W. | Hydrogen sulfide converter |
| US5347004A (en) | 1992-10-09 | 1994-09-13 | Baker Hughes, Inc. | Mixtures of hexahydrotriazines useful as H2 S scavengers |
| TW358820B (en) | 1995-04-11 | 1999-05-21 | Ciba Sc Holding Ag | Synergistic stabilizer mixture |
| DK0882112T3 (da) | 1996-07-12 | 2003-01-13 | Baker Hughes Inc | Bisoxazolidin-holdig hydrogensulfid-indfanger |
| DE19722858B4 (de) | 1997-05-23 | 2004-01-29 | Schülke & Mayr GmbH | Zusammensetzungen auf der Basis von Iodpropinyl- und Formaldehyd-Depot-Verbindungen und deren Verwendung als Konservierungsmittel |
| US6093743A (en) | 1998-06-23 | 2000-07-25 | Medinox Inc. | Therapeutic methods employing disulfide derivatives of dithiocarbamates and compositions useful therefor |
| DE19842116C2 (de) * | 1998-09-07 | 2001-02-08 | Schuelke & Mayr Gmbh | Verwendung von Derivaten von Methylenbisoxazolidin und dadurch erhaltene Zusammensetzungen |
| KR100779888B1 (ko) * | 2000-04-26 | 2007-11-28 | 미쓰비시 가가꾸 가부시키가이샤 | 케탈 및/또는 아세탈의 제조 방법 |
| GB0031710D0 (en) | 2000-12-27 | 2001-02-07 | Dyno Oil Field Chemicals | Process for the reduction or elimination of hydrogen sulphide |
| CN1242970C (zh) * | 2003-05-31 | 2006-02-22 | 中国石油化工股份有限公司 | 一种制备缩醛的固体催化剂及应用 |
| DE10340738A1 (de) * | 2003-09-04 | 2005-03-31 | Basf Ag | Verfahren zur Herstellung von 1,1,2,2-Tetramethoxyethan- und/oder Glyoxaldimethylacetal |
| DE102004014447A1 (de) | 2004-03-24 | 2005-10-20 | Schuelke & Mayr Gmbh | Emissionsarme Formaldehyd-Depot-Zubereitungen |
| US20060079720A1 (en) | 2004-10-13 | 2006-04-13 | Milliken & Company | Method for preparing acetal-containing compositions |
| CN101903449B (zh) | 2007-12-21 | 2013-05-22 | 巴斯夫欧洲公司 | 含有位阻胺的阻燃剂组合物 |
| EP2427257B1 (en) | 2009-05-05 | 2013-03-06 | Dorf Ketal Chemicals (I) Private Limited | Method of scavenging hydrogen sulfide from hydrocarbon stream |
| US20120157560A1 (en) | 2009-05-29 | 2012-06-21 | Xl Terra, Inc. | Ketal esters of anhydropentitols and uses thereof |
| EP2267098A1 (en) | 2009-06-26 | 2010-12-29 | M-i Swaco Norge As | Scavenger compositons and their use |
| US8765083B2 (en) | 2010-11-19 | 2014-07-01 | Nalco Company | Acid gas absorbent composition |
| PE20140464A1 (es) | 2010-11-22 | 2014-04-06 | Dorf Ketal Chemicals India Private Ltd | Composicion con aditivo y metodo para capturar sulfuro de hidrogeno en corrientes de hidrocarburos |
| US9260669B2 (en) | 2011-03-24 | 2016-02-16 | Baker Hughes Incorporated | Synergistic H2S/mercaptan scavengers using glyoxal |
| ES2589055T3 (es) | 2011-08-18 | 2016-11-08 | Basf Se | Procedimiento para preparar un sistema aglutinante acuoso |
| US9108899B2 (en) | 2011-12-30 | 2015-08-18 | General Electric Company | Sulfide scavengers, methods for making and methods for using |
| HK1210493A1 (zh) | 2012-08-21 | 2016-04-22 | 龙沙股份有限公司 | 清除硫化氫和/或巰基化合物的方法 |
| EP3080046A1 (en) | 2013-12-11 | 2016-10-19 | Nederlandse Organisatie voor toegepast- natuurwetenschappelijk onderzoek TNO | Process and apparatus for hydrogen sulfide removal |
| DE202014008415U1 (de) | 2014-02-19 | 2014-11-25 | Clariant International Ltd. | Wässrige Adjuvant-Zusammensetzung zur Wirkungssteigerung von Elektrolyt-Wirkstoffen |
| DE102014003215A1 (de) | 2014-03-06 | 2015-05-28 | Clariant International Ltd. | Korrosionsinhibierende Zusammensetzungen |
| CA2942276C (en) | 2014-03-17 | 2021-12-14 | Kuraray Co., Ltd. | Composition for removal of sulfur-containing compounds |
| DE102014014124A1 (de) | 2014-09-30 | 2016-03-31 | Clariant International Ltd. | Zusammensetzungen agrochemischer Wirkstoffe, deren Herstellung und Verwendung |
| RU2697360C2 (ru) | 2014-12-18 | 2019-08-13 | Хексион Инк. | Очистители газа |
| EP3064062A1 (en) | 2015-03-05 | 2016-09-07 | Clariant International Ltd | Use of a composition for reducing the drift when applying a plant treatment composition |
| JO3535B1 (ar) | 2015-03-30 | 2020-07-05 | Clariant Int Ltd | تركيبات أحماض دهنية ومشتقات ن – أسيل ساركوزين لطفو محسن لمعادن غير كبريتيدية |
| US10633573B2 (en) * | 2015-04-02 | 2020-04-28 | Clariant International Ltd. | Composition and method for inhibition of sulfide scales |
| KR101774443B1 (ko) | 2015-10-21 | 2017-09-13 | 한국화학연구원 | 바이오가스의 황화수소의 제거를 위한 액상촉매 조성물 |
| BR102015028532A2 (pt) | 2015-11-13 | 2017-05-23 | Oxiteno S A Indústria E Comércio | composição de sequestrante para aplicação na eliminação e/ou redução de sulfeto de hidrogênio e/ou mercaptanas em fluido |
| CN105749591B (zh) * | 2016-04-08 | 2018-02-02 | 徐州工程学院 | 一种旋流法处理污水中油污装置及其去除方法 |
| MY190322A (en) | 2016-07-01 | 2022-04-13 | Clariant Int Ltd | Synergized acetals composition and method for scavenging sulfides and mercaptans |
| US20190194551A1 (en) | 2017-12-22 | 2019-06-27 | Clariant International, Ltd. | Synergized acetals composition and method for scavenging sulfides and mercaptans |
| US11555140B2 (en) * | 2017-12-22 | 2023-01-17 | Clariant International Ltd | Synergized hemiacetals composition and method for scavenging sulfides and mercaptans |
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| EP3478789A1 (en) | 2019-05-08 |
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| US11530347B2 (en) | 2022-12-20 |
| CN109819658B (zh) | 2021-03-09 |
| DK3578622T3 (da) | 2020-10-19 |
| BR112018074975A2 (pt) | 2019-03-12 |
| CA3029452A1 (en) | 2018-01-04 |
| MX2018014216A (es) | 2019-09-06 |
| EP3578622B1 (en) | 2020-10-07 |
| WO2018001631A1 (en) | 2018-01-04 |
| AU2017291057A1 (en) | 2018-11-22 |
| BR122021017409A2 (enExample) | 2019-03-12 |
| EP3478789B1 (en) | 2020-02-26 |
| BR112018074975A8 (pt) | 2023-03-14 |
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