CZ20013966A3 - Způsob a kompozice k inhibici koroze ve vodných systémech - Google Patents

Způsob a kompozice k inhibici koroze ve vodných systémech Download PDF

Info

Publication number: CZ20013966A3
Authority: CZ; Czechia
Prior art keywords: acid; water; acids; tetrazolium; compounds
Prior art date: 1999-05-03

Application number

CZ20013966A

Other languages

Czech (cs)

English (en)

Inventor

William C. Ehrhardt

Longchun Cheng

Dawn Stasney

Kim A. Whitaker

Original Assignee

Betzdearborn Inc.

Priority date (The priority date 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 date listed.)

1999-05-03

Filing date

2000-05-02

Publication date

2002-05-15

1999-05-03 Priority claimed from US09/303,596 external-priority patent/US6585933B1/en

1999-05-03 Priority claimed from US09/304,181 external-priority patent/US6379587B1/en

2000-05-02 Application filed by Betzdearborn Inc. filed Critical Betzdearborn Inc.

2002-05-15 Publication of CZ20013966A3 publication Critical patent/CZ20013966A3/cs

Links

238000005260 corrosion Methods 0.000 title claims abstract description 76
230000007797 corrosion Effects 0.000 title claims abstract description 73
238000000034 method Methods 0.000 title claims abstract description 54
239000000203 mixture Substances 0.000 title claims description 58
230000002401 inhibitory effect Effects 0.000 title description 11
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XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 62
229910052751 metal Inorganic materials 0.000 claims abstract description 48
239000002184 metal Substances 0.000 claims abstract description 48
125000000217 alkyl group Chemical group 0.000 claims abstract description 25
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150000002739 metals Chemical class 0.000 claims abstract description 14
125000003118 aryl group Chemical group 0.000 claims abstract description 12
230000007935 neutral effect Effects 0.000 claims abstract description 11
125000002877 alkyl aryl group Chemical group 0.000 claims abstract description 10
125000003107 substituted aryl group Chemical group 0.000 claims abstract description 6
125000003831 tetrazolyl group Chemical group 0.000 claims description 63
239000000463 material Substances 0.000 claims description 49
239000002253 acid Substances 0.000 claims description 47
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125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 29
239000000178 monomer Substances 0.000 claims description 26
229910052739 hydrogen Inorganic materials 0.000 claims description 22
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 21
150000007513 acids Chemical class 0.000 claims description 20
229920002125 Sokalan® Polymers 0.000 claims description 19
150000001412 amines Chemical class 0.000 claims description 19
229920001577 copolymer Polymers 0.000 claims description 17
FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 claims description 16
230000008569 process Effects 0.000 claims description 16
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239000001257 hydrogen Substances 0.000 claims description 11
ZJAOAACCNHFJAH-UHFFFAOYSA-N phosphonoformic acid Chemical class OC(=O)P(O)(O)=O ZJAOAACCNHFJAH-UHFFFAOYSA-N 0.000 claims description 11
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239000011574 phosphorus Substances 0.000 claims description 11
GLDQAMYCGOIJDV-UHFFFAOYSA-N 2,3-dihydroxybenzoic acid Chemical compound OC(=O)C1=CC=CC(O)=C1O GLDQAMYCGOIJDV-UHFFFAOYSA-N 0.000 claims description 10
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 10
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VCESGVLABVSDRO-UHFFFAOYSA-L 2-[4-[4-[3,5-bis(4-nitrophenyl)tetrazol-2-ium-2-yl]-3-methoxyphenyl]-2-methoxyphenyl]-3,5-bis(4-nitrophenyl)tetrazol-2-ium;dichloride Chemical compound [Cl-].[Cl-].COC1=CC(C=2C=C(OC)C(=CC=2)[N+]=2N(N=C(N=2)C=2C=CC(=CC=2)[N+]([O-])=O)C=2C=CC(=CC=2)[N+]([O-])=O)=CC=C1[N+]1=NC(C=2C=CC(=CC=2)[N+]([O-])=O)=NN1C1=CC=C([N+]([O-])=O)C=C1 VCESGVLABVSDRO-UHFFFAOYSA-L 0.000 claims description 7
DZYHJDLBFUOKBD-UHFFFAOYSA-N 2-amino-2-hydroxybutanedioic acid Chemical compound OC(=O)C(O)(N)CC(O)=O DZYHJDLBFUOKBD-UHFFFAOYSA-N 0.000 claims description 7
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 7
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239000004584 polyacrylic acid Substances 0.000 claims description 7
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RGHNJXZEOKUKBD-SQOUGZDYSA-N D-gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 claims description 6
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KJUGUADJHNHALS-UHFFFAOYSA-N 1H-tetrazole Substances C=1N=NNN=1 KJUGUADJHNHALS-UHFFFAOYSA-N 0.000 claims description 4
RLHGFJMGWQXPBW-UHFFFAOYSA-N 2-hydroxy-3-(1h-imidazol-5-ylmethyl)benzamide Chemical group NC(=O)C1=CC=CC(CC=2NC=NC=2)=C1O RLHGFJMGWQXPBW-UHFFFAOYSA-N 0.000 claims description 4
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UQGFMSUEHSUPRD-UHFFFAOYSA-N disodium;3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane Chemical group [Na+].[Na+].O1B([O-])OB2OB([O-])OB1O2 UQGFMSUEHSUPRD-UHFFFAOYSA-N 0.000 claims description 4
150000002431 hydrogen Chemical group 0.000 claims description 4
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239000001301 oxygen Substances 0.000 claims description 4
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150000003536 tetrazoles Chemical class 0.000 claims description 4
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RWZYAGGXGHYGMB-UHFFFAOYSA-N anthranilic acid Chemical class NC1=CC=CC=C1C(O)=O RWZYAGGXGHYGMB-UHFFFAOYSA-N 0.000 claims description 3
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BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical class OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 claims description 3
150000004649 carbonic acid derivatives Chemical class 0.000 claims description 3
HDFRDWFLWVCOGP-UHFFFAOYSA-N carbonothioic O,S-acid Chemical class OC(S)=O HDFRDWFLWVCOGP-UHFFFAOYSA-N 0.000 claims description 3
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239000003518 caustics Substances 0.000 claims description 3
150000001805 chlorine compounds Chemical class 0.000 claims description 3
239000000539 dimer Substances 0.000 claims description 3
239000000174 gluconic acid Substances 0.000 claims description 3
235000012208 gluconic acid Nutrition 0.000 claims description 3
MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical compound C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 claims description 3
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239000003208 petroleum Substances 0.000 claims description 3
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HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
239000002689 soil Substances 0.000 description 1
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KGVYSMPUYYLGOM-UHFFFAOYSA-N triazine-4,5,6-tricarboxylic acid Chemical class OC(=O)C1=NN=NC(C(O)=O)=C1C(O)=O KGVYSMPUYYLGOM-UHFFFAOYSA-N 0.000 description 1
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QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
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Classifications

- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23F—NON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
- C23F11/00—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
- C23F11/08—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids
- C23F11/10—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids using organic inhibitors
- C23F11/14—Nitrogen-containing compounds
- C23F11/149—Heterocyclic compounds containing nitrogen as hetero atom
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23F—NON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
- C23F11/00—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
- C23F11/08—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23F—NON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
- C23F11/00—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
- C23F11/08—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids
- C23F11/10—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids using organic inhibitors
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2303/00—Specific treatment goals
- C02F2303/08—Corrosion inhibition

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Chemical & Material Sciences (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Mechanical Engineering (AREA)
Metallurgy (AREA)
Organic Chemistry (AREA)
Preventing Corrosion Or Incrustation Of Metals (AREA)
Compositions Of Macromolecular Compounds (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

CZ20013966A 1999-05-03 2000-05-02 Způsob a kompozice k inhibici koroze ve vodných systémech CZ20013966A3 (cs)

Applications Claiming Priority (4)

Application Number	Priority Date	Filing Date	Title
US09/303,596 US6585933B1 (en)	1999-05-03	1999-05-03	Method and composition for inhibiting corrosion in aqueous systems
US09/304,181 US6379587B1 (en)	1999-05-03	1999-05-03	Inhibition of corrosion in aqueous systems
US30956499A	1999-05-12	1999-05-12
US50572200A	2000-02-17	2000-02-17

Publications (1)

Publication Number	Publication Date
CZ20013966A3 true CZ20013966A3 (cs)	2002-05-15

Family

ID=27501833

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CZ20013966A CZ20013966A3 (cs)	1999-05-03	2000-05-02	Způsob a kompozice k inhibici koroze ve vodných systémech

Country Status (15)

Country	Link
EP (1)	EP1177331A1 (es)
JP (1)	JP2002543294A (es)
KR (1)	KR20020012564A (es)
CN (1)	CN1359430A (es)
AR (1)	AR023836A1 (es)
AU (1)	AU4972700A (es)
BR (1)	BR0010592A (es)
CA (1)	CA2369954A1 (es)
CZ (1)	CZ20013966A3 (es)
HK (1)	HK1044176A1 (es)
HU (1)	HUP0201012A3 (es)
MX (1)	MXPA01011087A (es)
NO (1)	NO20015307D0 (es)
PL (1)	PL352994A1 (es)
WO (1)	WO2000066810A1 (es)

Families Citing this family (70)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CA2398423C (en)	2001-09-04	2009-11-10	Rohm And Haas Company	Corrosion inhibiting compositions
WO2005028707A2 (en) *	2003-04-21	2005-03-31	The Johns Hopkins University	Methods for inhibiting microbiologically influenced corrosion of metals and alloys
US20050003978A1 (en) *	2003-05-28	2005-01-06	Lonza Inc.	Quaternary ammonium carbonates and bicarbonates as anticorrosive agents
CN1914356B (zh)	2004-02-05	2010-05-05	日矿金属株式会社	金属的表面处理剂
KR100725948B1 (ko) *	2005-11-04	2007-06-11	조우정	부식방지 및 스케일 제거용 화합물 및 그것을 함유한 조성물
CN101424887A (zh) *	2007-11-02	2009-05-06	安集微电子（上海）有限公司	一种半导体晶圆金属基材腐蚀防护液及其使用方法
CN101842747B (zh) *	2007-11-02	2012-07-25	安集微电子（上海）有限公司	一种半导体晶圆金属基材腐蚀防护液及其使用方法
US8771542B2 (en) *	2008-07-11	2014-07-08	Prestone Products Corporation	Heat transfer fluid, additive package, system and method
US8759265B2 (en) *	2008-07-15	2014-06-24	Ian D. Smith	Thermally stable subsea control hydraulic fluid compositions
CN101844888B (zh) *	2009-03-26	2012-04-11	北京纽维逊建筑工程技术有限公司	用于钢筋混凝土的有机复合钢筋阻锈剂及其制备方法
ES2812535T3 (es) *	2010-05-18	2021-03-17	Kurita Water Ind Ltd	Medio para la mejora de la transferencia de calor en instalaciones de generación de vapor
CN102558433B (zh) *	2010-12-28	2013-10-30	上海洗霸科技股份有限公司	一种阴离子聚丙烯酰胺及其制备方法和应用
US8236204B1 (en)	2011-03-11	2012-08-07	Wincom, Inc.	Corrosion inhibitor compositions comprising tetrahydrobenzotriazoles solubilized in activating solvents and methods for using same
US8236205B1 (en)	2011-03-11	2012-08-07	Wincom, Inc.	Corrosion inhibitor compositions comprising tetrahydrobenzotriazoles and other triazoles and methods for using same
ES2938544T3 (es) *	2011-07-29	2023-04-12	Kemira Oyj	Polímeros inhibidores de incrustaciones y métodos para prevenir la formación de incrustaciones
EP2804978B1 (en) *	2012-01-20	2019-01-09	Kemira Oyj	Device and method for monitoring biocide dosing in a machine
CN102730850B (zh) *	2012-07-11	2014-02-12	成都润兴消毒药业有限公司	一种环保型水处理缓蚀阻垢剂及其制备方法
KR101514715B1 (ko) *	2012-08-24	2015-04-23	유홍숙	스케일 및 녹 세정용 조성물
US9752105B2 (en)	2012-09-13	2017-09-05	Ecolab Usa Inc.	Two step method of cleaning, sanitizing, and rinsing a surface
US9023784B2 (en) *	2012-09-13	2015-05-05	Ecolab Usa Inc.	Method of reducing soil redeposition on a hard surface using phosphinosuccinic acid adducts
US9994799B2 (en)	2012-09-13	2018-06-12	Ecolab Usa Inc.	Hard surface cleaning compositions comprising phosphinosuccinic acid adducts and methods of use
US8871699B2 (en)	2012-09-13	2014-10-28	Ecolab Usa Inc.	Detergent composition comprising phosphinosuccinic acid adducts and methods of use
CA2952867C (en)	2013-06-18	2022-05-03	Chemgreen Innovation Inc.	An antimicrobial polymer wherein an aromatic moiety is covalently incorporated into the polymer backbone through loss of aromaticity
CN103409122B (zh) *	2013-08-28	2015-09-23	中国石油集团川庆钻探工程有限公司	一种水溶性抗硫化氢用缓蚀剂
US9309205B2 (en)	2013-10-28	2016-04-12	Wincom, Inc.	Filtration process for purifying liquid azole heteroaromatic compound-containing mixtures
JP6513091B2 (ja) *	2013-12-02	2019-05-15	エコラブユーエスエイインク	テトラゾール系腐食防止剤
CN103789774A (zh) *	2014-01-21	2014-05-14	山东省泰和水处理有限公司	一种咪唑啉衍生物缓蚀剂的制备方法
CN103820785B (zh) *	2014-01-28	2016-04-06	西安理工大学	用于碳钢的四元复配气相缓蚀剂及其制备方法
CN103924247B (zh) *	2014-04-12	2016-06-08	冯智勇	一种高效的燃煤锅炉缓蚀剂
CN103938213B (zh) *	2014-04-24	2017-09-05	姬光河	一种防锈液
US9752237B2 (en)	2014-05-29	2017-09-05	Ecolab Usa Inc.	Control of sugar evaporator scale using sugar or sugar moieties
CN104355418A (zh) *	2014-10-24	2015-02-18	中国海洋石油总公司	一种无磷缓蚀阻垢剂的制备方法
US20160145442A1 (en) *	2014-11-20	2016-05-26	Chemtreat, Inc.	Methods of pre-treating equipment used in water systems
CN107787380B (zh)	2015-05-28	2020-10-30	艺康美国股份有限公司	2-取代的咪唑和苯并咪唑腐蚀抑制剂
CN107667188B (zh) *	2015-05-28	2020-10-30	艺康美国股份有限公司	基于嘌呤的腐蚀抑制剂
US9404069B1 (en)	2015-06-12	2016-08-02	Crossford International, Llc	Systems and methods for cooling tower fill cleaning with a chemical gel
US10030216B2 (en)	2015-06-12	2018-07-24	Crossford International, Llc	Systems and methods for cooling tower fill cleaning with a chemical gel
CN106319528A (zh) *	2015-06-26	2017-01-11	埃科莱布美国股份有限公司	一种缓蚀剂组合物及其用途
CN105016490A (zh) *	2015-07-06	2015-11-04	安徽省蓝天能源环保科技有限公司	一种电力循环水系统用阻垢缓蚀剂
CN105039995B (zh) *	2015-07-09	2017-08-29	潍坊友容实业有限公司	一种盐碱地排盐暗管专用阻垢缓蚀剂及其制备方法
CN105603436B (zh) *	2015-12-18	2017-11-17	中国科学院长春应用化学研究所	一种复合缓蚀剂及其制备方法
CN105780011B (zh) *	2016-03-08	2018-11-13	克拉玛依中科恒信科技有限责任公司	一种含咪唑并[1,2-a]吡啶类化合物的缓蚀剂及其制备方法
CN106115945A (zh) *	2016-07-30	2016-11-16	山东胜伟园林科技有限公司	一种缓蚀性能好的阻垢剂在排盐暗管中的应用
CA3035448C (en)	2016-09-07	2023-05-09	Ecolab Usa Inc.	Solid detergent compositions and methods of adjusting the dispense rate of solid detergents using solid anionic surfactants
WO2018064721A1 (en)	2016-10-04	2018-04-12	Commonwealth Scientific And Industrial Research Organisation	Methods for inhibiting corrosion
CN108079981B (zh) *	2016-11-21	2021-06-08	中国科学院大连化学物理研究所	一种四氮唑/疏水基键合固定相及其制备方法
US11149202B1 (en)	2016-12-13	2021-10-19	Ecolab Usa Inc.	Tetracarboxylic acid combinations for corrosion inhibition
AU2018229264B2 (en)	2017-02-28	2021-04-01	Ecolab Usa Inc.	Alkaline cleaning compositions comprising an alkylamino hydroxy acid and/or secondary amine and methods of reducing metal corrosion
EP3589778A4 (en)	2017-02-28	2020-12-09	Ecolab USA Inc.	ALKALINE CLEANING COMPOSITION CONSISTING OF HYDROXYPHOSPHONO-CARBOXYLIC ACID AND METAL CORROSION REDUCTION METHODS
CN107254683B (zh) *	2017-07-03	2019-08-27	无锡市恒利弘实业有限公司	一种钢制件的强力除锈剂及其使用方法
TW201927706A (zh) *	2017-12-13	2019-07-16	美商藝康美國公司	經氫磷酸化之多羧酸及其協同組合作為腐蝕及積垢抑制劑
WO2019160131A1 (ja) *	2018-02-16	2019-08-22	株式会社日本触媒	金属腐食抑制剤
CN108623878B (zh) *	2018-04-20	2019-09-13	高松	一种水利工程浮漂用母粒的制备方法
CN109504973A (zh) *	2019-01-09	2019-03-22	奎克化学（中国）有限公司	一种用于轧钢领域的酸洗缓蚀剂的表面活性剂
CA3136427C (en) *	2019-04-16	2023-10-24	Ecolab Usa Inc.	Use of multiple charged cationic compounds derived from polyamines and compositions thereof for corrosion inhibition in a water system
US11525186B2 (en) *	2019-06-11	2022-12-13	Ecolab Usa Inc.	Corrosion inhibitor formulation for geothermal reinjection well
CN112682031B (zh) *	2019-10-18	2024-06-28	中国石油化工股份有限公司	一种油田井间示踪剂、示踪方法及压裂液
CN110670074B (zh) *	2019-11-05	2021-11-16	北美防锈技术（上海）有限公司	一种环保型螺纹钢表面防锈处理剂及其制备方法
EP4158080A1 (en)	2020-05-28	2023-04-05	Ecolab Usa Inc.	Closed loop cooling water corrosion inhibition employing polymaleates and non-borate buffers
JP7544523B2 (ja) *	2020-07-29	2024-09-03	東ソー・ファインケム株式会社	自然重合が抑制されたスチレンスルホン酸リチウムの極性有機溶剤溶液及び自然重合を抑制する方法
US20220127730A1 (en) *	2020-10-08	2022-04-28	Ecolab Usa Inc.	Corrosion Control Treatment Program
CN113667982A (zh) *	2021-07-27	2021-11-19	新疆金海德邦能源科技有限公司	一种预防碳钢应力腐蚀开裂的缓蚀剂及其制备方法
CN115959781A (zh) *	2021-10-12	2023-04-14	中国石油化工股份有限公司	无磷预膜剂及其应用和循环水处理方法
WO2024196346A1 (en) *	2023-03-17	2024-09-26	Baker Hughes Oilfield Operations Llc	Synergistic corrosion inhibitor blends
US12139662B2 (en)	2022-03-17	2024-11-12	Baker Hughes Oilfield Operations Llc	Synergistic corrosion inhibitor blends
CN114806529B (zh) *	2022-05-31	2023-07-28	中国石油化工股份有限公司	一种溶垢助溶剂及其制备方法
CN115094406B (zh) *	2022-06-20	2023-10-20	邢台旭阳科技有限公司	无磷预膜剂及其制备方法和应用
KR102627360B1 (ko) *	2023-10-20	2024-01-19	엔티스테크주식회사	부식억제 효과가 우수한 금속용 방식제 조성물
CN117447662B (zh) *	2023-12-22	2024-02-27	广东粤首新科技有限公司	一种水溶性聚合物阻垢剂的制备工艺
CN118791144B (zh) *	2024-07-22	2026-02-10	河北择赛生物科技有限公司	一种高硬度高碱度循环冷却水用缓蚀阻垢剂及其制备方法

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3867259A (en) *	1973-11-08	1975-02-18	American Cyanamid Co	Lactate dehydrogenase test material
US5635484A (en) *	1982-09-17	1997-06-03	The State Of Oregon Acting By And Through The Oregon State Board Of Higher Education On Behalf Of Oregon State University	Propionibacteria peptide microcin
US4683035A (en) *	1986-02-03	1987-07-28	Nalco Chemical Company	Method for in situ corrosion detection using electrochemically active compounds
NZ240442A (en) *	1990-11-07	1994-11-25	Cortech Inc	2-heterocyclic substituted aliphatic carboxylic acid esters of (optionally substituted) phenol and pharmaceutical compositions
DE4218585A1 (de) *	1992-03-02	1993-09-09	Henkel Kgaa	1,2,4-triazoliumsalze oder 1,2,3,4-tetrazoliumsalze, verfahren zu deren herstellung und deren verwendung
US5993852A (en) *	1997-08-29	1999-11-30	Pharmaderm Laboratories Ltd.	Biphasic lipid vesicle composition for transdermal administration of an immunogen
US6187262B1 (en) *	1998-08-19	2001-02-13	Betzdearborn Inc.	Inhibition of corrosion in aqueous systems

2000
- 2000-05-02 BR BR0010592-9A patent/BR0010592A/pt not_active IP Right Cessation
- 2000-05-02 AU AU49727/00A patent/AU4972700A/en not_active Abandoned
- 2000-05-02 MX MXPA01011087A patent/MXPA01011087A/es unknown
- 2000-05-02 KR KR1020017014019A patent/KR20020012564A/ko not_active Withdrawn
- 2000-05-02 PL PL00352994A patent/PL352994A1/xx unknown
- 2000-05-02 WO PCT/US2000/008750 patent/WO2000066810A1/en not_active Ceased
- 2000-05-02 EP EP00931920A patent/EP1177331A1/en not_active Withdrawn
- 2000-05-02 CA CA002369954A patent/CA2369954A1/en not_active Abandoned
- 2000-05-02 HK HK02105338.8A patent/HK1044176A1/zh unknown
- 2000-05-02 CN CN00809883A patent/CN1359430A/zh active Pending
- 2000-05-02 CZ CZ20013966A patent/CZ20013966A3/cs unknown
- 2000-05-02 HU HU0201012A patent/HUP0201012A3/hu unknown
- 2000-05-02 JP JP2000615429A patent/JP2002543294A/ja active Pending
- 2000-05-03 AR ARP000102114A patent/AR023836A1/es not_active Application Discontinuation
2001
- 2001-10-30 NO NO20015307A patent/NO20015307D0/no not_active Application Discontinuation

Also Published As

Publication number	Publication date
NO20015307D0 (no)	2001-10-30
AU4972700A (en)	2000-11-17
CN1359430A (zh)	2002-07-17
HK1044176A1 (zh)	2002-10-11
NO20015307L (no)	2001-01-02
WO2000066810A1 (en)	2000-11-09
MXPA01011087A (es)	2002-06-04
JP2002543294A (ja)	2002-12-17
EP1177331A1 (en)	2002-02-06
PL352994A1 (en)	2003-09-22
CA2369954A1 (en)	2000-11-09
KR20020012564A (ko)	2002-02-16
AR023836A1 (es)	2002-09-04
HUP0201012A2 (hu)	2002-07-29
BR0010592A (pt)	2002-02-05
HUP0201012A3 (en)	2003-08-28

Publication	Publication Date	Title
CZ20013966A3 (cs)	2002-05-15	Způsob a kompozice k inhibici koroze ve vodných systémech
US6585933B1 (en)	2003-07-01	Method and composition for inhibiting corrosion in aqueous systems
US6572789B1 (en)	2003-06-03	Corrosion inhibitors for aqueous systems
TWI527933B (zh)	2016-04-01	用於控制產業系統中銅排放及銅合金腐蝕之組合物及方法
EP0652305B1 (en)	1999-04-07	Corrosion inhibiting method for closed cooling systems
JP5835967B2 (ja)	2015-12-24	スライム剥離剤およびスライム剥離方法
KR960000311B1 (ko)	1996-01-04	급수 시스템에서 망간에 의한 스케일 형성 및 부식을 아미노포스폰산으로 억제하는 방법
US8236205B1 (en)	2012-08-07	Corrosion inhibitor compositions comprising tetrahydrobenzotriazoles and other triazoles and methods for using same
AU2002252089A1 (en)	2003-04-03	Corrosion inhibitors for aqueous systems
JPH05200397A (ja)	1993-08-10	高ｐＨスケール抑制のためのポリエーテルポリアミノメチレンホスホナート
EP0544345A1 (en)	1993-06-02	Corrosion and/or scale inhibition
US9447322B2 (en)	2016-09-20	Corrosion inhibitor compositions comprising tetrahydrobenzotriazoles solubilized in activating solvents and methods for using same
US6814930B1 (en)	2004-11-09	Galvanized metal corrosion inhibitor
EP0590879A1 (en)	1994-04-06	Method and composition for inhibiting silica and silicate deposition
ZA200109942B (en)	2003-03-03	Method and composition for inhibiting corrosion in aqueous systems.
KR20200020872A (ko)	2020-02-26	부식 및 스케일을 억제하기 위한 조성물 및 방법
JPS62256973A (ja)	1987-11-09	金属腐蝕抑制と燐酸カルシウム沈澱防止のためのホスホン酸／燐酸塩混合物
JPH05169094A (ja)	1993-07-09	水性系におけるスケール、腐蝕及び微生物の防止方法
US20250109504A1 (en)	2025-04-03	Heterocyclic non-triazole compounds and methods for inhibiting corrosion in industrial water treatment
JP2001049471A (ja)	2001-02-20	水系防食方法
UA139862U (uk)	2020-01-27	Антискалант із біоцидною дією для комплексного антикорозійного захисту у циркуляційних системах охолодження теплообмінників електростанцій та промислових підприємств