CS243481B2 - Anticorrosionnagent - Google Patents

Anticorrosionnagent Download PDF

Info

Publication number: CS243481B2
Authority: CS; Czechoslovakia
Prior art keywords: acid; corrosion; formula; aqueous solution; mol
Prior art date: 1983-02-08

Application number

CS84869A

Other languages

Czech (cs)

English (en)

Inventor

Werner Ritschel

Horst Lorka

Original Assignee

Hoechst Ag

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.)

1983-02-08

Filing date

1984-02-07

Publication date

1986-06-12

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=6190250&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=CS243481(B2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

1984-02-07 Application filed by Hoechst Ag filed Critical Hoechst Ag

1986-06-12 Publication of CS243481B2 publication Critical patent/CS243481B2/cs

Links

239000002253 acid Substances 0.000 claims description 20
239000007795 chemical reaction product Substances 0.000 claims description 8
239000007864 aqueous solution Substances 0.000 claims description 7
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
229910052739 hydrogen Inorganic materials 0.000 claims description 3
239000001257 hydrogen Substances 0.000 claims description 3
125000004429 atom Chemical group 0.000 claims description 2
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims 3
239000000779 smoke Substances 0.000 claims 2
241000269799 Perca fluviatilis Species 0.000 claims 1
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims 1
125000003710 aryl alkyl group Chemical group 0.000 claims 1
125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 claims 1
ZFCHNZDUMIOWFV-UHFFFAOYSA-N pyrimidine-2-carboxylic acid Chemical compound OC(=O)C1=NC=CC=N1 ZFCHNZDUMIOWFV-UHFFFAOYSA-N 0.000 claims 1
125000003396 thiol group Chemical group [H]S* 0.000 claims 1
ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 abstract description 9
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 abstract description 2
125000000008 (C1-C10) alkyl group Chemical group 0.000 abstract 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
230000007797 corrosion Effects 0.000 description 22
238000005260 corrosion Methods 0.000 description 22
239000000047 product Substances 0.000 description 16
239000000203 mixture Substances 0.000 description 10
230000000052 comparative effect Effects 0.000 description 9
239000000243 solution Substances 0.000 description 8
239000011814 protection agent Substances 0.000 description 7
239000012530 fluid Substances 0.000 description 6
244000005700 microbiome Species 0.000 description 6
230000004224 protection Effects 0.000 description 6
229930195733 hydrocarbon Natural products 0.000 description 5
150000002430 hydrocarbons Chemical class 0.000 description 5
239000007788 liquid Substances 0.000 description 5
125000003118 aryl group Chemical group 0.000 description 4
KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 4
239000004327 boric acid Substances 0.000 description 4
239000002173 cutting fluid Substances 0.000 description 4
230000000855 fungicidal effect Effects 0.000 description 4
125000000217 alkyl group Chemical group 0.000 description 3
150000001735 carboxylic acids Chemical class 0.000 description 3
239000003795 chemical substances by application Substances 0.000 description 3
239000002826 coolant Substances 0.000 description 3
230000000694 effects Effects 0.000 description 3
-1 ferrous metals Chemical class 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
241000233866 Fungi Species 0.000 description 2
241000223259 Trichoderma Species 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
239000013543 active substance Substances 0.000 description 2
230000000844 anti-bacterial effect Effects 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
239000007859 condensation product Substances 0.000 description 2
238000001816 cooling Methods 0.000 description 2
238000005520 cutting process Methods 0.000 description 2
238000005553 drilling Methods 0.000 description 2
238000005187 foaming Methods 0.000 description 2
238000010438 heat treatment Methods 0.000 description 2
229910052751 metal Inorganic materials 0.000 description 2
239000002184 metal Substances 0.000 description 2
238000005191 phase separation Methods 0.000 description 2
239000003755 preservative agent Substances 0.000 description 2
239000003223 protective agent Substances 0.000 description 2
238000005096 rolling process Methods 0.000 description 2
LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
239000000126 substance Substances 0.000 description 2
DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 1
SALYKAIZVOFAEJ-UHFFFAOYSA-N 2-(pentylamino)ethanol Chemical compound CCCCCNCCO SALYKAIZVOFAEJ-UHFFFAOYSA-N 0.000 description 1
IHCCLXNEEPMSIO-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperidin-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C1CCN(CC1)CC(=O)N1CC2=C(CC1)NN=N2 IHCCLXNEEPMSIO-UHFFFAOYSA-N 0.000 description 1
WTFUTSCZYYCBAY-SXBRIOAWSA-N 6-[(E)-C-[[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]methyl]-N-hydroxycarbonimidoyl]-3H-1,3-benzoxazol-2-one Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)C/C(=N/O)/C1=CC2=C(NC(O2)=O)C=C1 WTFUTSCZYYCBAY-SXBRIOAWSA-N 0.000 description 1
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
241000894006 Bacteria Species 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
239000004215 Carbon black (E152) Substances 0.000 description 1
FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
101100022176 Mus musculus Gstz1 gene Proteins 0.000 description 1
MKYBYDHXWVHEJW-UHFFFAOYSA-N N-[1-oxo-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propan-2-yl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(C(C)NC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 MKYBYDHXWVHEJW-UHFFFAOYSA-N 0.000 description 1
OPEPAPXSYGTENJ-UHFFFAOYSA-N NCC(C)O.C(C)(C)N Chemical compound NCC(C)O.C(C)(C)N OPEPAPXSYGTENJ-UHFFFAOYSA-N 0.000 description 1
IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 1
ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
230000002411 adverse Effects 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
150000001414 amino alcohols Chemical class 0.000 description 1
229910021529 ammonia Inorganic materials 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
238000009835 boiling Methods 0.000 description 1
239000002775 capsule Substances 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
238000004140 cleaning Methods 0.000 description 1
239000002131 composite material Substances 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
125000004122 cyclic group Chemical group 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
230000002500 effect on skin Effects 0.000 description 1
230000007613 environmental effect Effects 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
238000002474 experimental method 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
230000003993 interaction Effects 0.000 description 1
239000000314 lubricant Substances 0.000 description 1
238000003754 machining Methods 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
238000005555 metalworking Methods 0.000 description 1
230000003641 microbiacidal effect Effects 0.000 description 1
238000002156 mixing Methods 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
235000015097 nutrients Nutrition 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
150000004885 piperazines Chemical class 0.000 description 1
230000002335 preservative effect Effects 0.000 description 1
UIIIBRHUICCMAI-UHFFFAOYSA-N prop-2-ene-1-sulfonic acid Chemical compound OS(=O)(=O)CC=C UIIIBRHUICCMAI-UHFFFAOYSA-N 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
239000011435 rock Substances 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
239000012488 sample solution Substances 0.000 description 1
229930195734 saturated hydrocarbon Natural products 0.000 description 1
235000010288 sodium nitrite Nutrition 0.000 description 1
239000002904 solvent Substances 0.000 description 1
241000894007 species Species 0.000 description 1
238000003756 stirring Methods 0.000 description 1
DIORMHZUUKOISG-UHFFFAOYSA-N sulfoformic acid Chemical class OC(=O)S(O)(=O)=O DIORMHZUUKOISG-UHFFFAOYSA-N 0.000 description 1
229940124530 sulfonamide Drugs 0.000 description 1
230000008961 swelling Effects 0.000 description 1
229940066771 systemic antihistamines piperazine derivative Drugs 0.000 description 1
229940095064 tartrate Drugs 0.000 description 1
230000002110 toxicologic effect Effects 0.000 description 1
231100000027 toxicology Toxicity 0.000 description 1
150000004670 unsaturated fatty acids Chemical class 0.000 description 1
235000021122 unsaturated fatty acids Nutrition 0.000 description 1

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
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/02—Boron compounds
- C07F5/04—Esters of boric acids

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Mechanical Engineering (AREA)
Metallurgy (AREA)
Preventing Corrosion Or Incrustation Of Metals (AREA)
Lubricants (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

CS84869A 1983-02-08 1984-02-07 Anticorrosionnagent CS243481B2 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19833304164 DE3304164A1 (de)	1983-02-08	1983-02-08	Reaktionsprodukte aus borsaeure, diethanolamin und monoethanolaminen und deren verwendung als korrosionsschutzmittel

Publications (1)

Publication Number	Publication Date
CS243481B2 true CS243481B2 (en)	1986-06-12

Family

ID=6190250

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CS84869A CS243481B2 (en)	1983-02-08	1984-02-07	Anticorrosionnagent

Country Status (6)

Country	Link
EP (1)	EP0116348B2 (pt)
JP (1)	JPS59152351A (pt)
BR (1)	BR8400536A (pt)
CS (1)	CS243481B2 (pt)
DE (2)	DE3304164A1 (pt)
ZA (1)	ZA84885B (pt)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS62283197A (ja) *	1986-06-02	1987-12-09	Nippon Parkerizing Co Ltd	片面亜鉛メツキ鋼板用水溶性調質圧延剤
DE3808372A1 (de) *	1988-03-12	1989-09-21	Rewo Chemische Werke Gmbh	Reaktionsprodukte aus borsaeure und alkanoletheraminen und deren verwendung als korrosionsschutzmittel
GB9201165D0 (en) *	1992-01-18	1992-03-11	Ciba Geigy	Corrosion inhibiting compositions
US5507962A (en) *	1993-05-18	1996-04-16	The United States Of America As Represented By The Secretary Of Commerce	Method of fabricating articles
US7223299B2 (en) *	2003-09-02	2007-05-29	Atotech Deutschland Gmbh	Composition and process for improving the adhesion of a siccative organic coating compositions to metal substrates

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR1340167A (fr) *	1960-08-04	1963-10-18	Westinghouse Electric Corp	Procédé de préparation des composés de bore à coordination par l'azote obtenus par la réaction de monoalkanolamines
FR1558440A (pt) *	1967-12-04	1969-02-28
FR1546339A (fr) *	1967-12-05	1968-11-15		Préparation et utilisation d'esters boriques de diéthanolamine comme produits antirouille
DE2007229A1 (de) *	1969-02-19	1970-09-10	The Dow Chemical Company, Midland, Mich. (V.St.A.)	Borat-Korrosionsinhibitoren
CH629540A5 (de) *	1977-09-19	1982-04-30	Hoechst Ag	Wassermischbare korrosionsschutzmittel.

1983
- 1983-02-08 DE DE19833304164 patent/DE3304164A1/de not_active Withdrawn
1984
- 1984-02-03 EP EP84101088A patent/EP0116348B2/de not_active Expired - Lifetime
- 1984-02-03 DE DE8484101088T patent/DE3463931D1/de not_active Expired
- 1984-02-07 CS CS84869A patent/CS243481B2/cs unknown
- 1984-02-07 BR BR8400536A patent/BR8400536A/pt not_active IP Right Cessation
- 1984-02-07 JP JP59019555A patent/JPS59152351A/ja active Granted
- 1984-02-07 ZA ZA84885A patent/ZA84885B/xx unknown

Also Published As

Publication number	Publication date
EP0116348A2 (de)	1984-08-22
JPS59152351A (ja)	1984-08-31
DE3304164A1 (de)	1984-08-09
EP0116348A3 (en)	1984-10-10
DE3463931D1 (en)	1987-07-02
ZA84885B (en)	1984-09-26
EP0116348B1 (de)	1987-05-27
EP0116348B2 (de)	1993-11-03
JPH0582479B2 (pt)	1993-11-19
BR8400536A (pt)	1984-09-11

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EP2267098A1 (en)	2010-12-29	Scavenger compositons and their use
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JPH0377879B2 (pt)	1991-12-11
CS207675B2 (en)	1981-08-31	Means against the corrosion
EP0243016B1 (en)	1989-12-06	N, s containing corrosion inhibitors
BRPI0415183B1 (pt)	2015-05-19	Formulação anti-corrosão e anti-incrustação de sulfeto metálico e método para o tratamento de sistemas aquosos.
JPS63168495A (ja)	1988-07-12	低起泡性界面活性剤用可溶化剤
BR102015020543A2 (pt)	2017-01-24	inibidores de corrosão livres de boro para fluidos de usinagem de metais
RU2110613C1 (ru)	1998-05-10	Средство защиты от коррозии
JPH03176407A (ja)	1991-07-31	殺菌剤組成物
EP0364703A2 (en)	1990-04-25	Process for preparing sulfur solvent compositions
RU2166001C1 (ru)	2001-04-27	Состав для защиты нефтепромыслового оборудования от сероводородной и углекислотной коррозии
US4724124A (en)	1988-02-09	Use of alkenylsuccinic acid half-amides as anti-corrosion agents
CA1162409A (en)	1984-02-21	Use of alkoxylated compounds as nonionic emulsifiers in crop protection formulations
RU2038421C1 (ru)	1995-06-27	Ингибитор коррозии - бактерицид в минерализованных сероводородсодержащих водных средах
KR840002829A (ko)	1984-07-21	아졸릴-펜텐유도체의 제조방법
EP1059292B1 (en)	2003-09-24	New adamantane derivative and aqueous disinfectant composition containing it
US3976587A (en)	1976-08-24	Amino derivatives of tetrasubstituted benzene compounds
JPH10182318A (ja)	1998-07-07	安定化されたハロアセチレン化合物及びハロアセチレン化合物の保存方法
RU2236438C1 (ru)	2004-09-20	Концентрат смазочно-охлаждающей жидкости для механической обработки металлов
NL8300676A (nl)	1983-09-16	Samenstelling voor het verspreiden van koolwaterstoffen in water.