NO773601L - Kunstharpikskomponenter for fremstilling av biocide belegg - Google Patents

Kunstharpikskomponenter for fremstilling av biocide belegg

Info

Publication number: NO773601L
Authority: NO; Norway
Prior art keywords: compounds; triorganotin; glycidyl; hardeners; production
Prior art date: 1976-10-21

Application number

NO773601A

Other languages

English (en)

Norwegian (no)

Inventor

Bernd Neffgen

Hans Plum

Michael Richter

Ulrich Schroeer

Original Assignee

Schering 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.)

1976-10-21

Filing date

1977-10-20

Publication date

1978-04-24

1976-10-21 Priority claimed from DE19762647605 external-priority patent/DE2647605A1/de

1976-10-21 Priority claimed from DE19762647604 external-priority patent/DE2647604A1/de

1977-10-20 Application filed by Schering Ag filed Critical Schering Ag

1978-04-24 Publication of NO773601L publication Critical patent/NO773601L/no

Links

230000003115 biocidal effect Effects 0.000 title claims abstract description 17
238000004519 manufacturing process Methods 0.000 title claims abstract description 15
229920005989 resin Polymers 0.000 title claims description 7
239000011347 resin Substances 0.000 title claims description 7
239000003139 biocide Substances 0.000 title description 2
NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 title 1
238000000576 coating method Methods 0.000 claims abstract description 17
150000001875 compounds Chemical class 0.000 claims description 39
239000004848 polyfunctional curative Substances 0.000 claims description 26
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 21
-1 stannyl ester Chemical class 0.000 claims description 20
239000000047 product Substances 0.000 claims description 19
125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 claims description 17
125000004432 carbon atom Chemical group C* 0.000 claims description 12
239000000203 mixture Substances 0.000 claims description 10
150000004703 alkoxides Chemical class 0.000 claims description 8
125000003277 amino group Chemical group 0.000 claims description 7
150000001735 carboxylic acids Chemical class 0.000 claims description 7
125000001931 aliphatic group Chemical group 0.000 claims description 6
238000000034 method Methods 0.000 claims description 5
125000002029 aromatic hydrocarbon group Chemical group 0.000 claims description 4
239000007795 chemical reaction product Substances 0.000 claims description 4
239000000945 filler Substances 0.000 claims description 4
239000000049 pigment Substances 0.000 claims description 4
239000003795 chemical substances by application Substances 0.000 claims description 3
238000002360 preparation method Methods 0.000 claims description 3
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150000001298 alcohols Chemical class 0.000 claims 1
238000005728 strengthening Methods 0.000 claims 1
229920003002 synthetic resin Polymers 0.000 abstract description 2
239000000057 synthetic resin Substances 0.000 abstract description 2
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241000894006 Bacteria Species 0.000 description 4
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239000000126 substance Substances 0.000 description 4
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239000013543 active substance Substances 0.000 description 2
239000003513 alkali Substances 0.000 description 2
125000000217 alkyl group Chemical group 0.000 description 2
230000000844 anti-bacterial effect Effects 0.000 description 2
230000003373 anti-fouling effect Effects 0.000 description 2
230000008033 biological extinction Effects 0.000 description 2
230000000052 comparative effect Effects 0.000 description 2
239000007859 condensation product Substances 0.000 description 2
230000000694 effects Effects 0.000 description 2
230000000855 fungicidal effect Effects 0.000 description 2
238000005259 measurement Methods 0.000 description 2
LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 2
229920005862 polyol Polymers 0.000 description 2
239000001294 propane Substances 0.000 description 2
230000001105 regulatory effect Effects 0.000 description 2
239000012744 reinforcing agent Substances 0.000 description 2
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239000007858 starting material Substances 0.000 description 2
238000003756 stirring Methods 0.000 description 2
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238000012360 testing method Methods 0.000 description 2
DFNPRTKVCGZMMC-UHFFFAOYSA-M tributyl(fluoro)stannane Chemical compound CCCC[Sn](F)(CCCC)CCCC DFNPRTKVCGZMMC-UHFFFAOYSA-M 0.000 description 2
YSUXTNDMKYYZPR-UHFFFAOYSA-M tributylstannyl prop-2-enoate Chemical compound CCCC[Sn](CCCC)(CCCC)OC(=O)C=C YSUXTNDMKYYZPR-UHFFFAOYSA-M 0.000 description 2
230000007306 turnover Effects 0.000 description 2
239000008096 xylene Substances 0.000 description 2
GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-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
YSUQLAYJZDEMOT-UHFFFAOYSA-N 2-(butoxymethyl)oxirane Chemical compound CCCCOCC1CO1 YSUQLAYJZDEMOT-UHFFFAOYSA-N 0.000 description 1
WKJICCKTDQDONB-UHFFFAOYSA-N 2-(oxiran-2-ylmethoxycarbonyl)cyclohexane-1-carboxylic acid Chemical compound OC(=O)C1CCCCC1C(=O)OCC1OC1 WKJICCKTDQDONB-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
CUFXMPWHOWYNSO-UHFFFAOYSA-N 2-[(4-methylphenoxy)methyl]oxirane Chemical compound C1=CC(C)=CC=C1OCC1OC1 CUFXMPWHOWYNSO-UHFFFAOYSA-N 0.000 description 1
RNLHGQLZWXBQNY-UHFFFAOYSA-N 3-(aminomethyl)-3,5,5-trimethylcyclohexan-1-amine Chemical compound CC1(C)CC(N)CC(C)(CN)C1 RNLHGQLZWXBQNY-UHFFFAOYSA-N 0.000 description 1
RCXHRHWRRACBTK-UHFFFAOYSA-N 3-(oxiran-2-ylmethoxy)propane-1,2-diol Chemical compound OCC(O)COCC1CO1 RCXHRHWRRACBTK-UHFFFAOYSA-N 0.000 description 1
229920001817 Agar Polymers 0.000 description 1
LCFVJGUPQDGYKZ-UHFFFAOYSA-N Bisphenol A diglycidyl ether Chemical compound C=1C=C(OCC2OC2)C=CC=1C(C)(C)C(C=C1)=CC=C1OCC1CO1 LCFVJGUPQDGYKZ-UHFFFAOYSA-N 0.000 description 1
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
239000004386 Erythritol Substances 0.000 description 1
UNXHWFMMPAWVPI-UHFFFAOYSA-N Erythritol Natural products OCC(O)C(O)CO UNXHWFMMPAWVPI-UHFFFAOYSA-N 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
CTKINSOISVBQLD-UHFFFAOYSA-N Glycidol Chemical compound OCC1CO1 CTKINSOISVBQLD-UHFFFAOYSA-N 0.000 description 1
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CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
AQFLJCURVBBBFN-UHFFFAOYSA-N OC(O)(O)C(C1CO1)(C1=CC=CC=C1)OC(C1CO1)(C(O)(O)O)C1=CC=CC=C1 Chemical class OC(O)(O)C(C1CO1)(C1=CC=CC=C1)OC(C1CO1)(C(O)(O)O)C1=CC=CC=C1 AQFLJCURVBBBFN-UHFFFAOYSA-N 0.000 description 1
239000004698 Polyethylene Substances 0.000 description 1
229910000831 Steel Inorganic materials 0.000 description 1
AWMVMTVKBNGEAK-UHFFFAOYSA-N Styrene oxide Chemical compound C1OC1C1=CC=CC=C1 AWMVMTVKBNGEAK-UHFFFAOYSA-N 0.000 description 1
UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
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JCYTYSQYTAVAPU-UHFFFAOYSA-N [4-[[[4-(hydroxymethyl)phenyl]-(oxiran-2-yl)methoxy]-(oxiran-2-yl)methyl]phenyl]methanol Chemical compound C1=CC(CO)=CC=C1C(C1OC1)OC(C=1C=CC(CO)=CC=1)C1OC1 JCYTYSQYTAVAPU-UHFFFAOYSA-N 0.000 description 1
150000001253 acrylic acids Chemical class 0.000 description 1
239000008272 agar Substances 0.000 description 1
239000003570 air Substances 0.000 description 1
150000001299 aldehydes Chemical class 0.000 description 1
150000001338 aliphatic hydrocarbons Chemical group 0.000 description 1
IMUDHTPIFIBORV-UHFFFAOYSA-N aminoethylpiperazine Chemical compound NCCN1CCNCC1 IMUDHTPIFIBORV-UHFFFAOYSA-N 0.000 description 1
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150000004982 aromatic amines Chemical class 0.000 description 1
CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000000969 carrier Substances 0.000 description 1
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150000001879 copper Chemical class 0.000 description 1
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239000010949 copper Substances 0.000 description 1
230000007797 corrosion Effects 0.000 description 1
238000005260 corrosion Methods 0.000 description 1
LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
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239000000645 desinfectant Substances 0.000 description 1
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238000009792 diffusion process Methods 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
239000000539 dimer Substances 0.000 description 1
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238000004821 distillation Methods 0.000 description 1
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150000002170 ethers Chemical class 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
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239000000446 fuel Substances 0.000 description 1
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239000001257 hydrogen Substances 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 description 1
230000005764 inhibitory process Effects 0.000 description 1
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239000011976 maleic acid Substances 0.000 description 1
KJGLZJQPMKQFIK-UHFFFAOYSA-N methanolate;tributylstannanylium Chemical compound CCCC[Sn](CCCC)(CCCC)OC KJGLZJQPMKQFIK-UHFFFAOYSA-N 0.000 description 1
230000003641 microbiacidal effect Effects 0.000 description 1
238000002156 mixing Methods 0.000 description 1
150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 1
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Classifications

- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/14—Paints containing biocides, e.g. fungicides, insecticides or pesticides
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/20—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the epoxy compounds used
- C08G59/22—Di-epoxy compounds
- C08G59/30—Di-epoxy compounds containing atoms other than carbon, hydrogen, oxygen and nitrogen
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
- C08G59/50—Amines
- C08G59/504—Amines containing an atom other than nitrogen belonging to the amine group, carbon and hydrogen

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Chemical Kinetics & Catalysis (AREA)
Health & Medical Sciences (AREA)
Plant Pathology (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Wood Science & Technology (AREA)
Paints Or Removers (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

NO773601A 1976-10-21 1977-10-20 Kunstharpikskomponenter for fremstilling av biocide belegg NO773601L (no)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE19762647605 DE2647605A1 (de)	1976-10-21	1976-10-21	Kunstharzkomponenten zur herstellung von biozid ausgeruesteten beschichtungen
DE19762647604 DE2647604A1 (de)	1976-10-21	1976-10-21	Verwendung von kunstharzmischungen zur herstellung von biozid ausgeruesteten beschichtungen

Publications (1)

Publication Number	Publication Date
NO773601L true NO773601L (no)	1978-04-24

Family

ID=25771040

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO773601A NO773601L (no)	1976-10-21	1977-10-20	Kunstharpikskomponenter for fremstilling av biocide belegg

Country Status (9)

Country	Link
JP (1)	JPS5351236A (da)
DK (1)	DK426277A (da)
ES (1)	ES462158A1 (da)
FR (1)	FR2368522A1 (da)
IT (1)	IT1086150B (da)
LU (1)	LU78348A1 (da)
NL (1)	NL7710810A (da)
NO (1)	NO773601L (da)
SE (1)	SE7711818L (da)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS59142264A (ja) *	1983-02-02	1984-08-15	Nitto Electric Ind Co Ltd	液状活性物質含有被膜形成性塗布組成物
JPS59169879U (ja) *	1983-04-28	1984-11-13	株式会社学習研究社	文具ロボツト

1977
- 1977-09-06 ES ES462158A patent/ES462158A1/es not_active Expired
- 1977-09-27 DK DK426277A patent/DK426277A/da not_active Application Discontinuation
- 1977-09-28 IT IT28012/77A patent/IT1086150B/it active
- 1977-10-03 NL NL7710810A patent/NL7710810A/xx not_active Application Discontinuation
- 1977-10-19 LU LU78348A patent/LU78348A1/xx unknown
- 1977-10-20 JP JP12637177A patent/JPS5351236A/ja active Pending
- 1977-10-20 NO NO773601A patent/NO773601L/no unknown
- 1977-10-20 SE SE7711818A patent/SE7711818L/xx unknown
- 1977-10-20 FR FR7731576A patent/FR2368522A1/fr not_active Withdrawn

Also Published As

Publication number	Publication date
LU78348A1 (da)	1978-01-24
IT1086150B (it)	1985-05-28
ES462158A1 (es)	1979-01-01
JPS5351236A (en)	1978-05-10
DK426277A (da)	1978-04-22
FR2368522A1 (fr)	1978-05-19
NL7710810A (nl)	1978-04-25
SE7711818L (sv)	1978-04-22

Publication	Publication Date	Title
US3979354A (en)	1976-09-07	Non-polluting, antifouling composition and method
EP1788048B1 (en)	2010-10-06	High-solid anticorrosive coating composition, high-solid rapidly-curable anticorrosive coating composition, method of coating ship or the like, high-solid anticorrosive film and rapidly cured high-solid anticorrosive film obtained, and coated ship and underwater structure coated with these coating films
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JPS5536247A (en)	1980-03-13	Electrophoretic paint composition for cathode deposition
TW339352B (en)	1998-09-01	Coationic resin and capped polyisocyanate curing agent suitable for use in electrodeposition
JPS5590566A (en)	1980-07-09	Cationic electrodeposition coating resin composition
NO171683B (no)	1993-01-11	Aminogruppeholdig herdningskomponent, herdbar blanding paabasis av denne samt anvendelse av komponenten
JP6990241B2 (ja)	2022-01-12	エポキシ樹脂系防食塗料組成物、防食塗膜、積層防汚塗膜、および防汚基材、ならびにこれらの製造方法
US4692484A (en)	1987-09-08	Epoxy-phosphate/phenolic electrocoating compositions
WO1992012192A2 (en)	1992-07-23	Thermosetting reactive resin mixture, moulded article and coating made therefrom
CA1141499A (en)	1983-02-15	Electro-depositable corrosion resistant primers
JPWO2017094767A1 (ja)	2018-09-13	防汚性複合塗膜、防汚基材、および該防汚基材の製造方法
US5459180A (en)	1995-10-17	Polyol/epoxy adducts for use as emulsifier for liquid epoxy resins
US4104234A (en)	1978-08-01	Novel biologically active copolymers
KR102912223B1 (ko)	2026-01-13	에폭시 수지계 방식 도료 조성물, 방식 도막, 적층 방오 도막, 방오 기재 및 방오 기재의 제조방법
FR2472005A2 (fr)	1981-06-26	Procede de fabrication de liants deposables a la cathode
US6008314A (en)	1999-12-28	Aminourethane hardeners, epoxide-based coating media and the use thereof
US4064338A (en)	1977-12-20	Method for preparing biologically active copolymers of triorganotin acrylates
NO773601L (no)	1978-04-24	Kunstharpikskomponenter for fremstilling av biocide belegg
NO814423L (no)	1982-07-01	Beleggsammensetninger med dobbelt herdemekanisme
ES8205242A1 (es)	1982-06-01	Procedimiento para la obtencion de dispersiones acuosas de resina epoxidica.
KR900700551A (ko)	1990-08-16	도전성 기판을 코팅하기 위한 방법, 이 방법에 의해 코팅된 기판 및 수성전해코팅배드
US5101000A (en)	1992-03-31	Process for the preparation of binders for cathodically depositable paints, the binders produced, and to the use thereof in paints
US4272621A (en)	1981-06-09	Water thinnable coating compositions from aminoalkylated interpolymers
US4055517A (en)	1977-10-25	Process for producing water-soluble organic macromolecules, and the water-soluble organic macromolecules obtained