CH660749A5 - Compositions et procede pour le traitement oleophobe et hydrophobe des materiaux de construction. - Google Patents
Compositions et procede pour le traitement oleophobe et hydrophobe des materiaux de construction. Download PDFInfo
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- CH660749A5 CH660749A5 CH365/84A CH36584A CH660749A5 CH 660749 A5 CH660749 A5 CH 660749A5 CH 365/84 A CH365/84 A CH 365/84A CH 36584 A CH36584 A CH 36584A CH 660749 A5 CH660749 A5 CH 660749A5
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- CH
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- carbon atoms
- composition according
- parts
- composition
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- 239000000203 mixture Substances 0.000 title claims description 66
- 238000000034 method Methods 0.000 title claims description 14
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- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- XXROGKLTLUQVRX-UHFFFAOYSA-N hydroxymethylethylene Natural products OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 1
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- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
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- GIWKOZXJDKMGQC-UHFFFAOYSA-L lead(2+);naphthalene-2-carboxylate Chemical compound [Pb+2].C1=CC=CC2=CC(C(=O)[O-])=CC=C21.C1=CC=CC2=CC(C(=O)[O-])=CC=C21 GIWKOZXJDKMGQC-UHFFFAOYSA-L 0.000 description 1
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- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
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- VGIVLIHKENZQHQ-UHFFFAOYSA-N n,n,n',n'-tetramethylmethanediamine Chemical compound CN(C)CN(C)C VGIVLIHKENZQHQ-UHFFFAOYSA-N 0.000 description 1
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- OMNKZBIFPJNNIO-UHFFFAOYSA-N n-(2-methyl-4-oxopentan-2-yl)prop-2-enamide Chemical compound CC(=O)CC(C)(C)NC(=O)C=C OMNKZBIFPJNNIO-UHFFFAOYSA-N 0.000 description 1
- QNILTEGFHQSKFF-UHFFFAOYSA-N n-propan-2-ylprop-2-enamide Chemical compound CC(C)NC(=O)C=C QNILTEGFHQSKFF-UHFFFAOYSA-N 0.000 description 1
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- HMZGPNHSPWNGEP-UHFFFAOYSA-N octadecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C(C)=C HMZGPNHSPWNGEP-UHFFFAOYSA-N 0.000 description 1
- KZCOBXFFBQJQHH-UHFFFAOYSA-N octane-1-thiol Chemical compound CCCCCCCCS KZCOBXFFBQJQHH-UHFFFAOYSA-N 0.000 description 1
- 150000003961 organosilicon compounds Chemical class 0.000 description 1
- RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 description 1
- HVAMZGADVCBITI-UHFFFAOYSA-M pent-4-enoate Chemical compound [O-]C(=O)CCC=C HVAMZGADVCBITI-UHFFFAOYSA-M 0.000 description 1
- ICMWSAALRSINTC-UHFFFAOYSA-N penta-1,4-dien-3-ol Chemical compound C=CC(O)C=C ICMWSAALRSINTC-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- 150000003254 radicals Chemical class 0.000 description 1
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- 238000010992 reflux Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 238000007790 scraping Methods 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 229940047670 sodium acrylate Drugs 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 229950011008 tetrachloroethylene Drugs 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- GQIUQDDJKHLHTB-UHFFFAOYSA-N trichloro(ethenyl)silane Chemical compound Cl[Si](Cl)(Cl)C=C GQIUQDDJKHLHTB-UHFFFAOYSA-N 0.000 description 1
- FUSUHKVFWTUUBE-UHFFFAOYSA-N vinyl methyl ketone Natural products CC(=O)C=C FUSUHKVFWTUUBE-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
- C04B41/45—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements
- C04B41/46—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements with organic materials
- C04B41/48—Macromolecular compounds
- C04B41/4838—Halogenated polymers
- C04B41/4842—Fluorine-containing polymers
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/62—Polymers of compounds having carbon-to-carbon double bonds
- C08G18/6275—Polymers of halogen containing compounds having carbon-to-carbon double bonds; halogenated polymers of compounds having carbon-to-carbon double bonds
- C08G18/6279—Polymers of halogen containing compounds having carbon-to-carbon double bonds; halogenated polymers of compounds having carbon-to-carbon double bonds containing fluorine atoms
-
- 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
- C09K3/00—Materials not provided for elsewhere
- C09K3/18—Materials not provided for elsewhere for application to surfaces to minimize adherence of ice, mist or water thereto; Thawing or antifreeze materials for application to surfaces
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Ceramic Engineering (AREA)
- Materials Engineering (AREA)
- Medicinal Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Structural Engineering (AREA)
- Polymers & Plastics (AREA)
- Combustion & Propulsion (AREA)
- Paints Or Removers (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Polyurethanes Or Polyureas (AREA)
- Materials Applied To Surfaces To Minimize Adherence Of Mist Or Water (AREA)
- Silicon Polymers (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR8301346A FR2540131B1 (fr) | 1983-01-28 | 1983-01-28 | Compositions et procede pour le traitement oleophobe et hydrophobe des materiaux de construction |
Publications (1)
Publication Number | Publication Date |
---|---|
CH660749A5 true CH660749A5 (fr) | 1987-06-15 |
Family
ID=9285394
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH365/84A CH660749A5 (fr) | 1983-01-28 | 1984-01-26 | Compositions et procede pour le traitement oleophobe et hydrophobe des materiaux de construction. |
Country Status (14)
Country | Link |
---|---|
US (1) | US4478975A (forum.php) |
JP (1) | JPS59145274A (forum.php) |
BE (1) | BE898777A (forum.php) |
CA (1) | CA1225188A (forum.php) |
CH (1) | CH660749A5 (forum.php) |
DE (1) | DE3402935A1 (forum.php) |
DK (1) | DK164286C (forum.php) |
ES (1) | ES529228A0 (forum.php) |
FR (1) | FR2540131B1 (forum.php) |
GB (2) | GB2135317B (forum.php) |
GR (1) | GR81751B (forum.php) |
IT (1) | IT1179578B (forum.php) |
NL (1) | NL190752C (forum.php) |
SE (2) | SE461333B (forum.php) |
Families Citing this family (29)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3428023A1 (de) * | 1984-07-30 | 1986-02-06 | Werner & Mertz Gmbh | Impraegnierspray fuer leder und textilien sowie dessen verwendung |
JPH0768509B2 (ja) * | 1985-05-20 | 1995-07-26 | 日本メクトロン株式会社 | 防汚性撥水撥油剤 |
CA1336994C (en) * | 1986-07-09 | 1995-09-12 | Haruhiko Sawada | Coating composition |
EP0283892B1 (en) * | 1987-03-20 | 1993-06-09 | Asahi Glass Company Ltd. | Fluorine containing polyurethanes and polyisocyanate compound composition for its preparation |
JP3000580B2 (ja) * | 1988-12-23 | 2000-01-17 | 大日本インキ化学工業株式会社 | 硬化性樹脂組成物 |
WO1992016103A1 (en) * | 1991-03-15 | 1992-10-01 | Redline Products, Inc. | Protective compositions |
US6113925A (en) * | 1993-12-15 | 2000-09-05 | L'oreal | Method of forming a film using a composition containing a fluoroalkyl copolymer |
FR2713649B1 (fr) * | 1993-12-15 | 1996-08-02 | Oreal | Composition filmogène contenant un copolymère d'alkyle perfluoré, utilisable comme vernis à ongles. |
US5629372A (en) * | 1994-11-22 | 1997-05-13 | E. I. Du Pont De Nemours And Company | Acrylic fluorocarbon polymer containing coating |
FR2727417B1 (fr) | 1994-11-29 | 1997-01-03 | Atochem Elf Sa | Copolymeres fluores cationiques pour le traitement oleophobe et hydrophobe des materiaux de construction |
IT1273609B (it) * | 1995-04-28 | 1997-07-08 | Ausimont Spa | Procedimento per la protezione delle superfici lapidee o di rivestimento |
US5597874A (en) * | 1995-10-16 | 1997-01-28 | E. I. Du Pont De Nemours And Company | Coating compositions of an acrylic fluorocarbon polymer and a fluorinated polyisocyanate |
TW377370B (en) * | 1996-04-12 | 1999-12-21 | Du Pont | Waterborne fluoropolymer solutions for treating hard surfaces |
US5670573A (en) * | 1996-08-07 | 1997-09-23 | E. I. Du Pont De Nemours And Company | Coatings containing fluorinated esters |
US7268179B2 (en) * | 1997-02-03 | 2007-09-11 | Cytonix Corporation | Hydrophobic coating compositions, articles coated with said compositions, and processes for manufacturing same |
FR2762509B1 (fr) | 1997-04-28 | 2003-03-07 | Oreal | Composition cosmetique ou dermatologique comprenant un polymere filmogene, procede de maquillage et de traitement non therapeutique |
US6120892A (en) * | 1997-11-20 | 2000-09-19 | E. I. Du Pont De Nemours And Company | Waterborne fluoropolymer solutions for treating hard surfaces |
DE19806482A1 (de) * | 1998-02-17 | 1999-08-19 | Sueddeutsche Kalkstickstoff | Wasserlösliche oder wasserquellbare sulfogruppenhaltige Copolymere, Verfahren zu deren Herstellung und ihre Verwendung |
US6326447B1 (en) | 1998-06-19 | 2001-12-04 | E. I. Du Pont De Nemours And Company | Polymeric compositions for soil release on fabrics |
US6271289B1 (en) | 1999-11-16 | 2001-08-07 | E. I. Du Pont De Nemours And Company | Stain resistant compositions |
US6451717B1 (en) | 1999-12-14 | 2002-09-17 | E. I. Du Pont De Nemours And Company | Highly durable oil/water repellents for textiles |
WO2005074594A2 (en) | 2004-01-30 | 2005-08-18 | Great Lakes Chemical Corporation | Production processes and systems, compositions, surfactants, monomer units, metal complexes, phosphate esters, glycols, aqueous film forming foams, and foam stabilizers |
DE602004032231D1 (de) * | 2004-09-02 | 2011-05-26 | 3M Innovative Properties Co | Verfahren zur Behandlung von porösem Stein, bei dem eine fluorchemische Zusammensetzung verwendet wird |
DE102006011153A1 (de) * | 2006-03-10 | 2007-09-13 | Construction Research & Technology Gmbh | Fluormodifiziertes Zusatzmittel für zementäre Produkte, Verfahren zu seiner Herstellung und dessen Verwendung |
US20080308968A1 (en) * | 2007-06-13 | 2008-12-18 | Immordino Jr Salvatore C | Method of making a low-dust building panel |
US8318656B2 (en) | 2007-07-03 | 2012-11-27 | E. I. Du Pont De Nemours And Company | Production processes and systems, compositions, surfactants, monomer units, metal complexes, phosphate esters, glycols, aqueous film forming foams, and foam stabilizers |
WO2010072724A2 (en) | 2008-12-23 | 2010-07-01 | Basf Se | Process and aqueous formulation for the impregnation of non-living-materials imparting a protective activity against pests |
US8975348B2 (en) * | 2010-02-12 | 2015-03-10 | E I Du Pont De Nemours And Company | Non-aqueous composition comprising partially fluorinated methacrylic polymers |
FR3046463A1 (fr) * | 2015-12-30 | 2017-07-07 | Dominique Lestelle | Dispositif de mesure resistive de l'humidite d'un materiau mineral poreux, et application au monitoring hydrique des plantes |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1095900A (en) * | 1964-03-30 | 1967-12-20 | Daikin Ind Ltd | Fluorocarbon esters and polymers thereof |
CH1121365D (forum.php) * | 1964-08-14 | |||
GB1123829A (en) * | 1964-12-01 | 1968-08-14 | Minnesota Mining & Mfg | Fluorine containing copolymers |
US3356628A (en) * | 1964-12-01 | 1967-12-05 | Minnesota Mining & Mfg | Copolymers of perfluoro acrylates and hydroxy alkyl acrylates |
GB1188815A (en) * | 1966-04-15 | 1970-04-22 | Daikin Ind Ltd | Fluorocarbon Esters and Polymers thereof |
FR2034142B1 (forum.php) * | 1969-02-11 | 1975-07-04 | Ugine Kuhlmann | |
DE2526287C2 (de) * | 1975-06-12 | 1982-09-30 | Wacker-Chemie GmbH, 8000 München | Verfahren zum Öl- und Wasserabweisendmachen von offene Porosität aufweisenden Oberflächen normalerweise fester anorganischer Stoffe |
DE2713857A1 (de) * | 1977-03-29 | 1978-10-12 | Sager & Woerner | Verfahren zum impraegnieren der oberflaeche von mineralischen geformten baustoffen und mittel zur durchfuehrung des verfahrens |
DE2737406A1 (de) * | 1977-08-19 | 1979-02-22 | Bayer Ag | Strahlenhaertbare bindemittel |
FR2483447A1 (fr) * | 1980-06-03 | 1981-12-04 | Ugine Kuhlmann | Composition et procede pour la protection des materiaux contre les souillures |
JPS5834866A (ja) * | 1981-08-27 | 1983-03-01 | Dainippon Ink & Chem Inc | ウレタン塗料用組成物 |
-
1983
- 1983-01-28 FR FR8301346A patent/FR2540131B1/fr not_active Expired
-
1984
- 1984-01-19 US US06/572,026 patent/US4478975A/en not_active Expired - Lifetime
- 1984-01-26 CH CH365/84A patent/CH660749A5/fr not_active IP Right Cessation
- 1984-01-26 SE SE8400391A patent/SE461333B/sv not_active IP Right Cessation
- 1984-01-26 SE SE8400391D patent/SE8400391L/xx not_active Application Discontinuation
- 1984-01-27 ES ES529228A patent/ES529228A0/es active Granted
- 1984-01-27 IT IT67090/84A patent/IT1179578B/it active
- 1984-01-27 GR GR73639A patent/GR81751B/el unknown
- 1984-01-27 BE BE0/212293A patent/BE898777A/fr not_active IP Right Cessation
- 1984-01-27 NL NL8400255A patent/NL190752C/xx not_active IP Right Cessation
- 1984-01-27 GB GB08402243A patent/GB2135317B/en not_active Expired
- 1984-01-27 GB GB848402242A patent/GB8402242D0/en active Pending
- 1984-01-27 DK DK038584A patent/DK164286C/da active
- 1984-01-27 JP JP59013206A patent/JPS59145274A/ja active Pending
- 1984-01-27 CA CA000446190A patent/CA1225188A/fr not_active Expired
- 1984-01-28 DE DE19843402935 patent/DE3402935A1/de active Granted
Also Published As
Publication number | Publication date |
---|---|
BE898777A (fr) | 1984-07-27 |
GB2135317B (en) | 1986-07-09 |
GB8402242D0 (en) | 1984-02-29 |
SE8400391D0 (sv) | 1984-01-26 |
ES8500309A1 (es) | 1984-10-01 |
DE3402935A1 (de) | 1984-08-23 |
FR2540131B1 (fr) | 1986-04-04 |
NL190752B (nl) | 1994-03-01 |
DK164286C (da) | 1992-11-16 |
GB2135317A (en) | 1984-08-30 |
GR81751B (forum.php) | 1984-12-12 |
FR2540131A1 (fr) | 1984-08-03 |
SE461333B (sv) | 1990-02-05 |
NL8400255A (nl) | 1984-08-16 |
IT1179578B (it) | 1987-09-16 |
DE3402935C2 (forum.php) | 1988-12-01 |
NL190752C (nl) | 1994-08-01 |
ES529228A0 (es) | 1984-10-01 |
SE8400391L (sv) | 1984-07-29 |
CA1225188A (fr) | 1987-08-04 |
IT8467090A0 (it) | 1984-01-27 |
JPS59145274A (ja) | 1984-08-20 |
US4478975A (en) | 1984-10-23 |
DK38584D0 (da) | 1984-01-27 |
DK38584A (da) | 1984-08-30 |
DK164286B (da) | 1992-06-01 |
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