GB1528204A – Crosslinker platinum catalyst inhibitor and method of preparation thereof
– Google Patents
GB1528204A – Crosslinker platinum catalyst inhibitor and method of preparation thereof
– Google Patents
Crosslinker platinum catalyst inhibitor and method of preparation thereof
Info
Publication number
GB1528204A
GB1528204A
GB42203/75A
GB4220375A
GB1528204A
GB 1528204 A
GB1528204 A
GB 1528204A
GB 42203/75 A
GB42203/75 A
GB 42203/75A
GB 4220375 A
GB4220375 A
GB 4220375A
GB 1528204 A
GB1528204 A
GB 1528204A
Authority
GB
United Kingdom
Prior art keywords
radicals
hydrocarbon
atoms
crosslinker
average
Prior art date
1974-12-02
Legal status (The legal status 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 status listed.)
Expired
Application number
GB42203/75A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Dow Silicones Corp
Original Assignee
Dow Corning Corp
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.)
1974-12-02
Filing date
1975-10-15
Publication date
1978-10-11
1975-10-15
Application filed by Dow Corning Corp
filed
Critical
Dow Corning Corp
1978-10-11
Publication of GB1528204A
publication
Critical
patent/GB1528204A/en
Status
Expired
legal-status
Critical
Current
Links
Espacenet
Global Dossier
Discuss
BASFCYQUMIYNBI-UHFFFAOYSA-N
platinum
Chemical compound
[Pt]
BASFCYQUMIYNBI-UHFFFAOYSA-N
0.000
title
abstract
10
239000003060
catalysis inhibitor
Substances
0.000
title
abstract
5
229910052697
platinum
Inorganic materials
0.000
title
abstract
3
238000000034
method
Methods
0.000
title
abstract
2
239000004971
Cross linker
Substances
0.000
title
1
239000000203
mixture
Substances
0.000
abstract
11
239000004215
Carbon black (E152)
Substances
0.000
abstract
8
229930195733
hydrocarbon
Natural products
0.000
abstract
8
125000004429
atom
Chemical group
0.000
abstract
6
VYPSYNLAJGMNEJ-UHFFFAOYSA-N
Silicium dioxide
Chemical compound
O=[Si]=O
VYPSYNLAJGMNEJ-UHFFFAOYSA-N
0.000
abstract
5
150000002430
hydrocarbons
Chemical class
0.000
abstract
4
LFQSCWFLJHTTHZ-UHFFFAOYSA-N
Ethanol
Chemical compound
CCO
LFQSCWFLJHTTHZ-UHFFFAOYSA-N
0.000
abstract
3
125000001931
aliphatic group
Chemical group
0.000
abstract
3
239000003054
catalyst
Substances
0.000
abstract
3
KPUWHANPEXNPJT-UHFFFAOYSA-N
disiloxane
Chemical class
[SiH3]O[SiH3]
KPUWHANPEXNPJT-UHFFFAOYSA-N
0.000
abstract
3
RTZKZFJDLAIYFH-UHFFFAOYSA-N
ether
Substances
CCOCC
RTZKZFJDLAIYFH-UHFFFAOYSA-N
0.000
abstract
3
238000010438
heat treatment
Methods
0.000
abstract
3
-1
methylphenylvinylsiloxy
Chemical group
0.000
abstract
3
CEBKHWWANWSNTI-UHFFFAOYSA-N
2-methylbut-3-yn-2-ol
Chemical compound
CC(C)(O)C#C
CEBKHWWANWSNTI-UHFFFAOYSA-N
0.000
abstract
2
239000002253
acid
Substances
0.000
abstract
2
PNEYBMLMFCGWSK-UHFFFAOYSA-N
aluminium oxide
Inorganic materials
[O-2].[O-2].[O-2].[Al+3].[Al+3]
PNEYBMLMFCGWSK-UHFFFAOYSA-N
0.000
abstract
2
239000006229
carbon black
Substances
0.000
abstract
2
150000004820
halides
Chemical class
0.000
abstract
2
125000004430
oxygen atom
Chemical group
O*
0.000
abstract
2
239000000377
silicon dioxide
Substances
0.000
abstract
2
QYLFHLNFIHBCPR-UHFFFAOYSA-N
1-ethynylcyclohexan-1-ol
Chemical compound
C#CC1(O)CCCCC1
QYLFHLNFIHBCPR-UHFFFAOYSA-N
0.000
abstract
1
KSLSOBUAIFEGLT-UHFFFAOYSA-N
2-phenylbut-3-yn-2-ol
Chemical compound
C#CC(O)(C)C1=CC=CC=C1
KSLSOBUAIFEGLT-UHFFFAOYSA-N
0.000
abstract
1
NECRQCBKTGZNMH-UHFFFAOYSA-N
3,5-dimethylhex-1-yn-3-ol
Chemical compound
CC(C)CC(C)(O)C#C
NECRQCBKTGZNMH-UHFFFAOYSA-N
0.000
abstract
1
229910004298
SiO 2
Inorganic materials
0.000
abstract
1
239000004965
Silica aerogel
Substances
0.000
abstract
1
150000001298
alcohols
Chemical class
0.000
abstract
1
FSIJKGMIQTVTNP-UHFFFAOYSA-N
bis(ethenyl)-methyl-trimethylsilyloxysilane
Chemical compound
C[Si](C)(C)O[Si](C)(C=C)C=C
FSIJKGMIQTVTNP-UHFFFAOYSA-N
0.000
abstract
1
150000004649
carbonic acid derivatives
Chemical class
0.000
abstract
1
239000003610
charcoal
Substances
0.000
abstract
1
150000001875
compounds
Chemical class
0.000
abstract
1
229920001577
copolymer
Polymers
0.000
abstract
1
239000004205
dimethyl polysiloxane
Substances
0.000
abstract
1
239000000945
filler
Substances
0.000
abstract
1
239000012530
fluid
Substances
0.000
abstract
1
238000009472
formulation
Methods
0.000
abstract
1
239000003517
fume
Substances
0.000
abstract
1
125000004435
hydrogen atom
Chemical group
[H]*
0.000
abstract
1
239000007788
liquid
Substances
0.000
abstract
1
239000002184
metal
Substances
0.000
abstract
1
229910052751
metal
Inorganic materials
0.000
abstract
1
229910044991
metal oxide
Inorganic materials
0.000
abstract
1
150000004706
metal oxides
Chemical class
0.000
abstract
1
229910052914
metal silicate
Inorganic materials
0.000
abstract
1
QXLPXWSKPNOQLE-UHFFFAOYSA-N
methylpentynol
Chemical compound
CCC(C)(O)C#C
QXLPXWSKPNOQLE-UHFFFAOYSA-N
0.000
abstract
1
229920001558
organosilicon polymer
Polymers
0.000
abstract
1
229920000435
poly(dimethylsiloxane)
Polymers
0.000
abstract
1
229920000642
polymer
Polymers
0.000
abstract
1
239000010453
quartz
Substances
0.000
abstract
1
239000011369
resultant mixture
Substances
0.000
abstract
1
UHUUYVZLXJHWDV-UHFFFAOYSA-N
trimethyl(methylsilyloxy)silane
Chemical compound
C[SiH2]O[Si](C)(C)C
UHUUYVZLXJHWDV-UHFFFAOYSA-N
0.000
abstract
1
Classifications
C—CHEMISTRY; METALLURGY
C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
C08L83/04—Polysiloxanes
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
C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
C08G77/04—Polysiloxanes
C08G77/38—Polysiloxanes modified by chemical after-treatment
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
C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
C08G77/04—Polysiloxanes
C08G77/38—Polysiloxanes modified by chemical after-treatment
C08G77/382—Polysiloxanes modified by chemical after-treatment containing atoms other than carbon, hydrogen, oxygen or silicon
C08G77/398—Polysiloxanes modified by chemical after-treatment containing atoms other than carbon, hydrogen, oxygen or silicon containing boron or metal atoms
C—CHEMISTRY; METALLURGY
C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
C08K5/00—Use of organic ingredients
C08K5/0008—Organic ingredients according to more than one of the “one dot” groups of C08K5/01 – C08K5/59
C08K5/0025—Crosslinking or vulcanising agents; including accelerators
C—CHEMISTRY; METALLURGY
C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
C08K5/00—Use of organic ingredients
C08K5/04—Oxygen-containing compounds
C08K5/05—Alcohols; Metal alcoholates
C—CHEMISTRY; METALLURGY
C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
C08L83/04—Polysiloxanes
C08L83/06—Polysiloxanes containing silicon bound to oxygen-containing groups
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
C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
C08G77/04—Polysiloxanes
C08G77/12—Polysiloxanes containing silicon bound to hydrogen
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
C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
C08G77/04—Polysiloxanes
C08G77/20—Polysiloxanes containing silicon bound to unsaturated aliphatic groups
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
C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
C08G77/04—Polysiloxanes
C08G77/22—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen
C08G77/24—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen halogen-containing groups
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
C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
C08G77/04—Polysiloxanes
C08G77/22—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen
C08G77/26—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen nitrogen-containing groups
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
C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
C08G77/48—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule in which at least two but not all the silicon atoms are connected by linkages other than oxygen atoms
C08G77/50—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule in which at least two but not all the silicon atoms are connected by linkages other than oxygen atoms by carbon linkages
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
C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
C08G77/48—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule in which at least two but not all the silicon atoms are connected by linkages other than oxygen atoms
C08G77/50—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule in which at least two but not all the silicon atoms are connected by linkages other than oxygen atoms by carbon linkages
C08G77/52—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule in which at least two but not all the silicon atoms are connected by linkages other than oxygen atoms by carbon linkages containing aromatic rings
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
C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
C08G77/70—Siloxanes defined by use of the MDTQ nomenclature
Abstract
1528204 Crosslinker-platinum catalyst-inhibitor composition DOW CORNING CORP 15 Oct 1975 [2 Dec 1974] 42203/75 Headings C3T and C3S A crosslinker-platinum catalyst-inhibitor composition is prepared by a method comprising mixing a siloxane, an acetylenic alcohol and a Pt catalyst and heating the resultant mixture in a closed system for 10 to 30 hours at a temperature of from 50 C. to 90 C., said siloxane having an average of at least 3 Si-bonded hydrogen atoms per molecule, there being in addition an average of up to 2 monovalent organic radicals per Si atom selected from monovalent hydrocarbon and fluorinated hydrocarbon radicals free of aliphatic unsaturation,-the remaining valencies of the Si atoms being satisfied by divalent radicals selected from oxygen atoms, hydrocarbon and hydrocarbon ether radicals free of aliphatic unsaturation and fluorinated arylene radicals, wherein at least one divalent radical is -O-, the divalent radicals linking Si atoms, said siloxane being liquid at 50 to 90 C. in said mixture; the acetylenic alcohol preferably having a vapour pressure sufficient for the unreacted acetylenic alcohol to be removed from the mixture after the heating step by applyingareduced pressure of 700 to 750 mm.Hg.for at least 10 hours at a temperature of from 20 to 30C. Suitable acetylenic alcohols include 3- methyl-1-butyn-3-ol, 3-phenyl- 1 -butyn-3-ol, 1 – ethynylcyclohexan – 1 – ol, 3,5 – dimethyl – 1- hexyn – 3 – ol and 3 – methyl – 1 – pentyn – 3 – ol. Suitable Pt catalysts are chloroplatinic acid, Pt deposited on silica, alumina or charcoal, platinous halides, and complexes of platinous halides with olefinic compounds. The crosslinker-Pt catalyst-inhibitor composition can be used in a curable composition comprising an organosilicon polymer having an average of from 1-3 groups per Si atom selected from monovalent hydrocarbon radicals, aliphatic-unsaturationfree monovalent halohydrocarbon radicals and cyanoalkyl radicals, there being an average per molecule of said polymer of at least 2 monovalent hydrocarbon radicals containing aliphatic unsaturation, the remaining valencies of the Si atoms being satisfied by divalent radicals selected from oxygen atoms, hydrocarbon, hydrocarbon ether and haloarylene radicals, the divalent radicals linking Si atoms. The curable compositions may additionally contain fillers such as carbon black, silica aerogels, silica soots, treated silicas, alumina, clays, metal oxides, metal carbonates and metal silicates. In Examples 1 and 2 crosslinker-Pt catalystinhibitor compositions prepared by heating a mixture of 3-methyl-1-butyn-3-ol, a siloxane copolymer of average formula and a Pt complex catalyst of chloroplatinic acid, tetramethyldisiloxane and divinyltetramethyldisiloxane at 70 C. for 16 hours in tightly capped bottles and stripping the resultant product at room temperature under reduced pressure, are added to a base formulation comprising 76% wt. of methylphenylvinylsiloxy endblocked polydimethylsiloxane (400 c.p.); 19À3% wt. of 5 micron quartz, 2À8% wt. fume SiO 2 1À1 wt.% of an OH-terminated polyphenylmethylsiloxane fluid and 0À8 wt.% of Carbon black to form compositions which are cured at temperatures ranging from 25 to 150 C.
GB42203/75A
1974-12-02
1975-10-15
Crosslinker platinum catalyst inhibitor and method of preparation thereof
Expired
GB1528204A
(en)
Applications Claiming Priority (1)
Application Number
Priority Date
Filing Date
Title
US05/528,962
US3989666A
(en)
1974-12-02
1974-12-02
Crosslinker-platinum catalyst-inhibitor and method of preparation thereof
Publications (1)
Publication Number
Publication Date
GB1528204A
true
GB1528204A
(en)
1978-10-11
Family
ID=24107945
Family Applications (1)
Application Number
Title
Priority Date
Filing Date
GB42203/75A
Expired
GB1528204A
(en)
1974-12-02
1975-10-15
Crosslinker platinum catalyst inhibitor and method of preparation thereof
Country Status (10)
Country
Link
US
(1)
US3989666A
(en)
JP
(2)
JPS5177699A
(en)
AT
(1)
AT353482B
(en)
BE
(1)
BE836158A
(en)
CA
(1)
CA1049484A
(en)
DE
(1)
DE2552721C2
(en)
FR
(1)
FR2293243A1
(en)
GB
(1)
GB1528204A
(en)
IT
(1)
IT1042898B
(en)
NL
(1)
NL159702B
(en)
Cited By (1)
* Cited by examiner, † Cited by third party
Publication number
Priority date
Publication date
Assignee
Title
GB2184727A
(en)
*
1985-12-19
1987-07-01
Gen Electric
Hydrosilylation catalyst, method for making and use
Families Citing this family (35)
* Cited by examiner, † Cited by third party
Publication number
Priority date
Publication date
Assignee
Title
JPS5265556A
(en)
*
1975-11-27
1977-05-31
Shin Etsu Chem Co Ltd
Curable organopolysiloxane compositions
DE3040758C2
(en)
*
1980-10-29
1986-10-16
Wacker-Chemie GmbH, 8000 München
Process for rendering fibers water repellent
US4347346A
(en)
*
1981-04-02
1982-08-31
General Electric Company
Silicone release coatings and inhibitors
US4337332A
(en)
*
1981-04-09
1982-06-29
Minnesota Mining And Manufacturing Company
Latently curable organosilicone compositions
US4336364A
(en)
*
1981-07-20
1982-06-22
Dow Corning Corporation
Method of producing organosilicon composition with in situ produced cure inhibitor
DE3131734A1
(en)
*
1981-08-11
1983-02-24
Bayer Ag, 5090 Leverkusen
HEAT-CURABLE ORGANOPOLYSILOXANE MIXTURES
JPS5859260A
(en)
*
1981-10-02
1983-04-08
Toray Silicone Co Ltd
Organopolysiloxane composition
JPS59204526A
(en)
*
1983-05-09
1984-11-19
Toray Silicone Co Ltd
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US4504645A
(en)
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1983-09-23
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(en)
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1985-08-06
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US4603215A
(en)
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1984-08-20
1986-07-29
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Platinum (O) alkyne complexes
CA1282532C
(en)
*
1986-08-22
1991-04-02
Myron Timothy Maxson
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(en)
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(en)
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(en)
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Family Cites Families (5)
* Cited by examiner, † Cited by third party
Publication number
Priority date
Publication date
Assignee
Title
DE1103333B
(en)
*
1957-06-14
1961-03-30
Dow Corning A G
Process for the production of organic silicon compounds
NL129346C
(en)
*
1966-06-23
GB1293331A
(en)
*
1969-01-13
1972-10-18
Union Carbide Corp
Addition process for producing siloxane alcohols
US3715334A
(en)
*
1970-11-27
1973-02-06
Gen Electric
Platinum-vinylsiloxanes
US3842112A
(en)
*
1972-12-29
1974-10-15
Union Carbide Corp
Hydroxyalkenylsiloxane rigid urethane foam stabilizers
1974
1974-12-02
US
US05/528,962
patent/US3989666A/en
not_active
Expired – Lifetime
1975
1975-09-12
CA
CA235,317A
patent/CA1049484A/en
not_active
Expired
1975-09-22
IT
IT27491/75A
patent/IT1042898B/en
active
1975-10-15
GB
GB42203/75A
patent/GB1528204A/en
not_active
Expired
1975-11-12
JP
JP50135261A
patent/JPS5177699A/en
active
Granted
1975-11-24
AT
AT890275A
patent/AT353482B/en
active
1975-11-25
DE
DE2552721A
patent/DE2552721C2/en
not_active
Expired
1975-12-01
NL
NL7513973.A
patent/NL159702B/en
not_active
IP Right Cessation
1975-12-01
FR
FR7536716A
patent/FR2293243A1/en
active
Granted
1975-12-01
BE
BE162345A
patent/BE836158A/en
not_active
IP Right Cessation
1977
1977-12-13
JP
JP14889677A
patent/JPS53102362A/en
active
Granted
Cited By (2)
* Cited by examiner, † Cited by third party
Publication number
Priority date
Publication date
Assignee
Title
GB2184727A
(en)
*
1985-12-19
1987-07-01
Gen Electric
Hydrosilylation catalyst, method for making and use
GB2184727B
(en)
*
1985-12-19
1990-05-02
Gen Electric
Hydrosilylation catalyst, method for making and use
Also Published As
Publication number
Publication date
DE2552721A1
(en)
1976-06-24
AU8491175A
(en)
1977-03-24
FR2293243A1
(en)
1976-07-02
JPS53102362A
(en)
1978-09-06
JPS5518459B2
(en)
1980-05-19
JPS5324480B2
(en)
1978-07-20
CA1049484A
(en)
1979-02-27
NL159702B
(en)
1979-03-15
AT353482B
(en)
1979-11-12
FR2293243B1
(en)
1978-05-12
IT1042898B
(en)
1980-01-30
NL7513973A
(en)
1976-06-04
DE2552721C2
(en)
1982-10-21
BE836158A
(en)
1976-06-01
US3989666A
(en)
1976-11-02
JPS5177699A
(en)
1976-07-06
USB528962I5
(en)
1976-02-24
ATA890275A
(en)
1979-04-15
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Legal Events
Date
Code
Title
Description
1979-01-31
PS
Patent sealed [section 19, patents act 1949]
1995-06-14
PCNP
Patent ceased through non-payment of renewal fee
Effective date:
19941015
