GB1132821A

GB1132821A – Anaerobic curing compositions
– Google Patents

GB1132821A – Anaerobic curing compositions
– Google Patents
Anaerobic curing compositions

Info

Publication number
GB1132821A

GB1132821A
GB242/66A
GB24266A
GB1132821A
GB 1132821 A
GB1132821 A
GB 1132821A
GB 242/66 A
GB242/66 A
GB 242/66A
GB 24266 A
GB24266 A
GB 24266A
GB 1132821 A
GB1132821 A
GB 1132821A
Authority
GB
United Kingdom
Prior art keywords
radical
radicals
ureide
ester
acrylate
Prior art date
1965-01-27
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
GB242/66A
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.)

Henkel Loctite Corp

Original Assignee
Henkel Loctite 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.)
1965-01-27
Filing date
1966-01-04
Publication date
1968-11-06

1966-01-04
Application filed by Henkel Loctite Corp
filed
Critical
Henkel Loctite Corp

1968-11-06
Publication of GB1132821A
publication
Critical
patent/GB1132821A/en

Status
Expired
legal-status
Critical
Current

Links

Espacenet

Global Dossier

Discuss

Classifications

C—CHEMISTRY; METALLURGY

C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR

C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES

C09J175/00—Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers

C09J175/04—Polyurethanes

C09J175/14—Polyurethanes having carbon-to-carbon unsaturated bonds

C09J175/16—Polyurethanes having carbon-to-carbon unsaturated bonds having terminal carbon-to-carbon unsaturated bonds

C—CHEMISTRY; METALLURGY

C07—ORGANIC CHEMISTRY

C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS

C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups

C07C275/28—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton

C07C275/40—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton being further substituted by nitrogen atoms not being part of nitro or nitroso groups

C—CHEMISTRY; METALLURGY

C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON

C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS

C08F20/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof

C08F20/02—Monocarboxylic acids having less than ten carbon atoms, Derivatives thereof

C08F20/10—Esters

C08F20/34—Esters containing nitrogen, e.g. N,N-dimethylaminoethyl (meth)acrylate

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

C08G18/67—Unsaturated compounds having active hydrogen

C08G18/671—Unsaturated compounds having only one group containing active hydrogen

C08G18/672—Esters of acrylic or alkyl acrylic acid having only one group containing active hydrogen

C—CHEMISTRY; METALLURGY

C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR

C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES

C09J4/00—Adhesives based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; adhesives, based on monomers of macromolecular compounds of groups C09J183/00 – C09J183/16

Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS

Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC

Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS

Y10S525/00—Synthetic resins or natural rubbers — part of the class 520 series

Y10S525/92—Polyurethane having terminal ethylenic unsaturation

Abstract

1,132,821. Acrylate ester derivatives. LOCTITE CORP. 4 Jan., 1966 [27 Jan., 1965], No. 242/66. Heading C2C. [Also in Division C3] Polyacrylate ester monomers (stated to be new monomers) having terminal acrylate radicals and at least two non-terminal divalent urethane or ureide radicals, the number of terminal ester radicals not exceeding the number of urethane or ureide radicals, are prepared by reacting an organic polyisocyanate with a mono-acrylate ester having a group reactive with isocyanates (e.g. a hydroxy or amino group). (The term » acrylate » is used to include α- methyl, α-ethyl and α-haloacrylates in addition to the unsubstituted acrylates; and by » ureide radical » is meant the group -NH-CO-NH- or an N-substituted derivative thereof.) The polyisocyanate may be an aliphatic, cycloaliphatic or aromatic compound. Preferred polyacrylate products correspond to the formula or where X is-O-or and R is H or C 1 -C 7 alkyl; R1 is H, Cl, methyl or ethyl; R11 is a C 1 -C 8 alkylene radical or a phenylene or naphthylene radical; R111 is an alkylene, alkenylene, cycloalkylene, arylene, aralkylene or alkarylene radical of 2-20 carbon atoms; n is an integer greater than 1 (preferably 2-6); and B is an alkylene, alkenylene, cycloalkylene, arylene, aralkylene, alkarylene or polyvalent heterocyclic radical which may be substituted or unsubstituted or two such radicals linked by a ureide radical. In Example II a polyacrylate ester is obtained by the following reaction scheme:

GB242/66A
1965-01-27
1966-01-04
Anaerobic curing compositions

Expired

GB1132821A
(en)

Applications Claiming Priority (1)

Application Number
Priority Date
Filing Date
Title

US42854765A

1965-01-27
1965-01-27

Publications (1)

Publication Number
Publication Date

GB1132821A
true

GB1132821A
(en)

1968-11-06

Family
ID=23699348
Family Applications (1)

Application Number
Title
Priority Date
Filing Date

GB242/66A
Expired

GB1132821A
(en)

1965-01-27
1966-01-04
Anaerobic curing compositions

Country Status (5)

Country
Link

US
(1)

US3425988A
(en)

CH
(1)

CH494812A
(en)

DE
(1)

DE1745063C3
(en)

GB
(1)

GB1132821A
(en)

SE
(1)

SE351858B
(en)

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Publication date
Assignee
Title

FR2173130A1
(en)

*

1972-02-21
1973-10-05
I Khim
Oligourethane acrylate prepn – from polyol chloroformates with polyamines and telogens, and use in cross-linked polymer prodn

US4042413A
(en)

1972-02-28
1977-08-16
Imperial Chemical Industries Limited
Dispersing agents

US4070334A
(en)

1974-12-11
1978-01-24
Ciba-Geigy Corporation
Method of bonding

US4157266A
(en)

1972-02-28
1979-06-05
Imperial Chemical Industries Limited
Dispersion of pigment or dyestuff in organic liquid

US4348503A
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1980-06-04
1982-09-07
Bachmann Andrew G
Adhesive composition

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1967-02-10
1970-03-10
Textron Inc
Coating compositions containing polyol crosslinking agent and urethane prepolymers endblocked with ethylenic groups

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1970-05-06
1975-04-15
Ppg Industries Inc
Safety glass prepared by curing a b-stage polyurethane sheet

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1972-04-21
1975-03-25
Lord Corp
Adhesive bonding of polyvinyl chloride and other synthetic resin substrates

IE38322B1
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1972-05-29
1978-02-15
Loctite Ltd
Improvements in or relating to peroxide-initiated optical adhesives

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1972-08-18
1978-02-28
Ceskoslovenska Akademie Ved
Polyacrylates containing primary amino groups

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(en)

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1972-10-25
1976-06-08
Lord Corporation
Method for improving adhesion between adhesives and polyester or other thermoplastic substrates

IE37703B1
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1972-11-16
1977-09-28
Loctite Ltd
Protective adhesive-carrying tape

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1972-11-16
1977-09-28
Loctite Ltd
Dental filling composition and process for use thereof

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1974-02-19
1976-12-07
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1974-02-20
1976-05-25
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Acrylate adhesive composition

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1974-10-07
1976-11-23
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1975-03-12
1980-12-09
Louis J. Baccei
Curable poly(alkylene)ether polyol-based resins having improved properties

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1975-03-12
1979-10-30
Louis J. Baccei
Curable acrylate compositions having improved thermal properties

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1975-05-23
1981-09-01
Loctite Corporation
Accelerator for curable compositions

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1975-05-23
1982-03-23
Loctite Corporation
Accelerator for curable compositions

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1975-10-08
1982-01-05
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1978-01-03
1979-01-09
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1978-04-19
1979-10-26
Nitto Electric Ind Co Ltd
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1978-09-20
1985-11-15
Deltaglass Sa

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1979-08-07
1981-02-26
Bayer Ag

DENTAL MEASURES

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1981-03-03
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1980-06-04
1984-01-31
Bachmann Andrew G
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1980-06-04
1984-02-21
American Chemical & Engineering Co.
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(en)

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1980-07-23
1985-03-28
Blendax Werke Schneider Co
Adducts from diisocyanates and methacryloylalkylethers, -alcoxybenzenes resp. -alcoxycycloalcanes and their use

US4320221A
(en)

*

1980-12-12
1982-03-16
The Dow Chemical Company
Addition polymerizable isocyanate-polyol anaerobic adhesives

AU555141B2
(en)

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1980-12-12
1986-09-11
Dow Chemical Company, The
Addition polymerizable isocyanate-polyahl anaerobic adhesives

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1980-12-12
1983-02-22
The Dow Chemical Company
Addition polymerizable isocyanate-polyamine anaerobic adhesives

EP0151990B1
(en)

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1981-04-28
1990-02-07
Imperial Chemical Industries Plc
Copolymerisation of unsaturated urethane monomers

US4380613A
(en)

*

1981-07-02
1983-04-19
Loctite Corporation
Gasketing and sealing composition

US4500629A
(en)

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1982-04-08
1985-02-19
Ciba-Geigy Corporation
Method of forming images from liquid masses

IE54465B1
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1982-05-26
1989-10-25
Loctite Ltd
Two-part self-indicating adhesive composition

US4420306A
(en)

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1982-06-24
1983-12-13
Blendax-Werke R. Schneider Gmbh & Co.
Tetraacrylic and tetramethacrylic esters and dental materials containing same

US4451627A
(en)

*

1982-09-07
1984-05-29
The Dow Chemical Company
Addition polymerizable urethane-based anaerobic adhesives made from tin (II) organoesters

DE3316851A1
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1983-05-07
1984-11-08
Bayer Ag, 5090 Leverkusen

POLYMERIZABLE DENTAL MEASURES AND DENTAL MOLDED BODIES MADE THEREOF

US5073476A
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1983-05-18
1991-12-17
Ciba-Geigy Corporation
Curable composition and the use thereof

JPS61179216A
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1985-02-04
1986-08-11
Sanyo Kokusaku Pulp Co Ltd
Photocurable resin composition

DE3536246A1
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1985-10-10
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Acrylic and methacrylic acid derivatives, process for their preparation, and their use as flexibilisers for epoxy resin systems

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1986-05-13
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CURABLE TRANSVERSIBLE COMPOSITION FOR USE AS PLASTIC-STACKING MATERIAL

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1966-11-08
Dow Chemical Co
Polyurethane from ethylene-hydroxyalkyl acrylate copolymers

1965

1965-01-27
US
US428547A
patent/US3425988A/en
not_active
Expired – Lifetime

1966

1966-01-04
GB
GB242/66A
patent/GB1132821A/en
not_active
Expired

1966-01-25
CH
CH95066A
patent/CH494812A/en
not_active
IP Right Cessation

1966-01-25
SE
SE00940/66A
patent/SE351858B/xx
unknown

1966-01-26
DE
DE1745063A
patent/DE1745063C3/en
not_active
Expired

Cited By (5)

* Cited by examiner, † Cited by third party

Publication number
Priority date
Publication date
Assignee
Title

FR2173130A1
(en)

*

1972-02-21
1973-10-05
I Khim
Oligourethane acrylate prepn – from polyol chloroformates with polyamines and telogens, and use in cross-linked polymer prodn

US4042413A
(en)

1972-02-28
1977-08-16
Imperial Chemical Industries Limited
Dispersing agents

US4157266A
(en)

1972-02-28
1979-06-05
Imperial Chemical Industries Limited
Dispersion of pigment or dyestuff in organic liquid

US4070334A
(en)

1974-12-11
1978-01-24
Ciba-Geigy Corporation
Method of bonding

US4348503A
(en)

1980-06-04
1982-09-07
Bachmann Andrew G
Adhesive composition

Also Published As

Publication number
Publication date

US3425988A
(en)

1969-02-04

DE1745063C3
(en)

1979-06-28

CH494812A
(en)

1970-08-15

SE351858B
(en)

1972-12-11

DE1745063A1
(en)

1970-12-23

DE1745063B2
(en)

1978-11-02

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