NO773532L - Polyesterharpiksprodukt. - Google Patents

Polyesterharpiksprodukt.

Info

Publication number: NO773532L
Authority: NO; Norway
Prior art keywords: stated; resin mixture; polyester resin; mixture; solution
Prior art date: 1976-10-16

Application number

NO773532A

Other languages

English (en)

Norwegian (no)

Inventor

Brian York Downing

George Dennis Hamer

Original Assignee

British Industrial Plastics

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.)

1976-10-16

Filing date

1977-10-14

Publication date

1978-04-18

1977-10-14 Application filed by British Industrial Plastics filed Critical British Industrial Plastics

1978-04-18 Publication of NO773532L publication Critical patent/NO773532L/no

Links

229920001225 polyester resin Polymers 0.000 title claims description 22
239000004645 polyester resin Substances 0.000 title claims description 22
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 51
-1 aralkyl ester Chemical class 0.000 claims description 35
229920000642 polymer Polymers 0.000 claims description 35
229920005989 resin Polymers 0.000 claims description 34
239000011347 resin Substances 0.000 claims description 34
239000000178 monomer Substances 0.000 claims description 20
239000000203 mixture Substances 0.000 claims description 17
230000009974 thixotropic effect Effects 0.000 claims description 12
150000002148 esters Chemical class 0.000 claims description 7
239000002253 acid Substances 0.000 claims description 5
229920006337 unsaturated polyester resin Polymers 0.000 claims description 5
JBSLOWBPDRZSMB-BQYQJAHWSA-N dibutyl (e)-but-2-enedioate Chemical compound CCCCOC(=O)\C=C\C(=O)OCCCC JBSLOWBPDRZSMB-BQYQJAHWSA-N 0.000 claims description 4
125000000217 alkyl group Chemical group 0.000 claims description 3
GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 claims description 2
125000003118 aryl group Chemical group 0.000 claims description 2
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 claims description 2
150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 2
LNCPIMCVTKXXOY-UHFFFAOYSA-N hexyl 2-methylprop-2-enoate Chemical compound CCCCCCOC(=O)C(C)=C LNCPIMCVTKXXOY-UHFFFAOYSA-N 0.000 claims description 2
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims 1
JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 claims 1
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims 1
QISOBCMNUJQOJU-UHFFFAOYSA-N 4-bromo-1h-pyrazole-5-carboxylic acid Chemical compound OC(=O)C=1NN=CC=1Br QISOBCMNUJQOJU-UHFFFAOYSA-N 0.000 claims 1
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims 1
125000005907 alkyl ester group Chemical group 0.000 claims 1
125000004432 carbon atom Chemical group C* 0.000 claims 1
MULPEVDGMQIZMY-UHFFFAOYSA-N didecyl 2-methylidenebutanedioate Chemical compound CCCCCCCCCCOC(=O)CC(=C)C(=O)OCCCCCCCCCC MULPEVDGMQIZMY-UHFFFAOYSA-N 0.000 claims 1
125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 1
238000012360 testing method Methods 0.000 description 19
239000000654 additive Substances 0.000 description 8
239000013068 control sample Substances 0.000 description 7
229920000728 polyester Polymers 0.000 description 7
239000000523 sample Substances 0.000 description 7
238000000034 method Methods 0.000 description 6
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 5
230000000996 additive effect Effects 0.000 description 5
229910017052 cobalt Inorganic materials 0.000 description 5
239000010941 cobalt Substances 0.000 description 5
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 5
230000000694 effects Effects 0.000 description 5
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 4
238000002474 experimental method Methods 0.000 description 4
238000004519 manufacturing process Methods 0.000 description 4
239000002184 metal Substances 0.000 description 4
229910052751 metal Inorganic materials 0.000 description 4
230000001629 suppression Effects 0.000 description 4
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
239000004359 castor oil Substances 0.000 description 3
235000019438 castor oil Nutrition 0.000 description 3
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 3
238000010438 heat treatment Methods 0.000 description 3
239000007788 liquid Substances 0.000 description 3
239000000463 material Substances 0.000 description 3
230000003287 optical effect Effects 0.000 description 3
229920001610 polycaprolactone Polymers 0.000 description 3
229910002012 Aerosil® Inorganic materials 0.000 description 2
241001550224 Apha Species 0.000 description 2
239000004342 Benzoyl peroxide Substances 0.000 description 2
OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
235000019400 benzoyl peroxide Nutrition 0.000 description 2
230000000052 comparative effect Effects 0.000 description 2
SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 2
239000003112 inhibitor Substances 0.000 description 2
239000004632 polycaprolactone Substances 0.000 description 2
229920001223 polyethylene glycol Polymers 0.000 description 2
229920000129 polyhexylmethacrylate Polymers 0.000 description 2
HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 2
239000007787 solid Substances 0.000 description 2
WFUGQJXVXHBTEM-UHFFFAOYSA-N 2-hydroperoxy-2-(2-hydroperoxybutan-2-ylperoxy)butane Chemical compound CCC(C)(OO)OOC(C)(CC)OO WFUGQJXVXHBTEM-UHFFFAOYSA-N 0.000 description 1
LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
LGDAGYXJBDILKZ-UHFFFAOYSA-N [2-methyl-1,1-dioxo-3-(pyridin-2-ylcarbamoyl)-1$l^{6},2-benzothiazin-4-yl] 2,2-dimethylpropanoate Chemical compound CC(C)(C)C(=O)OC=1C2=CC=CC=C2S(=O)(=O)N(C)C=1C(=O)NC1=CC=CC=N1 LGDAGYXJBDILKZ-UHFFFAOYSA-N 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
238000012644 addition polymerization Methods 0.000 description 1
244000309464 bull Species 0.000 description 1
JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
CREMABGTGYGIQB-UHFFFAOYSA-N carbon carbon Chemical compound C.C CREMABGTGYGIQB-UHFFFAOYSA-N 0.000 description 1
239000011203 carbon fibre reinforced carbon Substances 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
230000001627 detrimental effect Effects 0.000 description 1
230000007613 environmental effect Effects 0.000 description 1
235000019441 ethanol Nutrition 0.000 description 1
239000011521 glass Substances 0.000 description 1
239000003999 initiator Substances 0.000 description 1
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
238000005259 measurement Methods 0.000 description 1
QJAOYSPHSNGHNC-UHFFFAOYSA-N octadecane-1-thiol Chemical compound CCCCCCCCCCCCCCCCCCS QJAOYSPHSNGHNC-UHFFFAOYSA-N 0.000 description 1
150000002978 peroxides Chemical class 0.000 description 1
231100000614 poison Toxicity 0.000 description 1
229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
239000004926 polymethyl methacrylate Substances 0.000 description 1
230000005180 public health Effects 0.000 description 1
150000003254 radicals Chemical class 0.000 description 1
239000012488 sample solution Substances 0.000 description 1
239000013049 sediment Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
238000010561 standard procedure Methods 0.000 description 1
239000003440 toxic substance Substances 0.000 description 1
229920006305 unsaturated polyester Polymers 0.000 description 1
239000002351 wastewater Substances 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
230000004580 weight loss Effects 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
- C08L67/06—Unsaturated polyesters

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Macromonomer-Based Addition Polymer (AREA)
Compositions Of Macromolecular Compounds (AREA)
Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Separation, Recovery Or Treatment Of Waste Materials Containing Plastics (AREA)
Developing Agents For Electrophotography (AREA)
Polyesters Or Polycarbonates (AREA)

NO773532A 1976-10-16 1977-10-14 Polyesterharpiksprodukt. NO773532L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
GB43076/76A GB1592352A (en)	1976-10-16	1976-10-16	Preparation of polyester resin/fibre laminates and compositions for use therein

Publications (1)

Publication Number	Publication Date
NO773532L true NO773532L (no)	1978-04-18

Family

ID=10427229

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO773532A NO773532L (no)	1976-10-16	1977-10-14	Polyesterharpiksprodukt.

Country Status (17)

Country	Link
US (1)	US4218546A (fr)
JP (1)	JPS5356253A (fr)
AU (1)	AU519321B2 (fr)
BE (1)	BE859773A (fr)
BR (1)	BR7706901A (fr)
CA (1)	CA1081890A (fr)
DE (1)	DE2746357A1 (fr)
DK (1)	DK458077A (fr)
FI (1)	FI773059A7 (fr)
FR (1)	FR2367796A1 (fr)
GB (1)	GB1592352A (fr)
IL (1)	IL53136A (fr)
NL (1)	NL7711300A (fr)
NO (1)	NO773532L (fr)
PT (1)	PT67158B (fr)
SE (1)	SE7711597L (fr)
ZA (1)	ZA776130B (fr)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4347170A (en) *	1979-10-12	1982-08-31	Internationale Octrooi Maatschappij "Octropa" B.V.	Unsaturated polyester compositions and their use
US4294941A (en) *	1979-12-14	1981-10-13	Owens-Corning Fiberglas Corporation	Compatible low shrink resin systems
US5198480A (en) *	1990-08-08	1993-03-30	The Standard Oil Company	Suppressants for unsaturated polyester resins
US5206077A (en) *	1991-11-25	1993-04-27	The Dow Chemical Company	Low vaporizable ethylenically unsaturated monomer emission vinyl ester and polyester resin compositions

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3014001A (en) *	1957-01-04	1961-12-19	Reichhold Chemicals Inc	Production of glossy, air-curing, noninhibited polyester coatings
NL235151A (fr)	1958-01-15
US3225117A (en) *	1962-06-15	1965-12-21	Cincinnati Milling Machine Co	Weather-resistant plastics
US3701748A (en) *	1966-07-20	1972-10-31	Rohm & Haas	Unsaturated polyester resinous compositions
US3449468A (en) *	1967-01-20	1969-06-10	Ppg Industries Inc	Method of reducing porosity and pinholes in unsaturated polyester resin coatings
JPS5222977B2 (fr) *	1971-08-06	1977-06-21
US3879318A (en) *	1972-06-02	1975-04-22	Rohm & Haas	Organic amide containing compositions and process for thickening control of polyesters
JPS5416693B2 (fr) *	1972-06-14	1979-06-25
IT1004335B (it)	1973-03-15	1976-07-10	Koppers Co Inc	Composizione da stampaggio di poliestere ritardante la fiamma
US4008294A (en) *	1974-11-27	1977-02-15	W. R. Grace & Co.	Thickened polyester composition containing ultrafine polypropylene fibers
DE2513255C2 (de)	1975-03-26	1982-10-14	Bayer Ag, 5090 Leverkusen	Stabile organische, schwundarm härtbare Dispersionen auf Basis ungesättigter Polyesterharze und thermoplastischer Polymerer

1976
- 1976-10-16 GB GB43076/76A patent/GB1592352A/en not_active Expired
1977
- 1977-10-14 NL NL7711300A patent/NL7711300A/xx not_active Application Discontinuation
- 1977-10-14 IL IL53136A patent/IL53136A/xx unknown
- 1977-10-14 FR FR7730929A patent/FR2367796A1/fr not_active Withdrawn
- 1977-10-14 ZA ZA00776130A patent/ZA776130B/xx unknown
- 1977-10-14 BR BR7706901A patent/BR7706901A/pt unknown
- 1977-10-14 BE BE181786A patent/BE859773A/fr unknown
- 1977-10-14 JP JP12342077A patent/JPS5356253A/ja active Granted
- 1977-10-14 NO NO773532A patent/NO773532L/no unknown
- 1977-10-14 FI FI773059A patent/FI773059A7/fi not_active Application Discontinuation
- 1977-10-14 SE SE7711597A patent/SE7711597L/xx not_active Application Discontinuation
- 1977-10-14 DK DK458077A patent/DK458077A/da unknown
- 1977-10-14 CA CA288,746A patent/CA1081890A/fr not_active Expired
- 1977-10-14 US US05/842,269 patent/US4218546A/en not_active Expired - Lifetime
- 1977-10-14 PT PT67158A patent/PT67158B/pt unknown
- 1977-10-14 DE DE19772746357 patent/DE2746357A1/de not_active Withdrawn
- 1977-10-17 AU AU29793/77A patent/AU519321B2/en not_active Expired

Also Published As

Publication number	Publication date
JPS5356253A (en)	1978-05-22
SE7711597L (sv)	1978-04-17
PT67158A (en)	1977-11-01
IL53136A (en)	1981-01-30
AU519321B2 (en)	1981-11-26
ZA776130B (en)	1978-06-28
FR2367796A1 (fr)	1978-05-12
US4218546A (en)	1980-08-19
FI773059A7 (fi)	1978-04-17
JPS571531B2 (fr)	1982-01-12
IL53136A0 (en)	1977-12-30
BR7706901A (pt)	1978-07-18
GB1592352A (en)	1981-07-08
CA1081890A (fr)	1980-07-15
DK458077A (da)	1978-04-17
NL7711300A (nl)	1978-04-18
DE2746357A1 (de)	1978-04-27
AU2979377A (en)	1979-04-26
BE859773A (fr)	1978-04-14
PT67158B (en)	1979-03-20

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