GB540168A - Resinous compositions and methods of preparing same - Google Patents
Resinous compositions and methods of preparing sameInfo
- Publication number
- GB540168A GB540168A GB33000/39A GB3300039A GB540168A GB 540168 A GB540168 A GB 540168A GB 33000/39 A GB33000/39 A GB 33000/39A GB 3300039 A GB3300039 A GB 3300039A GB 540168 A GB540168 A GB 540168A
- Authority
- GB
- United Kingdom
- Prior art keywords
- resin
- maleate
- diallyl
- acids
- glycol
- Prior art date
- 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
Links
- 239000000203 mixture Substances 0.000 title abstract 6
- 239000011347 resin Substances 0.000 abstract 16
- 229920005989 resin Polymers 0.000 abstract 16
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract 12
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 abstract 9
- ZPOLOEWJWXZUSP-WAYWQWQTSA-N bis(prop-2-enyl) (z)-but-2-enedioate Chemical compound C=CCOC(=O)\C=C/C(=O)OCC=C ZPOLOEWJWXZUSP-WAYWQWQTSA-N 0.000 abstract 8
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical class OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 abstract 6
- 239000002253 acid Substances 0.000 abstract 5
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 abstract 5
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 abstract 4
- 239000001913 cellulose Substances 0.000 abstract 4
- 229920002678 cellulose Polymers 0.000 abstract 4
- 235000021388 linseed oil Nutrition 0.000 abstract 4
- 239000000944 linseed oil Substances 0.000 abstract 4
- -1 #-benzoyl acrylic Chemical group 0.000 abstract 3
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 abstract 3
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 abstract 3
- 150000007513 acids Chemical class 0.000 abstract 3
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 abstract 3
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 abstract 3
- MKEPGIQTWYTRIW-ODZAUARKSA-N (z)-but-2-enedioic acid;ethane-1,2-diol Chemical compound OCCO.OC(=O)\C=C/C(O)=O MKEPGIQTWYTRIW-ODZAUARKSA-N 0.000 abstract 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 abstract 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 abstract 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical group Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 abstract 2
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 abstract 2
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 abstract 2
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical group FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 abstract 2
- 239000000428 dust Substances 0.000 abstract 2
- 244000144992 flock Species 0.000 abstract 2
- 239000003112 inhibitor Substances 0.000 abstract 2
- 239000003921 oil Substances 0.000 abstract 2
- 235000019198 oils Nutrition 0.000 abstract 2
- 150000007524 organic acids Chemical class 0.000 abstract 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 abstract 2
- 238000006116 polymerization reaction Methods 0.000 abstract 2
- 238000002360 preparation method Methods 0.000 abstract 2
- 235000013772 propylene glycol Nutrition 0.000 abstract 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 abstract 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 abstract 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 abstract 2
- 150000005846 sugar alcohols Polymers 0.000 abstract 2
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 abstract 2
- PVLVQTYSRICFCB-ODZAUARKSA-N (z)-but-2-enedioic acid;2-(2-hydroxyethoxy)ethanol Chemical compound OCCOCCO.OC(=O)\C=C/C(O)=O PVLVQTYSRICFCB-ODZAUARKSA-N 0.000 abstract 1
- PAOHAQSLJSMLAT-UHFFFAOYSA-N 1-butylperoxybutane Chemical group CCCCOOCCCC PAOHAQSLJSMLAT-UHFFFAOYSA-N 0.000 abstract 1
- FRPZMMHWLSIFAZ-UHFFFAOYSA-N 10-undecenoic acid Chemical compound OC(=O)CCCCCCCCC=C FRPZMMHWLSIFAZ-UHFFFAOYSA-N 0.000 abstract 1
- BYDRTKVGBRTTIT-UHFFFAOYSA-N 2-methylprop-2-en-1-ol Chemical compound CC(=C)CO BYDRTKVGBRTTIT-UHFFFAOYSA-N 0.000 abstract 1
- KHAHWKLZGBIAKT-UHFFFAOYSA-N 4-(4-methylpyrimidin-2-yl)benzaldehyde Chemical compound CC1=CC=NC(C=2C=CC(C=O)=CC=2)=N1 KHAHWKLZGBIAKT-UHFFFAOYSA-N 0.000 abstract 1
- MGYMHQJELJYRQS-UHFFFAOYSA-N Ascaridole Chemical group C1CC2(C)OOC1(C(C)C)C=C2 MGYMHQJELJYRQS-UHFFFAOYSA-N 0.000 abstract 1
- 229910015900 BF3 Chemical group 0.000 abstract 1
- KWMSJBQQSRWOEM-UHFFFAOYSA-N C(C=C/C(=O)O)(=O)O.C(CCCCCCCCCO)O Chemical compound C(C=C/C(=O)O)(=O)O.C(CCCCCCCCCO)O KWMSJBQQSRWOEM-UHFFFAOYSA-N 0.000 abstract 1
- 235000013162 Cocos nucifera Nutrition 0.000 abstract 1
- 244000060011 Cocos nucifera Species 0.000 abstract 1
- 229920000742 Cotton Polymers 0.000 abstract 1
- 239000004641 Diallyl-phthalate Substances 0.000 abstract 1
- 229910000831 Steel Inorganic materials 0.000 abstract 1
- 229910021627 Tin(IV) chloride Inorganic materials 0.000 abstract 1
- 229920002522 Wood fibre Polymers 0.000 abstract 1
- 229920002494 Zein Polymers 0.000 abstract 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract 1
- 239000000853 adhesive Substances 0.000 abstract 1
- 230000001070 adhesive effect Effects 0.000 abstract 1
- MGYMHQJELJYRQS-ZJUUUORDSA-N ascaridole Chemical group C1C[C@]2(C)OO[C@@]1(C(C)C)C=C2 MGYMHQJELJYRQS-ZJUUUORDSA-N 0.000 abstract 1
- 229960005070 ascorbic acid Drugs 0.000 abstract 1
- 239000011668 ascorbic acid Substances 0.000 abstract 1
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 abstract 1
- HABAXTXIECRCKH-UHFFFAOYSA-N bis(prop-2-enyl) butanedioate Chemical compound C=CCOC(=O)CCC(=O)OCC=C HABAXTXIECRCKH-UHFFFAOYSA-N 0.000 abstract 1
- 238000009835 boiling Methods 0.000 abstract 1
- KHAVLLBUVKBTBG-UHFFFAOYSA-N caproleic acid Natural products OC(=O)CCCCCCCC=C KHAVLLBUVKBTBG-UHFFFAOYSA-N 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 239000004927 clay Substances 0.000 abstract 1
- 239000008199 coating composition Substances 0.000 abstract 1
- IIGAELMXVLEZPM-GRVYQHKQSA-L cobalt(2+);(9z,12z)-octadeca-9,12-dienoate Chemical group [Co+2].CCCCC\C=C/C\C=C/CCCCCCCC([O-])=O.CCCCC\C=C/C\C=C/CCCCCCCC([O-])=O IIGAELMXVLEZPM-GRVYQHKQSA-L 0.000 abstract 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical class C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 abstract 1
- 235000014113 dietary fatty acids Nutrition 0.000 abstract 1
- 238000001035 drying Methods 0.000 abstract 1
- 239000000975 dye Substances 0.000 abstract 1
- 230000032050 esterification Effects 0.000 abstract 1
- 238000005886 esterification reaction Methods 0.000 abstract 1
- 239000004744 fabric Substances 0.000 abstract 1
- 239000000194 fatty acid Substances 0.000 abstract 1
- 229930195729 fatty acid Natural products 0.000 abstract 1
- 150000004665 fatty acids Chemical class 0.000 abstract 1
- 239000000945 filler Substances 0.000 abstract 1
- 235000013312 flour Nutrition 0.000 abstract 1
- 239000011491 glass wool Substances 0.000 abstract 1
- 150000002334 glycols Chemical class 0.000 abstract 1
- 239000010438 granite Substances 0.000 abstract 1
- 229940093915 gynecological organic acid Drugs 0.000 abstract 1
- 150000002689 maleic acids Chemical class 0.000 abstract 1
- 125000005395 methacrylic acid group Chemical group 0.000 abstract 1
- 125000005394 methallyl group Chemical group 0.000 abstract 1
- 239000010445 mica Substances 0.000 abstract 1
- 229910052618 mica group Inorganic materials 0.000 abstract 1
- 238000000465 moulding Methods 0.000 abstract 1
- GEMHFKXPOCTAIP-UHFFFAOYSA-N n,n-dimethyl-n'-phenylcarbamimidoyl chloride Chemical group CN(C)C(Cl)=NC1=CC=CC=C1 GEMHFKXPOCTAIP-UHFFFAOYSA-N 0.000 abstract 1
- 239000000025 natural resin Substances 0.000 abstract 1
- 235000005985 organic acids Nutrition 0.000 abstract 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 abstract 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 abstract 1
- 229920001568 phenolic resin Polymers 0.000 abstract 1
- 239000005011 phenolic resin Substances 0.000 abstract 1
- 239000000049 pigment Substances 0.000 abstract 1
- 239000002685 polymerization catalyst Substances 0.000 abstract 1
- 230000000379 polymerizing effect Effects 0.000 abstract 1
- 239000004576 sand Substances 0.000 abstract 1
- 229910010271 silicon carbide Inorganic materials 0.000 abstract 1
- 239000010959 steel Substances 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 229920003051 synthetic elastomer Polymers 0.000 abstract 1
- 229920003002 synthetic resin Polymers 0.000 abstract 1
- 239000000057 synthetic resin Substances 0.000 abstract 1
- 239000005061 synthetic rubber Substances 0.000 abstract 1
- 235000018553 tannin Nutrition 0.000 abstract 1
- 239000001648 tannin Substances 0.000 abstract 1
- 229920001864 tannin Polymers 0.000 abstract 1
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical group Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 abstract 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical group CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 abstract 1
- KQTIIICEAUMSDG-UHFFFAOYSA-N tricarballylic acid Chemical compound OC(=O)CC(C(O)=O)CC(O)=O KQTIIICEAUMSDG-UHFFFAOYSA-N 0.000 abstract 1
- XHGIFBQQEGRTPB-UHFFFAOYSA-N tris(prop-2-enyl) phosphate Chemical compound C=CCOP(=O)(OCC=C)OCC=C XHGIFBQQEGRTPB-UHFFFAOYSA-N 0.000 abstract 1
- 229960002703 undecylenic acid Drugs 0.000 abstract 1
- 239000002023 wood Substances 0.000 abstract 1
- 210000002268 wool Anatomy 0.000 abstract 1
- 239000005019 zein Substances 0.000 abstract 1
- 229940093612 zein Drugs 0.000 abstract 1
Classifications
-
- 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/66—Polyesters containing oxygen in the form of ether groups
- C08G63/668—Polyesters containing oxygen in the form of ether groups derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/676—Polyesters containing oxygen in the form of ether groups derived from polycarboxylic acids and polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation
-
- 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
- C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
- C08F283/01—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to unsaturated polyesters
-
- 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
- C08F290/00—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups
- C08F290/08—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups on to polymers modified by introduction of unsaturated side groups
- C08F290/14—Polymers provided for in subclass C08G
-
- 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/52—Polycarboxylic acids or polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation
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)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US540168XA | 1938-12-30 | 1938-12-30 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB540168A true GB540168A (en) | 1941-10-08 |
Family
ID=21988205
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB33000/39A Expired GB540168A (en) | 1938-12-30 | 1939-12-28 | Resinous compositions and methods of preparing same |
Country Status (4)
| Country | Link |
|---|---|
| BE (1) | BE474833A (enrdf_load_stackoverflow) |
| FR (1) | FR951560A (enrdf_load_stackoverflow) |
| GB (1) | GB540168A (enrdf_load_stackoverflow) |
| NL (1) | NL65945C (enrdf_load_stackoverflow) |
Cited By (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2419221A (en) * | 1942-05-11 | 1947-04-22 | Eastman Kodak Co | Copolymers of 2-halogeno-allyl alcohol or 2-halogeno-allyl esters |
| US2423042A (en) * | 1943-11-17 | 1947-06-24 | Marco Chemicals Inc | Polymerizable mixed ester of an unsaturated polycarboxylic acid, phthalic acid, and alower aliphatic glycol |
| US2431374A (en) * | 1943-12-30 | 1947-11-25 | Pro Phy Lac Tie Brush Company | Copolymers of diallyl maleate and saturated monohydric alcohol esters of maleic and fumaric acids |
| US2437232A (en) * | 1943-10-15 | 1948-03-02 | Resinous Prod & Chemical Co | Stabilization of polyesters from dihydric alcohols and both saturated and unsaturated dicarboxylic acids |
| US2437046A (en) * | 1943-10-15 | 1948-03-02 | Resinous Prod & Chemical Co | Stabilization of polyesters |
| US2448584A (en) * | 1943-11-24 | 1948-09-07 | Bell Telephone Labor Inc | Cured polyester synthetic rubbers formed from disecondary glycols |
| US2454210A (en) * | 1943-04-17 | 1948-11-16 | Westinghouse Electric Corp | Synthetic resin and members produced therefrom |
| US2462042A (en) * | 1944-01-12 | 1949-02-15 | Libbey Owens Ford Glass Co | Conjointly polymerized unsaturated substances |
| US2528235A (en) * | 1945-06-26 | 1950-10-31 | Gen Electric | Coating and impregnating compositions and articles produced from the same |
| US2530315A (en) * | 1944-10-21 | 1950-11-14 | Montclair Res Corp | Modified drying oil-alkyd resins and process of making them |
| US2530316A (en) * | 1944-10-21 | 1950-11-14 | Montclair Res Corp | Ester modified drying oil alkyd resins and process of making same |
| US2534617A (en) * | 1945-01-24 | 1950-12-19 | Monsanto Chemicals | Laminated product |
| US2563206A (en) * | 1946-12-23 | 1951-08-07 | Polymerisable Products Ltd | Cyclohexene carboxylic acid esters and process for preparing same |
| US2819243A (en) * | 1951-10-04 | 1958-01-07 | Allied Chem & Dye Corp | Method of making glass fiber filled alkyd resins |
| DE970557C (de) * | 1952-03-11 | 1958-10-02 | Ciba Geigy | Verfahren zur Herstellung einer gehaerteten Kunstharzmasse |
| US3151183A (en) * | 1960-01-18 | 1964-09-29 | Us Rubber Co | Flame resistant copolymer of an ester of a 2, 3-dihaloalkanol and an unsaturated polycarboxylic acid |
| CN113185652A (zh) * | 2021-06-17 | 2021-07-30 | 江西金石三维智能制造科技有限公司 | 一种类abs的立体光造型树脂以及制备方法 |
-
0
- BE BE474833D patent/BE474833A/xx unknown
- NL NL65945D patent/NL65945C/xx active
-
1939
- 1939-12-28 GB GB33000/39A patent/GB540168A/en not_active Expired
-
1947
- 1947-07-07 FR FR951560D patent/FR951560A/fr not_active Expired
Cited By (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2419221A (en) * | 1942-05-11 | 1947-04-22 | Eastman Kodak Co | Copolymers of 2-halogeno-allyl alcohol or 2-halogeno-allyl esters |
| US2454210A (en) * | 1943-04-17 | 1948-11-16 | Westinghouse Electric Corp | Synthetic resin and members produced therefrom |
| US2437232A (en) * | 1943-10-15 | 1948-03-02 | Resinous Prod & Chemical Co | Stabilization of polyesters from dihydric alcohols and both saturated and unsaturated dicarboxylic acids |
| US2437046A (en) * | 1943-10-15 | 1948-03-02 | Resinous Prod & Chemical Co | Stabilization of polyesters |
| US2423042A (en) * | 1943-11-17 | 1947-06-24 | Marco Chemicals Inc | Polymerizable mixed ester of an unsaturated polycarboxylic acid, phthalic acid, and alower aliphatic glycol |
| US2448584A (en) * | 1943-11-24 | 1948-09-07 | Bell Telephone Labor Inc | Cured polyester synthetic rubbers formed from disecondary glycols |
| US2431374A (en) * | 1943-12-30 | 1947-11-25 | Pro Phy Lac Tie Brush Company | Copolymers of diallyl maleate and saturated monohydric alcohol esters of maleic and fumaric acids |
| US2462042A (en) * | 1944-01-12 | 1949-02-15 | Libbey Owens Ford Glass Co | Conjointly polymerized unsaturated substances |
| US2530315A (en) * | 1944-10-21 | 1950-11-14 | Montclair Res Corp | Modified drying oil-alkyd resins and process of making them |
| US2530316A (en) * | 1944-10-21 | 1950-11-14 | Montclair Res Corp | Ester modified drying oil alkyd resins and process of making same |
| US2534617A (en) * | 1945-01-24 | 1950-12-19 | Monsanto Chemicals | Laminated product |
| US2528235A (en) * | 1945-06-26 | 1950-10-31 | Gen Electric | Coating and impregnating compositions and articles produced from the same |
| US2563206A (en) * | 1946-12-23 | 1951-08-07 | Polymerisable Products Ltd | Cyclohexene carboxylic acid esters and process for preparing same |
| US2819243A (en) * | 1951-10-04 | 1958-01-07 | Allied Chem & Dye Corp | Method of making glass fiber filled alkyd resins |
| DE970557C (de) * | 1952-03-11 | 1958-10-02 | Ciba Geigy | Verfahren zur Herstellung einer gehaerteten Kunstharzmasse |
| US3151183A (en) * | 1960-01-18 | 1964-09-29 | Us Rubber Co | Flame resistant copolymer of an ester of a 2, 3-dihaloalkanol and an unsaturated polycarboxylic acid |
| CN113185652A (zh) * | 2021-06-17 | 2021-07-30 | 江西金石三维智能制造科技有限公司 | 一种类abs的立体光造型树脂以及制备方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| FR951560A (fr) | 1949-10-28 |
| NL65945C (enrdf_load_stackoverflow) | |
| BE474833A (enrdf_load_stackoverflow) |
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