GB642414A - Improvements in and relating to modified rosin esters and compositions containing them - Google Patents
Improvements in and relating to modified rosin esters and compositions containing themInfo
- Publication number
- GB642414A GB642414A GB19527/47A GB1952747A GB642414A GB 642414 A GB642414 A GB 642414A GB 19527/47 A GB19527/47 A GB 19527/47A GB 1952747 A GB1952747 A GB 1952747A GB 642414 A GB642414 A GB 642414A
- Authority
- GB
- United Kingdom
- Prior art keywords
- diallyl
- abietate
- maleate
- rosin
- ester
- 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
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 title abstract 10
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 title abstract 9
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 title abstract 9
- 150000002148 esters Chemical class 0.000 title abstract 6
- 239000000203 mixture Substances 0.000 title abstract 5
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 abstract 18
- -1 unsaturated alcohol ester Chemical class 0.000 abstract 9
- 235000010985 glycerol esters of wood rosin Nutrition 0.000 abstract 8
- 239000000944 linseed oil Substances 0.000 abstract 7
- 235000021388 linseed oil Nutrition 0.000 abstract 7
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 abstract 6
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 abstract 6
- 239000000047 product Substances 0.000 abstract 5
- 229920005989 resin Polymers 0.000 abstract 5
- 239000011347 resin Substances 0.000 abstract 5
- YDRDTDKISFMAQR-SBGDMIGBSA-N 2,3-bis[[(1r,4ar,4br,10ar)-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carbonyl]oxy]propyl (1r,4ar,4br,10ar)-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylate Chemical compound C([C@@H]1[C@@]2(C)CCC3)CC(C(C)C)=CC1=CC[C@H]2[C@]3(C)C(=O)OC(COC(=O)[C@@]1(C)[C@@H]2CC=C3C=C(CC[C@@H]3[C@@]2(C)CCC1)C(C)C)COC(=O)[C@]1(C)CCC[C@@]2(C)[C@H]1CC=C1C=C(C(C)C)CC[C@@H]12 YDRDTDKISFMAQR-SBGDMIGBSA-N 0.000 abstract 4
- 239000004641 Diallyl-phthalate Substances 0.000 abstract 4
- 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 4
- 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 4
- 239000007795 chemical reaction product Substances 0.000 abstract 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 3
- BQSWWPVLPPRSPJ-FIKIKMCASA-N [3-[(1r,4ar,4br,10ar)-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carbonyl]oxy-2,2-bis[[(1r,4ar,4br,10ar)-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carbonyl]oxymethyl]propyl] (1r,4ar,4br,10ar)-1,4a Chemical compound C([C@@H]1[C@@]2(C)CCC3)CC(C(C)C)=CC1=CC[C@H]2[C@]3(C)C(=O)OCC(COC(=O)[C@@]1(C)[C@@H]2CC=C3C=C(CC[C@@H]3[C@@]2(C)CCC1)C(C)C)(COC(=O)[C@@]1(C)[C@@H]2CC=C3C=C(CC[C@@H]3[C@@]2(C)CCC1)C(C)C)COC(=O)[C@]1(C)CCC[C@@]2(C)[C@H]1CC=C1C=C(C(C)C)CC[C@@H]12 BQSWWPVLPPRSPJ-FIKIKMCASA-N 0.000 abstract 3
- DUTZBUOZKIIFTG-XWVZOOPGSA-N [3-hydroxy-2,2-bis(hydroxymethyl)propyl] (1r,4ar,4br,10ar)-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylate Chemical compound C([C@@H]12)CC(C(C)C)=CC1=CC[C@@H]1[C@]2(C)CCC[C@@]1(C)C(=O)OCC(CO)(CO)CO DUTZBUOZKIIFTG-XWVZOOPGSA-N 0.000 abstract 3
- ZPOLOEWJWXZUSP-AATRIKPKSA-N bis(prop-2-enyl) (e)-but-2-enedioate Chemical compound C=CCOC(=O)\C=C\C(=O)OCC=C ZPOLOEWJWXZUSP-AATRIKPKSA-N 0.000 abstract 3
- 238000001035 drying Methods 0.000 abstract 3
- 229910052500 inorganic mineral Inorganic materials 0.000 abstract 3
- 239000011707 mineral Substances 0.000 abstract 3
- 239000003921 oil Substances 0.000 abstract 3
- 235000019198 oils Nutrition 0.000 abstract 3
- 235000015096 spirit Nutrition 0.000 abstract 3
- 239000002966 varnish Substances 0.000 abstract 3
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 abstract 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 abstract 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 abstract 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 2
- HABAXTXIECRCKH-UHFFFAOYSA-N bis(prop-2-enyl) butanedioate Chemical compound C=CCOC(=O)CCC(=O)OCC=C HABAXTXIECRCKH-UHFFFAOYSA-N 0.000 abstract 2
- 239000010941 cobalt Substances 0.000 abstract 2
- 229910017052 cobalt Inorganic materials 0.000 abstract 2
- 239000002383 tung oil Substances 0.000 abstract 2
- PICABBUEHGURLB-XTICBAGASA-N (1r,4ar,4br,10ar)-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid;propane-1,2,3-triol Chemical compound OCC(O)CO.C([C@@H]12)CC(C(C)C)=CC1=CC[C@@H]1[C@]2(C)CCC[C@@]1(C)C(O)=O PICABBUEHGURLB-XTICBAGASA-N 0.000 abstract 1
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 abstract 1
- JSZOAYXJRCEYSX-UHFFFAOYSA-N 1-nitropropane Chemical compound CCC[N+]([O-])=O JSZOAYXJRCEYSX-UHFFFAOYSA-N 0.000 abstract 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 abstract 1
- UIYHUUARNKRKGV-UHFFFAOYSA-N 2-prop-2-enoxycarbonylbenzoic acid Chemical compound OC(=O)C1=CC=CC=C1C(=O)OCC=C UIYHUUARNKRKGV-UHFFFAOYSA-N 0.000 abstract 1
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 abstract 1
- BTXXTMOWISPQSJ-UHFFFAOYSA-N 4,4,4-trifluorobutan-2-one Chemical compound CC(=O)CC(F)(F)F BTXXTMOWISPQSJ-UHFFFAOYSA-N 0.000 abstract 1
- BQACOLQNOUYJCE-FYZZASKESA-N Abietic acid Natural products CC(C)C1=CC2=CC[C@]3(C)[C@](C)(CCC[C@@]3(C)C(=O)O)[C@H]2CC1 BQACOLQNOUYJCE-FYZZASKESA-N 0.000 abstract 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 abstract 1
- IHBJFNMTDJQXNV-UHFFFAOYSA-N C.NC(O)(O)O Chemical compound C.NC(O)(O)O IHBJFNMTDJQXNV-UHFFFAOYSA-N 0.000 abstract 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 abstract 1
- 229920000877 Melamine resin Polymers 0.000 abstract 1
- 239000000020 Nitrocellulose Substances 0.000 abstract 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 abstract 1
- 239000004372 Polyvinyl alcohol Substances 0.000 abstract 1
- 229920001807 Urea-formaldehyde Polymers 0.000 abstract 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 abstract 1
- FJWGYAHXMCUOOM-QHOUIDNNSA-N [(2s,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6s)-4,5-dinitrooxy-2-(nitrooxymethyl)-6-[(2r,3r,4s,5r,6s)-4,5,6-trinitrooxy-2-(nitrooxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-3,5-dinitrooxy-6-(nitrooxymethyl)oxan-4-yl] nitrate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O)O[C@H]1[C@@H]([C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@@H](CO[N+]([O-])=O)O1)O[N+]([O-])=O)CO[N+](=O)[O-])[C@@H]1[C@@H](CO[N+]([O-])=O)O[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O FJWGYAHXMCUOOM-QHOUIDNNSA-N 0.000 abstract 1
- RSWGJHLUYNHPMX-ONCXSQPRSA-N abietic acid Chemical compound C([C@@H]12)CC(C(C)C)=CC1=CC[C@@H]1[C@]2(C)CCC[C@@]1(C)C(O)=O RSWGJHLUYNHPMX-ONCXSQPRSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 150000007513 acids Chemical class 0.000 abstract 1
- FPODCVUTIPDRTE-UHFFFAOYSA-N bis(prop-2-enyl) hexanedioate Chemical compound C=CCOC(=O)CCCCC(=O)OCC=C FPODCVUTIPDRTE-UHFFFAOYSA-N 0.000 abstract 1
- BKXRKRANFLFTFU-UHFFFAOYSA-N bis(prop-2-enyl) oxalate Chemical compound C=CCOC(=O)C(=O)OCC=C BKXRKRANFLFTFU-UHFFFAOYSA-N 0.000 abstract 1
- 239000004359 castor oil Substances 0.000 abstract 1
- 235000019438 castor oil Nutrition 0.000 abstract 1
- 239000001913 cellulose Substances 0.000 abstract 1
- 229920002678 cellulose Polymers 0.000 abstract 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 abstract 1
- 229940018560 citraconate Drugs 0.000 abstract 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 abstract 1
- 229920001577 copolymer Polymers 0.000 abstract 1
- 150000001991 dicarboxylic acids Chemical class 0.000 abstract 1
- VVYDVQWJZWRVPE-UHFFFAOYSA-L dimethyltin(2+);diiodide Chemical compound C[Sn](C)(I)I VVYDVQWJZWRVPE-UHFFFAOYSA-L 0.000 abstract 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract 1
- VZCYOOQTPOCHFL-OWOJBTEDSA-L fumarate(2-) Chemical class [O-]C(=O)\C=C\C([O-])=O VZCYOOQTPOCHFL-OWOJBTEDSA-L 0.000 abstract 1
- 125000005456 glyceride group Chemical group 0.000 abstract 1
- 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 abstract 1
- 229940096886 glyceryl abietate Drugs 0.000 abstract 1
- 125000003976 glyceryl group Chemical group [H]C([*])([H])C(O[H])([H])C(O[H])([H])[H] 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 229930195733 hydrocarbon Natural products 0.000 abstract 1
- 150000002430 hydrocarbons Chemical class 0.000 abstract 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 abstract 1
- 150000002576 ketones Chemical class 0.000 abstract 1
- 239000004922 lacquer Substances 0.000 abstract 1
- 150000002688 maleic acid derivatives Chemical class 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- FYFFGSSZFBZTAH-UHFFFAOYSA-N methylaminomethanetriol Chemical compound CNC(O)(O)O FYFFGSSZFBZTAH-UHFFFAOYSA-N 0.000 abstract 1
- 229920001220 nitrocellulos Polymers 0.000 abstract 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 abstract 1
- PGMYKACGEOXYJE-UHFFFAOYSA-N pentyl acetate Chemical class CCCCCOC(C)=O PGMYKACGEOXYJE-UHFFFAOYSA-N 0.000 abstract 1
- 229920001568 phenolic resin Polymers 0.000 abstract 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 abstract 1
- 229920002451 polyvinyl alcohol Polymers 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 abstract 1
- 150000003900 succinic acid esters Chemical class 0.000 abstract 1
- 150000005846 sugar alcohols Polymers 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09F—NATURAL RESINS; FRENCH POLISH; DRYING-OILS; OIL DRYING AGENTS, i.e. SICCATIVES; TURPENTINE
- C09F1/00—Obtaining purification, or chemical modification of natural resins, e.g. oleo-resins
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Paints Or Removers (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Macromonomer-Based Addition Polymer (AREA)
Abstract
Modified rosin esters are prepared by reacting at between 200 DEG and 300 DEG C., a rosin ester of a polyhydric alcohol containing the conjugated unsaturation of abietic acid with an unsaturated alcohol ester of either (a) an alpha unsaturated alpha beta dicarboxylic acid, or (b) a saturated dicarboxylic acid. The reaction is preferably carried out in two stages, first at 200-250 DEG C. and when a preliminary reaction is over, at 250-300 DEG C. Esters of allyl, crotyl, propargyl and butenyl alcohols are suitable, preferably allyl and di-allyl phthalates, succinates, maleates, and fumarates. The products may be copolymerized with styrene, methyl methacrylate, or vinyl acetate, and the copolymers made into drying oils to form varnishes, or they may be blended with urea-, phenol-, or melamine-formaldehyde resins cellulose derivatives, or methyl methacrylate, acrylate, vinylidene chloride resins or polyvinyl alcohol. The products may be cooked into drying oils to form varnish bases, which may be thinned with mineral spirits, and driers added. In an example (1) glycerol abietate and diallyl maleate are heated and the temperature increased slowly from 200-300 DEG C. The product is dissolved in heated linseed oil (previously treated to produce conjugated unsaturation). The mixture is dissolved in mineral spirits and lead and cobalt naphthenates added. Alternatively a lacquer is obtained by dissolving the resin in a mixture of rosin, nitrocellulose, xylol, butyl-, ethyl-, and amyl acetates, and octyl alcohol. The resin is also soluble in esters, ketones, hydrocarbons, chlorinated hydrocarbons, glycol ethers, nitropropane, and butanol. The product of a similar example (2) is saponified with sodium hydroxide. Further examples describe heating together mixtures of (3) pentaerythrityl abietate and diallyl maleate; (4) pentaerythrityl abietate and diallyl fumarate; (5) ester gum and diallyl fumarate; (6) ester gum and diallyl chloromaleate; (7) ester gum and diallyl itaconate; (8) ester gum and diallyl citraconate; (9) the reaction product of glycerol and rosin and monoallyl maleate; (10) the reaction product of rosin and pentaerythritol and monoallyl maleate; (11) the reaction product of tri-hydroxymethyl-amino-methane and rosin and monoallyl maleate; (12) the reaction product of rosin and glycerol and monoallyl citracontate; (13) ester gum, glycerol, and monomethallyl maleate. Examples using esters of saturated polycarboxylic acids describe reacting mixtures of (14) and (15) glyceryl tri-abietate and diallyl phthalate; (16) pentaerythrityl tetra-abietate and diallyl phthalate; (17) pentaerythrityl tetra-abietate and diallyl succinate; (18) glyceryl tri-abietate and diallyl oxalate; (19) glyceryl tri-abietate and diallyl adipate; (20) glyceryl tri-abietate and diallyl succinate; (21) glyceryl diabietate and monoallyl phthalate; (22) pentaerythrityl triabietate and monomethallyl phthalate; (23) tri-hydroxy methylamine methane triabietate and monomethallyl succinate. Varnish bases are described in further examples, in which the product obtained from a resin ester and an unsaturated alcohol ester is afterwards heated with drying oils. Materials employed are, in examples (24) and (25) rosin glyceride, diallyl maleate, and linseed oil; (26) pentaerythritol tetra-abietate, diallyl fumarate, linseed oil, and china-wood oil; (27) glycerol diabietate, monoallyl maleate and raw tung oil; (28) ester gum, glycerol, monomethallyl maleate, and dehydrated castor oil; (29) glyceryl abietate, diallyl maleate, and alkali-refined linseed oil; (30) the resin of (23) and linseed oil; (31) ester gum, diallyl phthalate, and linseed oil; (32) pentaerythrityl abietate, diallyl phthalate, and linseed oil. The base is in each case thinned with mineral spirits and lead and cobalt naphenate driers are added.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US642414XA | 1944-04-14 | 1944-04-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB642414A true GB642414A (en) | 1950-09-06 |
Family
ID=22054544
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB19527/47A Expired GB642414A (en) | 1944-04-14 | 1947-07-21 | Improvements in and relating to modified rosin esters and compositions containing them |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB642414A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2757187A (en) * | 1955-11-14 | 1956-07-31 | Monsanto Chemicals | Polycarboxylates |
US3044998A (en) * | 1958-11-13 | 1962-07-17 | Standard Oil Co | Borated monomers and polymers |
US3182047A (en) * | 1961-06-02 | 1965-05-04 | Commerical Solvents Corp | Amino alcohol modified polyacrylates |
CN107964370A (en) * | 2018-01-04 | 2018-04-27 | 广东华林化工有限公司 | A kind of technology for producing colophony |
-
1947
- 1947-07-21 GB GB19527/47A patent/GB642414A/en not_active Expired
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2757187A (en) * | 1955-11-14 | 1956-07-31 | Monsanto Chemicals | Polycarboxylates |
US3044998A (en) * | 1958-11-13 | 1962-07-17 | Standard Oil Co | Borated monomers and polymers |
US3182047A (en) * | 1961-06-02 | 1965-05-04 | Commerical Solvents Corp | Amino alcohol modified polyacrylates |
CN107964370A (en) * | 2018-01-04 | 2018-04-27 | 广东华林化工有限公司 | A kind of technology for producing colophony |
CN107964370B (en) * | 2018-01-04 | 2020-05-05 | 广东华林化工有限公司 | Rosin production process |
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