GB339958A - Improvements in the manufacture and production of condensation products - Google Patents
Improvements in the manufacture and production of condensation productsInfo
- Publication number
- GB339958A GB339958A GB2461829A GB2461829A GB339958A GB 339958 A GB339958 A GB 339958A GB 2461829 A GB2461829 A GB 2461829A GB 2461829 A GB2461829 A GB 2461829A GB 339958 A GB339958 A GB 339958A
- Authority
- GB
- United Kingdom
- Prior art keywords
- parts
- acid
- colophony
- oil
- condensation products
- 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
- 239000007859 condensation product Substances 0.000 title abstract 3
- 238000004519 manufacturing process Methods 0.000 title 2
- 239000002253 acid Substances 0.000 abstract 6
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 3
- 150000007513 acids Chemical class 0.000 abstract 3
- 239000003921 oil Substances 0.000 abstract 3
- 239000004902 Softening Agent Substances 0.000 abstract 2
- 239000004359 castor oil Substances 0.000 abstract 2
- 235000019438 castor oil Nutrition 0.000 abstract 2
- 150000002148 esters Chemical class 0.000 abstract 2
- 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 2
- 238000010438 heat treatment Methods 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 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
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 abstract 1
- 229920002160 Celluloid Polymers 0.000 abstract 1
- 239000005662 Paraffin oil Substances 0.000 abstract 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 abstract 1
- 150000001298 alcohols Chemical class 0.000 abstract 1
- -1 aliphatic alcohols Chemical class 0.000 abstract 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- 239000004202 carbamide Substances 0.000 abstract 1
- 150000001735 carboxylic acids Chemical class 0.000 abstract 1
- 239000005018 casein Substances 0.000 abstract 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 abstract 1
- 235000021240 caseins Nutrition 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 230000032050 esterification Effects 0.000 abstract 1
- 238000005886 esterification reaction Methods 0.000 abstract 1
- ZNZUADCAUUUPHD-UHFFFAOYSA-N ethyl 2,2-dihydroxyoctadecanoate Chemical compound OC(C(=O)OCC)(CCCCCCCCCCCCCCCC)O ZNZUADCAUUUPHD-UHFFFAOYSA-N 0.000 abstract 1
- 239000011261 inert gas Substances 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- 150000002989 phenols Chemical class 0.000 abstract 1
- 239000000047 product Substances 0.000 abstract 1
- 239000012262 resinous product Substances 0.000 abstract 1
- WBHHMMIMDMUBKC-XLNAKTSKSA-N ricinelaidic acid Chemical compound CCCCCC[C@@H](O)C\C=C\CCCCCCCC(O)=O WBHHMMIMDMUBKC-XLNAKTSKSA-N 0.000 abstract 1
- 229960003656 ricinoleic acid Drugs 0.000 abstract 1
- FEUQNCSVHBHROZ-UHFFFAOYSA-N ricinoleic acid Natural products CCCCCCC(O[Si](C)(C)C)CC=CCCCCCCCC(=O)OC FEUQNCSVHBHROZ-UHFFFAOYSA-N 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Phenolic Resins Or Amino Resins (AREA)
Abstract
339,958. Johnson, J. Y., (I. G. Farbenindustrie Akt.-Ges.). Aug. 12, 1929. Ester condensation products; albumens.-Oily resinous products are obtained by esterifying the hydroxyl groups of aliphatic long chain carboxylic acids containing hydroxyl groups in the chain, or esters of such acids with alcohols, by heating these materials with colophony or other natural resinic acids until and under such conditions that the acid value of the resinic acids has practically disappeared. The esterification may be effected in vacuo or the water mav be removed as formed by the passage of an inert gas; acid or alkaline condensing agents may be used. The almost acid-free viscous oily products are stated to be useful as softening agents. According to examples, the parts being by weight, (1) 150 parts of castor oil and 50 parts of colophony are heated at 260‹ C. under reduced pressure to yield a viscous oil. A still more viscous oil is obtained by employing 100 to 150 parts colophony for the same quantity of castor oil, which is readily miscible in paraffin oil. It is suitable as a softening agent for celluloid, condensation products of formaldehyde with urea or phenols, or casein. (2) A brown viscous oil soluble in most organic solvents except the lower aliphatic alcohols, is obtained by heating 15 parts ricinoleic acid with 13.5 parts colophony for 10 hours under reduced pressure. (3) 3.4 parts of dihydroxystearic ethyl ester are heated with 3 parts of abietic acid at 260‹ C. in vacuo until the acid value has been reduced to zero.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2461829A GB339958A (en) | 1929-08-12 | 1929-08-12 | Improvements in the manufacture and production of condensation products |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2461829A GB339958A (en) | 1929-08-12 | 1929-08-12 | Improvements in the manufacture and production of condensation products |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB339958A true GB339958A (en) | 1930-12-12 |
Family
ID=10214515
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB2461829A Expired GB339958A (en) | 1929-08-12 | 1929-08-12 | Improvements in the manufacture and production of condensation products |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB339958A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2995890A1 (en) * | 2012-09-26 | 2014-03-28 | Colas Sa | Transparent hydrocarbon binder, useful in material comprising granules and optionally pigment for producing construction layers and/or coatings, comprises petroleum oil, and vegetable compound, preferably vegetable resin |
-
1929
- 1929-08-12 GB GB2461829A patent/GB339958A/en not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2995890A1 (en) * | 2012-09-26 | 2014-03-28 | Colas Sa | Transparent hydrocarbon binder, useful in material comprising granules and optionally pigment for producing construction layers and/or coatings, comprises petroleum oil, and vegetable compound, preferably vegetable resin |
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