GB1014678A - Improvements in or relating to sizing compositions - Google Patents
Improvements in or relating to sizing compositionsInfo
- Publication number
- GB1014678A GB1014678A GB1003863A GB1003863A GB1014678A GB 1014678 A GB1014678 A GB 1014678A GB 1003863 A GB1003863 A GB 1003863A GB 1003863 A GB1003863 A GB 1003863A GB 1014678 A GB1014678 A GB 1014678A
- Authority
- GB
- United Kingdom
- Prior art keywords
- terpene
- rosin
- polymers
- composition
- polymer
- 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
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/62—Rosin; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L93/00—Compositions of natural resins; Compositions of derivatives thereof
- C08L93/04—Rosin
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Paper (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Terpene polymers, e.g. dimers or higher polymer of allo-ocimene, carene, pinene, dipentene, terpinene, terpinolene or turpentine, a preferred material being "sulphate turpentine," are obtained with or without solvent and with known catalyst, e.g. H2SO4, H3PO4 fuller's earth, BF3, or chlorides of metals having amphoteric oxides.ALSO:A paper sizing composition comprises a neutralized modified rosin and a terpene polymer in aqueous dispersion. The rosin may be modified by hydrogenation, polymerization, heating or treatment with CH2O or an a ,b -unsaturated acid or a derivative thereof. Tall oil rosin is specified. It may be treated with the unsaturated acid before or after mixing with the terpene polymer. In the latter case a solvent may be used, e.g. tetrahydronaphthalene, decahydronaphthalene, an aromatic petroleum fraction, and chlorinated diphenyls. A peroxide catalyst may also be used, e.g. benzoyl, dicumyl, or di-tert-butyl peroxides or cumene hydroperoxide. a ,b unsaturated acids specified are acrylic, maleic, fumaric, itaconic, citraconic, aconitic, methacrylic, and a - and b -crotonic acids, anhydrides of these acids and acrylonitrile. 0.5-50% of this reaction product may be present in the composition. Terpene polymers specified are dimers or higher polymers of allo-ocimene, carene, pinene, dipentene, terpinene, terpinolene, or turpentines containing camphene, limonene and phellandrene, 0.5-45% may be used. The composition may also contain fatty acids, 0.5-27% of a terpene polymer treated with an a ,b -unsaturated acid and 1-5% of Al2(SO4)3. The terpene polymer may be treated with the acid before or after adding the rosin, the reactants being heated to 150-250 DEG C. in the presence of up to 15% of peroxide catalyst. The composition may be heated to 100-150 DEG C. with sufficient aqueous alkali, e.g. NaOH, KOH, Na2CO3 or K2CO3, t neutralize 70-95% of the acid groups in the rosin.ALSO:Reaction products are formed by reaction between terpene polymers and a ,b -unsaturated mono- or polybasic carboxylic acids or derivatives thereof. The polymer and acid reactants are mixed and heated for example to a temperature of 150-250 DEG C. with or without peroxide catalysts. The terpene polymers may be dimers or higher polymers of, e.g. allo-ocimene, carene, pinene, dipentene, terpinene, terpinolene or turpentine. The acid derivative may be the anhydride or nitrile, e.g. maleic anhydride or acrylonitrile. An example describes the reaction between a terpene polymer fraction containing dimers, trimers and tetramers and maleic anhydride.ALSO:Sized paper is made using a sizing composition comprising an aqueous dispersion of partially neutralized rosin, and 0.5-45% by weight, based on the rosin, of a terpene polymer. The term "rosin" includes modified rosins, e.g. hydrogenated, polymerized, or heat-treated rosins, and rosins that have been reacted with formaldehyde or a , b -unsaturated acids or derivatives thereof. The terpene polymers may be dimers or higher polymers of e.g. allo-ocimene, carene, pinene, dipentene, terpinene, terpinolene or turpentine, a preferred material being "sulphate turpentine". Products of the reaction of a , b -unsaturated acids or derivative thereof and the terpene polymers may be added to the composition. Paper may be made from pulp mixed with the composition. The composition may be dehydrated to a dry size.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US18209462A | 1962-03-23 | 1962-03-23 | |
US18213862A | 1962-03-23 | 1962-03-23 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1014678A true GB1014678A (en) | 1965-12-31 |
Family
ID=26877781
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1003863A Expired GB1014678A (en) | 1962-03-23 | 1963-03-13 | Improvements in or relating to sizing compositions |
Country Status (4)
Country | Link |
---|---|
BE (1) | BE629956A (en) |
FR (1) | FR1369015A (en) |
GB (1) | GB1014678A (en) |
NL (1) | NL290563A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2021253083A1 (en) * | 2020-06-16 | 2021-12-23 | Essential Queensland Pty Ltd | Method of extraction |
CN116473291A (en) * | 2023-05-17 | 2023-07-25 | 江苏富乐华功率半导体研究院有限公司 | Temperature-controllable electronic cigarette heating plate and preparation method thereof |
-
0
- BE BE629956D patent/BE629956A/xx unknown
-
1963
- 1963-03-13 GB GB1003863A patent/GB1014678A/en not_active Expired
- 1963-03-22 NL NL290563A patent/NL290563A/xx unknown
- 1963-07-11 FR FR69043801D patent/FR1369015A/en not_active Expired
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2021253083A1 (en) * | 2020-06-16 | 2021-12-23 | Essential Queensland Pty Ltd | Method of extraction |
CN115956107A (en) * | 2020-06-16 | 2023-04-11 | 伊森提尔昆士兰股份有限公司 | Extraction method |
CN116473291A (en) * | 2023-05-17 | 2023-07-25 | 江苏富乐华功率半导体研究院有限公司 | Temperature-controllable electronic cigarette heating plate and preparation method thereof |
CN116473291B (en) * | 2023-05-17 | 2023-11-24 | 江苏富乐华功率半导体研究院有限公司 | Temperature-controllable electronic cigarette heating plate and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
BE629956A (en) | |
NL290563A (en) | 1965-06-10 |
FR1369015A (en) | 1964-08-07 |
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