GB1014651A - Process for optically brightening natural or synthetic polymeric materials - Google Patents
Process for optically brightening natural or synthetic polymeric materialsInfo
- Publication number
- GB1014651A GB1014651A GB40601/61A GB4060161A GB1014651A GB 1014651 A GB1014651 A GB 1014651A GB 40601/61 A GB40601/61 A GB 40601/61A GB 4060161 A GB4060161 A GB 4060161A GB 1014651 A GB1014651 A GB 1014651A
- Authority
- GB
- United Kingdom
- Prior art keywords
- ether
- acid
- hydroquinone
- alkyl
- dimethoxy
- 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
- 238000005282 brightening Methods 0.000 title abstract 3
- 239000000463 material Substances 0.000 title abstract 2
- 238000000034 method Methods 0.000 title 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 14
- 150000003839 salts Chemical class 0.000 abstract 6
- OHBQPCCCRFSCAX-UHFFFAOYSA-N 1,4-Dimethoxybenzene Chemical compound COC1=CC=C(OC)C=C1 OHBQPCCCRFSCAX-UHFFFAOYSA-N 0.000 abstract 5
- RSEBUVRVKCANEP-UHFFFAOYSA-N 2-pyrroline Chemical compound C1CC=CN1 RSEBUVRVKCANEP-UHFFFAOYSA-N 0.000 abstract 4
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 abstract 4
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 abstract 4
- 239000002253 acid Substances 0.000 abstract 4
- 239000002657 fibrous material Substances 0.000 abstract 4
- 125000000623 heterocyclic group Chemical group 0.000 abstract 4
- 229920000642 polymer Polymers 0.000 abstract 4
- 150000004065 2-pyrrolines Chemical class 0.000 abstract 3
- 125000003118 aryl group Chemical group 0.000 abstract 3
- 229910052799 carbon Inorganic materials 0.000 abstract 3
- 229920001577 copolymer Polymers 0.000 abstract 3
- 229920000728 polyester Polymers 0.000 abstract 3
- AGIQIOSHSMJYJP-UHFFFAOYSA-N 1,2,4-Trimethoxybenzene Chemical compound COC1=CC=C(OC)C(OC)=C1 AGIQIOSHSMJYJP-UHFFFAOYSA-N 0.000 abstract 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N 1,4-Benzenediol Natural products OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 abstract 2
- HSBNNRSSNZGGRE-UHFFFAOYSA-N 1-(2,5-dimethoxyphenyl)pyrrolidine-2,5-dione Chemical compound COC1=CC=C(OC)C(N2C(CCC2=O)=O)=C1 HSBNNRSSNZGGRE-UHFFFAOYSA-N 0.000 abstract 2
- REFDOIWRJDGBHY-UHFFFAOYSA-N 2-bromobenzene-1,4-diol Chemical group OC1=CC=C(O)C(Br)=C1 REFDOIWRJDGBHY-UHFFFAOYSA-N 0.000 abstract 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 2
- XOBKSJJDNFUZPF-UHFFFAOYSA-N Methoxyethane Chemical compound CCOC XOBKSJJDNFUZPF-UHFFFAOYSA-N 0.000 abstract 2
- 239000004952 Polyamide Substances 0.000 abstract 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 abstract 2
- 150000001241 acetals Chemical class 0.000 abstract 2
- 150000007513 acids Chemical class 0.000 abstract 2
- 125000005396 acrylic acid ester group Chemical group 0.000 abstract 2
- 125000005011 alkyl ether group Chemical group 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid group Chemical group C(C1=CC=CC=C1)(=O)O WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 abstract 2
- 239000004305 biphenyl Substances 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 238000006243 chemical reaction Methods 0.000 abstract 2
- 239000003795 chemical substances by application Substances 0.000 abstract 2
- AJPXTSMULZANCB-UHFFFAOYSA-N chlorohydroquinone Chemical compound OC1=CC=C(O)C(Cl)=C1 AJPXTSMULZANCB-UHFFFAOYSA-N 0.000 abstract 2
- 239000006185 dispersion Substances 0.000 abstract 2
- FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical compound CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 abstract 2
- 125000001033 ether group Chemical group 0.000 abstract 2
- 229910000042 hydrogen bromide Inorganic materials 0.000 abstract 2
- 229910000041 hydrogen chloride Inorganic materials 0.000 abstract 2
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 abstract 2
- 150000002825 nitriles Chemical class 0.000 abstract 2
- 229920002401 polyacrylamide Polymers 0.000 abstract 2
- 229920002647 polyamide Polymers 0.000 abstract 2
- 229920002635 polyurethane Polymers 0.000 abstract 2
- 239000004814 polyurethane Substances 0.000 abstract 2
- 229920001290 polyvinyl ester Polymers 0.000 abstract 2
- 239000000243 solution Substances 0.000 abstract 2
- 239000000126 substance Substances 0.000 abstract 2
- CNHDIAIOKMXOLK-UHFFFAOYSA-N toluquinol Chemical compound CC1=CC(O)=CC=C1O CNHDIAIOKMXOLK-UHFFFAOYSA-N 0.000 abstract 2
- 229920002554 vinyl polymer Polymers 0.000 abstract 2
- RHHDMTSHWRREPK-UHFFFAOYSA-N 1,2-dimethoxynaphthalene Chemical compound C1=CC=CC2=C(OC)C(OC)=CC=C21 RHHDMTSHWRREPK-UHFFFAOYSA-N 0.000 abstract 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 abstract 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 abstract 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract 1
- SEKUASJMKSQCOB-UHFFFAOYSA-N 2-fluoro-1,4-bis[(5-methyl-2-propan-2-ylcyclohexyl)oxy]benzene Chemical compound C1(CC(C(CC1)C(C)C)OC1=C(C=C(OC2CC(CCC2C(C)C)C)C=C1)F)C SEKUASJMKSQCOB-UHFFFAOYSA-N 0.000 abstract 1
- WNCYZVMZKSOPMU-UHFFFAOYSA-N 2-fluoro-1,4-dimethoxybenzene Chemical compound COC1=CC=C(OC)C(F)=C1 WNCYZVMZKSOPMU-UHFFFAOYSA-N 0.000 abstract 1
- ALVJDUNBMKMTDC-UHFFFAOYSA-N 2-tert-butyl-1,4-dimethoxybenzene Chemical compound COC1=CC=C(OC)C(C(C)(C)C)=C1 ALVJDUNBMKMTDC-UHFFFAOYSA-N 0.000 abstract 1
- 229920000742 Cotton Polymers 0.000 abstract 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical group OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract 1
- 239000005864 Sulphur Substances 0.000 abstract 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 abstract 1
- 239000012670 alkaline solution Substances 0.000 abstract 1
- 125000002877 alkyl aryl group Chemical group 0.000 abstract 1
- 235000010290 biphenyl Nutrition 0.000 abstract 1
- 238000004061 bleaching Methods 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 125000002843 carboxylic acid group Chemical group 0.000 abstract 1
- 229920002678 cellulose Polymers 0.000 abstract 1
- 229920002301 cellulose acetate Polymers 0.000 abstract 1
- 229920003086 cellulose ether Polymers 0.000 abstract 1
- 229910001919 chlorite Inorganic materials 0.000 abstract 1
- 229910052619 chlorite group Inorganic materials 0.000 abstract 1
- QBWCMBCROVPCKQ-UHFFFAOYSA-N chlorous acid Chemical compound OCl=O QBWCMBCROVPCKQ-UHFFFAOYSA-N 0.000 abstract 1
- 239000008199 coating composition Substances 0.000 abstract 1
- 238000001035 drying Methods 0.000 abstract 1
- 239000000975 dye Substances 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 150000002170 ethers Chemical class 0.000 abstract 1
- 239000004744 fabric Substances 0.000 abstract 1
- 150000002334 glycols Chemical class 0.000 abstract 1
- 230000002209 hydrophobic effect Effects 0.000 abstract 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 abstract 1
- 239000011976 maleic acid Substances 0.000 abstract 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- IGJFZAGCHTVPGA-UHFFFAOYSA-N methyl 2,3-dimethoxy-2,3-diphenylpropanoate Chemical compound COC(C(C(C1=CC=CC=C1)OC)(C1=CC=CC=C1)OC)=O IGJFZAGCHTVPGA-UHFFFAOYSA-N 0.000 abstract 1
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 abstract 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- 230000003647 oxidation Effects 0.000 abstract 1
- 238000007254 oxidation reaction Methods 0.000 abstract 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 abstract 1
- 229920002239 polyacrylonitrile Polymers 0.000 abstract 1
- ZVJHJDDKYZXRJI-UHFFFAOYSA-N pyrroline Natural products C1CC=NC1 ZVJHJDDKYZXRJI-UHFFFAOYSA-N 0.000 abstract 1
- 239000004627 regenerated cellulose Substances 0.000 abstract 1
- 229920005989 resin Polymers 0.000 abstract 1
- 239000011347 resin Substances 0.000 abstract 1
- 238000005507 spraying Methods 0.000 abstract 1
- 238000010025 steaming Methods 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical group OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 abstract 1
- 229920002994 synthetic fiber Polymers 0.000 abstract 1
- 239000002562 thickening agent Substances 0.000 abstract 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 abstract 1
- 229940005605 valeric acid Drugs 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06L—DRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
- D06L4/00—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs
- D06L4/60—Optical bleaching or brightening
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Coloring (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEF32533A DE1220380B (de) | 1960-11-12 | 1960-11-12 | Optische Aufheller fuer Fasern und flaechige Gebilde bzw. UEberzuege aus hochpolymeren Natur- und Kunststoffen |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1014651A true GB1014651A (en) | 1965-12-31 |
Family
ID=7094672
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB40601/61A Expired GB1014651A (en) | 1960-11-12 | 1961-11-13 | Process for optically brightening natural or synthetic polymeric materials |
Country Status (4)
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2210374A (en) * | 1987-09-24 | 1989-06-07 | Acushnet Co | Improvements in clear coats |
US5018742A (en) * | 1987-09-24 | 1991-05-28 | Acushnet Company | Golf ball clear coating with optical brighteners |
US5160536A (en) * | 1991-04-18 | 1992-11-03 | Acushnet Company | Printing ink for golf balls |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2785133A (en) * | 1954-03-26 | 1957-03-12 | Gen Aniline & Film Corp | Compositions for a method of whitening fine fabrics |
-
1960
- 1960-11-12 DE DEF32533A patent/DE1220380B/de active Pending
-
1961
- 1961-11-10 CH CH923662A patent/CH399406A/de unknown
- 1961-11-10 CH CH1304761A patent/CH380074A/de unknown
- 1961-11-13 GB GB40601/61A patent/GB1014651A/en not_active Expired
- 1961-11-13 BE BE610232A patent/BE610232A/fr unknown
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2210374A (en) * | 1987-09-24 | 1989-06-07 | Acushnet Co | Improvements in clear coats |
US4865326A (en) * | 1987-09-24 | 1989-09-12 | Acushnet Company | Optical brightners in golf ball clear coatings |
US5018742A (en) * | 1987-09-24 | 1991-05-28 | Acushnet Company | Golf ball clear coating with optical brighteners |
GB2210374B (en) * | 1987-09-24 | 1991-12-18 | Acushnet Co | Improvements in clear coats |
US5160536A (en) * | 1991-04-18 | 1992-11-03 | Acushnet Company | Printing ink for golf balls |
Also Published As
Publication number | Publication date |
---|---|
CH399406A (de) | 1965-09-30 |
DE1220380B (de) | 1966-07-07 |
CH1304761A4 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1964-04-15 |
BE610232A (fr) | 1962-05-14 |
CH380074A (de) | 1964-09-30 |
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