JPH03402B2 - - Google Patents
Info
- Publication number
- JPH03402B2 JPH03402B2 JP16402384A JP16402384A JPH03402B2 JP H03402 B2 JPH03402 B2 JP H03402B2 JP 16402384 A JP16402384 A JP 16402384A JP 16402384 A JP16402384 A JP 16402384A JP H03402 B2 JPH03402 B2 JP H03402B2
- Authority
- JP
- Japan
- Prior art keywords
- alkylated
- polyvinyl alcohol
- polyvinyl acetal
- cyclohexanecarbaldehyde
- polyvinyl
- 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
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 20
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 19
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 claims description 14
- 125000001931 aliphatic group Chemical group 0.000 claims description 13
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 claims description 7
- 150000001875 compounds Chemical class 0.000 claims description 7
- 238000006482 condensation reaction Methods 0.000 claims description 7
- KVFDZFBHBWTVID-UHFFFAOYSA-N cyclohexanecarbaldehyde Chemical class O=CC1CCCCC1 KVFDZFBHBWTVID-UHFFFAOYSA-N 0.000 claims description 7
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 claims description 7
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 150000003934 aromatic aldehydes Chemical class 0.000 claims description 4
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 description 32
- 229920002554 vinyl polymer Polymers 0.000 description 32
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 29
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- 230000009102 absorption Effects 0.000 description 12
- 238000010521 absorption reaction Methods 0.000 description 12
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N Butyraldehyde Chemical compound CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 6
- 230000009477 glass transition Effects 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 230000003287 optical effect Effects 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 4
- 230000000704 physical effect Effects 0.000 description 4
- 238000001556 precipitation Methods 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 238000007127 saponification reaction Methods 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical group OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 3
- 238000006359 acetalization reaction Methods 0.000 description 3
- 150000001299 aldehydes Chemical class 0.000 description 3
- 238000012790 confirmation Methods 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 3
- 239000004417 polycarbonate Substances 0.000 description 3
- 229920000515 polycarbonate Polymers 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 239000004926 polymethyl methacrylate Substances 0.000 description 3
- 238000002834 transmittance Methods 0.000 description 3
- HGBOYTHUEUWSSQ-UHFFFAOYSA-N valeric aldehyde Natural products CCCCC=O HGBOYTHUEUWSSQ-UHFFFAOYSA-N 0.000 description 3
- FXZFFVCJWZTTMX-UHFFFAOYSA-N 1-methylcyclohexane-1-carbaldehyde Chemical compound O=CC1(C)CCCCC1 FXZFFVCJWZTTMX-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical group CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000011978 dissolution method Methods 0.000 description 2
- 235000019441 ethanol Nutrition 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 2
- 238000006386 neutralization reaction Methods 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- -1 polyvinyl formal Chemical class 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 229920003002 synthetic resin Polymers 0.000 description 2
- 239000000057 synthetic resin Substances 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- UAEPNZWRGJTJPN-UHFFFAOYSA-N Methylcyclohexane Natural products CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 description 1
- 238000000862 absorption spectrum Methods 0.000 description 1
- IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 150000001934 cyclohexanes Chemical class 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP16402384A JPS6142507A (ja) | 1984-08-03 | 1984-08-03 | アルキル化シクロヘキサンカルボアルデヒド−アセタ−ル化ポリビニルアルコ−ル |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP16402384A JPS6142507A (ja) | 1984-08-03 | 1984-08-03 | アルキル化シクロヘキサンカルボアルデヒド−アセタ−ル化ポリビニルアルコ−ル |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6142507A JPS6142507A (ja) | 1986-03-01 |
| JPH03402B2 true JPH03402B2 (enrdf_load_stackoverflow) | 1991-01-08 |
Family
ID=15785321
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP16402384A Granted JPS6142507A (ja) | 1984-08-03 | 1984-08-03 | アルキル化シクロヘキサンカルボアルデヒド−アセタ−ル化ポリビニルアルコ−ル |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6142507A (enrdf_load_stackoverflow) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20210060987A (ko) * | 2019-11-19 | 2021-05-27 | 농업회사법인 (주)생극양조 | 논 수위알림 장치 |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62141004A (ja) * | 1985-12-13 | 1987-06-24 | Sekisui Chem Co Ltd | シクロヘキサンカルボアルデヒド及びアルキル化シクロヘキサンカルボアルデヒド−アセタ−ル化ポリビニルアルコ−ル |
| WO2000003303A1 (fr) * | 1998-07-10 | 2000-01-20 | Clariant International Ltd. | Composition pour film empechant la reflexion de fond et nouveau colorant polymere utilise dans celle-ci |
| JP2006022160A (ja) * | 2004-07-06 | 2006-01-26 | Sekisui Chem Co Ltd | 変性ポリビニルアルコール |
| JP3802544B2 (ja) * | 2004-07-29 | 2006-07-26 | 日東電工株式会社 | 位相差板、及び新規ポリマー、及び光学フィルム、及び画像表示装置 |
| JP4828347B2 (ja) * | 2006-08-01 | 2011-11-30 | 株式会社クラレ | ポリビニルアセタール樹脂 |
-
1984
- 1984-08-03 JP JP16402384A patent/JPS6142507A/ja active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20210060987A (ko) * | 2019-11-19 | 2021-05-27 | 농업회사법인 (주)생극양조 | 논 수위알림 장치 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6142507A (ja) | 1986-03-01 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP4963331B2 (ja) | 官能化ポリアリルアミン及びその製造方法 | |
| US4611061A (en) | 2'-hydroxy-5'-(hydroxyalkyl)phenyl-2H-benzotriazoles | |
| US4889948A (en) | Acrylate ester ether derivatives | |
| US2945006A (en) | Reaction products of carbonyl containing polymers and aminoguanidine that are usefulas mordants | |
| JPH03402B2 (enrdf_load_stackoverflow) | ||
| JP2509622B2 (ja) | アダマンチルジアクリレ―トもしくはジメタクリレ―ト誘導体 | |
| JP2828699B2 (ja) | 高分子化合物及びそれよりなる光学成形品 | |
| JPS60255805A (ja) | シクロヘキサンカルボアルデヒド−アセタ−ル化ポリビニルアルコ−ル | |
| KR100191126B1 (ko) | 비닐4-t-부톡시카르보닐옥시벤잘-비닐 알코올-비닐 아세테이트 공중합체와 비닐 4-t-부톡시카르보닐옥시벤잘-비닐 4-히드록시벤잘-비닐 알코올-비닐 아세테이트 공중합체 및 그들의 제조방법 | |
| AU757140B2 (en) | Brominated materials | |
| US5847063A (en) | Resins for use in chemically amplified resists and manufacturing methods thereof | |
| JPS62141003A (ja) | 不飽和環カルボアルデヒド−アセタ−ル化ポリビニルアルコ−ル | |
| JP2868844B2 (ja) | ビニルフェニル化合物及びその製造方法 | |
| US2384124A (en) | Unsaturated esters and polymers thereof | |
| Nagase et al. | Control of thermal, mechanical, and optical properties of three‐component maleimide copolymers by steric bulkiness and hydrogen bonding | |
| JPS62141004A (ja) | シクロヘキサンカルボアルデヒド及びアルキル化シクロヘキサンカルボアルデヒド−アセタ−ル化ポリビニルアルコ−ル | |
| EP0302516B1 (en) | Optical article made of amorphous thermoplastic polyester resin | |
| US4999410A (en) | Acrylate ester ether derivatives | |
| JPH06805B2 (ja) | 高重合度ポリビニルアルコ−ルの製造法 | |
| JPS5867702A (ja) | 光不溶化性ポリビニルアルコ−ル誘導体の製造方法 | |
| JP2563267B2 (ja) | 多環式アルキル（メタ）アクリレ−トとその製造方法 | |
| JPH0318259B2 (enrdf_load_stackoverflow) | ||
| JPS60197670A (ja) | 新規１，３―ジオキソラン誘導体化合物 | |
| JPH0559115A (ja) | 高シンジオタクテイツクポリビニルアルコール系重合体の製造方法 | |
| US3776888A (en) | Carboxy poly(vinyl benzal)resins |