JPS61197615A - 新規な架橋性熱可逆高分子化合物の製造方法 - Google Patents
新規な架橋性熱可逆高分子化合物の製造方法Info
- Publication number
- JPS61197615A JPS61197615A JP3828885A JP3828885A JPS61197615A JP S61197615 A JPS61197615 A JP S61197615A JP 3828885 A JP3828885 A JP 3828885A JP 3828885 A JP3828885 A JP 3828885A JP S61197615 A JPS61197615 A JP S61197615A
- Authority
- JP
- Japan
- Prior art keywords
- polymer compound
- thermoreversible
- solution
- formula
- thermoreversible 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.)
- Granted
Links
- 229920000642 polymer Polymers 0.000 title claims abstract description 24
- 150000001875 compounds Chemical class 0.000 title claims abstract description 8
- 238000004519 manufacturing process Methods 0.000 title claims description 6
- CNCOEDDPFOAUMB-UHFFFAOYSA-N N-Methylolacrylamide Chemical compound OCNC(=O)C=C CNCOEDDPFOAUMB-UHFFFAOYSA-N 0.000 claims abstract description 9
- 238000007334 copolymerization reaction Methods 0.000 claims description 5
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract description 15
- 239000000463 material Substances 0.000 abstract description 8
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 abstract description 6
- RESPXSHDJQUNTN-UHFFFAOYSA-N 1-piperidin-1-ylprop-2-en-1-one Chemical compound C=CC(=O)N1CCCCC1 RESPXSHDJQUNTN-UHFFFAOYSA-N 0.000 abstract description 5
- 239000012528 membrane Substances 0.000 abstract description 4
- 238000000926 separation method Methods 0.000 abstract description 4
- 239000003463 adsorbent Substances 0.000 abstract description 3
- 239000000203 mixture Substances 0.000 abstract description 3
- 238000000465 moulding Methods 0.000 abstract description 3
- 239000002904 solvent Substances 0.000 abstract description 2
- YPHQUSNPXDGUHL-UHFFFAOYSA-N n-methylprop-2-enamide Chemical compound CNC(=O)C=C YPHQUSNPXDGUHL-UHFFFAOYSA-N 0.000 abstract 1
- 238000012216 screening Methods 0.000 abstract 1
- 229920001577 copolymer Polymers 0.000 description 14
- 230000007704 transition Effects 0.000 description 11
- 238000004132 cross linking Methods 0.000 description 9
- 238000000034 method Methods 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- 239000007864 aqueous solution Substances 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 6
- 239000000047 product Substances 0.000 description 4
- 230000035484 reaction time Effects 0.000 description 4
- 238000002834 transmittance Methods 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- 230000035945 sensitivity Effects 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 239000012429 reaction media Substances 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- 229920003169 water-soluble polymer Polymers 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- 239000004809 Teflon Substances 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- AJFDBNQQDYLMJN-UHFFFAOYSA-N n,n-diethylacetamide Chemical compound CCN(CC)C(C)=O AJFDBNQQDYLMJN-UHFFFAOYSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 239000007870 radical polymerization initiator Substances 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 230000029058 respiratory gaseous exchange Effects 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 238000002166 wet spinning Methods 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 |
|---|---|---|---|
| JP3828885A JPS61197615A (ja) | 1985-02-27 | 1985-02-27 | 新規な架橋性熱可逆高分子化合物の製造方法 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3828885A JPS61197615A (ja) | 1985-02-27 | 1985-02-27 | 新規な架橋性熱可逆高分子化合物の製造方法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS61197615A true JPS61197615A (ja) | 1986-09-01 |
| JPS635407B2 JPS635407B2 (enrdf_load_stackoverflow) | 1988-02-03 |
Family
ID=12521121
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP3828885A Granted JPS61197615A (ja) | 1985-02-27 | 1985-02-27 | 新規な架橋性熱可逆高分子化合物の製造方法 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS61197615A (enrdf_load_stackoverflow) |
-
1985
- 1985-02-27 JP JP3828885A patent/JPS61197615A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS635407B2 (enrdf_load_stackoverflow) | 1988-02-03 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Barsbay et al. | Verification of controlled grafting of styrene from cellulose via radiation-induced RAFT polymerization | |
| Nasef et al. | Radiation‐induced grafting of styrene onto poly (tetrafluoroethylene)(PTFE) films. I. Effect of grafting conditions and properties of the grafted films | |
| Gupta et al. | Crosslinked ion exchange membranes by radiation grafting of styrene/divinylbenzene into FEP films | |
| Singh et al. | Radiation‐induced grafting of N, N′‐dimethylaminoethylmethacrylate onto chitosan films | |
| Abd El-Mohdy et al. | Synthesis, characterization and properties of radiation-induced Starch/(EG-co-MAA) hydrogels | |
| JPH05331244A (ja) | 熱可逆性グラフト共重合体 | |
| SE448544B (sv) | Vattenabsorberande komposition och anvendning derav som berare for ett lekemedel | |
| Veen et al. | Photoregulation of polymer conformation by photochromic moieties–II. Cationic and neutral moieties on an anionic polymer | |
| CN103657448B (zh) | 一种阴离子交换膜的制备方法 | |
| US3634366A (en) | Polymerizing method | |
| Kminek et al. | A water-soluble poly (methylphenylsilylene) derivative as a photoinitiator of radical polymerization of hydrophilic vinyl monomers | |
| EP4092057A1 (en) | Thermosensitive fine particles | |
| Biswas et al. | Synthesis and characterization of stereoregular poly (N-ethylacrylamide) hydrogel by using Y (OTf) 3 Lewis acid | |
| JPS61197615A (ja) | 新規な架橋性熱可逆高分子化合物の製造方法 | |
| Xiang et al. | Preparation and characterization of alkali soluble polyacrylamide-g-polyaniline | |
| JPS6166707A (ja) | 新規アクリルアミド系共重合体及びその製造方法 | |
| JP2610089B2 (ja) | （メタ）アクリル酸（塩）系重合体の製造方法 | |
| RU2012147466A (ru) | Полиолефиновая композиция и способ ее изготовления | |
| Kamath et al. | Interpenetrating polymer networks of photocrosslinkable cellulose derivatives | |
| Paris et al. | Swelling and hydrolytic degradation behaviour of pH‐responsive hydrogels of poly [(N‐isopropylacrylamide)‐co‐(methacrylic acid)] crosslinked by biodegradable polycaprolactone chains | |
| JPS635411B2 (enrdf_load_stackoverflow) | ||
| Zhu et al. | Fabrication of LDPE/PS interpolymer resin particles through a swelling suspension polymerization approach | |
| US3813354A (en) | Copolymers of alkenylsulfonates and cation permoselective membranes based thereon | |
| Kaur et al. | Viscometric, conductometric, and ultrasonic studies of gelatin‐g‐polyacrylamide composite | |
| US3634370A (en) | Acrylonitrile polymerization in the presence of sulfuric acid followed by a neutralization step |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EXPY | Cancellation because of completion of term |