JPS6355527B2 - - Google Patents
Info
- Publication number
- JPS6355527B2 JPS6355527B2 JP60067735A JP6773585A JPS6355527B2 JP S6355527 B2 JPS6355527 B2 JP S6355527B2 JP 60067735 A JP60067735 A JP 60067735A JP 6773585 A JP6773585 A JP 6773585A JP S6355527 B2 JPS6355527 B2 JP S6355527B2
- Authority
- JP
- Japan
- Prior art keywords
- temperature
- polymer
- group
- poly
- formula
- 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
- 229920000642 polymer Polymers 0.000 claims description 23
- -1 vinyl compound Chemical class 0.000 claims description 20
- 229920002554 vinyl polymer Polymers 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 238000006116 polymerization reaction Methods 0.000 claims description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 15
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
- 238000000034 method Methods 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 229920002401 polyacrylamide Polymers 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- 230000007704 transition Effects 0.000 description 8
- 239000007864 aqueous solution Substances 0.000 description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- 239000000126 substance Substances 0.000 description 5
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 238000002834 transmittance Methods 0.000 description 4
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- NIHIVAISWHSKJZ-UHFFFAOYSA-N n-(3-ethoxypropyl)prop-2-enamide Chemical compound CCOCCCNC(=O)C=C NIHIVAISWHSKJZ-UHFFFAOYSA-N 0.000 description 3
- 238000010526 radical polymerization reaction Methods 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- HFBMWMNUJJDEQZ-UHFFFAOYSA-N acryloyl chloride Chemical compound ClC(=O)C=C HFBMWMNUJJDEQZ-UHFFFAOYSA-N 0.000 description 2
- 239000003463 adsorbent Substances 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000002209 hydrophobic effect Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000012528 membrane Substances 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- NGAATTKZMMWOBW-UHFFFAOYSA-N n-(3-ethoxypropyl)-2-methylprop-2-enamide Chemical compound CCOCCCNC(=O)C(C)=C NGAATTKZMMWOBW-UHFFFAOYSA-N 0.000 description 2
- VLZIDNWNQPRLFU-UHFFFAOYSA-N n-(3-propan-2-yloxypropyl)prop-2-enamide Chemical compound CC(C)OCCCNC(=O)C=C VLZIDNWNQPRLFU-UHFFFAOYSA-N 0.000 description 2
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 2
- 239000003505 polymerization initiator Substances 0.000 description 2
- 239000000700 radioactive tracer Substances 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- NTBSOSCZKLTOPF-UHFFFAOYSA-N 2-methyl-n-(3-propan-2-yloxypropyl)prop-2-enamide Chemical compound CC(C)OCCCNC(=O)C(C)=C NTBSOSCZKLTOPF-UHFFFAOYSA-N 0.000 description 1
- OLJBAHAQNWCHLV-UHFFFAOYSA-N 2-methyl-n-propan-2-yloxyprop-2-enamide Chemical compound CC(C)ONC(=O)C(C)=C OLJBAHAQNWCHLV-UHFFFAOYSA-N 0.000 description 1
- SOYBEXQHNURCGE-UHFFFAOYSA-N 3-ethoxypropan-1-amine Chemical compound CCOCCCN SOYBEXQHNURCGE-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 238000000862 absorption spectrum Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000003708 ampul Substances 0.000 description 1
- SLUNEGLMXGHOLY-UHFFFAOYSA-N benzene;hexane Chemical compound CCCCCC.C1=CC=CC=C1 SLUNEGLMXGHOLY-UHFFFAOYSA-N 0.000 description 1
- 238000012662 bulk polymerization Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000005034 decoration Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000001938 differential scanning calorimetry curve Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 239000000017 hydrogel Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- 125000003253 isopropoxy group Chemical group [H]C([H])([H])C([H])(O*)C([H])([H])[H] 0.000 description 1
- 238000001819 mass spectrum Methods 0.000 description 1
- VHRYZQNGTZXDNX-UHFFFAOYSA-N methacryloyl chloride Chemical compound CC(=C)C(Cl)=O VHRYZQNGTZXDNX-UHFFFAOYSA-N 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 239000003094 microcapsule Substances 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- RZJSNANAVOHGIY-UHFFFAOYSA-N n-(3-butoxypropyl)prop-2-enamide Chemical compound CCCCOCCCNC(=O)C=C RZJSNANAVOHGIY-UHFFFAOYSA-N 0.000 description 1
- ZEMHQYNMVKDBFJ-UHFFFAOYSA-N n-(3-hydroxypropyl)prop-2-enamide Chemical compound OCCCNC(=O)C=C ZEMHQYNMVKDBFJ-UHFFFAOYSA-N 0.000 description 1
- MNYSIPJUZUJRML-UHFFFAOYSA-N n-[3-(2-methylpropoxy)propyl]prop-2-enamide Chemical compound CC(C)COCCCNC(=O)C=C MNYSIPJUZUJRML-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000003504 photosensitizing agent Substances 0.000 description 1
- 229920003213 poly(N-isopropyl acrylamide) Polymers 0.000 description 1
- 229920002432 poly(vinyl methyl ether) polymer Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 239000007870 radical polymerization initiator Substances 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
Landscapes
- Separation Using Semi-Permeable Membranes (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6773585A JPS61225203A (ja) | 1985-03-29 | 1985-03-29 | 親水性−疎水性熱可逆型重合体及びその製造方法 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6773585A JPS61225203A (ja) | 1985-03-29 | 1985-03-29 | 親水性−疎水性熱可逆型重合体及びその製造方法 |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62314822A Division JPH066660B2 (ja) | 1987-12-11 | 1987-12-11 | 親水性−疎水性熱可逆材料 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS61225203A JPS61225203A (ja) | 1986-10-07 |
JPS6355527B2 true JPS6355527B2 (xx) | 1988-11-02 |
Family
ID=13353506
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP6773585A Granted JPS61225203A (ja) | 1985-03-29 | 1985-03-29 | 親水性−疎水性熱可逆型重合体及びその製造方法 |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS61225203A (xx) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5377042A (en) * | 1986-12-31 | 1994-12-27 | Chahroudi; Day | Structure and preparation of automatic light valves |
JPH066610B2 (ja) * | 1987-05-13 | 1994-01-26 | 工業技術院長 | 親水性―疎水性熱可逆型高分子材料及びその製造方法 |
JPH066611B2 (ja) * | 1987-05-27 | 1994-01-26 | 工業技術院長 | 親水性−疎水性熱可逆型高分子化合物及びその製造方法 |
JPH0618970B2 (ja) * | 1987-07-02 | 1994-03-16 | 工業技術院長 | 親水性―疎水性熱可逆型材料 |
US5404245A (en) * | 1989-11-28 | 1995-04-04 | Chahroudi; Day | Automatic light valves with polymeric layer containing network of bonds |
JPH0826295B2 (ja) * | 1992-09-16 | 1996-03-13 | エステー化学株式会社 | 揮散抑制剤 |
EP0692506A3 (en) | 1994-07-14 | 1996-04-10 | Miyoshi Yushi Kk | Heat sensitive polyether polyurethane, method of preparation and heat sensitive composition |
CN103215988B (zh) * | 2013-04-22 | 2015-01-21 | 胡明建 | 一种温差相变空气取水并用于栽培的方法 |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3421893A (en) * | 1967-05-26 | 1969-01-14 | Polaroid Corp | Acrylic polymer spacer layers for photographic elements |
-
1985
- 1985-03-29 JP JP6773585A patent/JPS61225203A/ja active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3421893A (en) * | 1967-05-26 | 1969-01-14 | Polaroid Corp | Acrylic polymer spacer layers for photographic elements |
Also Published As
Publication number | Publication date |
---|---|
JPS61225203A (ja) | 1986-10-07 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
EXPY | Cancellation because of completion of term |