JPS59186602A - 気体分離膜 - Google Patents
気体分離膜Info
- Publication number
- JPS59186602A JPS59186602A JP6054183A JP6054183A JPS59186602A JP S59186602 A JPS59186602 A JP S59186602A JP 6054183 A JP6054183 A JP 6054183A JP 6054183 A JP6054183 A JP 6054183A JP S59186602 A JPS59186602 A JP S59186602A
- Authority
- JP
- Japan
- Prior art keywords
- group
- membrane
- gas separation
- separation membrane
- atom
- 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
- 239000012528 membrane Substances 0.000 title claims abstract description 40
- 238000000926 separation method Methods 0.000 title claims abstract description 26
- 239000007789 gas Substances 0.000 claims abstract description 35
- 239000003431 cross linking reagent Substances 0.000 claims abstract description 10
- 229920000642 polymer Polymers 0.000 claims abstract description 4
- -1 polysiloxane Polymers 0.000 claims description 18
- 229920001296 polysiloxane Polymers 0.000 claims description 14
- 150000003377 silicon compounds Chemical class 0.000 claims description 10
- 238000007259 addition reaction Methods 0.000 claims description 8
- 125000004429 atom Chemical group 0.000 claims description 7
- 125000000524 functional group Chemical group 0.000 claims description 7
- 125000005843 halogen group Chemical group 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- 125000002252 acyl group Chemical group 0.000 claims description 3
- 125000003277 amino group Chemical group 0.000 claims description 3
- 238000006482 condensation reaction Methods 0.000 claims description 3
- 229920000573 polyethylene Polymers 0.000 claims description 3
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 2
- 239000005977 Ethylene Substances 0.000 claims description 2
- 125000004423 acyloxy group Chemical group 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000003700 epoxy group Chemical group 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- 125000003396 thiol group Chemical group [H]S* 0.000 claims description 2
- 210000003608 fece Anatomy 0.000 claims 1
- 239000010871 livestock manure Substances 0.000 claims 1
- 239000002861 polymer material Substances 0.000 claims 1
- 238000000034 method Methods 0.000 abstract description 14
- 239000001257 hydrogen Substances 0.000 abstract description 9
- 229910052739 hydrogen Inorganic materials 0.000 abstract description 9
- 239000000463 material Substances 0.000 abstract description 8
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 abstract description 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract description 6
- 229910052710 silicon Inorganic materials 0.000 abstract description 5
- 239000010703 silicon Substances 0.000 abstract description 5
- 239000003054 catalyst Substances 0.000 abstract description 4
- 230000035699 permeability Effects 0.000 abstract description 3
- 229920001577 copolymer Polymers 0.000 abstract description 2
- LCHWKMAWSZDQRD-UHFFFAOYSA-N silylformonitrile Chemical class [SiH3]C#N LCHWKMAWSZDQRD-UHFFFAOYSA-N 0.000 abstract description 2
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 abstract 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 2
- 229920002589 poly(vinylethylene) polymer Polymers 0.000 abstract 1
- 210000004379 membrane Anatomy 0.000 description 24
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 16
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical group CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 13
- 238000004132 cross linking Methods 0.000 description 11
- 238000006243 chemical reaction Methods 0.000 description 9
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Natural products C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 9
- 229910052757 nitrogen Inorganic materials 0.000 description 8
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 6
- 239000010408 film Substances 0.000 description 6
- 239000007788 liquid Substances 0.000 description 5
- 239000003960 organic solvent Substances 0.000 description 5
- QQQSFSZALRVCSZ-UHFFFAOYSA-N triethoxysilane Chemical compound CCO[SiH](OCC)OCC QQQSFSZALRVCSZ-UHFFFAOYSA-N 0.000 description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 238000011084 recovery Methods 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 229910052734 helium Inorganic materials 0.000 description 3
- 239000001307 helium Substances 0.000 description 3
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 3
- 150000002431 hydrogen Chemical class 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 239000010409 thin film Substances 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000001569 carbon dioxide Substances 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- 229910002090 carbon oxide Inorganic materials 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 210000004744 fore-foot Anatomy 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 1
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 1
- YQUSJXPLZZZDGP-UHFFFAOYSA-N 1-chlorosilyl-N,N-dimethylmethanamine Chemical compound Cl[SiH2]CN(C)C YQUSJXPLZZZDGP-UHFFFAOYSA-N 0.000 description 1
- IGWSIIBEBKJTKR-UHFFFAOYSA-N 2,4,6,8-tetrachloro-1,3,5,7,2,4,6,8-tetraoxatetrasilocane Chemical compound Cl[SiH]1O[SiH](O[SiH](O[SiH](O1)Cl)Cl)Cl IGWSIIBEBKJTKR-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- 241000283986 Lepus Species 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- UBAZGMLMVVQSCD-UHFFFAOYSA-N carbon dioxide;molecular oxygen Chemical compound O=O.O=C=O UBAZGMLMVVQSCD-UHFFFAOYSA-N 0.000 description 1
- 239000007809 chemical reaction catalyst Substances 0.000 description 1
- QABCGOSYZHCPGN-UHFFFAOYSA-N chloro(dimethyl)silicon Chemical compound C[Si](C)Cl QABCGOSYZHCPGN-UHFFFAOYSA-N 0.000 description 1
- SMLBKDGWTWVRBJ-UHFFFAOYSA-N chloro-dimethylsilyl-dimethylsilane Chemical compound C[SiH](C)[Si](C)(C)Cl SMLBKDGWTWVRBJ-UHFFFAOYSA-N 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 239000000567 combustion gas Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000000994 depressogenic effect Effects 0.000 description 1
- AONDIGWFVXEZGD-UHFFFAOYSA-N diacetyloxy(methyl)silicon Chemical compound CC(=O)O[Si](C)OC(C)=O AONDIGWFVXEZGD-UHFFFAOYSA-N 0.000 description 1
- 239000012975 dibutyltin dilaurate Substances 0.000 description 1
- 229940117389 dichlorobenzene Drugs 0.000 description 1
- XJTUNBKAWATELL-UHFFFAOYSA-N dichloromethyl(trimethyl)silane Chemical compound C[Si](C)(C)C(Cl)Cl XJTUNBKAWATELL-UHFFFAOYSA-N 0.000 description 1
- KZFNONVXCZVHRD-UHFFFAOYSA-N dimethylamino(dimethyl)silicon Chemical compound CN(C)[Si](C)C KZFNONVXCZVHRD-UHFFFAOYSA-N 0.000 description 1
- NYMVBZHJSKIHQK-UHFFFAOYSA-N dimethylsilyl acetate Chemical compound C[SiH](C)OC(C)=O NYMVBZHJSKIHQK-UHFFFAOYSA-N 0.000 description 1
- BMQHZMYHVVHFOJ-UHFFFAOYSA-N dimethylsilylmethanethiol Chemical compound SC[SiH](C)C BMQHZMYHVVHFOJ-UHFFFAOYSA-N 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 210000002615 epidermis Anatomy 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- DRUOQOFQRYFQGB-UHFFFAOYSA-N ethoxy(dimethyl)silicon Chemical compound CCO[Si](C)C DRUOQOFQRYFQGB-UHFFFAOYSA-N 0.000 description 1
- ZZRGHKUNLAYDTC-UHFFFAOYSA-N ethoxy(methyl)silane Chemical compound CCO[SiH2]C ZZRGHKUNLAYDTC-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 239000012456 homogeneous solution Substances 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 238000006459 hydrosilylation reaction Methods 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 210000004224 pleura Anatomy 0.000 description 1
- 229920000779 poly(divinylbenzene) Polymers 0.000 description 1
- 229920000548 poly(silane) polymer Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 239000010948 rhodium Substances 0.000 description 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical compound [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 description 1
- UQMGAWUIVYDWBP-UHFFFAOYSA-N silyl acetate Chemical class CC(=O)O[SiH3] UQMGAWUIVYDWBP-UHFFFAOYSA-N 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical class [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- IBOKZQNMFSHYNQ-UHFFFAOYSA-N tribromosilane Chemical compound Br[SiH](Br)Br IBOKZQNMFSHYNQ-UHFFFAOYSA-N 0.000 description 1
- ZDHXKXAHOVTTAH-UHFFFAOYSA-N trichlorosilane Chemical compound Cl[SiH](Cl)Cl ZDHXKXAHOVTTAH-UHFFFAOYSA-N 0.000 description 1
- 239000005052 trichlorosilane Substances 0.000 description 1
- YUYCVXFAYWRXLS-UHFFFAOYSA-N trimethoxysilane Chemical compound CO[SiH](OC)OC YUYCVXFAYWRXLS-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Separation Using Semi-Permeable Membranes (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6054183A JPS59186602A (ja) | 1983-04-06 | 1983-04-06 | 気体分離膜 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6054183A JPS59186602A (ja) | 1983-04-06 | 1983-04-06 | 気体分離膜 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS59186602A true JPS59186602A (ja) | 1984-10-23 |
| JPH0536093B2 JPH0536093B2 (cg-RX-API-DMAC7.html) | 1993-05-28 |
Family
ID=13145251
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP6054183A Granted JPS59186602A (ja) | 1983-04-06 | 1983-04-06 | 気体分離膜 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS59186602A (cg-RX-API-DMAC7.html) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4950314A (en) * | 1986-08-14 | 1990-08-21 | Toray Industries Inc. | Gas separation membrane |
| WO2018139134A1 (ja) * | 2017-01-30 | 2018-08-02 | 信越化学工業株式会社 | 室温硬化性シラン含有樹脂組成物及び実装回路基板 |
| WO2019163330A1 (ja) * | 2018-02-20 | 2019-08-29 | 信越化学工業株式会社 | 有機ケイ素化合物、並びにそれを用いたゴム用配合剤およびゴム組成物 |
-
1983
- 1983-04-06 JP JP6054183A patent/JPS59186602A/ja active Granted
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4950314A (en) * | 1986-08-14 | 1990-08-21 | Toray Industries Inc. | Gas separation membrane |
| WO2018139134A1 (ja) * | 2017-01-30 | 2018-08-02 | 信越化学工業株式会社 | 室温硬化性シラン含有樹脂組成物及び実装回路基板 |
| CN110234697A (zh) * | 2017-01-30 | 2019-09-13 | 信越化学工业株式会社 | 室温固化性含硅烷的树脂组合物及安装电路基板 |
| JPWO2018139134A1 (ja) * | 2017-01-30 | 2019-11-07 | 信越化学工業株式会社 | 室温硬化性シラン含有樹脂組成物及び実装回路基板 |
| US11274225B2 (en) | 2017-01-30 | 2022-03-15 | Shin-Etsu Chemical Co., Ltd. | Room temperature-vulcanizing silane-containing resin composition and mounting circuit substrate |
| CN110234697B (zh) * | 2017-01-30 | 2022-11-18 | 信越化学工业株式会社 | 室温固化性含硅烷的树脂组合物及安装电路基板 |
| WO2019163330A1 (ja) * | 2018-02-20 | 2019-08-29 | 信越化学工業株式会社 | 有機ケイ素化合物、並びにそれを用いたゴム用配合剤およびゴム組成物 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0536093B2 (cg-RX-API-DMAC7.html) | 1993-05-28 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Gomes et al. | Membranes for gas separation based on poly (1-trimethylsilyl-1-propyne)–silica nanocomposites | |
| Corriu et al. | Hybrid silica gels containing 1, 3-butadiyne bridging units. Thermal and chemical reactivity of the organic fragment | |
| EP0927736B1 (en) | Silphenylene polymer and composition containing same | |
| JP2007051152A (ja) | 柔軟な有機及び堅い無機部分を含む化合物の前駆体及びその製造法 | |
| JPH1171519A (ja) | 親水性及び疎水性のナノスコピックドメインを有するデンドリマーに基づく網状構造物を含む組成物 | |
| Kurayama et al. | Facile method for preparing organic/inorganic hybrid capsules using amino-functional silane coupling agent in aqueous media | |
| Aguilar-Lugo et al. | Highly permeable mixed matrix membranes of thermally rearranged polymers and porous polymer networks for gas separations | |
| CN110267730A (zh) | 用于重烃回收的改性硅氧烷复合膜 | |
| JP2799217B2 (ja) | 含フッ素ジアミノベンゼン誘導体およびポリイミド | |
| JPS59186602A (ja) | 気体分離膜 | |
| CN102061095B (zh) | 一种含氟硅氧烷/硅橡胶杂化膜及其制备方法和应用 | |
| Matteucci et al. | Desilylation of substituted polyacetylenes by nanoparticles | |
| JPS6284126A (ja) | ポリ二置換アセチレン／ポリオルガノシロキサングラフト共重合体 | |
| Huertas et al. | Polyimide-silica sol–gel membranes from a novel alkoxysilane functionalized polyimide: preparation, characterization and gas separation properties | |
| Adachi et al. | Pinacol Boronate Ester-Containing Polysilsesquioxane Membranes for CO2 Separation | |
| Flipsen et al. | Densely crosslinked polycarbosiloxanes. I. Synthesis | |
| JP3609753B2 (ja) | ポリアルキレングリコールに置換された多価反応性ケイ素化合物及びその製造方法 | |
| Lim et al. | Effect of polyether diamine on gas permeation properties of organic-inorganic hybrid membranes | |
| Achtel et al. | Synthesis of Biopolymer‐Based Precursors for the Formation of Organic–Inorganic Hybrid Materials | |
| US5171794A (en) | Modified poly(2,6-dimethyl-p-oxyphenylene), a process for its preparation and its use in gas mixture separation membranes | |
| Nasr et al. | Functionalization of polymethylhydrosiloxane gels with an allyl ureido benzocrown ether derivative: complexation properties | |
| JPH0436317A (ja) | 無定形の変性ポリ−（２，６−ジメチル−ｐ−オキシフェニレン）の製法 | |
| Yur'evich et al. | Methods for the Preparation of Modified Polyorganosiloxanes (A Review). | |
| JPH01242123A (ja) | 気体分離膜 | |
| JP5504591B2 (ja) | 水酸基含有ブロック共重合体を含む成形体の製造方法、水酸基含有ブロック共重合体を含む成形体、及び水酸基含有ブロック共重合体 |