JPWO2021201227A5 - - Google Patents
Download PDFInfo
- Publication number
- JPWO2021201227A5 JPWO2021201227A5 JP2022512702A JP2022512702A JPWO2021201227A5 JP WO2021201227 A5 JPWO2021201227 A5 JP WO2021201227A5 JP 2022512702 A JP2022512702 A JP 2022512702A JP 2022512702 A JP2022512702 A JP 2022512702A JP WO2021201227 A5 JPWO2021201227 A5 JP WO2021201227A5
- Authority
- JP
- Japan
- Prior art keywords
- properties
- polycarbonate resins
- polymer
- present
- ratio
- 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
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- 229920005668 polycarbonate resin Polymers 0.000 description 6
- 239000004431 polycarbonate resin Substances 0.000 description 6
- 239000004417 polycarbonate Substances 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 125000005439 maleimidyl group Chemical group C1(C=CC(N1*)=O)=O 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 108091008695 photoreceptors Proteins 0.000 description 3
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 2
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 2
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 2
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 238000007334 copolymerization reaction Methods 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- BGTOWKSIORTVQH-UHFFFAOYSA-N cyclopentanone Chemical compound O=C1CCCC1 BGTOWKSIORTVQH-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 150000004292 cyclic ethers Chemical class 0.000 description 1
- 150000003997 cyclic ketones Chemical class 0.000 description 1
- CGZZMOTZOONQIA-UHFFFAOYSA-N cycloheptanone Chemical compound O=C1CCCCCC1 CGZZMOTZOONQIA-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 231100000206 health hazard Toxicity 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- GJRQTCIYDGXPES-UHFFFAOYSA-N iso-butyl acetate Natural products CC(C)COC(C)=O GJRQTCIYDGXPES-UHFFFAOYSA-N 0.000 description 1
- FGKJLKRYENPLQH-UHFFFAOYSA-M isocaproate Chemical compound CC(C)CCC([O-])=O FGKJLKRYENPLQH-UHFFFAOYSA-M 0.000 description 1
- JMMWKPVZQRWMSS-UHFFFAOYSA-N isopropanol acetate Natural products CC(C)OC(C)=O JMMWKPVZQRWMSS-UHFFFAOYSA-N 0.000 description 1
- 229940011051 isopropyl acetate Drugs 0.000 description 1
- GWYFCOCPABKNJV-UHFFFAOYSA-N isovaleric acid Chemical compound CC(C)CC(O)=O GWYFCOCPABKNJV-UHFFFAOYSA-N 0.000 description 1
- OQAGVSWESNCJJT-UHFFFAOYSA-N isovaleric acid methyl ester Natural products COC(=O)CC(C)C OQAGVSWESNCJJT-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000004973 liquid crystal related substance Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2020066230 | 2020-04-01 | ||
| JP2020066230 | 2020-04-01 | ||
| PCT/JP2021/014163 WO2021201227A1 (ja) | 2020-04-01 | 2021-04-01 | 樹脂、樹脂前駆体組成物、塗液組成物、電子写真感光体、電子写真感光体の製造方法、成形物および電子デバイス |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JPWO2021201227A1 JPWO2021201227A1 (https=) | 2021-10-07 |
| JPWO2021201227A5 true JPWO2021201227A5 (https=) | 2023-08-14 |
| JP7562642B2 JP7562642B2 (ja) | 2024-10-07 |
Family
ID=77928127
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2022512702A Active JP7562642B2 (ja) | 2020-04-01 | 2021-04-01 | 樹脂、樹脂前駆体組成物、塗液組成物、電子写真感光体、電子写真感光体の製造方法、成形物および電子デバイス |
Country Status (5)
| Country | Link |
|---|---|
| JP (1) | JP7562642B2 (https=) |
| KR (1) | KR102770547B1 (https=) |
| CN (1) | CN115427479B (https=) |
| TW (1) | TWI879934B (https=) |
| WO (1) | WO2021201227A1 (https=) |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3435003A (en) | 1966-06-01 | 1969-03-25 | Du Pont | Cross-linked thermally reversible polymers produced from condensation polymers with pendant furan groups cross-linked with maleimides |
| DE3443091A1 (de) * | 1984-11-27 | 1986-05-28 | Bayer Ag, 5090 Leverkusen | Polycarbonate mit dimethylmaleinimid-endgruppen, gegebenenfalls im gemisch mit bekannten aromatischen polycarbonaten, ihre herstellung und modifizierung |
| EP0357110A1 (en) * | 1988-08-05 | 1990-03-07 | Akzo N.V. | Two component coating curable at ambient temperature via a Diels-Alder reaction |
| JPH0751625B2 (ja) * | 1989-03-08 | 1995-06-05 | 旭化成工業株式会社 | 末端官能化ポリフェニレンエーテル樹脂およびこれを用いた硬化性樹脂組成物 |
| JPH04117458A (ja) * | 1990-09-07 | 1992-04-17 | Sumitomo Bakelite Co Ltd | 半導体封止用樹脂組成物 |
| JP3201485B2 (ja) * | 1991-06-13 | 2001-08-20 | 住友ベークライト株式会社 | 半導体封止用樹脂組成物 |
| JP3081705B2 (ja) * | 1992-05-15 | 2000-08-28 | 株式会社リコー | 電子写真感光体 |
| US5495051A (en) * | 1994-08-22 | 1996-02-27 | Shell Oil Company | Phenolic allyl ethers |
| JP3786741B2 (ja) | 1996-05-28 | 2006-06-14 | 出光興産株式会社 | 電子写真感光体 |
| JP3584128B2 (ja) | 1996-08-30 | 2004-11-04 | 出光興産株式会社 | ポリカーボネート樹脂及びその製造方法 |
| JP4041591B2 (ja) | 1998-07-30 | 2008-01-30 | 出光興産株式会社 | 架橋ポリカーボネート樹脂組成物とそれを用いた吸収剤およびカラム充填剤 |
| JP2003286347A (ja) * | 2002-03-28 | 2003-10-10 | Toray Ind Inc | 鎖状熱可塑性樹脂およびその製造方法 |
| US7390857B2 (en) * | 2004-08-27 | 2008-06-24 | General Electric Company | Crosslinkable and crosslinked polymers |
| JP5214856B2 (ja) | 2006-05-29 | 2013-06-19 | 帝人化成株式会社 | 架橋ポリカーボネート樹脂組成物及びフィルム |
| JP5392531B2 (ja) | 2008-09-16 | 2014-01-22 | 株式会社リコー | 電子写真感光体、及びそれを用いた電子写真方法、電子写真装置、電子写真装置用プロセスカートリッジ |
| WO2019188330A1 (ja) * | 2018-03-29 | 2019-10-03 | Dic株式会社 | 硬化性組成物及びその硬化物 |
-
2021
- 2021-04-01 CN CN202180025308.XA patent/CN115427479B/zh active Active
- 2021-04-01 WO PCT/JP2021/014163 patent/WO2021201227A1/ja not_active Ceased
- 2021-04-01 KR KR1020227036080A patent/KR102770547B1/ko active Active
- 2021-04-01 TW TW110112195A patent/TWI879934B/zh active
- 2021-04-01 JP JP2022512702A patent/JP7562642B2/ja active Active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CA2974046C (en) | Intermediate transfer members | |
| US20180273685A1 (en) | Novel polysulfone amide compound, and resin composition containing same | |
| US6096850A (en) | Polyimides, process for producing the same and photosensitive composition containing the same | |
| JPWO2021201228A5 (https=) | ||
| JP2013091790A (ja) | コーティング組成物 | |
| US10971686B2 (en) | Organic semiconductor element, polymer, organic semiconductor composition, and organic semiconductor film | |
| JPWO2021201227A5 (https=) | ||
| JP2018164030A (ja) | 有機半導体素子、有機半導体組成物、有機半導体膜の製造方法、有機半導体膜、及びこれらに用いるポリマー | |
| JPS54141896A (en) | Photoconductive polymeric material | |
| US11081651B2 (en) | Organic semiconductor element, organic semiconductor composition, method of manufacturing organic semiconductor film, organic semiconductor film, and compound and polymer using the same | |
| JP6754126B2 (ja) | 有機半導体素子、有機半導体組成物、有機半導体膜の製造方法、有機半導体膜、並びに、これらに用いる化合物及びポリマー | |
| JP2012102236A (ja) | エレクトレット材料用重合体組成物 | |
| US3673155A (en) | Bis(organosilyl)hydrocarbon modified polyamides and methods for making them | |
| TWI761480B (zh) | 有機半導體元件、有機半導體組成物、有機半導體膜的製造方法、有機半導體膜、以及用於其的化合物及聚合物 | |
| TWI646150B (zh) | 感光樹脂組成物、感光樹脂及電子裝置 | |
| WO2018097496A2 (ko) | 화합물 | |
| JP6328790B2 (ja) | 有機半導体素子及び化合物 | |
| JPS6355562A (ja) | 電子写真感光体 | |
| JP2001335634A (ja) | 架橋性ポリイミド、架橋性ポリイミド塗料及び耐溶剤性ポリイミドフィルム | |
| JPS55111949A (en) | Electrophotographic material and manufacture thereof | |
| US9527224B2 (en) | Endless flexible members with a polymeric release agent for imaging devices | |
| JP2713056B2 (ja) | ポリイミド樹脂及びその製造方法 | |
| JPS5640837A (en) | Manufacture of electrophotographic receptor | |
| JPH0431404A (ja) | ヒドラゾン基を側鎖に有するスチレン系共重合体とその製造方法およびそれを用いた電子写真感光体 | |
| JP2002351172A (ja) | 半導電性シームレスベルト |