CN117209771A - 一种含氟有机硅聚合物的制备方法及其应用 - Google Patents
一种含氟有机硅聚合物的制备方法及其应用 Download PDFInfo
- Publication number
- CN117209771A CN117209771A CN202311182886.1A CN202311182886A CN117209771A CN 117209771 A CN117209771 A CN 117209771A CN 202311182886 A CN202311182886 A CN 202311182886A CN 117209771 A CN117209771 A CN 117209771A
- Authority
- CN
- China
- Prior art keywords
- chch
- fluorine
- hydrogen
- silicone oil
- carbon
- 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.)
- Pending
Links
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 title claims abstract description 46
- 239000011737 fluorine Substances 0.000 title claims abstract description 46
- 229910052731 fluorine Inorganic materials 0.000 title claims abstract description 46
- 229920001558 organosilicon polymer Polymers 0.000 title claims abstract description 21
- 238000002360 preparation method Methods 0.000 title claims abstract description 19
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 49
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 49
- 239000001257 hydrogen Substances 0.000 claims abstract description 49
- 239000003054 catalyst Substances 0.000 claims abstract description 36
- 229920002545 silicone oil Polymers 0.000 claims abstract description 36
- 238000006243 chemical reaction Methods 0.000 claims abstract description 23
- 239000011203 carbon fibre reinforced carbon Substances 0.000 claims abstract description 14
- 239000000178 monomer Substances 0.000 claims abstract description 13
- 238000000034 method Methods 0.000 claims abstract description 12
- 229910000510 noble metal Inorganic materials 0.000 claims abstract description 11
- GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 claims description 39
- 101150065749 Churc1 gene Proteins 0.000 claims description 39
- 102100038239 Protein Churchill Human genes 0.000 claims description 39
- -1 amino, carboxyl Chemical group 0.000 claims description 23
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Natural products CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 20
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 18
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 12
- 239000000243 solution Substances 0.000 claims description 12
- 239000011259 mixed solution Substances 0.000 claims description 10
- 238000000576 coating method Methods 0.000 claims description 9
- 239000011248 coating agent Substances 0.000 claims description 8
- 229920000642 polymer Polymers 0.000 claims description 7
- 239000010948 rhodium Substances 0.000 claims description 6
- 238000002156 mixing Methods 0.000 claims description 5
- 230000008569 process Effects 0.000 claims description 4
- 229910052697 platinum Inorganic materials 0.000 claims description 3
- 239000000126 substance Substances 0.000 claims description 3
- UUFQTNFCRMXOAE-UHFFFAOYSA-N 1-methylmethylene Chemical compound C[CH] UUFQTNFCRMXOAE-UHFFFAOYSA-N 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000000649 benzylidene group Chemical group [H]C(=[*])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 229910017052 cobalt Inorganic materials 0.000 claims description 2
- 239000010941 cobalt Substances 0.000 claims description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 2
- UMYVESYOFCWRIW-UHFFFAOYSA-N cobalt;methanone Chemical compound O=C=[Co] UMYVESYOFCWRIW-UHFFFAOYSA-N 0.000 claims description 2
- 125000003709 fluoroalkyl 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
- 229910052703 rhodium Inorganic materials 0.000 claims description 2
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 claims description 2
- 150000003613 toluenes Chemical class 0.000 claims description 2
- 239000006260 foam Substances 0.000 abstract description 27
- 239000000463 material Substances 0.000 abstract description 13
- 230000005764 inhibitory process Effects 0.000 abstract description 8
- 239000003795 chemical substances by application Substances 0.000 abstract description 5
- 238000013461 design Methods 0.000 abstract description 4
- 239000000047 product Substances 0.000 description 79
- 230000000052 comparative effect Effects 0.000 description 40
- 239000000839 emulsion Substances 0.000 description 27
- 230000000694 effects Effects 0.000 description 19
- 239000003973 paint Substances 0.000 description 16
- HBZFBSFGXQBQTB-UHFFFAOYSA-N 3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F HBZFBSFGXQBQTB-UHFFFAOYSA-N 0.000 description 13
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 13
- 239000007788 liquid Substances 0.000 description 13
- 239000000203 mixture Substances 0.000 description 13
- 238000012360 testing method Methods 0.000 description 11
- 238000009826 distribution Methods 0.000 description 10
- FYQFWFHDPNXORA-UHFFFAOYSA-N 3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooct-1-ene Chemical group FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C=C FYQFWFHDPNXORA-UHFFFAOYSA-N 0.000 description 9
- 238000011156 evaluation Methods 0.000 description 9
- 239000002904 solvent Substances 0.000 description 7
- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 6
- 238000006459 hydrosilylation reaction Methods 0.000 description 5
- 239000002210 silicon-based material Substances 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 4
- 230000035484 reaction time Effects 0.000 description 4
- 230000002829 reductive effect Effects 0.000 description 4
- 239000002966 varnish Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- NKAMGQZDVMQEJL-UHFFFAOYSA-N 3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodec-1-ene Chemical group FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C=C NKAMGQZDVMQEJL-UHFFFAOYSA-N 0.000 description 3
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 3
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 229910052710 silicon Inorganic materials 0.000 description 3
- 239000010703 silicon Substances 0.000 description 3
- HMUNWXXNJPVALC-UHFFFAOYSA-N 1-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)C(CN1CC2=C(CC1)NN=N2)=O HMUNWXXNJPVALC-UHFFFAOYSA-N 0.000 description 2
- FEWFXBUNENSNBQ-UHFFFAOYSA-N 2-hydroxyacrylic acid Chemical compound OC(=C)C(O)=O FEWFXBUNENSNBQ-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000006555 catalytic reaction Methods 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 230000002860 competitive effect Effects 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 230000010355 oscillation Effects 0.000 description 2
- 238000011056 performance test Methods 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 2
- 238000005086 pumping Methods 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 229920001909 styrene-acrylic polymer Polymers 0.000 description 2
- 230000001629 suppression Effects 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- IMVVEWPCRIJQCA-UHFFFAOYSA-N 1,1,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-icosafluorodec-1-ene Chemical compound FC(F)=C(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F IMVVEWPCRIJQCA-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- ATVJXMYDOSMEPO-UHFFFAOYSA-N 3-prop-2-enoxyprop-1-ene Chemical compound C=CCOCC=C ATVJXMYDOSMEPO-UHFFFAOYSA-N 0.000 description 1
- 239000005046 Chlorosilane Substances 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical class CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- 229920001774 Perfluoroether Polymers 0.000 description 1
- 239000004972 Polyurethane varnish Substances 0.000 description 1
- ZOXYLHRVLPYKPZ-UHFFFAOYSA-N [Pt]C=C Chemical compound [Pt]C=C ZOXYLHRVLPYKPZ-UHFFFAOYSA-N 0.000 description 1
- 238000007259 addition reaction Methods 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 150000001343 alkyl silanes Chemical class 0.000 description 1
- 125000005336 allyloxy group Chemical group 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- KOPOQZFJUQMUML-UHFFFAOYSA-N chlorosilane Chemical compound Cl[SiH3] KOPOQZFJUQMUML-UHFFFAOYSA-N 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- KTQYJQFGNYHXMB-UHFFFAOYSA-N dichloro(methyl)silicon Chemical compound C[Si](Cl)Cl KTQYJQFGNYHXMB-UHFFFAOYSA-N 0.000 description 1
- 238000010292 electrical insulation Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 150000002221 fluorine Chemical class 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000005048 methyldichlorosilane Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 231100000956 nontoxicity Toxicity 0.000 description 1
- 230000036961 partial effect Effects 0.000 description 1
- 229920001843 polymethylhydrosiloxane Polymers 0.000 description 1
- AZIQALWHRUQPHV-UHFFFAOYSA-N prop-2-eneperoxoic acid Chemical compound OOC(=O)C=C AZIQALWHRUQPHV-UHFFFAOYSA-N 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000007151 ring opening polymerisation reaction Methods 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- SCPYDCQAZCOKTP-UHFFFAOYSA-N silanol Chemical compound [SiH3]O SCPYDCQAZCOKTP-UHFFFAOYSA-N 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Landscapes
- Silicon Polymers (AREA)
Abstract
Description
实例2 | 对比例2 | 竞品 | |
接触角 | 107.299 | 106.186 | 106.114 |
Claims (10)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202311182886.1A CN117209771A (zh) | 2023-09-14 | 2023-09-14 | 一种含氟有机硅聚合物的制备方法及其应用 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202311182886.1A CN117209771A (zh) | 2023-09-14 | 2023-09-14 | 一种含氟有机硅聚合物的制备方法及其应用 |
Publications (1)
Publication Number | Publication Date |
---|---|
CN117209771A true CN117209771A (zh) | 2023-12-12 |
Family
ID=89034801
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202311182886.1A Pending CN117209771A (zh) | 2023-09-14 | 2023-09-14 | 一种含氟有机硅聚合物的制备方法及其应用 |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN117209771A (zh) |
-
2023
- 2023-09-14 CN CN202311182886.1A patent/CN117209771A/zh active Pending
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN111732720B (zh) | 含氟醚化合物、表面处理剂、含氟醚组合物、涂布液和物品 | |
CN105102505B (zh) | 含氟醚化合物、含氟醚组合物及涂布液,以及具有表面层的基材及其制造方法 | |
US10233331B2 (en) | Fluorinated ether composition, method for its production, coating liquid, substrate having surface-treated layer and method for its production | |
EP2399570B1 (en) | Polyether-modified polysiloxane containing a perfluoropolyether group and its production method | |
CN107922608A (zh) | 含氟醚化合物、含氟醚组合物、涂布液和物品 | |
JP5399604B2 (ja) | 新規フルオロシラン縮合生成物、それらの製造方法および表面改質のための使用方法。 | |
EP2780426B1 (en) | Fluorinated coatings with lubricious additive | |
CN100457803C (zh) | 一种新型含氟烷氧丙基甲基硅油及其制备方法 | |
JP5929919B2 (ja) | 含フッ素エーテル組成物、その製造方法、コーティング液、および表面処理層を有する基材の製造方法 | |
TW200922969A (en) | Surface treating agent, article, and novel fluorine-containing ether compound | |
CN112673050B (zh) | 一种化合物及其制备方法、用途和组成的组合物 | |
CN113912834A (zh) | 一种全氟聚醚硅氧烷产品的制备方法及其在防指纹涂料和防指纹涂层中的应用 | |
EP3981823A1 (en) | Fluoropolyether group-containing polymer and production method therefor | |
JP2017137511A (ja) | 含フッ素エーテル化合物の製造方法および含フッ素エーテル化合物 | |
CN117209771A (zh) | 一种含氟有机硅聚合物的制备方法及其应用 | |
JP7177030B2 (ja) | ポリエーテル変性シロキサン、塗料添加剤、塗料組成物、コーティング剤、コーティング層、及びポリエーテル変性シロキサンの製造方法 | |
CN115477758B (zh) | 一种含氟消泡剂及其制备方法 | |
CN114729227B (zh) | 水性涂料添加剂、水性涂料组合物及涂层剂 | |
JP2015189843A (ja) | 含フッ素アルコール化合物及びその製造方法 | |
EP0675152A2 (en) | Organosilicon polymers and method of preparation | |
JP5042165B2 (ja) | 含フッ素有機ケイ素化合物及びその製造方法 | |
EP4339225A1 (en) | Fluorine-including organohydrosilane compound | |
JP2011052170A (ja) | 硬化性塗布組成物および硬化被膜 | |
WO2024075458A1 (ja) | フルオロポリエーテル基含有ポリマー | |
JP2023128171A (ja) | 塗料組成物 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
CB02 | Change of applicant information |
Country or region after: China Address after: 200000 No. 220, Handan Road, Shanghai, Yangpu District Applicant after: FUDAN University Applicant after: Evkona (Nanchong) special polymer Co.,Ltd. Applicant after: Evkona polymer Co.,Ltd. Address before: No. 1 Zhibei Road, Hexi Town, Jialing District, Nanchong City, Sichuan Province, 637000 Applicant before: Evkona (Nanchong) special polymer Co.,Ltd. Country or region before: China Applicant before: Evkona polymer Co.,Ltd. Applicant before: FUDAN University |
|
CB02 | Change of applicant information |