CN108440734A - A kind of polyurethane eyeglass and its short route curing - Google Patents
A kind of polyurethane eyeglass and its short route curing Download PDFInfo
- Publication number
- CN108440734A CN108440734A CN201810186927.7A CN201810186927A CN108440734A CN 108440734 A CN108440734 A CN 108440734A CN 201810186927 A CN201810186927 A CN 201810186927A CN 108440734 A CN108440734 A CN 108440734A
- Authority
- CN
- China
- Prior art keywords
- bis
- eyeglass
- polyurethane
- methyl
- isocyanatomethyl
- 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
- 239000004814 polyurethane Substances 0.000 title claims abstract description 45
- 229920002635 polyurethane Polymers 0.000 title claims abstract description 45
- 238000010438 heat treatment Methods 0.000 claims abstract description 27
- 239000003054 catalyst Substances 0.000 claims abstract description 21
- 238000000034 method Methods 0.000 claims abstract description 21
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 claims abstract description 20
- 230000008569 process Effects 0.000 claims abstract description 15
- 239000002994 raw material Substances 0.000 claims abstract description 12
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 11
- 238000007711 solidification Methods 0.000 claims abstract description 10
- 230000008023 solidification Effects 0.000 claims abstract description 10
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims abstract description 9
- 229920000728 polyester Polymers 0.000 claims abstract description 9
- 239000003963 antioxidant agent Substances 0.000 claims abstract description 8
- 230000003078 antioxidant effect Effects 0.000 claims abstract description 8
- 229920001228 polyisocyanate Polymers 0.000 claims abstract description 8
- 239000005056 polyisocyanate Substances 0.000 claims abstract description 8
- 239000003086 colorant Substances 0.000 claims abstract description 6
- 238000000465 moulding Methods 0.000 claims abstract description 6
- 230000003197 catalytic effect Effects 0.000 claims abstract description 5
- 238000013036 cure process Methods 0.000 claims abstract description 4
- 230000000694 effects Effects 0.000 claims abstract description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 21
- -1 isocyanatomethyl Chemical group 0.000 claims description 21
- 238000001723 curing Methods 0.000 claims description 13
- 241000534944 Thia Species 0.000 claims description 8
- RJGHQTVXGKYATR-UHFFFAOYSA-L dibutyl(dichloro)stannane Chemical compound CCCC[Sn](Cl)(Cl)CCCC RJGHQTVXGKYATR-UHFFFAOYSA-L 0.000 claims description 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 7
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims description 6
- 239000012964 benzotriazole Substances 0.000 claims description 6
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims description 5
- 238000002360 preparation method Methods 0.000 claims description 5
- LOZWAPSEEHRYPG-UHFFFAOYSA-N 1,4-dithiane Chemical compound C1CSCCS1 LOZWAPSEEHRYPG-UHFFFAOYSA-N 0.000 claims description 4
- AXFVIWBTKYFOCY-UHFFFAOYSA-N 1-n,1-n,3-n,3-n-tetramethylbutane-1,3-diamine Chemical compound CN(C)C(C)CCN(C)C AXFVIWBTKYFOCY-UHFFFAOYSA-N 0.000 claims description 4
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 claims description 4
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 claims description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 4
- 150000001412 amines Chemical class 0.000 claims description 4
- 239000012752 auxiliary agent Substances 0.000 claims description 4
- 239000012965 benzophenone Substances 0.000 claims description 4
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 claims description 4
- 229910052797 bismuth Inorganic materials 0.000 claims description 4
- 150000002148 esters Chemical class 0.000 claims description 4
- 239000012948 isocyanate Substances 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- 150000003839 salts Chemical class 0.000 claims description 4
- 238000003756 stirring Methods 0.000 claims description 4
- 239000000758 substrate Substances 0.000 claims description 4
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 claims description 4
- FKTHNVSLHLHISI-UHFFFAOYSA-N 1,2-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC=C1CN=C=O FKTHNVSLHLHISI-UHFFFAOYSA-N 0.000 claims description 3
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 claims description 3
- 229910021529 ammonia Inorganic materials 0.000 claims description 3
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 claims description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 3
- 150000002513 isocyanates Chemical class 0.000 claims description 3
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical class OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims description 3
- GIWQSPITLQVMSG-UHFFFAOYSA-N 1,2-dimethylimidazole Chemical compound CC1=NC=CN1C GIWQSPITLQVMSG-UHFFFAOYSA-N 0.000 claims description 2
- PAMIQIKDUOTOBW-UHFFFAOYSA-N 1-methylpiperidine Chemical class CN1CCCCC1 PAMIQIKDUOTOBW-UHFFFAOYSA-N 0.000 claims description 2
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 claims description 2
- ZRXHQNQYIKVKNQ-UHFFFAOYSA-N 2-ethylhexanoic acid;zinc Chemical compound [Zn].CCCCC(CC)C(O)=O ZRXHQNQYIKVKNQ-UHFFFAOYSA-N 0.000 claims description 2
- XNZVPRAMMCVPSK-UHFFFAOYSA-N 2-methyl-1,4-dithiane-2,3-dithiol Chemical compound CC1(S)SCCSC1S XNZVPRAMMCVPSK-UHFFFAOYSA-N 0.000 claims description 2
- LXBGSDVWAMZHDD-UHFFFAOYSA-N 2-methyl-1h-imidazole Chemical compound CC1=NC=CN1 LXBGSDVWAMZHDD-UHFFFAOYSA-N 0.000 claims description 2
- DKIDEFUBRARXTE-UHFFFAOYSA-N 3-mercaptopropanoic acid Chemical class OC(=O)CCS DKIDEFUBRARXTE-UHFFFAOYSA-N 0.000 claims description 2
- NGKNMHFWZMHABQ-UHFFFAOYSA-N 4-chloro-2h-benzotriazole Chemical compound ClC1=CC=CC2=NNN=C12 NGKNMHFWZMHABQ-UHFFFAOYSA-N 0.000 claims description 2
- BRKHZWFIIVVNTA-UHFFFAOYSA-N 4-cyclohexylmorpholine Chemical class C1CCCCC1N1CCOCC1 BRKHZWFIIVVNTA-UHFFFAOYSA-N 0.000 claims description 2
- HVCNXQOWACZAFN-UHFFFAOYSA-N 4-ethylmorpholine Chemical compound CCN1CCOCC1 HVCNXQOWACZAFN-UHFFFAOYSA-N 0.000 claims description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 2
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 claims description 2
- SVYKKECYCPFKGB-UHFFFAOYSA-N N,N-dimethylcyclohexylamine Chemical compound CN(C)C1CCCCC1 SVYKKECYCPFKGB-UHFFFAOYSA-N 0.000 claims description 2
- SJRJJKPEHAURKC-UHFFFAOYSA-N N-Methylmorpholine Chemical group CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 claims description 2
- 239000004218 Orcein Substances 0.000 claims description 2
- 229910019142 PO4 Inorganic materials 0.000 claims description 2
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 claims description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 2
- SWHLOXLFJPTYTL-UHFFFAOYSA-N [2-methyl-3-(2-methylprop-2-enoyloxy)-2-(2-methylprop-2-enoyloxymethyl)propyl] 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(C)(COC(=O)C(C)=C)COC(=O)C(C)=C SWHLOXLFJPTYTL-UHFFFAOYSA-N 0.000 claims description 2
- 239000002253 acid Substances 0.000 claims description 2
- 150000001555 benzenes Chemical class 0.000 claims description 2
- 125000003354 benzotriazolyl group Chemical group N1N=NC2=C1C=CC=C2* 0.000 claims description 2
- NSPSPMKCKIPQBH-UHFFFAOYSA-K bismuth;7,7-dimethyloctanoate Chemical compound [Bi+3].CC(C)(C)CCCCCC([O-])=O.CC(C)(C)CCCCCC([O-])=O.CC(C)(C)CCCCCC([O-])=O NSPSPMKCKIPQBH-UHFFFAOYSA-K 0.000 claims description 2
- 239000001045 blue dye Substances 0.000 claims description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 239000004202 carbamide Substances 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 238000004140 cleaning Methods 0.000 claims description 2
- 238000013329 compounding Methods 0.000 claims description 2
- QVQGTNFYPJQJNM-UHFFFAOYSA-N dicyclohexylmethanamine Chemical compound C1CCCCC1C(N)C1CCCCC1 QVQGTNFYPJQJNM-UHFFFAOYSA-N 0.000 claims description 2
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 claims description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 2
- 125000000524 functional group Chemical group 0.000 claims description 2
- 239000001046 green dye Substances 0.000 claims description 2
- QZLKVQRFTHKQKP-UHFFFAOYSA-N hexadecanoic acid;tin Chemical compound [Sn].CCCCCCCCCCCCCCCC(O)=O QZLKVQRFTHKQKP-UHFFFAOYSA-N 0.000 claims description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 2
- 238000011416 infrared curing Methods 0.000 claims description 2
- FBAFATDZDUQKNH-UHFFFAOYSA-M iron chloride Chemical compound [Cl-].[Fe] FBAFATDZDUQKNH-UHFFFAOYSA-M 0.000 claims description 2
- DSSXKBBEJCDMBT-UHFFFAOYSA-M lead(2+);octanoate Chemical compound [Pb+2].CCCCCCCC([O-])=O DSSXKBBEJCDMBT-UHFFFAOYSA-M 0.000 claims description 2
- ZWRDBWDXRLPESY-UHFFFAOYSA-N n-benzyl-n-ethylethanamine Chemical compound CCN(CC)CC1=CC=CC=C1 ZWRDBWDXRLPESY-UHFFFAOYSA-N 0.000 claims description 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 claims description 2
- 235000019248 orcein Nutrition 0.000 claims description 2
- 235000021317 phosphate Nutrition 0.000 claims description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 claims description 2
- 239000001294 propane Substances 0.000 claims description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 2
- 125000000446 sulfanediyl group Chemical group *S* 0.000 claims description 2
- CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical class OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 claims description 2
- KSBAEPSJVUENNK-UHFFFAOYSA-L tin(ii) 2-ethylhexanoate Chemical compound [Sn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O KSBAEPSJVUENNK-UHFFFAOYSA-L 0.000 claims description 2
- 235000005074 zinc chloride Nutrition 0.000 claims description 2
- 239000011592 zinc chloride Substances 0.000 claims description 2
- 125000002462 isocyano group Chemical group *[N+]#[C-] 0.000 claims 3
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims 2
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 claims 2
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 claims 2
- CSUUDNFYSFENAE-UHFFFAOYSA-N (2-methoxyphenyl)-phenylmethanone Chemical compound COC1=CC=CC=C1C(=O)C1=CC=CC=C1 CSUUDNFYSFENAE-UHFFFAOYSA-N 0.000 claims 1
- XXZLJUHAFDUPOU-UHFFFAOYSA-N 1,2,3,5-tetrachloro-4,6-bis(isocyanatomethyl)benzene Chemical class ClC1=C(Cl)C(CN=C=O)=C(Cl)C(CN=C=O)=C1Cl XXZLJUHAFDUPOU-UHFFFAOYSA-N 0.000 claims 1
- KJQYDHSBSUHAID-UHFFFAOYSA-N 1,2,4,5-tetrabromo-3,6-bis(isocyanatomethyl)benzene Chemical class BrC1=C(Br)C(CN=C=O)=C(Br)C(Br)=C1CN=C=O KJQYDHSBSUHAID-UHFFFAOYSA-N 0.000 claims 1
- BSKHPKMHTQYZBB-UHFFFAOYSA-N 2-methylpyridine Chemical compound CC1=CC=CC=N1 BSKHPKMHTQYZBB-UHFFFAOYSA-N 0.000 claims 1
- 244000060011 Cocos nucifera Species 0.000 claims 1
- 235000013162 Cocos nucifera Nutrition 0.000 claims 1
- KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical class CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 claims 1
- URLKBWYHVLBVBO-UHFFFAOYSA-N Para-Xylene Chemical class CC1=CC=C(C)C=C1 URLKBWYHVLBVBO-UHFFFAOYSA-N 0.000 claims 1
- 150000008366 benzophenones Chemical class 0.000 claims 1
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 claims 1
- XLJMAIOERFSOGZ-UHFFFAOYSA-M cyanate Chemical compound [O-]C#N XLJMAIOERFSOGZ-UHFFFAOYSA-M 0.000 claims 1
- 235000013847 iso-butane Nutrition 0.000 claims 1
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 claims 1
- QATBRNFTOCXULG-UHFFFAOYSA-N n'-[2-(methylamino)ethyl]ethane-1,2-diamine Chemical compound CNCCNCCN QATBRNFTOCXULG-UHFFFAOYSA-N 0.000 claims 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N sec-butylidene Natural products CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 claims 1
- YTZKOQUCBOVLHL-UHFFFAOYSA-N tert-butylbenzene Chemical class CC(C)(C)C1=CC=CC=C1 YTZKOQUCBOVLHL-UHFFFAOYSA-N 0.000 claims 1
- 230000003287 optical effect Effects 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 5
- 239000000203 mixture Substances 0.000 description 4
- 238000005516 engineering process Methods 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 230000005855 radiation Effects 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 230000008901 benefit Effects 0.000 description 2
- 230000005540 biological transmission Effects 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 238000013007 heat curing Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 229920005749 polyurethane resin Polymers 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 230000035939 shock Effects 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- 238000002834 transmittance Methods 0.000 description 2
- OBETXYAYXDNJHR-SSDOTTSWSA-M (2r)-2-ethylhexanoate Chemical compound CCCC[C@@H](CC)C([O-])=O OBETXYAYXDNJHR-SSDOTTSWSA-M 0.000 description 1
- WZROIUBWZBSCSE-UHFFFAOYSA-N 1,2-bis(isocyanatomethyl)naphthalene Chemical class C1=CC=CC2=C(CN=C=O)C(CN=C=O)=CC=C21 WZROIUBWZBSCSE-UHFFFAOYSA-N 0.000 description 1
- AZYRZNIYJDKRHO-UHFFFAOYSA-N 1,3-bis(2-isocyanatopropan-2-yl)benzene Chemical compound O=C=NC(C)(C)C1=CC=CC(C(C)(C)N=C=O)=C1 AZYRZNIYJDKRHO-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- OBETXYAYXDNJHR-UHFFFAOYSA-N alpha-ethylcaproic acid Natural products CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 239000012975 dibutyltin dilaurate Substances 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- PYBNTRWJKQJDRE-UHFFFAOYSA-L dodecanoate;tin(2+) Chemical compound [Sn+2].CCCCCCCCCCCC([O-])=O.CCCCCCCCCCCC([O-])=O PYBNTRWJKQJDRE-UHFFFAOYSA-L 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 238000002594 fluoroscopy Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 1
- 230000008092 positive effect Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 150000003222 pyridines Chemical class 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 230000036632 reaction speed Effects 0.000 description 1
- 238000000518 rheometry Methods 0.000 description 1
- 239000011265 semifinished product Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000010105 thermoset forming Methods 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/38—Low-molecular-weight compounds having heteroatoms other than oxygen
- C08G18/3855—Low-molecular-weight compounds having heteroatoms other than oxygen having sulfur
- C08G18/3863—Low-molecular-weight compounds having heteroatoms other than oxygen having sulfur containing groups having sulfur atoms between two carbon atoms, the sulfur atoms being directly linked to carbon atoms or other sulfur atoms
- C08G18/3865—Low-molecular-weight compounds having heteroatoms other than oxygen having sulfur containing groups having sulfur atoms between two carbon atoms, the sulfur atoms being directly linked to carbon atoms or other sulfur atoms containing groups having one sulfur atom between two carbon atoms
- C08G18/3868—Low-molecular-weight compounds having heteroatoms other than oxygen having sulfur containing groups having sulfur atoms between two carbon atoms, the sulfur atoms being directly linked to carbon atoms or other sulfur atoms containing groups having one sulfur atom between two carbon atoms the sulfur atom belonging to a sulfide group
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
- C08K5/3472—Five-membered rings
- C08K5/3475—Five-membered rings condensed with carbocyclic rings
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B1/00—Optical elements characterised by the material of which they are made; Optical coatings for optical elements
- G02B1/04—Optical elements characterised by the material of which they are made; Optical coatings for optical elements made of organic materials, e.g. plastics
- G02B1/041—Lenses
Landscapes
- Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Polyurethanes Or Polyureas (AREA)
Abstract
The present invention relates to a kind of polyurethane eyeglass and its short route curing, polyurethane eyeglass, including the following raw material:Polythiaether mercaptan and polyester mercaptan, polyisocyanates, catalyst, antioxidant, releasing agent and coloring agent, raw material is reduced temperature manner and is cured to achieve the effect that the polyurethane eyeglass cure process time substantially shortens during curing molding is polyurethane eyeglass using catalyst complex process and infrared heating mode, circulation cold air.Mode of heating reduces temperature manner using infrared heating heating and circulation cold air and accurately controls urethane raw solidification process, and catalyst is compounded using two kinds or two or more catalyst, different to reach different temperatures catalytic effect.
Description
Technical field
The present invention relates to eyeglass production technical fields, are a kind of polyurethane eyeglass and its short route solidification side specifically
Method.
Background technology
Currently, international high-end spectacle lens assign eyeglass high refractive index, high transmission using heat curing type optical polyurethane as raw material
The excellent properties that a series of conventional lenses such as property, light and comfortable can not reach.The thermoset forming process of optical polyurethane is
Temperature field, flow field and chemical fields intercouple the complex process of intertexture.By stable state rheology and dynamic rheological property, the poly- ammonia of optics is studied
Before heat cure and the variation tendency of solidification process medium viscosity and viscoplasticity rule, know macromolecular chain clearly from microcosmic exists ester system
The submissive sex differernce of orientation, entanglement and strand in reaction process, before determining the gel point of different systems and establishing gel point,
Viscosity change model afterwards, by gel point occur time prediction needed for hardening time, to for short route process reason is provided
By foundation;By the characterization methods such as DSC, infrared, optical polyurethane thermosetting kinetics is studied, determines different material system
Curing initiation temperature, optimum temperature and stop temperature, by Kissinger equations, Ozawa equations etc. ask calculation system activation energy with
The order of reaction controls reaction speed to more efficient prediction reaction process, promotes the accuracy of abbreviated system route.It is logical
The systematization further investigation for crossing above-mentioned theory is explored and discloses from raw material, the forming of solidification cross-linked network and develop to final short
Flow industrialization process establishes the Integrated Model of structure --- abbreviated system --- product properties, to accurate pre-
The important turning point and key point for surveying reaction process provide foundation for the exploitation of polyurethane eyeglass curing process.
The short route processing of height refraction polyurethane, be thermodynamics of reactions, dynamics and mass transfer in preparation process, heat transfer,
The product that transmission engineering technology is combined.From the point of view of current patent retrieval, to the preparation research of high refraction polyurethane eyeglass
It is more, as CN201180042756 has studied the compounded technology with the refrangible polyurethane lens formulation of bloom;
CN201610270321 has studied a kind of polyurethane-type height refraction sulfur-bearing optical resin monomer and preparation method thereof;
CN201510862340 has studied a kind of improved method of polyurethane resin optical material heat resistance;CN201180027180 is ground
Study carefully with the urethane composition for improving impact resistance and optical property.In conclusion to polyurethane eyeglass curing molding mistake
The research of journey is less.
In the prior art, polyurethane eyeglass solidification process generally require cure twice, be cured as the first time 24 hours-
36 hours, it is more than hour that it is cured as 2 for the second time, it may be longer for the hardening time of semi-finished product.This patent is related to one kind
Polyurethane eyeglass short route curing process still belongs to study for the first time, polyurethane eyeglass of the invention, including the following raw material:Polythiaether
Mercaptan and polyester mercaptan, polyisocyanates, catalyst, antioxidant, releasing agent and coloring agent, raw material are poly- ammonia in curing molding
During ester eyeglass, using catalyst complex process and infrared heating mode and circulation cold air reduce temperature manner cured from
And achievees the effect that the polyurethane eyeglass cure process time and substantially shorten.It is using the present invention using infrared heating heating and
Circulation cold air reduces temperature manner, coordinates the preferred of catalyst, the urethane cures time can be reduced to 16-20 hours ranges
It is interior.
Invention content
It is an object of the invention to overcome the deficiencies of the prior art and provide a kind of polyurethane eyeglass and its short route solidification sides
Method.
The purpose of the present invention is achieved through the following technical solutions:
A kind of polyurethane eyeglass, the mass percent of raw material are:Polythiaether mercaptan or polyester mercaptan are 20%-
70%, polyisocyanates 30%-70%, catalyst are 1.0 ‰~10.0 ‰, antioxidant is 0.1%~2%, releasing agent
It is 0.1%~1%, coloring agent is 0.1 ‰~4 ‰.
Polythiaether mercaptan and polyester mercaptan include:4- mercapto methyl -1,8- dimercapto -3,6- dithias octane, 2,5- are bis-
Mercapto methyl -1,4- dithiane, 1,1,3,3- tetra- (mercapto methyl is thio) propane, 5,7- dimercapto methyl -1,11- dimercaptos -
Tri- thia hendecanes of 3,6,9-, three thia hendecanes of 4,7- dimercapto methyl -1,11- dimercaptos -3,6,9-, 4,8- dimercapto-methyls
Three thia hendecanes of base -1,11- dimercaptos -3,6,9-, trimethylolpropane tris (3-thiopropionate), trimethylolethane trimethacrylate
(2- mercaptoacetates), four (2- thioacetic acid) pentaerythritol esters and four (3- mercaptopropionic acids) pentaerythritol esters, two (2- hydroxyl second
Base) sulfide, bis- (the 2- hydroxyethyls sulfydryl) ethane of 1,2-, bis- (2- hydroxyethyls) disulphide and 1,4- dithiane -2,5-
One or more kinds of combinations in glycol.
Polyisocyanates include bis- (isocyanatomethyl) benzene of 1,3- (m- xyxylene-diisocyanate, m-XDI),
Bis- (the 2- isocyanato- propyl-s 2- of bis- (isocyanatomethyl) benzene of Isosorbide-5-Nitrae-(p- xyxylene-diisocyanate, p-XDI), 1,3-
Base) benzene (m- durol dimethyl-diisocyanate, m-TMXDI), bis- (the 2- isocyanato- propyl- 2- yls) benzene of Isosorbide-5-Nitrae-are (p-
Durol dimethyl-diisocyanate, p-TMXDI), bis- (the isocyanatomethyl) -4- methylbenzenes of 1,3-, 1,3- it is bis- (different
Cyanate radical close methyl) -4- ethylo benzenes, bis- (the isocyanatomethyl) -5- methylbenzenes of 1,3-, bis- (the isocyanato- first of 1,3-
Base) -4,5- dimethyl benzenes, bis- (the isocyanatomethyl) -2,5- dimethyl benzenes of 1,4-, 1,4- bis- (isocyanatomethyls) -
Bis- (the isocyanatomethyl) -4- of bis- (the isocyanatomethyl) -5- tert-butyl benzenes of 2,3,5,6- durols, 1,3-, 1,3-
Bis- (the isocyanatomethyl) -4,5- dichloro-benzenes of chlorobenzene, 1,3-, bis- (the isocyanatomethyl) -2,4,5,6- tetrachlorobenzenes of 1,3-, 1,
Bis- (the isocyanatomethyl) -2,3,5,6- tetrachlorobenzenes of 4-, bis- (the isocyanatomethyl) -2,3,5,6- tetrabromo-benzenes of 1,4-, 1,
One or more of bis- (2- isocyanatoethyls) benzene of 4-, bis- (isocyanatomethyl) naphthalenes of 1,4- combine.
Catalyst includes organic amine:Triethylamine, tri-butylamine, dimethyl benzyl amine, diethylbenzyl amine, pyridine, first
Yl pyridines, dicyclohexylmethylamine, dimethyl cyclohexyl amine, N, N, N', N'- tetramethyl diamino Anaesthetie Ether, double-(dimethyl
Aminopropyl)-urea, N- methyl-and N-ethylmorpholine, N- cocomorpholines, N- cyclohexyl morpholines, N, N, N', N'- tetramethyl second
Diamines, N, N, N', N'- tetramethyl -1,3- butanediamine, N, N, N', N'- tetramethyl -1,6- hexamethylene diamines, pentamethyl diethylidene three
Amine, N- methyl piperidines, N- dimethyl aminoethyl piperidines, N, N'- lupetazins, N- methyl-N'- dimethylaminos piperazine,
11 carbon -7- alkene (DBU) of 1,8- diazabicyclos (5.4.0), DMIZ 1,2 dimethylimidazole, 2-methylimidazole, N, N- dimethyl miaows
Azoles-beta-phenyl ethylamine, 1,4- diazabicyclos-(2,2,2)-octane, double-(N, N- dimethyl aminoethyl) adipate ester;
Metallic salt, frerrous chloride (II), iron chloride (III), 2 ethyl hexanoic acid bismuth (III), Bismuth Octoate (III), bismuth neodecanoate
(III), zinc chloride, 2 ethyl hexanoic acid zinc, tin octoate (II), thylhexoic acid tin (II), palmitic acid tin (II), two fourth of tin dilaurate
Ji Xi (IV) (DBTL), dibutyltin dichloride (IV) or lead octoate;Further preferred uses organic amine and metallic salt
It is compounded, to reach best catalytic effect.
Antioxidant is benzotriazole, benzophenone includes 2'~(2'~hydroxyl~3'~tertiary butyl~5'~methyl
Phenyl)~5~chlorobenzotriazole or or 2~(2'~hydroxyl~5'~t-octyl phenyl) benzotriazole or 2~hydroxyl~4~first
Oxygroup benzophenone or 2, the one or several kinds in 2'~dimethyl~4~methylamino benzophenone.
Releasing agent is organic phosphates releasing agent, and toner is orchil, one kind in green dye and blue dyes
Or several compounding.
A kind of preparation method of polyurethane eyeglass, the specific steps are:
Raw material is during curing molding is polyurethane eyeglass, using catalyst complex process;Mode of heating is using infrared
Heat temperature raising and circulation cold air reduce temperature manner to reach the effect that the polyurethane eyeglass cure process time substantially shortens
Fruit.Mode of heating reduces temperature manner using infrared heating heating and circulation cold air and accurately controls urethane raw solidification process,
Catalyst is compounded using two kinds or two or more catalyst, different to reach different temperatures catalytic effect.Using this
The infrared heating heating of invention and circulation cold air reduce temperature manner, coordinate the preferred of catalyst, when can be by urethane cures
Between be reduced in 16-20 hours ranges.
The infrared energy of infrared heating is penetrated by inside polyurethane resin eyeglass, and to the air in heating space, matchmaker
Jie's object does not heat substantially, therefore has the thermal efficiency is high, heating speed is fast, power consumption is few, heating quality is high, operating environment is good etc.
Advantage, especially in low temperature (50~650 DEG C) section, these features are especially pronounced.The solidification temperature of polyurethane eyeglass be 150 degree with
It is interior, therefore, solidification of the infrared heating particularly suitable for polyurethane eyeglass.In addition, in equipment aspect, electric infrared heating, which also has, to be set
The advantages that standby simple in structure, cost of equipment is low, easy care, floor space are small, easy realization serialization automated production.Infrared wavelength
Range is about 0.77~1000 μm, in the practical application of electric infrared heating, electric infra-red radiation generally only dividend external radiation with it is remote
Two wave bands of infra-red radiation.It is 2.5~30 μm that the electric infrared heating industrially applied, which mainly uses the latter, wave-length coverage,.
The infrared wavelength range of the present invention is 2.5~20 μm.
A kind of short route curing of polyurethane eyeglass, the specific steps are:
Stirring and dissolving in isocyanates is added in all auxiliary agents, until completely dissolved, polythiaether mercaptan is added while stirring
Or polyester mercaptan;All auxiliary agents are catalyst, antioxidant, releasing agent and coloring agent;And polythiaether mercaptan or polyester mercaptan and
The ratio of polyisocyanates is according to functional group's NCO/SH molar ratios 0.8:1~1.2:1;Raw material is poured into mold after vacuum defoamation
In, urethane raw is placed into specific infrared curing stove according to program curing and is cured, after curing completely cools to 60
Degree obtains the substrate of polyurethane eyeglass after demoulding cleaning;Program curing is:
25 DEG C~35 DEG C 0.5h~1h
35 DEG C~41 DEG C 2h~2.5h
41 DEG C~57 DEG C 2h~2.5h
57 DEG C~81 DEG C 3h~3.5h
81 DEG C~96 DEG C 2h~2.5h
96 DEG C~125 DEG C 2h~2.5h
125 DEG C~125 DEG C 2h~2.5h
125 DEG C~60 DEG C 2h~2.5h
60 DEG C~60 DEG C 0.5h~0.5h
At 60 DEG C, mold is removed, you can obtain polyurethane eyeglass substrate;New production program is simple and convenient, and assigns
Eyeglass good optical property.Used program curing has fully considered the heat release heat absorption problem of radical polymerization process,
Designed cure profile can more ensure the moulding process of eyeglass, ensure to fry mould from die sinking phenomenon control below 0.5%.
Time can control between 16 to 20 hours.
Polyurethane method for manufacturing lens obtained by production program, it is seen that x ray fluoroscopy x ratio is more than or equal to 93%, eyeglass
Glass transition temperature is 98 degree.The impact strength of eyeglass may be up to 60kJ/M2, can assemble no-frame glasses.
Compared with prior art, the positive effect of the present invention is:
Eyeglass hardening time shortens to 16-20 hours from original 24-36 hours.
Specific implementation mode
The specific implementation mode of a kind of polyurethane eyeglass of the present invention presented below and its short route curing.
Embodiment 1
Three thia hendecanes of 4,8- dimercapto methyl -1,11- dimercaptos -3,6,9-:480.0g
Between xyxylene isocyanates:515.0g
Dibutyl tin dichloride:1.0g
N, N, N', N'- tetramethyl -1,3- butanediamine:1.0g
2- (2'- hydroxyl -5'- t-octyls phenyl) benzotriazole:1.0g
Organic dyestuff blue and green:Each 1.0g
After being filtered with 0.5 μm of filter disc according to mixture obtained by above-mentioned formula, it is poured into preprepared glass
In mold, it is put into baking oven, Raolical polymerizable is carried out according to the program curing given.
At 60 DEG C, mold is removed, eyeglass is then subjected to stiffened and coating film treatment, you can obtain a kind of polyurethane mirror
Eyeglass prepared by piece, using ISO8980.3-1999《Flash eyeglass Part III:Diactinic requirement and test
Method》、QB2506-2001《Optical resin spectacles lens》Defined method is detected, as a result as follows:
1 original transmittance:93.2%
2 lens index 1.66;
3 shock resistances:It is provided by QB2506.
Embodiment 2
Three thia hendecanes of 5,7- dimercapto methyl -1,11- dimercaptos -3,6,9-:475.0g
Cyclohexanedimethyleterephthalate diisocyanate:520.0g
Dibutyl tin dichloride:1.0g
N, N, N', N'- tetramethyl -1,3- butanediamine:1.0g
2- (2'- hydroxyl -5'- t-octyls phenyl) benzotriazole:1.0g
Organic dyestuff blue and green:Each 1.0g
After being filtered with 0.5 μm of filter disc according to mixture obtained by above-mentioned formula, it is poured into preprepared glass
In mold, it is put into baking oven, Raolical polymerizable is carried out according to the program curing given.
At 60 DEG C, mold is removed, eyeglass is then subjected to stiffened and coating film treatment, you can obtain a kind of polyurethane mirror
Eyeglass prepared by piece, using ISO8980.3-1999《Flash eyeglass Part III:Diactinic requirement and test
Method》、QB2506-2001《Optical resin spectacles lens》Defined method is detected, as a result as follows:
1 original transmittance:93.2%
2 lens index 1.66;
3 shock resistances:It is provided by QB2506.
The above is only a preferred embodiment of the present invention, it is noted that for the ordinary skill people of the art
Member, without departing from the inventive concept of the premise, can also make several improvements and modifications, these improvements and modifications also should be regarded as
In protection scope of the present invention.
Claims (7)
1. a kind of polyurethane eyeglass, which is characterized in that the mass percent of its raw material is:Polythiaether mercaptan or polyester mercaptan are
20%-70%, polyisocyanates 30%-70%, catalyst are 1.0 ‰~10.0 ‰, antioxidant is 0.1%~2%, are taken off
Mould agent is 0.1%~1%, and coloring agent is 0.1 ‰~4 ‰.A kind of preparation method of polyurethane eyeglass, the specific steps are:
Raw material is during curing molding is polyurethane eyeglass, using catalyst complex process;Mode of heating uses infrared heating
Heating and circulation cold air reduce temperature manner to achieve the effect that the polyurethane eyeglass cure process time substantially shortens;Add
Hot mode reduces temperature manner using infrared heating heating and circulation cold air and accurately controls urethane raw solidification process, catalyst
It is compounded using two kinds or two or more catalyst, it is different to reach different temperatures catalytic effect;Using the application's
Infrared heating heats up and circulation cold air reduces temperature manner, coordinates the preferred of catalyst, the urethane cures time is reduced to 16-
Within the scope of 20 hours;Infrared wavelength range is 2.5~20 μm.
2. a kind of polyurethane eyeglass as described in claim 1, which is characterized in that polythiaether mercaptan and polyester mercaptan are 4- sulfydryls
Methyl-1,8- dimercapto -3,6- dithias octane, the bis- mercapto methyl -1,4- dithiane of 2,5-, tetra- (mercapto methyls of 1,1,3,3-
It is thio) propane, three thia hendecanes of 5,7- dimercapto methyl -1,11- dimercaptos -3,6,9-, 4,7- dimercapto methyl -1,11-
Three thia hendecanes of dimercapto -3,6,9-, three thia hendecanes of 4,8- dimercapto methyl -1,11- dimercaptos -3,6,9-, three hydroxyls
Methylpropane three (3-thiopropionate), trimethylolethane trimethacrylate (2- mercaptoacetates), four (2- thioacetic acid) pentaerythrites
Ester and bis- (the 2- hydroxyethyls sulfydryl) ethane of four (3- mercaptopropionic acids) pentaerythritol esters, two (2- hydroxyethyls) sulfide, 1,2-,
One or more kinds of combinations in bis- (2- hydroxyethyls) disulphide and 1,4- dithiane -2,5- glycol.
3. a kind of polyurethane eyeglass as described in claim 1, which is characterized in that polyisocyanates 1, the bis- (isocyanos of 3-
Close methyl) benzene (m- xyxylene-diisocyanate, m-XDI), bis- (isocyanatomethyl) benzene (the p- xyxylenes-two of Isosorbide-5-Nitrae-
Isocyanates, p-XDI), 1,3- bis- (2- isocyanato- propyl- 2- yls) benzene (m- durol dimethyl-diisocyanate, m-
TMXDI), bis- (the 2- isocyanato- propyl- 2- yls) benzene (p- durol dimethyl-diisocyanate, p-TMXDI) of Isosorbide-5-Nitrae-, 1,
Bis- (the isocyanatomethyl) -4- methylbenzenes of 3-, bis- (the isocyanatomethyl) -4- ethylo benzenes of 1,3-, the bis- (isocyanos of 1,3-
Close methyl) -5- methylbenzenes, bis- (the isocyanatomethyl) -4,5- dimethyl benzenes of 1,3-, 1,4- bis- (isocyanatomethyls) -
Bis- (the isocyanatomethyl) -2,3,5,6- durols of 2,5- dimethyl benzenes, 1,4-, 1,3- bis- (isocyanatomethyls) -
Bis- (the isocyanatomethyl) -4- chlorobenzenes of 5- tert-butyl benzenes, 1,3-, bis- (the isocyanatomethyl) -4,5- dichloro-benzenes of 1,3-, 1,3-
Bis- (isocyanatomethyl) -2,4,5,6- tetrachlorobenzenes, bis- (the isocyanatomethyl) -2,3,5,6- tetrachlorobenzenes of 1,4-, 1,4-
Bis- (2- isocyanatoethyls) benzene of bis- (isocyanatomethyl) -2,3,5,6- tetrabromo-benzenes, 1,4-, the bis- (isocyanos of 1,4-
Close methyl) combination of one or more of naphthalene.
4. a kind of polyurethane eyeglass as described in claim 1, which is characterized in that catalyst includes organic amine:Triethylamine, three
Butylamine, dimethyl benzyl amine, diethylbenzyl amine, pyridine, picoline, dicyclohexylmethylamine, dimethyl cyclohexyl amine, N,
N, N', N'- tetramethyl diamino Anaesthetie Ether, double-(dimethylaminopropyl)-urea, N- methyl-and N-ethylmorpholine, N- coconut palms
Oil base morpholine, N- cyclohexyl morpholines, N, N, N', N'- tetramethylethylenediamines, N, N, N', N'- tetramethyl -1,3- butanediamine, N, N,
N', N'- tetramethyl -1,6- hexamethylene diamines, five methyl diethylentriamine, N- methyl piperidines, N- dimethyl aminoethyl piperidines, N,
N'- lupetazins, N- methyl-N'- dimethylaminos piperazine, 11 carbon -7- alkene (DBU) of 1,8- diazabicyclos (5.4.0),
DMIZ 1,2 dimethylimidazole, 2-methylimidazole, N, N- methylimidazoles-beta-phenyl ethylamine, 1,4- diazabicyclos-(2,2,2)-
Octane, double-(N, N- dimethyl aminoethyl) adipate ester;Metallic salt, frerrous chloride (II), iron chloride (III), 2- ethyls
Caproic acid bismuth (III), Bismuth Octoate (III), bismuth neodecanoate (III), zinc chloride, 2 ethyl hexanoic acid zinc, tin octoate (II), thylhexoic acid
Tin (II), palmitic acid tin (II), dibutyl tin laurate (IV) (DBTL), dibutyltin dichloride (IV) or lead octoate;Into
One step preferably uses organic amine and metallic salt to be compounded, to reach best catalytic effect.
5. a kind of polyurethane eyeglass as described in claim 1, which is characterized in that antioxidant is benzotriazole, benzophenone
Class includes 2'~(2'~hydroxyl~3'~tertiary butyl~5'~aminomethyl phenyl)~5~chlorobenzotriazole or or 2~(2'~hydroxyl
~5'~t-octyl phenyl) benzotriazole or 2~hydroxyl~4~methoxy benzophenone or 2,2'~dimethyl~4~first ammonia
One or several kinds in base benzophenone.
6. a kind of polyurethane eyeglass as described in claim 1, which is characterized in that releasing agent is organic phosphates releasing agent, toning
Agent is orchil, one or several kinds of compoundings in green dye and blue dyes.
7. a kind of short route curing of polyurethane eyeglass, the specific steps are:
Stirring and dissolving in isocyanates is added in all auxiliary agents, until completely dissolved, polythiaether mercaptan or poly- is added while stirring
Ester mercaptan;All auxiliary agents are catalyst, antioxidant, releasing agent and coloring agent;And polythiaether mercaptan or polyester mercaptan and polyisocyanate
The ratio of cyanate is according to functional group's NCO/SH molar ratios 0.8:1~1.2:1;Raw material is poured into mold after vacuum defoamation,
Urethane raw specific infrared curing stove is placed into according to program curing to cure, after curing completely cools to 60 degree,
The substrate of polyurethane eyeglass is obtained after demoulding cleaning;Program curing is:
25 DEG C~35 DEG C 0.5h~1h
35 DEG C~41 DEG C 2h~2.5h
41 DEG C~57 DEG C 2h~2.5h
57 DEG C~81 DEG C 3h~3.5h
81 DEG C~96 DEG C 2h~2.5h
96 DEG C~125 DEG C 2h~2.5h
125 DEG C~125 DEG C 2h~2.5h
125 DEG C~60 DEG C 2h~2.5h
60 DEG C~60 DEG C 0.5h~0.5h
At 60 DEG C, mold is removed, you can obtain polyurethane eyeglass substrate.
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CN110078892A (en) * | 2019-05-21 | 2019-08-02 | 镇江利德尔复合材料有限公司 | A kind of lower shape memory polyurethane material of new infrared stimulation |
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