CH318461A - Procédé de fabrication de papier couché et appareil pour l'exécution de ce procédé - Google Patents
Procédé de fabrication de papier couché et appareil pour l'exécution de ce procédéInfo
- Publication number
- CH318461A CH318461A CH318461DA CH318461A CH 318461 A CH318461 A CH 318461A CH 318461D A CH318461D A CH 318461DA CH 318461 A CH318461 A CH 318461A
- Authority
- CH
- Switzerland
- Prior art keywords
- compounds
- malononitrile
- methoxy
- formula
- use according
- Prior art date
Links
- 238000000034 method Methods 0.000 title description 7
- 150000001875 compounds Chemical class 0.000 claims description 30
- 239000004753 textile Substances 0.000 claims description 15
- 239000000463 material Substances 0.000 claims description 7
- 239000000835 fiber Substances 0.000 claims description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 claims description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
- 230000001419 dependent effect Effects 0.000 claims 2
- -1 R '= CN Chemical group 0.000 description 32
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 18
- CUONGYYJJVDODC-UHFFFAOYSA-N malononitrile Chemical compound N#CCC#N CUONGYYJJVDODC-UHFFFAOYSA-N 0.000 description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- 239000006096 absorbing agent Substances 0.000 description 11
- 239000012965 benzophenone Substances 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- 125000003545 alkoxy group Chemical group 0.000 description 5
- 125000003118 aryl group Chemical group 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 230000004224 protection Effects 0.000 description 4
- 125000001424 substituent group Chemical group 0.000 description 4
- CSUUDNFYSFENAE-UHFFFAOYSA-N (2-methoxyphenyl)-phenylmethanone Chemical compound COC1=CC=CC=C1C(=O)C1=CC=CC=C1 CSUUDNFYSFENAE-UHFFFAOYSA-N 0.000 description 3
- CKGKXGQVRVAKEA-UHFFFAOYSA-N (2-methylphenyl)-phenylmethanone Chemical compound CC1=CC=CC=C1C(=O)C1=CC=CC=C1 CKGKXGQVRVAKEA-UHFFFAOYSA-N 0.000 description 3
- USFZMSVCRYTOJT-UHFFFAOYSA-N Ammonium acetate Chemical compound N.CC(O)=O USFZMSVCRYTOJT-UHFFFAOYSA-N 0.000 description 3
- 239000005695 Ammonium acetate Substances 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 229960000583 acetic acid Drugs 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 125000002947 alkylene group Chemical group 0.000 description 3
- 229940043376 ammonium acetate Drugs 0.000 description 3
- 235000019257 ammonium acetate Nutrition 0.000 description 3
- 150000008366 benzophenones Chemical class 0.000 description 3
- 239000012362 glacial acetic acid Substances 0.000 description 3
- 230000005855 radiation Effects 0.000 description 3
- RFWYJPXOKLPVND-UHFFFAOYSA-N (2-ethoxyphenyl)-phenylmethanone Chemical compound CCOC1=CC=CC=C1C(=O)C1=CC=CC=C1 RFWYJPXOKLPVND-UHFFFAOYSA-N 0.000 description 2
- VMFJVWPCRCAWBS-UHFFFAOYSA-N (3-methoxyphenyl)-phenylmethanone Chemical compound COC1=CC=CC(C(=O)C=2C=CC=CC=2)=C1 VMFJVWPCRCAWBS-UHFFFAOYSA-N 0.000 description 2
- JJVJYPSXZCEIEQ-UHFFFAOYSA-N (4-chlorophenyl)-(4-methoxyphenyl)methanone Chemical compound C1=CC(OC)=CC=C1C(=O)C1=CC=C(Cl)C=C1 JJVJYPSXZCEIEQ-UHFFFAOYSA-N 0.000 description 2
- OGTSHGYHILFRHD-UHFFFAOYSA-N (4-fluorophenyl)-phenylmethanone Chemical group C1=CC(F)=CC=C1C(=O)C1=CC=CC=C1 OGTSHGYHILFRHD-UHFFFAOYSA-N 0.000 description 2
- WXPWZZHELZEVPO-UHFFFAOYSA-N (4-methylphenyl)-phenylmethanone Chemical compound C1=CC(C)=CC=C1C(=O)C1=CC=CC=C1 WXPWZZHELZEVPO-UHFFFAOYSA-N 0.000 description 2
- BEDXTNBAFZMDAL-UHFFFAOYSA-N 2-[bis(4-hydroxyphenyl)methylidene]propanedinitrile Chemical compound C1=CC(O)=CC=C1C(=C(C#N)C#N)C1=CC=C(O)C=C1 BEDXTNBAFZMDAL-UHFFFAOYSA-N 0.000 description 2
- NPFYZDNDJHZQKY-UHFFFAOYSA-N 4-Hydroxybenzophenone Chemical compound C1=CC(O)=CC=C1C(=O)C1=CC=CC=C1 NPFYZDNDJHZQKY-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- NQSMEZJWJJVYOI-UHFFFAOYSA-N Methyl 2-benzoylbenzoate Chemical group COC(=O)C1=CC=CC=C1C(=O)C1=CC=CC=C1 NQSMEZJWJJVYOI-UHFFFAOYSA-N 0.000 description 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
- 125000004104 aryloxy group Chemical group 0.000 description 2
- LFABNOYDEODDFX-UHFFFAOYSA-N bis(4-bromophenyl)methanone Chemical compound C1=CC(Br)=CC=C1C(=O)C1=CC=C(Br)C=C1 LFABNOYDEODDFX-UHFFFAOYSA-N 0.000 description 2
- ZWPWLKXZYNXATK-UHFFFAOYSA-N bis(4-methylphenyl)methanone Chemical compound C1=CC(C)=CC=C1C(=O)C1=CC=C(C)C=C1 ZWPWLKXZYNXATK-UHFFFAOYSA-N 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- DGJMPUGMZIKDRO-UHFFFAOYSA-N cyanoacetamide Chemical compound NC(=O)CC#N DGJMPUGMZIKDRO-UHFFFAOYSA-N 0.000 description 2
- 125000004494 ethyl ester group Chemical group 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 150000002894 organic compounds Chemical class 0.000 description 2
- LYXOWKPVTCPORE-UHFFFAOYSA-N phenyl-(4-phenylphenyl)methanone Chemical compound C=1C=C(C=2C=CC=CC=2)C=CC=1C(=O)C1=CC=CC=C1 LYXOWKPVTCPORE-UHFFFAOYSA-N 0.000 description 2
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- ZWAJLVLEBYIOTI-OLQVQODUSA-N (1s,6r)-7-oxabicyclo[4.1.0]heptane Chemical compound C1CCC[C@@H]2O[C@@H]21 ZWAJLVLEBYIOTI-OLQVQODUSA-N 0.000 description 1
- QHNLFVNIJGHXLD-UHFFFAOYSA-N (2,4-dimethylphenyl)-(3,4-dimethylphenyl)methanone Chemical compound CC1=CC(C)=CC=C1C(=O)C1=CC=C(C)C(C)=C1 QHNLFVNIJGHXLD-UHFFFAOYSA-N 0.000 description 1
- COCNAUUGIBCANE-UHFFFAOYSA-N (2,4-dimethylphenyl)-(3-methylphenyl)methanone Chemical compound CC1=CC(C)=CC=C1C(=O)C1=CC=CC(C)=C1 COCNAUUGIBCANE-UHFFFAOYSA-N 0.000 description 1
- ZTTANZQQBIQFEG-UHFFFAOYSA-N (2-benzoylphenyl) acetate Chemical compound CC(=O)OC1=CC=CC=C1C(=O)C1=CC=CC=C1 ZTTANZQQBIQFEG-UHFFFAOYSA-N 0.000 description 1
- NDGSHOQCFOWVIW-UHFFFAOYSA-N (2-bromo-4-methylphenyl)-phenylmethanone Chemical compound BrC1=CC(C)=CC=C1C(=O)C1=CC=CC=C1 NDGSHOQCFOWVIW-UHFFFAOYSA-N 0.000 description 1
- KSTOVOWICRHLNC-UHFFFAOYSA-N (2-bromophenyl)-(2-methoxy-5-methylphenyl)methanone Chemical compound COC1=CC=C(C)C=C1C(=O)C1=CC=CC=C1Br KSTOVOWICRHLNC-UHFFFAOYSA-N 0.000 description 1
- LMHPMEIPNFBOES-UHFFFAOYSA-N (2-chloro-4-phenylphenyl)-phenylmethanone Chemical compound ClC1=C(C(=O)C2=CC=CC=C2)C=CC(=C1)C1=CC=CC=C1 LMHPMEIPNFBOES-UHFFFAOYSA-N 0.000 description 1
- WUIWHKKHOULZRK-UHFFFAOYSA-N (2-chlorophenyl)-(2,4-dimethylphenyl)methanone Chemical compound CC1=CC(C)=CC=C1C(=O)C1=CC=CC=C1Cl WUIWHKKHOULZRK-UHFFFAOYSA-N 0.000 description 1
- VMHYWKBKHMYRNF-UHFFFAOYSA-N (2-chlorophenyl)-phenylmethanone Chemical compound ClC1=CC=CC=C1C(=O)C1=CC=CC=C1 VMHYWKBKHMYRNF-UHFFFAOYSA-N 0.000 description 1
- DBCVWUIFYSBIJB-UHFFFAOYSA-N (2-ethoxy-5-methylphenyl)-phenylmethanone Chemical compound CCOC1=CC=C(C)C=C1C(=O)C1=CC=CC=C1 DBCVWUIFYSBIJB-UHFFFAOYSA-N 0.000 description 1
- DWFDQVMFSLLMPE-UHFFFAOYSA-N (2-fluorophenyl)-phenylmethanone Chemical compound FC1=CC=CC=C1C(=O)C1=CC=CC=C1 DWFDQVMFSLLMPE-UHFFFAOYSA-N 0.000 description 1
- ZSTOXXBHUBYMMY-UHFFFAOYSA-N (2-methoxy-5-methylphenyl)-phenylmethanone Chemical compound COC1=CC=C(C)C=C1C(=O)C1=CC=CC=C1 ZSTOXXBHUBYMMY-UHFFFAOYSA-N 0.000 description 1
- QWWJLMQOKZOTNX-UHFFFAOYSA-N (2-methoxyphenyl)-(4-methoxyphenyl)methanone Chemical compound C1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1OC QWWJLMQOKZOTNX-UHFFFAOYSA-N 0.000 description 1
- AAGUYRVFXRTPQG-UHFFFAOYSA-N (2-methyl-5-propan-2-ylphenyl)-phenylmethanone Chemical compound CC(C)C1=CC=C(C)C(C(=O)C=2C=CC=CC=2)=C1 AAGUYRVFXRTPQG-UHFFFAOYSA-N 0.000 description 1
- LERREUOVCXYKGR-UHFFFAOYSA-N (2-phenoxyphenyl)-phenylmethanone Chemical compound C=1C=CC=C(OC=2C=CC=CC=2)C=1C(=O)C1=CC=CC=C1 LERREUOVCXYKGR-UHFFFAOYSA-N 0.000 description 1
- LLUPHTAYNHAVQT-UHFFFAOYSA-N (3,4-dichlorophenyl)-phenylmethanone Chemical compound C1=C(Cl)C(Cl)=CC=C1C(=O)C1=CC=CC=C1 LLUPHTAYNHAVQT-UHFFFAOYSA-N 0.000 description 1
- XXLGSXCYXYPMHH-UHFFFAOYSA-N (3,4-dimethoxyphenyl)-(3-ethoxy-4-methoxyphenyl)methanone Chemical compound C1=C(OC)C(OCC)=CC(C(=O)C=2C=C(OC)C(OC)=CC=2)=C1 XXLGSXCYXYPMHH-UHFFFAOYSA-N 0.000 description 1
- YEYJXDBCSFBTSB-UHFFFAOYSA-N (3,5-dimethylphenyl)-(2,4,6-trimethylphenyl)methanone Chemical compound CC1=CC(C)=CC(C(=O)C=2C(=CC(C)=CC=2C)C)=C1 YEYJXDBCSFBTSB-UHFFFAOYSA-N 0.000 description 1
- FVSGBGVLSLEIMO-UHFFFAOYSA-N (3-benzoylphenyl) acetate Chemical compound CC(=O)OC1=CC=CC(C(=O)C=2C=CC=CC=2)=C1 FVSGBGVLSLEIMO-UHFFFAOYSA-N 0.000 description 1
- CPLWKNRPZVNELG-UHFFFAOYSA-N (3-chlorophenyl)-phenylmethanone Chemical compound ClC1=CC=CC(C(=O)C=2C=CC=CC=2)=C1 CPLWKNRPZVNELG-UHFFFAOYSA-N 0.000 description 1
- IIVNEWOXXBECGK-UHFFFAOYSA-N (3-ethoxyphenyl)-phenylmethanone Chemical compound CCOC1=CC=CC(C(=O)C=2C=CC=CC=2)=C1 IIVNEWOXXBECGK-UHFFFAOYSA-N 0.000 description 1
- MPRUUWLSXRQSKO-UHFFFAOYSA-N (3-iodo-4-methoxyphenyl)-(2-methylphenyl)methanone Chemical compound IC=1C=C(C=CC=1OC)C(C1=C(C=CC=C1)C)=O MPRUUWLSXRQSKO-UHFFFAOYSA-N 0.000 description 1
- LZKNYLDZTGMYFW-UHFFFAOYSA-N (3-iodo-4-methoxyphenyl)-phenylmethanone Chemical compound C1=C(I)C(OC)=CC=C1C(=O)C1=CC=CC=C1 LZKNYLDZTGMYFW-UHFFFAOYSA-N 0.000 description 1
- URBLVRAVOIVZFJ-UHFFFAOYSA-N (3-methylphenyl)-phenylmethanone Chemical compound CC1=CC=CC(C(=O)C=2C=CC=CC=2)=C1 URBLVRAVOIVZFJ-UHFFFAOYSA-N 0.000 description 1
- YJQAKTPJZFLSFL-UHFFFAOYSA-N (3-phenoxyphenyl)-phenylmethanone Chemical compound C=1C=CC(OC=2C=CC=CC=2)=CC=1C(=O)C1=CC=CC=C1 YJQAKTPJZFLSFL-UHFFFAOYSA-N 0.000 description 1
- HKCNCNXZAZPKDZ-UHFFFAOYSA-N (4,4-difluorocyclohexa-1,5-dien-1-yl)-phenylmethanone Chemical compound C1=CC(F)(F)CC=C1C(=O)C1=CC=CC=C1 HKCNCNXZAZPKDZ-UHFFFAOYSA-N 0.000 description 1
- DGBLQRCFBNFTSZ-UHFFFAOYSA-N (4-benzoylphenyl) acetate Chemical compound C1=CC(OC(=O)C)=CC=C1C(=O)C1=CC=CC=C1 DGBLQRCFBNFTSZ-UHFFFAOYSA-N 0.000 description 1
- FYMCXGILCMIOKD-UHFFFAOYSA-N (4-bromophenyl)-(4-chlorophenyl)methanone Chemical compound C1=CC(Cl)=CC=C1C(=O)C1=CC=C(Br)C=C1 FYMCXGILCMIOKD-UHFFFAOYSA-N 0.000 description 1
- CTFATYIGPWOEMM-UHFFFAOYSA-N (4-bromophenyl)-(4-ethoxyphenyl)methanone Chemical compound C1=CC(OCC)=CC=C1C(=O)C1=CC=C(Br)C=C1 CTFATYIGPWOEMM-UHFFFAOYSA-N 0.000 description 1
- YMDVVGLPIKIHRX-UHFFFAOYSA-N (4-chlorophenyl)-(3,4-dimethylphenyl)methanone Chemical compound C1=C(C)C(C)=CC=C1C(=O)C1=CC=C(Cl)C=C1 YMDVVGLPIKIHRX-UHFFFAOYSA-N 0.000 description 1
- FSHVUFAEQUBENQ-UHFFFAOYSA-N (4-dodecoxyphenyl)-phenylmethanone Chemical compound C1=CC(OCCCCCCCCCCCC)=CC=C1C(=O)C1=CC=CC=C1 FSHVUFAEQUBENQ-UHFFFAOYSA-N 0.000 description 1
- IBRIFDGHXDFGBY-UHFFFAOYSA-N (4-ethoxyphenyl)-phenylmethanone Chemical compound C1=CC(OCC)=CC=C1C(=O)C1=CC=CC=C1 IBRIFDGHXDFGBY-UHFFFAOYSA-N 0.000 description 1
- DKQYTWSXBRWWHQ-UHFFFAOYSA-N (4-fluoro-2-methylphenyl)-phenylmethanone Chemical compound CC1=CC(F)=CC=C1C(=O)C1=CC=CC=C1 DKQYTWSXBRWWHQ-UHFFFAOYSA-N 0.000 description 1
- OMZSPDPLNQUNBS-UHFFFAOYSA-N (4-methoxy-2,5-dimethylphenyl)-phenylmethanone Chemical compound C1=C(C)C(OC)=CC(C)=C1C(=O)C1=CC=CC=C1 OMZSPDPLNQUNBS-UHFFFAOYSA-N 0.000 description 1
- KDYYFNARCRZVDG-UHFFFAOYSA-N (4-methoxy-2-methylphenyl)-phenylmethanone Chemical compound CC1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1 KDYYFNARCRZVDG-UHFFFAOYSA-N 0.000 description 1
- XKQLZRYPUPMZHI-UHFFFAOYSA-N (4-methoxy-3-methylphenyl)-phenylmethanone Chemical compound C1=C(C)C(OC)=CC=C1C(=O)C1=CC=CC=C1 XKQLZRYPUPMZHI-UHFFFAOYSA-N 0.000 description 1
- FOVUIVBXXGGJMP-UHFFFAOYSA-N (4-methoxy-5-methyl-2-propan-2-ylphenyl)-phenylmethanone Chemical compound COC1=C(C=C(C(=O)C2=CC=CC=C2)C(=C1)C(C)C)C FOVUIVBXXGGJMP-UHFFFAOYSA-N 0.000 description 1
- VPAQGAOJFZBBTK-UHFFFAOYSA-N (4-methoxyphenyl)-(2-methylphenyl)methanone Chemical compound C1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1C VPAQGAOJFZBBTK-UHFFFAOYSA-N 0.000 description 1
- SWFHGTMLYIBPPA-UHFFFAOYSA-N (4-methoxyphenyl)-phenylmethanone Chemical compound C1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1 SWFHGTMLYIBPPA-UHFFFAOYSA-N 0.000 description 1
- ITVUPWDTDWMACZ-UHFFFAOYSA-N (4-phenoxyphenyl)-phenylmethanone Chemical compound C=1C=C(OC=2C=CC=CC=2)C=CC=1C(=O)C1=CC=CC=C1 ITVUPWDTDWMACZ-UHFFFAOYSA-N 0.000 description 1
- IRPCKIPNMKBCCI-UHFFFAOYSA-N (5-ethoxy-2,4-dimethylphenyl)-phenylmethanone Chemical compound C(C)OC=1C(=CC(=C(C(=O)C2=CC=CC=C2)C1)C)C IRPCKIPNMKBCCI-UHFFFAOYSA-N 0.000 description 1
- DATDSXLPCYAEOK-UHFFFAOYSA-N (5-fluoro-2-methoxyphenyl)-phenylmethanone Chemical compound COC1=CC=C(F)C=C1C(=O)C1=CC=CC=C1 DATDSXLPCYAEOK-UHFFFAOYSA-N 0.000 description 1
- SZKXPIUFDIGZMJ-UHFFFAOYSA-N (5-iodo-2-methoxyphenyl)-(2-methylphenyl)methanone Chemical compound COC1=CC=C(I)C=C1C(=O)C1=CC=CC=C1C SZKXPIUFDIGZMJ-UHFFFAOYSA-N 0.000 description 1
- GCDPERPXPREHJF-UHFFFAOYSA-N 1-iodododecane Chemical compound CCCCCCCCCCCCI GCDPERPXPREHJF-UHFFFAOYSA-N 0.000 description 1
- GELKGHVAFRCJNA-UHFFFAOYSA-N 2,2-Dimethyloxirane Chemical compound CC1(C)CO1 GELKGHVAFRCJNA-UHFFFAOYSA-N 0.000 description 1
- XFCNIRLJJYYGDW-UHFFFAOYSA-N 2-benzoyl-n-ethylbenzamide Chemical compound CCNC(=O)C1=CC=CC=C1C(=O)C1=CC=CC=C1 XFCNIRLJJYYGDW-UHFFFAOYSA-N 0.000 description 1
- WQVBZJXNXCEFJN-UHFFFAOYSA-N 2-benzoylbenzamide Chemical compound NC(=O)C1=CC=CC=C1C(=O)C1=CC=CC=C1 WQVBZJXNXCEFJN-UHFFFAOYSA-N 0.000 description 1
- AXJXRLHTQQONQR-UHFFFAOYSA-N 3-benzoylbenzoic acid Chemical compound OC(=O)C1=CC=CC(C(=O)C=2C=CC=CC=2)=C1 AXJXRLHTQQONQR-UHFFFAOYSA-N 0.000 description 1
- OKISUZLXOYGIFP-UHFFFAOYSA-N 4,4'-dichlorobenzophenone Chemical compound C1=CC(Cl)=CC=C1C(=O)C1=CC=C(Cl)C=C1 OKISUZLXOYGIFP-UHFFFAOYSA-N 0.000 description 1
- YSZWJJANSNFQMM-UHFFFAOYSA-N 4-benzoylbenzonitrile Chemical compound C=1C=C(C#N)C=CC=1C(=O)C1=CC=CC=C1 YSZWJJANSNFQMM-UHFFFAOYSA-N 0.000 description 1
- UGVRJVHOJNYEHR-UHFFFAOYSA-N 4-chlorobenzophenone Chemical compound C1=CC(Cl)=CC=C1C(=O)C1=CC=CC=C1 UGVRJVHOJNYEHR-UHFFFAOYSA-N 0.000 description 1
- TXOWBBUBRITKNS-UHFFFAOYSA-N 4-sulfonylcyclohexa-1,5-diene-1-carboxylic acid Chemical compound OC(=O)C1=CCC(=S(=O)=O)C=C1 TXOWBBUBRITKNS-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- UHKYXWSUTYAGLS-UHFFFAOYSA-N BrC1=C(C(=O)C2=C(C=C(C=C2C)C)C)C(=CC(=C1)C)C Chemical compound BrC1=C(C(=O)C2=C(C=C(C=C2C)C)C)C(=CC(=C1)C)C UHKYXWSUTYAGLS-UHFFFAOYSA-N 0.000 description 1
- SZFYDHGERHGQBN-UHFFFAOYSA-N BrC=1C=C(C(=O)C2=CC=CC=C2)C=C(C=1OCC)Br Chemical compound BrC=1C=C(C(=O)C2=CC=CC=C2)C=C(C=1OCC)Br SZFYDHGERHGQBN-UHFFFAOYSA-N 0.000 description 1
- BLKOTCYIMJZUOF-UHFFFAOYSA-N C(C)(=O)OC1=C(C=C(C(=O)C2=CC=CC=C2)C=C1C(C)C)C Chemical compound C(C)(=O)OC1=C(C=C(C(=O)C2=CC=CC=C2)C=C1C(C)C)C BLKOTCYIMJZUOF-UHFFFAOYSA-N 0.000 description 1
- YEFSBJPJVDNUNR-UHFFFAOYSA-N C(C)OC1=C(C=C(C(=O)C2=CC(=C(C=C2)OC)OC)C=C1)OC Chemical compound C(C)OC1=C(C=C(C(=O)C2=CC(=C(C=C2)OC)OC)C=C1)OC YEFSBJPJVDNUNR-UHFFFAOYSA-N 0.000 description 1
- DMYUJCPMRQPXHW-UHFFFAOYSA-N C(C1=CC=CC=C1)OC1=C(C=C(C=C1)C(=O)C1=CC(=C(C=C1)OCC1=CC=CC=C1)OC)OC Chemical compound C(C1=CC=CC=C1)OC1=C(C=C(C=C1)C(=O)C1=CC(=C(C=C1)OCC1=CC=CC=C1)OC)OC DMYUJCPMRQPXHW-UHFFFAOYSA-N 0.000 description 1
- AJQZGPFKDGYTCZ-UHFFFAOYSA-N C(CC(C)C)OC1=CC=C(C(=O)C2=CC=CC=C2)C=C1 Chemical compound C(CC(C)C)OC1=CC=C(C(=O)C2=CC=CC=C2)C=C1 AJQZGPFKDGYTCZ-UHFFFAOYSA-N 0.000 description 1
- LIVAFZGQBICBOO-UHFFFAOYSA-N CC1=C(C(=O)C2=C(C=CC(=C2)C(C)C)C)C=C(C=C1)C(C)C Chemical compound CC1=C(C(=O)C2=C(C=CC(=C2)C(C)C)C)C=C(C=C1)C(C)C LIVAFZGQBICBOO-UHFFFAOYSA-N 0.000 description 1
- UICNTHTUDKNNOQ-UHFFFAOYSA-N COC1=C(C(=O)C2=CC=CC=C2)C(=CC=C1C)OC Chemical compound COC1=C(C(=O)C2=CC=CC=C2)C(=CC=C1C)OC UICNTHTUDKNNOQ-UHFFFAOYSA-N 0.000 description 1
- NQXJKUXUMHAXBP-UHFFFAOYSA-N COC1=CC=C(C=C1)C1=CC=C(C(=O)C2=CC=C(C=C2)C2=CC=CC=C2)C=C1 Chemical compound COC1=CC=C(C=C1)C1=CC=C(C(=O)C2=CC=C(C=C2)C2=CC=CC=C2)C=C1 NQXJKUXUMHAXBP-UHFFFAOYSA-N 0.000 description 1
- DPRFTRFFNZDGJP-UHFFFAOYSA-N COC1=CC=C(OC2=CC=C(C(=O)C3=CC=C(C=C3)OC3=CC=C(C=C3)OC)C=C2)C=C1 Chemical compound COC1=CC=C(OC2=CC=C(C(=O)C3=CC=C(C=C3)OC3=CC=C(C=C3)OC)C=C2)C=C1 DPRFTRFFNZDGJP-UHFFFAOYSA-N 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- KSXHWOSTDXUVAH-UHFFFAOYSA-N ClC=1C(=C(C(=O)C2=C(C=C(C=C2OC)C)OC)C=C(C=1OC)Cl)OC Chemical compound ClC=1C(=C(C(=O)C2=C(C=C(C=C2OC)C)OC)C=C(C=1OC)Cl)OC KSXHWOSTDXUVAH-UHFFFAOYSA-N 0.000 description 1
- 240000000491 Corchorus aestuans Species 0.000 description 1
- 235000011777 Corchorus aestuans Nutrition 0.000 description 1
- 235000010862 Corchorus capsularis Nutrition 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- XZMCDFZZKTWFGF-UHFFFAOYSA-N Cyanamide Chemical compound NC#N XZMCDFZZKTWFGF-UHFFFAOYSA-N 0.000 description 1
- ZFIVKAOQEXOYFY-UHFFFAOYSA-N Diepoxybutane Chemical compound C1OC1C1OC1 ZFIVKAOQEXOYFY-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- CTKINSOISVBQLD-UHFFFAOYSA-N Glycidol Chemical compound OCC1CO1 CTKINSOISVBQLD-UHFFFAOYSA-N 0.000 description 1
- JGZWJYJYTNMOLP-UHFFFAOYSA-N IC=1C=C(C(=O)C2=CC=CC=C2)C=C(C=1)I Chemical compound IC=1C=C(C(=O)C2=CC=CC=C2)C=C(C=1)I JGZWJYJYTNMOLP-UHFFFAOYSA-N 0.000 description 1
- SOWBFZRMHSNYGE-UHFFFAOYSA-N Monoamide-Oxalic acid Natural products NC(=O)C(O)=O SOWBFZRMHSNYGE-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- AWMVMTVKBNGEAK-UHFFFAOYSA-N Styrene oxide Chemical compound C1OC1C1=CC=CC=C1 AWMVMTVKBNGEAK-UHFFFAOYSA-N 0.000 description 1
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 1
- 230000006750 UV protection Effects 0.000 description 1
- YPCASAXQFPRFPZ-UHFFFAOYSA-N [2-(2,3-dimethylphenoxy)phenyl]-phenylmethanone Chemical compound C1=C(C(=C(C=C1)OC1=C(C(=O)C2=CC=CC=C2)C=CC=C1)C)C YPCASAXQFPRFPZ-UHFFFAOYSA-N 0.000 description 1
- CSEADVGOSDRCEL-UHFFFAOYSA-N [4-(4-methoxyphenyl)phenyl]-phenylmethanone Chemical compound C1=CC(OC)=CC=C1C1=CC=C(C(=O)C=2C=CC=CC=2)C=C1 CSEADVGOSDRCEL-UHFFFAOYSA-N 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 125000004423 acyloxy group Chemical group 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 230000002152 alkylating effect Effects 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 150000005840 aryl radicals Chemical class 0.000 description 1
- CSKNSYBAZOQPLR-UHFFFAOYSA-N benzenesulfonyl chloride Chemical compound ClS(=O)(=O)C1=CC=CC=C1 CSKNSYBAZOQPLR-UHFFFAOYSA-N 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 125000000319 biphenyl-4-yl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 description 1
- SCBBVCPZAKTFJU-UHFFFAOYSA-N bis(2,4-dichlorophenyl)methanone Chemical compound ClC1=CC(Cl)=CC=C1C(=O)C1=CC=C(Cl)C=C1Cl SCBBVCPZAKTFJU-UHFFFAOYSA-N 0.000 description 1
- SYFPXYGMQIWYKK-UHFFFAOYSA-N bis(3,4,5-trimethoxyphenyl)methanone Chemical compound COC1=C(OC)C(OC)=CC(C(=O)C=2C=C(OC)C(OC)=C(OC)C=2)=C1 SYFPXYGMQIWYKK-UHFFFAOYSA-N 0.000 description 1
- RDGPYSMMOAURJB-UHFFFAOYSA-N bis(3-ethoxy-4-methoxyphenyl)methanone Chemical compound C1=C(OC)C(OCC)=CC(C(=O)C=2C=C(OCC)C(OC)=CC=2)=C1 RDGPYSMMOAURJB-UHFFFAOYSA-N 0.000 description 1
- FXLWAWKMFVSTOS-UHFFFAOYSA-N bis(3-fluoro-4-methoxyphenyl)methanone Chemical compound C1=C(F)C(OC)=CC=C1C(=O)C1=CC=C(OC)C(F)=C1 FXLWAWKMFVSTOS-UHFFFAOYSA-N 0.000 description 1
- SQQOQHHHNHBVEH-UHFFFAOYSA-N bis(4-propan-2-yloxyphenyl)methanone Chemical compound C1=CC(OC(C)C)=CC=C1C(=O)C1=CC=C(OC(C)C)C=C1 SQQOQHHHNHBVEH-UHFFFAOYSA-N 0.000 description 1
- 125000004799 bromophenyl group Chemical group 0.000 description 1
- 125000002837 carbocyclic group Chemical group 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 125000000068 chlorophenyl group Chemical group 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000005672 electromagnetic field Effects 0.000 description 1
- 125000005448 ethoxyethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 150000002497 iodine compounds Chemical class 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000002560 nitrile group Chemical group 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- QAHGFRPSVORUTJ-UHFFFAOYSA-N phenyl-(2,4,6-trichlorophenyl)methanone Chemical compound ClC1=CC(Cl)=CC(Cl)=C1C(=O)C1=CC=CC=C1 QAHGFRPSVORUTJ-UHFFFAOYSA-N 0.000 description 1
- HYTXMZZSNAJVGC-UHFFFAOYSA-N phenyl-(2-prop-2-enylphenyl)methanone Chemical compound C=CCC1=CC=CC=C1C(=O)C1=CC=CC=C1 HYTXMZZSNAJVGC-UHFFFAOYSA-N 0.000 description 1
- KOVXIYLMAMPQLP-UHFFFAOYSA-N phenyl-(3-phenylphenyl)methanone Chemical compound C=1C=CC(C=2C=CC=CC=2)=CC=1C(=O)C1=CC=CC=C1 KOVXIYLMAMPQLP-UHFFFAOYSA-N 0.000 description 1
- NMPNTBQOLRXPGK-UHFFFAOYSA-N phenyl-(4-phenylmethoxyphenyl)methanone Chemical compound C=1C=C(OCC=2C=CC=CC=2)C=CC=1C(=O)C1=CC=CC=C1 NMPNTBQOLRXPGK-UHFFFAOYSA-N 0.000 description 1
- CKFPWZPBRHQASN-UHFFFAOYSA-N phenyl-(4-propan-2-ylphenyl)methanone Chemical compound C1=CC(C(C)C)=CC=C1C(=O)C1=CC=CC=C1 CKFPWZPBRHQASN-UHFFFAOYSA-N 0.000 description 1
- JGIYVLYYGJBGIY-UHFFFAOYSA-N phenyl-(4-propylphenyl)methanone Chemical group C1=CC(CCC)=CC=C1C(=O)C1=CC=CC=C1 JGIYVLYYGJBGIY-UHFFFAOYSA-N 0.000 description 1
- OCIICNRVGIWCOF-UHFFFAOYSA-N phenyl-[4-(2-phenylethyl)phenyl]methanone Chemical compound C=1C=C(CCC=2C=CC=CC=2)C=CC=1C(=O)C1=CC=CC=C1 OCIICNRVGIWCOF-UHFFFAOYSA-N 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000003495 polar organic solvent Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000012192 staining solution Substances 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 150000003456 sulfonamides Chemical class 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
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H25/00—After-treatment of paper not provided for in groups D21H17/00 - D21H23/00
- D21H25/08—Rearranging applied substances, e.g. metering, smoothing; Removing excess material
- D21H25/12—Rearranging applied substances, e.g. metering, smoothing; Removing excess material with an essentially cylindrical body, e.g. roll or rod
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H5/00—Special paper or cardboard not otherwise provided for
- D21H5/0005—Processes or apparatus specially adapted for applying liquids or other fluent materials to finished paper or board, e.g. impregnating, coating
- D21H5/006—Controlling or regulating
- D21H5/0062—Regulating the amount or the distribution, e.g. smoothing, of essentially fluent material already applied to the paper; Recirculating excess coating material applied to paper
- D21H5/0067—Regulating the amount or the distribution, e.g. smoothing, of essentially fluent material already applied to the paper; Recirculating excess coating material applied to paper with an essentially cylindrical body, e.g. roll or rod
Landscapes
- Paper (AREA)
- Coating Apparatus (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US328840A US2729192A (en) | 1952-12-31 | 1952-12-31 | Doctor blade for paper coating apparatus |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH318461A true CH318461A (fr) | 1957-01-15 |
Family
ID=23282671
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH318461D CH318461A (fr) | 1952-12-31 | 1953-12-23 | Procédé de fabrication de papier couché et appareil pour l'exécution de ce procédé |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US2729192A (is") |
| BE (1) | BE525629A (is") |
| CH (1) | CH318461A (is") |
| DE (1) | DE1039827B (is") |
| FR (1) | FR1094628A (is") |
| GB (1) | GB759281A (is") |
Families Citing this family (43)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2830555A (en) * | 1954-10-29 | 1958-04-15 | Minnesota & Ontario Paper Co | Roller apparatus for coating paper |
| US2842092A (en) * | 1955-03-02 | 1958-07-08 | John Waldron Corp | Reverse roll coating machine with blade support for web |
| US2946307A (en) * | 1955-12-23 | 1960-07-26 | Champion Paper & Fibre Co | Apparatus for coating paper |
| US2970564A (en) * | 1955-12-23 | 1961-02-07 | Champion Paper & Fibre Co | Apparatus for coating paper |
| US3000760A (en) * | 1957-06-28 | 1961-09-19 | Eastman Kodak Co | Method and apparatus for coating a surface |
| US3143438A (en) * | 1960-07-26 | 1964-08-04 | West Virginia Pulp & Paper Co | Apparatus for coating web material |
| NL268472A (is") * | 1960-08-29 | |||
| NL268622A (is") * | 1960-09-19 | |||
| US3132048A (en) * | 1961-04-07 | 1964-05-05 | Higginson Norman | Wall paper pasting and paper hanging apparatus |
| US3182632A (en) * | 1962-02-05 | 1965-05-11 | Riegel Paper Corp | Coating apparatus with improved doctor means |
| US3245377A (en) * | 1962-06-20 | 1966-04-12 | Kimberly Clark Co | Apparatus for coating paper |
| US3187716A (en) * | 1962-09-19 | 1965-06-08 | Rice Barton Corp | Coating machinery |
| US3559572A (en) * | 1969-05-14 | 1971-02-02 | Us Plywood Champ Papers Inc | Method of inking a printing roll using a metering roll and revolving doctor rod |
| DE2008082B2 (de) * | 1970-02-21 | 1973-05-03 | Jagenberg-Werke AG, 4000 Düsseldorf | Vorrichtung zum regeln der auftragsstaerke beim beschichten laufender werkstoffbahnen |
| DE2438668B2 (de) * | 1973-08-28 | 1979-03-01 | Texogesa S.A., Genf (Schweiz) | Farbwerk für Druckmaschinen |
| DE2633145A1 (de) * | 1976-07-23 | 1978-06-08 | Agfa Gevaert Ag | Vorrichtung zur nassbehandlung fotografischer schichttraeger |
| US4192712A (en) * | 1977-12-13 | 1980-03-11 | Beloit Corporation | Combined breaker size press coater |
| DE2856088A1 (de) * | 1978-12-23 | 1980-07-03 | Maschf Augsburg Nuernberg Ag | Farbwerk |
| DE2935413C2 (de) * | 1979-09-01 | 1986-02-27 | Küsters, Eduard, 4150 Krefeld | Vorrichtung zum kontinuierlichen Behandeln einer textilen oder ähnlichen Warenbahn mit einem Behandlungsmedium in Schaumform |
| US4408527A (en) * | 1981-05-26 | 1983-10-11 | Bell Clinton C | Flexographic ink distribution system |
| US4425848A (en) | 1981-05-26 | 1984-01-17 | Bell Clinton C | Flexographic ink distribution system |
| US4527471A (en) * | 1983-05-06 | 1985-07-09 | Dahlgren Harold P | Dampening fluid removal device |
| DE3417487A1 (de) * | 1984-05-11 | 1985-11-21 | J.M. Voith Gmbh, 7920 Heidenheim | Vorrichtung zum auftragen einer fluessigkeit auf eine laufende bahn |
| FI853041A0 (fi) * | 1985-08-07 | 1985-08-07 | Valmet Oy | Anordning foer belaeggning av materialbana. |
| US4808445A (en) * | 1987-08-26 | 1989-02-28 | Beloit Corporation | Coating apparatus and method |
| SE463078B (sv) * | 1988-09-27 | 1990-10-08 | Btg Kaelle Inventing Ab | Paafoeringsanordning foer en- eller tvaasidig belaeggning av en loepande bana |
| US5340611A (en) * | 1989-07-25 | 1994-08-23 | J. M. Voith Gmbh | Process for coating travelling webs |
| US5264247A (en) * | 1990-09-14 | 1993-11-23 | Valmet Paper Machinery Inc. | Process for the manufacture of a coating bar for a bar coater |
| US5595601A (en) * | 1990-09-14 | 1997-01-21 | Valmet Corporation | Coating bar for a bar coater |
| DE4038874C2 (de) * | 1990-12-06 | 1997-01-23 | Kuesters Eduard Maschf | Vorrichtung zur Aufbringung einer Behandlungsflüssigkeit auf eine laufende Textilbahn |
| US5228920A (en) * | 1991-06-03 | 1993-07-20 | Thompson Iii Ernest E | Film coating unit |
| DE4131131C2 (de) * | 1991-09-19 | 1994-07-21 | Voith Gmbh J M | Vorrichtung zum Auftragen von Streichfarbe auf eine Faserstoffbahn |
| US6110281A (en) * | 1992-10-15 | 2000-08-29 | Dial-In Equipment Company | Preconditioning means for non-woven rolls |
| DE4302437A1 (en) * | 1993-01-29 | 1993-08-12 | Voith Gmbh J M | Paper web coating for low strength recycled paper material - by applying part of coating vol. at station with drying between stations, for strengthening |
| DE59405014D1 (de) * | 1993-08-07 | 1998-02-19 | Voith Gmbh J M | Vorrichtung zum Streichen einer Papierbahn |
| DE4402744C2 (de) * | 1994-01-31 | 1997-10-16 | Voith Gmbh J M | Vorrichtung zum Auftragen von Streichfarbe auf eine Faserstoffbahn |
| DE19606459A1 (de) | 1996-02-21 | 1997-08-28 | Voith Sulzer Papiermasch Gmbh | Verfahren und Vorrichtungen zum Auftragen eines flüssigen oder pastösen Mediums auf eine laufende Materialbahn |
| US7329437B2 (en) * | 2001-08-17 | 2008-02-12 | Fujifilm Corporation | Coating method and coating apparatus |
| US7527691B2 (en) * | 2003-01-17 | 2009-05-05 | Fujifilm Corporation | Coating apparatus and coating method |
| DE10316337A1 (de) * | 2003-04-10 | 2004-10-28 | Eduard Küsters Maschinenfabrik GmbH & Co. KG | Auftragswerk zur Applikation von Flotte auf eine laufende Bahn |
| EP1614483A3 (de) * | 2004-07-05 | 2006-11-15 | Jakob Weiss & Sohne Maschinenfabrik Gmbh | Rakelvorrichtung und Rakelverfahren |
| DE102012001956A1 (de) * | 2012-02-02 | 2013-08-08 | Olbrich Gmbh | Beschichtungssystem für flexible Bahnen |
| JP6222464B2 (ja) * | 2014-02-25 | 2017-11-01 | セイコーエプソン株式会社 | 液体吐出装置及び媒体の前処理方法 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1968911A (en) * | 1931-02-07 | 1934-08-07 | Potdevin Machine Co | Waxing machine |
| US2136739A (en) * | 1937-06-24 | 1938-11-15 | Canada Paper Company | Apparatus for making laminated wrapping papers |
| US2237068A (en) * | 1938-08-27 | 1941-04-01 | Champion Paper & Fibre Co | Method for making coated paper |
| US2334102A (en) * | 1940-08-26 | 1943-11-09 | Dow Chemical Co | Coating equipment |
| US2368176A (en) * | 1940-09-20 | 1945-01-30 | Trist Arthur Ronald | Machine for the coating of webs of paper and like absorbent material |
| US2534320A (en) * | 1946-05-16 | 1950-12-19 | Champion Paper & Fibre Co | Apparatus for coating paper |
| US2534321A (en) * | 1946-05-16 | 1950-12-19 | Champion Paper & Fibre Co | Coating method and apparatus |
| US2598733A (en) * | 1949-03-16 | 1952-06-03 | Champion Paper & Fibre Co | Wiping blade for coating devices |
| DE841544C (de) * | 1950-12-03 | 1952-06-16 | J W Zanders Feinpapierfabrik G | Schabemesser zum Abstreifen des UEberschusses an Streichfluessigkeit von Papier- oder Gewebebahnen |
-
0
- FR FR1094628D patent/FR1094628A/fr not_active Expired
- BE BE525629D patent/BE525629A/xx unknown
-
1952
- 1952-12-31 US US328840A patent/US2729192A/en not_active Expired - Lifetime
-
1953
- 1953-12-07 GB GB33954/53A patent/GB759281A/en not_active Expired
- 1953-12-23 CH CH318461D patent/CH318461A/de unknown
- 1953-12-31 DE DEC8690A patent/DE1039827B/de active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| BE525629A (is") | |
| DE1039827B (de) | 1958-09-25 |
| GB759281A (en) | 1956-10-17 |
| US2729192A (en) | 1956-01-03 |
| FR1094628A (is") | 1955-05-23 |
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