CN101087836A - 用于标记基材的涂料组合物 - Google Patents
用于标记基材的涂料组合物 Download PDFInfo
- Publication number
- CN101087836A CN101087836A CNA200580044394XA CN200580044394A CN101087836A CN 101087836 A CN101087836 A CN 101087836A CN A200580044394X A CNA200580044394X A CN A200580044394XA CN 200580044394 A CN200580044394 A CN 200580044394A CN 101087836 A CN101087836 A CN 101087836A
- Authority
- CN
- China
- Prior art keywords
- composition
- acid
- alkyl
- fluorane
- methyl
- 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
- 239000008199 coating composition Substances 0.000 title claims abstract description 36
- 239000000758 substrate Substances 0.000 title claims abstract description 8
- 239000000203 mixture Substances 0.000 claims abstract description 82
- 239000011230 binding agent Substances 0.000 claims abstract description 29
- 238000002360 preparation method Methods 0.000 claims abstract description 24
- 238000000034 method Methods 0.000 claims abstract description 22
- 150000003839 salts Chemical class 0.000 claims abstract description 17
- 239000003960 organic solvent Substances 0.000 claims abstract description 15
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims abstract description 12
- 229910000040 hydrogen fluoride Inorganic materials 0.000 claims description 81
- -1 4Be hydrogen Chemical class 0.000 claims description 68
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 claims description 49
- 239000000463 material Substances 0.000 claims description 31
- RHDGNLCLDBVESU-UHFFFAOYSA-N but-3-en-4-olide Chemical compound O=C1CC=CO1 RHDGNLCLDBVESU-UHFFFAOYSA-N 0.000 claims description 24
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 19
- 239000001257 hydrogen Substances 0.000 claims description 17
- 229910052739 hydrogen Inorganic materials 0.000 claims description 17
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 14
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 13
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 11
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 claims description 8
- XSQUKJJJFZCRTK-UHFFFAOYSA-N urea group Chemical group NC(=O)N XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 8
- 125000002252 acyl group Chemical group 0.000 claims description 7
- 239000003495 polar organic solvent Substances 0.000 claims description 7
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 claims description 6
- 150000002431 hydrogen Chemical class 0.000 claims description 6
- 230000005855 radiation Effects 0.000 claims description 6
- 229910052736 halogen Inorganic materials 0.000 claims description 5
- 150000002367 halogens Chemical class 0.000 claims description 5
- 125000001624 naphthyl group Chemical group 0.000 claims description 4
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims description 3
- CMLFRMDBDNHMRA-UHFFFAOYSA-N 2h-1,2-benzoxazine Chemical compound C1=CC=C2C=CNOC2=C1 CMLFRMDBDNHMRA-UHFFFAOYSA-N 0.000 claims description 3
- AGIJRRREJXSQJR-UHFFFAOYSA-N 2h-thiazine Chemical compound N1SC=CC=C1 AGIJRRREJXSQJR-UHFFFAOYSA-N 0.000 claims description 3
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims description 3
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims description 3
- 125000004076 pyridyl group Chemical group 0.000 claims description 3
- JWVCLYRUEFBMGU-UHFFFAOYSA-N quinazoline Chemical compound N1=CN=CC2=CC=CC=C21 JWVCLYRUEFBMGU-UHFFFAOYSA-N 0.000 claims description 3
- 150000001735 carboxylic acids Chemical class 0.000 claims description 2
- 229910052751 metal Inorganic materials 0.000 abstract description 7
- 239000002184 metal Substances 0.000 abstract description 7
- 238000004519 manufacturing process Methods 0.000 abstract description 4
- 239000000178 monomer Substances 0.000 description 41
- 239000002253 acid Substances 0.000 description 28
- 239000002585 base Substances 0.000 description 28
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical group [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 25
- 229910052725 zinc Inorganic materials 0.000 description 25
- 239000011701 zinc Substances 0.000 description 25
- 229920000642 polymer Polymers 0.000 description 21
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 19
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 18
- 239000000126 substance Substances 0.000 description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 17
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 15
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical group CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 15
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical group C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 13
- 238000010521 absorption reaction Methods 0.000 description 13
- 239000011248 coating agent Substances 0.000 description 13
- 238000000576 coating method Methods 0.000 description 13
- 239000000243 solution Substances 0.000 description 13
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 12
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 11
- 125000003368 amide group Chemical group 0.000 description 11
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 9
- 238000003384 imaging method Methods 0.000 description 9
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 9
- 229920002554 vinyl polymer Polymers 0.000 description 9
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 8
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 8
- 238000001035 drying Methods 0.000 description 8
- NQBWNECTZUOWID-UHFFFAOYSA-N (E)-cinnamyl (E)-cinnamate Natural products C=1C=CC=CC=1C=CC(=O)OCC=CC1=CC=CC=C1 NQBWNECTZUOWID-UHFFFAOYSA-N 0.000 description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Natural products OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 7
- 150000007513 acids Chemical class 0.000 description 7
- 150000001298 alcohols Chemical class 0.000 description 7
- IWYDHOAUDWTVEP-UHFFFAOYSA-N mandelic acid Chemical compound OC(=O)C(O)C1=CC=CC=C1 IWYDHOAUDWTVEP-UHFFFAOYSA-N 0.000 description 7
- 229960002510 mandelic acid Drugs 0.000 description 7
- 239000000123 paper Substances 0.000 description 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 6
- 150000001299 aldehydes Chemical class 0.000 description 6
- 239000012670 alkaline solution Substances 0.000 description 6
- BEFDCLMNVWHSGT-UHFFFAOYSA-N ethenylcyclopentane Chemical compound C=CC1CCCC1 BEFDCLMNVWHSGT-UHFFFAOYSA-N 0.000 description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 6
- 239000000049 pigment Substances 0.000 description 6
- 229920000728 polyester Polymers 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- 239000004334 sorbic acid Substances 0.000 description 6
- 235000010199 sorbic acid Nutrition 0.000 description 6
- 229940075582 sorbic acid Drugs 0.000 description 6
- 239000011592 zinc chloride Substances 0.000 description 6
- 235000005074 zinc chloride Nutrition 0.000 description 6
- SPMMMKHRSINRIN-UHFFFAOYSA-N 2-(4-methylphenyl)prop-2-enoic acid Chemical compound CC1=CC=C(C(=C)C(O)=O)C=C1 SPMMMKHRSINRIN-UHFFFAOYSA-N 0.000 description 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 5
- 238000001914 filtration Methods 0.000 description 5
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 5
- 229920000058 polyacrylate Polymers 0.000 description 5
- 239000004926 polymethyl methacrylate Substances 0.000 description 5
- 125000002348 vinylic group Chemical group 0.000 description 5
- LIZLYZVAYZQVPG-UHFFFAOYSA-N (3-bromo-2-fluorophenyl)methanol Chemical compound OCC1=CC=CC(Br)=C1F LIZLYZVAYZQVPG-UHFFFAOYSA-N 0.000 description 4
- MNAHQWDCXOHBHK-UHFFFAOYSA-N 1-phenylpropane-1,1-diol Chemical compound CCC(O)(O)C1=CC=CC=C1 MNAHQWDCXOHBHK-UHFFFAOYSA-N 0.000 description 4
- NRPFNQUDKRYCNX-UHFFFAOYSA-N 4-methoxyphenylacetic acid Chemical compound COC1=CC=C(CC(O)=O)C=C1 NRPFNQUDKRYCNX-UHFFFAOYSA-N 0.000 description 4
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N Butyraldehyde Chemical compound CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 4
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 4
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- 239000004743 Polypropylene Substances 0.000 description 4
- 239000004372 Polyvinyl alcohol Substances 0.000 description 4
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- FMFHUEMLVAIBFI-BQYQJAHWSA-N [(e)-2-phenylethenyl] acetate Chemical compound CC(=O)O\C=C\C1=CC=CC=C1 FMFHUEMLVAIBFI-BQYQJAHWSA-N 0.000 description 4
- 150000001408 amides Chemical class 0.000 description 4
- 150000001412 amines Chemical class 0.000 description 4
- 239000000460 chlorine Substances 0.000 description 4
- 229910052801 chlorine Inorganic materials 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N ethyl acetate Substances CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 4
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- TXXHDPDFNKHHGW-UHFFFAOYSA-N muconic acid Chemical compound OC(=O)C=CC=CC(O)=O TXXHDPDFNKHHGW-UHFFFAOYSA-N 0.000 description 4
- 229920005615 natural polymer Polymers 0.000 description 4
- 150000002924 oxiranes Chemical class 0.000 description 4
- DXGLGDHPHMLXJC-UHFFFAOYSA-N oxybenzone Chemical group OC1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1 DXGLGDHPHMLXJC-UHFFFAOYSA-N 0.000 description 4
- 229920001155 polypropylene Polymers 0.000 description 4
- 229920002451 polyvinyl alcohol Polymers 0.000 description 4
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 4
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 4
- 235000014347 soups Nutrition 0.000 description 4
- 150000003457 sulfones Chemical class 0.000 description 4
- IVSZLXZYQVIEFR-UHFFFAOYSA-N 1,3-Dimethylbenzene Natural products CC1=CC=CC(C)=C1 IVSZLXZYQVIEFR-UHFFFAOYSA-N 0.000 description 3
- YWPABLWXCWUIIT-UHFFFAOYSA-N 2-(2-phenylphenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC=C1C1=CC=CC=C1 YWPABLWXCWUIIT-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical group COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 239000004695 Polyether sulfone Substances 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Substances CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 229960000583 acetic acid Drugs 0.000 description 3
- 235000013877 carbamide Nutrition 0.000 description 3
- 239000011111 cardboard Substances 0.000 description 3
- 239000001913 cellulose Substances 0.000 description 3
- 229920002678 cellulose Polymers 0.000 description 3
- NQBWNECTZUOWID-QSYVVUFSSA-N cinnamyl cinnamate Chemical compound C=1C=CC=CC=1\C=C/C(=O)OC\C=C\C1=CC=CC=C1 NQBWNECTZUOWID-QSYVVUFSSA-N 0.000 description 3
- 229960000192 felbinac Drugs 0.000 description 3
- 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 3
- 150000002576 ketones Chemical class 0.000 description 3
- 239000003791 organic solvent mixture Substances 0.000 description 3
- 229920006393 polyether sulfone Polymers 0.000 description 3
- 229920000139 polyethylene terephthalate Polymers 0.000 description 3
- 239000005020 polyethylene terephthalate Substances 0.000 description 3
- 239000004800 polyvinyl chloride Substances 0.000 description 3
- 229920000915 polyvinyl chloride Polymers 0.000 description 3
- 238000007639 printing Methods 0.000 description 3
- 238000003892 spreading Methods 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 239000002966 varnish Substances 0.000 description 3
- FCBJLBCGHCTPAQ-UHFFFAOYSA-N 1-fluorobutane Chemical group CCCCF FCBJLBCGHCTPAQ-UHFFFAOYSA-N 0.000 description 2
- LNETULKMXZVUST-UHFFFAOYSA-N 1-naphthoic acid Chemical compound C1=CC=C2C(C(=O)O)=CC=CC2=C1 LNETULKMXZVUST-UHFFFAOYSA-N 0.000 description 2
- FRPZMMHWLSIFAZ-UHFFFAOYSA-N 10-undecenoic acid Chemical compound OC(=O)CCCCCCCCC=C FRPZMMHWLSIFAZ-UHFFFAOYSA-N 0.000 description 2
- 239000005995 Aluminium silicate Substances 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 2
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical group CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 2
- HYBBIBNJHNGZAN-UHFFFAOYSA-N Furaldehyde Natural products O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 2
- TXXHDPDFNKHHGW-CCAGOZQPSA-N Muconic acid Natural products OC(=O)\C=C/C=C\C(O)=O TXXHDPDFNKHHGW-CCAGOZQPSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 description 2
- 150000001336 alkenes Chemical class 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 239000004411 aluminium Substances 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 235000012211 aluminium silicate Nutrition 0.000 description 2
- APUPEJJSWDHEBO-UHFFFAOYSA-P ammonium molybdate Chemical compound [NH4+].[NH4+].[O-][Mo]([O-])(=O)=O APUPEJJSWDHEBO-UHFFFAOYSA-P 0.000 description 2
- 239000011609 ammonium molybdate Substances 0.000 description 2
- 235000018660 ammonium molybdate Nutrition 0.000 description 2
- 229940010552 ammonium molybdate Drugs 0.000 description 2
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 2
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- KHAVLLBUVKBTBG-UHFFFAOYSA-N caproleic acid Natural products OC(=O)CCCCCCCC=C KHAVLLBUVKBTBG-UHFFFAOYSA-N 0.000 description 2
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 2
- 239000010941 cobalt Substances 0.000 description 2
- 229910017052 cobalt Inorganic materials 0.000 description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 150000001896 cresols Chemical class 0.000 description 2
- 125000005442 diisocyanate group Chemical group 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 125000003700 epoxy group Chemical group 0.000 description 2
- 125000004494 ethyl ester group Chemical group 0.000 description 2
- FKRCODPIKNYEAC-UHFFFAOYSA-N ethyl propionate Chemical compound CCOC(=O)CC FKRCODPIKNYEAC-UHFFFAOYSA-N 0.000 description 2
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 238000005984 hydrogenation reaction Methods 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 229910000765 intermetallic Inorganic materials 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 2
- 239000004310 lactic acid Substances 0.000 description 2
- 235000014655 lactic acid Nutrition 0.000 description 2
- 125000000686 lactone group Chemical group 0.000 description 2
- 229920001684 low density polyethylene Polymers 0.000 description 2
- 239000004702 low-density polyethylene Substances 0.000 description 2
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 2
- 239000003550 marker Substances 0.000 description 2
- 239000011733 molybdenum Substances 0.000 description 2
- 229910052750 molybdenum Inorganic materials 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
- 239000005026 oriented polypropylene Substances 0.000 description 2
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 2
- 229920001490 poly(butyl methacrylate) polymer Polymers 0.000 description 2
- 229920002492 poly(sulfone) Polymers 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 2
- 239000011135 tin Substances 0.000 description 2
- 229910052718 tin Inorganic materials 0.000 description 2
- 229960002703 undecylenic acid Drugs 0.000 description 2
- 150000003672 ureas Chemical class 0.000 description 2
- HGBOYTHUEUWSSQ-UHFFFAOYSA-N valeric aldehyde Natural products CCCCC=O HGBOYTHUEUWSSQ-UHFFFAOYSA-N 0.000 description 2
- 229910052720 vanadium Inorganic materials 0.000 description 2
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 2
- 125000002256 xylenyl group Chemical class C1(C(C=CC=C1)C)(C)* 0.000 description 2
- 239000004246 zinc acetate Substances 0.000 description 2
- MEIRRNXMZYDVDW-MQQKCMAXSA-N (2E,4E)-2,4-hexadien-1-ol Chemical compound C\C=C\C=C\CO MEIRRNXMZYDVDW-MQQKCMAXSA-N 0.000 description 1
- 239000001602 (E)-hex-3-enoic acid Substances 0.000 description 1
- KJRRTHHNKJBVBO-AATRIKPKSA-N (e)-3-(2-chlorophenyl)prop-2-enoic acid Chemical compound OC(=O)\C=C\C1=CC=CC=C1Cl KJRRTHHNKJBVBO-AATRIKPKSA-N 0.000 description 1
- WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 description 1
- WIHIUTUAHOZVLE-UHFFFAOYSA-N 1,3-diethoxypropan-2-ol Chemical compound CCOCC(O)COCC WIHIUTUAHOZVLE-UHFFFAOYSA-N 0.000 description 1
- PTISZEDBAGUJSD-UHFFFAOYSA-N 1-(2-chlorophenyl)-1-fluorohydrazine Chemical compound NN(C1=CC=CC=C1Cl)F PTISZEDBAGUJSD-UHFFFAOYSA-N 0.000 description 1
- HNAGHMKIPMKKBB-UHFFFAOYSA-N 1-benzylpyrrolidine-3-carboxamide Chemical compound C1C(C(=O)N)CCN1CC1=CC=CC=C1 HNAGHMKIPMKKBB-UHFFFAOYSA-N 0.000 description 1
- UZKWTJUDCOPSNM-UHFFFAOYSA-N 1-ethenoxybutane Chemical compound CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
- SJJCQDRGABAVBB-UHFFFAOYSA-N 1-hydroxy-2-naphthoic acid Chemical compound C1=CC=CC2=C(O)C(C(=O)O)=CC=C21 SJJCQDRGABAVBB-UHFFFAOYSA-N 0.000 description 1
- PRPINYUDVPFIRX-UHFFFAOYSA-N 1-naphthaleneacetic acid Chemical compound C1=CC=C2C(CC(=O)O)=CC=CC2=C1 PRPINYUDVPFIRX-UHFFFAOYSA-N 0.000 description 1
- 239000005971 1-naphthylacetic acid Substances 0.000 description 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- GOJUJUVQIVIZAV-UHFFFAOYSA-N 2-amino-4,6-dichloropyrimidine-5-carbaldehyde Chemical group NC1=NC(Cl)=C(C=O)C(Cl)=N1 GOJUJUVQIVIZAV-UHFFFAOYSA-N 0.000 description 1
- ZCYXGVJUZBKJAI-UHFFFAOYSA-N 3,4,5-trimethoxydihydrocinnamic acid Chemical compound COC1=CC(CCC(O)=O)=CC(OC)=C1OC ZCYXGVJUZBKJAI-UHFFFAOYSA-N 0.000 description 1
- ALKYHXVLJMQRLQ-UHFFFAOYSA-N 3-Hydroxy-2-naphthoate Chemical compound C1=CC=C2C=C(O)C(C(=O)O)=CC2=C1 ALKYHXVLJMQRLQ-UHFFFAOYSA-N 0.000 description 1
- XMIIGOLPHOKFCH-UHFFFAOYSA-N 3-phenylpropionic acid Chemical compound OC(=O)CCC1=CC=CC=C1 XMIIGOLPHOKFCH-UHFFFAOYSA-N 0.000 description 1
- AWPROQFCCQOROZ-UHFFFAOYSA-N 4-(4-methylpentyl)phenol Chemical compound CC(C)CCCC1=CC=C(O)C=C1 AWPROQFCCQOROZ-UHFFFAOYSA-N 0.000 description 1
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 1
- OBKXEAXTFZPCHS-UHFFFAOYSA-N 4-phenylbutyric acid Chemical compound OC(=O)CCCC1=CC=CC=C1 OBKXEAXTFZPCHS-UHFFFAOYSA-N 0.000 description 1
- JCIDEANDDNSHQC-UHFFFAOYSA-N 4H-chromene Chemical compound C1=CC=C2CC=COC2=C1 JCIDEANDDNSHQC-UHFFFAOYSA-N 0.000 description 1
- 229920005789 ACRONAL® acrylic binder Polymers 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- MOZDKDIOPSPTBH-UHFFFAOYSA-N Benzyl parahydroxybenzoate Chemical compound C1=CC(O)=CC=C1C(=O)OCC1=CC=CC=C1 MOZDKDIOPSPTBH-UHFFFAOYSA-N 0.000 description 1
- CWXYHOHYCJXYFQ-UHFFFAOYSA-N Betamipron Chemical compound OC(=O)CCNC(=O)C1=CC=CC=C1 CWXYHOHYCJXYFQ-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- IWNDIAMCEDZCOS-UHFFFAOYSA-M C(C)(=O)[O-].C(=C\C1=CC=CC=C1)/[Zn+] Chemical compound C(C)(=O)[O-].C(=C\C1=CC=CC=C1)/[Zn+] IWNDIAMCEDZCOS-UHFFFAOYSA-M 0.000 description 1
- XXHDAWYDNSXJQM-UHFFFAOYSA-N Chloride-3-Hexenoic acid Natural products CCC=CCC(O)=O XXHDAWYDNSXJQM-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 1
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical group OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical group CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-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
- 108010010803 Gelatin Proteins 0.000 description 1
- CTKINSOISVBQLD-UHFFFAOYSA-N Glycidol Chemical compound OCC1CO1 CTKINSOISVBQLD-UHFFFAOYSA-N 0.000 description 1
- WZUVPPKBWHMQCE-UHFFFAOYSA-N Haematoxylin Chemical group C12=CC(O)=C(O)C=C2CC2(O)C1C1=CC=C(O)C(O)=C1OC2 WZUVPPKBWHMQCE-UHFFFAOYSA-N 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 description 1
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- PEEHTFAAVSWFBL-UHFFFAOYSA-N Maleimide Chemical compound O=C1NC(=O)C=C1 PEEHTFAAVSWFBL-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical class CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- 239000000020 Nitrocellulose Substances 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- YGSDEFSMJLZEOE-UHFFFAOYSA-N Salicylic acid Natural products OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 231100000768 Toxicity label Toxicity 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 241000405217 Viola <butterfly> Species 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- 150000001241 acetals Chemical class 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- GZCGUPFRVQAUEE-SLPGGIOYSA-N aldehydo-D-glucose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O GZCGUPFRVQAUEE-SLPGGIOYSA-N 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- YIYBQIKDCADOSF-UHFFFAOYSA-N alpha-Butylen-alpha-carbonsaeure Natural products CCC=CC(O)=O YIYBQIKDCADOSF-UHFFFAOYSA-N 0.000 description 1
- 239000005030 aluminium foil Substances 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 229910021502 aluminium hydroxide Inorganic materials 0.000 description 1
- JPNZKPRONVOMLL-UHFFFAOYSA-N azane;octadecanoic acid Chemical class [NH4+].CCCCCCCCCCCCCCCCCC([O-])=O JPNZKPRONVOMLL-UHFFFAOYSA-N 0.000 description 1
- 150000003851 azoles Chemical class 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical group C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- OBNCKNCVKJNDBV-UHFFFAOYSA-N butanoic acid ethyl ester Natural products CCCC(=O)OCC OBNCKNCVKJNDBV-UHFFFAOYSA-N 0.000 description 1
- 229940043232 butyl acetate Drugs 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 229920006218 cellulose propionate Polymers 0.000 description 1
- 238000005660 chlorination reaction Methods 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 229920001577 copolymer Polymers 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
- 150000004985 diamines Chemical class 0.000 description 1
- 238000003618 dip coating 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
- 239000003814 drug Substances 0.000 description 1
- 238000006735 epoxidation reaction Methods 0.000 description 1
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical group O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 1
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 125000000219 ethylidene group Chemical group [H]C(=[*])C([H])([H])[H] 0.000 description 1
- FWQHNLCNFPYBCA-UHFFFAOYSA-N fluoran Chemical compound C12=CC=CC=C2OC2=CC=CC=C2C11OC(=O)C2=CC=CC=C21 FWQHNLCNFPYBCA-UHFFFAOYSA-N 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexamethylene diamine Natural products NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical group O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000001863 hydroxypropyl cellulose Substances 0.000 description 1
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 1
- 125000000654 isopropylidene group Chemical group C(C)(C)=* 0.000 description 1
- 235000012204 lemonade/lime carbonate Nutrition 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 229910001507 metal halide Inorganic materials 0.000 description 1
- 150000005309 metal halides Chemical class 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 229940050176 methyl chloride Drugs 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 239000005078 molybdenum compound Substances 0.000 description 1
- 150000002752 molybdenum compounds Chemical class 0.000 description 1
- MGNPLIACIXIYJE-UHFFFAOYSA-N n-fluoroaniline Chemical compound FNC1=CC=CC=C1 MGNPLIACIXIYJE-UHFFFAOYSA-N 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
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- LYGJENNIWJXYER-UHFFFAOYSA-N nitromethane Chemical compound C[N+]([O-])=O LYGJENNIWJXYER-UHFFFAOYSA-N 0.000 description 1
- 125000001400 nonyl 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])[H] 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
- 238000007645 offset printing Methods 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- HDBWAWNLGGMZRQ-UHFFFAOYSA-N p-Vinylbiphenyl Chemical group C1=CC(C=C)=CC=C1C1=CC=CC=C1 HDBWAWNLGGMZRQ-UHFFFAOYSA-N 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 239000013034 phenoxy resin Substances 0.000 description 1
- 229920006287 phenoxy resin Polymers 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920005990 polystyrene resin Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 238000007650 screen-printing Methods 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 235000010215 titanium dioxide Nutrition 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- 150000004992 toluidines Chemical class 0.000 description 1
- WBYWAXJHAXSJNI-VOTSOKGWSA-N trans-cinnamic acid Chemical compound OC(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-N 0.000 description 1
- XXHDAWYDNSXJQM-ONEGZZNKSA-N trans-hex-3-enoic acid Chemical compound CC\C=C\CC(O)=O XXHDAWYDNSXJQM-ONEGZZNKSA-N 0.000 description 1
- YIYBQIKDCADOSF-ONEGZZNKSA-N trans-pent-2-enoic acid Chemical compound CC\C=C\C(O)=O YIYBQIKDCADOSF-ONEGZZNKSA-N 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 125000002948 undecyl 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])[H] 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- MECHNRXZTMCUDQ-RKHKHRCZSA-N vitamin D2 Chemical compound C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)/C=C/[C@H](C)C(C)C)=C\C=C1\C[C@@H](O)CCC1=C MECHNRXZTMCUDQ-RKHKHRCZSA-N 0.000 description 1
- 235000001892 vitamin D2 Nutrition 0.000 description 1
- 239000011653 vitamin D2 Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical group O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- C08K5/04—Oxygen-containing compounds
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
-
- 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
- C08K5/04—Oxygen-containing compounds
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
- C08K5/098—Metal salts of carboxylic acids
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/124—Duplicating or marking methods; Sheet materials for use therein using pressure to make a masked colour visible, e.g. to make a coloured support visible, to create an opaque or transparent pattern, or to form colour by uniting colour-forming components
- B41M5/132—Chemical colour-forming components; Additives or binders therefor
- B41M5/136—Organic colour formers, e.g. leuco dyes
- B41M5/145—Organic colour formers, e.g. leuco dyes with a lactone or lactam ring
- B41M5/1455—Organic colour formers, e.g. leuco dyes with a lactone or lactam ring characterised by fluoran compounds
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
- B41M5/262—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used recording or marking of inorganic surfaces or materials, e.g. glass, metal, or ceramics
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
- B41M5/267—Marking of plastic artifacts, e.g. with laser
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
- B41M5/30—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used using chemical colour formers
-
- 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
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/0041—Optical brightening agents, organic pigments
-
- 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
- C08K5/0091—Complexes with metal-heteroatom-bonds
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/50—Sympathetic, colour changing or similar inks
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/60—Additives non-macromolecular
- C09D7/63—Additives non-macromolecular organic
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Medicinal Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- General Chemical & Material Sciences (AREA)
- Ceramic Engineering (AREA)
- Paints Or Removers (AREA)
- Heat Sensitive Colour Forming Recording (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
本发明提供基材标记用涂料组合物,包含数量为0.01~50%的成色物质、数量为0.01~50%羧酸金属盐、数量为1~80%的粘结剂和数量为1~99%的有机溶剂,其中每个数量都以该组合物的重量为基准按重量计。本发明也提供本发明组合物的制备方法、涂布了这些组合物的基材、和使用这些组合物制备有标记基材的方法。
Description
本发明涉及基材标记用涂料组合物、涉及这些涂料组合物的制备方法、涉及涂布了这些组合物的基材、涉及使用这些组合物制备有标记基材的方法、还涉及有标记基材。
包装通常需要标记可见信息例如品牌标识、条形码、商品有效期或批号。做到这一点的一条途径是用一种包含成色物质和颜色展现剂的组合物涂布该包装,这些药剂当用热量等能量处理时发生反应形成一种可见颜色。
US 4,820,683描述涂料组合物,该组合物是包含下列成分的分散液:成色物质,羧酸金属盐例如二羧酸锌,附加酸性显色剂例如一种苯酚化合物,硬脂酸金属盐,粘结剂,和作为溶剂的水。将该组合物涂布在一种基材上、干燥,当用热量处理时产生一种影像。
WO 02/074548描述的涂料组合物包含一种多价金属的含氧阴离子例如八钼酸铵(AOM),一种典型地为聚合物的粘结剂,和一种溶剂例如水或乙醇。将这些组合物涂布在一种基材例如卡通纸板上、干燥、暴露于IR激光以产生一种影像。
WO 2004/043704描述的涂料组合物包含钼、钨或钒的一种胺化合物,一种有机溶剂,和任选地一种聚合物粘结剂。“钼酸铵”的一个实例是八钼酸二(2-乙基己基)胺。将该组合物涂布在基材例如聚对苯二甲酸乙二醇酯薄膜、铝箔或聚丙烯包装薄膜上,干燥,暴露于IR激光或热印刷机以产生一种影像。
US4,820,683和WO 02/074548中描述的涂料组合物的一个缺点是只能得到不透明涂层。WO 02/074548和WO 2004/043704中描述的涂料组合物的一个缺点是使用昂贵的钼化合物。WO 2004/043704的涂料组合物的一个进一步缺点是该“钼酸铵”的制备非常不方便,因为它涉及一种焦油状材料的生成,该焦油状材料的一部分会粘附到容器壁上。
本发明的一个目的是提供半透明到透明涂料组合物,该组合物能产生高强度和亮度的影像。同时,该涂料组合物将不需要制备不方便的、昂贵的金属化合物,而且在用能量处理之前将不易显色。
这个目的是由按照权利要求1的组合物、按照权利要求7和10的基材、和按照权利要求6、8和9的方法解决的。
本发明的组合物包含数量为0.01~50%的一种成色物质、数量为0.01~50%的一种羧酸金属盐、数量为1~80%的一种粘结剂、和数量为1~99%的一种有机溶剂,其中每个数量都是以该组合物的重量为基准按重量计的。
较好,该组合物包含数量为0.1~30%的成色物质、数量为0.1~30%的羧酸金属盐、数量为3~60%的粘结剂、和数量为20~95%的有机溶剂,其中每个数量都是以该组合物的重量为基准按重量计的。
更好,该组合物包含数量为1~20%的成色物质、数量为1~20%的羧酸金属盐、数量为5~30%的粘结剂、和数量为50~90%的有机溶剂,其中每个数量都是以该组合物的重量为基准按重量计的。
最好,该组合物包含数量为1~10%的成色物质、数量为1~10%的羧酸金属盐、数量为7~14%的粘结剂、和数量为75~85%的有机溶剂,其中每个数量都是以该组合物的重量为基准按重量计的。
较好,这四种成分即成色物质、羧酸金属盐、粘结剂和有机溶剂的总量是50~100%、更好80~100%、甚至更好95~100%、最好100%,每个数量都是以该组合物的重量为基准按重量计的。
该羧酸可以是式(I)的一种羧酸
或式(I)的羧酸混合物
式中
n是0、1、2、3、4、5、6、7、8、9、10、11、12、13或14,
m是0、1、2、3或4,
R1和R5相同或不同,可以是氢、羟基、C1-12烷基、羧基、C1-4烷氧羰基、氨基甲酰基、C1-4烷胺基羰基、酰基、氨基、(C1-4烷基)-CO-NH或脲基,
R2和R3相同或不同,可以是氢、C1-4烷基或(C1-4烷基)-CO-NH,
R4是氢、C1-12烷基、羧基、C1-4烷氧羰基、氨基甲酰基、C1-4烷胺基羰基、酰基、氨基、(C1-4烷基)-CO-NH、脲基、苯基、2-、3-或4-吡啶基、或者1-、2-或3-萘基,其中苯基、吡啶基或萘基可以是无取代的,也可以有C1-4烷基、苯基、C1-4烷氧基、羟基、二(C1-4烷基)氨基或卤素一取代、二取代或三取代。
C1-4烷氧基可以是甲氧基、乙氧基、丙氧基、异丙氧基、丁氧基、异丁氧基、仲丁氧基和叔丁氧基。C1-12烷基可以是甲基、乙基、丙基、异丙基、丁基、仲丁基、叔丁基、戊基、己基、庚基、辛基、壬基、癸基、十一烷基和十二烷基。酰基的实例是乙酰基和苯甲酰基。卤素可以是氯、氟或溴。
在较好的羧酸(I)中
n是0~9的整数,
m是0~3的整数,
R1和R5相同或不同,是氢、羟基、C1-4烷基、羧基、C1-4烷氧羰基、氨基甲酰基、C1-4烷胺基羰基、酰基、氨基、(C1-4烷基)-CO-NH或脲基,
R2和R3相同或不同,是氢、C1-4烷基或(C1-4烷基)-CO-NH,
R4是氢、C1-7烷基、羧基、C1-4烷氧羰基、氨基甲酰基、C1-4烷胺基羰基、酰基、氨基、(C1-4烷基)-CO-NH、脲基、苯基、2-、3-、或4-吡啶基、或1-、2-或3-萘基,其中苯基、吡啶基或萘基可以是无取代的,也可以有C1-4烷基、苯基、C1-4烷氧基、羟基、二(C1-4烷基)氨基或卤素一取代、二取代或三取代。
C1-4烷基可以是甲基、乙基、丙基、异丙基、丁基、异丁基、仲丁基和叔丁基。
C1-7烷基可以是甲基、乙基、丙基、异丙基、丁基、异丁基、仲丁基、叔丁基、苯基、己基或庚基。
在更好的羧酸(I)中
n是0~8的整数,
m是0、1或2,
R1是氢或羟基,
R5是氢,
R2和R3相同或不同,是氢或乙酰胺基,
R4是氢、C1-6烷基、羧基、氨基甲酰基、苯甲酰基、苯基或1-、2-或3-萘基,其中苯基可以是无取代的,也可以有C1-4烷基、苯基、C1-4烷氧基、羟基、二(C1-4烷基)氨基或卤素一取代、二取代或三取代;且其中萘基可以是无取代的,也可以有羟基取代。
C1-6烷基可以是甲基、乙基、丙基、异丙基、丁基、异丁基、仲丁基、叔丁基、苯基或己基。
更好的羧酸的实例是苯乙酸、对甲苯乙酸、4-联苯乙酸、扁桃酸、反式-苯乙烯基乙酸、山梨醇、α-乙酰胺基肉桂酸、4-甲基肉桂酸、4-甲氧基苯乙酸、十一碳烯酸、琥珀酸、阿魏酸、粘康酸、乳酸、反式-2-戊烯酸、反式-3-己烯酸、反式-2-辛烯酸、反式-肉桂酸、反式-3,4-二甲氧基肉桂酸、反式-3,4,5-三甲氧基肉桂酸、氢化肉桂酸、3,4,5-三甲氧基氢化肉桂酸、3,5-二叔丁基水杨酸、4-(二甲胺基)苯甲酸、4-苯丁酸、反式-2-氯肉桂酸、3,4-二甲氧基苯乙酸、3-羟基-2-萘甲酸、苯甲酸、1-羟基-2-萘甲酸、1-萘乙酸、3-苯甲酰丙酸、和1-萘甲酸或其混合物。
在甚至更好的羧酸(I)中
n是0~8的整数,
m是0、1或2,先决条件是n和m不同时为0,
R1是氢或羟基,
R5是氢,
R2和R3相同或不同,是氢或乙酰胺基,
R4是氢、甲基、羧基、氨基甲酰基或苯基,其中苯基可以是无取代的,也可以有甲基、苯基、甲氧基或羟基。
甚至更好的羧酸的实例是苯乙酸、对甲苯乙酸、4-联苯乙酸、扁桃酸、反式-苯乙烯基乙酸、山梨酸、α-乙酰胺基肉桂酸、4-甲基肉桂酸、4-甲氧基苯乙酸、十一碳烯酸、琥珀酸、阿魏酸、粘康酸、和乳酸或其混合物。
最好的羧酸是苯乙酸、对甲苯乙酸、4-联苯乙酸、扁桃酸、反式-苯乙烯基乙酸、山梨酸、α-乙酰胺基肉桂酸、和4-甲基肉桂酸或其混合物。
金属可以是碱土金属、过渡金属、或者主族III和IV中的金属。较好,它选自下列组成的一组:镁、钙、锶、钛、钒、铬、钼、锰、铁、钴、镍、铜、锌、铝和锡。更好,它选自下列组成的一组:钙、锰、钴、镍、铜、锌、铝和锡。最好,该金属是锌。
该羧酸金属盐可以通过使一种无机金属盐例如金属卤化物或硫酸盐与该羧酸的碱金属盐在水中反应来生成。
成色物质可以是任何一种适用的成色物质,例如2-苯并[c]呋喃酮、荧烷、三芳基甲烷、苯并嗪、喹唑啉、螺吡喃、醌、噻嗪、或嗪或其混合物。
2-苯并[c]呋喃酮的实例是结晶紫内酯(3,3-二(对二甲胺基苯基)-6-二甲胺基-2-苯并[c]呋喃酮)、3,3-二(对二甲胺基苯基)-2-苯并[c]呋喃酮、3,3-二(1-乙基-2-甲基吲哚-3-基)-2-苯并[c]呋喃酮、3,3-二(1-辛基-2-甲基吲哚-3-基)-2-苯并[c]呋喃酮、3-(4-二乙胺基苯基)-3-(1-乙基-2-甲基吲哚-3-基)-2-苯并[c]呋喃酮、7-(N-乙基-N-异戊基氨基)-3-甲基-1-苯基螺[4H-色烯并[2,3-c]吡唑-4(1H)-3’-2-苯并[c]呋喃酮]、3,6,6’-三(二甲胺基)螺[芴-9,3’-2-苯并[c]呋喃酮]、3,6,6’-三(二乙胺基)螺[芴-9,3’-2-苯并[c]呋喃酮]、3,3-二[2-(对二甲胺基苯基)-2-(对甲氧基苯基)乙烯基]-4,5,6,7-四溴-2-苯并[c]呋喃酮、3,3-二[2-(对二甲胺基苯基)-2-(对甲氧基苯基)乙烯基]-4,5,6,7-四氯-2-苯并[c]呋喃酮、3,3-二[1,1-二(4-吡咯烷酮基苯基)乙烯-2-基]-4,5,6,7-四溴-2-苯并[c]呋喃酮、3,3-二[1-(4-甲氧基苯基)-1-(4-吡咯烷酮基苯基)乙烯-2-基]-4,5,6,7-四氯-2-苯并[c]呋喃酮、3-(4-二乙胺基-2-乙氧基苯基)-3-(1-乙基-2-甲基吲哚-3-基)-4-氮杂-2-苯并[c]呋喃酮、3-(4-二乙胺基-2-乙氧基苯基)-3-(1-辛基-2-甲基吲哚-3-基)-4-氮杂-2-苯并[c]呋喃酮和3-(4-环己基乙基氨基-2-甲氧基苯基)-3-(1-乙基-2-甲基吲哚-3-基)-4-氮杂-2-苯并[c]呋喃酮。
该2-苯并[c]呋喃酮可以用业内已知的方法制备,例如,结晶紫内酮可以像GB 1,347,467中所述那样制备,3,3-二(1-乙基-2-甲基吲哚-3-基)-2-苯并[c]呋喃酮可以像GB 1,389,716中所述那样制备。
荧烷的实例是3-二(乙基)氨基-6-甲基-7-(叔丁氧羰基)苯胺基荧烷、3-二乙胺基-7-二苄胺基荧烷、3-二丁胺基-7-二苄胺基荧烷、3-二乙胺基-6-甲基-7-(二苄胺基)荧烷、3-二乙胺基-6-甲基荧烷、3-二乙胺基-6-氯-7-甲基荧烷、3-二乙胺基-6-甲基-7-氯荧烷、3-二乙胺基-7-叔丁基荧烷、3-二乙胺基-7-羧乙基荧烷、3-二乙胺基-7-甲基荧烷、3-二乙胺基-6,8-二甲基荧烷、3-二乙胺基-7-氯荧烷、3-二丁胺基-6-甲基荧烷、3-环己胺基-6-氯荧烷、3-二乙胺基苯并[a]荧烷、3-二乙胺基苯并[c]荧烷、3-二甲胺基-6-甲基-7-苯胺基荧烷、3-二乙胺基-6-甲基-7-苯胺基荧烷、3-二乙胺基-6-甲基-7-(2,4-二甲基苯胺基)荧烷、3-二甲胺基-6-甲基-7-(3-三氟甲基苯胺基)荧烷、3-二乙胺基-6-甲基-7-(2-氯苯胺基)荧烷、3-二乙胺基-6-甲基-7-(对氯苯胺基)荧烷、3-二乙胺基-6-甲基-7-(2-氟苯胺基)荧烷、3-二乙胺基-6-甲基-7-(对辛基苯胺基)荧烷、3-二乙胺基-7-(对辛基胺基)荧烷、3-二乙胺基-6-甲基-7-(对甲基苯胺基)荧烷、3-二乙胺基-6-乙氧乙基-7-苯胺基荧烷、3-二乙胺基-6-甲基-7-(3-甲基苯胺基)荧烷、3-二乙胺基-7-(3-三氟甲基苯胺基)荧烷、3-二乙胺基-7-(2-氯苯胺基)荧烷、3-二乙胺基-7-(2-氟苯胺基)荧烷、3-二乙胺基-6-氯-7-苯胺基荧烷、3-二丁胺基-6-甲基-7-苯胺基荧烷、3-二丁胺基-6-甲基-7-(2,4-二甲基苯胺基)荧烷、3-二丁胺基-6-甲基-7-(2-氯苯胺基)荧烷、3-二丁胺基-6-甲基-7-(4-氯苯胺基)荧烷、3-二丁胺基-6-甲基-7-(2-氟苯胺基)荧烷、3-二丁胺基-6-甲基-7-(3-三氟甲基苯胺基)荧烷、3-二丁胺基-6-乙氧乙基-7-苯胺基荧烷、3-二丁胺基-6-氯苯胺基荧烷、3-二丁胺基-6-甲基-7-(4-甲基苯胺基)荧烷、3-二丁胺基-7-(2-氯苯胺基)荧烷、3-二丁胺基-7-(2-氟苯胺基)荧烷、3-二戊胺基-6-甲基-7-苯胺基荧烷、3-二戊胺基-6-甲基-7-(4-2-氯苯胺基)荧烷、3-二戊胺基-7-(3-三氟甲基苯胺基)荧烷、3-二戊胺基-6-氯-7-苯胺基荧烷、3-二戊胺基-7-(4-氯苯胺基)荧烷、3-吡咯烷基-6-甲基-7-苯胺基荧烷、3-哌啶子基-6-甲基-7-苯胺基荧烷、3-(N-甲基-N-丙基氨基)-6-甲基-7-苯胺基荧烷、3-(N-甲基-N-环己基氨基)-6-甲基-7-苯胺基荧烷、3-(N-乙基-N-环己基氨基)-6-甲基-7-苯胺基荧烷、3-(N-乙基-N-己基氨基)-7-苯胺基荧烷、3-(N-乙基对甲苯胺基)氨基-6-甲基-7-苯胺基荧烷、3-(N-乙基对甲苯胺基)氨基-7-甲基荧烷、3-(N-乙基-N-异戊基氨基)-6-甲基-7-苯胺基荧烷、3-(N-乙基-N-异戊基氨基)-7-(2-氯苯胺基)荧烷、3-(N-乙基-N-异戊基氨基)-6-氯-7-苯胺基荧烷、3-(N-乙基-N-四氢糠基氨基)-6-甲基-7-苯胺基荧烷、3-(N-乙基-N-异丁基氨基)-6-甲基-7-苯胺基荧烷、3-(N-丁基-N-异戊基氨基)-6-甲基-7-苯胺基荧烷、3-(N-异丙基-N-3-戊基氨基)-6-甲基-7-苯胺基荧烷、3-(N-乙基-N-乙氧丙基氨基)-6-甲基-7-苯胺基荧烷、2-甲基-6-对(对二甲胺基苯基)氨基苯胺基荧烷、2-甲氧基-6-对(对二甲胺基苯基)氨基苯胺基荧烷、2-氯-3-甲基-6-对(对苯胺基苯基)氨基苯胺基荧烷、2-二乙胺基-6-对(对二甲胺基苯基)氨基苯胺基荧烷、2-苯基-6-甲基-6-对(对苯胺基苯基)氨基苯胺基荧烷、2-苄基-6-对(对苯胺基苯基)氨基苯胺基荧烷、3-甲基-6-对(对二甲胺基苯基)氨基苯胺基荧烷、3-二乙胺基-6-对(对二乙胺基苯基)氨基苯胺基荧烷、3-二乙胺基-6-对(对二丁胺基苯基)氨基苯胺基荧烷和2,4-二甲基-6-[4-(二甲胺基)苯胺基]荧烷。
荧烷类可以用业内已知的方法制备,例如,3-二乙胺基-7-二苄胺基荧烷、3-二乙胺基-7-叔丁基荧烷、3-二乙胺基-6-甲基-7-苯胺基荧烷和3-二乙胺基-6-甲基-7-(2,4-二甲基苯胺基)荧烷可以像US 5,166,350A中所述那样制备,3-二乙胺基-6-甲基-7-(3-甲基苯胺基)荧烷可以像EP 0546557A1中所述那样制备,3-二乙胺基-6-氯-7-苯胺基荧烷可以像DE 2130845中所述那样制备,3-吡咯烷基-6-甲基-7-苯胺基荧烷和3-哌啶子基-6-甲基-7-苯胺基荧烷可以像US 3,959,571A中所述那样制备,3-(N-乙基-N-异戊基氨基)-6-甲基-7-苯胺基荧烷可以像GB 2002801A中所述那样制备,且3-(N-甲基-N-丙基氨基)-6-甲基-7-苯胺基荧烷可以像GB 2154597A中所述那样制备。
苯并嗪的实例是2-苯基-4-(4-二乙胺基苯基)-4-(4-甲氧基苯基)-6-甲基-7-二甲胺基-3,1-苯并嗪-这可以像EP0187329A1中所述那样制备-和2-苯基-4-(4-二乙胺基苯基)-4-(4-甲氧基苯基)-8-甲基-7-二甲胺基-3,1-苯并嗪。
喹唑啉的实例是4,4’-[(1-甲基偏亚乙基)二(4,1-亚苯氧基-4,2-喹唑啉二基)]二[N,N-二乙基苯胺]。三芳基甲烷的实例是二(N-甲基二苯胺)-4-基(N-丁基咔唑)-3-基甲烷,这可以像GB1,548,059中所述那样制备。
螺吡喃的实例是1’,3’,3’-三甲基螺[2H-1-苯并吡喃-2,2’-吲哚啉]、1,3,3-三甲基螺[吲哚啉-2,3’-[3H]萘[2,1-b][1,4]唑啉]和1’,3’,3’-三甲基螺[2H-1-苯并噻喃-2,2’-吲哚啉]。
醌的实例是hematoxyline。嗪的实例是3,7-二(二甲胺基)-10-苯甲酰基吩嗪。噻嗪的实例是3,7-二(二甲胺基)-10-苯甲酰基吩噻嗪。
较好,该成色物质是2-苯并[c]呋喃酮或荧烷或其混合物。
更好,该成色物质是结晶紫内酯或诸如以商品名CibaPergascriptBlue 1-2RN销售的3,3-二(对二甲胺基苯基)-6-二甲胺基-2-苯并[c]呋喃酮、诸如以商品名CibaPergascriptRed I-6B销售的3,3-二(1-辛基-2-甲基吲哚-3-基)-2-苯并[c]呋喃酮或诸如以CibaPergascriptOrange 1-G销售的3-二乙胺基-7-(乙氧羰基)荧烷。
粘结剂可以是任何适用粘结剂。较好,该粘结剂是一种聚合物粘结剂。聚合物粘结剂的实例是丙烯酸类聚合物、苯乙烯类聚合物及其加氢产物、乙烯基类聚合物、聚烯烃及其加氢或环氧化产物、醛类聚合物、环氧类聚合物、聚酰胺类、聚酯类、聚氨酯类、砜系聚合物、和天然聚合物及其衍生物。该聚合物粘结剂也可以是聚合物粘结剂的混合物。
丙烯酸类聚合物是从至少一种丙烯酸类单体或从至少一种丙烯酸类单体和至少一种苯乙烯类单体、乙烯基类单体、烯烃类单体和/或马来酸类单体生成的聚合物。
丙烯酸类单体的实例是丙烯酸或其盐,丙烯酰胺,丙烯腈,丙烯酸C1-6烷酯例如丙烯酸乙酯、丙烯酸丁酯或丙烯酸己酯,丙烯酸二(C1-4烷胺基)C1-6烷酯例如丙烯酸二甲胺基乙酯或丙烯酸二乙胺基乙酯及其C1-4烷基卤加合物例如丙烯酸二甲胺基乙酯·甲基氯,从二(C1-4烷胺基)C1-6烷胺和丙烯酸生成的酰胺及其C1-4烷基卤加合物,甲基丙烯酸或其盐,甲基丙烯酰胺,甲基丙烯腈,甲基丙烯酸C1-6烷酯例如甲基丙烯酸甲酯或甲基丙烯酸乙酯,甲基丙烯酸二(C1-4烷胺基)C1-6烷酯及其C1-4烷基卤加合物,从二(C1-4烷胺基)C1-6烷胺和甲基丙烯酸生成的酰胺及其C1-4烷基卤加合物,和交联剂例如N,N’-亚甲基二丙烯酰胺。
苯乙烯类单体的实例是苯乙烯、4-甲基苯乙烯和4-乙烯基联苯。乙烯类单体的实例是乙烯醇、氯乙烯、偏二氯乙烯、乙烯基·丁基醚和乙酸乙烯酯。烯烃类单体的实例是乙烯、丙烯、丁二烯和异戊二烯及其氯化或氟化衍生物例如四氟乙烯。马来酸类单体的实例是马来酸、马来酸酐和马来酰亚胺。
丙烯酸类聚合物的实例是聚(甲基丙烯酸甲酯)、聚(甲基丙烯酸丁酯)和苯乙烯/丙烯类聚合物。
苯乙烯类聚合物是从至少一种苯乙烯类单体和至少一种乙烯类单体、烯烃单体和/或马来酸类单体生成的聚合物。苯乙烯类单体、乙烯基类单体、烯烃单体和马来酸类单体的实例是以上给出的。苯乙烯类聚合物的实例是苯乙烯/丁二烯/苯乙烯嵌段聚合物、苯乙烯/乙烯/丁二烯嵌段聚合物、苯乙烯/乙烯/丙烯/苯乙烯嵌段共聚物。
乙烯基类聚合物是从至少一种乙烯基类单体或从至少一种乙烯类单体和至少一种烯烃单体或马来酸类单体生成的聚合物。乙烯基类单体、烯烃单体和马来酸类单体是以上给出的。乙烯基类聚合物的实例是聚氯乙烯和聚乙烯醇。
聚烯烃是从至少一种烯烃单体生成的聚合物。烯烃单体的实例是以上给出的。聚烯烃的实例是聚乙烯、聚丙烯和聚丁二烯。
醛类聚合物是从至少一种醛类单体或聚合物和至少一种醇类单体或聚合物、胺类单体或聚合物和/或脲类单体或聚合物生成的聚合物。醛类单体的实例是甲醛、糠醛和丁醛。醇类单体和实例是苯酚、甲酚、间苯二酚和二甲苯酚。聚醇的实例是聚乙烯醇。胺类单体的实例是苯胺和蜜胺。脲类单体的实例是脲、硫脲和双氰胺。醛类聚合物的实例是从丁醛和聚乙烯醇生成的聚乙烯醇缩丁醛。
环氧类聚合物是从至少一种环氧类单体和至少一种醇类单体和/或胺类单体生成的聚合物。环氧类单体的实例是表氯醇和缩水甘油。醇类单体的实例是苯酚、甲酚、间苯二酚、二甲苯酚、双酚A和二醇类。环氧类聚合物的实例是从表氯醇和双酚A生成的苯氧基树脂。
聚酰胺是从至少一种有一个酰胺基或一个氨基以及一个羧基的单体或从至少一种有2个氨基的单体和至少一种有2个羧基的单体生成的聚合物。有一个酰胺基的单体的实例是己内酰胺。二胺的实例是1,6-二氨基己烷。二羧酸的实例是己二酸、对苯二甲酸、间苯二甲酸、和1,4-萘二羧酸。聚酰胺的实例是聚己二酰六亚甲基二胺和聚己内酰胺。
聚酯聚合物是从至少一种有一个羟基以及一个羧基的单体或从至少一种有2个羟基的单体和至少一种有2个羧基或一个内酯基的单体生成的。有一个羟基以及一个羧基的单体的实例是己二酸。二醇的实例是乙二醇。有内酯基的单体的实例是己内酯。二羧酸的实例是对苯二甲酸、间苯二甲酸和1,4-萘二羧酸。聚酯的实例是聚对苯二甲酸乙二醇酯。所谓醇酸树脂也视为属于聚酯聚合物。
聚氨酯是从至少一种二异氰酸酯单体和至少一种多醇单体和/或多胺单体生成的聚合物。二异氰酸酯单体的实例是六亚甲基二异氰酸酯、甲苯二异氰酸酯、和二苯甲烷二异氰酸酯。
砜系聚合物的实例是聚芳基砜、聚醚砜、聚苯基砜和聚砜。聚砜是从4,4’-二氯二苯砜和双酚A生成的聚合物。
天然聚合物可以是纤维素、天然橡胶或明胶。纤维素衍生物的实例是乙基纤维素、羟丙基纤维素、硝基纤维素、乙酸纤维素酯和丙酸纤维素酯。
该聚合物粘结剂是业内已知的而且可以用已知方法生产。该聚合物粘结剂也可以通过一种包含能自由基聚合的单体和紫外线敏感引发剂的组合物的紫外线照射原位生产。
较好的聚合物粘结剂是丙烯酸类聚合物、乙烯基类聚合物、醛类聚合物、环氧类聚合物、聚酰胺类、聚酯类、和天然聚合物类及其衍生物。更好的聚合物粘结剂是丙烯酸类聚合物、乙烯基类聚合物、天然聚合物类及其衍生物。
甚至更好的聚合物粘结剂是聚(甲基丙烯酸甲酯)、聚(甲基丙烯酸丁酯)、聚乙烯醇、和纤维素。
最好的聚合物粘结剂是聚(甲基丙烯酸甲酯)。
有机溶剂可以是任何适用的有机溶剂或有机溶剂混合物。较好,它是一种极性有机溶剂或极性有机溶剂混合物。
极性有机溶剂的实例是C1-4烷醇类、C1-4多醇类、C1-4烷酸C1-4烷酯类、C3-6酮类、C4-6醚类、C2-3腈类、硝基甲烷、二甲基亚砜、二甲基甲酰胺、二甲基乙酰胺、N-甲基吡咯烷酮和环丁砜,其中C1-4烷醇类、C1-4多醇类和C1-4烷酸C1-4烷酯可以有C1-4烷氧基取代。
C1-4烷醇类的实例是甲醇、乙醇、丙醇、异丙醇或丁醇、异丁醇、仲丁醇和叔丁醇。其C1-4烷氧基衍生物的实例是2-乙氧基乙醇和1-甲氧基-2-丙醇。C1-4多醇类的实例是乙二醇和甘油。C1-4烷酸C1-4烷酯类的实例是乙酸乙酯、乙酸丁酯、丙酸乙酯和丁酸乙酯。其C1-4烷氧基衍生物的实例是乙酸2-乙氧基乙酯和乙酸2-甲氧基乙酯。C3-6酮类的实例是丙酮和甲乙酮。C4-6醚类的实例是二甲氧基乙烷、二异丙醚和四氢呋喃。C2-3腈类的实例是乙腈。
更好,该有机溶剂是选自下列组成的一组的极性有机溶剂或极性有机溶剂混合物:C1-4烷醇类、C1-4烷酸C1-4烷酯类、和C3-6酮类。最好,该有机溶剂是C3-6酮或C3-6酮类混合物。
本发明的组合物也可以包含水,但较好没有水存在。
本发明的组合物还可以包含适用于改善性能的任何其它化合物,例如IR吸收剂、UV吸收剂、抗氧剂、颜料、稳定剂和标记剂。标记剂是添加到一种产品中以指出其制造原的各种物质。这些化合物之和的数量,以该组合物的重量为基准,可以有0.01~30wt%。较好,以该组合物的重量为基准,它是0.1~10wt%、更好它是1~5wt%。
IR吸收剂可以是能使IR光转化热量的任何化合物。较好的IR吸收剂在1064nm或10600nm有吸收最大值。UV吸收剂的实例是2-羟基-4-甲氧基苯甲酰苯。
可以添加颜料以增强未成像区与成像区之间的反差或作为一种安全特色。
为增强未成像区与成像区之间的反差而可以添加的颜料是实例是二氧化钛、碳酸钙、高岭土、煅烧高岭土、氢氧化铝、滑石、氧化锌、无定形硅石、硫酸钡、聚苯乙烯树脂、脲甲醛树脂、中空塑料颜料、及其混合物。
可以作为安全特色添加的颜料的实例是荧光颜料或磁性颜料。
该组合物除包含羧酸金属盐外也可以进一步包含显色剂。较好使用在用能量处理之前不引起该涂料组合物变色的附加显色剂。更好,不施用苯酚类化合物作为附加显色剂。苯酚类化合物的实例是2,2-二(4-羟基苯基)-4-甲基戊烷、4,4’-偏亚异丙基二苯酚(双酚A)和二(3-烯丙基-4-羟基苯基)砜及对羟基苯甲酸苄酯。
本发明的组合物可以是一种溶液或分散液例如乳状液或悬浮液。因所希望的应用而异,本发明的组合物可以用来得到要么透明的要么不透明的涂层。较好得到透明的涂层。
本发明的涂料组合物所形成的涂层可以涂布一个层压层或罩印清漆。若该层压层或罩印清漆的材料选择得使其在成像激光的波长上不吸收,则激光敏感涂层可以透过该层压层成像而不损害或标记该层压层。此外,该层压层或罩印清漆理想地选择得使其在能量处理之前不导致该涂层变色。
能得到透明涂层的本发明组合物的实例是包含下列成分的组合物:以该组合物的重量为基准3.1wt%结晶紫内酯作为成色物质,以该组合物的重量为基准3.1wt%要么苯乙酸锌、对甲苯乙酸锌、4-联苯乙酸锌、反式-苯乙烯基乙酸锌、山梨酸锌、α-乙酰胺基肉桂酸锌、4-甲基肉桂酸锌、要么扁桃酸锌作为羧酸金属盐,以该组合物的重量为基准10.6wt%聚甲基丙烯酸甲酯作为粘结剂,以及以该组合物的重量为基准26.7wt%丙酮和以该组合物的重量为基准54.7wt%甲乙酮作为有机溶剂混合物。
此外,本发明的一部分是本发明组合物的制备方法,包含使该羧酸金属盐、该显色剂、该粘结剂和该有机溶剂混合的步骤。较好,该方法包含下列步骤:i)使该羧酸金属盐和该有机溶剂混合,和ii)添加该成色物质、该聚合物粘结剂及任选的附加化合物例如IR或UV吸收剂、稳定剂等,和iii)任选地将该组合物稀释到所希望的浓度。
本发明的另一个方面是一种涂布了本发明涂料组合物的基材。
该基材可以是一种片材或任何其它三维物体,而且它可以是透明的或不透明的。该基材可以从纸、纸板、金属、木材、纺织品、玻璃、陶瓷和/或聚合物制造。聚合物的实例是聚对苯二甲酸乙二醇酯、低密度聚乙烯、聚丙烯、双轴取向聚丙烯、聚醚砜、聚氯乙烯、聚酯和聚乙烯。较好,该基材是从纸、纸板或聚合物制造的。更好,该基材是从下列制造的一种可挠曲聚合物薄膜:聚对苯二甲酸乙二醇酯、低密度聚乙烯、聚丙烯、双轴取向聚丙烯、聚醚砜或聚氯乙烯。
该基材可以使用标准涂料施用法例如棒涂器施用法、滚涂法、喷涂法、帘涂法、浸涂法、空气施用法、刀涂法、刮涂法或辊涂法来涂布本发明组合物。该组合物也可以由各种印刷方法例如丝网印刷、凹版印刷、胶版印刷、和苯胺印刷施用到该基材上。若该基材是纸,则该组合物也可以在施胶压机中或纸机的湿端施用。
该涂层的厚度通常在0.1~1000μm范围内选择。较好,它在1~500μm范围内。更好,它在1~250μm范围内。甚至更好,它在1~150μm范围内。
该涂料组合物可以,例如,在常温或高温下干燥。理想地选择高温,以避免过早成色。
此外,本发明的一部分是一种有标记基材的制备方法,包含下列步骤:i)用本发明组合物涂布一种基材,和ii)使有涂层的基材的那些部分-在以标记为意向的情况下-暴露于能量以期产生一种彩色标记。
该能量可以是当施加到涂布了本发明组合物的基材上时能产生一种标记的热量或任何其它能量。这样的能量的实例是紫外线、红外线、可见光或微波照射。
该能量可以以任何适用方式施加到有涂层的基材上,例如,热量可以使用一台热打印机施加,紫外线和红外线照射可以使用一台紫外或红外激光器施加。红外激光器的实例是CO2激光器、Nd:YAG激光器和红外半导体激光器。
较好,该能量是红外线照射。更好,该能量是其波长在0.78~1000μm范围内的红外线照射。最好,该能量是CO2激光器或Nd:YAG激光器发生的红外线照射。
典型地,该IR激光器的确切功率和线速度决定于该应用,而且选择得足以产生该影像,例如,当该红外激光器的波长是10600nm且该激光束的直径是0.35mm时,功率典型地是0.5~4W,且线速度典型地是300~1000mm/s。
本发明的又另一个方面是由本发明方法得到的、有标记的基材。
本发明的涂料组合物的优点是它们可以是要么透明的要么不透明的,而且它们能产生高强度和亮度的影像。本发明的涂料组合物的一个进一步优点是它们不需要昂贵的金属化合物,此外它们制备方便,而且它们在能量处理之前不容易成色。
实施例
实施例1
苯乙酸锌的制备
将47%(w/w)氢氧化钠溶液(5.5g)添加到70℃的苯乙酸(6.8g,0.05mol)水(100mL)浆状液中,给出一种清澈的微碱性溶液。添加氯化锌(3.4g,0.025mol)水(50mL)溶液,立即生成一种沉淀物。该混合物在70℃进一步搅拌2.5小时。然后将该沉淀物过滤、干燥,得到6.5g(78%)微细白色粉末状苯乙酸锌。IR吸收带:1528、1434和1388cm-1。
实施例2
扁桃酸锌的制备
将47%(w/w)氢氧化钠溶液(5.5g)添加到70℃的扁桃酸(7.6g,0.05mol)水(100mL)浆状液中,给出一种清澈的微碱性溶液。添加氯化锌(3.4g,0.025mol)水(50mL)溶液,立即生成一种沉淀物。该混合物在70℃进一步搅拌2.5小时。然后将该沉淀物过滤、干燥,得到5.6g(61%)微细白色粉末状扁桃酸锌。IR吸收带:1592、1404和1361cm-1。
实施例3
4-甲基肉桂酸锌的制备
将47%(w/w)氢氧化钠溶液(5.5g)添加到70℃的4-甲基肉桂酸(8.1g,0.05mol)水(100mL)浆状物中,给出一种清澈的微碱性溶液。添加氯化锌(3.4g,0.025mol)水(50mL)溶液,立即生成一种沉淀物。该混合物在70℃进一步搅拌2.5小时。然后将该沉淀物过滤、干燥,得到7.7g(80%)微细白色粉末状4-甲基肉桂酸锌。IR吸收带:1530、1509和1382cm-1。
实施例4
山梨酸锌的制备
将47%(w/w)氢氧化钠溶液(5.5g)添加到70℃的山梨酸(5.6g,0.05mol)水(100mL)浆状物中,给出一种清澈的微碱性溶液。添加氯化锌(3.4g,0.025mol)水(50mL)溶液,立即生成一种沉淀物。该混合物在70℃进一步搅拌2.5小时。然后将该沉淀物过滤、干燥,得到5.5g(76%)微细白色粉末状山梨酸锌。IR吸收带:1521和1418cm-1。
实施例5
α-乙酰胺基肉桂酸锌的制备
将47%(w/w)氢氧化钠溶液(5.5g)添加到70℃的α-乙酰胺基肉桂酸(10.3g,0.05mol)水(100mL)浆状物中,给出一种清澈的微碱性溶液。添加氯化锌(3.4g,0.025mol)水(50mL)溶液,立即生成一种沉淀物。该混合物在70℃进一步搅拌2.5小时。然后将该沉淀物过滤、干燥,得到9.4g(80%)微细白色粉末状α-乙酰胺基肉桂酸锌。IR吸收带:1560、1510、1402和1353cm-1。
实施例6
反式-苯乙烯基乙酸锌的制备
将47%(w/w)氢氧化钠溶液(5.5g)添加到70℃的反式-苯乙烯基乙酸(8.1g,0.05mol)水(100mL)浆状物中,给出清澈的微碱性溶液。添加氯化锌(3.4g,0.025mol)水(50mL)溶液,立即生成一种沉淀物。该混合物在70℃进一步搅拌2.5小时。然后将该沉淀物过滤、干燥,得到7.5g(77%)微细白色粉末状反式-苯乙烯基乙酸锌。IR吸收带:1526、1436和1385cm-1。
实施例7
涂料组合物的制备
像实施例1中所述那样制备的二羧酸锌(1.0g)在丙酮(8.6g)中搅拌。按以下顺序向此混合物中添加:诸如以商品名CibaPergascript Blue1-2RN销售的结晶紫内酯(1.0g),聚(甲基丙烯酸甲酯)(3.4g),2-羟基-4-甲氧基苯甲酰苯(0.6g)和甲乙酮(17.6g)。然后,该涂料组合物用一支涂布棒施用到素色平纹纸、涂布纸或聚对苯二甲酸乙二醇酯薄膜上,形成一个120μm的半透明涂层,在常温下干燥,使用一台CO2激光器(波长10600nm,功率0.5~4W,激光束直径0.35mm,线速度300~1000mm/s)成像,得到一种蓝色标记。
实施例8
涂料组合物的制备
像实施例7中所述那样制备一种涂料组合物,所不同的是使用像实施例2中所述那样制备的二羧酸锌(1.0g)。
实施例9
涂料组合物的制备
像实施例7中所述那样制备一种涂料组合物,所不同的是使用像实施例3中所述那样制备的二羧酸锌(1.0g)。
实施例10
涂料组合物的制备
像实施例7中所述那样制备一种涂料组合物,所不同的是使用像实施例4中所述那样制备的二羧酸锌(1.0g)。
实施例11
涂料组合物的制备
像实施例7中所述那样制备一种涂料组合物,所不同的是使用像实施例5中所述那样制备的二羧酸锌(1.0g)。
实施例12
涂料组合物的制备
像实施例7中所述那样制备一种涂料组合物,所不同的是使用像实施例6中所述那样制备的二羧酸锌(1.0g)。
实施例13
涂料组合物的制备
像实施例2中所述那样制备的二羧酸锌(1.0g)在丙酮(8.6g)中搅拌。按以下顺序向此混合物中添加:诸如以商品名CibaPergascriptRed I-6B销售的3,3-二(1-辛基-2-甲基吲哚-3-基)-2-苯并[c]呋喃酮(0.25g),聚(甲基丙烯酸甲酯)(3.4g),2-羟基-4-甲氧基苯甲酰苯(0.6g)和甲乙酮(17.6g)。然后,该涂料组合物用一支涂布棒施用到素色平纹纸、涂布纸或聚对苯二甲酸乙二醇酯薄膜上,形成一个120μm的半透明涂层,在常温下干燥,使用一台CO2激光器(波长10600nm,功率0.5~4W,激光束直径0.35mm,线速度300~1000mm/s)成像,得到一种红色标记。
实施例14
涂料组合物的制备
像实施例2中所述那样制备的二羧酸锌(1.0g)在丙酮(8.6g)中搅拌。按以下顺序向此混合物中添加:诸如以商品名CibaPergascriptOrange I-G销售的3-二乙胺基-7-(乙氧羰基)荧烷(0.25g)聚(甲基丙烯酸甲酯)(3.4g),2-羟基-4-甲氧基苯甲酰苯(0.6g)和甲乙酮(17.6g)。然后,该涂料组合物用一支涂布棒施用到素色平纹纸、涂布纸或聚对苯二甲酸乙二醇酯薄膜上,形成一个120μm的半透明涂层,在常温下干燥,使用一台CO2激光器(波长10600nm,功率0.5~4W,激光束直径0.35mm,线速度300~1000mm/s)成像,得到一种橙色标记。
Claims (13)
1.一种组合物,包含数量为0.01~50%的一种成色物质、数量为0.01~50%的一种羧酸金属盐、数量为1~80%的一种粘结剂、和数量为1~99%的一种有机溶剂,其中每个数量都是以该组合物的重量为基准按重量计的。
2.权利要求1的组合物,其中该羧酸是式(I)的一种羧酸
或式(I)的羧酸混合物
式中
n是0、1、2、3、4、5、6、7、8、9、10、11、12、13或14,
m是0、1、2、3或4,
R1和R5相同或不同,可以是氢、羟基、C1-12烷基、羧基、C1-4烷氧羰基、氨基甲酰基、C1-4烷胺基羰基、酰基、氨基、(C1-4烷基)-CO-NH或脲基,
R2和R3相同或不同,可以是氢、C1-4烷基或(C1-4烷基)-CO-NH,
R4是氢、C1-12烷基、羧基、C1-4烷氧羰基、氨基甲酰基、C1-4烷胺基羰基、酰基、氨基、(C1-4烷基)-CO-NH、脲基、苯基、2-、3-或4-吡啶基、或者1-、2-或3-萘基,其中苯基、吡啶基或萘基可以是无取代的,也可以有C1-4烷基、苯基、C1-4烷氧基、羟基、二(C1-4烷基)氨基或卤素一取代、二取代或三取代。
3.权利要求1或2的组合物,其中该成色物质选自下列组成的一组:2-苯并[c]呋喃酮、荧烷、三芳基甲烷、苯并嗪、喹唑啉、螺吡喃、醌、噻嗪、或嗪或其混合物。
4.权利要求1~3中任何一项的组合物,其中该粘结剂是一种聚合物粘结剂。
5.权利要求1~4中任何一项的组合物,其中该有机溶剂是一种极性有机溶剂或极性有机溶剂混合物。
6.权利要求1的组合物的制备方法,包含使羧酸金属盐、显色剂、粘结剂和有机溶剂混合的步骤。
7.一种基材,涂布了权利要求1~5中任何一项的涂料组合物。
8.一种有标记的基材的制备方法,包含下列步骤:i)用权利要求1~5中任何一项的组合物涂布一种基材,和ii)在以一种标记为意向的情况下,使有涂层的基材的那些部分暴露于能量,以便产生一种彩色标记。
9.权利要求8的方法,其中该能量是IR辐射。
10.一种有标记的基材,其是用权利要求8或9的方法得到的。
11.权利要求1~5中任何一项的组合物用于涂布基材的用途。
12.权利要求1~5中任何一项的组合物用于标记基材的用途。
13.权利要求12的用途,其中该标记是通过使用IR辐射得到的。
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB0428299.2A GB0428299D0 (en) | 2004-12-24 | 2004-12-24 | Coating compositions for marking substrates |
GB0428299.2 | 2004-12-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
CN101087836A true CN101087836A (zh) | 2007-12-12 |
Family
ID=34113221
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNA200580044394XA Pending CN101087836A (zh) | 2004-12-24 | 2005-12-14 | 用于标记基材的涂料组合物 |
Country Status (18)
Country | Link |
---|---|
US (1) | US8101544B2 (zh) |
EP (1) | EP1828296B1 (zh) |
JP (2) | JP5274841B2 (zh) |
KR (1) | KR20070090040A (zh) |
CN (1) | CN101087836A (zh) |
AU (1) | AU2005318208B2 (zh) |
BR (1) | BRPI0519408A2 (zh) |
CA (1) | CA2592426A1 (zh) |
ES (1) | ES2543959T3 (zh) |
GB (1) | GB0428299D0 (zh) |
MX (1) | MX2007007662A (zh) |
NO (1) | NO20073645L (zh) |
NZ (1) | NZ555573A (zh) |
RU (1) | RU2394691C2 (zh) |
SG (1) | SG158167A1 (zh) |
TW (1) | TW200634075A (zh) |
WO (1) | WO2006067073A1 (zh) |
ZA (1) | ZA200704288B (zh) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102575059A (zh) * | 2009-10-15 | 2012-07-11 | 美利肯公司 | 热塑性聚合物组合物 |
CN103076506A (zh) * | 2012-12-27 | 2013-05-01 | 浙江大学 | 电磁辐射源指示液及指示材料的制备、使用方法 |
CN108148464A (zh) * | 2018-02-07 | 2018-06-12 | 温州深奥科技有限公司 | 光变色墙贴专用环保油墨制备工艺 |
CN116218033A (zh) * | 2023-01-05 | 2023-06-06 | 四川大学 | 有机材料在制备可彩色色变聚合物材料中的应用 |
Families Citing this family (27)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0521513D0 (en) | 2005-10-21 | 2005-11-30 | Sherwood Technology Ltd | Laser marking on substrates |
WO2007088104A1 (en) * | 2006-01-31 | 2007-08-09 | Ciba Holding Inc. | Coating composition for marking substrates |
MX2009009394A (es) | 2007-03-15 | 2009-09-11 | Basf Se | Composiciones de revestimiento sensibles al calor a base de derivados de resorcinil triazina. |
GB0713655D0 (en) * | 2007-07-16 | 2007-08-22 | Blue Ltd T | Improvements in and relating to packaging |
CN101801676B (zh) | 2007-07-18 | 2012-10-03 | 巴斯夫欧洲公司 | 激光敏感涂料制剂 |
CN101784620B (zh) | 2007-08-22 | 2013-05-29 | 巴斯夫欧洲公司 | 激光敏感涂料组合物 |
CA2702732A1 (en) * | 2007-11-07 | 2009-05-14 | Basf Se | New fiber products |
US8853314B2 (en) | 2008-10-23 | 2014-10-07 | Datalase Ltd. | Heat absorbing additives |
EP2349734B1 (en) | 2008-10-27 | 2018-03-28 | DataLase Ltd | Aqueous laser-sensitive composition for marking substrates |
US9267042B2 (en) | 2008-10-27 | 2016-02-23 | Datalase Ltd. | Coating composition for marking substrates |
US8563641B2 (en) * | 2009-03-12 | 2013-10-22 | Fina Technology, Inc. | Ionomer compositions and methods of making and using same |
EP2714413B1 (en) | 2011-05-25 | 2018-01-17 | Tetra Laval Holdings & Finance SA | Improved near infrared absorbers |
CN103619606B (zh) | 2011-08-12 | 2016-04-27 | 利乐拉瓦尔集团及财务有限公司 | 含有氨基酸的过氧基钼复合物的用途、包含该复合物的组合物、基底以及标记该基底的方法 |
RU2582408C2 (ru) * | 2011-08-12 | 2016-04-27 | Тетра Лаваль Холдингз Энд Файнэнс С.А. | Новое маркировочное соединение |
ES2540786B1 (es) * | 2014-01-10 | 2016-05-13 | Chimigraf Ibérica, S.L. | Tinta indicadora de la frescura de alimentos y procedimiento para la fabricación de una tinta indicadora de la frescura de alimentos |
DE102015005672A1 (de) | 2015-05-04 | 2016-11-10 | Giesecke & Devrient Gmbh | Sicherheitsmerkmal und Verfahren zu dessen Herstellung |
DE102016002120A1 (de) | 2016-02-24 | 2017-08-24 | Giesecke & Devrient Gmbh | Sicherheitsmerkmal und Verfahren zu dessen Herstellung |
DE102016004424A1 (de) | 2016-04-12 | 2017-10-12 | Giesecke+Devrient Currency Technology Gmbh | Laserung einer Beschichtung mit Effektpigmenten |
DE102016006931A1 (de) | 2016-06-06 | 2017-12-07 | Giesecke+Devrient Currency Technology Gmbh | Sicherheitsmerkmal und Verfahren zu dessen Herstellung |
DE102016006929A1 (de) | 2016-06-06 | 2017-12-07 | Giesecke+Devrient Currency Technology Gmbh | Sicherheitsmerkmal und Verfahren zu dessen Herstellung |
US20200148907A1 (en) | 2017-07-03 | 2020-05-14 | Agfa Nv | Near infrared (nir) laser markable compositions |
EP3470134B1 (en) | 2017-10-13 | 2020-06-03 | Agfa Nv | A composition comprising solvent and heat resistant capsules |
EP3470135B1 (en) | 2017-10-13 | 2020-04-08 | Agfa Nv | A composition comprising solvent and heat resistant capsules |
EP3626472A1 (en) | 2018-09-24 | 2020-03-25 | Agfa Nv | Laser markable compositions |
EP3626471A1 (en) | 2018-09-24 | 2020-03-25 | Agfa Nv | Laser markable compositions |
EP3838610A1 (en) | 2019-12-17 | 2021-06-23 | Agfa Nv | Laser markable articles |
EP3838609A1 (en) | 2019-12-17 | 2021-06-23 | Agfa Nv | Laser markable articles |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5434909A (en) * | 1977-08-08 | 1979-03-14 | Yamada Chem Co | Colored recording material |
US4680598A (en) * | 1985-04-18 | 1987-07-14 | Shin Nisso Kako Co., Ltd. | Chromogenic materials employing fluoran compounds |
US4820683A (en) * | 1987-12-04 | 1989-04-11 | Appleton Papers Inc. | Thermally-responsive record material |
JPH01232093A (ja) * | 1988-03-14 | 1989-09-18 | Fuji Photo Film Co Ltd | 記録材料 |
JPH0717134A (ja) * | 1993-07-05 | 1995-01-20 | Fuji Photo Film Co Ltd | 感熱記録材料及びその製造方法 |
JP2004530576A (ja) * | 2001-05-30 | 2004-10-07 | ポラロイド コーポレイション | 熱画像化システム |
JP2004045549A (ja) * | 2002-07-09 | 2004-02-12 | Mitsubishi Paper Mills Ltd | 可逆性感熱記録材料への加筆方法と消去方法 |
JP2004160806A (ja) | 2002-11-12 | 2004-06-10 | Mitsubishi Paper Mills Ltd | 可逆性感熱記録材料および記録方法 |
-
2004
- 2004-12-24 GB GBGB0428299.2A patent/GB0428299D0/en not_active Ceased
-
2005
- 2005-12-14 NZ NZ555573A patent/NZ555573A/en not_active IP Right Cessation
- 2005-12-14 SG SG200908554-9A patent/SG158167A1/en unknown
- 2005-12-14 CA CA002592426A patent/CA2592426A1/en not_active Abandoned
- 2005-12-14 KR KR1020077017070A patent/KR20070090040A/ko not_active Application Discontinuation
- 2005-12-14 MX MX2007007662A patent/MX2007007662A/es active IP Right Grant
- 2005-12-14 BR BRPI0519408-3A patent/BRPI0519408A2/pt not_active IP Right Cessation
- 2005-12-14 EP EP05819361.6A patent/EP1828296B1/en active Active
- 2005-12-14 WO PCT/EP2005/056763 patent/WO2006067073A1/en active Application Filing
- 2005-12-14 RU RU2007128092/04A patent/RU2394691C2/ru not_active IP Right Cessation
- 2005-12-14 US US11/793,499 patent/US8101544B2/en active Active
- 2005-12-14 CN CNA200580044394XA patent/CN101087836A/zh active Pending
- 2005-12-14 AU AU2005318208A patent/AU2005318208B2/en not_active Expired - Fee Related
- 2005-12-14 ES ES05819361.6T patent/ES2543959T3/es active Active
- 2005-12-14 JP JP2007547456A patent/JP5274841B2/ja active Active
- 2005-12-22 TW TW094145709A patent/TW200634075A/zh unknown
-
2007
- 2007-05-25 ZA ZA200704288A patent/ZA200704288B/xx unknown
- 2007-07-16 NO NO20073645A patent/NO20073645L/no not_active Application Discontinuation
-
2013
- 2013-01-18 JP JP2013007444A patent/JP2013076091A/ja not_active Withdrawn
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102575059A (zh) * | 2009-10-15 | 2012-07-11 | 美利肯公司 | 热塑性聚合物组合物 |
CN103076506A (zh) * | 2012-12-27 | 2013-05-01 | 浙江大学 | 电磁辐射源指示液及指示材料的制备、使用方法 |
CN103076506B (zh) * | 2012-12-27 | 2015-05-20 | 浙江大学 | 电磁辐射源指示液及指示材料的制备、使用方法 |
CN108148464A (zh) * | 2018-02-07 | 2018-06-12 | 温州深奥科技有限公司 | 光变色墙贴专用环保油墨制备工艺 |
CN116218033A (zh) * | 2023-01-05 | 2023-06-06 | 四川大学 | 有机材料在制备可彩色色变聚合物材料中的应用 |
Also Published As
Publication number | Publication date |
---|---|
WO2006067073A1 (en) | 2006-06-29 |
SG158167A1 (en) | 2010-01-29 |
US20080207444A1 (en) | 2008-08-28 |
TW200634075A (en) | 2006-10-01 |
NZ555573A (en) | 2010-05-28 |
ES2543959T3 (es) | 2015-08-26 |
US8101544B2 (en) | 2012-01-24 |
RU2007128092A (ru) | 2009-01-27 |
AU2005318208B2 (en) | 2011-04-14 |
NO20073645L (no) | 2007-07-16 |
MX2007007662A (es) | 2007-09-12 |
RU2394691C2 (ru) | 2010-07-20 |
JP2008525217A (ja) | 2008-07-17 |
JP2013076091A (ja) | 2013-04-25 |
EP1828296B1 (en) | 2015-07-08 |
AU2005318208A1 (en) | 2006-06-29 |
KR20070090040A (ko) | 2007-09-04 |
EP1828296A1 (en) | 2007-09-05 |
ZA200704288B (en) | 2008-09-25 |
BRPI0519408A2 (pt) | 2009-01-20 |
GB0428299D0 (en) | 2005-01-26 |
CA2592426A1 (en) | 2006-06-29 |
JP5274841B2 (ja) | 2013-08-28 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN101087836A (zh) | 用于标记基材的涂料组合物 | |
CN101146878B (zh) | 用于标记底物的涂料组合物 | |
CN101228034B (zh) | 用于标记基材的水基透明涂料及其制备方法和产品 | |
CN101801676B (zh) | 激光敏感涂料制剂 | |
CN101374673A (zh) | 用于标记基材的涂料组合物 | |
US9045619B2 (en) | Laser-sensitive coating composition | |
US9267042B2 (en) | Coating composition for marking substrates | |
CN101626903A (zh) | 具有底涂层的激光敏感记录材料 | |
US20150361289A1 (en) | Aqueous laser-sensitive composition for marking substrates | |
US5888283A (en) | High solids direct thermal ink composition and method of making and using same | |
JP2016527345A (ja) | 黄色サーモクロミック染料、インキ組成物およびレベルインジケーター | |
JPH07304972A (ja) | フルオラン化合物およびこれを用いる記録材料、可逆性熱変色材料 | |
JPS5946126A (ja) | マイクロカプセルの製造方法 | |
JPS6114985A (ja) | 感熱記録紙用バインダ− |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C02 | Deemed withdrawal of patent application after publication (patent law 2001) | ||
WD01 | Invention patent application deemed withdrawn after publication |
Application publication date: 20071212 |