CN111087571A - Solvent-resistant diluted polyurethane ink binder and preparation method and application thereof - Google Patents
Solvent-resistant diluted polyurethane ink binder and preparation method and application thereof Download PDFInfo
- Publication number
- CN111087571A CN111087571A CN201911379893.4A CN201911379893A CN111087571A CN 111087571 A CN111087571 A CN 111087571A CN 201911379893 A CN201911379893 A CN 201911379893A CN 111087571 A CN111087571 A CN 111087571A
- Authority
- CN
- China
- Prior art keywords
- polyurethane
- solvent
- cross
- crosslinking
- resistant
- 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
- 229920002635 polyurethane Polymers 0.000 title claims abstract description 122
- 239000004814 polyurethane Substances 0.000 title claims abstract description 122
- 239000002904 solvent Substances 0.000 title claims abstract description 70
- 239000011230 binding agent Substances 0.000 title claims abstract description 42
- 238000002360 preparation method Methods 0.000 title claims abstract description 36
- 238000006243 chemical reaction Methods 0.000 claims abstract description 92
- 238000004132 cross linking Methods 0.000 claims abstract description 73
- 229920005862 polyol Polymers 0.000 claims abstract description 46
- 150000003077 polyols Chemical class 0.000 claims abstract description 46
- 239000003431 cross linking reagent Substances 0.000 claims abstract description 39
- 238000010790 dilution Methods 0.000 claims abstract description 20
- 239000012895 dilution Substances 0.000 claims abstract description 20
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 117
- 239000000976 ink Substances 0.000 claims description 107
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 59
- 239000002994 raw material Substances 0.000 claims description 42
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 27
- 239000004970 Chain extender Substances 0.000 claims description 22
- 125000004427 diamine group Chemical group 0.000 claims description 22
- 125000005442 diisocyanate group Chemical group 0.000 claims description 22
- 238000002156 mixing Methods 0.000 claims description 22
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 claims description 20
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 20
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims description 15
- 238000000034 method Methods 0.000 claims description 13
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims description 12
- 239000002253 acid Substances 0.000 claims description 12
- 238000005886 esterification reaction Methods 0.000 claims description 11
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 claims description 11
- 239000005057 Hexamethylene diisocyanate Substances 0.000 claims description 10
- 235000011037 adipic acid Nutrition 0.000 claims description 10
- 239000001361 adipic acid Substances 0.000 claims description 10
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 claims description 10
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 claims description 10
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 claims description 10
- RNLHGQLZWXBQNY-UHFFFAOYSA-N 3-(aminomethyl)-3,5,5-trimethylcyclohexan-1-amine Chemical compound CC1(C)CC(N)CC(C)(CN)C1 RNLHGQLZWXBQNY-UHFFFAOYSA-N 0.000 claims description 9
- 239000005058 Isophorone diisocyanate Substances 0.000 claims description 9
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 claims description 9
- OWBTYPJTUOEWEK-UHFFFAOYSA-N butane-2,3-diol Chemical compound CC(O)C(C)O OWBTYPJTUOEWEK-UHFFFAOYSA-N 0.000 claims description 8
- 235000013305 food Nutrition 0.000 claims description 8
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 claims description 7
- 239000003795 chemical substances by application Substances 0.000 claims description 7
- 238000009459 flexible packaging Methods 0.000 claims description 7
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 claims description 6
- UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 claims description 6
- BMVXCPBXGZKUPN-UHFFFAOYSA-N 1-hexanamine Chemical compound CCCCCCN BMVXCPBXGZKUPN-UHFFFAOYSA-N 0.000 claims description 5
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 claims description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 5
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 claims description 5
- 150000007519 polyprotic acids Polymers 0.000 claims description 5
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 claims description 5
- PISLZQACAJMAIO-UHFFFAOYSA-N 2,4-diethyl-6-methylbenzene-1,3-diamine Chemical compound CCC1=CC(C)=C(N)C(CC)=C1N PISLZQACAJMAIO-UHFFFAOYSA-N 0.000 claims description 4
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 claims description 4
- 230000032050 esterification Effects 0.000 claims description 4
- 239000011259 mixed solution Substances 0.000 claims description 4
- 239000000203 mixture Substances 0.000 claims description 4
- 239000003960 organic solvent Substances 0.000 claims description 4
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 claims description 3
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 claims description 3
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 238000006068 polycondensation reaction Methods 0.000 claims description 2
- 238000004321 preservation Methods 0.000 claims description 2
- 239000004971 Cross linker Substances 0.000 claims 1
- 229920000642 polymer Polymers 0.000 claims 1
- 150000005846 sugar alcohols Polymers 0.000 claims 1
- 229920005749 polyurethane resin Polymers 0.000 abstract description 35
- 239000002131 composite material Substances 0.000 abstract description 25
- 238000007646 gravure printing Methods 0.000 abstract description 23
- 230000015572 biosynthetic process Effects 0.000 abstract description 10
- 239000012948 isocyanate Substances 0.000 abstract description 10
- 150000002513 isocyanates Chemical class 0.000 abstract description 10
- 238000003786 synthesis reaction Methods 0.000 abstract description 10
- 239000012466 permeate Substances 0.000 abstract description 9
- 238000007639 printing Methods 0.000 abstract description 9
- 238000009835 boiling Methods 0.000 abstract description 8
- 230000000903 blocking effect Effects 0.000 abstract description 2
- 238000010438 heat treatment Methods 0.000 description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 16
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 10
- FPCJKVGGYOAWIZ-UHFFFAOYSA-N butan-1-ol;titanium Chemical compound [Ti].CCCCO.CCCCO.CCCCO.CCCCO FPCJKVGGYOAWIZ-UHFFFAOYSA-N 0.000 description 8
- 239000003054 catalyst Substances 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- 239000012153 distilled water Substances 0.000 description 7
- 238000001704 evaporation Methods 0.000 description 7
- 239000007788 liquid Substances 0.000 description 7
- 229920005906 polyester polyol Polymers 0.000 description 7
- 238000003756 stirring Methods 0.000 description 7
- 239000000463 material Substances 0.000 description 5
- 238000010998 test method Methods 0.000 description 5
- 239000003085 diluting agent Substances 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 238000010411 cooking Methods 0.000 description 3
- 229920002521 macromolecule Polymers 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 2
- 230000002159 abnormal effect Effects 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 125000004185 ester group Chemical group 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000011229 interlayer Substances 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 238000011056 performance test Methods 0.000 description 2
- 238000010025 steaming Methods 0.000 description 2
- JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- NWYDEWXSKCTWMJ-UHFFFAOYSA-N 2-methylcyclohexane-1,1-diamine Chemical compound CC1CCCCC1(N)N NWYDEWXSKCTWMJ-UHFFFAOYSA-N 0.000 description 1
- 241000219198 Brassica Species 0.000 description 1
- 235000003351 Brassica cretica Nutrition 0.000 description 1
- 235000003343 Brassica rupestris Nutrition 0.000 description 1
- 241000196324 Embryophyta Species 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
- 229920002125 Sokalan® Polymers 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000011127 biaxially oriented polypropylene Substances 0.000 description 1
- 229920006378 biaxially oriented polypropylene Polymers 0.000 description 1
- QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 229920006037 cross link polymer Polymers 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000011010 flushing procedure Methods 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- 235000010460 mustard Nutrition 0.000 description 1
- 125000004888 n-propyl amino group Chemical group [H]N(*)C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003672 ureas Chemical group 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/65—Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
- C08G18/66—Compounds of groups C08G18/42, C08G18/48, or C08G18/52
- C08G18/6633—Compounds of group C08G18/42
- C08G18/6637—Compounds of group C08G18/42 with compounds of group C08G18/32 or polyamines of C08G18/38
- C08G18/6648—Compounds of group C08G18/42 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/3225 or C08G18/3271 and/or polyamines of C08G18/38
- C08G18/6651—Compounds of group C08G18/42 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/3225 or C08G18/3271 and/or polyamines of C08G18/38 with compounds of group C08G18/3225 or polyamines of C08G18/38
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
- C08G18/4205—Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups
- C08G18/4208—Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups containing aromatic groups
- C08G18/4211—Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups containing aromatic groups derived from aromatic dicarboxylic acids and dialcohols
- C08G18/4216—Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups containing aromatic groups derived from aromatic dicarboxylic acids and dialcohols from mixtures or combinations of aromatic dicarboxylic acids and aliphatic dicarboxylic acids and dialcohols
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
- C08G18/4205—Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups
- C08G18/4208—Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups containing aromatic groups
- C08G18/4211—Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups containing aromatic groups derived from aromatic dicarboxylic acids and dialcohols
- C08G18/4219—Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups containing aromatic groups derived from aromatic dicarboxylic acids and dialcohols from aromatic dicarboxylic acids and dialcohols in combination with polycarboxylic acids and/or polyhydroxy compounds which are at least trifunctional
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
- C08G18/4236—Polycondensates having carboxylic or carbonic ester groups in the main chain containing only aliphatic groups
- C08G18/4238—Polycondensates having carboxylic or carbonic ester groups in the main chain containing only aliphatic groups derived from dicarboxylic acids and dialcohols
- C08G18/4241—Polycondensates having carboxylic or carbonic ester groups in the main chain containing only aliphatic groups derived from dicarboxylic acids and dialcohols from dicarboxylic acids and dialcohols in combination with polycarboxylic acids and/or polyhydroxy compounds which are at least trifunctional
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
- C08G18/4244—Polycondensates having carboxylic or carbonic ester groups in the main chain containing oxygen in the form of ether groups
- C08G18/4247—Polycondensates having carboxylic or carbonic ester groups in the main chain containing oxygen in the form of ether groups derived from polyols containing at least one ether group and polycarboxylic acids
- C08G18/425—Polycondensates having carboxylic or carbonic ester groups in the main chain containing oxygen in the form of ether groups derived from polyols containing at least one ether group and polycarboxylic acids the polyols containing one or two ether groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/65—Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
- C08G18/66—Compounds of groups C08G18/42, C08G18/48, or C08G18/52
- C08G18/6633—Compounds of group C08G18/42
- C08G18/6637—Compounds of group C08G18/42 with compounds of group C08G18/32 or polyamines of C08G18/38
- C08G18/664—Compounds of group C08G18/42 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/3203
- C08G18/6644—Compounds of group C08G18/42 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/3203 having at least three hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/16—Dicarboxylic acids and dihydroxy compounds
- C08G63/20—Polyesters having been prepared in the presence of compounds having one reactive group or more than two reactive groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/66—Polyesters containing oxygen in the form of ether groups
- C08G63/668—Polyesters containing oxygen in the form of ether groups derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/672—Dicarboxylic acids and dihydroxy compounds
-
- 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
- C09D11/02—Printing inks
- C09D11/10—Printing inks based on artificial resins
- C09D11/102—Printing inks based on artificial resins containing macromolecular compounds obtained by reactions other than those only involving unsaturated carbon-to-carbon bonds
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
Abstract
The invention belongs to the technical field of gravure ink printing, particularly relates to a solvent-resistant diluted polyurethane ink binder, and particularly relates to a polyurethane binder for flexible package gravure printing composite ink with excellent solvent dilution resistance, boiling resistance and blocking resistance, and further discloses a preparation method of the polyurethane binder. According to the polyurethane binder for the gravure printing composite ink, the cross-linked polyol and the isocyanate react, then the cross-linking agent is used for carrying out cross-linking reaction on the polyurethane resin again, and a double cross-linked network-shaped three-dimensional structure is introduced in the polyurethane synthesis, so that the movement of molecular chains is limited, solvent molecules are difficult to permeate, the solvent dilution resistance of the polyurethane resin is enhanced along with the improvement of the cross-linking degree, the heat resistance, the solvent solubility resistance and the solvent dilution resistance of the polyurethane are effectively improved, and the polyurethane binder is suitable for the performance requirements of the flexible package gravure printing composite ink.
Description
Technical Field
The invention belongs to the technical field of gravure ink printing, particularly relates to a solvent-resistant diluted polyurethane ink binder, and particularly relates to a polyurethane binder for flexible package gravure printing composite ink with excellent solvent dilution resistance, boiling resistance and blocking resistance, and further discloses a preparation method of the polyurethane binder.
Background
Along with the improvement of living standard, people have higher and higher requirements on food flexible packages, the attention on printing quality is improved, the attention on environmental pollution, printing workshop safety and the like in the production process is also paid, alcohol and ester soluble ink is gradually used for replacing benzene and ketone system ink in the market, and an environment-friendly ink system is gradually developed and formed so as to meet the market demand. The domestic flexible package gravure printing composite ink is mainly used by taking polyurethane resin as an ink binder, and with the rapid increase of economy, the domestic flexible package gravure printing composite ink, the food package printing ink and the like show an increasing trend. In the aspect of flexible packaging such as laundry powder bags, hot pickled mustard tuber bags and the like, the materials are mostly PET, BOPP and other materials, and certain steaming resistance and solvent resistance are required, so that the application requirement of the connecting material is higher and higher.
Since the main chain of the macromolecule of polyurethane contains a plurality of urethane groups, which are generated by stepwise polymerization of di (or poly) isocyanate, di (or poly) polyol and di (or poly) amine, the macromolecule chain also contains ether groups, ester groups, carbamide groups, amide groups and the like besides the urethane groups, so that hydrogen bonds are easily generated among the macromolecules. Therefore, the polyurethane resin has excellent wear resistance, scratch resistance, adhesive property, flexibility, good low-temperature performance, high gloss and gloss retention, particularly the aliphatic polyurethane also has ultraviolet light resistance and good chemical resistance, and the application performance of the polyurethane resin has wide adjustability, so that the polyurethane resin can meet various requirements and can be widely applied to various fields. Therefore, the use of polyurethane resins in inks is becoming active and an important ink vehicle.
At present, alcohol ester-soluble polyurethane ink binder occupies a very important position in ink, and after polyurethane resin is prepared into ink, ester or alcohol solvent is added to dilute the ink to a certain viscosity for printing on a printing machine, so that the dilution ratio of the ink and the solvent is particularly important, and more solvents capable of being diluted are more and more emphasized by more and more printing plants. Therefore, not only the quality and performance of polyurethane resin are more and more important, but also the durability and use performance of polyurethane resin are more and more concerned.
For example, chinese patent CN104204020A discloses a polyurethane resin composition for a printing ink binder, but the polyurethane ink binder does not pay attention to the performance such as dilution resistance and boiling resistance, and has certain use defects. For another example, chinese patent CN103012724A discloses a polyurethane resin for gravure composite ink, which has good solubility, but the solvent dilution resistance is not ideal. Further, as disclosed in chinese patent CN101781453A, the polyurethane resin obtained by this method contains isocyanate groups and is inferior in storage stability. For another example, chinese patent CN102746735A discloses a two-component alcohol-soluble polyurethane ink binder, but the method has a complex using process, is prone to error during blending, and is inconvenient to operate. For another example, chinese patent CN101921374A discloses a polyacrylate-polyurethane resin binder for single-liquid universal plastic gravure alcohol-water-soluble composite ink, which is obtained by modifying polyurethane with polyacrylic acid, but the method cannot be applied to the packaging of food or medicine due to the introduction of an initiator, and has certain application limitations.
Therefore, the development of the polyurethane ink binder which is suitable for gravure printing for food flexible packaging and has excellent solvent dilution resistance, steaming resistance and anti-blocking performance is of great significance.
Disclosure of Invention
Therefore, the technical problem to be solved by the invention is to provide a polyurethane ink binder suitable for gravure printing for food flexible packaging, wherein the polyurethane ink binder has better solvent dilution resistance, boiling resistance and anti-blocking performance;
the second technical problem to be solved by the invention is to provide a preparation method and application of the ink vehicle.
In order to solve the technical problems, the solvent-resistant diluted polyurethane ink binder provided by the invention comprises the following raw materials for preparing double-crosslinking polyurethane and an organic solvent; wherein,
the raw materials for preparing the double-crosslinking polyurethane comprise the following components in parts by weight:
specifically, the organic solvent includes ethyl acetate and/or isopropanol.
The solvent-resistant diluted polyurethane ink vehicle comprises the following preparation raw materials in total amount:
29-31 wt% of the double-crosslinking polyurethane;
0-70 wt% of ethyl acetate;
0-70 wt% of isopropanol.
Specifically, the cross-linked polyol is a cross-linked polymer which is formed by esterification, polycondensation and cross-linking by taking polyol and polybasic acid as raw materials in the presence of an esterification cross-linking agent;
the cross-linking type polyol comprises the following components in percentage by total amount of raw materials for preparing the cross-linking type polyol:
0-50 wt% of polyol;
0-50 wt% of polybasic acid;
0-10 wt% of esterified cross-linking agent.
Specifically, in the solvent-resistant diluted polyurethane ink vehicle:
the dibasic acid comprises adipic acid (structural formula is shown in the specification)
) Sebacic acid (structural formula is
) Terephthalic acid (structural formula is
) At least one of;
the dihydric alcohol comprises 1,6 hexanediol (with a structural formula shown in the specification)
) 1, 4-butanediol (structural formula is shown in the specification)
) Methyl propylene glycol (structural formula is shown in the specification)
) Diethylene glycol (structural formula is shown in the specification)
) At least one of;
the cross-linking agent comprises glycerol (structural formula is shown in the specification)
) Trimethylolpropane (structural formula
) At least one or more of;
the crosslinking polyol preferably has a hydroxyl value of 18.7 to 56.1mgKOH/g and an acid value of 0.05 to 0.5mgKOH/g, more preferably a hydroxyl value of 30.0mgKOH/g and an acid value of 0.2 mgKOH/g.
More preferably, the cross-linking polyol comprises the following components based on the total amount of raw materials for preparing the cross-linking polyol:
and adding a catalyst such as butyl orthotitanate in an amount of 0-1 wt% based on the total amount of the above raw materials.
Specifically, the solvent-resistant diluted polyurethane ink vehicle comprises:
the diisocyanate comprises isophorone diisocyanate (structural formula is shown in the specification)
) Toluene diisocyanate (structural formula is shown in the specification)
) 4,4' -diphenylmethane diisocyanate (structural formula is shown in the specification)
) Hexamethylene diisocyanate of the formula
) At least one of;
the diamine chain extender comprises isophorone diamine (structural formula is shown in the specification)
) Methyl cyclohexanediamine (structural formula is shown in the specification)
) Diethyl toluenediamine (structural formula is shown in the specification)
) Ethylenediamine (structural formula)
) At least one of;
the polyurethane crosslinking agent comprises glycerol (structural formula is shown in the specification)
) Diethylenetriamine (structural formula is
) Pentaerythritol (structural formula is
) At least one of;
the polyurethane terminator comprises n-butylamine (structural formula shown in the specification)
) Octadecylamine (structural formula is
) N-propylamine (structural formula is
) N-hexylamine (structural formula is shown in the specification)
) Ethanolamine (structural formula
) At least one of (1).
The invention also discloses a method for preparing the solvent-resistant diluted polyurethane ink binder, which comprises the following steps:
(1) uniformly mixing a selected amount of the cross-linking polyol, diisocyanate and part of ethyl acetate, and reacting at 80-100 ℃ to obtain a prepolymer;
(2) mixing a selected amount of the diamine chain extender, the polyurethane cross-linking agent and part of ethyl acetate and isopropanol uniformly to obtain a mixed solution;
(3) by N2Transferring the obtained prepolymer to the mixed liquid obtained in the step (2), adding a selected amount of the terminator, and continuing to react;
(4) and after the reaction is finished, continuing carrying out heat preservation reaction at 55-65 ℃, and adding the rest ethyl acetate and isopropanol and uniformly mixing to obtain the product.
Specifically, the step (2) further comprises the step of preserving the temperature of the obtained mixed solution at 40-55 ℃.
The invention also discloses application of the solvent-resistant diluted polyurethane ink binder in preparation of gravure printing ink for food flexible packaging. Specifically, the viscosity of the solvent-resistant diluted polyurethane ink binder is 1000-1600 mPas (25 ℃).
The invention also discloses gravure printing ink for food flexible packaging, which is prepared from the solvent-resistant diluted polyurethane ink binder.
According to the polyurethane connecting material for the gravure printing composite ink, the cross-linked polyol and the isocyanate react, then the cross-linking agent is used for carrying out cross-linking reaction on the polyurethane resin again, and a double cross-linked network-shaped three-dimensional structure is introduced in the polyurethane synthesis, so that the movement of a molecular chain is limited, solvent molecules are difficult to permeate, the solvent-resistant dilutability of the polyurethane resin is enhanced along with the improvement of the cross-linking degree, and the heat resistance, the solvent-resistant solubility and the solvent-resistant dilutability of the polyurethane are effectively improved; the terminator is introduced during chain extension, so that the risk of crosslinking caused by too fast reaction during polyurethane synthesis can be effectively controlled, and the reaction is easier to control. The polyurethane binder for the gravure printing composite ink has excellent solvent dilution resistance, boiling resistance and anti-blocking performance, and is suitable for the performance requirements of the flexible package gravure printing composite ink.
The polyurethane binder for gravure composite ink preferably selects the special cross-linking polyol with hydroxyl value of 30.0mgKOH/g and acid value of 0.2mgKOH/g, ensures enough ester groups and methylene in polyurethane resin, increases the crystallinity of chain segments along with the increase of hydrogen bonds, and improves the viscosity, tensile strength and bonding strength performance of the polyurethane resin; the hardness of the polyurethane resin is reduced, the flexibility of the polyurethane resin is improved, and the transferability and the leveling property of the polyurethane ink are ensured after the gravure printing composite ink is prepared.
Detailed Description
Example 1
The polyurethane binder for gravure printing composite ink in the embodiment comprises the following components in total amount of preparation raw materials:
30.3 wt% of raw materials for preparing the double-crosslinking polyurethane;
ethyl acetate 40.2 wt%;
and 29.5% of isopropanol.
The preparation method of the solvent-resistant diluted polyurethane ink vehicle comprises the following steps:
(1) uniformly mixing 100g of cross-linking polyol, 17.4g of diisocyanate and 10g of ethyl acetate in a reaction bottle 1, and heating to 90 ℃ to react for 2 hours to obtain a prepolymer;
(2) adding 12.8g of diamine chain extender, 1.5g of cross-linking agent, 1g of terminator, 157.4g of ethyl acetate and 120.2g of isopropanol into a reaction bottle 2, uniformly mixing, and keeping the temperature at 50 ℃;
(3) by N2Transferring the prepolymer from the reaction bottle 1 to the reaction bottle 2 for 15 min; adding 1g of terminating agent into the reaction bottle 2 continuously, and reacting for 20min continuously;
(4) after the reaction is finished, keeping the temperature at 60 ℃ for 4h, adding 10g of ethyl acetate and 10g of isopropanol, and stirring uniformly to obtain the product.
In the preparation raw materials of the solvent-resistant diluted polyurethane ink vehicle of the embodiment:
the cross-linked polyol is prepared by adding adipic acid (mass content of 58%), terephthalic acid (mass content of 5%), methyl propylene glycol (mass content of 35%), trimethylolpropane (mass content of 2%) and a catalyst (butyl orthotitanate accounting for 0.08% of the mass content of the raw materials) into a reaction bottle in sequence according to the mass of the prepared polyester polyol; heating to 200 ℃ for reaction for 4 hours, evaporating water generated in the reaction, continuously heating to 240 ℃ for reaction for 4 hours, wherein the reaction is esterification reaction, and the temperature rise process is controlled to be slow, and the temperature of distilled water is 100-; the hydroxyl value of the prepared crosslinking type polyol is 29.6mgKOH/g, and the acid value is 0.21 KOH/g;
the diisocyanate is isophorone diisocyanate and toluene diisocyanate, and the mass ratio of the diisocyanate to the toluene diisocyanate is 1.3: 1;
the diamine chain extender is isophorone diamine;
the polyurethane cross-linking agent is diethylenetriamine;
the polyurethane terminator is n-butylamine and ethanolamine, and the mass ratio is 1.2: 1.
in the polyurethane ink binder with the double-crosslinking structure, a crosslinking polyol and isocyanate react, then a crosslinking agent is used for carrying out a crosslinking reaction on polyurethane resin, and a crosslinking net-shaped three-dimensional structure is introduced in polyurethane synthesis, so that not only is the movement of a molecular chain limited, but also solvent molecules are difficult to permeate, and the solvent dilution resistance of the polyurethane resin is enhanced along with the improvement of the crosslinking degree; the viscosity of the polyurethane ink vehicle described in this example was 1200 mPas (25 ℃).
Example 2
The polyurethane binder for gravure printing composite ink in the embodiment comprises the following components in total amount of preparation raw materials:
29.5 wt% of raw materials for preparing the double-crosslinking polyurethane;
ethyl acetate 45.2 wt%;
24.5 percent of isopropanol.
The preparation method of the solvent-resistant diluted polyurethane ink vehicle comprises the following steps:
(1) uniformly mixing 100g of the cross-linking polyol, 24.7g of diisocyanate and 10g of ethyl acetate in a reaction bottle 1, and heating to 90 ℃ to react for 2.5 hours to obtain a prepolymer;
(2) adding 15.5g of diamine chain extender, 1.6g of cross-linking agent, 1.4g of terminator, 201.9g of ethyl acetate and 110.2g of isopropanol into a reaction bottle 2, uniformly mixing, and keeping the temperature at 50 ℃;
(3) by N2Transferring the prepolymer from the reaction bottle 1 to the reaction bottle 2 for 18 min; adding 1.6g of terminating agent into the reaction bottle 2, and continuing to react for 20 min;
(4) after the reaction is finished, preserving the heat for 4 hours at the temperature of 60 ℃, adding 10g of ethyl acetate and 10g of isopropanol, and uniformly stirring to obtain the product.
In the preparation raw materials of the solvent-resistant diluted polyurethane ink vehicle of the embodiment:
the preparation method comprises the following steps of taking adipic acid (40 wt%), sebacic acid (10 wt%), 1, 4-butanediol (25 wt%), methyl propylene glycol (21 wt%) and a crosslinking agent glycerol (4 wt%) as raw materials, and sequentially adding adipic acid (50 wt%), sebacic acid (12 wt%), 1, 4-butanediol (15 wt%), methyl propylene glycol (21 wt%), the crosslinking agent glycerol (2 wt%), and a catalyst (butyl orthotitanate, which accounts for 0.08 wt% of the raw materials) into a reaction bottle according to the mass of the prepared polyester polyol; heating to 200 ℃ for reaction for 4 hours, evaporating water generated in the reaction, continuously heating to 240 ℃ for reaction for 4 hours, wherein the reaction is esterification reaction, and the temperature rise process is controlled to be slow, and the temperature of distilled water is 100-; the hydroxyl value of the cross-linked polyol is 28.4mgKOH/g, and the acid value is 0.26 KOH/g;
the diisocyanate is isophorone diisocyanate and 4,4' -diphenylmethane diisocyanate, and the mass ratio is 0.9: 1;
the diamine chain extender is isophorone diamine and diethyl toluene diamine, and the mass ratio of the diamine chain extender to the diamine chain extender is 1: 1;
the polyurethane cross-linking agent is ethylene triamine;
the polyurethane terminator is composed of octadecylamine and ethanolamine in a mass ratio of 4.4: 1.
in the polyurethane ink binder with the double-crosslinking structure, a crosslinking polyol and isocyanate react, then a crosslinking agent is used for carrying out a crosslinking reaction on polyurethane resin, and a crosslinking net-shaped three-dimensional structure is introduced in polyurethane synthesis, so that not only is the movement of a molecular chain limited, but also solvent molecules are difficult to permeate, and the solvent dilution resistance of the polyurethane resin is enhanced along with the improvement of the crosslinking degree; the viscosity of the polyurethane ink vehicle described in this example was 1250 mPas (25 ℃).
Example 3
The polyurethane binder for gravure printing composite ink in the embodiment comprises the following components in total amount of preparation raw materials:
30.0 wt% of raw materials for preparing the double-crosslinking polyurethane;
ethyl acetate 50.3 wt%;
and 19.7% of isopropanol.
The preparation method of the solvent-resistant diluted polyurethane ink vehicle comprises the following steps:
(1) uniformly mixing 100g of novel special polyol, 23.5g of diisocyanate and 10g of ethyl acetate in a reaction bottle 1, heating to 85 ℃ and reacting for 3 hours to obtain a prepolymer;
(2) adding 16.5g of diamine chain extender, 1.5g of cross-linking agent, 1.6g of terminator, 222.6g of ethyl acetate and 95g of isopropanol into a reaction bottle 2, uniformly mixing, and keeping the temperature at 50 ℃;
(3) by N2Transferring the prepolymer A diluent from the reaction bottle 1 to the reaction bottle 2 for 20 min; adding 1.6g of terminating agent into the reaction bottle 2, and continuing to react for 20 min;
(4) after the reaction is finished, keeping the temperature at 60 ℃ for 4h, adding 10g of ethyl acetate and 10g of isopropanol, and stirring uniformly to obtain the product.
In the preparation raw materials of the solvent-resistant diluted polyurethane ink vehicle of the embodiment:
the preparation method of the cross-linked polyol comprises the following steps of adding adipic acid (55 wt% by mass), terephthalic acid (5 wt% by mass), 1, 4-butanediol (12 wt% by mass), diethylene glycol (26 wt% by mass), a cross-linking agent trimethylolpropane (2 wt% by mass) and a catalyst (butyl orthotitanate, accounting for 0.08% by mass of the raw materials) into a reaction bottle in sequence according to the mass of the prepared polyester polyol; heating to 200 ℃ for reaction for 4 hours, evaporating water generated in the reaction, continuously heating to 240 ℃ for reaction for 4 hours, wherein the reaction is esterification reaction, and the temperature rise process is controlled to be slow, and the temperature of distilled water is 100-; the hydroxyl value of the crosslinking polyol was 28.4mgKOH/g, and the acid value was 0.26 KOH/g.
The diisocyanate is isophorone diisocyanate and hexamethylene diisocyanate, and the mass ratio of the diisocyanate to the hexamethylene diisocyanate is 1.3: 1;
the diamine chain extender is isophorone diamine and methyl cyclohexane diamine, and the mass ratio is 1.3: 1;
the polyurethane cross-linking agent is glycerol;
the polyurethane terminator is n-butylamine and n-propylamine, and the mass ratio is 1.2: 1.
in the polyurethane ink binder with the double-crosslinking structure, a crosslinking polyol and isocyanate react, then a crosslinking agent is used for carrying out a crosslinking reaction on polyurethane resin, and a crosslinking net-shaped three-dimensional structure is introduced in polyurethane synthesis, so that not only is the movement of a molecular chain limited, but also solvent molecules are difficult to permeate, and the solvent dilution resistance of the polyurethane resin is enhanced along with the improvement of the crosslinking degree; the viscosity of the polyurethane ink vehicle described in this example was 1275mPa · s (25 ℃).
Example 4
The polyurethane binder for gravure printing composite ink in the embodiment comprises the following components in total amount of preparation raw materials:
30.8 wt% of raw materials for preparing the double-crosslinking polyurethane;
ethyl acetate 60.5 wt%;
8.7 percent of isopropanol.
The preparation method of the solvent-resistant diluted polyurethane ink vehicle comprises the following steps:
(1) uniformly mixing 100g of novel special polyol, 19.6g of diisocyanate and 10g of ethyl acetate in a reaction bottle 1, heating to 85 ℃ and reacting for 3 hours to obtain a prepolymer;
(2) adding 14.6g of diamine chain extender, 1.5g of cross-linking agent, 1.2g of terminator, 252.1g of ethyl acetate and 95g of isopropanol into a reaction bottle 2, uniformly mixing, and keeping the temperature at 50 ℃;
(3) by N2Mixing the prepolymerTransferring the diluent A from the reaction bottle 1 to the reaction bottle 2 for 20 min; adding 1.6g of terminating agent into the reaction bottle 2, and continuing to react for 20 min;
(4) after the reaction is finished, preserving the heat for 4 hours at the temperature of 60 ℃, adding 10g of ethyl acetate and 10g of isopropanol, and uniformly stirring to obtain the product.
In the preparation raw materials of the solvent-resistant diluted polyurethane ink vehicle of the embodiment:
the preparation method of the cross-linked polyol comprises the following steps of adding adipic acid (with the mass content of 58 wt%), sebacic acid (with the mass content of 6 wt%), 1, 6-hexanediol (with the mass content of 10 wt%), diethylene glycol (with the mass content of 22 wt%) and a cross-linking agent trimethylolpropane (with the mass content of 4%) into a reaction bottle in sequence according to the mass of the prepared polyester polyol, and adding a catalyst (butyl orthotitanate, which accounts for 0.08% of the mass content of the raw materials); heating to 200 ℃ for reaction for 4 hours, evaporating water generated in the reaction, continuously heating to 240 ℃ for reaction for 4 hours, wherein the reaction is esterification reaction, and the temperature rise process is controlled to be slow, and the temperature of distilled water is 100-; the hydroxyl value of the crosslinked polyol was 31.4mgKOH/g, and the acid value was 0.27 KOH/g.
The diisocyanate is isophorone diisocyanate, toluene diisocyanate and hexamethylene diisocyanate, and the mass ratio is 1.3: 1: 1;
the diamine chain extender is isophorone diamine and ethylene diamine, and the mass ratio is 2.8: 1;
the polyurethane cross-linking agent is diethylenetriamine;
the polyurethane terminator is composed of n-propylamine and n-hexylamine in a mass ratio of 0.6: 1.
in the polyurethane ink binder with the double-crosslinking structure, a crosslinking polyol and isocyanate react, then a crosslinking agent is used for carrying out a crosslinking reaction on polyurethane resin, and a crosslinking net-shaped three-dimensional structure is introduced in polyurethane synthesis, so that not only is the movement of a molecular chain limited, but also solvent molecules are difficult to permeate, and the solvent dilution resistance of the polyurethane resin is enhanced along with the improvement of the crosslinking degree; the viscosity of the polyurethane ink vehicle described in this example was 1350mPa · s (25 ℃).
Example 5
The polyurethane binder for gravure printing composite ink in the embodiment comprises the following components in total amount of preparation raw materials:
29.2 wt% of raw materials for preparing the double-crosslinking polyurethane;
26.5 wt% of ethyl acetate;
and 44.3 percent of isopropanol.
The preparation method of the solvent-resistant diluted polyurethane ink vehicle comprises the following steps:
(1) uniformly mixing 100g of novel special polyol, 26.3g of diisocyanate and 10g of ethyl acetate in a reaction bottle 1, heating to 95 ℃, and reacting for 3 hours to obtain a prepolymer;
(2) adding 16.5g of diamine chain extender, 1.5g of cross-linking agent, 1.8g of terminator, 75g of ethyl acetate and 224.4g of isopropanol into a reaction bottle 2, uniformly mixing, and keeping the temperature at 50 ℃;
(3) by N2Transferring the prepolymer A diluent from the reaction bottle 1 to the reaction bottle 2 for 20 min; adding 1.8g of terminating agent into the reaction bottle 2, and continuing to react for 20 min;
(4) after the reaction is finished, preserving the heat for 4 hours at the temperature of 60 ℃, adding 10g of ethyl acetate and 10g of isopropanol, and uniformly stirring to obtain the product.
In the preparation raw materials of the solvent-resistant diluted polyurethane ink vehicle of the embodiment:
the preparation method of the cross-linked polyol comprises the following steps of adding adipic acid (65 wt% in mass), 1, 6-hexanediol (8 wt% in mass), methyl propylene glycol (25 wt% in mass), a cross-linking agent glycerol (2 wt% in mass) and a catalyst (butyl orthotitanate, accounting for 0.08% in mass of raw materials) into a reaction bottle in sequence according to the mass of the prepared polyester polyol; heating to 200 ℃ for reaction for 4 hours, evaporating water generated in the reaction, continuously heating to 240 ℃ for reaction for 4 hours, wherein the reaction is esterification reaction, and the temperature rise process is controlled to be slow, and the temperature of distilled water is 100-; the hydroxyl value of the crosslinked polyol was 33.6mgKOH/g, and the acid value was 0.30 KOH/g.
The diisocyanate is isophorone diisocyanate and hexamethylene diisocyanate, and the mass ratio of the diisocyanate to the hexamethylene diisocyanate is 1.3: 1;
the diamine chain extender is isophorone diamine and diethyl toluene diamine, and the mass ratio of the diamine chain extender to the diamine chain extender is 1: 1;
the polyurethane cross-linking agent is pentaerythritol;
the polyurethane terminator is n-hexylamine and ethanolamine, and the mass ratio of the n-hexylamine to the ethanolamine is 1.7: 1.
in the polyurethane ink binder with the double-crosslinking structure, a crosslinking polyol and isocyanate react, then a crosslinking agent is used for carrying out a crosslinking reaction on polyurethane resin, and a crosslinking net-shaped three-dimensional structure is introduced in polyurethane synthesis, so that not only is the movement of a molecular chain limited, but also solvent molecules are difficult to permeate, and the solvent dilution resistance of the polyurethane resin is enhanced along with the improvement of the crosslinking degree; the viscosity of the polyurethane ink vehicle described in this example was 1250 mPas (25 ℃).
Example 6
The polyurethane binder for gravure printing composite ink in the embodiment comprises the following components in total amount of preparation raw materials:
29.8 wt% of raw materials for preparing the double-crosslinking polyurethane;
ethyl acetate 45.6 wt%;
24.6 percent of isopropanol.
The preparation method of the solvent-resistant diluted polyurethane ink vehicle comprises the following steps:
(1) uniformly mixing 100g of novel special polyol, 28.6g of diisocyanate and 10g of ethyl acetate in a reaction bottle 1, heating to 90 ℃, and reacting for 2.5 hours to obtain a prepolymer;
(2) adding 17.8g of diamine chain extender, 1.5g of cross-linking agent, 1.2g of terminator, 210.3g of ethyl acetate and 114.2g of isopropanol into a reaction bottle 2, uniformly mixing, and keeping the temperature at 50 ℃;
(3) by N2Transferring the prepolymer from the reaction bottle 1 to the reaction bottle 2 for 20 min; and in reactionAdding 1.4g of terminator into the bottle 2, and continuing to react for 20 min;
(4) after the reaction is finished, preserving the heat for 4 hours at the temperature of 60 ℃, adding 10g of ethyl acetate and 10g of isopropanol, and uniformly stirring to obtain the product.
In the preparation raw materials of the solvent-resistant diluted polyurethane ink vehicle of the embodiment:
the preparation method of the cross-linked polyol comprises the following steps of adding adipic acid (55 wt% by mass), terephthalic acid (7 wt% by mass), methyl propylene glycol (10 wt% by mass), diethylene glycol (25 wt% by mass), a cross-linking agent trimethylolpropane (3 wt% by mass) and a catalyst (butyl orthotitanate, accounting for 0.08% by mass of the raw materials) into a reaction bottle in sequence according to the mass of the prepared polyester polyol; heating to 200 ℃ for reaction for 4 hours, evaporating water generated in the reaction, continuously heating to 240 ℃ for reaction for 4 hours, wherein the reaction is esterification reaction, and the temperature rise process is controlled to be slow, and the temperature of distilled water is 100-; the hydroxyl value of the crosslinking polyol was 28.3mgKOH/g, and the acid value was 0.22 KOH/g.
The diisocyanate is a mixture of isophorone diisocyanate, 4' -diphenylmethane diisocyanate and hexamethylene diisocyanate, and the mass ratio is 1.3: 1.3: 1;
the diamine chain extender is isophorone diamine and methyl cyclohexane diamine, and the mass ratio is 1.5: 1;
the polyurethane cross-linking agent is glycerol;
the polyurethane terminator is n-propylamine and ethanolamine, and the mass ratio of the n-propylamine to the ethanolamine is 1: 1.
in the polyurethane ink binder with the double-crosslinking structure, a crosslinking polyol and isocyanate react, then a crosslinking agent is used for carrying out a crosslinking reaction on polyurethane resin, and a crosslinking net-shaped three-dimensional structure is introduced in polyurethane synthesis, so that not only is the movement of a molecular chain limited, but also solvent molecules are difficult to permeate, and the solvent dilution resistance of the polyurethane resin is enhanced along with the improvement of the crosslinking degree; the viscosity of the polyurethane ink vehicle described in this example was 1300 mPas (25 ℃).
Example 7
The polyurethane binder for gravure printing composite ink in the embodiment comprises the following components in total amount of preparation raw materials:
30.5 wt% of raw materials for preparing the double-crosslinking polyurethane;
47.6 wt% of ethyl acetate;
and 21.9% of isopropanol.
The preparation method of the solvent-resistant diluted polyurethane ink vehicle comprises the following steps:
(1) uniformly mixing 100g of novel special polyol, 22.5g of diisocyanate and 10g of ethyl acetate in a reaction bottle 1, heating to 95 ℃, and reacting for 3 hours to obtain a prepolymer;
(2) adding 14.6g of diamine chain extender, 1.6g of cross-linking agent, 1.2g of terminator, 200.8g of ethyl acetate and 91.6g of isopropanol into a reaction bottle 2, uniformly mixing, and keeping the temperature at 50 ℃;
(3) by N2Transferring the prepolymer A diluent from the reaction bottle 1 to the reaction bottle 2 for 20 min; adding 1.6g of terminating agent into the reaction bottle 2, and continuing to react for 20 min;
(4) after the reaction is finished, preserving the heat for 4 hours at the temperature of 60 ℃, adding 10g of ethyl acetate and 10g of isopropanol, and uniformly stirring to obtain the product.
In the preparation raw materials of the solvent-resistant diluted polyurethane ink vehicle of the embodiment:
the preparation method of the cross-linked polyol comprises the following steps of sequentially adding adipic acid (with the mass content of 60 wt%), terephthalic acid (with the mass content of 2 wt%), 1,6 hexanediol (with the mass content of 4 wt%), methyl propylene glycol (with the mass content of 31 wt%) and a cross-linking agent trimethylolpropane (with the mass content of 3%), and a catalyst (butyl orthotitanate, which accounts for 0.08% of the mass content of the raw materials) into a reaction bottle according to the mass of the prepared polyester polyol; heating to 200 ℃ for reaction for 4 hours, evaporating water generated in the reaction, continuously heating to 240 ℃ for reaction for 4 hours, wherein the reaction is esterification reaction, and the temperature rise process is controlled to be slow, and the temperature of distilled water is 100-; the hydroxyl value of the crosslinking polyol was 32.5mgKOH/g, and the acid value was 0.34 KOH/g.
The diisocyanate is isophorone diisocyanate and hexamethylene diisocyanate, and the mass ratio of the diisocyanate to the hexamethylene diisocyanate is 1.3: 1;
the diamine chain extender is isophorone diamine and ethylene diamine, and the mass ratio is 2.8: 1;
the polyurethane cross-linking agent is diethylenetriamine;
the polyurethane terminator is n-butylamine and ethanolamine, and the mass ratio of the n-butylamine to the ethanolamine is 1: 1.
in the polyurethane ink binder with the double-crosslinking structure, a crosslinking polyol and isocyanate react, then a crosslinking agent is used for carrying out a crosslinking reaction on polyurethane resin, and a crosslinking net-shaped three-dimensional structure is introduced in polyurethane synthesis, so that not only is the movement of a molecular chain limited, but also solvent molecules are difficult to permeate, and the solvent dilution resistance of the polyurethane resin is enhanced along with the improvement of the crosslinking degree; the viscosity of the polyurethane ink vehicle described in this example was 1350mPa · s (25 ℃).
Examples of the experiments
The polyurethane resin ink vehicles prepared in the above examples 1 to 6 were prepared into gravure composite inks according to the formulations shown in the following table 1, respectively, and the application properties thereof were tested using a conventional ink vehicle (model HZ1530B, a new material ltd, huang shan) of the related art as a comparative example.
TABLE 1 gravure composite ink formulation
The application performance of the prepared ink is detected by the following standard:
GB/T2024-2012 gravure plastic film composite ink;
GBT 13217.3-2008 liquid ink fineness test method;
GBT 13217.4-2008 liquid ink viscosity test method;
GBT 13217.6-2008 liquid ink tinting strength test method;
GBT 13217.7-2009 liquid ink adhesion test method;
GBT 13217.8-2009 liquid ink anti-blocking test method;
and (3) measuring dilution resistance: and (3) flushing the prepared ink to a fixed viscosity by using ethyl acetate to obtain the ratio of the mass of the diluted solvent to the mass of the ink. Note: the performance test is carried out until the viscosity of the prepared ink is 13 seconds/25 ℃;
and (3) measuring the water boiling performance: putting the sample into a water bath, setting the temperature at 100 ℃, boiling for 60min, cooling to room temperature after the test is finished, and observing whether the abnormal phenomena such as obvious deformation, interlayer peeling, heat-seal part peeling and the like exist;
and (3) determining the cooking performance: and (3) putting the sample into a cooking pot, setting the temperature at 121 ℃, cooking for 40min, cooling to room temperature after the test is finished, and observing whether the abnormal phenomena such as obvious deformation, interlayer peeling, heat-seal part peeling and the like exist.
The specific test results are shown in table 2 below.
TABLE 2 ink Performance test results
From the data in the table, the polyurethane binder for gravure printing composite ink has excellent solvent dilution resistance, boiling resistance and anti-blocking performance, and is suitable for the performance requirements of flexible package gravure printing composite ink.
It should be understood that the above examples are only for clarity of illustration and are not intended to limit the embodiments. Other variations and modifications will be apparent to persons skilled in the art in light of the above description. And are neither required nor exhaustive of all embodiments. And obvious variations or modifications therefrom are within the scope of the invention.
Claims (10)
1. A solvent-resistant diluted polyurethane ink binder is characterized in that the preparation raw materials comprise raw materials for preparing double-crosslinking polyurethane and an organic solvent; wherein,
the raw materials for preparing the double-crosslinking polyurethane comprise the following components in parts by weight:
2. the solvent-resistant dilution-type polyurethane ink vehicle of claim 1, wherein the organic solvent comprises ethyl acetate and/or isopropyl alcohol.
3. The solvent-resistant dilution-type polyurethane ink vehicle according to claim 1 or 2, characterized in that it is prepared from raw materials comprising, in total:
29-31 wt% of the double-crosslinking polyurethane;
0-70 wt% of ethyl acetate;
0-70 wt% of isopropanol.
4. The solvent-resistant dilution-type polyurethane ink vehicle according to any one of claims 1 to 3, wherein the crosslinking polyol is a crosslinking polymer obtained by esterification polycondensation and crosslinking using a polyol and a polybasic acid as raw materials in the presence of an esterification crosslinking agent;
the cross-linking type polyol comprises the following components in percentage by total amount of raw materials for preparing the cross-linking type polyol:
0-50 wt% of polyol;
0-50 wt% of polybasic acid;
0-10 wt% of esterified cross-linking agent.
5. A solvent-resistant, dilution-type polyurethane ink vehicle of claim 4, wherein:
the polyhydric alcohol comprises dihydric alcohol, and more preferably comprises at least one of 1, 6-hexanediol, 1, 4-butanediol, methyl propylene glycol and diethylene glycol;
the polybasic acid comprises dibasic acid, more preferably at least one of adipic acid, sebacic acid and terephthalic acid;
the esterified crosslinker comprises glycerol or trimethylolpropane.
6. A solvent dilution resistant polyurethane ink vehicle according to any one of claims 1 to 5, wherein:
the diisocyanate comprises at least one of isophorone diisocyanate, toluene diisocyanate, 4' -diphenylmethane diisocyanate and hexamethylene diisocyanate;
the diamine chain extender comprises at least one of isophorone diamine, methyl cyclohexane diamine, diethyl toluene diamine and ethylene diamine;
the polyurethane cross-linking agent comprises at least one of glycerol, diethylenetriamine and pentaerythritol;
the polyurethane terminator comprises at least one of n-butylamine, octadecylamine, n-propylamine, n-hexylamine and ethanolamine.
7. A method of making a solvent-resistant, dilution-type polyurethane ink vehicle according to any one of claims 1-6, comprising the steps of:
(1) uniformly mixing a selected amount of the cross-linking polyol, diisocyanate and part of ethyl acetate, and reacting at 80-100 ℃ to obtain a prepolymer;
(2) uniformly mixing a selected amount of the diamine chain extender, the polyurethane cross-linking agent, part of the terminating agent, and part of the ethyl acetate and the isopropanol to obtain a mixed solution;
(3) by N2Transferring the obtained prepolymer into the mixed solution obtained in the step (2), adding the rest amount of the terminator, and thenContinuing the reaction;
(4) and after the reaction is finished, continuing carrying out heat preservation reaction at 55-65 ℃, and adding the rest ethyl acetate and isopropanol and uniformly mixing to obtain the product.
8. The method for preparing the solvent-resistant dilution-type polyurethane ink vehicle as defined in claim 7, wherein the step (2) further comprises the step of maintaining the temperature of the obtained mixture at 40 to 55 ℃.
9. Use of the solvent-resistant diluted polyurethane ink vehicle of any one of claims 1-6 for the preparation of gravure inks for flexible packaging of foodstuffs.
10. Gravure ink for flexible packaging of foods prepared from the solvent-resistant diluted polyurethane ink vehicle of any one of claims 1 to 6.
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