CN105860656B - 一种环保水性油墨 - Google Patents
一种环保水性油墨 Download PDFInfo
- Publication number
- CN105860656B CN105860656B CN201610439099.4A CN201610439099A CN105860656B CN 105860656 B CN105860656 B CN 105860656B CN 201610439099 A CN201610439099 A CN 201610439099A CN 105860656 B CN105860656 B CN 105860656B
- Authority
- CN
- China
- Prior art keywords
- weight
- parts
- environmental
- water
- based ink
- 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.)
- Expired - Fee Related
Links
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims abstract description 40
- 239000004814 polyurethane Substances 0.000 claims abstract description 20
- 229920002635 polyurethane Polymers 0.000 claims abstract description 19
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 claims abstract description 14
- 239000000341 volatile oil Substances 0.000 claims abstract description 13
- 239000003921 oil Substances 0.000 claims abstract description 12
- 235000011203 Origanum Nutrition 0.000 claims abstract description 11
- 241001529744 Origanum Species 0.000 claims abstract description 11
- PCHRRCUWXAIEMW-UHFFFAOYSA-N decanedioic acid 2,2-dimethylpropane-1,3-diol hexane-1,6-diol Chemical compound C(CCCCCCCCC(=O)O)(=O)O.OCC(C)(CO)C.C(CCCCCO)O PCHRRCUWXAIEMW-UHFFFAOYSA-N 0.000 claims abstract description 11
- 241000723347 Cinnamomum Species 0.000 claims abstract description 10
- 235000017803 cinnamon Nutrition 0.000 claims abstract description 10
- 239000001289 litsea cubeba fruit oil Substances 0.000 claims abstract description 10
- 239000002994 raw material Substances 0.000 claims abstract description 8
- 229940051250 hexylene glycol Drugs 0.000 claims abstract description 7
- KSBAEPSJVUENNK-UHFFFAOYSA-L tin(ii) 2-ethylhexanoate Chemical compound [Sn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O KSBAEPSJVUENNK-UHFFFAOYSA-L 0.000 claims abstract description 5
- 238000006555 catalytic reaction Methods 0.000 claims abstract description 4
- PTBDIHRZYDMNKB-UHFFFAOYSA-N 2,2-Bis(hydroxymethyl)propionic acid Chemical compound OCC(C)(CO)C(O)=O PTBDIHRZYDMNKB-UHFFFAOYSA-N 0.000 claims abstract description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 24
- 238000006243 chemical reaction Methods 0.000 claims description 24
- -1 polypropylene Polymers 0.000 claims description 24
- JQVDAXLFBXTEQA-UHFFFAOYSA-N dibutylamine Chemical compound CCCCNCCCC JQVDAXLFBXTEQA-UHFFFAOYSA-N 0.000 claims description 12
- 239000004743 Polypropylene Substances 0.000 claims description 10
- 239000003795 chemical substances by application Substances 0.000 claims description 10
- 229920001155 polypropylene Polymers 0.000 claims description 10
- 239000006210 lotion Substances 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 9
- 239000000049 pigment Substances 0.000 claims description 9
- 229940051841 polyoxyethylene ether Drugs 0.000 claims description 9
- 229920000056 polyoxyethylene ether Polymers 0.000 claims description 9
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 7
- 229910052708 sodium Inorganic materials 0.000 claims description 7
- 239000011734 sodium Substances 0.000 claims description 7
- DUIOKRXOKLLURE-UHFFFAOYSA-N 2-octylphenol Chemical compound CCCCCCCCC1=CC=CC=C1O DUIOKRXOKLLURE-UHFFFAOYSA-N 0.000 claims description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 6
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 claims description 6
- 239000002518 antifoaming agent Substances 0.000 claims description 6
- 239000004952 Polyamide Substances 0.000 claims description 5
- 239000002216 antistatic agent Substances 0.000 claims description 5
- 239000004359 castor oil Substances 0.000 claims description 5
- 235000019438 castor oil Nutrition 0.000 claims description 5
- 239000002270 dispersing agent Substances 0.000 claims description 5
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 claims description 5
- 229920002647 polyamide Polymers 0.000 claims description 5
- 229920002125 Sokalan® Polymers 0.000 claims description 4
- 125000000118 dimethyl group Polymers [H]C([H])([H])* 0.000 claims description 4
- 239000006185 dispersion Substances 0.000 claims description 4
- 239000007789 gas Substances 0.000 claims description 4
- 229920002401 polyacrylamide Polymers 0.000 claims description 4
- 239000004584 polyacrylic acid Substances 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 4
- 229920005573 silicon-containing polymer Polymers 0.000 claims description 4
- 229910052786 argon Inorganic materials 0.000 claims description 3
- XUSLDCYELHANDT-UHFFFAOYSA-N bismuth;dodecanoic acid Chemical compound [Bi].CCCCCCCCCCCC(O)=O XUSLDCYELHANDT-UHFFFAOYSA-N 0.000 claims description 3
- 230000006837 decompression Effects 0.000 claims description 3
- 239000012153 distilled water Substances 0.000 claims description 3
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 claims description 3
- 229920000642 polymer Polymers 0.000 claims description 3
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical class [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 claims description 3
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 claims description 3
- 238000003756 stirring Methods 0.000 claims description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 2
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 claims 2
- BVPWNLKBGNMZRI-UHFFFAOYSA-N decanedioic acid;2,2-dimethylpropane-1,3-diol Chemical compound OCC(C)(C)CO.OC(=O)CCCCCCCCC(O)=O BVPWNLKBGNMZRI-UHFFFAOYSA-N 0.000 claims 2
- OBETXYAYXDNJHR-SSDOTTSWSA-M (2r)-2-ethylhexanoate Chemical compound CCCC[C@@H](CC)C([O-])=O OBETXYAYXDNJHR-SSDOTTSWSA-M 0.000 claims 1
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 claims 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 1
- 239000005864 Sulphur Substances 0.000 claims 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims 1
- 150000001336 alkenes Chemical class 0.000 claims 1
- OBETXYAYXDNJHR-UHFFFAOYSA-N alpha-ethylcaproic acid Natural products CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 claims 1
- MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical group CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 229920000609 methyl cellulose Polymers 0.000 claims 1
- 239000001923 methylcellulose Substances 0.000 claims 1
- 239000000376 reactant Substances 0.000 claims 1
- 238000010792 warming Methods 0.000 claims 1
- 239000000976 ink Substances 0.000 abstract description 28
- 239000011230 binding agent Substances 0.000 abstract description 9
- 230000000694 effects Effects 0.000 abstract description 5
- NMJFNVPVICIXBO-UHFFFAOYSA-N OC(O)(O)C(C)(C)C(O)(O)O Chemical compound OC(O)(O)C(C)(C)C(O)(O)O NMJFNVPVICIXBO-UHFFFAOYSA-N 0.000 abstract description 4
- 230000002421 anti-septic effect Effects 0.000 abstract description 3
- 230000007613 environmental effect Effects 0.000 abstract description 3
- 238000003860 storage Methods 0.000 abstract description 3
- 239000000853 adhesive Substances 0.000 abstract description 2
- 230000001070 adhesive effect Effects 0.000 abstract description 2
- 239000000758 substrate Substances 0.000 abstract description 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 244000005700 microbiome Species 0.000 description 4
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 3
- RCEAADKTGXTDOA-UHFFFAOYSA-N OS(O)(=O)=O.CCCCCCCCCCCC[Na] Chemical group OS(O)(=O)=O.CCCCCCCCCCCC[Na] RCEAADKTGXTDOA-UHFFFAOYSA-N 0.000 description 3
- 229920003063 hydroxymethyl cellulose Polymers 0.000 description 3
- 229940031574 hydroxymethyl cellulose Drugs 0.000 description 3
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical group CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 3
- 239000012855 volatile organic compound Substances 0.000 description 3
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000001299 aldehydes Chemical class 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- CZZYITDELCSZES-UHFFFAOYSA-N diphenylmethane Chemical compound C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 2
- 238000001802 infusion Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- JVYDLYGCSIHCMR-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)butanoic acid Chemical compound CCC(CO)(CO)C(O)=O JVYDLYGCSIHCMR-UHFFFAOYSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 235000019082 Osmanthus Nutrition 0.000 description 1
- 241000333181 Osmanthus Species 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 208000007502 anemia Diseases 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 238000009395 breeding Methods 0.000 description 1
- 230000001488 breeding effect Effects 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 239000003344 environmental pollutant Substances 0.000 description 1
- 230000003628 erosive effect Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 208000032839 leukemia Diseases 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 230000007096 poisonous effect Effects 0.000 description 1
- 231100000719 pollutant Toxicity 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
Classifications
-
- 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
-
- 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
- C08G18/08—Processes
- C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
- C08G18/12—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step using two or more compounds having active hydrogen in the first polymerisation step
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/34—Carboxylic acids; Esters thereof with monohydroxyl compounds
- C08G18/348—Hydroxycarboxylic acids
-
- 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
-
- 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
- C08G18/6659—Compounds of group C08G18/42 with compounds of group C08G18/34
-
- 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
- C09D11/03—Printing inks characterised by features other than the chemical nature of the binder
-
- 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
- C09D11/106—Printing inks based on artificial resins containing macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C09D11/107—Printing inks based on artificial resins containing macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds from unsaturated acids or derivatives thereof
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)
- General Chemical & Material Sciences (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
Abstract
本发明公开了一种环保水性油墨。本发明通过各组份的有效选择和配比组合的综合效果,提供了一个综合性能较佳的配方范围,使得各组分充分发挥作用,所用水性聚氨酯连接料以聚己二酸癸二酸新戊二醇‑1,6‑己二醇酯二醇和2,2‑二羟甲基丁酸为原料,在二苯基甲烷二异氰酸酯的催化下聚合,然后经由双(三羟甲基)丙烷在2‑乙基己酸亚锡的作用下发生交联,再经由己二醇进行扩链得到。得到的连接料的抗粘性及稳定性都得到了改善,且对基材具有优良的附着力;得到的水性油墨具有防静电、环保、保存时间长等特点,且具有很好的着色力和附着牢度,添加的牛至油、山苍子精油、肉桂精油具有广谱抗菌功效,有效解决了印刷制品由于霉变而影响贮存的问题。
Description
技术领域
本发明涉及一种油墨,更具体的说是涉及一种环保的水性油墨。
背景技术
PM2.5是大气中的一种污染物,形成PM2.5的物质中挥发性有机化合物占21%,而挥发性有机化合物中约18%是由溶剂型涂料、油墨排放产生的。溶剂型涂料、油墨要借助有机溶剂进行稀释处理,不仅需要消耗化石能源,有机溶剂还含有大量的苯、甲苯、二甲苯、甲醛等有毒有害物质,其挥发期有的长达十几年。有研究显示长期吸入这些挥发气体会导致再生障碍性贫血、白血病等严重疾病。
水性油墨以水为稀释剂,不含苯、甲苯、二甲苯,相对于传统溶剂型油墨能极大地减少挥发性有机化合物的排放。水性油墨主要是由连结料、色料、填料等材料分散混合均匀而成的胶体,油墨中连接料品质的好坏,直接决定了油墨的性能,因为油墨的干燥性、粘度、流动性等在很大程度上均由连接料所决定。连接料能使颜料牢固附着在承印物表面并使油墨具有一定的光泽、印刷转移性能及干燥性能等;提供了油墨必须的粘结及成膜性能,连接料就是油墨的“心脏”,所以选择合适的水性油墨连接料是保证油墨良好性能的关键之一。
尽管目前市场上已开发出多种类型的水性油墨,但往往功能单一,在分散性和稳定性上存在较多问题,另外,水性油墨在生产和储存过程中,有可能被生产原料带入的、生产设备污染的、因储存不当而被外界引入的微生物而污染,以及印刷品成品被外界引入的微生物而污染,由于水性油墨中所存在的水更适于微生物的生存和繁殖,使油墨很容易受到微生物的侵蚀而变质,严重影响包装制品的外观。
发明内容
针对现有技术存在的不足,本发明的目的在于提供一种环保水性油墨,无毒、防静电、保存时间长,且具有很好的着色力和附着牢度。
为实现上述目的,本发明提供了如下技术方案:一种环保水性油墨,包括以下组分:
水性聚氨酯 35~40重量份;
聚丙烯乳液 10~20重量份;
防沉剂 1~3重量份;
分散剂 0.5~1重量份;
流平剂 0.2~1重量份;
消泡剂 0.2~0.8重量份;
抗静电剂 0.5~1.5重量份;
颜料 10~20重量份;
水 10~20重量份;
乙酸乙酯 5~15重量份;
牛至油 0.3~0.4重量份;
山苍子精油 0.2~0.3重量份;
肉桂精油 0.1~0.2重量份;
所述水性聚氨酯以聚己二酸癸二酸新戊二醇-1,6-己二醇酯二醇和2,2-二羟甲基丁酸为原料,在二苯基甲烷二异氰酸酯的催化下聚合,然后经由双(三羟甲基)丙烷在2-乙基己酸亚锡的作用下发生交联,再经由己二醇进行扩链得到。所述牛至油、山苍子精油、肉桂精油中含有醛和酮类化合物,具有广谱抗菌功效,通过三者合适的配比,能有效防止油墨发生霉变。
作为本发明的进一步改进,所述水性聚氨酯由以下具体方法制备:
(1)原料预处理:先将聚己二酸癸二酸新戊二醇-1,6-己二醇酯二醇于100℃,0.1MPa真空度下减压除水1h,所述的聚己二酸癸二酸新戊二醇-1,6-己二醇酯二醇的数均分子量为2000,将二苯基甲烷二异氰酸酯用活化分子筛脱水干燥;
(2)预聚体的制备:将35重量份的聚己二酸癸二酸新戊二醇-1,6-己二醇酯二醇加入烧瓶中,所述烧瓶上装有搅拌器、冷凝管、温度计和通气管,通入干燥的氩气到反应体系,然后开动搅拌器,加入30重量份的2,2-二羟甲基丁酸,再加入3重量份的二苯基甲烷二异氰酸酯和0.01重量份的月桂酸铋,缓慢升温至80℃,恒温反应2h;
(3)交联:将15重量份的双(三羟甲基)丙烷和0.01重量份的2-乙基己酸亚锡加入到反应体系中,继续于80℃反应3h,通过二正丁胺法检测-NCO含量,待-NCO达到理论值之后降温至40℃;
(4)扩链:往反应体系中加入3重量份的丙酮和5重量份的己二醇,继续反应1.5h,通过二正丁胺法检测-NCO含量,至-NCO达到理论值;
(5)中和与乳化:将反应体系放入40℃的恒温水浴中,稳定10min,加入0.5重量份的三乙胺中和搅拌20min,继续降温至30℃,高速搅拌下加入蒸馏水进行分散30min,滴入消泡剂反应5min,反应结束,得到水性聚氨酯。
作为本发明的进一步改进,所述分散剂为十二烷基硫酸钠、聚丙烯酰胺或聚丙烯酸钠中的一种或几种。
作为本发明的进一步改进,所述流平剂为聚丙烯酸、羟甲基纤维素、或聚醚改性的聚二甲基硅氧烷中的一种或几种。
作为本发明的进一步改进,所述消泡剂为壬基酚聚氧乙烯醚或辛基酚聚氧乙烯醚中的一种或几种。
作为本发明的进一步改进,所述抗静电剂为烷基磺酸钠或聚氧乙烯中的一种或几种。
作为本发明的进一步改进,所述防沉剂为聚酰胺蜡、硫酸化蓖麻油或聚氧乙烯氢化蓖麻油中的一种或几种。
本发明水性聚氨酯连接料以聚己二酸癸二酸新戊二醇-1,6-己二醇酯二醇和2,2-二羟甲基丁酸为原料,在二苯基甲烷二异氰酸酯的催化下聚合,然后经由双(三羟甲基)丙烷在2-乙基己酸亚锡的作用下发生交联,再经由己二醇进行扩链得到。得到的水性聚氨酯连接料的抗粘性及稳定性都得到了改善,且对基材具有优良的附着力;本发明通过水性聚氨酯、聚丙烯乳液、防沉剂、分散剂、流平剂、消泡剂、抗静电剂的有效选择和配比组合的综合效果,提供了一个综合性能较佳的配方范围,使得各组分充分发挥作用,得到的水性油墨具有防静电、环保、保存时间长等特点,且具有很好的着色力和附着牢度,添加的牛至油、山苍子精油、肉桂精油具有广谱抗菌功效的植物精油,有效解决了印刷制品由于霉变而影响贮存时间的问题。
具体实施方式
下面将给出以下实施例对本发明做进一步的详述。
水性聚氨酯连接料的制备:
(1)原料预处理:先将聚己二酸癸二酸新戊二醇-1,6-己二醇酯二醇于100℃,0.1MPa真空度下减压除水1h,所述的聚己二酸癸二酸新戊二醇-1,6-己二醇酯二醇的数均分子量为2000,将二苯基甲烷二异氰酸酯用活化分子筛脱水干燥;
(2)预聚体的制备:将35重量份的聚己二酸癸二酸新戊二醇-1,6-己二醇酯二醇加入烧瓶中,所述烧瓶上装有搅拌器、冷凝管、温度计和通气管,通入干燥的氩气到反应体系,然后开动搅拌器,加入30重量份的2,2-二羟甲基丁酸,再加入3重量份的二苯基甲烷二异氰酸酯和0.01重量份的月桂酸铋,缓慢升温至80℃,恒温反应2h;
(3)交联:将15重量份的双(三羟甲基)丙烷和0.01重量份的2-乙基己酸亚锡加入到反应体系中,继续于80℃反应3h,通过二正丁胺法检测-NCO含量,待-NCO达到理论值之后降温至40℃;
(4)扩链:往反应体系中加入3重量份的丙酮和5重量份的己二醇,继续反应1.5h,通过二正丁胺法检测-NCO含量,至-NCO达到理论值;
(5)中和与乳化:将反应体系放入40℃的恒温水浴中,稳定10min,加入0.5重量份的三乙胺中和搅拌20min,继续降温至30℃,高速搅拌下加入蒸馏水进行分散30min,滴入消泡剂反应5min,反应结束,得到水性聚氨酯。
实施例1
水性聚氨酯 35重量份;
聚丙烯乳液 10重量份;
聚酰胺蜡 1重量份;
聚丙烯酸钠 0.5重量份;
羟甲基纤维素 0.2重量份;
辛基酚聚氧乙烯醚 0.2重量份;
烷基磺酸钠 0.5重量份;
颜料 10重量份;
水 10重量份;
乙酸乙酯 5重量份;
牛至油 0.3重量份;
山苍子精油 0.2重量份;
肉桂精油 0.1重量份。
实施例2
水性聚氨酯 40重量份;
聚丙烯乳液 20重量份;
聚酰胺蜡 3重量份;
聚丙烯酸钠 1重量份;
羟甲基纤维素 1重量份;
辛基酚聚氧乙烯醚 0.8重量份;
烷基磺酸钠 1.5重量份;
颜料 20重量份;
水 20重量份;
乙酸乙酯 15重量份;
牛至油 0.4重量份;
山苍子精油 0.3重量份;
肉桂精油 0.2重量份。
实施例3
水性聚氨酯 38重量份;
聚丙烯乳液 15重量份;
硫酸化蓖麻油 2重量份;
十二烷基硫酸钠 0.8重量份;
聚丙烯酸 0.5重量份;
辛基酚聚氧乙烯醚 0.6重量份;
烷基磺酸钠:1重量份;
颜料 15重量份;
水 15重量份;
乙酸乙酯 10重量份;
牛至油 0.3重量份;
山苍子精油 0.3重量份;
肉桂精油 0.2重量份。
实施例4
水性聚氨酯 36重量份;
聚丙烯乳液 12重量份;
硫酸化蓖麻油2重量份;
十二烷基硫酸钠 0.8重量份;
聚丙烯酸 0.6重量份;
辛基酚聚氧乙烯醚 0.5重量份;
聚氧乙烯:1.2重量份;
颜料 12重量份;
水 12重量份;
乙酸乙酯 10重量份;
牛至油 0.4重量份;
山苍子精油 0.3重量份;
肉桂精油 0.2重量份。
实施例5
水性聚氨酯 39重量份;
聚丙烯乳液 18重量份;
聚氧乙烯氢化蓖麻油 2重量份;
聚丙烯酰胺 0.6重量份;
聚醚改性的聚二甲基硅氧烷 0.5重量份;
壬基酚聚氧乙烯醚 0.3重量份;
聚氧乙烯:1.3重量份;
颜料 15重量份;
水 10重量份;
乙酸乙酯 12重量份;
牛至油 0.3重量份;
山苍子精油 0.2重量份;
肉桂精油 0.2重量份。
实施例6
水性聚氨酯 37重量份;
聚丙烯乳液 18重量份;
聚酰胺蜡 3重量份;
聚丙烯酰胺 0.7重量份;
聚醚改性的聚二甲基硅氧烷 0.6重量份;
壬基酚聚氧乙烯醚 0.4重量份;
聚氧乙烯:0.9重量份;
颜料 13重量份;
水 11重量份;
乙酸乙酯 8重量份;
牛至油 0.4重量份;
山苍子精油 0.3重量份;
肉桂精油 0.1重量份。
根据QB/T2024-94质量标准对以上实施例进行油墨性能测试,结果如下表所示:
由此可知,本发明提供的环保水性油墨在着色力、附着牢度和溶剂残留量方面具有突出的性能,各个实施例均具有较高的着色力,各个实施例的附着牢度均达到最高标准,各个实施例的溶剂残留量均达到较高标准。
以上所述仅是本发明的优选实施方式,本发明的保护范围并不仅局限于上述实施例,凡属于本发明思路下的技术方案均属于本发明的保护范围。应当指出,对于本技术领域的普通技术人员来说,在不脱离本发明原理前提下的若干改进和润饰,这些改进和润饰也应视为本发明的保护范围。
Claims (6)
1.一种环保水性油墨,其特征在于:包括以下组分:
水性聚氨酯35~40重量份;
聚丙烯乳液10~20重量份;
防沉剂1~3重量份;
分散剂0.5~1重量份;
流平剂0.2~1重量份;
消泡剂0.2~0.8重量份;
抗静电剂0.5~1.5重量份;
颜料10~20重量份;
水10~20重量份;
乙酸乙酯5~15重量份;
牛至油0.3~0.4重量份;
山苍子精油0.2~0.3重量份;
肉桂精油0.1~0.2重量份;
所述水性聚氨酯以聚己二酸癸二酸新戊二醇-1,6-己二醇酯二醇和2,2-二羟甲基丁酸为原料,在二苯基甲烷二异氰酸酯的催化下聚合,然后经由三羟甲基丙烷在2-乙基己酸亚锡的作用下发生交联,再经由己二醇进行扩链得到;
所述水性聚氨酯由以下具体方法制备:
(1)原料预处理:先将聚己二酸癸二酸新戊二醇-1,6-己二醇酯二醇于100℃,0.1MPa真空度下减压除水1h,所述的聚己二酸癸二酸新戊二醇-1,6-己二醇酯二醇的数均分子量为2000,将二苯基甲烷二异氰酸酯用活化分子筛脱水干燥;
(2)预聚体的制备:将35重量份的聚己二酸癸二酸新戊二醇-1,6-己二醇酯二醇加入烧瓶中,所述烧瓶上装有搅拌器、冷凝管、温度计和通气管,通入干燥的氩气到反应体系,然后开动搅拌器,加入30重量份的2,2-二羟甲基丁酸,再加入3重量份的二苯基甲烷二异氰酸酯和0.01重量份的月桂酸铋,升温至80℃,恒温反应2h;
(3)交联:将15重量份的三羟甲基丙烷和0.01重量份的2-乙基己酸亚锡加入到反应体系中,继续于80℃反应3h,通过二正丁胺法检测-NCO含量,待-NCO达到理论值之后降温至40℃;
(4)扩链:往反应体系中加入3重量份的丙酮和5重量份的己二醇,继续反应1.5h,通过二正丁胺法检测-NCO含量,至-NCO达到理论值;
(5)中和与乳化:将反应体系放入40℃的恒温水浴中,稳定10min,加入0.5重量份的三乙胺中和搅拌20min,继续降温至30℃,搅拌下加入蒸馏水进行分散30min,滴入消泡剂反应5min,反应结束,得到水性聚氨酯。
2.根据权利要求1所述的一种环保水性油墨,其特征在于:所述分散剂为十二烷基硫酸钠、聚丙烯酰胺或聚丙烯酸钠中的一种或几种。
3.根据权利要求2所述的一种环保水性油墨,其特征在于:所述流平剂为聚丙烯酸、羟甲基纤维素或聚醚改性的聚二甲基硅氧烷中的一种或几种。
4.根据权利要求3所述的一种环保水性油墨,其特征在于:所述消泡剂为壬基酚聚氧乙烯醚或辛基酚聚氧乙烯醚中的一种或几种。
5.根据权利要求4所述的一种环保水性油墨,其特征在于:所述抗静电剂为烷基磺酸钠或聚氧乙烯中的一种或几种。
6.根据权利要求5所述的一种环保水性油墨,其特征在于:所述防沉剂为聚酰胺蜡、硫酸化蓖麻油或聚氧乙烯氢化蓖麻油中的一种或几种。
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201610439099.4A CN105860656B (zh) | 2016-06-17 | 2016-06-17 | 一种环保水性油墨 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201610439099.4A CN105860656B (zh) | 2016-06-17 | 2016-06-17 | 一种环保水性油墨 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN105860656A CN105860656A (zh) | 2016-08-17 |
CN105860656B true CN105860656B (zh) | 2019-07-16 |
Family
ID=56650975
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201610439099.4A Expired - Fee Related CN105860656B (zh) | 2016-06-17 | 2016-06-17 | 一种环保水性油墨 |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN105860656B (zh) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107584916A (zh) * | 2017-10-08 | 2018-01-16 | 安徽省嘉瑞医药科技有限公司 | 医药包装袋绿色印刷工艺 |
CN107556813A (zh) * | 2017-10-08 | 2018-01-09 | 安徽省嘉瑞医药科技有限公司 | 专用于医药包装袋的绿色油墨印刷基材 |
CN109810569A (zh) * | 2018-12-27 | 2019-05-28 | 老鹰自动化设备有限公司 | 一种高解析喷码机墨水 |
CN113861366A (zh) * | 2021-10-15 | 2021-12-31 | 烟台德邦科技股份有限公司 | 一种耐霉变性水性聚氨酯树脂及其制备方法 |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0128221D0 (en) * | 2001-11-24 | 2002-01-16 | Avecia Ltd | Aqueous urethane dispersants |
JP2006022133A (ja) * | 2004-07-06 | 2006-01-26 | Nippon Polyurethane Ind Co Ltd | 水性ポリウレタンエマルジョン、並びにその製造方法及びその用途 |
CN1702124A (zh) * | 2005-06-06 | 2005-11-30 | 贺文海 | 一种水性铝箔油墨 |
JP2008101162A (ja) * | 2006-10-20 | 2008-05-01 | Mitsui Chemicals Polyurethanes Inc | 水性ポリウレタン樹脂、顔料分散液および水性インク |
US20090169748A1 (en) * | 2007-12-27 | 2009-07-02 | House Gary L | Inks for high speed durable inkjet printing |
CN104745001A (zh) * | 2015-03-30 | 2015-07-01 | 桐城市新丰彩印包装有限公司 | 一种环保型薄膜印刷油墨 |
-
2016
- 2016-06-17 CN CN201610439099.4A patent/CN105860656B/zh not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
CN105860656A (zh) | 2016-08-17 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN105860656B (zh) | 一种环保水性油墨 | |
CN105860012B (zh) | 一种环保水性油墨连接料 | |
CN101134864A (zh) | 一种烟标高速凹印水基油墨 | |
CN105038555B (zh) | 一种不用离型层的水性镭射电化铝涂料及其制备方法 | |
CN105524537A (zh) | 一种环保高耐磨型水性光油及其制造方法 | |
CN111499862B (zh) | 一种可降解聚氨酯及其制备方法 | |
CN108102458A (zh) | 一种柔性版水性油墨的制备方法 | |
CN109337568A (zh) | 一种金属基材长效防腐面漆及其制备方法 | |
CN109777198A (zh) | 环保可溶性油墨及其制备工艺 | |
CN109306226A (zh) | 一种金属基材长效防腐底漆及其制备方法 | |
CN106084988B (zh) | 一种多功能水性油墨 | |
CN109354933A (zh) | 一种竹木家具用耐磨涂料及其制备方法 | |
CN102363704B (zh) | 一种水性封闭剂及其制备方法 | |
CN102085678A (zh) | 木材保护涂料及其制备方法和应用 | |
CN110724447A (zh) | 一种水性数码印刷底胶及其制备方法 | |
CN114045074A (zh) | 水性铅笔抽涂哑光清漆及其制备方法 | |
CN105949875B (zh) | 一种水性油墨 | |
CN108913012A (zh) | 紫外光固化高耐污亚光地板涂料及其制备方法 | |
CN102585594A (zh) | 环保去粘剂 | |
CN109913032A (zh) | 一种环保型高稳定性抗粘水性油墨的制备方法 | |
CN107286744A (zh) | 一种快干热固油墨 | |
CN102220048A (zh) | 一种转移印花用环保型水性油墨配方及其制备方法 | |
CN109735173A (zh) | 阻湿型水性复合镭射镀铝涂料组合物及其制备方法 | |
CN105802331A (zh) | 一种新型胶印高光快干不结皮油墨 | |
CN101837692B (zh) | 超纤革或真皮或软木的湿法转印新方法及其湿法转印膜 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
TA01 | Transfer of patent application right |
Effective date of registration: 20190620 Address after: 341000 Xingcun Road, Xinfeng County Industrial Park, Ganzhou City, Jiangxi Province Applicant after: Xinfeng Hongmei Ink Technology Co.,Ltd. Address before: 325802 Dongcheng Road, Longgang, Wenzhou, Zhejiang Province, No. 351 Applicant before: CANGNAN BAOFENG PRINTING CO.,LTD. |
|
TA01 | Transfer of patent application right | ||
GR01 | Patent grant | ||
GR01 | Patent grant | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20190716 |