CN107287982A - A kind of preparation method of thermal transfer paint for papers - Google Patents
A kind of preparation method of thermal transfer paint for papers Download PDFInfo
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- CN107287982A CN107287982A CN201710520008.4A CN201710520008A CN107287982A CN 107287982 A CN107287982 A CN 107287982A CN 201710520008 A CN201710520008 A CN 201710520008A CN 107287982 A CN107287982 A CN 107287982A
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- Prior art keywords
- guar gum
- parts
- preparation
- papers
- thermal transfer
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- 238000012546 transfer Methods 0.000 title claims abstract description 24
- 239000003973 paint Substances 0.000 title claims abstract description 17
- 238000002360 preparation method Methods 0.000 title claims abstract description 11
- 229920002907 Guar gum Polymers 0.000 claims abstract description 36
- 239000000665 guar gum Substances 0.000 claims abstract description 36
- 229960002154 guar gum Drugs 0.000 claims abstract description 36
- 235000010417 guar gum Nutrition 0.000 claims abstract description 36
- 239000000243 solution Substances 0.000 claims abstract description 25
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 claims abstract description 20
- 239000000463 material Substances 0.000 claims abstract description 19
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims abstract description 18
- 238000004821 distillation Methods 0.000 claims abstract description 18
- 238000007639 printing Methods 0.000 claims abstract description 17
- 238000006243 chemical reaction Methods 0.000 claims abstract description 14
- 238000005406 washing Methods 0.000 claims abstract description 13
- 235000019270 ammonium chloride Nutrition 0.000 claims abstract description 11
- 238000003756 stirring Methods 0.000 claims abstract description 11
- 239000004115 Sodium Silicate Substances 0.000 claims abstract description 10
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims abstract description 10
- 235000019795 sodium metasilicate Nutrition 0.000 claims abstract description 10
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 claims abstract description 10
- 229910052911 sodium silicate Inorganic materials 0.000 claims abstract description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 10
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 claims abstract description 9
- 229910000013 Ammonium bicarbonate Inorganic materials 0.000 claims abstract description 9
- 235000012538 ammonium bicarbonate Nutrition 0.000 claims abstract description 9
- 239000001099 ammonium carbonate Substances 0.000 claims abstract description 9
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 claims abstract description 8
- 239000004359 castor oil Substances 0.000 claims abstract description 8
- 235000019438 castor oil Nutrition 0.000 claims abstract description 8
- 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 abstract description 8
- 229940051841 polyoxyethylene ether Drugs 0.000 claims abstract description 8
- 229920000056 polyoxyethylene ether Polymers 0.000 claims abstract description 8
- FDRCDNZGSXJAFP-UHFFFAOYSA-M sodium chloroacetate Chemical compound [Na+].[O-]C(=O)CCl FDRCDNZGSXJAFP-UHFFFAOYSA-M 0.000 claims abstract description 8
- 239000007864 aqueous solution Substances 0.000 claims abstract description 4
- -1 heating Chemical compound 0.000 claims abstract description 4
- 238000010438 heat treatment Methods 0.000 claims abstract description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 24
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 18
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 12
- 229910052757 nitrogen Inorganic materials 0.000 claims description 12
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 6
- 239000000376 reactant Substances 0.000 claims description 6
- 238000010792 warming Methods 0.000 claims description 6
- 229910001870 ammonium persulfate Inorganic materials 0.000 claims description 5
- YXYZMHGSOKYZAF-UHFFFAOYSA-M [Cl-].C(C(=C)C)(=O)OCC[N+](C(C)(C)C)(C)C Chemical class [Cl-].C(C(=C)C)(=O)OCC[N+](C(C)(C)C)(C)C YXYZMHGSOKYZAF-UHFFFAOYSA-M 0.000 claims description 3
- 238000007599 discharging Methods 0.000 claims description 3
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 claims description 2
- 240000000528 Ricinus communis Species 0.000 claims 1
- 235000004443 Ricinus communis Nutrition 0.000 claims 1
- LUZSPGQEISANPO-UHFFFAOYSA-N butyltin Chemical compound CCCC[Sn] LUZSPGQEISANPO-UHFFFAOYSA-N 0.000 claims 1
- 229960001777 castor oil Drugs 0.000 claims 1
- PYBNTRWJKQJDRE-UHFFFAOYSA-L dodecanoate;tin(2+) Chemical compound [Sn+2].CCCCCCCCCCCC([O-])=O.CCCCCCCCCCCC([O-])=O PYBNTRWJKQJDRE-UHFFFAOYSA-L 0.000 claims 1
- 239000011248 coating agent Substances 0.000 abstract description 16
- 238000000576 coating method Methods 0.000 abstract description 16
- 238000001035 drying Methods 0.000 abstract description 6
- 230000000740 bleeding effect Effects 0.000 abstract description 4
- 230000015572 biosynthetic process Effects 0.000 abstract description 2
- 239000003921 oil Substances 0.000 abstract description 2
- 230000035515 penetration Effects 0.000 abstract description 2
- 239000002861 polymer material Substances 0.000 abstract description 2
- YZCKVEUIGOORGS-OUBTZVSYSA-N Deuterium Chemical compound [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 abstract 1
- 238000002156 mixing Methods 0.000 abstract 1
- 230000000630 rising effect Effects 0.000 abstract 1
- 238000000859 sublimation Methods 0.000 description 7
- 230000008022 sublimation Effects 0.000 description 7
- 239000000975 dye Substances 0.000 description 4
- 150000003926 acrylamides Chemical class 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 229910052573 porcelain Inorganic materials 0.000 description 3
- ULWHHBHJGPPBCO-UHFFFAOYSA-N propane-1,1-diol Chemical class CCC(O)O ULWHHBHJGPPBCO-UHFFFAOYSA-N 0.000 description 3
- 238000002310 reflectometry Methods 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 238000010023 transfer printing Methods 0.000 description 3
- MPNXSZJPSVBLHP-UHFFFAOYSA-N 2-chloro-n-phenylpyridine-3-carboxamide Chemical compound ClC1=NC=CC=C1C(=O)NC1=CC=CC=C1 MPNXSZJPSVBLHP-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 230000008595 infiltration Effects 0.000 description 2
- 238000001764 infiltration Methods 0.000 description 2
- 125000005641 methacryl group Chemical group 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 238000001179 sorption measurement Methods 0.000 description 2
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 244000007835 Cyamopsis tetragonoloba Species 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 238000005660 chlorination reaction Methods 0.000 description 1
- AYOHIQLKSOJJQH-UHFFFAOYSA-N dibutyltin Chemical compound CCCC[Sn]CCCC AYOHIQLKSOJJQH-UHFFFAOYSA-N 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- IJKVHSBPTUYDLN-UHFFFAOYSA-N dihydroxy(oxo)silane Chemical compound O[Si](O)=O IJKVHSBPTUYDLN-UHFFFAOYSA-N 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229920001206 natural gum Polymers 0.000 description 1
- 238000011002 quantification Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H19/00—Coated paper; Coating material
- D21H19/36—Coatings with pigments
- D21H19/44—Coatings with pigments characterised by the other ingredients, e.g. the binder or dispersing agent
- D21H19/56—Macromolecular organic compounds or oligomers thereof obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D21H19/58—Polymers or oligomers of diolefins, aromatic vinyl monomers or unsaturated acids or derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B37/00—Preparation of polysaccharides not provided for in groups C08B1/00 - C08B35/00; Derivatives thereof
- C08B37/006—Heteroglycans, i.e. polysaccharides having more than one sugar residue in the main chain in either alternating or less regular sequence; Gellans; Succinoglycans; Arabinogalactans; Tragacanth or gum tragacanth or traganth from Astragalus; Gum Karaya from Sterculia urens; Gum Ghatti from Anogeissus latifolia; Derivatives thereof
- C08B37/0087—Glucomannans or galactomannans; Tara or tara gum, i.e. D-mannose and D-galactose units, e.g. from Cesalpinia spinosa; Tamarind gum, i.e. D-galactose, D-glucose and D-xylose units, e.g. from Tamarindus indica; Gum Arabic, i.e. L-arabinose, L-rhamnose, D-galactose and D-glucuronic acid units, e.g. from Acacia Senegal or Acacia Seyal; Derivatives thereof
- C08B37/0096—Guar, guar gum, guar flour, guaran, i.e. (beta-1,4) linked D-mannose units in the main chain branched with D-galactose units in (alpha-1,6), e.g. from Cyamopsis Tetragonolobus; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/52—Amides or imides
- C08F220/54—Amides, e.g. N,N-dimethylacrylamide or N-isopropylacrylamide
- C08F220/56—Acrylamide; Methacrylamide
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H19/00—Coated paper; Coating material
- D21H19/36—Coatings with pigments
- D21H19/38—Coatings with pigments characterised by the pigments
- D21H19/40—Coatings with pigments characterised by the pigments siliceous, e.g. clays
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H19/00—Coated paper; Coating material
- D21H19/36—Coatings with pigments
- D21H19/44—Coatings with pigments characterised by the other ingredients, e.g. the binder or dispersing agent
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Polymers & Plastics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Materials Engineering (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Dispersion Chemistry (AREA)
- Paper (AREA)
Abstract
The present invention relates to a kind of preparation method of thermal transfer paint for papers, belong to technical field of polymer materials.Guar gum, castor oil polyoxyethylene ether, ammonium hydrogen carbonate and 2 aqueous solution of propylene glycol etc. are carried out hybrid reaction by the present invention, and add sodium metasilicate and be stirred after preheating, add dibutyl tin laurate, heating, and ammonium chloride solution is added dropwise, stand follow-up temperature of continuing rising, and add after monoxone, stirring reaction, discharge, collect out material, and distilled to going out material, distillation residue is collected, after the washing of distillation residue, drying, dried object is collected, dried object, water, n-hexane etc. are finally stirred mixing.The oil absorbency of the coating of thermal transfer paint for papers formation prepared by the present invention is good, and image is less prone to heap ink and color bleeding phenomenon when printing is finished, while required drying time is short, ink penetration is in the speed of coating.
Description
Technical field
The present invention relates to a kind of preparation method of thermal transfer paint for papers, belong to technical field of polymer materials.
Background technology
Thermal transfer is an emerging typography, incoming by foreign countries.Thermal transfer is also referred to as heat sublimation, is by portrait, wind
Any images such as scape are added using thermal transfer ink printed on heat-transferring printing paper, then by corresponding thermal transfer equipment in several minutes
Heat arrives certain temperature, is transferred in the materials such as porcelain cup, porcelain dish, porcelain plate, clothes, metal the image color on paper is true to nature
A kind of special process.Heat-transferring printing paper is the carrier of transferred image, and he is in bright gay color degree, the image fidelity after the transfer of image
It is most important.
Influence of the quality of thermal dye sublimation transfer printing paper to product printing quality plays direct effect.The ink of paper absorbs
Uniform type, the speed degree for absorbing ink determines the print quality of heat sublimation printing paper, and good print quality is to ensure production
The basis of product printing quality, excellent transfer performance, it is desirable to which thermal dye sublimation transfer printing paper has larger tightness, control dyestuff is heated to be risen
Will not be from the back side diffusion of page when magnificent.Meanwhile, thermal dye sublimation transfer printing paper will also have preferable page stability, otherwise be become by heat
Shape, causes the ghost image of image smudgy.However, the inferior quality of current heat-transferring printing paper body paper, is mainly shown as that body paper is needed
Carry out the coating of special coating, the absorbency of coating is bad, ink droplet infiltration rate is slow, and image has obvious heap ink when printing is finished
And color bleeding phenomenon.
In summary, a kind of coating of research invention, the coating ink absorption that it is formed is good, and ink absorption speed is existing soon
There is the most important thing that technical staff studies.
The content of the invention
The technical problems to be solved by the invention:Need to carry out the coating of special coating, the suction of coating for current body paper
Ink is bad, ink droplet infiltration rate slow, and there is provided a kind of heat for the problem of image has obvious heap ink and color bleeding phenomenon when printing is finished
Transfer the preparation method of paint for papers.
In order to solve the above technical problems, the present invention is using technical scheme as described below:
(1)Take guar gum, castor oil polyoxyethylene ether, ammonium hydrogen carbonate and aqueous solution of propylene glycol to be put into reactor, use nitrogen
Protection, reuses sodium hydroxide solution regulation pH to 8.5~9.0, adds sodium metasilicate, preheated at 35~40 DEG C;
(2)After preheating terminates, dibutyl tin laurate is added, 45~50 DEG C are warming up to, and ammonium chloride solution is added dropwise, it is quiet
Put, then heating, add monoxone, stirring reaction;
(3)After the completion of reaction, room temperature is cooled to, discharges, collects out material, and is distilled to going out material, distillation is collected surplus
Excess, is washed to distillation residue using ethanol solution, collects washings, washings is dried, collect dried object;
(4)Count by weight, take 50~60 parts of dried objects, 30~35 parts of water, 12~15 parts of n-hexanes, 10~15 parts of acryloyls
Amine, 7~10 parts of MethacryloyloxyethylTrimethyl Trimethyl Ammonium Chlorides and 1~2 part of ammonium persulfate, are put into reactor, use nitrogen
Protection, is reacted at 70~75 DEG C, and reactant mixture is collected in discharging, you can obtain thermal transfer paint for papers.
The step(1)Middle guar gum, castor oil polyoxyethylene ether, the mass ratio of ammonium hydrogen carbonate and propylene glycol solution are 4
~5:0.4~0.8:1:7~9.
The step(1)The addition of middle sodium metasilicate is the 20~25% of guar gum quality.
The step(2)The addition of middle dibutyl tin laurate is guar gum quality 0.6~0.9%, and ammonium chloride is molten
The dripping quantity of liquid is guar gum quality 30~35%, and chloroacetic addition is guar gum quality 30~35%.
The present invention is compared with other method, and advantageous effects are:
The present invention in the presence of catalyst dibutyltin dilaurylate, passes through chlorination using the guar gum of low viscosity as matrix
Ammonium and monoxone are modified to guar gum, are obtained the guar gum of anionic property, are made modified guar gum have high electric charge close
Degree, can rest on paper surface rather than penetrate into inside paper fibre, prevent ink from oozing using electrostatic repulsion
Enter in paper fibre, improve transferring rate, while in modifying process, using sodium metasilicate as raw material, forming Bio-sil, being modified
Guar gum is wrapped up, and improves space therein, and then adds the adsorption efficiency to ink, then with acrylamide, metering system
Acyloxyethyl trimethyl ammonium chloride is as raw material, and the space in silica gel and modified guar is polymerize, in increase space
Cations, further improve the adsorption capacity to ink, also increase the rate of drying of ink, are carried while adding n-hexane
Height volatilization efficiency, and the present invention is degradable from the guar gum in natural gum, it is environmentally safe.
Embodiment
The preparation method of thermal transfer paint for papers of the present invention, comprises the following steps:
(1)In mass ratio 4~5:0.4~0.8:1:7~9, take guar gum, castor oil polyoxyethylene ether, ammonium hydrogen carbonate and
2.0mol/L aqueous solution of propylene glycol is put into reactor, is protected using nitrogen, reuse sodium hydroxide solution regulation pH to 8.5~
After 9.0, the sodium metasilicate of guar gum quality 20~25% is added, with 30~40min of 200r/min stirring preheatings at 35~40 DEG C;
(2)After preheating terminates, the dibutyl tin laurate of guar gum quality 0.6~0.9% is added, 45~50 DEG C are warming up to,
And 1.8mol/L ammonium chloride solutions are added dropwise, 4~8h is stood, 60~70 DEG C, addition guar gum quality 30~35% are then raised temperature to
Monoxone, 7~9h of stirring reaction;
(3)After the completion of reaction, room temperature is cooled to, discharges, collects out material, and is distilled to going out material, vapo(u)rizing temperature is
100~105 DEG C, distillation residue is collected, the use of the mass fraction of 6~8 times of residue quality of distillation is 60% ethanol solution pair
Distillation residue is washed, and collects washings, and washings is dried at 80 DEG C, dried object is collected;
(4)Count by weight, take 50~60 parts of dried objects, 30~35 parts of water, 12~15 parts of n-hexanes, 10~15 parts of acryloyls
Amine, 7~10 parts of MethacryloyloxyethylTrimethyl Trimethyl Ammonium Chlorides and 1~2 part of ammonium persulfate, are put into reactor, use nitrogen
Protection, reacts 4~8h at 70~75 DEG C, and reactant mixture is collected in discharging, you can obtain thermal transfer paint for papers.
Example 1
(1)In mass ratio 5:0.8:1:9, take guar gum, castor oil polyoxyethylene ether, ammonium hydrogen carbonate and 2.0mol/L propane diols water
Solution is put into reactor, is protected using nitrogen, is reused after sodium hydroxide solution regulation pH to 9.0, is added guar gum quality
25% sodium metasilicate, with 200r/min stirring preheatings 40min at 40 DEG C;
(2)After preheating terminates, the dibutyl tin laurate of guar gum quality 0.9% is added, 50 DEG C are warming up to, and be added dropwise
1.8mol/L ammonium chloride solutions, stand 8h, then raise temperature to 70 DEG C, the monoxone of addition guar gum quality 35%, stirring reaction
9h;
(3)After the completion of reaction, room temperature is cooled to, discharges, collects out material, and is distilled to going out material, vapo(u)rizing temperature is
105 DEG C, distillation residue is collected, it is remaining to distillation for 60% ethanol solution using the mass fraction of 8 times of residue quality of distillation
Thing is washed, and collects washings, and washings is dried at 80 DEG C, dried object is collected;
(4)Count by weight, take 60 parts of dried objects, 35 parts of water, 15 parts of n-hexanes, 15 parts of acrylamides, 10 parts of metering systems
Acyloxyethyl trimethyl ammonium chloride and 2 parts of ammonium persulfates, are put into reactor, are protected using nitrogen, reacted 8h at 75 DEG C, go out
Material, collects reactant mixture, you can obtain thermal transfer paint for papers.
Example 2
(1)In mass ratio 5:0.8:1:9, take guar gum, castor oil polyoxyethylene ether, ammonium hydrogen carbonate and 2.0mol/L propane diols water
Solution is put into reactor, is protected using nitrogen, is reused after sodium hydroxide solution regulation pH to 9.0, is added guar gum quality
25% sodium metasilicate, with 200r/min stirring preheatings 40min at 40 DEG C;
(2)After preheating terminates, the dibutyl tin laurate of guar gum quality 0.9% is added, 50 DEG C are warming up to, and be added dropwise
1.8mol/L ammonium chloride solutions, stand 8h, then raise temperature to 70 DEG C, the monoxone of addition guar gum quality 35%, stirring reaction
9h;
(3)After the completion of reaction, room temperature is cooled to, discharges, collects out material, and is distilled to going out material, vapo(u)rizing temperature is
105 DEG C, distillation residue is collected, it is remaining to distillation for 60% ethanol solution using the mass fraction of 8 times of residue quality of distillation
Thing is washed, and collects washings, and washings is dried at 80 DEG C, dried object is collected;
(4)Count by weight, take 50 parts of dried objects, 30 parts of water, 12 parts of n-hexanes, 10 parts of acrylamides, 7 parts of methacryls
Oxy-ethyl-trimethyl salmiac and 1 part of ammonium persulfate, are put into reactor, are protected using nitrogen, reacted 4h at 70 DEG C, go out
Material, collects reactant mixture, you can obtain thermal transfer paint for papers.
Example 3
(1)In mass ratio 5:0.8:1:9, take guar gum, castor oil polyoxyethylene ether, ammonium hydrogen carbonate and 2.0mol/L propane diols water
Solution is put into reactor, is protected using nitrogen, is reused after sodium hydroxide solution regulation pH to 9.0, is added guar gum quality
25% sodium metasilicate, with 200r/min stirring preheatings 40min at 40 DEG C;
(2)After preheating terminates, the dibutyl tin laurate of guar gum quality 0.9% is added, 50 DEG C are warming up to, and be added dropwise
1.8mol/L ammonium chloride solutions, stand 8h, then raise temperature to 70 DEG C, the monoxone of addition guar gum quality 35%, stirring reaction
9h;
(3)After the completion of reaction, room temperature is cooled to, discharges, collects out material, and is distilled to going out material, vapo(u)rizing temperature is
105 DEG C, distillation residue is collected, it is remaining to distillation for 60% ethanol solution using the mass fraction of 8 times of residue quality of distillation
Thing is washed, and collects washings, and washings is dried at 80 DEG C, dried object is collected;
(4)Count by weight, take 55 parts of dried objects, 32 parts of water, 13 parts of n-hexanes, 13 parts of acrylamides, 8 parts of methacryls
Oxy-ethyl-trimethyl salmiac and 1 part of ammonium persulfate, are put into reactor, are protected using nitrogen, reacted 6h at 72 DEG C, go out
Material, collects reactant mixture, you can obtain thermal transfer paint for papers.
Reference examples:The thermal transfer paint for papers of Dongguan City new material Co., Ltd production.
Example and the thermal transfer paint for papers of reference examples are applied in thermal transfer, and it tested, concrete application
And test as follows:
Concrete application is as follows:Example and the coating of reference examples are coated on heat-transferring printing paper using airblade coating mode(Zhejiang Jinchang
The production of speciality paper limited company)On, control quantification of 95g/m2, after end to be coated, it is dried, applied
There is the heat-transferring printing paper of coating.
Specific test is as follows:
(1)The absorbability of ink is determined:Using the dirty test method(s) of ink, excessive heat sublimation ink is coated on above-mentioned scribble
The heat-transferring printing paper surface of material, and kept for the regular hour, then unnecessary ink wiping is fallen with soft cloth, dirty area is determined respectively
Domain and the paper reflectivity of white space, the absorbability of ink is represented with K&N values, and calculation formula is as follows:
R in formula∞For the reflectivity of sufficiently thick white space(%);RFMean the reflectivity in the dirty region of ink.
(2)Drying time determines:Designed pattern is printed to using piezoelectric type digital-code printer and heat sublimation ink
On the above-mentioned heat-transferring printing paper for scribbling coating, its drying time is determined.
Specific testing result such as table 1.
Table 1
As shown in Table 1, the oil absorbency of the coating for the thermal transfer paint for papers formation that prepared by the present invention is good, when printing is finished
Image is less prone to heap ink and color bleeding phenomenon, while required drying time is short, shows ink penetration in the speed of coating, and
Guar gum is degradable, environmentally safe.
Claims (4)
1. a kind of preparation method of thermal transfer paint for papers, it is characterised in that the preparation method comprises the following steps:
(1)Take guar gum, castor oil polyoxyethylene ether, ammonium hydrogen carbonate and aqueous solution of propylene glycol to be put into reactor, use nitrogen
Protection, reuses sodium hydroxide solution regulation pH to 8.5~9.0, adds sodium metasilicate, preheated at 35~40 DEG C;
(2)After preheating terminates, dibutyl tin laurate is added, 45~50 DEG C are warming up to, and ammonium chloride solution is added dropwise, it is quiet
Put, then heating, add monoxone, stirring reaction;
(3)After the completion of reaction, room temperature is cooled to, discharges, collects out material, and is distilled to going out material, distillation is collected surplus
Excess, is washed to distillation residue using ethanol solution, collects washings, washings is dried, collect dried object;
(4)Count by weight, take 50~60 parts of dried objects, 30~35 parts of water, 12~15 parts of n-hexanes, 10~15 parts of acryloyls
Amine, 7~10 parts of MethacryloyloxyethylTrimethyl Trimethyl Ammonium Chlorides and 1~2 part of ammonium persulfate, are put into reactor, use nitrogen
Protection, is reacted at 70~75 DEG C, and reactant mixture is collected in discharging, you can obtain thermal transfer paint for papers.
2. the preparation method of heat-transferring printing paper according to claim 1, it is characterised in that the step(1)Middle guar gum, castor-oil plant
The mass ratio of oily APEO, ammonium hydrogen carbonate and propylene glycol solution is 4~5:0.4~0.8:1:7~9.
3. the preparation method of heat-transferring printing paper according to claim 1, it is characterised in that the step(1)Middle sodium metasilicate plus
It is the 20~25% of guar gum quality to enter amount.
4. the preparation method of heat-transferring printing paper according to claim 1, it is characterised in that the step(2)Middle tin dilaurate two
The addition of butyl tin is guar gum quality 0.6~0.9%, and the dripping quantity of ammonium chloride solution is guar gum quality 30~35%,
Chloroacetic addition is guar gum quality 30~35%.
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CN104875518A (en) * | 2014-02-27 | 2015-09-02 | 金东纸业(江苏)股份有限公司 | Coating material, thermal transfer printing paper, and thermal transfer printing paper preparation method |
CN106592326A (en) * | 2016-12-27 | 2017-04-26 | 东升新材料(山东)有限公司 | Heat transfer printing paper coating and heat transfer printing paper applying same |
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CN1593935A (en) * | 2004-06-30 | 2005-03-16 | 乐凯集团第二胶片厂 | Ink-ejecting acceptance material and back jetting lamp house sheet using the same |
CN102877360A (en) * | 2012-09-05 | 2013-01-16 | 喻小琦 | Coating component for heat transfer paper, heat transfer paper and manufacturing method thereof |
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Application publication date: 20171024 |