CN102965912B - Be suitable for cotton type fabric thermal transfer printing alkaline reaction type silicon titanium colloidal sol preparation method - Google Patents
Be suitable for cotton type fabric thermal transfer printing alkaline reaction type silicon titanium colloidal sol preparation method Download PDFInfo
- Publication number
- CN102965912B CN102965912B CN201210516631.XA CN201210516631A CN102965912B CN 102965912 B CN102965912 B CN 102965912B CN 201210516631 A CN201210516631 A CN 201210516631A CN 102965912 B CN102965912 B CN 102965912B
- Authority
- CN
- China
- Prior art keywords
- parts
- weight
- solution
- cotton
- transfer printing
- 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
- 239000004744 fabric Substances 0.000 title claims abstract description 50
- 238000010023 transfer printing Methods 0.000 title claims abstract description 26
- UGACIEPFGXRWCH-UHFFFAOYSA-N [Si].[Ti] Chemical compound [Si].[Ti] UGACIEPFGXRWCH-UHFFFAOYSA-N 0.000 title claims abstract description 21
- 229920000742 Cotton Polymers 0.000 title claims description 22
- 238000006757 chemical reactions by type Methods 0.000 title claims description 6
- 238000002360 preparation method Methods 0.000 title description 2
- 238000000034 method Methods 0.000 claims abstract description 13
- 239000000243 solution Substances 0.000 claims description 48
- 238000003756 stirring Methods 0.000 claims description 35
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 claims description 17
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 15
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 15
- 125000002091 cationic group Chemical group 0.000 claims description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 14
- 239000008367 deionised water Substances 0.000 claims description 12
- 229910021641 deionized water Inorganic materials 0.000 claims description 12
- 238000012546 transfer Methods 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 10
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 claims description 9
- PEDCQBHIVMGVHV-UHFFFAOYSA-N glycerol group Chemical group OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 9
- 239000000986 disperse dye Substances 0.000 claims description 8
- -1 cationic quaternary ammonium salt Chemical class 0.000 claims description 7
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 claims description 5
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 claims description 5
- 235000011114 ammonium hydroxide Nutrition 0.000 claims description 5
- YHWCPXVTRSHPNY-UHFFFAOYSA-N butan-1-olate;titanium(4+) Chemical compound [Ti+4].CCCC[O-].CCCC[O-].CCCC[O-].CCCC[O-] YHWCPXVTRSHPNY-UHFFFAOYSA-N 0.000 claims description 5
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 4
- 239000011259 mixed solution Substances 0.000 claims description 4
- 238000005507 spraying Methods 0.000 claims description 4
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 3
- 239000004202 carbamide Substances 0.000 claims description 3
- 229920003086 cellulose ether Polymers 0.000 claims description 3
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 3
- 229910052719 titanium Inorganic materials 0.000 claims description 3
- 239000010936 titanium Substances 0.000 claims description 3
- PUVAFTRIIUSGLK-UHFFFAOYSA-M trimethyl(oxiran-2-ylmethyl)azanium;chloride Chemical group [Cl-].C[N+](C)(C)CC1CO1 PUVAFTRIIUSGLK-UHFFFAOYSA-M 0.000 claims description 3
- 235000019270 ammonium chloride Nutrition 0.000 claims description 2
- 239000007822 coupling agent Substances 0.000 claims description 2
- 238000004528 spin coating Methods 0.000 claims description 2
- 238000005516 engineering process Methods 0.000 abstract description 5
- 238000007639 printing Methods 0.000 abstract description 3
- 239000010865 sewage Substances 0.000 abstract description 2
- 239000004753 textile Substances 0.000 abstract description 2
- 238000004043 dyeing Methods 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 229920000728 polyester Polymers 0.000 description 5
- 239000002759 woven fabric Substances 0.000 description 4
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 238000000859 sublimation Methods 0.000 description 2
- 230000008022 sublimation Effects 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000004044 disperse dyeing Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 239000002105 nanoparticle Substances 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
Landscapes
- Coloring (AREA)
Abstract
本发明公开了一种适用棉型织物热转移印花碱性反应型硅钛溶胶制备方法,属于纺织化工技术领域。预处理后的棉型织物热转移印花后其颜色深度和色泽鲜艳度显著提高,而且织物柔软耐洗、穿着舒服。同时该方法为无污水排放、对人体皮肤无伤害的清洁印染技术,具有普遍的推广和应用价值。The invention discloses a method for preparing an alkali-reactive silicon-titanium sol suitable for thermal transfer printing of cotton-type fabrics, and belongs to the technical field of textile chemicals. The color depth and color brightness of the pretreated cotton-type fabric are significantly improved after thermal transfer printing, and the fabric is soft, washable and comfortable to wear. At the same time, the method is a clean printing and dyeing technology without sewage discharge and no harm to human skin, and has universal promotion and application value.
Description
技术领域 technical field
一种适用棉型织物热转移印花碱性反应型硅钛溶胶制备方法,属于纺织化学技术领域。The invention discloses a method for preparing an alkali-reactive silicon-titanium sol suitable for thermal transfer printing of cotton-type fabrics, belonging to the technical field of textile chemistry.
背景技术 Background technique
热转移印花是利用分散染料的热升华性能将织物与印有图案的转移印花纸相接触,在转移印花机上进行热压,分散染料通过升华作用离开转移纸,再凝华到织物上,从而实现染料从印花纸到织物的转移。该印花技术不耗水、也不产生污水,清洁无污染。但是该印花技术只能应用于涤纶织物上,因分散染料对棉型织物无亲合力,所以不能应用于棉型织物上。为了实现棉型织物的转移印花,专利CN02159176.81公开了一种棉织物热转移印花的方法,该方法以织物浸轧FY-3架桥剂进行预处理,从而实现图案向棉织物上的转移。热转移印制的织物图案色泽鲜艳,花色图案牢度好,且织物柔软可洗。专利CN200710048901.8公开了一种棉织物分散染料转移印花用表面改性剂的制备和转移印花预处理的方法,该方法用架桥剂、pH调节剂、改良剂、膨化剂和稀释剂对棉织物进行预处理。印制的织物图案鲜艳,色牢度高,而且对人体无害。目前现有的对织物的预处理技术一般采用成分复杂的有机聚合物或复配物作为架桥剂,其合成工艺较复杂,且存在人体和环境安全隐患,因此普遍推广和应用价值受到限制。Thermal transfer printing is to use the heat sublimation performance of disperse dyes to contact the fabric with the transfer printing paper printed with patterns, and heat press on the transfer printing machine. The disperse dyes leave the transfer paper through sublimation and then condense on the fabric. The transfer of dyestuff from printed paper to fabric. The printing technology does not consume water, does not produce sewage, and is clean and pollution-free. But this printing technology can only be applied on polyester fabric, because disperse dye has no affinity to cotton fabric, so can not be applied on cotton fabric. In order to realize the transfer printing of cotton-type fabrics, patent CN02159176.81 discloses a method for thermal transfer printing of cotton fabrics, which uses fabric padding FY-3 bridging agent for pretreatment, thereby realizing the transfer of patterns to cotton fabrics . The fabric pattern printed by heat transfer is bright in color, the pattern fastness is good, and the fabric is soft and washable. Patent CN200710048901.8 discloses a method for the preparation of a surface modifier for cotton fabric disperse dye transfer printing and transfer printing pretreatment. The fabric is pretreated. The printed fabric has bright patterns, high color fastness, and is harmless to the human body. At present, the existing fabric pretreatment technology generally uses organic polymers or complexes with complex components as bridging agents. The synthesis process is relatively complicated, and there are hidden dangers to human and environmental safety, so the general promotion and application value are limited.
通过溶胶-凝胶掺杂技术将反应型的环氧烷型季铵盐杂化到以无机纳米颗粒为主要成分的硅钛溶胶中,制备碱性反应型硅钛溶胶,并用于织物处理以实现分散染印制的转移印花纸上的图案到棉型织物上的转移。Through the sol-gel doping technology, the reactive alkylene oxide quaternary ammonium salt is hybridized into the silicon-titanium sol mainly composed of inorganic nanoparticles, and the alkaline reactive silicon-titanium sol is prepared and used for fabric treatment to achieve The transfer of the pattern on the transfer printing paper printed by disperse dyeing to the cotton type fabric.
发明内容Contents of the invention
本发明目的在于提供一种适用棉型织物热转移印花碱性反应型硅钛溶胶制备方法,具体实验方法如下:The purpose of the present invention is to provide a method for preparing an alkali-reactive silicon-titanium sol suitable for thermal transfer printing of cotton-type fabrics. The specific experimental method is as follows:
1.向锥形瓶中依次加入21-30重量份正硅酸乙酯、9-21重量份无水乙醇,搅拌均匀,为溶液A;将10-25重量份无水乙醇、10-30重量份去离子水和8-13重量份1mol/L氨水溶液混合并搅拌均匀,为溶液B;将2-5重量份的偶合剂和1-5重量份阳离子季铵盐在室温下溶于5-15份去离子水中,搅拌均匀,为溶液C;在搅拌条件下,将溶液B逐滴滴加到溶液A中,搅拌30min,然后将溶液C逐滴滴加到上述混合液中,在室温下连续搅拌48h,即得碱性阳离子二氧化硅溶胶;1. Add 21-30 parts by weight of ethyl orthosilicate and 9-21 parts by weight of absolute ethanol to the Erlenmeyer flask in sequence, and stir evenly to form solution A; mix 10-25 parts by weight of absolute ethanol, 10-30 parts Parts of deionized water and 8-13 parts by weight of 1mol/L ammonia solution are mixed and stirred uniformly to be solution B; 2-5 parts by weight of coupling agent and 1-5 parts by weight of cationic quaternary ammonium salt are dissolved in 5- 15 parts of deionized water, stirred evenly, is solution C; under stirring condition, add solution B dropwise to solution A, stir for 30min, then add solution C dropwise to the above mixed solution, at room temperature Stir continuously for 48 hours to obtain alkaline cationic silica sol;
所述偶合剂为聚乙二醇、丙三醇、尿素;Described coupler is polyethylene glycol, glycerol, urea;
所述阳离子季铵盐为2,3-环氧丙基三甲基氯化铵、环氧丙基苯乙基二(十八酰胺乙基)氯化铵、氯化-2-羟基-3-(三甲氨基)丙基聚环氧乙烷纤维素醚、3′-甲撑基双[2,3-环氧丙基二甲基-4′-羟基苄基]氯化铵;The cationic quaternary ammonium salt is 2,3-epoxypropyl trimethylammonium chloride, epoxypropyl phenethyl bis(octadecylaminoethyl) ammonium chloride, chloride-2-hydroxyl-3- (Trimethylamino) propyl polyethylene oxide cellulose ether, 3'-methylenebis[2,3-epoxypropyldimethyl-4'-hydroxybenzyl] ammonium chloride;
将5-12重量份的钛酸四丁酯溶于8-15重量份的无水乙醇中,搅拌均匀,为溶液D;将5-10重量份的0.5mol/L的醋酸和18-31重量份的去离子水混合,搅拌均匀,为溶液E;取碱性阳离子二氧化硅溶胶43-54重量份置于锥形瓶中,将上述溶液D和溶液E依次缓慢滴加到碱性阳离子二氧化硅溶胶中,室温条件下搅拌12h,然后陈化120h,即得碱性反应型硅钛溶胶。Dissolve 5-12 parts by weight of tetrabutyl titanate in 8-15 parts by weight of absolute ethanol and stir evenly to obtain solution D; mix 5-10 parts by weight of 0.5 mol/L acetic acid and 18-31 parts by weight 43-54 parts by weight of the basic cationic silica sol is placed in a conical flask, and the above solution D and solution E are slowly added dropwise to the basic cationic silica sol successively. In the silica sol, stir at room temperature for 12 hours, and then age for 120 hours to obtain the alkaline reaction type silicon titanium sol.
2.所述一种适用热转移印花碱性反应型硅钛溶胶,其特征是采用的棉型织物为棉及其混纺织物。2. The alkaline reactive silicon-titanium sol suitable for thermal transfer printing is characterized in that the cotton fabric used is cotton and its blended fabric.
3.所述适用一种热转移印花碱性反应型硅钛溶胶其在棉型织物上的应用,其特征是采用喷涂或旋涂的方法;处理后织物在50-60℃预烘15-40min。3. The application of a thermal transfer printing alkaline reaction type silicon-titanium sol on cotton fabrics is characterized in that it adopts the method of spraying or spin coating; after the treatment, the fabric is prebaked at 50-60°C for 15-40min .
4.所述的一种适用热转移印花碱性反应型硅钛溶胶在棉型织物上的应用,其热转移工艺为:将印有图案的转移纸与经预处理的棉型织物贴合、铺平,然后在200-220℃下热处理25-40s。4. The application of the alkaline reaction type silica-titanium sol suitable for heat transfer printing on cotton fabrics, the heat transfer process is as follows: the transfer paper printed with patterns is bonded to the pretreated cotton fabric, Lay flat, then heat treat at 200-220°C for 25-40s.
具体实施方式 detailed description
通过以下的实施例将有助于进一步的理解本发明,但不能限定本发明的内容。The following examples will help to further understand the present invention, but cannot limit the content of the present invention.
测试方法,具体分析如下:The test method, the specific analysis is as follows:
(1)K/S值测试(1) K/S value test
将印花织物样品折叠4层,用X-rite8400型测色仪CIE-lab测色系统在D65光源,10°视场条件下测试织物颜色表观深度(K/S值)。测量前仪器选用中型孔径,并经黑白板校正仪器。每个样品测试8次,结果取平均值。Fold the printed fabric sample into 4 layers, and use the X-rite8400 colorimeter CIE-lab colorimetric system to test the apparent color depth (K/S value) of the fabric under the condition of D65 light source and 10° field of view. Before the measurement, the instrument uses a medium-sized aperture, and the instrument is calibrated by black and white boards. Each sample was tested 8 times, and the results were averaged.
实施例1Example 1
向锥形瓶中依次加入23重量份正硅酸乙酯、18重量份无水乙醇,搅拌均匀,为溶液A;将11重量份无水乙醇、16重量份去离子水和9重量份1mol/L氨水溶液混合并搅拌均匀,为溶液B;将3重量份的聚乙二醇和3重量份2,3-环氧丙基三甲基氯化铵在室温下溶于15重量份去离子水中,搅拌均匀,为溶液C;在搅拌条件下,将溶液B逐滴滴加到溶液A中,搅拌30min,然后将溶液C逐滴滴加到上述混合液中,在室温下连续搅拌48h,即得碱性阳离子二氧化硅溶胶。Add 23 parts by weight of tetraethyl orthosilicate and 18 parts by weight of absolute ethanol to the Erlenmeyer flask in sequence, and stir evenly to form solution A; mix 11 parts by weight of absolute ethanol, 16 parts by weight of deionized water and 9 parts by weight of 1mol The L ammonia solution is mixed and stirred uniformly to be solution B; 3 parts by weight of polyethylene glycol and 3 parts by weight of 2,3-epoxypropyltrimethylammonium chloride are dissolved in 15 parts by weight of deionized water at room temperature, Stir evenly to obtain solution C; under stirring conditions, add solution B dropwise to solution A, stir for 30 minutes, then add solution C dropwise to the above mixture, and continue stirring at room temperature for 48 hours to obtain Alkaline cationic silica sol.
将6重量份的钛酸四丁酯溶于11重量份的无水乙醇中,搅拌均匀,为溶液D;将6重量份的0.5mol/L的醋酸和26重量份的去离子水混合,搅拌均匀,为溶液E;取碱性阳离子二氧化硅溶胶51重量份置于锥形瓶中,将上述溶液D和溶液E依次缓慢滴加到碱性阳离子二氧化硅溶胶中,室温条件下搅拌12h,然后陈化120h,,即得碱性反应型硅钛溶胶。Dissolve 6 parts by weight of tetrabutyl titanate in 11 parts by weight of absolute ethanol, and stir evenly to form solution D; mix 6 parts by weight of 0.5 mol/L acetic acid with 26 parts by weight of deionized water, and stir Evenly, it is solution E; take 51 parts by weight of alkaline cationic silica sol and place it in a conical flask, slowly add the above solution D and solution E to the alkaline cationic silica sol successively, and stir for 12 hours at room temperature , and then aged for 120h, to obtain an alkaline reactive silicon-titanium sol.
用上述碱性反应型硅钛溶胶对纯棉机织物进行喷涂预处理,然后织物在50℃预烘25min。将印有分散染料红色色块的转移纸与经预处理的纯棉机织物贴合、铺平,然后在205℃下热处理35s。The pure cotton woven fabric was pre-treated by spraying with the above-mentioned alkaline reactive silica titanium sol, and then the fabric was pre-baked at 50°C for 25 minutes. Lay the transfer paper printed with the red color block of disperse dyes with the pretreated pure cotton woven fabric, pave it flat, and then heat-treat it at 205°C for 35s.
未经预处理的纯棉机织物热转移印花后K/S值为2.45,而经碱性反应型硅钛溶胶预处理的纯棉机织物热转移印花后K/S值为10.05。The K/S value of the unpretreated pure cotton woven fabric was 2.45 after thermal transfer printing, while the K/S value of the pure cotton woven fabric pretreated with alkaline reactive silicon titanium sol was 10.05 after thermal transfer printing.
实施例2Example 2
向锥形瓶中依次加入28重量份正硅酸乙酯、14重量份无水乙醇,搅拌均匀,为溶液A;将14重量份无水乙醇、22重量份去离子水和10重量份1mol/L氨水溶液混合并搅拌均匀,为溶液B;将4重量份尿素和2重量份环氧丙基苯乙基二(十八酰胺乙基)氯化铵在室温下溶于6重量份去离子水中,搅拌均匀,为溶液C;在搅拌条件下,将溶液B逐滴滴加到溶液A中,搅拌30min,然后将溶液C逐滴滴加到上述混合液中,在室温下连续搅拌48h,即得碱性阳离子二氧化硅溶胶。Add 28 parts by weight of tetraethyl orthosilicate and 14 parts by weight of absolute ethanol to the Erlenmeyer flask in sequence, and stir evenly to form solution A; mix 14 parts by weight of absolute ethanol, 22 parts by weight of deionized water and 10 parts by weight of L ammonia solution is mixed and stirred evenly, is solution B; 4 parts by weight of urea and 2 parts by weight of epoxypropyl phenethyl bis(octadecylaminoethyl) ammonium chloride are dissolved in 6 parts by weight of deionized water at room temperature , stir evenly, it is solution C; under stirring condition, add solution B dropwise to solution A, stir for 30min, then add solution C dropwise to the above mixed solution, stir continuously at room temperature for 48h, that is Obtain alkaline cationic silica sol.
将10重量份的钛酸四丁酯溶于14重量份的无水乙醇中,搅拌均匀,为溶液D;将7重量份的0.5mol/L的醋酸和23重量份的去离子水混合,搅拌均匀,为溶液E;取碱性阳离子二氧化硅溶胶46重量份置于锥形瓶中,将上述溶液D和溶液E依次缓慢滴加到碱性阳离子二氧化硅溶胶中,室温条件下搅拌12h,然后陈化120h,即得碱性反应型硅钛溶胶。Dissolve 10 parts by weight of tetrabutyl titanate in 14 parts by weight of absolute ethanol, and stir evenly to form solution D; mix 7 parts by weight of 0.5 mol/L acetic acid with 23 parts by weight of deionized water, and stir Evenly, it is solution E; take 46 parts by weight of alkaline cationic silica sol and place it in a conical flask, slowly add the above solution D and solution E to the alkaline cationic silica sol successively, and stir for 12 hours at room temperature , and then aged for 120h to obtain an alkaline reactive silicon-titanium sol.
用上述碱性反应型硅钛溶胶对棉涤混纺织物进行旋涂预处理,然后织物在60℃预烘23min。将印有分散染料红色色块的转移纸与经预处理的棉涤混纺织贴合、铺平,然后在210℃下热处理28s。Spin-coat the cotton-polyester blended fabric with the above-mentioned alkaline-reactive silicon-titanium sol, and then pre-dry the fabric at 60°C for 23 minutes. Lay the transfer paper printed with the red color block of disperse dyes with the pretreated cotton-polyester blended fabric, lay it flat, and then heat-treat it at 210°C for 28s.
未经预处理的棉涤混纺织物热转移印花后K/S值为4.18,而经碱性反应型硅钛溶胶预处理的棉涤混纺织物热转移印花后K/S值为11.67。The K/S value of the non-pretreated cotton-polyester blended fabric was 4.18 after thermal transfer printing, while the K/S value of the cotton-polyester blended fabric pretreated with alkaline reactive silicon titanium sol was 11.67 after thermal transfer printing.
实施例3Example 3
向锥形瓶中依次加入25重量份正硅酸乙酯、10重量份无水乙醇,搅拌均匀,为溶液A;将20重量份无水乙醇、15重量份去离子水和12重量份1mol/L氨水溶液混合并搅拌均匀,为溶液B;将5重量份的丙三醇和1重量份氯化-2-羟基-3-(三甲氨基)丙基聚环氧乙烷纤维素醚在室温下溶于12重量份去离子水中,搅拌均匀,为溶液C;溶液A在磁力搅拌器搅拌条件下,将溶液B逐滴滴加到溶液A中,搅拌30min,然后将溶液C逐滴滴加到上述混合液中,在室温下连续搅拌48h,即得碱性阳离子二氧化硅溶胶。Add 25 parts by weight of tetraethyl orthosilicate and 10 parts by weight of absolute ethanol in turn to the Erlenmeyer flask, and stir evenly to form solution A; mix 20 parts by weight of absolute ethanol, 15 parts by weight of deionized water and 12 parts by weight of The L ammonia solution is mixed and stirred evenly, which is solution B; 5 parts by weight of glycerol and 1 part by weight of chlorinated-2-hydroxyl-3-(trimethylamino)propyl polyethylene oxide cellulose ether are dissolved at room temperature In 12 parts by weight of deionized water, stir evenly to form solution C; solution A is added dropwise to solution A under the stirring condition of a magnetic stirrer, and stirred for 30 minutes, then solution C is added dropwise to the above The mixed solution was continuously stirred at room temperature for 48 hours to obtain an alkaline cationic silica sol.
将9重量份的钛酸四丁酯溶于15重量份的无水乙醇中,搅拌均匀,为溶液D;将6重量份的0.5mol/L的醋酸和25重量份的去离子水混合,搅拌均匀,为溶液E;取碱性阳离子二氧化硅溶胶45重量份置于锥形瓶中,将上述溶液D和溶液E依次缓慢滴加到碱性阳离子二氧化硅溶胶中,室温条件下搅拌12h,然后陈化120h,即得碱性反应型硅钛溶胶。Dissolve 9 parts by weight of tetrabutyl titanate in 15 parts by weight of absolute ethanol, and stir evenly to form solution D; mix 6 parts by weight of 0.5 mol/L acetic acid with 25 parts by weight of deionized water, and stir Evenly, it is solution E; take 45 parts by weight of alkaline cationic silica sol and place it in a conical flask, slowly add the above solution D and solution E to the alkaline cationic silica sol successively, and stir for 12 hours at room temperature , and then aged for 120h to obtain an alkaline reactive silicon-titanium sol.
用上述碱性反应型硅钛溶胶对棉麻混纺织物进行喷涂预处理,然后织物在55℃预烘24min。将印有分散染料蓝色色块的转移纸与经预处理的棉麻混纺织物贴合、铺平,然后在215℃下热处理26s。Cotton and linen blended fabrics were pretreated by spraying with the above-mentioned alkaline reactive silicon titanium sol, and then the fabrics were prebaked at 55°C for 24 minutes. Lay the transfer paper printed with the blue color block of disperse dyes with the pretreated cotton and linen blended fabric, lay it flat, and then heat-treat it at 215°C for 26s.
未经预处理的棉麻混纺织物热转移印花后K/S值为5.32,而经碱性反应型硅钛溶胶预处理的棉麻混纺织物热转移印花后K/S值为9.86。The K/S value of the cotton-linen blended fabric without pretreatment was 5.32 after thermal transfer printing, while the K/S value of the cotton-linen blended fabric pretreated with alkaline reactive silicon titanium sol was 9.86 after thermal transfer printing.
Claims (4)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201210516631.XA CN102965912B (en) | 2012-11-20 | 2012-11-20 | Be suitable for cotton type fabric thermal transfer printing alkaline reaction type silicon titanium colloidal sol preparation method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201210516631.XA CN102965912B (en) | 2012-11-20 | 2012-11-20 | Be suitable for cotton type fabric thermal transfer printing alkaline reaction type silicon titanium colloidal sol preparation method |
Publications (2)
Publication Number | Publication Date |
---|---|
CN102965912A CN102965912A (en) | 2013-03-13 |
CN102965912B true CN102965912B (en) | 2016-05-25 |
Family
ID=47796329
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201210516631.XA Expired - Fee Related CN102965912B (en) | 2012-11-20 | 2012-11-20 | Be suitable for cotton type fabric thermal transfer printing alkaline reaction type silicon titanium colloidal sol preparation method |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN102965912B (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103640350A (en) * | 2013-11-25 | 2014-03-19 | 江南大学 | Method for giving turned edge painted design of jeans wear through reverse side transfer printing |
CN105346295B (en) * | 2015-11-06 | 2018-06-05 | 苏州市智汇宝数码科技有限公司 | A kind of functional distillation transfer printing paper and its preparation method and application |
CN105862414B (en) * | 2016-04-16 | 2018-06-26 | 山东黄河三角洲纺织科技研究院有限公司 | A kind of method for improving the rich and gaudy degree of pigment printing color and fastness |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5296299A (en) * | 1988-04-23 | 1994-03-22 | Matsubishi Paper Mills Ltd. | Thermal transfer film |
CN1417405A (en) * | 2002-12-30 | 2003-05-14 | 北京服装学院 | Cotton fabric thermal transfer printing method |
CN1546781A (en) * | 2003-12-05 | 2004-11-17 | 东华大学 | Composite hydrosol color-fixing finishing agent, synthesis method and use thereof |
CN101046060A (en) * | 2007-04-19 | 2007-10-03 | 四川大学 | Surface modifier for transfer printing with dispersive cotton fabric dye and its pre-treatment method |
CN101117765A (en) * | 2007-07-23 | 2008-02-06 | 江南大学 | A kind of Gemini type cationic sol and the method for improving fabric color fastness |
CN101302730A (en) * | 2008-06-06 | 2008-11-12 | 陕西科技大学 | A kind of preparation method of surface sizing reinforcing agent |
CN101363190A (en) * | 2008-09-26 | 2009-02-11 | 江南大学 | Preparation of a Gemini type composite sol and its application in UV protection/antibacterial finishing |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3259078B2 (en) * | 1993-04-27 | 2002-02-18 | 倉庫精練株式会社 | Method for producing printing base fabric having microporous film |
-
2012
- 2012-11-20 CN CN201210516631.XA patent/CN102965912B/en not_active Expired - Fee Related
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5296299A (en) * | 1988-04-23 | 1994-03-22 | Matsubishi Paper Mills Ltd. | Thermal transfer film |
CN1417405A (en) * | 2002-12-30 | 2003-05-14 | 北京服装学院 | Cotton fabric thermal transfer printing method |
CN1546781A (en) * | 2003-12-05 | 2004-11-17 | 东华大学 | Composite hydrosol color-fixing finishing agent, synthesis method and use thereof |
CN101046060A (en) * | 2007-04-19 | 2007-10-03 | 四川大学 | Surface modifier for transfer printing with dispersive cotton fabric dye and its pre-treatment method |
CN101117765A (en) * | 2007-07-23 | 2008-02-06 | 江南大学 | A kind of Gemini type cationic sol and the method for improving fabric color fastness |
CN101302730A (en) * | 2008-06-06 | 2008-11-12 | 陕西科技大学 | A kind of preparation method of surface sizing reinforcing agent |
CN101363190A (en) * | 2008-09-26 | 2009-02-11 | 江南大学 | Preparation of a Gemini type composite sol and its application in UV protection/antibacterial finishing |
Also Published As
Publication number | Publication date |
---|---|
CN102965912A (en) | 2013-03-13 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN104493937B (en) | Method for increasing dyeing and fixation rate of reactive dye to wood | |
CN102965912B (en) | Be suitable for cotton type fabric thermal transfer printing alkaline reaction type silicon titanium colloidal sol preparation method | |
CN102634992A (en) | Method for dyeing cyclodextrin cross-linked modified polyester, cotton and blended fabric by cationic dyes | |
CN101363195B (en) | A preparation method of composite sol for improving inkjet printing fastness | |
CN102936859A (en) | One-bath one-step dyeing method for cotton and nitrile blended fabric | |
CN108252130A (en) | The pad dyeing colouring method of alginate fibre/polyester fiber blended fabric | |
CN106192463A (en) | A kind of protein fibre fabric natural dye ecology printing method | |
CN109281208B (en) | Low-temperature white discharge printing method for cotton fabric | |
CN108797157B (en) | Plateless multi-color-register printed fabric with simple process and obvious outline characteristics and preparation method thereof | |
CN109233337B (en) | Black dye composition and dye product | |
CN100535236C (en) | Fibroin protein coating fabric dying method | |
CN103469618B (en) | A kind of without urea printing with reactive dye mill base, manufacture method and dyeing method | |
CN103628333B (en) | Digit printing dyeing finishing agent and preparation method and application process | |
CN108729269A (en) | A kind of active dye fixing agent and preparation method thereof | |
CN101349015B (en) | Preparation and application of colloidal sol dyeing liquor | |
KR101230699B1 (en) | One bath dyeing method of complex fabric with polyester-cotton | |
CN101381964B (en) | Comprehensive coating screen printing method | |
CN102493224B (en) | A kind of auxiliary for pad stack dyeing of reactive dye | |
CN109403070B (en) | Preparation method of radiation-proof heat-preservation composite fabric based on double-sided heterochromatic digital printing | |
CN101649563A (en) | Room temperature wool pad dyeing microwave color fixing method | |
CN109338747B (en) | Dyeing method for reducing dye thiourea dioxide at low temperature | |
CN101235599A (en) | A kind of dyeing method of ordinary polypropylene fiber products | |
CN103397542A (en) | Preparation method of near-infrared camouflage painting fabric | |
CN104589444A (en) | Alkaline silica soil color fixing agent and preparation method thereof | |
CN108166252A (en) | A kind of digit printing cotton pretreatment agent and preparation method thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20160525 Termination date: 20181120 |
|
CF01 | Termination of patent right due to non-payment of annual fee |