CN117701060A - A kind of preparation method of edge pressure printer ink - Google Patents
A kind of preparation method of edge pressure printer ink Download PDFInfo
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- 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
- C09D11/037—Printing inks characterised by features other than the chemical nature of the binder characterised by the pigment
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- 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
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- C09D11/03—Printing inks characterised by features other than the chemical nature of the binder
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- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
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- 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
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- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
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- 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
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Abstract
本发明公开了一种边压式打印机油墨的制备方法,包括:将颜料放入乙醇‑乙醚液中浸泡,急速搅拌,过滤后烘干得到洁净的颜料颗粒;将甲基三氯硅烷加入至乙醚中,形成硅醚液,然后将洁净的颜料颗粒放入硅醚液低温超声分散,烘干得到镀膜颜料;将以含水空气为气体,将镀膜颗粒喷洒至反应釜中沉积,得到包裹型颜料;将包裹型颜料放入有机溶剂中,然后依次加入树脂材料、防腐剂和填料,形成均质浆料;将固化剂加入至均质浆料内研磨细化,得到边压式打印机油墨。本发明解决了现有油墨中的颜料变质的问题,利用甲基三氯硅烷形成硅氧结构均质包裹在整个颜料表面,形成颜料结构稳定性,且甲基三氯硅烷形成包裹层具有透明性,并不会产生颜色遮蔽。The invention discloses a preparation method for edge pressure printer ink, which includes: soaking pigments in ethanol-ether liquid, stirring rapidly, filtering and drying to obtain clean pigment particles; adding methyltrichlorosilane to ether In the process, a silicon ether liquid is formed, and then the clean pigment particles are put into the silicon ether liquid for low-temperature ultrasonic dispersion, and dried to obtain the coating pigment; using water-containing air as gas, the coating particles are sprayed into the reactor for deposition to obtain the wrapped pigment; Put the wrapped pigment into an organic solvent, then add resin materials, preservatives and fillers in sequence to form a homogeneous slurry; add the curing agent into the homogeneous slurry and grind and refine it to obtain edge pressure printer ink. The present invention solves the problem of pigment deterioration in existing inks. Methyltrichlorosilane is used to form a silicon-oxygen structure that is uniformly wrapped on the entire pigment surface to form a stable pigment structure, and the wrapping layer formed by methyltrichlorosilane is transparent. , and will not produce color masking.
Description
技术领域Technical field
本发明属于油墨技术领域,具体涉及一种边压式打印机油墨的制备方法。The invention belongs to the technical field of inks, and specifically relates to a method for preparing ink for an edge-pressure printer.
背景技术Background technique
油墨是用于印刷的重要材料,它通过印刷或喷绘将图案、文字表现在承印物上。油墨中包括主要成分和辅助成分,它们均匀地混合并经反复轧制而成一种黏性胶状流体。由连结料(树脂)、颜料、填料、助剂和溶剂等组成。用于书刊、包装装潢、建筑装饰及电子线路板材等各种印刷。随着社会需求增大,油墨品种和产量也相应扩展和增长。然而,热转印碳带随着使用时间的延长,油墨颜色极易发生变化,难以在电子、塑胶、陶瓷等领域广泛性使用。Ink is an important material used for printing. It expresses patterns and text on the substrate through printing or inkjet printing. The ink includes main components and auxiliary components, which are uniformly mixed and rolled repeatedly to form a viscous colloidal fluid. It is composed of binder (resin), pigments, fillers, additives and solvents. Used for various printing of books, periodicals, packaging and decoration, architectural decoration and electronic circuit boards. As social demand increases, ink varieties and output have also expanded and grown accordingly. However, as thermal transfer ribbons are used for extended periods of time, the ink color is easily changed, making it difficult to be widely used in electronics, plastics, ceramics and other fields.
发明内容Contents of the invention
针对现有技术中的问题,本发明提供一种边压式打印机油墨的制备方法,解决了现有油墨中的颜料变质的问题,利用甲基三氯硅烷形成硅氧结构均质包裹在整个颜料表面,形成颜料结构稳定性,且甲基三氯硅烷形成包裹层具有透明性,并不会产生颜色遮蔽。In view of the problems in the prior art, the present invention provides a preparation method of edge pressure printer ink, which solves the problem of pigment deterioration in the existing ink. Methyltrichlorosilane is used to form a silicon-oxygen structure that is uniformly wrapped around the entire pigment. On the surface, the pigment structure is stabilized, and the wrapping layer formed by methyltrichlorosilane is transparent and will not cause color shading.
为实现以上技术目的,本发明的技术方案是:In order to achieve the above technical objectives, the technical solution of the present invention is:
一种边压式打印机油墨的制备方法,包括如下步骤:A method for preparing ink for an edge-pressure printer, including the following steps:
步骤1,将颜料放入乙醇-乙醚液中浸泡10-20min,急速搅拌30-60min,过滤后烘干得到洁净的颜料颗粒,所述颜料采用氧化铬、四氧化三铁、氧化钴中的一种,所述乙醇-乙醚液中的乙醇与乙醚的体积比为1:2-3,所述颜料在乙醇-乙醚液中的浓度为200-400g/L,浸泡的温度为5-10℃,所述急速搅拌的搅拌速度为500-800r/min,所述烘干在氮气氛围下烘干,且烘干的温度为90-100℃;该步骤利用乙醇-乙醚液的洗涤作用,实现了颜料的表面洗涤,并通过浸泡与急速搅拌的方式降低颜料表面的气泡,有效的提升了颜料的表面洁净度;Step 1: Soak the pigment in ethanol-ether liquid for 10-20 minutes, stir rapidly for 30-60 minutes, filter and dry to obtain clean pigment particles. The pigment is made of one of chromium oxide, ferric oxide, and cobalt oxide. kind, the volume ratio of ethanol to ether in the ethanol-ether liquid is 1:2-3, the concentration of the pigment in the ethanol-ether liquid is 200-400g/L, and the soaking temperature is 5-10°C. The stirring speed of the rapid stirring is 500-800r/min, the drying is done in a nitrogen atmosphere, and the drying temperature is 90-100°C; this step utilizes the washing effect of ethanol-ether liquid to realize the pigment Surface cleaning, and reducing bubbles on the surface of the paint through soaking and rapid stirring, effectively improving the surface cleanliness of the paint;
步骤2,将甲基三氯硅烷加入至乙醚中搅拌均匀,形成硅醚液,然后将洁净的颜料颗粒放入硅醚液低温超声分散2-4h,烘干得到镀膜颜料,所述甲基三氯硅烷在乙醚中的浓度为100-200g/L,搅拌均匀的搅拌速度为100-200r/min,所述颜料颗粒在硅醚液中的浓度为60-100g/L,低温超声的超声频率为60-90kHz,温度为5-10℃;所述烘干的温度为40-45℃;该步骤利用溶液镀膜的方式在颜料表面形成稳定的液膜,同时,三氯甲基硅烷自身的液体状态能够均质分散在颜料表面,形成液膜包裹;Step 2: Add methyltrichlorosilane to diethyl ether and stir evenly to form a silicon ether liquid. Then put the clean pigment particles into the silicon ether liquid for low-temperature ultrasonic dispersion for 2-4 hours, and dry to obtain a coating pigment. The methyltrichlorosilane The concentration of chlorosilane in diethyl ether is 100-200g/L, the stirring speed for uniform stirring is 100-200r/min, the concentration of the pigment particles in the silicon ether liquid is 60-100g/L, and the ultrasonic frequency of low-temperature ultrasound is 60-90kHz, the temperature is 5-10°C; the drying temperature is 40-45°C; this step uses solution coating to form a stable liquid film on the surface of the pigment, and at the same time, the liquid state of trichloromethylsilane itself Can be dispersed homogeneously on the surface of the pigment to form a liquid film;
步骤3,将以含水空气为气体,将镀膜颗粒喷洒至反应釜中沉积2-3h,得到包裹型颜料,所述镀膜颗粒与含水空气的质量体积比为1-2g/mL,含水空气的含水量为8%,喷洒速度为10-20mL/min,沉积的温度为90-100℃;该步骤利用含水空气吹动镀膜颗粒时,含水空气中的水分子与镀膜颗粒上的三氯甲基硅烷形成反应,得到三羟基甲基硅烷,并在沉积过程的温度中,三羟基甲基硅烷形成缩聚,得到包裹型颜料;Step 3: Using water-containing air as gas, spray the coated particles into the reaction kettle and deposit them for 2-3 hours to obtain the wrapped pigment. The mass-to-volume ratio of the coating particles to the water-containing air is 1-2g/mL, and the content of the water-containing air is 1-2g/mL. The water volume is 8%, the spraying speed is 10-20mL/min, and the deposition temperature is 90-100°C; in this step, when water-containing air is used to blow the coated particles, the water molecules in the water-containing air interact with the trichloromethylsilane on the coated particles. Formation reaction produces trihydroxymethylsilane, and at the temperature of the deposition process, trihydroxymethylsilane forms condensation polymerization to obtain encapsulated pigment;
步骤4,将包裹型颜料放入有机溶剂中搅拌均匀,然后依次加入树脂材料、防腐剂和填料,急速搅拌形成均质浆料;所述有机溶剂采用环己烷和环己酮的混合液,且环己烷和环己酮的体积比为1-3:1,所述包裹型颜料与有机溶剂的质量比为1:2-4,所述树脂材料采用丙烯酸树脂与环氧树脂的混合物,且丙烯酸树脂与环氧树脂的质量比为2-3:2,所述树脂材料与包裹型颜料的质量比为2-3:2,所述防腐剂采用Proxel GXL,且防腐剂的加入量是包裹型颜料质量的5-10%,所述填料采用气相白炭黑,且所述气相白炭黑与包裹型颜料的质量比为3:3-4,急速搅拌的温度为70-80℃,搅拌速度为1000-2000r/min;Step 4: Put the wrapped pigment into an organic solvent and stir evenly, then add resin materials, preservatives and fillers in sequence, and stir rapidly to form a homogeneous slurry; the organic solvent is a mixture of cyclohexane and cyclohexanone. And the volume ratio of cyclohexane and cyclohexanone is 1-3:1, the mass ratio of the wrapped pigment and organic solvent is 1:2-4, and the resin material is a mixture of acrylic resin and epoxy resin, And the mass ratio of acrylic resin to epoxy resin is 2-3:2, the mass ratio of the resin material to the wrapped pigment is 2-3:2, the preservative is Proxel GXL, and the amount of preservative added is 5-10% of the mass of the wrapped pigment, the filler is gas phase silica, and the mass ratio of the gas phase silica to the wrapped pigment is 3:3-4, and the temperature of rapid stirring is 70-80°C. The stirring speed is 1000-2000r/min;
步骤5,将固化剂加入至均质浆料内研磨细化,得到边压式打印机油墨,所述固化剂采用ZL-1环氧固化剂,所述固化剂的加入量是均质浆料质量的1-2%,所述研磨处理的温度为40-50℃,研磨时间为3-5h。Step 5: Add the curing agent into the homogeneous slurry and grind and refine it to obtain edge pressure printer ink. The curing agent is ZL-1 epoxy curing agent. The amount of the curing agent added is the mass of the homogeneous slurry. 1-2%, the temperature of the grinding treatment is 40-50°C, and the grinding time is 3-5h.
从以上描述可以看出,本发明具备以下优点:As can be seen from the above description, the present invention has the following advantages:
1.本发明解决了现有油墨中的颜料变质的问题,利用甲基三氯硅烷形成硅氧结构均质包裹在整个颜料表面,形成颜料结构稳定性,且甲基三氯硅烷形成包裹层具有透明性,并不会产生颜色遮蔽。1. The present invention solves the problem of pigment deterioration in existing inks. Methyltrichlorosilane is used to form a silicon-oxygen structure that is uniformly wrapped on the entire pigment surface to form a stable pigment structure. The wrapping layer formed by methyltrichlorosilane has Transparency and no color blocking.
2.本发明以气相白炭黑作为填料,能够利用气相白炭黑自身的细小结构形成快速渗透,提高油墨固化后的紧密性,特别能够穿插在环氧树脂固化过程中形成的网络结构内,同时气相白炭黑具有反射光线等效果和不遮蔽的特性,能够保证油墨的正常使用,降低光损伤对树脂的影响。2. The present invention uses fumed silica as a filler, which can utilize the fine structure of the fumed silica itself to form rapid penetration and improve the tightness of the ink after curing. It can especially be inserted into the network structure formed during the curing process of the epoxy resin. At the same time, fumed silica has the effect of reflecting light and not blocking, which can ensure the normal use of the ink and reduce the impact of light damage on the resin.
具体实施方式Detailed ways
结合实施例详细说明本发明,但不对本发明的权利要求做任何限定。The present invention will be described in detail with reference to the examples, but the claims of the present invention will not be limited in any way.
实施例1Example 1
一种边压式打印机油墨的制备方法,包括如下步骤:A method for preparing ink for an edge-pressure printer, including the following steps:
步骤1,将颜料放入乙醇-乙醚液中浸泡10min,急速搅拌30min,过滤后烘干得到洁净的颜料颗粒,所述颜料采用氧化铬,所述乙醇-乙醚液中的乙醇与乙醚的体积比为1:2,所述颜料在乙醇-乙醚液中的浓度为200g/L,浸泡的温度为5℃,所述急速搅拌的搅拌速度为500r/min,所述烘干在氮气氛围下烘干,且烘干的温度为90℃;Step 1: Soak the pigment in ethanol-ether liquid for 10 minutes, stir rapidly for 30 minutes, filter and dry to obtain clean pigment particles. The pigment is chromium oxide. The volume ratio of ethanol to ether in the ethanol-ether liquid is is 1:2, the concentration of the pigment in the ethanol-ether liquid is 200g/L, the soaking temperature is 5°C, the stirring speed of the rapid stirring is 500r/min, and the drying is done under a nitrogen atmosphere , and the drying temperature is 90℃;
步骤2,将甲基三氯硅烷加入至乙醚中搅拌均匀,形成硅醚液,然后将洁净的颜料颗粒放入硅醚液低温超声分散2h,烘干得到镀膜颜料,所述甲基三氯硅烷在乙醚中的浓度为100g/L,搅拌均匀的搅拌速度为100r/min,所述颜料颗粒在硅醚液中的浓度为60g/L,低温超声的超声频率为60kHz,温度为5℃;所述烘干的温度为40℃;Step 2: Add methyltrichlorosilane to diethyl ether and stir evenly to form a silicon ether liquid. Then put the clean pigment particles into the silicon ether liquid for low-temperature ultrasonic dispersion for 2 hours, and dry to obtain a coating pigment. The methyltrichlorosilane The concentration in diethyl ether is 100g/L, the stirring speed for uniform stirring is 100r/min, the concentration of the pigment particles in the silicon ether liquid is 60g/L, the ultrasonic frequency of low-temperature ultrasound is 60kHz, and the temperature is 5°C; The drying temperature is 40℃;
步骤3,将以含水空气为气体,将镀膜颗粒喷洒至反应釜中沉积2h,得到包裹型颜料,所述镀膜颗粒与含水空气的质量体积比为1g/mL,含水空气的含水量为8%,喷洒速度为10mL/min,沉积的温度为90℃;Step 3: Using water-containing air as gas, spray the coated particles into the reaction kettle for deposition for 2 hours to obtain the wrapped pigment. The mass-volume ratio of the coating particles to the water-containing air is 1g/mL, and the water content of the water-containing air is 8%. , the spraying speed is 10mL/min, and the deposition temperature is 90°C;
步骤4,将包裹型颜料放入有机溶剂中搅拌均匀,然后依次加入树脂材料、防腐剂和填料,急速搅拌形成均质浆料;所述有机溶剂采用环己烷和环己酮的混合液,且环己烷和环己酮的体积比为1:1,所述包裹型颜料与有机溶剂的质量比为1:2,所述树脂材料采用丙烯酸树脂与环氧树脂的混合物,且丙烯酸树脂与环氧树脂的质量比为2:2,所述树脂材料与包裹型颜料的质量比为2:2,所述防腐剂采用Proxel GXL,且防腐剂的加入量是包裹型颜料质量的5%,所述填料采用气相白炭黑,且所述气相白炭黑与包裹型颜料的质量比为3:3,急速搅拌的温度为70℃,搅拌速度为1000r/min;Step 4: Put the wrapped pigment into an organic solvent and stir evenly, then add resin materials, preservatives and fillers in sequence, and stir rapidly to form a homogeneous slurry; the organic solvent is a mixture of cyclohexane and cyclohexanone. And the volume ratio of cyclohexane and cyclohexanone is 1:1, the mass ratio of the encapsulated pigment and organic solvent is 1:2, the resin material is a mixture of acrylic resin and epoxy resin, and the acrylic resin and The mass ratio of epoxy resin is 2:2, the mass ratio of the resin material to the wrapped pigment is 2:2, the preservative is Proxel GXL, and the amount of preservative added is 5% of the mass of the wrapped pigment, The filler uses gas phase silica, and the mass ratio of the gas phase silica to the wrapped pigment is 3:3, the temperature of rapid stirring is 70°C, and the stirring speed is 1000r/min;
步骤5,将固化剂加入至均质浆料内研磨细化,得到边压式打印机油墨,所述固化剂采用ZL-1环氧固化剂,所述固化剂的加入量是均质浆料质量的1%,所述研磨处理的温度为40℃,研磨时间为3h。Step 5: Add the curing agent into the homogeneous slurry and grind and refine it to obtain edge pressure printer ink. The curing agent is ZL-1 epoxy curing agent. The amount of the curing agent added is the mass of the homogeneous slurry. 1%, the temperature of the grinding treatment is 40°C, and the grinding time is 3h.
将该实施例制备的油墨通过边压式打印机打印,得到的打印印迹在300℃下放置2h,依然完好,表面清晰,经耐磨试验仪测试,耐摩擦28次,其常温下放置1个月,基本没变化。The ink prepared in this example was printed with an edge pressure printer. The resulting print was still intact and had a clear surface after being placed at 300°C for 2 hours. It was tested with a wear-resistant tester and was resistant to friction 28 times. It was placed at room temperature for 1 month. , basically unchanged.
实施例2Example 2
一种边压式打印机油墨的制备方法,包括如下步骤:A method for preparing ink for an edge-pressure printer, including the following steps:
步骤1,将颜料放入乙醇-乙醚液中浸泡20min,急速搅拌60min,过滤后烘干得到洁净的颜料颗粒,所述颜料采用四氧化三铁,所述乙醇-乙醚液中的乙醇与乙醚的体积比为1:3,所述颜料在乙醇-乙醚液中的浓度为400g/L,浸泡的温度为10℃,所述急速搅拌的搅拌速度为800r/min,所述烘干在氮气氛围下烘干,且烘干的温度为100℃;Step 1: Soak the pigment in the ethanol-ether liquid for 20 minutes, stir rapidly for 60 minutes, filter and dry to obtain clean pigment particles. The pigment is ferric oxide, and the ethanol and ether in the ethanol-ether liquid are equal to each other. The volume ratio is 1:3, the concentration of the pigment in the ethanol-ether liquid is 400g/L, the soaking temperature is 10°C, the stirring speed of the rapid stirring is 800r/min, and the drying is under a nitrogen atmosphere Drying, and the drying temperature is 100℃;
步骤2,将甲基三氯硅烷加入至乙醚中搅拌均匀,形成硅醚液,然后将洁净的颜料颗粒放入硅醚液低温超声分散4h,烘干得到镀膜颜料,所述甲基三氯硅烷在乙醚中的浓度为200g/L,搅拌均匀的搅拌速度为200r/min,所述颜料颗粒在硅醚液中的浓度为100g/L,低温超声的超声频率为90kHz,温度为10℃;所述烘干的温度为45℃;Step 2: Add methyltrichlorosilane to diethyl ether and stir evenly to form a silicon ether liquid. Then put the clean pigment particles into the silicon ether liquid for low-temperature ultrasonic dispersion for 4 hours, and dry to obtain a coating pigment. The methyltrichlorosilane The concentration in diethyl ether is 200g/L, the stirring speed for uniform stirring is 200r/min, the concentration of the pigment particles in the silicon ether liquid is 100g/L, the ultrasonic frequency of low-temperature ultrasound is 90kHz, and the temperature is 10°C; so The drying temperature is 45℃;
步骤3,将以含水空气为气体,将镀膜颗粒喷洒至反应釜中沉积3h,得到包裹型颜料,所述镀膜颗粒与含水空气的质量体积比为2g/mL,含水空气的含水量为8%,喷洒速度为20mL/min,沉积的温度为100℃;Step 3: Using water-containing air as gas, spray the coated particles into the reaction kettle for deposition for 3 hours to obtain the wrapped pigment. The mass-to-volume ratio of the coating particles to the water-containing air is 2g/mL, and the water content of the water-containing air is 8%. , the spraying speed is 20mL/min, and the deposition temperature is 100℃;
步骤4,将包裹型颜料放入有机溶剂中搅拌均匀,然后依次加入树脂材料、防腐剂和填料,急速搅拌形成均质浆料;所述有机溶剂采用环己烷和环己酮的混合液,且环己烷和环己酮的体积比为3:1,所述包裹型颜料与有机溶剂的质量比为1:4,所述树脂材料采用丙烯酸树脂与环氧树脂的混合物,且丙烯酸树脂与环氧树脂的质量比为3:2,所述树脂材料与包裹型颜料的质量比为3:2,所述防腐剂采用Proxel GXL,且防腐剂的加入量是包裹型颜料质量的10%,所述填料采用气相白炭黑,且所述气相白炭黑与包裹型颜料的质量比为3:4,急速搅拌的温度为80℃,搅拌速度为2000r/min;Step 4: Put the wrapped pigment into an organic solvent and stir evenly, then add resin materials, preservatives and fillers in sequence, and stir rapidly to form a homogeneous slurry; the organic solvent is a mixture of cyclohexane and cyclohexanone. And the volume ratio of cyclohexane and cyclohexanone is 3:1, the mass ratio of the encapsulated pigment and organic solvent is 1:4, the resin material is a mixture of acrylic resin and epoxy resin, and the acrylic resin and The mass ratio of epoxy resin is 3:2, the mass ratio of the resin material to the wrapped pigment is 3:2, the preservative is Proxel GXL, and the amount of preservative added is 10% of the mass of the wrapped pigment, The filler uses gas phase silica, and the mass ratio of the gas phase silica to the wrapped pigment is 3:4, the temperature of rapid stirring is 80°C, and the stirring speed is 2000r/min;
步骤5,将固化剂加入至均质浆料内研磨细化,得到边压式打印机油墨,所述固化剂采用ZL-1环氧固化剂,所述固化剂的加入量是均质浆料质量的2%,所述研磨处理的温度为50℃,研磨时间为5h。Step 5: Add the curing agent into the homogeneous slurry and grind and refine it to obtain edge pressure printer ink. The curing agent is ZL-1 epoxy curing agent. The amount of the curing agent added is the mass of the homogeneous slurry. 2%, the temperature of the grinding treatment is 50°C, and the grinding time is 5h.
将该实施例制备的油墨通过边压式打印机打印,得到的打印印迹在300℃下放置2h,依然完好,表面清晰,经耐磨试验仪测试,耐摩擦35次,其常温下放置1个月,基本没变化。The ink prepared in this example was printed with an edge pressure printer. The resulting print was still intact and had a clear surface after being placed at 300°C for 2 hours. It was tested by a wear-resistant tester and was resistant to friction 35 times. It was placed at room temperature for 1 month. , basically unchanged.
实施例3Example 3
一种边压式打印机油墨的制备方法,包括如下步骤:A method for preparing ink for an edge-pressure printer, including the following steps:
步骤1,将颜料放入乙醇-乙醚液中浸泡15min,急速搅拌50min,过滤后烘干得到洁净的颜料颗粒,所述颜料采用氧化钴,所述乙醇-乙醚液中的乙醇与乙醚的体积比为1:3,所述颜料在乙醇-乙醚液中的浓度为300g/L,浸泡的温度为8℃,所述急速搅拌的搅拌速度为700r/min,所述烘干在氮气氛围下烘干,且烘干的温度为95℃;Step 1: Soak the pigment in ethanol-ether liquid for 15 minutes, stir rapidly for 50 minutes, filter and dry to obtain clean pigment particles. The pigment is cobalt oxide, and the volume ratio of ethanol to ether in the ethanol-ether liquid is is 1:3, the concentration of the pigment in the ethanol-ether liquid is 300g/L, the soaking temperature is 8°C, the stirring speed of the rapid stirring is 700r/min, and the drying is done under a nitrogen atmosphere , and the drying temperature is 95℃;
步骤2,将甲基三氯硅烷加入至乙醚中搅拌均匀,形成硅醚液,然后将洁净的颜料颗粒放入硅醚液低温超声分散3h,烘干得到镀膜颜料,所述甲基三氯硅烷在乙醚中的浓度为150g/L,搅拌均匀的搅拌速度为150r/min,所述颜料颗粒在硅醚液中的浓度为80g/L,低温超声的超声频率为80kHz,温度为8℃;所述烘干的温度为43℃;Step 2: Add methyltrichlorosilane to diethyl ether and stir evenly to form a silicon ether liquid. Then put the clean pigment particles into the silicon ether liquid for low-temperature ultrasonic dispersion for 3 hours, and dry to obtain a coating pigment. The methyltrichlorosilane The concentration in diethyl ether is 150g/L, the stirring speed for uniform stirring is 150r/min, the concentration of the pigment particles in the silicon ether liquid is 80g/L, the ultrasonic frequency of low-temperature ultrasound is 80kHz, and the temperature is 8°C; The drying temperature is 43℃;
步骤3,将以含水空气为气体,将镀膜颗粒喷洒至反应釜中沉积3h,得到包裹型颜料,所述镀膜颗粒与含水空气的质量体积比为2g/mL,含水空气的含水量为8%,喷洒速度为15mL/min,沉积的温度为95℃;Step 3: Using water-containing air as gas, spray the coated particles into the reaction kettle for deposition for 3 hours to obtain the wrapped pigment. The mass-to-volume ratio of the coating particles to the water-containing air is 2g/mL, and the water content of the water-containing air is 8%. , the spraying speed is 15mL/min, and the deposition temperature is 95℃;
步骤4,将包裹型颜料放入有机溶剂中搅拌均匀,然后依次加入树脂材料、防腐剂和填料,急速搅拌形成均质浆料;所述有机溶剂采用环己烷和环己酮的混合液,且环己烷和环己酮的体积比为2:1,所述包裹型颜料与有机溶剂的质量比为1:3,所述树脂材料采用丙烯酸树脂与环氧树脂的混合物,且丙烯酸树脂与环氧树脂的质量比为3:2,所述树脂材料与包裹型颜料的质量比为3:2,所述防腐剂采用Proxel GXL,且防腐剂的加入量是包裹型颜料质量的8%,所述填料采用气相白炭黑,且所述气相白炭黑与包裹型颜料的质量比为3:4,急速搅拌的温度为75℃,搅拌速度为1500r/min;Step 4: Put the wrapped pigment into an organic solvent and stir evenly, then add resin materials, preservatives and fillers in sequence, and stir rapidly to form a homogeneous slurry; the organic solvent is a mixture of cyclohexane and cyclohexanone. And the volume ratio of cyclohexane and cyclohexanone is 2:1, the mass ratio of the encapsulated pigment and organic solvent is 1:3, the resin material is a mixture of acrylic resin and epoxy resin, and the acrylic resin and The mass ratio of epoxy resin is 3:2, the mass ratio of the resin material to the wrapped pigment is 3:2, the preservative is Proxel GXL, and the amount of preservative added is 8% of the mass of the wrapped pigment, The filler uses gas phase silica, and the mass ratio of the gas phase silica to the wrapped pigment is 3:4, the temperature of rapid stirring is 75°C, and the stirring speed is 1500r/min;
步骤5,将固化剂加入至均质浆料内研磨细化,得到边压式打印机油墨,所述固化剂采用ZL-1环氧固化剂,所述固化剂的加入量是均质浆料质量的2%,所述研磨处理的温度为45℃,研磨时间为4h。Step 5: Add the curing agent into the homogeneous slurry and grind and refine it to obtain edge pressure printer ink. The curing agent is ZL-1 epoxy curing agent. The amount of the curing agent added is the mass of the homogeneous slurry. 2%, the temperature of the grinding treatment is 45°C, and the grinding time is 4h.
将该实施例制备的油墨通过边压式打印机打印,得到的打印印迹在300℃下放置2h,依然完好,表面清晰,经耐磨试验仪测试,耐摩擦30次,其常温下放置1个月,基本没变化。The ink prepared in this example was printed with an edge-pressure printer. The resulting print was still intact and had a clear surface after being placed at 300°C for 2 hours. It was tested with a wear-resistant tester and was resistant to rubbing for 30 times. It was placed at room temperature for 1 month. , basically unchanged.
可以理解的是,以上关于本发明的具体描述,仅用于说明本发明而并非受限于本发明实施例所描述的技术方案。本领域的普通技术人员应当理解,仍然可以对本发明进行修改或等同替换,以达到相同的技术效果;只要满足使用需要,都在本发明的保护范围之内。It can be understood that the above specific description of the present invention is only used to illustrate the present invention and is not limited to the technical solutions described in the embodiments of the present invention. Those of ordinary skill in the art should understand that the present invention can still be modified or equivalently substituted to achieve the same technical effect; as long as the requirements for use are met, they are all within the protection scope of the present invention.
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Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0753545A2 (en) * | 1995-07-13 | 1997-01-15 | Basf Aktiengesellschaft | Goniochromatic brilliant pigments based on transparent non-metallic platy substrates |
| US5653794A (en) * | 1995-12-01 | 1997-08-05 | Scm Chemicals, Inc. | Silane treated inorganic pigments |
| US6120596A (en) * | 1997-01-23 | 2000-09-19 | Marconi Data Systems Inc. | Method for treating pigment particles to improve dispersibility and particle size distribution |
| US20040131527A1 (en) * | 2002-12-20 | 2004-07-08 | Wacker-Chemie Gmbh | Water-wettable silylated metal oxides |
| CN102239117A (en) * | 2008-12-05 | 2011-11-09 | 赢创德固赛有限公司 | Iron-silicon oxide particles with a core-shell structure |
| CN102844384A (en) * | 2010-02-05 | 2012-12-26 | 埃卡特有限公司 | Metal effect pigments coated with SiO2, method for producing said metal effect pigments and use |
| JP2013095888A (en) * | 2011-11-04 | 2013-05-20 | Jgc Catalysts & Chemicals Ltd | Method for producing pigment-encapsulated silica-based particles, pigment-encapsulated silica-based particles, and cosmetics containing the particles |
| CN106243781A (en) * | 2016-07-27 | 2016-12-21 | 升华集团德清华源颜料有限公司 | A kind of preparation method of easy dispersion lipophile iron oxide yellow |
-
2023
- 2023-12-27 CN CN202311821187.7A patent/CN117701060A/en not_active Withdrawn
Patent Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0753545A2 (en) * | 1995-07-13 | 1997-01-15 | Basf Aktiengesellschaft | Goniochromatic brilliant pigments based on transparent non-metallic platy substrates |
| US5653794A (en) * | 1995-12-01 | 1997-08-05 | Scm Chemicals, Inc. | Silane treated inorganic pigments |
| US6120596A (en) * | 1997-01-23 | 2000-09-19 | Marconi Data Systems Inc. | Method for treating pigment particles to improve dispersibility and particle size distribution |
| US20040131527A1 (en) * | 2002-12-20 | 2004-07-08 | Wacker-Chemie Gmbh | Water-wettable silylated metal oxides |
| CN102239117A (en) * | 2008-12-05 | 2011-11-09 | 赢创德固赛有限公司 | Iron-silicon oxide particles with a core-shell structure |
| CN102844384A (en) * | 2010-02-05 | 2012-12-26 | 埃卡特有限公司 | Metal effect pigments coated with SiO2, method for producing said metal effect pigments and use |
| JP2013095888A (en) * | 2011-11-04 | 2013-05-20 | Jgc Catalysts & Chemicals Ltd | Method for producing pigment-encapsulated silica-based particles, pigment-encapsulated silica-based particles, and cosmetics containing the particles |
| CN106243781A (en) * | 2016-07-27 | 2016-12-21 | 升华集团德清华源颜料有限公司 | A kind of preparation method of easy dispersion lipophile iron oxide yellow |
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