WO2017066974A1 - 一种色母粒制备工艺 - Google Patents

一种色母粒制备工艺 Download PDF

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Publication number
WO2017066974A1
WO2017066974A1 PCT/CN2015/092609 CN2015092609W WO2017066974A1 WO 2017066974 A1 WO2017066974 A1 WO 2017066974A1 CN 2015092609 W CN2015092609 W CN 2015092609W WO 2017066974 A1 WO2017066974 A1 WO 2017066974A1
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grinding
masterbatch
parts
mixing
mixed
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PCT/CN2015/092609
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English (en)
French (fr)
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陈少双
黄怀光
黄海灏
黄怀裕
黄麒翁
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揭东巴黎万株纱华纺织有限公司
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Priority to PCT/CN2015/092609 priority Critical patent/WO2017066974A1/zh
Publication of WO2017066974A1 publication Critical patent/WO2017066974A1/zh

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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/25Component parts, details or accessories; Auxiliary operations
    • B29C48/92Measuring, controlling or regulating
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J3/00Processes of treating or compounding macromolecular substances
    • C08J3/20Compounding polymers with additives, e.g. colouring
    • C08J3/22Compounding polymers with additives, e.g. colouring using masterbatch techniques

Definitions

  • the invention relates to the technical field of masterbatch and its preparation process, in particular to a preparation process of masterbatch, in particular to a process for preparing high-speed textile fiber masterbatch.
  • Color masterbatch coloring is the most commonly used plastic coloring method.
  • the masterbatch is generally composed of three parts, namely coloring agent, carrier and dispersing agent. After mixing by high-speed mixing machine, it is broken, extruded and granulated, and colored. Masterbatch has significant advantages in high concentration, good dispersibility and cleanness in plastic processing.
  • the traditional coloring masterbatch production process is usually: PET slice grinding, stirring into the toner, mixing evenly, putting it into a screw extruder, melting the strip, and cutting the pellet to obtain the finished product.
  • This kind of production process requires the PET chips to be mixed into the toner, so the working environment is dusty and dusty.
  • the color masterbatch commonly used in the market has poor dispersibility, tinting strength and hiding power performance, and there are problems such as non-weathering, acid-proof, heat-resistant, and cold-resistant. Many of the existing masterbatch are difficult to mix with the product in actual production, and the color of the product after coloring is not uniform, which does not meet the required requirements.
  • the object of the present invention is to overcome the defects in the prior art and to provide a masterbatch preparation process, and the prepared masterbatch can be easily mixed with the PET product plastic to achieve uniform coloration. It not only improves dispersibility, coloring power, hiding power, but also has weather resistance, acid resistance, heat resistance and cold resistance properties and maintains chemical stability of the pigment.
  • the present invention provides a masterbatch preparation process, and the preparation steps thereof are as follows:
  • carrier grinding mixing polyolefin, polyterephthalate and polyamide resin according to the mixing ratio to obtain a mixed carrier, mixing the carrier and water at a mass ratio of 8:5 and grinding, the grinding time is 30-40 min. ,spare;
  • color material grinding the color material and water are mixed at a mass ratio of 8:5, and then placed in a grinder for grinding for 30 minutes, and then reserved;
  • auxiliary agent grinding the antibacterial agent, the antioxidant and the additive are mixed in proportion, and the mixture is mixed with water at a mass ratio of 8:5, and the grinding time is 40 min, and is reserved;
  • step S7 extrusion granulation: the mixture obtained in step S6 is sent to a screw extruder, the temperature in the screw extruder is controlled at 270-290 ° C, the rotation speed is 360-400 r / min, and the granulation is carried out. Sieve to obtain masterbatch;
  • step S8 Drying: The masterbatch obtained in step S7 is dried in a dryer at a drying temperature of 60 to 80 ° C, and the water content of the masterbatch after drying is controlled to be 3% to 5%.
  • step S4 there is a heating step between the step S4 and the step S5. Specifically, the components after the steps S1 to S4 are mixed, and then placed in a heating dish for heating, and the heating temperature is controlled at 80 ° C, and the heating is performed. 20-30min.
  • the content of each raw material component is in parts by weight: 20-80 parts of the carrier, 5-30 parts of the toner, 5-25 parts of the dispersing agent, and 1-8 parts of the heat stabilizer. 1 to 8 parts of antibacterial agent, 1 to 8 parts of antioxidant, and 1 to 5 parts of additive.
  • the mixture carrier is prepared from the following raw materials in parts by weight: 10-20 parts of polyolefin, 8-15 parts of polyterephthalate, and 5-15 parts of polyamide resin.
  • the polyterephthalate is polyethylene terephthalate, polybutylene terephthalate or polyethylene terephthalate.
  • the toner is one of phthalocyanine red, phthalocyanine blue, phthalocyanine green, light fast red, macromolecular red, macromolecular yellow, permanent yellow, permanent violet, and azo red.
  • the dispersing agent is any one of polyethylene wax, oxidized polyethylene wax, EVA wax, ethylene-vinyl acetate wax, ethylene bis-stearyl amide, and pentaerythritol stearate.
  • the heat stabilizer is epoxy glyceride, epoxy fatty ester, calcium stearate or zinc stearate.
  • the antibacterial agent is chitosan, carboxymethyl chitosan or nano silver.
  • the antioxidant is one of tea polyphenols, phytic acid, tocopherol, flavonoids or Several.
  • the additive is a mixture of a benzotriazole-based ultraviolet absorber and a brightener, and the benzotriazole-based ultraviolet absorber and the brightener are mixed at a mass ratio of 1:1.
  • the preparation process of the invention adopts a mixed carrier to make a synergistic effect between the mixed carrier and the mixed dispersant and the heat stabilizer, ensuring the stability of the material during processing and long-term outdoor use, and the mechanical properties of the material are better. Use color masterbatch to achieve uniform dispersion.
  • the antibacterial agent, the antioxidant and the additive are added to the preparation process of the invention, which can further strengthen the anti-aging property of the masterbatch, improve the antibacterial property of the masterbatch, and achieve the antibacterial and antibacterial effects.
  • the preparation process of the invention uses a plurality of dispersing agents to combine various dispersing agents and mixed carriers to produce a synergistic effect, improve the dispersibility, tinting strength, hiding power of the masterbatch, and has weather resistance, Resistance to acid, heat and cold and maintain the chemical stability of the pigment.
  • the natural antibacterial agent and natural antioxidant are used in the preparation process of the invention to make the masterbatch more environmentally friendly and healthier during use.
  • the invention also adds an anti-ultraviolet absorption additive, which can reduce the temperature of the colored product when used outdoors, and further strengthen the anti-aging property.
  • a masterbatch preparation process the preparation steps are as follows:
  • carrier grinding 10 parts of polyolefin, 8 parts of polyterephthalate, 5 parts of polyamide resin are mixed to prepare a mixed carrier, 20 parts of the mixed carrier and water are mixed at a mass ratio of 8:5, and then ground.
  • the grinding time is 30-40 min, and the polyterephthalate is polyethylene terephthalate, polybutylene terephthalate or polyethylene terephthalate;
  • color material grinding mixing 5 parts of color material and water according to mass ratio of 8:5, and then grinding in a grinder for 30 minutes, and then standby;
  • the toner is phthalocyanine red, phthalocyanine blue, phthalocyanine green
  • the heating temperature is controlled at 80 ° C, heating for 20 min;
  • step S7 high-speed grinding: the components after the mixing and grinding in step S6 are put into a high-speed mixer for high-speed grinding and stirring, and the grinding time is 20 min;
  • step S8 extrusion granulation: the mixture obtained in step S7 is sent to a screw extruder, the temperature in the screw extruder is controlled at 270 ° C, the rotation speed is 360 r / min, extrusion, granulation, sieving, color Masterbatch
  • the masterbatch obtained in the step S8 is dried in a dryer at a drying temperature of 60 to 80 ° C, and the water content of the masterbatch after drying is controlled to 5%.
  • a masterbatch preparation process the preparation steps are as follows:
  • carrier grinding 13 parts of polyolefin, 10 parts of polyterephthalate, 8 parts of polyamide resin are mixed to prepare a mixed carrier, 40 parts of the mixed carrier and water are mixed at a mass ratio of 8:5, and then ground.
  • the grinding time is 30-40 min, and the polyterephthalate is polyethylene terephthalate, polybutylene terephthalate or polyethylene terephthalate;
  • color material grinding 10 parts of the color material and water are mixed at a mass ratio of 8:5, and then placed in a grinder for grinding for 30 minutes, and then reserved; the toner is phthalocyanine red, phthalocyanine blue, phthalocyanine green One of light fast red, macromolecular red, macromolecular yellow, permanent yellow, permanent violet, and azo red;
  • the dispersing agent is polyethylene wax, Any two of oxidized polyethylene wax, EVA wax, ethylene-vinyl acetate wax, ethylene bis-stearyl amide, and pentaerythritol stearate;
  • the heating temperature is controlled at 80 ° C, heating for 25 min;
  • step S7 high-speed grinding: the components after the mixing and grinding in step S6 are put into a high-speed mixer for high-speed grinding and stirring, and the grinding time is 20 min;
  • step S8 extrusion granulation: the mixture obtained in step S7 is sent to a screw extruder, the temperature in the screw extruder is controlled at 280 ° C, the rotation speed is 380 r / min extrusion, granulation, sieving, color Masterbatch
  • the masterbatch obtained in the step S8 is dried in a dryer at a drying temperature of 60 to 80 ° C, and the water content of the masterbatch after drying is controlled to 4%.
  • a masterbatch preparation process the preparation steps are as follows:
  • carrier grinding 16 parts of polyolefin, 13 parts of polyterephthalate, 12 parts of polyamide resin are mixed to prepare a mixed carrier, 60 parts of the mixed carrier and water are mixed at a mass ratio of 8:5, and then ground.
  • the grinding time is 30-40 min, and the polyterephthalate is polyethylene terephthalate, polybutylene terephthalate or polyethylene terephthalate;
  • color material grinding 20 parts of the color material and water are mixed at a mass ratio of 8:5, and then placed in a grinder for grinding for 30 minutes, and then reserved; the toner is phthalocyanine red, phthalocyanine blue, phthalocyanine green One of light fast red, macromolecular red, macromolecular yellow, permanent yellow, permanent violet, and azo red;
  • the dispersing agent is polyethylene wax, Any two of oxidized polyethylene wax, EVA wax, ethylene-vinyl acetate wax, ethylene bis-stearyl amide, and pentaerythritol stearate;
  • the components after the steps S1 to S4 are mixed, and then placed in a heating dish for heating, the heating temperature is controlled at 80 ° C, heating for 30 min;
  • step S7 high-speed grinding: the components after the mixing and grinding in step S6 are put into a high-speed mixer for high-speed grinding and stirring, and the grinding time is 20 min;
  • step S8 extrusion granulation: the mixture obtained in step S7 is sent to a screw extruder, the temperature in the screw extruder is controlled at 285 ° C, the rotation speed is 400 r / min extrusion, granulation, sieving, color Masterbatch
  • the masterbatch obtained in the step S8 is dried in a dryer at a drying temperature of 60 to 80 ° C, and the water content of the masterbatch after drying is controlled to 3%.
  • a masterbatch preparation process the preparation steps are as follows:
  • carrier grinding 20 parts of polyolefin, 15 parts of polyterephthalate, 15 parts of polyamide resin are mixed to prepare a mixed carrier, 80 parts of the mixed carrier and water are mixed at a mass ratio of 8:5, and then ground.
  • the grinding time is 30-40 min, and the polyterephthalate is polyethylene terephthalate, polybutylene terephthalate or polyethylene terephthalate;
  • color material grinding 30 parts of color material and water are mixed at a mass ratio of 8:5, and then placed in a grinder for grinding for 30 minutes, and then reserved; the toner is phthalocyanine red, phthalocyanine blue, phthalocyanine green One of light fast red, macromolecular red, macromolecular yellow, permanent yellow, permanent violet, and azo red;
  • the dispersing agent is polyethylene wax, Any two of oxidized polyethylene wax, EVA wax, ethylene-vinyl acetate wax, ethylene bis-stearyl amide, and pentaerythritol stearate;
  • the components after the steps S1 to S4 are mixed, and then placed in a heating dish for heating, the heating temperature is controlled at 80 ° C, heating for 30 min;
  • step S7 high-speed grinding: the components after the mixing and grinding in step S6 are put into a high-speed mixer for high-speed grinding and stirring, and the grinding time is 20 min;
  • step S8 extrusion granulation: the mixture obtained in step S7 is sent to a screw extruder, the temperature in the screw extruder is controlled at 290 ° C, the rotation speed is 400 r / min, extrusion, granulation, sieving, color Masterbatch
  • the masterbatch obtained in the step S8 is dried in a dryer at a drying temperature of 60 to 80 ° C, and the water content of the masterbatch after drying is controlled to 3%.
  • the preparation of the masterbatch of the present invention produces a synergistic effect between the mixed carrier and the mixed dispersant and the heat stabilizer, ensuring the stability of the material during processing and long-term outdoor use, and the mechanics of the material.
  • Better performance use color masterbatch to achieve uniform dispersion effect; use synergistic dispersant and mixed carrier to produce synergistic effect, improve the dispersibility, tinting strength and hiding power of masterbatch; at the same time, add antibacterial agent, antioxidant and The additive can further strengthen the anti-aging property of the masterbatch, improve the antibacterial property of the masterbatch, and achieve the antibacterial and antibacterial effects.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
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Abstract

一种色母粒制备工艺包括:载体研磨、色料研磨、配料研磨、辅助剂研磨、混合研磨、高速研磨、挤出造粒、干燥步骤。采用该工艺制备的色母粒能够与PET制品塑料容易混合,达到着色均匀的效果。不仅提高了分散性、着色力、遮盖力,而且具有耐候性、耐酸性、耐热性和耐寒性的性能和保持颜料的化学稳定性,色母粒在使用过程中更环保、更健康。

Description

一种色母粒制备工艺 技术领域
本发明涉及色母粒及其制备工艺技术领域,具体涉及一种色母粒制备工艺,尤其是一种用于高速纺织纤维色母粒制备工艺。
背景技术
色母粒着色是现今最普遍采用的塑料着色法,色母粒一般由三部分组成,即着色剂、载体和分散剂,通过高速混练机混炼后,破碎,挤出拉成粒,色母粒在塑料加工过程中,具有浓度高、分散性好、清洁等显著优点。
传统的着色母粒生产工艺通常为:PET切片磨粉,搅入色粉,混合均匀,投入螺杆挤出机,熔化后拉条,切粒得成品。这种生产工艺由于需将PET切片磨粉再混入色粉,因此生产过程中,工作环境灰尘、粉尘多。
市面上常用色母粒的分散性、着色力、遮盖力性能方面比较差,同时存在不耐候、不耐酸、不耐热、不耐寒等问题。现有的很多色母粒在实际生产中却难以与制品混合,制品着色后颜色不均匀,达不到所需要的要求。
发明内容
本发明的目的在于克服现有技术中的缺陷,提供一种色母粒制备工艺,制备得到的色母粒能够与PET制品塑料容易混合,达到着色均匀的效果。不仅提高了分散性、着色力、遮盖力,而且具有耐候性、耐酸性、耐热性和耐寒性的性能和保持颜料的化学稳定性。
为了实现上述目的,本发明提供的一种色母粒制备工艺,其制备步骤依次为:
S1、载体研磨:将聚烯烃、聚对苯二甲酸脂、聚酰胺树脂按配比混合后制得混合载体,混合载体与水按质量比为8:5混合后进行研磨,研磨时间为30~40min,备用;
S2、色料研磨:将色料与水按质量比为8:5混合后放入研磨机进行研磨30min后,备用;
S3、配料研磨:将分散剂和热稳定剂按比例混合后,与水按质量比为8:5混 合进行研磨,研磨时间为30min,备用;
S4、辅助剂研磨:将抗菌剂、抗氧化剂和添加剂按比例混合,与水按质量比为8:5混合进行研磨,研磨时间为40min,备用;
S5、混合研磨:将步骤S1~S4研磨后的各组分混合后,搅拌10min,进行混合研磨,研磨时间为30min;
S6、高速研磨:将经过步骤S5混合研磨后的各组分投入高速拌和机中进行高速研磨和搅拌,研磨时间为20min;
S7、挤出造粒:将步骤S6所得的混合物料输送至螺杆挤出机内,螺杆挤出机内的温度控制在270~290℃,转速为360~400r/min挤出,造粒,过筛,得到色母粒;
S8、干燥:将步骤S7得到的色母粒在干燥机内进行干燥处理,干燥温度为60~80℃,干燥后的色母粒含水量控制在3%-5%。
进一步的,所述步骤S4与步骤S5之间还有加热步骤,具体为:将步骤S1~S4研磨后的各组分混合后,置于加热皿中进行加热,加热温度控制在80℃,加热20-30min。
更进一步的,所述的色母粒制备工艺中各原料成分含量按重量份数计:载体20~80份,色粉5~30份,分散剂5~25份,热稳定剂1~8份,抗菌剂1~8份,抗氧化剂1~8份,添加剂1~5份。
更进一步的,所述步骤S1中混合物载体由按重量份数计的以下原料制备而成:聚烯烃10~20份,聚对苯二甲酸脂8~15份,聚酰胺树脂5~15份。
优选的,所述的聚对苯二甲酸脂为聚对苯二甲酸乙二酯、聚对苯二甲酸丁二酯或聚对苯二甲酸乙二醇酯。
优选的,所述的色粉为酞菁红、酞菁蓝、酞菁绿、耐晒大红、大分子红、大分子黄、永固黄、永固紫、偶氮红中的一种。
优选的,所述的分散剂为聚乙烯蜡、氧化聚乙烯蜡、EVA蜡、乙烯-醋酸乙烯蜡、乙撑双硬酯酰胺、季戊四醇硬脂酸酯中的任意两种。
优选的,所述的热稳定剂为环氧甘油酯、环氧脂肪酯、硬脂酸钙或硬脂酸锌。
优选的,所述的抗菌剂为壳聚糖、羧甲基壳聚糖或纳米银。
优选的,所述的抗氧化剂为茶多酚、植酸、生育酚、黄酮类物质中的一种或 几种。
优选的,所述的添加剂为苯并三唑类紫外线吸收剂和增亮剂的混合物,苯并三唑类紫外线吸收剂和增亮剂按质量比为1:1混合。
本发明的有益效果:
1、本发明制备工艺采用混合型载体,使混合载体与混合分散剂、热稳定剂产生协同效应,确保材料在加工过程中和在户外长期使用中都能保证稳定性,材料的力学性能更佳,使用色母粒着色达到均匀分散的效果。
2、本发明制备工艺中加入了抗菌剂、抗氧化剂和添加剂,可以进一步强化色母粒抗老化性能,提高色母粒的抗菌性能,达到抗菌、抑菌的作用。
3、本发明制备工艺使用多种分散剂的复配,使各种分散剂和混合载体结合使用,产生协同效果,提高了色母粒的分散性、着色力、遮盖力,而且具有耐候性、耐酸性、耐热性和耐寒性的性能和保持颜料的化学稳定性。
4、本发明制备工艺中使用天然的抗菌剂和天然抗氧化剂,使色母粒在使用过程中更环保、更健康。
5、本发明同时添加了抗紫外吸收添加剂,可以降低着色制品在户外使用时的温度,进一步强化其抗老化性能。
具体实施方式
以下对本发明的实施方式作详细说明。应该强调的是,下述说明仅仅是示例性的,而不是为了限制本发明的范围及其应用。
实施例1
一种色母粒制备工艺,其制备步骤依次为:
S1、载体研磨:将10份聚烯烃,8份聚对苯二甲酸脂,5份聚酰胺树脂混合后制得混合载体,20份混合载体与水按质量比为8:5混合后进行研磨,研磨时间为30~40min,备用;所述的聚对苯二甲酸脂为聚对苯二甲酸乙二酯、聚对苯二甲酸丁二酯或聚对苯二甲酸乙二醇酯;
S2、色料研磨:将5份色料与水按质量比为8:5混合后放入研磨机进行研磨30min后,备用;所述的色粉为酞菁红、酞菁蓝、酞菁绿、耐晒大红、大分子红、大分子黄、永固黄、永固紫、偶氮红中的一种;
S3、配料研磨:将5份分散剂和1份环氧甘油酯混合后,与水按质量比为 8:5混合后进行研磨,研磨时间为30min,备用;所述的分散剂为聚乙烯蜡、氧化聚乙烯蜡、EVA蜡、乙烯-醋酸乙烯蜡、乙撑双硬酯酰胺、季戊四醇硬脂酸酯中的任意两种;
S4、辅助剂研磨:将1份壳聚糖,1份茶多酚,1份苯并三唑类紫外线吸收剂和1份增亮剂混合后,与水按质量比为8:5混合后进行研磨,研磨时间为40min,备用;
S5、将步骤S1~S4研磨后的各组分混合后,置于加热皿中进行加热,加热温度控制在80℃,加热20min;
S6、混合研磨:将经过步骤S5加热的混合搅拌10min,进行混合研磨,研磨时间为30min;
S7、高速研磨:将经过步骤S6混合研磨后的各组分投入高速拌和机中进行高速研磨和搅拌,研磨时间为20min;
S8、挤出造粒:将步骤S7所得的混合物料输送至螺杆挤出机内,螺杆挤出机内的温度控制在270℃,转速为360r/min挤出,造粒,过筛,得到色母粒;
S9、干燥:将步骤S8得到的色母粒在干燥机内进行干燥处理,干燥温度为60~80℃,干燥后的色母粒含水量控制在5%。
实施例2
一种色母粒制备工艺,其制备步骤依次为:
S1、载体研磨:将13份聚烯烃,10份聚对苯二甲酸脂,8份聚酰胺树脂混合后制得混合载体,40份混合载体与水按质量比为8:5混合后进行研磨,研磨时间为30~40min,备用;所述的聚对苯二甲酸脂为聚对苯二甲酸乙二酯、聚对苯二甲酸丁二酯或聚对苯二甲酸乙二醇酯;
S2、色料研磨:将10份色料与水按质量比为8:5混合后放入研磨机进行研磨30min后,备用;所述的色粉为酞菁红、酞菁蓝、酞菁绿、耐晒大红、大分子红、大分子黄、永固黄、永固紫、偶氮红中的一种;
S3、配料研磨:将10份分散剂和3份环氧脂肪酯混合后,与水按质量比为8:5混合进行研磨,研磨时间为30min,备用;所述的分散剂为聚乙烯蜡、氧化聚乙烯蜡、EVA蜡、乙烯-醋酸乙烯蜡、乙撑双硬酯酰胺、季戊四醇硬脂酸酯中的任意两种;
S4、辅助剂研磨:将3份羧甲基壳聚糖,3份植酸,2份苯并三唑类紫外线吸收剂和3份增亮剂混合后,与水按质量比为8:5混合进行研磨,研磨时间为40min,备用;
S5、将步骤S1~S4研磨后的各组分混合后,置于加热皿中进行加热,加热温度控制在80℃,加热25min;
S6、混合研磨:将经过步骤S5加热的混合搅拌10min,进行混合研磨,研磨时间为30min;
S7、高速研磨:将经过步骤S6混合研磨后的各组分投入高速拌和机中进行高速研磨和搅拌,研磨时间为20min;
S8、挤出造粒:将步骤S7所得的混合物料输送至螺杆挤出机内,螺杆挤出机内的温度控制在280℃,转速为380r/min挤出,造粒,过筛,得到色母粒;
S9、干燥:将步骤S8得到的色母粒在干燥机内进行干燥处理,干燥温度为60~80℃,干燥后的色母粒含水量控制在4%。
实施例3
一种色母粒制备工艺,其制备步骤依次为:
S1、载体研磨:将16份聚烯烃,13份聚对苯二甲酸脂,12份聚酰胺树脂混合后制得混合载体,60份混合载体与水按质量比为8:5混合后进行研磨,研磨时间为30~40min,备用;所述的聚对苯二甲酸脂为聚对苯二甲酸乙二酯、聚对苯二甲酸丁二酯或聚对苯二甲酸乙二醇酯;
S2、色料研磨:将20份色料与水按质量比为8:5混合后放入研磨机进行研磨30min后,备用;所述的色粉为酞菁红、酞菁蓝、酞菁绿、耐晒大红、大分子红、大分子黄、永固黄、永固紫、偶氮红中的一种;
S3、配料研磨:将20份分散剂和6份硬脂酸钙混合后,与水按质量比为8:5混合进行研磨,研磨时间为30min,备用;所述的分散剂为聚乙烯蜡、氧化聚乙烯蜡、EVA蜡、乙烯-醋酸乙烯蜡、乙撑双硬酯酰胺、季戊四醇硬脂酸酯中的任意两种;
S4、辅助剂研磨:将6份纳米银,6份生育酚,4份苯并三唑类紫外线吸收剂和4份增亮剂混合后,与水按质量比为8:5混合进行研磨,研磨时间为40min,备用;
S5、将步骤S1~S4研磨后的各组分混合后,置于加热皿中进行加热,加热温度控制在80℃,加热30min;
S6、混合研磨:将经过步骤S5加热的混合搅拌10min,进行混合研磨,研磨时间为30min;
S7、高速研磨:将经过步骤S6混合研磨后的各组分投入高速拌和机中进行高速研磨和搅拌,研磨时间为20min;
S8、挤出造粒:将步骤S7所得的混合物料输送至螺杆挤出机内,螺杆挤出机内的温度控制在285℃,转速为400r/min挤出,造粒,过筛,得到色母粒;
S9、干燥:将步骤S8得到的色母粒在干燥机内进行干燥处理,干燥温度为60~80℃,干燥后的色母粒含水量控制在3%。
实施例4
一种色母粒制备工艺,其制备步骤依次为:
S1、载体研磨:将20份聚烯烃,15份聚对苯二甲酸脂,15份聚酰胺树脂混合后制得混合载体,80份混合载体与水按质量比为8:5混合后进行研磨,研磨时间为30~40min,备用;所述的聚对苯二甲酸脂为聚对苯二甲酸乙二酯、聚对苯二甲酸丁二酯或聚对苯二甲酸乙二醇酯;
S2、色料研磨:将30份色料与水按质量比为8:5混合后放入研磨机进行研磨30min后,备用;所述的色粉为酞菁红、酞菁蓝、酞菁绿、耐晒大红、大分子红、大分子黄、永固黄、永固紫、偶氮红中的一种;
S3、配料研磨:将25份分散剂和8份硬脂酸锌混合后,与水按质量比为8:5混合进行研磨,研磨时间为30min,备用;所述的分散剂为聚乙烯蜡、氧化聚乙烯蜡、EVA蜡、乙烯-醋酸乙烯蜡、乙撑双硬酯酰胺、季戊四醇硬脂酸酯中的任意两种;
S4、辅助剂研磨:将8份壳聚糖,8份黄酮类物质,5份苯并三唑类紫外线吸收剂和5份增亮剂混合后,与水按质量比为8:5混合进行研磨,研磨时间为40min,备用;
S5、将步骤S1~S4研磨后的各组分混合后,置于加热皿中进行加热,加热温度控制在80℃,加热30min;
S6、混合研磨:将经过步骤S5加热的混合搅拌10min,进行混合研磨,研 磨时间为30min;
S7、高速研磨:将经过步骤S6混合研磨后的各组分投入高速拌和机中进行高速研磨和搅拌,研磨时间为20min;
S8、挤出造粒:将步骤S7所得的混合物料输送至螺杆挤出机内,螺杆挤出机内的温度控制在290℃,转速为400r/min挤出,造粒,过筛,得到色母粒;
S9、干燥:将步骤S8得到的色母粒在干燥机内进行干燥处理,干燥温度为60~80℃,干燥后的色母粒含水量控制在3%。
为验证本发明制备的色母粒是否达到预期的发明效果,对本发明制备的色母粒进行性能试验分析,结果如下所示:
Figure PCTCN2015092609-appb-000001
从上表可以看出,本发明制备色母粒中使混合载体与混合分散剂、热稳定剂产生协同效应,确保材料在加工过程中和在户外长期使用中都能保证稳定性,材料的力学性能更佳,使用色母粒着色达到均匀分散的效果;使用复配分散剂和混合载体产生协同效果,提高了色母粒的分散性、着色力、遮盖力;同时,加入抗菌剂、抗氧化剂和添加剂,可以进一步强化色母粒抗老化性能,提高色母粒的抗菌性能,达到抗菌、抑菌的作用。
最后应说明的是:显然,上述实施例仅仅是为清楚地说明本发明所作的举例,而并非对实施方式的限定。对于所属领域的普通技术人员来说,在上述说明的基 础上还可以做出其它不同形式的变化或变动。这里无需也无法对所有的实施方式予以穷举。而由此所引申出的显而易见的变化或变动仍处于本发明的保护范围之中。

Claims (10)

  1. 一种色母粒制备工艺,其特征在于,其制备步骤依次为:
    S1、载体研磨:将聚烯烃、聚对苯二甲酸脂、聚酰胺树脂按配比混合后制得混合载体,混合载体与水按质量比为8:5混合后进行研磨,研磨时间为30~40min,备用;
    S2、色料研磨:将色料与水按质量比为8:5混合后放入研磨机进行研磨30min后,备用;
    S3、配料研磨:将分散剂和热稳定剂按比例混合后,与水按质量比为8:5混合后进行研磨,研磨时间为30min,备用;
    S4、辅助剂研磨:将抗菌剂、抗氧化剂和添加剂按比例混合,与水按质量比为8:5混合后进行研磨,研磨时间为40min,备用;
    S5、混合研磨:将步骤S1~S4研磨后的各组分混合后,搅拌10min,进行混合研磨,研磨时间为30min;
    S6、高速研磨:将经过步骤S5混合研磨后的各组分投入高速拌和机中进行高速研磨和搅拌,研磨时间为20min;
    S7、挤出造粒:将步骤S6所得的混合物料输送至螺杆挤出机内,螺杆挤出机内的温度控制在270~290℃,转速为360~400r/min挤出,造粒,过筛,得到色母粒;
    S8、干燥:将步骤S7得到的色母粒在干燥机内进行干燥处理,干燥温度为60~80℃,干燥后的色母粒含水量控制在3%-5%。
  2. 根据权利要求1所述的一种色母粒制备工艺,其特征在于,所述步骤S4与步骤S5之间还有加热步骤,具体为:将步骤S1~S4研磨后的各组分混合后,置于加热皿中进行加热,加热温度控制在80℃,加热20-30min。
  3. 根据权利要求1所述的一种色母粒制备工艺,其特征在于,所述的色母粒制备工艺中各原料成分含量按重量份数计:载体20~80份,色粉5~30份,分散剂5~25份,热稳定剂1~8份,抗菌剂1~8份,抗氧化剂1~8份,添加剂1~5份。
  4. 根据权利要求1所述的一种色母粒制备工艺,其特征在于,所述步骤S1中混合物载体由按重量份数计的以下原料制备而成:聚烯烃10~20份,聚对苯二 甲酸脂8~15份,聚酰胺树脂5~15份;所述的聚对苯二甲酸脂为聚对苯二甲酸乙二酯、聚对苯二甲酸丁二酯或聚对苯二甲酸乙二醇酯。
  5. 根据权利要求1-4任一项所述的一种色母粒制备工艺,其特征在于,所述的色粉为酞菁红、酞菁蓝、酞菁绿、耐晒大红、大分子红、大分子黄、永固黄、永固紫、偶氮红中的一种。
  6. 根据权利要求1-4任一项所述的一种色母粒制备工艺,其特征在于,所述的分散剂为聚乙烯蜡、氧化聚乙烯蜡、EVA蜡、乙烯-醋酸乙烯蜡、乙撑双硬酯酰胺、季戊四醇硬脂酸酯中的任意两种。
  7. 根据权利要求1-4任一项所述的一种色母粒制备工艺,其特征在于,所述的热稳定剂为环氧甘油酯、环氧脂肪酯、硬脂酸钙或硬脂酸锌。
  8. 根据权利要求1-4任一项所述的一种色母粒制备工艺,其特征在于,所述的抗菌剂为壳聚糖、羧甲基壳聚糖或纳米银。
  9. 根据权利要求1-4任一项所述的一种色母粒制备工艺,其特征在于,所述的抗氧化剂为茶多酚、植酸、生育酚、黄酮类物质中的一种或几种。
  10. 根据权利要求1-4任一项所述的一种色母粒制备工艺,其特征在于,所述的添加剂为苯并三唑类紫外线吸收剂和增亮剂的混合物,苯并三唑类紫外线吸收剂和增亮剂按质量比为1:1混合。
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Publication number Priority date Publication date Assignee Title
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CN111077089A (zh) * 2020-01-16 2020-04-28 北京龙苑伟业新材料有限公司 一种冲压模具检测用刮削显示剂及其制备方法
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Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB774078A (en) * 1953-04-30 1957-05-08 Laszlo Auer Improvements in textile decoration and compositions therefor
CN102010539A (zh) * 2010-11-12 2011-04-13 上海剑徽塑胶科技有限公司 一种塑料着色微珠色母粒的组成及其加工工艺
CN103131158A (zh) * 2013-01-31 2013-06-05 杜县南 一种抗静电色母粒及其制备方法
CN102516691B (zh) * 2011-10-28 2013-12-11 江苏昊华光伏科技有限公司 聚偏二氟乙烯太阳能背板膜专用白色母粒的制造方法

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB774078A (en) * 1953-04-30 1957-05-08 Laszlo Auer Improvements in textile decoration and compositions therefor
CN102010539A (zh) * 2010-11-12 2011-04-13 上海剑徽塑胶科技有限公司 一种塑料着色微珠色母粒的组成及其加工工艺
CN102516691B (zh) * 2011-10-28 2013-12-11 江苏昊华光伏科技有限公司 聚偏二氟乙烯太阳能背板膜专用白色母粒的制造方法
CN103131158A (zh) * 2013-01-31 2013-06-05 杜县南 一种抗静电色母粒及其制备方法

Cited By (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109061818A (zh) * 2018-08-23 2018-12-21 镇江荣诚管业有限公司 一种硅芯管的制作方法
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