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CN107955358A - A kind of special light LED material of optical electron and preparation method thereof - Google Patents

A kind of special light LED material of optical electron and preparation method thereof Download PDF

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CN107955358A
CN107955358A CN201711344654.6A CN201711344654A CN107955358A CN 107955358 A CN107955358 A CN 107955358A CN 201711344654 A CN201711344654 A CN 201711344654A CN 107955358 A CN107955358 A CN 107955358A
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施享
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Maanshan Songhe Information Technology Co Ltd
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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    • C08L63/00Compositions of epoxy resins; Compositions of derivatives of epoxy resins
    • HELECTRICITY
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    • H10HINORGANIC LIGHT-EMITTING SEMICONDUCTOR DEVICES HAVING POTENTIAL BARRIERS
    • H10H20/00Individual inorganic light-emitting semiconductor devices having potential barriers, e.g. light-emitting diodes [LED]
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Abstract

本发明涉及一种光学电子专用发光二极管材料及其制备方法,原料组成成分按重量份数由以下比例组成:聚碳酸酯10‑15份、聚丙烯3‑5份、砷化镓4‑6份、磷化镓5‑7份、磷砷化镓4‑5份、纳米光纤4‑6份、环氧树脂10‑15份、聚氧乙烯聚氧丙醇胺醚3‑5份、酸酣3‑4份、离模剂2‑3份、氢氧化镁2‑3份、白炭黑2‑4份、乙醇20‑30份。本发明材料易得,成本低,环保安全,结构密度小,固化效果强,具有良好的抗压能力,耐磨性强,电能转换率高,发光效果好,可呈现多种颜色的光束,耐高温高压,绝缘阻燃,防水防潮,化学性质稳定,延长使用寿命,适用范围广,可回收利用,提高综合经济效益,保护环境卫生。The invention relates to a special light-emitting diode material for optical electronics and a preparation method thereof. The composition of the raw materials is composed of the following proportions in parts by weight: 10-15 parts of polycarbonate, 3-5 parts of polypropylene, and 4-6 parts of gallium arsenide , 5-7 parts of gallium phosphide, 4-5 parts of gallium arsenide phosphide, 4-6 parts of nano-fiber, 10-15 parts of epoxy resin, 3-5 parts of polyoxyethylene polyoxypropanolamine ether, 3 parts of acid ‑4 parts, 2‑3 parts of release agent, 2‑3 parts of magnesium hydroxide, 2‑4 parts of white carbon black, 20‑30 parts of ethanol. The material of the present invention is easy to obtain, low in cost, environmentally friendly and safe, low in structure density, strong in curing effect, good in compression resistance, strong in wear resistance, high in electric energy conversion rate, good in luminous effect, can present beams of various colors, and is durable High temperature and high pressure, insulation and flame retardant, waterproof and moisture-proof, stable chemical properties, extended service life, wide application range, recyclable, improve comprehensive economic benefits, and protect environmental hygiene.

Description

一种光学电子专用发光二极管材料及其制备方法A light-emitting diode material for optical electronics and its preparation method

技术领域technical field

本发明涉及电子光学材料领域,具体涉及一种光学电子专用发光二极管材料及其制备方法。The invention relates to the field of electronic optical materials, in particular to a light-emitting diode material dedicated to optical electronics and a preparation method thereof.

背景技术Background technique

随着社会的发展,电子光学的发展很迅速,不仅在光学转化率上具有很大的提高,且在去配套的材料上也有很大的突破,现有的发光二极管材料的技术也在不断的提高,就目前而言,发光二极管的材料上由于热稳定性不显著,易发生氧化等现象,造成阻燃效果的降低,从而降低工作效率。With the development of society, the development of electron optics is very rapid. Not only has the optical conversion rate been greatly improved, but also there has been a great breakthrough in the matching materials. The existing technology of light-emitting diode materials is also constantly improving. Improvement, as far as the current situation is concerned, due to the insignificant thermal stability of the material of the light-emitting diode, oxidation and other phenomena are prone to occur, resulting in a reduction in the flame-retardant effect, thereby reducing work efficiency.

发明内容Contents of the invention

本发明的目的是为了克服以上的不足而提供一种光学电子专用发光二极管材料及其制备方法。The object of the present invention is to provide a light-emitting diode material for optical electronics and a preparation method thereof in order to overcome the above disadvantages.

本发明的技术方案包括:一种光学电子专用发光二极管材料及其制备方法,原料组成成分按重量份数由以下比例组成:聚碳酸酯10-15份、聚丙烯3-5份、砷化镓4-6份、磷化镓5-7份、磷砷化镓4-5份、纳米光纤4-6份、环氧树脂10-15份、聚氧乙烯聚氧丙醇胺醚3-5份、酸酣3-4份、离模剂2-3份、氢氧化镁2-3份、白炭黑2-4份、乙醇20-30份。The technical scheme of the present invention includes: a special light-emitting diode material for optical electronics and its preparation method, the raw material components are composed of the following proportions in parts by weight: 10-15 parts of polycarbonate, 3-5 parts of polypropylene, gallium arsenide 4-6 parts, 5-7 parts of gallium phosphide, 4-5 parts of gallium arsenide phosphide, 4-6 parts of nanofiber, 10-15 parts of epoxy resin, 3-5 parts of polyoxyethylene polyoxypropanolamine ether , 3-4 parts of acid, 2-3 parts of release agent, 2-3 parts of magnesium hydroxide, 2-4 parts of white carbon black, 20-30 parts of ethanol.

本发明的进一步改进在于:其制备方法如下:The further improvement of the present invention is: its preparation method is as follows:

A、将砷化镓、磷化镓和磷砷化镓进行搅拌均匀,搅拌速率为380-420r/min,将其投入反应釜中加入纳米光纤进行高温缩聚,适量乙醇为溶剂,压力为1.5-1.8MPa,温度设为380-420℃,以白炭黑为催化剂,20-30min后得混合物A;A. Stir gallium arsenide, gallium phosphide and gallium arsenide phosphide evenly at a stirring rate of 380-420r/min, put them into the reaction kettle and add nano-fibers for high-temperature polycondensation, with an appropriate amount of ethanol as a solvent, and a pressure of 1.5- 1.8MPa, set the temperature at 380-420°C, use white carbon black as the catalyst, and obtain mixture A after 20-30min;

B、将聚碳酸酯、聚丙烯和环氧树脂进行聚合反应,温度设为220-240℃,压力为1.3-1.5MPa,15-20min后冷却至65-80℃时,依次加入聚氧乙烯聚氧丙醇胺醚、酸酐、离模剂和氢氧化镁进行搅拌,搅拌速率为480-540r/min,得混合物B;B. Polymerize polycarbonate, polypropylene and epoxy resin, set the temperature at 220-240°C, pressure at 1.3-1.5MPa, cool to 65-80°C after 15-20min, then add polyoxyethylene poly Oxypropanolamine ether, acid anhydride, release agent and magnesium hydroxide are stirred at a stirring rate of 480-540r/min to obtain mixture B;

C、将混合物B投入模具中,再将混合物A浸泡其中,浸泡2-3h后进行脱模,投入烘干机中进行烘干处理,烘干温度为200-220℃,将其进行挤压、锻造,受力为180-200N/cm2,得产物。C. Put the mixture B into the mold, then soak the mixture A in it, soak it for 2-3 hours, remove the mold, put it into the dryer for drying treatment, the drying temperature is 200-220°C, and squeeze it, Forging, with a force of 180-200N/cm 2 , to obtain a product.

本发明的有益效果:本发明材料易得,成本低,环保安全,结构密度小,固化效果强,具有良好的抗压能力,耐磨性强,电能转换率高,提高工作效率,发光效果好,可呈现多种颜色的光束,耐高温高压,绝缘阻燃,防水防潮,化学性质稳定,延长使用寿命,适用范围广,可回收利用,提高综合经济效益,保护环境卫生。Beneficial effects of the present invention: the material of the present invention is easy to obtain, low in cost, environmentally safe, small in structure density, strong in curing effect, good in compressive capacity, strong in wear resistance, high in electric energy conversion rate, improves work efficiency, and has good luminous effect , can present a variety of colors of light beams, high temperature and high pressure resistance, insulation and flame retardant, waterproof and moisture-proof, stable chemical properties, extended service life, wide application range, recyclable, improve comprehensive economic benefits, and protect environmental sanitation.

具体实施方式:Detailed ways:

为了加深对本发明的理解,下面将结合实施例对本发明作进一步详述,该实施例仅用于解释本发明,并不构成对本发明保护范围的限定。In order to deepen the understanding of the present invention, the present invention will be further described below in conjunction with examples, which are only used to explain the present invention and do not constitute a limitation to the protection scope of the present invention.

实施例1Example 1

一种光学电子专用发光二极管材料及其制备方法,原料组成成分按重量份数由以下比例组成:聚碳酸酯13份、聚丙烯4份、砷化镓5份、磷化镓6份、磷砷化镓5份、纳米光纤5份、环氧树脂12份、聚氧乙烯聚氧丙醇胺醚4份、酸酣3份、离模剂2份、氢氧化镁3份、白炭黑3份、乙醇22份。A special light-emitting diode material for optical electronics and a preparation method thereof. The raw materials are composed of the following proportions in parts by weight: 13 parts of polycarbonate, 4 parts of polypropylene, 5 parts of gallium arsenide, 6 parts of gallium phosphide, and phosphorous arsenic 5 parts of gallium chloride, 5 parts of nanofiber, 12 parts of epoxy resin, 4 parts of polyoxyethylene polyoxypropanolamine ether, 3 parts of acid, 2 parts of release agent, 3 parts of magnesium hydroxide, 3 parts of white carbon black , 22 parts of ethanol.

其制备方法如下:Its preparation method is as follows:

A、将砷化镓、磷化镓和磷砷化镓进行搅拌均匀,搅拌速率为390r/min,将其投入反应釜中加入纳米光纤进行高温缩聚,适量乙醇为溶剂,压力为1.6MPa,温度设为400℃,以白炭黑为催化剂,24min后得混合物A;A. Stir gallium arsenide, gallium phosphide and gallium arsenide phosphide evenly at a stirring rate of 390r/min, put them into the reaction kettle and add nano-fibers for high-temperature polycondensation, appropriate amount of ethanol as solvent, pressure 1.6MPa, temperature Set at 400°C, use white carbon black as catalyst, and obtain mixture A after 24 minutes;

B、将聚碳酸酯、聚丙烯和环氧树脂进行聚合反应,温度设为230℃,压力为1.4MPa,18min后冷却至75℃时,依次加入聚氧乙烯聚氧丙醇胺醚、酸酐、离模剂和氢氧化镁进行搅拌,搅拌速率为530r/min,得混合物B;B. Polymerize polycarbonate, polypropylene and epoxy resin, set the temperature at 230°C, and the pressure at 1.4MPa. After cooling to 75°C after 18 minutes, add polyoxyethylene polyoxypropanolamine ether, acid anhydride, Release agent and magnesium hydroxide are stirred, and stirring speed is 530r/min, obtains mixture B;

C、将混合物B投入模具中,再将混合物A浸泡其中,浸泡2.5h后进行脱模,投入烘干机中进行烘干处理,烘干温度为210℃,将其进行挤压、锻造,受力为1950N/cm2,得产物。C. Put the mixture B into the mold, then soak the mixture A in it, remove the mold after soaking for 2.5 hours, put it into the dryer for drying treatment, the drying temperature is 210°C, extrude and forge it, and The force was 1950 N/cm 2 and the product was obtained.

实施例2Example 2

一种光学电子专用发光二极管材料及其制备方法,原料组成成分按重量份数由以下比例组成:聚碳酸酯15份、聚丙烯3份、砷化镓6份、磷化镓5份、磷砷化镓5份、纳米光纤4份、环氧树脂15份、聚氧乙烯聚氧丙醇胺醚3份、酸酣4份、离模剂2份、氢氧化镁3份、白炭黑2份、乙醇30份。A special light-emitting diode material for optical electronics and a preparation method thereof. The raw materials are composed of the following proportions in parts by weight: 15 parts of polycarbonate, 3 parts of polypropylene, 6 parts of gallium arsenide, 5 parts of gallium phosphide, and phosphorus arsenic 5 parts of gallium chloride, 4 parts of nano-fiber, 15 parts of epoxy resin, 3 parts of polyoxyethylene polyoxypropanolamine ether, 4 parts of acid alcohol, 2 parts of release agent, 3 parts of magnesium hydroxide, 2 parts of white carbon black , 30 parts of ethanol.

其制备方法如下:Its preparation method is as follows:

A、将砷化镓、磷化镓和磷砷化镓进行搅拌均匀,搅拌速率为420r/min,将其投入反应釜中加入纳米光纤进行高温缩聚,适量乙醇为溶剂,压力为1.5MPa,温度设为420℃,以白炭黑为催化剂,20min后得混合物A;A. Stir gallium arsenide, gallium phosphide and gallium arsenide phosphide evenly at a stirring rate of 420r/min, put them into the reaction kettle and add nano-fibers for high-temperature polycondensation, appropriate amount of ethanol as solvent, pressure 1.5MPa, temperature Set at 420°C, use white carbon black as catalyst, and obtain mixture A after 20 minutes;

B、将聚碳酸酯、聚丙烯和环氧树脂进行聚合反应,温度设为240℃,压力为1.3MPa,20min后冷却至65℃时,依次加入聚氧乙烯聚氧丙醇胺醚、酸酐、离模剂和氢氧化镁进行搅拌,搅拌速率为540r/min,得混合物B;B. Polymerize polycarbonate, polypropylene and epoxy resin, set the temperature at 240°C, and the pressure at 1.3MPa. After cooling to 65°C after 20 minutes, add polyoxyethylene polyoxypropanolamine ether, acid anhydride, Release agent and magnesium hydroxide are stirred, and stirring speed is 540r/min, obtains mixture B;

C、将混合物B投入模具中,再将混合物A浸泡其中,浸泡2h后进行脱模,投入烘干机中进行烘干处理,烘干温度为220℃,将其进行挤压、锻造,受力为180N/cm2,得产物。C. Put the mixture B into the mold, then soak the mixture A in it, remove the mold after soaking for 2 hours, put it into the dryer for drying treatment, the drying temperature is 220°C, squeeze it, forge it, and force it It was 180N/cm 2 , and the product was obtained.

实施例3Example 3

一种光学电子专用发光二极管材料及其制备方法,原料组成成分按重量份数由以下比例组成:聚碳酸酯10份、聚丙烯5份、砷化镓4份、磷化镓7份、磷砷化镓4份、纳米光纤6份、环氧树脂10份、聚氧乙烯聚氧丙醇胺醚5份、酸酣3份、离模剂3份、氢氧化镁2份、白炭黑4份、乙醇20份。A special light-emitting diode material for optical electronics and a preparation method thereof. The raw material components are composed of the following proportions in parts by weight: 10 parts of polycarbonate, 5 parts of polypropylene, 4 parts of gallium arsenide, 7 parts of gallium phosphide, and phosphorus arsenic 4 parts of gallium chloride, 6 parts of nano-fiber, 10 parts of epoxy resin, 5 parts of polyoxyethylene polyoxypropanolamine ether, 3 parts of acid liquor, 3 parts of release agent, 2 parts of magnesium hydroxide, 4 parts of white carbon black , 20 parts of ethanol.

其制备方法如下:Its preparation method is as follows:

A、将砷化镓、磷化镓和磷砷化镓进行搅拌均匀,搅拌速率为380r/min,将其投入反应釜中加入纳米光纤进行高温缩聚,适量乙醇为溶剂,压力为1.8MPa,温度设为380℃,以白炭黑为催化剂,30min后得混合物A;A. Stir gallium arsenide, gallium phosphide and gallium arsenide phosphide evenly at a stirring rate of 380r/min, put them into the reaction kettle and add nano-fibers for high-temperature polycondensation, appropriate amount of ethanol as solvent, pressure 1.8MPa, temperature Set at 380°C, use white carbon black as catalyst, and obtain mixture A after 30 minutes;

B、将聚碳酸酯、聚丙烯和环氧树脂进行聚合反应,温度设为220℃,压力为1.5MPa,15min后冷却至80℃时,依次加入聚氧乙烯聚氧丙醇胺醚、酸酐、离模剂和氢氧化镁进行搅拌,搅拌速率为480r/min,得混合物B;B. Polymerize polycarbonate, polypropylene and epoxy resin, set the temperature at 220°C, and the pressure at 1.5MPa. After cooling to 80°C after 15 minutes, add polyoxyethylene polyoxypropanolamine ether, acid anhydride, Release agent and magnesium hydroxide are stirred, and stirring rate is 480r/min, obtains mixture B;

C、将混合物B投入模具中,再将混合物A浸泡其中,浸泡3h后进行脱模,投入烘干机中进行烘干处理,烘干温度为200℃,将其进行挤压、锻造,受力为200N/cm2,得产物。C. Put the mixture B into the mold, then soak the mixture A in it, remove the mold after soaking for 3 hours, put it into the dryer for drying treatment, the drying temperature is 200°C, squeeze it, forge it, and press it 200N/cm 2 , the product was obtained.

实施例4Example 4

一种光学电子专用发光二极管材料及其制备方法,原料组成成分按重量份数由以下比例组成:聚碳酸酯14份、聚丙烯5份、砷化镓5份、磷化镓6份、磷砷化镓4份、纳米光纤5份、环氧树脂13份、聚氧乙烯聚氧丙醇胺醚4份、酸酣3份、离模剂2份、氢氧化镁3份、白炭黑3份、乙醇28份。A special light-emitting diode material for optical electronics and a preparation method thereof. The raw material components are composed of the following proportions in parts by weight: 14 parts of polycarbonate, 5 parts of polypropylene, 5 parts of gallium arsenide, 6 parts of gallium phosphide, and phosphorous arsenic 4 parts of gallium chloride, 5 parts of nano-fiber, 13 parts of epoxy resin, 4 parts of polyoxyethylene polyoxypropanolamine ether, 3 parts of acid, 2 parts of release agent, 3 parts of magnesium hydroxide, 3 parts of white carbon black , 28 parts of ethanol.

其制备方法如下:Its preparation method is as follows:

A、将砷化镓、磷化镓和磷砷化镓进行搅拌均匀,搅拌速率为390r/min,将其投入反应釜中加入纳米光纤进行高温缩聚,适量乙醇为溶剂,压力为1.7MPa,温度设为400℃,以白炭黑为催化剂,26min后得混合物A;A. Stir gallium arsenide, gallium phosphide and gallium arsenide phosphide evenly at a stirring rate of 390r/min, put them into the reaction kettle and add nano-fibers for high-temperature polycondensation, appropriate amount of ethanol as solvent, pressure 1.7MPa, temperature Set at 400°C, use white carbon black as catalyst, and obtain mixture A after 26 minutes;

B、将聚碳酸酯、聚丙烯和环氧树脂进行聚合反应,温度设为230℃,压力为1.4MPa,19min后冷却至75℃时,依次加入聚氧乙烯聚氧丙醇胺醚、酸酐、离模剂和氢氧化镁进行搅拌,搅拌速率为510r/min,得混合物B;B. Polycarbonate, polypropylene and epoxy resin are polymerized, the temperature is set at 230°C, the pressure is 1.4MPa, and after cooling to 75°C after 19 minutes, polyoxyethylene polyoxypropanolamine ether, acid anhydride, Release agent and magnesium hydroxide are stirred, and stirring speed is 510r/min, obtains mixture B;

C、将混合物B投入模具中,再将混合物A浸泡其中,浸泡2h后进行脱模,投入烘干机中进行烘干处理,烘干温度为215℃,将其进行挤压、锻造,受力为195N/cm2,得产物。C. Put the mixture B into the mold, then soak the mixture A in it, remove the mold after soaking for 2 hours, put it into the dryer for drying treatment, the drying temperature is 215°C, squeeze it, forge it, and force it It was 195 N/cm 2 , and the product was obtained.

以上实施例中,实施例4为最佳实施例,耐磨效果强,通过改性,加强结构的稳定性和抗压能力。Among the above embodiments, embodiment 4 is the best embodiment, which has a strong wear resistance effect, and the stability and compression resistance of the structure can be enhanced through modification.

以上所述仅为说明本发明的实施方式,并不用于限制本发明,对于本领域的技术人员来说,凡在本发明的精神和原则之内,所作的任何修改、等同替换、改进等,均应包含在本发明的保护范围之内。The above is only to illustrate the implementation of the present invention, and is not intended to limit the present invention. For those skilled in the art, any modifications, equivalent replacements, improvements, etc. made within the spirit and principles of the present invention, All should be included within the protection scope of the present invention.

Claims (2)

  1. A kind of 1. special light LED material of optical electron and preparation method thereof, it is characterised in that:Raw material constituent is by weight Amount number is made of following ratio:10-15 parts of makrolon, 3-5 parts of polypropylene, 4-6 parts of GaAs, 5-7 parts of gallium phosphide, phosphorus arsenic Change 4-5 part of gallium, 4-6 parts of nano optical fibers, 10-15 parts of epoxy resin, 3-5 parts of polyoxyethylene polyoxy propyl alcohol amidogen ether, it is intoxicated 3-4 parts sour, 2-3 parts of release agent, 2-3 parts of magnesium hydroxide, 2-4 parts of white carbon, 20-30 parts of ethanol.
  2. 2. special light LED material of a kind of optical electron according to claim 1 and preparation method thereof, its feature exists In:Its preparation method is as follows:
    A, GaAs, gallium phosphide and gallium arsenide phosphide are stirred uniformly, stir speed (S.S.) 380-420r/min, are put into anti- Answer and nano optical fibers are added in kettle carry out high-temperature polycondensation, ethanol in proper amount is solvent, pressure 1.5-1.8MPa, and temperature is set to 380- 420 DEG C, using white carbon as catalyst, mixture A is obtained after 20-30min;
    B, makrolon, polypropylene and epoxy resin are subjected to polymerisation, temperature is set to 220-240 DEG C, pressure 1.3- When 1.5MPa, 15-20min postcooling are to 65-80 DEG C, polyoxyethylene polyoxy propyl alcohol amidogen ether, acid anhydrides, release agent and hydrogen are sequentially added Magnesia is stirred, and stir speed (S.S.) 480-540r/min, obtains mixture B;
    C, mixture B is put into mould, then by mixture A immersions wherein, is demoulded after soaking 2-3h, put into dryer Drying and processing is carried out, drying temperature is 200-220 DEG C, is extruded, forged, stress 180-200N/cm2, obtain product.
CN201711344654.6A 2017-12-15 2017-12-15 A kind of special light LED material of optical electron and preparation method thereof Withdrawn CN107955358A (en)

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Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1369920A (en) * 2001-02-12 2002-09-18 国联光电科技股份有限公司 Light-emitting diode and its manufacturing method
CN102850750A (en) * 2012-09-21 2013-01-02 常熟市凯力达蜂窝包装材料有限公司 Preparation method of halogen-free flame retardant polypropylene modified polycarbonate alloy material
CN103554876A (en) * 2013-10-25 2014-02-05 安徽省富光实业股份有限公司 Polycarbonate composite material for water cup shells and preparation method thereof
CN107286588A (en) * 2017-08-02 2017-10-24 方政 A kind of special encapsulating material of LED and its preparation technology
CN107418154A (en) * 2017-08-07 2017-12-01 方碧水 A kind of environment friendly halogen-free fireproof section bar material and preparation method thereof
CN107446313A (en) * 2017-08-23 2017-12-08 伊婕 A kind of New LED encapsulating material and preparation method thereof

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1369920A (en) * 2001-02-12 2002-09-18 国联光电科技股份有限公司 Light-emitting diode and its manufacturing method
CN102850750A (en) * 2012-09-21 2013-01-02 常熟市凯力达蜂窝包装材料有限公司 Preparation method of halogen-free flame retardant polypropylene modified polycarbonate alloy material
CN103554876A (en) * 2013-10-25 2014-02-05 安徽省富光实业股份有限公司 Polycarbonate composite material for water cup shells and preparation method thereof
CN107286588A (en) * 2017-08-02 2017-10-24 方政 A kind of special encapsulating material of LED and its preparation technology
CN107418154A (en) * 2017-08-07 2017-12-01 方碧水 A kind of environment friendly halogen-free fireproof section bar material and preparation method thereof
CN107446313A (en) * 2017-08-23 2017-12-08 伊婕 A kind of New LED encapsulating material and preparation method thereof

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
杨武等: "《改变世界的信息材料》", 30 April 2012 *

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