CN115073874A - Polypropylene composite material for automobile spoiler and preparation method thereof - Google Patents
Polypropylene composite material for automobile spoiler and preparation method thereof Download PDFInfo
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- 239000004743 Polypropylene Substances 0.000 title claims abstract description 82
- -1 Polypropylene Polymers 0.000 title claims abstract description 60
- 229920001155 polypropylene Polymers 0.000 title claims abstract description 60
- 239000002131 composite material Substances 0.000 title claims abstract description 34
- 238000002360 preparation method Methods 0.000 title claims abstract description 6
- 239000003963 antioxidant agent Substances 0.000 claims abstract description 44
- 230000003078 antioxidant effect Effects 0.000 claims abstract description 44
- 239000000155 melt Substances 0.000 claims abstract description 27
- 239000011256 inorganic filler Substances 0.000 claims abstract description 24
- 229910003475 inorganic filler Inorganic materials 0.000 claims abstract description 24
- 239000002245 particle Substances 0.000 claims abstract description 14
- 239000002994 raw material Substances 0.000 claims abstract description 12
- 229920001577 copolymer Polymers 0.000 claims abstract description 11
- 238000001125 extrusion Methods 0.000 claims description 30
- 229920001971 elastomer Polymers 0.000 claims description 28
- 239000000806 elastomer Substances 0.000 claims description 27
- 238000000034 method Methods 0.000 claims description 17
- 238000001035 drying Methods 0.000 claims description 11
- PWWSSIYVTQUJQQ-UHFFFAOYSA-N distearyl thiodipropionate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCCCCCCCC PWWSSIYVTQUJQQ-UHFFFAOYSA-N 0.000 claims description 10
- 238000005469 granulation Methods 0.000 claims description 10
- 230000003179 granulation Effects 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 7
- 229910052623 talc Inorganic materials 0.000 claims description 6
- 239000000454 talc Substances 0.000 claims description 6
- 238000003756 stirring Methods 0.000 claims description 2
- FPAFDBFIGPHWGO-UHFFFAOYSA-N dioxosilane;oxomagnesium;hydrate Chemical compound O.[Mg]=O.[Mg]=O.[Mg]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O FPAFDBFIGPHWGO-UHFFFAOYSA-N 0.000 abstract description 14
- 239000000463 material Substances 0.000 abstract description 12
- 239000004033 plastic Substances 0.000 abstract description 7
- 229920003023 plastic Polymers 0.000 abstract description 7
- 239000000956 alloy Substances 0.000 abstract description 5
- 229910045601 alloy Inorganic materials 0.000 abstract description 5
- 229920007019 PC/ABS Polymers 0.000 abstract description 4
- 238000004519 manufacturing process Methods 0.000 abstract description 2
- 229920006124 polyolefin elastomer Polymers 0.000 abstract 3
- 229920001225 polyester resin Polymers 0.000 abstract 1
- 239000004645 polyester resin Substances 0.000 abstract 1
- 230000000052 comparative effect Effects 0.000 description 9
- 235000012222 talc Nutrition 0.000 description 5
- 230000007423 decrease Effects 0.000 description 4
- 238000005452 bending Methods 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000011056 performance test Methods 0.000 description 2
- NIPNSKYNPDTRPC-UHFFFAOYSA-N N-[2-oxo-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 NIPNSKYNPDTRPC-UHFFFAOYSA-N 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 238000005034 decoration Methods 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L53/00—Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K2201/00—Specific properties of additives
- C08K2201/002—Physical properties
- C08K2201/005—Additives being defined by their particle size in general
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Abstract
Description
技术领域technical field
本发明涉及高分子改性技术领域,具体涉及一种用于汽车扰流板的聚丙烯复合材料及其制备方法。The invention relates to the technical field of polymer modification, in particular to a polypropylene composite material used for an automobile spoiler and a preparation method thereof.
背景技术Background technique
为了有效地减少汽车高速行驶时空气阻力的影响,汽车尾部设计了扰流板(也叫尾翼),其作用是使空气对汽车产生对地面的附着力,以抵消一部分气动升力,控制汽车上浮,使汽车能紧贴着道路行驶,从而起到提高汽车行驶稳定性的作用。In order to effectively reduce the impact of air resistance when the car is running at high speed, a spoiler (also called a rear wing) is designed at the rear of the car. Its function is to make the air adhere to the car to the ground to offset part of the aerodynamic lift and control the car to float. So that the car can drive close to the road, so as to improve the driving stability of the car.
目前主流的汽车扰流板材料为PC/ABS(塑料合金),成本非常高。聚丙烯作为一种通用塑料,由于其成本低、密度小、耐化学性能好、加工工艺性好、易回收利用等优点,广泛地应用于汽车内外饰中,如汽车仪表板、保险杠、立柱、侧围、副仪表板等,汽车装饰件聚烯烃化已经成为一种趋势。The current mainstream car spoiler material is PC/ABS (plastic alloy), and the cost is very high. As a general-purpose plastic, polypropylene is widely used in automobile interior and exterior decorations, such as automobile dashboards, bumpers, pillars, due to its advantages of low cost, low density, good chemical resistance, good processability, and easy recycling. , side panels, sub-dashboards, etc., the polyolefinization of automotive decorative parts has become a trend.
然而,聚丙烯也有力学强度不高,冲击性能差,收缩率大、材料成本高等缺点,因此在实际使用过程中需要对其进行改性,以满足各类零部件的性能需求。However, polypropylene also has the disadvantages of low mechanical strength, poor impact performance, high shrinkage rate, and high material cost. Therefore, it needs to be modified in the actual use process to meet the performance requirements of various parts.
发明内容SUMMARY OF THE INVENTION
有鉴于此,本发明提出了一种用于汽车扰流板的聚丙烯复合材料及其制备方法,制备所得的聚丙烯复合材料不仅具有高强度、高韧性,还具有较低的线性膨胀系数,可以直接垂直切换目前的PC/ABS(塑料合金)扰流板,降低材料成本。In view of this, the present invention proposes a polypropylene composite material for an automobile spoiler and a preparation method thereof. The prepared polypropylene composite material not only has high strength, high toughness, but also has a low coefficient of linear expansion, The current PC/ABS (plastic alloy) spoiler can be directly switched vertically, reducing material costs.
在本发明的一个方面,本发明提出了一种用于汽车扰流板的聚丙烯复合材料,包括:In one aspect of the present invention, the present invention proposes a polypropylene composite material for an automobile spoiler, comprising:
聚丙烯PP、高性能无机填料、弹性体POE、抗氧剂A、抗氧剂B。Polypropylene PP, high performance inorganic filler, elastomer POE, antioxidant A, antioxidant B.
根据本发明的实施例,所述聚丙烯PP、高性能无机填料、弹性体POE、抗氧剂A、抗氧剂B的质量百分比为(39.4-54.4):(30-35):(15-25):(0.25-0.35):(0.25-0.35)。According to an embodiment of the present invention, the mass percentages of the polypropylene PP, high-performance inorganic filler, elastomer POE, antioxidant A, and antioxidant B are (39.4-54.4): (30-35): (15- 25): (0.25-0.35): (0.25-0.35).
其中,所述聚丙烯PP为上海石化生产的嵌段共聚聚丙烯,商品名为PP M2600R,其在230℃,2.16kg的测试条件下熔融指数为10-30g/10min。所述聚丙烯PP的重量百分比为39.4-54.4%,具体地,可以为39.4%、44.4%、49.4%、54.4%以及此范围内的其他数值。Wherein, the polypropylene PP is a block copolymerized polypropylene produced by Shanghai Petrochemical, with a trade name of PP M2600R, and its melt index is 10-30g/10min under the test conditions of 230°C and 2.16kg. The weight percentage of the polypropylene PP is 39.4-54.4%, specifically, it can be 39.4%, 44.4%, 49.4%, 54.4% and other values within this range.
所述高性能无机填料为超细滑石粉,其粒径范围均为1-3μm。具体的,粒径的数值可以为1μm、1.5μm、2μm、2.5μm、3μm以及此范围内的其他数值。此粒径范围的超细滑石粉添加后可显著提高所得材料的刚性、耐表面划伤性、热稳定性,并且还具有润滑作用,能提高材料的加工工艺性。The high-performance inorganic filler is ultra-fine talc powder, and the particle size range is 1-3 μm. Specifically, the numerical value of the particle size can be 1 μm, 1.5 μm, 2 μm, 2.5 μm, 3 μm and other numerical values within this range. The addition of ultrafine talc in this particle size range can significantly improve the rigidity, surface scratch resistance and thermal stability of the obtained material, and also has a lubricating effect, which can improve the processability of the material.
所述弹性体POE为美国陶氏公司生产的一类线性乙烯-辛烯共聚物,因其特殊的分子链段结构,具有橡胶和塑料的双重特性,所述的弹性体POE密度为0.88-0.90g/cm3,其在190℃,2.16kg的测试条件下熔融指数为0.5-10g/10min,所述弹性体POE的重量百分比为15-25%,具体地,可以为15%、20%、25%以及此范围内的其他数值。添加混合后可提高所得材料的力学性能和耐热老化性能。The elastomer POE is a type of linear ethylene-octene copolymer produced by Dow Company in the United States. Because of its special molecular segment structure, it has the dual characteristics of rubber and plastic. The elastomer POE density is 0.88-0.90 g/cm 3 , its melt index is 0.5-10 g/10min under the test condition of 190° C. and 2.16kg, and the weight percentage of the elastomer POE is 15-25%, specifically, it can be 15%, 20%, 25% and other values within this range. After adding and mixing, the mechanical properties and heat aging resistance of the obtained material can be improved.
所述的抗氧剂A包括Ciba公司生产的3114、1010以及英国ICE公司生产的DSTP中的一种或者几种,所述抗氧剂A的重量百分比为0.25-0.35%,具体地,可以为0.25%、0.3%、0.35%以及此范围内的其他数值。The antioxidant A includes one or more of 3114 and 1010 produced by Ciba company and DSTP produced by British ICE company, and the weight percentage of the antioxidant A is 0.25-0.35%, specifically, can be 0.25%, 0.3%, 0.35% and other values within this range.
所述的抗氧剂B包括Ciba公司生产的618和168中的一种或两种,所述抗氧剂B的重量百分比为0.25-0.35%,具体地,可以为0.25%、0.3%、0.35%以及此范围内的其他数值。The antioxidant B includes one or both of 618 and 168 produced by Ciba company, and the weight percentage of the antioxidant B is 0.25-0.35%, specifically, can be 0.25%, 0.3%, 0.35% % and other values within this range.
在本发明的一些实施例中,通过在聚丙烯复合材料配方体系中添加高性能的超细滑石粉以及弹性体POE,制备所得的聚丙烯复合材料的线性膨胀系数明显降低,因此,材料的热稳定性、抗热震性能有明显提升。此外,高性能滑石粉和弹性体POE的增加还使制得的聚丙烯复合材料具有更强的刚性和韧性,抗冲击性变强,从而提高了汽车行驶过程中的稳定性。In some embodiments of the present invention, by adding high-performance ultra-fine talc and elastomer POE into the polypropylene composite material formulation system, the linear expansion coefficient of the prepared polypropylene composite material is significantly reduced. Therefore, the thermal The stability and thermal shock resistance have been significantly improved. In addition, the increase of high-performance talcum powder and elastomer POE also makes the obtained polypropylene composite material have stronger rigidity and toughness, and stronger impact resistance, thereby improving the stability of automobiles during driving.
在本发明的第二个方面,本发明提出了一种制备上述用于汽车扰流板的聚丙烯复合材料的方法,其包括:In a second aspect of the present invention, the present invention proposes a method for preparing the above-mentioned polypropylene composite material for an automobile spoiler, comprising:
(1)将各组分原料按配比在高速混合机中充分混合,得到混合物;(1) fully mixing each component raw material in a high-speed mixer according to the proportioning ratio to obtain a mixture;
(2)将得到的混合物输送到双螺杆挤出机中进行熔融挤出、造粒、干燥,即得所述聚丙烯复合材料。(2) The obtained mixture is transported to a twin-screw extruder for melt extrusion, granulation and drying to obtain the polypropylene composite material.
在本发明的一些实施例中,所述步骤(1)中,高速混合机的转速为600-1800转/分钟,搅拌时间为2-4分钟。In some embodiments of the present invention, in the step (1), the rotational speed of the high-speed mixer is 600-1800 rpm, and the stirring time is 2-4 minutes.
在本发明的一些实施例中,所述步骤(2)中,双螺杆挤出机中熔融挤出的条件为:一区190-200℃、二区200-210℃、三区210-230℃、四区205-220℃,压力15-20MPa。In some embodiments of the present invention, in the step (2), the conditions for melt extrusion in the twin-screw extruder are: 190-200°C in the first zone, 200-210°C in the second zone, and 210-230°C in the third zone , Four zones 205-220℃, pressure 15-20MPa.
在本发明的一些实施例中,所述步骤(2)中,双螺杆挤出机螺杆转速为150-300转/分钟,整个挤出过程的停留时间为1-3分钟。In some embodiments of the present invention, in the step (2), the screw speed of the twin-screw extruder is 150-300 rpm, and the residence time of the entire extrusion process is 1-3 minutes.
本发明的附加方面和优点将在下面的描述中部分给出,部分将从下面的描述中变得明显,或通过本发明的实践了解到。Additional aspects and advantages of the present invention will be set forth, in part, from the following description, and in part will be apparent from the following description, or may be learned by practice of the invention.
具体实施方式Detailed ways
下面参考具体实施例,对本发明进行描述,需要说明的是,这些实施例仅仅是描述性的,而不以任何方式限制本发明。The present invention will be described below with reference to specific embodiments. It should be noted that these embodiments are merely illustrative and do not limit the present invention in any way.
实施例1Example 1
称取54.4%的聚丙烯PP、15%的弹性体POE、30%的高性能无机填料A、0.3%的抗氧化剂A、0.3%的抗氧化剂B,需要说明的是,在本实施例中,所述聚丙烯PP的熔体流动速率为25g/10min(测试条件:230℃,2.16kg),所述弹性体POE为线性乙烯-辛烯共聚物,密度为0.88-0.90g/cm3,其在190℃,2.16kg的测试条件下,熔融指数为0.5-10g/10min,所述无机填料A为5000目滑石粉,平均粒径为2.5μm,所述抗氧剂A为DSTP和3114,所述抗氧剂B为168。将上述原料在高速混合器中,以高于600转/分钟的转速搅拌2-4分钟,混合均匀得到预混料,将预混料置于双螺杆挤出机中进行熔融挤出,造粒干燥,即得所述聚丙烯复合材料。Weigh 54.4% of polypropylene PP, 15% of elastomer POE, 30% of high-performance inorganic filler A, 0.3% of antioxidant A, and 0.3% of antioxidant B. It should be noted that in this example, The melt flow rate of the polypropylene PP is 25g/10min (test condition: 230° C., 2.16kg), the elastomer POE is a linear ethylene-octene copolymer, and the density is 0.88-0.90g/cm 3 . Under the test conditions of 190°C and 2.16kg, the melt index is 0.5-10g/10min, the inorganic filler A is 5000 mesh talcum powder, the average particle size is 2.5μm, and the antioxidant A is DSTP and 3114, so The antioxidant B is 168. The above-mentioned raw materials are stirred in a high-speed mixer for 2-4 minutes at a speed higher than 600 r/min, mixed uniformly to obtain a premix, and the premix is placed in a twin-screw extruder for melt extrusion and granulation. After drying, the polypropylene composite material is obtained.
双螺杆挤出机的熔融挤出的条件为:一区190-200℃、二区200-210℃、三区210-230℃、四区205-220℃,压力15~20MPa。螺杆的转速为150-300转/分钟,整个挤出过程的停留时间为1-3分钟。The melt extrusion conditions of the twin-screw extruder are: 190-200°C in the first zone, 200-210°C in the second zone, 210-230°C in the third zone, 205-220°C in the fourth zone, and pressure 15-20MPa. The rotation speed of the screw is 150-300 rpm, and the residence time of the whole extrusion process is 1-3 minutes.
实施例2Example 2
称取49.4%的聚丙烯PP、20%的弹性体POE、30%的高性能无机填料A、0.3%的抗氧化剂A、0.3%的抗氧化剂B,需要说明的是,在本实施例中,所述聚丙烯PP的熔体流动速率为25g/10min(测试条件:230℃,2.16kg),所述弹性体POE为线性乙烯-辛烯共聚物,密度为0.88-0.90g/cm3,其在190℃,2.16kg的测试条件下,熔融指数为0.5-10g/10min,所述无机填料A为5000目滑石粉,平均粒径为2.5μm,所述抗氧剂A为DSTP和3114,所述抗氧剂B为168。将上述原料在高速混合器中,以高于600转/分钟的转速搅拌2-4分钟,混合均匀得到预混料,将预混料置于双螺杆挤出机中进行熔融挤出,造粒干燥,即得所述聚丙烯复合材料。Weigh 49.4% polypropylene PP, 20% elastomer POE, 30% high-performance inorganic filler A, 0.3% antioxidant A, and 0.3% antioxidant B. It should be noted that in this example, The melt flow rate of the polypropylene PP is 25g/10min (test condition: 230° C., 2.16kg), the elastomer POE is a linear ethylene-octene copolymer, and the density is 0.88-0.90g/cm 3 . Under the test conditions of 190°C and 2.16kg, the melt index is 0.5-10g/10min, the inorganic filler A is 5000 mesh talcum powder, the average particle size is 2.5μm, and the antioxidant A is DSTP and 3114, so The antioxidant B is 168. The above-mentioned raw materials are stirred in a high-speed mixer for 2-4 minutes at a speed higher than 600 r/min, mixed uniformly to obtain a premix, and the premix is placed in a twin-screw extruder for melt extrusion and granulation. After drying, the polypropylene composite material is obtained.
双螺杆挤出机的熔融挤出的条件为:一区190-200℃、二区200-210℃、三区210-230℃、四区205-220℃,压力15-20MPa。螺杆的转速为150-300转/分钟,整个挤出过程的停留时间为1-3分钟。The melt extrusion conditions of the twin-screw extruder are: 190-200°C in the first zone, 200-210°C in the second zone, 210-230°C in the third zone, 205-220°C in the fourth zone, and pressure 15-20MPa. The rotation speed of the screw is 150-300 rpm, and the residence time of the whole extrusion process is 1-3 minutes.
实施例3Example 3
称取44.4%的聚丙烯PP、25%的弹性体POE、30%的高性能无机填料A、0.3%的抗氧化剂A、0.3%的抗氧化剂B,需要说明的是,在本实施例中,所述聚丙烯PP的熔体流动速率为25g/10min(测试条件:230℃,2.16kg),所述弹性体POE为线性乙烯-辛烯共聚物,密度为0.88-0.90g/cm3,其在190℃,2.16kg的测试条件下,熔融指数为0.5-10g/10min,所述无机填料A为5000目滑石粉,平均粒径为2.5μm,所述抗氧剂A为DSTP和3114,所述抗氧剂B为168。将上述原料在高速混合器中,以高于600转/分钟的转速搅拌2-4分钟,混合均匀得到预混料,将预混料置于双螺杆挤出机中进行熔融挤出,造粒干燥,即得所述聚丙烯复合材料。Weigh 44.4% polypropylene PP, 25% elastomer POE, 30% high-performance inorganic filler A, 0.3% antioxidant A, and 0.3% antioxidant B. It should be noted that in this example, The melt flow rate of the polypropylene PP is 25g/10min (test condition: 230° C., 2.16kg), the elastomer POE is a linear ethylene-octene copolymer, and the density is 0.88-0.90g/cm 3 . Under the test conditions of 190°C and 2.16kg, the melt index is 0.5-10g/10min, the inorganic filler A is 5000 mesh talcum powder, the average particle size is 2.5μm, and the antioxidant A is DSTP and 3114, so The antioxidant B is 168. The above-mentioned raw materials are stirred in a high-speed mixer for 2-4 minutes at a speed higher than 600 r/min, mixed uniformly to obtain a premix, and the premix is placed in a twin-screw extruder for melt extrusion and granulation. After drying, the polypropylene composite material is obtained.
双螺杆挤出机的熔融挤出的条件为:一区190-200℃、二区200-210℃、三区210-230℃、四区205-220℃,压力15~20MPa。螺杆的转速为150-300转/分钟,整个挤出过程的停留时间为1-3分钟。The melt extrusion conditions of the twin-screw extruder are: 190-200°C in the first zone, 200-210°C in the second zone, 210-230°C in the third zone, 205-220°C in the fourth zone, and pressure 15-20MPa. The rotation speed of the screw is 150-300 rpm, and the residence time of the whole extrusion process is 1-3 minutes.
实施例4Example 4
称取49.4%的聚丙烯PP、15%的弹性体POE、35%的高性能无机填料A、0.3%的抗氧化剂A、0.3%的抗氧化剂B,需要说明的是,在本实施例中,所述聚丙烯PP的熔体流动速率为25g/10min(测试条件:230℃,2.16kg),所述弹性体POE为线性乙烯-辛烯共聚物,密度为0.88-0.90g/cm3,其在190℃,2.16kg的测试条件下,熔融指数为0.5-10g/10min,所述无机填料A为5000目滑石粉,平均粒径为2.5μm,所述抗氧剂A为DSTP和3114,所述抗氧剂B为168。将上述原料在高速混合器中,以高于600转/分钟的转速搅拌2-4分钟,混合均匀得到预混料,将预混料置于双螺杆挤出机中进行熔融挤出,造粒干燥,即得所述聚丙烯复合材料。Weigh 49.4% polypropylene PP, 15% elastomer POE, 35% high-performance inorganic filler A, 0.3% antioxidant A, and 0.3% antioxidant B. It should be noted that in this example, The melt flow rate of the polypropylene PP is 25g/10min (test condition: 230° C., 2.16kg), the elastomer POE is a linear ethylene-octene copolymer, and the density is 0.88-0.90g/cm 3 . Under the test conditions of 190°C and 2.16kg, the melt index is 0.5-10g/10min, the inorganic filler A is 5000 mesh talcum powder, the average particle size is 2.5μm, and the antioxidant A is DSTP and 3114, so The antioxidant B is 168. The above-mentioned raw materials are stirred in a high-speed mixer for 2-4 minutes at a speed higher than 600 r/min, mixed uniformly to obtain a premix, and the premix is placed in a twin-screw extruder for melt extrusion and granulation. After drying, the polypropylene composite material is obtained.
双螺杆挤出机的熔融挤出的条件为:一区190-200℃、二区200-210℃、三区210-230℃、四区205-220℃,压力15-20MPa。螺杆的转速为150-300转/分钟,整个挤出过程的停留时间为1-3分钟。The melt extrusion conditions of the twin-screw extruder are: 190-200°C in the first zone, 200-210°C in the second zone, 210-230°C in the third zone, 205-220°C in the fourth zone, and pressure 15-20MPa. The rotation speed of the screw is 150-300 rpm, and the residence time of the whole extrusion process is 1-3 minutes.
实施例5Example 5
称取44.4%的聚丙烯PP、20%的弹性体POE、35%的高性能无机填料A、0.3%的抗氧化剂A、0.3%的抗氧化剂B,需要说明的是,在本实施例中,所述聚丙烯PP的熔体流动速率为25g/10min(测试条件:230℃,2.16kg),所述弹性体POE为线性乙烯-辛烯共聚物,密度为0.88-0.90g/cm3,其在190℃,2.16kg的测试条件下,熔融指数为0.5-10g/10min,所述无机填料A为5000目滑石粉,平均粒径为2.5μm,所述抗氧剂A为DSTP和3114,所述抗氧剂B为168。将上述原料在高速混合器中,以高于600转/分钟的转速搅拌2-4分钟,混合均匀得到预混料,将预混料置于双螺杆挤出机中进行熔融挤出,造粒干燥,即得所述聚丙烯复合材料。Weigh 44.4% polypropylene PP, 20% elastomer POE, 35% high-performance inorganic filler A, 0.3% antioxidant A, and 0.3% antioxidant B. It should be noted that in this example, The melt flow rate of the polypropylene PP is 25g/10min (test condition: 230° C., 2.16kg), the elastomer POE is a linear ethylene-octene copolymer, and the density is 0.88-0.90g/cm 3 . Under the test conditions of 190°C and 2.16kg, the melt index is 0.5-10g/10min, the inorganic filler A is 5000 mesh talcum powder, the average particle size is 2.5μm, and the antioxidant A is DSTP and 3114, so The antioxidant B is 168. The above-mentioned raw materials are stirred in a high-speed mixer for 2-4 minutes at a speed higher than 600 r/min, mixed uniformly to obtain a premix, and the premix is placed in a twin-screw extruder for melt extrusion and granulation. After drying, the polypropylene composite material is obtained.
双螺杆挤出机的熔融挤出的条件为:一区190-200℃、二区200-210℃、三区210-230℃、四区205-220℃,压力15-20MPa。螺杆的转速为150-300转/分钟,整个挤出过程的停留时间为1-3分钟。The melt extrusion conditions of the twin-screw extruder are: 190-200°C in the first zone, 200-210°C in the second zone, 210-230°C in the third zone, 205-220°C in the fourth zone, and pressure 15-20MPa. The rotation speed of the screw is 150-300 rpm, and the residence time of the whole extrusion process is 1-3 minutes.
实施例6Example 6
称取39.4%的聚丙烯PP、25%的弹性体POE、35%的高性能无机填料A、0.3%的抗氧化剂A、0.3%的抗氧化剂B,需要说明的是,在本实施例中,所述聚丙烯PP的熔体流动速率为25g/10min(测试条件:230℃,2.16kg),所述弹性体POE为线性乙烯-辛烯共聚物,密度为0.88-0.90g/cm3,其在190℃,2.16kg的测试条件下,熔融指数为0.5-10g/10min,所述无机填料A为5000目滑石粉,平均粒径为2.5μm,所述抗氧剂A为DSTP和3114,所述抗氧剂B为168。将上述原料在高速混合器中,以高于600转/分钟的转速搅拌2-4分钟,混合均匀得到预混料,将预混料置于双螺杆挤出机中进行熔融挤出,造粒干燥,即得所述聚丙烯复合材料。Weigh 39.4% polypropylene PP, 25% elastomer POE, 35% high-performance inorganic filler A, 0.3% antioxidant A, and 0.3% antioxidant B. It should be noted that in this example, The melt flow rate of the polypropylene PP is 25g/10min (test condition: 230° C., 2.16kg), the elastomer POE is a linear ethylene-octene copolymer, and the density is 0.88-0.90g/cm 3 . Under the test conditions of 190°C and 2.16kg, the melt index is 0.5-10g/10min, the inorganic filler A is 5000 mesh talcum powder, the average particle size is 2.5μm, and the antioxidant A is DSTP and 3114, so The antioxidant B is 168. The above-mentioned raw materials are stirred in a high-speed mixer for 2-4 minutes at a speed higher than 600 rpm, and the premix is uniformly mixed to obtain a premix. The premix is placed in a twin-screw extruder for melt extrusion and granulation. After drying, the polypropylene composite material is obtained.
双螺杆挤出机的熔融挤出的条件为:一区190-200℃、二区200-210℃、三区210-230℃、四区205-220℃,压力15-20MPa。螺杆的转速为150-300转/分钟,整个挤出过程的停留时间为1-3分钟。The melt extrusion conditions of the twin-screw extruder are: 190-200°C in the first zone, 200-210°C in the second zone, 210-230°C in the third zone, 205-220°C in the fourth zone, and pressure 15-20MPa. The rotation speed of the screw is 150-300 rpm, and the residence time of the whole extrusion process is 1-3 minutes.
对比例1Comparative Example 1
称取49.4%的聚丙烯PP、20%的弹性体POE、30%的高性能无机填料B、0.3%的抗氧化剂A、0.3%的抗氧化剂B,需要说明的是,在本对比例中,所述聚丙烯PP的熔体流动速率为25g/10min(测试条件:230℃,2.16kg),所述弹性体POE为线性乙烯-辛烯共聚物,密度为0.88-0.90g/cm3,其在190℃,2.16kg的测试条件下,熔融指数为0.5-10g/10min,所述高性能无机填料B为1250目滑石粉,平均粒径为10μm,所述抗氧剂A为DSTP和3114,所述抗氧剂B为168。将上述原料在高速混合器中,以高于600转/分钟的转速搅拌2-4分钟,混合均匀得到预混料,将预混料置于双螺杆挤出机中进行熔融挤出,造粒干燥,即得所述聚丙烯复合材料。Weigh 49.4% polypropylene PP, 20% elastomer POE, 30% high-performance inorganic filler B, 0.3% antioxidant A, and 0.3% antioxidant B. It should be noted that in this comparative example, The melt flow rate of the polypropylene PP is 25g/10min (test condition: 230° C., 2.16kg), the elastomer POE is a linear ethylene-octene copolymer, and the density is 0.88-0.90g/cm 3 . Under the test conditions of 190°C and 2.16kg, the melt index is 0.5-10g/10min, the high-performance inorganic filler B is 1250 mesh talcum powder, the average particle size is 10μm, the antioxidant A is DSTP and 3114, The antioxidant B is 168. The above-mentioned raw materials are stirred in a high-speed mixer for 2-4 minutes at a speed higher than 600 r/min, mixed uniformly to obtain a premix, and the premix is placed in a twin-screw extruder for melt extrusion and granulation. After drying, the polypropylene composite material is obtained.
双螺杆挤出机的熔融挤出的条件为:一区190-200℃、二区200-210℃、三区210-230℃、四区205-220℃,压力15-20MPa。螺杆的转速为150-300转/分钟,整个挤出过程的停留时间为1-3分钟。The melt extrusion conditions of the twin-screw extruder are: 190-200°C in the first zone, 200-210°C in the second zone, 210-230°C in the third zone, 205-220°C in the fourth zone, and pressure 15-20MPa. The rotation speed of the screw is 150-300 rpm, and the residence time of the whole extrusion process is 1-3 minutes.
对比例2Comparative Example 2
称取44.4%的聚丙烯PP、20%的弹性体POE、35%的高性能无机填料B、0.3%的抗氧化剂A、0.3%的抗氧化剂B,需要说明的是,在本对比例中,所述聚丙烯PP的熔体流动速率为25g/10min(测试条件:230℃,2.16kg),所述弹性体POE为线性乙烯-辛烯共聚物,密度为0.88-0.90g/cm3,其在190℃,2.16kg的测试条件下,熔融指数为0.5-10g/10min,所述高性能无机填料B为1250目滑石粉,平均粒径为10μm,所述抗氧剂A为DSTP和3114,所述抗氧剂B为168。将上述原料在高速混合器中,以高于600转/分钟的转速搅拌2-4分钟,混合均匀得到预混料,将预混料置于双螺杆挤出机中进行熔融挤出,造粒干燥,即得所述聚丙烯复合材料。Weigh 44.4% polypropylene PP, 20% elastomer POE, 35% high-performance inorganic filler B, 0.3% antioxidant A, and 0.3% antioxidant B. It should be noted that in this comparative example, The melt flow rate of the polypropylene PP is 25g/10min (test condition: 230° C., 2.16kg), the elastomer POE is a linear ethylene-octene copolymer, and the density is 0.88-0.90g/cm 3 . Under the test conditions of 190°C and 2.16kg, the melt index is 0.5-10g/10min, the high-performance inorganic filler B is 1250 mesh talcum powder, the average particle size is 10μm, the antioxidant A is DSTP and 3114, The antioxidant B is 168. The above-mentioned raw materials are stirred in a high-speed mixer for 2-4 minutes at a speed higher than 600 r/min, mixed uniformly to obtain a premix, and the premix is placed in a twin-screw extruder for melt extrusion and granulation. After drying, the polypropylene composite material is obtained.
双螺杆挤出机的熔融挤出的条件为:一区190-200℃、二区200-210℃、三区210-230℃、四区205-220℃,压力15-20MPa。螺杆的转速为150-300转/分钟,整个挤出过程的停留时间为1-3分钟。The melt extrusion conditions of the twin-screw extruder are: 190-200°C in the first zone, 200-210°C in the second zone, 210-230°C in the third zone, 205-220°C in the fourth zone, and pressure 15-20MPa. The rotation speed of the screw is 150-300 rpm, and the residence time of the whole extrusion process is 1-3 minutes.
表1实施例1-6及对比例1-2配方(单位:%)Table 1 Formulations of Examples 1-6 and Comparative Examples 1-2 (unit: %)
将实施例1-6及对比例1-2得到的聚丙烯复合材料进行测试,对其缺口冲击强度、拉伸强度、弯曲模量和线性膨胀系数进行评价,测试方法及标准如下:The polypropylene composite materials obtained in Examples 1-6 and Comparative Examples 1-2 were tested, and their notched impact strength, tensile strength, flexural modulus and coefficient of linear expansion were evaluated. The test methods and standards are as follows:
将按上述方法制造的塑料粒子材料置于100℃的鼓风干燥箱中干燥2-4小时,然后再将干燥好的粒料在注射成型机上进行注射成型制样。拉伸性能按照ISO 527进行,试样尺寸为170×10×4mm哑铃型样条,拉伸速度为50mm/min;弯曲性能测试按照ISO 178进行,试样尺寸为80×10×4mm,弯曲速度为2mm/min,跨距为64mm;简支梁缺口冲击强度按ISO 179进行,试样尺寸为80×10×4mm,缺口类型采用该标准中的A型缺口,线性膨胀系数按ISO11359,试样尺寸为8×8×4mm。The plastic particle material produced by the above method is placed in a blast drying oven at 100° C. to dry for 2-4 hours, and then the dried pellets are injected into an injection molding machine for sample preparation. Tensile properties were carried out according to ISO 527, the size of the specimen was 170×10×4mm dumbbell-shaped splines, and the tensile speed was 50mm/min; the bending performance test was carried out according to ISO 178, and the size of the specimen was 80×10×4mm, and the bending speed was The notch is 2mm/min, the span is 64mm; the impact strength of the simply supported beam is carried out according to ISO 179, the size of the sample is 80×10×4mm, the type of notch is the A-notch in this standard, the coefficient of linear expansion is according to ISO11359, the sample is The size is 8×8×4mm.
实施例1-6、对比例1-2各项性能测试结果如表2所示:The performance test results of Examples 1-6 and Comparative Examples 1-2 are shown in Table 2:
表2实施例1-6及对比例1-2测试结果Table 2 Test results of Examples 1-6 and Comparative Examples 1-2
从实施例1-6与对比例1-2的测试结果对比可以看出,通过添加高性能的滑石粉,也就是无机填料A,制备出的聚丙烯复合材料的拉伸强度、弯曲模量明显升高,而线性膨胀系数明显降低,说明高性能的滑石粉的添加可以提升所得材料的刚性和韧性,从实施案例1-3和实施例4-6均可以看出,随着弹性体POE含量的增加,线性膨胀系数逐渐减小,冲击性能逐渐增强,说明弹性体POE的增加能够增强所得材料的热稳定性能和抗冲击性能;从实施例4-6对比于实施例1-3可以看出,随着滑石粉含量的增加,拉伸强度和弯曲模量逐渐增强,但冲击性能逐渐减小,线性膨胀系数部分减小,说明,高性能的滑石粉并不是添加的越多越好,要在一个合适范围。因此,本发明通过添加适量的高性能超细滑石粉、弹性体POE,以及各组分配比的合理搭配,使得制备的聚丙烯复合材料具有了高强度、高韧性以及良好的热稳定性,符合汽车扰流板材料的要求。From the comparison of the test results of Examples 1-6 and Comparative Examples 1-2, it can be seen that by adding high-performance talc, namely inorganic filler A, the tensile strength and flexural modulus of the prepared polypropylene composite material are obvious. increases, while the linear expansion coefficient decreases significantly, indicating that the addition of high-performance talc can improve the rigidity and toughness of the resulting material. It can be seen from examples 1-3 and 4-6 that with the POE content of the elastomer With the increase of , the linear expansion coefficient gradually decreases, and the impact performance gradually increases, indicating that the increase of the POE of the elastomer can enhance the thermal stability performance and impact resistance performance of the obtained material; it can be seen from the comparison of Example 4-6 with Example 1-3 , with the increase of talc content, the tensile strength and flexural modulus gradually increase, but the impact performance gradually decreases, and the linear expansion coefficient decreases partially, indicating that high-performance talc powder is not added as much as possible. within a suitable range. Therefore, in the present invention, by adding an appropriate amount of high-performance ultrafine talcum powder, elastomer POE, and a reasonable combination of the proportions of each component, the prepared polypropylene composite material has high strength, high toughness and good thermal stability, which meets the requirements of Requirements for automotive spoiler materials.
本发明提出的聚丙烯复合材料可用于汽车扰流板中,可以直接垂直切换目前的PC/ABS(塑料合金)扰流板,无需增加开模费用,除此之外,在PC/ABS(塑料合金)材料方案领域的零件,均可进行有效替换,降低制造成本。The polypropylene composite material proposed by the present invention can be used in automobile spoilers, and the current PC/ABS (plastic alloy) spoilers can be directly and vertically switched without increasing the cost of mold opening. Parts in the field of alloy) material solutions can be effectively replaced to reduce manufacturing costs.
尽管上面已经示出和描述了本发明的实施例,可以理解的是,上述实施例是示例性的,不能理解为对本发明的限制,本领域的普通技术人员在本发明的范围内可以对上述实施例进行变化、修改、替换和变型。Although the embodiments of the present invention have been shown and described above, it should be understood that the above-mentioned embodiments are exemplary and should not be construed as limiting the present invention. Embodiments are subject to variations, modifications, substitutions and variations.
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Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103923381A (en) * | 2013-12-28 | 2014-07-16 | 上海普利特复合材料股份有限公司 | High-modulus and ultrahigh-impact polypropylene composite material and its preparation method |
CN104592645A (en) * | 2014-12-22 | 2015-05-06 | 上海普利特复合材料股份有限公司 | Low-density low-shrinkage high-impact polypropylene composite material and preparation method thereof |
CN105542375A (en) * | 2015-12-30 | 2016-05-04 | 上海普利特复合材料股份有限公司 | High-performance polypropylene composite material applicable to thin-walled part injection molding and preparation method thereof |
CN105602179A (en) * | 2015-12-30 | 2016-05-25 | 上海普利特复合材料股份有限公司 | High-rigidity, low-shrinkage and good-appearance polypropylene composite material and preparation method thereof |
CN108546385A (en) * | 2018-03-13 | 2018-09-18 | 上海普利特复合材料股份有限公司 | A kind of automobile seamless gasbag instrument board high-performance polypropylene compound material and preparation method thereof |
-
2021
- 2021-03-12 CN CN202110271434.5A patent/CN115073874A/en active Pending
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103923381A (en) * | 2013-12-28 | 2014-07-16 | 上海普利特复合材料股份有限公司 | High-modulus and ultrahigh-impact polypropylene composite material and its preparation method |
CN104592645A (en) * | 2014-12-22 | 2015-05-06 | 上海普利特复合材料股份有限公司 | Low-density low-shrinkage high-impact polypropylene composite material and preparation method thereof |
CN105542375A (en) * | 2015-12-30 | 2016-05-04 | 上海普利特复合材料股份有限公司 | High-performance polypropylene composite material applicable to thin-walled part injection molding and preparation method thereof |
CN105602179A (en) * | 2015-12-30 | 2016-05-25 | 上海普利特复合材料股份有限公司 | High-rigidity, low-shrinkage and good-appearance polypropylene composite material and preparation method thereof |
CN108546385A (en) * | 2018-03-13 | 2018-09-18 | 上海普利特复合材料股份有限公司 | A kind of automobile seamless gasbag instrument board high-performance polypropylene compound material and preparation method thereof |
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