CN106519622B - A kind of macromolecule Polycarbonate alloy material and preparation method thereof - Google Patents

A kind of macromolecule Polycarbonate alloy material and preparation method thereof Download PDF

Info

Publication number
CN106519622B
CN106519622B CN201510584022.1A CN201510584022A CN106519622B CN 106519622 B CN106519622 B CN 106519622B CN 201510584022 A CN201510584022 A CN 201510584022A CN 106519622 B CN106519622 B CN 106519622B
Authority
CN
China
Prior art keywords
area
compatilizer
alloy material
polycarbonate alloy
weight
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
CN201510584022.1A
Other languages
Chinese (zh)
Other versions
CN106519622A (en
Inventor
葛腾杰
高宇新
曹婷婷
宋磊
于占元
姜进宪
王熺
张明强
安彦杰
李�瑞
国海峰
张德英
王世华
赵吉娜
梁立伟
李岩
于波
李景新
黄影
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
China Petroleum and Natural Gas Co Ltd
Original Assignee
China Petroleum and Natural Gas Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by China Petroleum and Natural Gas Co Ltd filed Critical China Petroleum and Natural Gas Co Ltd
Priority to CN201510584022.1A priority Critical patent/CN106519622B/en
Publication of CN106519622A publication Critical patent/CN106519622A/en
Application granted granted Critical
Publication of CN106519622B publication Critical patent/CN106519622B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Compositions Of Macromolecular Compounds (AREA)
  • Processes Of Treating Macromolecular Substances (AREA)

Abstract

The present invention relates to a kind of macromolecule Polycarbonate alloy materials and preparation method thereof, and the raw material of the alloy material includes:The PC of 60 80 parts by weight, the ABS of 20 30 parts by weight, the compatilizer a of 14 parts by weight, the antioxidant of the compatilizer b of 14 parts by weight and 0.2 0.4 parts by weight, compatilizer a and compatilizer b be maleic anhydride grafted polyethylene, be used for be grafted polyethylene softening point≤85 DEG C;First, a melting extrusion is blended in PC and compatilizer a, obtains PC/PE g MAH, then, it after PC/PE g MAH are sufficiently mixed again with ABS, compatilizer b, antioxidant in high-speed mixer, is granulated by double screw extruder second melting, obtains macromolecule Polycarbonate alloy material.Polycarbonate alloy performance prepared by the present invention is stablized, and material erosion-resisting characteristics is good, improves and there are problems that being layered serious, surface decorative pattern occurs in actual processing process in which materials.

Description

A kind of macromolecule Polycarbonate alloy material and preparation method thereof
Technical field
The present invention relates to polycarbonate alloy technology preparation field, more particularly to a kind of polyphosphazene polymer carbonic ester alloy material Material and preparation method thereof.
Background technology
Blend using ABS and PC as primary raw material is a kind of important engineering plastic alloy, has the excellent of ABS and PC concurrently Point, i.e., with good shaping mobile performance and higher heat distortion temperature and stability.It reduces melt compared with PC and glues Degree, improves processing performance, improves low temperature impact strength and reduce thickness-sensitive and price;Compared with ABS, improve Heat distortion temperature and its mechanical property is improved, automobile, electronics, office machine-tool industry etc. can be preferably applied for.
However have the presence of benzene ring structure in PC, and in ABS the styrene-content of main component SAN generally 70% with On, therefore, PC and ABS can only partially compatible.In order to which PC is made to can be good at merging with ABS, the excellent of alloy material is given full play to Gesture using the modified PC alloy materials such as all kinds of compatilizers, coupling agent, improves material compatibility and has become the heat studied now Point.
The patent of Application No. 201210275477.3 provides a kind of preparation method and application of PC/ABS alloys, can be with Significantly improve the mechanical performance of alloy.But patent provide method be by all auxiliary agents and melt pelletization of basis material, There is the problems such as decorative pattern, not easy to be processed in the presence of serious, surface is layered in actual processing process in which materials.
The content of the invention
It is an object of the invention to solve in the prior art, material exists during actual processing is layered serious, surface There is the problems such as decorative pattern, not easy to be processed, and a kind of macromolecule Polycarbonate alloy material haveing excellent performance and its preparation side are provided Method.
A kind of macromolecule Polycarbonate alloy material provided by the invention, the raw material of the alloy material include:60-80 weight Compatilizer b and the 0.2-0.4 parts by weight of compatilizer a, 1-4 parts by weight of ABS, 1-4 parts by weight of PC, 20-30 parts by weight of part Antioxidant, the compatilizer a and compatilizer b are maleic anhydride grafted polyethylene, are used for the softening point for the polyethylene being grafted ≤ 85 DEG C.
Preferably, the compatilizer a and compatilizer b is identical or different maleic anhydride grafted polyethylene
Preferably, the maleic anhydride grafted polyethylene is to be grafted LLDPE, maleic anhydride grafting by maleic anhydride VLDPE, maleic anhydride grafting HDPE or maleic anhydride grafting LDPE.
Preferably, the antioxidant is Hinered phenols antioxidant and/or phosphite ester kind antioxidant.
The preparation method of macromolecule Polycarbonate alloy material provided by the invention, the macromolecule Polycarbonate alloy material It is above-mentioned macromolecule Polycarbonate alloy material, comprises the following steps:
S1:A melting extrusion is blended in PC and compatilizer a, obtains PC/PE-g-MAH;
S2:After PC/PE-g-MAH is sufficiently mixed again with ABS, compatilizer b, antioxidant in high-speed mixer, pass through double spiral shells Bar extruder second melting is granulated, and obtains macromolecule Polycarbonate alloy material.
Preferably, in step S1, the extrusion temperature once melted is 180~250 DEG C.
Preferably, in step S2, the extrusion temperature of the second melting is 180~230 DEG C.
Beneficial effects of the present invention:
The macromolecule Polycarbonate alloy material, due to selecting the polyethylene of softening point≤85 DEG C as grafting high score Son, hence it is evident that the compatibility of PC and ABS are improved, and the polyethylene co-monomer content therein of low softening point is relatively high, On the premise of PC alloy materials other mechanical properties are not destroyed, the impact strength of material is significantly improved.It is in addition, special Compatilizer addition manner and secondary granulation technique preferably improve the compatibility of PC and ABS, reduce the dosage of compatilizer.
The preparation method of the macromolecule Polycarbonate alloy material, hence it is evident that improve the compatibility of alloy system, make material Expect that performance is more stablized, significantly improve the erosion-resisting characteristics of material, improve and there is layering sternly in actual processing process in which materials There is the problem of decorative pattern in weight, surface.
Specific embodiment
It further illustrates the present invention by the following examples, but the present invention is not limited to these embodiments.
Embodiment 1
The raw material of the macromolecule Polycarbonate alloy material of the present invention includes, in parts by weight:
First, by after PC and compatilizer a mixed at high speed, melt pelletization of double screw extruder, processing technology are passed through It is as follows:The extrusion temperature once melted is 220~245 DEG C, is specially 220 DEG C of one area of double screw extruder, 235 DEG C of 2nd area, three 235 DEG C of area, 235 DEG C of 4th area, 240 DEG C of 5th area, 245 DEG C of 6th area, 240 DEG C of 7th area, 235 DEG C of 8th area, screw speed 300r/min are obtained To PC/PE-g-MAH;
Then, by after obtained PC/PE-g-MAH particles and ABS, compatilizer b, antioxidant mixed at high speed, twin-screw is passed through Extruder second melting is granulated, and processing technology is as follows:The extrusion temperature of second melting is 210~230 DEG C, is specially twin-screw 210 DEG C of one area of extruder, 225 DEG C of 2nd area, 225 DEG C of 3rd area, 225 DEG C of 4th area, 230 DEG C of 5th area, 230 DEG C of 6th area, 230 DEG C of 7th area, Eight 225 DEG C of areas, screw speed 300r/min obtain macromolecule polycarbonate alloy, and test performance is shown in Table 1.
Comparative example 1
The raw material of macromolecule Polycarbonate alloy material includes, in parts by weight:
First, by after PC and compatilizer a mixed at high speed, melt pelletization of double screw extruder, processing technology are passed through It is as follows:The extrusion temperature once melted is 220~245 DEG C, is specially 220 DEG C of one area of double screw extruder, 235 DEG C of 2nd area, three 235 DEG C of area, 235 DEG C of 4th area, 240 DEG C of 5th area, 245 DEG C of 6th area, 240 DEG C of 7th area, 235 DEG C of 8th area, screw speed 300r/min are obtained To PC/PE-g-MAH.
Then, by after obtained PC/PE-g-MAH particles and ABS, compatilizer b, antioxidant mixed at high speed, twin-screw is passed through Extruder second melting is granulated, and processing technology is as follows:The extrusion temperature of second melting is 210~230 DEG C, is specially twin-screw 210 DEG C of one area of extruder, 225 DEG C of 2nd area, 225 DEG C of 3rd area, 225 DEG C of 4th area, 230 DEG C of 5th area, 230 DEG C of 6th area, 230 DEG C of 7th area, Eight 225 DEG C of areas, screw speed 300r/min obtain macromolecule polycarbonate alloy, and test performance is shown in Table 1.
Embodiment 2
The raw material of the macromolecule Polycarbonate alloy material of the present invention includes, in parts by weight:
First, by after PC and compatilizer a mixed at high speed, melt pelletization of double screw extruder, processing technology are passed through It is as follows:The extrusion temperature once melted is 220~245 DEG C, is specially 220 DEG C of one area of double screw extruder, 235 DEG C of 2nd area, three 235 DEG C of area, 235 DEG C of 4th area, 240 DEG C of 5th area, 245 DEG C of 6th area, 240 DEG C of 7th area, 235 DEG C of 8th area, screw speed 300r/min are obtained To PC/PE-g-MAH.
Then, by after obtained PC/PE-g-MAH particles and ABS, compatilizer b, antioxidant mixed at high speed, twin-screw is passed through Extruder second melting is granulated, and processing technology is as follows:The extrusion temperature of second melting is 210~230 DEG C, is specially twin-screw 210 DEG C of one area of extruder, 225 DEG C of 2nd area, 225 DEG C of 3rd area, 225 DEG C of 4th area, 230 DEG C of 5th area, 230 DEG C of 6th area, 230 DEG C of 7th area, Eight 225 DEG C of areas, screw speed 300r/min obtain macromolecule polycarbonate alloy, and test performance is shown in Table 1.
Comparative example 2
The raw material of macromolecule Polycarbonate alloy material includes, in parts by weight:
First, by after PC and compatilizer a mixed at high speed, melt pelletization of double screw extruder, processing technology are passed through It is as follows:The extrusion temperature once melted is 220~245 DEG C, is specially 220 DEG C of one area of double screw extruder, 235 DEG C of 2nd area, three 235 DEG C of area, 235 DEG C of 4th area, 240 DEG C of 5th area, 245 DEG C of 6th area, 240 DEG C of 7th area, 235 DEG C of 8th area, screw speed 300r/min are obtained To PC/PE-g-MAH.
Then, by after obtained PC/PE-g-MAH particles and ABS, compatilizer b, antioxidant mixed at high speed, twin-screw is passed through Extruder second melting is granulated, and processing technology is as follows:The extrusion temperature of second melting is 210~230 DEG C, is specially twin-screw 210 DEG C of one area of extruder, 225 DEG C of 2nd area, 225 DEG C of 3rd area, 225 DEG C of 4th area, 230 DEG C of 5th area, 230 DEG C of 6th area, 230 DEG C of 7th area, Eight 225 DEG C of areas, screw speed 300r/min obtain macromolecule polycarbonate alloy, and test performance is shown in Table 1.
Embodiment 3
The raw material of the macromolecule Polycarbonate alloy material of the present invention includes, in parts by weight:
First, by after PC and compatilizer a mixed at high speed, melt pelletization of double screw extruder, processing technology are passed through It is as follows:The extrusion temperature once melted is 180~245 DEG C, is specially 180 DEG C of one area of double screw extruder, 190 DEG C of 2nd area, three 200 DEG C of area, 235 DEG C of 4th area, 240 DEG C of 5th area, 245 DEG C of 6th area, 240 DEG C of 7th area, 235 DEG C of 8th area, screw speed 300r/min are obtained To PC/PE-g-MAH.
Then, by after obtained PC/PE-g-MAH particles and ABS, compatilizer b, antioxidant mixed at high speed, twin-screw is passed through Extruder second melting is granulated, and processing technology is as follows:The extrusion temperature of second melting is 210~230 DEG C, is specially twin-screw 210 DEG C of one area of extruder, 225 DEG C of 2nd area, 225 DEG C of 3rd area, 225 DEG C of 4th area, 230 DEG C of 5th area, 230 DEG C of 6th area, 230 DEG C of 7th area, Eight 225 DEG C of areas, screw speed 300r/min obtain macromolecule polycarbonate alloy, and test performance is shown in Table 1.
Comparative example 3
The raw material of macromolecule Polycarbonate alloy material includes, in parts by weight:
First, by after PC and compatilizer a mixed at high speed, melt pelletization of double screw extruder, processing technology are passed through It is as follows:The extrusion temperature once melted is 180~245 DEG C, is specially 180 DEG C of one area of double screw extruder, 190 DEG C of 2nd area, three 200 DEG C of area, 235 DEG C of 4th area, 240 DEG C of 5th area, 245 DEG C of 6th area, 240 DEG C of 7th area, 235 DEG C of 8th area, screw speed 300r/min are obtained To PC/PE-g-MAH.
Then, by after obtained PC/PE-g-MAH particles and ABS, compatilizer b, antioxidant mixed at high speed, twin-screw is passed through Extruder second melting is granulated, and processing technology is as follows:The extrusion temperature of second melting is 210~230 DEG C, is specially twin-screw 210 DEG C of one area of extruder, 225 DEG C of 2nd area, 225 DEG C of 3rd area, 225 DEG C of 4th area, 230 DEG C of 5th area, 230 DEG C of 6th area, 230 DEG C of 7th area, Eight 225 DEG C of areas, screw speed 300r/min obtain macromolecule polycarbonate alloy, and test performance is shown in Table 1.
Embodiment 4
The raw material of the macromolecule Polycarbonate alloy material of the present invention includes, in parts by weight:
First, by after PC and compatilizer a mixed at high speed, melt pelletization of double screw extruder, processing technology are passed through It is as follows:The extrusion temperature once melted is 180~245 DEG C, is specially 180 DEG C of one area of double screw extruder, 190 DEG C of 2nd area, three 200 DEG C of area, 235 DEG C of 4th area, 240 DEG C of 5th area, 245 DEG C of 6th area, 240 DEG C of 7th area, 235 DEG C of 8th area, screw speed 300r/min are obtained To PC/PE-g-MAH.
Then, by after obtained PC/PE-g-MAH particles and ABS, compatilizer b, antioxidant mixed at high speed, twin-screw is passed through Extruder second melting is granulated, and processing technology is as follows:The extrusion temperature of second melting is 210~230 DEG C, is specially twin-screw 210 DEG C of one area of extruder, 225 DEG C of 2nd area, 225 DEG C of 3rd area, 225 DEG C of 4th area, 230 DEG C of 5th area, 230 DEG C of 6th area, 230 DEG C of 7th area, Eight 225 DEG C of areas, screw speed 300r/min obtain macromolecule polycarbonate alloy, and test performance is shown in Table 1.
Comparative example 4
The raw material of macromolecule Polycarbonate alloy material includes, in parts by weight:
First, by after PC and compatilizer a mixed at high speed, melt pelletization of double screw extruder, processing technology are passed through It is as follows:The extrusion temperature once melted is 180~245 DEG C, is specially 180 DEG C of one area of double screw extruder, 190 DEG C of 2nd area, three 200 DEG C of area, 235 DEG C of 4th area, 240 DEG C of 5th area, 245 DEG C of 6th area, 240 DEG C of 7th area, 235 DEG C of 8th area, screw speed 300r/min are obtained To PC/PE-g-MAH.
Then, by after obtained PC/PE-g-MAH particles and ABS, compatilizer b, antioxidant mixed at high speed, twin-screw is passed through Extruder second melting is granulated, and processing technology is as follows:The extrusion temperature of second melting is 210~230 DEG C, is specially twin-screw 210 DEG C of one area of extruder, 225 DEG C of 2nd area, 225 DEG C of 3rd area, 225 DEG C of 4th area, 230 DEG C of 5th area, 230 DEG C of 6th area, 230 DEG C of 7th area, Eight 225 DEG C of areas, screw speed 300r/min obtain macromolecule polycarbonate alloy, and test performance is shown in Table 1.
Embodiment 5
The raw material of the macromolecule Polycarbonate alloy material of the present invention includes, in parts by weight:
First, by after PC and compatilizer a mixed at high speed, melt pelletization of double screw extruder, processing technology are passed through It is as follows:The extrusion temperature once melted is 180~245 DEG C, is specially 180 DEG C of one area of double screw extruder, 190 DEG C of 2nd area, three 200 DEG C of area, 235 DEG C of 4th area, 240 DEG C of 5th area, 245 DEG C of 6th area, 240 DEG C of 7th area, 235 DEG C of 8th area, screw speed 300r/min are obtained To PC/PE-g-MAH.
Then, then by after obtained PC/PE-g-MAH particles and ABS, compatilizer b, antioxidant mixed at high speed, double spiral shells are passed through Bar extruder second melting is granulated, and processing technology is as follows:The extrusion temperature of second melting is 210~230 DEG C, is specially double spiral shells 210 DEG C of one area of bar extruder, 225 DEG C of 2nd area, 225 DEG C of 3rd area, 225 DEG C of 4th area, 230 DEG C of 5th area, 230 DEG C of 6th area, seven areas 230 DEG C, 225 DEG C, screw speed 300r/min of 8th area, obtain macromolecule polycarbonate alloy, test performance is shown in Table 1.
Embodiment 6
The raw material of the macromolecule Polycarbonate alloy material of the present invention includes, in parts by weight:
First, by after PC and compatilizer a mixed at high speed, melt pelletization of double screw extruder, processing technology are passed through It is as follows:The extrusion temperature once melted is 180~245 DEG C, is specially 180 DEG C of one area of double screw extruder, 190 DEG C of 2nd area, three 200 DEG C of area, 235 DEG C of 4th area, 240 DEG C of 5th area, 245 DEG C of 6th area, 240 DEG C of 7th area, 235 DEG C of 8th area, screw speed 300r/min are obtained To PC/PE-g-MAH.
Then, by after obtained PC/PE-g-MAH particles and ABS, compatilizer b, antioxidant mixed at high speed, twin-screw is passed through Extruder second melting is granulated, and processing technology is as follows:The extrusion temperature of second melting is 210~230 DEG C, is specially twin-screw 210 DEG C of one area of extruder, 225 DEG C of 2nd area, 225 DEG C of 3rd area, 225 DEG C of 4th area, 230 DEG C of 5th area, 230 DEG C of 6th area, 230 DEG C of 7th area, Eight 225 DEG C of areas, screw speed 300r/min obtain macromolecule polycarbonate alloy, and test performance is shown in Table 1.
Embodiment 7
The raw material of the macromolecule Polycarbonate alloy material of the present invention includes, in parts by weight:
First, by after PC and compatilizer a mixed at high speed, melt pelletization of double screw extruder, processing technology are passed through It is as follows:The extrusion temperature once melted is 180~245 DEG C, is specially 180 DEG C of one area of double screw extruder, 190 DEG C of 2nd area, three 200 DEG C of area, 235 DEG C of 4th area, 240 DEG C of 5th area, 245 DEG C of 6th area, 240 DEG C of 7th area, 235 DEG C of 8th area, screw speed 300r/min are obtained To PC/PE-g-MAH.
Then, by after obtained PC/PE-g-MAH particles and ABS, compatilizer b, antioxidant mixed at high speed, twin-screw is passed through Extruder second melting is granulated, and processing technology is as follows:The extrusion temperature of second melting is 180~245 DEG C, is specially twin-screw 180 DEG C of one area of extruder, 190 DEG C of 2nd area, 200 DEG C of 3rd area, 235 DEG C of 4th area, 240 DEG C of 5th area, 245 DEG C of 6th area, 240 DEG C of 7th area, Eight 235 DEG C of areas, screw speed 300r/min obtain macromolecule polycarbonate alloy, and test performance is shown in Table 1.
Embodiment 8
The raw material of the macromolecule Polycarbonate alloy material of the present invention includes, in parts by weight:
First, by after PC and compatilizer a mixed at high speed, melt pelletization of double screw extruder, processing technology are passed through It is as follows:The extrusion temperature once melted is 220~245 DEG C, is specially 220 DEG C of one area of double screw extruder, 235 DEG C of 2nd area, three 235 DEG C of area, 235 DEG C of 4th area, 240 DEG C of 5th area, 245 DEG C of 6th area, 240 DEG C of 7th area, 235 DEG C of 8th area, screw speed 300r/min are obtained To PC/PE-g-MAH.
Then, by after obtained PC/PE-g-MAH particles and ABS, compatilizer b, antioxidant mixed at high speed, twin-screw is passed through Extruder second melting is granulated, and processing technology is as follows:The extrusion temperature of second melting is 210~230 DEG C, is specially twin-screw 210 DEG C of one area of extruder, 225 DEG C of 2nd area, 225 DEG C of 3rd area, 225 DEG C of 4th area, 230 DEG C of 5th area, 230 DEG C of 6th area, 230 DEG C of 7th area, Eight 225 DEG C of areas, screw speed 300r/min obtain macromolecule polycarbonate alloy, and test performance is shown in Table 1.
Embodiment 9
The raw material of the macromolecule Polycarbonate alloy material of the present invention includes, in parts by weight:
First, by after PC and compatilizer a mixed at high speed, melt pelletization of double screw extruder, processing technology are passed through It is as follows:The extrusion temperature once melted is 220~245 DEG C, is specially 220 DEG C of one area of double screw extruder, 235 DEG C of 2nd area, three 235 DEG C of area, 235 DEG C of 4th area, 240 DEG C of 5th area, 245 DEG C of 6th area, 240 DEG C of 7th area, 235 DEG C of 8th area, screw speed 300r/min are obtained To PC/PE-g-MAH.
Then, by after obtained PC/PE-g-MAH particles and ABS, compatilizer b, antioxidant mixed at high speed, twin-screw is passed through Extruder second melting is granulated, and processing technology is as follows:The extrusion temperature of second melting is 210~230 DEG C, is specially twin-screw 210 DEG C of one area of extruder, 225 DEG C of 2nd area, 225 DEG C of 3rd area, 225 DEG C of 4th area, 230 DEG C of 5th area, 230 DEG C of 6th area, 230 DEG C of 7th area, Eight 225 DEG C of areas, screw speed 300r/min obtain macromolecule polycarbonate alloy, and test performance is shown in Table 1.
Embodiment 10
The raw material of the macromolecule Polycarbonate alloy material of the present invention includes, in parts by weight:
First, by after PC and compatilizer a mixed at high speed, melt pelletization of double screw extruder, processing technology are passed through It is as follows:The extrusion temperature once melted is 220~245 DEG C, is specially 220 DEG C of one area of double screw extruder, 235 DEG C of 2nd area, three 235 DEG C of area, 235 DEG C of 4th area, 240 DEG C of 5th area, 245 DEG C of 6th area, 240 DEG C of 7th area, 235 DEG C of 8th area, screw speed 300r/min are obtained To PC/PE-g-MAH.
Then, by after obtained PC/PE-g-MAH particles and ABS, compatilizer b, antioxidant mixed at high speed, twin-screw is passed through Extruder second melting is granulated, and processing technology is as follows:The extrusion temperature of second melting is 210~230 DEG C, is specially twin-screw 210 DEG C of one area of extruder, 225 DEG C of 2nd area, 225 DEG C of 3rd area, 225 DEG C of 4th area, 230 DEG C of 5th area, 230 DEG C of 6th area, 230 DEG C of 7th area, Eight 225 DEG C of areas, screw speed 300r/min obtain macromolecule polycarbonate alloy, and test performance is shown in Table 1.
Embodiment 11
The raw material of the macromolecule Polycarbonate alloy material of the present invention includes, in parts by weight:
First, by after PC and compatilizer a mixed at high speed, melt pelletization of double screw extruder, processing technology are passed through It is as follows:The extrusion temperature once melted is 220~245 DEG C, is specially 220 DEG C of one area of double screw extruder, 235 DEG C of 2nd area, three 235 DEG C of area, 235 DEG C of 4th area, 240 DEG C of 5th area, 245 DEG C of 6th area, 240 DEG C of 7th area, 235 DEG C of 8th area, screw speed 300r/min are obtained To PC/PE-g-MAH.
Then, by after obtained PC/PE-g-MAH particles and ABS, compatilizer b, antioxidant mixed at high speed, twin-screw is passed through Extruder second melting is granulated, and processing technology is as follows:The extrusion temperature of second melting is 210~230 DEG C, is specially twin-screw 210 DEG C of one area of extruder, 225 DEG C of 2nd area, 225 DEG C of 3rd area, 225 DEG C of 4th area, 230 DEG C of 5th area, 230 DEG C of 6th area, 230 DEG C of 7th area, Eight 225 DEG C of areas, screw speed 300r/min obtain macromolecule polycarbonate alloy, and test performance is shown in Table 1.
Embodiment 12
The raw material of the macromolecule Polycarbonate alloy material of the present invention includes, in parts by weight:
First, by after PC and compatilizer a mixed at high speed, melt pelletization of double screw extruder, processing technology are passed through It is as follows:The extrusion temperature once melted is 220~245 DEG C, is specially 220 DEG C of one area of double screw extruder, 235 DEG C of 2nd area, three 235 DEG C of area, 235 DEG C of 4th area, 240 DEG C of 5th area, 245 DEG C of 6th area, 240 DEG C of 7th area, 235 DEG C of 8th area, screw speed 300r/min are obtained To PC/PE-g-MAH.
Then, by after obtained PC/PE-g-MAH particles and ABS, compatilizer b, antioxidant mixed at high speed, twin-screw is passed through Extruder second melting is granulated, and processing technology is as follows:The extrusion temperature of second melting is 210~230 DEG C, is specially twin-screw 210 DEG C of one area of extruder, 225 DEG C of 2nd area, 225 DEG C of 3rd area, 225 DEG C of 4th area, 230 DEG C of 5th area, 230 DEG C of 6th area, 230 DEG C of 7th area, Eight 225 DEG C of areas, screw speed 300r/min obtain macromolecule polycarbonate alloy, and test performance is shown in Table 1.
Embodiment 13
The raw material of the macromolecule Polycarbonate alloy material of the present invention includes, in parts by weight:
First, by after PC and compatilizer a mixed at high speed, melt pelletization of double screw extruder, processing technology are passed through It is as follows:The extrusion temperature once melted is 220~245 DEG C, is specially 220 DEG C of one area of double screw extruder, 235 DEG C of 2nd area, three 235 DEG C of area, 235 DEG C of 4th area, 240 DEG C of 5th area, 245 DEG C of 6th area, 240 DEG C of 7th area, 235 DEG C of 8th area, screw speed 300r/min are obtained To PC/PE-g-MAH.
Then, by after obtained PC/PE-g-MAH particles and ABS, compatilizer b, antioxidant mixed at high speed, twin-screw is passed through Extruder second melting is granulated, and processing technology is as follows:The extrusion temperature of second melting is 210~230 DEG C, is specially twin-screw 210 DEG C of one area of extruder, 225 DEG C of 2nd area, 225 DEG C of 3rd area, 225 DEG C of 4th area, 230 DEG C of 5th area, 230 DEG C of 6th area, 230 DEG C of 7th area, Eight 225 DEG C of areas, screw speed 300r/min obtain macromolecule polycarbonate alloy, and test performance is shown in Table 1.
Embodiment 14
The raw material of the macromolecule Polycarbonate alloy material of the present invention includes, in parts by weight:
First, by after PC and compatilizer a mixed at high speed, melt pelletization of double screw extruder, processing technology are passed through It is as follows:The extrusion temperature once melted is 220~245 DEG C, is specially 220 DEG C of one area of double screw extruder, 235 DEG C of 2nd area, three 235 DEG C of area, 235 DEG C of 4th area, 240 DEG C of 5th area, 245 DEG C of 6th area, 240 DEG C of 7th area, 235 DEG C of 8th area, screw speed 300r/min are obtained To PC/PE-g-MAH.
Then, by after obtained PC/PE-g-MAH particles and ABS, compatilizer b, antioxidant mixed at high speed, twin-screw is passed through Extruder second melting is granulated, and processing technology is as follows:The extrusion temperature of second melting is 210~230 DEG C, is specially twin-screw 210 DEG C of one area of extruder, 225 DEG C of 2nd area, 225 DEG C of 3rd area, 225 DEG C of 4th area, 230 DEG C of 5th area, 230 DEG C of 6th area, 230 DEG C of 7th area, Eight 225 DEG C of areas, screw speed 300r/min obtain macromolecule polycarbonate alloy, and test performance is shown in Table 1.
Embodiment 15
The raw material of the macromolecule Polycarbonate alloy material of the present invention includes, in parts by weight:
First, by after PC and compatilizer a mixed at high speed, melt pelletization of double screw extruder, processing technology are passed through It is as follows:The extrusion temperature once melted is 220~245 DEG C, is specially 220 DEG C of one area of double screw extruder, 235 DEG C of 2nd area, three 235 DEG C of area, 235 DEG C of 4th area, 240 DEG C of 5th area, 245 DEG C of 6th area, 240 DEG C of 7th area, 235 DEG C of 8th area, screw speed 300r/min are obtained To PC/PE-g-MAH.
Then, by after obtained PC/PE-g-MAH particles and ABS, compatilizer b, antioxidant mixed at high speed, twin-screw is passed through Extruder second melting is granulated, and processing technology is as follows:The extrusion temperature of second melting is 210~230 DEG C, is specially twin-screw 210 DEG C of one area of extruder, 225 DEG C of 2nd area, 225 DEG C of 3rd area, 225 DEG C of 4th area, 230 DEG C of 5th area, 230 DEG C of 6th area, 230 DEG C of 7th area, Eight 225 DEG C of areas, screw speed 300r/min obtain macromolecule polycarbonate alloy, and test performance is shown in Table 1.
Embodiment 16
The raw material of the macromolecule Polycarbonate alloy material of the present invention includes, in parts by weight:
First, by after PC and compatilizer a mixed at high speed, melt pelletization of double screw extruder, processing technology are passed through It is as follows:The extrusion temperature once melted is 220~245 DEG C, is specially 220 DEG C of one area of double screw extruder, 235 DEG C of 2nd area, three 235 DEG C of area, 235 DEG C of 4th area, 240 DEG C of 5th area, 245 DEG C of 6th area, 240 DEG C of 7th area, 235 DEG C of 8th area, screw speed 300r/min are obtained To PC/PE-g-MAH.
Then, by after obtained PC/PE-g-MAH particles and ABS, compatilizer b, antioxidant mixed at high speed, twin-screw is passed through Extruder second melting is granulated, and processing technology is as follows:The extrusion temperature of second melting is 210~230 DEG C, is specially twin-screw 210 DEG C of one area of extruder, 225 DEG C of 2nd area, 225 DEG C of 3rd area, 225 DEG C of 4th area, 230 DEG C of 5th area, 230 DEG C of 6th area, 230 DEG C of 7th area, Eight 225 DEG C of areas, screw speed 300r/min obtain macromolecule polycarbonate alloy, and test performance is shown in Table 1.
Embodiment 17
The raw material of the macromolecule Polycarbonate alloy material of the present invention includes, in parts by weight:
First, by after PC and compatilizer a mixed at high speed, melt pelletization of double screw extruder, processing technology are passed through It is as follows:The extrusion temperature once melted is 220~245 DEG C, is specially 220 DEG C of one area of double screw extruder, 235 DEG C of 2nd area, three 235 DEG C of area, 235 DEG C of 4th area, 240 DEG C of 5th area, 245 DEG C of 6th area, 240 DEG C of 7th area, 235 DEG C of 8th area, screw speed 300r/min are obtained To PC/PE-g-MAH.
Then, by after obtained PC/PE-g-MAH particles and ABS, compatilizer b, antioxidant mixed at high speed, twin-screw is passed through Extruder second melting is granulated, and processing technology is as follows:The extrusion temperature of second melting is 210~230 DEG C, is specially twin-screw 210 DEG C of one area of extruder, 225 DEG C of 2nd area, 225 DEG C of 3rd area, 225 DEG C of 4th area, 230 DEG C of 5th area, 230 DEG C of 6th area, 230 DEG C of 7th area, Eight 225 DEG C of areas, screw speed 300r/min obtain macromolecule polycarbonate alloy, and test performance is shown in Table 1.
1 embodiment product mechanical property of table compares
As shown in table 1, the shadow to alloy material mechanical performance with the base resin softening point of maleic anhydride grafting is illustrated It rings.Embodiment 1-17 and comparative example 1-4 has chosen softening point respectively less than or equal to 85 DEG C and at least one softening point is more than 85 DEG C The compatilizer of base resin, and the performance to alloy is made is tested.As can be seen that softening point is big from comparative example 1-4 In showing impact strength and tensile strength decline on alloy material prepared by 85 DEG C of compatilizers, mechanical property, material is adding The problem of layering, decorative pattern being there is also during work.It, can compared to alloy material prepared by compatilizer of the softening point less than 85 DEG C Meet the compatibility requirements of alloy system well, the mechanical property of material protrudes.
In conclusion the macromolecule Polycarbonate alloy material of the present invention, due to selecting the polyethylene of softening point≤85 DEG C As grafting polymer, hence it is evident that improve the compatibility of PC and ABS, and the polyethylene comonomer therein of low softening point contains It measures relatively high, on the premise of PC alloy materials other mechanical properties are not destroyed, significantly improves the impact strength of material. In addition, special compatilizer addition manner and secondary granulation technique, preferably improve the compatibility of PC and ABS, reduce phase Hold the dosage of agent.
The preparation method of the macromolecule Polycarbonate alloy material, hence it is evident that improve the compatibility of alloy system, make material Expect that performance is more stablized, significantly improve the erosion-resisting characteristics of material, improve and there is layering sternly in actual processing process in which materials There is the problem of decorative pattern in weight, surface.
Certainly, the present invention can also have other various embodiments, without deviating from the spirit and substance of the present invention, ripe Various corresponding changes and deformation, but these corresponding changes and deformation can be made according to the present invention by knowing those skilled in the art It should all belong to the scope of protection of the present invention.

Claims (7)

1. a kind of macromolecule Polycarbonate alloy material, it is characterised in that:The raw material of the alloy material includes:60-80 parts by weight PC, 20-30 parts by weight ABS, 1-4 parts by weight compatilizer a, 1-4 parts by weight compatilizer b and 0.2-0.4 parts by weight Antioxidant, the compatilizer a and compatilizer b are maleic anhydride grafted polyethylene, and the softening point for being used for the polyethylene being grafted is equal ≤85℃。
2. macromolecule Polycarbonate alloy material according to claim 1, it is characterised in that:The compatilizer a and compatible Agent b is identical or different maleic anhydride grafted polyethylene.
3. macromolecule Polycarbonate alloy material according to claim 1, it is characterised in that:The maleic anhydride grafting Polyethylene is grafted LLDPE for maleic anhydride, maleic anhydride is grafted VLDPE, maleic anhydride is grafted HDPE or maleic anhydride grafting LDPE。
4. macromolecule Polycarbonate alloy material according to claim 1, it is characterised in that:The antioxidant is hindered phenol Kind antioxidant and/or phosphite ester kind antioxidant.
5. a kind of preparation method of macromolecule Polycarbonate alloy material, which is claim 1-4 any one of them alloy materials, it is characterised in that:Comprise the following steps:
S1:A melting extrusion is blended in PC and compatilizer a, obtains PC/PE-g-MAH;
S2:After PC/PE-g-MAH is sufficiently mixed again with ABS, compatilizer b, antioxidant in high-speed mixer, squeezed by twin-screw Go out the granulation of machine second melting, obtain macromolecule Polycarbonate alloy material.
6. the preparation method of macromolecule Polycarbonate alloy material according to claim 5, it is characterised in that:Step S1 In, the extrusion temperature once melted is 180~250 DEG C.
7. the preparation method of macromolecule Polycarbonate alloy material according to claim 5, it is characterised in that:Step S2 In, the extrusion temperature of the second melting is 180~230 DEG C.
CN201510584022.1A 2015-09-14 2015-09-14 A kind of macromolecule Polycarbonate alloy material and preparation method thereof Active CN106519622B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201510584022.1A CN106519622B (en) 2015-09-14 2015-09-14 A kind of macromolecule Polycarbonate alloy material and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201510584022.1A CN106519622B (en) 2015-09-14 2015-09-14 A kind of macromolecule Polycarbonate alloy material and preparation method thereof

Publications (2)

Publication Number Publication Date
CN106519622A CN106519622A (en) 2017-03-22
CN106519622B true CN106519622B (en) 2018-06-01

Family

ID=58348462

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201510584022.1A Active CN106519622B (en) 2015-09-14 2015-09-14 A kind of macromolecule Polycarbonate alloy material and preparation method thereof

Country Status (1)

Country Link
CN (1) CN106519622B (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112662154B (en) * 2019-10-16 2023-03-31 惠州比亚迪电子有限公司 Spot-decorated halogen-free flame-retardant PC/ABS plastic alloy and preparation method thereof
CN110903626B (en) * 2019-12-12 2022-10-14 湖南绿燊环保科技有限公司 Polycarbonate composite material and preparation method thereof
CN112175278A (en) * 2020-10-16 2021-01-05 青岛汉缆股份有限公司 Thermoplastic halogen-free flame-retardant polyolefin sheath material for ultrahigh-voltage cable and preparation method and application thereof

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101591468A (en) * 2008-05-28 2009-12-02 上海仲真材料科技有限公司 A kind of low-smoke halogen-free flame retardant PC/ABS Alloy And Preparation Method
CN101875768A (en) * 2009-11-30 2010-11-03 中国蓝星(集团)股份有限公司 Antiaging glass fiber-reinforced polycarbonate composition and preparation method thereof

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04502646A (en) * 1989-10-31 1992-05-14 ゼネラル・エレクトリック・カンパニイ Polymer blend of polycarbonate, styrene terpolymer and glass fiber

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101591468A (en) * 2008-05-28 2009-12-02 上海仲真材料科技有限公司 A kind of low-smoke halogen-free flame retardant PC/ABS Alloy And Preparation Method
CN101875768A (en) * 2009-11-30 2010-11-03 中国蓝星(集团)股份有限公司 Antiaging glass fiber-reinforced polycarbonate composition and preparation method thereof

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
"共混体系相容性的研究";唐颂超等;《功能高分子学报》;20100315(第1期);第24-28页 *
"改性PC/ABS 塑料合金的制备及力学性能研究";司春雷等;《石油化工高等学校学报》;20080615;第21卷(第2期);第45-47+52页 *

Also Published As

Publication number Publication date
CN106519622A (en) 2017-03-22

Similar Documents

Publication Publication Date Title
WO2018107969A1 (en) Pc/abs composition, preparation method therefor and use thereof
CN106519622B (en) A kind of macromolecule Polycarbonate alloy material and preparation method thereof
CN105860316A (en) ASA resin composition with improved low temperature impact toughness and preparation method thereof
CN108129767B (en) Graphene oxide reinforced PVC/ABS composite pipe and preparation method thereof
CN103897268A (en) Medical antibacterial toughened anti-static polypropylene composite material and preparation method thereof
CN102936372A (en) Polypropylene composite material, preparation method and applications thereof
CN105348623A (en) Polyethylene plum blossom pipe material
CN105400053B (en) A kind of micro- permeability low viscosity PE alloy materials and preparation method thereof
CN107177074A (en) A kind of high-strength wood plastic composite and preparation method thereof
CN102558711B (en) Wood plastic composite material and production method thereof
CN104513429A (en) Wear-resistant PP (propene polymer) material and preparation method thereof
CN111073553A (en) High-strength high-fluidity polypropylene bonding resin and preparation method thereof
CN107118421A (en) A kind of high temperature resistant wood plastic composite and preparation method thereof
CN108676274A (en) A kind of film and preparation method thereof
CN102807698A (en) Material special for blowing packaging film and preparation method for material
CN104497444A (en) PVC filler and preparation method, product and application thereof
CN103865179A (en) Impact-resistant low temperature-resistant protection box material and preparation method thereof
CN107418030A (en) A kind of high-temperature-resistant high wood plastic composite and preparation method thereof
CN107903499A (en) A kind of transparent toughening modifying polypropylene plastics and its preparation
CN106905633A (en) A kind of reinforced PVC composite and preparation method thereof
CN103351529B (en) A kind of high workability high temperature UHMWPE/LCP/PP alloy material and preparation method thereof
CN106633570B (en) A kind of polymethylmethacrylacomposition composition of high transparency and preparation method thereof
CN107987378A (en) One kind is used for high comfortable feel non-woven fabrics modified polypropylene material and preparation method thereof
CN104312047B (en) A kind of heat-proof impact-resistant polrvinyl chloride-poly 1-butene complex and preparation method thereof
CN103911011A (en) Molybdenum waste residue-reinforced wood-plastic composite material and preparation method thereof

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant