CN103613876A - High-gloss toughening AS (acrylonitrile-styrene) composite material and preparation method thereof - Google Patents

High-gloss toughening AS (acrylonitrile-styrene) composite material and preparation method thereof Download PDF

Info

Publication number
CN103613876A
CN103613876A CN201310567255.1A CN201310567255A CN103613876A CN 103613876 A CN103613876 A CN 103613876A CN 201310567255 A CN201310567255 A CN 201310567255A CN 103613876 A CN103613876 A CN 103613876A
Authority
CN
China
Prior art keywords
resin
high gloss
matrix material
toughness reinforcing
preparation
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.)
Granted
Application number
CN201310567255.1A
Other languages
Chinese (zh)
Other versions
CN103613876B (en
Inventor
徐东
张博
徐永
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.)
Polymer Science Shenzhen New Materials Co Ltd
Original Assignee
Polymer Science Shenzhen New Materials 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 Polymer Science Shenzhen New Materials Co Ltd filed Critical Polymer Science Shenzhen New Materials Co Ltd
Priority to CN201310567255.1A priority Critical patent/CN103613876B/en
Publication of CN103613876A publication Critical patent/CN103613876A/en
Application granted granted Critical
Publication of CN103613876B publication Critical patent/CN103613876B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Extrusion Moulding Of Plastics Or The Like (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

The invention discloses a high-gloss toughening AS (acrylonitrile-styrene) composite material and a preparation method thereof. The high-gloss toughening AS composite material comprises the following components by weight percent: 68.08-92.6% of AS resin, 5-25% of K resin, 2-6% of compatilizer, 0.2-0.6% of lubricating agent and 0.2-0.32% of antioxidant. The AS composite material uses the AS resin and the K resin as matrix components and various components carry out synergism in a melt extrusion process, so that the high-gloss toughening AS composite material has high transparency and excellent processing properties and mechanical properties. The high-gloss toughening AS composite material is simple in process, easy in control of conditions and low in cost, has low requirements for equipment, and is suitable for industrial production.

Description

Toughness reinforcing AS matrix material of a kind of high gloss and preparation method thereof
Technical field
The present invention relates to technical field of polymer materials, relate in particular to toughness reinforcing AS matrix material of a kind of high gloss and preparation method thereof.
Background technology
Because the low price of household electrical appliances market is lasting active, global ABS material market demand growth speed, supply falls short of demand.For supplementing the demand in ABS market, the applied research of AS material is more and more important.AS resin has good transparency, intensity, and chemical resistant properties, more in the application of household electrical appliances, field of food, but its notched Izod impact strength is low, poor toughness.In view of above feature, engineering plastics industry is carried out modification to AS resin, as AS/ high glue powder, and AS/PC alloy etc., above method has been expanded the Application Areas of AS resin.
To AS(, being AS resin) in study on the modification, the inventor finds that K resin material has good processibility and tinting strength.But its market application is limitation comparatively, utilizes the method for its alloying and through engineering approaches not yet to develop.
The present invention is by suitable material ratio and adopt blend method to make AS and K Resin by Resin Alloying, has improved intensity, the toughness of mixture, and glossiness.The material that adopts above invention, industrial designers can design cheap double-shot moulding flat panel TV, for high-endization and the universalness of flat panel TV provides good selection.
Summary of the invention
The object of the invention is to overcome the above-mentioned deficiency of prior art, provide a kind of have excellent in strength, toughness and glossiness, by the matrix material of AS and K Resin by Resin Alloying.
Another object of the present invention is to provide a kind of technique simple, cost is low, the preparation method of the toughness reinforcing AS matrix material of high gloss being easy to operate and control.
In order to realize foregoing invention object, technical scheme of the present invention is as follows:
The toughness reinforcing AS matrix material of high gloss, comprises the component of following weight percent:
And the preparation method of the toughness reinforcing AS matrix material of a kind of high gloss, comprises the following steps:
According to the toughness reinforcing AS composite-material formula of above-mentioned high gloss, take respectively each component;
Described in inciting somebody to action, take each component and carry out mixing treatment, obtain mixture;
Described mixture is melt extruded, and granulation, obtains the toughness reinforcing AS matrix material of described high gloss.
The toughness reinforcing AS matrix material of above-mentioned high gloss is by K resin and AS resin-bonded, AS resin is carried out to modification, realized the alloying of AS and K resin, improved intensity, the toughness of mixture, and glossiness, can when mixing mutually with arbitrary proportion with ABS, keep better the background color of mixture.
The preparation method of the toughness reinforcing AS matrix material of above-mentioned high gloss only need melt extrude mixed being incorporated at suitable temperature of each component can obtain product by formula, its preparation method technique is simple, and condition is easily controlled, with low cost, feature low for equipment requirements, is suitable for suitability for industrialized production.
Embodiment
In order to make the technical problem to be solved in the present invention, technical scheme and beneficial effect clearer, below in conjunction with embodiment, the present invention is further elaborated.Should be appreciated that specific embodiment described herein, only in order to explain the present invention, is not intended to limit the present invention.
The embodiment of the present invention provides a kind of high gloss toughness reinforcing AS matrix material, comprises the component of following weight percent:
Figure BDA0000414373610000022
Figure BDA0000414373610000031
Particularly, above-mentioned AS resin is fine-cinnamic multipolymer of propylene, is by vinyl cyanide and the styrene copolymerized macromolecular compound forming, and generally containing vinylbenzene 15%-50%, is transparent and the yellow solid to amber pin look of band, the present blend composition mainly as ABS.Preferably shock strength is 30 ± 5J/M, and density is 1.04-1.07g/cm 3aS resin, LG chemistry 80HF for example, platform NF2200.
Above-mentioned K resin is styrene-butadiene transparent anti-impact resin, claim again K-Resin(K-resin), that to take vinylbenzene, divinyl be monomer, take lithium alkylide as initiator, adopt the synthetic a kind of segmented copolymer of anionic solution polymerization technology, it is transparent, bright, also has high toughness and shock resistance simultaneously.In a preferred embodiment, described K resin is the styrene-butadiene copolymer that transmittance is greater than 88%, and shock strength is (or being about) 40 ± 5J/M, and density is 1.01-1.03g/cm 3, for example strange beautiful PB-5903 or PB-5910.
Above-mentioned K resin and AS resin are combined through hybrid junctions, make matrix material have good color effects, reach well transparent, gloss intensity, can be used as the selection of high-end electronic product material.
Above-mentioned compatilizer can combine each component of matrix material and bring into play synergy.Conventional compatilizer is ABS grafted maleic anhydride compatilizer.In a preferred embodiment, the AS resin that described compatilizer is 98-99:0.2-0.3:1.6-1.7:0.2-0.3 by weight ratio, white oil, maleic anhydride and tasteless DCP form, can be described as AS grafted maleic anhydride, it can be by extruding each component mixed melting to make, wherein, extrusion temperature is 140-170 ℃.Specifically can pass through twin-screw extrusion fusion-grafting, screw speed is made as to 270-300 rev/min.In above-mentioned compatilizer system by using, the above-mentioned AS resin base material of the optional use of AS resin, white oil is selected technical grade, and the rank that maleic anhydride and tasteless DCP all can select purity to be greater than 98%, can reduce mixing of other impurity like this, guarantees the purity of color.Its key index is DCP content, can control the color of compatilizer after adjustment, for follow-up use is laid the groundwork.Preferably, the weight ratio of AS resin, white oil, maleic anhydride and tasteless DCP is 98:0.2:1.6:0.2-0.3.
Traditional method is prepared AS class mixture, all uses ABS grafted maleic anhydride, and matrix is ABS, but when ABS mixes with AS arbitrary proportion, has a strong impact on the background color transparency of mixture.The present invention is by the above-mentioned AS grafted maleic anhydride of self-control, and adjust by the consumption to initiator DCP, make compatilizer color reach ideal effect, and the background color that can keep better mixture, adopt AS grafted maleic anhydride can make main body A S be combined with glass interface tightr, composite strength reaches best effect simultaneously.
Above-mentioned lubricant is conducive to melt extruding of matrix material, can improve the physicals of extruded product, makes product surface smooth good-looking.The preferred fusing point of described lubricant is the amide waxe class modifier of 141.5 ℃-144.5 ℃, and concrete example is as Guangzhou Ou Ying chemical industry TAF, EBS.
Above-mentioned oxidation inhibitor can delay or suppress the carrying out of polymkeric substance oxidising process, thereby stops the aging of polymkeric substance and extend its work-ing life.Preferably, described oxidation inhibitor is Hinered phenols antioxidant, and fusing point 115-150 ℃, as vapour bar IRGANOX1098, IRGANOX1010.
The preferred above-mentioned self-control maleic anhydride graft AS of the present invention plays synergistic effect as compatilizer, because the main body of whole invention is AS material, toughened system is K resin, maleic anhydride graft AS can with two reach completely compatible, it is ultimate attainment that thereby the effect that makes AS compatilizer performs to, the shock strength of matrix material is obviously improved, and higher than two material of main parts, obtain the toughness reinforcing AS matrix material of high gloss of excellent performance.
Correspondingly, the embodiment of the present invention also provides the preparation method of the toughness reinforcing AS matrix material of a kind of high gloss, comprises the following steps:
S01, according to the toughness reinforcing AS composite-material formula of above-mentioned high gloss, take respectively each component;
Described in S02, general, take each component and carry out mixing treatment, obtain mixture;
S03, described mixture is melt extruded, granulation, obtains the toughness reinforcing AS matrix material of described high gloss.
Particularly, each component preferred content in the formula of the toughness reinforcing AS matrix material of high gloss in above-mentioned steps S01 and formula and kind as described above, in order to save length, do not repeat them here.
In above-mentioned steps S02, each component is carried out the time of mixing treatment and can be adjusted flexibly according to actual production conditions, as long as each component premix fully, if the equipment of mixing can be mixing machine etc.In a preferred embodiment, mixing treatment be by each component (as rotating speed is greater than 300r/min) combination treatment at a high speed 10~15 minutes, each component is mixed.
In above-mentioned steps S03, mixture melt extrude the technique that can adopt this area routine.For each component is better acted synergistically in melt extruding, give the toughness reinforcing AS matrix material of above-mentioned high gloss more excellent gloss transparency and mechanical property, in a preferred embodiment, it is to adopt twin screw extruder to melt extrude that mixture melt extrudes, extrusion temperature is 170-230 ℃, screw speed 270-300 rev/min.
The toughness reinforcing AS composite material and preparation method thereof of above-mentioned high gloss only need melt extrude mixed being incorporated at suitable temperature of each component can obtain product by formula, in melt extruding process, only need to control the temperature and time melt extruding, therefore, its preparation method technique is simple, condition is easily controlled, feature with low cost, low for equipment requirements, is suitable for suitability for industrialized production.
The toughness reinforcing AS matrix material of concrete high gloss and preparation method thereof of now take is example, and the present invention is further elaborated.The toughness reinforcing AS matrix material of high gloss that the present invention proposes, need to use following starting material: AS resin, K resin, compatilizer, lubricant, oxidation inhibitor.
Wherein, the 80HF of AS Choice of Resin LG or the NF2200 of platform; K Choice of Resin strange beautiful PB-5903 or PB-5910; Compatilizer is selected self-control AS grafted maleic anhydride; Oxidation inhibitor is selected the IRGANOX1098(or 1010 of vapour bar chemical industry); Lubricant is selected Guangzhou Ou Ying chemical industry TAF(or EBS).
Embodiment is all used the given raw material of the present invention and preparation method; The unit of each component concentration of following examples be all weight percentage (wt%).
Embodiment 1
Take AS resin 92.6, K resin 5, compatilizer 2, lubricant 0.2, oxidation inhibitor 0.2, pre-mixing starting material, then raw material is placed in twin screw extruder through melt extruding, granulation, its expressing technique is: 170 ℃, 170 190 200 ℃, 4th district, ℃, 3rd district, ℃, 2nd district, a district, 230 ℃ of heads.
Embodiment 2
Take AS resin 86.46, K resin 10, compatilizer 3, lubricant 0.3, oxidation inhibitor 0.24, premix starting material, then raw material is placed in twin screw extruder through melt extruding, granulation, its expressing technique is: 180 ℃, 180 170 190 ℃, 4th district, ℃, 3rd district, ℃, 2nd district, a district, 220 ℃ of heads.
Embodiment 3
Take AS resin 80.34, K resin 15, compatilizer 4, lubricant 0.4, oxidation inhibitor 0.26, premix starting material, then raw material is placed in twin screw extruder through melt extruding, granulation, its expressing technique is: 190 ℃, 170 200 200 ℃, 4th district, ℃, 3rd district, ℃, 2nd district, a district, 210 ℃ of heads.
Embodiment 4
Take AS resin 74.2, K resin 20, compatilizer 5, lubricant 0.5, oxidation inhibitor 0.3, premix starting material, then raw material is placed in twin screw extruder through melt extruding, granulation, its expressing technique is: 175 ℃, 175 195 205 ℃, 4th district, ℃, 3rd district, ℃, 2nd district, a district, 225 ℃ of heads.
Embodiment 5
Take AS resin 68.08, K resin 25, compatilizer 6, lubricant 0.6, oxidation inhibitor 0.32, premix starting material, then raw material is placed in twin screw extruder through melt extruding, granulation, its expressing technique is: 170 ℃, 185 185 200 ℃, 4th district, ℃, 3rd district, ℃, 2nd district, a district, 205 ℃ of heads.
Comparative example 1
Take ABS resin 80, K resin 20, premix starting material, then raw material is placed in twin screw extruder through melt extruding, granulation, its expressing technique is: 160 ℃, 185 220 210 ℃, 4th district, ℃, 3rd district, ℃, 2nd district, a district, 200 ℃ of heads.
Comparative example 2
Take ABS resin 100, do not add other, by raw material be placed in twin screw extruder through melt extruding, granulation, its expressing technique is: 170 ℃, 185 185 200 ℃, 4th district, ℃, 3rd district, ℃, 2nd district, a district, 205 ℃ of heads.
Comparative example 3
Take K resin 100, do not add other, by raw material be placed in twin screw extruder through melt extruding, granulation, its expressing technique is: 190 ℃, 170 200 200 ℃, 4th district, ℃, 3rd district, ℃, 2nd district, a district, 210 ℃ of heads.
Performance test:
Tensile strength is tested by ASTMD-638 standard.Specimen types is I type, batten size (mm): (176 ± 2) (length) * (12.6 ± 0.2) (end width) * (3.05 ± 0.2) (thickness), and draw speed is 50mm/min;
Flexural strength and modulus in flexure are tested by ASTM D-790 standard.Specimen types is specimen size (mm): (128 ± 2) * (12.67 ± 0.2) * (3.11 ± 0.2), and rate of bending is 20mm/min;
Socle girder notched Izod impact strength is tested by ASTM D-256 standard.Specimen types is I type, specimen size (mm): (63 ± 2) * (12.45 ± 0.2) * (3.1 ± 0.2); Breach type is category-A, and breach residual thickness is 1.9mm;
The performance test results of embodiment 1-5 is in Table 1:
Table 1
Figure BDA0000414373610000071
Figure BDA0000414373610000081
The performance test of comparative example 1,2,3 is in Table 2:
Table 2
Figure BDA0000414373610000082
By embodiment in table 1, can find out compatilizer, AS resin, the ratio of K resin is determining mechanical property and the outward appearance of mixture jointly, raising along with K resin and compatilizer ratio, the shock strength of mixture obviously improves, consider tensile strength, the flexural strength of matrix material, and shock strength needs the performance of balance, from above data, we think at AS resin 74.2%, K resin 20%, the proportioning of compatilizer 5% is optimum proportion, now the shock strength of mixture is higher, and stretch, flexural strength reduces moderately, overall performance is excellent.
Three of whole comparative example kinds of typical result as can be seen from Table 2, comparative example 1 is selected 80% AS and 20% K resin alloy, does not use compatilizer, can find out all more weaker than the performance of any embodiment from data; Comparative example 2 is used pure AS resin; Comparative example 3 is used pure K resin.Known above, use thinking of the present invention can make two performances all lower resin for the mixture of excellent combination property, when K resin and AS grafted maleic anhydride, select when suitable, whole diagram of system reveals good consistency.
The foregoing is only preferred embodiment of the present invention, not in order to limit the present invention, all any modifications of doing within the spirit and principles in the present invention, be equal to and replace and improvement etc., within all should being included in protection scope of the present invention.

Claims (9)

1. the toughness reinforcing AS matrix material of high gloss, is characterized in that, comprises the component of following weight percent:
Figure FDA0000414373600000011
2. the toughness reinforcing AS matrix material of high gloss as claimed in claim 1, is characterized in that, the AS resin that described compatilizer is 98-99:0.2-0.3:1.6-1.7:0.2-0.3 by weight ratio, white oil, maleic anhydride and tasteless DCP form.
3. the toughness reinforcing AS matrix material of high gloss as claimed in claim 2, is characterized in that, described compatilizer is extruded by mixed melting, and extrusion temperature is 140-170 ℃.
4. the toughness reinforcing AS matrix material of high gloss as claimed in claim 1, is characterized in that, described K resin is the styrene-butadiene copolymer that transmittance is greater than 88%, and shock strength is 40 ± 5J/M.
5. the toughness reinforcing AS matrix material of high gloss as described in claim 1-4 any one, is characterized in that, the shock strength of described AS resin is 30 ± 5J/M, and density is 1.04-1.07g/cm 3.
6. the toughness reinforcing AS matrix material of high gloss as described in claim 1-4 any one, is characterized in that, described oxidation inhibitor is Hinered phenols antioxidant, and fusing point is 115-150 ℃.
7. the toughness reinforcing AS matrix material of high gloss as described in claim 1-4 any one, is characterized in that, described lubricant is amide waxe class modifier, and fusing point is 141.5-144.5 ℃.
8. a preparation method for the toughness reinforcing AS matrix material of high gloss, is characterized in that, comprises following preparation process:
According to the toughness reinforcing AS composite-material formula of the arbitrary described high gloss of claim 1~7, take respectively each component;
Described in inciting somebody to action, take each component and carry out mixing treatment, obtain mixture;
Described mixture is melt extruded, and granulation, obtains the toughness reinforcing AS matrix material of described high gloss.
9. the preparation method of the toughness reinforcing AS matrix material of high gloss as claimed in claim 8, is characterized in that, described in to melt extrude be to adopt twin-screw extrusion, its extrusion temperature is 170-230 ℃.
CN201310567255.1A 2013-11-13 2013-11-13 Toughness reinforcing AS matrix material of a kind of high gloss and preparation method thereof Expired - Fee Related CN103613876B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201310567255.1A CN103613876B (en) 2013-11-13 2013-11-13 Toughness reinforcing AS matrix material of a kind of high gloss and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201310567255.1A CN103613876B (en) 2013-11-13 2013-11-13 Toughness reinforcing AS matrix material of a kind of high gloss and preparation method thereof

Publications (2)

Publication Number Publication Date
CN103613876A true CN103613876A (en) 2014-03-05
CN103613876B CN103613876B (en) 2015-09-09

Family

ID=50164598

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201310567255.1A Expired - Fee Related CN103613876B (en) 2013-11-13 2013-11-13 Toughness reinforcing AS matrix material of a kind of high gloss and preparation method thereof

Country Status (1)

Country Link
CN (1) CN103613876B (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107266808A (en) * 2017-08-20 2017-10-20 苏建 A kind of high glaze toughness reinforcing AS composites and preparation method thereof
CN107446291A (en) * 2017-08-20 2017-12-08 佛山市北朝源科技服务有限公司 A kind of high glaze toughness reinforcing AS composites and preparation method thereof
CN115286877A (en) * 2022-08-31 2022-11-04 金发科技股份有限公司 Reinforced AS alloy material with low powder content and high transparency AS well AS preparation method and application thereof

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103044797A (en) * 2013-01-22 2013-04-17 贵州省复合改性聚合物材料工程技术研究中心 Transparent K glue composite AS (Acrylonitrile-Styrene Copolymers) alloy material and preparation method thereof
CN103333453A (en) * 2013-06-28 2013-10-02 广东银禧科技股份有限公司 High-light-shading acrylonitrile butadiene styrene (ABS) composite material and preparation method thereof

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103044797A (en) * 2013-01-22 2013-04-17 贵州省复合改性聚合物材料工程技术研究中心 Transparent K glue composite AS (Acrylonitrile-Styrene Copolymers) alloy material and preparation method thereof
CN103333453A (en) * 2013-06-28 2013-10-02 广东银禧科技股份有限公司 High-light-shading acrylonitrile butadiene styrene (ABS) composite material and preparation method thereof

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
蒋登高等: "PS/K树脂合金的制备及表征", 《郑州大学学报(工学版)》, vol. 34, no. 3, 31 May 2013 (2013-05-31), pages 42 - 45 *

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107266808A (en) * 2017-08-20 2017-10-20 苏建 A kind of high glaze toughness reinforcing AS composites and preparation method thereof
CN107446291A (en) * 2017-08-20 2017-12-08 佛山市北朝源科技服务有限公司 A kind of high glaze toughness reinforcing AS composites and preparation method thereof
CN115286877A (en) * 2022-08-31 2022-11-04 金发科技股份有限公司 Reinforced AS alloy material with low powder content and high transparency AS well AS preparation method and application thereof
CN115286877B (en) * 2022-08-31 2023-11-03 金发科技股份有限公司 Reinforced AS alloy material with low powder content and high transparency, and preparation method and application thereof

Also Published As

Publication number Publication date
CN103613876B (en) 2015-09-09

Similar Documents

Publication Publication Date Title
CN101831136B (en) High-strength high-toughness flame-resistant ABS (Acrylonitrile Butadiene Styrene) composite material and preparation method thereof
CN101508817B (en) High-light ABS alloy and method for producing the same
CN102219927B (en) Nucleating agent composite capable of increasing rigidity and toughness of polypropylene
CN103013089B (en) Flame-retardant glass fiber reinforced PC (Polycarbonate)/ABS (Acrylonitrile Butadiene Styrene) composite material and preparation method thereof
CN103435950A (en) PMMA/ABS composite material, and preparation method and application thereof
CN102108181B (en) Thermoplastic alloy and preparation method thereof
CN105419142B (en) A kind of plating PC/ABS alloy materials and preparation method thereof
CN104559108A (en) Spray-free PC/ABS composite material with high gloss and high impact resistance and preparation method of spray-free PC/ABS composite material
CN102627830B (en) ABS/attapulgite composite material and preparation method thereof
CN102757613A (en) Faint-odor polypropylene stem grafting maleic anhydride extruded by double screws and preparation method thereof
CN102731921A (en) Weatherproof polymer alloy used for replacing ABS
CN103613876B (en) Toughness reinforcing AS matrix material of a kind of high gloss and preparation method thereof
CN104004279A (en) High gloss modified polystyrene and preparation method thereof
CN102936372B (en) Polypropylene composite material, its preparation method and application
CN102746631B (en) Low temperature impact resistant polycarbonate/ABS (acrylonitrile, butadiene and styrene) resin plastic alloy
CN103709681B (en) A kind of high tenacity, high-heat-resisting glass-fiber strengthen PBT composite and preparation method thereof
CN105542380A (en) ABS noctilucent masterbatches and preparation method thereof
CN103524981A (en) Modified PBT/ABS (polybutylene terephthalate/acrylonitrile-butadiene-styrene) alloy material
CN103525038A (en) Glass fiber-reinforced PBT/ABS (Polybutylece Terephthalate/Acrylonitrile Butadiene Styrene) alloy material and preparation method thereof
CN102382413B (en) ABS (acrylonitrile butadiene styrene) alloy for multi-rib highly-smooth base and preparation method thereof
CN103613853A (en) Transparent glass fiber reinforced polypropylene (PP) composite material and preparation method thereof
CN103554870A (en) Polycarbonate/ABS (Acrylonitrile-Butadiene-Styrene copolymer) alloy composition and preparation method thereof
CN107266808A (en) A kind of high glaze toughness reinforcing AS composites and preparation method thereof
CN101885894B (en) Modified abs resin and preparation method thereof
CN103709583A (en) Glass fiber enhanced K resin composite material and preparation method thereof

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
PE01 Entry into force of the registration of the contract for pledge of patent right
PE01 Entry into force of the registration of the contract for pledge of patent right

Denomination of invention: High-gloss toughening AS (acrylonitrile-styrene) composite material and preparation method thereof

Effective date of registration: 20180912

Granted publication date: 20150909

Pledgee: Bank of Shizuishan Limited by Share Ltd Yinchuan branch

Pledgor: Polymer Science (Anhui) New Material Co., Ltd.|Shenzhen Keju New Material Co., Ltd.

Registration number: 2018440020055

CF01 Termination of patent right due to non-payment of annual fee
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20150909

Termination date: 20181113