KR100972667B1 - Polypropylene compound composition having quality of heat stroage and radiation, and its products - Google Patents

Polypropylene compound composition having quality of heat stroage and radiation, and its products Download PDF

Info

Publication number
KR100972667B1
KR100972667B1 KR1020090054764A KR20090054764A KR100972667B1 KR 100972667 B1 KR100972667 B1 KR 100972667B1 KR 1020090054764 A KR1020090054764 A KR 1020090054764A KR 20090054764 A KR20090054764 A KR 20090054764A KR 100972667 B1 KR100972667 B1 KR 100972667B1
Authority
KR
South Korea
Prior art keywords
polypropylene
weight
rubber
parts
wax
Prior art date
Application number
KR1020090054764A
Other languages
Korean (ko)
Inventor
박종순
이경철
Original Assignee
(주)대웅
박종순
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 (주)대웅, 박종순 filed Critical (주)대웅
Priority to KR1020090054764A priority Critical patent/KR100972667B1/en
Application granted granted Critical
Publication of KR100972667B1 publication Critical patent/KR100972667B1/en

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/10Homopolymers or copolymers of propene
    • C08L23/12Polypropene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00Manufacture of articles or shaped materials containing macromolecular substances
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L9/00Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
    • C08L9/02Copolymers with acrylonitrile
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L9/00Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
    • C08L9/06Copolymers with styrene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L91/00Compositions of oils, fats or waxes; Compositions of derivatives thereof
    • C08L91/06Waxes

Abstract

PURPOSE: A polypropylene composition is provided to prevent the damage of electronic products by quickly absorbing, storing, and emitting heat which is generated from the electronic products and to extend the lifespan of the electronic product by reducing fluctuation of thermal load. CONSTITUTION: A polypropylene composition includes 10~50 parts by weight of a rubber and 10~80 parts by weight of wax based on 100.0 parts by weight of the polypropylene. The rubber is a nitrile butadiene rubber or a styrene butadiene rubber. The wax is composed of paraffin wax having a melting point of 30~100 °C. A method for manufacturing polypropylene products comprises the following steps: putting the paraffin wax and rubber into the polypropylene and mixing the materials for 30 minutes using a super mixer; obtaining pellets by extruding the mixed material in a twin extruder; and obtaining a desired product by extruding and injecting the pellets.

Description

열저장 및 방출 특성을 갖는 폴리프로필렌 조성물 및 이의 제품{POLYPROPYLENE COMPOUND COMPOSITION HAVING QUALITY OF HEAT STROAGE AND RADIATION, AND ITS PRODUCTS}POLYPROPYLENE COMPOUND COMPOSITION HAVING QUALITY OF HEAT STROAGE AND RADIATION, AND ITS PRODUCTS}

본 발명은 열저장 및 방출 특성을 갖는 폴리프로필렌 조성물 및 이의 제품에 관한 것으로 보다 상세하게는 열가소성 폴리프로필렌 100 중량부에 니트릴부타디엔러버(NBR) 또는 스티렌부타디엔러버(SBR) 10~50 중량부, 파라핀왁스 또는 염화파라핀 10~80 중량부로 이루어진 조성물로 특별히 용도를 한정하는 것은 아니지만, 사용 환경에 있어서 발열 작용으로 인하여 성능저하가 우려되는 경우 열을 적절히 흡수 저장 및 방출하는 특성을 갖는 것으로 밧데리 케이스, 핸드폰 케이스, 노트북 케이스, 방열판 등에 사용할 수 있다. The present invention relates to a polypropylene composition having heat storage and releasing properties, and more particularly, to 10 parts by weight of nitrile butadiene rubber (NBR) or styrene butadiene rubber (SBR) in 100 parts by weight of thermoplastic polypropylene, and paraffin. It is a composition composed of 10 to 80 parts by weight of wax or paraffin chloride, but the use thereof is not particularly limited. However, if the performance is deteriorated due to the exothermic action in the use environment, it has the property of properly absorbing and storing heat and discharging the battery. It can be used for cases, laptop cases, heat sinks, etc.

일반적으로 합성수지 조성물에 융점이 다르거나 용융시 서로 혼합되어 서로 섞일 수 있는 상용성이 적은 물질을 사용하는 경우 압축강도, 굴곡강도 등 기계적 물성이 나빠지므로 잘 사용하지 않는다. In general, when a synthetic resin composition has a low melting point or a material having low compatibility with each other when mixed with each other when melted, the mechanical properties such as compressive strength and flexural strength deteriorate.

특히 파라핀왁스로 불리는 곧은 사슬 탄화수소 혼합물의 경우 융점이 48~66℃ 영역이지만 용도에 따라 증류 재결정과정을 거쳐 녹는 영역을 세분할 수 있고, 이와같은 파라핀왁스는 용융 및 응고되면서 흡수 및 방출하는데 그 열량 변화를 시차주사열분석기로 분석한 결과 210J/g으로 매우 높은 열량을 갖는 상변화물질에 해당된다. 또한 정제된 파라핀왁스는 용융시 투명한 무색 액체로 취기를 나타내지 않으며 접착성이 없고 윤활성이 있어 이형제, 코팅제, 광택제, 전기절연체 등으로 사용된다. 석탄가스를 탄화수소로 바꾸는 방법을 사용한 합성 파라핀왁스 생산공정으로 얻어진 염화파라핀은 폴리에틸렌 같은 합성수지의 변형제로 사용되기도 하였다.Especially in the case of straight chain hydrocarbon mixture called paraffin wax, melting point is 48 ~ 66 ℃, but it can be subdivided into melting zone through distillation recrystallization process depending on the use. Such paraffin wax is absorbed and released as it melts and solidifies. The change was analyzed by differential scanning calorimetry and it was 210J / g, which is a phase change material with very high calorific value. In addition, the purified paraffin wax is a transparent colorless liquid when melted, does not exhibit odor, adhesiveness and lubricity and is used as a release agent, coating agent, varnish, electrical insulator and the like. Synthetic paraffin wax obtained by converting coal gas into hydrocarbon has been used as a modifier of synthetic resin such as polyethylene.

파라핀왁스의 상변화특성을 이용하면 48~66℃ 영역에서 발생하는 열을 흡수저장하기도 하며 방출하는 특성을 갖는 열저장 물질로 활용이 가능하지만 윤활성을 갖기 때문에 상용성이 낮아 합성수지에 적용이 어려웠다. By using the phase change characteristic of paraffin wax, it can absorb and store the heat generated in the 48 ~ 66 ℃ range and can be used as a heat storage material having the characteristic of being released, but it is difficult to apply to synthetic resin because of its low compatibility.

파라핀왁스는 일반적인 열가소성 합성수지와는 융점이 50℃ 이상 차이가 나며 용융시 점도가 낮고 흐름성이 좋을 뿐만 아니라 윤활성을 가지므로 합성수지 조성물에 많은 양을 혼입할 수 없었다. The paraffin wax has a melting point of 50 ° C. or higher than a general thermoplastic resin, and has a low viscosity and good flowability when melted, and has a lubricating property. Therefore, a large amount of paraffin wax could not be incorporated into the synthetic resin composition.

특히 압출이나 사출과정에서 익스트루더의 온도는 합성수지의 융점 이상으로 가열되어지지만 익스트루더의 온도가 70℃만 되어도 파라핀왁스는 점성을 잃고 유동성이 매우 높은 액체로 되어 흐르게 되므로 합성수지와 과량의 파라핀왁스를 혼합하는 것은 불가능하였다. In particular, the extruder's temperature is heated above the melting point of the resin during extrusion or injection.However, even if the extruder's temperature is only 70 ° C, the paraffin wax loses its viscosity and flows into a highly fluid liquid. It was not possible to mix the wax.

이상과 같은 문제를 해결하기 위하여 니트릴부타디엔러버(NBR)나 스티렌부타 디엔러버(SBR)에 파라핀왁스를 혼합하는 방법을 사용하였다. 대부분의 고무는 오일을 흡수하는 능력이 매우 좋으며 특히 합성고무인 니트릴부타디엔러버(NBR)나 스티렌부타디엔러버(SBR)는 중량비로 120% 까지 오일을 흡수할 수 있다.In order to solve the above problems, a method of mixing paraffin wax with nitrile butadiene rubber (NBR) or styrene butadiene rubber (SBR) was used. Most rubbers have a very good ability to absorb oil, especially synthetic rubber nitrile butadiene rubber (NBR) and styrene butadiene rubber (SBR), which can absorb up to 120% by weight.

이와 같은 니트릴부타디엔러버(NBR)나 스티렌부타디엔러버(SBR)의 특성을 이용하여 수퍼믹서에 니트릴부타디엔러버(NBR)나 스티렌부타디엔러버(SBR)를 넣고 파라핀왁스를 넣은 후 30분 이상을 교반하면 니트릴부타디엔러버(NBR)나 스티렌부타디엔러버(SBR)에 파라핀왁스가 녹아 들어가게 된다.Using nitrile butadiene rubber (NBR) or styrene butadiene rubber (SBR), nitrile butadiene rubber (NBR) or styrene butadiene rubber (SBR) is added to the supermixer, and paraffin wax is added. Paraffin wax is dissolved in butadiene rubber (NBR) or styrene butadiene rubber (SBR).

또한 합성수지는 니트릴부타디엔러버(NBR)나 스티렌부타디엔러버(SBR)와 같은 고무 재질과는 상용성을 갖으므로 파라핀왁스가 녹아든 러버를 폴리프로필렌와 혼합하여 압출하거나 압출된 컴파운드를 사출하는 것이 가능하다. In addition, synthetic resins are compatible with rubber materials such as nitrile butadiene rubber (NBR) and styrene butadiene rubber (SBR), so that the rubber in which paraffin wax is dissolved can be mixed with polypropylene and extruded or extruded compound.

상술한 본 발명에 따른 폴리프로필렌 조성물을 이용한 제품은 모터, 핸드폰, 노트북 등과 같이 전기, 전자제품의 사용에 따른 발열작용이 과도하게 일어나 사용에 제약을 받게 될 때, 발생 된 열을 신속히 흡수 저장하였다가 방출하도록 함으로써 기기의 손상이나 사용제한을 막을 뿐만 아니라 열적 부하의 변동 강도를 줄여줌으로써 기기 및 제품의 수명을 연장할 수 있도록 도와준다. 가령 폴리프로필렌 제품이 자연에 노출된 경우 태양열이 영향을 미치는 주간에는 열을 받아 뜨거워지지만 야간에는 냉각되는데, 이때 파라핀왁스가 들어 있는 경우 주간에 폴리프로필렌의 온도는 파라핀왁스가 열을 흡수 저장하여 가열되는 시간이 지연되며, 야간에는 용융되어 있던 파라핀왁스가 응고되며 열을 방출하므로 냉각되는 기간이 길어지게 된다. 따라서 가열 및 냉각기간이 지연되며, 파라핀왁스의 용량증가시 온도 편차를 거의 없앨 수 있으므로 열적 부하의 반복으로 인한 폴리프로필렌의 물성저하를 막을 수도 있다.When the product using the polypropylene composition according to the present invention described above is excessively exothermic due to the use of electric and electronic products such as a motor, a mobile phone, a notebook, and is restricted in use, the generated heat is quickly absorbed and stored. This prevents damage to the device and limits on its use, as well as reducing the intensity of fluctuations in thermal loads, helping to prolong the life of the device and product. For example, when a polypropylene product is exposed to nature, it is heated and heated during the day when solar heat is affected, but it is cooled at night.In the case of paraffin wax, the temperature of the polypropylene during the day is absorbed by paraffin wax to absorb and store heat. At this time, the molten paraffin wax is solidified at night and releases heat, which increases the cooling period. Therefore, the heating and cooling periods are delayed, and the temperature variation can be almost eliminated when the capacity of paraffin wax is increased, thereby preventing the degradation of the properties of polypropylene due to repeated thermal loads.

폴리프로필렌에 파라핀왁스 고무를 넣고 슈퍼믹서로 30분간 강하게 교반한 후 트윈압출기에 넣어 압출하여 펠렛화 하였으며 이렇게 얻어진 펠렛을 압출 및 사출하여 원하는 제품을 얻도록 한다.Paraffin wax rubber was added to polypropylene, and then stirred vigorously with a super mixer for 30 minutes, and then extruded and pelletized in a twin extruder. The obtained pellet was extruded and injected to obtain a desired product.

실시예1Example 1

폴리프로필렌 수지 100중량부에 스티렌부타디엔러버(SBR) 40중량부, 파라핀왁스 40중량부, 탈크 20 중량부를 넣고 수퍼믹서에서 30분간 강하게 교반하여 얻어진 혼합물을 트윈압출기로 펠렛화 하였다. 또 이 과정을 통하여 얻어진 펫렛을 시편용 사출기로 시편을 제작하여 물성을 측정한 결과는 다음과 같았다.40 parts by weight of styrene butadiene rubber (SBR), 40 parts by weight of paraffin wax, and 20 parts by weight of talc were added to 100 parts by weight of polypropylene resin, and the mixture obtained by vigorous stirring in a supermixer for 30 minutes was pelletized by a twin extruder. In addition, the result of measuring the physical properties of the pellets obtained through this process using the specimen injection machine was as follows.

흐름지수Flow index 재(%)ashes(%) 아이조드충격강도
kgf/cm
Izod impact strength
kgf / cm
비중importance 인장강도
MPa
The tensile strength
MPa
신율(%)% Elongation 굴곡강도
MPa
Flexural strength
MPa
탄성율
MPa
Modulus
MPa
경도Hardness
3737 88 12.912.9 0.980.98 160160 558558 104104 80008000 2727

실시예2Example 2

또 폴리프로필렌 수지 100중량부에 스티렌부타디엔러버(SBR) 60중량부, 스테아린산 30중량부, 탈크 10중량부를 수퍼믹서에서 강하게 30분간 교반한 혼합물을 트윈압출기로 펠렛화하여 시편용 사출기로 시편을 제작, 물성을 측정한 결과는 다음과 같다. In addition, 100 parts by weight of polypropylene resin, 60 parts by weight of styrene-butadiene rubber (SBR), 30 parts by weight of stearic acid, and 10 parts by weight of talc were pelletized by a twin extruder, and the test piece was prepared by using a specimen extruder. The measurement results of the physical properties are as follows.

흐름지수Flow index 재(%)ashes(%) 아이조드충격강도
kgf/cm
Izod impact strength
kgf / cm
비중importance 인장강도
MPa
The tensile strength
MPa
신율(%)% Elongation 굴곡강도
MPa
Flexural strength
MPa
탄성율
MPa
Modulus
MPa
경도Hardness
2626 3.53.5 3939 0.9580.958 180180 832832 156156 1560015600 4242

실시 예1의 열 흡수 및 방출 특성을 시차주사열량계로 분석한 결과를 그림1과 그림2에 나타내었다. The heat absorption and release characteristics of Example 1 were analyzed with a differential scanning calorimeter.

실시 예2의 열 흡수 및 방출 특성을 시차주사열량계로 분석한 결과를 그림3, 그림4에 나타내었다.The heat absorption and release characteristics of Example 2 were analyzed by differential scanning calorimetry.

그림1에서 보는 바와 같이 실시예1의 폴리프로필렌 조성물은 55℃에서 24.6J/g으로 열을 흡수하며 그림2에서 보는 바와 같이 응고될 때 24.4J/g의 열을 방출하는 것을 알 수 있다. As shown in Fig. 1, the polypropylene composition of Example 1 absorbs heat at 24.6 J / g at 55 ° C and releases 24.4 J / g of heat when solidified as shown in Fig. 2.

또 그림3에서 보는 바와 같이 실시예2의 폴리프로필렌 조성물은 120℃ 영역에서 적은 양의 열 흡수가 일어 났으나 열적으로는 거의 의미 없는 양이었으며, 그림4에서 보는 바와 같이 응고시에는 일반 폴리프로필렌과 같은 양상을 나타 내었다.In addition, as shown in Fig. 3, the polypropylene composition of Example 2 had a small amount of heat absorption in the region of 120 ° C., but was almost insignificant thermally. The same aspect was shown.

따라서 표와 그림에서 보는 바와 같이 파라핀 왁스를 혼합한 조성물은 열의 흡수 및 방출 특성을 갖으며 고무계 화합물을 부가함으로써 열가소성 폴리프로필렌와 잘 결합하여 요구하는 물성을 갖는 폴리프로필렌 조성물을 얻을 수 있다는 사실을 확인하였다.Therefore, as shown in the table and the figure, it was confirmed that the mixture of paraffin wax has heat absorption and release characteristics, and by adding a rubber compound, a polypropylene composition having a desired physical property can be obtained by combining with a thermoplastic polypropylene. .

제1도는 실시 예1의 열흡수 시차주사열분석 결과도 1 is a heat absorption differential scanning thermal analysis results of Example 1

제2도는 실시 예1의 열방출 시차주사열분석 결과도2 is a thermal emission differential scanning sequence analysis of Example 1

제3도는 실시 예2의 열흡수 시차주사열분석 결과도3 is a heat absorption differential scanning thermal analysis results of Example 2

제4도는 실시 예2의 열방출 시차주사열분석 결과도4 is a result of the thermal emission differential scanning sequence analysis of Example 2

Claims (8)

폴리프로필렌 100 중량부에 대하여 러버 10~50 중량부와 왁스10~80 중량부가 혼합된 것을 특징으로 하는 폴리프로필렌 조성물.A polypropylene composition comprising 10 to 50 parts by weight of rubber and 10 to 80 parts by weight of wax based on 100 parts by weight of polypropylene. 삭제delete 제1항에 있어서, 상기 러버는 니트릴부타디엔러버(NBR) 또는 스티렌부타디엔러버(SBR)인 것을 특징으로 하는 폴리프로필렌 조성물. The polypropylene composition of claim 1, wherein the rubber is nitrile butadiene rubber (NBR) or styrene butadiene rubber (SBR). 제1항에 있어서, 상기 왁스는 융점이 30~100℃인 파라핀왁스로 이루어진 것을 특징으로 하는 폴리프로필렌 조성물. The polypropylene composition according to claim 1, wherein the wax is made of paraffin wax having a melting point of 30 to 100 ° C. 폴리프로필렌 100 중량부에 대하여 러버 10~50 중량부와 왁스10~80 중량부가 혼합된 폴리프로필렌 조성물을 이용하여 제조되는 것을 특징으로 하는 폴리프로필렌 제품.A polypropylene product, which is prepared using a polypropylene composition in which 10 to 50 parts by weight of rubber and 10 to 80 parts by weight of wax are mixed with respect to 100 parts by weight of polypropylene. 삭제delete 제5항에 있어서, 상기 러버는 니트릴부타디엔러버(NBR) 또는 스티렌부타디엔러버(SBR)인 것을 특징으로 하는 폴리프로필렌 제품.6. The polypropylene article according to claim 5, wherein the rubber is nitrile butadiene rubber (NBR) or styrene butadiene rubber (SBR). 제5항에 있어서, 상기 왁스는 융점이 30~100℃인 파라핀왁스로 이루어진 것을 특징으로 하는 폴리프로필렌 제품.6. The polypropylene product according to claim 5, wherein the wax is made of paraffin wax having a melting point of 30 to 100 ° C.
KR1020090054764A 2009-06-19 2009-06-19 Polypropylene compound composition having quality of heat stroage and radiation, and its products KR100972667B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
KR1020090054764A KR100972667B1 (en) 2009-06-19 2009-06-19 Polypropylene compound composition having quality of heat stroage and radiation, and its products

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
KR1020090054764A KR100972667B1 (en) 2009-06-19 2009-06-19 Polypropylene compound composition having quality of heat stroage and radiation, and its products

Publications (1)

Publication Number Publication Date
KR100972667B1 true KR100972667B1 (en) 2010-07-27

Family

ID=42646078

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1020090054764A KR100972667B1 (en) 2009-06-19 2009-06-19 Polypropylene compound composition having quality of heat stroage and radiation, and its products

Country Status (1)

Country Link
KR (1) KR100972667B1 (en)

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5023301A (en) * 1990-03-05 1991-06-11 The Goodyear Tire & Rubber Company Polypropylene reinforced rubber
KR920012279A (en) * 1990-12-17 1992-07-25 공정곤 Electroconductive Composite Resin Composition for Electromagnetic Shielding
KR20010051044A (en) * 1999-10-20 2001-06-25 후지 폴리머 인더스트리즈 가부시키가이샤 Thermally conductive composition and method of forming thermally conductive film with use of same
US6906144B2 (en) 2003-03-27 2005-06-14 Hyundai Motor Company Polypropylene-based resin composition for powder slush molding

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5023301A (en) * 1990-03-05 1991-06-11 The Goodyear Tire & Rubber Company Polypropylene reinforced rubber
KR920012279A (en) * 1990-12-17 1992-07-25 공정곤 Electroconductive Composite Resin Composition for Electromagnetic Shielding
KR20010051044A (en) * 1999-10-20 2001-06-25 후지 폴리머 인더스트리즈 가부시키가이샤 Thermally conductive composition and method of forming thermally conductive film with use of same
US6906144B2 (en) 2003-03-27 2005-06-14 Hyundai Motor Company Polypropylene-based resin composition for powder slush molding

Similar Documents

Publication Publication Date Title
US9447575B2 (en) Polyamide resin composition, expanded polyamide resin molding, and automotive resin molding
US8388869B2 (en) Thermally conductive resin composition including a milled pitch based carbon fiber
KR101155869B1 (en) Thermo-reversible Crosslinked elastomer and Method producing thereof
CN1162504C (en) Heat-conducting polymer material and its prepn
Uthaipan et al. Effects of cooling rates on crystallization behavior and melting characteristics of isotactic polypropylene as neat and in the TPVs EPDM/PP and EOC/PP
CN105229068A (en) Nucleating composition and the thermoplastic polymer composition comprising this nucleating composition
CN104974418A (en) Polyropylene composite material and preparation method thereof
JP5939843B2 (en) How to use polyacetal resin molded products
CN102617908B (en) Thermal-conductivity nano-composite material and preparation method thereof
CA2716056A1 (en) Thermally conductive polymer compositions
Bahari et al. Thermal stability of processed PVC/bamboo blends: effect of compounding procedures
CN104292732A (en) Polycarbonate-containing styrene thermoplastic elastomer composite material, and preparation method of formed body made of composite material
Wang et al. Superior stretchable, low thermal resistance and efficient self-healing composite elastomers for thermal management
CN103732682A (en) Process for production of a heat - stabilised polyamide - filled acrylatepolymer
EP3992240A1 (en) Polyamide resin composition for foam molding and foam molded body
KR100972667B1 (en) Polypropylene compound composition having quality of heat stroage and radiation, and its products
CN106398234A (en) Halogen-free flame-retardant and cold-resistant PC material suitable for charging pile charging gun and preparation method thereof
KR101795294B1 (en) Polyamide6,6 Resin Composition having Toughness, Abrasion Resistance and Frictional Resistance
CA1212494A (en) Non-mold depositing polyethylene terephthalate molding compositions
CN101838462A (en) Glass-fiber reinforced polyphenyl thioether composite material with humidity resistance and high resistivity and preparation method thereof
CN103275375A (en) Special material for hot spraying of ultra-high molecular weight polyethylene and preparation method thereof
KR101385379B1 (en) Polypropylene resin composition for high flexural modulus, high impact strength and low volatile organic compounds and manufactured by using the same
KR101812367B1 (en) Wholly aromatic liquid crystalline polyester resin compound with excellent releasing property and measurability and method for preparing the same
JPS62138542A (en) Polyolefin composition
CN104650451A (en) Preparation method of novel flame-retardant polypropylene

Legal Events

Date Code Title Description
A201 Request for examination
A302 Request for accelerated examination
E902 Notification of reason for refusal
E902 Notification of reason for refusal
E701 Decision to grant or registration of patent right
GRNT Written decision to grant
FPAY Annual fee payment

Payment date: 20130529

Year of fee payment: 4

FPAY Annual fee payment

Payment date: 20140610

Year of fee payment: 5

FPAY Annual fee payment

Payment date: 20150715

Year of fee payment: 6

FPAY Annual fee payment

Payment date: 20170720

Year of fee payment: 8

FPAY Annual fee payment

Payment date: 20180822

Year of fee payment: 9

FPAY Annual fee payment

Payment date: 20190530

Year of fee payment: 10