KR100648974B1 - Method for processing polypropylene/polyester fiber composite - Google Patents
Method for processing polypropylene/polyester fiber composite Download PDFInfo
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- KR100648974B1 KR100648974B1 KR1020050120437A KR20050120437A KR100648974B1 KR 100648974 B1 KR100648974 B1 KR 100648974B1 KR 1020050120437 A KR1020050120437 A KR 1020050120437A KR 20050120437 A KR20050120437 A KR 20050120437A KR 100648974 B1 KR100648974 B1 KR 100648974B1
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- polyester fiber
- polypropylene
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- 239000000835 fiber Substances 0.000 title claims abstract description 60
- 229920000728 polyester Polymers 0.000 title claims abstract description 57
- -1 polypropylene Polymers 0.000 title claims abstract description 29
- 239000004743 Polypropylene Substances 0.000 title claims abstract description 28
- 229920001155 polypropylene Polymers 0.000 title claims abstract description 28
- 239000002131 composite material Substances 0.000 title claims abstract description 26
- 238000000034 method Methods 0.000 title claims abstract description 16
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims abstract description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 9
- 239000007864 aqueous solution Substances 0.000 claims abstract description 8
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims abstract description 6
- 239000003637 basic solution Substances 0.000 claims abstract description 6
- 238000004519 manufacturing process Methods 0.000 claims description 7
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical group OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 6
- 238000004381 surface treatment Methods 0.000 claims description 6
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 6
- 239000000243 solution Substances 0.000 claims description 4
- 229920002943 EPDM rubber Polymers 0.000 claims description 2
- 239000005977 Ethylene Substances 0.000 claims 1
- 239000011259 mixed solution Substances 0.000 abstract 1
- 239000003365 glass fiber Substances 0.000 description 5
- 239000011256 inorganic filler Substances 0.000 description 4
- 229910003475 inorganic filler Inorganic materials 0.000 description 4
- 229920005629 polypropylene homopolymer Polymers 0.000 description 4
- 239000004594 Masterbatch (MB) Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000005484 gravity Effects 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 238000000635 electron micrograph Methods 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000012765 fibrous filler Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
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- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
- D06M11/32—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond
- D06M11/36—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond with oxides, hydroxides or mixed oxides; with salts derived from anions with an amphoteric element-oxygen bond
- D06M11/38—Oxides or hydroxides of elements of Groups 1 or 11 of the Periodic Table
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- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
- D06M11/01—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with hydrogen, water or heavy water; with hydrides of metals or complexes thereof; with boranes, diboranes, silanes, disilanes, phosphines, diphosphines, stibines, distibines, arsines, or diarsines or complexes thereof
- D06M11/05—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with hydrogen, water or heavy water; with hydrides of metals or complexes thereof; with boranes, diboranes, silanes, disilanes, phosphines, diphosphines, stibines, distibines, arsines, or diarsines or complexes thereof with water, e.g. steam; with heavy water
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- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M2101/00—Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
- D06M2101/16—Synthetic fibres, other than mineral fibres
- D06M2101/30—Synthetic polymers consisting of macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M2101/32—Polyesters
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- D—TEXTILES; PAPER
- D10—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B2321/00—Fibres made from polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D10B2321/02—Fibres made from polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds polyolefins
- D10B2321/022—Fibres made from polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds polyolefins polypropylene
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- D—TEXTILES; PAPER
- D10—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B2331/00—Fibres made from polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polycondensation products
- D10B2331/04—Fibres made from polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polycondensation products polyesters, e.g. polyethylene terephthalate [PET]
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- D—TEXTILES; PAPER
- D10—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B2401/00—Physical properties
- D10B2401/06—Load-responsive characteristics
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Abstract
Description
도 1은 표면처리되지 않은 폴리에스테르 섬유가 함유되고 PP-g-MA가 첨가된 폴리프로필렌/폴리에스테르 섬유의 전자현미경 사진이다.1 is an electron micrograph of a polypropylene / polyester fiber containing untreated polyester fiber and containing PP-g-MA.
도 2는 표면처리된 폴리에스테르 섬유가 함유되고 PP-g-MA가 첨가된 폴리프로필렌/폴리에스테르 섬유의 전자현미경 사진이다.FIG. 2 is an electron micrograph of polypropylene / polyester fiber containing surface treated polyester fiber and containing PP-g-MA. FIG.
본 발명은 폴리프로필렌/폴리에스테르 섬유 복합재료 및 그 제조방법에 관한 것으로서, 보다 상세하게는 염기성 용액 또는 물을 이용하여 폴리에스테르 섬유의 표면을 가수분해시켜 섬유표면에 수산기를 용이하게 도입시킨 후 상용화제를 첨가하여 인장강도를 향상시킨 폴리프로필렌/폴리에스테르 섬유 복합재료 및 그 제조방법에 관한 것이다.The present invention relates to a polypropylene / polyester fiber composite material and a method for manufacturing the same. More specifically, the surface of the polyester fiber is hydrolyzed using a basic solution or water to easily introduce hydroxyl groups on the surface of the fiber, and then commercialized. The present invention relates to a polypropylene / polyester fiber composite material in which a tensile strength is added to improve a tensile strength, and a method of manufacturing the same.
기존의 폴리프로필렌 복합재료의 기계적 물성을 향상시키는 방법으로는 한국특허출원 제10-2005-0040493호에서 밝힌 바와 같이 유리섬유를 사용하는 경우 제품 의 변형이 발생할 수 있고 이것을 개선하기 위해 탈크 등의 판상 무기 필러를 사용하는 것이 대표적이나 이렇게 무기필러를 과량으로 사용할 경우 오히려 인장강도가 저하되는 단점을 가지고 있다. 이러한 단점을 보완하기 위하여 말레이트 폴리프로필렌(이하, "PP-g-MA"라 함)을 사용하여 상용성을 개선하는 방법이 사용된다. PP-g-MA와 같은 상용화제는 무기 필러 표면의 수산기와 반응하여 수소결합 또는 공유결합을 이루어 무기 필러와 상용성을 갖게 된다. 그러나 유리섬유와 같은 섬유상 필러를 첨가할 경우 유리섬유의 배향에 의해 사출성형품의 변형이 발생하게 되고 복합재료의 비중이 높아지는 단점이 생기게 된다. 재료의 높은 비중은 제품의 부피당 재료의 사용량을 증가시키고 제품의 가격을 증가시키는 원인이 된다.As a method of improving the mechanical properties of the existing polypropylene composite material, as described in Korean Patent Application No. 10-2005-0040493, deformation of the product may occur when glass fiber is used, and in order to improve the plate shape of talc, etc. The use of the inorganic filler is typical, but when the inorganic filler is used in an excessive amount, the tensile strength is rather deteriorated. In order to compensate for this disadvantage, a method of improving compatibility using maleate polypropylene (hereinafter referred to as "PP-g-MA") is used. Compatibilizers such as PP-g-MA react with hydroxyl groups on the surface of the inorganic filler to form hydrogen bonds or covalent bonds, thereby making them compatible with the inorganic filler. However, when a fibrous filler such as glass fiber is added, deformation of the injection molded product occurs due to the orientation of the glass fiber, and the specific gravity of the composite material increases. The high specific gravity of the material increases the amount of material used per volume of the product and increases the price of the product.
폴리에스테르 섬유는 유리섬유보다 낮은 비중을 갖고 있고 폴리프로필렌보다 높은 인장강도를 갖고 있기 때문에 폴리에스테르 섬유를 폴리프로필렌에 첨가하면 유리섬유보다는 인장강도가 낮지만 폴리프로필렌보다는 높은 인장강도를 가지게 될 것이다. 그러나 결과적으로 폴리에스테르 섬유는 폴리프로필렌과의 상용성이 낮기 때문에 낮은 인장강도를 갖는다. 이것은 폴리프로필렌/폴리에스테르 섬유 복합재료는 폴리에스테르의 화학적 특성상 PP-g-MA와 반응성이 없기 때문에 이것을 첨가하여도 폴리에스테르 섬유의 표면에서 계면의 젖음 효과를 얻을 수 없기 때문이다. 따라서, 상용화제와 화학적 반응을 통하여 인장강도를 향상시키기 위해서는 상용화제와 반응할 수 있는 반응성기를 도입할 필요가 있으며 이러한 반응성기를 도입하는 방법으로서 폴리에스테르 섬유의 표면처리 등의 전처리 절차가 요구된다. Because polyester fibers have a lower specific gravity than glass fibers and have higher tensile strength than polypropylene, adding polyester fibers to polypropylene will result in lower tensile strength than glass fibers but higher tensile strength than polypropylene. As a result, however, polyester fibers have low tensile strength because of their low compatibility with polypropylene. This is because the polypropylene / polyester fiber composite material is not reactive with PP-g-MA due to the chemical properties of the polyester, and even if it is added, the wetting effect of the interface cannot be obtained on the surface of the polyester fiber. Therefore, in order to improve the tensile strength through the chemical reaction with the compatibilizer, it is necessary to introduce a reactive group capable of reacting with the compatibilizer and a pretreatment procedure such as surface treatment of a polyester fiber is required as a method of introducing such a reactive group.
한국특허출원 제10-2005-0071403호와 같이 합성섬유를 포함하여 고분자로부 터 제조되는 섬유는 복합재료를 제조하는 과정에서 보푸라기로 쉽게 변하여 취급이 용이하지 않고 첨가할 수 있는 양도 크게 제한되어 적층 등의 방법으로 사용될 수 밖에 없다. Fibers prepared from polymers, including synthetic fibers, are easily changed to lint during the manufacture of composite materials, such as Korean Patent Application No. 10-2005-0071403. It can only be used in such a way.
이러한 단점을 갖는 폴리에스테르 섬유를 효과적으로 활용하기 위해서는 폴리에스테르 섬유보다 비교적 낮은 용융온도를 갖는 폴리프로필렌 또는 폴리에틸렌과 같은 재료를 매트릭스로 하여 섬유상의 폴리에스테르를 용융온도보다 낮은 온도에서 복합재료를 제조할 필요가 있다. 이것은 연신공정을 통하여 고분자 사슬이 배향되어 섬유의 강도가 매우 우수하기 때문에 이 특성을 복합재료의 기계적 물성에 반영하기 위해서는 섬유의 형상이 유지되어야 할 필요가 있기 때문이다. In order to effectively utilize polyester fibers having such disadvantages, it is necessary to prepare a composite material at a temperature lower than the melting temperature of the fibrous polyester using a material such as polypropylene or polyethylene having a lower melting temperature than the polyester fiber as a matrix. There is. This is because the shape of the fiber needs to be maintained in order to reflect this property in the mechanical properties of the composite material because the polymer chain is oriented through the stretching process and the fiber strength is very excellent.
이에 본 발명자들은 폴리에스테르 섬유의 화학적 특성상 PP-g-MA와 같은 상용화제의 영향이 없고 폴리에스테르 섬유의 취급이 곤란하며 고함량의 첨가가 어려운 문제를 개선하기 위하여 폴리에스테르 섬유에 상용화제와 쉽게 반응하여 상용화제의 효과를 개선시킬 수 있도록 폴리에스테르 섬유 표면에 극성기를 도입시키는 표면처리를 함으로써 인장강도를 향상시킨 폴리프로필렌/폴리에스테르 섬유 복합재료를 제조할 수 있음을 발견하고 본 발명을 완성하게 되었다.Accordingly, the present inventors have no influence of a compatibilizer such as PP-g-MA due to the chemical properties of the polyester fiber, and it is easy to handle the polyester fiber and improve the difficulty of adding a high content. The present invention was completed by discovering that a polypropylene / polyester fiber composite material having improved tensile strength can be prepared by performing a surface treatment to introduce a polar group on the surface of a polyester fiber so as to improve the effect of the compatibilizer. It became.
따라서, 본 발명의 목적은 염기성 용액 또는 물을 처리하여 폴리에스테르 섬유에 극성기를 도입시키는 표면처리 방법을 제공하고자 한다.Accordingly, an object of the present invention is to provide a surface treatment method of introducing a polar group into a polyester fiber by treating a basic solution or water.
또한 본 발명의 목적은 상기 표면처리된 폴리에스테르 섬유에 상용화제를 첨 가하여 인장강도를 비롯한 기계적 물성을 향상시킨 폴리프로필렌/폴리에스테르 섬유 복합재료 및 그 제조방법을 제공하고자 한다.It is also an object of the present invention to provide a polypropylene / polyester fiber composite material and a method of manufacturing the same by adding a compatibilizer to the surface-treated polyester fiber to improve mechanical properties including tensile strength.
상기 목적을 달성하기 위하여, 본 발명에서는 폴리에스테르 섬유에 염기성 용액을 처리하여 폴리에스테르 섬유 표면에 극성기를 도입시키는 방법을 제공한다.In order to achieve the above object, the present invention provides a method for introducing a polar group to the polyester fiber surface by treating the polyester fiber with a basic solution.
상기 과정을 상세히 살펴보면, 폴리에스테르 섬유를 0.01 내지 1.0 노르말의 염기성 수용액 중에서 0.5 내지 3.0시간동안 침지한 후 물로 세척한 다음 80℃에서 24시간 건조한다.Looking at the process in detail, the polyester fiber is immersed in a basic aqueous solution of 0.01 to 1.0 normal for 0.5 to 3.0 hours, washed with water and dried at 80 ℃ for 24 hours.
본 발명에서 사용하는 염기성 용액으로는 수산화나트륨 수용액 및 수산화칼륨 수용액 등을 들 수 있다.Examples of the basic solution used in the present invention include an aqueous sodium hydroxide solution and an aqueous potassium hydroxide solution.
또한 본 발명에서는 폴리에스테르 섬유를 60∼90℃의 물 중에서 24∼48시간 동안 침지하여 표면처리할 수도 있다.In the present invention, the polyester fiber may also be surface treated by immersing the polyester fiber in water at 60 to 90 ° C for 24 to 48 hours.
또한 본 발명에서는 상기 표면처리된 폴리에스테르 섬유와 폴리프로필렌을 4:6에서 6:4 사이의 중량비로 혼합한 마스터배치를 제조하여 폴리에스테르 섬유의 취급이 용이하도록 한 다음 상용화제를 첨가하여 인장 강도 및 기계적 물성을 향상시킨 폴리프로필렌/폴리에스테르 섬유 복합재료 및 그 제조방법을 제공한다.In addition, in the present invention, the masterbatch is prepared by mixing the surface-treated polyester fibers and polypropylene in a weight ratio of 4: 6 to 6: 4 to facilitate the handling of polyester fibers and then adding a compatibilizer to tensile strength And it provides a polypropylene / polyester fiber composite material and a method of manufacturing the improved mechanical properties.
본 발명에서 사용하는 상용화제로는 PP-g-MA, 말레이트 에틸렌-프로필렌-다이엔-터폴리머(이하, "EPDM-g-MA"라 한다) 또는 말레이트 폴리(스티렌-b-에틸렌- co-부틸렌-b-스티렌)(이하, "SEBS-g-MA"라 한다)를 들 수 있다. 이들 상용화제는 복합 재료의 전체 중량에 대하여 0.5∼5.0 wt%로 첨가될 수 있다.Compatibilizers used in the present invention include PP-g-MA, maleate ethylene-propylene-diene-terpolymer (hereinafter referred to as "EPDM-g-MA") or maleate poly (styrene-b-ethylene-co -Butylene-b-styrene) (henceforth "SEBS-g-MA"). These compatibilizers may be added at 0.5 to 5.0 wt% based on the total weight of the composite material.
이하, 실시예 및 시험예를 들어 본 발명의 구성 및 작용효과를 보다 구체적으로 설명한다. 그러나, 이들 실시예는 본 발명을 설명하기 위한 것으로, 본 발명이 이들 실시예로만 한정되는 것은 아니다.Hereinafter, the configuration and effect of the present invention will be described in more detail with reference to Examples and Test Examples. However, these examples are for illustrating the present invention, and the present invention is not limited only to these examples.
[실시예 1]Example 1
폴리에스테르 섬유는 0.01 노르말 수산화나트륨 수용액에서 3시간 동안 침지하여 표면처리한 다음 물로 세척한 후 80℃에서 24시간 건조하였다. 건조된 폴리에스테르 섬유는 서로 다른 회전비를 갖는 이축 용융혼합기에서 30 wt%의 폴리에스테르 섬유와 용융흐름지수가 0.5 내지 60g/min인 호모 폴리프로필렌 70 wt%를 6Kgf/㎠의 압력으로 170℃까지 용융, 혼합하여 폴리에스테르 섬유 마스터배치를 제조하였다. The polyester fibers were surface treated by immersion in 0.01 normal sodium hydroxide aqueous solution for 3 hours, washed with water, and dried at 80 ° C. for 24 hours. The dried polyester fibers were 30 wt% polyester fiber and 70 wt% homopolypropylene with melt flow index of 0.5 to 60 g / min in a twin screw melter with different rotation ratios up to 170 ° C at a pressure of 6 Kg f / cm2. Melting and mixing were performed to prepare a polyester fiber masterbatch.
[실시예 2]Example 2
상기 실시예 1에서 0.01 노르말의 수산화나트륨 수용액 대신에 0.1 노르말의 수산화칼륨 수용액을 사용하여 0.5시간동안 침지하여 표면처리를 하는 것을 제외하고 실시예 1과 동일한 방법으로 제조하였다.In Example 1 was prepared in the same manner as in Example 1 except that the surface treatment by immersion for 0.5 hours using 0.1 normal potassium hydroxide solution instead of 0.01 normal sodium hydroxide solution.
[실시예 3]Example 3
상기 실시예 1에서 0.01 노르말의 수산화나트륨 수용액 대신에 60℃의 물에서 48시간동안 표면처리를 하는 것을 제외하고 실시예 1과 동일한 방법으로 제조하였다.In Example 1 was prepared in the same manner as in Example 1, except that the surface treatment for 48 hours in 60 ℃ water instead of 0.01 normal sodium hydroxide solution.
[실시예 4]Example 4
상기 실시예 1에서 제조한 폴리에스테르 섬유 마스터배치를 용융흐름지수가 10 g/min인 호모 폴리프로필렌에 폴리에스테르 섬유를 혼합한 후 PP-g-MA를 첨가하였다. 이때, 상기 폴리프로필렌:폴리에스테르 섬유:PP-g-MA를 각각 95:5:3.0, 90:10:3.0, 85:15:3.0, 80:20:3.0 및 50:50:3.0의 중량비로 혼합하였다. 상기 혼합물을 L/D가 40인 이축압출기에서 170℃의 온도에서 복합재료를 제조하였으며, 하기 표 1에 기계적 물성을 나타내었다. The polyester fiber masterbatch prepared in Example 1 was mixed with homopolypropylene having a melt flow index of 10 g / min, and then PP-g-MA was added. At this time, the polypropylene: polyester fiber: PP-g-MA is mixed in a weight ratio of 95: 5: 3.0, 90: 10: 3.0, 85: 15: 3.0, 80: 20: 3.0 and 50: 50: 3.0, respectively It was. The mixture was prepared for the composite material at a temperature of 170 ° C. in a twin screw extruder having an L / D of 40, and the mechanical properties are shown in Table 1 below.
[실시예 5]Example 5
상기 실시예 4에서 PP-g-MA 대신 EPDM-g-MA를 3.0 wt% 첨가한 것을 제외하고 동일한 방법으로 복합재료를 제조하였으며, 하기 표 1에 기계적 물성을 나타내었다. The composite material was manufactured in the same manner as in Example 4, except that 3.0 wt% of EPDM-g-MA was added instead of PP-g-MA, and the mechanical properties thereof are shown in Table 1 below.
[실시예 6]Example 6
상기 실시예 4에서 PP-g-MA 대신 SEBS-g-MA를 3.0 wt% 첨가한 것을 제외하고 동일한 방법으로 복합재료를 제조하였으며, 하기 표 1에 기계적 물성을 나타내었다. The composite material was manufactured in the same manner as in Example 4, except that 3.0 wt% of SEBS-g-MA was added instead of PP-g-MA, and the mechanical properties thereof are shown in Table 1 below.
[비교예 1]Comparative Example 1
표면처리되지 않은 폴리에스테르 섬유를 용융흐름지수가 0.5 내지 60 g/min인 호모 폴리프로필렌에 폴리에스테르 섬유를 혼합한 후 PP-g-MA를 첨가하였다. 이때, 상기 폴리프로필렌:폴리에스테르 섬유:PP-g-MA를 각각 95:5:3.0, 90:10:3.0, 85:15:3.0, 80:20:3.0 및 50:50:3.0의 중량비로 혼합하였다. 상기 혼합물을 L/D가 40인 이축압출기에서 170℃의 온도에서 복합재료를 제조하였으며, 하기 표 1에 기계적 물성을 나타내었다.The untreated polyester fibers were mixed with homopolypropylene having a melt flow index of 0.5 to 60 g / min, and then PP-g-MA was added. At this time, the polypropylene: polyester fiber: PP-g-MA is mixed in a weight ratio of 95: 5: 3.0, 90: 10: 3.0, 85: 15: 3.0, 80: 20: 3.0 and 50: 50: 3.0, respectively It was. The mixture was prepared for the composite material at a temperature of 170 ° C. in a twin screw extruder having an L / D of 40, and the mechanical properties are shown in Table 1 below.
[표 1]TABLE 1
실시예 4-6 및 비교예 1에 의한 복합재료의 물성 비교Comparison of physical properties of the composite material according to Example 4-6 and Comparative Example 1
※ (1) 항복강도(Yield Strength), (2) 신율(Elongation), ※ (1) Yield Strength, (2) Elongation,
(3) 굴곡탄성율(Flexural Modulus), (4) 충격강도(notched IZOD impact strength) (3) Flexural Modulus, (4) notched IZOD impact strength
상기에서 살펴 본 바와 같이, 본 발명은 염기성 수용액 또는 물을 이용하여 폴리에스테르 섬유의 표면을 가수분해시켜 섬유표면에 수산기를 용이하게 도입하였으며 이를 통하여 상용화제의 특성을 향상시키고 폴리프로필렌/폴리에스테르 섬유 복합재료의 기계적 물성을 효과적으로 개선하였다. 또한 EPDM-g-MA 또는 SEBS-g-MA도 효과적인 인장강도의 개선을 나타내었으며 PP-g-MA보다 우수한 충격강도를 갖고 있음을 확인하였고, 폴리에스테르 섬유 마스터배치를 제조함에 따라 섬유의 취급을 용이하게 할 수 있을 뿐 아니라 고함량의 섬유를 첨가할 수 있다는 장점을 가지고 있었다.As described above, the present invention hydrolyzed the surface of the polyester fiber using a basic aqueous solution or water to easily introduce a hydroxyl group on the surface of the fiber, thereby improving the properties of the compatibilizer and the polypropylene / polyester fiber The mechanical properties of the composites were effectively improved. In addition, EPDM-g-MA or SEBS-g-MA also showed effective tensile strength improvement and better impact strength than PP-g-MA. Not only can it be easily made, but it has the advantage of adding a high content of fibers.
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KR920703717A (en) * | 1989-10-06 | 1992-12-18 | 해롤드 에인혼 | Polyolefin / Thermoplastic Blend |
KR950010747B1 (en) * | 1993-07-06 | 1995-09-22 | 주식회사코오롱 | Composite fiber and its manufacturing method |
KR100221956B1 (en) | 1996-04-29 | 1999-10-01 | 김윤 | The polyester-polypropylene division conjugated fiber superior the dyeing nature and working nature |
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KR920703717A (en) * | 1989-10-06 | 1992-12-18 | 해롤드 에인혼 | Polyolefin / Thermoplastic Blend |
KR950010747B1 (en) * | 1993-07-06 | 1995-09-22 | 주식회사코오롱 | Composite fiber and its manufacturing method |
KR100221956B1 (en) | 1996-04-29 | 1999-10-01 | 김윤 | The polyester-polypropylene division conjugated fiber superior the dyeing nature and working nature |
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