JPH04145158A - Photo-degradable heat-resistant interior cover of automobile - Google Patents
Photo-degradable heat-resistant interior cover of automobileInfo
- Publication number
- JPH04145158A JPH04145158A JP26789790A JP26789790A JPH04145158A JP H04145158 A JPH04145158 A JP H04145158A JP 26789790 A JP26789790 A JP 26789790A JP 26789790 A JP26789790 A JP 26789790A JP H04145158 A JPH04145158 A JP H04145158A
- Authority
- JP
- Japan
- Prior art keywords
- weight
- automobile
- modified polyethylene
- polypropylene
- carbon monoxide
- 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.)
- Pending
Links
- -1 polyethylene Polymers 0.000 claims abstract description 49
- 239000004698 Polyethylene Substances 0.000 claims abstract description 31
- 229920000573 polyethylene Polymers 0.000 claims abstract description 31
- 239000004743 Polypropylene Substances 0.000 claims abstract description 17
- 229920001155 polypropylene Polymers 0.000 claims abstract description 17
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims abstract description 16
- 229910002091 carbon monoxide Inorganic materials 0.000 claims abstract description 16
- 239000011342 resin composition Substances 0.000 claims abstract description 13
- 239000004611 light stabiliser Substances 0.000 claims abstract description 10
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims abstract description 7
- 239000005977 Ethylene Substances 0.000 claims abstract description 7
- 239000003963 antioxidant agent Substances 0.000 claims abstract description 6
- VNWKTOKETHGBQD-AKLPVKDBSA-N carbane Chemical compound [15CH4] VNWKTOKETHGBQD-AKLPVKDBSA-N 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 abstract description 8
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 abstract description 5
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 abstract description 5
- 238000007334 copolymerization reaction Methods 0.000 abstract description 5
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 abstract description 5
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 abstract description 5
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 abstract description 5
- 239000000203 mixture Substances 0.000 abstract description 3
- 238000001782 photodegradation Methods 0.000 abstract description 2
- 239000004711 α-olefin Substances 0.000 abstract description 2
- 230000003078 antioxidant effect Effects 0.000 abstract 2
- 239000003054 catalyst Substances 0.000 abstract 1
- 239000011347 resin Substances 0.000 description 13
- 229920005989 resin Polymers 0.000 description 13
- 230000000052 comparative effect Effects 0.000 description 9
- 238000000034 method Methods 0.000 description 9
- 239000003381 stabilizer Substances 0.000 description 8
- 238000004519 manufacturing process Methods 0.000 description 6
- 229910002090 carbon oxide Inorganic materials 0.000 description 5
- 229920001577 copolymer Polymers 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 230000001590 oxidative effect Effects 0.000 description 3
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 238000006303 photolysis reaction Methods 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 1
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 241000972773 Aulopiformes Species 0.000 description 1
- YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
- NHOGGUYTANYCGQ-UHFFFAOYSA-N ethenoxybenzene Chemical compound C=COC1=CC=CC=C1 NHOGGUYTANYCGQ-UHFFFAOYSA-N 0.000 description 1
- 229940117927 ethylene oxide Drugs 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 229920001684 low density polyethylene Polymers 0.000 description 1
- 239000004702 low-density polyethylene Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000002667 nucleating agent Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 235000019515 salmon Nutrition 0.000 description 1
- 238000007613 slurry method Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- PFBLRDXPNUJYJM-UHFFFAOYSA-N tert-butyl 2-methylpropaneperoxoate Chemical compound CC(C)C(=O)OOC(C)(C)C PFBLRDXPNUJYJM-UHFFFAOYSA-N 0.000 description 1
- SWAXTRYEYUTSAP-UHFFFAOYSA-N tert-butyl ethaneperoxoate Chemical compound CC(=O)OOC(C)(C)C SWAXTRYEYUTSAP-UHFFFAOYSA-N 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
- 238000011179 visual inspection Methods 0.000 description 1
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は、自動車の内装品を包装するのに用いられる光
崩壊性耐熱性自動車内装品カバーに関する。DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a photodegradable heat-resistant automobile interior cover used for packaging automobile interior components.
[従来の技術]
自動車産業は、代表的なアセンブリー産業であり、多く
の部品、たとえば、ぎ装量、電装品、車体構造体、懸架
装置、拘束装置、換気装置、変速装置、排気装置、タイ
ヤ、ホイール、がじ取装置、ブレーキ制御装置、エンジ
ン、燃料系装置などを集合し、組立ラインで順次部品を
組入れて作られる。[Prior Art] The automobile industry is a typical assembly industry, and many parts such as fittings, electrical components, body structures, suspension systems, restraint systems, ventilation systems, transmission systems, exhaust systems, tires, It is made by assembling wheels, steering gear, brake control equipment, engine, fuel system, etc., and assembling the parts one by one on an assembly line.
これらの部品または構造体は、自動車製造会社で内装さ
れるものと、外部の会社で製造されて自動車製造会社に
納入されるものとがある。これらの部品または構造体の
うち、ぎ装量、特に座席、ドア、内壁、天井、日除けな
どは樹脂フィルムのカバーで覆われた状態で使用者に提
供されている。Some of these parts or structures are installed internally by automobile manufacturing companies, while others are manufactured by external companies and delivered to automobile manufacturing companies. Among these parts or structures, the fittings, particularly seats, doors, inner walls, ceilings, sunshades, etc., are provided to the user in a state covered with a resin film cover.
この自動車内装品カバーには、従来、安価で加工性、透
明性、強度に優れたポリエチレンのフィルムが使用され
いる。Conventionally, polyethylene films, which are inexpensive and have excellent processability, transparency, and strength, have been used for automobile interior parts covers.
近年、自動車産業に対して、安全性、コストダウン、環
境保護などが要請されており、自動車内装カバーについ
て・もこの要請に応じていかなければならず、従来のポ
リエチレンでは対応が回能になってきた。In recent years, the automobile industry has been required to improve safety, reduce costs, and protect the environment, and automobile interior covers must also meet these demands, and conventional polyethylene is no longer able to meet these demands. It's here.
すなわち、■安全性については自動車内部が高温になっ
ても耐熱性があること、■コストダウンについては外部
の会社で作られたぎ装量を自動車製造ラインに受入れる
とき規格に合格しているか否かを自動車内装品カバーを
通して目視検査をおこなっているが、自動車内装品カバ
ーの透明性が悪いと検査に手間取り時間がかかりコスト
アップとなるので透明性が十分であること、■環境保護
については、自動車がユーザーに渡り自動車の使用を開
始するとき、これらの自動車内装品カバーは、ぎ装量か
ら取除かれ廃棄されるが、これが自然環境中で崩壊しな
いと環境破壊につながるので光崩゛壊性であること、な
どの要件を満足することが、近年特に要請されるように
なってきた。従来のポリエチレン製のカバーは、自然環
境中で光崩壊しない。In other words, ■For safety, we need to be able to withstand heat even when the inside of the car reaches high temperatures.■For cost reduction, we need to ensure that the fittings made by an outside company meet the standards when they are accepted into the automobile manufacturing line. Visual inspections are conducted through automobile interior covers, but if the transparency of automobile interior covers is poor, the inspection will take time and increase costs, so it is important to have sufficient transparency. When the car is handed over to the user and the car starts to be used, these car interior parts covers are removed from the equipment and discarded, but if they do not disintegrate in the natural environment, it will lead to environmental damage, so they must not be photo-degradable. In recent years, it has become particularly important to satisfy requirements such as: Traditional polyethylene covers do not photodegrade in the natural environment.
ところで、光崩壊性のポリオレフィン組成物としては、
たとえば、特開昭50−34044号公報に酸化安定剤
を含むポリオレフィンを主成分とし、これにエチレンと
一酸化炭素との共重合体を配合して光崩壊性を付与した
樹脂組成物の開示がある。しかしこの樹脂組成物では光
崩壊性を有するが耐熱性、透明性が不十分である。By the way, as a photodegradable polyolefin composition,
For example, Japanese Patent Application Laid-Open No. 50-34044 discloses a resin composition which has a polyolefin containing an oxidation stabilizer as its main component, and which is blended with a copolymer of ethylene and carbon monoxide to impart photodegradability. be. However, although this resin composition has photodegradability, it has insufficient heat resistance and transparency.
[発明が解決し・ようとする課題]
本発明は上記の事情に鑑みてなされたもので、ポリエチ
レンフィルムで作られた自動車内装品カバーに替えて、
耐熱性、透明性および光崩壊性に優れた自動車内装品カ
バーを提供することを目的とする。[Problems to be solved by the invention] The present invention has been made in view of the above circumstances, and provides a method for replacing automobile interior parts covers made of polyethylene film.
The purpose of the present invention is to provide an automobile interior cover with excellent heat resistance, transparency, and photodegradability.
[課題を解決するための手段]
本発明者らは、自動車内装品カバーに要求される耐熱性
、透明性および光崩壊性などの性質を同時に満足させ適
度の強度と加工性を有する数多くの素材と、それらの組
合せについて検討をおこなって以下の本発明の構成の自
動車内装品カバーを見出し完成したものである。[Means for Solving the Problems] The present inventors have developed a number of materials that simultaneously satisfy the properties such as heat resistance, transparency, and photodegradability required for automobile interior parts covers, and have appropriate strength and processability. After studying these combinations, we discovered and completed an automobile interior parts cover having the following structure according to the present invention.
本発明の自動車内装品カバーは、エチレンを主たる構成
成分とし0.5〜10重量%の一酸化炭素が共重合され
た変性ポリエチレン70〜85重量%と、光安定剤およ
び酸化防止剤を含まないポリプロピレン15〜30重量
%とからなる樹脂組成物で形成されている。The automobile interior parts cover of the present invention contains 70 to 85% by weight of modified polyethylene copolymerized with ethylene as a main component and 0.5 to 10% by weight of carbon monoxide, and does not contain light stabilizers or antioxidants. It is formed from a resin composition consisting of 15 to 30% by weight of polypropylene.
この変性ポリエチレンは、エチレンを主たる構成成分と
し、−酸化炭素または一酸化炭素とエチレン性不飽和化
合物を共重合したものであって、成形品の透明性と光崩
壊性を保持する。This modified polyethylene has ethylene as its main component and is a copolymer of carbon oxide or carbon monoxide and an ethylenically unsaturated compound, and maintains the transparency and photodegradability of molded products.
変性ポリエチレン中の一酸化炭素の量は0.5〜10重
量%である。−酸化炭素の共重合割合が、0.5重量%
未満であると光分解速度が著しく小さくなり、10重間
%を超えると光分解速度が大きくなりすぎて、短時間で
強度が低下するので成形品としては好ましくない。また
、−酸化炭素に共重合されるエチレン性不飽和化合物と
しては、酢酸ビニル、アクリル酸、アクリル酸メチル、
アクリル酸エチル、メタクリル酸、メタクリル酸メチル
、マレイン酸、フマル酸、アクリロニトリル、アクリル
アミド、ビニルメチルエーテル、ビニルフェニルエーテ
ル、スチレン、塩化ビニル、プロピレン、ブテン−1、
ヘキセン−1、オクテン1、デセン−1,4−メチルペ
ンテン−1などがあげられるがコスト、フィルム強度、
耐熱性、光沢、曇価などの点で酢酸ビニルおよびアクリ
ル酸エチルが特に好ましい。The amount of carbon monoxide in the modified polyethylene is 0.5-10% by weight. -The copolymerization ratio of carbon oxide is 0.5% by weight
If it is less than 10% by weight, the photodecomposition rate will be extremely low, and if it exceeds 10% by weight, the photodecomposition rate will be too high and the strength will decrease in a short time, which is not preferable for molded products. In addition, examples of ethylenically unsaturated compounds copolymerized with -carbon oxide include vinyl acetate, acrylic acid, methyl acrylate,
Ethyl acrylate, methacrylic acid, methyl methacrylate, maleic acid, fumaric acid, acrylonitrile, acrylamide, vinyl methyl ether, vinyl phenyl ether, styrene, vinyl chloride, propylene, butene-1,
Examples include hexene-1, octene-1, decene-1,4-methylpentene-1, but cost, film strength, etc.
Vinyl acetate and ethyl acrylate are particularly preferred in terms of heat resistance, gloss, haze value, and the like.
また−酸化炭素と共に酢酸ビニルやアクリル酸エチルな
どのエチレン性不飽和化合物を共重合した変性ポリエチ
レンは、自動車内装品カバーの透明性をざらによくする
と共に、一定期間経過後に光分解を急激に起こす。この
エチレン性不飽和化合物を共重合させる場合は、その共
重合割合は1〜20重量%の範囲が好ましい。1重量%
未満であると共重合による効果が発揮されず、20重量
%を超えるとフィルムの強度が低下し加工性が悪くなる
ので好ましくない。Additionally, modified polyethylene, which is made by copolymerizing ethylenically unsaturated compounds such as vinyl acetate and ethyl acrylate with carbon oxide, not only improves the transparency of automobile interior parts covers, but also causes rapid photodegradation after a certain period of time. . When this ethylenically unsaturated compound is copolymerized, the copolymerization ratio is preferably in the range of 1 to 20% by weight. 1% by weight
If it is less than 20% by weight, the effect of copolymerization will not be exhibited, and if it exceeds 20% by weight, the strength of the film will decrease and processability will deteriorate, which is not preferable.
本発明において、光安定剤および酸化防止剤を含有しな
いポリプロピレンとは、チーグラー・ナツタ系などの公
知のα−オレフィンの立体規則性触媒を用いてスラリー
法、溶液法、気相法またはそれらの(jf用などの公知
の方法でプロピレンを単独重合させるか、またはプロピ
レンと他のα−オレフィンを共重合させることによって
得られるものである。そしてこの重合体は、光安定剤お
よび酸化安定剤を全く添加していないものである。In the present invention, polypropylene that does not contain light stabilizers and antioxidants is produced using a slurry method, solution method, gas phase method, or their ( It is obtained by homopolymerizing propylene or copolymerizing propylene and other α-olefins by a known method such as for JF.This polymer is completely free of light stabilizers and oxidative stabilizers. It is not added.
通常市販されているポリプロピレンは、重合ざれたベー
スレジンのままでは熱や光線により励起されやすく、ラ
ジカルを発生し、このラジカルに酸素が反応し、酸化劣
化が進行覆るので光安定剤および酸化安定剤が配合され
ている。本発明においては光崩壊性の成形品を作ること
を目的としているので、前記の安定剤を全く添加してい
ないポリプロピレンを使用する。この安定剤を含まない
ポリプロピレンを配合することにより樹脂全体に光崩壊
性が適度にバランスされることができる。Normally commercially available polypropylene is a polymerized base resin that is easily excited by heat or light, generating radicals, which react with oxygen and oxidative deterioration progresses. is blended. Since the purpose of the present invention is to produce a photodegradable molded article, polypropylene to which no stabilizer is added is used. By blending polypropylene that does not contain this stabilizer, the photodegradability of the entire resin can be appropriately balanced.
このポリプロピレンは、樹脂組成物の耐熱性と強度およ
び加工性を高めるもので、変性ポリエチレン70〜85
重量%に対して15〜30重量%配合される。変性ポリ
エチレンの配合量が70重量%未満で、かつポリプロピ
レンの配合量が30重量%を超えると、自動車内装品カ
バーとしての機械的強度が不十分となり、透明性も劣り
、加工時にメルトフラクチャーを生じるので好ましくな
い。This polypropylene is used to improve the heat resistance, strength, and processability of the resin composition, and is a modified polyethylene of 70 to 85%.
It is blended in an amount of 15 to 30% by weight. If the amount of modified polyethylene is less than 70% by weight and the amount of polypropylene is more than 30% by weight, the mechanical strength as an automobile interior parts cover will be insufficient, the transparency will be poor, and melt fracture will occur during processing. So I don't like it.
また変性ポリエチレンの配合量が85重量%を超えかつ
ポリプロピレンの配合量が15重量%未満であると、自
動車内装品カバーとしての耐熱性基準に適合せず、光崩
壊性も遅くなるの好ましくない。If the amount of modified polyethylene is more than 85% by weight and the amount of polypropylene is less than 15% by weight, it will not meet the heat resistance standards for automobile interior parts covers and the photodegradability will be slow, which is undesirable.
変性ポリエチレンは以下の方法により製造できる。たと
えば、ポリエチレン製造装置を用いて、反応温度150
〜300℃、圧力500〜8000気圧の条件下に、ジ
ラウロイルパーオキサイド、ターシャリ−ブチルパーオ
キサイド、ターシャリ−ブチルパーイソブチレート、タ
ーシャリ−ブチルパーアセテートまたはα、α′−アゾ
ビスイソブチロニトリルなどのラジカル開始剤をベンゼ
ン、ケロセンまたは鉱油などの不活性有機溶媒に溶解し
たものを反応器に注入し、エチレンと一酸化炭素および
必要に応じて伯のエチレン性不飽和化合物とを共重合さ
せる方法、ポリエチレン製造装置を用いて、反応温度5
0〜300℃、圧力O〜200気圧の条件下に、配位触
媒または金属触媒(チーグラー型、ナツタ型、フィリッ
プス型など)の存在下で、スラリー法、溶液法、気相法
などでエチレンと一酸化炭素および必要に応じて他のエ
チレン性不飽和化合物とを共重合させる方法で製造する
ことができる。Modified polyethylene can be produced by the following method. For example, using a polyethylene manufacturing equipment, the reaction temperature is 150
Dilauroyl peroxide, tert-butyl peroxide, t-butyl perisobutyrate, t-butyl peracetate or α,α'-azobisisobutyronitrile under conditions of ~300°C and a pressure of 500-8000 atm. A radical initiator, such as , dissolved in an inert organic solvent such as benzene, kerosene or mineral oil, is injected into the reactor to copolymerize ethylene with carbon monoxide and optionally an ethylenically unsaturated compound. method, using a polyethylene manufacturing equipment, reaction temperature 5
Ethylene and It can be produced by copolymerizing carbon monoxide and, if necessary, other ethylenically unsaturated compounds.
樹脂組成物には、光崩壊性、耐熱性および透明性を阻害
しない範囲で、顔料、架橋剤、滑剤、加工性改良剤、帯
電防止剤、核形成剤、霧発生防止剤、難燃剤、抗菌剤、
防臭剤、芳香剤、鮭度保持剤、赤外線放射剤などを配合
してもよい。The resin composition contains pigments, cross-linking agents, lubricants, processability improvers, antistatic agents, nucleating agents, antifogging agents, flame retardants, and antibacterial agents to the extent that they do not impair photodegradability, heat resistance, and transparency. agent,
Deodorizers, fragrances, salmon temperature retaining agents, infrared radiation agents, etc. may also be added.
この樹脂組成物は、樹脂成分、上記配合物などをバンバ
リーミキサー、加圧ニーダ−1二軸押出し機、ブスコニ
ーダー、ヘンシェルミキサー、ロルニーダーなどを用い
て通常の混練法で製造できる。This resin composition can be produced by a conventional kneading method using a Banbury mixer, a pressure kneader-1 twin-screw extruder, a Busco kneader, a Henschel mixer, a Roll kneader, etc., by mixing the resin component, the above-mentioned compound, and the like.
この樹脂組成物より、自動車内装品カバーを製造するに
は、インフレーション法、カレンダー法、キャスティン
グ法などによりフィルムをつくり所定の形状に切断して
、ヒートシールして作製することができる。In order to manufacture an automobile interior parts cover from this resin composition, a film can be made by an inflation method, a calendar method, a casting method, etc., cut into a predetermined shape, and heat-sealed.
[実施例コ 以下、実施例により具体的に説明する。[Example code] Hereinafter, this will be explained in detail using examples.
(実施例1)
一酸化炭素含有量が0.9%のエヂレンーーーーー酸化
炭素共重合体[ユニオンカーバイド社製、DXM−43
9、メルトインデックス(MI)0.7(190℃)]
88重量%と、光安定剤及び酸化防止剤が添加されてい
ないポリプロピレン[東燃石油化学社製、メルトフロー
レイト(MFR)9(230℃)]15重間%をバンバ
リーミキサ−により混練し、ペレット化した樹脂組成物
を得た。(Example 1) Edylene carbon oxide copolymer with a carbon monoxide content of 0.9% [manufactured by Union Carbide, DXM-43]
9. Melt index (MI) 0.7 (190°C)]
88% by weight and 15% by weight of polypropylene without light stabilizers and antioxidants [Melt Flow Rate (MFR) 9 (230°C) manufactured by Tonen Petrochemical Co., Ltd.] were kneaded in a Banbury mixer to form pellets. A resin composition was obtained.
この樹脂組成物を用いて、50m/m径のインフレーシ
ョン押出し機により190℃で50μの厚みのフィルム
を作製した。このフィルムについて下記の評価法で評価
した。結果を第1表に示す。Using this resin composition, a film with a thickness of 50 μm was produced at 190° C. using an inflation extruder with a diameter of 50 m/m. This film was evaluated using the following evaluation method. The results are shown in Table 1.
配向性:フィルムの縦方向と横方向の引裂き強度の比率
が0.4以上を○、0.4以下をXとしフィルムの強度
を判定した。Orientation: The strength of the film was evaluated using a ratio of 0.4 or more as ○ and a ratio of 0.4 or less as X.
光崩壊性:サンシャイン型ウェザ−オーメータでフィル
ムを70時間暴露させた後の伸び残率を測定し、50%
以上のものをX、30〜10%のものを○、10%以下
のものを◎とした。Photodegradability: Measure the remaining elongation after exposing the film for 70 hours using a sunshine type weather-o-meter, and it is 50%.
Those above were rated as X, those with 30 to 10% were rated as ○, and those with 10% or less were rated as ◎.
加工性:フィルム成形においてメルトフラクチャーが生
じる場合×、生じない場合を○とした。Processability: When melt fracture occurred during film molding, it was evaluated as ×, and when it did not occur, it was evaluated as ○.
耐熱性:フィルムを120℃のチャンバーに入れ、10
分後に取出したとき、元のままであったものを○、収縮
しているものをXとした。Heat resistance: Place the film in a chamber at 120°C,
When taken out after a minute, those that remained intact were marked as ○, and those that had shrunk were marked as X.
透明性:曇値が8以上のものを×、8以下のものをOと
した。Transparency: Those with a cloudy value of 8 or more were rated as ×, and those with a cloudy value of 8 or less were rated as O.
(実施例2〜6)
実施例2は変性ポリエチレン中の一酸化炭素の量を0.
5重量%、MI=0.7を80重量%にした他は、実施
例1と同様にして樹脂フィルムを作製した。(Examples 2 to 6) In Example 2, the amount of carbon monoxide in modified polyethylene was 0.
A resin film was produced in the same manner as in Example 1, except that 5% by weight and MI=0.7 were changed to 80% by weight.
実施例3は変性ポリエチレンの一酸化炭素の量を3重量
%、MI=2を75重量%にした他は、実施例1と同様
にして樹脂フィルムを作製した。In Example 3, a resin film was produced in the same manner as in Example 1, except that the amount of carbon monoxide in the modified polyethylene was 3% by weight and the MI=2 was 75% by weight.
実施例4は変性ポリエチレンの一酸化炭素の量を10重
量%、MI=5を70重量%にした他は、実施例1と同
様にして樹脂フィルムを作製した。In Example 4, a resin film was produced in the same manner as in Example 1, except that the amount of carbon monoxide in the modified polyethylene was 10% by weight and the MI=5 was 70% by weight.
実施例5は変性ポリエチレンの一酸化炭素を5重量%と
酢酸ビニルを7重量%を共重合した共重合体でMI=6
を75重口%にした他は、実施例1と同様にして樹脂フ
ィルムを作製した。Example 5 is a copolymer prepared by copolymerizing modified polyethylene with 5% by weight of carbon monoxide and 7% by weight of vinyl acetate, and has an MI of 6.
A resin film was produced in the same manner as in Example 1, except that the amount was changed to 75% by weight.
実施例6は変性ポリエチレンを一酸化炭素を2重量%と
アクリル酸エチル5重量%の共重合体でMI=3を80
重重量にした他は、実施例1と同様にして樹脂フィルム
を作製した。In Example 6, modified polyethylene was made of a copolymer of 2% by weight of carbon monoxide and 5% by weight of ethyl acrylate, and the MI=3 was 80.
A resin film was produced in the same manner as in Example 1 except that the weight was increased.
(比較例)
比較例1は変性ポリエチレンが実施例1より多く95重
量%にした他は、実施例1と同様にして樹脂フィルムを
作製した。(Comparative Example) In Comparative Example 1, a resin film was produced in the same manner as in Example 1, except that the modified polyethylene was increased to 95% by weight, which was higher than in Example 1.
比較例2は変性ポリエチレンが実施例3と同じで量が6
5重量%と少なくにした他は、実施例1と同様にして樹
脂フィルムを作製した。In Comparative Example 2, the modified polyethylene was the same as in Example 3, but the amount was 6.
A resin film was produced in the same manner as in Example 1, except that the amount was reduced to 5% by weight.
比較例3は変性ポリエチレンが実施例4と同じで量が8
0重量%で光安定剤および酸化安定剤を含むポリプロピ
レンを使用にした伯は、実施例1と同様にして樹脂フィ
ルムを作製した。In Comparative Example 3, the modified polyethylene was the same as in Example 4, but the amount was 8.
A resin film was produced in the same manner as in Example 1 using polypropylene containing 0% by weight of a light stabilizer and an oxidation stabilizer.
比較例4は一酸化炭素を共重合してないポリエチレンを
80重量%用いた他は実施例1と同様にして樹脂フィル
ムを作製した。In Comparative Example 4, a resin film was produced in the same manner as in Example 1, except that 80% by weight of polyethylene not copolymerized with carbon monoxide was used.
(評価結果)
第1表の評価結果によれば、実施例1〜6は配向性、光
崩壊性、加工性、耐熱性、透明性のいずれをも満足して
いる。一方比較例1の変性ポリエチレンの量が95重量
%となると耐熱性が低下する。比較例2の変性ポリエチ
レンの最が65重量%となると光崩壊性は良好であるが
配向性、加工性、透明性が低下する。比較例3の安定剤
を配合したポリプロピレンを用いた場合では光崩壊性を
示さなくなる。また比較例4のように変性ポリエチレン
の代りに高圧法低密度ポリエチレンを用いた場合は光崩
壊性とならない。(Evaluation Results) According to the evaluation results in Table 1, Examples 1 to 6 satisfied all of orientation, photodegradability, processability, heat resistance, and transparency. On the other hand, when the amount of modified polyethylene in Comparative Example 1 reaches 95% by weight, the heat resistance decreases. When the modified polyethylene of Comparative Example 2 reaches 65% by weight, the photodegradability is good, but the orientation, processability, and transparency deteriorate. When the polypropylene blended with the stabilizer of Comparative Example 3 is used, it no longer exhibits photodegradability. Further, when high-pressure low-density polyethylene is used instead of modified polyethylene as in Comparative Example 4, photodegradability does not occur.
したがって、−1化炭素を共重合した変性ポリエチレン
の特定量と、光安定剤および酸化安定剤を含まないポリ
プロピレンとの樹脂組成物で作製された自動車内装品カ
バーは、光崩壊性耐熱性および透明性をもち適度の強度
と加工性を有する。Therefore, an automobile interior cover made of a resin composition of a specific amount of modified polyethylene copolymerized with -carbon monide and polypropylene free of light stabilizers and oxidation stabilizers has photodegradable heat resistance and transparency. It has moderate strength and workability.
[発明の効果コ
本発明の自動車内装品カバーは、光崩壊性を有し透明性
で適度の強度をもつ変性ポリエチレンの耐熱性を高める
ためにポリプロピレンが配合されている。そして光崩壊
性を促進するためにポリプロピレンには、光安定剤およ
び酸化安定剤が配合されていない。したがってこの両者
が特定の割合で配合されることにより、所望の強度と耐
熱性および透明性をもち光崩壊性をもあわせもつ自動車
内装品カバーを形成することができる。[Effects of the Invention] The automobile interior parts cover of the present invention contains polypropylene in order to improve the heat resistance of modified polyethylene, which is photodegradable, transparent, and has an appropriate strength. In order to promote photodegradability, polypropylene does not contain light stabilizers or oxidative stabilizers. Therefore, by blending both of them in a specific ratio, it is possible to form an automobile interior parts cover that has desired strength, heat resistance, transparency, and photodegradability.
また、自動車が気温の高い地域において使用される場合
でもこの樹脂組成物で形成された自動車内装品カバーは
、変形して外観が悪くなることがない。また透明性がよ
いので製品の納入検査も楽にできる。さらにこのカバー
が自然環境中に聞棄されたとぎに光崩壊性が良いので容
易に分解して原形のまま残存しないので、環境美化に貢
献することができる。Moreover, even when a car is used in a region with high temperatures, the car interior cover made of this resin composition will not be deformed and its appearance will not deteriorate. Also, since it is highly transparent, it is easy to inspect products upon delivery. Furthermore, even if this cover is discarded in the natural environment, it has good photodegradability, so it easily disintegrates and does not remain in its original form, contributing to environmental beautification.
特許出願人 トヨタ自動車株式会社Patent applicant: Toyota Motor Corporation
Claims (1)
酸化炭素が共重合された変性ポリエチレン70〜85重
量%と、光安定剤および酸化防止剤を含まないポリプロ
ピレン15〜30重量%とからなる樹脂組成物で形成さ
れた光崩壊性耐熱性自動車内装品カバー。Consists of 70-85% by weight of modified polyethylene, which is copolymerized with ethylene as the main component and 0.5-10% by weight of carbon monoxide, and 15-30% by weight of polypropylene that does not contain light stabilizers or antioxidants. A photodegradable heat-resistant automobile interior parts cover made of a resin composition.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP26789790A JPH04145158A (en) | 1990-10-04 | 1990-10-04 | Photo-degradable heat-resistant interior cover of automobile |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP26789790A JPH04145158A (en) | 1990-10-04 | 1990-10-04 | Photo-degradable heat-resistant interior cover of automobile |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH04145158A true JPH04145158A (en) | 1992-05-19 |
Family
ID=17451142
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP26789790A Pending JPH04145158A (en) | 1990-10-04 | 1990-10-04 | Photo-degradable heat-resistant interior cover of automobile |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH04145158A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113385210A (en) * | 2021-06-08 | 2021-09-14 | 太原理工大学 | Photocatalytic hydrogen production catalyst and preparation method and application thereof |
-
1990
- 1990-10-04 JP JP26789790A patent/JPH04145158A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113385210A (en) * | 2021-06-08 | 2021-09-14 | 太原理工大学 | Photocatalytic hydrogen production catalyst and preparation method and application thereof |
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