JPS63172758A - Polypropylene resin composition for bumper - Google Patents
Polypropylene resin composition for bumperInfo
- Publication number
- JPS63172758A JPS63172758A JP178587A JP178587A JPS63172758A JP S63172758 A JPS63172758 A JP S63172758A JP 178587 A JP178587 A JP 178587A JP 178587 A JP178587 A JP 178587A JP S63172758 A JPS63172758 A JP S63172758A
- Authority
- JP
- Japan
- Prior art keywords
- weight
- propylene
- ethylene
- component
- content
- 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
Links
- -1 Polypropylene Polymers 0.000 title claims abstract description 12
- 239000011342 resin composition Substances 0.000 title claims description 12
- 239000004743 Polypropylene Substances 0.000 title claims description 10
- 229920001155 polypropylene Polymers 0.000 title claims description 10
- 239000000454 talc Substances 0.000 claims abstract description 13
- 229910052623 talc Inorganic materials 0.000 claims abstract description 13
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims abstract description 11
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims abstract description 11
- 239000005977 Ethylene Substances 0.000 claims abstract description 9
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims abstract description 8
- 229920001971 elastomer Polymers 0.000 claims abstract description 8
- 229920001577 copolymer Polymers 0.000 claims abstract description 6
- 229920001400 block copolymer Polymers 0.000 claims abstract description 5
- 238000009835 boiling Methods 0.000 claims abstract description 5
- OJOWICOBYCXEKR-KRXBUXKQSA-N (5e)-5-ethylidenebicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(=C/C)/CC1C=C2 OJOWICOBYCXEKR-KRXBUXKQSA-N 0.000 claims abstract description 4
- PRBHEGAFLDMLAL-GQCTYLIASA-N (4e)-hexa-1,4-diene Chemical compound C\C=C\CC=C PRBHEGAFLDMLAL-GQCTYLIASA-N 0.000 claims abstract description 3
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 claims abstract 5
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 6
- 238000002156 mixing Methods 0.000 claims description 6
- 150000002894 organic compounds Chemical class 0.000 claims description 6
- 229910000077 silane Inorganic materials 0.000 claims description 6
- 229920002943 EPDM rubber Polymers 0.000 claims description 5
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 claims description 3
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 abstract description 3
- 150000001282 organosilanes Chemical class 0.000 abstract description 3
- 238000001035 drying Methods 0.000 abstract description 2
- 150000001993 dienes Chemical class 0.000 abstract 1
- 229920000642 polymer Polymers 0.000 abstract 1
- 238000000576 coating method Methods 0.000 description 9
- 239000011248 coating agent Substances 0.000 description 8
- 230000007423 decrease Effects 0.000 description 7
- 238000000034 method Methods 0.000 description 6
- 230000000704 physical effect Effects 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- 238000000227 grinding Methods 0.000 description 4
- 238000001746 injection moulding Methods 0.000 description 4
- 238000000465 moulding Methods 0.000 description 3
- 239000008188 pellet Substances 0.000 description 3
- 238000010298 pulverizing process Methods 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 238000004381 surface treatment Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 239000011256 inorganic filler Substances 0.000 description 2
- 229910003475 inorganic filler Inorganic materials 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 229920002545 silicone oil Polymers 0.000 description 2
- QJVOZXGJOGJKPT-IGHBBLSQSA-N (1r,2r,5s,11ar)-2-(prop-2-en-1-yl)-1,2,3,4,5,6,11,11a-octahydro-10h-1,5-methanopyrido[1,2-a][1,5]diazocin-10-one Chemical compound C([C@@H]12)C(=O)C=CN1C[C@@H]1CN[C@H](CC=C)[C@H]2C1 QJVOZXGJOGJKPT-IGHBBLSQSA-N 0.000 description 1
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 1
- RYPKRALMXUUNKS-UHFFFAOYSA-N 2-Hexene Natural products CCCC=CC RYPKRALMXUUNKS-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- QJVOZXGJOGJKPT-UHFFFAOYSA-N albine Natural products C12CC(=O)C=CN2CC2CNC(CC=C)C1C2 QJVOZXGJOGJKPT-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000009837 dry grinding Methods 0.000 description 1
- 229920005676 ethylene-propylene block copolymer Polymers 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- DPUXQWOMYBMHRN-UHFFFAOYSA-N hexa-2,3-diene Chemical compound CCC=C=CC DPUXQWOMYBMHRN-UHFFFAOYSA-N 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 210000003127 knee Anatomy 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 238000005453 pelletization Methods 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 229920005629 polypropylene homopolymer Polymers 0.000 description 1
- 229920005630 polypropylene random copolymer Polymers 0.000 description 1
- 238000001175 rotational moulding Methods 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- 239000012756 surface treatment agent Substances 0.000 description 1
- 239000000326 ultraviolet stabilizing agent Substances 0.000 description 1
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は高剛性、低温耐衝γ性を存し、塗装性、製品外
観にすぐれるバンパー用ポリプロピレン樹脂組成物に関
する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a polypropylene resin composition for bumpers that has high rigidity, low-temperature impact γ resistance, and has excellent paintability and product appearance.
(従来の技術〕
ポリプロピレン樹脂、エチレン・プロピレン共重合体ゴ
ム、および各種無機フィラーから成る樹脂組成物は、剛
性、耐衝祭性等の物性バランス及び塗装性が良好でかつ
成形性にすぐれるため、現在、自動車外装用の大型部品
特にバンパーに広く使用されている(特開昭57−55
952号公報、同57−159842号公報、同58−
213043号公報等)。(Prior art) A resin composition composed of polypropylene resin, ethylene-propylene copolymer rubber, and various inorganic fillers has a good balance of physical properties such as rigidity and impact resistance, and has good paintability and excellent moldability. Currently, it is widely used in large parts for automobile exteriors, especially bumpers (Japanese Patent Laid-Open No. 57-55
No. 952, No. 57-159842, No. 58-
213043, etc.).
しかしながら、従来のポリプロピレン樹脂組成物を用い
てバンパーのような形状の製品を成形した場合、ウェル
ドラインが非常に目立ち易く、また塗装を施すと、さら
にウェルドラインが目立つため外観が見劣りし、商品価
値を下げていた。However, when a conventional polypropylene resin composition is used to mold a product shaped like a bumper, the weld lines are very noticeable, and when painted, the weld lines become even more noticeable, resulting in a poor appearance and poor product value. was lowered.
本発明は上記問題点を解決すべくなされたもので、バン
パー材としての諸物性を損なうことなく外観の良好なバ
ンパー用ポリプロピレン樹脂組成物を提供することを目
的とする。The present invention was made to solve the above problems, and an object of the present invention is to provide a polypropylene resin composition for a bumper that has a good appearance without impairing various physical properties as a bumper material.
すなわち、本発明は下記a)〜C)成分より成り、各成
分の配合割合がa)〜C)の合計量を100重量%とじ
てa)が65〜55重量%、b)が30〜35重量%お
よびC)が5〜lO重量%であることを特徴とするバン
パー用ポリプロピレン樹脂組成物である。That is, the present invention consists of the following components a) to C), and the blending ratio of each component is 65 to 55% by weight of a) and 30 to 35% of b), taking the total amount of a) to C) as 100% by weight. A polypropylene resin composition for a bumper, characterized in that C) is 5 to 10% by weight.
a)エチレン含有量4〜8重量%、沸an−ヘブタン不
溶分85重量%以上、メルトフローインデックス(M
I ) 10〜15g/minの結晶性エチレン・プロ
ピレンブロック共重合体。a) Ethylene content 4-8% by weight, boiling an-hebutane insoluble content 85% by weight or more, melt flow index (M
I) 10-15 g/min crystalline ethylene-propylene block copolymer.
b) プロピレン含有量45〜60重量%、ムーニー粘
度(ML100℃
1+4)が20〜50であるエチレン・プロピレン共重
合体ゴムおよび/または同様のプロピレン含有量、ムー
ニー粘度を有し、かつ第3成分がジシクロペンタジェン
、エチリデンノルボルネンまたは1.4−へキサジエン
であるエチレン・プロピレン・チェ23元共重合体ゴム
。b) Ethylene-propylene copolymer rubber having a propylene content of 45 to 60% by weight and a Mooney viscosity (ML100°C 1+4) of 20 to 50 and/or a third component having a similar propylene content and Mooney viscosity; is dicyclopentadiene, ethylidene norbornene or 1,4-hexadiene.
C) 乾式ないし半乾式の粉砕機中でシラン系有機化合
物により表面処理されたタルク。C) Talc surface-treated with a silane-based organic compound in a dry or semi-dry grinder.
そして、本発明の好ましい実施態様としては前記の粉砕
機がジェット気流式粉砕機であることであり、さらには
流動層式ジェット粉砕機であることである。In a preferred embodiment of the present invention, the pulverizer is a jet stream type pulverizer, and furthermore, it is a fluidized bed type jet pulverizer.
本発明に用いるエチレン・プロピレンブロック共重合体
はエチレン含有量4〜8重量%、沸騰n−ベブタン不溶
分85重量%以上、MIION15g/10m1nのも
のに限られる。The ethylene/propylene block copolymer used in the present invention is limited to one having an ethylene content of 4 to 8% by weight, a boiling n-bebutane insoluble content of 85% by weight or more, and a MIION of 15g/10ml.
ポリプロピレン単独重合体やランダム共重合体では耐衝
撃性が低く好ましくない。Polypropylene homopolymers and random copolymers have low impact resistance and are not preferred.
エチレン・プロピレンブロック共重合体中のエチレン含
有量が4重量%未満では耐衝撃性が低く、8重量%を超
えた場合、剛性が低く、又、耐傷付性が悪くなる。沸1
1n−ヘプタン不溶分が85重量%未満のものを用いる
と剛性が低く、耐傷付性も悪くなり好ましくない。MI
がlOg / 10m1n未満では成形性が低下し、製
品にフローマークが起き易く、15g / 10a+i
nを超えた場合、耐衝撃性が低下する他、製品に凹みが
発生し易く好ましくない。If the ethylene content in the ethylene/propylene block copolymer is less than 4% by weight, the impact resistance will be low, and if it exceeds 8% by weight, the rigidity will be low and the scratch resistance will be poor. boiling 1
If the 1n-heptane insoluble content is less than 85% by weight, the rigidity will be low and the scratch resistance will be poor, which is not preferable. M.I.
If it is less than lOg / 10m1n, the moldability will decrease and flow marks will easily occur on the product.
If it exceeds n, the impact resistance will deteriorate and the product will be more likely to be dented, which is not preferable.
本発明に用いるゴム成分としてはプロピレン含有量が4
5〜60重量%、ムーニー粘度100℃
(ML )が20〜50であるエチレン・プロ1
+4
とレン共重合体ゴム(EPR)および/または同様のプ
ロピレン含有量とムーニー粘度を有し、第3成分がジシ
クロペンタジェン、エチリデンノルボルネンまたは 1
.4−ヘキサジエンであるエチレン・プロピレン・チェ
23元共重合体ゴム(EPDM)に限られる。The rubber component used in the present invention has a propylene content of 4
Ethylene Pro 1 having a Mooney viscosity of 5 to 60% by weight and a Mooney viscosity of 100°C (ML) of 20 to 50.
+4 and ren copolymer rubber (EPR) and/or have similar propylene content and Mooney viscosity, and the third component is dicyclopentadiene, ethylidene norbornene or 1
.. It is limited to ethylene-propylene-che 23-component copolymer rubber (EPDM), which is 4-hexadiene.
前記EPR,EPDM中のプロピレン含有量が45重量
%未満ではEPR,EPDMの分散が悪く外観が低下す
る他、耐#軍性も低下する。一方、60fifi%を超
えた場合、耐傷付性が低下する。If the propylene content in the EPR or EPDM is less than 45% by weight, the dispersion of the EPR or EPDM will be poor, resulting in poor appearance and also poor #mildew resistance. On the other hand, when it exceeds 60 fifi%, scratch resistance decreases.
4−ニー粘度(Mt、 100℃
1+4 )が20未満°の
EPR,EPDMを用いると塗装した場合の塗膜剥離強
度が低下するほか、ウェルドラインが目立ち易く、50
を超えたものを用いると成形性が低下しフローマークが
起き易く、またウェルドラインもかえって目立ち易くな
り、いずれの場合も好ましくない。4- If EPR or EPDM with a knee viscosity (Mt, 100°C 1+4) of less than 20° is used, the peeling strength of the coating will decrease, and weld lines will be more noticeable.
If it exceeds the above range, moldability decreases, flow marks are more likely to occur, and weld lines become more noticeable, which is undesirable in either case.
タルクは、乾式ないし半乾式の粉砕機中で、シラン系有
機化合物と共に粉砕して表面処理するか、あるいは上記
粉砕機中でシラン系有機化合物で表面処理されたもので
ある。このようなタルクは例えば有機シラン系カップリ
ング剤、シリコンオイル、変性シリコンオイル、各種シ
ラン化合物等のシラン系有機化合物とタルクを予備混合
して、あるいは別々に粉砕機に供給し、粉砕と同時に表
面処理を行なうことによって得られる。Talc is surface-treated by being ground together with a silane-based organic compound in a dry or semi-dry grinding machine, or surface-treated with a silane-based organic compound in the above-mentioned grinding machine. Such talc can be prepared by pre-mixing talc with a silane-based organic compound such as an organosilane-based coupling agent, silicone oil, modified silicone oil, or various silane compounds, or by supplying the talc separately to a grinder. Obtained by processing.
ここでタルクとシラン系有機化合物との割合は通常タル
ク100重量部に対して0.O1〜5重量部程度が好ま
しい。すなわち、表面処理効果を大きくする点で0.0
1重量部以上が好ましく、一方、得られる樹脂組成物の
剛性、耐衝撃性、耐熱性、表面特性等の物性バランスの
向上の点で5重量部以下が好ましい。そして5重量部を
越えると、かえって剛性、耐衝撃性等が低下する場合が
あるばかりでなくコストも高くなるので、いずれにして
も好ましくない。Here, the ratio of talc and silane-based organic compound is usually 0.00 parts per 100 parts by weight of talc. About 1 to 5 parts by weight of O is preferable. In other words, 0.0 in terms of increasing the surface treatment effect.
The amount is preferably 1 part by weight or more, while the amount is preferably 5 parts by weight or less in terms of improving the balance of physical properties such as rigidity, impact resistance, heat resistance, and surface properties of the resulting resin composition. If the amount exceeds 5 parts by weight, not only the rigidity, impact resistance, etc. may deteriorate, but also the cost will increase, which is not preferable in any case.
上記粉砕機としては通常乾式あるいは半乾式で細粉砕微
粉砕できるものであれば良く、例えばミクロンミル、ジ
ェット気流式粉砕機、ボールミル、ミクロナイザー、タ
ーボミル、アトマイザ−等の粉砕機が挙げられるが、粉
砕効率、粉砕時間、作業性の点からミクロナイザー型、
リダクショナイザー型、衝撃型、対向型、流動層型等の
ジェット気流式粉砕機が好ましく、中でも表面処理がよ
り均一に行なわれる流動層型ジェット粉砕機がとりわけ
好ましい。The above-mentioned pulverizer may be one that can perform fine pulverization using a dry or semi-dry method, such as a micron mill, a jet stream pulverizer, a ball mill, a micronizer, a turbo mill, an atomizer, etc. Micronizer type in terms of grinding efficiency, grinding time, and workability.
Jet-flow type mills such as reductionizer type, impact type, opposing type, and fluidized bed type are preferred, and among them, fluidized bed type jet mills are particularly preferred because surface treatment can be performed more uniformly.
このようなタルクを用いることにより、得られる成形品
の外観(フローマーク、ウェルトライン)が改善される
ほか、耐衝撃性も大巾に向トする。本発明における各成
分の配合割合はa)〜C)成分の合計量100重量%に
対しa)が65〜55ffi量%、b)が30〜35重
量%、C)が5〜IO重量%である。By using such talc, not only the appearance (flow marks, welt lines) of the resulting molded product is improved, but also the impact resistance is greatly improved. The blending ratio of each component in the present invention is 65 to 55% by weight of a), 30 to 35% by weight of b), and 5 to IO% by weight of C) based on 100% by weight of the total amount of components a) to C). be.
a)が65重量%を越えた場合、耐衝撃性、塗膜剥離強
度が低下し、55重量%未満の場合剛性が低下し好まし
くない。If a) exceeds 65% by weight, impact resistance and coating peel strength will decrease, and if it is less than 55% by weight, rigidity will decrease, which is not preferable.
b)が30重量%未満の場合、耐衝撃性、塗膜剥離強度
が低下し、35重量%を越えた場合、剛性が低く、製品
外観も低下(凹み、フローマーク、ウェルドライン)す
るため好ましくない。If b) is less than 30% by weight, the impact resistance and coating peel strength will decrease, and if it exceeds 35% by weight, the rigidity will be low and the product appearance will deteriorate (dents, flow marks, weld lines), so it is preferable. do not have.
C)が5重量%未満の場合、剛性が低く、10重量%を
越えた場合、耐衝撃性が低下し、製品外観(フローマー
ク、ウェルドライン)も低下するためいずれの場合も好
ましくない。When C) is less than 5% by weight, the rigidity is low, and when it exceeds 10% by weight, impact resistance and product appearance (flow marks, weld lines) are also deteriorated, so both cases are unfavorable.
本発明においては、酸化防止剤、滑剤、紫外線吸収剤、
紫外線安定剤、熱安定剤、帯電防止剤、有機もしくは無
機顔料等の各種添加剤を単独あるいは組合わせて添加し
ても良い。これら各種添加剤の例としては、ポリオレフ
ィン樹脂に通常添加されるものを挙げることができ、本
発明の効果を著しく損なわない範囲で用いればよい。ま
た必要に応じて本発明で用いるポリプロピレン樹脂以外
の樹脂(例えばポリエチレン)およびタルク以外の無機
フィラーを本発明の効果を著しく損なわない範囲であれ
ば併用することもできる。In the present invention, antioxidants, lubricants, ultraviolet absorbers,
Various additives such as ultraviolet stabilizers, heat stabilizers, antistatic agents, and organic or inorganic pigments may be added alone or in combination. Examples of these various additives include those commonly added to polyolefin resins, and they may be used within a range that does not significantly impair the effects of the present invention. Further, if necessary, resins other than the polypropylene resin used in the present invention (for example, polyethylene) and inorganic fillers other than talc may be used in combination as long as they do not significantly impair the effects of the present invention.
本発明の樹脂組成物は、通常は各成分をあらかじめヘン
シェルミキサー等の混合機で予備混合後、1軸あるいは
2軸押比機等で溶融混練してベレット化することにより
得られ、該ベレットを用いて押出成形、射出成形、回転
成形、圧縮成形等の成形方法により製品に成形しつる。The resin composition of the present invention is usually obtained by premixing each component in a mixer such as a Henschel mixer, and then melt-kneading it into pellets using a single-screw or twin-screw presser. The material is then molded into a product using extrusion molding, injection molding, rotational molding, compression molding, or other molding methods.
以下実施例により本発明を具体的に説明する。 The present invention will be specifically explained below using Examples.
以下の記載においてMlはA S T M D −1
238、曲げ弾性率はASTM D−790、アイゾ
ツト衝撃値はA S T M D −256に従って
測定した。実施例および比較例において使用した各成分
は以下の通りである。In the following description, Ml is ASTMD-1
238, flexural modulus was measured according to ASTM D-790, and Izod impact value was measured according to ASTM D-256. The components used in the Examples and Comparative Examples are as follows.
タルク−A
平均粒を径約10pの通常の粒度分布を有するタルク1
0(1重量部と、ジメチルポリシロキシラザン1.0重
量部を西独アルビネ社製の流動層式カウンタージェット
ミル”400A F G型”粉砕機に別々に供給し、下
記条件で粉砕表面処理を行なった。Talc-A Talc 1 having a normal particle size distribution with an average particle size of about 10p
0 (1 part by weight) and 1.0 part by weight of dimethylpolysiloxylazan were separately supplied to a fluidized bed counterjet mill "400A F G type" pulverizer manufactured by Albine, West Germany, and subjected to pulverization surface treatment under the following conditions. Ta.
処理条件 風量 1B20tn3/Hr粉砕圧
6kg/crn”
(圧縮空気使用)
分級機回転数 4000rpm
タルク−B
タルク−Aにおけるジメチルポリシロキシシラザンの代
わりにr−アミノプロピルトリエトキシシランを用いた
もの。Processing conditions Air flow rate 1B20tn3/Hr Grinding pressure 6kg/crn'' (compressed air used) Classifier rotation speed 4000rpm Talc-B Talc-A using r-aminopropyltriethoxysilane instead of dimethylpolysiloxysilazane.
タルク−C 表面処理剤を用いずに粉砕のみ行なフたもの。Talc-C A type that only performs pulverization without using a surface treatment agent.
タルク−D
タルク−C100重量部とジメチルポリシロキシシラザ
ン1.0重量部とをヘンシェルミキサー中で混合したも
の。Talc-D 100 parts by weight of Talc-C and 1.0 parts by weight of dimethylpolysiloxysilazane were mixed in a Henschel mixer.
実施例1〜4
前述の成分a)〜C)を表−4で示す割合にて配合し、
それの100重量部に対し、2,6−シーLert−ブ
チル−4−メチルフェノール0.05重量部、ステアリ
ン酸カルシウム0.1重量部、およびテトラキス〔メチ
レン−3−(3,5−ジーtert、−ブチルー4−ヒ
ドロキシフェニル)プロピオネート]メタン0.1重量
部を加えてヘンシェルミキサーで混合した後、40mm
φ1軸押出機全押出、210℃でペレット化を行なった
。得られたベレットを射出成形機を用い210℃で所定
の試験片に成形し各々の物性を測定した。結果を表−4
に示す。Examples 1 to 4 The aforementioned components a) to C) were blended in the proportions shown in Table 4,
To 100 parts by weight of the same, 0.05 part by weight of 2,6-C-Lert-butyl-4-methylphenol, 0.1 part by weight of calcium stearate, and 0.1 part by weight of 2,6-C-Lert-butyl-4-methylphenol, -Butyl-4-hydroxyphenyl)propionate] After adding 0.1 part by weight of methane and mixing with a Henschel mixer, 40 mm
Complete extrusion was performed using a φ single-screw extruder, and pelletization was performed at 210°C. The obtained pellets were molded into predetermined test pieces at 210° C. using an injection molding machine, and the physical properties of each test piece were measured. Table 4 shows the results.
Shown below.
ウェルドラインの評価は次の方法により行なった。The weld line was evaluated by the following method.
前記のペレットを100トンの射出成形機によって成形
温度210℃、射出圧力800kg / crn’、金
型温度50℃の条件において射出成形し、80X240
X3mmの平板状の試験片を成形した。この試験片は
80mmの一辺にあるゲート部から80mmでかつ、2
40mmの辺から40m+nの距離にある点を中心とす
る直径201mの穴を有する。この穴から長手方向に発
生するウェルドラインを目視により、下記の判定基準に
より評価した。The above pellets were injection molded using a 100 ton injection molding machine under conditions of a molding temperature of 210°C, an injection pressure of 800 kg/crn', and a mold temperature of 50°C.
A flat test piece with a size of 3 mm was molded. This test piece is 80 mm from the gate part on one side of 80 mm and 2
It has a hole with a diameter of 201 m centered at a point located at a distance of 40 m+n from a 40 mm side. The weld line generated in the longitudinal direction from this hole was visually observed and evaluated according to the following criteria.
○:ニラエルドライン実質的に認められない。○: Niraeld line is not substantially observed.
△:ニラエルドラインやや認められる。△: Niraeld line is slightly observed.
×:ウェルドラインがかなり認められる。×: Weld lines are considerably observed.
塗装性の評価は次の塗装方法により得られた試験片を用
いて剥離強度および耐温水性の測定を行なった。Paintability was evaluated by measuring peel strength and hot water resistance using test pieces obtained by the following painting method.
塗装方法
射出成形機を用いて得たaox 160 X 2mmの
平板を試験片とし、これをトリクロルエタン蒸気により
60秒間洗浄を行ない次いで2液型のアクリル−塩素化
ポリプロピレン系の下塗り塗料を膜厚15μとなるよう
に塗装し90℃で30分乾燥した後、ざらに2液型のウ
レタン系の上塗り塗料を膜厚約100−となるように塗
装し、90℃で40分乾燥し、さらに室温で48時間放
置して塗装性試験片を得た。Coating method: A flat plate of AOX 160 x 2 mm obtained using an injection molding machine was used as a test piece. It was washed with trichloroethane vapor for 60 seconds, and then a two-component acrylic-chlorinated polypropylene base coat was applied to a film thickness of 15 μm. After drying at 90°C for 30 minutes, apply a two-component urethane top coat to a film thickness of approximately 100°C, dry at 90°C for 40 minutes, and then leave at room temperature. A paintability test piece was obtained after being left for 48 hours.
剥離強度
上記方法にて得た試験片にカッターナイフにより巾1.
Ocmの切り込みを入れ、インストロン引張試験機にて
30mm/minの速度で引っ張り、塗膜の180°剥
離強度を測定した。Peel strength The test piece obtained by the above method was peeled with a cutter knife to a width of 1.
A cut of 0 cm was made and the film was pulled at a speed of 30 mm/min using an Instron tensile tester to measure the 180° peel strength of the coating film.
耐温水性
上記方法にて得た試験片を40℃の温水中に240時間
浸した後、塗膜面の状態を観察した。Hot Water Resistance The test piece obtained by the above method was immersed in hot water at 40°C for 240 hours, and then the state of the coating surface was observed.
○:塗膜のふくれ等全くなし。○: No blistering of the coating film.
△:塗膜のふくれややあり。△: There is some blistering in the coating film.
×:塗膜のふくれかなりあり。×: There was considerable blistering of the coating film.
比較例1〜II
成分a)〜C)の種類と配合量を表−4に示す割合とし
、実施例−1と同様に試験した。得られた結果を同表に
示す。Comparative Examples 1 to II Components a) to C) were tested in the same manner as in Example 1 using the types and blending amounts shown in Table 4. The obtained results are shown in the same table.
本発明によるポリプロピレン樹脂組成物は、剛−性、耐
衝掌性が高く物性バランスが良好で、成形性、塗装性、
製品外観に優れることより、自動車のバンパー、サイド
モール等の大型外装部品に適する。The polypropylene resin composition according to the present invention has high rigidity and impact resistance, has a good balance of physical properties, and has good moldability, paintability,
Due to its excellent product appearance, it is suitable for large exterior parts such as automobile bumpers and side moldings.
特許出願人 三井東圧化学株式会社 本田技研工業株式会社Patent applicant: Mitsui Toatsu Chemical Co., Ltd. Honda motor industry stock company
Claims (1)
a)〜c)の合計量を100重量%として、a)が65
〜55重量%、b)が30〜35重量%およびc)が5
〜10重量%であることを特徴とするバンパー用ポリプ
ロピレン樹脂組成物。 a)エチレン含有量4〜8重量%、沸騰n−ヘプタン不
溶分85重量%以上、メルトフローインデックス(MI
)10〜15g/10minの結晶性エチレン・プロピ
レンブロック共重合 体。 b)プロピレン含有量45〜60重量%、ムーニー粘度
(ML^1^0^0^℃_1_+_4)が20〜50で
あるエチレン・プロピレン共重合体ゴムおよび/または
同様のプロピレン含有量、ムーニー粘度を有 し、かつ第3成分がジンクロペンタジエン、エチリデン
ノルボルネンまたは1,4−ヘキサジエンであるエチレ
ン・プロピレン・ジエン3元共重合体ゴム。 c)乾式ないし半乾式の粉砕機中で、シラン系有機化合
物により表面処理されたタルク。 2、前記粉砕機がジェット気流式粉砕機である特許請求
の範囲第1項記載の樹脂組成物。 3、前記ジェット気流式粉砕機が流動層式ジェット粉砕
機である特許請求の範囲第2項記載の樹脂組成物。[Scope of Claims] 1. Consisting of the following components a) to c), where the blending ratio of each component is 65% by weight, assuming that the total amount of a) to c) is 100% by weight.
~55 wt%, b) 30-35 wt% and c) 5
A polypropylene resin composition for a bumper, characterized in that the content thereof is 10% by weight. a) Ethylene content 4-8% by weight, boiling n-heptane insoluble content 85% by weight or more, melt flow index (MI
) 10-15 g/10 min of crystalline ethylene/propylene block copolymer. b) Ethylene-propylene copolymer rubber with a propylene content of 45 to 60% by weight and a Mooney viscosity (ML^1^0^0^℃_1_+_4) of 20 to 50 and/or a similar propylene content and a Mooney viscosity of ethylene-propylene-diene terpolymer rubber, wherein the third component is zinclopentadiene, ethylidenenorbornene or 1,4-hexadiene. c) Talc surface-treated with a silane-based organic compound in a dry or semi-dry grinder. 2. The resin composition according to claim 1, wherein the pulverizer is a jet stream type pulverizer. 3. The resin composition according to claim 2, wherein the jet stream type pulverizer is a fluidized bed type jet pulverizer.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP178587A JPS63172758A (en) | 1987-01-09 | 1987-01-09 | Polypropylene resin composition for bumper |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP178587A JPS63172758A (en) | 1987-01-09 | 1987-01-09 | Polypropylene resin composition for bumper |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63172758A true JPS63172758A (en) | 1988-07-16 |
JPH0588865B2 JPH0588865B2 (en) | 1993-12-24 |
Family
ID=11511228
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP178587A Granted JPS63172758A (en) | 1987-01-09 | 1987-01-09 | Polypropylene resin composition for bumper |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63172758A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4960823A (en) * | 1989-02-13 | 1990-10-02 | Tonen Sekiyukagaku Kabushiki Kaisha | Resin composition for bumpers |
-
1987
- 1987-01-09 JP JP178587A patent/JPS63172758A/en active Granted
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4960823A (en) * | 1989-02-13 | 1990-10-02 | Tonen Sekiyukagaku Kabushiki Kaisha | Resin composition for bumpers |
Also Published As
Publication number | Publication date |
---|---|
JPH0588865B2 (en) | 1993-12-24 |
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