JPH023424B2 - - Google Patents
Info
- Publication number
- JPH023424B2 JPH023424B2 JP57040390A JP4039082A JPH023424B2 JP H023424 B2 JPH023424 B2 JP H023424B2 JP 57040390 A JP57040390 A JP 57040390A JP 4039082 A JP4039082 A JP 4039082A JP H023424 B2 JPH023424 B2 JP H023424B2
- Authority
- JP
- Japan
- Prior art keywords
- weight
- component
- parts
- propylene polymer
- carbon atoms
- 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.)
- Expired - Lifetime
Links
- 150000001875 compounds Chemical class 0.000 claims description 11
- 229920001155 polypropylene Polymers 0.000 claims description 10
- 125000004432 carbon atom Chemical group C* 0.000 claims description 7
- 239000000203 mixture Substances 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 229910052751 metal Inorganic materials 0.000 claims description 5
- 239000002184 metal Substances 0.000 claims description 5
- 150000003839 salts Chemical class 0.000 claims description 5
- 125000003545 alkoxy group Chemical group 0.000 claims description 4
- 125000005233 alkylalcohol group Chemical group 0.000 claims description 4
- 229910052736 halogen Inorganic materials 0.000 claims description 4
- 150000002367 halogens Chemical class 0.000 claims description 4
- 238000002347 injection Methods 0.000 claims description 4
- 239000007924 injection Substances 0.000 claims description 4
- UKGRTCZMPQERFQ-UHFFFAOYSA-N octadecyl 2-hydroxypropanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C(C)O UKGRTCZMPQERFQ-UHFFFAOYSA-N 0.000 claims description 4
- 239000000155 melt Substances 0.000 claims description 3
- 238000002156 mixing Methods 0.000 claims description 2
- -1 polypropylene Polymers 0.000 description 10
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000000600 sorbitol Substances 0.000 description 5
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 4
- 239000008188 pellet Substances 0.000 description 4
- 239000003963 antioxidant agent Substances 0.000 description 3
- 230000000740 bleeding effect Effects 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 239000002667 nucleating agent Substances 0.000 description 3
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- HUTIVPWAVQGKQA-UHFFFAOYSA-N calcium;octadecyl 2-hydroxypropanoate Chemical compound [Ca].CCCCCCCCCCCCCCCCCCOC(=O)C(C)O HUTIVPWAVQGKQA-UHFFFAOYSA-N 0.000 description 2
- 229940087101 dibenzylidene sorbitol Drugs 0.000 description 2
- 238000001746 injection moulding Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- LQAFKEDMOAMGAK-RLCYQCIGSA-N (1r)-1-[(4r,4ar,8as)-2,6-bis(4-methylphenyl)-4,4a,8,8a-tetrahydro-[1,3]dioxino[5,4-d][1,3]dioxin-4-yl]ethane-1,2-diol Chemical compound C1=CC(C)=CC=C1C1O[C@H]2[C@@H]([C@H](O)CO)OC(C=3C=CC(C)=CC=3)O[C@H]2CO1 LQAFKEDMOAMGAK-RLCYQCIGSA-N 0.000 description 1
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-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
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 239000008395 clarifying agent Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000003349 gelling agent Substances 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910001463 metal phosphate Inorganic materials 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 229920001384 propylene homopolymer Polymers 0.000 description 1
- 229920005604 random copolymer Polymers 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Description
【発明の詳細な説明】
本発明は、高度に透明性の改良されたプロピレ
ン重合体組成物射出成形品に関する。
アイソタクチツクポリプロピレンは、実用性能
が優れる為に広い分野で簡便に利用されている
が、結晶性であるため、透明性が不良となつて商
品価値を損ねる場合がある。
この欠点を改善するのに、従来より種々の核剤
を添加する方法が試みられている。核剤として
は、例えば芳香族カルボン酸のアルミニウム塩、
芳香族カルボン酸、芳香族リン酸金属塩、多価ア
ルコールとアルデヒドとの縮合物などが知られて
いる。
特に、1,3,2,4―ジベンジリデンソルビ
トールは比較的効果が大きいが、未だ最近の高度
な要求を満足するレベルに到達していない。
また、1,3,2,4―ジベンジリデンソルビ
トールよりも透明性の改良効果が大きい核剤とし
てジ―置換ベンジリデンソルビトールがあるが
(特公昭55―12460、特開昭56―30449、同56―
30450、同56―45934各号公報参照)、このものは
高価である上、多く用いるとブリードの問題を生
じてくるので、極力少量の添加で透明性の改良を
果たす技術の確立は是非必要な課題である。
本発明は、この課題に解決を与えることを目的
としたものであり、プロピレン重合体に、特定の
ジ―置換ベンジリデンソルビトールと特定の化合
物を併用配合することにより意外にも高度に透明
性が改良された射出成形品が得られることが判明
して為されたものである。
すなわち本発明は、下記の(A)〜(C)成分を配合し
てなることを特徴とするプロピレン重合体組成物
射出成形品である。
(A) メルトフローレートが0.1〜100g/10分のプ
ロピレン重合体100重量部
(B) 次式で表される化合物0.01〜0.5重量部
(式中、Rは炭素数1〜8のアルキル、同アル
コキシ又はハロゲンのいずれかであり、同一化
合物中で異なつていても良い。mおよびnはそ
れぞれ独立に0〜3の整数で、かつm+n≧1
である。)
(C) ステアリル乳酸金属塩および炭素数8〜30の
アルキルアルコールから選ばれる少なくとも1
つの化合物0.01〜1重量%
(式中、R1は炭素数8〜30のアルキル基、k
およびlはそれぞれ独立に0〜10の整数であ
り、k+l≧1である。)
本発明で用いる上記(A)成分であるプロピレン重
合体は、メルトフローレート(MFR)が0.1〜
100g/10分のものであり、結晶性のものにおい
て、本発明の効果が顕著に発揮される。具体的に
は、たとえば、プロピレンの単独重合体のほか、
過半数(好ましくは70重量%以上)のプロピレン
と他のα―オレフイン(例えばエチレン、ブテン
―1、4―メチルペンテン―1、ヘキセン―1
等)とのランダム又はブロツク共重合体が好適で
ある。MFRが上記以外のものは成形不良となつ
て好ましくない。
また、本発明で用いる上記(B)成分であるジ―置
換ベンジリデンソルビトールは、次式で表される
化合物である。
(式中、Rは炭素数1〜8のアルキル、同アルコ
キシ又はハロゲンのいずれかであり、同一化合物
中で異なつていても良い。mおよびnはそれぞれ
独立に0〜3の整数で、かつm+n≧1である。)
具体的には、Rとしてメチル、エチル、n―プ
ロピル、i―プロピル、t―ブチル等のアルキル
又はメトキシ、エトキシ、n―プロポキシ等のア
ルコキシないしは塩素、臭素等のハロゲンが適当
である。
更に、本発明で用いる上記(C)成分であるステア
リル乳酸金属塩としては、ステアリル乳酸カルシ
ウム等がある。また、炭素数8〜30のアルキルア
ルコールとしては、ステアリルアルコール、ラウ
リルアルコール等がある。
上記3成分の配合割合は、(A)成分のプロピレン
重合体100重量部に対して、(B)成分のジ―置換ベ
ンジリデンソルビトールが0.01〜0.5重量部、好
ましくは0.05〜0.3重量部および(C)成分の化合物
が0.01〜1重量部、好ましくは0.01〜0.5重量部、
特に好ましくは、上記のステアリル乳酸金属塩に
ついては0.01〜0.3重量部、また、上記のアルキ
ルアルコールについては、0.05〜0.5重量部であ
る。
(B)成分は高価であり、又量が多ければそれだけ
ブリードが問題となる可能性が高くなるので上記
の如く少ない量で用いるべきである。
しかし、上記の量未満では効果が不満足とな
る。また、(C)成分は上記量超過では着色やブリー
ドの原因となり、上記量未満では効果が低過ぎ
る。
本発明で用いる組成物には、他の成分として、
通常用いられる酸化防止剤、上記(C)成分以外の金
属塩、紫外線吸収剤、滑剤、帯電防止剤、分散
剤、顔料、透明化剤、ゲル化剤、分子量調整剤等
を本発明の効果を著しく損わない範囲で添加する
ことができる。
本発明で用いる組成物は、通常の混練方法で製
造することができる。
すなわち、例えば(A)成分のプロピレン重合体粉
末に(B)成分および(C)成分、更に必要に応じて酸化
防止剤等他の添加剤を配合し、ミキサー等で混合
後、押出機にて熔融混練してペレツトとする。こ
のペレツトを用いて射出成形法により、型物の成
形品にする。もちろん上記のミキサー等で混合し
た粉末物を直接に成形に供しても良い。
また、上記(B)または(C)成分のみを(A)成分に配合
してペレツトとした組成物に、(C)または(B)成分を
付着あるいは添加配合して成形に供する方法によ
つても良い。
実施例
(A)成分としてのプロピレン―エチレンランダム
共重合体(MFR14g/10分、エチレン含量2.5重
量%)100重量部に対し、第1表に示す如く、(B)
成分としてのジ―置換ベンジリデンソルビトール
および(C)成分を酸化防止剤と共に配合し、スーパ
ーミキサーで混合後、30mm径押出機(230℃)で
ペレツトにした。このペレツトを射出成形機
(280℃)で100×100×1各mmのシートに成形し、
JIS―K6714に準拠して、このシートの透明性
(ヘイズ)を評価した。結果を第1表に示す。
表中の名称の化合物は以下のとおりである。
ゲルオールMD:新日本理化社製、1,3,2,
4―ジ(p―メチルベンジリデン)ソルビトー
ル。
LAA:(株)武蔵野化学研究所製のステアリル乳酸
カルシウム。
St―OH:ステアリルアルコール(試薬)。
【表】DETAILED DESCRIPTION OF THE INVENTION The present invention relates to highly transparent propylene polymer composition injection molded articles. Isotactic polypropylene is conveniently used in a wide range of fields because of its excellent practical performance, but because it is crystalline, its transparency may be poor and its commercial value may be impaired. In order to improve this drawback, various methods of adding nucleating agents have been tried. Examples of nucleating agents include aluminum salts of aromatic carboxylic acids,
Known examples include aromatic carboxylic acids, aromatic metal phosphates, and condensates of polyhydric alcohols and aldehydes. In particular, 1,3,2,4-dibenzylidene sorbitol is relatively effective, but has not yet reached a level that satisfies recent advanced demands. In addition, di-substituted benzylidene sorbitol is a nucleating agent that has a greater effect on improving transparency than 1,3,2,4-dibenzylidene sorbitol (Japanese Patent Publication No. 55-12460, JP-A No. 56-30449, JP-A No. 56-30449).
30450, Publications Nos. 56-45934), this material is expensive, and if used in large quantities, it may cause bleeding problems, so it is absolutely necessary to establish a technology that improves transparency with the addition of as little amount as possible. This is a challenge. The present invention aims to provide a solution to this problem, and has surprisingly improved transparency by combining a specific di-substituted benzylidene sorbitol and a specific compound with a propylene polymer. This was done after it was discovered that it was possible to obtain injection molded products. That is, the present invention is an injection molded product of a propylene polymer composition, which is characterized by containing the following components (A) to (C). (A) 100 parts by weight of a propylene polymer with a melt flow rate of 0.1 to 100 g/10 minutes (B) 0.01 to 0.5 parts by weight of a compound represented by the following formula (In the formula, R is either alkyl, alkoxy or halogen having 1 to 8 carbon atoms, and may be different in the same compound. m and n are each independently an integer of 0 to 3, and m+n≧1
It is. ) (C) At least one selected from stearyl lactate metal salt and alkyl alcohol having 8 to 30 carbon atoms.
0.01-1% by weight of one compound (In the formula, R 1 is an alkyl group having 8 to 30 carbon atoms, k
and l are each independently an integer of 0 to 10, and k+l≧1. ) The propylene polymer that is the component (A) used in the present invention has a melt flow rate (MFR) of 0.1 to
100 g/10 minutes, and the effects of the present invention are significantly exhibited in crystalline products. Specifically, for example, in addition to propylene homopolymers,
The majority (preferably 70% by weight or more) of propylene and other α-olefins (e.g. ethylene, butene-1, 4-methylpentene-1, hexene-1
etc.) are suitable. MFRs other than those listed above are undesirable as they result in poor molding. Further, the di-substituted benzylidene sorbitol, which is the component (B) used in the present invention, is a compound represented by the following formula. (In the formula, R is either alkyl, alkoxy or halogen having 1 to 8 carbon atoms, and may be different in the same compound. m and n are each independently an integer of 0 to 3, and (m+n≧1.) Specifically, R is alkyl such as methyl, ethyl, n-propyl, i-propyl, t-butyl, alkoxy such as methoxy, ethoxy, n-propoxy, or halogen such as chlorine or bromine. is appropriate. Furthermore, examples of the stearyl lactate metal salt used in the present invention as the component (C) include calcium stearyl lactate and the like. Further, examples of the alkyl alcohol having 8 to 30 carbon atoms include stearyl alcohol and lauryl alcohol. The blending ratio of the above three components is 0.01 to 0.5 parts by weight, preferably 0.05 to 0.3 parts by weight, of di-substituted benzylidene sorbitol as component (B) and 100 parts by weight of propylene polymer as component (A), and (C ) component compound is 0.01 to 1 part by weight, preferably 0.01 to 0.5 part by weight,
Particularly preferably, the amount is 0.01 to 0.3 parts by weight for the stearyl lactate metal salt, and 0.05 to 0.5 part by weight for the alkyl alcohol. Component (B) is expensive, and the greater the amount, the greater the possibility that bleeding will become a problem, so it should be used in a small amount as described above. However, if the amount is less than the above, the effect will be unsatisfactory. Furthermore, if component (C) exceeds the above amount, it will cause coloring or bleeding, and if it is less than the above amount, the effect will be too low. The composition used in the present invention includes, as other ingredients,
The effects of the present invention can be achieved by adding commonly used antioxidants, metal salts other than component (C) above, ultraviolet absorbers, lubricants, antistatic agents, dispersants, pigments, clarifying agents, gelling agents, molecular weight regulators, etc. It can be added within a range that does not cause significant damage. The composition used in the present invention can be manufactured by a conventional kneading method. That is, for example, component (A), propylene polymer powder, is blended with component (B) and component (C), as well as other additives such as antioxidants if necessary, mixed in a mixer, etc., and then processed in an extruder. Melt and knead to make pellets. The pellets are molded into molded articles by injection molding. Of course, the powder mixed in the above-mentioned mixer or the like may be directly subjected to molding. In addition, a method in which component (C) or (B) is attached or added to a composition in which only component (B) or (C) above is blended with component (A) to form a pellet, and then subjected to molding. Also good. Example As shown in Table 1, (B) was added to 100 parts by weight of propylene-ethylene random copolymer (MFR 14 g/10 minutes, ethylene content 2.5% by weight) as component (A).
The components di-substituted benzylidene sorbitol and component (C) were blended together with an antioxidant, mixed in a super mixer, and pelletized in a 30 mm diameter extruder (230°C). The pellets were molded into sheets of 100 x 100 x 1 mm each using an injection molding machine (280°C).
The transparency (haze) of this sheet was evaluated in accordance with JIS-K6714. The results are shown in Table 1. The compounds with names in the table are as follows. Gel All MD: manufactured by Shin Nippon Rika Co., Ltd., 1, 3, 2,
4-di(p-methylbenzylidene) sorbitol. LAA: Calcium stearyl lactate manufactured by Musashino Chemical Research Institute. St-OH: Stearyl alcohol (reagent). 【table】
Claims (1)
とするプロピレン重合体組成物射出成形品。 (A) メルトフローレートが0.1〜100g/10分のプ
ロピレン重合体100重量部 (B) 次式で表される化合物0.01〜0.5重量部 (式中、Rは炭素数1〜8のアルキル、同アル
コキシ又はハロゲンのいずれかであり、同一化
合物中で異なつていても良い。mおよびnはそ
れぞれ独立に0〜3の整数で、かつm+n≧1
である。) (C) ステアリル乳酸金属塩および炭素数8〜30の
アルキルアルコールから選ばれる少なくとも1
つの化合物0.01〜1重量%。[Scope of Claims] 1. An injection molded product of a propylene polymer composition, characterized by blending the following components (A) to (C). (A) 100 parts by weight of a propylene polymer with a melt flow rate of 0.1 to 100 g/10 minutes (B) 0.01 to 0.5 parts by weight of a compound represented by the following formula (In the formula, R is either alkyl, alkoxy or halogen having 1 to 8 carbon atoms, and may be different in the same compound. m and n are each independently an integer of 0 to 3, and m+n≧1
It is. ) (C) At least one selected from stearyl lactate metal salt and alkyl alcohol having 8 to 30 carbon atoms.
0.01-1% by weight of one compound.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4039082A JPS58157840A (en) | 1982-03-15 | 1982-03-15 | Molded article of propylene polymer composition by injection |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4039082A JPS58157840A (en) | 1982-03-15 | 1982-03-15 | Molded article of propylene polymer composition by injection |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3174399A Division JPH06874B2 (en) | 1991-06-19 | 1991-06-19 | Propylene polymer composition injection molded product |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS58157840A JPS58157840A (en) | 1983-09-20 |
JPH023424B2 true JPH023424B2 (en) | 1990-01-23 |
Family
ID=12579324
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP4039082A Granted JPS58157840A (en) | 1982-03-15 | 1982-03-15 | Molded article of propylene polymer composition by injection |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS58157840A (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6119646A (en) * | 1984-07-06 | 1986-01-28 | Mitsubishi Petrochem Co Ltd | Polypropylene composition |
JPS62138545A (en) * | 1985-12-11 | 1987-06-22 | Tokuyama Soda Co Ltd | Polypropylene based resin composition |
US4845137A (en) * | 1987-11-05 | 1989-07-04 | Becton, Dickinson And Company | Polyolefin compositions of high clarity and resistance to oxidation |
US5135975A (en) * | 1989-09-20 | 1992-08-04 | Milliken Research Corporation | Bis(3,4-dialkylbenzylidene) sorbitol acetals and compositions containing same |
US5049605A (en) * | 1989-09-20 | 1991-09-17 | Milliken Research Corporation | Bis(3,4-dialkylbenzylidene) sorbitol acetals and compositions containing same |
KR100418564B1 (en) * | 2001-04-30 | 2004-02-14 | 선구케미칼(주) | Nucleating agent containing metaparadimethylbenzylidene paramethylbenzylidene sorbitol and the preparation method thereof |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5630449A (en) * | 1979-08-21 | 1981-03-27 | Mitsui Toatsu Chem Inc | Polypropylene composition |
JPS5665034A (en) * | 1979-11-02 | 1981-06-02 | Musashino Kagaku Kenkyusho:Kk | Stabilized polyolefin composition |
-
1982
- 1982-03-15 JP JP4039082A patent/JPS58157840A/en active Granted
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5630449A (en) * | 1979-08-21 | 1981-03-27 | Mitsui Toatsu Chem Inc | Polypropylene composition |
JPS5665034A (en) * | 1979-11-02 | 1981-06-02 | Musashino Kagaku Kenkyusho:Kk | Stabilized polyolefin composition |
Also Published As
Publication number | Publication date |
---|---|
JPS58157840A (en) | 1983-09-20 |
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