JPS5971353A - thermoplastic resin composition - Google Patents
thermoplastic resin compositionInfo
- Publication number
- JPS5971353A JPS5971353A JP18166782A JP18166782A JPS5971353A JP S5971353 A JPS5971353 A JP S5971353A JP 18166782 A JP18166782 A JP 18166782A JP 18166782 A JP18166782 A JP 18166782A JP S5971353 A JPS5971353 A JP S5971353A
- Authority
- JP
- Japan
- Prior art keywords
- methylstyrene
- vinyl chloride
- resistance
- vinyl
- alpha
- 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
- 239000011342 resin composition Substances 0.000 title claims abstract description 6
- 229920005992 thermoplastic resin Polymers 0.000 title claims abstract 3
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims abstract description 17
- 229920001577 copolymer Polymers 0.000 claims abstract description 15
- 229920005989 resin Polymers 0.000 claims abstract description 13
- 239000011347 resin Substances 0.000 claims abstract description 13
- 239000004609 Impact Modifier Substances 0.000 claims abstract description 8
- 229920001971 elastomer Polymers 0.000 claims abstract description 7
- 239000000203 mixture Substances 0.000 abstract description 10
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 abstract description 7
- 229920002943 EPDM rubber Polymers 0.000 abstract description 7
- -1 aromatic vinyl compound Chemical class 0.000 abstract description 6
- 229920002554 vinyl polymer Polymers 0.000 abstract description 6
- 238000006116 polymerization reaction Methods 0.000 abstract description 5
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 abstract description 4
- 238000002156 mixing Methods 0.000 abstract description 4
- 125000005397 methacrylic acid ester group Chemical group 0.000 abstract description 3
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 abstract 1
- 238000010559 graft polymerization reaction Methods 0.000 abstract 1
- 238000000034 method Methods 0.000 description 5
- 238000004898 kneading Methods 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 3
- ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical class C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- 150000001993 dienes Chemical class 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 229920000578 graft copolymer Polymers 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- PRBHEGAFLDMLAL-GQCTYLIASA-N (4e)-hexa-1,4-diene Chemical compound C\C=C\CC=C PRBHEGAFLDMLAL-GQCTYLIASA-N 0.000 description 1
- XHAFIUUYXQFJEW-UHFFFAOYSA-N 1-chloroethenylbenzene Chemical compound ClC(=C)C1=CC=CC=C1 XHAFIUUYXQFJEW-UHFFFAOYSA-N 0.000 description 1
- 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 description 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- BTOVVHWKPVSLBI-UHFFFAOYSA-N 2-methylprop-1-enylbenzene Chemical compound CC(C)=CC1=CC=CC=C1 BTOVVHWKPVSLBI-UHFFFAOYSA-N 0.000 description 1
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 1
- NWNPESVXYXCGLH-UHFFFAOYSA-N 4-ethenylbicyclo[2.2.1]hept-2-ene Chemical compound C1CC2C=CC1(C=C)C2 NWNPESVXYXCGLH-UHFFFAOYSA-N 0.000 description 1
- WTQBISBWKRKLIJ-UHFFFAOYSA-N 5-methylidenebicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(=C)CC1C=C2 WTQBISBWKRKLIJ-UHFFFAOYSA-N 0.000 description 1
- 239000004709 Chlorinated polyethylene Substances 0.000 description 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 229920000800 acrylic rubber Polymers 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は耐衝撃性、耐熱変形性、耐候性に優れた塩化ビ
ニル系樹脂組成物に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a vinyl chloride resin composition that has excellent impact resistance, heat deformation resistance, and weather resistance.
塩化ビニル系樹脂は、耐候性、耐薬品性、難燃性などの
優れた性質を有する反面、耐衝撃性、耐熱変形性などに
欠点を持っている。こうした欠点を改良するため、従来
種々の提案がなされており、例えば耐衝撃性を改良する
代表的な方法としては、ABS樹脂あるいはMBS樹脂
をブレンドする方法等があるが、耐候性に大きな欠点が
ある。Although vinyl chloride resins have excellent properties such as weather resistance, chemical resistance, and flame retardancy, they have drawbacks such as impact resistance and heat deformation resistance. In order to improve these drawbacks, various proposals have been made in the past. For example, a typical method to improve impact resistance is to blend ABS resin or MBS resin, but this method has a major drawback in weather resistance. be.
一方、耐候性を考慮して、塩素化ポリエチレン、エチレ
ン・酢酸ビニル共重合体に塩化ビニルをグラフト重合せ
しめたグラフト共重合体、アクリルゴム、エチレン−プ
ロピレン−非共役ジエン共重合ゴム(以下、EPDMと
いう)系等の耐衝撃改良剤をブレンドする方法があるが
、耐衝撃性、耐候性で満足するものは得られるけれども
、耐熱変形性が低下する。On the other hand, in consideration of weather resistance, chlorinated polyethylene, graft copolymer obtained by grafting vinyl chloride onto ethylene/vinyl acetate copolymer, acrylic rubber, ethylene-propylene-nonconjugated diene copolymer rubber (hereinafter referred to as EPDM) There is a method of blending impact modifiers such as those of the above-mentioned type, but although satisfactory impact resistance and weather resistance can be obtained, the heat deformation resistance decreases.
一般に塩化ビニル系樹脂の耐候性を損なわずに、耐衝撃
性を改良し、同時に耐熱変形性を大巾に向上させるポリ
マーブレンド系は知られていない。In general, there is no known polymer blend system that improves the impact resistance and at the same time greatly improves the heat deformation resistance of vinyl chloride resins without impairing their weather resistance.
本発明者等は鋭意検討した結果、塩化ビニル系樹脂と、
EPDM系耐衝撃改良剤と、α−メチルスチレン−アク
リロニトリル共重合体との三元混合系にすることにより
、耐衝撃性、耐候性、耐熱変形性に優れた樹脂組成物が
得られることを見出した。As a result of intensive study, the present inventors found that vinyl chloride resin and
It has been discovered that a resin composition with excellent impact resistance, weather resistance, and heat deformation resistance can be obtained by creating a ternary mixture system of an EPDM-based impact modifier and an α-methylstyrene-acrylonitrile copolymer. Ta.
即ち、本発明の組成物は55ないし90重量部の塩化ビ
ニル系樹脂と、5ないし40重量部のEP6M系耐衝撃
改良剤と、5ないし40重掻部ノα−メチルスチレンー
アクリロニトリル共重合体とから成り、該組成物を混合
、混線、成形することによって耐衝撃性、耐候性、耐熱
変形性の良好な成形体が得られる。That is, the composition of the present invention comprises 55 to 90 parts by weight of a vinyl chloride resin, 5 to 40 parts by weight of an EP6M impact modifier, and 5 to 40 parts by weight of α-methylstyrene-acrylonitrile copolymer. By mixing, cross-wiring, and molding the composition, a molded article with good impact resistance, weather resistance, and heat deformation resistance can be obtained.
さらに本発明の組成物は、耐薬品性、難燃性にも優れ、
かつ真空成形性、射出成形性、押出成形性等の成形性等
に於いても優れているという特徴を有する。Furthermore, the composition of the present invention has excellent chemical resistance and flame retardancy,
Moreover, it is characterized by excellent moldability such as vacuum moldability, injection moldability, and extrusion moldability.
本発明に用いられる塩化ビニル系樹脂は、塩化ビニル単
独重合体のばか塩化ビニルを少(とも75重ta%以上
含む共重合体であっても差支えない。The vinyl chloride resin used in the present invention may be a copolymer of vinyl chloride homopolymer containing a small amount of vinyl chloride (at least 75% by weight and ta).
また塩化ビニル系樹脂の平均重合度は成形法によっても
異なるが400ないし2,000程度のものが一般に用
いられる。Furthermore, the average degree of polymerization of the vinyl chloride resin varies depending on the molding method, but is generally used to have an average degree of polymerization of about 400 to 2,000.
EPDM系耐衝撃改良剤は、EPDMに芳香属ビニル、
シアン化ビニル、並びにメタアクリル酸エステル等の化
合物をグラフト重合してなるグラフト共重合体である。EPDM-based impact modifiers include EPDM, aromatic vinyl,
It is a graft copolymer obtained by graft polymerizing compounds such as vinyl cyanide and methacrylic acid ester.
なお、芳香属ビニル、シアン化ビニル、メタアクリル酸
エステルの代りに塩化ビニル、塩化ビニリデン等を用い
てもよい。Note that vinyl chloride, vinylidene chloride, etc. may be used instead of aromatic vinyl, vinyl cyanide, and methacrylic acid ester.
EPDMは、エチレン、プロピレン−非共役ジエンの共
重合ゴムであって、非共役ジエン成分として、5−メチ
レン−2−ノルボルネン、5エチリテン−2−ノルボル
ネン、5−インプロピリデン−2−ノルボルネン、5−
ビニル−2−ノルボルネン等のノルボルネン類、シクロ
ペンタジェン、ジシクロペンタジェン等のシクロペンタ
ジェン類、1.4−へキサジエン等の鎖状ジエン類のも
のが用いられる。芳香属ビニル化合物としては、スチレ
ン、α−メチルスチレン、α−クロルスチレン、ジメチ
ルスチレン等を用いることが出来る。EPDM is a copolymer rubber of ethylene, propylene-non-conjugated diene, and contains 5-methylene-2-norbornene, 5-ethythelene-2-norbornene, 5-impropylidene-2-norbornene, 5-impropylidene-2-norbornene, and 5-impropylidene-2-norbornene. −
Norbornenes such as vinyl-2-norbornene, cyclopentadienes such as cyclopentadiene and dicyclopentadiene, and chain dienes such as 1,4-hexadiene are used. As the aromatic vinyl compound, styrene, α-methylstyrene, α-chlorostyrene, dimethylstyrene, etc. can be used.
シアン化ビニル化合物としては、アクリロニトリル、メ
タアクリロニトリル等が用いられる。As the vinyl cyanide compound, acrylonitrile, methacrylonitrile, etc. are used.
メタアクリル酸エステル化合物としては、アルキル基の
炭素数が1〜8個のメタアクリル酸アルキルエステル等
があげられる。Examples of the methacrylic acid ester compound include methacrylic acid alkyl esters in which the alkyl group has 1 to 8 carbon atoms.
これらビニル化合物とゴムとの重合比は、その目的に応
じて適当な範囲を選ぶことが出来るが通常ビニル化合物
95重i%に対しゴム分5〜60重量%が用いられる。The polymerization ratio of these vinyl compounds and rubber can be selected within an appropriate range depending on the purpose, but usually a rubber content of 5 to 60% by weight is used based on 95% by weight of the vinyl compound.
σ−メチルスチレンーアクリロニトリル共重合体は90
ないし60重量%のび一メチルスチレンと10ないし、
4o重fi−%のアクリロニトリルからなる共重合体が
用いられる。σ-methylstyrene-acrylonitrile copolymer is 90
10 to 60% by weight of methyl styrene;
A copolymer of 40% acrylonitrile is used.
本発明の組成物の成形加工にあたっては、塩化ビニル系
樹脂の加工に通常用いられている公知の安定剤、滑剤、
紫外線吸収剤、酸化防止剤等を適宜添加し、また必要に
応じて充填材の使用も可能である。In molding the composition of the present invention, known stabilizers and lubricants commonly used in processing vinyl chloride resins,
Ultraviolet absorbers, antioxidants, etc. can be added as appropriate, and fillers can also be used if necessary.
該組成物の物性を十分に発揮さすためには、できるだけ
均一に混練することが望ましく、混練方法としてはロー
ル混線、バンバリー混練、押出機混練等周知の方法がと
られ、粉末から直接押出成形することも可能である。In order to fully exhibit the physical properties of the composition, it is desirable to knead it as uniformly as possible, and kneading methods include well-known methods such as roll kneading, Banbury kneading, and extruder kneading, and direct extrusion molding from powder. It is also possible.
以下に実施例により本発明をさらに具体的に説明するが
本発明はこれらに限定されるものではない。The present invention will be explained in more detail with reference to Examples below, but the present invention is not limited thereto.
実施例1
平均重合度1.100のポリ塩化ビニル(住友化学工業
製 スミリット■5x−11)とEPDM/アクリロニ
トリル/スチレン共重合体(ゴム含M52%)トゲ−メ
チルスチレン/アクリロニトリル共重合体(単量体比7
o:30)とを第1表の割合で配合し、鉛系安定剤5重
最部、TlO23重量部を添加し、200°Cの2本ロ
ールで7分間混練した後、205℃で10分間圧縮成形
して物性試験用シートを得た。Example 1 Polyvinyl chloride with an average degree of polymerization of 1.100 (Sumitomo Chemical Co., Ltd., Sumilit ■5x-11), EPDM/acrylonitrile/styrene copolymer (rubber content M52%), thorn-methylstyrene/acrylonitrile copolymer (synthetic Mass ratio 7
o: 30) in the proportions shown in Table 1, add the 5-layer lead stabilizer and 23 parts by weight of TlO, knead for 7 minutes with two rolls at 200°C, and then knead at 205°C for 10 minutes. Compression molding was performed to obtain a sheet for physical property testing.
第1表から明らかなように、本発明の組成物は、塩化ビ
ニル樹脂、および塩化ビニル樹脂と衝撃改良剤との2成
分混合に比べ、衝撃強度、耐熱変形性、高温時の伸び特
性を大巾に向上させている。As is clear from Table 1, the composition of the present invention has greater impact strength, heat deformation resistance, and elongation properties at high temperatures than a vinyl chloride resin or a two-component mixture of a vinyl chloride resin and an impact modifier. It has improved significantly.
実施例2
実施例1で用いた組成物について耐候劣化後のシャルピ
ー衝撃強度を測定した結果を第2表に示す。Example 2 Table 2 shows the results of measuring the Charpy impact strength of the composition used in Example 1 after weathering.
Claims (1)
部の塩化ビニル系樹脂と(b)5ないし40重量部のエ
チレン−プロピレン−非共役ジエン共重合ゴム系面子衝
撃改良剤と(C)5ないし40重量部のα−メチルスチ
レン−アクリロニトリル共重合体とより成る熱可塑性樹
脂組成物。100 parts by weight of the resin composition contains (a) 55 to 90 parts by weight of a vinyl chloride resin, (b) 5 to 40 parts by weight of an ethylene-propylene-nonconjugated diene copolymer rubber-based face impact modifier, and (C) A thermoplastic resin composition comprising 5 to 40 parts by weight of an α-methylstyrene-acrylonitrile copolymer.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57181667A JPH062857B2 (en) | 1982-10-15 | 1982-10-15 | Thermoplastic resin composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57181667A JPH062857B2 (en) | 1982-10-15 | 1982-10-15 | Thermoplastic resin composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5971353A true JPS5971353A (en) | 1984-04-23 |
JPH062857B2 JPH062857B2 (en) | 1994-01-12 |
Family
ID=16104756
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP57181667A Expired - Lifetime JPH062857B2 (en) | 1982-10-15 | 1982-10-15 | Thermoplastic resin composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH062857B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62167347A (en) * | 1986-01-18 | 1987-07-23 | Sumitomo Naugatuck Co Ltd | Inpact-resistance weather-resistant resin composition having low orientation |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5371146A (en) * | 1976-12-06 | 1978-06-24 | Nippon Zeon Co Ltd | Mat thermoplastic resin composition |
JPS5753546A (en) * | 1980-08-08 | 1982-03-30 | Stamicarbon | Polymer composition |
-
1982
- 1982-10-15 JP JP57181667A patent/JPH062857B2/en not_active Expired - Lifetime
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5371146A (en) * | 1976-12-06 | 1978-06-24 | Nippon Zeon Co Ltd | Mat thermoplastic resin composition |
JPS5753546A (en) * | 1980-08-08 | 1982-03-30 | Stamicarbon | Polymer composition |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62167347A (en) * | 1986-01-18 | 1987-07-23 | Sumitomo Naugatuck Co Ltd | Inpact-resistance weather-resistant resin composition having low orientation |
Also Published As
Publication number | Publication date |
---|---|
JPH062857B2 (en) | 1994-01-12 |
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