JPS5998152A - Vinyl chloride resin composition - Google Patents
Vinyl chloride resin compositionInfo
- Publication number
- JPS5998152A JPS5998152A JP19658882A JP19658882A JPS5998152A JP S5998152 A JPS5998152 A JP S5998152A JP 19658882 A JP19658882 A JP 19658882A JP 19658882 A JP19658882 A JP 19658882A JP S5998152 A JPS5998152 A JP S5998152A
- Authority
- JP
- Japan
- Prior art keywords
- vinyl chloride
- methyl methacrylate
- weight
- polymer
- parts
- 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
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- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は耐熱変形性および加工性に優れた塩化ビニル系
樹脂組成物に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a vinyl chloride resin composition having excellent heat deformation resistance and processability.
塩化ビニルは従来から安価なうえ、難燃性。Vinyl chloride has traditionally been inexpensive and flame-retardant.
耐薬品性など多くの長所を有する汎用樹脂であるが、同
時に耐衝撃性、加工性、耐熱変形性に劣る欠点を有する
。Although it is a general-purpose resin that has many advantages such as chemical resistance, it also has the disadvantages of poor impact resistance, processability, and heat deformation resistance.
かかる耐衝撃性の改良として、いわゆるMBS樹脂のよ
うな改質剤を添加することが開発された。また加工性の
改質として主に還元粘度が0.3以上なる高分子量のア
クリル系ポリマーを添加することが行われてきた。In order to improve the impact resistance, it has been developed to add a modifier such as a so-called MBS resin. Furthermore, as a modification of processability, addition of a high molecular weight acrylic polymer having a reduced viscosity of 0.3 or more has been carried out.
一方耐熱変形性の改質にFi特公昭45−24867号
公報、特公昭48 18101号公報に示されるように
α−メチルスチレンを共重合させた共重合体が提案され
てきたが加工性の点で未だ問題が残されている。On the other hand, copolymers in which α-methylstyrene is copolymerized have been proposed for improving heat deformation resistance, as shown in Fi Patent Publication No. 45-24867 and Japanese Patent Publication No. 48-18101, but there are problems with processability. There still remains a problem.
また上記加工性改質として用いられる高分子量のアクリ
ル系ポリマーは高分子量であるためその使用量が5重量
部以上では配合組成物の溶融粘度を著しく増大させ、そ
の結果成形機の負荷の増大、ひいては熱安定性の低下を
もたらす欠点を有する。Furthermore, since the high molecular weight acrylic polymer used to modify the processability has a high molecular weight, if the amount used is 5 parts by weight or more, the melt viscosity of the compounded composition will increase significantly, resulting in an increase in the load on the molding machine. Furthermore, it has the disadvantage of decreasing thermal stability.
本発明者らはかかる現状に鑑み塩化ビニル樹脂の特性を
損なわずして、その耐熱変形性および加工性を改質すべ
く鋭意検討の結果本発明に到達した。即ち本発明は少な
くとも80重量%が塩化ビニルから成る塩化ビニル系重
合体の少なくとも一種40〜95重量部と還元粘度が0
.005〜0.2で、かつ少なくとも75重量%がメタ
クリル酸メチルから成るメタクリル酸メチル系重合体の
少なくとも一種60〜5重量部から成る耐熱変形性およ
び加工性に優れた塩化ビニル系樹脂組成物である。In view of the current situation, the present inventors have arrived at the present invention as a result of intensive studies aimed at improving the heat deformation resistance and processability of vinyl chloride resin without impairing its properties. That is, the present invention uses 40 to 95 parts by weight of at least one type of vinyl chloride polymer containing at least 80% by weight of vinyl chloride and a reduced viscosity of 0.
.. A vinyl chloride resin composition having excellent heat deformation resistance and processability and comprising 60 to 5 parts by weight of at least one kind of methyl methacrylate polymer having a molecular weight of 0.005 to 0.2 and at least 75% by weight of methyl methacrylate. be.
本発明における塩化ビニル系重合体は少なくとも80重
量%が塩化ビニルから構成されるもので塩化ビニル単独
重合体、または20重量%まで他の共重合性単量体と共
重合した塩化ビニル共重合体であり、これら単独重合体
および共重合体は単独で、または混合して用いることが
できる。共重合性単量体としては酢酸ビニル。The vinyl chloride polymer in the present invention is composed of at least 80% by weight of vinyl chloride, and is a vinyl chloride homopolymer or a vinyl chloride copolymer copolymerized with up to 20% by weight of other copolymerizable monomers. These homopolymers and copolymers can be used alone or in combination. Vinyl acetate is used as a copolymerizable monomer.
エチレン、プロピレンなどが用いられるが、その共重合
体中の構成含量は20重量%までであり、20重量%を
超える場合には本発明の目的である耐熱変形性の付与が
困難となるので好ましくない。Ethylene, propylene, etc. are used, but the constituent content in the copolymer is up to 20% by weight, and if it exceeds 20% by weight, it is difficult to impart heat deformation resistance, which is the objective of the present invention, so it is preferable. do not have.
次に本発明におけるメタクリル酸メチル系重合体は少な
くとも75重量%がメタクリル酸メチルから構成される
ものでメタクリル酸メチル単独重合体、または25重量
%まで他の共重合性単量体と共重合したメタクリル酸メ
チル共重合体であり、これら単独重合体および共重合体
は単独で、捷たは混合して用いることができ名。Next, the methyl methacrylate-based polymer in the present invention is composed of at least 75% by weight of methyl methacrylate and is copolymerized with methyl methacrylate homopolymer or with other copolymerizable monomers up to 25% by weight. It is a methyl methacrylate copolymer, and these homopolymers and copolymers can be used alone, or in combination.
一方このメタクリル酸メチル系重合体はその12を11
のクロロホルムに溶解した溶液を25℃にて測定した還
元粘度が0.005〜0.2.好ましくけ0.03〜0
.06の範囲であることが必要であり、還元粘度が0.
005未満のものでは本発明の目的である耐熱変形性の
付与が困難となるので奸才しくない。また還元粘度が0
.2を超えるものでは得られる樹脂組成物を成形する際
の負荷が大になり、加工性が低下するため好ましくない
。On the other hand, this methyl methacrylate polymer has 12 as 11
The reduced viscosity of a solution dissolved in chloroform measured at 25°C is 0.005 to 0.2. Preferably 0.03~0
.. It is necessary that the reduced viscosity is within the range of 0.06 and the reduced viscosity is 0.06.
If it is less than 005, it will be difficult to impart heat deformation resistance, which is the objective of the present invention, and thus it is unskillful. Also, the reduced viscosity is 0
.. If it exceeds 2, the load when molding the resulting resin composition becomes large and processability decreases, which is not preferable.
メタクリル酸メチル共重合体の共重合性単量体としては
炭素数が1〜8のアルキル基を有するアクリル酸アルキ
ルエステル、スチレン、α−メチルスチレン、アクリロ
ニトリルなどを使用することができ、エチルアクリレー
ト、ブチルアクリレートなどが好ましいものである。共
重合体中の共重合性単量体の構成含量は25重量%まで
であり、25重量%を超える場合には耐熱変形性の付与
が困難となるので好ましくない。共重合性単量体の構成
含量は10重重量板下が好ましいものである。As the copolymerizable monomer of the methyl methacrylate copolymer, acrylic acid alkyl ester having an alkyl group having 1 to 8 carbon atoms, styrene, α-methylstyrene, acrylonitrile, etc. can be used, and ethyl acrylate, Butyl acrylate and the like are preferred. The constituent content of the copolymerizable monomer in the copolymer is up to 25% by weight, and if it exceeds 25% by weight, it becomes difficult to impart heat deformation resistance, which is not preferred. The content of the copolymerizable monomer is preferably less than 10% by weight.
本発明の塩化ビニル系樹脂組成物は上記塩化ビニル系重
合体の少なく七も一種を40〜95重量部、上記メタク
リル酸メチル系重合体の少なくとも一種を60〜5重量
部それぞれ配合して成るものであり、メタクリル酸メチ
ル系重合体の配合量が5重量部未満では耐熱変形性付与
の効果が充分でなく、捷だ60重量部を超える場合には
難燃性、耐薬品性など塩化ビニル系重合体が本来有する
特徴が損なわれてしまうため好1しくない。The vinyl chloride resin composition of the present invention contains 40 to 95 parts by weight of at least seven of the above vinyl chloride polymers and 60 to 5 parts by weight of at least one of the methyl methacrylate polymers. If the blending amount of the methyl methacrylate polymer is less than 5 parts by weight, the effect of imparting heat deformation resistance will not be sufficient, and if it exceeds 60 parts by weight, the vinyl chloride polymer will have poor flame retardancy, chemical resistance, etc. This is not preferable because the characteristics originally possessed by the polymer are impaired.
本発明の特徴は本発明で使用するメタクリル酸メチル系
重合体が従来から用いられている高分子量のアクリル系
ポリマーの加工性改質剤に比較し配合した樹脂組成物の
溶融粘度を上げる心配がないため上述した如き高添加量
の配合も可能であり、耐熱変形性の他、真空成形性など
の加工性も著しく向上したものとできたことである。The feature of the present invention is that the methyl methacrylate-based polymer used in the present invention does not have to worry about increasing the melt viscosity of the blended resin composition compared to conventionally used processability modifiers for high molecular weight acrylic polymers. Because of this, it is possible to mix in the high addition amount as described above, and it has been possible to significantly improve processability such as vacuum formability in addition to heat deformation resistance.
本発明の塩化ビニル系樹脂組成物は雨樋、パイプ継手々
との射出成形分野、シート、プレートナどの真空成形分
野の成形材料として使用することができる。The vinyl chloride resin composition of the present invention can be used as a molding material in the field of injection molding of rain gutters and pipe joints, and in the field of vacuum forming of sheets, plates, and the like.
本発明の塩化ビニル系樹脂組成物には必要に応じて熱安
定剤、光安定剤、滑剤、充填剤などを添加することがで
きる。A heat stabilizer, a light stabilizer, a lubricant, a filler, etc. can be added to the vinyl chloride resin composition of the present invention, if necessary.
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.
なお実施例および比較例において「部」はすべて1重量
部」である。In the Examples and Comparative Examples, all "parts" are 1 part by weight.
実施例1〜5.比較例1〜2
攪拌根細反応容器に蒸留水250部、オレイン酸カリウ
l、1.0部、過硫酸カリウム肌5部および表1に示し
た単量体ならびにオードデシルメルカプタンのそれぞれ
の量を投入し、60℃で5時間重合させた。反応完了後
得られたラテックスを凝固、洗浄、乾燥して各種のメタ
クリル酸メチル系重合体を得た。Examples 1-5. Comparative Examples 1 to 2 250 parts of distilled water, 1.0 part of potassium oleate, 5 parts of potassium persulfate, and the respective amounts of the monomers and ordodecyl mercaptan shown in Table 1 were placed in a stirred root cell reaction vessel. and polymerized at 60°C for 5 hours. After the reaction was completed, the resulting latex was coagulated, washed, and dried to obtain various methyl methacrylate polymers.
かかる各種のメタクリル酸メチル系重合体30部、ポリ
塩化ビニル(平均重合度800)70部、ジプチル錫メ
ルカプチド2.0部、ステアリン酸ブチル0.5部。モ
ンタンワックス0.5部をブレンドし、しかる後40町
ψ押出機を用いて5調厚の各種シートに成形し/(。30 parts of the various methyl methacrylate polymers, 70 parts of polyvinyl chloride (average degree of polymerization 800), 2.0 parts of diptyltin mercaptide, and 0.5 parts of butyl stearate. 0.5 part of montan wax is blended and then formed into various sheets of 5 thicknesses using a 40 mm ψ extruder.
得られた各種シートの耐熱性、加工性を評価した結果を
表1に示1〜だ。加工性は40胴φ押出機の負荷(A)
で示しlこ。首だ真空成形性の目安として100℃にお
けるシートの伸度を測定した。この結果を表1に示した
。伸度が大きいことは優れた真空成形性を示すものであ
る。Table 1 shows the results of evaluating the heat resistance and processability of the various sheets obtained. Processability is the load (A) of a 40 cylinder φ extruder
Indicate by . The elongation of the sheet at 100° C. was measured as a measure of vacuum formability. The results are shown in Table 1. A high elongation indicates excellent vacuum formability.
実施例6〜8.比較例3〜4
実施例1で得られたメタクリル酸メチル単独重合体を表
2に示した各部数をポリ塩化ビニルと配合し夫々100
部とした。これらの配合物の特性を表1に示した方法に
より求めたものを表2に示す。Examples 6-8. Comparative Examples 3 to 4 Each part of the methyl methacrylate homopolymer obtained in Example 1 shown in Table 2 was blended with polyvinyl chloride, and 100% of each
Department. Table 2 shows the properties of these formulations determined by the method shown in Table 1.
なお配合物には実施例1と同様にジプチル錫メルカプチ
ド2.0部、ステアリン酸ブチル0.5部、モンタンワ
ックス0.5部を配合しである。As in Example 1, the formulation contained 2.0 parts of diptyltin mercaptide, 0.5 parts of butyl stearate, and 0.5 parts of montan wax.
表 2 手続補正書 特許庁長官 若杉和夫 殿 1、事件の表示 特願昭57−196588号 2、発明の名称 塩化ビニル系樹脂組成物 3、補正をする者 事件との関係 特許出願人 東京都中央区京橋二丁目3番19号 (603)三菱レイヨン株式会社 取締役社長 河 崎 晃 夫 4、代 理 人 東京都中央区京橋二丁目3番19号 および「発明の詳細な説明」の欄 7、補正の内容 (13%許請求の範囲を別紙の通り訂正する。Table 2 Procedural amendment Mr. Kazuo Wakasugi, Commissioner of the Patent Office 1.Display of the incident Patent application No. 196588, 1988 2. Name of the invention Vinyl chloride resin composition 3. Person who makes corrections Relationship to the incident: Patent applicant 2-3-19 Kyobashi, Chuo-ku, Tokyo (603) Mitsubishi Rayon Co., Ltd. President and Director Akio Kawasaki 4. Deputy manager 2-3-19 Kyobashi, Chuo-ku, Tokyo and “Detailed Description of the Invention” column. 7. Contents of correction (The scope of the 13% claim is corrected as shown in the attached sheet.
(2) 明細書第2頁第2行目の[0,3jを「0.
3M/ Jに訂正する。(2) Replace [0, 3j in the second line of page 2 of the specification with “0.
Corrected to 3M/J.
(3)同第3頁第1行目の[0,2Jをr 0.21/
p Jに訂正する。(3) Page 3, line 1, [0,2J r 0.21/
P Correct to J.
(4)同第4負第7行目の[0,2Jをr 0.21/
l Jに訂正する。(4) 4th negative 7th line [0,2J r 0.21/
l Correct to J.
(5)同第4頁第8行目の「0.06Jをro、061
//」に訂正する。(5) On page 4, line 8, “0.06J is ro, 061
//” to be corrected.
(6)同第4頁第9行目の[0,o05JをrO,00
51/p Jに訂正する。(6) [0,o05J on page 4, line 9] rO,00
51/p Corrected to J.
(7) 同第4頁第11行目のl−0,2Jをr O,
211/f Jに訂正する。(7) l-0, 2J on page 4, line 11 of the same page is r O,
Corrected to 211/f J.
(8) 同第6頁第17行目の「オードデシル」を「
t−ドデシル」に訂正する。(8) “Eau de decyl” on page 6, line 17 of the same page is changed to “
Corrected to "t-dodecyl".
(9)同第7頁第4行目の「ヌテアリ」を「ステアリJ
K訂正する。(9) “Nuteari” on page 7, line 4 of the same page was changed to “Steari J”
K Correct.
1)
(10)同第8頁表1中の「ηsp/c」を[ηQ/c
(It//) Jに訂正する。1) (10) "ηsp/c" in Table 1 on page 8 of the same page is changed to [ηQ/c
(It//) Correct to J.
「特許請求の範囲“Claims
Claims (1)
系重合体の少なくとも一種40〜95重量部と還元粘度
が0.005〜0.2で、かつ少なくとも75重量%が
メタクリル酸メチルから成るメタクリル酸メチル系重合
体の少なくとも一種60〜5重量部から成る耐熱変形性
および加工性に優れた塩化ビニル系樹脂組成物。A methyl methacrylate system consisting of 40 to 95 parts by weight of at least one type of vinyl chloride polymer comprising at least 80% by weight of vinyl chloride, a reduced viscosity of 0.005 to 0.2, and at least 75% by weight comprising methyl methacrylate. A vinyl chloride resin composition having excellent heat deformation resistance and processability and comprising 60 to 5 parts by weight of at least one kind of polymer.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP19658882A JPS5998152A (en) | 1982-11-09 | 1982-11-09 | Vinyl chloride resin composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP19658882A JPS5998152A (en) | 1982-11-09 | 1982-11-09 | Vinyl chloride resin composition |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS5998152A true JPS5998152A (en) | 1984-06-06 |
Family
ID=16360230
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP19658882A Pending JPS5998152A (en) | 1982-11-09 | 1982-11-09 | Vinyl chloride resin composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5998152A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61162543A (en) * | 1985-01-10 | 1986-07-23 | Nippon Shokubai Kagaku Kogyo Co Ltd | Thermoplastic resin composition |
JPS62131049A (en) * | 1985-11-30 | 1987-06-13 | バイエル・アクチエンゲゼルシヤフト | Vinyl chhloride molding material |
EP0277831A2 (en) * | 1987-02-04 | 1988-08-10 | Morton International, Inc. | Lubricant composition and process |
JPS6426660A (en) * | 1987-07-22 | 1989-01-27 | Chisso Corp | Vinyl chloride polymer composition |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5552336A (en) * | 1978-10-13 | 1980-04-16 | Kureha Chem Ind Co Ltd | Vinyl chloride-based resin composition |
JPS5774347A (en) * | 1980-10-28 | 1982-05-10 | Mitsubishi Rayon Co Ltd | Vinyl chloride resin composition |
JPS57159836A (en) * | 1981-03-11 | 1982-10-02 | Du Pont | Forming blend component |
-
1982
- 1982-11-09 JP JP19658882A patent/JPS5998152A/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5552336A (en) * | 1978-10-13 | 1980-04-16 | Kureha Chem Ind Co Ltd | Vinyl chloride-based resin composition |
JPS5774347A (en) * | 1980-10-28 | 1982-05-10 | Mitsubishi Rayon Co Ltd | Vinyl chloride resin composition |
JPS57159836A (en) * | 1981-03-11 | 1982-10-02 | Du Pont | Forming blend component |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61162543A (en) * | 1985-01-10 | 1986-07-23 | Nippon Shokubai Kagaku Kogyo Co Ltd | Thermoplastic resin composition |
JPS6357460B2 (en) * | 1985-01-10 | 1988-11-11 | Nippon Shokubai Kagaku Kogyo Kk | |
JPS62131049A (en) * | 1985-11-30 | 1987-06-13 | バイエル・アクチエンゲゼルシヤフト | Vinyl chhloride molding material |
EP0277831A2 (en) * | 1987-02-04 | 1988-08-10 | Morton International, Inc. | Lubricant composition and process |
JPS6426660A (en) * | 1987-07-22 | 1989-01-27 | Chisso Corp | Vinyl chloride polymer composition |
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