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JP2512569B2 - Hard vinyl chloride resin composition - Google Patents

Hard vinyl chloride resin composition

Info

Publication number
JP2512569B2
JP2512569B2 JP1282185A JP28218589A JP2512569B2 JP 2512569 B2 JP2512569 B2 JP 2512569B2 JP 1282185 A JP1282185 A JP 1282185A JP 28218589 A JP28218589 A JP 28218589A JP 2512569 B2 JP2512569 B2 JP 2512569B2
Authority
JP
Japan
Prior art keywords
vinyl chloride
weight
parts
chloride resin
resin composition
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
Application number
JP1282185A
Other languages
Japanese (ja)
Other versions
JPH03143942A (en
Inventor
孝政 福岡
和弘 森田
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sekisui Chemical Co Ltd
Original Assignee
Sekisui Chemical Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Sekisui Chemical Co Ltd filed Critical Sekisui Chemical Co Ltd
Priority to JP1282185A priority Critical patent/JP2512569B2/en
Publication of JPH03143942A publication Critical patent/JPH03143942A/en
Application granted granted Critical
Publication of JP2512569B2 publication Critical patent/JP2512569B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は、特に成形加工性の改良された硬質塩化ビニ
ル系樹脂組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a hard vinyl chloride resin composition having improved moldability.

(従来の技術) 無可塑ポリ塩化ビニル等の硬質塩化ビニル系樹脂は、
機械的強度、難燃性、耐候性、耐薬品性等に優れてお
り、パイプ、板等に広く用いられている。
(Prior Art) Hard vinyl chloride resins such as unplasticized polyvinyl chloride are
It has excellent mechanical strength, flame retardancy, weather resistance, chemical resistance, etc. and is widely used for pipes, plates, etc.

しかし、欠点もある。例えば成形加工性(成形時の流
れ特性)に問題がある。特に、耐熱性を向上させるため
に後塩素化した硬質塩化ビニル系樹脂を用いる場合は、
成形加工性がさらに悪くなる。
However, there are drawbacks. For example, there is a problem in moldability (flow characteristics during molding). Especially when using a post-chlorinated hard vinyl chloride resin to improve heat resistance,
Moldability becomes worse.

硬質塩化ビニル系樹脂の成形加工性を改善する方法
は、多数提案されている、その中の一つの方法として、
塩化ビニル系樹脂に硬質性を保持する範囲内で可塑剤や
内部滑剤を添加する方法がある。
A number of methods have been proposed to improve the moldability of hard vinyl chloride resins, among which,
There is a method of adding a plasticizer and an internal lubricant to the vinyl chloride resin within the range of maintaining the hardness.

(発明が解決しようとする課題) ところが、塩化ビニル系樹脂に可塑剤や内部滑剤を添
加する場合、添加量は多い程成形加工性が改善される
が、添加量の増加につれて特に耐熱性の低下が著しく、
充分な改善効果が得られない。
(Problems to be solved by the invention) However, when a plasticizer or an internal lubricant is added to a vinyl chloride resin, the moldability is improved as the added amount increases, but the heat resistance particularly decreases as the added amount increases. Is significantly
Sufficient improvement effect cannot be obtained.

本発明は、上記の問題を解決するものであり、その目
的とするところは、耐熱性をあまり低下させることな
く、成形加工性が改善され、しかも耐衝撃性も改善され
得る硬質塩化ビニル系樹脂組成物を提供することにあ
る。
The present invention is to solve the above problems, and an object of the invention is to improve the processability of the molding and to improve the impact resistance of the hard vinyl chloride resin without significantly lowering the heat resistance. To provide a composition.

(課題を解決するための手段) 本発明の硬質塩化ビニル系樹脂組成物は、塩化ビニル
系樹脂100重量部と下記の一般式(a)及び(b)の群
から選ばれた少なくとも一種の化合物2〜20重量部とか
らなり、そのことにより上記の目的が達成される。
(Means for Solving the Problems) The hard vinyl chloride resin composition of the present invention comprises 100 parts by weight of a vinyl chloride resin and at least one compound selected from the group of the following general formulas (a) and (b). 2 to 20 parts by weight, whereby the above object is achieved.

(a)(R1−CONH)2C6H4(但し、R1は炭素数7〜23のア
ルキル基又はその任意の水素が水酸基で置換されたアル
キル基である。) (b)(R2−NHCO)2C6H4(但し、R2は炭素数7〜23の
アルキル基又はその任意の水素が水酸基で置換されたア
ルキル基である。) 本発明でいう塩化ビニル系樹脂とは、塩化ビニルの単
独重合体、塩化ビニルと他のモノマーとの共重合体、塩
化ビニルと他のポリマーとのグラフト重合体、上記単独
重合体や共重合体やグラフト重合体の塩素化物、及びこ
れ等の混合物を指す。特に、塩素含有率(塩素化度)が
62〜70重量%の塩素化ポリ塩化ビニルは、耐熱性が優れ
ているので、好適に使用される。
(A) (R 1 -CONH) 2 C 6 H 4 (wherein R 1 is an alkyl group having 7 to 23 carbon atoms or an alkyl group in which any hydrogen thereof is substituted with a hydroxyl group.) (B) (R 2- NHCO) 2 C 6 H 4 (wherein R 2 is an alkyl group having 7 to 23 carbon atoms or an alkyl group in which any hydrogen thereof is substituted with a hydroxyl group.) The vinyl chloride resin in the present invention is A homopolymer of vinyl chloride, a copolymer of vinyl chloride with another monomer, a graft polymer of vinyl chloride with another polymer, a chlorinated product of the above homopolymer, copolymer or graft polymer, and the like. And the like. Especially, the chlorine content (chlorination degree)
Chlorinated polyvinyl chloride of 62 to 70% by weight has excellent heat resistance and is therefore preferably used.

また、本発明でいう硬質とは、塩化ビニル系樹脂に可
塑剤を全く配合しないか、或いは塩化ビニル系樹脂に10
重量%以下の可塑剤を配合したものを意味する。
Further, the term "hard" in the present invention means that no plasticizer is added to the vinyl chloride resin, or the vinyl chloride resin contains 10
It means a mixture of plasticizer in an amount of not more than wt%.

塩化ビニル系樹脂は、その重量度が低くなると機械的
強度が低下し、高くなると成形加工性(成形時の流れ特
性)や透明性が低下するので、重合度は300〜2000、好
ましくは350〜1500程度のものを用いるのが適当であ
る。
The vinyl chloride resin has a lower degree of mechanical strength as its weight decreases, and its moldability (flow characteristics during molding) and transparency decrease as its weight increases. Therefore, the degree of polymerization is 300 to 2000, preferably 350 to It is suitable to use the one of about 1500.

本発明において用いる前記化合物(a)は、ビスアミ
ド系化合物と呼ばれ、例えばカプリン酸、ラウリン酸、
ステアリン酸、イソステアリン酸、12ヒドロキシステア
リン酸、ベヘン酸等の高級脂肪酸と、フェニレンジアミ
ンとの反応により得ることができる。
The compound (a) used in the present invention is called a bisamide compound and includes, for example, capric acid, lauric acid,
It can be obtained by reacting higher fatty acids such as stearic acid, isostearic acid, 12-hydroxystearic acid and behenic acid with phenylenediamine.

このような化合物(a)の例としては、o−フェニレ
ンビスステアリン酸アミド、m−フェニレンビスステア
リン酸アミド、等がある。
Examples of such a compound (a) include o-phenylenebisstearic acid amide and m-phenylenebisstearic acid amide.

また、前記化合物(b)は、ジアルキルフタル酸アミ
ド系化合物と呼ばれ、例えばカプリルアミン、ラウリル
アミン、ステアリルアミン、12−ヒドロキシステアリル
アミン、ベヘニルアミン等のアルキルアミンと、フタル
酸又はイソフタル酸又はテレフタル酸との反応により得
ることができる。
The compound (b) is called a dialkylphthalic acid amide compound, and includes, for example, an alkylamine such as caprylamine, laurylamine, stearylamine, 12-hydroxystearylamine, behenylamine, phthalic acid, isophthalic acid, or terephthalic acid. It can be obtained by reaction with an acid.

このような化合物(b)の例としては、N,N′−ジス
テアリルフタル酸アミド、N,N′−ジラウリルイソフタ
ル酸アミド、N,N′−ジステアリルイソフタル酸アミ
ド、N,N′−ジベヘニルイソフタル酸アミド、N,N′−ジ
ステアリルテレフタル酸アミド等がある。
Examples of such compound (b) include N, N'-distearyl phthalic acid amide, N, N'-dilauryl isophthalic acid amide, N, N'-distearyl isophthalic acid amide, N, N'- Examples include dibehenyl isophthalic acid amide and N, N'-distearyl terephthalic acid amide.

前記化合物(a)及び(b)において、R1、R2の炭素
数が7を下回ると、耐熱性が悪くなり、逆にR1、R2の炭
素数が23を上回ると、樹脂組成物の溶融に要する時間が
長くなり、樹脂が熱分解し易くなる。R1、R2の炭素数は1
2〜21が好ましい。
In the compounds (a) and (b), when the carbon number of R 1 and R 2 is less than 7, the heat resistance becomes poor, and conversely, when the carbon number of R 1 and R 2 exceeds 23, the resin composition The time required for melting the resin becomes long, and the resin is easily decomposed by heat. The carbon number of R 1 and R 2 is 1
2 to 21 is preferable.

上記の化合物(a)及び(b)群から選ばれた少なく
とも一種の化合物は、その配合量が少なくなると樹脂の
溶融粘度の低下が小さくなり、配合量が多くなると樹脂
の溶融速度が遅くなる。したがって、化合物(a)及び
(b)の群から選ばれた少なくとも一種の化合物は、塩
化ビニル系樹脂100重量部に対して2〜20重量部、好ま
しくは3〜20重量部、さらに好ましくは5〜15重量部配
合される。
At least one compound selected from the above-mentioned compounds (a) and (b) will decrease the melt viscosity of the resin when the compounding amount is small, and the melting rate of the resin will be slow when the compounding amount is large. Therefore, at least one compound selected from the group of compounds (a) and (b) is 2 to 20 parts by weight, preferably 3 to 20 parts by weight, and more preferably 5 parts by weight based on 100 parts by weight of the vinyl chloride resin. ~ 15 parts by weight is compounded.

本発明の硬質塩化ビニル系樹脂組成物の構成は、上述
の通りであるが、配合組成物から成形体を成形するに
は、熱安定剤、滑剤、耐衝撃性改良剤、帯電防止剤、着
色剤、充填剤など、一般に硬質塩化ビニル樹脂に用いら
れている配合剤が、必要に応じて配合される。そして、
例えば押出成形法や射出成形法により所望の形状に成形
される。
The composition of the hard vinyl chloride resin composition of the present invention is as described above, but in order to form a molded article from the compounding composition, a heat stabilizer, a lubricant, an impact resistance improver, an antistatic agent, a coloring Compounding agents generally used for hard vinyl chloride resins such as agents and fillers are compounded as necessary. And
For example, it is molded into a desired shape by an extrusion molding method or an injection molding method.

(作用) 本発明において、塩化ビニル系樹脂100重量部に対
し、前記の一般式(a)及び(b)の群から選ばれた少
なくとも一種の化合物2〜20重量部が配合されると、樹
脂の耐熱性をあまり低下させることなく、成形時の流れ
特性が改善され、しかも耐衝撃性も改善される。
(Function) In the present invention, when 2 to 20 parts by weight of at least one compound selected from the group of the general formulas (a) and (b) is mixed with 100 parts by weight of the vinyl chloride resin, the resin is The flow characteristics at the time of molding are improved, and the impact resistance is also improved, without significantly lowering the heat resistance of.

このような特性が得られる理由は必ずしも明らかでは
ないが、成形時の加熱により上記の化合物が溶けて樹脂
の溶融粘度を低下させ、それにより成形時の流れ特性が
改善され、そして、上記化合物は、得られる成型体の中
では固体状で相分離の状態で存在しており、そのため耐
衝撃性が向上しまた耐熱性にはあまり影響しないものと
推察される。
Although the reason why such characteristics are obtained is not always clear, the above compound is melted by heating during molding to reduce the melt viscosity of the resin, thereby improving the flow characteristics during molding, and the above compound is In the obtained molded product, it exists in a solid state and in a phase-separated state, so that it is presumed that impact resistance is improved and heat resistance is not significantly affected.

(実施例) 以下、本発明の実施例及び比較例を示す。(Example) Hereinafter, the Example and comparative example of this invention are shown.

実施例1〜5 平均重合度400、塩素含有率63.5%の塩素化ポリ塩化
ビニル樹脂100重量部に、熱安定剤としてRC−40FT1.5重
量部及びJF−9B1.5重量部(いずれも三共有機合成社
製)、滑剤としてエキセパールBS0.4重量部及びカルコ
ール86 0.4重量部(いずれも花王社製)、さらにロキシ
オールG70S 0.1重量部(ヘンケル白水社製)を添加し、
ヘンシェルミキサーで80℃以下で5分間混合し、樹脂混
合物を調製した。
Examples 1 to 5 100 parts by weight of a chlorinated polyvinyl chloride resin having an average degree of polymerization of 400 and a chlorine content of 63.5%, 1.5 parts by weight of RC-40FT and 1.5 parts by weight of JF-9B as heat stabilizers (both three Addition of 0.4 parts by weight of Exepearl BS and 0.4 parts by weight of Calcol 86 (both manufactured by Kao Corporation) as a lubricant, 0.1 part by weight of Roxyol G70S (manufactured by Henkel Hakusui Co., Ltd.),
A resin mixture was prepared by mixing at 80 ° C. or lower for 5 minutes with a Henschel mixer.

この樹脂混合物に第1表に示した化合物(a)及び
(b)を、第1表に示すように上記樹脂100重量部に対
し、2重量部、5重量部、10重量部、(15重量部)とな
るように添加し、充分に混合し塩素化ポリ塩化ビニル樹
脂配合組成物を得た。
Compounds (a) and (b) shown in Table 1 were added to this resin mixture, as shown in Table 1, with respect to 100 parts by weight of the resin, 2 parts by weight, 5 parts by weight, 10 parts by weight, (15 parts by weight). Parts) and mixed well to obtain a chlorinated polyvinyl chloride resin compounding composition.

この配合組成物を190℃のロールで3分間混練した
後、200℃でプレス成形して厚さ3mm及び5mmのシートを
調製した。このシートについて下記の方法で、耐熱性、
成形加工性及び耐衝撃性を測定した。その結果を第1表
に示す。
This compounded composition was kneaded with a roll at 190 ° C. for 3 minutes and then press-molded at 200 ° C. to prepare sheets having thicknesses of 3 mm and 5 mm. About this sheet, the heat resistance,
Molding processability and impact resistance were measured. The results are shown in Table 1.

(1)耐熱性 厚さ5mmのシートを用い、耐熱性の指標である熱変形
温度(HDT)(JIS K−7207に準拠、荷重18.5kg/cm2)を
測定した。
(1) Heat resistance A sheet with a thickness of 5 mm was used to measure the heat distortion temperature (HDT) (conforming to JIS K-7207, load 18.5 kg / cm 2 ) which is an index of heat resistance.

(2)成形加工性 厚さ3mmのシートを2mm角に切断し、これを高化式フロ
ーテスターに供給し、1mmΦ×10mmのノズルを用い荷重1
60kg/cm2、温度190℃の条件で、成形加工性の指標であ
るフロー値(吐出量)を測定した。
(2) Forming processability A sheet with a thickness of 3 mm is cut into 2 mm squares, and this is supplied to a Koka type flow tester, and a load of 1 mmΦ x 10 mm is used.
The flow value (discharge amount), which is an index of moldability, was measured under the conditions of 60 kg / cm 2 and temperature of 190 ° C.

(3)耐衝撃性 厚さ3mmのシートを用い、JIS K−7111に準拠して耐衝
撃性の指標であるシャルピー衝撃強度(ノッチ付き)を
測定した。
(3) Impact resistance Using a sheet having a thickness of 3 mm, the Charpy impact strength (with a notch), which is an index of impact resistance, was measured according to JIS K-7111.

比較例1〜7 実施例で調製した混合物に実施例で用いた化合物
(a)及び(b)を全く添加しないか、或いはこれ等の
化合物以外の比較化合物を第2表に示すように上記樹脂
100重量部に対し、2重量部、5重量部(8重量部)、1
0重量部となるように添加したこと以外は、実施例と同
様に行った。その結果を第2表に示す。
Comparative Examples 1 to 7 Compounds (a) and (b) used in Examples were not added to the mixture prepared in Examples, or comparative compounds other than these compounds were used as shown in Table 2 above.
2 parts by weight, 5 parts by weight (8 parts by weight), 100 parts by weight, 1
The same procedure as in Example was carried out except that the addition amount was 0 part by weight. Table 2 shows the results.

(発明の効果) 上述の通り、塩化ビニル系樹脂100重量部に前記の一
般式(a)及び(b)の群から選ばれた少なくとも一種
の化合物2〜20重量部を配合すると、耐熱性をあまり低
下させることなく、成形加工性が改善され、しかも耐衝
撃性度も改善され得る。
(Effect of the invention) As described above, when 100 parts by weight of the vinyl chloride resin is mixed with 2 to 20 parts by weight of at least one compound selected from the group of the general formulas (a) and (b), heat resistance is improved. The molding processability can be improved and the impact resistance can also be improved without significantly reducing it.

したがって、本発明の硬質塩化ビニル系樹脂組成物
は、オートメーション機器のハウジング、パイプ継手、
バルブ等の射出成形品、工業用板、パイプ、雨樋、窓枠
等の押出成形品として好適に使用される。
Therefore, the hard vinyl chloride resin composition of the present invention is used for the housing of automation equipment, pipe fittings,
It is suitably used as an injection molded product such as a valve, an industrial plate, a pipe, a gutter, an extrusion molded product such as a window frame.

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】塩化ビニル系樹脂100重量部と下記の一般
式(a)及び(b)の群から選ばれた少なくとも一種の
化合物2〜20重量部とからなる硬質塩化ビニル系樹脂組
成物。 (a)(R1−CONH)2C6H4(但し、R1は炭素数7〜23のア
ルキル基又はその任意の水素が水酸基で置換されたアル
キル基である。) (b)(R2−NHCO)2C6H4(但し、R2は炭素数7〜23のア
ルキル基又はその任意の水素が水酸基で置換されたアル
キル基である。)
1. A hard vinyl chloride resin composition comprising 100 parts by weight of a vinyl chloride resin and 2 to 20 parts by weight of at least one compound selected from the group of the following general formulas (a) and (b). (A) (R 1 -CONH) 2 C 6 H 4 (wherein R 1 is an alkyl group having 7 to 23 carbon atoms or an alkyl group in which any hydrogen thereof is substituted with a hydroxyl group.) (B) (R 2- NHCO) 2 C 6 H 4 (wherein R 2 is an alkyl group having 7 to 23 carbon atoms or an alkyl group in which any hydrogen thereof is substituted with a hydroxyl group.)
JP1282185A 1989-10-30 1989-10-30 Hard vinyl chloride resin composition Expired - Lifetime JP2512569B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1282185A JP2512569B2 (en) 1989-10-30 1989-10-30 Hard vinyl chloride resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1282185A JP2512569B2 (en) 1989-10-30 1989-10-30 Hard vinyl chloride resin composition

Publications (2)

Publication Number Publication Date
JPH03143942A JPH03143942A (en) 1991-06-19
JP2512569B2 true JP2512569B2 (en) 1996-07-03

Family

ID=17649185

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1282185A Expired - Lifetime JP2512569B2 (en) 1989-10-30 1989-10-30 Hard vinyl chloride resin composition

Country Status (1)

Country Link
JP (1) JP2512569B2 (en)

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS532453B2 (en) * 1974-01-14 1978-01-28

Also Published As

Publication number Publication date
JPH03143942A (en) 1991-06-19

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