JPH03152147A - Rigid chlorinated vinyl chloride-based resin composition for injection molding - Google Patents

Rigid chlorinated vinyl chloride-based resin composition for injection molding

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Publication number
JPH03152147A
JPH03152147A JP28942089A JP28942089A JPH03152147A JP H03152147 A JPH03152147 A JP H03152147A JP 28942089 A JP28942089 A JP 28942089A JP 28942089 A JP28942089 A JP 28942089A JP H03152147 A JPH03152147 A JP H03152147A
Authority
JP
Japan
Prior art keywords
vinyl chloride
weight
chlorinated vinyl
parts
pref
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
Application number
JP28942089A
Other languages
Japanese (ja)
Inventor
Takamasa Fukuoka
福岡 孝政
Kazuhiro Morita
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 JP28942089A priority Critical patent/JPH03152147A/en
Publication of JPH03152147A publication Critical patent/JPH03152147A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To obtain the title composition excellent, in particular, in molding processability and resistance to heat and impact by incorporating a specific chlorinated vinyl chloride-based resin with an impact resistance improver and a specific bisamide compound. CONSTITUTION:The objective composition can be obtained by incorporating (A) 100 pts.wt. of a chlorinated vinyl chloride-based resin 400-1200 (pref. 600-1000) in average polymerization degree and 62-70 (pref. 62-68)wt.% in chlorine content with (B) 3-15 pts.wt. of an impact resistance improver (pref. chlorinated polyethylene, ABS resin or MBS resin) and (C) 4-20 (pref. 5-15) pts.wt. of a bisamide compound of the formula (R is 7-23C pref. 7-21C alkyl or OH-substituted alkyl; n is 1-10 pref. 1-6) (e.g. methylenebisstearic amide) and, where appropriate, (D) other ingredient(s).

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、耐熱性、耐衝撃性の良好な
射出成形用硬質塩素化塩化ビニル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 chlorinated vinyl chloride resin composition for injection molding, particularly having good moldability, heat resistance, and impact resistance.

(従来の技術) 硬質の塩化ビニル樹脂は、機械的強度、寸法安定性、難
燃性、耐候性、耐薬品性等に優れており、継手、フラン
ジ、バルブ、ボルト、ナツト、容器等の射出成形品とし
て広く用いられている。
(Prior art) Hard vinyl chloride resin has excellent mechanical strength, dimensional stability, flame retardancy, weather resistance, chemical resistance, etc., and is suitable for injection molding of joints, flanges, valves, bolts, nuts, containers, etc. Widely used as molded products.

しかし、硬質の塩化ビニル樹脂は、耐熱性が充分でなく
熱湯等の高温下では熱変形を起こすという欠点がある。
However, hard vinyl chloride resin has the disadvantage that it does not have sufficient heat resistance and may undergo thermal deformation under high temperatures such as boiling water.

かかる欠点を改良するために、塩化ビニル樹脂を後塩素
化した塩素化塩化ビニル樹脂が用いられているが、硬質
の塩素化塩化ビニル樹脂は成形加工性(射出成形時の流
れ特性)に問題がある。
In order to improve these drawbacks, chlorinated vinyl chloride resin, which is obtained by post-chlorinating vinyl chloride resin, has been used, but hard chlorinated vinyl chloride resin has problems with moldability (flow characteristics during injection molding). be.

成形加工性を改善する方法として、塩素化塩化ビニル樹
脂に内部滑剤や加工助剤を添加する方法がある。
As a method of improving molding processability, there is a method of adding an internal lubricant or a processing aid to chlorinated vinyl chloride resin.

(発明が解決しようとする課H) ところが、塩素化塩化ビニル樹脂に内部滑剤や加工助剤
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耐熱性の低下が著しく、実
際には少量しか添加できず充分な改善効果が得られない
(Question H to be solved by the invention) However, when adding an internal lubricant or processing aid to chlorinated vinyl chloride resin, the moldability improves as the amount added increases, but the heat resistance decreases as the amount added increases. The decrease in the amount of carbon dioxide is significant, and in reality, only a small amount can be added and a 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、特に成形加工性、耐熱性、耐衝撃性の
良好な射出成形用硬質塩素化塩化ビニル樹脂組成物を提
供することにある。
The present invention solves the above problems, and its purpose is to provide a hard chlorinated vinyl chloride resin composition for injection molding that has particularly good moldability, heat resistance, and impact resistance. It is in.

(課題を解決するための手段) 本発明の射出成形用硬質塩化ビニル樹脂組成物は、平均
重合度が400〜1200で且つ塩素含有率が62〜7
0重量%の塩素化塩化ビニル樹脂100重量部と、耐衝
撃性改良剤3〜15重量部と、−般式(R−CONH)
1(CFIり、 (但し、R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、nは1〜10である。)で示されるビスアミド系化
合物4〜20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 for injection molding of the present invention has an average degree of polymerization of 400 to 1200 and a chlorine content of 62 to 7.
100 parts by weight of 0% by weight chlorinated vinyl chloride resin, 3 to 15 parts by weight of an impact modifier, -general formula (R-CONH)
Bisamide-based compounds 4 to 20 represented by 1 (CFI) (wherein R 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, and n is 1 to 10) parts by weight, thereby achieving the above objective.

本発明においては、平均重合度が400〜1200好ま
しくは600〜1000で且つ塩素含有率が62〜70
重量%好ましくは62〜68重量%の塩素化塩化ビニル
樹脂を用いる。平均重合度が400を下回ると機械的強
度や耐衝撃性が悪くなり、逆に平均重合度が1200を
上回ると成形加工性(射出成形時の流動性)や溶融ゲル
化特性が悪くなる。
In the present invention, the average degree of polymerization is 400 to 1200, preferably 600 to 1000, and the chlorine content is 62 to 70.
Weight percent preferably 62 to 68 weight percent of chlorinated vinyl chloride resin is used. If the average degree of polymerization is less than 400, mechanical strength and impact resistance will deteriorate, and if the average degree of polymerization exceeds 1200, moldability (fluidity during injection molding) and melt gelling properties will deteriorate.

また、塩素含有率が62重量%を下回ると耐熱性が塩化
ビニル樹脂とさほど変わらず、逆に塩素含有率が70重
量%を上回ると熱分解しやすくなる。
Further, when the chlorine content is less than 62% by weight, the heat resistance is not much different from that of vinyl chloride resin, and conversely, when the chlorine content is more than 70% by weight, thermal decomposition becomes easy.

なお、平均重合度はJIS K−6721に準拠して測
定され、塩素含有率は酸素フラスコ燃焼法による塩素重
量分析により測定される。
Note that the average degree of polymerization is measured in accordance with JIS K-6721, and the chlorine content is measured by chlorine weight analysis using an oxygen flask combustion method.

また、本発明でいう硬質とは、塩素化塩化ビニル樹脂に
可塑剤を全く配合しないか、或いは塩素化塩化ビニル樹
脂に10重量%以下の可塑剤を配合したものを意味する
Furthermore, hard as used in the present invention means a chlorinated vinyl chloride resin containing no plasticizer at all, or a chlorinated vinyl chloride resin containing 10% by weight or less of a plasticizer.

耐衝撃改良剤としては、一般に塩素化塩化ビニル樹脂や
塩化ビニル樹脂に用いられているものが全て使用可能で
ある。その中でも塩素化ポリエチレン、ABS樹脂、M
BS樹脂が好適である。かかる耐衝撃改良剤は、塩素化
塩化ビニル樹脂100重量部に対して3〜15重量部の
範囲で配合される。配合量が3重量部を下回ると耐衝撃
性が不足し、逆に配合量が15重量部を上回ると機械的
強度の低下を招く恐れがあり、また後述のビスアミド系
化合物の配合により耐衝撃性が改善されるので、20重
量部以下の配合で充分である。
As the impact modifier, all those commonly used for chlorinated vinyl chloride resins and vinyl chloride resins can be used. Among them, chlorinated polyethylene, ABS resin, M
BS resin is preferred. The impact modifier is blended in an amount of 3 to 15 parts by weight based on 100 parts by weight of the chlorinated vinyl chloride resin. If the amount is less than 3 parts by weight, the impact resistance will be insufficient, and if the amount is more than 15 parts by weight, there is a risk of a decrease in mechanical strength. is improved, so it is sufficient to add 20 parts by weight or less.

一般式(R−CONH) s (CH3)7て示される
ビスアミド系化合物において、Rの炭素数が23を上回
るか、nが10を上回ると、樹脂組成物の溶融(ゲル化
)に要する時間が長くなり、樹脂が熱分解し易くなる。
In the bisamide compound represented by the general formula (R-CONH) s (CH3)7, when the number of carbon atoms in R exceeds 23 or when n exceeds 10, the time required for melting (gelling) the resin composition increases. As the length increases, the resin becomes easier to thermally decompose.

Rの炭素数は7〜21、nは1〜6が好ましい、このよ
うなビスアミド系化合物は、nが2以上の場合は脂肪酸
とアルキルアミンとの反応により得ることができる。ま
た、nが1の場合は脂肪酸アミドとホルマリンとの反応
により得ることができる。
The number of carbon atoms in R is preferably 7 to 21, and n is preferably 1 to 6. Such a bisamide compound can be obtained by reacting a fatty acid with an alkylamine when n is 2 or more. Moreover, when n is 1, it can be obtained by reaction of fatty acid amide and formalin.

かかるビスアミド系化合物の例としては、メチレンビス
ステアリン酸アミド、エチレンビスカプリン酸アミド、
エチレンビスラウリン酸アミド、エチレンビスステ、ア
リン酸アミド、エチレンビスイソステアリン酸アミド、
エチレンビス12ヒドロキシステアリン酸アミド、エチ
レンビスベヘン酸アミド、ヘキサメチレンビスステアリ
ン酸アミド、ヘキサメチレンビス12ヒドロキシステア
リン酸アミド、ヘキサメチレンビスベヘン酸アミド等が
ある。
Examples of such bisamide compounds include methylene bisstearamide, ethylene biscapric acid amide,
Ethylene bislauric acid amide, ethylene bisstearic acid amide, ethylene bisisostearic acid amide,
Examples include ethylene bis-12-hydroxystearamide, ethylene-bis-behenic acid amide, hexamethylene-bis-stearic acid amide, hexamethylene-bis-12-hydroxystearic acid amide, hexamethylene-bis-behenic acid amide, and the like.

これ等のビスアミド系化合物は単独或いは二種以上を組
み合わせて使用され、塩素化塩化ビニル樹脂100重量
部に対して4〜20重量部、好ましくは5〜15重量部
配合される。配合量が4重量部を下回ると樹脂の溶融粘
度が充分に低下せず、逆に配合量が20重量部を上回る
と樹脂の溶融ゲル化速度が遅(なる。
These bisamide compounds may be used alone or in combination of two or more, and are blended in an amount of 4 to 20 parts by weight, preferably 5 to 15 parts by weight, per 100 parts by weight of the chlorinated vinyl chloride resin. If the amount is less than 4 parts by weight, the melt viscosity of the resin will not be sufficiently reduced, and if the amount is more than 20 parts by weight, the melt gelation rate of the resin will be slow.

本発明の射出成形用硬質塩素化塩化ビニル樹脂組成物の
構成は上述の通りであるが、配合組成物から成形品を成
形するには、従来公知の射出成形機が使用され、一般に
樹脂配合粉を混練し一旦ペレット化して射出成形機に供
給される。
The structure of the hard chlorinated vinyl chloride resin composition for injection molding of the present invention is as described above, but a conventionally known injection molding machine is used to mold a molded article from the compounded composition, and generally a resin compound powder is used. The mixture is kneaded, pelletized, and then supplied to an injection molding machine.

この場合、樹脂配合粉には、熱安定剤、滑剤、加工助剤
、帯電防止剤、紫外線吸収剤、着色剤、充填剤など、一
般に硬質塩素化塩化ビニル樹脂や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。
In this case, the resin compound powder contains heat stabilizers, lubricants, processing aids, antistatic agents, ultraviolet absorbers, colorants, fillers, etc. that are generally used in hard chlorinated vinyl chloride resins and vinyl chloride resins. Compounding agents are added as necessary.

(作用) 本発明のように、特定の塩素化塩化ビニル樹脂に、所定
範囲量の耐衝撃強化剤が配合されると樹脂の耐衝撃性が
改善され、さらに所定範囲量の特定ビスアミド系化合物
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、射出成形時の流れ特性が改善される。また、上記ビ
スアミド系化合物は樹脂の耐衝撃性改善にも寄与する。
(Function) As in the present invention, when a specific chlorinated vinyl chloride resin is blended with an impact strength enhancer in a predetermined range, the impact resistance of the resin is improved, and further, when a specific bisamide compound is added in a predetermined range, the impact resistance of the resin is improved. When blended, the flow characteristics during injection molding are improved without significantly reducing the heat resistance of the resin. Furthermore, the above-mentioned bisamide compound also contributes to improving the impact resistance of the resin.

上記ビスアミド系化合物の配合により、上記のような特
性が得られる理由は必ずしも明らかではないが、射出成
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、それにより射出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。
The reason why the above properties are obtained by blending the above bisamide compounds is not necessarily clear, but the above compound melts due to heating during injection molding and lowers the melt viscosity of the resin. The flow characteristics are improved, and the above compound exists in a solid state in a phase-separated state in the resulting molded product, which is expected to improve impact resistance and not significantly affect heat resistance. be done.

(実施例) 以下、本発明の実施例及び比較例を示す。(Example) Examples and comparative examples of the present invention are shown below.

爽隨■上 平均重合度が800で塩素含有率が67重量%の塩素化
ポリ塩化ビニル100重量部と、耐衝撃性改良剤として
BT八−1[[N(呉羽化学社製のMBS樹脂)7重量
部と、熱安定剤としてTVS−8831(日東化成社製
のジオクチル錫メルカプト)2重量部及びTVS−88
13(日東化成社製のジオクチル錫マレート1重量部と
、滑剤として1八X−0P(ヘキストジャバン社製の複
合滑剤)1重量部と、加工助剤としてメタブレンP−7
00(三菱レーヨン社製のアクリル系)1重量部と、ビ
スアミド系化合物としてエチレンビスステアリン酸アミ
ドを7重量部とをヘンシェルミキサーで80°C以下で
5分間混合し、樹脂配合粉を調製した。
100 parts by weight of chlorinated polyvinyl chloride with an average degree of polymerization of 800 and a chlorine content of 67% by weight, and BT8-1 [[N (MBS resin manufactured by Kureha Chemical Co., Ltd.) as an impact modifier] 7 parts by weight, 2 parts by weight of TVS-8831 (dioctyltin mercapto manufactured by Nitto Kasei Co., Ltd.) as a heat stabilizer, and TVS-88.
13 (1 part by weight of dioctyltin malate manufactured by Nitto Kasei Co., Ltd., 1 part by weight of 18X-0P (composite lubricant manufactured by Hoechst Java Co., Ltd.) as a lubricant, and Metablane P-7 as a processing aid.
00 (acrylic type manufactured by Mitsubishi Rayon Co., Ltd.) and 7 parts by weight of ethylene bisstearic acid amide as a bisamide compound were mixed in a Henschel mixer at 80° C. or lower for 5 minutes to prepare a resin blend powder.

この樹脂配合粉を二軸混練押出機でバレル最高温度19
0℃でストランド状に押出し、直ちにペレタイザーによ
り切断してペレット状コンパウンドを製造した。このペ
レット状コンパウンドを射出成形機(東芝機械社製1s
−850B)に供給し、射出圧力1840kg/cj、
成形温度170〜180℃、スクリュー回転数60rp
lI、金型温度30℃の条件で縦450鴫×横900w
X厚さ3鵬及び5■の板を成形した。
This resin blended powder is processed into a twin-screw kneading extruder at a maximum barrel temperature of 19.
The mixture was extruded into strands at 0°C and immediately cut with a pelletizer to produce a pelleted compound. This pellet-like compound was molded into an injection molding machine (1s manufactured by Toshiba Machine Co., Ltd.).
-850B), injection pressure 1840kg/cj,
Molding temperature 170-180℃, screw rotation speed 60rp
lI, height 450mm x width 900w under conditions of mold temperature 30℃
A plate with a thickness of 3 cm and a thickness of 5 cm was molded.

この場合の樹脂の充填率(完全充填の場合を100%と
する)を測定した。また、上記成形板について樹脂焼け
の有無、及び下記の方法で成形加工性、耐熱性、耐衝撃
性を測定した。その結果を第1表に示す。
The filling rate of the resin in this case (complete filling is taken as 100%) was measured. In addition, the molded plates were checked for resin burn, and their moldability, heat resistance, and impact resistance were measured using the following methods. The results are shown in Table 1.

(1)成形加工性 上記ペレット状コンパウンドを高化式フローテスターに
供給し、1mΦX 10mのノズルを用い荷重100 
kg/cd、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。
(1) Molding processability The above pellet-like compound was supplied to a Koka-type flow tester, and a load of 100 was applied using a nozzle of 1 mΦ x 10 m.
The flow value (discharge amount), which is an index of moldability, was measured under the conditions of kg/cd and temperature of 190°C.

(2)耐熱性 上記厚さ5■の成形板を用い、耐熱性の指標である熱変
形温度(H(IT) (JIS K−7207に準拠、
荷重18 、5 kg / cd)゛を測定した。
(2) Heat resistance Using a molded plate with a thickness of 5 cm, the heat distortion temperature (H (IT)), which is an index of heat resistance (according to JIS K-7207,
A load of 18,5 kg/cd) was measured.

(3)耐衝撃性 上記厚さ3r!mの成形板を用い、JIS K−711
1に準拠して耐衝撃性の指標であるシャルピー衝撃強度
(ノツチ付き)を測定した。
(3) Impact resistance Above thickness 3r! JIS K-711 using a molded plate of
1, Charpy impact strength (notched), which is an index of impact resistance, was measured.

1族性( ビスアミド系化合物のエチレンビスステアリン酸アミド
の配合量を12重量部に変更したこと以外は、実施例1
と同様に行った。その結果を第1表に示す。
Group 1 (Example 1 except that the amount of ethylene bisstearamide as a bisamide compound was changed to 12 parts by weight)
I did the same thing. The results are shown in Table 1.

夾隨LL ビスアミド系化合物としてエチレンビス12ヒドロキシ
ステアリン酸アミドを7重量部配合したこと以外は、実
施例1と同様に行った。その結果を第1表に示す。
The same procedure as in Example 1 was carried out except that 7 parts by weight of ethylene bis-12-hydroxystearamide was added as the bisamide compound. The results are shown in Table 1.

裏隨■土 ビスアミド系化合物としてエチレンビスベヘン酸アミド
を7重量部配合したこと以外は、実施例1と同様に行っ
た。その結果を第1表に示す。
The same procedure as in Example 1 was carried out except that 7 parts by weight of ethylene bisbehenic acid amide was added as the bisamide compound. The results are shown in Table 1.

1m ビスアミド系化合物としてヘキサメチレンビスステアリ
ン酸アミドを7重量部配合したこと以外は、実施例1と
同様に行った。その結果を第1表に示す。
Example 1 was carried out in the same manner as in Example 1, except that 7 parts by weight of hexamethylene bisstearamide was blended as the bisamide compound. The results are shown in Table 1.

ル較■土 ビスアミド系化合物のエチレンビスステアリン酸アミド
の配合量を3重量部に変更したこと以外は、実施例1と
同様に行った。その結果を第1表に示す。
Example 1 was carried out in the same manner as in Example 1, except that the amount of ethylene bisstearamide as a bisamide-based compound was changed to 3 parts by weight. The results are shown in Table 1.

ル較桝l ビスアミド系化合物のエチレンビスステアリン酸アミド
の代わりに、従来使用のモノステアリン酸グリセライド
を7重量部配合したこと以外は、実施例1と同様に行っ
た。その結果を第1表に示す。
Example 1 The same procedure as in Example 1 was carried out, except that 7 parts by weight of conventionally used monostearic acid glyceride was added instead of the bisamide-based compound ethylene bisstearic acid amide. The results are shown in Table 1.

且較11 耐衝撃性改良剤のBT八−1[[N(呉羽化学社製のM
BS樹脂)の配合量を2重量部に変更したこと以外は、
実施例1と同様に行った。その結果を第1表に示す。
Comparison 11 Impact modifier BT8-1 [[N (M manufactured by Kureha Chemical Co., Ltd.)
Except for changing the blending amount of BS resin to 2 parts by weight.
The same procedure as in Example 1 was carried out. The results are shown in Table 1.

(発明の効果) 上述の通り、平均重合度が400〜1200で且つ塩素
含有率が62〜70重量%の塩素化塩化ビニル樹脂10
0重量部と、耐衝撃性改良剤3〜15重量部と、一般式
(R−CON)I)x(C)It)fi(但し、R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、nは1−10である。)で示
されるビスアミド系化合物4〜20重量部とを配合する
ことにより、特に成形加工性、耐熱性、耐衝撃性の良好
な射出成形に適した硬質塩素化塩化ビニル樹脂組成物が
得られる。
(Effect of the invention) As mentioned above, the chlorinated vinyl chloride resin 10 has an average degree of polymerization of 400 to 1200 and a chlorine content of 62 to 70% by weight.
0 parts by weight, 3 to 15 parts by weight of an impact modifier, and general formula (R-CON) By blending 4 to 20 parts by weight of a bisamide compound represented by an alkyl group in which hydrogen is substituted with a hydroxyl group (n is 1-10), particularly good moldability, heat resistance, and impact resistance can be achieved. A hard chlorinated vinyl chloride resin composition suitable for injection molding is obtained.

したがって、本発明の射出成形用硬質塩素化塩化ビニル
樹脂組成物は、継手、フランジ、バルブ、ボルト、ナツ
ト、容器等の射出成形品として、硬質の塩化ビニル樹脂
では耐熱性の点で使用できなかった用途に好適に使用さ
れる。
Therefore, the hard chlorinated vinyl chloride resin composition for injection molding of the present invention cannot be used as injection molded products such as joints, flanges, valves, bolts, nuts, containers, etc. due to the heat resistance of hard vinyl chloride resins. It is suitable for use in various applications.

Claims (1)

【特許請求の範囲】[Claims] 1、平均重合度が400〜1200で且つ塩素含有率が
62〜70重量%の塩素化塩化ビニル樹脂100重量部
と、耐衝撃性改良剤3〜15重量部と、一般式(R−C
ONH)_2(CH_2)_n(但し、R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、nは1〜10である。)で示されるビ
スアミド系化合物4〜20重量部とからなる射出成形用
硬質塩素化塩化ビニル樹脂組成物。
1. 100 parts by weight of a chlorinated vinyl chloride resin with an average degree of polymerization of 400 to 1200 and a chlorine content of 62 to 70% by weight, 3 to 15 parts by weight of an impact modifier, and a compound of the general formula (R-C
ONH)_2(CH_2)_n (However, R has 7 to 7 carbon atoms
23 alkyl group or an alkyl group in which any hydrogen thereof is substituted with a hydroxyl group; n is 1 to 10; ) A hard chlorinated vinyl chloride resin composition for injection molding, comprising 4 to 20 parts by weight of a bisamide compound represented by:
JP28942089A 1989-11-07 1989-11-07 Rigid chlorinated vinyl chloride-based resin composition for injection molding Pending JPH03152147A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP28942089A JPH03152147A (en) 1989-11-07 1989-11-07 Rigid chlorinated vinyl chloride-based resin composition for injection molding

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP28942089A JPH03152147A (en) 1989-11-07 1989-11-07 Rigid chlorinated vinyl chloride-based resin composition for injection molding

Publications (1)

Publication Number Publication Date
JPH03152147A true JPH03152147A (en) 1991-06-28

Family

ID=17743014

Family Applications (1)

Application Number Title Priority Date Filing Date
JP28942089A Pending JPH03152147A (en) 1989-11-07 1989-11-07 Rigid chlorinated vinyl chloride-based resin composition for injection molding

Country Status (1)

Country Link
JP (1) JPH03152147A (en)

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5584347A (en) * 1978-12-21 1980-06-25 Kanegafuchi Chem Ind Co Ltd Improved vinyl chloride resin composition
JPS5695944A (en) * 1979-12-28 1981-08-03 Kanegafuchi Chem Ind Co Ltd Reinforced polyvinyl chloride resin composition
JPS63251449A (en) * 1987-04-06 1988-10-18 Nippon Carbide Ind Co Ltd Heat-resistant thermoplastic resin composition
JPH01263143A (en) * 1988-04-15 1989-10-19 Kanegafuchi Chem Ind Co Ltd Resin composition excellent in heat resistance and processability for thermoplasticated molding

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5584347A (en) * 1978-12-21 1980-06-25 Kanegafuchi Chem Ind Co Ltd Improved vinyl chloride resin composition
JPS5695944A (en) * 1979-12-28 1981-08-03 Kanegafuchi Chem Ind Co Ltd Reinforced polyvinyl chloride resin composition
JPS63251449A (en) * 1987-04-06 1988-10-18 Nippon Carbide Ind Co Ltd Heat-resistant thermoplastic resin composition
JPH01263143A (en) * 1988-04-15 1989-10-19 Kanegafuchi Chem Ind Co Ltd Resin composition excellent in heat resistance and processability for thermoplasticated molding

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