JPS6088066A - Polyamide resin composition - Google Patents

Polyamide resin composition

Info

Publication number
JPS6088066A
JPS6088066A JP19611083A JP19611083A JPS6088066A JP S6088066 A JPS6088066 A JP S6088066A JP 19611083 A JP19611083 A JP 19611083A JP 19611083 A JP19611083 A JP 19611083A JP S6088066 A JPS6088066 A JP S6088066A
Authority
JP
Japan
Prior art keywords
polyamide
ratio
nylon
relative viscosity
aliph
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
Application number
JP19611083A
Other languages
Japanese (ja)
Other versions
JPH051304B2 (en
Inventor
Hironobu Kawasaki
川崎 洪伸
Kenichi Higami
樋上 健一
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.)
Asahi Kasei Corp
Asahi Chemical Industry Co Ltd
Original Assignee
Asahi Chemical Industry Co Ltd
Asahi Kasei Kogyo KK
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 Asahi Chemical Industry Co Ltd, Asahi Kasei Kogyo KK filed Critical Asahi Chemical Industry Co Ltd
Priority to JP19611083A priority Critical patent/JPS6088066A/en
Publication of JPS6088066A publication Critical patent/JPS6088066A/en
Publication of JPH051304B2 publication Critical patent/JPH051304B2/ja
Granted legal-status Critical Current

Links

Abstract

PURPOSE:To provide a compsn. which gives lamellar moldings which have excellent mechanical properties and little suffer environmental stress cracking caused by metal halides, by mixing two aliph. polyamides having a specified ratio of the number of methylene groups to that of amide groups and a specified relative viscosity ratio. CONSTITUTION:A polyamide resin compsn. consists of 10-90pts.wt. aliph. polyamide (A) in which the ratio of the number of methylene groups to that of amide groups in the main polymer chain is 4-5, and 90-10pts.wt. higher aliph. polyamide (B) in which the ratio of the number of methylene groups to that of amide groups is 6-11, and has a ratio of the relative viscosity of A to that of B of 1.16-2.70. Optionally, other polymers and additives such as colorant, antioxidant, thermal stabilizer, ultraviolet light absorber, antistatic agent, lubricant, plasticizer, flame retarder, etc. may be added to the compsn. according to purpose, so long as the desired properties are not deteriorated.

Description

【発明の詳細な説明】 本発明はポリアミド佃脂組成物に関する6、さらに詳し
くは金に4ハロゲン化物による環境応力亀裂が少なく、
かつ機械的性質に優れた1層状体成形品を提供するポリ
アミド4111脂組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a polyamide tsukuzai composition that has less environmental stress cracking due to 6, more specifically 4 halides on gold, and
The present invention also relates to a polyamide 4111 resin composition that provides a single-layer molded article with excellent mechanical properties.

ポリアミドはその強靭性、電気特性、 nj(熱性を生
かして、自動車や電気製品の部品として巾広く利用され
ている1、シかし、汎用的に用いられていスボIJ了ミ
ド、イlIlりtfε−カプロラクタムのNl珊重合で
得られるナイロン6やヘキサメチレンジアミンとアジピ
ン酸の重縮合反応で得られるナイロン66など、では金
属ハロゲン化物によって環境応力亀裂が生じるという重
大な欠点がある。特に塩化亜鉛や塩化カルシウムとの接
触では、ポリアミド樹脂成形品にクラックを生じ成形品
の劣化を引き起こすことが知られている。
Due to its toughness, electrical properties, and thermal properties, polyamide is widely used as parts for automobiles and electrical products. - Nylon 6 obtained by Nl silicon polymerization of caprolactam and nylon 66 obtained by polycondensation reaction of hexamethylene diamine and adipic acid have a serious drawback of environmental stress cracking caused by metal halides. It is known that contact with calcium chloride causes cracks in polyamide resin molded products and causes deterioration of the molded products.

この環境応力亀裂を改善するため、研究がなされておシ
、ナイロン66に高級脂肪「快ポリアミドを配合するこ
とが効果的であることが知られている。(特開昭57−
80449、!r¥開昭57−212252)。
In order to improve this environmental stress cracking, research has been carried out, and it is known that it is effective to blend high-grade fat "Kai-polyamide" into nylon 66.
80449,! r¥ Kaisho 57-212252).

本発明者らは、更にこの間)、Ωを改善すべく鋭意挽割
した結果、カ”d肪族ポリアミド〔A〕に、1YHj級
脂肪族ポリアミド〔13〕を配合するに際し〔N〕と(
B〕の分子量(相対溶液粘度)を特定することが、彫く
べきことに、この改善に大きな効果を発J’ltするこ
とを見出した3、 又、当該組成物社層状体を為していることが、倍率14
倍の顕微鏡写真でIj(a認されており、本発明はこの
層状体を 当該環境応力色・fグ改善に効果あらしめる
ものにしたものである。
During this time, the present inventors also worked diligently to improve Ω, and as a result, when blending 1YHj class aliphatic polyamide [13] with Ka'd aliphatic polyamide [A], [N] and (
It has been found that specifying the molecular weight (relative solution viscosity) of B) has a significant effect on this improvement3. Being there is a magnification of 14
Ij (a) is recognized in the micrograph at 2x magnification, and the present invention makes this layered material effective in improving the environmental stress color and fg.

すなわち、本発明は、ポリマー主鎖中のメチレン基数と
アミド基数の比(CH2/NHCO)が4〜5である脂
肪族ポリアミド(Au1o〜90重量部と(Cl−12
/N1−IC0)が6〜11の高級脂肪族ポリアミドC
B)90〜10重量部とからなり、ポリアミド(A)と
〔B〕の相対粘度比(〔A〕の相対粘度/〔B〕の相対
粘度)が、1.16〜2.70であるポリアミド樹脂組
成物に関するものである。
That is, the present invention provides an aliphatic polyamide (Au10 to 90 parts by weight and (Cl-12
/N1-IC0) is 6 to 11 higher aliphatic polyamide C
B) A polyamide consisting of 90 to 10 parts by weight and having a relative viscosity ratio of polyamide (A) and [B] (relative viscosity of [A]/relative viscosity of [B]) of 1.16 to 2.70. This invention relates to a resin composition.

本発明のポリアミド樹脂組成物は、2種の脂肪族ポリア
ミドからなる組成物であるが、この種別は、ポリマー主
鎖中のメチレン基数とアミド基数の比(Cl−12/ 
NHCO)で行うこと、ができる。脂肪族ポリアミド〔
A〕は、(CH2/ NlIC0)が、4〜5であるポ
リアミドであフ、かかるポリアミドとしては、ナイロン
4、ナイロン6、ナイロン46、ナイロン66等または
それらの混合物、共重合体があげられる。
The polyamide resin composition of the present invention is a composition consisting of two types of aliphatic polyamides, and this type is characterized by the ratio of the number of methylene groups to the number of amide groups in the polymer main chain (Cl-12/
NHCO). Aliphatic polyamide [
A] is a polyamide in which (CH2/NlIC0) is 4 to 5. Examples of such polyamide include nylon 4, nylon 6, nylon 46, nylon 66, etc., or mixtures and copolymers thereof.

高級脂肪族ポリアミド(B)は、(CH2/NHCO)
が、6〜11であるポリアミドでおυ、かかるポリアミ
ドとして(rl、、ナイロン11.ナイロン12゜ナイ
ロン69.ナイロン610.ナイロン612、ナイロン
613等またはそれらの混合物、共重合体があげられる
Higher aliphatic polyamide (B) is (CH2/NHCO)
is 6 to 11. Such polyamides include (rl, nylon 11, nylon 12, nylon 69, nylon 610, nylon 612, nylon 613, etc., or mixtures and copolymers thereof.

〔A〕において、主鎖中のメチレン基!、zとアミド基
数の比が4未aすの場合、〔13〕において七の比が1
2以上の1ハ合は、いづれの場合も(A、)と〔+(〕
との相溶性が損われ、組成物の性質が損われる1、本発
明において使用する脂肪族ポリアミドCA、)と高級脂
肪族ポリアミド〔13〕の相対粘度比は1.16〜2.
70であり、好ましくは1−50〜2.50である。1
.16未満では、金属ハロゲン化物によるu゛(境応力
亀裂に対する抵抗性改善への寄与が不充分であシ、2,
70を越えると押出し、成形加工性が悪く実用的でない
。又、脂肪族ポリアミド(A、)の相対粘度は、常用の
粘度のものでも良いが、好ましくは、3.5〜5.0の
ものが良く、又更に好°ましいのは4.0〜5.0のも
のである。。
In [A], methylene group in the main chain! , when the ratio of z and the number of amide groups is 4 less than a, then in [13] the ratio of 7 is 1
In any case, the combination of 2 or more is (A,) and [+(]
The relative viscosity ratio of the aliphatic polyamide CA used in the present invention (1) and the higher aliphatic polyamide [13] is between 1.16 and 2.
70, preferably 1-50 to 2.50. 1
.. If it is less than 16, the contribution of the metal halide to improving resistance to boundary stress cracking is insufficient;
If it exceeds 70, extrusion and molding properties are poor and it is not practical. Further, the relative viscosity of the aliphatic polyamide (A) may be a commonly used viscosity, but is preferably 3.5 to 5.0, and more preferably 4.0 to 5.0. 5.0. .

ここでいう相対粘度とは、 JIS K−6810に基
づいて測定した相対粘度をいう1、 本発明のポリアミド樹脂組成物は、脂肪族ポリアミド(
A)と高級脂肪族ポリアミド〔B〕の粘度比が1.16
〜2.70となるよう選ばれ、ポリアミド〔A110〜
90重量部好ましくは30〜60重量部とポリアミド〔
B〕90〜10重景部好まし重量70〜40重は部から
なるものである。
The relative viscosity here refers to the relative viscosity measured based on JIS K-68101. The polyamide resin composition of the present invention is composed of aliphatic polyamide (
The viscosity ratio of A) and higher aliphatic polyamide [B] is 1.16
~2.70, polyamide [A110~
90 parts by weight, preferably 30 to 60 parts by weight, and polyamide [
B] 90 to 10 parts by weight, preferably 70 to 40 parts by weight.

組成物中の脂肪族ポリアミドC,B)の量が10重量部
よシ少ないと、金属ハロゲン化物による環境応力亀裂に
対しての改善が充分でなく、又90重量部を越えると、
脂肪族ポリアミド(A)の有する機械的性質を低下させ
る。
If the amount of aliphatic polyamide C, B) in the composition is less than 10 parts by weight, the improvement against environmental stress cracking caused by metal halides will not be sufficient, and if it exceeds 90 parts by weight,
The mechanical properties of the aliphatic polyamide (A) are reduced.

本発明の組成物は、周知の製造方法によって製造できる
。例えば常用の単軸または二軸押出機のような、押出機
中で溶融ブレンドする方法、射出成形でブレンドする方
法等が挙げられる。
The composition of the present invention can be manufactured by well-known manufacturing methods. Examples include a method of melt blending in an extruder such as a conventional single-screw or twin-screw extruder, a method of blending by injection molding, and the like.

また本発明の目的を損わない範囲において、これら組成
物にさらに他の樹脂ポリマー、着色剤、酸化劣化防止剤
、熱安定剤、紫外線吸収剤、帯電防止剤、滑剤、可塑剤
%難燃剤などを目的に応じて添加することができる。
In addition, to the extent that the purpose of the present invention is not impaired, these compositions may further include other resin polymers, colorants, oxidative deterioration inhibitors, heat stabilizers, ultraviolet absorbers, antistatic agents, lubricants, plasticizers, flame retardants, etc. can be added depending on the purpose.

このように本発明は極めて特徴的である。即ち。In this way, the present invention is extremely distinctive. That is.

先に公開された文献(特開昭57−80449、特開昭
57−212252 )には、脂肪族ポリアミド[A)
に高級脂肪族ポリアミドCB)を配合することが示さJ
lているが、[A″]、[:B]の相対粘度比に言及さ
れていない。
Previously published documents (JP-A-57-80449, JP-A-57-212252) describe aliphatic polyamide [A]
It has been shown that higher aliphatic polyamide CB) is blended into J
However, the relative viscosity ratio of [A''] and [:B] is not mentioned.

これに対して1本発明は、[A) 1O−=90好まし
くは30〜60重量部と(B]90〜10好ましくは7
0〜40重量部からなる配合組成において、CA)とC
B)の相対粘度比を1.16〜2.70にすることが、
環境応力亀裂に効果大なることを見いだしたものであり
、全く新規な発明である。
On the other hand, in the present invention, [A] 1O-=90, preferably 30 to 60 parts by weight, and (B) 90 to 10, preferably 7
In a compounding composition consisting of 0 to 40 parts by weight, CA) and C
Setting the relative viscosity ratio of B) to 1.16 to 2.70,
This is a completely new invention that has been found to be highly effective against environmental stress cracks.

次に本発明を実施例によシ具体的に説明する。Next, the present invention will be specifically explained using examples.

実施例−1 相対粘度ηrが2.58.3.80.4.01.4.7
8のナイロン66と相対粘度ηrが2.18.2.76
のナイロン610を第1表に示す組み合わせにて、ナイ
ロン66にナイロン610を重叶比で60対40の割合
で加え。
Example-1 Relative viscosity ηr is 2.58.3.80.4.01.4.7
8 nylon 66 and relative viscosity ηr is 2.18.2.76
In the combination of nylon 610 shown in Table 1, nylon 610 was added to nylon 66 at a ratio of 60:40.

タンブラ−型混合機にてブレンドした。当混合物をTO
mnφ単軸押出機にて溶融混練しボリアミド樹脂組成物
を得た。得られたポリアミド組成物を射出成形機を用い
て物性測定用試験片に成形し、耐環境応力亀裂性を調べ
た。その結果を3(r、 1表に示す。
Blended using a tumbler type mixer. This mixture is TO
A polyamide resin composition was obtained by melt-kneading using an mnφ single-screw extruder. The obtained polyamide composition was molded into a test piece for measuring physical properties using an injection molding machine, and its resistance to environmental stress cracking was examined. The results are shown in Table 1.

比較例−1 相対粘度ηrが2.58.4.78.6.00のナイロ
ン66と相対粘度ηrが1.70.2.26.2.76
のナイロン61Gを第1表に示す組み合わせにして、ナ
イロン66にナイロン610を重量比で60対4oの割
合で加え、実施例1と同様の方法でポリアミド組成物を
得て、嗣薫境応力亀裂性を調べた。その結果を第実施例
−2 ベレット状のナイロン66 (相対粘度ηr = 4.
01 )にペレット状のナイロン612(相対粘度ηr
=2−22)を加えて、実施例−1と同様の方法でポリ
アミド樹脂組成物を得た。この際、ナイロン66/ナイ
ロン6!2を重量比で15/85.25/75.35/
65゜so、’so、 To/30.85/15 の組
成物を作成した。得られたポリアミド組成物を射出成形
機を用いて物性測定用試験片に成形し、 i−1環境応
力亀裂性と引張強度を調べた。その結果を第2表に示す
Comparative Example-1 Nylon 66 with relative viscosity ηr of 2.58.4.78.6.00 and relative viscosity ηr of 1.70.2.26.2.76
Nylon 61G was combined as shown in Table 1, and nylon 610 was added to nylon 66 at a weight ratio of 60:4 to obtain a polyamide composition in the same manner as in Example 1. I looked into gender. The results are shown in Example 2: pellet-shaped nylon 66 (relative viscosity ηr = 4.
01) and pelletized nylon 612 (relative viscosity ηr
=2-22) to obtain a polyamide resin composition in the same manner as in Example-1. At this time, the weight ratio of nylon 66/nylon 6!2 was 15/85.25/75.35/
Compositions of 65°so, 'so, To/30.85/15 were prepared. The obtained polyamide composition was molded into a test piece for measuring physical properties using an injection molding machine, and the i-1 environmental stress cracking property and tensile strength were examined. The results are shown in Table 2.

比較例−2 実施例−2と同じナイロン66とナイロン612を用い
て、ナイロン66とナイロン612の配合割合を重量比
で10010.9515.5/95.0/Zoo の割
に混合し、実施例−2と同様の方法でポリアミド組成物
を得て、実施例−2と同様に評価した。その結果を第2
表に示す。
Comparative Example-2 Using the same nylon 66 and nylon 612 as in Example-2, the weight ratio of nylon 66 and nylon 612 was 10010.9515.5/95.0/Zoo. A polyamide composition was obtained in the same manner as in Example-2, and evaluated in the same manner as in Example-2. The result is the second
Shown in the table.

以下余白Below margin

Claims (1)

【特許請求の範囲】 ポリマー主鎖中のメチレン基数とアミド基数の比(CH
2/ NHCO)が4〜5である脂肪族ポリアミドCA
ll0〜90重デ14部と(CH2/NHCO)が6〜
11の高級脂肪族ポリアミド〔B〕90〜10重邦5部
とからなり、かつ〔A〕と(B)の相対粘度比(〔A〕
の相対粘度/ [Jりの相対粘度が、1.16〜2−7
0であることを特徴とするポリアミド樹脂組成物
[Claims] The ratio of the number of methylene groups to the number of amide groups in the polymer main chain (CH
2/Aliphatic polyamide CA whose NHCO) is 4 to 5
ll0~90 heavy de14 parts and (CH2/NHCO) is 6~
11 higher aliphatic polyamide [B] consisting of 5 parts of 90-10
Relative viscosity of / [Relative viscosity of J is 1.16 to 2-7
A polyamide resin composition characterized in that
JP19611083A 1983-10-21 1983-10-21 Polyamide resin composition Granted JPS6088066A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP19611083A JPS6088066A (en) 1983-10-21 1983-10-21 Polyamide resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP19611083A JPS6088066A (en) 1983-10-21 1983-10-21 Polyamide resin composition

Publications (2)

Publication Number Publication Date
JPS6088066A true JPS6088066A (en) 1985-05-17
JPH051304B2 JPH051304B2 (en) 1993-01-07

Family

ID=16352401

Family Applications (1)

Application Number Title Priority Date Filing Date
JP19611083A Granted JPS6088066A (en) 1983-10-21 1983-10-21 Polyamide resin composition

Country Status (1)

Country Link
JP (1) JPS6088066A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5869099A (en) * 1996-08-26 1999-02-09 Basf Aktiengesellschaft Cosmetic composition with polymer-bound benzophenone chromophores
US6001337A (en) * 1996-08-26 1999-12-14 Basf Aktiengesellschaft Cosmetic composition with polymer-bound benzophenone chromophores
WO2011120949A1 (en) 2010-03-30 2011-10-06 Basf Se Use of polyamides that are resistant to corrosion and stress cracking
JP2017203151A (en) * 2016-05-06 2017-11-16 旭化成株式会社 Polyamide resin composition and chemical resistance improving method

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20130171394A1 (en) 2011-12-30 2013-07-04 E. I. Du Pont De Nemours And Company Polyamide Composition Containing Ionomer
US8906479B2 (en) 2011-12-30 2014-12-09 E I Du Pont De Nemours And Company Compositions of polyamide and ionomer

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57212252A (en) * 1981-06-25 1982-12-27 Ube Ind Ltd Polyamide composition resistant to calcium chloride

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57212252A (en) * 1981-06-25 1982-12-27 Ube Ind Ltd Polyamide composition resistant to calcium chloride

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5869099A (en) * 1996-08-26 1999-02-09 Basf Aktiengesellschaft Cosmetic composition with polymer-bound benzophenone chromophores
US6001337A (en) * 1996-08-26 1999-12-14 Basf Aktiengesellschaft Cosmetic composition with polymer-bound benzophenone chromophores
WO2011120949A1 (en) 2010-03-30 2011-10-06 Basf Se Use of polyamides that are resistant to corrosion and stress cracking
JP2017203151A (en) * 2016-05-06 2017-11-16 旭化成株式会社 Polyamide resin composition and chemical resistance improving method

Also Published As

Publication number Publication date
JPH051304B2 (en) 1993-01-07

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