JPS60215053A - Transparent polyamide resin composition - Google Patents

Transparent polyamide resin composition

Info

Publication number
JPS60215053A
JPS60215053A JP7001884A JP7001884A JPS60215053A JP S60215053 A JPS60215053 A JP S60215053A JP 7001884 A JP7001884 A JP 7001884A JP 7001884 A JP7001884 A JP 7001884A JP S60215053 A JPS60215053 A JP S60215053A
Authority
JP
Japan
Prior art keywords
polyamide
transparent polyamide
weight
parts
nylon
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
JP7001884A
Other languages
Japanese (ja)
Other versions
JPH0532427B2 (en
Inventor
Hiroaki Kamei
亀井 裕晃
Moriyuki Yokoyama
盛之 横山
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.)
DAISERU HIYURUSU KK
Daicel Evonik Ltd
Original Assignee
DAISERU HIYURUSU KK
Daicel Huels 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 DAISERU HIYURUSU KK, Daicel Huels Ltd filed Critical DAISERU HIYURUSU KK
Priority to JP7001884A priority Critical patent/JPS60215053A/en
Publication of JPS60215053A publication Critical patent/JPS60215053A/en
Publication of JPH0532427B2 publication Critical patent/JPH0532427B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:The titled composition having improved flexibility, comprising a specified transparent polyamide and a copolyamide. CONSTITUTION:Lauryl lactam, 12-aminododecanoic acid or 11-aminoundecanoic acid, and bis(4-aminocyclohexyl)methane, as essential monomer components, are copolymerized with monomers such as isophthalic acid, terephthalic acid, or isophoronediamine to obtain a transparent polyamide containing a cyclic compound. 100pts.wt. polyamide is incorporated with 5-200pts.wt. copolyamide consisting of nylon 12 or nylon 11 as an essential component, which is different from the polyamide and has a modulus of elasticity of 15,000kg/cm<2> or lower and lower than that of component A.

Description

【発明の詳細な説明】 本発明は柔軟性の改善された透明ポリアミド樹脂組成V
lJ中に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention provides a transparent polyamide resin composition V with improved flexibility.
Regarding the middle of lJ.

透明ポリアミドは、その耐薬品性、耐熱性、耐衝撃性、
耐寒性の故にシャワーハンドル、オイルフィルター、各
種カバー、ハウジング、眼鏡フレーム等に使用される。
Transparent polyamide is characterized by its chemical resistance, heat resistance, impact resistance,
Because of its cold resistance, it is used for shower handles, oil filters, various covers, housings, eyeglass frames, etc.

その中でも特にフレームには好適に使用される。Among these, it is particularly suitable for use in frames.

透明ポリアミドは化学組成上、環状化合物を多く含有し
、剛性が高く、耐衝撃性、耐熱性におし・て優れている
。しかし、眼鏡フレームに使用する場合、剛性が高すぎ
るとレンズを装着するとき、レンズが入らない、又はフ
レーム及びレンズを破損する等のトラブルを生じる。
Due to its chemical composition, transparent polyamide contains a large amount of cyclic compounds, has high rigidity, and has excellent impact resistance and heat resistance. However, when used in eyeglass frames, if the rigidity is too high, problems such as the lens not being inserted or damage to the frame and lens occur when the lens is attached.

この為フレームの形状、厚み等によって使用する樹脂の
弾性率を変更し、柔軟化させる必要がある。この問題を
解決する為各メーカーでは重合組成を変更することによ
り、剛性又は弾性率を変化させることを試みている。し
かし重合に逆のぼって物性を改善する場合、ユーザーの
ニーズにこまかく対応することが難しく、又、グレード
が増すことはコストアップの要因になり、経済的でない
For this reason, it is necessary to make the resin flexible by changing the elastic modulus of the resin depending on the shape, thickness, etc. of the frame. To solve this problem, manufacturers are trying to change the rigidity or elastic modulus by changing the polymer composition. However, if the physical properties are improved by going against the polymerization process, it is difficult to respond precisely to the needs of users, and increasing the grade increases the cost, which is not economical.

本発明者らは、上記問題を解決すべ(鋭意検討を行なっ
た結果、透明ポリアミドにナイロン12又はナイロン1
1共重合体をブレンドし、成形することにより、透明性
を損なわずに柔軟性が改良された透明ポリアミドを供給
することが可能となった0 μ・ 即ち、本発明はラウリルラクタム、12アミノデカン酸
、又は11アミノウンデカン酸及びビス(4−アミノシ
クロヘキシル)メタンを必須モノマー成分とする透明ポ
リアミド100重量部に上記透明ポリアミドと異なり、
弾性率が上記ポリアミドより小さい、具体的には15.
00 okg7c4以下のナイロン12又はナイロン1
1のモノマーを必須成分とする共重合ポリアミド5〜2
00重量部を配合することを特徴とする、透明性を損な
わずに、任意の柔軟性が得られ、尚かつ安価な透明ポリ
アミド樹脂組成物に関する。
The inventors of the present invention have solved the above problem (as a result of intensive studies, they have found that nylon 12 or nylon 1 is made of transparent polyamide.
By blending and molding 1 copolymer, it has become possible to supply a transparent polyamide with improved flexibility without impairing transparency. , or 100 parts by weight of a transparent polyamide containing 11-aminoundecanoic acid and bis(4-aminocyclohexyl)methane as essential monomer components, unlike the above transparent polyamide,
The elastic modulus is smaller than the above polyamide, specifically 15.
00 okg7c4 or less nylon 12 or nylon 1
Copolyamide 5 to 2 containing monomer 1 as an essential component
The present invention relates to a transparent polyamide resin composition which is characterized by containing 0.00 parts by weight, which provides desired flexibility without impairing transparency, and which is inexpensive.

本発明に言う透明ポリアミドとは、ラウリルラクタム、
12アミノドデカン酸又は11アミノウンデカン酸、ビ
ス(4−アミノシクロヘキシル)メタンを必須モノマー
成分とし、さらにイソフタル酸、テレフタル酸、インホ
ロンジアミン等のモノマーを共重合することによって得
られる分子中に環状化合物を有する剛性、耐熱性、透明
性にすぐれたポリアミド樹脂である。具体的には特開昭
56−45924などに開示されたものが利用できる。
The transparent polyamide referred to in the present invention includes lauryllactam,
A cyclic compound in the molecule obtained by copolymerizing 12-aminododecanoic acid or 11-aminoundecanoic acid and bis(4-aminocyclohexyl)methane as essential monomer components and further monomers such as isophthalic acid, terephthalic acid, and inphorondiamine. It is a polyamide resin with excellent rigidity, heat resistance, and transparency. Specifically, the one disclosed in Japanese Unexamined Patent Publication No. 56-45924 can be used.

本発明中に言うポリアミド12又はポリアミド11のモ
ノマーを必須成分とする共重合ポリアミモノマーを1種
又はそれ以上共重合して得られるポリアミド樹脂を言う
It refers to a polyamide resin obtained by copolymerizing one or more types of copolymerized polyamide monomers having monomers of polyamide 12 or polyamide 11 as an essential component in the present invention.

上記共重合ポリアミドは、透明ポリアミドとは異なり弾
性率が小さいものである。配合の組合せは、ナイロン1
1系同志、ナイロン12系同志が好ましい。
The above-mentioned copolyamide has a small elastic modulus, unlike transparent polyamide. The combination is nylon 1
1 series comrades and nylon 12 series comrades are preferred.

透明ポリアミドに共重合ポリアミドを配合する場合、共
重合ポリアミドの量は該透明ポリアミド100重量部に
対して5〜200重量部、好ましくは5〜100重量部
であり、共重合ポリアミドが5重量部より少ないと柔軟
化効果が充分でなく200重量部より多いと透明性を損
うばかりが、本来の耐熱性を損う場合がある。該透明ポ
リアミドに共重合ポリアミドを混練配合する方法につい
ては特に制限はな(、公知の配合方法を採用することが
できるが、トライブレンドした樹脂をそのまま射出成形
することもできる。
When blending copolyamide with transparent polyamide, the amount of copolyamide is 5 to 200 parts by weight, preferably 5 to 100 parts by weight, based on 100 parts by weight of the transparent polyamide, and the amount of copolyamide is 5 to 100 parts by weight. If it is too little, the softening effect will not be sufficient, and if it is more than 200 parts by weight, not only will transparency be impaired, but the original heat resistance may also be impaired. There are no particular limitations on the method of kneading and blending the copolymerized polyamide with the transparent polyamide (although any known blending method may be employed, but the triblended resin may also be injection molded as it is.

定則又は顔料を添加しても良い。A regular or pigment may be added.

次に、本発明を実施例をもって説明する。Next, the present invention will be explained using examples.

実施例1゜ ラウリルラクタム35重量部、ビス(4−アミノシクロ
ヘキシル)メタン19重量部、インホロンジアミン15
重量部、イソフタル酸30重量部を共重合してなる透明
ポリアミド100重量部にナイロン6−ナイロン12共
重合体(共重合比20/80)25重量部混練し、14
〃×捺“×5″の曲げ試験片を成形し、透明性及び曲げ
弾性率の測定を行なった。
Example 1 35 parts by weight of lauryl lactam, 19 parts by weight of bis(4-aminocyclohexyl)methane, 15 parts by weight of inphorondiamine
25 parts by weight of a nylon 6-nylon 12 copolymer (copolymerization ratio 20/80) was kneaded with 100 parts by weight of a transparent polyamide obtained by copolymerizing 30 parts by weight of isophthalic acid.
A bending test piece of "×5" was molded, and its transparency and bending elastic modulus were measured.

実施例2 実施例1における透明ポリアミド100重量部に実施例
1における共重合ポリアミドを50重量部配合し、実施
例1と同様の試験を行なった。
Example 2 50 parts by weight of the copolyamide in Example 1 was blended with 100 parts by weight of the transparent polyamide in Example 1, and the same test as in Example 1 was conducted.

実施例& 実施例1における透明ポリアミド100重量部に実施例
1における共重合ポリアミドを100重量部配合し、実
施例1と同様の試験を行なった。
Examples & 100 parts by weight of the copolyamide in Example 1 was blended with 100 parts by weight of the transparent polyamide in Example 1, and the same test as in Example 1 was conducted.

実施例生 実施例1における透明ポリアミド100重量部に実施例
1における共重合ポリアミドを200重量部配合した。
EXAMPLE 100 parts by weight of the transparent polyamide in Example 1 was blended with 200 parts by weight of the copolyamide in Example 1.

比較例1゜ 実施例1における透明ポリアミドだけで実施例1と同様
の試験を行なった。
Comparative Example 1 A test similar to that of Example 1 was conducted using only the transparent polyamide of Example 1.

比較例2゜ 実施例1における透明ポリアミド100重量部にナイロ
ン用可塑剤ブチルベンゼンスルポンアミドを20重量部
配合した。
Comparative Example 2 20 parts by weight of butylbenzenesulponamide, a plasticizer for nylon, was added to 100 parts by weight of the transparent polyamide in Example 1.

以上の結果を表1に示す。The above results are shown in Table 1.

Claims (1)

【特許請求の範囲】[Claims] ラウリルラクタム、12−アミドデカン酸又は11−ア
ミノウンデカン酸とビス(4−アミノシクロヘキシル)
メタンを必須モノマー成分とする環状化合物を含有する
透明性ポリアミド100重量部に上記透明性ポリアミド
と異なり弾性率が上記ポリアミドより小さ℃・ナイロン
12又はナイロン11のモノマーを必須成分とする共重
合ポリアミド5〜200重量部を配合してなることを特
徴とする柔軟性の改善された透明性ポリアミド樹脂組成
物。
Lauryllactam, 12-amidodecanoic acid or 11-aminoundecanoic acid and bis(4-aminocyclohexyl)
100 parts by weight of a transparent polyamide containing a cyclic compound containing methane as an essential monomer component and a copolymerized polyamide 5 containing a monomer of nylon 12 or nylon 11 as an essential component, which has a lower elastic modulus than the above polyamide, unlike the above transparent polyamide. 200 parts by weight of a transparent polyamide resin composition with improved flexibility.
JP7001884A 1984-04-10 1984-04-10 Transparent polyamide resin composition Granted JPS60215053A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7001884A JPS60215053A (en) 1984-04-10 1984-04-10 Transparent polyamide resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7001884A JPS60215053A (en) 1984-04-10 1984-04-10 Transparent polyamide resin composition

Publications (2)

Publication Number Publication Date
JPS60215053A true JPS60215053A (en) 1985-10-28
JPH0532427B2 JPH0532427B2 (en) 1993-05-17

Family

ID=13419445

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7001884A Granted JPS60215053A (en) 1984-04-10 1984-04-10 Transparent polyamide resin composition

Country Status (1)

Country Link
JP (1) JPS60215053A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH05311067A (en) * 1991-12-31 1993-11-22 Elf Atochem Sa Transparent polyamide composition with high resistance to chemical agent
KR100294136B1 (en) * 1997-09-18 2001-07-12 아토피나 Copolyamide and polyamide compositions, process of manufacture and applications
US6528560B2 (en) 2000-03-01 2003-03-04 Ems-Chemie Ag Colorless, highly transparent polyamide blends with improved stress cracking resistance

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH05311067A (en) * 1991-12-31 1993-11-22 Elf Atochem Sa Transparent polyamide composition with high resistance to chemical agent
KR100294136B1 (en) * 1997-09-18 2001-07-12 아토피나 Copolyamide and polyamide compositions, process of manufacture and applications
US6528560B2 (en) 2000-03-01 2003-03-04 Ems-Chemie Ag Colorless, highly transparent polyamide blends with improved stress cracking resistance

Also Published As

Publication number Publication date
JPH0532427B2 (en) 1993-05-17

Similar Documents

Publication Publication Date Title
JPS6023435A (en) Antistatic resin composition
JP2825602B2 (en) Thermoplastic molding material resistant to low-temperature impact and miscible with pigment, method for producing the same, method for producing molded parts
GB1602692A (en) Thermoplastic moulding compositions based on polyamides obtained from w-aminocarboxylic acids or lactams of more than 10 carbon atoms and possessing flexibility and low temperature impact strength
JPH039444B2 (en)
WO2011030788A1 (en) Polyamide copolymer and molded article
CN106188534B (en) A kind of polyamide and preparation method thereof, polyamide material prepared therefrom
CA2105567A1 (en) Flexible thermoplastic compositions comprising nylon
JPS60215053A (en) Transparent polyamide resin composition
JP2693531B2 (en) Soft, thermoplastically processable polymer alloy containing polyamide
JPS60215054A (en) Transparent polyamide composition
JPH01101352A (en) Polymer blend consisting of methacrylate polymer and vinylidene fluoride/propylene hexafluoride copolymer and molded product
JPH03258850A (en) Thermoplastic resin composition
JP2018024877A (en) Tough polyamide moulding material
KR910003017A (en) Single Phase Amorphous Polymer Blends and Methods for Making the Same
JP2546093B2 (en) Polyamide resin composition
GB2291062A (en) Polyketone polymers as polyamide tougheners
JP2866995B2 (en) Polyamide resin composition
JPH027969B2 (en)
JP2525106B2 (en) Acrylic resin composition
JPS6023447A (en) Antistatic resin composition
JPS62215656A (en) Polyamide composition
JPS5949252A (en) Thermoplastic resin composition
JPH06340810A (en) High-impact poly(arylene sulfide) resin composition
JPH08225644A (en) Trielement copolyamide
CA1248674A (en) Methylmethacrylate/n-phenylmaleimide copolymer- containing polymer alloys