JPH0320359A - Monomer cast nylon - Google Patents

Monomer cast nylon

Info

Publication number
JPH0320359A
JPH0320359A JP15446689A JP15446689A JPH0320359A JP H0320359 A JPH0320359 A JP H0320359A JP 15446689 A JP15446689 A JP 15446689A JP 15446689 A JP15446689 A JP 15446689A JP H0320359 A JPH0320359 A JP H0320359A
Authority
JP
Japan
Prior art keywords
nylon
monomer
wollastonite
monomer cast
cast 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
JP15446689A
Other languages
Japanese (ja)
Other versions
JP3057497B2 (en
Inventor
Saburo Sano
三郎 佐野
Masaaki Hiramoto
平本 雅明
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.)
NIPPON PORIPENKO KK
Original Assignee
NIPPON PORIPENKO 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 NIPPON PORIPENKO KK filed Critical NIPPON PORIPENKO KK
Priority to JP1154466A priority Critical patent/JP3057497B2/en
Publication of JPH0320359A publication Critical patent/JPH0320359A/en
Application granted granted Critical
Publication of JP3057497B2 publication Critical patent/JP3057497B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Polyamides (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:To form a monomer cast nylon with excellent strength in a high temp. range at a glass transition temp. or higher by incorporating wollastonite with a specified particle size and a crystalline morphology in a nylon at a specified ration when a monomer cast nylon is prepd. CONSTITUTION:A monomer cast nylon formed by monomer casting is incorporated with 5-40 pts.wt. wollastonite with a particle size of 200-400 mesh and an acicular crystal dispersed in the nylon based on 100 pts.wt. nylon. As the monomer cast nylon, nylon 6 wherein epsilon-caprolactam is used as a raw material and nylon 12 wherein omega-laurolactam is used as a raw material are cited.

Description

【発明の詳細な説明】 (産業上の利用分野〉 この発明はモ/マーキャスティングによって生威された
モノマーキャストナイa冫、特に、高温下、高荷重を受
ける、例えばローラー、パレット、ライナー、車輪、ガ
イドなどの用途に好適な、モノマーキャストナイロンに
係わるものである.(従来の技術、及び発明が解決しよ
うとする課題) モノマーキャストナイロンは機械的強度に優れた特性を
有するが、ガラス転移点前後の温度において、at威的
強度、弾性率に大きな開きがあり、使用環境によって優
れた特性が発揮できないという不都合がある.即ち、〃
ラス転移温度及びそれ以上の高温域で強度面、熱安定性
に欠けるという問題がある. そこでモノマーキャストナイロン中に無m系の充填剤を
混合、分散させて注型することにより、強度の向上をは
かることが考えられるが、この場合、重合開始後、原料
の粘度が上がりだす前に、充填剤が沈澱してしまう問題
があり、そのため添加量が制限され、期待される効果が
発揮されない。
DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) This invention is applicable to monomer cast materials produced by monomer casting, especially those that are subjected to high temperatures and high loads, such as rollers, pallets, liners, and wheels. This invention relates to monomer cast nylon, which is suitable for uses such as guides. (Prior art and problems to be solved by the invention) Monomer cast nylon has excellent mechanical strength, but has a low glass transition point. There is a large difference in the strength and modulus of elasticity at different temperatures, and there is a disadvantage that excellent properties cannot be exhibited depending on the usage environment.
The problem is that it lacks strength and thermal stability at the lath transition temperature and higher temperatures. Therefore, it is possible to improve the strength by mixing and dispersing a m-free filler into monomer cast nylon and casting it, but in this case, after the start of polymerization and before the viscosity of the raw material starts to increase, However, there is a problem that the filler precipitates, which limits the amount added and does not produce the expected effect.

このような背景にかんがみ、ガラス転移温度以上の高温
域においても、強度面などにおいて優れた特性を有し、
使用条件下で高温、高荷重を受ける用途に対しても有効
に使用でさるモノマーキャストナイロンの出現が!望さ
れる. (課題を解決するための手段) 本発明は上記要望を解決するものであって、その要胃と
するところはモノマーキャスティングによって生1&さ
れた七ノマーキャストナイロンであって、ナイロンに、
200〜400メッシュの粒子大きさの針状結晶のウオ
ラストナイトが分散されており、かつ上記ウオラストナ
イトはナイロン100重量部当り5〜40重量部の割合
で含有されていることを特徴とするモノマーキャストナ
イロンに存する. 本発明のモノマーキャストナイロンとしては、ε一カプ
ロラクタムを原料とする6−ナイロンや、ω−ラウロラ
クタムを原料とする12−ナイロン等が挙げられる. 本発明は、か)るナイロンをマトリックスとし、これに
特定のウオラス}ナイト(珪灰石)の微粉結晶を特定量
分散させてなるものである.即ち、ここで用いられるウ
オラス}ナイトは針状結晶のものであり、粒子大きさは
200〜400メッシュであり、か1るウオラストナイ
トを、マトリックスのナイロンの100重量部につき5
〜40重量部の割合で含存させる.針状結晶であるウオ
ラストナイトは比重2.9であり、また嵩比重が0.8
6前後と、無磯充填剤としては小さく、130〜170
℃に維持したC一カブロラクタム、ω−ラウロラクタム
によく分散し、しかも沈降が極めて僅少という製造上の
利点のほかに、針状結晶でるため、圧縮、曲げ強度、弾
性率の大幅な向上がみられる.更にアニオン重合反応を
阻害しないので、七ノマーキャストナイロンの製造に好
都合である. 本発明で用いられるウォラストナイトは200〜400
メッシュ(好ましくは200〜300メッシュ)の範囲
のものから選ばれる.400メッシュより細かいと、粒
子の総表面積が大きくなりすぎ、吸油量が増えてナイロ
ンモノマーの流動性が低下し、強度袖強の効果が出る程
多く充填剤を混入することができない.また、ウォラス
トナイトの粒大きさが200メッシュより大きくなると
、原料のモ/マーと混合撹拌するとき、又は注型時に金
型内で沈澱するものの量が増え、充填剤を多量充填して
も、期待するほどの強度補強効果は得られず、また同一
製品において、製品の上部と下部で物性のパラツキが生
じ、製品として好ましくない.なお、本発明におけるウ
オラストナイトの粒大きさが200〜400メッシュと
いうのは、実質上、200〜400メッシュの範囲とい
うことであり、例えば200メッシュのふるいで処理す
るとさ、完全に全量がふるいを通過することをいうので
なく、少量(5%程度)がふるい上に残る場合、また、
400メッシュのふるいで処理するとき、このふるいを
通過するものが完全に0であることをいうものでなく、
少量(5%程度)通過するものがあってもよいことをい
うものである.なお、ここでメッシュはタイラー式ふる
いによるものをいう. 本発明において、ウオラストナイトは、マトリックスの
ナイロン100重量部に対し、5〜40重量部、好まし
くは10〜25重量部の割合で含存されるように用いら
れる.この量が5重量部未満であると、機械的特性にお
いて期待される効果が出す、一方40重量部を越えると
、モノマーと混合するとさ、及び注型金型内で沈降する
量が多くなり、好ましくない. 本発明のモノマーキャストナイロンを製造するには、ウ
オラストナイトを原料モノマーに添加する以外は、従未
知られているモノマーキャスティング方法に準じて行な
えば上い. ウオラストナイトの配合は、あらかじめ原料タンク内で
原料モノマーとウォラストナイトを混合すると、原料タ
ンク内で沈降する可能性があるので、注型直前に両者を
混合し、注型するのがよい.〈実施例〉 実施例1 ステンレスビーカーに無水のε一カブロラクタム2k.
を採り、140〜160℃に調整する。
Considering this background, it has excellent properties such as strength even at high temperatures above the glass transition temperature.
The advent of monomer cast nylon that can be effectively used in applications that are subject to high temperatures and high loads under usage conditions! desired. (Means for Solving the Problems) The present invention solves the above-mentioned needs, and its main feature is a heptanomeric cast nylon produced by monomer casting.
Wollastonite in the form of acicular crystals with a particle size of 200 to 400 mesh is dispersed therein, and the wollastonite is contained in a proportion of 5 to 40 parts by weight per 100 parts by weight of nylon. It consists of monomer cast nylon. Examples of the monomer cast nylon of the present invention include 6-nylon made from ε-caprolactam and 12-nylon made from ω-laurolactam. The present invention uses such nylon as a matrix, and a specific amount of fine crystals of a specific wollastonite (wollastonite) is dispersed therein. That is, the wollastonite used here is of needle-like crystals, and the particle size is 200 to 400 mesh, and the wollastonite used here is 5 parts by weight per 100 parts by weight of the nylon matrix.
It is contained in a proportion of ~40 parts by weight. Wollastonite, which is a needle-shaped crystal, has a specific gravity of 2.9 and a bulk specific gravity of 0.8.
Around 6, which is small for a non-iso filler, 130-170
In addition to the manufacturing advantages of being well dispersed in C-cabrolactam and ω-laurolactam maintained at ℃ and with extremely little sedimentation, it also has the advantage of producing needle-shaped crystals, which significantly improves compressive strength, bending strength, and elastic modulus. It will be done. Furthermore, since it does not inhibit anionic polymerization reactions, it is convenient for producing heptanomer cast nylon. The wollastonite used in the present invention has a molecular weight of 200 to 400
Selected from a range of mesh (preferably 200 to 300 mesh). If it is finer than 400 mesh, the total surface area of the particles becomes too large, the amount of oil absorbed increases, the fluidity of the nylon monomer decreases, and it is not possible to mix in enough filler to have the effect of increasing strength. In addition, when the grain size of wollastonite becomes larger than 200 mesh, the amount of precipitates in the mold increases when mixing with the raw material mo/mer or during casting, and even when a large amount of filler is filled. However, the expected strength reinforcement effect was not obtained, and the physical properties of the upper and lower parts of the same product varied, making it undesirable as a product. Note that the particle size of wollastonite in the present invention of 200 to 400 mesh means that it is substantially in the range of 200 to 400 mesh. This does not mean that it passes through, but if a small amount (about 5%) remains on the sieve,
When processing through a 400 mesh sieve, this does not mean that the amount of material passing through the sieve is completely zero;
This means that a small amount (about 5%) may pass through. Note that the mesh here refers to a Tyler sieve. In the present invention, wollastonite is used in an amount of 5 to 40 parts by weight, preferably 10 to 25 parts by weight, based on 100 parts by weight of the nylon matrix. If this amount is less than 5 parts by weight, the expected effect on mechanical properties will be achieved, while if it exceeds 40 parts by weight, a large amount will settle when mixed with the monomer and in the casting mold. I don't like it. The monomer cast nylon of the present invention can be produced by following a previously unknown monomer casting method, except for adding wollastonite to the raw material monomer. When blending wollastonite, if you mix the raw material monomer and wollastonite in the raw material tank in advance, there is a possibility that they will settle in the raw material tank, so it is better to mix the two immediately before casting and then casting. <Example> Example 1 Anhydrous ε-cabrolactam 2k in a stainless steel beaker.
and adjust the temperature to 140-160°C.

これに重合助触媒としてトリレンジイソン7ネート15
gを加え、予め120℃程度に加熱しておいたウオラス
トナイト〔面品名ケそりット、(株)丸和バイオケミカ
ル製、300メッシュのふるいで95%通過)400.
を加え、均一に分散するよう撹件する. 一方、別のステンレスビーカーに無水のε一カプロラク
タムlkgを採り、これに重合触媒としての水素化ナト
リウム(抽性63%>6gを加え、更に熱安定剤15.
を加え、140〜160℃に加熱する. 次いで上記両者を混合して系を均一に攪拌した後、15
0℃の金型に注型してウオラストナイトが分散したモノ
マーキャストナイロンを得た.基づき、試験機としてイ
ンストロン型万能試験磯を用いて測定した。その結果得
られた圧縮特性値をf51表に、曲げ待性侭をttS2
表に示す。
Tolylene diisone hepnate 15 was added to this as a polymerization cocatalyst.
wollastonite (Mengen name Kesorit, manufactured by Maruwa Biochemical Co., Ltd., 95% passed through a 300 mesh sieve) 400.
Add and stir to disperse evenly. On the other hand, take 1 kg of anhydrous ε-caprolactam in another stainless steel beaker, add 6 g of sodium hydride as a polymerization catalyst (extractivity 63%), and add 15 g of heat stabilizer.
Add and heat to 140-160℃. Next, after mixing the above two and stirring the system uniformly, 15
Monomer cast nylon with wollastonite dispersed was obtained by casting into a mold at 0°C. Based on this, measurements were made using an Instron type universal testing rock as a testing machine. The resulting compression characteristic values are shown in the f51 table, and the bending properties are shown in the ttS2 table.
Shown in the table.

なお、第1〜2表における数値の単位はkg/C1であ
る。
Note that the units of numerical values in Tables 1 and 2 are kg/C1.

弟1表 た点を除き、その他は実施例1と同様にしてモノマーキ
ャストナイロンを得た. 上記実施例1及び比較例1で得られた板状樹脂(厚さ1
5曽曽、幅3001111、長さ400mm)それぞれ
を切削加工して、測定に必要な寸法の試験片を調製し、
これらにつき、次の方法によって圧縮特性(測定温度2
3〜150℃における5%変形時の圧縮強度及び圧縮弾
性率)並びに曲げ特性(測定温度23〜150℃におけ
る曲げ強度及び曲げ弾性率)を測定した.圧縮特性はA
STM−D6951に基づき、曲げ特性はASTM−D
?90に#2fi 1.5倍と#1段に向上した。
Monomer cast nylon was obtained in the same manner as in Example 1 except for the following points. The plate-shaped resins obtained in Example 1 and Comparative Example 1 (thickness 1
5 Soso, width 3001111, length 400mm) were each cut to prepare test pieces with the dimensions required for measurement,
For these, the compression characteristics (measurement temperature 2
Compressive strength and compressive elastic modulus at 5% deformation at 3 to 150°C) and bending properties (bending strength and bending elastic modulus at measurement temperature of 23 to 150°C) were measured. Compression characteristics are A
Based on STM-D6951, bending properties are ASTM-D
? In 90, #2fi improved by 1.5 times and #1 step.

出穎人 日本ボリペンコ株式会社 1ζ−,’l”,:I (発明の効果〉 (イ)本発明のモノマーキャストナイロンにおいては、
結晶形態及び粒子大きさを規定したウォラストナイトを
用いることにより、これをナイロンマトリックス中に均
一に分散させることがでさ、高充填のキャストナイロン
を得ることが可能になった.
(Effect of the invention) (a) In the monomer cast nylon of the present invention,
By using wollastonite with a defined crystal morphology and particle size, we were able to uniformly disperse it in the nylon matrix, making it possible to obtain highly filled cast nylon.

Claims (1)

【特許請求の範囲】[Claims] (1)モノマーキャスティングによって生成されたモノ
マーキャストナイロンであって、ナイロンに、200〜
400メッシュの粒子大きさの針状結晶のウオラストナ
イトが分散されており、かつ上記ウオラストナイトはナ
イロン100重量部当り5〜40重量部の割合で含有さ
れていることを特徴とするモノマーキャストナイロン。
(1) Monomer cast nylon produced by monomer casting, which has a nylon content of 200 to
A monomer cast characterized in that wollastonite in the form of acicular crystals with a particle size of 400 mesh is dispersed, and the wollastonite is contained in a ratio of 5 to 40 parts by weight per 100 parts by weight of nylon. Nylon.
JP1154466A 1989-06-19 1989-06-19 Monomer cast nylon Expired - Fee Related JP3057497B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1154466A JP3057497B2 (en) 1989-06-19 1989-06-19 Monomer cast nylon

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1154466A JP3057497B2 (en) 1989-06-19 1989-06-19 Monomer cast nylon

Publications (2)

Publication Number Publication Date
JPH0320359A true JPH0320359A (en) 1991-01-29
JP3057497B2 JP3057497B2 (en) 2000-06-26

Family

ID=15584862

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1154466A Expired - Fee Related JP3057497B2 (en) 1989-06-19 1989-06-19 Monomer cast nylon

Country Status (1)

Country Link
JP (1) JP3057497B2 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0639613A1 (en) * 1993-08-19 1995-02-22 General Electric Company A mineral filled moldable thermoplastic composition
JP2008214398A (en) * 2007-02-28 2008-09-18 Nippon Polypenco Ltd Thermally conductive monomer cast nylon molded body
JP2009242673A (en) * 2008-03-31 2009-10-22 Nippon Polypenco Ltd Monomer cast nylon molded body
CN114933699A (en) * 2022-06-06 2022-08-23 镇江市营房塑电有限公司 Preparation method of carbon quantum dot-MC nylon 6 composite material

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0639613A1 (en) * 1993-08-19 1995-02-22 General Electric Company A mineral filled moldable thermoplastic composition
US5965655A (en) * 1993-08-19 1999-10-12 General Electric Company Mineral filled moldable thermoplastic composition
EP1439207A1 (en) * 1993-08-19 2004-07-21 General Electric Company A mineral filled moldable thermoplastic composition
JP2008214398A (en) * 2007-02-28 2008-09-18 Nippon Polypenco Ltd Thermally conductive monomer cast nylon molded body
JP2009242673A (en) * 2008-03-31 2009-10-22 Nippon Polypenco Ltd Monomer cast nylon molded body
CN114933699A (en) * 2022-06-06 2022-08-23 镇江市营房塑电有限公司 Preparation method of carbon quantum dot-MC nylon 6 composite material

Also Published As

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