JPH0456863B2 - - Google Patents

Info

Publication number
JPH0456863B2
JPH0456863B2 JP858484A JP858484A JPH0456863B2 JP H0456863 B2 JPH0456863 B2 JP H0456863B2 JP 858484 A JP858484 A JP 858484A JP 858484 A JP858484 A JP 858484A JP H0456863 B2 JPH0456863 B2 JP H0456863B2
Authority
JP
Japan
Prior art keywords
weight
parts
lithium chloride
nylon
same manner
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
Application number
JP858484A
Other languages
Japanese (ja)
Other versions
JPS60173045A (en
Inventor
Masami Kita
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.)
Daicel Corp
Original Assignee
Daicel Chemical Industries 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 Daicel Chemical Industries Ltd filed Critical Daicel Chemical Industries Ltd
Priority to JP858484A priority Critical patent/JPS60173045A/en
Publication of JPS60173045A publication Critical patent/JPS60173045A/en
Publication of JPH0456863B2 publication Critical patent/JPH0456863B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Compositions Of Macromolecular Compounds (AREA)

Description

【発明の詳細な説明】 本発明は、安価かつ簡便に製造可能で、しかも
ナイロン本来の優れた機械的・化学的性質を損う
ことく、良好な成形性を有する高衝撃性透明ナイ
ロン樹脂組成物に関するものである。 従来、透明性ポリアミドは主として環状モノマ
ーとナイロンモノマーの共縮合重合により製造さ
れており(例えば特開昭51−119794、西独国公開
公報2743515参照)、ナイロン本来の優れた耐薬品
性をも保持しているため一般の透明性樹脂(例え
ば、ポリメチルメタクリレート、ポリスチレン、
アクリロニトリルスチレン樹脂、ポリカーボネー
トなど)が、通常の有機薬品で失透したり、クラ
ツクが発生したりして適用できない分野に使用さ
れつつある。ただし、特殊環状モノマーを使用す
るためコストが高くなり、また共重合体中の環状
モノマーセグメントが高い溶融温度であるため、
得られた共重合体の成形加工性も悪いなどの問題
があつた。 そこで本発明は、上述した欠点を解決すべく鋭
意努力した結果、ポリアミド樹脂と特定の添加剤
の組合せにより、安価で成形加工性が良好で、し
かもポリアミド樹脂本来の優れた化学的性質を保
持した高衝撃性透明ナイロンが製造できることを
見出し、本発明に到達した。 すなわち、本発明は炭素原子数100個当りアミ
ド基数が14個以下のポリアミド樹脂100重量部に、
ハロゲン化リチウムを1.0重量部以上10.0重量部
未満、好ましくは4.0重量部以上10.0重量部未満、
更に好ましくは5.0重量部以上10.0重量部配合し
てなる高衝撃性透明ナイロン樹脂組成物を提供す
るものである。 従来ポリアミドに塩化リチウムを配合した組成
物そのものは、特開昭56−61454号公報に見られ
るように公知であるが、これは熱感応性素子とし
ての応用のみを目的として塩化リチウムを少量配
合したものであり、成形品の高衝撃性、透明性に
ついての記述は全く見あたらない。また、特開昭
57−185349号公報には、ポリε−カプロラクタム
(ナイロン6)に塩化リチウムを配合した組成物
についての記載が見られるが、ここでも高衝撃
性、透明性についての記述はない。 本発明で使用するポリアミド樹脂とは、ナイロ
ン11、ナイロン12あるいはナイロン6・10、ナイ
ロン6・12で代表されるアミド基濃度の低いポリ
アミド、さらに詳しく述べるならば炭素原子数
100個当りのアミド基数が14個以下のホモポリア
ミドまたはコポリアミドである。 また、本発明における添加剤成分であるハロゲ
ン化リチウムのなかで、フツ化リチウム、ヨウ化
リチウム、臭化リチウムなども効果があるが、特
に効果があるのは塩化リチウムである。 本発明で使用するハロゲン化リチウムの添加量
は、ポリアミド樹脂に対し1.0重量部以上10.0重
量部未満、好ましくは4.0重量部以上10.0重量部
未満、更に好ましくは5.0重量部以上10.0重量部
未満であり、1.0重量部以下では十分な透明性、
高い耐衝撃性が得られず、また10重量部以上では
ハロゲン化リチウム自体が固体粒子としてポリア
ミド樹脂中に分散してしまい、透明性は急激に低
下してしまうため好ましくない。 本発明におけるポリアミド樹脂への塩化リチウ
ムの添加方法特に限定されず、塩化リチウム水溶
液にポリアミドペレツトまたは粉末を浸漬する方
法、塩化リチウムとポリアミドペレツトまたは粉
末を混合後、押出機で溶融混練する方法、ポリア
ミドの重合段階で添加する方法など、任意の方法
が実施できる。 本発明のハロゲン化リチウムを含有する高衝撃
性透明ナイロン組成物は、プレス成形、押出し成
形、射出成形などの方法で任意の形状に成形した
後、実用に供される。 また、本発明による高衝撃性透明ナイロン組成
物には、常用の樹脂添加物、例えば酸化安定剤、
防炎剤、紫外線安定剤、熱安定剤等を配合しても
よい。 こうして得られた本発明の高衝撃性透明ナイロ
ン組成物は、きわめて高い耐衝撃性、きわめて良
好な透明性、良好な加工性および機械的性質、き
わめて良好な耐有機薬品性を有する。 以下に実施例及び比較例を示して本発明の効果
を説明するが、本発明はこれらの実施例に限定さ
れるものではない。 実施例 1 ナイロン12(ダイセルヒユルス社製ダイアミド
L1901)100重量部に対し、塩化リチウム(半井
化学薬品製特級)を3重量部添加し、ヘンシエル
ミキサーを用いて混合してから押出機により溶融
混練した後、ペレタイザーによりペレツト化し
た。このペレツトから220℃でプレス成形により
厚さ約0.5mmのシートを作成したところ、透明性
の良好なものであつた。また、ASTM D256に
従がつて射出成形法により試験片を作り、Izod衝
撃強度を測定したところ、非常に耐衝撃性が優れ
ていた。このものの性質を表1に示す。 実施例 2 ナイロン6・12(ダイセルヒユルス社製D1700)
100重量部に対し、塩化リチウムを5重量部添加
し、実施例と全く同様の方法で厚さ約0.5mmのシ
ートを作成したところ、透明性の良好なものであ
つた。また、実施例1と全く同様にしてIzod衝撃
強度を測定したところ非常に耐衝撃性が優れてい
た。 このものの性質を表1に示す。 実施例 3 ナイロン11(ATO社製リルサンBESNO)100
重量部に対し、塩化リチウムを4重量部添加し、
実施例1と全く同様の方法で厚さ約0.5mmのシー
トを作成したところ、透明性の良好なものであつ
た。また、実施例1と全く同様にして、Izod衝撃
強度を測定したところ、非常に耐衝撃性が優れて
いた。 このものの性質を表1に示す。 実施例 4 ナイロン12(ダイセルヒユルス社製L1840Y;耐
熱安定剤入り)100重量部に対し塩化リチウムを
5重量部添加し、実施例1と全く同様の方法で厚
さ約0.5mmのシートを作成したところ透明性の良
好なものであつた。 また、実施例1と全く同様にしてIzod衝撃強度
を測定したところ、非常に耐衝撃性が優れてい
た。 このものの性質を表1に示す。 比較例 1 実施例1おいて塩化リチウムを加えないこと以
外は実施例1と全く同様にして厚さ約0.5mmのシ
ートとIzod衝撃試験片を得た。 このものは透明性を示さず、耐衝撃性も低くか
つた。 このものの性質を表1に示す。 比較例 2 実施例3において塩化リチウムを添加しないこ
と以外は実施例2と全く同様にして厚さ約0.5mm
のシートとIzod衝撃試験片を得た。このものは透
明性を示さず、耐衝撃性も低くかつた。このもの
の性質を表1に示す。 比較例 3 実施例1において塩化リチウムの添加量を5重
量部から0.5重量部に変えたこと以外は比較例1
と全く同様にして厚さ約0.5mmのシートを得た。
このシートは全く透明性を有していなかつた。 このものの性質を表1に示す。 比較例 4 実施例1において塩化リチウムの添加量を3重
量部から12重量部に変えたこと以外は実施例1と
全く同様にしてシートを得た。得られたシート
は、一面に塩化リチウムと思われる小さな粒子が
分散していた。 このものの性質を表1に示す。 実施例 5 実施例1において塩化リチウムの添加量が7重
量部であること以外は、実施例1と全く同じ方法
で厚さ約0.5mmのシートを作成したところ透明性
の良好なものであつた。また、実施例1と全く同
様にしてIzod衝撃強度を測定したところ、非常に
耐衝撃性が優れていた。 このものの性質を表1に示す。 実施例 6 実施例1において塩化リチウムの添加量が9重
量部であること以外は、実施例1と全く同じ方法
で厚さ約0.5mmのシートを作成したところ透明性
の良好なものであつた。また、実施例1と全く同
様にしてIzod衝撃強度を測定したところ、非常に
耐衝撃性が優れていた。このものの性質を表1に
示す。 【表】
DETAILED DESCRIPTION OF THE INVENTION The present invention provides a high-impact transparent nylon resin composition that can be produced easily at low cost and has good moldability without impairing the excellent mechanical and chemical properties inherent to nylon. It is about things. Conventionally, transparent polyamides have been mainly produced by cocondensation polymerization of cyclic monomers and nylon monomers (see, for example, Japanese Patent Laid-Open No. 51-119794 and West German Publication No. 2743515), and they also maintain the excellent chemical resistance inherent to nylon. Because of this, common transparent resins (e.g., polymethyl methacrylate, polystyrene,
(acrylonitrile styrene resin, polycarbonate, etc.) are being used in fields where they cannot be used because they devitrify or crack with regular organic chemicals. However, the cost is high due to the use of special cyclic monomers, and the cyclic monomer segments in the copolymer have a high melting temperature.
There were also problems such as poor moldability of the obtained copolymer. Therefore, as a result of intensive efforts to solve the above-mentioned drawbacks, the present invention has been developed by combining a polyamide resin and specific additives, which is inexpensive and has good moldability, while still retaining the excellent chemical properties inherent to polyamide resin. It was discovered that high impact transparent nylon can be produced and the present invention was achieved. That is, in the present invention, 100 parts by weight of a polyamide resin having 14 or less amide groups per 100 carbon atoms,
1.0 parts by weight or more and less than 10.0 parts by weight of lithium halide, preferably 4.0 parts by weight or more and less than 10.0 parts by weight,
More preferably, a high impact transparent nylon resin composition containing 5.0 parts by weight or more and 10.0 parts by weight is provided. Conventionally, a composition in which lithium chloride is blended with polyamide is publicly known as seen in Japanese Patent Application Laid-open No. 56-61454, but this is a composition in which a small amount of lithium chloride is blended for the sole purpose of application as a heat-sensitive element. However, there is no mention of high impact resistance or transparency of the molded product. Also, Tokukai Akira
No. 57-185349 describes a composition in which lithium chloride is blended with polyε-caprolactam (nylon 6), but there is no mention of high impact strength or transparency here either. The polyamide resin used in the present invention is a polyamide with a low concentration of amide groups such as nylon 11, nylon 12, nylon 6/10, or nylon 6/12, and more specifically, a polyamide with a low carbon atom concentration.
Homopolyamide or copolyamide with 14 or less amide groups per 100 amide groups. Among the lithium halides that are additive components in the present invention, lithium fluoride, lithium iodide, lithium bromide, and the like are also effective, but lithium chloride is particularly effective. The amount of lithium halide used in the present invention is at least 1.0 parts by weight and less than 10.0 parts by weight, preferably at least 4.0 parts by weight and less than 10.0 parts by weight, and more preferably at least 5.0 parts by weight and less than 10.0 parts by weight. , sufficient transparency at 1.0 parts by weight or less;
High impact resistance cannot be obtained, and if it exceeds 10 parts by weight, the lithium halide itself will be dispersed as solid particles in the polyamide resin, resulting in a sharp drop in transparency, which is not preferable. The method of adding lithium chloride to the polyamide resin in the present invention is not particularly limited, but includes a method of immersing polyamide pellets or powder in an aqueous lithium chloride solution, a method of mixing lithium chloride and polyamide pellets or powder, and then melt-kneading the mixture using an extruder. Any method can be used, such as adding it at the stage of polyamide polymerization. The high-impact transparent nylon composition containing lithium halide of the present invention is put into practical use after being molded into an arbitrary shape by a method such as press molding, extrusion molding, or injection molding. The high impact transparent nylon compositions of the present invention may also contain conventional resin additives such as oxidative stabilizers,
Flame retardants, ultraviolet stabilizers, heat stabilizers, etc. may be added. The high-impact transparent nylon composition of the present invention thus obtained has extremely high impact resistance, very good transparency, good processability and mechanical properties, and very good resistance to organic chemicals. The effects of the present invention will be explained below with reference to Examples and Comparative Examples, but the present invention is not limited to these Examples. Example 1 Nylon 12 (Diamid manufactured by Daicel Hyulus)
To 100 parts by weight of lithium chloride (L1901), 3 parts by weight of lithium chloride (special grade manufactured by Hanui Chemical Co., Ltd.) was added, mixed using a Henschel mixer, melt-kneaded using an extruder, and then pelletized using a pelletizer. When a sheet with a thickness of about 0.5 mm was made from this pellet by press molding at 220°C, it had good transparency. In addition, test specimens were made by injection molding according to ASTM D256, and the Izod impact strength was measured, and the impact resistance was extremely excellent. The properties of this product are shown in Table 1. Example 2 Nylon 6/12 (D1700 manufactured by Daicel Hyulus)
When 5 parts by weight of lithium chloride was added to 100 parts by weight and a sheet with a thickness of about 0.5 mm was prepared in exactly the same manner as in the example, it had good transparency. Further, when the Izod impact strength was measured in exactly the same manner as in Example 1, the impact resistance was extremely excellent. The properties of this product are shown in Table 1. Example 3 Nylon 11 (Rilsan BESNO manufactured by ATO) 100
Adding 4 parts by weight of lithium chloride to the parts by weight,
When a sheet with a thickness of about 0.5 mm was prepared in exactly the same manner as in Example 1, it had good transparency. Further, when the Izod impact strength was measured in exactly the same manner as in Example 1, the impact resistance was extremely excellent. The properties of this product are shown in Table 1. Example 4 5 parts by weight of lithium chloride was added to 100 parts by weight of nylon 12 (L1840Y manufactured by Daicel Hyulus; containing a heat-resistant stabilizer), and a sheet with a thickness of approximately 0.5 mm was prepared in exactly the same manner as in Example 1. It had good transparency. Further, when the Izod impact strength was measured in exactly the same manner as in Example 1, the impact resistance was extremely excellent. The properties of this product are shown in Table 1. Comparative Example 1 A sheet with a thickness of about 0.5 mm and an Izod impact test piece were obtained in exactly the same manner as in Example 1 except that lithium chloride was not added. This material did not exhibit transparency and had low impact resistance. The properties of this product are shown in Table 1. Comparative Example 2 The same procedure as in Example 2 was made except that lithium chloride was not added in Example 3, and the thickness was approximately 0.5 mm.
sheets and Izod impact specimens were obtained. This material did not exhibit transparency and had low impact resistance. The properties of this product are shown in Table 1. Comparative Example 3 Comparative Example 1 except that the amount of lithium chloride added in Example 1 was changed from 5 parts by weight to 0.5 parts by weight.
A sheet with a thickness of about 0.5 mm was obtained in exactly the same manner as above.
This sheet had no transparency at all. The properties of this product are shown in Table 1. Comparative Example 4 A sheet was obtained in exactly the same manner as in Example 1 except that the amount of lithium chloride added was changed from 3 parts by weight to 12 parts by weight. The resulting sheet had small particles that appeared to be lithium chloride dispersed all over it. The properties of this product are shown in Table 1. Example 5 A sheet with a thickness of approximately 0.5 mm was prepared in the same manner as in Example 1, except that the amount of lithium chloride added was 7 parts by weight, and the sheet had good transparency. . Further, when the Izod impact strength was measured in exactly the same manner as in Example 1, the impact resistance was extremely excellent. The properties of this product are shown in Table 1. Example 6 A sheet with a thickness of approximately 0.5 mm was prepared in the same manner as in Example 1, except that the amount of lithium chloride added was 9 parts by weight, and the sheet had good transparency. . Further, when the Izod impact strength was measured in exactly the same manner as in Example 1, the impact resistance was extremely excellent. The properties of this product are shown in Table 1. 【table】

Claims (1)

【特許請求の範囲】[Claims] 1 炭素原子数100個当たりのアミド基数が14個
以下のポリアミド樹脂100重量部にハロゲン化リ
チウムを1.0重量部以上10.0重量部未満配合して
る透明ナイロン組成物。
1. A transparent nylon composition containing 1.0 parts by weight or more and less than 10.0 parts by weight of lithium halide in 100 parts by weight of a polyamide resin having 14 or less amide groups per 100 carbon atoms.
JP858484A 1984-01-23 1984-01-23 Transparent nylon composition Granted JPS60173045A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP858484A JPS60173045A (en) 1984-01-23 1984-01-23 Transparent nylon composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP858484A JPS60173045A (en) 1984-01-23 1984-01-23 Transparent nylon composition

Publications (2)

Publication Number Publication Date
JPS60173045A JPS60173045A (en) 1985-09-06
JPH0456863B2 true JPH0456863B2 (en) 1992-09-09

Family

ID=11697052

Family Applications (1)

Application Number Title Priority Date Filing Date
JP858484A Granted JPS60173045A (en) 1984-01-23 1984-01-23 Transparent nylon composition

Country Status (1)

Country Link
JP (1) JPS60173045A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62215146A (en) * 1986-03-12 1987-09-21 Daiseru Hiyurusu Kk Flywheel

Also Published As

Publication number Publication date
JPS60173045A (en) 1985-09-06

Similar Documents

Publication Publication Date Title
US4554320A (en) Nylon molding materials having high impact strength
JPS6058257B2 (en) High heat resistant thermoplastic resin composition
JPS6058463A (en) Modified blend of polyphenylene resin and polyamide
JPH04506829A (en) Fire-resistant polycarbonate blend
JPH01313557A (en) Resin composition for molding material
CA1272824A (en) Thermoplastic moulding compositions with flame- resistant properties
EP0752448B1 (en) Impact modified thermoplastic molding composition containing a silicone rubber powder
US4525513A (en) Flame retardant polyamide composition
JP3456501B2 (en) Polyamide resin composition
JPH0456863B2 (en)
EP0179175B1 (en) Methylmethacrylate/n-phenylmaleimide copolymer-containing polymer alloys
JP2670775B2 (en) Impact resistant flame retardant resin composition
KR101233383B1 (en) Antistatic thermoplastic resin composition
JPH0532429B2 (en)
JPS63135442A (en) Flame-retarding rubber-reinforced resin composition
JPH0532425B2 (en)
JP2634844B2 (en) Impact resistant resin composition having antistatic properties
JPS5837333B2 (en) Flame-retardant styrenic resin composition
JPS5819355A (en) Polyamide sliding material
JPH06340810A (en) High-impact poly(arylene sulfide) resin composition
JPH0532426B2 (en)
JPH0456862B2 (en)
JP2875168B2 (en) Antistatic resin composition
JPS5949252A (en) Thermoplastic resin composition
JPS60238361A (en) Transparent nylon composition