JPH04246442A - Antistatic resin composition resistant against water washing - Google Patents
Antistatic resin composition resistant against water washingInfo
- Publication number
- JPH04246442A JPH04246442A JP3031326A JP3132691A JPH04246442A JP H04246442 A JPH04246442 A JP H04246442A JP 3031326 A JP3031326 A JP 3031326A JP 3132691 A JP3132691 A JP 3132691A JP H04246442 A JPH04246442 A JP H04246442A
- Authority
- JP
- Japan
- Prior art keywords
- parts
- resin
- component
- antistatic
- resin composition
- 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
Links
- 239000011342 resin composition Substances 0.000 title claims description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title description 10
- 238000005406 washing Methods 0.000 title description 8
- 229910052751 metal Inorganic materials 0.000 claims description 9
- 239000002184 metal Substances 0.000 claims description 9
- 229920005990 polystyrene resin Polymers 0.000 claims description 9
- 229920006122 polyamide resin Polymers 0.000 claims description 6
- 229920005672 polyolefin resin Polymers 0.000 claims description 6
- 150000003839 salts Chemical class 0.000 claims description 6
- 238000002156 mixing Methods 0.000 claims description 4
- 150000005846 sugar alcohols Polymers 0.000 claims description 4
- 230000000737 periodic effect Effects 0.000 claims description 3
- JAXFJECJQZDFJS-XHEPKHHKSA-N gtpl8555 Chemical group OC(=O)C[C@H](N)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](C(C)C)C(=O)N1CCC[C@@H]1C(=O)N[C@H](B1O[C@@]2(C)[C@H]3C[C@H](C3(C)C)C[C@H]2O1)CCC1=CC=C(F)C=C1 JAXFJECJQZDFJS-XHEPKHHKSA-N 0.000 claims 1
- 229920005989 resin Polymers 0.000 description 17
- 239000011347 resin Substances 0.000 description 17
- 239000004677 Nylon Substances 0.000 description 11
- 229920001778 nylon Polymers 0.000 description 11
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 9
- 230000000694 effects Effects 0.000 description 9
- -1 polyethylene Polymers 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 5
- 229920005992 thermoplastic resin Polymers 0.000 description 5
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- 235000011187 glycerol Nutrition 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- ZNNZYHKDIALBAK-UHFFFAOYSA-M potassium thiocyanate Chemical compound [K+].[S-]C#N ZNNZYHKDIALBAK-UHFFFAOYSA-M 0.000 description 4
- 239000006229 carbon black Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
- 239000000806 elastomer Substances 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- 229940116357 potassium thiocyanate Drugs 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000002216 antistatic agent Substances 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 238000004806 packaging method and process Methods 0.000 description 2
- 239000008188 pellet Substances 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 1
- PYSRRFNXTXNWCD-UHFFFAOYSA-N 3-(2-phenylethenyl)furan-2,5-dione Chemical compound O=C1OC(=O)C(C=CC=2C=CC=CC=2)=C1 PYSRRFNXTXNWCD-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- XTEGARKTQYYJKE-UHFFFAOYSA-M Chlorate Chemical class [O-]Cl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-M 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 241000283220 Odobenus rosmarus Species 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 229920000147 Styrene maleic anhydride Polymers 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- SXDBWCPKPHAZSM-UHFFFAOYSA-M bromate Chemical class [O-]Br(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-M 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- NJLLQSBAHIKGKF-UHFFFAOYSA-N dipotassium dioxido(oxo)titanium Chemical compound [K+].[K+].[O-][Ti]([O-])=O NJLLQSBAHIKGKF-UHFFFAOYSA-N 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- 229920006244 ethylene-ethyl acrylate Polymers 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 229920001903 high density polyethylene Polymers 0.000 description 1
- 229920005669 high impact polystyrene Polymers 0.000 description 1
- 239000004700 high-density polyethylene Substances 0.000 description 1
- 239000004797 high-impact polystyrene Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 229920000554 ionomer Polymers 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- MHCFAGZWMAWTNR-UHFFFAOYSA-M lithium perchlorate Chemical compound [Li+].[O-]Cl(=O)(=O)=O MHCFAGZWMAWTNR-UHFFFAOYSA-M 0.000 description 1
- 229910001486 lithium perchlorate Inorganic materials 0.000 description 1
- HGPXWXLYXNVULB-UHFFFAOYSA-M lithium stearate Chemical compound [Li+].CCCCCCCCCCCCCCCCCC([O-])=O HGPXWXLYXNVULB-UHFFFAOYSA-M 0.000 description 1
- INHCSSUBVCNVSK-UHFFFAOYSA-L lithium sulfate Inorganic materials [Li+].[Li+].[O-]S([O-])(=O)=O INHCSSUBVCNVSK-UHFFFAOYSA-L 0.000 description 1
- ZJZXSOKJEJFHCP-UHFFFAOYSA-M lithium;thiocyanate Chemical compound [Li+].[S-]C#N ZJZXSOKJEJFHCP-UHFFFAOYSA-M 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 239000002667 nucleating agent Substances 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- LLYCMZGLHLKPPU-UHFFFAOYSA-N perbromic acid Chemical class OBr(=O)(=O)=O LLYCMZGLHLKPPU-UHFFFAOYSA-N 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical class OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- 150000003016 phosphoric acids Chemical class 0.000 description 1
- 238000001782 photodegradation Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920000306 polymethylpentene Polymers 0.000 description 1
- 239000011116 polymethylpentene Substances 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- VGTPCRGMBIAPIM-UHFFFAOYSA-M sodium thiocyanate Chemical compound [Na+].[S-]C#N VGTPCRGMBIAPIM-UHFFFAOYSA-M 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- RBTVSNLYYIMMKS-UHFFFAOYSA-N tert-butyl 3-aminoazetidine-1-carboxylate;hydrochloride Chemical compound Cl.CC(C)(C)OC(=O)N1CC(N)C1 RBTVSNLYYIMMKS-UHFFFAOYSA-N 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 150000003567 thiocyanates Chemical class 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Conductive Materials (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【0001】0001
【産業上の利用分野】本発明はポリオレフイン系樹脂及
び/又はポリスチレン系樹脂に,ポリアミド系樹脂を配
合した熱可塑性樹脂を基体とし,恒常的な優れた帯電防
止性を有する耐水帯電防止性樹脂組成物に関するもので
ある。[Industrial Application Field] The present invention is a water-resistant antistatic resin composition that has a constant and excellent antistatic property and is based on a thermoplastic resin that is a mixture of a polyolefin resin and/or a polystyrene resin and a polyamide resin. It is about things.
【0002】0002
【従来の技術】従来より帯電防止効果の優れた導電性樹
脂は,ICやLSI等保護のためキャリアケースや電子
部品の包装等に使用されている。そして,この際に使用
する帯電防止性(導電性)樹脂としては,価格,電気特
性,機械的物性等の問題から導電性付与剤としてカーボ
ンブラックを配合したものが殆どである。しかし,熱可
塑性樹脂にカーボンブラックを配合したものは導電性は
良好であるが,得られる成形品の色調が黒色となり,色
分けを求められる場合の導電性樹脂としては不適当であ
り,又,カーボンブラックによる汚れを嫌う用途にも使
用出来ないのが現状である。2. Description of the Related Art Conventionally, conductive resins with excellent antistatic effects have been used for carrier cases and packaging of electronic parts to protect ICs, LSIs, etc. Most of the antistatic (conductive) resins used in this case contain carbon black as a conductivity imparting agent due to issues such as price, electrical properties, and mechanical properties. However, although a thermoplastic resin containing carbon black has good conductivity, the color tone of the resulting molded product is black, making it unsuitable as a conductive resin when color separation is required. Currently, it cannot be used in applications where stains caused by black are averse.
【0003】又,帯電防止剤を使用したものとして,樹
脂に練り込んだり,成形品表面に塗布したりする方法も
あるが,いずれも,その効果(導電性)は短期間で消滅
しまう欠点がある。このため近年,帯電防止性樹脂とし
て,熱可塑性樹脂に親水性樹脂を配合したものが,いろ
いろと開発検討されている。しかし,親水性樹脂を配合
したものに共通する欠点として,成形品の物性(例:伸
び率,引張強度)が著しく低下したり,成形品の表面に
ベタツキが生じやすくなり,ほこりが吸着し易いなどの
欠点がある。[0003]Also, there are methods of using antistatic agents, such as kneading them into resin or coating them on the surface of molded products, but both methods have the disadvantage that the effect (conductivity) disappears in a short period of time. be. For this reason, in recent years, various antistatic resins in which hydrophilic resins are blended with thermoplastic resins have been developed and studied. However, the common drawbacks of products containing hydrophilic resins are that the physical properties of the molded product (e.g., elongation, tensile strength) are significantly reduced, and the surface of the molded product tends to become sticky and attract dust. There are drawbacks such as.
【0004】そこで本発明者らは,以前,ICやLSI
等保護のためキャリアケースや包装材の着色が可能であ
り,しかも,成形が容易であり,得られる成形品の機械
的物性の優れた着色可能な帯電防止性熱可塑性樹脂組成
物(特願平2−295277号)を出願したのである。[0004] Therefore, the present inventors previously developed IC and LSI
A colorable antistatic thermoplastic resin composition (patent application patent) that can be used to color carrier cases and packaging materials for protection, etc., is easy to mold, and has excellent mechanical properties of the resulting molded products. No. 2-295277).
【0005】[0005]
【発明が解決しようとする課題】しかし,上記製品の用
途の一つであるIC包装用品では,水洗洗浄工程を取り
入れるケースが近年増加しており,このため帯電防止剤
を使用した成形品のように水洗後,瞬時にその効果が消
滅してしまうことは無いが,水洗を多数回行うと帯電防
止効果が減少する傾向がある。そこで,本発明者らは使
用用途の大きな汎用樹脂であるポリオレフイン系樹脂や
ポリスチレン系樹脂について,耐水洗性に優れた着色可
能な導電性(帯電防止性)樹脂の開発を検討したのであ
る。[Problem to be solved by the invention] However, in recent years, there has been an increase in the number of cases in which a water-washing process is adopted for IC packaging supplies, which is one of the applications of the above products, and as a result, molded products using antistatic agents, etc. After washing with water, the antistatic effect does not disappear instantly, but the antistatic effect tends to decrease if washing is repeated many times. Therefore, the present inventors investigated the development of colorable conductive (antistatic) resins with excellent water wash resistance for polyolefin resins and polystyrene resins, which are general-purpose resins with a wide range of uses.
【0006】[0006]
【課題を解決するための手段】上記目的を達成するため
に,本発明は(A)ポリオレフイン系樹脂及び/又はポ
リスチレン系樹脂100重量部(以後,部と略)に対し
て,(B)周期律表第▲1▼族及び/又は第▲2▼族の
金属及び/又は金属塩のうち1種もしくは2種以上を0
.01〜15部,(C)多価アルコール系化合物を0.
5〜20部,(D)ポリアミド系樹脂2〜90部以上,
(B),(C)及び(D)の3成分を(A)成分に配合
することを特徴とする耐水洗帯電防止性樹脂組成物であ
る。[Means for Solving the Problems] In order to achieve the above object, the present invention provides (A) a polyolefin resin and/or a polystyrene resin with a period of 0 of the metals and/or metal salts of group ▲1▼ and/or group ▲2▼ of the Table of Laws
.. 01 to 15 parts, (C) 0.01 to 15 parts of polyhydric alcohol compound.
5 to 20 parts, (D) 2 to 90 parts or more of polyamide resin,
This is a wash-resistant and antistatic resin composition characterized by blending three components (B), (C), and (D) into component (A).
【0007】本発明に用いる(A)成分の熱可塑性樹脂
としては,ポリオレフイン系樹脂及びポリスチレン系樹
脂を使用する。そして詳しくはポリオレフイン系樹脂で
は,直鎖状ポリエチレン,高圧ポリエチレン,ポリプロ
ピレン,エチレンとα−オレフインの共重合体,エチレ
ン酢酸ビニル共重合体,エチレン・エチルアクリレート
共重合体,アイオノマー,ポリブテン,ポリメチルペン
テン等が挙げられる。[0007] As the thermoplastic resin of component (A) used in the present invention, polyolefin resins and polystyrene resins are used. In detail, polyolefin resins include linear polyethylene, high-pressure polyethylene, polypropylene, copolymers of ethylene and α-olefin, ethylene-vinyl acetate copolymers, ethylene-ethyl acrylate copolymers, ionomers, polybutene, and polymethylpentene. etc.
【0008】又,ポリスチレン系樹脂としては,ポリス
チレン,ハイインパクト・ポリスチレン,AS樹脂,A
BS樹脂,スチレン無水マレイン酸共重合体等が挙げら
れる。尚,(A)成分の樹脂は単独でも,2種以上を混
合して使用しても良い。[0008] Polystyrene resins include polystyrene, high impact polystyrene, AS resin, A
Examples include BS resin, styrene maleic anhydride copolymer, and the like. Note that the resin as component (A) may be used alone or in combination of two or more.
【0009】(B)成分の周期律表第▲1▼族及び第▲
2▼族の金属としては,リチウム,ナトリウム,カリウ
ム,ベリウム,カルシウム,マグネシウム,アルミニウ
ム等が挙げられる。又,第▲1▼族及び第▲2▼族の金
属塩としては,ハロゲン化物,過塩素酸塩,過臭素酸塩
,塩素酸塩,臭素酸塩,チオシアン酸塩,硝酸塩,硫酸
塩,燐酸塩,脂肪酸塩等が挙げられ,具体的な化合物と
しては,チオシアン酸カリウム,チオシアン酸ナトリウ
ム,チオシアン酸リチウム,硫酸リチウム,ステアリン
酸リチウム,塩化リチウム,過塩素酸リチウム等が挙げ
られる。(B) Groups ▲1▼ and ▲ of the periodic table of components
Examples of group 2▼ metals include lithium, sodium, potassium, beryum, calcium, magnesium, and aluminum. In addition, metal salts of groups ▲1▼ and ▲2▼ include halides, perchlorates, perbromates, chlorates, bromates, thiocyanates, nitrates, sulfates, and phosphoric acids. salts, fatty acid salts, etc., and specific compounds include potassium thiocyanate, sodium thiocyanate, lithium thiocyanate, lithium sulfate, lithium stearate, lithium chloride, lithium perchlorate, and the like.
【0010】(C)成分の多価アルコール系化合物とし
ては,ポリエチレングリコール,ポリプロピレングリコ
ール,グリセリン,ポリビニルアルコール,ソルビトー
ル等及びこれらの誘導体が挙げられる。(D)成分のポ
リアミド系樹脂としては,6−ナイロン,66−ナイロ
ン,12−ナイロン,6−ナイロン系エラストマー,1
2−ナイロン系エラストマー等が挙げられる。特に,本
発明では,(C)成分と(D)成分の配合により,(B
)成分が(A)成分樹脂への分散が極めて良好となり,
このため導電性が著しく向上する。Examples of the polyhydric alcohol compound (C) include polyethylene glycol, polypropylene glycol, glycerin, polyvinyl alcohol, sorbitol, and derivatives thereof. The polyamide resin of component (D) includes 6-nylon, 66-nylon, 12-nylon, 6-nylon elastomer, 1
Examples include 2-nylon elastomer. In particular, in the present invention, by blending component (C) and component (D), (B
) component is extremely well dispersed in component (A) resin,
Therefore, the conductivity is significantly improved.
【0011】本発明では,(A)成分の樹脂100重量
部に対して,(B)成分の周期律表第▲1▼族及び/又
は第▲2▼族の金属及び/又はその金属塩のうち1種も
しくは2種以上を0.01〜15部配合する。この際に
,(B)成分の使用量が0.01部より少ないと,十分
な導電性効果が得られず好ましくない。一方,15部よ
り多く配合しても,導電性効果は特に向上せず,むしろ
樹脂組成物の機械的物性が低下して好ましくない。尚,
特に好ましくは(B)成分が0.1〜10部のときに電
気的物性及び成形性のバランスが特に良好であり好まし
い。In the present invention, a metal of group (1) and/or group (2) of the periodic table as component (B) and/or a metal salt thereof is added to 100 parts by weight of the resin as component (A). 0.01 to 15 parts of one or more of these are blended. In this case, if the amount of component (B) used is less than 0.01 part, a sufficient conductive effect cannot be obtained, which is not preferable. On the other hand, if more than 15 parts are added, the conductivity effect will not be particularly improved, but rather the mechanical properties of the resin composition will deteriorate, which is not preferable. still,
Particularly preferably, component (B) is contained in an amount of 0.1 to 10 parts because the balance between electrical properties and moldability is particularly good.
【0012】(C)成分の多価アルコールは,0.5〜
20部を配合する。(C)成分の使用量が0.5部より
少ないと,(B)成分の(A)成分の樹脂中への分散性
が向上せず,優れた導電性が得られず好ましくない。一
方,(C)成分を20部より配合しても,(B)成分の
分散性及び導電性は特には向上せず,むしろ組成物の機
械的物性が低下して好ましくない。(D)成分のポリア
ミド系樹脂は2〜90部配合する。この際に(D)成分
の使用量が2部より少ないと,本発明の最大特徴である
優れた耐水洗性が得られず好ましくない。一方,(D)
成分を90部より多く配合しても耐水洗性は向上せず得
られる製品がコスト高になり好ましくない。本発明の耐
水洗帯電防止性樹脂組成物の製造法には,特別な制限は
なく通常の方法で,各種添加剤を配合しても良い。[0012] The polyhydric alcohol of component (C) has a content of 0.5 to
Blend 20 parts. If the amount of component (C) used is less than 0.5 parts, the dispersibility of component (B) into the resin of component (A) will not improve, and excellent conductivity will not be obtained, which is not preferable. On the other hand, even if 20 parts of component (C) is added, the dispersibility and conductivity of component (B) are not particularly improved, and the mechanical properties of the composition are rather deteriorated, which is not preferable. Component (D), a polyamide resin, is blended in an amount of 2 to 90 parts. In this case, if the amount of component (D) used is less than 2 parts, it is not preferable because the excellent water wash resistance, which is the most important feature of the present invention, cannot be obtained. On the other hand, (D)
Even if more than 90 parts of the ingredients are blended, the water wash resistance will not improve and the resulting product will be expensive, which is not preferable. There are no particular restrictions on the method for producing the water-washable, antistatic resin composition of the present invention, and various additives may be added using conventional methods.
【0013】本発明の組成物を着色する際に使用する染
顔料は,従来より使用されているものであれば,どれで
も良い。そして染顔料の易分散化の目的で脂肪酸,脂肪
酸金属塩,低分子量ポリマー,脂肪酸ワックス等を配合
しても良い。又,必要により他の添加剤,例えば酸化防
止剤,光劣化防止剤,可塑剤,滑剤,相溶化剤,難燃剤
,核剤等を適当な時点で配合することも可能である。
他にフイラーや充填剤として,ガラスフアイバー,カー
ボンブラック,シリカ,炭酸カルシウム,ケイ酸カルシ
ウム,チタン酸カリウム,ウオラスナイト等を任意に使
用しても良い。以下に実施例及び比較例を述べる[0013] Any dye or pigment used in coloring the composition of the present invention may be used as long as it is conventionally used. For the purpose of easily dispersing the dye and pigment, fatty acids, fatty acid metal salts, low molecular weight polymers, fatty acid waxes, etc. may be added. Further, if necessary, other additives such as antioxidants, photodegradation inhibitors, plasticizers, lubricants, compatibilizers, flame retardants, nucleating agents, etc. can be added at an appropriate time. Other fillers or fillers that may be used include glass fiber, carbon black, silica, calcium carbonate, calcium silicate, potassium titanate, and walrus night. Examples and comparative examples are described below.
【00
14】実施例1
(A)粉末状のポリスチレン樹脂
100部(B)チオシアン酸カリウム
5部(C)グリセリン
3部(D)
粉末状の6−ナイロン
10部以上,4成分をヘンシエルミキサーを使用
して配合し,その後単軸押出機を用いて混練押し出し,
本発明の耐水洗帯電防止性樹脂組成物のペレットを得る
。次いで,上記ペレットを使用して射出成形機により,
40×40×2mmの試験用試料を作成する。以後,実
施例1と同様な方法により,実施例2〜4,及び比較例
1〜2についても行う。以後,その際に使用する(A)
,(B),(C)及び(D)成分の配合割合のみを示す
。00
14] Example 1 (A) Powdered polystyrene resin
100 parts (B) Potassium thiocyanate
Part 5 (C) Glycerin
Part 3 (D)
Powdered 6-nylon
10 parts or more of 4 ingredients are blended using a Henschel mixer, then kneaded and extruded using a single screw extruder,
Pellets of the washable and antistatic resin composition of the present invention are obtained. Next, using an injection molding machine using the above pellets,
A test sample of 40 x 40 x 2 mm is prepared. Thereafter, Examples 2 to 4 and Comparative Examples 1 to 2 are also conducted in the same manner as in Example 1. From now on, use (A)
, (B), (C) and (D) components only.
【0015】実施例2
(A)粉末状のポリスチレン樹脂
100部(B)NaI
5部(C)グリセ
リン
3部(D)粉末状の12−ナイロン系エラストマー
5部実施例3
(A)粉末状のABS樹脂
100部(B)チオシアン酸カリウム
3部(C)グリセリンモノ
ステアレート 6部(D)粉末
状の6−ナイロン
10部実施例4
(A)粉末状のポリプロピレン樹脂
100部(B)チオシアン酸カリウム
5部(C)デカポリグリセリン
9部(D)
粉末状の6−ナイロン
20部Example 2 (A) Powdered polystyrene resin
100 copies (B) NaI
Part 5 (C) Glycerin
3 parts (D) Powdered 12-nylon elastomer 5 parts Example 3 (A) Powdered ABS resin
100 parts (B) Potassium thiocyanate
3 parts (C) Glycerin monostearate 6 parts (D) Powdered 6-nylon
10 parts Example 4 (A) Powdered polypropylene resin
100 parts (B) Potassium thiocyanate
5 parts (C) decapolyglycerin 9 parts (D)
Powdered 6-nylon
20 copies
【0016】比較例1
(A)粉末状のポリスチレン樹脂
100部(B)KI
5部(C)グリ
セリン
3部(D)粉末状の6−ナイロン
1部比較例2
(A)粉末状の高密度ポリエチレン樹脂 1
00部(B)NaI
8部(C)グリセリ
ン
7部(D)粉末状の6−ナイロン
0.5部Comparative Example 1 (A) Powdered polystyrene resin
100 copies (B) KI
Part 5 (C) Glycerin
3 parts (D) Powdered 6-nylon
1 part Comparative Example 2 (A) Powdered high-density polyethylene resin 1
00 parts (B) NaI
Part 8 (C) Glycerin
7 parts (D) Powdered 6-nylon
0.5 part
【0017】次ぎに実施例1
〜4,及び比較例1〜2で得られた各試料について,下
記の(イ)の試験法で測定し,その結果をNext, Example 1
~4, and each sample obtained in Comparative Examples 1 and 2, was measured using the test method in (a) below, and the results were
【表1】
に示す。
(イ)半減期の測定
試料を水道水で洗浄する,その際の洗浄は1分間を1回
として毎回ガーゼで表面の付着水分を取り除き,温度2
3℃,相対湿度55%の雰囲気下で測定する。尚,測定
には宍戸商会製スタチックオネストメーターを使用し,
帯電圧減衰時間(半減期)を測定する。評価の基準は,
半減期2秒未満……帯電防止効果は良好,半減期2秒以
上……帯電防止効果は不良。It is shown in [Table 1]. (b) Wash the half-life measurement sample with tap water. Wash the sample for 1 minute each time, remove the moisture on the surface with gauze, and
Measured in an atmosphere of 3°C and 55% relative humidity. In addition, a static honest meter manufactured by Shishido Shokai was used for the measurement.
Measure the charged voltage decay time (half-life). The evaluation criteria are:
Half-life less than 2 seconds...The antistatic effect is good; half-life 2 seconds or more...The antistatic effect is poor.
【0018】[0018]
【表1】[Table 1]
【0019】[0019]
【発明の効果】本発明品は,(A)成分に(B)成分と
(C)成分のみを使用したものよりも帯電防止機能が向
上する。特に,[Effects of the Invention] The product of the present invention has improved antistatic function compared to a product using only components (B) and (C) in addition to component (A). especially,
【表1】でも示すように成形品の耐水洗性が著しく向上
し,水洗回数が50回となっても半減期の変化が殆ど見
られず優れた導電性を保持安定していることを示してい
る。 これは(D)成分のポリアミド系樹脂を配合する
ことにより,(B)成分と(C)成分の(A)成分に対
する親和性を増し,これにより水洗による(B)成分と
(C)成分の溶出を押えている,又,ポリアミド基によ
る吸水性も寄与しているのである。As shown in [Table 1], the washing resistance of the molded product has significantly improved, and even after washing 50 times, there is almost no change in half-life, indicating that it maintains excellent conductivity and remains stable. ing. By blending the polyamide resin of the (D) component, the affinity of the (B) and (C) components for the (A) component is increased. This suppresses elution, and the water absorbing properties of the polyamide group also contribute.
【0020】この性質は,IC用トレー,マガジン等の
帯電防止製品や,半導体関係製品の収納容器等の水洗を
必要とする製品について,水洗後も同じ機能(帯電防止
性)を有し,半永久的な耐水洗性を保持するものである
。もちろん得られる成形品は,着色剤を配合することで
,任意に着色可能でありカラフルな成形品を容易に製造
できる。This property means that antistatic products such as IC trays and magazines, and products that require washing with water, such as storage containers for semiconductor-related products, retain the same function (antistatic property) even after washing with water, and are semi-permanent. It maintains water wash resistance. Of course, the resulting molded product can be colored as desired by adding a coloring agent, making it easy to produce colorful molded products.
Claims (1)
はポリスチレン系樹脂100重量部に対して,(B)周
期律表第▲1▼族及び/又は第▲2▼族の金属及び/又
はその金属塩のうち1種もしくは2種以上を0.01〜
15重量部,(C)多価アルコール系化合物を0.5〜
20重量部,(D)ポリアミド系樹脂2〜90重量部,
以上(B),(C)及び(D)の3成分を配合すること
を特徴とする耐水洗帯電防止性樹脂組成物。Claim 1: Based on 100 parts by weight of (A) polyolefin resin and/or polystyrene resin, (B) metal of group (1) and/or group (2) of the periodic table and/or the metal thereof. One or more types of salt from 0.01 to
15 parts by weight, (C) 0.5 to 0.5 parts by weight of polyhydric alcohol compound
20 parts by weight, (D) 2 to 90 parts by weight of polyamide resin,
A washable and antistatic resin composition characterized by blending the above three components (B), (C), and (D).
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3031326A JPH04246442A (en) | 1991-02-01 | 1991-02-01 | Antistatic resin composition resistant against water washing |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3031326A JPH04246442A (en) | 1991-02-01 | 1991-02-01 | Antistatic resin composition resistant against water washing |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH04246442A true JPH04246442A (en) | 1992-09-02 |
Family
ID=12328141
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP3031326A Pending JPH04246442A (en) | 1991-02-01 | 1991-02-01 | Antistatic resin composition resistant against water washing |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH04246442A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH06313078A (en) * | 1993-03-03 | 1994-11-08 | Sanyo Chem Ind Ltd | Resin composition |
-
1991
- 1991-02-01 JP JP3031326A patent/JPH04246442A/en active Pending
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH06313078A (en) * | 1993-03-03 | 1994-11-08 | Sanyo Chem Ind Ltd | Resin composition |
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