JPS5938982B2 - Methacrylic resin composition with excellent antistatic properties - Google Patents
Methacrylic resin composition with excellent antistatic propertiesInfo
- Publication number
- JPS5938982B2 JPS5938982B2 JP2897577A JP2897577A JPS5938982B2 JP S5938982 B2 JPS5938982 B2 JP S5938982B2 JP 2897577 A JP2897577 A JP 2897577A JP 2897577 A JP2897577 A JP 2897577A JP S5938982 B2 JPS5938982 B2 JP S5938982B2
- Authority
- JP
- Japan
- Prior art keywords
- methacrylic resin
- weight
- parts
- resin composition
- acid monoglyceride
- 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
Links
- 239000000113 methacrylic resin Substances 0.000 title claims description 30
- 239000000203 mixture Substances 0.000 title claims description 17
- 229920001577 copolymer Polymers 0.000 claims description 16
- LDVVTQMJQSCDMK-UHFFFAOYSA-N 1,3-dihydroxypropan-2-yl formate Chemical compound OCC(CO)OC=O LDVVTQMJQSCDMK-UHFFFAOYSA-N 0.000 claims description 12
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 12
- 229930195729 fatty acid Natural products 0.000 claims description 12
- 239000000194 fatty acid Substances 0.000 claims description 12
- 150000004665 fatty acids Chemical class 0.000 claims description 11
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 10
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 7
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 5
- 229910052783 alkali metal Inorganic materials 0.000 claims description 5
- -1 alkali metal salt Chemical class 0.000 claims description 5
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 238000000465 moulding Methods 0.000 description 5
- 239000008188 pellet Substances 0.000 description 5
- 239000000654 additive Substances 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- LLLCSBYSPJHDJX-UHFFFAOYSA-M potassium;2-methylprop-2-enoate Chemical compound [K+].CC(=C)C([O-])=O LLLCSBYSPJHDJX-UHFFFAOYSA-M 0.000 description 4
- RZRNAYUHWVFMIP-KTKRTIGZSA-N 1-oleoylglycerol Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(O)CO RZRNAYUHWVFMIP-KTKRTIGZSA-N 0.000 description 3
- 238000001746 injection moulding Methods 0.000 description 3
- 238000004898 kneading Methods 0.000 description 3
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- 229920000297 Rayon Polymers 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 239000002216 antistatic agent Substances 0.000 description 2
- VBICKXHEKHSIBG-UHFFFAOYSA-N beta-monoglyceryl stearate Natural products CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 125000005395 methacrylic acid group Chemical group 0.000 description 2
- RZRNAYUHWVFMIP-UHFFFAOYSA-N monoelaidin Natural products CCCCCCCCC=CCCCCCCCC(=O)OCC(O)CO RZRNAYUHWVFMIP-UHFFFAOYSA-N 0.000 description 2
- UTOPWMOLSKOLTQ-UHFFFAOYSA-N octacosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCC(O)=O UTOPWMOLSKOLTQ-UHFFFAOYSA-N 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- SONHXMAHPHADTF-UHFFFAOYSA-M sodium;2-methylprop-2-enoate Chemical compound [Na+].CC(=C)C([O-])=O SONHXMAHPHADTF-UHFFFAOYSA-M 0.000 description 2
- 230000003068 static effect Effects 0.000 description 2
- DMBUODUULYCPAK-UHFFFAOYSA-N 1,3-bis(docosanoyloxy)propan-2-yl docosanoate Chemical compound CCCCCCCCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCCCCCC DMBUODUULYCPAK-UHFFFAOYSA-N 0.000 description 1
- WECGLUPZRHILCT-GSNKCQISSA-N 1-linoleoyl-sn-glycerol Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(=O)OC[C@@H](O)CO WECGLUPZRHILCT-GSNKCQISSA-N 0.000 description 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
- WDQMWEYDKDCEHT-UHFFFAOYSA-N 2-ethylhexyl 2-methylprop-2-enoate Chemical compound CCCCC(CC)COC(=O)C(C)=C WDQMWEYDKDCEHT-UHFFFAOYSA-N 0.000 description 1
- VAPQAGMSICPBKJ-UHFFFAOYSA-N 2-nitroacridine Chemical compound C1=CC=CC2=CC3=CC([N+](=O)[O-])=CC=C3N=C21 VAPQAGMSICPBKJ-UHFFFAOYSA-N 0.000 description 1
- 229920005506 ACRYPET® MD Polymers 0.000 description 1
- 229920005497 Acrypet® Polymers 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- PVNIQBQSYATKKL-UHFFFAOYSA-N Glycerol trihexadecanoate Natural products CCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCC PVNIQBQSYATKKL-UHFFFAOYSA-N 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
- ARIWANIATODDMH-UHFFFAOYSA-N Lauric acid monoglyceride Natural products CCCCCCCCCCCC(=O)OCC(O)CO ARIWANIATODDMH-UHFFFAOYSA-N 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- DCBSHORRWZKAKO-UHFFFAOYSA-N alpha-glycerol monomyristate Natural products CCCCCCCCCCCCCC(=O)OCC(O)CO DCBSHORRWZKAKO-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 238000005034 decoration Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000005453 pelletization Methods 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- ZLMJMSJWJFRBEC-OUBTZVSYSA-N potassium-40 Chemical compound [40K] ZLMJMSJWJFRBEC-OUBTZVSYSA-N 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Description
【発明の詳細な説明】
本発明は、帯電防止性に優れたメタクリル樹脂組成物に
関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a methacrylic resin composition with excellent antistatic properties.
メタクリル樹脂は、その卓越した透明性、良好な機械的
性質、加工性並びに成形品の美麗さによつて照明器具、
看板、各種装飾品および銘板などに広く使用されている
が、その表面固有抵抗が非常に高いために、接触または
摩擦等で誘起された静電気が逃散、消失しにくく、その
ため使用中の樹脂表面にほこり等が付着して汚れ易く、
美しい外観を損う結果となつている。Methacrylic resin is used in lighting equipment, due to its excellent transparency, good mechanical properties, processability, and beautiful molded products.
It is widely used for signboards, various decorations, and nameplates, etc., but because its surface resistivity is extremely high, static electricity induced by contact or friction is difficult to dissipate and disappear, so the resin surface during use is Easy to get dirty due to dust etc.
This results in spoiling the beautiful appearance.
従来、合成樹脂に帯電防止性を付与する方法として、界
面活性剤類、多価アルコールの脂肪酸エステル等を添加
して練込する添加練込法が数多く提案されているが、メ
タクリル樹脂にこれらを適用する場合、ほとんど効果を
示さないか、成形加工条件が制約されるか、もしくは成
形品に外観上の欠陥が発生し、もし帯電防止性能が付与
されたとしても、メタクリル樹脂特有の無色透明性、表
面光沢の良さが著しく減じ、実用に供し得ない。Conventionally, as a method of imparting antistatic properties to synthetic resins, many additive kneading methods have been proposed in which surfactants, fatty acid esters of polyhydric alcohols, etc. are added and kneaded. When applied, there is little effect, the molding conditions are restricted, or defects in the appearance of the molded product occur, and even if antistatic performance is imparted, the colorless transparency characteristic of methacrylic resin , the quality of the surface gloss is significantly reduced and it cannot be put to practical use.
そこで、本発明者は上記の欠点を除去するため、先にメ
タクリル樹脂に高級脂肪酸モノグリセラードを添加して
帯電防止性能を付与する方法として、高級脂肪酸モノグ
リセラードの一部を懸濁重合時のモノマーに溶解し、さ
らにその残量部を賦形時に混合する方法を提案した。し
かしながら、このような方法を採用することにより、優
れた帯電防止性能を付与できるが、メタクリル樹脂に対
して多量添加することが必要であり、この添加量では、
ややもすればメタクリル樹脂のもつ本来の物性値を低下
させたり、また過剰の滑性による押出成形時のトラブル
をもたらす等の欠点を有していた。Therefore, in order to eliminate the above-mentioned drawbacks, the present inventor proposed a method of first adding higher fatty acid monoglyceride to a methacrylic resin to impart antistatic properties. We proposed a method in which the remaining amount is mixed with the monomer during molding. However, by adopting such a method, excellent antistatic performance can be imparted, but it is necessary to add a large amount to the methacrylic resin, and with this addition amount,
However, they have disadvantages such as lowering the original physical properties of the methacrylic resin and causing problems during extrusion molding due to excessive slipperiness.
本発明者らは、これらの欠点をさらに改良すべく鋭意検
討を行なつた結果、特殊の組成物を形成させることによ
り、これらの欠点が一挙に解決できることを兄い出し本
発明を完成した。The present inventors conducted intensive studies to further improve these drawbacks, and as a result, they discovered that these drawbacks could be solved all at once by forming a special composition, and completed the present invention.
即ち、本発明の要旨とするところは、メタクリル樹脂〔
A〕100重量部と、メタクリル酸及び/又はアクリル
酸のアルカリ金属塩30〜90重量%とメタクリル酸メ
チル70〜10重量%とからなる共重合体〔B〕0.0
3〜2.0重量と、炭素数8〜22の高級脂肪酸モノグ
リセラード〔C〕2〜6重量部とよりなる帯電防止性の
優れたメタクリル樹脂組成物にある。That is, the gist of the present invention is that methacrylic resin [
Copolymer consisting of 100 parts by weight of A], 30 to 90% by weight of an alkali metal salt of methacrylic acid and/or acrylic acid, and 70 to 10% by weight of methyl methacrylate [B] 0.0
3 to 2.0 parts by weight and 2 to 6 parts by weight of higher fatty acid monoglycerade [C] having 8 to 22 carbon atoms, and has excellent antistatic properties.
本発明において用いられるメタクリル樹脂〔A〕は、メ
タクリル酸メチル単独重合体もしくはメタクリル酸メチ
ルと他の共重合可能な単量体との共重合体である。The methacrylic resin [A] used in the present invention is a methyl methacrylate homopolymer or a copolymer of methyl methacrylate and another copolymerizable monomer.
この共重合体を製するに用いられる他の共重合可能な単
量体としては、特に限定されないが、本発明においては
、炭素数1〜10のアルキル基をもつアクリル酸エステ
ルもしくは炭素数2〜10のアルキル基をもつメタアク
リル酸エステル、例えばアクリル酸メチル、アクリル酸
エチル、アクリル酸ブチル、アクリル酸2一エチルヘキ
シル、メタクリル酸エチル、メタクリル酸ブチル、メタ
クリル酸2−エチルヘキシル等が好ましい例として挙げ
られる。これらは1種もしくは2種以上を用いて、メタ
アクリル酸メチルとの混合物中20重量%まで使用する
ことができる。本発明の実施に際して用いられるメタク
リル酸及び/又はアクリル酸のアルカリ金属塩とメタア
クリル酸メチルとからなる共重合体〔B〕(以T1(メ
タ)アクリル酸塩共重合体〔B〕という)はメタクリル
酸及び/又はアクリル酸をリチウム、ナトリウム及びカ
リウム等のアルカリ金属で置換した金属塩30〜90重
量%とメタクリル酸メチル70〜10重量%とを重合さ
せることにより得られる共重合体である。Other copolymerizable monomers used to produce this copolymer are not particularly limited, but in the present invention, acrylic esters having an alkyl group having 1 to 10 carbon atoms or acrylic esters having 2 to 10 carbon atoms are used. Preferred examples include methacrylic esters having 10 alkyl groups, such as methyl acrylate, ethyl acrylate, butyl acrylate, 2-ethylhexyl acrylate, ethyl methacrylate, butyl methacrylate, and 2-ethylhexyl methacrylate. . One or more of these can be used in a mixture with methyl methacrylate up to 20% by weight. The copolymer [B] consisting of an alkali metal salt of methacrylic acid and/or acrylic acid and methyl methacrylate (hereinafter referred to as T1 (meth)acrylate copolymer [B]) used in carrying out the present invention is It is a copolymer obtained by polymerizing 30 to 90% by weight of a metal salt obtained by substituting methacrylic acid and/or acrylic acid with an alkali metal such as lithium, sodium, and potassium, and 70 to 10% by weight of methyl methacrylate.
この(メタ)アクリル酸塩共重合体〔B〕において、メ
タクリル酸及び/又はアクリル酸のアルカリ金属塩の量
が30重量%未満の場合はメタクリル樹脂との親和性が
良くなりすぎ、表面移行性が悪くなり、帯電防止効果が
低丁する点で好ましくなく、またその量が90重量%を
こえる場合には、逆にメタクリル樹脂との親和性が悪く
なり、成形品の表面光沢および透明性が低下する点で好
ましくない。また本発明において用いられる高級脂肪酸
モノグリセラード〔C〕としては、グリセリンと炭素数
8〜22の高級脂肪酸とのモノエステル化物であつて、
例えばラウリン酸モノグリセラード、ミリスチン酸モノ
グリセラード、バルミチン酸モノグリセラード、オレイ
ン酸モノグリセラード、ステアリン酸モノグリセラード
、モンタン酸モノグリセラード、リノール酸モノグリセ
ラード及びベヘン酸モノグリセラードが好ましい例とし
てあげられる。In this (meth)acrylate copolymer [B], if the amount of the alkali metal salt of methacrylic acid and/or acrylic acid is less than 30% by weight, the affinity with the methacrylic resin becomes too good, resulting in surface migration. If the amount exceeds 90% by weight, the compatibility with methacrylic resin will deteriorate and the surface gloss and transparency of the molded product will deteriorate. This is not preferable in that it causes a decrease in the temperature. Further, the higher fatty acid monoglycerade [C] used in the present invention is a monoester of glycerin and a higher fatty acid having 8 to 22 carbon atoms,
For example, lauric acid monoglyceride, myristic acid monoglyceride, valmitic acid monoglyceride, oleic acid monoglyceride, stearic acid monoglyceride, montanic acid monoglyceride, linoleic acid monoglyceride and behenic acid monoglyceride are preferred. This can be given as an example.
これらは単独でまた必要に応じて2種以上を混合して用
いることもできる。メタクリル樹脂組成物中の(メタ)
アクリル酸塩共重合体〔B〕と高級脂肪酸モノグリセラ
ード〔C〕との併用は、単に両者の加成性を示すのでは
なく、両者を併用することによつて、メタクリル樹脂の
帯電防止性能への相乗効果が認められ、帯電防止剤の全
添加量を著しく減することが可能となる。These can be used alone or in combination of two or more types if necessary. (meth) in methacrylic resin composition
The combined use of acrylate copolymer [B] and higher fatty acid monoglyceride [C] does not simply show the additivity of both, but also improves the antistatic performance of methacrylic resin by using both together. A synergistic effect on the antistatic agent was observed, making it possible to significantly reduce the total amount of antistatic agent added.
また、(メタ)アクリル酸塩共重合体〔B〕はメタクリ
ル酸エステルの懸濁重合の分散安定剤として使用される
ものであり、一方高級脂肪酸モノグリセラード〔C〕は
、メタクリル樹脂の滑剤として有用なものであるから、
得られたメタクリル樹脂組成物の耐熱性が良く、さらに
通常の成形温度(180℃〜260良C)での成形加工
においても、従来のメタクリル樹脂成形品と何ら変らな
い無色透明の成形品をうることができる。In addition, (meth)acrylate copolymer [B] is used as a dispersion stabilizer for suspension polymerization of methacrylic acid ester, while higher fatty acid monoglyceride [C] is used as a lubricant for methacrylic resin. Because it is useful,
The resulting methacrylic resin composition has good heat resistance, and even when molded at normal molding temperatures (180°C to 260°C), colorless and transparent molded products that are no different from conventional methacrylic resin molded products can be obtained. be able to.
本組成物中の(メタ)アタリル酸塩共重合体〔B〕及び
高級脂肪酸モノグリセラード〔C〕の使用割合はメタク
リル樹脂〔A〕100重量部に対して、前記共重合体〔
B〕が0.03〜2.0重量部、好ましくは0.0〜1
.5重量部であり、また高級脂肪酸モノグリセラード〔
C〕が2〜6重量部、好ましくは3〜5重量部である。The ratio of the (meth)acrylate copolymer [B] and higher fatty acid monoglyceride [C] in this composition is based on 100 parts by weight of the methacrylic resin [A].
B] is 0.03 to 2.0 parts by weight, preferably 0.0 to 1 part by weight.
.. 5 parts by weight, and higher fatty acid monoglyceride [
C] is 2 to 6 parts by weight, preferably 3 to 5 parts by weight.
メタクリル樹脂組成物中、(メタ)アクリル酸塩共重合
体〔B〕がメタクリル樹脂〔A〕100重量部に対して
、0.03重量部未満の場合には帯電防止効果がなく、
また一方その添加量が2重量部をこえる場合には成形品
の透明性を著しく損い、かつ成形加工条件の制約を受け
実用性を受け実用性に乏しくなるので好ましくない。ま
た、メタクリル樹脂組成物中、高級脂肪酸モノグリセラ
ード〔C〕がメタクリル樹脂〔A〕100重量部に対し
て、2重量%未満では、実質な帯電防止効果はなく、ま
た6重量部をこえると、賦形時の押出条件巾が狭くなり
、成形加工性の低下をきたすのみならず、メタクリル樹
脂の物性をも低下させるので好ましくない。In the methacrylic resin composition, if the (meth)acrylate copolymer [B] is less than 0.03 parts by weight based on 100 parts by weight of the methacrylic resin [A], there is no antistatic effect;
On the other hand, if the amount added exceeds 2 parts by weight, the transparency of the molded product will be significantly impaired and the practicality will be poor due to restrictions on molding processing conditions, which is not preferable. In addition, if the higher fatty acid monoglyceride [C] in the methacrylic resin composition is less than 2% by weight based on 100 parts by weight of the methacrylic resin [A], there is no substantial antistatic effect, and if it exceeds 6 parts by weight, This is not preferable because the extrusion condition width during shaping becomes narrower, which not only causes a decrease in molding processability but also deteriorates the physical properties of the methacrylic resin.
本発明に係る帯電防止性能を有するメタクリル樹脂組成
物は、(メタ)アクリル酸塩共重合体〔B〕と高級脂肪
酸モノグリセラード〔C〕とをメタクリル樹脂粉末に添
加混合し、押出機を通してペレツト化して製造されるか
、あるいは前記添加物を直接メタクリル樹脂ペレツトに
添加混合して成形加工を行うか、もしくは前記添加物を
あらかじめモノマーに溶解混合し、重合せしめることに
よつて製造される。The methacrylic resin composition having antistatic properties according to the present invention is produced by adding and mixing a (meth)acrylate copolymer [B] and a higher fatty acid monoglyceride [C] to methacrylic resin powder, and pelletizing the mixture through an extruder. Alternatively, the additives may be directly added to and mixed with methacrylic resin pellets and molded, or the additives may be dissolved and mixed in monomers in advance and polymerized.
また、本発明において、もし必要あれば、組成物中に他
の添加剤例えば酸化防止剤、滑剤、紫外線吸収剤、可塑
剤及び各種の顔料を添加することもできる。In addition, in the present invention, other additives such as antioxidants, lubricants, ultraviolet absorbers, plasticizers, and various pigments may be added to the composition, if necessary.
本発明組成物によつて得られる成形品は計器のメーター
カバー、銘板、電気機器部品、水準器の外枠、その他高
級雑貨類等に用いられ、すぐれた帯電防止効果を発揮す
ることができる。Molded articles obtained from the composition of the present invention can be used for meter covers of instruments, name plates, electrical equipment parts, outer frames of spirit levels, and other high-end miscellaneous goods, and can exhibit excellent antistatic effects.
次に実施例により、本発明を更に詳しく説明するが、実
施例中部は重量部を、%は重量%を示す。Next, the present invention will be explained in more detail with reference to Examples, in which the middle part of the example indicates parts by weight, and % indicates weight %.
例1メタクリル樹脂(三菱し・イヨン株式会社製、商標
名「アクリペツトH」 )〔A1〕100部に対して、
メタクリル酸カリウム70%を含むメタクリル酸メチル
とメタクリル酸カリウムの共重合体〔B1〕とステアリ
ン酸モノグリセラード〔C1〕を第1表に示したような
割合で混合しこれを40φ押出機にて240′Cで混練
ペレツト化後、50z射出成形機によつて220℃で2
顛板(110×110mm)を作製した。Example 1 For 100 parts of methacrylic resin (manufactured by Mitsubishi Shiyo Corporation, trade name "Acrypet H") [A1],
A copolymer of methyl methacrylate and potassium methacrylate containing 70% potassium methacrylate [B1] and stearic acid monoglyceride [C1] were mixed in the proportions shown in Table 1, and this was mixed in a 40φ extruder. After kneading into pellets at 240'C, the pellets were kneaded at 220°C by a 50Z injection molding machine.
A crest plate (110 x 110 mm) was prepared.
成形板を射出成形後23℃、5001)湿度の恒温室に
3日間放置後、極超絶縁計SM−10型(東亜電波工業
製)にて、表面固有抵抗を測定した。またスタテイツク
オネストメータ一(宍戸商会製)にて電圧1万ボルトを
試料に印加後、印加電圧を零とし、帯電圧が半減するま
での時間を測定した。その結果を第1表に示す。例2
メタクリル樹脂(三菱レイヨン株式会社製、商標名[ア
クリペツトMD」)〔A2〕100部に対して、メタク
リル酸ナトリウム4001)を含むメタクリル酸メチル
とメタクリル酸ナトリウムの共重合体〔B2〕とパルミ
チン酸モノグリセラード〔C2〕を第2表に示すような
組成割合で混合し、これを40φ押出機にて220℃で
混練ペレツト化後、50z射出成形機によつて210℃
で2mm板(110×110mm)を作製した。After the molded plate was injection-molded, it was left in a constant temperature room at 23° C. and 5001°C humidity for 3 days, and then the surface resistivity was measured using a ultra-super megohmmeter SM-10 model (manufactured by Toa Denpa Kogyo). Further, after applying a voltage of 10,000 volts to the sample using a static honest meter (manufactured by Shishido Shokai), the applied voltage was reduced to zero, and the time until the charged voltage was halved was measured. The results are shown in Table 1. Example 2 Copolymer of methyl methacrylate and sodium methacrylate containing sodium methacrylate 4001) [B2] and palmitin per 100 parts of methacrylic resin (manufactured by Mitsubishi Rayon Co., Ltd., trade name [Acrypet MD]) [A2] Acid monoglyceride [C2] was mixed in the composition ratio shown in Table 2, kneaded into pellets at 220°C using a 40φ extruder, and then pelletized at 210°C using a 50Z injection molding machine.
A 2 mm plate (110 x 110 mm) was prepared.
得られた成形板を例1と同様にして表面固有抵抗と半減
期を測定した。結果を第2表に示す。例3
メタクリル樹脂(三菱レイヨン株式会社製、商標名「ア
クリペツトMF」)〔A3〕100部に対して、アクリ
ル酸カリウム30%、メタクリル酸カリウム30%、メ
タクリル酸メチル40%からなる共重合体〔B3〕とオ
レイン酸モノグリセラード〔C3〕を第3表に示すよう
な組成割合で混合し、これを40φ押出機にて210℃
で混練ペレツト化後、50z射出成形機によつて210
℃で2mm板(110×110mm)を作製した。The surface resistivity and half-life of the obtained molded plate were measured in the same manner as in Example 1. The results are shown in Table 2. Example 3 A copolymer consisting of 30% potassium acrylate, 30% potassium methacrylate, and 40% methyl methacrylate based on 100 parts of methacrylic resin (manufactured by Mitsubishi Rayon Co., Ltd., trade name "Acripet MF") [A3]. B3] and oleic acid monoglyceride [C3] were mixed in the composition ratio shown in Table 3, and the mixture was heated at 210°C in a 40φ extruder.
After kneading into pellets with 50z injection molding machine, 210
A 2 mm plate (110 x 110 mm) was prepared at °C.
Claims (1)
酸及び/又はアクリル酸のアルカリ金属塩30〜90重
量%とメタクリル酸メチル70〜10重量%とからなる
共重合体〔B〕0.03〜2.0重量部と、炭素数8〜
22の高級脂肪酸モノグリセラード〔C〕2〜6重量部
とよりなる帯電防止性の優れたメタクリル樹脂組成物。[Scope of Claims] 1. A copolymer [B] consisting of 100 parts by weight of methacrylic resin [A], 30-90% by weight of an alkali metal salt of methacrylic acid and/or acrylic acid, and 70-10% by weight of methyl methacrylate. ] 0.03 to 2.0 parts by weight and carbon number 8 to
A methacrylic resin composition having excellent antistatic properties and comprising 2 to 6 parts by weight of higher fatty acid monoglyceride [C] of No. 22.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2897577A JPS5938982B2 (en) | 1977-03-16 | 1977-03-16 | Methacrylic resin composition with excellent antistatic properties |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2897577A JPS5938982B2 (en) | 1977-03-16 | 1977-03-16 | Methacrylic resin composition with excellent antistatic properties |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS53113852A JPS53113852A (en) | 1978-10-04 |
| JPS5938982B2 true JPS5938982B2 (en) | 1984-09-20 |
Family
ID=12263412
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2897577A Expired JPS5938982B2 (en) | 1977-03-16 | 1977-03-16 | Methacrylic resin composition with excellent antistatic properties |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5938982B2 (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60175283U (en) * | 1984-05-01 | 1985-11-20 | 神明電機株式会社 | winning ball detector |
| JPS61177685U (en) * | 1985-04-24 | 1986-11-06 |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5912957A (en) * | 1982-07-15 | 1984-01-23 | Asahi Chem Ind Co Ltd | Antistatic methacrylic resin composition |
-
1977
- 1977-03-16 JP JP2897577A patent/JPS5938982B2/en not_active Expired
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60175283U (en) * | 1984-05-01 | 1985-11-20 | 神明電機株式会社 | winning ball detector |
| JPS61177685U (en) * | 1985-04-24 | 1986-11-06 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS53113852A (en) | 1978-10-04 |
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