JP5170735B2 - Plastic molded product - Google Patents
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- JP5170735B2 JP5170735B2 JP2007165850A JP2007165850A JP5170735B2 JP 5170735 B2 JP5170735 B2 JP 5170735B2 JP 2007165850 A JP2007165850 A JP 2007165850A JP 2007165850 A JP2007165850 A JP 2007165850A JP 5170735 B2 JP5170735 B2 JP 5170735B2
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- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 48
- 239000011347 resin Substances 0.000 claims description 35
- 229920005989 resin Polymers 0.000 claims description 35
- 239000002216 antistatic agent Substances 0.000 claims description 25
- 239000000377 silicon dioxide Substances 0.000 claims description 23
- 239000011342 resin composition Substances 0.000 claims description 17
- -1 polypropylene Polymers 0.000 claims description 13
- 229920013716 polyethylene resin Polymers 0.000 claims description 12
- 229920001155 polypropylene Polymers 0.000 claims description 10
- 239000004743 Polypropylene Substances 0.000 claims description 9
- 239000002245 particle Substances 0.000 claims description 6
- 235000013305 food Nutrition 0.000 description 24
- 230000000052 comparative effect Effects 0.000 description 9
- 239000000428 dust Substances 0.000 description 7
- 238000000465 moulding Methods 0.000 description 7
- 230000000694 effects Effects 0.000 description 6
- 238000002156 mixing Methods 0.000 description 6
- 238000011156 evaluation Methods 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- 238000000034 method Methods 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- 238000007542 hardness measurement Methods 0.000 description 3
- 239000011256 inorganic filler Substances 0.000 description 3
- 229910003475 inorganic filler Inorganic materials 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 239000002344 surface layer Substances 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 235000010724 Wisteria floribunda Nutrition 0.000 description 2
- 239000012792 core layer Substances 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- 230000002209 hydrophobic effect Effects 0.000 description 2
- 239000002440 industrial waste Substances 0.000 description 2
- 238000001746 injection moulding Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 230000003373 anti-fouling effect Effects 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 239000011162 core material Substances 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000003595 mist Substances 0.000 description 1
- 239000010705 motor oil Substances 0.000 description 1
- 239000002667 nucleating agent Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
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- Manufacture Of Macromolecular Shaped Articles (AREA)
Description
本発明は、たとえば、自動車部品、産業用コンテナ、食品用コンテナ、食品容器等の樹脂成形品に関する。 The present invention relates to resin molded products such as automobile parts, industrial containers, food containers, and food containers.
自動車部品、産業用コンテナ、食品用コンテナ、食品容器等には、ポリエチレン系樹脂やポリプロピレン系樹脂を主成分とする樹脂組成物からなる樹脂成形品が多用されている。
ポリエチレン系樹脂やポリプロピレン系樹脂は、表面硬度が2B〜4Bと、柔らかいため簡単にキズがつきやすい。
For automobile parts, industrial containers, food containers, food containers and the like, resin molded products made of a resin composition mainly composed of polyethylene resin or polypropylene resin are frequently used.
Polyethylene resins and polypropylene resins have a surface hardness of 2B to 4B and are soft and easily scratched.
そこで、自動車部品、産業用コンテナ、食品用コンテナ、食品容器等の樹脂成形品を成形するのにタルク等の無機充填材が配合されている樹脂組成物を用いて、樹脂成形品の表面硬度を上げるようにしている(特許文献1参照)。 Therefore, the surface hardness of the resin molded product is increased by using a resin composition containing an inorganic filler such as talc for molding resin molded products such as automobile parts, industrial containers, food containers and food containers. (See Patent Document 1).
一方、ポリエチレン樹脂やポリプロピレン樹脂は、親油性であるので、油性の物質が付着すると簡単には脱落しない。したがって、従来のポリエチレン系樹脂やポリプロピレン系樹脂を主成分とする樹脂組成物からなる樹脂成形品の場合、時間の経過とともに黒色の汚れが目立ってくるという問題がある。
この黒色の汚れは、排気ガス中のオイルミストとカーボン、空気中の粉塵(砂ぼこり、粘土類の微粉)等の空気中の浮遊物が、成形品の静電気により引き寄せられ付着することが原因である。
On the other hand, since polyethylene resin and polypropylene resin are oleophilic, they do not easily fall off when an oily substance adheres. Therefore, in the case of a resin molded product made of a resin composition containing a conventional polyethylene resin or polypropylene resin as a main component, there is a problem that black stains become conspicuous over time.
This black dirt is caused by airborne dust such as oil mist and carbon in the exhaust gas, dust in the air (dust dust, clay fines) attracted by the static electricity of the molded product. .
従来、上記のような汚れがあると、食品等のコンテナにおいては不潔に見えて使用できなくなる。また、自動車部品においては、自動車自体の価値が低下するという問題があった。
そこで、食品等のコンテナにおいては70℃〜80℃のお湯を使い、頻繁に洗浄し、目立った汚れをなくすようにしていたが、洗浄の際、ブラシ等で表面を摩擦して汚れを落とすため、上記のように無機充填材の配合によって表面硬度を上げていたとしても、やはり表面にキズが付き、その結果、キズに汚れが食い込む、より強い力で洗浄するとの悪循環を繰り返していた。
Conventionally, when there is dirt as described above, it looks unclean in a container such as food and cannot be used. In addition, there is a problem that the value of the automobile itself is lowered in the automobile parts.
Therefore, in containers for foods, hot water of 70 ° C to 80 ° C was used and washed frequently to eliminate noticeable dirt. However, when washing, the surface is rubbed with a brush to remove dirt. Even if the surface hardness was increased by the blending of the inorganic filler as described above, the surface was still scratched, and as a result, the scratch was contaminated, and the vicious cycle of washing with a stronger force was repeated.
他方、樹脂組成物中に帯電防止剤を配合することによって、樹脂成形品表面へのゴミ等の付着を防止する方法もある。
そして、帯電防止剤として樹脂に対して相溶性が悪いものを配合すれば、拭き取りや洗浄によって樹脂成形品表面の帯電防止剤が無くなると、樹脂成形品内側の帯電防止剤が表面側に移行して汚れの付着を防ぐことができる。
On the other hand, there is also a method for preventing adhesion of dust or the like to the surface of a resin molded product by blending an antistatic agent in the resin composition.
If an antistatic agent with poor compatibility with the resin is blended, the antistatic agent inside the resin molded product will move to the surface side when the antistatic agent on the surface of the resin molded product disappears due to wiping or washing. Can prevent the adhesion of dirt.
しかし、成形品内側の帯電防止剤がすべて消費されてしまうと、ゴミの付着防止効果がなくなってしまうため、長期間汚れの付着を防止するには、樹脂組成物中に帯電防止剤を多量に配合しておく必要があるが、樹脂組成物中に多量の帯電防止剤を配合させると、成形品表面がベタベタとなり、不潔感、不快感を抱かせる。そのため、多くの成形品は、約1年間の使用でしだいに付着したゴミが堆積し、汚れが濃くなるのが現状である。 However, if all of the antistatic agent inside the molded product is consumed, the effect of preventing the adhesion of dust will be lost, so to prevent the adhesion of dirt for a long period of time, a large amount of antistatic agent is added to the resin composition. Although it is necessary to mix | blend, when a lot of antistatic agents are mix | blended with a resin composition, the surface of a molded article will become sticky and will have a dirty feeling and discomfort. For this reason, in many molded products, the attached dust accumulates gradually after use for about one year, and the dirt is thick.
本発明は、上記事情に鑑みて、使用感がよく、表面に傷が付きにくいとともに、長期間安定して汚れ成分の付着を防止することができる樹脂成形品を提供することを目的としている。 In view of the above circumstances, an object of the present invention is to provide a resin molded article that has a good feeling of use, is hardly scratched on the surface, and can stably prevent adhesion of dirt components for a long period of time.
上記目的を達成するために、本発明にかかる樹脂成形品は、ポリエチレン系樹脂またはポリプロピレン系樹脂を主成分として含む樹脂組成物からなる層を少なくとも表面に有する樹脂成形品において、前記樹脂組成物が主成分100重量部に対し、平均粒子径3μm以上5μm以下の多孔質シリカを2〜6重量部、帯電防止剤を0.1〜1重量部の割合で含み、鉛筆硬度HB以上の硬度を備えていることを特徴としている。 In order to achieve the above object, the resin molded product according to the present invention is a resin molded product having at least a layer comprising a resin composition containing a polyethylene resin or a polypropylene resin as a main component on the surface. It contains 2 to 6 parts by weight of porous silica having an average particle diameter of 3 μm or more and 5 μm or less and 0.1 to 1 part by weight of an antistatic agent with respect to 100 parts by weight of the main component, and has a hardness of pencil hardness HB or more. It is characterized by having.
本発明において、多孔質シリカは、その一部の粒子が樹脂成形品の表面に露出していることが好ましい。
すなわち、一部の多孔質シリカ粒子が露出していることによって、より高い表面硬度を得ることができるとともに、臭いの吸着性も備えたものとすることができる。
In the present invention, the porous silica preferably has some particles exposed on the surface of the resin molded product.
That is, by exposing some of the porous silica particles, it is possible to obtain higher surface hardness and to have odor adsorptivity.
上記ポリエチレン系樹脂またはポリプロピレン系樹脂としてはホモポリマーだけでなく、エチレン−プロピレン共重合体やそれらの混合物も含まれる。また、MFRが過度に大きいと、樹脂溶融時に樹脂中でのシリカの分散が不均一となって、効果の発現が小さくなることがあり、MFRが過度に小さいと、樹脂の流動性が不足して充填性不足となることがあるので、MFRが3〜30g/10分程度のとき本発明の効果を十分に発現できる。 The polyethylene resin or polypropylene resin includes not only homopolymers but also ethylene-propylene copolymers and mixtures thereof. In addition, if the MFR is excessively large, the dispersion of the silica in the resin becomes non-uniform when the resin is melted, and the effect may be reduced. If the MFR is excessively small, the fluidity of the resin is insufficient. Therefore, the effect of the present invention can be sufficiently exhibited when the MFR is about 3 to 30 g / 10 minutes.
多孔質シリカとしては、特に限定されないが、平均粒子径が3μm以上5μm以下のものが好ましい。平均粒子径が小さ過ぎると、粒子が微細なために表面への露出が少なくなり、効果発現が小さくなることがあり、大き過ぎると、成形品表面のザラツキ感が発生することがある。 Although it does not specifically limit as a porous silica, A thing with an average particle diameter of 3 micrometers or more and 5 micrometers or less is preferable. If the average particle size is too small, the particles are fine, so that the exposure to the surface is reduced and the effect expression may be reduced. If it is too large, the surface of the molded product may be rough.
帯電防止剤としては、特に限定されないが、例えば、グリセリン脂肪酸エステル、ポリオキシエチレンアルキルアミン、アルキルジエタノールアミン等が使用できる。特に、ポリプロピレン樹脂、ポリエチレン樹脂に対する相溶性に優れるグリセリン脂肪酸エステルの場合、効果の発現性が良好である。 Although it does not specifically limit as an antistatic agent, For example, glycerin fatty acid ester, polyoxyethylene alkylamine, alkyl diethanolamine etc. can be used. In particular, in the case of a glycerin fatty acid ester having excellent compatibility with a polypropylene resin and a polyethylene resin, the effect is excellent.
本発明の樹脂成形品の製造方法は、特に限定されないが、射出成形が一般的で、単一樹脂組成物で成形されていても構わないが、サンドイッチ成形によってコア層を他の樹脂組成物で形成しても構わないし、金属板等の芯材をインサートするようにしても構わない。 The method for producing the resin molded product of the present invention is not particularly limited, but injection molding is common and may be molded with a single resin composition, but the core layer may be formed with other resin composition by sandwich molding. It may be formed or a core material such as a metal plate may be inserted.
また、多孔質シリカおよび帯電防止剤の配合量は、特に限定されないが、主成分100重量部に対し、多孔質シリカを2〜6重量部、帯電防止剤を0.1〜1重量部の割合とすることが好ましい。 The blending amount of the porous silica and the antistatic agent is not particularly limited, but the ratio of 2 to 6 parts by weight of the porous silica and 0.1 to 1 part by weight of the antistatic agent with respect to 100 parts by weight of the main component. It is preferable that
すなわち、多孔質シリカが主成分100重量部に対し、2重量部未満であると、多孔質シリカ単独では表面硬度が十分確保できず、6重量部を越えると、添加の効果がそれ以上期待できないとともに、得られる成形品の曲げ強度、引っ張り強度等の物性を低下させる恐れがある。
一方、帯電防止剤が主成分100重量部に対し、0.1重量部未満であると、帯電防止剤による汚れ防止効果の耐久性の点で問題が生じ、1重量部を越えると、多孔質シリカの配合量によっては成形品表面がべとつく恐れがある。
That is, when the porous silica is less than 2 parts by weight relative to 100 parts by weight of the main component, the surface hardness cannot be sufficiently secured with the porous silica alone, and when it exceeds 6 parts by weight, the effect of addition cannot be expected any more. In addition, physical properties such as bending strength and tensile strength of the obtained molded product may be reduced.
On the other hand, if the antistatic agent is less than 0.1 part by weight relative to 100 parts by weight of the main component, there is a problem in terms of durability of the antifouling effect by the antistatic agent, and if it exceeds 1 part by weight, the porous material is porous. Depending on the amount of silica, the surface of the molded product may become sticky.
また、本発明にかかる樹脂成形品に用いられる樹脂組成物中には、本発明の目的を阻害しない範囲で、必要に応じて、他の無機充填材、顔料、酸化防止剤、光安定剤、紫外線吸収剤、核剤、難燃剤、分散剤等を配合することができる。 Further, in the resin composition used for the resin molded product according to the present invention, other inorganic fillers, pigments, antioxidants, light stabilizers, and the like, as long as the purpose of the present invention is not impaired. An ultraviolet absorber, a nucleating agent, a flame retardant, a dispersing agent, etc. can be mix | blended.
以上のように、本発明にかかる樹脂成形品は、樹脂組成物が多孔質シリカおよび帯電防止剤を含み、鉛筆硬度HB以上の硬度を備えているので、表面に傷がつきにくい。しかも、帯電防止剤が多孔質シリカに適度に吸着されるため、徐々にブリードアウトする。すなわち、帯電防止剤のブリードアウト速度を抑制でき、帯電防止性能を長期にわたり維持できる。したがって、汚れを長期間防止することができ、樹脂成形品も長期間きれいな状態で使用できる。そして、これまで、付着した汚れが落ちないために産業廃棄物となっていた樹脂成形品が、汚れが付きにくくなることで使用できる期間が長くなり、産業廃棄物を削減できる。 As mentioned above, since the resin composition contains porous silica and an antistatic agent and has a hardness equal to or higher than pencil hardness HB, the surface of the resin molded product according to the present invention is hardly damaged. In addition, the antistatic agent is moderately adsorbed on the porous silica, and therefore gradually bleeds out. That is, the bleed-out speed of the antistatic agent can be suppressed, and the antistatic performance can be maintained for a long time. Therefore, the contamination can be prevented for a long time, and the resin molded product can be used in a clean state for a long time. And until now, since the adhered dirt does not come off, the resin molded product that has become industrial waste can be used for a longer period of time because it becomes difficult to get dirty, and industrial waste can be reduced.
また、食品等のコンテナの汚れを落とすため、コンテナ使用のたびに70℃〜80℃のお湯で洗浄を行っていたが、汚れの付着が低減することで、洗浄回数を少なくでき、水資源を有効に生かせ、環境への負荷を低減できる。 In addition, in order to remove dirt from containers such as food, washing was performed with hot water of 70 ° C to 80 ° C every time the container was used. It can be used effectively and the load on the environment can be reduced.
以下に、本発明を、その具体的な実施例を参照しつつ詳しく説明する。 Hereinafter, the present invention will be described in detail with reference to specific examples thereof.
(実施例1)
ポリプロピレン樹脂(プライムポリマー社製商品名プライムポリプロJ−830HV)100重量部に対し、多孔質シリカ(トクヤマ社製商品名レオロシール QS−102(親水性))を3重量部、帯電防止剤(花王社製商品名エレクトロストッパー12N)を0.2重量部それぞれ含む樹脂組成物を用いて射出成形によって各部の寸法が図1に示すとおりの色目が黄色の食品用コンテナを成形した。
(Example 1)
3 parts by weight of porous silica (trade name Leoroseal QS-102 (hydrophilic) made by Tokuyama Co., Ltd.) and 100 parts by weight of an antistatic agent (Kao Corporation) with respect to 100 parts by weight of polypropylene resin (trade name Prime Polypro J-830HV, manufactured by Prime Polymer Co., Ltd.) A food container having a yellow color as shown in FIG. 1 was molded by injection molding using a resin composition containing 0.2 parts by weight of the electro-stopper 12N).
(実施例2)
多孔質シリカとして、多孔質シリカ(トクヤマ社製商品名レオロシール QS−102(親水性))3重量部に代えて、多孔質シリカ(富士シリシア社製サイロホービック100(疎水性))を5重量部配合した以外は、実施例1と同様にして図1に示す食品用コンテナを成形した。
(Example 2)
Instead of 3 parts by weight of porous silica (trade name Leoroseal QS-102 (hydrophilic)) manufactured by Tokuyama Corporation, 5 weights of porous silica (Silo Hovic 100 (hydrophobic) manufactured by Fuji Silysia) was used as the porous silica. A food container shown in FIG. 1 was molded in the same manner as in Example 1 except that the ingredients were mixed.
(実施例3)
多孔質シリカの配合量を2重量部とした以外は、上記実施例1と同様にして図1に示す食品用コンテナを成形した。
(Example 3)
A food container shown in FIG. 1 was molded in the same manner as in Example 1 except that the amount of porous silica was 2 parts by weight.
(実施例4)
多孔質シリカの配合量を6重量部とした以外は、上記実施例1と同様にして図1に示す食品用コンテナを成形した。
Example 4
A food container shown in FIG. 1 was molded in the same manner as in Example 1 except that the amount of porous silica was 6 parts by weight.
(実施例5)
帯電防止剤の配合量を0.1重量部とした以外は、上記実施例1と同様にして図1に示す食品用コンテナを成形した。
(Example 5)
A food container shown in FIG. 1 was molded in the same manner as in Example 1 except that the blending amount of the antistatic agent was 0.1 parts by weight.
(実施例6)
帯電防止剤の配合量を1重量部とした以外は、上記実施例1と同様にして図1に示す食品用コンテナを成形した。
Example 6
A food container shown in FIG. 1 was molded in the same manner as in Example 1 except that the blending amount of the antistatic agent was 1 part by weight.
(実施例7)
多孔質シリカの配合量を10重量部とした以外は、上記実施例1と同様にして図1に示す食品用コンテナを成形した。
(Example 7)
A food container shown in FIG. 1 was molded in the same manner as in Example 1 except that the amount of porous silica was 10 parts by weight.
(実施例8)
帯電防止剤の配合量を1.5重量部とした以外は、上記実施例1と同様にして図1に示す食品用コンテナを成形した。
(Example 8)
A food container shown in FIG. 1 was molded in the same manner as in Example 1 except that the blending amount of the antistatic agent was 1.5 parts by weight.
(比較例1)
多孔質シリカを配合しなかった以外は、上記実施例1と同様にして図1に示す食品用コンテナを成形した。
(Comparative Example 1)
A food container shown in FIG. 1 was molded in the same manner as in Example 1 except that the porous silica was not blended.
(比較例2)
多孔質シリカの配合量を1重量部とした以外は、上記実施例1と同様にして図1に示す食品用コンテナを成形した。
(Comparative Example 2)
A food container shown in FIG. 1 was molded in the same manner as in Example 1 except that the amount of porous silica was 1 part by weight.
(比較例3)
多孔質シリカの配合量を1重量部とした以外は、上記実施例2と同様にして図1に示す食品用コンテナを成形した。
(Comparative Example 3)
The food container shown in FIG. 1 was molded in the same manner as in Example 2 except that the amount of porous silica was 1 part by weight.
(比較例4)
帯電防止剤を配合しなかった以外は、上記実施例1と同様にして図1に示す食品用コンテナを成形した。
(Comparative Example 4)
A food container shown in FIG. 1 was molded in the same manner as in Example 1 except that no antistatic agent was added.
上記実施例1〜8および比較例1〜4で得られた食品用コンテナについて、コンテナ表面の鉛筆硬度測定、帯電防止性評価および汚れ評価を以下に示す方法でそれぞれ実施し、その結果を表1および表2に示した。
〔鉛筆硬度測定〕
JIS K 5600−5−4の引っかき硬度(鉛筆法)に準拠した。
〔帯電性〕
表面固有抵抗測定機 (ACI Incorporated製 Surface Resistivity Meter MODEL475 )にて、成形直後、成形1週間後、成形1ヶ月後、並びに成形3ヶ月後のコンテナ表面の表面固有抵抗値を測定した。
〔汚れ評価〕
汚れ物質(代用物)としてのエンジンオイル(エクソンモービル社製4サイクルエンジン用 10W−30 )50重量%とカーボン粉50重量%とを混合したものを薄膜状にコンテナ表面に塗布し、恒温室内で、60℃×8時間、20℃×16時間を1サイクルの繰り返し保管条件で保管して、保管1週間後、保管2週間後、保管3週間後、保管1ヶ月後、保管2ヶ月後、保管3ヶ月後に汚れ物質をきれいな綿布で拭き取り、その後「色差計」にてΔEを測定した。
For the food containers obtained in Examples 1 to 8 and Comparative Examples 1 to 4, pencil hardness measurement, antistatic property evaluation, and dirt evaluation on the container surface were carried out by the following methods, and the results are shown in Table 1. And in Table 2.
[Pencil hardness measurement]
It was based on the scratch hardness (pencil method) of JIS K 5600-5-4.
[Chargeability]
The surface specific resistance value of the container surface immediately after molding, after 1 week of molding, after 1 month of molding, and after 3 months of molding was measured using a surface resistivity measuring machine (Surface Resistivity Meter MODEL 475 manufactured by ACI Incorporated).
[Dirt evaluation]
A mixture of 50% by weight of engine oil (10W-30 for 4-cycle engine manufactured by ExxonMobil Corporation) and 50% by weight of carbon powder as a dirty substance (substitute) is applied to the container surface in a thin film form, Store at 60 ° C x 8 hours, 20 ° C x 16 hours under repeated storage conditions of 1 cycle, 1 week after storage, 2 weeks after storage, 3 weeks after storage, 1 month after storage, 2 months after storage After 3 months, the dirt substance was wiped off with a clean cotton cloth, and then ΔE was measured with a “color difference meter”.
上記表1,2から、本発明の樹脂成形品は、従来の樹脂成形品に比べ、傷つきにくく、かつ汚れもつきにくいことがよくわかる。 From the above Tables 1 and 2, it can be seen that the resin molded product of the present invention is less likely to be scratched and dirty than the conventional resin molded product.
(実施例9)
ポリエチレン樹脂(プライムポリマー社製商品名ハイゼックス 2208G)100重量部に対し、多孔質シリカ(水澤化学社製商品名ミズカシルP73(親水性))を3重量部、帯電防止剤(花王社製商品名エレクトロストッパー12N)を0.2重量部それぞれ含む表層用樹脂組成物と、コア層用ポリエチレン樹脂(プライムポリマー社製商品名ハイゼックス 2208G)とを用いて射出サンドイッチ成形によって各部の寸法が図2に示すとおりの色目が青色のバケツを成形した。
Example 9
3 parts by weight of porous silica (trade name Mizukasil P73 (hydrophilic) made by Mizusawa Chemical Co., Ltd.) and 100 parts by weight of an antistatic agent (trade name Electro produced by Kao Co., Ltd.) are added to 100 parts by weight of polyethylene resin (trade name Hi-Zex 2208G made by Prime Polymer Co., Ltd.). The dimensions of each part are shown in FIG. 2 by injection sandwich molding using a resin composition for surface layer containing 0.2 parts by weight of stopper 12N) and a polyethylene resin for core layer (trade name Hi-Zex 2208G manufactured by Prime Polymer Co., Ltd.). A bucket with a blue color was molded.
(実施例10)
表層用樹脂組成物として、ポリエチレン樹脂(プライムポリマー社製商品名ハイゼックス 2208G)100重量部に対し、(富士シリシア社製サイロホービック100(疎水性))を5重量部、帯電防止剤(花王社製商品名エレクトロストッパー12N)を0.2重量部それぞれ含むものを用いた以外は、上記実施例9と同様にして図2に示すとおりの色目が青色のバケツを成形した。
(Example 10)
As a resin composition for the surface layer, 5 parts by weight of (Silo Hovic 100 (hydrophobic) manufactured by Fuji Silysia) and 100 parts by weight of an antistatic agent (Kao Corporation) with respect to 100 parts by weight of polyethylene resin (trade name Hi-Zex 2208G manufactured by Prime Polymer Co., Ltd.) A bucket having a blue color as shown in FIG. 2 was formed in the same manner as in Example 9 except that 0.2 wt part of the product name electro stopper 12N) was used.
(比較例5)
表層用樹脂組成物として、 ポリエチピレン樹脂(プライムポリマー社製商品名ハイゼックス 2208G)100重量部に対し帯電防止剤(花王社製商品名エレクトロストッパー12N)を0.2重量部それぞれ含むものを用いた以外は、上記実施例9と同様にして図2に示すとおりの色目が青色のバケツを成形した。
(Comparative Example 5)
As the resin composition for the surface layer, one containing 0.2 parts by weight of an antistatic agent (trade name: Electrostopper 12N, manufactured by Kao Corporation) with respect to 100 parts by weight of polyethylene resin (trade name: Hi-Zex 2208G, manufactured by Prime Polymer Co., Ltd.) was used. Except for the above, a bucket having a blue color as shown in FIG.
上記実施例9,10および比較例5で得られたバケツについて、バケツ表面の鉛筆硬度測定、帯電防止性評価および汚れ評価を上記した方法でそれぞれ実施し、その結果を表3および表4に示した。 For the buckets obtained in Examples 9 and 10 and Comparative Example 5, the pencil hardness measurement, the antistatic property evaluation, and the dirt evaluation on the bucket surface were performed by the methods described above, and the results are shown in Table 3 and Table 4. It was.
本発明の樹脂成形品は、たとえば、自動車部品、産業用コンテナ、食品用コンテナ、食品容器等に用いることができる。 The resin molded product of the present invention can be used for, for example, automobile parts, industrial containers, food containers, food containers and the like.
Claims (1)
前記樹脂組成物が主成分100重量部に対し、平均粒子径3μm以上5μm以下の多孔質シリカを2〜6重量部、帯電防止剤を0.1〜1重量部の割合で含み、鉛筆硬度HB以上の硬度を備えていることを特徴とする樹脂成形品。 In a resin molded article having at least a layer formed of a resin composition containing a polyethylene resin or a polypropylene resin as a main component,
The resin composition contains 2 to 6 parts by weight of porous silica having an average particle diameter of 3 μm or more and 5 μm or less and 0.1 to 1 part by weight of an antistatic agent with respect to 100 parts by weight of the main component, and has a pencil hardness of HB A resin molded product having the above hardness.
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| JP2007165850A JP5170735B2 (en) | 2007-06-25 | 2007-06-25 | Plastic molded product |
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| JP5170735B2 true JP5170735B2 (en) | 2013-03-27 |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| JP3067328B2 (en) * | 1991-10-22 | 2000-07-17 | 三菱化学株式会社 | Food packaging sheet or film |
| JP3036932B2 (en) * | 1991-11-07 | 2000-04-24 | 三菱化学株式会社 | Food packaging sheet or film |
| JP2878099B2 (en) * | 1993-12-28 | 1999-04-05 | 株式会社トクヤマ | Toilet seat and toilet lid |
| JPH1045964A (en) * | 1996-08-02 | 1998-02-17 | Tosoh Corp | Polypropylene resin composition and home appliance housing material comprising the same |
| JP2000109637A (en) * | 1998-10-05 | 2000-04-18 | Grand Polymer:Kk | Polypropylene resin composition and injection molded product |
| JP2000154285A (en) * | 1998-11-20 | 2000-06-06 | Grand Polymer:Kk | Polypropylene resin composition for injection molding and injection molded article using the same |
| JP3832129B2 (en) * | 1999-02-05 | 2006-10-11 | 株式会社プライムポリマー | Polypropylene resin composition and injection molded product |
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