JPH01306429A - Resin composition for coloring - Google Patents
Resin composition for coloringInfo
- Publication number
- JPH01306429A JPH01306429A JP13707188A JP13707188A JPH01306429A JP H01306429 A JPH01306429 A JP H01306429A JP 13707188 A JP13707188 A JP 13707188A JP 13707188 A JP13707188 A JP 13707188A JP H01306429 A JPH01306429 A JP H01306429A
- Authority
- JP
- Japan
- Prior art keywords
- pigment
- masterbatch
- coloring
- resin
- weight
- 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
- 238000004040 coloring Methods 0.000 title claims description 14
- 239000011342 resin composition Substances 0.000 title claims description 7
- 239000000049 pigment Substances 0.000 claims abstract description 16
- 239000001993 wax Substances 0.000 claims abstract description 9
- 239000002270 dispersing agent Substances 0.000 claims abstract description 5
- 229920000098 polyolefin Polymers 0.000 claims abstract description 4
- 239000000344 soap Substances 0.000 claims abstract description 3
- 239000000155 melt Substances 0.000 claims abstract 2
- -1 polyethylene Polymers 0.000 claims description 18
- 239000004698 Polyethylene Substances 0.000 claims description 16
- 229920000573 polyethylene Polymers 0.000 claims description 15
- 229920005992 thermoplastic resin Polymers 0.000 claims description 9
- 229910052751 metal Inorganic materials 0.000 claims description 3
- 239000002184 metal Substances 0.000 claims description 3
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 2
- 239000005977 Ethylene Substances 0.000 claims description 2
- FTQWRYSLUYAIRQ-UHFFFAOYSA-N n-[(octadecanoylamino)methyl]octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCNC(=O)CCCCCCCCCCCCCCCCC FTQWRYSLUYAIRQ-UHFFFAOYSA-N 0.000 claims description 2
- 239000004594 Masterbatch (MB) Substances 0.000 abstract description 23
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 abstract description 4
- 239000000203 mixture Substances 0.000 abstract description 3
- 235000019359 magnesium stearate Nutrition 0.000 abstract description 2
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 abstract description 2
- 229920005989 resin Polymers 0.000 description 21
- 239000011347 resin Substances 0.000 description 21
- 238000000465 moulding Methods 0.000 description 19
- 239000008188 pellet Substances 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- 229930182556 Polyacetal Natural products 0.000 description 3
- 239000004743 Polypropylene Substances 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 229920006324 polyoxymethylene Polymers 0.000 description 3
- 229920001155 polypropylene Polymers 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 239000000454 talc Substances 0.000 description 3
- 229910052623 talc Inorganic materials 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000005038 ethylene vinyl acetate Substances 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 229920001903 high density polyethylene Polymers 0.000 description 2
- 239000004700 high-density polyethylene Substances 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 2
- 229920005672 polyolefin resin Polymers 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- 239000004332 silver Substances 0.000 description 2
- JTXMVXSTHSMVQF-UHFFFAOYSA-N 2-acetyloxyethyl acetate Chemical compound CC(=O)OCCOC(C)=O JTXMVXSTHSMVQF-UHFFFAOYSA-N 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- 229920005177 Duracon® POM Polymers 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- CEGOLXSVJUTHNZ-UHFFFAOYSA-K aluminium tristearate Chemical compound [Al+3].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CEGOLXSVJUTHNZ-UHFFFAOYSA-K 0.000 description 1
- 229940063655 aluminum stearate Drugs 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 235000013405 beer Nutrition 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000012784 inorganic fiber Substances 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920005668 polycarbonate resin Polymers 0.000 description 1
- 239000004431 polycarbonate resin Substances 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 229920005606 polypropylene copolymer Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 229920006163 vinyl copolymer Polymers 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
Abstract
Description
【発明の詳細な説明】
〔発明の目的〕
(産業上の利用分野)
本発明は、熱可塑性樹脂の着色用樹脂組成物(マスター
バッチ)に関する。DETAILED DESCRIPTION OF THE INVENTION [Object of the Invention] (Field of Industrial Application) The present invention relates to a resin composition (masterbatch) for coloring a thermoplastic resin.
(従来の技術) 熱可塑性樹脂のマスターバッチのベースレジンは。(Conventional technology) Base resin for thermoplastic resin masterbatch.
被着色熱可塑性樹脂への分散1分配性を考慮し、−般に
被着色樹脂と同一の樹脂が使用されている。In consideration of dispersibility into the thermoplastic resin to be colored, the same resin as the resin to be colored is generally used.
しかしながら、これらのマスターバッチは異なる種類の
被着色樹脂に対しては9分散性や物性低下の問題で使用
出来なかった。又近年着色コスト低減の要求が厳しく、
マスターバッチ中の顔料含有率を高くする必要があるが
、単に顔料含有率を高くする事はマスターバンチの粘度
が高くなり顔料分散も難しく、成形品表面にも色むらが
出やすくなる。そのためマスターバッチの主要3成分(
顔料1分散剤およびベースレジン)のうちベースレジン
の粘度をさげマスターバッチ中のベースレジンの含有率
をマスターバッチの生産に支障がない限界まで少な(シ
、成形品物性に与える影響を少なくシ、成形品表面の色
むらを改良することが行われてきた。例えば、特開昭5
7−114042号公報では、ベースレジンとしてエチ
レン−酢酸ビニル共重合体を使用することが提案された
が、耐熱性に問題があり、摩擦発熱の大きな成形機で成
形する場合やメルトフローレート(MFR)が小さな高
密度ポリエチレン、ポリプロピレンあるいはフィラー入
り樹脂を成形する場合に成形品表面に色むらが発生する
ことがあった。また。However, these masterbatches could not be used for different types of colored resins due to problems with dispersibility and deterioration of physical properties. In addition, in recent years there has been a strong demand for reducing coloring costs.
It is necessary to increase the pigment content in the masterbatch, but simply increasing the pigment content increases the viscosity of the masterbatch, making it difficult to disperse the pigment and making color unevenness more likely to appear on the surface of the molded product. Therefore, the three main components of the masterbatch (
Pigment 1 (dispersant and base resin), the content of the base resin in the masterbatch is reduced to the limit that does not interfere with the production of the masterbatch by reducing the viscosity of the base resin. Efforts have been made to improve color unevenness on the surface of molded products.
Publication No. 7-114042 proposed the use of ethylene-vinyl acetate copolymer as a base resin, but it had problems with heat resistance, and it was difficult to use when molding with a molding machine that generates a lot of frictional heat or when melt flow rate (MFR) was used. ) When molding high-density polyethylene, polypropylene, or filler-containing resin with a small diameter, uneven coloring may occur on the surface of the molded product. Also.
成形を中断した場合にも樹脂が成形機内に滞留する結果
9色むらが発生することがあった。Even when molding was interrupted, resin remained in the molding machine, resulting in uneven coloring.
さらに、従来のマスターバッチでは、ポリアセクールの
着色成形する場合、成形機の温度をポリアセタールを成
形する温度より高くするとシルバーの発生の原因となる
ため、生産性が悪かった。Furthermore, with conventional masterbatches, when coloring polyacecool and molding, if the temperature of the molding machine is higher than the temperature at which polyacetal is molded, it causes the generation of silver, resulting in poor productivity.
(発明が解決しようとする課題)
本発明は、上記の種々の欠点を改良し、多種多様な成形
条件及び樹脂の着色に汎用性が存り2色むらのない成形
品が得られ、特に均一な着色が困難な大型の射出成形品
においても均一な着色が可能なマスターバンチを提供す
るものである。(Problems to be Solved by the Invention) The present invention improves the various drawbacks mentioned above, has versatility in a wide variety of molding conditions and resin coloring, and can obtain molded products with no unevenness in two colors, and is particularly uniform. The present invention provides a master bunch that can uniformly color even large injection molded products that are difficult to color.
(課題を解決するための手段)
本発明において(a)l料としては、従来から樹脂の着
色に使用されている公知のすべての染顔料が使用出来る
。(Means for Solving the Problems) In the present invention, as the material (a), all known dyes and pigments conventionally used for coloring resins can be used.
(b)成分のベースレジンとしては、MFRが100〜
500.好ましくは200〜400の範囲にあるポリエ
チレンが用いられる。MFRが100未満の時はマスタ
ーバッチの粘度が高くなり色むらが発生し易くなり、M
FRが500を超える場合には。The base resin for component (b) has an MFR of 100~
500. Preferably polyethylene in the range of 200 to 400 is used. When MFR is less than 100, the viscosity of the masterbatch becomes high and color unevenness tends to occur.
If FR exceeds 500.
マスターバッチの粘度が低過ぎるためマスターバッチの
ベレット化が難しくなる。The viscosity of the masterbatch is too low, making it difficult to form the masterbatch into pellets.
(c)fM料骨分散剤してはポリエチレンワックス。(c) Polyethylene wax as fM bone dispersant.
ポリプロピレンワックス等のポリオレフインワンクス及
びこれら誘4体や、ステアリン酸亜鉛、ステアリン酸マ
グネシウム、ステアリン酸アルミニウム。Polyolefin waxes such as polypropylene wax and derivatives thereof, zinc stearate, magnesium stearate, and aluminum stearate.
ステアリン酸カルシウム等の金属石ケン類、エチレンビ
スアマイド等から選ばれる1種又は2種以上が用いられ
る。One or more types selected from metal soaps such as calcium stearate, ethylene bisamide, etc. are used.
本発明の(a)、 (b)および(c)の配合割合は
(a)、 (b)および(c)の総和に対して、それ
ぞれ10〜50重量%、5〜30重量%、10〜50重
量%の範囲である。The proportions of (a), (b) and (c) in the present invention are 10 to 50% by weight, 5 to 30% by weight, and 10 to 30% by weight, respectively, based on the total of (a), (b) and (c). It is in the range of 50% by weight.
<a)の配合量が10重量%未満では近年のマスターバ
ッチの高濃度化、つまり30倍以上の希釈による熱可塑
性樹脂の着色が可能とは言い難(,50重量%以上の場
合にはマスターバッチの流動性が悪くなり色むらを生じ
る。If the blending amount of <a) is less than 10% by weight, it is difficult to say that it is possible to color thermoplastic resins by diluting the masterbatch at a high concentration of 30 times or more, as has been the case in recent years. The fluidity of the batch deteriorates, resulting in uneven color.
(b)の配合量が5重量%未満ではマスターパンチ製造
時の押出ベレット等の加工が困難となり、30重量%を
超える場合は同じポリエチレン及びポリプロピレン等の
オレフィン系の樹脂には有用であるがその他の樹脂に対
して汎用性がなくなる。If the amount of (b) is less than 5% by weight, it will be difficult to process extrusion pellets during master punch production, and if it exceeds 30% by weight, it will be useful for olefin resins such as polyethylene and polypropylene, but other than that. It loses its versatility for other resins.
(c)の配合量が10重量%未満ではマスターバッチの
流動性が悪く色むらを生じ、50重量%を超えると9着
色される樹脂の機械物性、耐熱性等に悪影響を及ぼず。When the amount of (c) is less than 10% by weight, the masterbatch has poor fluidity and uneven coloring occurs, and when it exceeds 50% by weight, it does not adversely affect the mechanical properties, heat resistance, etc. of the resin to be colored.
本発明の樹脂組成物には2本発明の効果を阻害しない範
囲で酸化防止剤、紫外線吸収剤等の各種の添加剤を添加
する事も出来、又炭酸カルシウム、タルク、微粉末酸化
ケイ素等も低コスト化。To the resin composition of the present invention, various additives such as antioxidants and ultraviolet absorbers can be added as long as they do not impede the effects of the present invention, and calcium carbonate, talc, finely powdered silicon oxide, etc. can also be added. lowering cost.
粘度調整剤として添加出来る。Can be added as a viscosity modifier.
本発明の樹脂組成物が着色出来る熱可塑性樹脂はポリオ
レフィン樹脂、EVA、EMMA、ポリメチルヘンテン
、ポリブテン−1,ポリスチレン、 PVC,PET
、PBT、ABS、AES、 ポリアミド。Thermoplastic resins that can be colored with the resin composition of the present invention include polyolefin resins, EVA, EMMA, polymethylhentene, polybutene-1, polystyrene, PVC, and PET.
, PBT, ABS, AES, polyamide.
ポリカーボネート、ポリアセタール、ポリウレタンなど
がある。又これらの樹脂に対し、タルク、マイカ、硫酸
バリウム、炭酸カルシウム等の無機光テン剤やガラス繊
維、有機繊維、金属繊維、炭素繊維等を添加したフィラ
ー入り樹脂又は繊維強化樹脂であってもよい。Examples include polycarbonate, polyacetal, and polyurethane. In addition, filler-containing resins or fiber-reinforced resins may be added to these resins with inorganic photo-tensifying agents such as talc, mica, barium sulfate, and calcium carbonate, glass fibers, organic fibers, metal fibers, carbon fibers, etc. .
(実施例)
以下、実施例により本発明を説明する。例中1部とは重
量部を2%とは重量%をそれぞれ表わす。(Example) The present invention will be explained below with reference to Examples. In the examples, 1 part means part by weight, and 2% means % by weight.
実施例1
ポリエチレン「スミ力センG−808J(住友化学工業
住局製 MFR200) 20%ポリエチレンワッ
クス「サンワックス131 PJ(三洋化成工業■製)
50%カーボンブラック「三菱カー
ボン#44」(三菱化成工業■製) 3
0%上記3成分をニーグーで混練後、押出機でベレット
化しマスターバッチを得た。Example 1 Polyethylene "Sumi-Rikisen G-808J (manufactured by Sumitomo Chemical Industry Co., Ltd., MFR200)" 20% polyethylene wax "Sunwax 131 PJ (manufactured by Sanyo Chemical Industries, Ltd.)
50% carbon black “Mitsubishi Carbon #44” (manufactured by Mitsubishi Chemical Corporation) 3
0% The above three components were kneaded using a Ni-Goo, and then pelletized using an extruder to obtain a masterbatch.
実施例2
実施例1のポリエチレンの代りに「ミラリンJ−443
J (三井石油化学工業■製 MFR150)を用い
た以外は実施例1と同様にしてマスターバッチを得た。Example 2 Instead of the polyethylene in Example 1, “Mirarin J-443” was used.
A masterbatch was obtained in the same manner as in Example 1 except that J (MFR150 manufactured by Mitsui Petrochemical Industries, Ltd.) was used.
実施例3
実施例1のポリエチレンの代りにMFR400(試作品
)を用いた以外は実施例1と同様にしてマスターバッチ
を得た。Example 3 A masterbatch was obtained in the same manner as in Example 1 except that MFR400 (prototype) was used instead of the polyethylene in Example 1.
実施例4
ポリエチレン[スミ力センG−808J 15%ポリ
エチレンワックス「ハイワックス4400GJ(三井石
油化学工業側製) 45%フタロシアニ
ンブルー「リオノールプルーP OB S J(東洋イ
ンキ製造側製) 10%酸化チタン[
タイベークCR−80J
(石層産業■製) 30%ポリエ
チレンワックスと顔料を3本ロールで混練後、ポリエチ
レンと配合し押出ベレット化しマスターバッチを得た。Example 4 Polyethylene [Sumikisen G-808J 15% polyethylene wax "Hiwax 4400GJ (manufactured by Mitsui Petrochemical Industries) 45% phthalocyanine blue""Lionol Blue POB S J (manufactured by Toyo Ink Manufacturing) 10% titanium oxide [
Tybake CR-80J (manufactured by Ishiya Sangyo ■) 30% polyethylene wax and pigment were kneaded with three rolls, then blended with polyethylene and extruded into pellets to obtain a masterbatch.
このマスターバッチ3部をl(D PEハイゼックス2
208J (三井石油化学工業■製MFR5,,5)1
00部と混合しボトルコンテナーを成形したところ色む
らのない成形品が得られた。Add 3 parts of this masterbatch (D PE Hi-Zex 2
208J (MFR5, 5 manufactured by Mitsui Petrochemical Industries) 1
00 parts and molded into a bottle container, a molded product with no uneven color was obtained.
比較例1
実施例1のポリエチレンの代りにエチレン−酢IIビニ
ル共重合体「エバフレックス420J (三井デュポ
ンポリケミカル側製 MFRI50)を用いた以外は実
施例1と同様にしてマスターバンチを得た。Comparative Example 1 A master bunch was obtained in the same manner as in Example 1, except that the ethylene-acetate II vinyl copolymer "Evaflex 420J (MFRI50, manufactured by DuPont Mitsui Polychemicals)" was used instead of the polyethylene in Example 1.
比較例2
実施例1のポリエチレンの代りにスミカセンG−807
MFR75を用いた以外は実施例1と同様にしてマスタ
ーバッチを得た。Comparative Example 2 Sumikasen G-807 instead of polyethylene in Example 1
A masterbatch was obtained in the same manner as in Example 1 except that MFR75 was used.
比較例3
スミ力センG−80820%
ハイワックス4400G 20%リオ
ノールブルーPoB5 10%タイベーク
CR−8050%
上記4成分を実施例1と同様にしてマスターバッチを得
た。Comparative Example 3 Sumirikisen G-80820% Hiwax 4400G 20% Lionol Blue PoB5 10% Thai Bake CR-8050% A masterbatch was obtained using the above four components in the same manner as in Example 1.
比較例4
ポリエチレン「スミ力セン(、−808J 4%サ
ンワックス131P 60%三菱カ
ーボン144 36%実施例1と同
様にしてベレット化しようとしたが押出しベレット化が
出来なかった。Comparative Example 4 Polyethylene Sumirikisen (-808J) 4% Sunwax 131P 60% Mitsubishi Carbon 144 36% An attempt was made to make pellets in the same manner as in Example 1, but extrusion could not be made into pellets.
各実施例および比較例1〜3で得られたマスターバッチ
を表1に記載した希釈樹脂に重量割合で3/100添加
し9表1記載の条件で成形試験を行った。The masterbatches obtained in Examples and Comparative Examples 1 to 3 were added to the diluted resins listed in Table 1 at a weight ratio of 3/100, and a molding test was conducted under the conditions listed in Table 1.
表中、希釈樹脂と成形条件は以下のとおりである。In the table, the diluted resin and molding conditions are as follows.
■:高密度ポリエチレンハイゼソクス2208Jを使用
し、成形機は来遊l5−75を使用し220℃と240
℃で平板を成形し色むらを評価シ2゜た。■: High-density polyethylene Hizesox 2208J is used, and the molding machine is Raiyu 15-75 at 220℃ and 240℃.
A flat plate was molded at 2°C and color unevenness was evaluated.
■:ハイゼックス2208Jを使用し、大型成形機によ
りビールのコンテナーを成形し色むらを評価した。■: A beer container was molded using a large molding machine using HIZEX 2208J, and color unevenness was evaluated.
■:タルク10%入ポリプロピレンコポリマーにマスタ
ーバッチを混合し、成形機は来遊1s−75を使用し2
20℃で滞留なしと15分滞留後の成形品(平板)で色
むらを評価した。■: Mix the masterbatch with polypropylene copolymer containing 10% talc, and use the molding machine Raiyu 1s-75.
Color unevenness was evaluated for molded products (flat plates) without retention at 20°C and after retention for 15 minutes.
■:ポリアセクール樹脂「ジュラコンM90−02」
(ポリプラスチック■製)にマスターバッチを混合し2
00℃で押出成形した時のホルマリン臭によるポリアセ
クールの分解の状況と。■: Polysecure resin “Duracon M90-02”
(made of polyplastic ■) and mix the masterbatch 2
Decomposition of polyacecool due to formalin odor when extruded at 00°C.
来遊l5−75で押出ししたベレットを成形した時の成
形品へのシルバーの出方で評価した。Evaluation was made based on the appearance of silver in the molded product when a pellet extruded using 15-75 was molded.
V:ABS樹脂「タララスチックMHJ (住友ノー
ガタック特製)とマスターバッチを混合し来遊l5−7
5で平板を成形し色むらを評価した。V: ABS resin "Tallastic MHJ (specially made by Sumitomo Naugatac) and masterbatch are mixed and used" 15-7
A flat plate was molded in No. 5 and color unevenness was evaluated.
■:ボリカーボネート樹脂[タフロンA−200J(出
光石油化学■製)を使用し、■と同じ成形条件と評価を
行った。■: Polycarbonate resin [Taflon A-200J (manufactured by Idemitsu Petrochemical ■) was used, and the same molding conditions and evaluation as in ■ were performed.
■:ナイロン[ダイアミドL−1940J (ダイセ
ル0菊製)を使用し、■と同じ成形条件と評価を行った
。■: Nylon [Diamid L-1940J (manufactured by Daicel 0 Kiku) was used, and the same molding conditions and evaluation as in ■ were conducted.
表1
〔発明の効果〕
本発明の熱可塑性樹脂の着色用樹脂組成物は。顔料濃度
が高く、添加量が従来のマスターバンチに較べはるかに
少なくても十分な着色が可能であり、多種多様な熱可塑
性樹脂の着色が出来るだけでなく。Table 1 [Effects of the Invention] The resin composition for coloring a thermoplastic resin of the present invention is as follows. It has a high pigment concentration and can provide sufficient coloring even if the amount added is much smaller than conventional master bunches, and it is not only capable of coloring a wide variety of thermoplastic resins.
無機充填剤や繊維等を含む熱可塑性樹脂にもを効でなお
かつ顔料分散性に優れ熱的にも安定である。It is also effective for thermoplastic resins containing inorganic fillers and fibers, and has excellent pigment dispersibility and thermal stability.
本発明の着色用樹脂組成物は、従来のマスターバッチの
欠点であった。摩擦発熱の大きな成形品や。The coloring resin composition of the present invention has the drawbacks of conventional masterbatches. Molded products that generate a lot of frictional heat.
成形機を10分以上滞留させた後続けて成形する場合に
発生する色むらや、ポリアセタールの成形では成形温度
を下げて操業しなければならないため生産性に劣るとい
う欠点を解消するものである。This eliminates the disadvantages of color unevenness that occurs when molding is continued after being left in the molding machine for 10 minutes or more, and of poor productivity when molding polyacetal because it must be operated at a lower molding temperature.
Claims (1)
レートが100〜500の範囲にあるポリエチレン5〜
30重量%、(c)ポリオレフィンワックスおよびこれ
らの誘導体、金属石ケン類およびエチレンビスアマイド
からなる群から選ばれる1種または2種以上の顔料分散
剤10〜50重量%からなることを特徴とする熱可塑性
樹脂の着色用樹脂組成物。1. (a) 10 to 50% by weight of pigment, (b) polyethylene with a melt flow rate in the range of 100 to 500
30% by weight, (c) 10 to 50% by weight of one or more pigment dispersants selected from the group consisting of polyolefin waxes and their derivatives, metal soaps, and ethylene bisamide. A resin composition for coloring thermoplastic resin.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13707188A JPH01306429A (en) | 1988-06-03 | 1988-06-03 | Resin composition for coloring |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13707188A JPH01306429A (en) | 1988-06-03 | 1988-06-03 | Resin composition for coloring |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01306429A true JPH01306429A (en) | 1989-12-11 |
Family
ID=15190222
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP13707188A Pending JPH01306429A (en) | 1988-06-03 | 1988-06-03 | Resin composition for coloring |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01306429A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0931206A (en) * | 1995-07-14 | 1997-02-04 | Toyo Ink Mfg Co Ltd | Composition for coloration |
JP2009256446A (en) * | 2008-04-16 | 2009-11-05 | Asahi Kasei Chemicals Corp | Polyacetal resin composition |
WO2010058673A1 (en) * | 2008-11-21 | 2010-05-27 | 東洋アルミニウム株式会社 | Master batch for coloring synthetic resin |
JP2013518616A (en) * | 2010-02-01 | 2013-05-23 | マテル,インコーポレイテッド | Compositions for forming dolls and dolls |
JP2016084387A (en) * | 2014-10-23 | 2016-05-19 | 株式会社プライムポリマー | Polypropylene resin composition and use thereof |
JP2017507233A (en) * | 2014-03-04 | 2017-03-16 | ダウ コーニング コーポレーションDow Corning Corporation | Thermoplastic polymer masterbatch |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5540703A (en) * | 1978-09-14 | 1980-03-22 | Dainichi Seika Kogyo Kk | Pigment composition for coloring of polyolefin resin |
JPS5620053A (en) * | 1979-07-30 | 1981-02-25 | Dainichi Seika Kogyo Kk | Colored resin composition |
JPS56143231A (en) * | 1980-04-10 | 1981-11-07 | Nippon Petrochem Co Ltd | Carbon black composition for coloring |
JPS58167624A (en) * | 1982-03-29 | 1983-10-03 | Tokyo Ink Kk | Preparation of granular master batch for polyolefin resin |
JPS6144943A (en) * | 1984-08-09 | 1986-03-04 | Mitsubishi Petrochem Co Ltd | Colored resin composition |
-
1988
- 1988-06-03 JP JP13707188A patent/JPH01306429A/en active Pending
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5540703A (en) * | 1978-09-14 | 1980-03-22 | Dainichi Seika Kogyo Kk | Pigment composition for coloring of polyolefin resin |
JPS5620053A (en) * | 1979-07-30 | 1981-02-25 | Dainichi Seika Kogyo Kk | Colored resin composition |
JPS56143231A (en) * | 1980-04-10 | 1981-11-07 | Nippon Petrochem Co Ltd | Carbon black composition for coloring |
JPS58167624A (en) * | 1982-03-29 | 1983-10-03 | Tokyo Ink Kk | Preparation of granular master batch for polyolefin resin |
JPS6144943A (en) * | 1984-08-09 | 1986-03-04 | Mitsubishi Petrochem Co Ltd | Colored resin composition |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0931206A (en) * | 1995-07-14 | 1997-02-04 | Toyo Ink Mfg Co Ltd | Composition for coloration |
JP2009256446A (en) * | 2008-04-16 | 2009-11-05 | Asahi Kasei Chemicals Corp | Polyacetal resin composition |
WO2010058673A1 (en) * | 2008-11-21 | 2010-05-27 | 東洋アルミニウム株式会社 | Master batch for coloring synthetic resin |
CN102216374A (en) * | 2008-11-21 | 2011-10-12 | 东洋铝株式会社 | Master batch for coloring synthetic resin |
US8513344B2 (en) | 2008-11-21 | 2013-08-20 | Toyo Aluminium Kabushiki Kaisha | Masterbatch for coloring synthetic resin |
JP2013518616A (en) * | 2010-02-01 | 2013-05-23 | マテル,インコーポレイテッド | Compositions for forming dolls and dolls |
JP2017507233A (en) * | 2014-03-04 | 2017-03-16 | ダウ コーニング コーポレーションDow Corning Corporation | Thermoplastic polymer masterbatch |
US10246580B2 (en) | 2014-03-04 | 2019-04-02 | Dow Silicones Corporation | Thermoplastic polymer masterbatch |
JP2016084387A (en) * | 2014-10-23 | 2016-05-19 | 株式会社プライムポリマー | Polypropylene resin composition and use thereof |
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