JPS5934738B2 - granular pigment - Google Patents
granular pigmentInfo
- Publication number
- JPS5934738B2 JPS5934738B2 JP9255881A JP9255881A JPS5934738B2 JP S5934738 B2 JPS5934738 B2 JP S5934738B2 JP 9255881 A JP9255881 A JP 9255881A JP 9255881 A JP9255881 A JP 9255881A JP S5934738 B2 JPS5934738 B2 JP S5934738B2
- Authority
- JP
- Japan
- Prior art keywords
- pigment
- weight
- resin
- dispersant
- resins
- 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
- 239000000049 pigment Substances 0.000 title claims description 29
- 239000002270 dispersing agent Substances 0.000 claims description 17
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 10
- 239000000194 fatty acid Substances 0.000 claims description 10
- 229930195729 fatty acid Natural products 0.000 claims description 10
- 150000004665 fatty acids Chemical class 0.000 claims description 10
- 229910052751 metal Inorganic materials 0.000 claims description 5
- 239000002184 metal Substances 0.000 claims description 5
- 239000000203 mixture Substances 0.000 claims description 5
- 150000003839 salts Chemical class 0.000 claims description 5
- FTQWRYSLUYAIRQ-UHFFFAOYSA-N n-[(octadecanoylamino)methyl]octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCNC(=O)CCCCCCCCCCCCCCCCC FTQWRYSLUYAIRQ-UHFFFAOYSA-N 0.000 claims description 4
- RKISUIUJZGSLEV-UHFFFAOYSA-N n-[2-(octadecanoylamino)ethyl]octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCCNC(=O)CCCCCCCCCCCCCCCCC RKISUIUJZGSLEV-UHFFFAOYSA-N 0.000 claims description 3
- 229920005989 resin Polymers 0.000 description 18
- 239000011347 resin Substances 0.000 description 18
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 10
- 238000000034 method Methods 0.000 description 9
- 238000000465 moulding Methods 0.000 description 6
- 239000008187 granular material Substances 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 229920006026 co-polymeric resin Polymers 0.000 description 4
- 239000003086 colorant Substances 0.000 description 4
- 238000004040 coloring Methods 0.000 description 4
- 230000006866 deterioration Effects 0.000 description 4
- 239000000975 dye Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 230000000704 physical effect Effects 0.000 description 3
- 229920005992 thermoplastic resin Polymers 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- -1 acrylonitrile-butadiene-styrene-d-methylstyrene Chemical compound 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- VKOBVWXKNCXXDE-UHFFFAOYSA-N icosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCC(O)=O VKOBVWXKNCXXDE-UHFFFAOYSA-N 0.000 description 2
- 239000011261 inert gas Substances 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-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
- 239000005639 Lauric acid Substances 0.000 description 1
- 239000004594 Masterbatch (MB) Substances 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 description 1
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 description 1
- 159000000009 barium salts Chemical class 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical class CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- DGBWPZSGHAXYGK-UHFFFAOYSA-N perinone Chemical compound C12=NC3=CC=CC=C3N2C(=O)C2=CC=C3C4=C2C1=CC=C4C(=O)N1C2=CC=CC=C2N=C13 DGBWPZSGHAXYGK-UHFFFAOYSA-N 0.000 description 1
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 description 1
- CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920005668 polycarbonate resin Polymers 0.000 description 1
- 239000004431 polycarbonate resin Substances 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- IZMJMCDDWKSTTK-UHFFFAOYSA-N quinoline yellow Chemical compound C1=CC=CC2=NC(C3C(C4=CC=CC=C4C3=O)=O)=CC=C21 IZMJMCDDWKSTTK-UHFFFAOYSA-N 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Pigments, Carbon Blacks, Or Wood Stains (AREA)
Description
【発明の詳細な説明】
本発明は、熱可塑性樹脂用の粒状顔料、特にABS系樹
脂の着色用に適した粒状顔料に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a granular pigment for thermoplastic resins, particularly a granular pigment suitable for coloring ABS resins.
3以下例としてABS系樹脂について説明するが、これ
に限定されるものではない。3. ABS resin will be described below as an example, but the invention is not limited thereto.
従来からABS系樹脂の着色は予め樹脂と着色剤との混
合物を押出機により混練したカラーペレット法が一般的
に行われている。そのコストダウン対策として成形加工
時に着色剤と樹脂とを混合して着色成形加工を行なうい
わゆる自家着色成形法が要望されている。一般的に、着
色剤はABS系樹脂に対して難分散性であるため、その
着色法について、いろいろ提案されている。例えば(1
)ABS系樹脂とドライカラーの混合物を、直接に成形
するドライカラー法、(2)顔料を液状媒体に分散させ
るリキッドカラー法(3顔料を顆粒状に造粒し易崩壊性
とする粒状カラー法(4)ABS系樹脂に予め高濃度に
顔料を分散させたマスターバッチカラー法などがある。Conventionally, ABS resins have been generally colored by a color pellet method in which a mixture of resin and colorant is kneaded in advance using an extruder. As a cost reduction measure, there is a demand for a so-called self-coloring molding method in which a coloring agent and a resin are mixed during molding to perform coloring molding. In general, colorants have difficulty dispersing in ABS resins, and various methods have been proposed for coloring them. For example (1
) A dry color method in which a mixture of ABS resin and dry color is directly molded, (2) a liquid color method in which the pigment is dispersed in a liquid medium (a granular color method in which the three pigments are granulated into granules to make them easily disintegrating) (4) There is a masterbatch color method in which pigments are dispersed in ABS resin in advance at a high concentration.
しかし、(1)は、カラーの飛散により作業環境が悪化
すると共に色変更が難かしく、(2)は液状媒体がその
成形品中に残存するので物性が低下すること、(3)は
成形時の被着色樹脂の喰込み不良を起しやすく、又顆粒
破壊が困難なため混練不足により色ムラ、層剥離、フラ
ッシュなどの外観不良となること、(4)は製造工程が
増加する他樹脂が熱履歴を受けるので、その物性が低下
するなどの欠点がある。However, (1) causes deterioration of the working environment due to color scattering and makes it difficult to change the color, (2) causes deterioration of physical properties as the liquid medium remains in the molded product, and (3) causes deterioration of physical properties during molding. (4) It is easy to cause poor biting of the resin to be colored, and it is difficult to break the granules, resulting in poor appearance such as color unevenness, layer peeling, and flash due to insufficient kneading. Since it is subjected to thermal history, it has disadvantages such as deterioration of its physical properties.
本発明は、これらの欠点を解決したもので顔料に高級脂
肪酸と特定の脂肪酸アミドとを配合した溶融混合物粒状
にすることにより安価で色変更操作も容易であり、樹脂
自体が熱履歴を受けることなく、色ムラなどの全くない
すぐれた成形用樹脂の顔料を提供しようとするものであ
る。The present invention solves these drawbacks, and by forming a molten mixture of pigments with a higher fatty acid and a specific fatty acid amide into granules, it is inexpensive and easy to change the color, and the resin itself does not undergo heat history. The purpose is to provide an excellent pigment for molding resin that is completely free of color unevenness.
すなわち本発明は顔料25〜75重量%と分散剤75〜
25重量%との混合物であつて、しかもその分散剤が高
級脂肪酸の金属塩とメチレンビスステアロアミド又はエ
チレンビスステアロアミドからなり、かつ、その割合が
重量で5〜95:95〜5である粒状顔料である。That is, the present invention uses 25 to 75% by weight of pigment and 75 to 75% by weight of dispersant.
25% by weight, and the dispersing agent consists of a metal salt of a higher fatty acid and methylene bis stearamide or ethylene bis stearamide, and the ratio by weight is 5 to 95:95 to 5. It is a particulate pigment.
以下さらに本発明を詳しく説明する。The present invention will be further explained in detail below.
本発明の粒状顔料は、熱可塑性樹脂例えば、ABS系樹
脂、塩化ビニル樹脂、エチレン樹脂、プロピレン樹脂、
スチレン樹脂、ポリカーボネート樹脂、ポリアミド樹脂
、ジエン系樹脂及びエステル樹脂などに用いることがで
きるが、特にABS系樹脂に対して有利に使用されるも
のである。The granular pigment of the present invention is made of thermoplastic resins such as ABS resins, vinyl chloride resins, ethylene resins, propylene resins,
It can be used for styrene resins, polycarbonate resins, polyamide resins, diene resins, ester resins, etc., and is particularly advantageous for ABS resins.
さらに前記のABS系樹脂の具体例としては、アクリロ
ニトリル−ブタジエン−スチレン共重合樹脂、アクリロ
ニトリル−ブタジエン−スチレン−dメチルスチレン共
重合樹脂、アクリロニトリル−ブタジエン−スチレン−
アクリル酸エステル共重合樹脂、およびアクリロニトリ
ル−ブタジエン−スチレン−dメチルスチレン−アクリ
ル酸エステル共重合樹脂などがあげられるが、これらに
限られるものではない。Furthermore, specific examples of the above-mentioned ABS resin include acrylonitrile-butadiene-styrene copolymer resin, acrylonitrile-butadiene-styrene-d-methylstyrene copolymer resin, acrylonitrile-butadiene-styrene-
Examples include, but are not limited to, acrylic ester copolymer resins, acrylonitrile-butadiene-styrene-d-methylstyrene-acrylic ester copolymer resins, and the like.
本発明において、顔料とは、公知の染料および顔料の両
者を意味するもので、例えば、カーボンブラツク、酸化
チタン、酸化亜鉛、酸化鉄、炭酸カルシウム、シリカ、
酸化クロム、タルクなどの無機物質からなる顔料フタロ
シアニン系、アンスラキノン系、キナクリドン系、アゾ
系、キノフタロン系、ペリノン系、ペリレン系などの有
機顔料及び染料等であり一般に熱可塑性樹脂用として使
用されているものであればよい。In the present invention, pigment means both known dyes and pigments, such as carbon black, titanium oxide, zinc oxide, iron oxide, calcium carbonate, silica,
Pigments made of inorganic substances such as chromium oxide and talc Organic pigments and dyes such as phthalocyanine, anthraquinone, quinacridone, azo, quinophthalone, perinone, and perylene, and are generally used for thermoplastic resins. It's fine as long as it's available.
次に顔料と分散剤との割合は、重量比で25〜75対7
5〜25であり、分散剤の配合割合がこれより大なる場
合は樹脂に対する粒状顔料組成物の添加量が増加するの
で経済的でなく、逆に小さい場合は着色剤の粒状化が困
難となる。Next, the ratio of pigment to dispersant is 25 to 75 to 7 by weight.
5 to 25, and if the blending ratio of the dispersant is larger than this, the amount of the granular pigment composition added to the resin will increase, which is not economical.On the other hand, if it is smaller, it will be difficult to granulate the colorant. .
また、本発明は、分散剤の種類及び配合比において特徴
とするものであつて、その分散剤としては高級脂肪酸金
属塩と特定の脂肪酸アミドとからなるものである。Further, the present invention is characterized by the type and blending ratio of the dispersant, and the dispersant consists of a higher fatty acid metal salt and a specific fatty acid amide.
また、その割合は重量比で5〜95対95〜5である。
このように特定した理由は、高級脂肪酸金属塩単独又は
その割合が小さい場合は成形時に被着色樹脂の喰込み不
良となりやすく、混練不足によるフラツシユ、層ハクリ
等の外観不良となる。また脂肪酸アミドが単独又はその
割合が小さい場合は喰込みは良好であるが色ムラが発生
するので好ましくない。Moreover, the weight ratio is 5 to 95 to 95 to 5.
The reason for this specification is that when a higher fatty acid metal salt is used alone or in a small proportion, the resin to be colored tends to be poorly penetrated during molding, resulting in poor appearance such as flashing and layer peeling due to insufficient kneading. Furthermore, if the fatty acid amide is used alone or in a small proportion, the biting is good, but color unevenness occurs, which is not preferable.
高級脂肪酸金属塩の具体例としては、ラウリン酸、ミリ
スチン酸、パルミチン酸、ステアリン酸、アラキン酸、
オレイン酸のカルシウム塩、バリウム塩、アルミニウム
塩、亜鉛塩、マグネシウム塩などがあげられ、これら1
種以上用いることができる。Specific examples of higher fatty acid metal salts include lauric acid, myristic acid, palmitic acid, stearic acid, arachidic acid,
Examples include calcium salts, barium salts, aluminum salts, zinc salts, and magnesium salts of oleic acid.
More than one species can be used.
また本発明で用いられる脂肪酸アミドはメチレンビスス
テアロアミドとエチレンビスステアロアミドの群から選
ばれたもので、これらの1種以上を用いる。Further, the fatty acid amide used in the present invention is selected from the group of methylene bis stearamide and ethylene bis stearamide, and one or more of these is used.
本発明は顔料分散剤の種類及びその含有量に特徴づけら
れ、粒状顔料を構成する必須成分は顔料及び該分散剤で
あるが、その他必要に応じて各播の添加剤、例えば紫外
線吸収剤・酸化防止剤・難燃剤・帯電防止剤等を添加す
ることができる。The present invention is characterized by the type and content of the pigment dispersant, and the essential components constituting the granular pigment are the pigment and the dispersant, but other additives may be added as necessary, such as ultraviolet absorbers and Antioxidants, flame retardants, antistatic agents, etc. can be added.
本発明品を製造する方法は、例えば染料または顔料と分
散剤とをタンブラ一や高速攪拌機などを用い混合攪拌し
て、その発熱を利用し溶融体とし粒状化する方法または
前記原料を混合しこれを不活性ガスの存在下、分散剤の
融点から約40℃の温度で溶融し、冷却粉砕する方法な
どあげられるが、これらに限られるものではなく、混合
して粒状化される方法であればよい。以下実施例をあげ
てさらに本発明を具体的に説明する。The product of the present invention can be manufactured by, for example, mixing and agitating a dye or pigment and a dispersant using a tumbler or a high-speed stirrer, and utilizing the heat generated to form a melt into granules, or by mixing the above-mentioned raw materials. Examples include, but are not limited to, a method in which the material is melted in the presence of an inert gas at a temperature of about 40°C below the melting point of the dispersant, cooled and pulverized, as long as it is mixed and granulated. good. EXAMPLES The present invention will be explained in more detail below with reference to Examples.
実施例 1
カーボンブラツク50重量部と第1表に示す分散剤50
重量部をペンシルミキサーにより2分間攪拌混合しミキ
サーより取り出し次いでこれを不活性ガス中で分散剤の
融点より約40℃高い温度で加熱し溶融し冷却し、これ
を粉砕し粒径0.1〜3mmの粒状顔料とした。Example 1 50 parts by weight of carbon black and 50 parts by weight of the dispersant shown in Table 1
Parts by weight are stirred and mixed for 2 minutes using a pencil mixer, taken out from the mixer, heated in an inert gas at a temperature approximately 40°C higher than the melting point of the dispersant, melted, cooled, and pulverized to obtain particles with a particle size of 0.1 to It was made into a 3 mm granular pigment.
この粒状顔料1重量部と電気化学(株)商品名「デンカ
ABSGR−200」100重量部とを三井三池製作所
FM−20型のペンシルミキサーにより撹拌数900r
pmで2分間混合した。1 part by weight of this granular pigment and 100 parts by weight of "Denka ABSGR-200" manufactured by Denki Kagaku Co., Ltd. were stirred for 900 r using a Mitsui Miike Seisakusho FM-20 type pencil mixer.
Mixed for 2 minutes at pm.
次いで日精(株)商品名「日精TS−50」、(スクリ
ユ一L/T=18、フルフライトタイプスクリュ一)の
射出成形機により80×50mmのプレートを成形し、
プレート外観性及び層ハクリを調べた。Next, a plate of 80 x 50 mm was molded using an injection molding machine manufactured by Nissei Co., Ltd. under the trade name "Nissei TS-50" (screw 1 L/T = 18, full flight type screw 1).
The plate appearance and layer peeling were examined.
その結果を第1表に示す。実施例 2
第2表に示す分散剤及びその割合を変えた他実施例1と
同様に粒状顔料を製造した。The results are shown in Table 1. Example 2 A granular pigment was produced in the same manner as in Example 1 except that the dispersants and their proportions shown in Table 2 were changed.
次いで電気化学(株)商品名「デンカABSQF」を用
いた以外実施例1と同様に行つた。これらの結果を第2
表に示す。分散剤に占めるステアリン酸亜鉛量が95重
量%を超える粒状顔料による成形品は層ハクリを示し、
5重量%未満の粒状顔料による戒形品は色ムラを呈しい
ずれも劣りステアリン酸亜鉛/メチレ8Cンビスステア
ロアミドの配合比5/95〜95/5の分散剤からなる
粒状顔料による成形品は顔料無含有QFによる成形品と
同様に良好な外観を示した。Next, the same procedure as in Example 1 was carried out except that "Denka ABSQF" manufactured by Denki Kagaku Co., Ltd. was used. These results are the second
Shown in the table. Molded products made of granular pigments in which the amount of zinc stearate in the dispersant exceeds 95% by weight exhibit layer peeling,
Molded products made of granular pigments containing less than 5% by weight of granular pigments exhibit color unevenness and are inferior.Molded products made of granular pigments containing a dispersant with a blending ratio of zinc stearate/methylene bisstearamide of 5/95 to 95/5. The molded product had the same good appearance as the molded product made of pigment-free QF.
○・・・・・・良好フラツシユなし。○...Good condition, no flashing.
△・・・・・・樹脂の流れ方向にヘアーライン状のシル
バ一あり。△・・・・・・There is hairline-like silver in the flow direction of the resin.
×・・・・・・フラツシユ部分が顕著である。(3)層
ハクリ性(DIS値)プレート(3mm厚)を樹脂の流
れ方向及び流れの直角方向の2方向から8mm×20m
mの小片をそれぞれ6本切出し、ダインスタツト衝撃強
度を測定した。×...The flash portion is noticeable. (3) Layer peelability (DIS value) Plate (3 mm thick) is 8 mm x 20 m from two directions: the flow direction of the resin and the direction perpendicular to the flow.
Six small pieces of m were cut out, and the die stud impact strength was measured.
樹脂の流れ方向、直角方向のダインスタツト衝撃強度の
平均値をそれぞれXT、XYとし次の式からDiS値を
求めた。The DiS value was determined from the following equation, with the average values of the die-stud impact strength in the resin flow direction and the right angle direction being XT and XY, respectively.
DiS値=又Y/又TDiS値が1.0に近いもの程衝
撃強度の方向性がなく層ハクリのない均質な樹脂と判断
できる。DiS value = Y/Also, the closer the TDiS value is to 1.0, the more directional the impact strength is and it can be judged that the resin is homogeneous without layer peeling.
(4)ハクリ試験
ゲート形状がタブ式のプレートを使用しタブ部分を折り
曲げた後樹脂の流れ方向に引きはがしはがれた面積の多
少を目視判定した。(4) Peeling test A plate with a tab-shaped gate was used, and after the tab portion was bent, the plate was peeled off in the flow direction of the resin, and the peeled area was visually judged.
Claims (1)
の混合物であつて、しかもその分散剤が高級脂肪酸の金
属塩とメチレンビスステアロアミド又はエチレンビスス
テアロアミドからなり、かつ、3その割合が重量で5〜
95:95〜5である粒状顔料。1 A mixture of 25 to 75% by weight of a pigment and 75 to 25% by weight of a dispersant, in which the dispersant consists of a metal salt of a higher fatty acid and methylene bisstearamide or ethylene bisstearamide, and 3 The ratio is 5~ by weight
95: Particulate pigment having a ratio of 95 to 5.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9255881A JPS5934738B2 (en) | 1981-06-16 | 1981-06-16 | granular pigment |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9255881A JPS5934738B2 (en) | 1981-06-16 | 1981-06-16 | granular pigment |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS57207652A JPS57207652A (en) | 1982-12-20 |
| JPS5934738B2 true JPS5934738B2 (en) | 1984-08-24 |
Family
ID=14057740
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP9255881A Expired JPS5934738B2 (en) | 1981-06-16 | 1981-06-16 | granular pigment |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5934738B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS61234817A (en) * | 1986-03-17 | 1986-10-20 | 松下電器産業株式会社 | electric coffee brewer |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0619055B2 (en) * | 1986-08-29 | 1994-03-16 | 水澤化学工業株式会社 | Filler for resin molded products |
| JPS6366247A (en) * | 1986-09-05 | 1988-03-24 | Toyo Tire & Rubber Co Ltd | Production of rubber composition |
| JPH02105835A (en) * | 1988-08-24 | 1990-04-18 | Pluss Stauffer Ag | Coated inorganic filler or coated inorganic flameproofing agent |
| ES2156213T3 (en) * | 1994-07-12 | 2001-06-16 | Cabot Corp | GRANULES AVAILABLE FROM SMOKE BLACK. |
| US6204319B1 (en) | 1998-10-30 | 2001-03-20 | E.I. Du Pont De Nemours And Company | Aqueous coating compositions |
| IT201600109323A1 (en) | 2016-10-28 | 2018-04-28 | Giovanni Broggi | UNIVERSAL PIGMENTARY PREPARATIONS FOR COLORING AND REINFORCING PLASTIC MATERIALS |
-
1981
- 1981-06-16 JP JP9255881A patent/JPS5934738B2/en not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS61234817A (en) * | 1986-03-17 | 1986-10-20 | 松下電器産業株式会社 | electric coffee brewer |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS57207652A (en) | 1982-12-20 |
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