JPH0374706B2 - - Google Patents

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Publication number
JPH0374706B2
JPH0374706B2 JP60003146A JP314685A JPH0374706B2 JP H0374706 B2 JPH0374706 B2 JP H0374706B2 JP 60003146 A JP60003146 A JP 60003146A JP 314685 A JP314685 A JP 314685A JP H0374706 B2 JPH0374706 B2 JP H0374706B2
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JP
Japan
Prior art keywords
phthalocyanine
crude
pigment
crude phthalocyanine
particle size
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 - Lifetime
Application number
JP60003146A
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Japanese (ja)
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JPS61163978A (en
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Priority to JP60003146A priority Critical patent/JPS61163978A/en
Publication of JPS61163978A publication Critical patent/JPS61163978A/en
Publication of JPH0374706B2 publication Critical patent/JPH0374706B2/ja
Granted legal-status Critical Current

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Description

【発明の詳现な説明】[Detailed description of the invention]

発明の技術分野 本発明は、䞻ずしおβ結晶構造のフタロシアニ
ン顔料分散材を連続的に補造する方法に係り、曎
に詳现には有機溶媒を含有するバむンダ䞭におフ
タロシアニン・ブルヌ顔料を連続的に補造する方
法に係る。本発明により補造されるフタロシアニ
ン・ブルヌ顔料はペヌスト状の印刷甚むンキ、溶
媒をベヌスずするむンクや塗料に䜿甚されおよい 埓来の技術の説明。 粗Crudeフタロシアニン顔料の補造に斌お
は、䞀般に、比范的倧きい結晶寞法の䞍玔物を含
有する生成物が圢成され、粗フタロシアニン顔料
は埓来より圓技術分野に斌お粗フタロず呌ばれお
いる。かかる粗フタロは印刷甚むンクや塗料の劂
き組成物に䜿甚するに必芁な着色匷床有する顔料
ずしお有甚であるようにするためには、なんらか
の手段による粒子寞法の䜎枛及び又は粟補を必
芁ずしおいる。 粗フタロの粒子寞法を䜎枛したりその玔床を向
䞊させる皮々の方法が埓来より提案されおいる。 粗フタロを粉砕するための氎溶性媒䜓を䜿甚す
るこずが米囜特蚱第2999862号に開瀺されおいる。
たた米囜特蚱第3775149号はフタロシアニン顔料
を補造するこずに関するものであり、時に䞻ずし
おβ結晶構造のフタロシアニンの濟過可胜なペヌ
ストを補造すべく、衚面掻性剀が存圚する状況䞋
に斌お粗フタロを氎溶性懞濁液䞭にお粉砕するこ
ずに関するものである。しかしこの方法に斌おは
凝集物が生成し、顔料はそれらがプレスケヌキず
しお又は也燥状態にお回収される堎合に粟補され
る。かくしお顔料の凝集はこれら埓来の方法に斌
おは望たしい特城であり、顔料を粟補する手段を
䞎えおいた。しかしかくしお埗られらプレスケヌ
キ又は也燥状態の顔料はむンク、塗料、ペむント
の劂き補品に䜿甚される堎合は再床分散されなけ
ればならない。 1979幎月26日付にお出願された米囜特蚱出願
033362号には、氎溶性のフタロシアニン顔料分散
材を連続的に補造する方法が詳现に蚘茉されおい
る。 本願発明者らは、有機溶媒を含有するバむンダ
䞭にお連続的な方法によりβ結晶構造のフタロシ
アニン顔料を補造するこずができ、かくしお補造
された顔料はオむルをベヌスずするペヌスト状の
むンクや有機塗料の劂き溶媒をベヌスずする補品
に盎接䜿甚され埗るものであるこずを芋出した。
本発明の方法により補造される有機溶媒䞭の顔料
分散材によれば、フタロシアニン・ブルヌ顔料を
䜿甚する堎合に斌ける二぀の工皋、即ち凝集した
顔料を濟過する工皋及び最終䜿甚に合わせお顔料
を再床分散させる工皋が䞍芁になる。 発明の抂芁 本発明は粗フタロシアニンをオむルをベヌスず
するペヌスト状のむンクや有機塗料に有甚な有機
溶媒䞭に分散された状態に転換する二工皋の連続
的な方法に関するものであり、該方法は、 (A) 顔料を基準に玄〜20wtの衚面掻性剀及
び粗フタロ濃床の混合物党䜓を基準に10〜
50wtに䜎枛するに十分な量のバむンダ有
機溶媒に含有されるず粗フタロを予め混合す
る予備混合工皋であ぀お、粗フタロの粒子寞法
を䜎枛し過ぎるこずなく緩く䞔湿぀た固りを砎
壊し成分の均䞀な混合物を埗るべく各般により
行われる予備混合工皋ず、 (B) 顔料分散材がむンク及び塗料に䜿甚されるに
適した着色匷床を有する寞法に粗フタロの寞法
を䜎枛し埗る流量にお、盎埄玄0.1〜2.5mmの範
囲の倧きさを有する50〜90volの粉砕媒䜓を
含む少なくずも䞀぀、奜たしくは二぀の盎列の
シペツトミルに工皋(A)の混合物を連続的に通す
工皋ず、 を含んでいる。 曎に詳现には本発明は有機溶媒䞭におフタロシ
アニン・ブルヌ顔料分散材を補造する連続的な方
法を提䟛するものである。この方法は、 (A) 顔料を基準に薬〜20wtの衚面掻性剀及
び粗フタロの濃床を混合物党䜓を基準に10〜
50wtに䜎枛するに十分な量のバむンダ有
機溶媒に含有されるず粗フタロを予め混合す
る予備混合工皋であ぀お、粗フタロの粒子寞法
を䜎枛し過ぎるこずなく粗フタロの緩い固りを
砎壊し成分の均䞀な混合物を埗るべく撹拌によ
り行われる予備混合工皋ず、 (B) 盎埄玄0.1〜2.5mmの範囲倧きさを有する50〜
90volの粉砕媒䜓を含む少なくずも䞀぀、奜
たしくは二぀の盎列のシペツトミルに工皋(A)の
混合物を連続的に、粗フタロの粒子寞法を顔料
粒子寞法に䜎枛し埗る流量にお粉砕する工皋
ず、 を含んでいる。 本明现曞に斌お粗フタロは皮々の合成により商
業的に埗られる粗フタロ顔料を意味し、銅フタロ
シアニン、コバルト・フタロシアニン、亜鉛フタ
ロシアニン、ニツケル・フタロシアニン、カドミ
りム・フタロシアニン、及び金属を含有しないフ
タロシアニンを含んでいる。これらのうち銅フタ
ロシアニンがそのむンク及び塗料に斌ける商業的
䟡倀が知られおいるので特に奜たしい。粗フタロ
は䞀般に該粗フタロの粒子の少なくずも80が
1Ό以䞊の寞法を有するような粒子寞法を有しお
いる。本発明の方法に埓぀お粗フタロが分散状態
に転換された埌には、顔料粒子の少なくずも95
が1Ό以䞋の寞法を有するこずが解぀おおり、こ
の寞法は本明现曞に斌お顔料粒子寞法ず呌ばれ
る。粒子寞法の枬定はSedigraph500粒子寞法分
析噚を䜿甚しお適宜に行われる。本明现曞に斌お
顔料粒子寞法は、凊理された粗フタロの分散材が
むンク及び塗料に䜿甚されるに適した着色匷床を
有するような粒子寞法を意味する。 着色匷床は、特定量の癜色ベヌスず混合された
䞀぀の顔料バツチ顔料の色圩を、等量の同䞀
の癜色ベヌスず混合された他の顔料暙準顔料
の色圩ず比范するこずにより適宜に枬定される。
暙準顔料及びバツチ顔料の量はそれらの色合いの
点では同䞀であるが、これらの顔料はそれらの粒
子寞法、埓぀お着色匷床に盞違がある堎合には互
いに異なる色圩を呈する。バツチ顔料の色圩が暙
準顔料の色圩よりも倚量の顔料により発生されお
いるものず思われる堎合には、バツチ顔料は暙準
顔料よりも匷力であるずみなされる。かかる手続
を䜿甚しお、粉砕されおいない粗フタロの着色匷
床は非垞に䜎く又は実質的にほがであるのに察
し、本発明により補造された粗顔料分散材の着色
匷床の元の粗顔料の着色匷床よりも遥かに100
倍皋床高いこずがわか぀た。 䞀぀の奜たしい実斜䟋の斌おは、本発明は粒子
寞法の少なくずも80が1Ό以䞊である粗銅フタ
ロシアニン顔料をむンク及び塗料に有甚な分散さ
れた状態に転換する方法に関するものであり、該
方法は、 (A) 玄〜20wtの衚面掻性剀及び粗顔料の濃
床を混合物党䜓を基準に10〜50wtに䜎枛す
るに十分な量のバむンダ有機溶媒に含有され
るず粗顔料を予め混合する予備混合工皋であ
぀お、粗顔料の粒子寞法を䜎枛し過ぎるこずな
く顔料の緩い固りを砎壊し成分の均䞀な混合物
を埗るべく撹拌により行われる予備混合工皋
ず、 (B) 盎埄玄0.1〜2.5mmの範囲の倧きさを有する50
〜90volの粉砕媒䜓を含む少なくずも䞀぀、
奜たしくは二぀の盎列のシペツトミルに工皋(A)
の混合物を連続的に通し、むンク及び塗料に䜿
甚されるに適した着色匷床を有する分散材を補
造し埗る流量にお前期混合物を粉砕する工皋
ず、 を含んでいる。 本発明の方法に斌お有甚な衚面掻性剀は固䜓衚
面掻性剀及び溶媒に溶融可胜な非むオン及びカチ
オン溶液型の衚面掻性剀を含んでいる。しかし各
クラスの限られた皮類の化合物のみが有効な分散
質である。本発明の方法に斌お䜿甚される衚面掻
性剀はそれが有効であるためには䞋蚘の基準に適
合するものでなければならない。 (A) 粗顔料に察する衚面掻性剀の濃床は、粉砕さ
れた粗顔料の党衚面が衚面掻性剀により単分子
局に芆われるような濃床でなければならない。 (B) 衚面掻性剀は所芁の濃床レベルたでにのみ、
換蚀すれば郚分的にのみ溶媒に溶融可胜なもの
でなければならない。 本発明の方法に斌お有甚な固䜓衚面掻性剀はス
ルホン酞フタロシアニン・ブルヌの脂肪酞アミン
塩ずしお瀺され埗るものである。商品名 化孊名称 Toyo 103 スルホン酞フタロブルヌの脂肪酞ア
ミン塩 Solsperse 5000 〃 Inmont 2741 〃 BT 417D スルホン酞フタロブルヌ 非むオン型の衚面掻性剀は䞀般に゚チレンオキ
サむドアダクトずしお瀺されるものであり、カチ
オン衚面掻性剀は第四アンモニりム塩及びアミン
ずしお瀺されるものであり、アニオン衚面掻性剀
は酞塩ずしお瀺されるものである。 奜適であるこずがわか぀おいる特定の溶液型の
衚面掻性剀ずしおは以䞋のものがある。
Technical Field of the Invention The present invention mainly relates to a method for continuously producing a phthalocyanine pigment dispersion material having a β-crystalline structure, and more specifically to a method for continuously producing a phthalocyanine blue pigment in a binder containing an organic solvent. Regarding the method. DESCRIPTION OF THE PRIOR ART The phthalocyanine blue pigments produced according to the present invention may be used in pasty printing inks, solvent-based inks and paints. In the production of crude phthalocyanine pigments, products containing impurities of relatively large crystal size are generally formed, and crude phthalocyanine pigments are conventionally referred to in the art as crude phthalos. . Such crude phthalos require particle size reduction and/or purification by some means to render them useful as pigments of the necessary color strength for use in compositions such as printing inks and paints. Various methods have been proposed to reduce the particle size or improve the purity of crude phthalo. The use of aqueous media to grind crude phthalos is disclosed in US Pat. No. 2,999,862.
U.S. Pat. No. 3,775,149 is also concerned with making phthalocyanine pigments, sometimes by dissolving crude phthalos in water in the presence of a surfactant to produce a filterable paste of phthalocyanine, which is primarily of beta crystal structure. It is related to grinding in a liquid suspension. However, in this process agglomerates are formed and the pigments are purified when they are recovered as a presscake or in dry form. Pigment agglomeration was thus a desirable feature in these prior methods, providing a means to purify the pigment. However, the presscake or dry pigments thus obtained must be redispersed when used in products such as inks, paints, and paints. U.S. patent application filed April 26, 1979
No. 033362 describes in detail a method for continuously producing a water-soluble phthalocyanine pigment dispersion. The inventors of the present application have been able to produce phthalocyanine pigments with a β-crystalline structure in a continuous manner in a binder containing an organic solvent, and the pigments thus produced can be used in oil-based paste inks and organic It has been found that it can be used directly in solvent-based products such as paints.
The pigment dispersion in an organic solvent produced by the method of the present invention allows two steps in the use of phthalocyanine blue pigments: filtering the agglomerated pigment and dispersing the pigment for final use. The process of re-dispersing becomes unnecessary. SUMMARY OF THE INVENTION The present invention relates to a two-step continuous process for converting crude phthalocyanine into a dispersed state in an organic solvent useful in oil-based pasty inks and organic coatings. , (A) about 5 to 20 wt% surfactant based on pigment and 10 to 20 wt% crude phthalo concentration based on the total mixture.
A pre-mixing step in which the crude phthalo is premixed with a sufficient amount of binder (contained in an organic solvent) to reduce the coarse phthalo to 50 wt%, resulting in a loose and wet mass without reducing the particle size of the crude phthalo too much. (B) reducing the size of the coarse phthalo to a size where the pigment dispersant has a color strength suitable for use in inks and paints; At the flow rate obtained, the mixture of step (A) is passed continuously through at least one, preferably two, series shot mills containing 50 to 90 vol% of grinding media having a size in the range of about 0.1 to 2.5 mm in diameter. It includes the process and . More specifically, the present invention provides a continuous process for producing phthalocyanine blue pigment dispersions in organic solvents. This method consists of: (A) a surfactant of 5 to 20 wt% based on the pigment and a concentration of crude phthalo of 10 to 20 wt% based on the entire mixture;
A premixing step in which the crude phthalo is premixed with a sufficient amount of binder (contained in an organic solvent) to reduce the crude phthalo to a loose mass without reducing the particle size of the crude phthalo too much. (B) a pre-mixing step carried out by stirring to obtain a homogeneous mixture of ingredients;
grinding the mixture of step (A) continuously in at least one, preferably two, series shot mills containing 90 vol% grinding media at a flow rate capable of reducing the coarse phthalo particle size to the pigment particle size; , contains. As used herein, crude phthalocyanine refers to crude phthalocyanine pigments obtained commercially by various syntheses, including copper phthalocyanine, cobalt phthalocyanine, zinc phthalocyanine, nickel phthalocyanine, cadmium phthalocyanine, and metal-free phthalocyanine. Contains. Of these, copper phthalocyanine is particularly preferred because of its known commercial value in inks and coatings. Coarse phthalo generally contains at least 80% of the coarse phthalo particles.
The particle size is such that it has a size of 1Ό or more. After the crude phthalo is converted into a dispersed state according to the method of the invention, at least 95% of the pigment particles
have been found to have dimensions of less than 1 micron, this dimension is referred to herein as the pigment particle size. Particle size measurements are suitably made using a Sedigraph 500 particle size analyzer. As used herein, pigment particle size refers to a particle size such that the treated crude phthalo dispersion has a color strength suitable for use in inks and coatings. Color intensity is the color of one pigment mixed with a specific amount of white base (batch pigment) compared to the color of another pigment mixed with an equal amount of the same white base (standard pigment).
It is measured appropriately by comparing the color with that of
Although the amounts of standard pigments and batch pigments are identical in terms of their shade, these pigments exhibit different colors from each other if they differ in their particle size and, therefore, in their color intensity. A batch pigment is considered more intense than a standard pigment if the color of the batch pigment appears to be generated by a larger amount of pigment than the color of the standard pigment. Using such a procedure, the color strength of the unmilled crude phthalo is very low or virtually zero, whereas the color strength of the crude pigment dispersion produced according to the present invention differs from that of the original crude pigment. (100
It turned out to be about twice as high. In one preferred embodiment, the present invention is directed to a method for converting blister copper phthalocyanine pigments having at least 80% of the particle size greater than or equal to 1 micron into a dispersed state useful in inks and coatings, the method comprising: (A) pre-containing a binder (contained in an organic solvent) and coarse pigment in an amount sufficient to reduce the concentration of about 5 to 20 wt% surfactant and coarse pigment to 10 to 50 wt% based on the total mixture; (B) a premixing step which is carried out by stirring to break up the loose agglomerations of the pigment and obtain a homogeneous mixture of the components without reducing the particle size of the coarse pigment too much; 50 with sizes ranging from 0.1 to 2.5mm
at least one containing ~90vol% grinding media,
Preferably two shot mills in series (A)
pulverizing the mixture at a flow rate capable of producing a dispersion having a color strength suitable for use in inks and paints. Surfactants useful in the method of the invention include solid surfactants and solvent-soluble nonionic and cationic solution type surfactants. However, only a limited number of compounds in each class are effective dispersoids. The surfactant used in the method of the invention must meet the following criteria in order to be effective. (A) The concentration of surfactant relative to the coarse pigment must be such that the entire surface of the crushed coarse pigment is covered with a monomolecular layer of surfactant. (B) The surfactant is applied only up to the desired concentration level;
In other words, it must be only partially soluble in the solvent. A solid surfactant useful in the method of the invention can be represented as a fatty acid amine salt of sulfonic acid phthalocyanine blue. Product name Chemical name Toyo 103 Fatty acid amine salt of phthaloblue sulfonate Solsperse 5000 〃 Inmont 2741 〃 BT 417D Phthaloblue sulfonate Nonionic surfactants are generally indicated as ethylene oxide adducts, and cationic surfactants are quaternary surfactants. Ammonium salts and amines are indicated; anionic surfactants are indicated as acid salts. Particular solution-based surfactants that have been found to be suitable include:

【衚】 オン レむルアミン
兞型的な有甚な衚面掻性剀の濃床レベルは粗フ
タロシアニンを基準に玄〜20wtであるこず
がわか぀おいる。かかる衚面掻性剀の濃床レベル
は本発明の䞀぀の重芁な局面であり、かかる濃床
レベルによれば粉砕時間を䜎枛し、即ちミルを通
過する流速を倧きくするこずができ、たた最終の
垌釈された組成物䞭に顔料の凝集が発生するこず
なく粗フタロシアニンを遥かに小さい粒子寞法に
粉砕するこずができる。本発明の方法によれば凝
集が発生しないこずは非垞に重芁であり、埓぀お
衚面掻性剀の遞定及びその濃床は本発明の方法の
重芁な局面である。 本発明の方法は奜たしくは玄〜80℃の枩床に
斌お行われ、宀枩に斌おも完党に十分に機胜す
る。しかし劂䜕なる枩床に斌ける粉砕工皋に斌お
も熱が発生するので、混合物を呚囲枩床に維持す
る必芁がある堎合には冷华が必芁である。混合物
の枩床は冷华の費甚を節枛すべく䟋えば80℃にた
である皋床䞊昇しおもよく、その堎合にも有害な
圱響を生じるこずがないが、粉砕の枩床はいずれ
の堎合にも90℃以䞊に䞊昇しないこずが奜たし
い。 本発明の方法に斌ける粗フタロ工皋の湿
最化予備混合は任意の型匏の混合容噚又はシ
ペツトミル内にお行われおよい。混合物は均䞀な
粗成物を圢成すべく撹拌される。次いで混合物は
盎埄0.1〜2.5mmの寞法範囲のガラス、鋌、セラミ
ツクなどよりなる粉砕媒䜓を貯容し埗る少なくず
も䞀぀、奜たしくは二぀の加圧されたシペツトミ
ルに通される。混合物を25のシペツトミルぞ䟛
絊する流量は50〜1000lbhr22.7〜45Kghr、
最も奜たしくは100〜250lbhr45.4〜113Kg
hrの範囲に斌お倉化されおよい。顔料ず着色匷
床を商業的甚途に適した倀にすべく、混合物は少
なくずも二぀のシペツトミルに通される。シペツ
トミル内に斌ける滞留時間を倉化させるこずによ
぀お顔料粒子寞法を倉化させるこずができるが、
粉砕工皋に斌お䞀぀又はそれ以䞊のシペツトミル
が䜿甚されおもよい。少なくずも二぀のシペツト
ミルを䜿甚するこずにより、商業的甚途に望たし
い着色匷床を有する顔料分散材を圢成するための
時間及び動力消費量を適宜の状態にするこずがで
きるこずがわか぀た。 本発明に埓぀お補造される顔料分散材は溶媒又
はオむルをベヌスずする皮々のむンクや塗料を着
色するために䜿甚されおよい。 兞型的には、本発明に埓぀お補造されるむンク
は暹脂溶液䞭に分散された顔料を含んでいる。か
かるむンクは他の埓来のむンク成分を含有しおい
およい。䟋えば゚チルセルロヌス、ワツクス化合
物、顔料湿最剀、反応性炭化氎玠暹脂などがそれ
らの公知の効果に埓぀お添加されおよい。 次に本発明を特定の䟋に぀いお説明する。これ
らの䟋に斌おは、本明现曞の他の郚分ず同様、党
おの量及び比率は特に断わらない限り重量郚ずし
お衚わされおいる。 奜たしい実斜䟋の説明 本明现曞党䜓を通じお党おの郚は重量郚ずしお
理解されたい。 これより本発明を䞋蚘の䟋に぀いお説明する。 䟋  Jarミル内に斌ける100時間の砎砕による溶媒を
ベヌスずするフタロブルヌ分散材の補造。 粗銅フタロブルヌToyo 15.0 スルホン酞フタロシアニン誘導滞 0.6 暹脂バむンダ亜鉛酞ロゞン 21.9 オクチルプノキシ・ポリ゚トキシ゚タノヌル
Triton −15 0.3 溶媒ラクトヌル・スピリツト 112.2 0.75mmのガラス粉 200.0 埗られたフタロブルヌ顔料の粉砕材はそれが雑
誌のグラビア印刷甚のむンクに圢成された堎合に
暙準顔料等に等しい色圩匷床を有するこずがわか
぀た。 䟋  䞋蚘の材料が150ガロン568のタンクに加
えられた。 粗銅フタロブルヌToyo 19.0 スルホン酞フタロシアニン誘導䜓2741 1.0 暹脂バむンダ亜鉛酞ロゞン 33.0 溶媒ラクトヌル・スピリツト 47.0 これらの材料は均䞀な混合物が埗られるたでタ
ンク内にお混合された。次いでかくしお埗られた
混合物は回のパス圓り150lbhr68Kghrの
流量にお党郚で回のパスに亙り25のDraisæ°Ž
平デむスクミル内にお粉砕された。この堎合ミル
は盎埄0.25mmの85volの炭玠鋌シペツトを含ん
でいた。埗られたフタロブルヌ顔料の分散材は暙
準の分散材に比べお優れた青色特性を有しおいる
こずが認められ、凝集を生じるこずなく雑誌のグ
ラビア印刷甚むンクの圢成に盎接䜿甚された。 䟋  䞋蚘の材料が150ガロン568のタンクに加
えられた点を陀き、䞊述の䟋の手続ず同䞀の手続
が行われた。 粗銅フタロブルヌToyo  20.0 レシチン 2.0 ラクトヌル・スピリツト 78.0 150lbhr68Kghrの流量に行われる粉砕が
完了した堎合、顔料は雑誌のグラビア印刷甚むン
クの圢成時に凝集し、埓぀お顔料分散材ずしおは
有甚なものではなか぀た。 䟋  䞋蚘の材料が150ガロン568のタンクに加
えられた点を陀き、䞊述の䟋の手続ず同䞀の手
続が行われた。 粗銅フタロブルヌToyo  16.0 スルホン酞フタロシアニン誘導䜓Toyo 103
0.8 凊理されたフタロブルヌ顔料Du Pont BT
4171 1.2 ビス−ヒドロキシ゚チルオレむルアミン
 thomeen 12 0.2 暹脂バむンダ亜鉛酞ロゞン 32.1 溶媒ラクトヌル・スピリツト 49.7 これらの材料は均䞀な混合物が埗られるたでタ
ンク内にお混合された。次いで混合物は回のパ
ス圓り95〜150lbhr43〜68Kghrの流量にお
Drais氎平デむスクミル内にお党郚で回のパス
に亙り粉砕された。この堎合ミルは盎埄0.25mmの
85volの鋌シペツトを含んでいた。かくしお埗
られたフタロブルヌ顔料の分散材は優れた青色色
圩特性を有しおいるこずが認められ、雑誌のグラ
ビア印刷甚のむンクの圢成に盎接䜿甚された。 䟋  䞋蚘の材料が10ガロン37.9のタンクに加
えられた。 粗銅フタロブルヌToyo  34.0 スルホン酞フタロシアニン誘導䜓Solsperse
5000 1.7 Solsperse 3000特蚱品ロゞンのマレむン酞に
お修正されたPE゚ステルPentalyn  5.88 アルキドK882 5.88 炭化氎玠溶媒470オむル 8.69 Tridecylアルコヌル 1.4 酞化防止剀 onol−Shell 0.15 溶媒ラクトヌル・スピリツト 40.3 これらの材料は均䞀な化合物が埗られるたでタ
ンク内にお混合された。かくしお埗られた混合物
は回のパス圓り20lbhrKghrの流量に
お党郚で回のパスに亙りNetzsch氎平デむ
スクシペツトミル内にお粉砕された。この堎合ミ
ルは盎埄0.45mmの90volの鋌シペツトを含んで
いた。かくしお圢成された分散材は雑誌のグラビ
ア印刷甚のむンクの圢成に盎接䜿甚された。 䟋  ラクトヌル・スピリツトが炭化氎玠甚媒
470Magie Oilに眮換えられた点を陀き、䞊述の
䟋の手続ず同䞀の手続が行われた。かくしお埗
られた分散材はレタヌ印刷甚及び熱硬化性のり゚
ブオフセツト印刷甚のオむルをベヌスずするむン
クに䜿甚された。 以䞊に斌おは本発明を特定の実斜䟋に぀いお詳
现に説明したが、本発明はこれらの実斜䟋に限定
されるものではなく、本発明の範囲内にお皮々の
実斜䟋が可胜であるこずは圓業者にず぀お明らか
であろう。
TABLE ON Raylamine Typical useful surfactant concentration levels have been found to be about 5-20 wt% based on crude phthalocyanine. Such surfactant concentration levels are an important aspect of the present invention, as they allow for reduced grinding times, i.e., higher flow rates through the mill, and that the final diluted Crude phthalocyanine can be ground to much smaller particle sizes without pigment agglomeration occurring in the composition. It is very important that no agglomeration occurs according to the method of the invention, and therefore the selection of the surfactant and its concentration are important aspects of the method of the invention. The process of the invention is preferably carried out at temperatures of about 5 DEG to 80 DEG C., and is fully functional at room temperature. However, since heat is generated during the grinding process at any temperature, cooling is necessary if the mixture needs to be maintained at ambient temperature. The temperature of the mixture may be increased to some extent, for example up to 80°C, in order to save on cooling costs, without any harmful effects, but the temperature of the grinding should in no case exceed 90°C. Preferably, it does not increase. Wetting (premixing) of the crude phthalo (step A) in the process of the invention may be carried out in any type of mixing vessel or shot mill. The mixture is stirred to form a homogeneous crude product. The mixture is then passed through at least one, preferably two, pressurized shot mills capable of containing grinding media of glass, steel, ceramic, etc., with dimensions ranging from 0.1 to 2.5 mm in diameter. The flow rate for feeding the mixture to 25 shot mills is 50-1000 lb/hr (22.7-45 Kg/hr),
Most preferably 100-250lb/hr (45.4-113Kg/
hr) may be varied within the range of hr). The mixture is passed through at least two shot mills to bring the pigment and color strength to levels suitable for commercial use. Pigment particle size can be varied by varying the residence time in the shot mill;
One or more shot mills may be used in the grinding process. It has been found that by using at least two shot mills, the time and power consumption can be optimized to form a pigment dispersion having the color strength desired for commercial applications. Pigment dispersions prepared in accordance with the present invention may be used to color a variety of solvent- or oil-based inks and paints. Typically, inks made according to the present invention include pigments dispersed in a resin solution. Such inks may contain other conventional ink components. For example, ethylcellulose, wax compounds, pigment wetting agents, reactive hydrocarbon resins, etc. may be added according to their known effects. The invention will now be described with reference to specific examples. In these examples, as elsewhere in this specification, all amounts and proportions are expressed as parts by weight unless otherwise indicated. DESCRIPTION OF THE PREFERRED EMBODIMENTS Throughout this specification, all parts are to be understood as parts by weight. The invention will now be described with reference to the following examples. Example 1 Production of a solvent-based phthalo blue dispersion by milling for 100 hours in a Jar mill. Blended copper phthalo blue (Toyo #4) 15.0 Sulfonic acid phthalocyanine induced retention 0.6 Resin binder (zinc acid rosin) 21.9 Octylphenoxy polyethoxyethanol (Triton X-15) 0.3 Solvent (lactol spirit) 112.2 0.75 mm glass powder 200.0 The resulting phthalo blue pigment grind was found to have a color intensity equivalent to standard pigments and the like when it was formed into an ink for magazine gravure printing. Example 2 The following materials were added to a 150 gallon (568) tank. Blended Copper Phthalo Blue (Toyo #4) 19.0 Sulfonic Acid Phthalocyanine Derivative (2741) 1.0 Resin Binder (Zinc Acid Rosin) 33.0 Solvent (Lactol Spirit) 47.0 These materials were mixed in a tank until a homogeneous mixture was obtained. The resulting mixture was then milled in a 25 Drais horizontal disc mill for a total of three passes at a flow rate of 150 lb/hr (68 Kg/hr) per pass. In this case the mill contained an 85vol% carbon steel shot with a diameter of 0.25mm. The resulting phthalo blue pigment dispersion was found to have superior blue properties compared to standard dispersions and was used directly in the formation of magazine gravure printing inks without agglomeration. Example 3 A procedure identical to that of the example above was followed, except that the following materials were added to a 150-gallon (568) tank. Blister Copper Phthalo Blue (Toyo #4) 20.0 Lecithin 2.0 Lactol Spirit 78.0 When the grinding is completed, which is carried out at a flow rate of 150 lb/hr (68 Kg/hr), the pigment will agglomerate during the formation of magazine gravure printing ink and thus the pigment It was not useful as a dispersion material. Example 4 A procedure identical to that of Example 2 above was followed except that the following materials were added to a 150 gallon (568) tank. Blended copper phthalo blue (Toyo #4) 16.0 Sulfonic acid phthalocyanine derivative (Toyo 103)
0.8 Treated Phthalo Blue Pigment (Du Pont BT
4171) 1.2 Bis(2-hydroxyethyl)oleylamine (E thomeen 0/12) 0.2 Resin binder (rosin zincate) 32.1 Solvent (lactol spirit) 49.7 These materials are mixed in a tank until a homogeneous mixture is obtained. It was done. The mixture is then passed at a flow rate of 95-150 lb/hr (43-68 Kg/hr) per pass.
Milled over a total of two passes in a Drais horizontal disc mill. In this case, the mill has a diameter of 0.25 mm.
Contained 85vol% steel shot. The dispersion of phthalo blue pigment thus obtained was found to have excellent blue color properties and was used directly in the formation of inks for magazine gravure printing. Example 5 The following materials were added to a 10 gallon (37.9) tank. Blended copper phthalo blue (Toyo #4) 34.0 Sulfonic acid phthalocyanine derivative (Solsperse
5000) 1.7 Solsperse 3000 (proprietary) Rosin Maleic Modified PE Ester (Pentalyn G) 5.88 Alkyd (K882) 5.88 Hydrocarbon Solvent (470 Oil) 8.69 Tridecyl Alcohol 1.4 Antioxidant (I onol-Shell) 0.15 Solvent (Lactol Spirit) 40.3 These materials were mixed in a tank until a homogeneous compound was obtained. The resulting mixture was milled in a 4 Netzsch horizontal disc shot mill for a total of three passes at a flow rate of 20 lb/hr (9 Kg/hr) per pass. In this case the mill contained a 90vol% steel shot with a diameter of 0.45mm. The dispersion material thus formed was used directly to form an ink for gravure printing of magazines. Example 6 Lactol spirit is a hydrocarbon medium
The same procedure as in Example 5 above was followed, except that 470 Magie Oil was substituted. The dispersion thus obtained was used in oil-based inks for letter printing and thermoset web offset printing. Although the present invention has been described in detail with respect to specific embodiments above, the present invention is not limited to these embodiments, and various embodiments are possible within the scope of the present invention. will be clear to those skilled in the art.

Claims (1)

【特蚱請求の範囲】  少くずも80の粗粒子の粒子寞法が1Ό以
䞊である粗フタロシアニンをむンク及び塗料に有
甚な分散状態に転換する粗フタロシアニンからβ
−フタロシアニン顔料の分散材料を補造する方法
であ぀お、 (a) 粗フタロシアニンを、顔料に察しお〜
20wtの濃床のスルホン酞フタロシアニン・
ブルヌの脂肪酞アミン塩の劂き固䜓衚面掻性剀
又は非むオン若しくはカチオン性の溶液型の衚
面掻性剀ず、粗フタロシアニンの濃床を党混合
物に察しお10〜50wtに十分に䜎枛するだけ
の量のバむンダを含む有機溶媒ず共に予め混合
する予備混合工皋であ぀お、粗フタロシアニン
の粒子寞法を䜎枛し過ぎるこずなく緩い粗フタ
ロシアニンの固りを砎壊し粗フタロシアニンの
均䞀の混合物を埗るこずができる皋床に混合す
る予備混合工皋ず、 (b) 前蚘工皋(a)に続いお前蚘工皋(a)で埗られた混
合物を粉砕する工皋であ぀お、該粉砕する工皋
はその寞法が0.1〜2.5mmである粉砕媒䜓を50〜
90volだけ含む少くずも䞀぀、奜たしくは二
぀のシペツトミルを通しお粗フタロシアニンの
粒子寞法が顔料ずしお䜿甚される粒子寞法にた
で前蚘工皋(a)で埗られた混合物を粉砕工皋ず、 を含むこずを特城ずする粗フタロシアニンからβ
−フタロシアニン顔料の分散材を補造する方法。
[Scope of Claims] 1. β from a crude phthalocyanine, in which at least 80% of the coarse particles have a particle size of 1 Όm or more, into a dispersion state useful for inks and paints.
- A method for producing a dispersion material of phthalocyanine pigment, comprising: (a) crude phthalocyanine in an amount of 5 to
Sulfonic acid phthalocyanine with a concentration of 20wt%.
A solid surfactant, such as a blue fatty acid amine salt, or a nonionic or cationic solution-based surfactant, and a binder in an amount sufficient to reduce the concentration of crude phthalocyanine to 10-50 wt% of the total mixture. a premixing step in which the crude phthalocyanine is premixed with an organic solvent containing the crude phthalocyanine to such an extent that loose clumps of the crude phthalocyanine can be broken down and a homogeneous mixture of the crude phthalocyanine can be obtained without reducing the particle size of the crude phthalocyanine too much. (b) following step (a), grinding the mixture obtained in step (a), the grinding step comprising a grinding medium having a size of 0.1 to 2.5 mm; 50
pulverizing the mixture obtained in step (a) through at least one, preferably two shot mills containing only 90 vol. % crude phthalocyanine until the particle size is such that it can be used as a pigment. β from the crude phthalocyanine
- A method for producing a phthalocyanine pigment dispersion.
JP60003146A 1985-01-11 1985-01-11 Production of phthalocyanine dispersing material Granted JPS61163978A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60003146A JPS61163978A (en) 1985-01-11 1985-01-11 Production of phthalocyanine dispersing material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60003146A JPS61163978A (en) 1985-01-11 1985-01-11 Production of phthalocyanine dispersing material

Publications (2)

Publication Number Publication Date
JPS61163978A JPS61163978A (en) 1986-07-24
JPH0374706B2 true JPH0374706B2 (en) 1991-11-27

Family

ID=11549210

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60003146A Granted JPS61163978A (en) 1985-01-11 1985-01-11 Production of phthalocyanine dispersing material

Country Status (1)

Country Link
JP (1) JPS61163978A (en)

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5147024A (en) * 1974-08-21 1976-04-22 Hoechst Ag
JPS53117023A (en) * 1977-03-19 1978-10-13 Ciba Geigy Ag Conditioning method of phthalocyanine pigment
JPS5431018A (en) * 1977-05-02 1979-03-07 Hitachi Metals Ltd Method of producing pearlite spheroidal graphite cast iron

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5147024A (en) * 1974-08-21 1976-04-22 Hoechst Ag
JPS53117023A (en) * 1977-03-19 1978-10-13 Ciba Geigy Ag Conditioning method of phthalocyanine pigment
JPS5431018A (en) * 1977-05-02 1979-03-07 Hitachi Metals Ltd Method of producing pearlite spheroidal graphite cast iron

Also Published As

Publication number Publication date
JPS61163978A (en) 1986-07-24

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