CN103483915B - Preparation method of pigment yellow 17 emulsion - Google Patents

Preparation method of pigment yellow 17 emulsion Download PDF

Info

Publication number
CN103483915B
CN103483915B CN201310411001.0A CN201310411001A CN103483915B CN 103483915 B CN103483915 B CN 103483915B CN 201310411001 A CN201310411001 A CN 201310411001A CN 103483915 B CN103483915 B CN 103483915B
Authority
CN
China
Prior art keywords
pigment yellow
parts
preparation
add
container
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 - Fee Related
Application number
CN201310411001.0A
Other languages
Chinese (zh)
Other versions
CN103483915A (en
Inventor
李小福
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Wujiang Huacheng Composite Technology Co Ltd
Original Assignee
Wujiang Huacheng Composite Technology Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Wujiang Huacheng Composite Technology Co Ltd filed Critical Wujiang Huacheng Composite Technology Co Ltd
Priority to CN201310411001.0A priority Critical patent/CN103483915B/en
Publication of CN103483915A publication Critical patent/CN103483915A/en
Application granted granted Critical
Publication of CN103483915B publication Critical patent/CN103483915B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Cosmetics (AREA)

Abstract

The invention relates to a preparation method of a pigment yellow 17 emulsion. The preparation method comprises the steps of (1) putting 10-12 parts of pigment yellow 17 powder of which the mesh number is 400-500 meshes into a container; (2) adding 5-9 parts of caprylic capric triglyceride into the container, and uniformly mixing pigment yellow 17 with caprylic capric triglyceride to obtain a mixture A; (3) adding 20-24 parts of rosin-polythylene oxide ester, 18-25 parts of petroleum sodium sulfonate and 160-170 parts of water into another container, and uniformly mixing to obtain liquid B; (4) mixing the mixture A with the liquid B, and shearing for 10-20 minutes by using a shearing machine at a rotating speed of 6000-8000rpm; (5) preserving after shearing. The particle size of the pigment yellow 17 emulsion prepared by the preparation method disclosed by the invention is 10-16 mum, and the application space of the pigment yellow 17 is expanded.

Description

一种颜料黄17乳液的制备方法A kind of preparation method of pigment yellow 17 emulsion

技术领域 technical field

本发明涉及一种乳液的制备方法,特别是涉及一种颜料黄17乳液的制备方法。 The invention relates to a method for preparing an emulsion, in particular to a method for preparing a Pigment Yellow 17 emulsion.

背景技术 Background technique

颜料黄17为一种偶氮颜料,具有不溶于水的特点。由于其不溶于水,在一些水体系下,就会制约了颜料黄17的用途和空间。为了拓展颜料黄17的应用领域,很多人尝试将颜料黄17作为微乳液或者乳液,目前将其做成为微乳液的没有,因为其结构所决定做成为微乳液难度较大。作为乳液,目前的研究也较少,而且取得的效果不甚显著,依然存在很多的缺点,制约了其的大规模应用。 Pigment Yellow 17 is an azo pigment that is insoluble in water. Because it is insoluble in water, in some water systems, the use and space of Pigment Yellow 17 will be restricted. In order to expand the application field of Pigment Yellow 17, many people try to use Pigment Yellow 17 as a microemulsion or emulsion. At present, there is no such thing as a microemulsion, because its structure determines that it is difficult to make a microemulsion. As an emulsion, the current research is less, and the effect obtained is not very significant, and there are still many shortcomings, which restrict its large-scale application.

发明内容 Contents of the invention

要解决的技术问题:常规颜料黄17乳液粒径大、稳定性差的问题。 The technical problem to be solved: the problem of large particle size and poor stability of conventional pigment yellow 17 emulsion.

技术方案:本发明公开了一种颜料黄17乳液的制备方法,制备方法包括以下步骤:(1)取目数为400~500目的颜料黄17粉末为10~12份,将颜料黄17放入容器中;(2)向容器中加入辛癸酸甘油酯为5~9份,将颜料黄17与辛癸酸甘油酯混合均匀,为A混合体;(3)另取一容器,向容器中加入松香酸聚氧乙烯酯为20~24份,再加入石油磺酸钠为18~25份,再加入水为160至170份,混合均匀为B液;(4)将A混合体与B液混合,使用剪切机剪切10~20min,转速为6000rpm至8000rpm;(5)剪切结束后保藏。颜料黄17粉末目数优选为500目。颜料黄17粉末优选为12份辛癸酸甘油酯优选为5份。剪切机剪切时间优选为20min。 Technical solution: The invention discloses a preparation method of Pigment Yellow 17 emulsion. The preparation method includes the following steps: (1) Take 10-12 parts of Pigment Yellow 17 powder with a mesh number of 400-500 mesh, put Pigment Yellow 17 into (2) Add 5-9 parts of caprylic acid glycerin to the container, mix Pigment Yellow 17 and caprylic capric acid glycerin evenly, and form A mixture; Add 20-24 parts of polyoxyethylene rosin acid, then add 18-25 parts of sodium petroleum sulfonate, and then add 160-170 parts of water, mix well to form B liquid; (4) Mix A mixture with B liquid Mix and shear with a shear for 10 to 20 minutes at a speed of 6,000 to 8,000 rpm; (5) Store after shearing. The mesh number of Pigment Yellow 17 powder is preferably 500 mesh. Pigment Yellow 17 powder is preferably 12 parts . Caprylic capric acid glyceride is preferably 5 parts. Shear shearing time is preferably 20min.

有益效果:本制备方法制备得到颜料黄17乳液粒径非常小,为10um~16um。同时具有良好热稳定性和离心稳定性。乳液在50℃下加热5~10h没有发生分层现象。另外在转速为4000rpm下离心30min~60min也未有分层和破乳现象产生。 Beneficial effects: the particle size of the pigment yellow 17 emulsion prepared by the preparation method is very small, ranging from 10um to 16um. At the same time, it has good thermal stability and centrifugal stability. The emulsion did not delaminate when heated at 50°C for 5-10 hours. In addition, there was no delamination and demulsification when centrifuged at 4000rpm for 30min to 60min.

具体实施方式 Detailed ways

实施例1 Example 1

(1)取目数为400目的颜料黄17粉末为10kg,将颜料黄17放入容器中;(2)向容器中加入辛癸酸甘油酯为9kg,将颜料黄17与辛癸酸甘油酯混合均匀,为A混合体;(3)另取一容器,向容器中加入松香酸聚氧乙烯酯为24kg,再加入石油磺酸钠为25kg,再加入水为160kg,混合均匀为B液;(4)将A混合体与B液混合,使用剪切机剪切10min,转速为6000rpm;(5)剪切结束后保藏。 (1) Take 10kg of Pigment Yellow 17 powder with a mesh number of 400, and put Pigment Yellow 17 into the container; (2) Add caprylic capric acid glyceride to the container to make 9kg, mix Pigment Yellow 17 and caprylic capric glyceride Mix well, it is A mixture; (3) Take another container, add polyoxyethylene rosin acid to the container to make 24kg, add petroleum sodium sulfonate to make 25kg, add water to make 160kg, mix evenly to make B liquid; (4) Mix A mixture with B liquid, and use a shearing machine to shear for 10 minutes at a speed of 6000 rpm; (5) Store after shearing.

实施例2 Example 2

(1)取目数为500目的颜料黄17粉末为11kg,将颜料黄17放入容器中;(2)向容器中加入辛癸酸甘油酯为5kg,将颜料黄17与辛癸酸甘油酯混合均匀,为A混合体;(3)另取一容器,向容器中加入松香酸聚氧乙烯酯为20kg,再加入石油磺酸钠为23kg,再加入水为170kg,混合均匀为B液;(4)将A混合体与B液混合,使用剪切机剪切20min,转速为7000rpm;(5)剪切结束后保藏。 (1) Take 11kg of Pigment Yellow 17 powder with a mesh number of 500, and put Pigment Yellow 17 into the container; (2) Add caprylic capric acid glyceride to the container to make 5kg, mix Pigment Yellow 17 and caprylic capric glycerin Mix evenly, it is A mixture; (3) Take another container, add polyoxyethylene rosin acid to the container to make 20kg, then add petroleum sodium sulfonate to make 23kg, then add water to make 170kg, mix evenly to make B liquid; (4) Mix A mixture with B liquid, and use a shearing machine to shear for 20 minutes at a speed of 7000 rpm; (5) Store after shearing.

实施例3 Example 3

(1)取目数为450目的颜料黄17粉末为12kg,将颜料黄17放入容器中;(2)向容器中加入辛癸酸甘油酯为7kg,将颜料黄17与辛癸酸甘油酯混合均匀,为A混合体;(3)另取一容器,向容器中加入松香酸聚氧乙烯酯为22kg,再加入石油磺酸钠为18kg,再加入水为165kg,混合均匀为B液;(4)将A混合体与B液混合,使用剪切机剪切15min,转速为8000rpm;(5)剪切结束后保藏。 (1) Take 12kg of Pigment Yellow 17 powder with a mesh number of 450, put Pigment Yellow 17 into the container; (2) add caprylic capric acid glyceride to the container to make 7kg, mix Pigment Yellow 17 and caprylic capric glycerin Mix well, it is A mixture; (3) Take another container, add polyoxyethylene rosin acid to the container to make 22kg, then add petroleum sodium sulfonate to make 18kg, then add water to make 165kg, mix evenly to make B liquid; (4) Mix A mixture with B liquid, and use a shearing machine to shear for 15 minutes at a speed of 8000 rpm; (5) Store after shearing.

对实施例1、实施例2、实施例3的产品进行了粒径、热稳定性、离心稳定性测定。结果如下表。 The products of embodiment 1, embodiment 2 and embodiment 3 have carried out particle diameter, thermal stability, centrifugal stability measurement. The results are shown in the table below.

制备得到的产品具备了良好的热稳定性和离心稳定性。 The prepared product has good thermal stability and centrifugal stability.

Claims (5)

1. 一种颜料黄17乳液的制备方法,其特征在于制备方法包括以下步骤:(1)取目数为400~500目的颜料黄17粉末为10~12份,将颜料黄17粉末放入容器中;(2)向容器中加入辛癸酸甘油酯为5~9份,将颜料黄17粉末与辛癸酸甘油酯混合均匀,为A混合体;(3)另取一容器,向容器中加入松香酸聚氧乙烯酯为20~24份,再加入石油磺酸钠为18~25份,再加入水为160至170份,混合均匀为B液;(4)将A混合体与B液混合,使用剪切机剪切10~20min,转速为6000rpm至8000rpm;(5)剪切结束后保藏。 1. A method for preparing Pigment Yellow 17 emulsion, characterized in that the preparation method comprises the following steps: (1) Take 10-12 parts of Pigment Yellow 17 powder with a mesh size of 400-500 mesh, and put the Pigment Yellow 17 powder into a container (2) Add 5-9 parts of caprylic acid glyceride to the container, mix Pigment Yellow 17 powder and caprylic capric acid glycerin evenly to form A mixture; Add 20-24 parts of polyoxyethylene rosin acid, then add 18-25 parts of sodium petroleum sulfonate, and then add 160-170 parts of water, mix well to form B liquid; (4) Mix A mixture with B liquid Mix and shear with a shear for 10 to 20 minutes at a speed of 6,000 to 8,000 rpm; (5) Store after shearing. 2.根据权利要求1所述的一种颜料黄17乳液的制备方法,其特征在于颜料黄17粉末目数为500目。 2. the preparation method of a kind of pigment yellow 17 emulsion according to claim 1 is characterized in that pigment yellow 17 powder mesh number is 500 orders. 3.根据权利要求1所述的一种颜料黄17乳液的制备方法,其特征在于颜料黄17粉末为12份 3. the preparation method of a kind of Pigment Yellow 17 emulsion according to claim 1 is characterized in that Pigment Yellow 17 powder is 12 parts . 4.根据权利要求1所述的一种颜料黄17乳液的制备方法,其特征在于辛癸酸甘油酯为5份。 4. the preparation method of a kind of Pigment Yellow 17 emulsion according to claim 1 is characterized in that caprylyl capric acid glyceride is 5 parts. 5.根据权利要求1所述的一种颜料黄17乳液的制备方法,其特征在于剪切机剪切时间为20min。 5. the preparation method of a kind of Pigment Yellow 17 emulsion according to claim 1 is characterized in that the shearing machine shearing time is 20min.
CN201310411001.0A 2013-09-11 2013-09-11 Preparation method of pigment yellow 17 emulsion Expired - Fee Related CN103483915B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201310411001.0A CN103483915B (en) 2013-09-11 2013-09-11 Preparation method of pigment yellow 17 emulsion

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201310411001.0A CN103483915B (en) 2013-09-11 2013-09-11 Preparation method of pigment yellow 17 emulsion

Publications (2)

Publication Number Publication Date
CN103483915A CN103483915A (en) 2014-01-01
CN103483915B true CN103483915B (en) 2015-01-21

Family

ID=49824532

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201310411001.0A Expired - Fee Related CN103483915B (en) 2013-09-11 2013-09-11 Preparation method of pigment yellow 17 emulsion

Country Status (1)

Country Link
CN (1) CN103483915B (en)

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2048206A1 (en) * 2006-07-31 2009-04-15 DIC Corporation Process for producing aqueous pigment dispersion and ink for ink-jet recording
CN101469155A (en) * 2007-12-24 2009-07-01 深圳市海川实业股份有限公司 Environment friendly transparent iron oxide yellow superfine aqueous color sizing dispersion and preparation thereof
CN101597446A (en) * 2008-12-25 2009-12-09 天津兆阳纳米科技有限公司 A kind of stable-type yellow nanometer water-type pigment dispersion

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101597443A (en) * 2008-12-25 2009-12-09 天津兆阳纳米科技有限公司 A kind of Yellow nanometer water-type pigment dispersion

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2048206A1 (en) * 2006-07-31 2009-04-15 DIC Corporation Process for producing aqueous pigment dispersion and ink for ink-jet recording
CN101469155A (en) * 2007-12-24 2009-07-01 深圳市海川实业股份有限公司 Environment friendly transparent iron oxide yellow superfine aqueous color sizing dispersion and preparation thereof
CN101597446A (en) * 2008-12-25 2009-12-09 天津兆阳纳米科技有限公司 A kind of stable-type yellow nanometer water-type pigment dispersion

Also Published As

Publication number Publication date
CN103483915A (en) 2014-01-01

Similar Documents

Publication Publication Date Title
CN104855548B (en) A kind of preparation method of load carrotene grease gel
CN103059095B (en) A kind of green extraction of yellow ginger resource comprehensive efficiency utilization
RU2012102830A (en) METHOD FOR PRODUCING LIQUID FOR ELECTRONIC CIGARETTES
CN103111315A (en) A preparation method of bismuth phosphate (BiPO4) photocatalyst with different structures
CN103520209B (en) A kind of grease of compound colla corii asini slurry processing method
CN108864242B (en) Extraction method and application of ursolic acid
CN102492307A (en) Hydration degumming method for hot pepper extract
CN109852474A (en) A kind of water-soluble product of carnosic acid and preparation method thereof
CN103483915B (en) Preparation method of pigment yellow 17 emulsion
CN103642276B (en) A kind of preparation method of high concentration capsicum red pigment
CN103704737A (en) Pot-stewed beef for benefiting qi and nourishing blood and processing method thereof
CN103739650B (en) A kind of preparation method of β monoammonium glycyrrhizinate
CN103382409A (en) Mould oil for pharmaceutical grade capsule and preparation method thereof
CN104479926A (en) Natural plant detergent and preparation method thereof
CN106336971A (en) Chinese herbal sunscreen handmade soap
CN102260587A (en) Method for extracting grape seed oil and proantho cyanidins
CN102512452B (en) Process method for preparing sea cucumber glycosides by using sea cucumber coelomic fluid
CN102899161B (en) Process for extracting shrimp oil crude product from dried antarctic krill and treating foam
CN106586967B (en) The safe extracting method of ammonium perchlorate in a kind of solid cloud detonator
CN103483196B (en) Method for extracting oleocanthal from olive oil
CN103446185A (en) Method for preparing soluble pearl calcium by use of pearl shells
CN102669679B (en) Method for preparing chrysanthemum morifolium ramat extract in microwave-assisted way
TWI501787B (en) A preparation method of American ginseng broken wall preparation
CN103519317A (en) Method for preparing feed preservative
CN103520389A (en) Extracting method of flavone in vine tea

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
ASS Succession or assignment of patent right

Owner name: WUJIANG HUACHENG COMPOSITE TECHNOLOGY CO., LTD.

Free format text: FORMER OWNER: WUJIANG BINGXIN CULTURAL + EDUCATIONAL GOODS CO., LTD.

Effective date: 20141126

C41 Transfer of patent application or patent right or utility model
COR Change of bibliographic data

Free format text: CORRECT: ADDRESS; FROM: 215221 SUZHOU, JIANGSU PROVINCE TO: 215000 SUZHOU, JIANGSU PROVINCE

TA01 Transfer of patent application right

Effective date of registration: 20141126

Address after: 215000 Jiangsu Province, Wujiang District of Suzhou city with Wu Road No. 22

Applicant after: WUJIANG HUACHENG COMPOSITE MATERIAL SCIENCE & TECHNOLOGY Co.,Ltd.

Address before: The village Pingwang town Wujiang District Suzhou City, Jiangsu province 215221

Applicant before: WUJIANG BINGXIN CULTURAL & EDUCATIONAL GOODS Co.,Ltd.

C14 Grant of patent or utility model
GR01 Patent grant
CF01 Termination of patent right due to non-payment of annual fee
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20150121