CN104231755A - Grapheme modified color paste material and preparation method thereof - Google Patents
Grapheme modified color paste material and preparation method thereof Download PDFInfo
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Abstract
The invention discloses a grapheme modified color paste material. The grapheme modified color paste material is prepared from the following components in part by weight: 20 to 40 parts of ethyl acrylate, 10 to 25 parts of glycidyl acrylate, 10 to 20 parts of dipropylene glycol dimethyl ether, 10 to 15 parts of grapheme, 3 to 12 parts of amylopectin, 5 to 12 parts of maleic anhydride grafted polypropylene, 0.8 to 2 parts of 2-Octyl-2H-isothiazol-3-one and 0.8 to 1.5 parts of carbon black. The grapheme modified color paste material prepared by a method disclosed by the invention has not only a good dispersing effect, but also a good adhesive force.
Description
Technical field
The invention belongs to mill base Material Field, particularly a kind of Graphene modification mill base material and preparation method thereof.
Background technology
In the process used, often there is the problem of consistency, usually also can solve the compatibility problem of mill base and coating by adding auxiliary agent, but in general, can not reach and separate flocculation completely in mill base.The solution flocculating degree of the mill base of superperformance is higher, so just can have good particle uniformity, good tinting strength and storage stability.Due to the otherness of composition in pigment in mill base and base-material, thus can cause the uneven distribution of mill base, make the product after mill base film forming occur coming off and cleavage phenomenon because of the change of the factor such as ambient temperature and humidity.If mill base dispersing property is good, then the generation can avoided loose colour He grow dim.The quality of the dispersiveness of another coating self also directly affects the loose colour of colored paint and grows dim.
Acrylate materials has good ozone resistants, resistance to air loss, resistance toly to subdue and resistance to breach growth property, and uvioresistant discolouration etc., but simultaneously acrylate materials also exists the shortcomings such as tack difference and low temperature become fragile, and causes its use to receive a lot of restriction.
Summary of the invention
For above-mentioned demand, the object of this invention is to provide a kind of Graphene modification mill base material and preparation method thereof, the mill base material obtained by present method not only has good dispersion effect, and has good sticking power.
Object of the present invention can be achieved through the following technical solutions:
A kind of Graphene modification mill base material, be made up of the component comprising following weight part:
Ethyl propenoate 20-40 part,
Glycidyl acrylate 10-25 part,
Dimethyl ether 10-20 part,
Graphene 10-15 part,
Amylopectin 3-12 part,
Maleic anhydride inoculated polypropylene 5-12 part,
N-octyl-isothiazolin ketone 0.8-2 part,
Carbon black 0.8-1.5 part.
The percentage of grafting of described amylopectin is 30-50%.
The percentage of grafting of described maleic anhydride inoculated polypropylene is 25%.
A preparation method for Graphene modification mill base material, the method comprises the following steps:
(1) ethyl propenoate 20-40 part, glycidyl acrylate 10-25 part, dimethyl ether 10-20 part, amylopectin 3-12 part, maleic anhydride inoculated polypropylene 5-12 part and n-octyl-isothiazolin ketone 0.8-2 part is taken, add in clarifixator, at 50-80 DEG C, mix 1-3 hour, obtain a homogeneous mixture;
(2) mixture of step 1 is added Graphene 10-15 part and carbon black 0.8-1.5 part under with the agitation condition of 600-800 rev/min of rotating speed, mix;
(3) 1M sodium carbonate adjust ph will be added in above-mentioned mixed solution to 8-8.5, deaeration 1 hour in vacuum defoamation machine, obtain Graphene modification mill base material.
PH value in described step 3 is 8.2.
Compared with prior art, its beneficial effect is: in the present invention in the present invention, owing to adding Graphene, makes mill base have preferably evenly performance, improves the tack of mill base simultaneously.Present invention adds amylopectin and coordinate with certain temperature, make the mill base obtained not only have the weather resistance of ethyl propenoate, while there is good tack, there is good dispersiveness simultaneously, thus can be used as the surface spraying mill base of less article, such as stationery, toy etc.
Embodiment
Below in conjunction with embodiment, the present invention is further illustrated.
Embodiment 1
(1) take ethyl propenoate 20kg, glycidyl acrylate 10kg, maleic anhydride inoculated polypropylene 5kg and n-octyl-isothiazolin ketone 0.8kg that amylopectin 8kg that dimethyl ether 15kg, percentage of grafting are 30%, percentage of grafting are 25%, add in clarifixator, at 50 DEG C, mix 3 hours, obtain a homogeneous mixture;
(2) mixture of step 1 is added Graphene 10kg and carbon black 0.8kg under with the agitation condition of 600 revs/min of rotating speeds, mix;
(3) 1M sodium carbonate adjust ph to 8 will be added in above-mentioned mixed solution, deaeration 1 hour in vacuum defoamation machine, obtain Graphene modification mill base material.
Obtained Graphene modification mill base coated materials is in frosting, and the performance test results obtained is as shown in table 1.
Embodiment 2
(1) take ethyl propenoate 40kg, glycidyl acrylate 15kg, maleic anhydride inoculated polypropylene 12kg and n-octyl-isothiazolin ketone 2kg that amylopectin 10kg that dimethyl ether 20kg, percentage of grafting are 50%, percentage of grafting are 25%, add in clarifixator, at 60 DEG C, mix 1 hour, obtain a homogeneous mixture;
(2) mixture of step 1 is added Graphene 10kg and carbon black 0.8kg under with the agitation condition of 800 revs/min of rotating speeds, mix;
(3) 1M sodium carbonate adjust ph to 8.5 will be added in above-mentioned mixed solution, deaeration 1 hour in vacuum defoamation machine, obtain Graphene modification mill base material.
Obtained Graphene modification mill base coated materials is in frosting, and the performance test results obtained is as shown in table 1.
Embodiment 3
(1) take ethyl propenoate 25kg, glycidyl acrylate 25kg, maleic anhydride inoculated polypropylene 10kg and n-octyl-isothiazolin ketone 1.4kg that amylopectin 12kg that dimethyl ether 15kg, percentage of grafting are 30%, percentage of grafting are 25%, add in clarifixator, at 80 DEG C, mix 2 hours, obtain a homogeneous mixture;
(2) mixture of step 1 is added Graphene 15kg and carbon black 1kg under with the agitation condition of 700 revs/min of rotating speeds, mix;
(3) 1M sodium carbonate adjust ph to 8.2 will be added in above-mentioned mixed solution, deaeration 1 hour in vacuum defoamation machine, obtain Graphene modification mill base material.
Obtained Graphene modification mill base coated materials is in frosting, and the performance test results obtained is as shown in table 1.
Embodiment 4
(1) take ethyl propenoate 28kg, glycidyl acrylate 20kg, maleic anhydride inoculated polypropylene 8kg and n-octyl-isothiazolin ketone 1kg that amylopectin 3kg that dimethyl ether 10kg, percentage of grafting are 40%, percentage of grafting are 25%, add in clarifixator, at 70 DEG C, mix 1 hour, obtain a homogeneous mixture;
(2) mixture of step 1 is added Graphene 10kg and carbon black 1.5kg under with the agitation condition of 650 revs/min of rotating speeds, mix;
(3) 1M sodium carbonate adjust ph to 8.2 will be added in above-mentioned mixed solution, deaeration 1 hour in vacuum defoamation machine, obtain Graphene modification mill base material.
Table 1
| Test event | Embodiment 1 | Embodiment 2 | Embodiment 3 |
| Fineness | < 4 microns | < 4 microns | < 4 microns |
| Bonding strength (MPa) | 15 | 14 | 17 |
The invention is not restricted to embodiment here, those skilled in the art, according to announcement of the present invention, do not depart from improvement that scope makes and amendment all should within protection scope of the present invention.
Claims (5)
1. a Graphene modification mill base material, is characterized in that, is made up of the component comprising following weight part:
Ethyl propenoate 20-40 part,
Glycidyl acrylate 10-25 part,
Dimethyl ether 10-20 part,
Graphene 10-15 part,
Amylopectin 3-12 part,
Maleic anhydride inoculated polypropylene 5-12 part,
N-octyl-isothiazolin ketone 0.8-2 part,
Carbon black 0.8-1.5 part.
2. Graphene modification mill base material according to claim 1, is characterized in that, the percentage of grafting of described amylopectin is 30-50%.
3. Graphene modification mill base material according to claim 1, is characterized in that, the percentage of grafting of described maleic anhydride inoculated polypropylene is 25%.
4. a preparation method for Graphene modification mill base material, it is characterized in that, the method comprises the following steps:
(1) ethyl propenoate 20-40 part, glycidyl acrylate 10-25 part, dimethyl ether 10-20 part, amylopectin 3-12 part, maleic anhydride inoculated polypropylene 5-12 part and n-octyl-isothiazolin ketone 0.8-2 part is taken, add in clarifixator, at 50-80 DEG C, mix 1-3 hour, obtain a homogeneous mixture;
(2) mixture of step 1 is added Graphene 10-15 part and carbon black 0.8-1.5 part under with the agitation condition of 600-800 rev/min of rotating speed, mix;
(3) 1M sodium carbonate adjust ph will be added in above-mentioned mixed solution to 8-8.5, deaeration 1 hour in vacuum defoamation machine, obtain Graphene modification mill base material.
5. the preparation method of Graphene modification mill base material according to claim 4, it is characterized in that, the pH value in described step 3 is 8.2.
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Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
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| CN105543993A (en) * | 2016-01-13 | 2016-05-04 | 济南圣泉集团股份有限公司 | Graphene modified color paste, preparation method and application |
| CN105803830A (en) * | 2016-04-05 | 2016-07-27 | 吴江市林旺纺织厂 | Color paste material for textiles and preparation method of color paste material |
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| JP2009221052A (en) * | 2008-03-17 | 2009-10-01 | Teijin Ltd | Composite powder |
| CN103113786A (en) * | 2013-03-07 | 2013-05-22 | 苏州牛剑新材料有限公司 | Graphene conductive ink and preparation method thereof |
| WO2013073259A1 (en) * | 2011-11-16 | 2013-05-23 | 東ソー有機化学株式会社 | High-purity parastyrene sulfonic acid (salt); polystyrene sulfonic acid (salt) using same; dispersant, conductive polymer dopant, aqueous nanocarbon material dispersion and aqueous conductive polymer dispersion each using polystyrene sulfonic acid (salt); and method for producing polystyrene sulfonic acid (salt) |
| CN103733271A (en) * | 2011-08-22 | 2014-04-16 | 拜耳知识产权有限责任公司 | Dispersion comprising carbon nanotubes and graphene platelets |
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Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
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| JP2009221052A (en) * | 2008-03-17 | 2009-10-01 | Teijin Ltd | Composite powder |
| CN103733271A (en) * | 2011-08-22 | 2014-04-16 | 拜耳知识产权有限责任公司 | Dispersion comprising carbon nanotubes and graphene platelets |
| WO2013073259A1 (en) * | 2011-11-16 | 2013-05-23 | 東ソー有機化学株式会社 | High-purity parastyrene sulfonic acid (salt); polystyrene sulfonic acid (salt) using same; dispersant, conductive polymer dopant, aqueous nanocarbon material dispersion and aqueous conductive polymer dispersion each using polystyrene sulfonic acid (salt); and method for producing polystyrene sulfonic acid (salt) |
| CN103113786A (en) * | 2013-03-07 | 2013-05-22 | 苏州牛剑新材料有限公司 | Graphene conductive ink and preparation method thereof |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105543993A (en) * | 2016-01-13 | 2016-05-04 | 济南圣泉集团股份有限公司 | Graphene modified color paste, preparation method and application |
| CN105543993B (en) * | 2016-01-13 | 2018-03-30 | 济南圣泉集团股份有限公司 | A kind of graphene is modified mill base, preparation method and its usage |
| CN105803830A (en) * | 2016-04-05 | 2016-07-27 | 吴江市林旺纺织厂 | Color paste material for textiles and preparation method of color paste material |
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| CN104231755B (en) | 2016-02-10 |
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Inventor after: Zhan Binghui Inventor before: Li Bingxin |
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Effective date of registration: 20160115 Address after: 518033 Guangdong city of Shenzhen province Futian District Futian Street Binhe love to building No. 5003 West Block 19 Building ABC room Applicant after: SHENZHEN KEEN ENVIRONMENTAL PROTECTION Co.,Ltd. Address before: The village Pingwang town Wujiang District Suzhou City, Jiangsu province 215221 Applicant before: SUZHOU BINGXIN STATIONERY Co.,Ltd. |
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Address after: Room 301, Building B, Yingdali Technology Digital Park, No. 8 Hongmian Road, Fubao Community, Futian District, Shenzhen City, Guangdong Province, 518000 Patentee after: SHENZHEN KEEN ENVIRONMENTAL PROTECTION Co.,Ltd. Address before: 518033 room ABC, 19th floor, west block, Aidi building, 5003 Binhe Avenue, Futian street, Futian District, Shenzhen City, Guangdong Province Patentee before: SHENZHEN KEEN ENVIRONMENTAL PROTECTION Co.,Ltd. |