CN105153940A - Production method of rosin derivative for pigment industry - Google Patents
Production method of rosin derivative for pigment industry Download PDFInfo
- Publication number
- CN105153940A CN105153940A CN201510562125.8A CN201510562125A CN105153940A CN 105153940 A CN105153940 A CN 105153940A CN 201510562125 A CN201510562125 A CN 201510562125A CN 105153940 A CN105153940 A CN 105153940A
- Authority
- CN
- China
- Prior art keywords
- rosin
- rosin derivative
- production method
- tannin
- pigment
- 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
Landscapes
- Inks, Pencil-Leads, Or Crayons (AREA)
Abstract
The invention discloses a production method of a rosin derivative for the pigment industry and relates to the technical field of rosin deep processing. The production method comprises the steps of adding alkylphenol disulphide and tannin into rosin, firstly heating to 120 to 150 DEG C, agitating for 0.5h, and then increasing the temperature to 230 to 270 DEG C, agitating for 2 to 6h; then decreasing the temperature to 180 to 200 DEG C, continuously adding tannin, agitating for 1h and discharging the material to obtain the rosin derivative. By adding two batches of tannin for compounding before and after the disproportionation reaction stage of the rosin and by utilizing the high molecular weight of the batches of tannin and the anti-oxidation effect of contained polyphenols, not only can the thermal stability of the product be improved, but also the pigment coloring power can be further improved, the transparency is higher, and the rosin derivative further has the characteristics of nature, environmental friendliness and environmental protection.
Description
Technical field
The present invention relates to rosin deep process technology field, especially a kind of production method of the rosin derivative for pigment industry.
Background technology
Conventional offset printing ink benzidine yellow pigment needs a large amount of interpolation nilox resin or staybelite to obtain high transparency, high tinting strength, pigment with low cost.Nilox resin on the market and staybelite are substantially all manufacture by precious metal palladium carbon catalyzed reaction.Inevitably there is a certain amount of catalyst residue in the product, there is great potential safety hazard in the rosin derivative that this precious metal catalyst obtains, very easily catching fire in production and transportation.Having there is the serious fire much caused because using this kind of rosin in domestic and international pigment industry, suffers heavy losses.Have people to adopt interpolation antioxidant in large quantities to solve above safety issue in some methods improved, but regrettably this method thoroughly can not be dealt with problems, and sacrifice the color development performance of pigment, have impact on the drying property of ink.
Summary of the invention
The invention provides one and can improve pigmenting power further, have higher transparency, also there is the production method of the rosin derivative for pigment industry of natural, green, environmental protection.
In order to solve the problems of the technologies described above, the technical solution adopted in the present invention is:
Add in rosin account for rosin total mass 0.1% ~ 1.0% alkyl phenol disulfide and account for rosin total mass 0.1% ~ 0.2% Weibull, first be heated to 120 DEG C ~ 150 DEG C stir 0.5 hour, and then be warming up to 230 DEG C ~ 270 DEG C stirrings 2 hours ~ 6 hours; Then be cooled to 180 DEG C ~ 200 DEG C again, and continue to add account for rosin total mass 0.2% ~ 0.4% Weibull, stir 1 hour, discharging, obtains this rosin derivative.
In technique scheme, scheme can also be more specifically: described alkyl phenol disulfide can be the one in Pentaphen disulphide, p-tert-butylphenol disulphide.
Owing to adopting technique scheme, the present invention has following beneficial effect:
1, the present invention is composite by adding two batches of Weibull before and after the present rosin generation disproportionation reaction stage respectively, utilize the macromolecule of Weibull in batches with the antioxygenation of contained polyphenol, not only can strengthen the thermostability of product, the present invention also can be further made to improve pigmenting power, there is higher transparency, also there is feature that is natural, green, environmental protection.
2, the present invention is mainly used in the industries such as the synthesis of pigment, and be particularly suitable for the benzidine yellow pigment manufacturing high addition, its quality index meets the service requirements of pigment industry.
3, the present invention adopts non-metallic catalyst to replace precious metal palladium C catalyst, solve the safety problem that precious metal palladium C catalyst brings, obtain the rosin derivative of high heat stability, and compared with conventional disproportionation, hydrogenation, can pigmenting power be improved, have higher transparency.
Embodiment
Below in conjunction with specific examples, the invention will be further described:
Embodiment 1
Add in rosin account for rosin total mass 0.1% Pentaphen disulphide and account for rosin total mass 0.1% Weibull, be first heated to 120 DEG C stir 0.5 hour, and then be warming up to 230 DEG C stir 6 hours; Then be cooled to 200 DEG C again, and continue to add account for rosin total mass 0.4% Weibull, stir 1 hour, discharging, obtains this rosin derivative.
Compared with existing rosin derivative, by rosin derivative obtained for the present embodiment for the preparation of pigment, the pigmenting power obtained can be made to improve 50%.
Embodiment 2
Add in rosin account for rosin total mass 0.5% alkyl phenol disulfide and account for rosin total mass 0.15% Weibull, be first heated to 150 DEG C stir 0.5 hour, and then be warming up to 270 DEG C stir 2 hours; Then be cooled to 180 DEG C again, and continue to add account for rosin total mass 0.2% Weibull, stir 1 hour, discharging, obtains this rosin derivative.
Compared with existing rosin derivative, by rosin derivative obtained for the present embodiment for the preparation of pigment, the pigmenting power obtained can be made to improve 50%.
Embodiment 3
Add in rosin account for rosin total mass 1.0% alkyl phenol disulfide and account for rosin total mass 0.2% Weibull, be first heated to 130 DEG C stir 0.5 hour, and then be warming up to 250 DEG C stir 4 hours; Then be cooled to 190 DEG C again, and continue to add account for rosin total mass 0.3% Weibull, stir 1 hour, discharging, obtains this rosin derivative.
Compared with existing rosin derivative, by rosin derivative obtained for the present embodiment for the preparation of pigment, the pigmenting power obtained can be made to improve 50%.
Technical indicator of the present invention is as table 1:
Table 1
。
Claims (2)
1. the production method for the rosin derivative of pigment industry, it is characterized in that its preparation process is: add in rosin account for rosin total mass 0.1% ~ 1.0% alkyl phenol disulfide and account for rosin total mass 0.1% ~ 0.2% Weibull, first be heated to 120 DEG C ~ 150 DEG C stir 0.5 hour, and then be warming up to 230 DEG C ~ 270 DEG C stirrings 2 hours ~ 6 hours; Then be cooled to 180 DEG C ~ 200 DEG C again, and continue to add account for rosin total mass 0.2% ~ 0.4% Weibull, stir 1 hour, discharging, obtains this rosin derivative.
2. the production method of the rosin derivative for pigment industry according to claim 1, is characterized in that described alkyl phenol disulfide is the one in Pentaphen disulphide, p-tert-butylphenol disulphide.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201510562125.8A CN105153940A (en) | 2015-09-07 | 2015-09-07 | Production method of rosin derivative for pigment industry |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201510562125.8A CN105153940A (en) | 2015-09-07 | 2015-09-07 | Production method of rosin derivative for pigment industry |
Publications (1)
Publication Number | Publication Date |
---|---|
CN105153940A true CN105153940A (en) | 2015-12-16 |
Family
ID=54795006
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201510562125.8A Pending CN105153940A (en) | 2015-09-07 | 2015-09-07 | Production method of rosin derivative for pigment industry |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN105153940A (en) |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101570664A (en) * | 2009-05-28 | 2009-11-04 | 东莞市英科水墨有限公司 | Acrylic acid modified rosin ester for water-based ink and preparation method thereof |
CN103450809A (en) * | 2013-08-27 | 2013-12-18 | 广西梧州松脂股份有限公司 | Method for preparing rosin derivative for pigment industry |
CN103601876A (en) * | 2013-11-18 | 2014-02-26 | 广东科茂林产化工股份有限公司 | High molecular weight modified rosin resin for water-based ink and preparation method thereof |
-
2015
- 2015-09-07 CN CN201510562125.8A patent/CN105153940A/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101570664A (en) * | 2009-05-28 | 2009-11-04 | 东莞市英科水墨有限公司 | Acrylic acid modified rosin ester for water-based ink and preparation method thereof |
CN103450809A (en) * | 2013-08-27 | 2013-12-18 | 广西梧州松脂股份有限公司 | Method for preparing rosin derivative for pigment industry |
CN103601876A (en) * | 2013-11-18 | 2014-02-26 | 广东科茂林产化工股份有限公司 | High molecular weight modified rosin resin for water-based ink and preparation method thereof |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN104084518A (en) | Heatproof precoated sand and preparation method thereof | |
CN103642245A (en) | Silicone rubber preparation method | |
CN103450809B (en) | Method for preparing rosin derivative for pigment industry | |
CN107312307A (en) | A kind of polycarbonate compositions of high durable and preparation method thereof | |
CN105153940A (en) | Production method of rosin derivative for pigment industry | |
CN101381505B (en) | Synthetic resin produced by renewable resource and preparation method thereof | |
CN102675974A (en) | Connection material for high-viscosity offset printing high-gloss quick drying ink and preparation method thereof | |
CN104152048A (en) | Novel rosin resin for oil paints | |
CN102633969B (en) | Thermosetting environment-friendly phenolic resin and manufacturing method thereof | |
CN104559185A (en) | Compound type microencapsulated ammonium polyphosphate master batch | |
CN104448709B (en) | Masterbatch material for stationery and preparation method thereof | |
CN105585683A (en) | Method for preparing melamine formaldehyde resin flocculating agent | |
CN104877096A (en) | Preparation method of modified phenol formaldehyde resin | |
CN103865328A (en) | Formula, preparation technology and application of gummy oil | |
CN103044657B (en) | Nano-modified epoxy resin and preparation method thereof | |
CN104130362A (en) | Preparation method of rosin modified phenolic resin | |
CN102912233A (en) | Preparation method of high corrosion resistance iron alloy | |
CN104164050B (en) | A kind of heat resistant type Environmental protection phenol formaldehyde resin and the preparation method of composite thereof | |
CN103387819B (en) | Chemosynthesis aromatic hydrocarbons heat transfer oil and preparation method thereof | |
CN102504484B (en) | Gel coat resin and preparation method thereof | |
CN102561102A (en) | Light oil formula and preparation process thereof | |
CN101659827A (en) | Long-afterglow luminescent paint | |
CN109336399A (en) | A kind of decorative devitrified glass material | |
CN107344991B (en) | Low-cost and environment-friendly phenolic amide epoxy curing agent and preparation method thereof | |
CN104910022A (en) | Preparation method of rubber antioxidant |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
RJ01 | Rejection of invention patent application after publication |
Application publication date: 20151216 |
|
RJ01 | Rejection of invention patent application after publication |