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Heat-resistant yellow-stain-resistant epoxy acrylate low polymer and preparation method of UV (ultraviolet) ink

A technology for changing epoxy acrylate and glycerol acrylate, which is applied in the field of synthesis and its application in UV ink, can solve the problems of poor yellowing resistance, hardness and chemical resistance, and achieve stable performance and improved alkali resistance. Soluble, wide range of effects

Active Publication Date: 2015-10-07
FOSHAN SOUTHERN PACKAGING +2
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Although these technologies have indeed achieved satisfactory results in improving the flexibility and thermal stability of epoxy acrylate, the modified epoxy acrylate has decreased in terms of hardness and chemical resistance, and it is still Unable to solve the problem of poor yellowing resistance

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0049] (1) Synthesis of epoxy acrylate oligomer TGICAHHPA

[0050] Add 14.8g (0.05mol) TGIC and 10.8g (0.15mol) AA to a 100mL four-neck flask equipped with an overhead stirrer, a thermometer, and a spherical condenser, and heat the oil bath to 90°C. After TGIC and AA are completely dissolved, raise the temperature to 100°C, start the stirrer, add 0.15g of triethylamine catalyst at the same time, react for 4h, add 0.1g of polymerization inhibitor hydroquinone, and obtain a transparent viscous substance. Add 15.4g (0.1mol) HHPA to the reaction bottle, heat the oil bath to 100°C, react for 30min, then add 15g of acetone as a solvent to reduce viscosity, continue to react for 90min, add 5g HDDA as active diluent to adjust the viscosity of the system, cool out Material, obtains transparent viscous material, and its GPC survey weight-average molecular weight is 1031, and molecular weight distribution coefficient is 1.02.

[0051] (2) Preparation and test method of ink

[0052] ...

Embodiment 2

[0064] (1) Synthesis of epoxy acrylate oligomer TGICAMA

[0065] Add 14.8g (0.05mol) TGIC and 10.8g (0.15mol) AA to a 100mL four-neck flask equipped with an overhead stirrer, a thermometer, and a spherical condenser device, and add 0.1g of inhibitor hydroquinone at the same time . Heat the oil bath to 90°C, after TGIC and AA are completely dissolved, raise the temperature to 100°C, start the stirrer, add 0.15g of triethylamine catalyst at the same time, react for 4h, and obtain a transparent viscous substance. Add 9.8g (0.1mol) MA to the reaction bottle, heat the oil bath to 100°C, react for 30min, then add 15g of acetone as a solvent to reduce the viscosity, continue the reaction for 90min, add 5g of 1,6-hexanediol diacrylate ( HDDA) was used as a reactive diluent to adjust the viscosity of the system, and the material was cooled and discharged to obtain a transparent viscous substance with a GPC weight-average molecular weight of 1525 and a molecular weight distribution coe...

Embodiment 3

[0079] (1) Synthesis of epoxy acrylate oligomer TGICATMA

[0080] Add 14.8g (0.05mol) TGIC and 10.8g (0.15mol) AA to a 100mL four-neck flask equipped with an overhead stirrer, a thermometer, and a spherical condenser device, and add 0.1g of inhibitor hydroquinone at the same time . Heat the oil bath to 90°C, after TGIC and AA are completely dissolved, raise the temperature to 100°C, start the stirrer, add 0.15g of triethylamine catalyst at the same time, react for 4h, and obtain a transparent viscous substance. Add 19.2g (0.1mol) TMA to the reaction bottle, heat the oil bath to 100°C, react for 30min, then add 15g of acetone as a solvent to reduce the viscosity, continue the reaction for 90min, add 5g of 1,6-hexanediol diacrylate ( HDDA) was used as a reactive diluent to adjust the viscosity of the system, and the material was cooled and discharged to obtain a transparent viscous substance with a GPC weight-average molecular weight of 1428 and a molecular weight distribution ...

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PUM

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Abstract

The invention discloses a heat-resistant yellow-stain-resistant epoxy acrylate low polymer and a preparation method of UV (ultraviolet) ink. The heat-resistant yellow-stain-resistant epoxy acrylate low polymer is prepared through a following method comprising the following steps of carrying out an addition-esterification reaction on triglycidyl isocyanurate and an acrylic organic acid under the action of a catalyst, so as to obtain triglycidyl isocyanurate acrylate, then reacting the triglycidyl isocyanurate acrylate with an acid anhydride to obtain an acid anhydride modified triglycidyl isocyanurate acrylate, finally, adding a viscosity reducer and a reactive thinning agent into the acid anhydride modified triglycidyl isocyanurate acrylate, and regulating system viscosity to obtain the heat-resistant yellow-stain-resistant epoxy acrylate low polymer. The heat-resistant yellow-stain-resistant epoxy acrylate low polymer is adopted for the UV ink prepared by the invention; the defect that conventional UV ink is easy to yellow is overcome; moreover the UV ink is high in adhesive force, is wide in the serviceable range to base materials, and can be printed on the upper surfaces of base materials of PE (polyethylene), PP (polypropylene), PET (polyethylene terephthalate), glass, a circuit board and the like in a screen printing manner. The UV ink prepared by the invention has high glossiness, excellent heat resistance and yellow stain resistance, and is further wide in application range.

Description

technical field [0001] The invention relates to the field of inks, in particular to the synthesis of a heat-resistant and yellowing-resistant epoxy acrylate oligomer and its application in UV inks. Background technique [0002] Ultraviolet (UV) curing means that under the action of ultraviolet light, the photosensitive substances in the system undergo chemical reactions to produce active fragments, which trigger the polymerization and crosslinking of active monomers or oligomers in the system, so that the system has a liquid coating instantly into a solid coating. Since Bayer in Germany developed the first generation of UV curing coatings in 1967, UV curing technology has developed rapidly worldwide, mainly because it cures quickly and meets the needs of modern automatic production; it is non-polluting and complies with the requirements of modern coatings and inks. Development direction; high coating film quality, high hardness, scratch resistance, corrosion resistance and ...

Claims

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Application Information

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IPC IPC(8): C09D11/101C09D11/03C07D251/34
Inventor 彭斯敏毕明珠王小妹郑日安张桂祥万彬方利平丘日才
Owner FOSHAN SOUTHERN PACKAGING
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