Liquid, hybrid UV/vis radiation curable resin compositions for additive fabrication
US-9708442-B1 · Jul 18, 2017 · US
US10647823B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10647823-B2 |
| Application number | US-201815981840-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 16, 2018 |
| Priority date | May 16, 2018 |
| Publication date | May 12, 2020 |
| Grant date | May 12, 2020 |
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The current process relates to an adiabatic gel polymerization process for the production of water-soluble polyelectrolytes using UV LED modules or a combination of a UV tube light sources and UV LED modules wherein the resulting polymer has increased throughput, lower residual monomer content as well as lower insolubles compared with current photoinitiated polymerization processes.
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What is claimed is: 1. An adiabatic gel polymerization process for the production of water-soluble polyelectrolytes comprising: providing a monomer solution comprising an aqueous acrylamide, an ethylenically unsaturated monomer, and a photoinitiator; purging the monomer solution to remove oxygen and adjusting the pH to about 3-7 and a temperature below 25° C.; initiating photopolymerization utilizing a UV light source having a wavelength of from about 365 nanometer (nm) to about 395 nm and an intensity of from about 0.1 mW/cm 2 to about 2.5 mW/cm 2 until the temperature reaches from about 40° C. to about 80° C.; increasing the intensity of the UV light source to from about 5 mW/cm 2 @365±10 nm to about 50 mW/cm 2 @365±10 nm until reaching the maximum reaction temperature of from about 60° C. to about 150° C.; producing a gelatinous polymer; drying the gelatinous polymer and comminuting the dried product to a desired particle size. 2. The process according to claim 1 , wherein the gelatinous polymer is cut prior to drying. 3. The process according to claim 1 , wherein the adiabatic gel polymerization process is a continuous process. 4. The process according to claim 1 , wherein the monomer solution is purged at a temperature below 10 degrees Celsius. 5. The process according to claim 1 , wherein the monomer solution is purged at a temperature below minus 5 degrees Celsius. 6. The process according to claim 1 , wherein photopolymerization is initiated utilizing a UV light source having an intensity of from about 0.2 mW/cm 2 to about 2.0 mW/cm 2 . 7. The process according to claim 1 , wherein the intensity of the UV light source is increased when the reaction temperature reaches from about 50° C. to about 60° C. 8. The process according to claim 1 , wherein the intensity of the UV light source is increased to from about 10 mW/cm 2 @365±10 nm to about 50 mW/cm 2 @365±10 nm. 9. The process according to claim 8 , wherein the intensity of the UV light source is increased to from about 15 mW/cm 2 @365±10 nm to about 30 mW/cm 2 @365±10 nm. 10. The process according to claim 1 , wherein the reaction is continued until a reaction temperature of from about 80° C. to 120° C. 11. The process according to claims 1 , wherein the initial UV light source is a tube light source or an LED light source. 12. The process according to claims 1 , wherein the UV light source is a combination of tube and LED light sources. 13. The process according to claim 1 , wherein the gelatinous polymer gel is dried at a temperature of from about from about 70° C. to 150° C. 14. The process according to claim 1 , wherein the gelatinous polymer gel is dried over a temperature profile of about 110° C. to about 120° C. for about 10 minutes, followed by a temperature of about 95° C. to about 105° C. for about 40 minutes followed by a temperature of about 85° C. to about 95° C. for about 30 minutes. 15. The process according to claim 1 , wherein the product is ground to a particle-size fraction of from about 100 micron to about 1400 micron. 16. The process according to claim 15 , wherein the particles size fraction is from about 200 micron to about 1,200 micron. 17. The process according to claim 16 , wherein the particles size fraction is from about 500 micron to about 800 micron. 18. The process according to claim 1 , wherein when the temperature of the reaction reaches from about 40° C. to about 80° C., the intensity of the initial UV light source is increased at least about 10 -fold higher. 19. The process according to claim 18 , wherein when the temperature of the reaction reaches from about 40° C. to about 80° C., the intensity of the initial UV light source is increased by at least about 30-fold. 20. The process according to claim 19 , wherein when the temperature of the reaction reaches from about 40° C. to about 80° C., the intensity of the initial UV light source is increased at least about 60-fold higher.
Azo-compounds · CPC title
by ultraviolet or visible light · CPC title
use in electrical or conductive gadgets · CPC title
Homopolymers or copolymers of acrylamide or methacrylamide · CPC title
Emulsion polymerisation · CPC title
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