Hybrid sustainable composites and methods of making and using thereof
US-2016229997-A1 · Aug 11, 2016 · US
US10414880B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10414880-B2 |
| Application number | US-201515126187-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 13, 2015 |
| Priority date | Mar 14, 2014 |
| Publication date | Sep 17, 2019 |
| Grant date | Sep 17, 2019 |
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Biocarbon is presented as an alternative to synthetic carbon black. Master batches having biocarbon for usage in raw plastics and/or the production of composites. Biocarbon is mainly derived from plant biomass, but other sources can be used. A method of producing the master batch: (a) pyrolyzing processed biomass in an oxygen-starved environment to produced biocarbon; (b) comminuting the biocarbon in a reduced oxygen atmosphere; (c) cooling the comminuted biocarbon; (d) mixing the cooled comminuted biocarbon with a carrier resin, thereby producing the master batch.
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What is claimed is: 1. A master batch for the production of composites, the master batch comprising a blend of carbonized biomass and a carrier resin, wherein the carbonized biomass has a particle size lower than about 100 microns, and wherein the concentration of the carbonized biomass in the master batch is from about 25% wt. to about 75% wt., and the concentration of the carrier resin in the master batch is from about 25% wt. to about 75% wt. 2. The master batch of claim 1 , wherein the biomass is selected from: plant fibers, municipal solid waste, agricultural biomass, forest biomass, and animal manure. 3. The master batch of claim 1 , wherein the carrier resin is a synthetic polymer. 4. The master batch of claim 2 , wherein the synthetic polymer is selected from polyethylene (PE), crosslinked-polyethylene (PEX), polypropylene (PP), impact polypropylene, and polybutylene (PB); polyvinylchloride (PVC), chlorinated polyvinyl chloride (CPVC), polyvinylidene fluoride (PVDF), polystyrene (PS), acrylic polymers, nylon, acrylonitrile butadiene styrene, thermoplastic polyurethanes, polycarbonates, or combinations thereof. 5. The master batch of claim 1 , wherein the carrier resin is a bioplastic. 6. The master batch of claim 5 , wherein the bioplastic is selected from poly(lactic acid) (PLA), polyglycolic acid (PGA), poly(lactic acid-co-glycolic acid (PLGA), polycaprolactone, polyhydroxyalkanoates or combinations thereof. 7. The master batch of claim 1 , wherein the blend further comprises an additive. 8. A composite comprising a polymer compounded with a master batch of claim 1 . 9. The composite of claim 8 , wherein the concentration of the carbonized biomass in the composite comprises between 1% wt. and 6% wt. 10. A product comprising the composite of claim 8 . 11. The master batch of claim 1 , wherein the carbonized biomass is biochar. 12. The master batch of claim 1 , wherein the carbonized biomass has a particle size ranging from about 50 nanometers to about 100 microns. 13. The composite of claim 8 , wherein the carbonized biomass is biochar. 14. The composite of claim 8 , wherein the carbonized biomass has a particle size ranging from about 50 nanometers to about 100 microns. 15. A master batch for the production of composites, the master batch comprising a blend of carbonized biomass and a carrier resin, wherein the carbonized biomass has a particle size lower than about 100 microns, and wherein the carrier resin is a bioplastic. 16. A composite comprising a polymer compounded with a master batch of claim 15 . 17. A method of producing a master batch according to claim 1 , the method comprising: (a) pyrolizing processed biomass in an oxygen-starved environment to produced biocarbon; (b) communiting the biocarbon; (c) mixing the communited biocarbon with a carrier resin, thereby producing the master batch. 18. The method of claim 17 , wherein the pyrolysis is carried out at a temperature of about 400° C. to about 900° C. 19. The method of claim 18 , wherein the biocarbon is comminuted while the biocarbon is at about 350° C. 20. The method of claim 17 , wherein the comminuting of step (b) takes place in a reduced oxygen atmosphere. 21. The method of claim 20 , wherein the method further comprises cooling the comminuted biocarbon. 22. The method of claim 21 , wherein the comminuted biocarbon is cooled to about 200° C. 23. The method of claim 17 , wherein the biocarbon is comminuted to a particle size ranging from about 100 microns to about 50 nanometers. 24. The method of claim 17 , wherein from about 25% wt. to about 70% wt of the carrier resin is mixed with from about 30% wt. to about 75% wt. of the biocarbon. 25. The method of claim 17 , wherein the method further comprises adding an additive.
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