Abstract:
Paraffin compositions including mainly even carbon number paraffins, and a method for manufacturing the same, is disclosed herein. In one embodiment, the method involves contacting naturally occurring fatty acid/glycerides with hydrogen in a slurry bubble column reactor containing bimetallic catalysts with equivalent particle diameters from about 10 to about 400 micron. The even carbon number compositions are particularly useful as phase change material.
Abstract:
Paraffin compositions including mainly even carbon number paraffins, and a method for manufacturing the same, is disclosed herein. In one embodiment, the method involves contacting naturally occurring fatty acid/glycerides with hydrogen in a slurry bubble column reactor containing bimetallic catalysts with equivalent particle diameters from about 10 to about 400 micron. The even carbon number compositions are particularly useful as phase change material.
Abstract:
Disclosed is a method of producing an estolide having high structural stability, including: a) preparing a fatty acid mixture from biomass-derived oil; b) separating the fatty acid mixture into a C16 fatty acid and a C18 fatty acid; c) converting the C18 fatty acid into a C18 or C17 linear internal olefin; and d) subjecting the C18 or C17 linear internal olefin and the C16 fatty acid to an estolide reaction, thus obtaining an estolide.
Abstract:
The disclosed invention relates to a process for converting ethylbenzene to styrene, comprising: flowing a feed composition comprising ethylbenzene in at least one process microchannel in contact with at least one catalyst to dehydrogenate the ethylbenzene and form a product comprising styrene; exchanging heat between the process microchannel and at least one heat exchange channel in thermal contact with the process microchannel; and removing product from the process microchannel. Also disclosed is an apparatus comprising a process microchannel, a heat exchange channel, and a heat transfer wall positioned between the process microchannel and heat exchange channel wherein the heat transfer wall comprises a thermal resistance layer.
Abstract:
Disclosed is a method of producing an estolide having high structural stability, including: a) preparing a fatty acid mixture from biomass-derived oil; b) separating the fatty acid mixture into a C16 fatty acid and a C18 fatty acid; c) converting the C18 fatty acid into a C18 or C17 linear internal olefin; and d) subjecting the C18 or C17 linear internal olefin and the C16 fatty acid to an estolide reaction, thus obtaining an estolide.
Abstract:
Provided herein are methods of processing polyester-containing feedstocks to provide hydrocarbon products. Exemplary feedstocks include those containing estolide compounds, which may be processed under thermal and/or catalytic conditions to provide at least one hydrocarbon product.
Abstract:
A process for making a bio-diesel and a bio-naphtha from a complex mixture of natural occurring fats & oils may include subjecting the complex mixture to a refining treatment for removing non-triglyceride and non-fatty acid components, thereby obtaining refined oils. The complex mixture or refined oils may be subjected hydrolysis for obtaining glycerol and free fatty acids. The free fatty acids may be subjected to fractionation for obtaining: a liquid part (phase L); and a solid part (phase S). The phase L may be transformed into alkyl-esters as bio-diesel by an esterification. The phase S may be transformed into linear paraffins as the bio-naphtha by: hydrodeoxygenation or decarboxylation of the free fatty acids; or obtaining fatty acids soaps from the phase S and decarboxylation of the fatty acids soaps.
Abstract:
The present application discloses low temperature, low pressure methods (LTLP) for upgrading and/or stabilizing bio-oil or a bio-oil fraction. One method comprises providing a bio-oil or bio-oil fraction and hydrogen, which are reacted in the presence of a catalyst at a temperature of less than 150° C. and a pressure of less than 100 bar (absolute) to produce a hydrogenated liquid oil at a carbon yield of over 75%. Another method comprises providing a bio-oil or bio-oil fraction, providing oxygen reducing reaction conditions, and reacting the bio-oil or bio-oil fraction under the oxygen reducing reaction conditions at LTLP to produce an upgraded bio-oil product containing fewer carbonyls than the bio-oil or bio-oil fraction. Yet another method comprises providing a bio-oil or bio-oil fraction and a solution comprising one or more fermentation organisms and a sugar source. The solution and bio-oil or bio-oil fraction are combined to obtain a fermentation mixture, which is incubated at 15° C. to 30° C. for 16 to 72 hours to produce an upgraded bio-oil fermentation product containing fewer carbonyls than the bio-oil or bio-oil fraction.
Abstract:
A process is described for producing a hydrocarbon product. In examples, the process comprising contacting a feedstock with a catalyst composition in the presence of hydrogen, the feedstock including a lipid, and the catalyst composition being active for conversion of the lipid to the hydrocarbon product in a single step. The catalyst composition comprises an M1-8 Sup] catalyst, where M1 is an active metal and [Sup] comprises an acidic support. In examples described, the process is used in the production of diesel-range fuel and/or jet fuel from lipid having a high yield of C11-C24 branched alkanes with high cetane value and low freeing point. In examples, the hydrocarbon product includes greater than 70% measured by weight of C11-C24 alkanes based on the weight of the lipid, and the content of branched alkanes of the C11-C24 alkanes is greater than 60% measured by weight of branched C11-C24 alkanes based on the weight of the C11-C24 alkanes.
Abstract:
A catalyst comprising NiO, a metal mixture comprising at least one of MoO3 or WO3, a mixture comprising at least one of SiO2 and Al2O3, and P2O5. In this embodiment the metal sites on the catalyst are sulfided and the catalyst is capable of removing tar from a synthesis gas while performing methanation and water gas shift reactions at a temperature range from 300° C. to 600° C.
Abstract translation:包含NiO的催化剂,包含MoO 3或WO 3中的至少一种的金属混合物,包含SiO 2和Al 2 O 3中的至少一种的混合物和P 2 O 5。 在该实施方案中,催化剂上的金属部位被硫化,并且催化剂能够在300℃至600℃的温度范围内进行甲烷化和水煤气变换反应从合成气中除去焦油。