The utilization of non-edible and low-cost feedstock in bioenergy research is getting more attention in recent decades. Catalytic deoxygenation of fatty acids from waste oil feedstocks is a promising route to produce diesel-like hydrocarbons. Here we report the conversion of palm fatty acid distillate (PFAD), a low-value side product of physical refining of crude palm oil, into green diesel using a solventless and hydrogen-free deoxygenation (DO) reaction using catalytic deoxygenation over solid acid catalysts (Co/SBA-15, Ni/SBA-15, and Ni-Co/SBA-15) with total metal loadings of 5 wt%. Metal precursors (Ni, Co, Ni-Co) were doped on the mesostructured catalyst supporter, SBA-15 by wet impregnation. The catalysts were characterized by nitrogen adsorption-desorption isotherm analysis, X-ray diffraction, X-ray fluorescence, infrared spectroscopy, and highresolution transmission electron microscopy with elemental mapping. The DO reaction was carried out in a semi-batch reactor with a catalyst loading of 10 wt% at 350 °C for 3 h. The use of both Ni/SBA-15 and Ni-Co/SBA-15 afforded products with high contents of liquid hydrocarbons (C8-C17) with yields of 85.8% and 88.1%, respectively, and selectivity for diesel-range hydrocarbons (C13-C17) above 85% were achieved. Cobalt seems to have a larger particle size, then associates with the carbon formation and introduces coke formation. It blocks some pores and deactivates the active sites of the catalyst, thus reducing the catalytic activity.
Poly(ω-hydroxy pelargonate) or P(ω-OHP) is a potential biodegradable plastic which was prepared by melt condensation of its monomer (ω-hydroxy pelargonic acid). In this study, the performances of P(ω-OHP) in thermal and mechanical aspects, as well as the method employed for the monomer preparation was presented. Although this type of monomer is well established for pharmaceutical and cosmetic application, its possibility to be applied in bioplastic has not been extensively studied. Previous research also showed that the monomer preparation was rather complicated, expansive, and hazardous. Thus, this study offers the safe method through chemical modification which conducted in mild condition. The monomer structure was verified by using ESI-MS at 173.1 m/z with 92% purity. After melt-condensation process was carried out at 190 °C for 4 h, the formation of P(ω-OHP) was identified by the present of methylene ester bond indicated on 1H NMR peak at 4.05 ppm. The thermal properties were analyzed by DSC, TGA,and rheometer. P(ω-OHP) was melted at 72.8 °C and start to degrade at 220 °C with rheology analysis represented Newtonian flow at 80 and 180 °C.P(ω-OHP) contains 73.5% degree of crystallinity as determined by XRD with fewer amorphous area has affecting low mechanical value in hardness (31) and compressive strength (modulus 47.3 MPa, yield 1.03 MPa). The results suggest that P(ω-OHP) is thermally stable and physically hard and brittle. The findings have implications for bioplastic custom and subjected to improvement via polymer blending or block co-polymerization for application flexibility.
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