Acrocomia aculeata is a palm tree typical of the Brazilian savanna. Oils extracted from the pulp and kernel of Acrocomia aculeata fruits have gained considerable attention mainly due to their nutritional and medicinal features. Despite their potential applications, a detailed analysis of their oxidative stability is still needed. The present study shows a close analysis of the oxidative stability of the oils obtained from the kernel and pulp of Acrocomia aculeata fruits, evaluating the influence of the intrinsic antioxidants and the fatty acid composition on the oil's thermal stability. A complete characterization of the physical-chemical and optical properties of the oils was performed. The results showed that 66% of the fatty acids present in the pulp oil are unsaturated, while 75% are saturated in the kernel oil. A higher content of intrinsic antioxidants was obtained in the pulp oil, and an induction period (at 110 • C) of 65 and 43 h was determined for the pulp and kernel oil, respectively. Additionally, oil absorption increases due to the formation of degradation products, and a new fluorescent compound was formed during the oil oxidation process at 110 • C. Even though the pulp presented a high content of unsaturated fatty acids, the pulp oil was more stable than the kernel oil due to its higher content of intrinsic antioxidant, especially carotenoids. The results also demonstrated that oil oxidation can be optically determined by analyzing the absorption at 232 and 270 nm, as well as the emission at 424 nm.
Cellulosic ethanol is one of the most important biotechnological products to mitigate the consumption of fossil fuels and to increase the use of renewable resources for fuels and chemicals. By performing this process at high total solids (TS) and low enzyme loadings (EL), one can achieve significant improvements in the overall cellulosic ethanol production process. In this work, steam-exploded materials were obtained from Eucalyptus urograndis chips and sugarcane bagasse to be subsequently used for enzymatic hydrolysis at high TS (20 wt%) and relatively low EL (13.3 FPU g −1 TS of Cellic CTec3 from Novozymes). Also, the fermentability of their corresponding hydrolysates was tested using an industrial strain of Saccharomyces cerevisiae (Thermosacc Dry from Lallemand). Enzymatic hydrolysis of steam-treated E. urograndis reached 125 g L −1 of glucose in 72 h, while steam-treated bagasse gave yields 25 % lower. Both substrate hydrolysates were easily converted to ethanol, giving yields above 25 g L −1 and productivities of 2.3 g L −1 h −1 for eucalypt and 2.2 g L −1 h −1 for bagasse after only 12 h of fermentation. Under the conditions used in this study, sugarcane bagasse glucans showed the potential to boost the ethanol production from sugarcane culms by 31 %, from the 80 L t −1 of first generation to a total production of 105 L t −1. On the other hand, E. urograndis plantations are able to achieve cellulosic ethanol productivities of 2832.2 L ha −1 year −1 , which was 57.8 % higher than the projected value of 1794.5 L ha −1 year −1 that was obtained for sugarcane bagasse.
Cellulosic ethanol is one of the most important biotechnological products to mitigate the consumption of fossil fuels and to increase the use of renewable resources for fuels and chemicals. By performing this process at high total solids (TS) and low enzyme loadings (EL), one can achieve significant improvements in the overall cellulosic ethanol production process. In this work, steam-exploded materials were obtained from Eucalyptus urograndis chips and sugarcane bagasse to be subsequently used for enzymatic hydrolysis at high TS (20 wt%) and relatively low EL (13.3 FPU g −1 TS of Cellic CTec3 from Novozymes). Also, the fermentability of their corresponding hydrolysates was tested using an industrial strain of Saccharomyces cerevisiae (Thermosacc Dry from Lallemand). Enzymatic hydrolysis of steam-treated E. urograndis reached 125 g L −1 of glucose in 72 h, while steam-treated bagasse gave yields 25 % lower. Both substrate hydrolysates were easily converted to ethanol, giving yields above 25 g L −1 and productivities of 2.3 g L −1 h −1 for eucalypt and 2.2 g L −1 h −1 for bagasse after only 12 h of fermentation. Under the conditions used in this study, sugarcane bagasse glucans showed the potential to boost the ethanol production from sugarcane culms by 31 %, from the 80 L t −1 of first generation to a total production of 105 L t −1. On the other hand, E. urograndis plantations are able to achieve cellulosic ethanol productivities of 2832.2 L ha −1 year −1 , which was 57.8 % higher than the projected value of 1794.5 L ha −1 year −1 that was obtained for sugarcane bagasse.
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