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The cell wall compositional (lignin and polysaccharides) variation of two sweet sorghum varieties, Della (D) and its variant REDforGREEN (RG), was evaluated at internodes (IN) and nodes (N) using high-performance liquid chromatography (HPLC), pyrolysis-gas chromatography-mass spectrometry (Py-GCMS), X-ray diffraction (XRD), and two-dimensional (2D) 1 H- 13 C nuclear magnetic resonance (NMR). The stalks were grown in 2018 (D1 and RG1) and 2019 (D2 and RG2) seasons. In RG1, Klason lignin reductions by 16-44 and 2-26% were detected in IN and N, respectively. The analyses also revealed that lignin from the sorghum stalks was enriched in guaiacyl units and the syringyl/guaiacyl ratio was increased in RG1 and RG2, respectively, by 96% and more than 2-fold at IN and 61 and 23% at N. The glucan content was reduced by 23-27% for RG1 and by 17-22% for RG2 at internodes. Structural variations due to changes in both cellulose- and hemicellulose-based sugars were detected. The nonacylated and γ-acylated β-O-4 linkages were the main interunit linkages detected in lignin. These results indicate compositional variation of stalks due to the RG variation, and the growing season could influence their mechanical and lodging behavior.

A non-isothermal decomposition of Moringa oleifera husk and Delonix regia seed pod was carried out in an N 2 pyrolytic condition with the primary objective of undertaking the kinetics modeling, thermodynamics and thermal performance analyses of the identified samples. Three different isoconversional models, namely, differential Friedman, Flynn-Wall-Ozawa, and Starink techniques were utilized for the deduction of the kinetics data. The thermodynamic parameters were deduced from the kinetic data based on a first-order chemical reaction model. In the kinetics study, a strong correlation (R 2  > 0.9) was observed throughout the conversion range for all the kinetic models. The activation energy profiles showed two distinctive regions. In the first region, the average activation energy values were relatively higher-a typical example is in the Flynn-Wall-Ozawa technique-MH (199 kJ/mol) and RP (194 kJ/mol), while in the second region, MH (292 kJ/mol) and RP (234 kJ/mol). It was also demonstrated that the thermal process for the samples experienced endothermic reactions thought the conversion range. In summary, both the kinetic and thermodynamic parameters vary significantly with conversion-underscoring the complexity associated with the thermal conversion of lignocellulosic biomass samples.

The effects of Al 2 O 3 coating on the performance of silica nanospring (NS) supported Co catalysts for Fischer-Tropsch synthesis (FTS) were evaluated in a quartz fixed-bed microreactor. The Co/NS-Al 2 O 3 catalysts were synthesized by coating the Co/NS and NS with Al 2 O 3 by an alkoxide-based sol-gel method (NS-Al-A and NS-Al-B, respectively) and then by decorating them with Co. Co deposition was via an impregnation method. Catalysts were characterized before the FTS reaction by the Brunauer-Emmett-Teller (BET) method, X-ray diffraction, transmission electron microscopy, temperature programmed reduction, X-ray photoelectron spectroscopy, differential thermal analysis and thermogravimetric analysis in order to find correlations between physico-chemical properties of catalysts and catalytic performance. The products of the FTS were trapped and analyzed by GC-TCD and GC-MS to determine the CO conversion and reaction selectivity. The Al 2 O 3 coated NS catalyst had a significant affect in FTS activity and selectivity in both Co/NS-Al 2 O 3 catalysts. A high CO conversion (82.4%) and Σ > C 6 (86.3%) yield were obtained on the Co/NS-Al-B catalyst, whereas the CO conversion was 62.8% and Σ > C 6 was 58.5% on the Co/NS-Al-A catalyst under the same FTS experimental condition. The Co/NS-Al-A catalyst yielded the aromatic selectivity of 10.2% and oxygenated compounds.