77 research outputs found

    Thermal and catalytic decomposition studies of microalgal residue using pyrolysis-GC/MS and TG/MS

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    The marine algal biomass is one of the most promising candidates for the raw material of sustainable biofuel production. Biofuels of different phases can be converted by bio- or thermochemical methods. In this study thermogravimetry/mass spectrometry (TG/MS) and pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS) were used to analyze the main decomposition products of the deoiled algal cake (DAC). Two mesoporous silica catalysts (SBA-15 and FSM-16) were applied to modify the composition of the evolving gas phase products. The yield of the evolving volatile gas products was enhanced by the use of the SBA-15. This catalyst promoted the decomposition of the inorganic carbonates into carbon dioxide. The formation of hydrocarbons during the fast pyrolysis simple alcohol molecules were formed from the deoiled algal residue. The yields of the anhydro-sugar derivatives were strongly affected by the presence of both catalysts. The intensity of the aromatic and aliphatic decomposition products were influenced by the catalytic decomposition procedure

    Spectral microscopic mechanisms and quantum phase transitions in a 1D correlated problem

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    In this paper we study the dominant microscopic processes that generate nearly the whole one-electron removal and addition spectral weight of the one-dimensional Hubbard model for all values of the on-site repulsion UU. We find that for the doped Mott-Hubbard insulator there is a competition between the microscopic processes that generate the one-electron upper-Hubbard band spectral-weight distributions of the Mott-Hubbard insulating phase and finite-doping-concentration metallic phase, respectively. The spectral-weight distributions generated by the non-perturbative processes studied here are shown elsewhere to agree quantitatively for the whole momentum and energy bandwidth with the peak dispersions observed by angle-resolved photoelectron spectroscopy in quasi-one-dimensional compounds.Comment: 18 pages, 2 figure

    Thermoanalytical characterization and catalytic conversion of de-oiled micro algae and jatropha seed cake

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    The thermal decomposition of the by-products of the biodiesel process was studied by thermoanalytical methods. De-oiled algae cake and jatropha seed de-oiled cake were pyrolyzed and the catalytic effects of silica supported iron catalysts (Fe/FSM-16 and Fe/SBA-15) and magnetite (Fe3O4) were tested. The evolution profiles of the decomposition products as well as the thermal stability of the samples were determined by thermogravimetry/mass spectrometry (TG/MS). The formation of the volatile products was monitored by pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS). The composition and the amounts of the gaseous products changed significantly in the presence of the silica supported iron catalysts: the yield of hydrogen and carbon monoxide considerably increased above the decomposition temperature of 400 °C. Both silica supported iron catalysts had important effects on the yield of the products originating from carbohydrates and lignins. The formation of anhydrosugars and phenolic compounds was hindered, while the evolution of aromatic and aliphatic hydrocarbons was enhanced. Fe/FSM-16 proved to be more efficient than Fe/SBA-15 and Fe3O4 catalysts. The thermal decomposition of the protein content of the samples resulted in the formation of 2,5 diketopiperazines and smaller molecules (e.g., ammonia). The silica supported iron catalysts had a special effect: their presence promoted the reaction of fatty acid esters and ammonia resulting in the formation of alkyl nitriles during the thermal decomposition

    Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort

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    Background: As gene-targeted therapies are increasingly being developed for Parkinson's disease (PD), identifying and characterizing carriers of specific genetic pathogenic variants is imperative. Only a small fraction of the estimated number of subjects with monogenic PD worldwide are currently represented in the literature and availability of clinical data and clinical trial-ready cohorts is limited. Objective: The objectives are to (1) establish an international cohort of affected and unaffected individuals with PD-linked variants; (2) provide harmonized and quality-controlled clinical characterization data for each included individual; and (3) further promote collaboration of researchers in the field of monogenic PD. Methods: We conducted a worldwide, systematic online survey to collect individual-level data on individuals with PD-linked variants in SNCA, LRRK2, VPS35, PRKN, PINK1, DJ-1, as well as selected pathogenic and risk variants in GBA and corresponding demographic, clinical, and genetic data. All registered cases underwent thorough quality checks, and pathogenicity scoring of the variants and genotype–phenotype relationships were analyzed. Results: We collected 3888 variant carriers for our analyses, reported by 92 centers (42 countries) worldwide. Of the included individuals, 3185 had a diagnosis of PD (ie, 1306 LRRK2, 115 SNCA, 23 VPS35, 429 PRKN, 75 PINK1, 13 DJ-1, and 1224 GBA) and 703 were unaffected (ie, 328 LRRK2, 32 SNCA, 3 VPS35, 1 PRKN, 1 PINK1, and 338 GBA). In total, we identified 269 different pathogenic variants; 1322 individuals in our cohort (34%) were indicated as not previously published. Conclusions: Within the MJFF Global Genetic PD Study Group, we (1) established the largest international cohort of affected and unaffected individuals carrying PD-linked variants; (2) provide harmonized and quality-controlled clinical and genetic data for each included individual; (3) promote collaboration in the field of genetic PD with a view toward clinical and genetic stratification of patients for gene-targeted clinical trials. © 2023 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society

    Using global team science to identify genetic parkinson's disease worldwide.

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    Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)

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