The wet biomass brewer's spent grain was subjected to hydrothermal carbonization to produce biocoal. Mass balance considerations indicate for about two thirds of the organic carbon of the input biomass to be transferred into the biocoal. The van Krevelen plot refers to a high degree of defunctionalization with decarboxylation prevailing over dehydration.
View Article and Find Full Text PDFOrganic components in olive mill wastewater (OMW) were analyzed by exhaustive solvent extraction of the lyophilisate followed by pre-chromatographic derivatization techniques and GC/MS-analysis of the extracts. Simple biophenols including tyrosol (Tyr), hydroxytyrosol (OH-Tyr) and homovanillic alcohol as well as complex biophenols including decarbomethoxy ligostride aglycon and decarbomethoxy oleuropein aglycon proved most abundant analytes. Hydroxylated benzoic and cinnamic acids are less abundant, which may indicate a humification process to have occurred.
View Article and Find Full Text PDFThe degree of degradation of 12 organic compounds from various classes, comprising of pharmaceuticals, pesticides, and industrial chemicals, was analyzed after hydrothermal treatment at 200°C for 4 or 16h, or 255°C for 16h. The reactions were conducted in water, aqueous H2SO4, or sucrose solution in aqueous H2SO4 as a representative matrix of hydrothermal carbonization (HTC) of wet biomasses. The impact of the sucrose-matrix, which formed during the HTC reaction as a solid hydrochar material and a complex pattern of dissolved organic matter in the aqueous phase, was found to be insignificant for the degree of conversion of most compounds.
View Article and Find Full Text PDFHydrothermal carbonization (HTC) is an emerging technology to treat wet biomasses aimed at producing a biochar material. Herein, olive mill wastewater (OMW) was subjected to HTC. Mass balance considerations provide evidence that the yield of biochar is low (~30%, w/w), which is associated with a low fraction of carbohydrates in OMW.
View Article and Find Full Text PDFThe gated decoupled (13)C NMR spectra of a dipeptide (Glu-Trp) and a tetrapeptide (NAc-Ser-Phe-Val-Gly-OMe) were recorded in D(2)O and in a lyotropic alignment medium (pentaethylene glycol monododecyl ether/n-hexanol). The residual dipolar couplings were extracted as the differences between the observed couplings for the magnetic nuclei dissolved in the latter and former media. Using a computational optimization, the spatial structures of the compounds were calculated starting from their respective low energy conformations obtained on a semiempirical basis.
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