Facile preparation protocol of magnetic mesoporous carbon acid catalysts via soft-template self-assembly method and their applications in conversion of xylose into furfural

Furfural is a valuable dehydration product of xylose. It has a broad spectrum of industrial applications. Various catalysts containing SO 3 H have been reported for the conversion of xylose into furfural. Nevertheless, the multi-step preparation is tedious, and the catalysts are usually fine powders that are difficult to separate from the suspension. Novel magnetic mesoporous carbonaceous materials (Fe/MC) were successfully prepared via facile self-assembly in a single step. A facile subsequent hydrothermal sulfonation of Fe/MC with concentrated H 2 SO 4 at 180°C gave mesoporous carbon bearing SO 3 H groups (SO 3 H@Fe/MC) without loss of the magnetic properties. Various techniques were employed to characterize the SO 3 H@Fe/MC as a candidate catalyst. It showed strong magnetism due to its Fe particles and possessed a 243 m 2 g −1 BET-specific surface area and a 90% mesopore volume. The sample contained 0.21 mmol g −1 of SO 3 H and gave a high conversion and an acceptable furfural yield and selectivity (100%, 45% and 45%, respectively) when used at 170°C for 1 h with γ-valerolactone as solvent. The catalyst was easily separated after the catalytic tests by using a magnet, confirming sufficient magneticstability. This article is part of the theme issue ‘Bio-derived and bioinspired sustainable advanced materials for emerging technologies (part 2)’.

Diagenetic Processes in Aquaculture Ponds Showing Metal Accumulation on Shrimp Gills

The gill is the organ by which many toxic metals are taken up by crustaceans. Iron is known to precipitate at its surface, a phenomenon recently observed in some tropical aquaculture ponds. The present study uses a field approach to understand better the environmental conditions and ecological processes involved in this deposit. Because shrimp are exposed to reduced products originating from organic waste accumulated in the sediment, spatial variation in pH, redox potential and concentrations of dissolved metals in pore water were investigated in these ponds. Total organic carbon, acid volatile sulfide and pyrite were also analyzed in the solid phase. Fe2+ in pore waters showed high spatial variability between ponds and within the same pond with concentrations up to 1,193 μmol l–1. Behaviors of Fe2+, Mn2+ and Co2+ in pore water were similar. Four geochemical environments were identified, based on their physico-chemical characteristics. Highest concentrations for Fe2+, Mn2+ and Co2+ in sediment pore water occurred in slightly acidic and suboxic conditions. When the sediment became anoxic, the H2S produced reacted with Fe2+ and/or Co2+ to form acid volatile sulfide and pyrite. When pH increased, the concentration of free H2S rose up to 736 μmol l–1. With neutral and suboxic conditions, dissolved metal concentrations could be controlled by their precipitation as oxides and hydroxides. The production of pyrite suggested the existence of a possible process of sediment acidification between two crop periods through the production of sulfuric acid. This acidification could increase with pond age and be the cause of the accumulation of reduced metal after 30 years of aquaculture activity.

The green synthesis of a palm empty fruit bunch-derived sulfonated carbon acid catalyst and its performance for cassava peel starch hydrolysis

A sulfonated carbon acid catalyst (C–SO3H) was successfully generated from palm empty fruit bunch (PEFB) carbon via hydrothermal sulfonation via the addition of hydroxyethylsulfonic acid and citric acid.

Cross-Linking Modification of Ammonium Polyphosphate via Ionic Exchange and Self-Assembly for Enhancing the Fire Safety Properties of Polypropylene

Modified ammonium polyphosphate (MAPP) was prepared as a novel mono-component intumescent flame retardant (IFR) via the ionic exchange between ammonium polyphosphate (APP) and piperazine sulfonate, which is synthesized by self-assembly using 1-(2-aminoethyl) piperazine (AEP) and p-aminobenzene sulfonic acid (ASC) as raw materials. This all-in-one IFR integrating three functional elements (carbon, acid, and gas source) showed more efficient flame retardancy and excellent smoke suppression as well as better mechanical properties than the conventional APP. The incorporation of 22.5 wt.% MAPP into polypropylene (PP) eliminated the melt dripping phenomenon and passed the UL-94 V-0 rating. The results of the cone calorimetry test (CCT) revealed that the release of heat, smoke, and CO is significantly decreased, demonstrating that this novel IFR endows PP with excellent fire safety more effectively. For PP/MAPP composites, a possible IFR mechanism was proposed based on the analysis of the pyrolysis gas and char residues.

Cross-Linking Modification of Ammonium Polyphosphate via Ionic Exchange and Self-Assembly for Enhancing Fire Safety Properties of Polypropylene

Modified ammonium polyphosphate (MAPP) as a novel mono-component intumescent flame retardant (IFR) was prepared via the ionic exchange between ammonium polyphosphate (APP) and piperazine sulfonate, which is synthesized by self-assembly using 1-(2-Amioethyl) piperazine (AEP) and p-amino benzene sulfonic acid (ASC) as raw materials. This all-in-one IFR integrating three functional elements (carbon, acid, and gas source) showed more efficient flame retardancy and excellent smoke suppression as well as better mechanical properties than the conventional APP. The incorporation of 22.5 wt.% MAPP into polypropylene (PP) eliminated the melt dripping phenomenon and passed the UL-94 V-0 rating. The results of the cone calorimetry test (CCT) revealed that the release of heat, smoke, and CO is significantly decreased, demonstrating that this novel IFR endows PP with excellent fire safety more effectively. For PP/MAPP composites, a possible IFR mechanism was proposed based on the analysis of the pyrolysis gas and char residues.