Metal Triflates Incorporated in Mesoporous Catalysts for Green Synthesis of Fine Chemicals

Strong Lewis acid SnTf-MCM-41 and SnTf-UVM-7 catalysts with unimodal and bimodal pore systems were prepared in a two-step synthesis in which the triflic acid (Tf) was incorporated into previously synthesized mesoporous tin-containing silicas. The Sn incorporation inside the pore walls was carried out through the Atrane method. The SnTf-UVM-7 catalysts were prepared by aggregating nanometric mesoporous particles defining a hierarchic textural-type additional pore system. Catalysts with different Si/Sn ratios in the range 21.8–50.8 for SnTf-MCM-41 and 18.4 for SnTf-UVM-7 were found to be efficient catalysts for the acylation of aromatics and heteroaromatics. Under microwave irradiation the reaction was possible even with acetic acid. The selectivity to the desired product (o-hydroxyacetophenone for phenol) or the unfavored three-substituted five ring heterocycles was dramatically increased under these conditions. The process is green, environmentally safe, and heterogeneous.     

Cellulose nanocomposites based on silane reinforced 3-butynoate-substituted zirconium-oxocluster copolymers: Mechanical,thermal and hydrophobic properties

Silica based cellulose nanocomposites obtained from (3-mercaptopropyl)trimethoxysilane or vinyltrimethoxysilane and 3-butynoate-substituted zirconium-oxoclusters were prepared and their surface morphology, wettability, and thermo-mechanical properties were studied. The composites showed a hydrophobic surface, high strength, and resistance to thermal degradation and aging; in comparison to the untreated paper they required a higher temperature to activate combustion and generated less heat during all thermal processes.     

Defined Conjugation of Glycans to the Lysines of CRM197 Guided by their Reactivity Mapping

Systematic characterisation of the reactivity of the lysine moieties in CRM₁₉₇ towards N‐hydroxysuccinimide linkers bearing alkynes or azides is described. This involves two‐step conjugation of various glycans to CRM₁₉₇ by click chemistry in a well‐defined manner. By semiquantitative LC‐MS/MS analysis of proteolytic digests of the conjugates formed, the reactivity of lysine residues in the protein was mapped and ranked. Computational analysis of the solvent accessibility of each lysine residue (based on the CRM₁₉₇ crystal structure) established a correlation between reactivity and surface exposure. By this approach, conjugation involving lysine residues (normally a random process) can be controlled. It enables the preparation of lysine‐mediated glycoconjugates with improved batch‐to‐batch reproducibility, thereby producing neo‐glycoconjugates with more‐consistent biological activity.     

A chemically enhanced biological process for lowering operative costs and solid residues of industrial recalcitrant wastewater treatment

An innovative process based on ozone-enhanced biological degradation, carried out in an aerobic granular biomass system (SBBGR - Sequencing Batch Biofilter Granular Reactor), was tested at pilot scale for tannery wastewater treatment chosen as representative of industrial recalcitrant wastewater. The results have shown that the process was able to meet the current discharge limits when the biologically treated wastewater was recirculated through an adjacent reactor where a specific ozone dose of 120 mg O₃/L_influent was used. The benefits produced by using ozone were appreciable even visually since the final effluent of the process looked like tap water. In comparison with the conventional treatment, the proposed process was able to reduce the sludge production by 25-30 times and to save 60% of operating costs.Molecular in situ detection methods were employed in combination with the traditional measurements (oxygen uptake rate, total protein content, extracellular polymeric substances and hydrophobicity) to evaluate microbial activity and composition, and the structure of the biomass. A stable presence of active bacterial populations was observed in the biomass with the simultaneous occurrence of distinctive functional microbial groups involved in carbon, nitrogen and sulphate removal under different reaction environments established within the large microbial aggregates. The structure and activity of the biomass were not affected by the use of ozone.