Enhancements of dimethyl carbonate synthesis from methanol and carbon dioxide:The in situ hydrolysis of 2-cyanopyridine and crystal face effect of ceria

This paper describes the effect of the in situ hydrolysis of 2-cyanopyridine and its derivatives on the synthesis of dimethyl carbonate（DMC） from CO2 and methanol over CeO2.2-Cyanopyridine.with the highest electronic charge number of the carbon in the cyanogroup,is the most effective agent to accelerate the desired reaction by a decrease of water.CeO2（110） planes are active for the hydrolysis of 2-cyanopyridine,further enhancing the DMC formation by in situ removal of water effectively.The DMC yield is improved drastically up to 378.5 mmol g cat^-1 from 12.8 mmol g cat^-1 with the in situ hydrolysis of 2-cyanopyridine over rod-CeO2（1 1 0） catalyst.

Nitrogen-doped flower-like porous carbon materials directed by in situ hydrolysed MgO： Promising support for Ru nanoparticles in catalytic hydrogenations

The development of novel simple, and convenient techniques for the fabrication of porous carbon materials with desirable properties, such as tunable pore structures and the presence of nitrogen functionalities, from renewable and abundant biomasses is required. We herein describe an in situ directing method for the preparation of a nitrogen-doped flower-like porous carbon （NFPC） employing arbitrarily shaped MgO from bio-derived glucosamine chloride （GAH）. Experimental evidence demonstrated that the structure directing effect of the Mg（OH）2 nanosheets formed in situ from MgO hydrolysis was key to this process, with the original MgO morphology being irrelevant. Furthermore, this method was applicable for a wide variety of biomass-derived carbon precursors. The resulting NFPC exhibited a high nitrogen content of 〈9 wt.%, and was employed as a support to anchor small Ru nanoparticles （average size = 2.7 nm）. The resulting Ru/NFPC was highly active in heterogeneous hydrogenations of toluene and benzoic acid, which demonstrated the advantages of nitrogen doping in terms of boosting catalytic performance.

Improving biodegradation potential of domestic wastewater by manipulating the size distribution of organic matter

Carbon source is a critical constraint on nutrient removal in domestic wastewater treatment.However,the functions of particulate organic matter（POM） and some organics with high molecular weight（HMW） are overlooked in the conventional process,as they cannot be directly assimilated into cells during microbial metabolism.This further aggravates the problem of carbon source shortage and thus affects the effluent quality.Therefore,to better characterize organic matter（OM） based MW distribution,microfiltration/ultrafiltration/nanofiltration（MF/UF/NF） membranes were used in parallel to fractionate OM,which obtained seven fractions.Hydrolysis acidification（HA） was adopted to manipulate the MW distribution of dissolved organic matter（DOM） and further explore the correlation between molecular size and biodegradability.Results showed that HA pretreatment of wastewater not only promoted transformation from POM to DOM,but also boosted biodegradability.After 8 hr of HA,the concentration of dissolved organic carbon（DOC） increased by 65%,from the initial value of20.25 to 33.48 mg/L,and the biodegradability index（BOD5（biochemical oxygen demand）/SCOD（soluble chemical oxygen demand）） increased from 0.52 to 0.74.Using MW distribution analysis and composition optimization,a new understanding on the characteristics of organics in wastewater was obtained,which is of importance to solving low C/N wastewater treatment in engineering practice.