Performance of Catalytically Active Membrane Reactors with Different A/V Ratios

Although the performance of membrane reactors(MR) is highly affected by the ratio of membrane area-toreaction volume, there are few studies on this effect owing to the difficulties associated with reactor manufacture. In this study, an MR with high A/V ratio, a diameter of 35 m,and a height of 0.8 mm was fabricated. Separation performance of this MR was investigated in an n-butanol/water system. Esterification of acetic acid and n-butanol was used as the model reaction to investigate the performance of catalytically active membrane reactors(CAMR)with different A/V ratios. The reaction conversion was 38.59% in the CAMR with the high A/V ratio of 12,497/m,which was much higher than that in other CAMRs, for reaction time of 60 min and W/Vfratio of 0.093 g/mL.Excellent catalytic stability of the CAMR was confirmed by performing long-term stability experiments.

Enhanced charge separation by continuous homojunction with spatially separated redox sites for hydrogen evolution

Photocatalytic hydrogen generation represents a promising strategy for the establishment of a sustainable and environmentally friendly energy reservoir.However,the current solar-to-hydrogen conversion efficiency is not yet sufficient for practical hydrogen production,highlighting the need for further research and development.Here,we report the synthesis of a Sn-doped TiO_(2)continuous homojunction hollow sphere,achieved through controlled calcination time.The incorporation of a gradient doping profile has been demonstrated to generate a gradient in the band edge energy,facilitating carrier orientation migration.Furthermore,the hollow sphere’s outer and inner sides provide spatially separated reaction sites allowing for the separate acceptance of holes and electrons,which enables the rapid utilization of carriers after separation.As a result,the hollow sphere TiO_(2)with gradient Sn doping exhibits a significantly increased hydrogen production rate of 20.1 mmol·g^(−1)·h^(−1).This study offers a compelling and effective approach to the designing and fabricating highly efficient nanostructured photocatalysts for solar energy conversion applications.

The Ame2020 atomic mass evaluation(II).Tables,graphs and references

This is the second part of the new evaluation of atomic masses,Ame2020.Using least-squares adjustments to all evaluated and accepted experimental data,described in Part I,we derived tables with numerical values and graphs which supersede those given in Ame2016.The first table presents the recommended atomic mass values and their uncertainties.It is followed by a table of the influences of data on primary nuclides,a table of various reaction and decay energies,and finally,a series of graphs of separation and decay energies.The last section of this paper provides all input data references that were used in the Ame2020 and the Nubase2020 evaluations.

The AME2016 atomic mass evaluation (Ⅱ).Tables,graphs and references

This paper is the second part of the new evaluation of atomic masses, AME2016. Using least-squares adjustments to all evaluated and accepted experimental data, described in Part I, we derive tables with numerical values and graphs to replace those given in AME2012. The first table lists the recommended atomic mass values and their uncertainties. It is followed by a table of the influences of data on primary nuclides, a table of various reaction and decay energies, and finally, a series of graphs of separation and decay energies. The last section of this paper lists all references of the input data used in the AME2016 and the NUBASE2016 evaluations （first paper in this issue）.

Fabrication of morphology-controlled TiO_2 photocatalyst nanoparticles and improvement of photocatalytic activities by modification of Fe compounds

Our previous studies suggested that redox reaction proceeded separately on specific exposed crystal faces of TiO2 nanoparticles. Site-selective deposition of metal or metal oxide on TiO2 specific exposed crystal faces successfully proceeded using the unique reactivity properties on the surface of TiO2 nanoparticles under photoexcitation. A remarkable improvement ofphotocatalytic activity of shape- controlled brookite and rutile TiO2 nanorods with modification of Fe^3＋ compounds was observed under visible light. Crystal face-selective metal compound modification on exposed crystal faces of TiO2 nanorods with brookite and futile phases was successfully prepared. Brookite and rutile TiO2 nanorods prepared by site-selective modification with metal compounds should be ideal visible-light responsive TiO2 photocatalysts because of the remarkable suppression of back electron transfer from TiO2 to oxidized metal com- pounds on the surface of the TiO2 nanorod with a brookite or rutile phase. In this paper, the development of exposed crystal face-controlled TiO2 nanorods with rutile and brookite phases was described. The obtained rutile and brookite TiO2 nanorod, showing remarkably high activity for degra- dation of organic compounds compared with the photocatalytic activities of anatase fine particles （ST-01）, is one of the most active commercially available photocatalysts for environmental cleanup in Japan. The technology of visiblelight responsive treatment for morphology-controlled rutile and brookite TiO2 nanorods by crystal face-selective modification of Fe^3＋ compounds was also discussed in this paper. The Fe^3＋ compound-modified rutile and brookite TiO2 nanorods show much higher activity than conventional visible-light responsive N-doped TiO2, which is commercially available in Japan.