Improvement of thermoelectric properties of Cu3SbSe4 hierarchical with in-situ second phase synthesized by microwave-assisted solvothermal method

2019 ◽  
Vol 806 ◽  
pp. 676-682 ◽  
Author(s):  
Boyi Wang ◽  
Yongli Wang ◽  
Shuqi Zheng ◽  
Shichao Liu ◽  
Juan Li ◽  
...  
Nanoscale ◽  
2018 ◽  
Vol 10 (30) ◽  
pp. 14546-14553 ◽  
Author(s):  
Dandan Xie ◽  
Bin Zhang ◽  
Aijuan Zhang ◽  
Yongjin Chen ◽  
Yanci Yan ◽  
...  

The Cu2–xSe nanoinclusions lead to reduced κL and enhanced zT in Cu3SbSe4.


1999 ◽  
Vol 564 ◽  
Author(s):  
P. W. DeHaven ◽  
K. P. Rodbell ◽  
L. Gignac

AbstractThe effectiveness of a TiN capping layer to prevent the conversion of α-titantium to titanium nitride when annealed in a nitrogen ambient has been studied over the temperature range 300–700°C using in-situ high temperature diffraction and transmission electron microscopy. Over the time range of interest (four hours), no evidence of Ti reaction was observed at 300°C. At 450°C. nitrogen was found to diffuse into the Ti to form a Ti(N) solid solution. Above 500°C the titanium is transformed to a second phase: however this reaction follows two different kinetic paths, depending on the annealing temperature. Below 600°C. the reaction proceeds in two stages, with the first stage consisting of Ti(N) formation, and the second stage consisting of the conversion of the Ti(N) with a transformation mechanism characteristic of short range diffusion (grain edge nucleation). Above 600°C, a simple linear transformation rate is observed.


ChemInform ◽  
2011 ◽  
Vol 43 (1) ◽  
pp. no-no
Author(s):  
Thomas O. Painter ◽  
Paul D. Thornton ◽  
Mario Orestano ◽  
Conrad Santini ◽  
Michael G. Organ ◽  
...  

2018 ◽  
Vol 247 ◽  
pp. 851-858 ◽  
Author(s):  
Liangliang Fan ◽  
Paul Chen ◽  
Nan Zhou ◽  
Shiyu Liu ◽  
Yaning Zhang ◽  
...  

2012 ◽  
Vol 9 (3) ◽  
pp. 1033-1040 ◽  
Author(s):  
M. Barlett ◽  
K. Zhuang ◽  
R. Mahadevan ◽  
D. Lovley

Abstract. Enhancing microbial U(VI) reduction with the addition of organic electron donors is a promising strategy for immobilizing uranium in contaminated groundwaters, but has yet to be optimized because of a poor understanding of the factors controlling the growth of various microbial communities during bioremediation. In previous field trials in which acetate was added to the subsurface, there were two distinct phases: an initial phase in which acetate-oxidizing, U(VI)-reducing Geobacter predominated and U(VI) was effectively reduced and a second phase in which acetate-oxidizing sulfate reducing bacteria (SRB) predominated and U(VI) reduction was poor. The interaction of Geobacter and SRB was investigated both in sediment incubations that mimicked in situ bioremediation and with in silico metabolic modeling. In sediment incubations, Geobacter grew quickly but then declined in numbers as the microbially reducible Fe(III) was depleted whereas the SRB grow more slowly and reached dominance after 30–40 days. Modeling predicted a similar outcome. Additional modeling in which the relative initial percentages of the Geobacter and SRB were varied indicated that there was little to no competitive interaction between Geobacter and SRB when acetate was abundant. Further simulations suggested that the addition of Fe(III) would revive the Geobacter, but have little to no effect on the SRB. This result was confirmed experimentally. The results demonstrate that it is possible to predict the impact of amendments on important components of the subsurface microbial community during groundwater bioremediation. The finding that Fe(III) availability, rather than competition with SRB, is the key factor limiting the activity of Geobacter during in situ uranium bioremediation will aid in the design of improved uranium bioremediation strategies.


Sign in / Sign up

Export Citation Format

Share Document