Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Crystal growth electrochemical synthesis

She G, Zhang X, Shi W, Cai Y, Wang N, Liu P, Chen D (2008) Template-free electrochemical synthesis of single-crystal CuTe nanoribbons. Cryst Growth Des 8 1789-1791... [Pg.206]

The subhalides of tellurium are an especially important class of solid state compounds, and they have been the subject of intensive studies, so that a rather complete picture of their chemistry and their properties has been obtained in recent years. Because of their high tellurium content they contain fragments of the homonuclear tellurium chains their modified tellurium structures are of great current interest with respect to possibly significant physical properties. Consequently, the results of various investigations on the synthesis of the compounds, on phase analysis by thermal methods, on crystal growth, on the structures, on spectroscopic, thermodynamic, optical, photoelectric, electrochemical properties have been reported in the last two decades. In a comprehensive review (237) all significant results are reported and discussed in detail so that the present chapter will be restricted to some selected and chemically important features. [Pg.301]

Some work has been reported on deposition of hydroxyapatite under hydrothermal conditions, that is much above 100 °C. This includes a study by Liu, Savino and Yates (2011) who coated hydroxyapatite on titanium, stainless steel, aluminium and copper substrates by a seeded hydrothermal deposition method. The deposition strategy included an electrochemical reaction to form quickly a thin layer of HAp seed crystals. Subsequent hydrothermal crystal growth from the seed layer resulted in dense and durable HAp films. In a typical hydrothermal synthesis, a solution of Na2EDTA (0.20 M) and Ca(NOs)2 (0.20 M) was prepared in 15 ml water and a solution of (NH4)2HP04 (0.12 M) in 15 ml water was prepared in a second container. The two source solutions were mixed together after the pH of each solution was raised to 10.0 with ammonium hydroxide. The resulting combined solution was stirred at room temperature for about 20 min and then transferred to a Teflon-lined stainless steel pressure vessel of 40 ml internal volume. [Pg.162]


See other pages where Crystal growth electrochemical synthesis is mentioned: [Pg.84]    [Pg.358]    [Pg.239]    [Pg.212]    [Pg.534]    [Pg.241]    [Pg.122]    [Pg.461]    [Pg.81]    [Pg.241]    [Pg.373]    [Pg.234]    [Pg.832]    [Pg.255]    [Pg.323]    [Pg.120]    [Pg.210]    [Pg.236]    [Pg.51]    [Pg.193]    [Pg.139]    [Pg.183]    [Pg.128]    [Pg.276]    [Pg.11]    [Pg.399]    [Pg.107]    [Pg.285]    [Pg.6]    [Pg.397]    [Pg.7]    [Pg.258]    [Pg.278]    [Pg.102]    [Pg.308]   
See also in sourсe #XX -- [ Pg.212 ]




SEARCH



Crystals synthesis

Electrochemical crystal growth

Electrochemical growth

Synthesis crystal growth

© 2024 chempedia.info