Ternary
compounds (nano- and microparticles) of AgAsSe2 and Ag3AsSe3
have been synthesized from approximately equimolar mixtures of silver
nitrate, sodium metaarsenite and sodium selenosulfate with prepared by
refluxing selen powder with concentrated sodium sulfite solution under
hydrothermal conditions in ethylene glycol medium. The solutions were put into
a 100 mL Teflon-lined stainless steel autoclave Speedwave
four BERGHOF and sealed and then heated at the temperature of 443 K during 8
hours (pH = 5-4). The products were filtered via the glass filter and washed by
deionized water and absolute ethanol for several times, then dried at 353 K in
vacuum oven for at least 1 hour for analysis. The thermogravimetric (TG) and
electron microprobe analysis have been carried out. The results showed that the
composition of silver selenoarsenates
compounds corresponding to the formule AgAsSe2 and Ag3AsSe3.
The results of SEM image and shows the typical morphologies of
synthesized products in which tubular and stick shaped like nano-particles can
be observed and their size can be estimated from 140 nm to 310 nm. The compound
of AgAsSe2 and Ag3AsSe3 was constructed using
X-ray phase and differential-thermal analyses. It is ascertained by X-ray
powder diffraction (XRD) that the parameters of AgAsSe2 crystallized in the tetragonal space group R3-m
with a = 12.54 Å, c = 11.14 Å, α = 900, β = 900,γ = 900,
Z = 5, Ag3AsSe3 (this compound is an allotrope of β-Ag3AsSe3) crystallizes
in the orthorhombic space group Pnma, a = 8.11 Å, b = 11.34 Å, c = 20.73 Å, α = 900, β = 900,γ
= 900, Z = 8. The results of differential thermal analysis (DTA) AgAsSe2
compound is melting congruently at Tg =
683 K,
Ag3AsSe3 with incongruent type of melting at Tg = 663 K was established.
hydrothermal synthesis organic solvent arsenic (III) selenide XRD scanning electron microscopy
Primary Language | English |
---|---|
Subjects | Chemical Engineering |
Journal Section | Articles |
Authors | |
Publication Date | July 13, 2017 |
Submission Date | May 24, 2017 |
Acceptance Date | February 28, 2018 |
Published in Issue | Year 2017 Volume: 4 Issue: 1 |