X-ray diffraction, high-resolution transmission electron microscopy and Fourier-transform infrared study of Ca-doped Al2O3

1993 ◽  
Vol 89 (1) ◽  
pp. 135 ◽  
Author(s):  
Claudio Morterra ◽  
Giuliana Magnacca ◽  
Giuseppina Cerrato ◽  
Nadia Del Favero ◽  
Francesca Filippi ◽  
...  
2015 ◽  
Vol 19 (56) ◽  
Author(s):  
Muflihatun ◽  
Siti Shofiah ◽  
Edi Suharyadi

Nanopartikel Nikel Ferit (NiFe2O4) telah disintesis dengan metode kopresipitasi dengan memvariasi konsentrasi NaOH dan suhu sintesis. Struktur kristal, ukuran partikel, dan morfologi dari sampel dianalisa menggunakan X-ray diffraction (XRD) dan transmission electron microscopy (TEM). Ukuran butir pada konsentrasi NaOH 3, 5, dan 10 M masing-masing adalah 5,7; 4,3; dan 4,2 nm, sedangkan pada suhu 60, 80, dan 150°C berturut-turut adalah 4,2; 4,9; dan 5,5 nm. Analisa fourier transform infrared (FTIR) menunjukkan dua puncak serapan pada rentang ~400-600 cm-1 yang terkait dengan site oktahedral dan tetrahedral pada struktur NiFe2O4. Sifat magnetik NiFe2O4 hasil analisa vibrating sample magnetometer (VSM) menunjukkan bahwa sampel berperilaku ferromagnetik dengan nilai koersivitasnya pada rentang 42-47 Oe. Sampel dengan variasi konsentrasi NaOH, koersivitasnya cenderung menurun dengan menurunnya ukuran partikel. Sementara sampel dengan variasi suhu, semakin kecil ukuran partikel, koersivitasnya cenderung meningkat. Pada 15 kOe, nilai magnetisasi terbesar (6,17 emu/g) diperoleh pada sampel dengan rasio fasa α-Fe2O3 paling rendah.


Author(s):  
R. Gronsky

The phenomenon of clustering in Al-Ag alloys has been extensively studied since the early work of Guinierl, wherein the pre-precipitation state was characterized as an assembly of spherical, ordered, silver-rich G.P. zones. Subsequent x-ray and TEM investigations yielded results in general agreement with this model. However, serious discrepancies were later revealed by the detailed x-ray diffraction - based computer simulations of Gragg and Cohen, i.e., the silver-rich clusters were instead octahedral in shape and fully disordered, atleast below 170°C. The object of the present investigation is to examine directly the structural characteristics of G.P. zones in Al-Ag by high resolution transmission electron microscopy.


Clay Minerals ◽  
2004 ◽  
Vol 39 (4) ◽  
pp. 391-404 ◽  
Author(s):  
J. E. F. C. Gardolinski ◽  
G. Lagaly ◽  
M. Czank

AbstractKaolinite and synthetic γ-Al(OH)3 (gibbsite or hydrargillite) were reacted with phenylphosphonic, phenylphosphinic and 2-nitrophenol-4-arsonic acids. The products were studied by powder X-ray diffraction, transmission electron microscopy/selected area electron diffraction/ energy dispersive X-ray/Fourier transform infrared and simultaneous thermogravimetric/differential thermal analysis. The acids were not intercalated but, instead, easily destroyed the structure of the minerals. Lamellar Al phenylphosphonate and aluminium phenylphosphinate and phenylarsonate with polymeric linear-chain structures were formed from kaolinite. The reaction between gibbsite and the same acids yielded almost identical products. No evidence of formation of grafted kaolinite derivatives after the reaction with phenylphosphonic acid was found.


2001 ◽  
Vol 16 (7) ◽  
pp. 1960-1966 ◽  
Author(s):  
K. Miyazawa ◽  
H. Satsuki ◽  
M. Kuwabara ◽  
M. Akaishi

The structure and hardness of C60 bulk specimens compressed under 5.5 GPa at room temperature to 600 °C are investigated by high-resolution transmission electron microscopy, x-ray diffraction, and micro-Vickers hardness tests. A strong accumulation of the [1 1 0]tr orientation of high-pressure-treated C60 specimens was developed along the compression axis, and stacking faults and nano-sized deformation twins were introduced into the C60 specimens compressed at 450–600 °C. Curved lattice planes indicating a polymerization of C60 were observed by high resolution transmission electron microscopy (HRTEM). The polymerization of the high-pressure-compressed C60 is also supported by the computer simulation of HRTEM images.


1995 ◽  
Vol 399 ◽  
Author(s):  
M. Shima ◽  
L. Salamanca-Riba ◽  
G. Springholz ◽  
G. Bauer

ABSTRACTMolecular beam epitaxy was used to grow EuTe(x)/PbTe(y) short period superlattices with x=1-4 EuTe(111) monolayers alternating with y≈3x PbTe monolayers. The superlattices were characterized by transmission electron microscopy and high resolution x-ray diffraction. Regions with double periodicity were observed coexisting with areas of nominal periodicity. The sample with x=3.5 and y=9, for example, contains regions with double periodicity of x=7 and y=17. X-ray diffraction measurements confirm the formation of the double periodicity in these samples by the appearance of weak satellites in between the satellites of the nominal periodicity. The double periodicity in the superlattice is believed to result from interdiffusion during the growth. A model for this process is presented.


Sign in / Sign up

Export Citation Format

Share Document