Morphology, crystallography and origin of needle fiber calcite in quaternary pedogenic calcretes of South Australia

Soil Research ◽  
1987 ◽  
Vol 25 (4) ◽  
pp. 429 ◽  
Author(s):  
SE Phillips ◽  
PG Self

In several calcrete profiles from South Australia, needle-fibre calcite is concentrated in the channels and voids of nodules, hardpans, carbonate silt and platy calcrete. The morphology, spatial arrangements and crystallography of the needle-fibre calcite were determined using scanning and transmission electron microscopy. Needle-fibre calcite is composed of single crystals of calcite containing less than 0 5 wt % Mg. Two distinct morphological classes are evident: (1) small single rods or micro-rods, 1 �m in length and 0.1 �m or less in diameter and (2) larger needle-fibres 2-120 �m in length and 0.5-6 �m in diameter which display a variety of habits including multiple rods and serrated forms. The basic unit for the second group is that of a double rod which may be modified by cementation to other rods, and by epitaxial growth or dissolution. Spatial arrangements of needle-fibre calcite are determined by their association with organic matter. The large fibres form within mycelial strands. Lysis of the strand by rod-shaped bacteria releases the needle-fibres for redistribution in the profile. The micro-rods are calcified rod-shaped bacteria.

Author(s):  
J.G. Wen ◽  
K.K. Fung

Bi-based superconducting phases have been found to be members of a structural series represented by Bi2Sr2Can−1Cun−1On+4, n=1,2,3, and are referred to as 2201, 2212, 2223 phases. All these phases are incommensurate modulated structures. The super space groups are P2/b, NBbmb 2201, 2212 phases respectively. Pb-doped ceramic samples and single crystals and Y-doped single crystals have been studied by transmission electron microscopy.Modulated structures of all Bi-based superconducting phases are in b-c plane, therefore, it is the best way to determine modulated structure and c parameter in diffraction pattern. FIG. 1,2,3 show diffraction patterns of three kinds of modulations in Pb-doped ceramic samples. Energy dispersive X-ray analysis (EDAX) confirms the presence of Pb in the three modulated structures. Parameters c are 3 0.06, 38.29, 30.24Å, ie 2212, 2223, 2212 phases for FIG. 1,2,3 respectively. Their average space groups are all Bbmb.


Author(s):  
K. Seshan ◽  
H.-R. Wenk

Asbestos fibre texture occurs in various mineral groups (e.g. chrysotile, crocidolite, tremolite, grunerite, tourmaline) and it has been established that at least chrysotile is carcinogenic. We are investigating various aspects of the asbestos structure, with transmission electron microscopy (TEM) (1) in order to develop methods for unequivocal asbestos identification using minute samples and also to determine defects responsible for the fibre structure in these minerals which often occur as large, we 11-developed single crystals.In order to do this, we have started by investigating clinoamphibole asbestos such as tremolite Ca2Mg5[Si8O22] (OH, F)2 and crocidolite Na2 (Mg, Al, Fe3+, Fe2+) (Si8O22) (OH, F )2 , from California localities. In crocidoli te - asbestos we observed a high density of very narrow microtwins parallel to the fibre axis [001] (Fig. 1). They are often only 50-100Å wide. Diffraction patterns display the typical twin arrangement of spots and although preliminary contrast experiments are not yet conclusive the twin plane appears to be (100).


2009 ◽  
Vol 64 (8) ◽  
pp. 922-928 ◽  
Author(s):  
Manuel Christian Schaloske ◽  
Hansjürgen Mattausch ◽  
Viola Duppel ◽  
Lorenz Kienle ◽  
Arndt Simon

The compounds Pr6(C2)Br10, Pr10(C2)2Br15 and Pr14(C2)3Br20 were prepared from PrBr3 and the appropriate amounts of Pr and C and characterized by X-ray structure analyses of single crystals. All three compounds crystallize in space group P1 with lattice parameters a = 7.571(2), b = 9.004(2), c = 9.062(2) Å ,α = 108.57(3), β = 97.77(3), γ = 106.28(3)◦ for Pr6(C2)Br10; a = 9.098(2), b = 10.127(2), c = 10.965(2) A° , α = 70.38(3), β = 66.31(3), γ = 70.84(3)◦ for Pr10(C2)2Br15; a = 9.054(2), b = 10.935(2), c = 13.352(3) Å , α = 86.27(3), β = 72.57(3), γ = 66.88(3)◦ for Pr14(C2)3Br20. They are members of a general series Ln4n+2(C2)nBr5n+5 and isostructural with the corresponding iodides known for Ln = La, Ce, Pr. Pr6(C2)Br10 was further characterized via transmission electron microscopy techniques


2016 ◽  
Vol 858 ◽  
pp. 225-228 ◽  
Author(s):  
Ren Wei Zhou ◽  
Xue Chao Liu ◽  
Hui Jun Guo ◽  
H.K. Kong ◽  
Er Wei Shi

Triangle-shaped defects are one of the most common surface defects on epitaxial growth of 4H-SiC epilayer on nearly on-axis SiC substrate. In this paper, we investigate the feature and structure of such defects using Nomarski optical microscopy (NOM), micro-Raman spectroscopy and high resolution transmission electron microscopy (HR-TEM). It is found that triangle-shaped defects were composed of a thick 3C-SiC polytype, as well as 4H-SiC epilayer.


1992 ◽  
Vol 263 ◽  
Author(s):  
Ting-Yen Chiang ◽  
En-Huery Liu ◽  
Der-Hwa Yiin ◽  
Tri-Rung Yew

ABSTRACTThis paper presents results of the low—temperature epitaxial growth of GaAs on Si substrates with orientation 1°—4° off (100) by molecular beam epitaxy (MBE). The epitaxial growth ·is carried out on Si wafers subjected to HF solution treatment by “spin-etch” technique before the wafer is transferred to the entry chamber of MBE system. Methods used for reducing defect density in the epitaxial layers are proposed. The characterization techniques include cross-sectional transmission electron microscopy (XTEM), plan-view transmission electron microscopy, scanning electron microscopy (S EM), and double crystal X-ray diffraction (DCXRD). Epitaxial films with a full width at half—maximum (FWHM) of about 310 arcsec measured by DCXRD are obtained without annealing.-


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