MINERALOGY OF SURFACE SOIL SAMPLES OF SOME QUEBEC SOILS WITH REFERENCE TO K STATUS

1984 ◽  
Vol 64 (1) ◽  
pp. 107-113 ◽  
Author(s):  
T. AL-KANANI ◽  
A. F. MacKENZIE ◽  
G. J. ROSS

Surface samples of five Quebec soils (St. Bernard, Ormstown, Howick, Dalhousie and Bearbrook) were selected to represent typical agricultural soils with a range of parent material. Soil minerals were fractionated by size into five separates and examined using X-ray diffraction (XRD) techniques and chemical analyses. In nearly all cases the non-clay separates (250–2.0 μm) contained feldspars, amphiboles and quartz as dominant minerals with only small amounts of layer silicates. Feldspars, amphiboles and quartz were also relatively abundant in the clay separates. The layer silicates in the clay separates consisted mainly of mica, chlorite and vermiculite. The soils had similar mineral suites, considered indicative of a low degree of weathering. Considering the mineral composition and the low degree of weathering, it is proposed that primary K-bearing minerals, including K-feldspars, are important sources of K in these soils. Key words: K release, particle size, soil mineralogy

Clay Minerals ◽  
2001 ◽  
Vol 36 (3) ◽  
pp. 277-294 ◽  
Author(s):  
B. Velde

AbstractA survey of the clay fraction at the surface of 86 loam and silt loam agricultural soils from the Central United States was undertaken to observe the possible influences of climate and parent material (dominantly phyllosilicates in this study) on the clay mineralogy of the upper portions of the soils, for the most part in Mollisol–Alfisol order soils.Decomposed X-ray diffraction spectra show that the most abundant clay minerals are two disordered illite-smectite (I-S) minerals, one with ∼50% smectite layers and another, less abundant, disordered I-S phase with 20% smectite. These minerals usually co-exist in the same samples. The charge site in both of these I-S minerals is both beidellitic and montmorillonitic in the expanding layers. A relatively large proportion of these smectite layers (up to 20%) are of high charge.There seems to be a convergence in mineralogy towards mixed-layer phases formed under a range of mid-Continent climates from a range of phyllosilicate parent materials.


2012 ◽  
Vol 600 ◽  
pp. 174-177 ◽  
Author(s):  
Jian Fei Xia ◽  
Zong Hua Wang ◽  
Yan Zhi Xia ◽  
Fei Fei Zhang ◽  
Fu Qiang Zhu ◽  
...  

Zirconia-graphene composite (ZrO2-G) has been successfully synthesized via decomposition of ZrOCl2•6H2O in a water-isopropanol system with dispersed graphene oxide (GO) utilizing Na2S as a precursor could enable the occurrence of the deposition of Zr4+ and the deoxygenation of GO at the same time. Transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR) and X-ray diffraction (XRD) techniques were used to characterize the samples. It was found that graphene were fully coated with ZrO2, and the ZrO2 existing in tetragonal phase, which resulted in the formation of two-dimensional composite.


2011 ◽  
Vol 465 ◽  
pp. 259-262 ◽  
Author(s):  
M. Rogante ◽  
Pavol Mikula ◽  
Miroslav Vrána

The residual stress (RS) status induced in the substrate of coated materials by the coating process plays frequently a major role in lending the component’s characteristics. RS assessment can give, thus, a substantial contribution in justifying different cases of failure or else bad performance of coated components due to e.g. the coating delamination or to other occurrences which are not simply interpretable via the conventional mechanical tests or microstructure analyses. The adoption of both neutron diffraction (ND) and X-ray diffraction (XRD) techniques has revealed its usefulness in assessing the RS values in proximity of the coating interface area, respectively, without any layer removal or hole drilling at the extreme surface. In this paper, some real cases of RS determination in coated materials by using these techniques and exploiting their complementarity are described. ND, in particular, is very suitable for crucial applications, where a much different stress situation than that assessed by XRD could be present at some depth below the surface. The results achieved can yield trends adoptable in monitoring of the coating features.


Molecules ◽  
2019 ◽  
Vol 24 (24) ◽  
pp. 4431 ◽  
Author(s):  
Lingshu Meng ◽  
Lun Zhao ◽  
Guanlin Guo ◽  
Xin Liu ◽  
Zhijun Liang ◽  
...  

In this study, three new 3D coordination polymers (CPs), {[Cd3(L)(H2O)6]·H2O}n (1), {[Cu1.5(L)0.5(bimb)1.5]·5H2O·DMF}n (2), and {[Mn1.5(H3L)(bibp)0.5(H2O)2]·3H2O}n (3) (bimb= 1,3-bis(imidazol-1-yl)benzene, bibp= 1,4-bis((4-imidazol-1-yl)benzyl)piperazine), were prepared under solvothermal or hydrothermal conditions based on a hexadentate ligand (1,3,5-triazine-2,4,6-triamine hexa-acetic acid (H6L)). Structural elucidations were carried out by IR spectra along with single-crystal X-ray diffraction analysis, while thermogravimetric analysis (TGA) (dynamic and isothermal) and XRD techniques were used for property evaluations of the polymers. Furthermore, the fluorescence properties and detection of the Fe3+ ions in 1 were tested at room temperature, and the electrochemical behavior of 2 is also stated in this article.


2019 ◽  
Vol 969 ◽  
pp. 93-97
Author(s):  
S. Manivannan ◽  
B. Narenthiran ◽  
A. Sivanantham ◽  
S.P. Kumaresh Babu

The experimatal alloys were aged at different temperatures of 180°C, 200°C, 220°C, and 240º C with calcium addition levels of (X=0.5, 1, 1.5, 2%) on Mg-6Al-1Zn-XCa alloy were investigated in 3.5% NaCl solution. All the experimatal alloys were immersed in 3.5% NaCl solutions and the resulted surface were analyzed to study the corrosion behaviour and its surface topography by optical microscopy (OM), scanning electron microscopy (SEM), energy dispersed spectroscopy (EDS) and X-ray diffraction (XRD) techniques. The result shows that corrosion attack occurred predominantly on ß phase and α phase exhibit relatively minor corrosion. In addition to that the increased aging temperature coarsens the intermetallic as well as α- Mg grains, which shows adverse effect to corrosion resistances and the best result were obtained at composition of 0.5wt.% Ca aged at 200°C.


2016 ◽  
Vol 6 (4) ◽  
pp. 544-552 ◽  
Author(s):  
H. Godini ◽  
F. Hashemi ◽  
L. Mansuri ◽  
M. Sardar ◽  
Ghasem Hassani ◽  
...  

The present paper aims to investigate water purification of phenol by walnut green hull adsorbent. The surface characteristics of the adsorbent were studied using Fourier transform infra-red (FTIR), scanning electron microscope, and X-ray diffraction (XRD) techniques. The presence of functional groups such as hydroxyl and carbonyl onto walnut green hull surface was proved by FTIR analysis. Also quartz, cellulose and hematite were detected in the XRD analysis of samples by an X-ray diffractometer. The maximum sorption was achieved at pH 4.0. Data were evaluated for compliance with the Langmuir, Freundlich, Temkin and Dubinin–Radushkevich isotherm models. The results indicate that the data for adsorption of phenol onto walnut green hull fitted well with the Langmuir isotherm. The maximum adsorption capacity of the adsorbent was achieved by Langmuir isotherm 17.8 mg g–1. Also, the adsorption kinetics of phenol on the adsorbent were studied. The rates of sorption were found to conform to pseudo-second-order kinetics with good correlation.


e-Polymers ◽  
2009 ◽  
Vol 9 (1) ◽  
Author(s):  
Guido Scavia ◽  
William Porzio ◽  
Silvia Destri ◽  
Alberto Giacometti Schieroni ◽  
Fabio Bertini

AbstractThe morphology and structure of the overlying poly(3-hexylthiophene) (P3HT) layer onto differently silanized silicon oxide has been studied by Atomic Force Microscopy (AFM) and X-Ray Diffraction (XRD) techniques. By increasing the silanizer alkyl chain length, the layer morphology evolves from a filament like to globular needle like as a consequence of the different SAM organization, while the P3HT conformation remains edge-on. For each case the effect of the annealing temperature has been studied. For all the cases a particular attention has been paid to the first thin layers close to the interface P3HT/SiOx. The effect of a polar substituent and presence of aromatic ring has been also studied.


2013 ◽  
Vol 753-755 ◽  
pp. 388-391
Author(s):  
Ying Na Zhao ◽  
Xiong Feng Zeng ◽  
Gui Qin Hou ◽  
Wen Li Zhang

Nanometer Si powders were used as interlayer materials, which were expected to be microwave heated rapidly and reacted with the surface of Al2O3ceramics to form the low eutectoid compound. The phenomena of element migration of joint samples were investigated by energy dispersive spectroscopy (EDS) and the interface phase transition was analyzed by X-ray diffraction (XRD). The results indicated that the low eutectoid compound of the joint interface wetted and penetrated to the ceramic surface. The variation of micro-hardness at the interface across the parent material was measured by micro-hardness instrument and the interfacial microstructure and the fracture surface were investigated by scanning electron microscopy (SEM).


2012 ◽  
Vol 48 (2) ◽  
pp. 259-264 ◽  
Author(s):  
E. Güler ◽  
M. Güler

Deformation induced martensite properties were examined according to existing martensite morphology, crystallography and formation temperatures for different prior austenite homogenization conditions in Fe-30%Ni-5%Cu alloy. Scanning electron microscope (SEM), differential scanning calorimetry (DSC) and X-ray diffraction (XRD) techniques were employed to investigation. Scanning electron microscope observations showed elongated deformation induced martensite morphology in the austenite phase of alloy. As well, after deformation martensite start temperatures (Ms) were determined as -101?C and -105?C from DSC measurements for different homogenization conditions. In addition, X-ray diffraction analysis revealed the face centred cubic (fcc) of austenite phases and body centred cubic (bcc) deformation induced martensite phases for all studied samples.


2013 ◽  
Vol 91 (3) ◽  
pp. 196-205 ◽  
Author(s):  
A. Shanavas ◽  
T. Narasimhaswamy ◽  
B.V.N. Phani Kumar ◽  
A. Sultan Nasar

Novel star mesogens based on trimesic acid and symmetrical side arm cores with terminal alkoxy groups were synthesized via a divergent approach. The central core and side arms were connected through alkyl spacers. All the synthesized mesogens and their intermediates were characterized thoroughly using Fourier transform infrared (FT-IR), 1H nuclear magnetic resonance (NMR), 13C NMR, and mass spectrometers. One representative mesogen was subjected to the two-dimensional (2D) NMR experiments to ascertain the structure of the mesogens. The mesophase characterization was carried out using hot-stage optical polarizing microscopy (HOPM), differential scanning calorimetry (DSC), and X-ray diffraction (XRD) techniques. Many of the molecules with an ethyloxy spacer were found to be nonmesogenic, whereas all the molecules with a butyloxy spacer showed liquid crystalline phases. The increase of terminal chain length decreased the transition temperatures. The nematic phase was observed for the mesogens with short terminal chain length, whereas smectic polymorphism was observed on increasing the terminal chain length. The results of a variable temperature powder X-ray diffraction of the representative sample support the smectic layer ordering.


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