scholarly journals An experimental study on improvement of cohesive soil with eco-friendly guar gum

2021 ◽  
Vol 44 (2) ◽  
pp. 1-9
Author(s):  
Baki Bagriacik ◽  
Bahadir Ok ◽  
Mustafa Tahseen Mohamed Ali Kahiyah
Keyword(s):  
Guar Gum ◽  
Comprehensive Evaluation ◽  
Environmentally Friendly ◽  
Fluorescence Analysis ◽  
Cohesive Soil ◽  
Mixing Ratio ◽  
X Ray ◽  
Mixing Ratios ◽  
Compressive Strength Test ◽  
Sem Analyses

Recently, the demand for environmentally friendly products has been increasing worldwide. In this study, the improvement of cohesive soil with a biopolymer material (Guar Gum), which is a type of additive and organic, environmentally friendly, is investigated. For this purpose, various laboratory tests have been conducted on the biopolymer-added soils, including the compaction test, the Atterberg limits test, and the unconfined compressive strength test. The samples for tests have been prepared that the biopolymer has been mixed with the soil in three different proportions to determine the optimum mixing ratio. Also, in the biopolymer-added soils, some samples have been cured at varying times to determine the effect of curing periods on their strength. For comparison, the tests performed on improved soils have been also carried out on the untreated cohesive soil. For a comprehensive evaluation, scanning electron microscopy analyses (SEM analyses) was carried out on some samples. On the other hand, X-ray fluorescence analysis (XRF analysis) was performed to have an idea about the composition of the cohesive soil. Consequently, the biopolymer additive material has improved the geotechnical properties of the cohesive soil in all mixing ratios and curing times. Moreover, the optimum mixing ratio has been obtained at 1% according to the results of tests.

scholarly journals Synthesis of Tungsten-Doped Vanadium Dioxide Using a Modified Polyol Method Involving 1-Dodecanol

Materials ◽  
2020 ◽  
Vol 13 (23) ◽  
pp. 5384
Author(s):  
Yonghyun Lee ◽  
Sang Won Jung ◽  
Sang Hwi Park ◽  
Jung Whan Yoo ◽  
Juhyun Park
Keyword(s):  
Linear Growth ◽  
Mixing Ratio ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Metal Insulator ◽  
X Ray ◽  
Mixing Ratios ◽  
The Difference ◽  
Modified Polyol Method ◽  
Optimal Mixing

The doping of tungsten into VO2 (M) via a polyol process that is based on oligomerization of ammonium metavanadate and ethylene glycol (EG) to synthesize a vanadyl ethylene glycolate (VEG) followed by postcalcination was carried out by simply adding 1-dodecanol and the tungsten source tungstenoxytetrachloride (WOCl4). Tungsten-doped VEGs (W-VEGs) and their calcinated compounds (WxVO2) were prepared with varying mixing ratios of EG to 1-dodecanol and WOCl4 concentrations. Characterizations of W-VEGs by powder X-ray diffraction, differential scanning calorimetry, scanning electron microscopy, and infrared and transmittance spectroscopy showed that tungsten elements were successfully doped into WxVO2, thereby decreasing the metal-insulator transition temperature from 68 down to 51 °C. Our results suggested that WOCl4 variously combined with 1-dodecanol might interrupt the linear growth of W-VEGs, but that such an interruption might be alleviated at the optimal 1:1 mixing ratio of EG to 1-dodecanol, resulting in the successful W doping. The difference in the solar modulations of a W0.0207VO2 dispersion measured at 20 and 70 °C was increased to 21.8% while that of a pure VO2 dispersion was 2.5%. It was suggested that WOCl4 coupled with both EG and 1-dodecanol at an optimal mixing ratio could improve the formation of W-VEG and WxVO2 and that the bulky dodecyl chains might act as defects to decrease crystallinity.

An x-ray microprobe based upon a close-coupled focal-spot / glass capillary arrangement

1992 ◽  
Vol 50 (2) ◽  
pp. 1758-1759
Author(s):  
D. A. Carpenter ◽  
M. A. Taylor
Keyword(s):  
Imaging Techniques ◽  
Fluorescence Analysis ◽  
High Sensitivity ◽  
Specimen Preparation ◽  
X Rays ◽  
Glass Capillary ◽  
Close Coupling ◽  
X Ray ◽  
Point To Point ◽  
Beam Damage

The development of intense sources of x rays has led to renewed interest in the use of microbeams of x rays in x-ray fluorescence analysis. Sparks pointed out that the use of x rays as a probe offered the advantages of high sensitivity, low detection limits, low beam damage, and large penetration depths with minimal specimen preparation or perturbation. In addition, the option of air operation provided special advantages for examination of hydrated systems or for nondestructive microanalysis of large specimens.The disadvantages of synchrotron sources prompted the development of laboratory-based instrumentation with various schemes to maximize the beam flux while maintaining small point-to-point resolution. Nichols and Ryon developed a microprobe using a rotating anode source and a modified microdiffractometer. Cross and Wherry showed that by close-coupling the x-ray source, specimen, and detector, good intensities could be obtained for beam sizes between 30 and 100μm. More importantly, both groups combined specimen scanning with modern imaging techniques for rapid element mapping.

XRMF applications of a monolithic, polycapillary, focusing x-ray optic

1996 ◽  
Vol 54 ◽  
pp. 240-241
Author(s):  
D. A. Carpenter ◽  
Ning Gao ◽  
G. J. Havrilla
Keyword(s):  
Trace Elements ◽  
Point Source ◽  
Focal Spot ◽  
Fluorescence Analysis ◽  
X Rays ◽  
Focal Distance ◽  
Spot Diameter ◽  
X Ray ◽  
Focal Spot Diameter

A monolithic, polycapillary, x-ray optic was adapted to a laboratory-based x-ray microprobe to evaluate the potential of the optic for x-ray micro fluorescence analysis. The polycapillary was capable of collecting x-rays over a 6 degree angle from a point source and focusing them to a spot approximately 40 µm diameter. The high intensities expected from this capillary should be useful for determining and mapping minor to trace elements in materials. Fig. 1 shows a sketch of the capillary with important dimensions.The microprobe had previously been used with straight and with tapered monocapillaries. Alignment of the monocapillaries with the focal spot was accomplished by electromagnetically scanning the focal spot over the beveled anode. With the polycapillary it was also necessary to manually adjust the distance between the focal spot and the polycapillary.The focal distance and focal spot diameter of the polycapillary were determined from a series of edge scans.

Sorption of Se (IV) from aqueous solutions with subsequent determination by X-ray fluorescence analysis

2020 ◽  
Vol 86 (10) ◽  
pp. 5-9
Author(s):  
D. G. Filatova ◽  
A. A. Arkhipenko ◽  
M. A. Statkus ◽  
V. V. Es’kina ◽  
V. B. Baranovskaya ◽  
...  
Keyword(s):  
Inductively Coupled Plasma ◽  
Fluorescence Analysis ◽  
Standard Samples ◽  
Phase Contact Time ◽  
Sorbent Phase ◽  
X Ray ◽  
Fundamental Parameters ◽  
Inductively Coupled ◽  
Subsequent Determination

An approach to sorptive separation of Se (IV) from solutions on a novel S,N-containing sorbent with subsequent determination of the analyte in the sorbent phase by micro-x-ray fluorescence method is presented. The sorbent copolymethylenesulfide-N-alkyl-methylenamine (CMA) was synthesized using «snake in the cage» procedure and proven to be stable in acid solutions. Conditions for quantitative extraction of Se (IV) were determined: sorption in 5 M HCl or 0.05 M HNO3 solutions when heated to 60°C, phase contact time being 1 h. The residual selenium content in the solution was determined by inductively coupled plasma mass spectrometry (ICP-MS) using 82Se isotope. The absence of selenium losses is proved and the mechanism of sorption interaction under specified conditions is proposed. The method of micro-x-ray fluorescence analysis (micro-RFA) with mapping revealed a uniform distribution of selenium on the sorbent surface. The possibility of determining selenium in the sorbent phase by micro-RFA is shown. When comparing the obtained results with the results of calculations by the method of fundamental parameters, it is shown the necessity of using standard samples of sorbates to obtain correct results of RFA determination of selenium in the sorbent phase.

scholarly journals An X-ray CT study of miniature clay sample preparation techniques

2019 ◽  
Vol 92 ◽  
pp. 01004
Author(s):  
Christopher Ibeh ◽  
Matteo Pedrotti ◽  
Alessandro Tarantino ◽  
Rebecca Lunn
Keyword(s):  
Sample Preparation ◽  
Shear Plane ◽  
Cohesive Soil ◽  
Image Resolution ◽  
Particle Orientation ◽  
X Ray ◽  
High Resolution Images ◽  
X Ray Computed ◽  
Sample Disturbance ◽  
Relationship Of

The quality and reliability of cohesive soil laboratory test data can be significantlyaffected by sample disturbance during sampling or sample preparation. Sample disturbance may affect key design and modelling parameters such as stiffness, preconsolidation stress, compressibility and undrained shear strength, and ultimately determine particle mobilization and shear plane development. The use of X-ray computed tomography (X-CT) in the study of soil is restricted by the inverse relationship of specimen size and obtainable image resolution. This has led to the testing of miniature specimen sizes which are far less than conventional laboratory sample size in a bid to obtain high resolution images and detailed particle-scale soil properties; however, these miniature soil specimens are more prone to sample disturbance. In this work 2% muscovite was mixed with speswhite kaolin clay as a strain marker for use in X-CT. The clay soil sample was prepared from slurry and either consolidated using an oedometer or a gypsum mould. Specimens obtained from a 7 mm tube sampler were compared to lathe trimmed specimens with a diameter (Ø) of 7 mm. Results from X-CT imaging were used to study the influence of sampler type on specimen disturbance, by analysing the muscovite particle orientation of the obtained 3D images. The results show that; for samples subjected to large consolidation stress (>200kpa) lathe trimmed specimens may be subject to lesser disturbance compared to tube sampled specimens.

Energy-Dispersive X-ray Fluorescence Analysis as a Rapid Method for Identifying Tephras

1983 ◽  
Vol 19 (2) ◽  
pp. 201-211 ◽  
Author(s):  
A. B. Cormie ◽  
D. E. Nelson
Keyword(s):  
Reliable Method ◽  
Fluorescence Analysis ◽  
Energy Dispersive ◽  
Bulk Glass ◽  
X Ray ◽  
Additional Tool ◽  
White River ◽  
Routine Identification ◽  
Weathering Effects ◽  
Mount St Helens

AbstractThe use of energy-dispersive X-ray fluorescence analysis (XES) for the routine identification of three tephras (Mazama, Bridge River, Mount St. Helens Yn) commonly found in archeological sites in British Columbia has been investigated. Researchers have often assumed that chemical analysis of bulk samples of glass separates would be hampered by contamination and weathering effects. Our results indicate that XES of bulk glass separates provides a very reliable method for rapidly identifying the three tephras in question, even with a very simple sample preparation. This should enable persons not skilled in geology or in tephrochronology to collect and to identify samples of these tephras. Finally, as a part of the study, similar measurements were made on the separated glass portions of these three tephras and of three others (Glacier Peak B and G, White River) from northwest North America. The results suggest that this method may provide tephrochronologists with a useful additional tool for studying tephras in other regions.

scholarly journals Environmentally Friendly Nafion-Catalyzed Synthesis of Substituted 2-Ethyl-3-Methylquinolines from Aniline and Propionaldehyde under Microwave Irradiation

Catalysts ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 877
Author(s):  
Chieh-Kai Chan ◽  
Chien-Yu Lai ◽  
Cheng-Chung Wang
Keyword(s):  
Reaction Mechanism ◽  
Microwave Irradiation ◽  
Single Crystal ◽  
Diffraction Analysis ◽  
Environmentally Friendly ◽  
Single Crystal Diffraction ◽  
X Ray ◽  
Related Data ◽  
Heating Source ◽  
Chemical Structures

Herein, we report a facile synthetic methodology for the preparation of 2,3-dialkylquinolines from anilines and propionaldehydes. This cyclization involved environmentally friendly Nafion® NR50 as an acidic catalyst with microwave irradiation as the heating source. A series of substituted 2-ethyl-3-methylquinolines were prepared from various anilines and propionaldehyde derivatives through this protocol with good to excellent yields. Some new chemical structures were confirmed by X-ray single-crystal diffraction analysis and the related data were provided. The plausible reaction mechanism studies are also discussed.

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