Cadmium sulfide nanoparticles were grown using wet chemical method by dissolving the reactants of cadmium acetate and sodium sulfide in the presence of thioglycerol (TG) as capping agent in ethanol solvent. Different nanoparticle sizes and size distribution were obtained through varying the molarities of thioglycerol. At higher TG concentration, synthesis provides a nearly monodisperse nanoparticles. Also this method reveals high stability of nanoparticles in ethanol solvent. Samples properties were investigated using UV-VIS absorption, photoluminescence spectroscopy and X-ray diffraction (XRD) methods.

Because of the important role of rock mass Structural properties on its mechanical behavior, determining the qualitative and quantitative properties of has been a subject of intense research. In this regard, numerous techniques such as scanline surveying, cell mapping, and geologic structure mapping have been proposed. However, applying such field surveying techniques for rock mass properties involves spending substantial costs and times and high risks. Besides, due to the errors induced by operations, measurements, systematic errors, etc., the results of these techniques are not accurate and precise enough. Short-range digital photogrammetry is an state-of-art technique applied for surveying rock mass characteristics. Through this novel approach, rock mass surface is imaged, the obtained images are analyzed, and rock mass characteristics are determined, and finally, the technique is validated by comparing the obtained results with field surveys. In the present work, two digital photogrammetry based methods including digital image processing and laser-based imaging are implemented in rock mass Characterization. The results show that short-range digital photogrammetry can be effectively employed in rock mass structure Characterization. Moreover, this approach, unlike the existing traditional ones, involves low costs, high speed, and sufficiently accurate and precise results.

Structural changes of mechanically-activated ilmenite during milling by a planetary mill are monitored and determined as a function of the milling time. The maximum specific BET surface area of 10. 76 m2/g is obtained after 150 min of milling. The results obtained indicate that agglomeration of the particles occurs after 45 min of milling. The maximum X-ray amorphization degree of ca. 95% has been calculated after 150 min of milling. Estimation of the stored energy reveals that the X-ray amorphization degree has a dominant contribution to the excess enthalpy of the activated materials. The surface-weighted crystallite size in the ground ilmenite reaches 4. 45 nm, which corresponds to the volume-weighted crystallite size of 8 nm and 11. 18 nm obtained by the Williamson-Hall and Rietveld methods, respectively. After 150 min of mechanical activation, the root mean square strain, , increases to 0. 78%, which corresponds to the strains of 1. 43% and 1. 04% obtained from the Williamson-Hall and Rietveld methods, respectively. Reduction in the crystallite size leads to the contraction of the ilmenite unit cell after 150 min. The reaction rate constant of the ilmenite dissolution increases by over 58 times after 150 min of milling. Activation energy of the dissolution reaction decreases from 57. 45 kJ/mol to 41. 09 kJ/mol after 150 min of milling.

Competition law is a newcomer to the legal system recently. A sound understanding of competition policy can provide us with sufficient bases to apply a fundamental and normative view of the issues of competition law. The difference in supervision and regulation determines how the market functions and in order to understand this difference one must understand competition policy. Competition policy may be based on governmental support for national production and industry or on a non-interventional and regulatory posture. Moreover, supervision, based on the principle of non-intervention in the market mechanism, is rooted in liberal ideas; however, regulation, whether as a rule or an exception, is based on the assertion that the market has been ineffective in attaining its goals. Therefore, the government will resort to interventions to regulate inefficiencies.  This paper aims to analyze Supervisory Authority in Implementing Competitive Policy by employing the description method. In this article the author tries to first delineate competition policy, its related requirements and imposed deviations to the market. Then, by defining the supervisory entity and clarifying its distinction from the regulatory institutions, the author considers the characteristics of an appropriate supervisory entity conducting a comparative study of this issue in Iran and the U.S.A. This form of Competition policy because of its applicable experiences which have been well described by recent scholarship is considered suitable for the native system.

In this research, zinc oxide quantum dots and graphene nanocomposites were synthesized via two different methods; In the first (direct) method, ZnO-graphene Nanocomposites were made mixing the synthesized zinc oxide and graphene. In the second (indirect) method, zinc nitrate, graphene, and sodium hydroxide were used to made ZnO-graphene Nanocomposites. XRD, FTIR and Raman spectroscopy analyses were used for phase and Structural evaluations. The morphology of the nanocomposites w::as char::acterized by SEM. The specific surface area and porosity of the samples were characterized by BET analysis. The optical properties of the samples were investigated by photoluminescence and ultraviolet-visible spectroscopy analyses. Results showed that using graphene, increased the photoluminescence property and shifted the photoluminescence spectrum of the composites towards the visible light spectrum. The photoluminescence of the synthesized graphene-zinc oxide composite, in the visible light region, was closer to white light than that of pure zinc oxide. According to the results of BET test, the nanocomposite synthesized by direct method had a higher surface area (25.7 m2.g-1) and a higher porosity (0.32 cm3.g-1) than the nanocomposite synthesized by the indirect method with a specific surface area of (16.5 m2.g-1) and a porosity of 0.23 cm3.g-1).