61 research outputs found

    Moving from evaluation to trial: how do SMEs start adopting cloud ERP?

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    The advent of cloud technology involving low subscription overheads cost has provided small and medium-sized enterprises (SMEs) with the opportunity to adopt new cloud-based corporate-wide systems (i.e., cloud ERP). This technology, operating through subscriptionbased services, has now provided SMEs with a complete range of IT applications that were once restricted to large organisations. As anecdotal evidences suggest, SMEs are increasingly adopting cloud-based ERP software. The selection of an ERP is a complex process involving multiple stages and stakeholders, suggesting the importance of closer examination of cloud ERP adoption in SMEs. Yet, prior studies have predominantly treated technology adoption as a single activity and largely ignored the issue of ERP adoption in SMEs. Understanding of the process nature of the adoption and the factors that are important in each stage of the adoption potentially may result in guiding SMEs to make well-informed decisions throughout the ERP selection process. Thus, our study proposes that the adoption of cloud ERP should be examined as a multi-stage process. Using the theory of planned behaviour (TPB) and Ettlie’s adoption stages, as well as employing data gathered from 162 owners of SMEs, our findings show that the factors that influence the intention to adopt cloud ERP vary significantly across adoptive stages

    Assessing geochemical and natural radioactivity impacts of Hamadat phosphatic mine through radiological indices

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    The utilization of phosphorite deposits as an industrial resource is of paramount importance, and its sustainability largely depends on ensuring safe and responsible practices. This study aims to evaluate the suitability of phosphorite deposits for industrial applications such as the production of phosphoric acid and phosphatic fertilizers. To achieve this goal, the study meticulously examines the geochemical characteristics of the deposits, investigates the distribution of natural Radioactivity within them, and assesses the potential radiological risk associated with their use. The phosphorites are massive and collected from different beds within the Duwi Formation at the Hamadat mining area. They are grain-supported and composed of phosphatic pellets, bioclasts (bones), non-phosphatic minerals, and cement. Geochemically, phosphorites contain high concentrations of P2O5 (23.59-28.36 wt.%) and CaO (40.85-44.35 wt.%), with low amounts of Al2O3 (0.23-0.51 wt.%), TiO2 (0.01-0.03 wt.%), Fe2O3 (1.14-2.28 wt.%), Na2O (0.37-1.19 wt.%), K2O (0.03-0.12 wt.%), and MnO (0.08- 0.18 wt.%), suggesting the low contribution of the detrital material during their deposition. Moreover, they belong to contain enhanced U concentration (55-128 ppm). They are also enriched with Sr, Ba, Cr, V, and Zn and depleted in Th, Zr, and Rb, which strongly supports the low detrital input during the formation of the Hamadat phosphorites. The high Radioactivity of the studied phosphorites is probably due to the widespread occurrence of phosphatic components (e.g., apatite) that accommodate U in high concentrations. Gamma spectrometry based on NaI (Tl) crystal 3×3 has been used to measure occurring radionuclides in the phosphorite samples. The results indicate that the radioactive concentrations' average values of 226Ra, 232Th, and 40K are 184.18±9.19, 125.82±6.29, and 63.82±3.19 Bq Kg-1 , respectively. Additionally, evaluations have been made of the radiological hazards. The calculated risk indicators exceeded the recommended national and world averages. The data obtained will serve as a reference for follow-up studies to evaluate the effectiveness of the Radioactivity of phosphatic materials collected from the Hamdat mine area. © 2023 Fathy et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited

    Physico-mechanical properties and shielding efficiency in relation to mineralogical and geochemical compositions of Um Had granitoid, Central Eastern Desert, Egypt

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    The current work aims to describe the physico-mechanical characteristics and shielding efficiency with reference to the mineralogical and geochemical compositions of the Neoproterozoic Um Had composite granitoid pluton in order to deduce their favorability as dimension stones. The Um Had granitoid pluton has an elliptical outline with a mean diameter of about 10 km. This pluton is a composite (ranging from white to reddish pink color), hard, massive, and medium- to coarse-grained granitoid body. It is classified as syenogranite according to their modal and bulk chemical compositions. Geochemically, the granitoid pluton is a highly calc-alkaline, peraluminous granite, formed by low degree partial melting of tonalitic source rock in a post-collisional tectonic setting. The physico-mechanical properties of the granitoid pluton under study satisfy the requirements of dimension stone in terms of their bulk density (from 2561 to 2564 kg/m3), and to some extent water absorption capacity (from 0.38% to 0.55%). However, their compressive strength values (50.4–113.4 MPa) do not achieve the minimum requirement for interior use and light duty exterior use. This study delves into the potential of some of our syenogranite samples (I, IIA, IIS, and 10) as gamma radiation shielding materials. We have assessed the mass attenuation coefficient (GMAC), effective atomic number (Zeff), exposure build-up factor (EBF), and energy absorption build-up factor (EABF) for each of these samples. The GMAC and Zeff calculations were performed using the Phy-X online software, across a photon energy range of 0.015–15 MeV. Our findings suggest an inverse relationship between photon energy and GMAC, with the highest values observed for the (I) granite sample (∼18). This study shows the promising radiation shielding capacity of our samples. The insights derived from GMAC, Zeff, EBF, and EABF can serve as a guide for the development of effective, naturally sourced radiation shielding materials. Copyright © 2023 Rashwan, Lasheen, Abdelwahab, Azer, Zakaly, Alarifi, Ene and Thabet.King Saud University, KSUThis research was supported by the Researchers Supporting Project number (RSP2023R496), King Saud University, Riyadh, Saudi Arabia

    Petrogenesis and Tectonic Implications of the Cryogenian I-Type Granodiorites from Gabgaba Terrane (NE Sudan)

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    The widely distributed granitic intrusions in the Nubian Shield can provide comprehensive data for understanding its crustal evolution. We present new bulk-rock geochemistry and isotopic (zircon U-Pb and Lu-Hf) data from the Haweit granodiorites in the Gabgaba Terrane (NE Sudan). The dated zircons presented a 206Pb/238U Concordia age of 718.5 ± 2.2 Ma, indicating that they crystallized during the Cryogenian. The granodiorites contain both biotite and amphibole as the main mafic constituents. The samples exhibit metaluminous (A/CNK = 0.84–0.94) and calc-alkaline signatures. Their mineralogical composition and remarkable low P2O5, Zr, Ce, and Nb concentrations confirm that they belong to I-type granites. They exhibit subduction-related magma geochemical characters such as enrichment in LILEs and LREEs and depletion in HFSEs and HREEs, with a low (La/Yb)N ratio (3.0–5.9) and apparent negative Nb anomaly. The positive Hf(t) values (+7.34 to +11.21) and young crustal model age (TDMC = 734–985 Ma) indicates a juvenile composition of the granodiorites. The data suggest that the Haweit granodiorites may have formed from partially melting a juvenile low-K mafic source. During subduction, the ascending asthenosphere melts might heat and partially melt the pre-existing lower crust mafic materials to generate the Haweit granodiorites in the middle segment of the Nubian Shield. © 2023 by the authors.King Saud University, KSUThis research was supported by Researchers Supporting Project number (RSP2023R496), King Saud University, Riyadh, Saudi Arabia. The author AE would like to thank “Dunarea de Jos” University of Galati, Romania, INPOLDE infrastructure, for the material and technical support.This research was supported by Researchers Supporting Project number (RSP2023R496), King Saud University, Riyadh, Saudi Arabia. The author A.E. would like to thank “Dunarea de Jos” University of Galati, Romania, INPOLDE infrastructure, for the material and technical support. The authors would like to thank the editors and the reviewers for their precious time, detailed and constructive reviews, and additional comments which significantly improved the manuscript

    The role of ceria in promoting Ni catalysts supported on phosphate‐modified zirconia for the partial oxidation of methane

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    The catalytic partial oxidation of methane (POM) is aimed at the mitigation of CH4 (a highly potent greenhouse gas) from the environment and the synthesis of syngas with a high H2/CO ratio. Herein, to enhance the POM reaction, Ni-supported phosphate-modified-zirconia were synthesized with promotor “Ce” to achieve high H2/CO ratio (2.4–3.2). The catalysts were characterized by surface area and porosity, X-ray diffraction, RAMAN, temperature-programmed experiments (TPR, CO2-TPD, and TPO), and TEM. Increasing the ceria addition over 10Ni/PO4 + ZrO2 resulted in lower crystallinity, higher dispersion of active sites, and enhanced the surface area of catalyst. The unique and prominent reducibility and basicity of NiO-species and surface oxide ions, respectively, are particularly notable at 4 wt.% ceria loading. At a reaction temperature of 600°C, the highest concentration of active sites and a unique concentration of moderate strength basic sites can be achieved with 4 wt.% ceria loading over 10Ni/PO4 + ZrO2. This leads to 44% conversion of CH4, 36% yield of H2, 35% yield of CO2, and H2/CO ratio of 3.16 for the POM reaction. The cyclic H2TPR-O2TPO-H2TPR experiment confirms the reorganization of the active site towards high temperature under oxidizing gas O2 and reducing gas H2 gas stream during the POM reaction.<br/
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