Determinants of energy demand in the French service sector: A decomposition analysis

This paper analyzes the changes in the energy consumption of the service sector in France over the period 1995–2006, using the logarithmic mean Divisia index I (LMDI I) decomposition method. The analysis is carried out at various disaggregation levels to highlight the specifics of each sub-sector and end-use according to their respective determinants. The results show that in this period the economic growth of the service sector was the main factor that led to the increase in total energy consumption. Structure, productivity, substitution and intensity effects restricted this growth, but with limited effect. By analyzing each end-use, this paper enables a more precise understanding of the impact of these factors. The activity effect was the main determinant of the increase in energy consumption for all end-uses except for air conditioning, for which the equipment rate effect was the main factor. Structural changes in the service sector primarily impacted energy consumption for space heating and cooking. Improvements in productivity limited the growth of energy consumption for all end-uses except for cooking. Finally, energy efficiency improvements mainly affected space-heating energy use.     

基于Livermore模型CT图片构建人体躯干数字体模及其在肺部计数器虚拟刻度中的应用

基于Livermore 人体躯干物理模型CT图片构建数字体模,并结合蒙特卡罗程序MCNP对一套由四个宽能高纯锗探测器(BEGe)构成的肺部计数器进行了虚拟刻度.首先,利用点源(241Am,137Cs,60Co,54Mn,57Co,109Cd) 实验数据,对高纯锗晶体尺寸进行调整以获得正确的探测器几何参数,在γ射线能量13.9 keV～1332.5 keV范围内,调整后四个探测器全能峰效率实验测量的平均值与蒙特卡罗计算值的差别在±10%范围内.之后,对不同胸壁厚度(CWT=19 mm, 25 mm, 30 mm, 43 mm)躯干体模进行CT扫描获得其CT图片,利用Dosigray软件对CT图片进行分割后,连同探测器几何描述文件输入到OEDIPE软件,生成数字体模虚拟刻度用MCNP输入程序.最后,利用241Am、152Eu肺部源对数字体模虚拟刻度结果进行了实验验证,结果表明:在59.5 keV～1408 keV能量范围内,虚拟刻度结果与实验结果的差别在±10%之间;对于17.5 keV能量,差别在±30%之间.     

Nickel phosphonate MOF as efficient water splitting photocatalyst

A novel microporous two-dimensional(2D)Ni-based phosphonate metal-organic framework(MOF;denoted as IEF-13)has been successfully synthesized by a simple and green hydrothermal method and fully characterized using a combination of experimental and computational techniques.Structure resolution by single-crystal X-ray diffraction reveals that IEF-13 crystallizes in the triclinic space group Pi having bi-octahedra nickel nodes and a photo/electroactive tritopic phosphonate ligand.Remarkably,this material exhibits coordinatively unsaturated nickel(II)sites,free-P0₃H₂and-P0₃H acidic groups,a C0₂accessible microporosity,and an exceptional thermal and chemical stability.Further,its in-deep optoelectronic characterization evidences a photoresponse suitable for photocatalysis.In this sense,the photocatalytic activity for challenging H₂generation and overall water splitting in absence of any co-catalyst using UV-Vis irradiation and simulated sunlight has been evaluated,constituting the first report for a phosphonate-MOF photocatalyst.IEF-13 is able to produce up to 2,200 fimol of H₂per gram using methanol as sacrificial agent,exhibiting stability,maintaining its crystal structure and allowing its recycling.Even more,170μmol of H₂per gram were produced using IEF-13 as photocatalyst in the absence of any co-catalyst for the overall water splitting,being this reaction limited by the 0₂reduction.The present work opens new avenues for further optimization of the photocatalytic activity in this type of multifunctional materials.     

Maximum power tracking for photovoltaic power system: Development and experimental comparison of two algorithms

This work presents an experimental comparison of two algorithms developed in order to maximize the output power from a photovoltaic (PV) system for the same given set of conditions. The maximum power point tracking (MPPT) methods proposed in this study are two extended algorithms: Perturb and Observe and Incremental Conductance. The numerical modelling of the PV system shows the MPPT interest and then the extended MPPT algorithms are highlighted. In this paper, a PV system based on a boost converter as MPPT device is considered. A programmable DC electronic load is fed by two identical PV systems in which the MPPT control converter algorithms are different. This experimental platform operates under the same conditions such as changing solar radiation and cell temperature. The experimental results obtained with a dSPACE controller board show the MPPT energy efficiency of the proposed algorithms.     

Intergranular Oxidation of Nickel-Base Alloys: Potentialities of Focused Ion Beam Tomography

Oxidation of Metals - The present work focuses on the intergranular oxidation of Alloy 600 and its weld material Alloy 82 after exposure in simulated primary water at 340–360 °C...     

Fucoxanthin,a Marine-Derived Carotenoid from Brown Seaweeds and Microalgae: A Promising Bioactive Compound for Cancer Therapy

Fucoxanthin is a well-known carotenoid of the xanthophyll family, mainly produced by marine organisms such as the macroalgae of the fucus genus or microalgae such as Phaeodactylum tricornutum. Fucoxanthin has antioxidant and anti-inflammatory properties but also several anticancer effects. Fucoxanthin induces cell growth arrest, apoptosis, and/or autophagy in several cancer cell lines as well as in animal models of cancer. Fucoxanthin treatment leads to the inhibition of metastasis-related migration, invasion, epithelial–mesenchymal transition, and angiogenesis. Fucoxanthin also affects the DNA repair pathways, which could be involved in the resistance phenotype of tumor cells. Moreover, combined treatments of fucoxanthin, or its metabolite fucoxanthinol, with usual anticancer treatments can support conventional therapeutic strategies by reducing drug resistance. This review focuses on the current knowledge of fucoxanthin with its potential anticancer properties, showing that fucoxanthin could be a promising compound for cancer therapy by acting on most of the classical hallmarks of tumor cells.     

Coupling osmotic dehydration with heat treatment for green papaya impregnated with blackberry juice solution

Slices (1.5 mm thick) of green papaya were impregnated through osmotic dehydration with a blackberry juice–sucrose solution to produce an intermediate moisture product. The effect of processing temperature (T) and sucrose-added molality (m_sucrose) on mass transfer during the operation was assessed, using a response surface methodology (RSM). The RSM was used to model water loss, sugar and anthocyanin gain during the process. Increasing sucrose molality resulted in increasing water loss and sugar gain, but decreasing anthocyanin gain. Water transfer therefore limits anthocyanin impregnation, but not sucrose incorporation. Afterwards, the impact of heat treatment at high temperatures was analysed, using numerical simulation. The conditions of the combined process, designed to achieve an anthocyanin-rich final product, are low sucrose-added molalities (sucrose molality < 1 mol kg^–1) and high processing temperatures (T > 50 ºC) for osmotic dehydration, coupled with high-temperature, short-time (HTST) heat treatments for product stabilisation.     

Structural evolution at short and medium range distances during crystallization of a P2O5-Li2O-Al2O3-SiO2 glass

Li₂O-Al₂O₃-SiO₂ (LAS) glass-ceramics have important industrial applications and bulk nucleation is usually achieved by using nucleating agents. In particular, P₂O₅ is an efficient agent in glasses containing a low level of Al₂O₃ but its role in the first stages of nucleation is not well established. In this study, we combine structural investigations from local to mesoscales to describe the structural evolution during crystallization of LAS glass-ceramics. Local environment is probed using ²⁹Si and ³¹P MAS-NMR, indicating organization of P in poorly crystallized Li₃PO₄ species prior to any crystallization. To better understand the detailed nanoscale changes of the glass structure, ³¹P-³¹P DQ-DRENAR homonuclear correlation experiments have been carried out, revealing the gradual segregation of P atoms associated with the formation of disordered Li₃PO₄. Small-angle neutron scattering data also show the apparition of nanoscale heterogeneities associated with Li₃PO₄ species upon heating treatments and allow the determination of their average sizes. These new structural information enhance our understanding of the role of P in nucleation mechanisms. Nucleation is initiated by gradual change in P environment implying P segregation upon heating treatments, forming disordered Li₃PO₄ heterogeneities. The segregation of P atoms enables the precipitation of meta- and disilicate phases.