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Summary Past climatic fluctuations have played a major role in shaping the current plant biodiversity. Although harbouring an exceptional biota, oceanic islands have received little attention in studies on species demographic history and past vegetation patterns. We investigated the impact of past climatic changes on the effective population size of a tree (Coffea mauritiana) that is endemic to Reunion Island, located in the south‐western Indian Ocean (SWIO). Demographic changes were inferred using summary statistics calculated from genomic data. Using ecological niche modelling and the current distribution of genetic diversity, the paleodistribution of the species was also assessed. A reduction in the effective population size of C. mauritiana during the last glaciation maximum was inferred. The distribution of the species was reduced on the western side of the island, due to low rainfall. It appeared that a major reduction in rainfall and a slight temperature decrease prevailed in the SWIO. Our findings indicated that analyses on the current patterns of intraspecific genetic variations can efficiently contribute to past climatic changes characterisation in remote islands. Identifying area with higher resilience in oceanic islands could provide guidance in forest management and conservation faced to the global climate change.

Abstract The hybrid pneumatic power system (HPPS) proposed in this research replaces the battery’s electric-chemical energy with flow work and optimizes the management and utilization of the energy. This power system is able to keep the internal-combustion engine working at its optimal condition and turn its waste energy into effective mechanical energy and so enhance the thermal efficiency of the whole system. Using computer simulation software ITI-SIM, this study simulates the overall dynamic characteristics of the system in accordance with the regulated running-vehicle test-mode ECE47, and, with experimental verification and analysis, proves that this system can meet the requirements of the standard running-car mode. As for recycling the waste energy, the experimental results show that this design could offset the shortcomings of the low-density of pneumatic power and so effectively enhance the efficiency of the whole system.

The fast decay in PEM fuel cells of a highly active, high performance, but unstable Fe/N/C catalyst like our NC_Ar + NH3 follows a chemical, not an electrochemical, demetallation mechanism for its ORR active FeN4 sites in the catalyst micropores.

Abstract This paper gives an experimental investigation of the effect of climatic conditions on the performance and degradation of crystalline silicon photovoltaic modules under Saharan environment in Adrar region in the south of Algeria. The first part of this study is focused on the analysis and assessment of UDTS 50 PV modules degradation after a long term outdoor exposure to these conditions (more than 12 years). The visual inspection of 62 PV modules has allowed to observe and determine the degradation modes such as, EVA discoloration, delamination, busbar corrosion, cracking of solar cell, glass breakage, AR coating and solder bond. The degradation evaluation of three modules with different defects was also performed, using (I-V/P-V) characteristics and the degradation rates of the parameters (Pmax, Imp, Vmp, Isc, Voc, FF) at Standard test conditions (STC) in order to compare with the nominal data delivered by the manufacturer of photovoltaic panels. Finally, the combination of the partial shading effect and the presence of EVA browning defect was examined to assess the changes in I-V and P-V curves caused by the drop in electrical parameters.

AbstractCellulose and lignin nanoparticles are high‐value‐added products obtained from lignocellulosic biomasses through several steps of cellulose purification and lignin extraction. These steps drastically reduce the potential feedstock revenue when carried out as stand‐alone methodologies. To increase biomass yields, we describe here a strategy to design a biorefinery focused on producing cellulose and lignin nanoparticles as main products, but also aim to recover and benefit from other biomass components using only water‐based processes. Sequential pressurized liquid extractions and diluted acid and alkaline treatments were carried out to fractionate elephant grass biomass, yielding (for every 100 g of biomass): 30 g of cellulose pulp (converted to 9 g of cellulose nanocrystals and 9 g of cellulose nanofibers); 10 g of lignin (used to produce 8.5 g of stable colloidal lignin nanoparticles by probe‐sonication in water); 7.5 g of extractives (e.g. sterols and phenolics) and 23 g of xylose (converted to 4.1 g of furfural). Alternatively, to allow for the flexible use of the cellulose fraction in the proposed biorefinery, 22 g of glucose could be produced by enzymatic hydrolysis. The results demonstrate that water‐based processes are suitable for a holistic use of biomass, providing a comprehensive set of high‐value‐added co‐products that are renewable and cost‐effective chemical, cosmetic, food, polymer and pharmaceutical solutions.

Abstract This work presents a numerical study on the performance of a stand-alone adsorption cooling system based on the silica gel/water couple driven by hybrid photovoltaic/thermal (PVT) collectors. This system is intended for the conservation of perishable agricultural products which require air-conditioned premises to preserve them. The weather conditions are those of North Africa (Algiers). Considering the above, this paper aims at analyzing the PVT-Adsorption system with energy storage to guarantee a stabilized production and increase the solar coverage. trnsys was used to simulate the system taking into account hourly series of irradiation and ambient temperature covering one year. The performance study reveals that the DualSun PVT hybrid collectors used provide optimal annual production and that the adsorption cooling system offers more reliable production during summer. The temperature difference between the inside and outside of the cooled enclosure balances supply and demand. The loss analysis of the storage device indicates that losses depend, on the one hand, on the interior/exterior temperature difference of the storage tank with more significant values during the summer season. On the other hand, the losses also depend on the volume of the storage tank which was optimized in order to limit the heat exchange with the surroundings.

Biodiesel is a fuel generally consisting of a mixture of fatty acid methyl esters (FAMEs) which is used in alternative or in combination with petroleum diesel for its environmental benefits. Biodiesel is conveniently manufactured from vegetable oils by transesterification of triglycerides with methanol. However, the process brings about the concurrent formation of glycerol, which may become an oversupplied chemical if biodiesel production keeps growing. A novel biodiesel-like material (abbreviated as DMC-BioD) was developed by reacting soybean oil with dimethyl carbonate (DMC), which avoided the co-production of glycerol. The main difference between DMC-BioD and biodiesel produced from vegetable oil and methanol (MeOH-biodiesel) was the presence of fatty acid glycerol carbonate monoesters (FAGCs) in addition to FAMEs. In the following study, details regarding synthesis and composition of DMC-BioD are provided along with physical properties relevant for its use as a fuel. In addition, the production of potential pyrogenic contaminants was investigated by analytical pyrolysis and compared with those from MeOH-biodiesel, and the model compounds tristearin, triolein, trilinolein and oleic acid glycerol carbonate ester (OAGC). The presence of FAGCs influenced both fuel and flow properties, while the distribution of main pyrogenic compounds, including polycyclic aromatic hydrocarbons (PAHs), was little affected. Benefits and drawbacks of DMC as a candidate transmethylating reagent for producing biofuel from renewable resources and alternative co-products (glycerol carbonate and glycerol dicarbonate) are discussed.

The phosphate (P) fertilizer industry generates a highly hazardous and acidic wastewater. The present study reports the evaluation of an integrated precipitation and Enhanced Biological Phosphorus Removal (EBPR) process for the treatment of fertilizer plant wastewater and effluent detoxification, assessed by microtoxicity and seed germination tests. Effluent samples were collected from a local P fertilizer industry and were characterized by their high fluoride and P content. First, the samples were pre‐treated by precipitation of P and fluoride ions using hydrated lime. The resulting low‐fluoride and phosphorus effluent was then treated with the EBPR process to monitor the simultaneous removal of carbon, nitrogen, and phosphorus. Phosphorus removal included a two‐stage anaerobic/aerobic system operating under continuous flow. Pre‐treated wastewater was added to the activated sludge and operated for 160 days in the reactor. The operating strategy included increasing the organic loading rate from 0.3 to 1.2 g chemical oxygen demand (COD)/L day. The stable and high removal rates of COD, NH4+‐N, and PO43−‐P were then recorded. The mean concentrations of the influent were approximately 3600 mg COD/L, 60 mg N/L and 14 mg P/L, which corresponded to removal efficiencies of approximately 98%, 86%, and 92%, respectively. The microtoxicity of the treated wastewater was then monitored by LUMIStox and its phytotoxicity was investigated on cress, tomato, wheat, maize, ryegrass, and alfalfa seed germination. LUMIStox tests showed that treatment allowed a significant toxicity removal. Moreover, the untreated wastewater inhibited the species germination even when diluted 10 times, whereas a positive effect of treated wastewater was noticed. © 2013 American Institute of Chemical Engineers Environ Prog, 33: 463–471, 2014

Mercury (Hg) represents a growing environmental and health major concern. It originates from natural sources and mainly from anthropogenic processes and it is widely distributed in the natural media. According to the last Global Mercury Assessment (2013), annual global emissions from both sources were estimated to be from 5,000 to 8,000 metric tons per year. Among the different mercury species released to the environment, methylmercury (MeHg) is considered as the most toxic form due to its ability to bioaccumulate, being then threatening even at very low concentrations.Its presence depends onHg(II) bioavailability and global amount.This explains the urgent need to ensure a continuous Hg(II) monitoring. Many efforts have been made in order to develop reliable systems able to deliver quick data and to comply with low detection limits, in accordance with the threshold value delivered by the World Health Organization (1µg L-1/ 5 nM). Spectroscopic techniques such as CV-AFS and CV-AAS are routinely used for Hg(II) determination. Although these methods can afford good sensitivity and low concentrations determination, they require sample preparation step, complex procedures and expensive material, which limits their use for on-site measurements. In this context, electrochemical sensors present excellent candidates for in situ Hg(II) trace analysis, taking in account their numerous advantages compared to spectroscopic techniques: easier handling, simple procedure, low energy consuming, low cost material and portability. In this work, we will propose a new electrochemical approach aiming to conceive and optimize an electrochemical Hg(II) sensor. The method consists in the functionalization of a glassy carbon electrode (GC) with gold nanoparticles (AuNPs) and Diazonium Salts. The main idea is to combine the interesting properties of both AuNPs and Diazonium salts. AuNPs were chosen for their electrocatalytic effect, large surface area, mass transport enhancement and for the strong affinity to mercury which will improve the sensor sensitivity. On the other hand, diazonium salts are used to improve the sensor stability by anchoring the AuNPs to the GC surface. First, nanometricorganic layer were grafted of the polished GC surface, by electrochemical reduction of 1.5 mM4-thiophenol diazonium (SH) using Constant Potential Electrolysis (CPE) in 0.1 M HCl solution at -0.55 V for 300 seconds. Electrochemical characterization performed by Cyclic Voltammetry (CV) and redox probes (ferricyanide and hexaamineruthenium(III)) revealed a total suppression of the signal, confirming the formation of a continuous blocking layer. This was confirmed by Atomic Force Microscopy (AFM)used to estimate the layer thickness, which was found to be 4 nm. Second, AuNPs were electrodeposited, for the first time, onto the diazonium multilayer by CPE in NaNO3 solution containing 0.25 mM HAuCl4for 300 seconds. Once more, redox probes were used to characterize the resulting interface and a total signal restauration and enhancement was observed after AuNPs electrodeposition, which highlights the effective AuNPs onto the organic layers. Field emission gun scanning microscopy (FEG-SEM) was used to provided further evidence and to quantify particle size and density of the AuNPs deposits. Both size and density are dependent on the CPE duration. Small homogeneous AuNPs with 27±3 nm average diameter and 158 NPs/µm2density were observed when the CPE was carried out during 300 seconds, while larger particles with 63±6 nm average diameter and lower density (63 NPs/µm2) were obtained when a longer CPE duration (600 seconds) is used. Finally, AuNPs were activated by cyclic voltammetry in H2SO4 prior to Hg(II) detection in order to homogenize the surface and to rearrange the crystallographic plans of the AuNPs. Herein, the well-known gold oxides reduction peak was observed and used to calculate the electroactive surface area (ESA) of the functionlized electrode. The electrochemical response of the final generated GC/SH/AuNPs interface towards Hg(II) was recorded by Square Wave Anodic Stripping Voltammetry (SWASV) in 0.01 M HCl solution containing different amounts of Hg(II). The SWASV procedure consists on the Hg(II) preconcentration at the electrode surface followed by the preconcentrated Hg(0) reoxidation in Hg(II). Under optimized conditions, and for a preconcentration time of 300 seconds, a well-defined peak, corresponding to Hg(0) reoxidation, was observed around 0.5 V/ECS. The sensor showed a linearity range from 1 up to 10 nM and allowed to reach picomolar level. The stability in HCl, phosphate buffer and air was also studied over several weeks: Once a week, the activation procedure was performed and followed by Hg(II) determination in order to evaluate the analytical performances of the sensor over time. Finally, Hg(II) detection assays were conducted in natural water samples collected from different sampling points. Figure 1