Contributing authors

Contributing authors     

Monitoring and control of the biogas process based on propionate concentration using online VFA measurement.

Simple logic control algorithms were tested for automatic control of a lab-scale CSTR manure digester. Using an online VFA monitoring system, propionate concentration in the reactor was used as parameter for control of the biogas process. The propionate concentration was kept below a threshold of 10 mM by manipulating the feed flow. Other online parameters such as pH, biogas production, total VFA, and other individual VFA were also measured to examine process performance. The experimental results showed that a simple logic control can successfully prevent the reactor from overload, but with fluctuations of the propionate level due to the nature of control approach. The fluctuation of propionate concentration could be reduced, by adding a lower feed flow limit into the control algorithm to prevent undershooting of propionate response. It was found that use of the biogas production as a main control parameter, rather than propionate can give a more stable process, since propionate was very persistent and only responded very slowly to the decrease of the feed flow which lead to high fluctuation of biogas production. Propionate, however, was still an excellent parameter to indicate process stress under gradual overload and thus recommended as an alarm in the control algorithm.     

Vibrational spectroscopy and periodic DFT studies of LaMg2PdH7: A material with two types of hydride

The need for a safe, reliable and cheap method for hydrogen transportation has prompted an intense effort in the synthesis of novel hydrides. To direct the search for better materials, it is essential to understand the bonding present in these systems. A newly synthesized material is LaMg₂PdH₇ which is best formulated as {La³⁺}{Mg²⁺}₂{[PdH₄]⁴⁻}{H⁻}₃. Thus hydrogen is formally present both as a free hydride ion and also as a covalently bound ligand. The combination of inelastic neutron scattering (INS), infrared and Raman spectroscopies and periodic density functional theory (DFT) has been used to characterise the material. We find that the material is less ionic than Ba₂[PdH₄], which also contains [PdH₄]⁴⁻. The charges carried by both the coordinating and free hydrides are similar which hints at a degree of covalency in the interactions between the interstitial hydrides and the lanthanum and magnesium ions.     

Separation of particles from hot gases using metallic foams

One of the most complicated tasks in the field of hot gas cleaning is the removal of particles from a complex mixture of degradation products formed during thermal treatment. A robust and completely reliable technology is still to be developed to achieve high efficiencies. In the past few years, significant improvements have been brought to gas cleaning technologies. Nevertheless, none of the existing processes has proved fully successful.The aim of this work is to perform the filtration of particles generated in fluidized bed gasification experiments using metallic foams. The gasified material used is dried sewage sludge. Nickel–chromium metallic foams are likely to have inherent properties that would make them suitable for use in structures where strength, high temperature-resistance and corrosion resistance are required. Moreover, metallic foams are characterized structurally by their cell topology, relative density, high porosity (? = 0.95) and cell size. In hot gas filtration, high temperature-resistance and low pressure drop to specific area ratio are essential characteristics. In the present work, several experimental operating conditions (heating time, temperature, washing method and metallic foam thickness) are investigated. The pressure drops in the metallic foams during filtration are calculated. The experimental results obtained are compared with numerical simulation results and a good agreement is obtained. The metallic foams are simulated from tomography results and a model is created.     

Chlorination of bromide-containing waters: Enhanced bromate formation in the presence of synthetic metal oxides and deposits formed in drinking water distribution systems

Bromate formation from the reaction between chlorine and bromide in homogeneous solution is a slow process. The present study investigated metal oxides enhanced bromate formation during chlorination of bromide-containing waters. Selected metal oxides enhanced the decay of hypobromous acid (HOBr), a requisite intermediate during the oxidation of bromide to bromate, via (i) disproportionation to bromate in the presence of nickel oxide (NiO) and cupric oxide (CuO), (ii) oxidation of a metal to a higher valence state in the presence of cuprous oxide (Cu₂O) and (iii) oxygen formation by NiO and CuO. Goethite (α-FeOOH) did not enhance either of these pathways. Non-charged species of metal oxides seem to be responsible for the catalytic disproportionation which shows its highest rate in the pH range near the pK_a of HOBr. Due to the ability to catalyze HOBr disproportionation, bromate was formed during chlorination of bromide-containing waters in the presence of CuO and NiO, whereas no bromate was detected in the presence of Cu₂O and α-FeOOH for analogous conditions. The inhibition ability of coexisting anions on bromate formation at pH 8.6 follows the sequence of phosphate >> sulfate > bicarbonate/carbonate. A black deposit in a water pipe harvested from a drinking water distribution system exerted significant residual oxidant decay and bromate formation during chlorination of bromide-containing waters. Energy dispersive spectroscopy (EDS) analyses showed that the black deposit contained copper (14%, atomic percentage) and nickel (1.8%, atomic percentage). Cupric oxide was further confirmed by X-ray diffraction (XRD). These results indicate that bromate formation may be of concern during chlorination of bromide-containing waters in distribution systems containing CuO and/or NiO.     

Coupling dark fermentation and microbial electrolysis to enhance bio-hydrogen production from agro-industrial wastewaters and by-products in a bio-refinery framework

The aim of this work is to evaluate biohydrogen production from agro-industrial wastewaters and by-products, by combining dark fermentation and microbial electrolysis in a two-step cascade process. Such coupling of both technologies constitutes a technological building block within a concept of environmental biorefinery where sustainable production of renewable energy is expected.Six different wastewaters and industrial by-products coming from cheese, fruit juice, paper, sugar, fruit processing and spirits factories were evaluated for the feasibility of hydrogen production in a two-step process. The overall hydrogen production when coupling dark fermentation and microbial electrolysis was increased up to 13 times when compared to fermentation alone, achieving a maximum overall hydrogen yield of 1608.6 ± 266.2 mLH₂/gCOD_consumed and a maximum of 78.5 ± 5.7% of COD removal.These results show that dark fermentation coupled with microbial electrolysis is a highly promising option to maximize the conversion of agro-industrial wastewaters and by-products into bio-hydrogen.     

Simulated annealing-based fitting of CAD models to point clouds of mechanical parts’ assemblies

Engineering with Computers - This paper introduces a new fitting approach to allow an efficient part-by-part reconstruction or update of editable CAD models fitting the point cloud of a digitized...     

Overlapping community detection using core label propagation algorithm and belonging functions

Applied Intelligence - The community detection in complex networks has become a major field of research. Disjoint community detection deals often with getting a partition of nodes where every node...     

Comparison Between Equivalent Architectures of Complex-valued and Real-valued Neural Networks - Application on Polarimetric SAR Image Segmentation

Journal of Signal Processing Systems - We present an in-depth statistical comparison among several Complex-Valued Neural Network (CVNN) models on the Oberpfaffenhofen Polarimetric Synthetic...     

Hydrocarbons in the Ant <Emphasis Type="Italic">Lasius niger</Emphasis>: From the Cuticle to the Nest and Home Range Marking

The cuticular hydrocarbons (CHCs) of the ant Lasius niger are described. We observe a high local colony specificity of the body cuticular profile as predicted for a monogynous and multicolonial species. The CHCs show a low geographical variation among different locations in France. The CHCs on the legs also are colony specific, but their relative quantities are slightly different from those on the main body. For the first time, we demonstrate that the inner walls of the ant nest are coated with the same hydrocarbons as those found on the cuticle but in different proportions. The high amount of inner-nest marking and its lack of colony-specificity may explain why alien ants are not rejected once they succeed in entering the nest. The cuticular hydrocarbons also are deposited in front of the nest entrance and on the foraging arena, with a progressive increase in n-alkanes relative amounts. Chemical marks laid over the substrate are colony specific only when we consider methyl-branched alkanes. Our data confirm that these “footprint hydrocarbons” are probably deposited passively by the contact of ant tarsae with the substrate. These results suggest that the CHCs chemical profiles used by ants in colony recognition are much more complex than a single template: ants have to learn and memorize odors that vary depending on their context of perception.