Indirect electrochemical treatment of bisphenol A in water via electrochemically generated Fenton's reagent

Bisphenol A (BPA) has been treated with electrochemically generated Fenton's reagent in aqueous medium. Hydroxyl radicals that were formed in Fenton's reagent reacted with the organic substrate producing two different isomers of monohydroxylated product and, upon successive hydroxylation, mainly one dihydroxylated product. Further hydroxylation first degraded one of the aromatic rings, and the side chain thus formed was then cleaved off the other aromatic ring. The second aromatic ring was also degraded upon successive hydroxylations. Small saturated and unsaturated aliphatic acids were the last products prior to mineralization. It was found that use of cuprous/cupric ion pair resulted a faster conversion of BPA and faster mineralization when compared using ferrous/ferric ions, but this happened at the expence of excess electrical charge utilized for an equivalent conversion or mineralization. Degradation by using ferrous/ferric ions was more efficient than cuprous/cupric ions case in terms of total mineralization versus charge utilized, and a mineralization of 82% had been achieved by applying 107.8 mF of charge to a 0.7 mM BPA solution of 0.200 dm3. The rate constant of the monohydroxylation of BPA in the presence of ferrous/ferric ions had been determined as 1.0 x 10(10) M(-1) s(-1) where BPA and salicylic acid competitively reacted with hydroxyl radicals in aqueous medium with the initial concentrations of Fe2+, BPA, and SA of 1.0, 0.5, and 0.5 mM, respectively. In a similar experiment where the initial concentrations of Cu2+, BPA, and SA were 1.0, 0.5, and 0.5 mM, respectively, the corresponding rate constant was determined to be the same as the rate constant obtained for Fe2+ (i.e., 1.0 x 10(10) M(-1) s(-1)). While the use of Cu2+ cannot be advised for processing BPA and similar substrates by using the electro-Fenton technique for both technical and economical reasons, the use of [Fe2+]/[BPA]0 values in the range 3-4 will be sufficient to achieve an efficient mineralization of BPA and similar substrates by the electro-Fenton process in aqueous medium.     

Evaluation of various carbon materials supported Pt catalyts for aqueous-phase reforming of lignocellulosic biomass hydrolysate

Currently, under huge pressure from energy demands and environmental problems, much attention is being paid to produce fuel and chemicals from lignocellulosic biomass. In this matter, development of active and also recyclable catalysts are essential. In the present study, various types of carbon supported Pt reforming catalysts were prepared for use in gasification of wheat straw biomass hydrolysate by aqueous-phase reforming. The supports tested were various carbon materials having different surface and structures that were activated carbon (AC), single- and multi-walled carbon nanotubes (SWCNT and MWCNT), superdarco carbon (SDC) and graphene oxide (GO). The catalysts prepared using these supports were evaluated based on gasification yield, carbon amount consumed in the process, sugar alcohols formation and breaking down of organic compounds in the hydrolysate.     

Network Polydiacetylene Films: Preparation,Patterning, and Sensor Applications

The synthesis, characterization, and functionalization of polydiacetylene (PDA) networks on solid substrates is presented. A highly transparent and cross‐linked diacetylene film of DCDDA‐bis‐BA on a solid substrate is prepared first by tailoring the monomers with organoboronic acid moieties as pendant side groups and consequent drop‐casting and dehydration steps. Precisely controlled thermal curing plays a key role to obtain properly aligned diacetylene monomers that are closely packed between the boronic acid derived anhydride structures. A second cross‐linking, which occurs by polymerization of the diacetylene monomers with UV irradiation, induces a transparent to blue color shift. Accordingly, colored image patterns are readily available by polymerization through a photomask. The color change that takes place as a response to various organic solvents can be simply detected by naked eyes. The thermofluorescence change of PDA networks is demonstrated to be an effective method by which to obtain the microscale temperature distribution of thermal systems. The ease of film formation and stress‐induced blue‐to‐red color change with a simultaneous fluorescence generation features of the network structure should find a great utility in a wide range of chemical and thermal sensing platforms.     

Inkjet printing of conjugated polymer precursors on paper substrates for colorimetric sensing and flexible electrothermochromic display

Inkjet-printable aqueous suspensions of conjugated polymer precursors are developed for fabrication of patterned color images on paper substrates. Printing of a diacetylene (DA)-surfactant composite ink on unmodified paper and photopaper, as well as on a banknote, enables generation of latent images that are transformed to blue-colored polydiacetylene (PDA) structures by UV irradiation. Both irreversible and reversible thermochromism with the PDA printed images are demonstrated and applied to flexible and disposable sensors and to displays.     

Estimating graph distance and centrality on shared nothing architectures

We present a parallel toolkit for pairwise distance computation in massive networks. Computing the exact shortest paths between a large number of vertices is a costly operation, and serial algorithms are not practical for billion‐scale graphs. We first describe an efficient parallel method to solve the single source shortest path problem on commodity hardware with no shared memory. Using it as a building block, we introduce a new parallel algorithm to estimate the shortest paths between arbitrary pairs of vertices. Our method exploits data locality, produces highly accurate results, and allows batch computation of shortest paths with 7% average error in graphs that contain billions of edges. The proposed algorithm is up to two orders of magnitude faster than previously suggested algorithms and does not require large amounts of memory or expensive high‐end servers. We further leverage this method to estimate the closeness and betweenness centrality metrics, which involve systems challenges dealing with indexing, joining, and comparing large datasets efficiently. In one experiment, we mined a real‐world Web graph with 700 million nodes and 12 billion edges to identify the most central vertices and calculated more than 63 billion shortest paths in 6 h on a 20‐node commodity cluster. Copyright © 2014 John Wiley & Sons, Ltd.     

Inhibition of polyphenol oxidase obtained from various sources by 2,3‐diaminopropionic acid

This paper reports for the first time the inhibition of the catecholase activities of mushroom, artichoke (Cynara scolymus L) and Ocimum basilicum L polyphenol oxidase by 2,3‐diaminopropionic acid. Polyphenol oxidases from artichoke and O basilicum L were purified by ammonium sulfate precipitation, dialysis and a Sepharose 4B‐L ‐tyrosine‐p‐aminobenzoic acid‐affinity column. In inhibition studies, 2,3‐diaminopropionic acid showed uncompetitive inhibition for mushroom PPO using catechol and pyrogallol as substrates, competitive inhibition for O basilicum L PPO using catechol as a substrate, and uncompetitive inhibition for artichoke PPO using catechol as a substrate. Furthermore, sodium azide, which is an inhibitor of PPO, was used as an inhibitor for comparison with the inhibition potency of 2,3‐diaminopropionic acid. The highest 2,3‐diaminopropionic acid inhibition observed with O basilicum L (K_i = 0.89 mM ), followed by artichoke (K_i = 1.42 mM ) and mushroom (K_i = 2.47 mM ), respectively. Copyright © 2005 Society of Chemical Industry     

An empirical analysis of the main drivers affecting the buyer surplus in E-auctions

We empirically examine the impacts of the product category, the auction format, the 2008 global financial crisis, the group purchasing, the contract type, the platform ownership, and the number of participating suppliers on the buyer surplus obtained from e-auctions. To this end, we collect a unique dataset from a purchasing organisation that offers e-auction solutions to its corporate customers. By using a standard Tobit model, we show that the product categories, the auction type, and the number of participating suppliers have significant effects on the decrease in the procurement prices with respect to the minimum of the initial submitted bids. It is observed that the 2008 global financial crisis led to an increase in the buyer surplus. We classify the product categories into three groups based on their impacts on the average of the decrease in the procurement prices. We show that the average decrease in procurement prices is higher for the group purchasing option than for the individual buying option. It is concluded that the types of contract between buyers and auctioneer and the platform ownership have no statistically significant effects on the average decrease in procurement prices.     

In situ Van der Pauw measurements of the Ni/YSZ anode during exposure to syngas with phosphine contaminant

Solid oxide fuel cells (SOFCs) represent an option to provide a bridging technology for energy conversion (coal syngas) as well as a long-term technology (hydrogen from biomass). Whether the fuel is coal syngas or hydrogen from biomass, the effect of impurities on the performance of the anode is a vital question. The anode resistivity during SOFC operation with phosphine-contaminated syngas was studied using the in situ Van der Pauw method. Commercial anode-supported solid oxide fuel cells (Ni/YSZ composite anodes, YSZ electrolytes) were exposed to a synthetic coal syngas mixture (H₂, H₂O, CO, and CO₂) at a constant current and their performance evaluated periodically with electrochemical methods (cyclic voltammetry, impedance spectroscopy, and polarization curves). In one test, after 170 h of phosphine exposure, a significant degradation of cell performance (loss of cell voltage, increase of series resistance and increase of polarization resistance) was evident. The rate of voltage loss was 1.4 mV h⁻¹. The resistivity measurements on Ni/YSZ anode by the in situ Van der Pauw method showed that there were no significant changes in anode resistivity both under clean syngas and syngas with 10 ppm PH₃. XRD analysis suggested that Ni₅P₂ and P₂O₅ are two compounds accumulated on the anode. XPS studies provided support for the presence of two phosphorus phases with different oxidation states on the external anode surface. Phosphorus, in a positive oxidation state, was observed in the anode active layer. Based on these observations, the effect of 10 ppm phosphine impurity (or its reaction products with coal syngas) is assigned to the loss of performance of the Ni/YSZ active layer next to the electrolyte, and not to any changes in the thick Ni/YSZ support layer.