Investigation of maximum lifetime and minimum delay trade‐off in underwater sensor networks

Underwater acoustic sensor networks (UASNs) are subjected to harsh characteristics of underwater acoustic channel such as severe path losses, noise, and high propagation delays. Among these constraints, propagation delay (more generally, end‐to‐end delay) is the most dominating limitation especially for time‐critical UASN applications. Although the minimization of end‐to‐end delay can be achieved by using the minimum hop routing, this solution cannot lead prolonged lifetimes since nodes consume excessive energy for transmission over long links. On the other hand, the maximization of network lifetime is possible by using energy efficient paths, which consist of relatively short links but high number of hops. However, this solution results in long end‐to‐end delays. Hence, there is a trade‐off between maximizing the network lifetime and minimizing the end‐to‐end delay in UASNs. In this work, we develop a novel multi‐objective–optimization (MOO) model that jointly maximizes the network lifetime while minimizing the end‐to‐end delay. We systematically analyze the effects of limiting the end‐to‐end delay on UASN lifetime. Our results reveal that the minimum end‐to‐end delay routing solution results in at most 72.93% reduction in maximum network lifetimes obtained without any restrictions on the end‐to‐end delay. Nevertheless, relaxing the minimum end‐to‐end delay constraint at least by 30.91% yields negligible reductions in maximum network lifetimes.     

A new Schiff base: Synthesis,characterization and optimization of metal ions-binding properties

In this study, a new Schiff base (H₄TSTE) was synthesized and characterized by elemental analysis, FT-IR, NMR and MS spectral data. Liquid–liquid extraction process was performed for removal of Cu(II), Mn(II), Ni(II), Pb(II) and Zn(II) from aqueous solutions by means of H₄TSTE. The extractions were investigated depending on the concentration of picric acid, metal ion and H₄TSTE ligand. Response surface methodology (RSM) was first applied to optimize metal ion-binding properties of H₄TSTE. The extraction efficiency was estimated to be >98% for all metals by models. Under the same conditions, the extraction efficiency was experimentally found to be >97% with a relative standard deviation within ±0.10 (N = 4), indicating the suitability of the models.     

Effect of Cobalt and Nickel Doping on Structural and Magnetic Properties of Iron Oxide Nanoparticles

Two series samples of Iron Oxide nanoparticles doped with nickel and cobalt with different doping values (x?=?0.01; 0.03; 0.05 and 0.07), were successfully synthesized by using sol–gel method, and then they were characterized by X-ray diffraction, scanning electron and vibrating sample magnetometer (VSM). X-ray diffraction analysis of two series samples showed the formation α-Fe₂O₃ nanoparticles, accompanied by two phases iron spinels, CoFe₂O₄ and NiFe₂O₄. In addition, the variations in grain size were observed for both two series. The observation by scanning electron microscopy reveals a change in the morphology of the grains of all the samples doped, which confirm the cobalt and nickel effect on the morphology of iron oxide nanoparticles. Magnetic measurements which were measured by VSM showed significant magnetic parameters such as coercivity and magnetization besides the ferromagnetic behavior of both two series doped with Cobalt and Nickel.

     

Electrochemical measurements for studying the polymerization process and critical point behaviors of hydrogels

We propose a new technique based on electrochemical measurements for studying the critical point behaviors of the sol–gel transition of acrylamide–N,N′‐methylene bisacrylamide hydrogels. In this technique, no chemical activator is used for accelerating the polymerization reaction. However, a potential difference is applied by means of silver and calomel electrodes placed in the reaction mixture. The silver electrode begins to be ionized and loses its electrons. The free radicals, ^?O₃S? O^?, H^?, and ^?OH, form on the silver electrode via persulfate dissociation. The polymerization is initiated by means of these free radicals. The current measured during the gelation processes passes through a maximum (a Gaussian‐like behavior) and varies linearly with the reaction time during linear polymerization. All the parameters (the monomer, initiator, and crosslinker concentrations, the applied voltage, and the stirring rate of the reacting mixture) affecting the current have been studied in detail. We show that the maxima appearing in the current–time plots correspond to the gelation thresholds, the so‐called sol–gel transition points. We also analytically prove that the current monitors the weight‐average degree of polymerization (DP_w) and the gel fraction (G) below and above the threshold, respectively. The scaling behaviors of DP_w and G have been tested near the gelation thresholds, and we have observed that the critical exponents γ and β, defined for DP_w and G, agree with the predictions by mean‐field theory. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Immobilization of invertase in conducting polypyrrole/PMMA‐co‐PMTM graft copolymers

In this study, invertase was immobilized in copolymer electrodes constructed. Three different types of polymethyl methacrylate‐co‐polymethyl thienyl methacrylate matrices were used to obtain copolymers that were characterized by FT‐IR spectroscopy. Immobilization of enzymes was carried out by the entrapment of the enzyme in conducting polymer matrices during electrochemical polymerization of pyrrole through thiophene moieties of polymers. Immobilization of the enzyme was achieved by application of 1.0 V constant potential on a platinum electrode for 30 min in solution. The effects of temperature and pH on the activity of the enzyme electrodes were examined and operational stability studies were done. The changes in the maximum reaction rate and the variations in the Michaelis–Menten constant were studied. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 96: 502–507, 2005     

Biodegradation kinetics of the soluble slowly biodegradable substrate in polyamide carpet finishing wastewater

BACKGROUND: Carpet manufacturing and finishing with purely synthetic fibers has received relatively little attention, compared to other textile processing types. This study evaluates the biodegradation kinetics of organic compounds generated from polyamide‐based carpet manufacturing. RESULTS: Experiments were conducted on pre‐washing and dyeing/softening wastewater effluents. Model evaluation of oxygen uptake rate profiles with dual hydrolysis kinetics revealed that the soluble slowly hydrolysable chemical oxygen demand (COD) was the major fraction, constituting nearly 97% of the biodegradable COD and 78% of total COD content. Degradation of the slowly hydrolysable COD fraction was characterized with a rate coefficient of 0.72 day^?1, a significant rate limiting step for substrate utilization. Model simulation of system performance indicated that an unusually long hydraulic retention time was required for an activated sludge system to reduce the effluent COD concentration. CONCLUSION: Compared to domestic wastewater, two additional hydrolysable COD fractions with different degradation kinetics were characterized. The dyeing and softening step had the highest slowly biodegradable organic matter content, with the lowest degradation rate. Simulation results showed that soluble slowly hydrolysable COD degradation did not cause any problem in terms of effluent quality. With the system operated under reduced solids retention time, the effluent COD quality was significantly influenced by the slow hydrolysis rate of soluble hydrolysable matter. Copyright © 2007 Society of Chemical Industry     

N‐(hydroxymethyl) acrylamide as a multifunctional finish to cotton and a tether for grafting methacrylamide for biocidal coatings

N‐(hydroxymethyl) acrylamide (NMA) was immobilized on cotton surfaces through etherification, and then methacrylamide (MA) was grafted onto the treated surface. The coatings were characterized by ATR‐IR spectroscopy and were rendered biocidal upon exposure to dilute household bleach. The treated fabrics were challenged with Gram‐negative and Gram‐positive bacteria; both NMA and NMA/MA‐treated fabrics inactivated about 8 logs of Escherichia coli O157:H7 and Staphylococcus aureus within only 5 min of contact time. The coatings were also quite stable toward ultraviolet (UVA) light exposure and repeated laundering. Moreover, a substantial improvement in wrinkle recovery angle was obtained for the NMA/MA‐treated fabrics. The new acyclic acrylamide N‐halamine coating should be less expensive to produce and use than previous cyclic N‐halamine coatings developed in these laboratories. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Heat-resistance characteristics of ascospores of Eurotium chevalieri isolated from apricot juice

A heat-resistant fungus was isolated from aseptically packaged apricot pulp. The fungus was identified as Eurotium chevalieri. Heat resistance of the fungus was studied at four different temperatures (70, 75, 80 and 83 degrees C) after activation of its ascospores for 30 min at 70 degrees C. D70, D75, D80 and D83 values of ascospores of Eurotium chevalieri were estimated by linear regression (log-survival vs. heating time) as 118.58, 34.15, 5.50 and 3.77 min, respectively. The z-value was determined in the same way (regression of log-D values vs. heating temp.) and was found as 8.23 degrees C.