The desalting and recycling of wastewaters from textile dyeing operations using reverse osmosis

The wastewater from the textile dyeing operations was separated into a concentrate stream, rich in salts and dyes, and a purified product water stream using reverse osmosis membranes. Three membrane materials and three module configurations were used, namely : polyamide (hollow fine fiber configuration ), cellulose acetate ( spiral wound and tubular configurations ) and hydrous Zr(IV)- polyacrylate ( tubular configuration ). The modules were tested for periods ranging from 600 hours to more than 1000 hours under actual field conditions. Membrane flux and rejection were monitored throughout the operation and samples of the feed and product water were analysed chemically. The successful operation of the R.O. equipment under field conditions demonstrated the applicability of this process in the desalination of dyeing wastewater.     

Synthesis of copolymers of tert‐butyl vinyl ether with maleic and citraconic anhydrides

In the present study, the effects of charge‐transfer complex formation and intramolecular fragmentation (side‐chain lactonization) in radical copolymerization of tert‐butyl vinyl ether (t‐BVE) with anhydrides of maleic (MA) and citraconic (CA) acids and the structure–thermal behavior relationships of the resulting copolymers were examined using the ¹H‐NMR, FTIR, DSC, and TGA analysis methods. It was shown that copolymerization under the chosen conditions proceeded through intramolecular fragmentation with the formation of γ‐lactone units. Side‐chain fragmentation of t‐BVE–MA and t‐BVE–CA copolymers also was confirmed by TGA and DSC analysis. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 2455–2463, 2006 2006     

Thermal characterization of n‐alkyl maleate‐styrene‐allyl propionate terpolymers

Thermal characterization of maleic anhydride‐styrene‐allyl propionate (MA‐St‐AP) terpolymer and its ester derivatives named as n‐alkyl maleate and shown as nPr MA‐St‐AP, nBu MA‐St‐AP, nPn MA‐St‐AP, and nBz MA‐St‐AP was carried out. The thermal characterization was performed using thermal analysis techniques such as TGA, DTA, DSC, and TMA. Different results were observed between the original terpolymer and its ester derivatives. Thermal stabilities of the terpolymer and its ester derivatives were compared by using various measurements plotted as TGA, DTA, DSC, and TMA curves. The increase in the alcohols' carbon numbers added to the original terpolymer results in ester derivatives with different thermal stability behavior. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 600–604, 2007     

Synergic influence of a surfactant and ultrasonication on the preparation of soluble,conducting polydiphenylamine/silica‐nanoparticle composites

Conducting polydiphenylamine was used to encapsulate silica nanoparticles through the oxidative polymerization of diphenylamine in the presence of ultrasonic irradiation. The polymerization was performed in the presence of sodium lauryl sulfate as a surfactant. Experiments performed in the absence of ultrasound clearly demonstrated that the application of ultrasonication played multiple roles in the preparation of a composite of polydiphenylamine with silica nanoparticles. Ultrasonication dispersed the silica nanoparticles, converted sodium lauryl sulfate to lauryl alcohol, and augmented the dispersion of the silica‐nanoparticle/polydiphenylamine composite in an organic medium. Silica‐nanoparticle/polydiphenylamine composites were also prepared in the absence of ultrasound and/or sodium lauryl sulfate. The silica‐nanoparticle/polydiphenylamine composites were characterized with Fourier trans form infrared spectroscopy, ultraviolet–visible/near‐infrared spectroscopy, and thermogravimetric analysis. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 3912–3918, 2006     

Electrodeposition of smooth and adherent film of polypyrrole on lead electrode

Electropolymerization of pyrrole on lead substrate electrode was studied. Due to electrochemical activity of Pb in acidic media, this process is only possible at basic pHs. For this purpose, electropolymerization process was performed in an aqueous solution of Na₂SO₄ with pH 12. Potentiodynamic cycling shows the Pb oxidation at the first cycles. In subsequent cycles, polypyrrole film grows on the oxidized lead substrate. Of course, as the passive film is highly porous, a composite of polypyrrole/PbSO₄ is formed in the first layers. However, subsequent cycling leads to the formation of pure polypyrrole film. According to this structure and strong connection of the polymer film to the substrate surface via this composite layer, the polypyrrole film deposited on the lead surface has enhanced mechanical stability. AFM measurements showed peculiar smoothness of both composite and lateral polypyrrole films. This synthesis approach is of particular interest for the preparation of highly stable polymer films and fabrication of supercapacitors with a polymer/PbSO₄ conductive structure.     

Ellipsoidal neighbourhood outlier factor for distributed anomaly detection in resource constrained networks

Anomaly detection in resource constrained wireless networks is an important challenge for tasks such as intrusion detection, quality assurance and event monitoring applications. The challenge is to detect these interesting events or anomalies in a timely manner, while minimising energy consumption in the network. We propose a distributed anomaly detection architecture, which uses multiple hyperellipsoidal clusters to model the data at each sensor node, and identify global and local anomalies in the network. In particular, a novel anomaly scoring method is proposed to provide a score for each hyperellipsoidal model, based on how remote the ellipsoid is relative to their neighbours. We demonstrate using several synthetic and real datasets that our proposed scheme achieves a higher detection performance with a significant reduction in communication overhead in the network compared to centralised and existing schemes.     

Variations in fat content and lipid class composition in ten different mango varieties

The kernels of 10 different mango varieties were extracted. The physico-chemical characteristics and lipid class composition of fats were studied. The fat content of mango kernels grown under the soil and climatic conditions of Bangladesh varied from 7.1% to 10%, depending on the variety. The total lipid extracts were fractionated into lipid classes by a combination of column and thin layer chromatography (TLC). The hydrocarbon and sterol esters varied from 0.3% to 0.7%, triglycerides from 55.6% to 91.5%, partial glycerides from 2.3% to 4% and free sterol from 0.3% to 0.6%. Free fatty acids amounted to 3.0–37% as oleic; glycolipids were 0.6–1.2% and phospholipids 0.11–0.8%. The fatty acid composition of triglyceride (TG) fractions was analyzed by gas liquid chromatography (GLC). Palmitic acid varied from 7.9 molar % to 10.0 molar %, stearic from 38.2% to 40.2%, oleic from 41.1% to 43.8%, linoleic from 6.0% to 7.6%, linolenic from 0.6% to 1.0% and arachidic acid from 1.7% to 2.6%. TLC revealed the presence of lyso-phosphatidylcholine, phosphatidylcholine, phosphatidylinositol, phosphatidylethanolamine and phosphatidic acid in the phospholipid fraction.     

Thermoplastic interpenetrating polymer networks based on a poly(styrene-b-butadiene) copolymer and an ionically-terminated polybutadiene ionomer

Thermoplastic interpenetrating polymer networks (IPN) are mixtures of two physically crosslinked polymers. Thermoplastic IPNs were prepared by blending an SBS triblock elastomer with a 1,2-polybutadiene that was ionically-terminated at both ends. The morphologies of these IPNs were studied using differential scanning calorimetry and dynamic mechanical thermal analysis. It was concluded that the ionomer was incompatible with the SBS elastomer, since the T_gs of both the 1,2-polybutadiene from the ionomer and the essentially 1,4-polybutadiene from the SBS component were observable at temperatures that were close to those of the individual components. The addition of the polybutadiene material had, however, an influence on the relaxation processes of the polystyrene blocks. The polystyrene glass transition in the pure SBS copolymer is broadened by the interfacial region between polystyrene and polybutadiene. The low temperature shoulder was much more pronounced when the ion-terminated polybutadiene was present, indicating it has a preference to be located in these interfacial regions. © 1994 John Wiley & Sons, Inc.     

H ∞ filtering for singular bilinear systems with application to a single-link flexible-joint robot

In this paper, we consider the H _∞ filters design for singular bilinear systems. The approach is based on the parameterized solution of a set of constrained Sylvester equations. The exponential convergence and l ₂ gain attenuation problems are solved by using the bounded real lemma, which leads to linear matrix inequalities (LMI) formulation. Finally, a detailed design procedure is given for the estimation of the states of a flexible joint robot, which demonstrates the effectiveness of the proposed method.     

Synthesis,characterization, and antitumor activity of poly(maleic anhydride‐co‐vinyl acetate‐co‐acrylic acid)

The ternary copolymerization of maleic anhydride (MA), vinyl acetate (VA), and acrylic acid (AA) [P(MA‐co‐VA‐co‐AA)], which is considered to be an acceptor–donor–acceptor system, was carried out in 1,4‐dioxane with benzoyl peroxide as an initiator at 70°C under a nitrogen atmosphere. Constants of complex formation for the monomer systems in the study were determined by UV–visible (hydrogen‐bonding complex) and ¹H‐NMR (charge transfer complex) methods, respectively. The results show that polymerization of the P(MA‐co‐VA‐co‐AA) system proceeds by an alternating terpolymerization mechanism. It is shown that the synthesized copolymers have typical polyelectrolyte behavior, ability for reversible hydrolysis–anhydrization reactions, and semicrystalline structures. In these cases, including radical polymerization, and formation of semicrystalline structures, the hydrogen‐bonding effect plays a significant role. The in vitro cytotoxicities of the synthesized terpolymer and alternating copolymer were evaluated using Raji cells (human Burkitt lymphoma cell line). The antitumor activities of prepared anion‐active copolymers were studied using methyl–thiazol–tetrazolium colorimetric assay and 50% of the cytotoxic dose of each copolymer and terpolymer were calculated. Hydrolyzed P(MA‐co‐VA‐co‐AA) and P(MA‐alt‐AA) copolymers have sufficiently high antitumor activity, which depends on the amount of hydrogen‐bonding carboxylic groups and their regular distribution in the side chain of functional macromolecules. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 3425–3432, 2006