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.     

Stabilization of positive switched systems with time-varying delays under asynchronous switching

This paper investigates the state feedback stabilization problem for a class of positive switched systems with time-varying delays under asynchronous switching in the frameworks of continuous-time and discrete-time dynamics. The so-called asynchronous switching means that the switches between the candidate controllers and system modes are asynchronous. By constructing an appropriate co-positive type Lyapunov-Krasovskii functional and further allowing the functional to increase during the running time of active subsystems, sufficient conditions are provided to guarantee the exponential stability of the resulting closed-loop systems, and the corresponding controller gain matrices and admissible switching signals are presented. Finally, two illustrative examples are given to show the effectiveness of the proposed methods.     

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     

Adsorption of Cr(III), Ni(II), Zn(II), Co(II) ions onto phenolated wood resin

In this study, phenolated wood resin was used an adsorbent for the removal of Cr(III), Ni(II), Zn(II), Co(II) ions by adsorption from aqueous solution. The adsorption of metal ions from solution was carried at different contact times, concentrations and pHs at room temperature (25°C). For individual metal ion, the amount of metal ions adsorbed per unit weight of phenolated wood resin at equilibrium time increased with increasing concentration and pH. Also, when the amounts of metal ions adsorbed are compared to each other, it was seen that this increase was order of Cr(III) > Ni(II) > Zn(II) > Co(II). This increase was order of Cr(III) > Ni(II) > Co(II) > Zn(II) for commercial phenol–formaldehyde resin. Kinetic studies showed that the adsorption process obeyed the intraparticle diffusion model. It was also determined that adsorption isotherm followed Langmuir and Freundlich models. Adsorption isotherm obtained for commercial phenol–formaldehyde resin was consistent with Freundlich model well. Adsorption capacities from Langmuir isotherm for commercial phenol–formaldehyde resin were higher than those of phenolated wood resin, in the case of individual metal ions. Original adsorption isotherm demonstrated the monolayer coverage of the surface of phenolated wood resin. Adsorption kinetic followed the intraparticle diffusion model. The positive values of ΔG° determined using the equilibrium constants showed that the adsorption was not of spontaneous nature. It was seen that values of distribution coefficient (K_D) decreasing with metal ion concentration in solution at equilibrium (C_e) indicated that the occupation of active surface sites of adsorbent increased with metal ions. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 2838–2846, 2006     

Characterization and preparation of new multiwall carbon nanotube/conducting polymer composites by in situ polymerization

Composites based on poly(diphenyl amine) (PDPA) and multiwall carbon nanotubes (MWNTs) were prepared by chemical oxidative polymerization through two different approaches: in situ polymerization and intimate mixing. In in situ polymerization, DPA was polymerized in the presence of dispersed MWNTs in sulfuric acid medium for different molar composition ratios of MWNT and DPA. Intimate mixing of synthesized PDPA with MWNT was also used for the preparation of PDPA/MWNT composites. Transmission electron microscopy revealed that the diameter of the tubular structure for the composite was 10–20 nm higher than the diameter of pure MWNT. Scanning electron microscopy provided evidence for the differences in the morphology between the MWNTs and the composites. Raman and Fourier transform IR (FTIR) spectroscopy, thermogravimetric analysis, X‐ray diffraction, and UV–visible spectroscopy were used to characterize the composites and reveal the differences in the molecular level interactions between the components in the composites. The Raman and FTIR spectral results revealed doping‐type molecular interactions and coordinate covalent‐type interactions between MWNT and PDPA in the composite prepared by in situ polymerization and intimate mixing, respectively. The backbone structure of PDPA in the composite decomposed at a higher temperature (>340°C) than the pristine PDPA (～300°C). This behavior also favored the molecular level interactions between MWNT and PDPA in the composite. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 3721–3729, 2006     

Magnetic Behavior of Trinuclear Vanadium(II)–Diamine Complexes. Part 2. Large Intramolecular Antiferromagnetic Exchange Interactions in a Triangular Unit

This study reports the magnetic structures of newly reported trinuclear vanadium(II)–diamine complexes. Using the isotropic Heisenberg exchange Hamiltonian, it is suggested that there are strong intramolecular antiferromagnetic interactions among the vanadium(II) ions. It is also suggested that these complexes are good candidates to the geometrically frustrated systems. For part 1 see A. Bayri, J. Inorg. Organomet. Polym. Mater., (in press) An erratum to this article can be found at     

Antiferromagnetic Exchange Interactions. Part 1. Newly Reported Nickel(II) Complex of the Antiprine Schiff Base of 3-Formylsalicylic Acid

This study reports the magnetic properties of newly reported nickel(II) complex of the antiprine Schiff base of 3-formylsalicylic acid. Using the isotropic magnetic interaction model it is suggested that there is a strong antiferromagnetic interactions between metal centers in dimeric units. It is also suggested that the system become demagnetized below a certain temperature. An erratum to this article can be found at     

Profile based routing in vehicular ad-hoc networks

One of the main problems in the VANET(vehicular ad-hoc network)routing algorithms is how to establish the stable routes.The link duration in these networks is often very short because of the frequent changes in the network topology.Short link duration reduce the network efficiency.Different speeds of the vehicles and choosing different directions by the vehicles in the junctions are the two reasons that lead to link breakage and a reduction in link duration.Several routing protocols have been proposed for VANET in order to improve the link duration,while none of them avoids the link breakages caused by the second reason.In this paper,a new method for routing algorithms is proposed based on the vehicles trips history.Here,each vehicle has a profile containing its movement patterns extracted from its trips history.The next direction which each vehicle may choose at the next junction is predicted using this profile and is sent to other vehicles.Afterward each vehicle selects a node the future direction of which is the same as its predicted direction.Our case study indicates that applying our proposed method to ROMSGP(receive on most stable group-path)routing protocol reduces the links breakages and increases the link duration time.