A novel electronic micro-viscometer

Microsystem Technologies - This paper reports the development of a novel electronic micro-viscometer capable of measuring viscosity of different Newtonian fluids using less than 100 µl which...     

Cationic surfactant-selective potentiometric sensors based on neutral ion-pair carrier complexes

Poly(vinyl chloride) (PVC) membrane electrodes to determine monomer concentrations of tetradecyltrimethylammonium ion (TTA⁺) and hexadecylpyridinium ion (HPy⁺) based on neutral ion-pair carrier complexes of tetradecyltrimethylammonium dodecyl sulfate (TTA⁺-DS⁻) and hexadecylpyridinium dodecyl sulfate (HPy⁺-DS⁻), respectively, are reported here. The electrodes exhibit a Nernstian slope of 59 mV per decade for TTA⁺ and a sub-Nernstian slope of 34.5 mV per decade for HPy⁺ ions. The TTA⁺ ion-selective electrode (ISE) and the HPy⁺-ISE can determine the monomer units down to concentrations as low as 4.0×10⁻⁴M and 1.66×10⁻⁵ M, respectively. The effect of various additives, such as the anionic polyelectrolyte sodium dextran sulfate and macrocyclic β-cyclodextrin, on the surface activity exhibited by the cationic surfactants TTA⁺-DS⁻ and HPy⁺-DS⁻, in the presence of background concentrations of NaCl was also examined with surfactant-selective sensors. The Gibbs free energy of micelle formation (ΔG _m ) of both surfactants in the presence of various additives was calculated and found to be less favorable with respect to an increase in the amount of additives due to less availability of cationic surfactant monomer units. The ion-pair complexes TTA⁺-DS⁻ and HPy⁺-DS⁻ were found to behave as selective carrier compounds in PVC membranes in determining the concentration of monomer units of both TTA⁺ and HPy⁺, respectively. The proposed sensors worked well at a fairly acidic pH of 1–6.5 with response time of 60 s. The sensors responded well to the surfactant ions even in the presence of additives at lower concentration. The lifetime of the sensors is 3 mon.     

Phase‐transfer‐agent‐aided polymerization and graft copolymerization of acrylamide

The use of phase‐transfer catalysts, with water‐insoluble initiators, for polymerization and graft copolymerization reactions was explored. The polymerization of a water‐soluble vinyl monomer, acrylamide (AAm), and the graft copolymerization of AAm onto a water‐insoluble polymer backbone, isotactic polypropylene (IPP), with a water‐insoluble initiator, benzoyl peroxide (BPO), and a phase‐transfer catalyst, tetrabutyl ammonium bromide (Bu₄N⁺Br^?), were carried out in a water/xylene binary solvent system. The conversion percentage of AAm into polyacrylamide (PAAm) and the percentage of grafting of AAm onto IPP were determined as functions of various reaction parameters, such as the BPO, AAm, and phase‐transfer‐catalyst concentrations, the amounts of water and xylene in the water/xylene mixture, the time, and the temperature. The graft copolymer, IPP‐g‐PAAm, was characterized with IR spectroscopy and thermogravimetric analysis. By a comparison of the results of the phase‐transfer‐catalyzed graft copolymerization of AAm onto IPP and the preirradiation method, it was observed that the optimum reaction conditions were milder for the phase‐transfer‐catalyst‐aided graft copolymerization. Milder reaction conditions, including the temperature, the time of reaction, and a moderate initiator (BPO), in comparison with high‐energy γ‐rays, led to better quality products, and the reaction proceeded smoothly with high productivity. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 91: 2364–2375, 2004     

Synthesis,characterization and use of polymer‐supported phase transfer catalyst in organic reactions

A polymer‐supported (PS) phase transfer catalyst, polyethylene‐g‐quaternary ammonium salt (PE‐g‐Q_N⁺), is prepared through a three‐step graft copolymerization of maleic anhydride (MAn) onto polyethylene (PE) by photochemical method using 1% benzophenone (Bz) as photosensitizer. Post grafted acid hydrolysis of polyethylene‐g‐maleic anhydride (PE‐g‐MAn) results in the preparation of PE‐g‐succinic acid which on further treatment with tetrabutylammonium bromide (TBAB) under basic conditions in tetrahydrofuran (THF) gives PE‐g‐Q_N⁺. Optimum conditions pertaining to maximum percentage of grafting have been evaluated as a function of concentration of maleic anhydride, amount of photosensitizer, and time of reaction. Maximum percentage of grafting (25%) was obtained using 3.57 mol of MAn and 0.5 mL of 1% Bz in 120 min. The PE and graft copolymers, PE‐g‐MAn, and PE‐g‐Q_N⁺ were characterized by FTIR Spectroscopy and thermogravimetric analysis (TGA). The ionic nature of quaternary ammonium salt, PE‐g‐Q_N⁺ has also been confirmed by conductance measurements. PE‐g‐Q_N⁺ reagent have been used successfully for polymerization, amidation, and esterification reactions. The products obtained were characterized by FTIR and H¹NMR spectral methods. The reagent was reused for the further reactions and it was observed that the polymeric reagent polymerize, amidate, and esterificate the compounds successfully but with little lower product yield. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Spin valve effect in sputtered FL-MoS2 and ferromagnetic shape memory alloy based magnetic tunnel junction

In the last decade, two-dimensional (2D) transition metal dichalcogenides have been introduced with great significance in the spintronic devices for their extraordinary electrical, optical, and spin-dependent properties. In this work, we have fabricated a few-layer molybdenum disulfide (FL-MoS₂) (~6 nm) as a non-magnetic spacer layer in Ni–Mn–In/FL-MoS₂/Ni–Mn–In magnetic tunnel junction (MTJ) using DC magnetron sputtering. FL-MoS₂ thin film sandwiched between two ferromagnetic shape memory alloy based electrodes exhibit semiconducting behavior, confirmed by current-voltage (I–V) characteristics and temperature dependent resistance measurement. The fabricated MTJ shows spin valve effect in the presence of an external magnetic field. The tunneling magnetoresistance (TMR) has been recorded in 10 K–300 K temperature range. The highest TMR ratio of 0.51% was obtained at a low temperature ~10 K, corresponding to the spin polarization of ~5%. This TMR ratio reduces to a value of 0.032% as the temperature of the device increases up to 300 K, displaying a finite TMR at room temperature. A detailed study of thickness and temperature-dependent magnetization versus magnetic field (M ? H) hysteresis loops of Ni–Mn–In thin films has been performed to understand the complex TMR behavior. The present study paves the way for the use of sputtered FL-MoS₂ and ferromagnetic shape memory alloy in ultrafast spintronics for advanced magnetic devices application.     

Analysis of Fatty Acid and Lignan Composition of Indian Germplasm of Sesame to Evaluate Their Nutritional Merits

An attempt was made to individually analyze a germplasm collection of 54 indigenous Indian sesame cultivars for fatty acid and lignan composition of their seed oil by gas chromatography and high performance liquid chromatography, respectively. The entries varied in their fatty acid and lignan composition. The mean percentage contents of palmitic, stearic, oleic, linoleic and α‐linolenic acids ranged between 10–22, 5–10, 38–50, 18–43 and less than 1 whereas sesamol, sesamin and sesamolin scored between 3–37, 27–67, 20–59 of the total percentage of lignan, respectively. The highest percentage of α‐linolenic acid (ALA) was obtained in Var‐9 (1.3 % of the total fatty acids). Among the lignans, high sesamin content is considered to be significant, particularly in terms of long shelf life and nutraceutical value of sesame seed oil. The study has broadened our understanding related to differential biochemical composition of the rich sesame germplasms, thereby providing us with a useful groundwork for identifying potential targets and suitable cultivars for genetic engineering approaches to be undertaken in order to improve the nutritional quality of sesame oil, which in turn would be beneficial towards human health.     

Synthesis,optimization and characterization of PVA-co-poly(methacrylic acid) green adsorbents and applications in environmental remediation

Polymer Bulletin - The present paper is focused on the synthesis and optimization of a green PVA-co-poly(MAA) adsorbent by free radical polymerization using N,N′-methylene-bis-acrylamide and...     

Polymers from renewable resources: Kinetics studies of the radiochemical graft copolymerization of styrene onto cellulose extracted from pine needles and the effect of some additives on the grafting parameters in an aqueous medium

In an attempt to develop an alternative to petro‐based polymers, we graft‐copolymerized cellulose isolated from the needles of Pinus roxburghii with styrene in a limited aqueous medium in air by simultaneous irradiation using gamma rays as the initiator. The optimum conditions for obtaining maximum grafting were determined as a function of monomer concentration, total dose of irradiation, and amount of water. Maximum percentage of grafting (P_g; 79.9) was obtained at a total dose of 1.152 × 10⁴ Gy with 1.325 × 10^?4 mol of styrene. The effect of methanol, LiNO₃, Cu(NO₃)₂, Mohr's salt, H₂SO₄, HNO₃, and AcOH on P_g was studied. All the additives were found to decrease graft yield, contrary to some reported studies. Total percentage conversion and rates of polymerization, grafting, and homopolymerization were evaluated. Evidence of grafting was provided by the characterization of cellulose and its graft copolymers by Fourier transform infrared spectroscopy, thermogravimetry, and observation of the swelling behavior in some solvents. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 83: 1490–1500, 2002     

Aza-Michael Addition of <Emphasis Type="Italic">γ</Emphasis>-Aminopropylsilatranes to Substituted N-Phenylmaleimides: Design and Synthesis of a Heterocyclic Amine Receptor and Their Preliminary Antimicrobial Studies

An efficient method for C-N bond formation via aza-Michael addition of γ-aminopropylsilatranes to substituted N-phenylmaleimides under mild conditions is described. The five receptors enclosing the maleimide moiety have been synthesized by the aza-Michael addition to strong nucleophile γ-aminopropylsilatrane producing silatranes possessing substituted N-phenylsuccinimide at the axial position without any catalyst. All the compounds have been characterized by elemental analysis, spectroscopic techniques and thermo-gravimetric analysis. The synthesized compounds have been screened for possible antimicrobial properties and results have shown modest activity.     

Moisture Adsorption Isotherms of Watermelon Seed and Kernels

The moisture adsorption isotherms of watermelon seeds and kernels from Citrullus lanatus Cv Mateera and Citrullus vulgaris Cv Sugar baby were obtained using standard static method with saturated salt solutions over a range of water activities from 0.113 to 0.92 at 20–60°C. The adsorption capacity of seeds decreased with the increase in temperature at constant water activity. Sorption models were used to explain the adsorption behavior involving water activity and moisture content (Type I) and also temperature (Type II). Oswin's models gave best fit among Type I with coefficient of determination of 0.953–0.995, standard error of 0.031–0.0571, mean relative error of 0.071–0.152, and scattered residual plots. Modified Oswin was the best fit model among Type II for the seeds and kernels of both the cultivars with coefficient of determination of 0.997–0.999, standard error of 0.151–0.255, mean relative error of 0.018–0.244, and scattered residual plots. The net isoelectric heat of adsorption, estimated from Clausius-Clapeyron decreased from about 27.0 to 0.5 kJ/mol in kernels and 18.0 to 0.5 kJ/mol in seeds of both the cultivars as the moisture content increased from 5 to 25% (dry basis).