Studies on the copolymerization of methyl methacrylate with N‐(o/m/p‐chlorophenyl) itaconimides

The article describes the synthesis and characterization of N‐aryl itaconimide monomers such as: N‐(p‐chlorophenyl) itaconimide (PI)/N‐(m‐chlorophenyl) itaconimide (MI)/N‐(o‐chlorophenyl) itaconimide (OI) and its copolymerization behavior with MMA. The homopolymers and copolymers of N‐aryl itaconimides and methyl methacrylate (MMA, M₂) were synthesized by varying the mol fraction of N‐aryl itaconimides in the initial feed from 0.1 to 0.5 using azobisisobutyronitrile (AIBN) as an initiator and tetrahydrofuran (THF) as the solvent. Copolymer composition was determined using ¹H‐NMR spectroscopy [by taking the ratio of intensities of signals due to ? OCH₃ of MMA (δ = 3.59 ppm) and the aromatic proton (δ = 7.2–7.5 ppm) of N‐aryl itaconimides] and percent nitrogen content. The reactivity ratios were found to be r₁ = 1.33 and r₂ = 0.36 (PI‐MMA) r₁ = 1.15 and r₂ = 0.32 (MI‐MMA) and r₁ = 0.81 and r₂ = 0.35 (OI‐MMA). Molecular weight as determined using high‐performance liquid chromatography decreased with increasing mol fraction of itaconimides in copolymers. All the polymers had a polydisperstivity index in the range of 1.5–2.6.Thermal characterization was done using differential scanning calorimetry and dynamic thermogravimetry in nitrogen atmosphere. Incorporation of these N‐aryl itaconimides in PMMA backbone resulted in an improvement in glass transition temperature (T_g) and thermal stability. Percent char increased with the increase of PI/MI/OI content in the copolymers. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 82: 2078–2086, 2001     

Optimization of Lithium Content and Sintering Aid for Maximized Li+ Conductivity and Density in Ta‐Doped Li7La3Zr2O12

Ta‐doped cubic phase Li₇La₃Zr₂O₁₂ (LLZ) lithium garnet received considerable attention in recent times as prospective electrolyte for all‐solid‐state lithium battery. Although the conductivity has been improved by stabilizing the cubic phase with the Ta⁵⁺ doping for Zr⁴⁺ in LLZ, the density of the pellet was found to be relatively poor with large amount of pores. In addition to the high Li⁺ conductivity, density is also an essential parameter for the successful application of LLZ as solid electrolyte membrane in all‐solid‐state lithium battery. Systematic investigations carried out through this work indicated that the optimal Li concentration of 6.4 (i.e., Li_6.4La₃Zr_1.4Ta_0.6O₁₂) is required to obtain phase pure, relatively dense and high Li⁺ conductive cubic phase in Li_7?xLa₃Zr_2?xTa_xO₁₂ solid solutions. Effort has been also made in this work to enhance the density and Li⁺ conductivity of Li_6.4La₃Zr_1.4Ta_0.6O₁₂ further through the Li₄SiO₄ addition. A maximized room‐temperature (33°C) total (bulk + grain boundary) Li⁺ conductivity of 3.7 × 10^?4 S/cm and maximized relative density of 94% was observed for Li_6.4La₃Zr_1.4Ta_0.6O₁₂ added with 1 wt% of Li₄SiO₄.     

Synthesis of urea-pyridyl ligand functionalized mesoporous silica hybrid material for hydrophobic and hydrophilic drug delivery application

In this work, we propose the synthesis of urea-pyridyl (UPy) ligand functionalized mesoporous silica hybrid material as novel and effective drug delivery system for loading/release of both hydrophobic and hydrophilic drugs. For the synthesis of UPy ligand functionalized mesoporous silica hybrid material, the combination of sol–gel co-condensation technique and post silica surface modification method were adapted. The prepared UPy ligand functionalized mesoporous silica hybrid (UPy-MSH) material was characterized by X-ray diffraction, Fourier-transform infrared, N₂ adsorption–desorption analysis. The material morphology and mesopore channels were observed by scanning and transmission electron microscopic analyses. The content of modified organic ligand functionalities present in the UPy-MSH material surface was determined by thermogravimetric analysis. The hydrophilic anticancer drug, 5-Fluorouracil and the hydrophobic anti-inflammatory drug, Ibuprofen was used as a model drugs to determine the loading and pH-responsive release efficiency of the synthesized UPy-MSH material under different pH (pH 7.4 and 5.0) conditions, respectively. In addition, the biocompatibility of the UPy-MSH material was evaluated on MDA-MB-231 cells. The experimental results depicted that the synthesized UPy-MSH material is biocompatible and has high drug loading capacity, selective and controlled release of specific drug with respect to the pH condition.     

Citrulline malate supplementation does not improve German Volume Training performance or reduce muscle soreness in moderately trained males and females

Background

Use of supplements to aid performance is common practice amongst recreationally active individuals, including those without a sufficient evidence base. This investigation sought to assess whether acute supplementation with 8 g of citrulline malate (CM) (1.11: 1 ratio) would improve anaerobic performance.

Methods

A randomised double blind placebo control trial was employed, using a counterbalanced design. We recruited recreationally active men and women to take part in an isokinetic chair protocol, based on German Volume Training (GVT) whereby participants attempted to perform 10 sets of 10 repetitions against a force representing 70% of their peak concentric force.

Results

The number of repetitions achieved over the course of the GVT was 94.0?±?7.9 and 90.9?±?13.9 for placebo and CM respectively. There was no significant difference between the placebo and CM treatment for number of repetitions (P?=?0.33), isometric (P?=?0.60), concentric (P?=?0.38), or eccentric (P?=?0.65) peak force following the GVT. Total muscle soreness was significantly higher in the CM compared to the placebo treatment following the GVT protocol over 72 h (P?=?0.01); although this was not accompanied by a greater workload/number of repetitions in the CM group.

Conclusions

We conclude that an acute dose of CM does not significantly affect anaerobic performance using an isokinetic chair in recreational active participants. Practical implications include precaution in recommending CM supplementation. Coaches and athletes should be aware of the disparity between the chemical analyses of the products reviewed in the present investigation versus the manufacturers’ claims.

     

A novel method of unburned hydrocarbons and NOx gases capture from vehicular exhaust using natural biosorbent

Automobile emissions are composed of NO_x and unburned hydrocarbon that contribute significantly to major environmental and health issues. In this study, encapsulated Moringa oleifera beads (EMBs) were synthesized using Moringa oleifera pod powder that was cross-linked with calcium alginate and used as a biosorbent for reducing the emission gas concentrations from the single-cylinder diesel engine. The breakthrough curve was attained from single and double stage of fixed bed column by the influence of temperature ranging from (80°C–120°C) ± 5°C with a feed flow rate varying from 8 to 10 kg hr^–1 and bed height varying from 15 to 30 cm. Based on the experimental results, the maximum biosorption capacity (q_o) was found to be 14.45 and 123.51 mg g^–1 for HC and NO_x, respectively, and was obtained at 80°C–90°C with double stage of BH–30cm under flow rate of 8 kg hr^–1. Further, breakthrough curves were investigated, and the experimental data were fitted using well-established models like Thomas, Yoon–Nelson, and Wang models. In addition, mass transfer models like Weber–Morris and Boyd were investigated to identify the rate-limiting step of the overall biosorption process.     

Isolation of High Oleate Recombinants in Peanut by Near Infra‐Red Spectroscopy and Confirmation With Allele Specific Polymerase Chain Reaction Marker

Near infrared (NIR) spectrophotometer offers rapid, noninvasive, nondestructive, and high‐throughput phenotyping of seed samples for use in agriculture and industry. In this study, a reflectance‐based NIR spectrophotometer was calibrated and used for the isolation of desirable higher‐oleic‐acid peanut recombinants from single‐seed‐derived segregating populations at F₇ and F₈ generations. A calibration model was developed through partial least‐square regression using wet chemistry data from 158 peanut genotypes. Desirable prediction for oil, palmitic acid, oleic acid, and linoleic acid in intact seed was obtained based on this calibration. It detected significant high correlations (r) and coefficient of determination (R²) between the actual gas chromatography values and NIR predicted values of fatty acid profile in another 123 peanut genotypes that were generated from crosses involving a high‐oleate mutant and Spanish bunch varieties with early maturity. From this recombinant single‐seed‐derived progenies, 15 higher‐oleate recombinants were isolated and later genotyped through an in‐house developed polymerase chain reaction‐based allele specific marker. The present study has generated high‐oleate peanut recombinants with early maturity in Spanish bunch background. The breeding materials generated here will be evaluated for yield attributing traits at different locations in future.     

Structural,magnetic, and textural properties of iron oxide-reduced graphene oxide hybrids and their use for the electrochemical detection of chromium

Superparamagnetic Fe₃O₄ nanoparticles were anchored on reduced graphene oxide (RGO) nanosheets by co-precipitation of iron salts in the presence of different amounts of graphene oxide (GO). A pH dependent zeta potential and good aqueous dispersions were observed for the three hybrids of Fe₃O₄ and RGO. The structure, morphology and microstructure of the hybrids were examined by X-ray diffraction, transmission electron microscopy (TEM), Fourier transform infrared spectroscopy, Raman and X-ray photoelectron spectroscopy. TEM images reveal lattice fringes (d₃₁₁ = 0.26 nm) of Fe₃O₄ nanoparticles with clear stacked layers of RGO nanosheets. The textural properties including the pore size distribution and loading of Fe₃O₄ nanoparticles to form Fe₃O₄–RGO hybrids have been controlled by changing the concentration of GO. An observed maximum (～10 nm) in pore size distribution for the sample with 0.25 mg ml^?1 of GO is different from that prepared using 1.0 mg ml^?1 GO. The superparamagnetic behavior is also lost in the latter and it exhibits a ferrimagnetic nature. The electrochemical behavior of the hybrids towards chromium ion was assessed and a novel electrode system using cyclic voltammetry for the preparation of an electrochemical sensor platform is proposed. The textural properties seem to influence the electrochemical and magnetic behavior of the hybrids.     

Transport phenomena in the electrodeionization of cesium from AMP-PAN

Electrodeionization (EDI) of cesium from cesium-sorbed ammonium molybdophosphate-polyacrylonitrile (AMP-PAN) was investigated by passing eluant through the packed bed of ion-exchange resin in an electrodialysis cell. The deionized cesium from the packed bed was recovered in catholyte by migration and in the eluant by convection. Recovery percentage of Cs by migration increased while the recovery by convection decreased with increase in current density from 20 to 40 mA/cm². Increased eluant concentration resulted in low migration percentage of cesium. Increased catholyte concentration had a negligible effect on total recovery. Apparent diffusion coefficients evaluated using the Nernst–Plank relation increased with increase in current density and catholyte concentration while a decreasing trend was observed with increase in eluant concentration.     

Modeling Critical Air Exchange Rates (CAERs) for aerosol number concentrations from nano-particle sources using an “effective coagulation coefficient” approach

An important issue in the context of air pollution by indoor combustion sources pertains to the joint effect of source strength, coagulation, and ventilation rate on the ultrafine particle exposure metrics. It was recently predicted by detailed numerical analysis of the Smoluchowski coagulation equation with continuous source and sink terms that the ultrafine particle number, mass, and surface area concentrations do not monotonically decrease with increasing air exchange rate, but display peak concentrations at certain Critical Air Exchange Rates (CAERs). As these results are of considerable significance for exposure assessment as well as for implementing particle control technologies, it is necessary to assess the CAER for different aerosol characteristics. Given the fact that the numerical method of solving coagulation equation with realistic Fuchs kernel is computationally intensive, simpler semi-analytical approaches are desired for providing reasonable estimates of CAER and clearer insight into the counter-intuitive, peaking behavior. In this article, we present such an approach by replacing the Fuchs kernel by a spectrum-averaged effective coagulation coefficient, within the framework of the steady-state model. The effective coagulation coefficient is size independent but depends implicitly on the aerosol concentration thus capturing the combined effect of coagulation and removal processes. The number concentrations obtained from this method have been compared and validated against the numerical solutions. The model predicts more pronounced effects on the peaking behavior as well as larger CAER values for fractal particles as compared to compact particles. The results are further discussed.

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