Methacrylate-functionalized POSS influence on cross-linking and mechanical properties of styrene-butadiene rubber

Iranian Polymer Journal - The addition of methacrylate-functional polyhedral oligomeric silsesquioxane (MA-POSS) nanoparticles to styrene-butadiene rubber (SBR) composites was evaluated in terms of...     

Investigation of the Equivalence of National Dew-Point Temperature Realizations in the ?50?°C to +?20?°C Range

In the field of humidity quantities, the first CIPM key comparison, CCT-K6 is at its end. The corresponding European regional key comparison, EUROMET.T-K6, was completed in early 2008, about 4?years after the starting initial measurements in the project. In total, 24 NMIs from different countries took part in the comparison. This number includes 22 EURAMET countries, and Russia and South Africa. The comparison covered the dew-point temperature range from ?50?°C to +20?°C. It was carried out in three parallel loops, each with two chilled mirror hygrometers as transfer standards in each loop. The comparison scheme was designed to ensure high quality results with evenly spread workload for the participants. It is shown that the standard uncertainty due to the long-term instability was smaller than 0.008?°C in all loops. The standard uncertainties due to links between the loops were found to be smaller than 0.025?°C at ?50?°C and 0.010?°C elsewhere. Conclusions on the equivalence of the dew-point temperature standards are drawn on the basis of calculated bilateral degrees of equivalence and deviations from the EURAMET comparison reference values (ERV). Taking into account 16 different primary dew-point realizations and 8 secondary realizations, the results demonstrate the equivalence of a large number of laboratories at an uncertainty level that is better than achieved in other multilateral comparisons so far in the humidity field.     

Power‐law conductivity in polythiophene/copper(II) acetylacetonate composites

This paper reports the charge transport mechanism of polythiophene (PT) matrix composites having various concentrations of copper(II) acetylacetonate. Characterization and structural analyses of the samples were carried out via Fourier transform infrared spectroscopy, atomic absorption spectroscopy, differential scanning calorimetry, thermogravimetric analysis and scanning electron microscopy (SEM). The alternating current electrical properties were investigated as a function of temperature. The change of free energy of adsorption calculated from the Langmuir adsorption isotherm showed that metal ions were electrostatically adsorbed onto polymer chains. Significant morphological changes were observed from SEM images of PT depending on doping process which in turn affected the thermal degradation of PT. The charge transport mechanism determined from a power law showed that there was one frequency‐dependent conductivity region for PT, while there were two regions for the composites in contrast to studies reported in the literature. © 2013 Society of Chemical Industry     

Formulation studies for mirtazapine orally disintegrating tablets

Abstract

Objective: Orally disintegrating tablets (ODTs) recently have gained much attention to fulfill the needs for pediatric, geriatric, and psychiatric patients with dysphagia. Aim of this study was to develop new ODT formulations containing mirtazapine, an antidepressant drug molecule having bitter taste, by using simple and inexpensive preparation methods such as coacervation, direct compression and to compare their characteristics with those of reference product (Remereon SolTab).

Materials and methods: Coacervation method was chosen for taste masking of mirtazapine. In vitro characterization studies such as diameter and thickness, weight variation, tablet hardness, tablet friability and disintegration time were performed on tablet formulations. Wetting time and in vitro dissolution tests of developed ODTs also studied using 900?mL 0.1?N HCl medium, 900?mL pH 6.8 phosphate buffer or 900?mL pH 4.5 acetate buffer at 37?±?0.2?°C as dissolution medium.

Results: Ratio of Eudragit® E-100 was chosen as 6% (w/w) since the dissolution profile of A1 (6% Eudragit® E-100) was found closer to the reference product than A2 (4% Eudragit® E-100) and A3 (8% Eudragit® E-100). Group D, E and F formulations were presented better results in terms of disintegration time. Dissolution results indicated that Group E and F formulations showed optimum properties in all three dissolution media.

Discussion: Formulations D1, D4, D5, E3, E4, F1 and F5 found suitable as ODT formulations due to their favorable disintegration times and dissolution profiles.

Conclusion: Developed mirtazapine ODTs were found promising in terms of showing the similar characteristics to the original formulation.     

Comprehensibility of universal healthcare symbols for wayfinding in healthcare facilities

Healthcare facilities are often complex and overwhelming for visitors, and wayfinding in healthcare facilities can be challenging. As there is an increasing number of global citizens who travel to seek medical care in another country, it is critical to make wayfinding easy for visitors who are not familiar with the language in a foreign country. Among many wayfinding aids, symbols are helpful for those visitors who have limited ability to understand written language. This study tested universal healthcare symbols in the United States, South Korea, and Turkey to compare the comprehension of symbols cross-country and identify predictors of the correct comprehension. To explore statistically significant relationships between symbol comprehension and countries, Pearson's Chi-square tests, logistic regression, and ANOVA were conducted. The test results showed that ten symbols among 14 tested have significant relationship with countries. Results of this study demonstrate that symbol comprehension can be varied significantly in different countries.     

Tungsten(VI) oxide supported rhodium(0) nanoparticles; highly efficient catalyst for H2 production from dimethylamine borane

It reports the preparation and characterization of tungsten(VI) oxide supported rhodium(0) nanoparticles (Rh⁰/WO₃ NPs) being used as catalysts in releasing H₂ from dimethylamine borane (DMAB). The reducible nature of WO₃ plays a significant role in the catalytic efficiency of rhodium(0) nanoparticles in the dehydrogenation of DMAB. The Rh⁰/WO₃ NPs were in-situ generated from the reduction of Rh²⁺ ions on the surface of WO₃ during the catalytic dehydrogenation of dimethylamine borane in toluene and isolated from the reaction solution after the dehydrogenation to be characterized by using SEM, TEM, XPS, ATR-IR and XRD. The results reveal the formation of Rh⁰ NPs with a mean particle size of 1.92 ± 0.34 nm dispersed on the surface of tungsten(VI) oxide. Rh⁰/WO₃ NPs are found to be very active catalyst releasing 1.0 equiv. H₂ per mole of dimethylamine borane under ambient conditions. Among the various WO₃ supported Rh⁰ NPs with different metal loadings, the sample with 0.1% wt. Rh provide the record catalytic activity (TOF = 2816 h^?1) which is one of the highest value ever reported for rhodium-based catalysts in H₂ generation from DMAB at 60.0 ± 0.5 °C. Rh⁰/WO₃ NPs were also reusable catalyst in dehydrogenation of DMAB retaining 55% of their initial catalytic activity in the 3rd run of the dehydrogenation reaction. Control experiments were performed at various catalyst concentrations and temperatures to investigate the kinetics of dehydrogenation and to calculate the activation parameters for the reaction.     

Prioritization methodology of dangerous substances for water quality monitoring with scarce data

Monitoring and control of dangerous substances discharged into receiving waters have attracted more attention lately. Since it is not possible to analyze every single substance, a prioritization methodology is needed for the selection of those to be monitored. Existing well-developed models require significant amount of data for reliable outcomes. This paper presents a methodology to prioritize the dangerous substances having adverse effects on freshwaters in Turkey, where data are scarce. Such a methodology will also serve as a solid model for other countries with limited background data. The adopted methodology enabled the elimination of chemicals to generate a candidate list composed of 608 substances among more than 5000 substances. Further screening and prioritization were conducted using different assessment methods (i.e., Total Hazard Value, Total Impact Value, Combined Monitoring-based, and Modelling-based Priority Setting) to obtain a proposed Final Candidate Specific Pollutants List of 150 dangerous substances. The proposed Candidate National Pollutant List of Turkey was established by combining 45 priority pollutants of the European Union with a list of candidate specific pollutants. According to the outcomes of this study, monitoring and controlling of 195 dangerous substances in freshwaters are recommended. Further detailed studies should be conducted in order to observe the actual levels of these dangerous substances in freshwaters followed by a review of the monitoring list accordingly. Moreover, further revisions might be required in the proposed list due to some possible versatile conditions in terms of sampling points (i.e., change in the location of industries).     

Comparison of additive effects on the PVA/starch cryogels: Synthesis,characterization, cytotoxicity,and genotoxicity studies

The research goal of this study is to produce suitable scaffolds for tissue engineering applications. Different ratios of polyvinyl alcohol (PVA)/starch (90:10, 70:30, 50:50) and crosslinking methods have been used to prepare cryogels. Chemically crosslinked cryogels were synthesized using glutaraldehyde as the crosslinking agent. For the physically crosslinked cryogels, sodium dodecyl sulfate was used during cryogelation as the foaming agent. Chemical structure and pore morphology were demonstrated by Fourier transform infrared spectroscopy and scanning electron microscopy (SEM). Swelling ratio and degradation profile of the scaffolds were also determined. 3-(4,5-dimethylthiazoyl-2-yl)-2,5-diphenyltetrazolium bromide assay and SEM were used to investigate the biocompatibility of the scaffolds and cell morphology. Genotoxicity test was performed to show DNA fragmentation. The overall results demonstrated that PVA/starch cryogels could have potentially appealing application as scaffolds for tissue engineering applications and additives affect the architecture and characteristic properties of the cryogels.