Delayed release matrix pellet preparation containing an alkalizing pore-former agent

The aim of this study was to develop a delayed-release matrix pellet containing atenolol as active pharmaceutical ingredient. The matrix additionally contained trisodium phosphate dodecahydrate as alkalizing pore-former agent to enhance the dissolution of the atenolol at pH 6.8. The delayed release was ensured by coating with a gastro-resistant polymer. For this purpose, an acryl EZE MP aqueous dispersion was used, which is suggested in the literature for pellet coating. Before this functional film coating, a protective polymer layer was developed, to prevent direct contact between the alkalizing layer and the acryl EZE. The results of in vitro dissolution tests demonstrated that the double-coated pellet preparation is a delayed-release solid dosage form.     

Dendrimer finishing influence on CO/PES blended fabrics color assessment

Textile finishing includes all processes that help to maintain the value or increase the value of the textile material. It encompasses dyeing, printing, and all the finishing treatments to realize durable press, soil release, flame retardant, antistatic, antimicrobial, or water/oil repellency properties. When these properties are realized on dyed textile fabric, one effect could be ascribed to the color change induced by finishing operations. This research focuses on the assessment of color alterations occurring on the dyed cotton/polyester blended fabrics due to the nanoparticle‐sized dendrimer (DWR), dendrimer–fluorocarbon (DWOR), and fluorocarbon (FWOR) finishing onto their surfaces. The dependence of color on the surface state of treated textiles is calculated in the context of spectrophotometric measurements. Modification of the surface roughness by reflectance spectrum and the absorbance of finishes in visible range were investigated to determine color changes between the original (control fabric, dyed but not treated) and treated fabrics. As a result of color matching calculated by CIE‐Lab values, color change is related to the surface roughness associated with absorbance values of applied finishes. In addition, fabrics mechanical properties were evaluated to estimate if finishing agents application gives rise to other changes, besides color alterations. The fabrics mechanical properties have been found not significantly altered by the aforementioned finishing treatments. These results could be applied for industrial needs (quality control), or in the artistic field of conservation, or restoration (to follow the color of paintings). © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Analysis of solution polybutadiene polymerizations performed with a neodymium catalyst

This article is regarding the polymerization of 1,3‐butadiene with a neodymium catalyst activated by diisobutylaluminum‐hydride and diethylaluminum chloride (DEAC). The effects of the polymerization conditions (ratio between DEAC and neodymium molar concentrations, polymerization temperature, catalyst concentration, and butadiene concentration) on the polymer yield and molecular weight distribution (MWD) of polybutadiene (PB) samples were evaluated. It is shown that the DEAC/Nd ratio and the polymerization temperature are the reaction variables that influence the MWD and the catalyst performance most significantly. PBs with broad and sometimes bimodal MWD were produced at the analyzed reaction conditions. For this reason, the MWD of the obtained polymer materials was deconvoluted with the help of the Flory most probable distribution, indicating that three or more catalyst sites are required to explain the final MWD of the polymer samples. Finally, it was observed that the analyzed neodymium catalyst is able to produce branched PBs at mild reaction conditions and that the branching frequency depends on the polymerization conditions, which may be useful for development of operation policies at plant site and production of materials with improved performances. POLYM. ENG. SCI., 2011. © 2010 Society of Plastics Engineers     

Measurement and numerical prediction of fiber‐reinforced thermoplastics' thermal conductivity in injection molded parts

Recent improvements in injection molding numerical simulation software have led to the possibility of computing fiber orientation in fiber reinforced materials during and at the end of the injection molding process. However, mechanical, thermal, and electrical properties of fiber reinforced materials are still largely measured experimentally. While theoretical models that consider fiber orientation for the prediction of those properties exist, estimating them numerically has not yet been practical. In the present study, two different models are used to estimate the thermal conductivity of fiber reinforced thermoplastics (FRT) using fiber orientation obtained by injection molding numerical simulation software. Experimental data were obtained by measuring fiber orientation in injection molded samples' micrographs by image processing methods. The results were then compared with the numerically obtained prediction and good agreement between numerical and experimental fiber orientation was found. Thermal conductivity for the same samples was computed by applying two different FRT thermal conductivity models using numerically obtained fiber orientation. In the case of thermal conductivity, predicted results were consistent with experimental data measurements, showing the validity of the models. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 39811.     

MS和MSE的特性及其在化妆品中的应用

本文较详细地介绍了甲基葡萄糖苷倍半硬脂酸酯（MS）和聚氧乙烯（20EO）甲基葡萄糖苷倍半硬脂酸酯（MSE）的结构、合成、质量指标和特性及其在化妆品中的应用。     

化工专业《试验设计与数据处理》教学方法探讨

经过几十年的发展与实践,试验设计与数据处理在我国经济发展中的重要性有目共睹。目前,大多数高校化学相关专业的本科生和研究生均开设了这门工具课。本文从教材的选择、教学内容、教学方式和课程考查方式等几方面进行了探讨。探讨该课程的教学方法,有利于激发学生的学习热情和学习兴趣,从而提高教学质量。     

Structural symmetry breaking of silicon‐containing poly(amide‐imide) oligomers and its relation to electrical conductivity and Raman‐active vibrations

Optically active poly(amide‐imide) oligomers were synthesized by direct polycondensation between an aromatic diamine and a dicarboxylic acid both containing a diphenylsilylene unit. The reaction was carried out using triphenyl phosphite/pyridine in the presence of CaCl₂ and N‐methyl‐2‐pyrrolidone as solvent. Oligomers were obtained in good yields and showed high solubility in common aprotic polar solvents. The precursors, monomers and poly(amide‐imide) oligomers were characterized using elemental analysis and Fourier transform infrared and NMR (¹H, ¹³C, ²⁹Si) spectroscopy. Additionally, the main vibrations of the functional groups (C?O, C?C or N? H) in the oligomers with respect to temperature were characterized using Raman spectroscopy. The glass transition temperature was determined by studying the Raman spectra and corroborated using differential scanning calorimetry. The thermal stability was studied using thermogravimetric analysis. The molecular mass of the compounds was obtained from matrix‐assisted laser desorption ionization time‐of‐flight mass spectrometry and their optical properties were analyzed using UV‐visible diode array spectrophotometry. The electronic properties of the oligomers as well as the delocalization of charge carriers within their structures were analyzed using conductance‐voltage curves, which showed that these materials are excellent candidates for integrated optoelectronic applications. Copyright © 2011 Society of Chemical Industry     

Thiophene‐ and silarylene‐containing polyesters. Resonance effect on conductivity after polarization in an external electric field

Polyesters were synthesized by direct polycondensation of thiophene‐2,5‐dicarboxylic acid and five different silarylene‐containing diphenols using a tosyl chloride/pyridine/N,N‐dimethylformamide system as a condensing agent. Polymers were obtained in good yields and were characterized using Fourier transform infrared and NMR (¹H, ¹³C, 135‐DEPT and ²⁹Si) spectroscopy and elemental analysis. All polymers were completely soluble in aprotic organic polar solvents such as dimethylformamide, dimethylsulfoxide and N‐methyl‐2‐pyrrolidone. The range of effective mass of the polymers (m/z) was 1 × 10⁵–2 × 10⁵, determined using electrospray ionization mass spectrometry. Asymmetry and steric hindrance prevented dense packing of the polymeric chains, showing glass transition temperatures between ? 78 and ? 51 °C and loss of thermal stability at 177–199 °C (10% weight loss). Additionally, the melting points of the polyesters were found to be in the range 62–67 °C. Because of this, the samples were semi‐solid at room temperature. The optical band gaps of the polymers were observed between 4.54 and 4.48 eV, corresponding in all cases to insulator behavior. The molecular structure of the samples was studied using X‐ray diffraction, showing a degree of order that was associated with two monoclinic lattices. Additionally, the conductivity was studied using a two‐point method with contacts on top of polymer films. Prior to the electrical measurement, the samples were polarized in an external electric field of 0.8 to 6.4 V cm^?1, and the alignment of the dipoles increased the electrical conductivity. Copyright © 2012 Society of Chemical Industry