In this study, the effect of activator ZnO and heating time at 190 C on foaming, gelation, and dehydrochlorination of poly(vinyl chloride) (PVC) plastisol was investigated. For this purpose, a PVC plastisol was prepared by mixing PVC, dioctyl phthalate (DOP), azodicarbonamide (ADC), ZnO, and the heat stabilizers calcium stearate (CaSt 2 ) and zinc stearate(ZnSt 2 ). PVC plastisol films were heated for 3, 6, 12, and 24 min periods at 190 C to see the effect of heating time on the gelation and foaming processes of the PVC foam. The time of 12 min was determined to be optimum for the completion of gelation and foaming processes without thermal degradation of PVC. No foaming was observed under the same conditions for the samples without ZnO. ZnO had a significant catalytic effect on ADC decomposition, accelerating the foaming of the films. Average porosity measurement showed a consistent increase in porosity with heating time up to 76% and the average density decreased from 1.17 to 0.29 g/cm 3 on foaming. Tensile tests showed that the tensile strength and tensile strain both increased considerably up to 0.98 MPa and 207%, respectively, with heating time and the elastic modulus was seen to gradually decrease from 4.7 to 0.7 MPa with heating time. Films without ZnO had higher tensile strength since there were no pores. PVC thermomat tests showed that ZnO lowered the stability time of plastigel film with azodicarbonamide.
The aqueous phase adsorption of fuel oxygenates methyl tertiary butyl ether (MTBE) and ethyl tertiary butyl ether (ETBE) onto commercially available granular activated carbon (GAC; Norit GAC 1240) was investigated in a batch system at 27°C. The oxygenate concentrations were determined by headspace gas chromatography/mass spectrometry analyses. The experimental data were used with four two-parameter isotherm models (Langmuir, Freundlich, Temkin, and DubininRadushkevich) and two kinetic models (pseudo firstorder and pseudo second-order) to determine equilibrium and kinetic parameters. Considering the correlation coefficient and root mean square error, Dubinin-Radushkevich isotherm showed better fit with the equilibrium data for MTBE. However, the performances of Langmuir and Dubinin-Radushkevich models were comparable for ETBE. The adsorption capacities were calculated as 5.50 and 6.92 mg/g for MTBE and ETBE, respectively, at an equilibrium solution concentration of 1 mg/L using Dubinin-Radushkevich isotherm. The differences between the model predictions and experimental data were similar for the pseudo first-order and pseudo secondorder kinetic models. Gibbs free-energy changes of adsorption were found to be −22.59 and −28.55 kJ/mol for MTBE-GAC and ETBE-GAC systems, respectively, under the experimental conditions studied.
DNA adsorption is the initial stage of gene therapy for drug delivery systems and solid phase extraction methods of DNA purification. High pore volume and high adsorption capacity are simple requirements not only for producing 'smart' drug delivery systems but also the development of purification kits. Silica is the most used material for this purpose. The present study aimed at elucidating the calf thymus DNA biosorption process by the characterization of calf thymus DNA and silica to increase the efficiency of the currently used silica material. Mesoporous silica has long been used for DNA adsorption and silica aerogel is the new adsorbent investigated in the present study. When DNA solution was freeze dried on a silica wafer, self-assembled super helices formed as shown by atomic microscopy (AFM). Thus DNA existed not as single molecules but as large sized agglomerates in water. Thus it could be adsorbed in the macropores and on the external surface of adsorbents. Adsorption of calf thymus DNA to a silica aerogel, a mesoporous silica gel and a silica wafer was investigated in the present study. Silica aerogel was synthesized from TEOS by a supercritical ethanol drying process. The DNA adsorption capacity of the silica aerogel was nearly two times that of the mesoporous silica gel due to its macroporous structure and its higher silanol content. Silica aerogel was found to be a very promising material for DNA adsorption. Therefore silica aerogel can be considered as a good candidate for the delivery of DNA.
Flexible PVC films are statically charged due to their low electrical conductivity. This creates fire threat during its handling. Conductive materials are added to films to prevent this. In the present study it was aimed to prepare PVC- copper composite films by sol gel technique and characterize the prepared films. It was aimed to increase the electrical conductivity of the films by adding copper powder. However, the copper particles settled down to bottom instead of forming a conductive network that covers the whole cross section. Thus at the film cross-section a plastic upper phase and a copper rich lower phase were present. The film did not conduct electricity due to this uneven distribution. The minimum volumetric and surface resistivities of the films were at the order of 109 ohm-cm and 1010 ohm square respectively.
Methylene blue (MB) adsorption studies were performed with poly(vinyl chloride)-(dioctyl phthalate)-silica composites, which were obtained by using plastisol-plastigel technology. The films were flexible, having elastic modulus of 1.0-1.5 GPa. Diminishing MB concentration in the aqueous phase was followed as the adsorption process advanced by using visible spectroscopy. Contributions of the individual components of the composites to adsorption were also investigated. Although the MB adsorption capacity was extensively high for silica, it was moderate for the composite, most likely owing to the occlusion of pores of silica by plasticizer to some extent. The improvement of MB adsorption capacity of the composites as the silica ratio increased was explicitly deduced from the optical microscopy photographs. The diffusion coefficients of MB through the composites were 5 3 10 213 , 6 3 10 213 , and 3 3 10 213 m 2 s 21 with regression coefficients of 0.73, 0.89, and 0.88 for 0, 2, and 16% silica-containing composites, respectively. Because of the slow diffusion of MB in poly(vinyl chloride)-silica composites, using them as dynamic column adsorbent was not practical. However, these versatile plastics can be used as plastic labels, colored clothing, leather substitutes, antimicrobial medical devices, and laser printable surfaces. J. VINYL ADDIT. TECHNOL., 21:42-50, 2015.
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