Chemical Engineering / Kimya Mühendisliği
Permanent URI for this collectionhttps://hdl.handle.net/11147/14
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Article Citation - WoS: 15Citation - Scopus: 18Preparation and Characterization of Magnesium Stearate, Cobalt Stearate, and Copper Stearate and Their Effects on Poly(vinyl Chloride) Dehydrochlorination(John Wiley and Sons Inc., 2015) Gönen, Mehmet; Egbuchunam, Theresa Obuajulu; Balköse, Devrim; İnal, Fikret; Ülkü, SemraPreparation and characterization of pure metal soaps and investigation of their effects on poly(vinyl chloride) (PVC) dehydrochlorination were the objectives of the present study. Magnesium stearate (MgSt2), cobalt stearate (CoSt2), and copper stearate (CuSt2) were prepared by a precipitation method. An aqueous sodium stearate (NaSt) solution was mixed at 500 rpm with respective metal salt solutions at 75oC. The precipitates that formed were collected by filtration, washed with water, and ultimately dried at 105oC under reduced pressure. Lamellar crystals that melted on heating were obtained. Solid-liquid phase transitions were observed by optical microscopy at 160oC, 159oC, and 117oC for MgSt2, CoSt2, and CuSt2, respectively. However, the melting points of MgSt2, CoSt2, and CuSt2 were determined as 115oC, 159oC, and 111oC, respectively, by analysis by differential scanning calorimetry. The onset temperature of the mass loss was the lowest at 255oC for CuSt2 and the lowest activation energy for thermal decomposition was 18 kJ/mol for CuSt2. CoSt2 was effective in extending the induction time of PVC dehydrochlorination at both 140oC and 160oC. The activation energy calculated from stability time decreased from 175 kJ/mol for a blank PVC sample to 114, 105, and 107 kJ/mol for MgSt2, CoSt2, and CuSt2-containing PVC samples, respectively. All three metal soaps accelerated the dehydrochlorination of PVC. J. VINYL ADDIT. TECHNOL., 21:235-244, 2015.Article Citation - WoS: 5Citation - Scopus: 5Methylene Blue Adsorption From Aqueous Solutions To Flexible Poly(vinyl Chloride) Silica Composites(John Wiley and Sons Inc., 2015) Yetgin, Senem; Ulutan, Sevgi; Balköse, DevrimMethylene 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 × 10-13, 6 × 10-13, and 3 × 10-13 m2 s-1 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.Conference Object Citation - WoS: 22Citation - Scopus: 24Characterization of Poly(vinyl Chloride) Powder Produced by Emulsion Polymerization(Springer Verlag, 2010) Atakul Savrık, Sevdiye; Balköse, Devrim; Ulutan, Sevgi; Ülkü, SemraThe effect of emulsion process formulation ingredients on the morphology, structure, and properties of polyvinyl chloride (PVC) powder has been considered in this study. PVC powder was extracted with ethanol and films were obtained by solvent casting from tetrahydrofurane. Characterization of powders, films, and ethanol extract was performed through FTIR spectroscopy, DSC, AFM, SEM, EDX analysis, methylene blue, and nitrogen adsorption. PVC powder was composed of spheres of a large particle size range from 10 nm to 20 μm as shown by SEM. The specific surface area of the PVC powder was determined as 16 and 12 m 2 g-1 from methylene blue adsorption at 25 °C and from N2 adsorption at -196 °C, respectively. AFM indicated the surface roughness of the films obtained by pressing the particles was 25.9 nm. Density of PVC powder was determined by helium pycnometry as 1.39 g cm -3. FTIR spectroscopy indicated that it contained carbonyl and carboxylate groups belonging to additives such as surface active agents, plasticizers, and antioxidants used in production of PVC. These additives were 1.6% in mass of PVC as determined by ethanol extraction. EDX analysis showed PVC particles surfaces were coated with carbon-rich materials. The coatings had plasticizer effect since, glass transition temperature was lower than 25 °C for PVC powder and it was 80 °C for ethanol extracted powders as found by using differential scanning calorimetry. These additives from polymerization process made PVC powder more thermally stable as understood from Metrom PVC thermomat tests as well. © 2010 Akadémiai Kiadó, Budapest, Hungary.Article Citation - WoS: 2Citation - Scopus: 1Stabilizing Effect of Biobased Additives on the Thermal Degradation of Pvc(Trans Tech Publications, 2010) Egbuchunam, Theresa Obuajulu; Okieimen, Felix Ebhodaghe; Balköse, DevrimNovel biobased additives prepared from rubber seed oil were evaluated as thermal stabilizer for PVC. Divalent metal (barium and cadmium) soaps of rubber seed oil were prepared by metathesis in aqueous alcohol and characterized by thermal methods (differential scanning calorimetry and thermogravimetry). The stabilizing effect of the soaps and their admixtures on the thermal degradation of PVC powder and plasticized PVC was examined by dynamic thermogravimetry and dehydrochlorination studies at 160°C using the Thermomat equipment. The metal soaps showed multiple decomposition endotherms but were generally stable (with weight loss less than 5%) within the temperature range (180-220°C) frequently used in the processing of PVC. Using the Broido model, values of apparent activation energy of decomposition of between 50 and 200 kJmol-1 were obtained for the soaps. The biobased additives were found to be relatively effective in stabilizing PVC in powder and plasticized forms against thermal degradation. Using inhibition/retardation time, temperature of incipient decomposition, and temperature at which various extents of decomposition was attained as indices of thermal stabilization, the results from this study indicate a potential for the application of the biobased additives as thermal stabilizer for PVC in rigid and flexible formulations. © (2010) Trans Tech Publications, Switzerland.Conference Object Citation - WoS: 18Citation - Scopus: 19Development of Synergistic Heat Stabilizers for Pvc From Zinc Borate-Zinc Phosphate(Taylor and Francis Ltd., 2009) Erdoğdu, Cem Aykut; Atakul, Sevdiye; Balköse, Devrim; Ülkü, SemraThe importance of flame-retardant and smoke-suppressed poly(vinyl chloride) (PVC) compositions is increasing gradually in the polymer industry since PVC releases smoke and toxic gases (hydrogen chloride, HCl) during heating at temperatures above 140°C with the result of dehydrochlorination reaction. In this study, the synergistic effects of zinc borate (ZB)-zinc phosphate (ZP) on the thermal stability of PVC were investigated using thermal techniques. The induction and stability time values of PVC plastigels were obtained at 140°C and 160°C. The results revealed that PVC plastigels having only ZP and ZB retarded dehydrochlorination of PVC compared with the unstabilized sample. However, the plastigels with both ZB and ZP had a superior synergistic effect on char formation of PVC. Since the induction periods of the samples having both ZB and ZP were higher than those of the unstabilized samples having only ZB or only ZP, the synergistic effect was observed.Conference Object Citation - WoS: 2Citation - Scopus: 2Studies in the Utilization of Biobased Additives as Thermal Stabilizer for Plasticized Pvc(Trans Tech Publications, 2009) Okieimen, Felix Ebhodaghe; Egbuchunam, Theresa Obuajulu; Balköse, DevrimDivalent metal (barium, cadmium, calcium and zinc) soaps of rubber seed oil and their binary mixtures (BaJCd and CaJZn) and epoxidized rubber seed oil (4.5% epoxide content) and its admixtures with the single divalent metal soaps were evaluated as thermal stabilizer for dioctylphthalate plasticized PVC using changes in discolouration indices (yellowness index and UV absorption at 360nm) and initial rates of dehydrochlorination measured at 140 and 160°C. The results obtained showed that the divalent metal soaps were relatively effective in stabilizing the dioctylphthalate plasticized PVC against thermal degradation and that the binary soap mixtures enhanced the heat stabilizing effectiveness: marked reduction in the values of the discolouration indices; longer dehydrochiorination induction period and smaller values of rate constant of initial rate of dehydrochlorination. It was found that epoxidized rubber seed oil was less effective in comparison with the divalent metal soaps in stabilizing plasticized PVC against thermal degradation. These results show that the bio-based additives are compatible with dioctylphthalate plasticized PVC, stable to heat within the range of temperature used in the processing of plasticized PVC, inhibitlretard dehydrochlorination and reduce the extent of degradation.Article Citation - WoS: 15Citation - Scopus: 18Formulation and Properties' Evaluation of Pvc/(dioctyl Phthalate)/ (epoxidized Rubber Seed Oil) Plastigels(John Wiley and Sons Inc., 2008) Balköse, Devrim; Egbuchunam, Theresa Obuajulu; Okieimen, Felix EbhodagheEpoxidized rubber seed oil (4.5% oxirane content, ERSO) was prepared by treating the oil with peracetic acid generated in situ by reacting glacial acetic acid with hydrogen peroxide. The thermal behavior of the ERSO was determined by differential scanning calorimetry. The effect of the epoxidized oil on the thermal stability of poly (vinyl chloride) (PVC) plastigels, formulated to contain dioctyl phthalate (DOP) plasticizer and various amounts of the epoxidized oil, was evaluated by using discoloration indices of the polymer samples degraded at 1600C for 30 min and thermogravimetry at a constant heating rate of 10°C/min up to 600°C. The thermal behavior of the ERSO was characterized by endothermic peaks at about 150°C, which were attributed to the formation of network structures via epoxide groups, and at temperatures above 300°C, which were due to the decomposition of the material. Up to 50% of the DOP plasticizer in the PVC plastisol formulation could be substituted by ERSO without a marked deleterious effect on the consistency of the plastigel formed. In the presence of the epoxidized oil, PVC plastigel samples showed a marked reduction in discoloration and the number of conjugated double bonds, as well as high temperatures for the attainment of specific extents of degradation. These results showed that the ERSO retarded/inhibited thermal dehydrochlorination and the formation of long (n > 6) polyene sequences in PVC plastigels. The plasticizer efficiency/permanence of ERSO in PVC/DOP plastigels was evaluated from mechanical properties' measurements, leaching/migration tests, and water vapor permeability studies. The results showed that a large proportion of DOP could be substituted by ERSO in a PVC plastisol formulation without deleterious effects on the properties of the plastigels.Article Citation - WoS: 19Flexible Poly(vinyl Chloride)-Zeolite Composites for Dye Adsorption From Aqueous Solutions(Taylor and Francis Ltd., 1996) Balköse, Devrim; Ulutan, Sevgi; Çakıcıoğlu Özkan, Seher Fehime; Ülkü, Semra; Köktürk, UğurFlexible poly(vinyl chloride) (PVC) composites having natural zeolite clinoptillolite were prepared by plastisol-plastigel technology. Adsoption of methylene blue on each raw material and on composites was studied both from an equilibrium and a rate approach. It was observed that the adsorption capacity of zeolite decreased when it was embedded in composites. The equilibrium uptake of methylene blue increased with an increasing zeolite fraction in composites. Methylene blue was adsorbed from a 0.02 g·cm-3 aqueous solution slowly, but was nearly adsorbed completely with a composite having a 0.3 volume fraction of zeolite. The effective diffusion coefficient of methylene blue in composites was of the order of 10-13 m2·s-1 and decreased with increasing filler fraction.