Browsing by Subject "Polystyrene"

Now showing 1 - 6 of 6

Open Access
Assessment of PMMA and polystyrene based microfluidic chips fabricated using CO2 laser machining
(Elsevier, 2020-08-19) Bilican, İsmail; Güler, Mustafa Tahsin
Laser machining could be an alternative way for the fabrication of microchannels. In this study, laser machining of polymethylmethacrylate (PMMA) and polystyrene (PS) substrates were characterized in detail. A fabrication method preventing leakage at PS microchannel inlets was developed. The effect of laser parameters (power, speed and frequency) on engraving was analyzed by scanning electron microscopy. Laser ablation mechanism of both materials was explained through thermal analysis and material properties. Defocusing the laser beam was also analyzed as an additional parameter affecting the channel profile. Two parameters affecting the resolution were analyzed which are the minimum channel size that can be achieved by the laser beam and x-y stage of the laser engraver for straight and complex microchannel geometries. The hydrophilicity of the surface before and after laser machining was tested with contact angle measurements. The capabilities/limitations of machining were revealed through some complex channel structures. Finally, a passive micromixer and a droplet generator microfluidic devices were manufactured and tested, and promising results were obtained.
Open Access
Bacteria-immobilized electrospun fibrous polymeric webs for hexavalent chromium remediation in water
(Springer Berlin Heidelberg, 2016) Sarioglu, O.F.; Celebioglu A.; Tekinay, T.; Uyar, Tamer
The development of hexavalent chromium remediating fibrous biocomposite mats through the immobilization of a hexavalent chromium reducing bacterial strain, Morganella morganiiSTB5, on the surfaces of electrospun polystyrene and polysulfone webs is described. The bacteria-immobilized biocomposite webs have shown removal yields of 93.60 and 93.79 % for 10 mg/L, 99.47 and 90.78 % for 15 mg/L and 70.41 and 68.27 % for 25 mg/L of initial hexavalent chromium within 72 h, respectively, and could be reused for at least five cycles. Storage test results indicate that the biocomposite mats can be stored without losing their bioremoval capacities. Scanning electron microscopy images of the biocomposite webs demonstrate that biofilms of M. morganii STB5 adhere strongly to the fibrous polymeric surfaces and are retained after repeated cycles of use. Overall, the results suggest that reusable bacteria-immobilized fibrous biocomposite webs might be applicable for continuous hexavalent chromium remediation in water systems.
Open Access
Functional electrospun polystyrene nanofibers incorporating α-, β-, and γ-cyclodextrins: Comparison of molecular filter performance
(2010) Uyar, Tamer; Havelund, R.; Hacaloglu, J.; Besenbacher, F.; Kingshott, P.
Electrospinning has been used to successfully create polystyrene (PS) nanofibers containing either of three different types of cyclodextrin (CD); α-CD, β-CD, and γ-CD. These three CDs are chosen because they have different sized cavities that potentially allow for selective inclusion complex (IC) formation with molecules of different size or differences in affinity of IC formation with one type of molecule. The CD containing electrospun PS nanofibers (PS/CD) were initially characterized by scanning electron microscopy (SEM) to determine the uniformity of the fibers and their fiber diameter distributions. X-ray photoelectron spectroscopy (XPS) was used to quantitatively determine the concentration of each CD on the different fiber surfaces. Static time-of-flight secondary ion mass spectrometry (static-ToF-SIMS) showed the presence of each type of CD on the PS nanofibers by the detection of both the CD sodium adduct molecular ions (M + Na+) and lower molecular weight oxygen containing fragment ions. The comparative efficiency of the PS/CD nanofibers/nanoweb for removing phenolphthalein, a model organic compound, from solution was determined by UV-vis spectrometry, and the kinetics of phenolphthalein capture was shown to follow the trend PS/α-CD > PS/β-CD > PS/γ-CD. Direct pyrolysis mass spectrometry (DP-MS) was also performed to ascertain the relative binding strengths of the phenolphthalein for the CD cavities, and the results showed the trend in the interaction strength was β-CD > γ-CD > α-CD. Our results demonstrate that nanofibers produced by electrospinning that incorporate cyclodextrins with different sized cavities can indeed filter organic molecules and can potentially be used for filtration, purification, and/or separation processes. © 2010 American Chemical Society.
Open Access
Mixing challenges for SiO2/polystyrene nanocomposites
(SAGE Publications, 2018) Kourki, H.; Famili, M. H. N.; Mortezaei, M.; Malekipirbazari, M.
Morphology of a nanocomposite, which has indisputable effects on its properties, is determined by its dynamic and thermodynamic conditions. While physical properties of the components of a nanocomposite as well as the interaction between them are the parameters controlling the morphology thermodynamically, their dynamic condition is related to the issues like intensity of mixing and geometry of mixer. In this research, we investigate the mixing process of solution casting method by studying the effects of mixing intensity on the dynamics of the particle structure and hereby its morphology using sedimentation test. In these experiments, mixing is performed at various durations, input energies, and energy types for suspensions containing different particle sizes and concentrations as well as diverse polymer concentrations. We found that increasing mixing time and input energy along with using ultrasonic wave decrease the size of aggregates. Sedimentation test revealed improvements of dispersion and distribution states of suspension by using ultrasonic waves and high shear mixing, respectively. Finally, particle-particle interaction data show increase in the probability of restructuring after mixing with reduction in particle size and increase in particle volume fraction.
Open Access
Pyrolysis mass spectrometric analysis of styrene-butadiene block and random copolymers
(Elsevier, 1997-02) Hacaloglu, J.; Ersen, T.; Ertugrul, N.; Fares, M. M.; Süzer, Şefik
Direct pyrolysis mass spectrometric analysis of a styrene-butadiene-styrene block copolymer indicated that thermal decomposition of each block shows a resemblance to the related homopolymer, giving a possibility of differentiation of blocks. However, the random analog, the styrene butadiene rubber, degraded in a manner that is somewhat in between in nature of the thermal characteristics of both homopolymers. This technique shows promise to differentiate thermal behaviors of each sequence in block polymers if any exist. Indirect pyrolysis mass spectrometric analysis gave no clear evidence for differentiation of the nature and the composition of the copolymers. © 1997 Elsevier Science Ltd. All rights reserved.
Open Access
Pyrolysis mass spectrometric analysis of styrene-isoprene-styrene copolymers
(Elsevier, 1999-05) Hacaloglu, J.; Fares, M. M.; Süzer, Şefik
Thermal analysis of styrene±isoprene±styrene block copolymer, using the direct pyrolysis mass spectrometry (MS) technique, indicated that each block showed very similar thermal behavior with the corresponding homopolymer. The isoprene block was found to be thermally less stable, decomposing by random scissions followed by cyclization reactions. The more stable styrene block degraded by a radical depolymerization mechanism. With an indirect pyrolysis MS technique, it was found that production of benzene, toluene, 1-methyl cyclopentene and 1-methyl cyclohexene was more e ective when degradation was carried out in a closed reactor. # 1999 Elsevier Science Ltd. All rights reserved.