UV-irradiated parylene surfaces for proliferation and differentiation of PC-12 cells.

PC-12 cells originate from neuroblastic cells, which have an ability to differentiate into neuronlike cells. In this work, the purpose was to estimate the influence of microenvironments on cell attachment and neuritogenesis capacity of PC-12 cells on parylene-N and parylene-C films with and without ultraviolet (UV) light treatment. The estimate of total cell number after incubation for 72h, the ratio of adherent to suspended cells, counting of neurite outgrowths on parylene-N or parylene-C films after UV exposure suggested that these films were suitable for proliferation as well as differentiation of PC-12 cells. The differences in surface properties of parylene-N and parylene-C films with and without UV exposure were analyzed by contact angle measurement, Fourier-transform infrared spectrometry, and X-ray photoelectron spectroscopy. According to these analyses, introduction of oxygen-related chemical functional groups was presumed to result in increased hydrophilicity and efficiency of protein immobilization on parylene-N and parylene-C films after UV treatment. According to fluorescent staining, western blotting, and cell cycle analysis, UV-treated parylene-C and parylene-N films appear to effectively facilitate simultaneous proliferation and differentiation of PC-12 cells with neurite outgrowth.

Parylene-coated metal tracks for neural electrode arrays - fabrication approaches and improvements utilizing different laser systems.

In the past we developed a method for the fabrication of neural electrodes based on laser-structuring metal foil to form tracks and electrode sites within a silicone rubber substrate. Here, this process was refined by an additional coating of the laser-patterned metal tracks to improve their mechanical properties. Parylene C has been found to be the coating material of choice due to excellent electrical and mechanical characteristics and its well known biocompatibility. An almost ten times increased tensile strength compared to uncoated tracks could be achieved. Investigating the electrical properties of parylene C and silicone rubber attested both materials excellent insulating capabilities by withstanding voltages of more than 400 V(DC) for layer thicknesses as intended to be used in electrode array fabrication (some 10 µm). This paper outlines the feasibility of the manufacturing process using a 1064 nm Nd:YAG laser in the nanosecond pulse regime. However, an improvement of the whole processing was demonstrated when a 355 nm Nd:YVO(4) laser in the picosecond regime is used. Benefits of this short pulse duration range from ablating materials independent of their optical properties to increased manufacturing speed and superior processing quality.

Plasma surface modified TiO2 nanoparticles: improved photocatalytic oxidation of gaseous m-xylene.

Titanium dioxide (TiO(2)) is a preferred catalyst for photocatalytic oxidation of many air pollutants. In an effort to enhance its photocatalytic activity, TiO(2) was modified by pulsed plasma treatment. In this work, TiO(2) nanoparticles, coated on a glass plate, were treated with a plasma discharge of hexafluoropropylene oxide (HFPO) gas. By appropriate adjustment of discharge conditions, it was discovered that the TiO(2) particles can be either directly fluorinated (Ti-F) or coated with thin perfluorocarbon films (C-F). Specifically, under relatively high power input, the plasma deposition process favored direct surface fluorination. The extent of Ti-F formation increased with increasing power input. In contrast, at lower average power inputs, perfluorocarbon films are deposited on the surface of the TiO(2) particles. The plasma surface modified TiO(2) nanoparticles were subsequently employed as catalysts in the photocatalytic oxidation of m-xylene in air, as carried out inside a batch reactor with closed loop constant gas circulation. Both types of modified TiO(2) were significantly more catalytically active than that of the unmodified particles. For example, the rate constant of m-xylene degradation was increased from 0.012 min(-1) with untreated TiO(2) to 0.074 min(-1) with fluorinated TiO(2). Although it is not possible to provide unequivocal reasons for this increased photocatalytic activity, it is noted that the plasma surface treatment converted the TiO(2) from hydrophilic to highly hydrophobic, which would provide more facile catalyst adsorption of the xylene from the flowing air. Also, based on literature reports, the use of fluorinated TiO(2) reduces electron-hole recombination rates, thus increasing the photocatalytic activity.

Effect of gamma-irradiation on some chemical characteristics and volatile content of linseed.

The effect of irradiation (2.5, 4.0, 5.5, and 7.0 kGy) on chemical properties and volatile contents of linseed was investigated. Consistent decreases were observed in both protein and oil content of the irradiated linseed samples with increasing irradiation doses. The ash content of the irradiated linseed samples increased significantly (P<.05) with increasing irradiation doses except for 5.5 kGy. Irradiation treatment caused irregular changes in palmitic and stearic acid content. Although styrene and p-xylene content decreased as a result of irradiation, 1-hexanol content only decreased at 7.0 kGy. Benzaldehyde, p-cymene, and nonanol were not determined at irradiation doses above 4.0 kGy.

Degradation of m-xylene solution using ultrasonic irradiation.

This study is to apply ultrasound to remove m-xylene, a volatile compound from aqueous solutions which causes environmental damage. High frequency ultrasound was used to investigate the effect of different operational parameters, such as m-xylene initial concentration, ultrasonic frequency and ultrasonic power. The degradation rate of m-xylene was increased with decreasing initial concentration of m-xylene and increasing frequency and power. Optimal conditions include 26.07 mg/L, 806.3 kHz and 70±1 W, in which MnO(2), Cu(2+), Fe(2+), and H(2)O(2) had little or no effect on the degradation. Moreover, the effect of radical scavengers such as Na(2)CO(3) and t-butyl was not obvious, which indicates that direct pyrolysis inside the collapsing bubbles has an important role in m-xylene ultrasonic removal. In addition, the degradation of m-xylene was observed to behave under pseudo-first-order kinetics with different experimental conditions tested in the present work.

Real-time monitoring of benzene, toluene, and p-xylene in a photoreaction chamber with a tunable mid-infrared laser and ultraviolet differential optical absorption spectroscopy.

We describe the implementation of a mid-infrared laser-based trace gas sensor with a photoreaction chamber, used for reproducing chemical transformations of benzene, toluene, and p-xylene (BTX) gases that may occur in the atmosphere. The system performance was assessed in the presence of photoreaction products including aerosol particles. A mid-infrared external cavity quantum cascade laser (EC-QCL)-tunable from 9.41-9.88 µm (1012-1063 cm(-1))-was used to monitor gas phase concentrations of BTX simultaneously and in real time during chemical processing of these compounds with hydroxyl radicals in a photoreaction chamber. Results are compared to concurrent measurements using ultraviolet differential optical absorption spectroscopy (UV DOAS). The EC-QCL based system provides quantitation limits of approximately 200, 200, and 600 parts in 10(9) (ppb) for benzene, toluene, and p-xylene, respectively, which represents a significant improvement over our previous work with this laser system. Correspondingly, we observe the best agreement between the EC-QCL measurements and the UV DOAS measurements with benzene, followed by toluene, then p-xylene. Although BTX gas-detection limits are not as low for the EC-QCL system as for UV DOAS, an unidentified by-product of the photoreactions was observed with the EC-QCL, but not with the UV DOAS system.

Light intensity and light source influence on secondary organic aerosol formation for the m-xylene/NO(x) photooxidation system.

A series of m-xylene/NO(x) photooxidation experiments were conducted to determine the influence of light intensity and radiation spectrum on secondary organic aerosol (SOA) formation within the UC Riverside/CE-CERT environmental chamber. The environmental chamber is equipped with 80 115-W black lights and a variable voltage 200 kW argon arc lamp that emits a wavelength spectrum more similar to natural light. SOA formation increased significantly with light intensity, measured as the photolysis rate of NO2 to NO (k1), increased from 0.09 to 0.26 min(-1). The argon arc lamp produced approximately 20% more SOA than black lights at a k1 of 0.09 min(-1) for similar amounts of m-xylene consumed. These results may help explain the variation of SOA formation between environmental chambers and the differences between measured SOA in the ambient atmosphere versus environmental chamber predictions.

Phase control of molecular fragmentation with a pair of femtosecond-laser pulses.

We demonstrate the control of molecular fragmentation of o-xylene (C(8)H(10)) on a femtosecond time scale in two-pulse measurements with a pair of femtosecond-laser pulses. Parent and fragment-ion yields were recorded as a function of interpulse delays, i.e., different relative phases of the excitation pulses. The experiments revealed different fragmentation mechanisms in the temporal region of direct overlapping pulses and for separated pulses. For overlapping pulses all ion yields followed the excitation intensity which oscillated as a function of interpulse delay due to the change of constructive and destructive interference of the light fields. For larger delays, in particular, the oscillations of the C(+) and CH(3) (+) fragment-ion yield showed a significant deviation from each other. The results are interpreted as a manifestation of optical phase-dependent electronic excitations mapped onto the nuclear fragmentation dynamics.

Matrix isolation, spectroscopic characterization, and photoisomerization of m-xylylene.

A new efficient synthesis of m-xylylene 1 is reported. The diradical 1 was trapped in argon matrices at 10 K and characterized by IR, UV-vis, and EPR spectroscopy. The syntheses reported before only allowed generation of 1 in organic glasses, and the spectroscopic identification was limited to fluorescence and EPR spectroscopy. Diradical 1 proved to be highly photolabile, and irradiation results in the formation of three isomeric hydrocarbons 7, 9, and 11 which could be identified by comparison of their IR spectra with the results of DFT calculations.

Secondary organic aerosol formation from the photooxidation of p- and o-xylene.

The formation of secondary organic aerosol (SOA) from the photooxidation of xylene isomers (m-, p-, and o-xylenes) has been extensively investigated. The dependence of SOA aerosol formation on the structure of xylene isomers in the presence of NO was confirmed. Generally, SOA formation of p-xylene was less than that of m- and o-xylenes. This discrepancy varies significantly with initial NOx levels. In a NOx-free environment, the difference of aerosol formation between o- and p-xylenes becomes insignificant. Several chemical pathways for the SOA dependence on structure and NOx are explored, with the experimental findings indicating that organic peroxides may be a major key to explaining SOA formation from aromatic hydrocarbons.

Secondary organic aerosol formation from m-xylene in the absence of NOx.

Formation of secondary organic aerosol (SOA) from m-xylene photoxidation in the absence of NOx was investigated in a series of smog chamber experiments. Experiments were performed in dry air and in the absence of seed aerosol with H2O2 photolysis providing a stable hydroxyl radical (OH radical) source. SOA formation from this study is exceptionally higher than experiments with existence of NOx. The experiments with elevated HO2 levels indicate that organic hydroperoxide compounds should contribute to SOA formation. Nitrogen oxide (NO) is shown to reduce aerosol formation; the constant aerosol formation rate obtained before addition of NO and after consumption of NO strongly suggests that aerosol formation is mainlythrough reactions with OH and HO2 radicals. In addition, a density of 1.40 +/- 0.1 g cm(-3) for the SOA from the photooxidation of m-xylene in the absence of NOx has been measured, which is significantly higherthan the currently used unit density.

Using UV pretreatment to enhance biofiltration of mixtures of aromatic VOCs.

Mixtures of airborne toluene and o-xylene, two relatively recalcitrant volatile organic compounds (VOCs), were treated effectively using integrated UV-biofiltration. The set-up consisted of a biofilter receiving UV-pretreated stream and a reference biofilter receiving no pretreatment. Experimental conditions included UV fluences of 6 and 12 mJcm(-2) as well as air flow rates of 6.3 and 9.4 Lmin(-1), corresponding to biofilter empty bed retention times (EBRTs) of 45 and 30s, respectively. The inlet concentration of organics (toluene and o-xylene) ranged between 70 and 650 mg(carbon)m(-3). The UV-biofilter consistently provided removal efficiencies of greater than 95% over the range of toluene and o-xylene inlet concentrations. Also, the coupled UV-biofiltration system provided up to 60% additional contaminant removal compared to the sum of that offered by UV and reference biofilter, demonstrating the synergistic effect of UV on biofilter performance. The UV photooxidation partially oxidized a fraction of toluene and o-xylene into water soluble and more biodegradable intermediates, such as acetaldehyde and formaldehyde, which were readily removed in the downstream biofilter. These intermediates along with up to 20ppmv ozone, formed through the photolysis of oxygen by 185 nm UV, contributed to the enhanced degradation of parent VOCs in the biofilter as well as the absence of any inhibitory effects of the VOCs on one another. Also, the presence of ozone helped control the growth of excess biofilm in the UV-coupled biofilter. While the standalone biofilter showed significant pressure drop increase (of up to 14 mm H(2)Om(-1) of the bed) over the course of experiment, the UV-coupled biofilter maintained a relatively low pressure drop of less than 3 mmH(2)Om(-1) of the bed.

Study on the resonance light-scattering spectrum of anionic dye xylenol orange-cetyltrimethylammonium-nucleic acids system and determination of nucleic acids at nanogram levels.

The interaction of xylenol orange (XO) and nucleic acids in the presence of cetyltrimethylammonium bromide (CTMAB) in aqueous solution has been studied by a resonance light-scattering (RLS) technique with a common spectrofluorometer. In hexamethylenetetramine (HMTA) buffer (pH7.30), XO and nucleic acids react with cetyltrimethylammonium bromide to form large particles of three-component complex, which results in strong enhanced RLS signals characterized by three peaks at 295.9, 335.5 and 542 nm, Mechanistic studies showed that the enhanced RLS stems from the aggregation of XO on DNA through the bridged and synergistic effect of CTMAB. With the enhanced RLS signals at the three wavelengths, the enhanced RLS intensity is proportional to the concentration of nucleic acids in an appropriate range. The lowest limit of determination was 5.31 ng ml(-1), three synthetic samples of yDNA were analyzed satisfactorily.

Kinetics of nitromusk compounds degradation in water by ultraviolet radiation and hydrogen peroxide.

The photodegradation of five representative nitromusk compounds in water has been performed in a stirred batch photoreactor with a UV low-pressure immersed mercury lamp, at constant temperature and different doses of hydrogen peroxide. The rate constants have been calculated on the basis of experimental data and a postulated first-order kinetic model. The rate constants, at 298 K and a dose of 1.1746 micromol l(-1) H2O2 ranges from 0.3567 x 10(-3) s(-1) for musk tibetene, to 1.785 x 10(-3) s(-1) for musk ambrette.