Photocatalytic oxidation of selected gas-phase VOCs using UV light, TiO2, and TiO2/Pd.

Heterogeneous photocatalytic oxidation systems using titanium dioxide (TiO2) have been extensively studied for the removal of several volatile organic compounds (VOCs). The addition of noble metals such as palladium on TiO2 may improve photocatalytic activity by increasing charge separation efficiency. In this work, palladium was impregnated on TiO2 and the efficiency of the new catalyst was tested and compared with that of pure TiO2. Pd was impregnated on TiO2 by the reduction method, using NaBH4, and was characterized by XRD, XPS, UV-Vis, and H2 chemisorption. The photocatalytic tests were performed in an annular coated-wall reactor using octane, isooctane, n-hexane, and cyclohexane at inlet concentrations varying from 100 to 120 ppmv. Compared with pure TiO2 film, the photocatalytic activity of TiO2 impregnated with 1 wt% of palladium was improved. All the aforementioned analytical techniques confirmed the presence of Pd incorporated into the structure of TiO2, and the conversion rates were studied in a broad range of residence times, yielding up to 90 % or higher rates in 40 s of residence time, thus underscoring the relevant contribution of the technology.

Four new phenolic acid with unusual bicycle [2.2.2] octane moiety from Clerodendranthus spicatus and their anti-inflammatory activity.

Four new phenolic acids, clerodens A-D (1-4) possessing an unusual bicycle [2.2.2] octane moiety were isolated from the whole plants of Clerodendranthus spicatus. Their structures were elucidated by extensive spectroscopic methods, including NMR, MS, and ECD data. All isolates were evaluated for their anti-inflammatory activities on lipopolysaccharide (LPS)-induced nitric oxide (NO) production in RAW 264.7, and compound 4 showed significant inhibitory activities with IC50 value of 6.8 µM.

Removal of airborne toxic chemicals by porous organic polymers containing metal-catecholates.

Porous organic polymers bearing metal-catecholate groups were evaluated for their ability to remove airborne ammonia, cyanogen chloride, sulphur dioxide, and octane by micro-breakthrough analysis. For ammonia, the metal-catecholate materials showed remarkable uptake under humid conditions.

An unusual caffeic acid derived bicyclic [2.2.2] octane lignan and other constituents from Cordia rufescens.

This work reports isolation of an unusual lignan with a bicyclic [2.2.2] octene skeleton, named rufescenolide (1), from stems of Cordia rufescens, along with ß-sitosterol, stigmasterol, syringaldehyde, 3-ß-O-D-glucopyranosyl-sitosterol, methyl caffeate, 4-methoxy-protocatechuic acid and methyl rosmarinate. Structural characterizations employed IR spectroscopic, ESIHRMS and mono and dimensional NMR spectroscopy.

Measuring gas-liquid partition coefficients of aroma compounds by solid phase microextraction, sampling either headspace or liquid.

Hydrophobic compounds are important odorants and nutrients in foods and beverages, as well as environmental contaminants and pharmaceuticals. Factors influencing their partitioning within multi-component systems and/or from the bulk liquid phase to the air are critical for understanding aroma quality and nutrient bioavailability. The equilibrium partitioning of hydrophobic analytes between air and water was analyzed using solid phase microextraction (SPME) in the headspace (HS-SPME) and via direct immersion in the liquid (DI-SPME). The compounds studied serve as models for hydrophobic aroma compounds covering a range of air-water partition coefficients that extends over four orders of magnitude. By varying the total amount of analyte as well as the ratio of vapor to liquid in the closed, static system, the partition coefficient, K(vl), can be determined without the need for an external calibration, eliminating many potential systematic errors. K(vl) determination using DI-SPME in this manner has not been demonstrated before. There was good agreement between results determined by DI-SPME and by HS-SPME over the wide range of partitioning behavior studied. This shows that these two methods are capable of providing accurate, complementary measurements. Precision in K(vl) determination depends strongly on K(vl) magnitude and the ratio of the air and liquid phases.

Effect of fibrous filter properties on the oil-in-water-emulsion separation and filtration performance.

Separation of secondary emulsions of dispersed droplet size less than 10 µm, by means of fibrous medium is a very complex but important process. The study investigates the influence of thin fibrous filter properties, i.e. surface energy, pore size and porosity on the separation performance of an isooctane in water emulsion (0.2%, mean drop size 2 µm). Experiments were carried out on five different filter media with a wide variation in their pore size (2-51 µm), surface energy (14-46 mN/m) and porosity (0.46-0.87) at similar process conditions. Filter media with different wettability are obtained by applying various hydrophobic and hydrophilic coatings. All the used coatings contain nanoparticles (25 nm) to impart nanoscale surface roughness at the single fiber surface. Besides emulsion properties and operating conditions, the phase separation mechanism and performance highly depends on pore size, surface energy and porosity of the filter media. More complete coalescence takes place at reduced pore size and at a surface preferentially wetted by the dispersed phase. Whereas when the pore size equals to the influent droplet size, then the surface wettability of filter is less effective and the separation mechanism is governed by inflow velocity. The emulsion inflow velocity and pressure drop are significantly affected by the filter media air permeability but do not depend on filter surface energy.

A short and facile synthesis of 2-(1Z)-(3-hydroxy-3,7-dimethylocta-1,6-dienyl)-1,4-benzenediol and 1-(3'-methoxypropanoyl)-2,4,5-trimethoxybenzene isolated from Cordia alliodora.

A novel synthesis of 2-(1Z)-(3-hydroxy-3,7-dimethylocta-1,6-dienyl)-1,4-benzenediol and 1-(3'-methoxypropanoyl)-2,4,5-trimethoxybenzene has been carried out by making use of an easily available starting material, acceleration by MW irradiation and the use of water as a green solvent in the key steps.

Rate-limited mass transfer of octane, decane, and dodecane into nonionic surfactants solutions under laminar flow conditions.

A key component to predicting the success of utilizing surfactants to enhance the removal of organic liquids from soil system is quantifying micellar solubilization kinetics. In this study, a flow reactor was employed to investigate the influence of surfactant ethoxylate chain length on the rates of solubilization of octane, decane, and dodecane in micellar solutions of a homologous series of purified dodecyl alcohol ethoxylates. Effluent concentration data were fit using a finite element model utilizing a linear-driving-force model to represent mass transfer at the interface. For flow rates between 0.1 and 2 ml min(-1), mass transfer coefficients ranged from 5 x 10(-8) to 7 x 10(-7)m s(-1) and did not vary in a systematic way with either solute structure or surfactant ethoxylate chain length and were lower than those found in pure water. Correlations developed for the Sherwood number based on diffusion coefficients of surfactant micelles containing organic material (organic-laden micelle) exhibit a velocity dependence similar to that found for systems based on aqueous diffusion. These results suggest that under gentle flowing conditions, the mass transfer is limited by diffusion of the organic-laden micelle. Although these trends are specific for this experimental system, the results demonstrate the importance of selecting the proper diffusion coefficient when modeling surfactant solubilization processes.

Contribution to linearly programmed temperature gas chromatography. Further application of the Van den Dool-Kratz equation, and a new utilization of the Sadtler retention index library.

Programmed temperature retention indices (PTRIs) calculated according to the equations of Van den Dool and Kratz, Golovnya and Uraletz, and Erdey et al. (also referred to as Antoine's integrated equation) are used in this work. Precalculation of isotherm retention indices from the results of a linearly programmed temperature GC is also presented. Deviations between experimental and calculated isothermal retention indices are below 2 retention index units. A relative "volatility" retention index is defined, as a function of the "volatilities"of the solute and the bracket reference n-alkanes. The comparison of the "volatility" retention indices with the PTRIs obtained with the other above equations shows absolute deviations of up to 4 retention index units. Based on an earlier "equivalent" temperature concept and on Tekler's proviso, a novel way for the utilization of Sadtler's retention index database, which takes advantage of the 3 data supplied by the library, is proposed.

DC corona electric discharges for air pollution control. Part 1. Efficiency and products of hydrocarbon processing.

A large (ca 0.7 L) wire-cylinder benchtop reactor was developed and tested for DC corona processing of VOC (volatile organic compound)-contaminated air at room temperature and pressure. The aim of our research is the identification and rationalization of the chemical reactions responsible for VOC removal. Model hydrocarbons, n-hexane and 2,2,4-trimethylpentane (i-octane), were used to characterize the process and compare the effects of DC corona polarity and of humidity on its energy efficiency and products. n-Hexane and i-octane behave very similarly. For both, the energy efficiency is significantly better with negative than with positive DC corona, especially in humid air. The effect of humidity is most interesting. Thus, while with -DC corona the process efficiency is significantly better in humid air, a slight inhibition is observed with +DC corona. Differences between +DC and -DC corona are also found in the amounts of volatile products formed, which include CO2, CO, and minor quantities of organic byproducts (aldehydes, ketones, alcohols, and lower hydrocarbons). A significant fraction of the carbon originally present as VOC is, however, unaccounted for by the analysis of gaseous and volatile organic products and must, therefore, end up as nonvolatile materials and aerosols.

Unknown bisethylisooctanollactone isomers in industrial waste water. Isolation, identification and occurrence in surface water.

Unknown bisethylisooctanollactone isomers (BIOL isomers) which are chemical by-products of butyraldehyde synthesis, were isolated from industrial waste water applying various purification methods with subsequent semi-preparative high-performance liquid chromatography. Through interpretation of mass spectra after gas chromatographic separation the individual BIOL isomers were identified as stereoisomers of 2,4-diethyl-3-n-propyl-delta-valerolactone. Thus, it was possible for the first time to quantify the BIOL isomers in the river Rhine, Germany, with a mean sum concentration of 1.6 microg l(-1). A regular analysis performed over a period of almost two years of the river Rhine always gave the same ratio among the individual isomers. Drinking water production out of such water was studied, revealing that activated carbon filtration led to a 95% reduction of the BIOL concentration. Additional subsoil passage and a subsequent slowsand filtration led to a total elimination due to microbial degradation. Even if the BIOL isomers proved not to be relevant to drinking water, their behavior in the aquatic environment needs to be more thoroughly investigated since these compounds have been discharged for many years in high amounts into the river Rhine.

Antifungal and larvicidal compounds from the root bark of Cordia alliodora.

Two new natural products, a phenylpropanoid derivative characterized as 1-(3'-methoxypropanoyl)-2,4,5-trimethoxybenzene (1) and a prenylated hydroquinone, 2-(2Z)-(3-hydroxy-3,7-dimethylocta-2, 6-dienyl)-1,4-benzenediol (2), have been isolated from the root bark of Cordia alliodora. Both compounds exhibited antifungal properties against the phytopathogenic mold Cladosporium cucumerinum. The phenylpropanoid derivative (1), whose structure is closely related to beta-asarone, also demonstrated a marked activity against larvae of the yellow-fever-transmitting mosquito Aedes aegypti.