RESIDENCE TIME MEASUREMENTS IN PILOT-SCALE ELECTROLYTIC CELLS: APPLICATION OF LASER-INDUCED FLUORESCENCE

The flow distribution in the rectangular channel of a pilot-scale electrolytic cell was observed using an imperfect tracer-pulse injection technique in order to study residence time distribution (RTD), back-mixing effects, and velocity profiles of the electrolyte liquids within the cathode compartment. The electrolytic cell was operated under cold flow and at process conditions. While residence time studies performed in a vast number of applications are mainly based on classical conductometric measurements, alternative measurement methods have to be applied in electrochemical systems. Hence, this study deals with the investigation of RTD using laser-induced fluorescence (LIF) visualization. Back-mixing effects of the electrolyte are quantified using the axial dispersion flow model. RTD studies for the overall cell as well as velocity profile analysis for selected individual regions are conducted. Additionally, the effects of the nonstabilized membrane and of the membrane-stabilizing spacer grid are investigated.     

Comparison of the Structures of Triacylglycerols from Native and Transgenic Medium-Chain Fatty Acid-Enriched Rape Seed Oil by Liquid Chromatography–Atmospheric Pressure Chemical Ionization Ion-Trap Mass Spectrometry (LC–APCI-ITMS)

The sn position of fatty acids in seed oil lipids affects physiological function in pharmaceutical and dietary applications. In this study the composition of acyl-chain substituents in the sn positions of glycerol backbones in triacylglycerols (TAG) have been compared. TAG from native and transgenic medium-chain fatty acid-enriched rape seed oil were analyzed by reversed-phase high performance liquid chromatography coupled with online atmospheric-pressure chemical ionization ion-trap mass spectrometry. The transformation of summer rape with thioesterase and 3-ketoacyl-[ACP]-synthase genes of Cuphea lanceolata led to increased expression of 1.5% (w/w) caprylic acid (8:0), 6.7% (w/w) capric acid (10:0), 0.9% (w/w) lauric acid (12:0), and 0.2% (w/w) myristic acid (14:0). In contrast, linoleic (18:2n6) and alpha-linolenic acid (18:3n3) levels decreased compared with the original seed oil. The TAG sn position distribution of fatty acids was also modified. The original oil included eleven unique TAG species whereas the transgenic oil contained sixty. Twenty species were common to both oils. The transgenic oil included trioctadecenoyl-glycerol (18:1/18:1/18:1) and trioctadecatrienoyl-glycerol (18:3/18:3/18:3) whereas the native oil included only the latter. The transgenic TAG were dominated by combinations of caprylic, capric, lauric, myrisitic, palmitic (16:0), stearic (18:0), oleic (18:1n9), linoleic, arachidic (20:0), behenic (22:0), and lignoceric acids (24:0), which accounted for 52% of the total fat. In the original TAG palmitic, stearic, oleic, and linoleic acids accounted for 50% of the total fat. Medium-chain triacylglycerols with capric and lauric acids combined with stearic, oleic, linoleic, alpha-linolenic, arachidic, and gondoic acids (20:1n9) accounted for 25% of the transgenic oil. The medium-chain fatty acids were mainly integrated into the sn-1/3 position combined with the essential linoleic and alpha-linolenic acids at the sn-2 position. Eight species contained caprylic, capric, and lauric acids in the sn-2 position. The appearance of new TAG in the transgenic oil illustrates the extensive effect of genetic modification on fat metabolism by transformed plants and offers interesting possibilities for improved enteral applications.     

CH3-ReO3 on γ-Al2O3: Activity,selectivity, active site and deactivation in olefin metathesis

The active sites (15% of total Re) of CH₃ReO₃ supported on alumina arise solely from the reaction of the CH bond of CH₃ReO₃ with reactive Al_SO_S sites of a γ-Al₂O₃ surface to yield [Al_SCH₂ReO₃], whereas the major species, inactive, corresponds to MeReO₃ chemisorbed through its oxo ligand(s) on Lewis acid sites of alumina. Monitoring the active sites of CH₃ReO₃ supported on alumina by solid-state NMR spectroscopy shows that no carbenic signals are observed and that the resting states of the catalyst in the metathesis of propene correspond to μ-methylene and μ-ethylidene species, so that the propagating carbenic species are likely formed only in the presence of olefins. Although this system is highly active in the metathesis of propene, with initial rates similar to some of the best catalysts, it undergoes fast deactivation, which is due to the propene metathesis products, most likely ethene.     

Model of microbial transport and inactivation in the surf zone and application to field measurements of total coliform in Northern Orange County, California

The classic model of pollutant transport in the surf zone of a long, sandy beach developed by Inman et al. (J. Geophys. Res. 1971, 76, 3493) is altered to account for first-order pollutant inactivation in an effort to understand how rip cell dilution and bacterial inactivation control the length of shoreline adversely impacted by microbial pollution from a point source. A dimensionless number gamma dictates whether physical processes (dilution of microbes in the surf zone by rip cell mixing) or biological processes (microbial inactivation) control the distribution of pollution along the shoreline. Estimates of gamma for beaches in Northern Orange County, California, indicate that dilution is the primary factor controlling total coliform levels surrounding two drains that release nuisance runoff directly onto the beach. It is also shown that, even when alongshore currents are fast, pollutant levels will drop e-fold at distances under 4000 m from the point source due to dilution alone. Because dilution is ultimately controlled by wave climate and shoreline morphology, the results suggest the strategic position of drains and other point sources in high dilution wave environments will reduce potential adverse effects on beach water quality. In addition, the results stress the importance of understanding hydrodynamics when conducting microbial source tracking at wave-dominated marine beaches.     

Source allocation by least-squares hydrocarbon fingerprint matching

There has been much controversy regarding the origins of the natural polycyclic aromatic hydrocarbon (PAH) and chemical biomarker background in Prince William Sound (PWS), Alaska, site of the 1989 Exxon Valdez oil spill. Different authors have attributed the sources to various proportions of coal, natural seep oil, shales, and stream sediments. The different probable bioavailabilities of hydrocarbons from these various sources can affect environmental damage assessments from the spill. This study compares two different approaches to source apportionment with the same data (136 PAHs and biomarkers) and investigate whether increasing the number of coal source samples from one to six increases coal attributions. The constrained least-squares (CLS) source allocation method that fits concentrations meets geologic and chemical constraints better than partial least-squares (PLS) which predicts variance. The field data set was expanded to include coal samples reported by others, and CLS fits confirm earlier findings of low coal contributions to PWS.     

Tidal forcing of enterococci at marine recreational beaches at fortnightly and semidiurnal frequencies

Marine beach water quality is typically monitored in early morning once a week without respect to tidal condition. To assess the effect of tide on this public health warning system, we analyzed enterococci (ENT) data from 60 southern California marine beaches with differing geomorphology, orientation, and proximity to runoff sources. ENT concentrations during spring tides were significantly higher (p < 0.1) than those during neap tides at 50 of the beaches, and at the majority of these, water samples were also more than twice as likely to be out of compliance with the ENT single-sample standard during spring tides compared to neap tides. When tide range (spring/neap) and tide stage (ebb/flood) conditions were considered together, spring-ebb tides yielded the highest ENT concentrations and the greatest chance of exceeding the single-sample standard at the majority of beaches. The proximity to a terrestrial runoff source, the slope of the runoff source, the slope of the beach, and the orientation of the beach had minimal influence on the tidal modulation of ENT concentrations. The presence of spring and spring-ebb tide signals at such a great percentage of beaches suggests that tide should be considered in the design and interpretation of beach monitoring program data. It also suggests that ENT delivered by tidally forced sources other than terrestrial surficial runoff are widespread. Possibilities include ENT-laden groundwater (saline and fresh) from the beach aquifer as well as ENT-enriched sands, decaying wrack, and bird feces near the high water line.     

Preparation of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) particles in O/W emulsion

In the present paper, we investigate the preparation of polymeric particles based on the biodegradable polyester poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV). A new technique for PHBV particle preparation has been developed. This method utilizes the thermoreversible gelation of PHBV in toluene. Particles have been obtained by the secondary dispersion technique in a three-step procedure: (a) preparation of PHBV solution in toluene; (b) preparation of O/W emulsion by ultrasound followed by the gel formation in toluene/PHBV droplets; and (c) toluene extraction. In the present study we investigated the influence of the stabilizer type and its concentration in the aqueous phase, ultrasound power, and PHBV concentration in toluene on the size and stability of the formed droplets as well as the final PHBV particles. It has been found that PEO/PS block copolymers are the best stabilizers for the present system as compared to conventional tensides such as SDS or CTAB. It has been found that PEO/PS block copolymers allow obtaining PHBV particles with a regular shape and controlled dimensions after toluene extraction. The minimal size of the PHBV particles obtained by this technique was ca. 100 nm. The obtained particles exhibit a relatively broad particle size distribution and the particle shape is strongly affected by the block copolymer composition, ultrasound power and the way of toluene extraction.     

Carbon as a catalyst in oxidation reactions and hydrogen halide elimination reactions

Carbon catalyses many reactions, mainly oxidation reactions with oxygen and with halogens, e.g. $\text{SO}{}_2\text{+}\text{1}\text{20}{}_2\text{→ SO}{}_3$, or CO + Cl₂→ COCl₂. It is known, however, that different carbons behave quite differently in the reduction of oxygen on fuel cell cathodes. Therefore the catalytic activity of carbons has been studied in other reactions. A convenient test reaction is the oxidation of dilute aqueous sulphurous acid. It became apparent that all catalytically active carbons contain small quantities of nitrogen, and inactive carbons such as wood charcoal or carbon blacks can be rendered highly active by treatment with N H₃ or HCN at elevated temperatures. Photoelectron spectra indicate that the catalytic activity increases parallel to the incorporation of a nitrogen species which is pyridine-like, i.e. incorporated in the aromatic layers. Treatment with NH₃ at 900 °C leads also to massive gasification of the carbons, increasing their surface area. Other reactions studied included the oxidation of aqueous oxalic acid and of methanol to formaldehyde. A quite different type of reaction is the elimination of hydrogen chloride from 1-chloroalkanes, e.g. 1 -chlorobutane. Again, activity changes in parallel to nitrogen content. Reaction products are olefins, dimers of the alkyl groups, and a polymer on the catalyst surface. The formation of alkyl dimers, e.g. n-octane in the case of n-butylchloride, suggests that radicals are involved in the reaction.     

Growth and Viability of Cutaneous Squamous Cell Carcinoma Cell Lines Display Different Sensitivities to Isoform-Specific Phosphoinositide 3-Kinase Inhibitors

Cutaneous squamous cell carcinomas (cSCCs) account for about 20% of keratinocyte carcinomas, the most common cancer in the UK. Therapeutic options for cSCC patients who develop metastasis are limited and a better understanding of the biochemical pathways involved in cSCC development/progression is crucial to identify novel therapeutic targets. Evidence indicates that the phosphoinositide 3-kinases (PI3Ks)/Akt pathway plays an important role, in particular in advanced cSCC. Questions remain of whether all four PI3K isoforms able to activate Akt are involved and whether selective inhibition of specific isoform(s) might represent a more targeted strategy. Here we determined the sensitivity of four patient-derived cSCC cell lines to isoform-specific PI3K inhibitors to start investigating their potential therapeutic value in cSCC. Parallel experiments were performed in immortalized keratinocyte cell lines. We observed that pan PI3Ks inhibition reduced the growth/viability of all tested cell lines, confirming the crucial role of this pathway. Selective inhibition of the PI3K isoform p110α reduced growth/viability of keratinocytes and of two cSCC cell lines while affecting the other two only slightly. Importantly, p110α inhibition reduced Akt phosphorylation in all cSCC cell lines. These data indicate that growth and viability of the investigated cSCC cells display differential sensitivity to isoform-specific PI3K inhibitors.