Spectral discrimination of phytoplankton colour groups: The effect of suspended particulate matter and sensor spectral resolution

Remote sensing has been used extensively to provide quantitative information on the distribution of phytoplankton in inland waters through the surrogate mapping of chlorophyll a, but as chlorophyll a is common to almost all species of phytoplankton it cannot provide any information on the taxonomic composition of phytoplankton communities. However, the varied optical properties of phytoplankton taxa may present a means to their discrimination via remote sensing data. This paper presents the results of an experimental study in which the spectral dissimilarities of brown, green, blue-green and red algae were examined with a view to establishing a basis upon which broad changes in phytoplankton communities might be monitored through remote sensing. Pseudo phytoplankton communities were simulated in a series of mesocosm experiments from which spectral reflectance measurements were acquired. The results demonstrated that the phytoplankton colour groups examined were indeed spectrally dissimilar. The spectral distinction between colour groups was noted to be greatest at high concentrations of chlorophyll a and between pseudo-communities dominated by a single species; spectral differences were lower in mixed pseudo-communities with co-dominant species. Moreover, it proved possible to quantify the concentration of two potential biomarker pigments, fucoxanthin and C-phycocyanin, through the derivation of simple spectral indices. The coincidental presence of varying concentrations of SPM (SPIM and SPOM) caused significant attenuation of the spectral response of the pseudo-communities and affected the accuracy of biomarker pigment estimation. It is considered that the realisation of a remote sensing technique for the discrimination of phytoplankton taxa in inland waters would be an extremely useful tool for limnological research and water resource management and thus the future application of this research to inland waters is also discussed.     

Electrosynthesis of benzoquinone from phenol on α and β surfaces of PbO2

Electrosynthesis of benzoquinone from phenol was investigated in acetonitrile-water mixtures on α-PbO₂ and β-PbO₂ electrodes. The influence of water concentration, electrolysis potential, initial phenol concentration and temperature on benzoquinone production was also studied. Different electrocatalytic activities of α and β structures of PbO₂ were determined.     

Comparison of planktonic and reed biofilm bacteria in different riverine water bodies of river Danube

As the submerged shoot parts of common reed (Phragmites australis) can provide large surfaces for biofilm‐forming bacteria, extensive reed stands can effectively contribute to the self‐purification in the littoral zones of freshwaters. However, bacterial biofilm developed on reed surfaces have been studied only in still waters. In the present study, comparative examinations were performed on the planktonic and reed biofilm bacterial communities from two different riverine water bodies. Water and reed biofilm samples were taken at the beginning and end of the vegetation period from (a) a regulated side arm and (b) a separated oxbow of River Danube. Besides measuring physical and chemical environmental variables, planktonic bacterial cell numbers were detected by 4′,6‐diamidino‐2‐phenylindole staining method, and the bacterial communities were compared by denaturing gradient gel electrophoresis. Our results demonstrated that the structure and composition of bacterial communities correlated with different environmental variables and were different regarding both the habitats (planktonic vs. reed biofilm) and the types of riverine water bodies. The seasonal differences in the bacterial community structures were smaller in the river side arm than in the separated oxbow. In the water column, representatives of widespread and typical freshwater planktonic bacteria (“Candidatus Planktophila,” Limnohabitans, and Polynucleobacter), whereas, in the reed biofilm samples, phototrophic and plant associated bacteria were identified.     

In situ chlorination of poly(vinyl chloride) in aqueous hydrochloric acid

Based on environmental, safety, corrosion and technological considerations a new method has been developed for chlorination of PVC in aqueous hydrochloric acid solvent by controlled electrolytic in situ generation of chlorine using graphite and chlorine-selective Ti-RuO₂ electrodes. The byproduct, HCl gas, is dissolved at the moment of its formation and acts as starting material of further chlorination. This way, the application of corrosive chlorine gas is avoided. The chlorination conditions have been optimized. The highest chlorine content was found at 5.5 h reaction time using a graphite electrode. The obtained chlorinated PVC did not contain any CCl₂ units.     

The effects of pH on the molecular distribution of water soluble ruthenium(II) hydrides and its consequences on the selectivity of the catalytic hydrogenation of unsaturated aldehydes

The effect of pH on the formation and equilibrium distribution of the water soluble ruthenium hydrides [HRuCl(TPPMS)₂]₂, [HRuCl(TPPMS)₃] and [H₂Ru(TPPMS)₄] (TPPMS=(3-sulfonatophenyl)diphenylphosphine sodium salt) was studied in aqueous solution by pH-potentiometric and

Full-size image

and

Full-size image

NMR methods. Depending on the pH, [RuCl₂(TPPMS)₂]₂ and its hydrido-derivatives hydrolyse extensively, giving rise to formation of hydroxo-ruthenium complexes. It was established that at pH≤3.3 the dominant ruthenium(II) species was [HRuCl(TPPMS)₃], while at pH≥7 it was [H₂Ru(TPPMS)₄]. While [HRuCl(TPPMS)₃] catalyzed the slow, selective hydrogenation of the C=C bond in trans-cinnamaldehyde, [H₂Ru(TPPMS)₄] was found an active and selective catalyst for C=O reduction. Consequently, the selectivity of the hydrogenation of trans-cinnamaldehyde could be completely inverted by minor changes in the solution pH, shifting the equilibrium between [HRuCl(TPPMS)₃] and [H₂Ru(TPPMS)₄].     

Thermal and Mechanical Properties of Poly(arylene ether ketone)s Based on 5‐tert‐Butyl‐1,3‐bis(4‐fluorobenzoyl)benzene

An aromatic bishalide, 5‐tert‐butyl‐1,3‐bis(4‐fluorobenzoyl)benzene ( 2 ) was synthesized in high yield and purity by the reaction of 5‐tert‐butylisophthaloyl chloride ( 1 ) and fluorobenzene and polymerized by nucleophilic substitution reaction with commercially available aromatic bisphenols to prepare a series of high molecular weight poly(arylene ether ketone)s containing pendant tertiary butyl groups. The effect of molecular structure on the physical, thermal, mechanical and adhesion properties of the polymers was investigated.     

Interaction of Aqueous Bovine Serum Albumin with Silica Aerogel Microparticles: Sorption Induced Aggregation

Mesoporous silica aerogels have a wide range of potential applications in biotechnology, the food industry, pharmacy and medicine. Understanding the nature of the interactions of biomolecules with these porous nanostructured materials is essential for achieving optimum performance in the targeted applications. In this study, the well-characterized bovine serum albumin (BSA) was chosen as a model protein to probe protein–aerogel interactions in the solution phase. Aqueous BSA was mixed with suspended silica aerogel microparticles, and the colloid system was monitored on-line by UV–vis spectrophotometry and turbidimetry. The global mathematical analysis of the time-resolved data reveals that the fast sorption of the protein on the aerogel microparticles follows a multistep binding mechanism. The extensive sorption of the protein eventually induces the aggregation of the covered aerogel due to the alteration of the electrical double layer of the particles. The interaction of BSA and silica aerogel is the strongest between pH = 4 and 5, because their native surface charges are the opposite in this pH range, as indicated by their respective zeta potentials.     

Chemiresistive response of silicon nanowires to trace vapor of nitro explosives

Silicon nanowires are observed to behave as chemically modulated resistors and exhibit sensitive and fast electrical responses to vapors of common nitro explosives and their degradation by-products. The nanowires were prepared with a top-down nano-fabrication process on a silicon-on-insulator wafer. The surface of the silicon nanowires was modified by plasma treatments. Both hydrogen and oxygen plasma treatments can significantly improve the responses, and oxygen plasma changes the majority carrier from p- to n-type on the surface of silicon nanowire thin films. The sensitivity is found to increase when the cross-section of the nanowires decreases.     

Poly(N-ethylaniline) coatings on 304 stainless steel for corrosion protection in aqueous HCl and NaCl solutions

Poly(N-ethylaniline) (PNEA) coatings were grown by potentiodynamic synthesis technique on 304 stainless steel (SS) alloy from 0.1 M of N-ethylaniline (NEA) in 0.3 M oxalic acid solution. Characterization of adhesive and electroactive PNEA coatings was carried out by cyclic voltammetry, FT-IR spectroscopy and scanning electron microscopy (SEM) techniques. The protective properties of PNEA coatings on SS were elucidated using linear anodic potentiodynamic polarization, Tafel and electrochemical impedance spectroscopy (EIS) test techniques, in highly aggressive 0.5 M HCl and 0.5 M NaCl solutions. Linear anodic potentiodynamic polarization test results proved that PNEA coating improved the degree of protection against pitting corrosion in HCl and NaCl solutions. Tafel test results showed that PNEA coating appears to enhancement protection for SS in 0.5 M NaCl and 0.5 M HCl solutions. However, according to long-term EIS results, PNEA coating is better for the protection of SS electrodes during the long immersion period in NaCl compared to that in HCl medium.