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Strong Adsorption (strong + adsorption)
Selected AbstractsElectrode Reactions of Catechol at Tyrosinase-Immobilized Latex SuspensionsELECTROANALYSIS, Issue 8 2004Patsamon Rijiravanich Abstract Tyrosinase was immobilized on polystyrene latex particles in order to control amounts of the enzyme. The tyrosinase-coated latex particles were composed of the core polystyrene and four successive coating layers: polystyrene sulfonate, polyallylamine, tyrosinase and polyallylamine again, built up by the layer-by-layer technique. They showed catalytic currents for the enzymatic oxidation of catechol to o -quinone. The enzyme activity per particle was evaluated as 2.3×10,7 units from UV absorption of o -quinone. The relation between the catalytic current and the concentration of catechol leads to a Michaelis-Menten type kinetic equation. The layer-by-layer method was found to have a deactivating effect on enzyme catalysis. In spite of this, the catechol oxidation current was larger than the current from free tyrosinase at a common value of enzyme units per volume. This is ascribed to strong adsorption of the latex particles on the electrode, leading to the enhancement of the local concentration of tyrosinase. [source] Prediction of large variation in biota to sediment accumulation factors due to concentration-dependent black carbon adsorption of planar hydrophobic organic compoundsENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 3 2005Gerard Cornelissen Abstract Biota-to-sediment accumulation factors (BSAFs) sometimes show large variations between sites for a given planar hydrophobic organic compound (pHOC) in a given organism. We present a framework in which strong adsorption to soot/charcoal (black carbon [BC]) explains such BSAF variations. Recently constrained parameters on environmental BC sorption were used in a dual-mode sorption model of BSAF. Variations in sedimentary BC content are shown to explain variations in BSAF of one to two orders of magnitude. In addition, strong BC sorption can explain the often-observed difference in BSAF between polycyclic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs). The strong nonlinearity of BC sorption can render BSAF values strongly concentration-dependent for a given sediment/organism/compound combination, so it is of paramount importance to carry out uptake and toxicity tests at the relevant environmental concentrations. [source] Microbial transformation of pyrethroid insecticides in aqueous and sediment phasesENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 1 2004Sangjin Lee Abstract Recent studies showed that synthetic pyrethroids(SPs)can move via surface runoff into aquatic systems. Fifty-six of SP-degrading bacteria strains were isolated from contaminated sediments, of which six were evaluated for their ability to transform bifenthrin and permethrin in the aqueous phase and bifenthrin in the sediment phase. In the aqueous phase, bifenthrin was rapidly degraded by strains of Stenotrophomonas acidaminiphila, and the half-life (t1/2) was reduced from >700 h to 30 to 131 h. Permethrin isomers were degraded by Aeromonas sobria, Erwinia carotovora, and Yersinia frederiksenii. Similar to bifenthrin, the t1/2 of cis - and trans -permethrin was reduced by approximately 10-fold after bacteria inoculation. However, bifenthrin degradation by S. acidaminiphila was significantly inhibited in the presence of sediment, and the effect was likely caused by strong adsorption to the solid phase. Bifenthrin t1/2 was 343 to 466 h for a field sediment, and increased to 980 to 1200 h for a creek sediment. Bifenthrin degradation in the inoculated slurry treatments was not greatly enhanced when compared with the noninoculated system. Therefore, although SP-degrading bacteria may be widespread in aquatic systems, adsorption to sediment could render SPs unavailable to the degraders, thus prolonging their persistence. [source] Graphite Oxides Obtained from Porous Graphite: The Role of Surface Chemistry and Texture in Ammonia Retention at Ambient ConditionsADVANCED FUNCTIONAL MATERIALS, Issue 10 2010Mykola Seredych Abstract Graphite oxides (GO) synthesized using Brodie and Hummers methods are tested for ammonia adsorption at ambient conditions with different contents of water in the system. Surface characterization before and after exposure to ammonia is performed using XRD, FTIR spectroscopy, potentiometric titration, thermal analysis, adsorption of nitrogen, and XPS. Oxidation of the same porous graphite using two methods results in materials with different textural and chemical features. On GO obtained using the Brodie method mainly epoxy and carboxylic groups are present whereas on the GO obtained using the Hummers method chemisorbed oxygen is also found. The contribution of the carboxylic groups in the latter material is greater. It also contains sulfur either in sulfones or as residual sulfuric acid. Ammonia is adsorbed either via reaction with surface groups or dissolution in water. The former is responsible for strong adsorption. The evidence of the catalytic effect of the carbon surface on activation of oxygen leading to surface oxidation is also observed. [source] Simple Purification of Immunoglobulins from Whey Proteins ConcentrateBIOTECHNOLOGY PROGRESS, Issue 2 2006Benevides C. C. Pessela We have developed a new protocol with only two steps for purification of immunoglobulins (Ig) from a protein concentrate of whey. Following this protocol, we have an 80% recovery of immunoglobulins, fairly pure. The purification was achieved by eliminating the BSA, via a strong adsorption on DEAE-agarose. Full desoprtion of the other serum proteins could be achieved without contamination with BSA. Thus, a protein solution containing only Ig and very small proteins (e.g., ,-lactoglobulins and ,-lactalbumin) was obtained. Offering this protein mixture to a lowly activated aminated support, only Ig adsorbed on the support. It has been shown that BSA is able to interact with other proteins (including Ig and lactalbumins). This ability to form complexes with other proteins prevented the success of the direct adsorption of Ig on this mildly activated support, even although Ig should be the largest protein presented in dairy whey. [source] Interaction of Flavin Adenine Dinucleotide (FAD) with a Glassy Carbon Electrode SurfaceCHEMISTRY & BIODIVERSITY, Issue 8 2008Haizhen Wei Abstract The interaction of flavin adenine dinucleotide (FAD) with a glassy carbon electrode (GCE) surface was investigated in terms of the FAD adsorption thermodynamics and kinetics, the subsequent electroreduction mechanism, and the corresponding electron-transfer rate. The kinetics of FAD electroreduction at the GCE was found to be an adsorption-controlled process. A set of electroreduction kinetic parameters was calculated: the true number of electrons involved in the FAD reduction, n=1.76, the apparent transfer coefficient, ,app=0.41, and the apparent heterogeneous electron-transfer rate constant, kapp=1.4,s,1. The deviation of the number of exchanged electrons from the theoretical value for the complete reduction of FAD to FADH2 (n=2) indicates that a small portion of FAD goes to a semiquinone state during the redox process. The FAD adsorption was well described by the Langmuir adsorption isotherm. The large negative apparent Gibbs energy of adsorption (,Gads=,39.7 ±0.4,kJmol,1) indicated a highly spontaneous and strong adsorption of FAD on the GCE. The energetics of the adsorption process was found to be independent of the electrode surface charge in the electrochemical double-layer region. The kinetics of FAD adsorption was modeled using a pseudo -first-order kinetic model. [source] | |||||||||||||