Cobalt and nickel uptake by silica-based extractants

The pK_as of ethyl/butyl phosphonate silica (EBP-Si) have been determined, and the removal of cobalt and nickel from solution was investigated as a function of various parameters and compared with those of Purolite S950. pH uptake experiments suggested a combination of ion exchange and acid dissociation of the surface occurring. Isotherm data, fitted using the Langmuir and Dubinin–Radushkevich (D-R) models, indicated that stronger complexes formed with S950 than with EBP-Si. Kinetic data, fitted using a pseudo-second-order model, suggested that the rate-determining process is the reaction of metal ions with the chelating functionality of the resin. Uptake by EBP-Si is two to three times faster than that on S950.     

Relationship between the presence of newborn and the house dust endotoxin

Background

Exposure to house dust endotoxin induces of airways' inflammation. Endotoxin are produced by the Gram-negative bacteria, which are released into the stools and could contaminate domestic environment.

Objective

The newborn could contaminate his mattress by endotoxin.

Methods

The dusts of mattress and carpets of 97 newborn' dwellings were sampled at birth and after six months of life. Samplings were made in the bedroom from the baby and in the second place where the baby spent the longer time. The endotoxin concentration was measured by a quantitative Limulus assay and the bacterial contamination was evaluated using 3 selective agar media.

Results

Endotoxin concentration at birth was positively associated with the presence of both sibling and the number of inhabitants (p < 0.01). At 6 months of life, the endotoxin concentration raised significantly not only in the mattresses (from a median of 17.6 (ranges: 0.4-346.7) to 79.6 (3.8-518.8) EU/mg) (p < 0.0001), but also in the dust from the second place where the baby is sleeping (from 20.4 (0.8-226.3) to 101.8 (6.5-634.3) EU/mg) (p < 0.001). Importantly, there was no change in endotoxin concentration from the carpets dust, and the environmental dwelling characteristics remained unchanged. The total bacterial contamination was also positively associated with endotoxin concentration in newborn mattress at birth (p < 0.01) and showed a significant increase at 6 months of life of the newborn (p < 0.01).

Conclusion

The newborn is a significant source of house dust's endotoxin.     

Relationship between the structure,physicochemical properties and in vitro digestibility of rice starches with different amylose contents

The in vitro digestibility and molecular and crystalline structures of rice starches (Long-grain, Arborio, Calrose, and Glutinous) differing in amylose content were investigated and the relationship between the structure and in vitro digestibility of starch was studied. Long-grain showed the highest amylose content (27.2%), whereas Glutinous showed the lowest amylose content (4.2%). Long-grain had the highest average amylopectin branch chain length (18.8) and proportion (8.7%) of long branch chains (DP ≥ 37), and the lowest proportion (26.9%) of short branch chains (DP 6–12). Among the non-waxy rice starches (Long-grain, Arborio, and Calrose), Calrose had the lowest average chain length (17.7) and the lowest proportion (7.1%) of long branch chains (DP ≥ 37). The relative crystallinity of rice starch followed the order: Glutinous (33.5%) > Calrose (31.4%) > Arborio (31.0%) > Long-grain (29.9%). Long-grain had the highest gelatinization temperature and the lowest gelatinization temperature range, whereas Glutinous showed the highest gelatinization temperature range and gelatinization enthalpy. Arborio had the highest melting enthalpy for amylose–lipid complex among the tested rice starches. Pasting temperature, setback, and final viscosity increased with increasing amylose content, whereas the peak viscosity and breakdown showed negative correlations with amylose content. The rapidly digestible starch (RDS) content of the tested rice starches followed the order: Glutinous (71.4%) > Calrose (52.2%) > Arborio (48.4%) > Long-grain (39.4%). Contrary to this, the slowly digestible starch (SDS) and resistant starch (RS) contents showed an opposite trend compared to RDS. Digestibility (RDS, SDS, and RS) of the rice starches was significantly correlated (p ≤ 0.05) with amylose content, proportions of DP 6–12 and DP 13–24, relative crystallinity, intensity ratio (of 1047 cm⁻¹ to 1022 cm⁻¹ from Fourier transform infrared spectroscopy), swelling factor, amylose leaching, onset temperature of gelatinization, gelatinization temperature range, gelatinization enthalpy, pasting temperature, peak viscosity, breakdown, setback, and final viscosity.     

Effects of light on sediment nutrient flux and water column nutrient stoichiometry in a shallow lake

The effects of light and temperature on nutrient cycling (silica (Si), nitrogen (N) and phosphorus (P)) between sediments and water in a shallow eutrophic lake (Loch Leven, Scotland), and consequent effects on water column nutrient stoichiometry, were assessed using a series of intact sediment core incubation experiments. Estimates of actual seasonal dark and light P-fluxes were assessed using 24-h incubations. Sediment-P uptake was observed in spring (7 degrees C) and release in autumn (12 degrees C) and summer (17 degrees C), with the highest release rates ( approximately 17 mgPO4-Pm(-2) sediment surface area d(-1)) occurring in summer. In a longer (21-day) experiment in which the effects of light (light (n=6) and dark (n=6)) and temperature (five 4-day cycles to represent: 7 degrees C-->13 degrees C-->23 degrees C-->13 degrees C-->7 degrees C) on water column nutrient concentrations were assessed, PO(4-)-P, total P (TP), SiO2 and total silica (TSi) concentrations in the water column were all significantly higher under dark conditions (ANOVA, alpha=0.05). NH4-N (ammonium N) water column concentrations were observed to be higher under dark conditions at low temperatures and higher under light conditions following a high-temperature (23 degrees C) treatment. No significant light effects were observed for water column total N (TN) concentration. Flux estimates for all nutrients measured are given. In terms of water column nutrient stoichiometry, TN:TP ratio was significantly higher under light conditions, TSi:TN was significantly lower under light conditions, and TSi:TP did not vary significantly between the dark and light treatments. The main processes acting to regulate diffusive nutrient release appeared to be photosynthetic elevation of bottom water pH and dissolved oxygen concentration (both significantly higher under light conditions) and direct microalgal sequestration. Thus, a feedback mechanism exists in recovering shallow lakes where benthic microalgae can affect the stoichiometry (to favour P/Si limitation) of the plankton, and also of the main source of nutrients back to the sediments via the disproportionate regulation of sediment P, Si and N release.     

Perfluorinated compounds in the Cape Fear Drainage Basin in North Carolina

Concern over perfluorinated organic compounds (PFCs), e.g., perfluorooctane sulfonate (PFOS) and perfluorooctanoic acid (PFOA), is due to a number of recent studies which show that the PFCs are persistent, bioaccumulative, and toxic in animals. Despite sustained interest in this topic, little information is available concerning the environmental distributions of the compounds. In this study, a new method was developed for the analysis of 10 target PFCs and its performance was examined in a systematic evaluation of surface water in the Cape Fear River Basin in North Carolina. One hundred samples from 80 different locations were collected during the spring of 2006. Detectable levels of the target PFCs were found in all samples, and were comparable to values reported previously, with maximum PFOS at 132 ng/L, PFOA at 287 ng/L, perfluorononanoic acid (C9) at 194 ng/L, and perfluoroheptanoic acid (C7) at 329 ng/L. In general, the lowest concentrations of the PFCs were found in the smallest tributaries while the highest levels were found in middle reaches of the Drainage Basin. Variability of PFC concentrations suggests a series of source inputs throughout the Basin. Seventeen sample sites (22%) had PFOS concentrations greater than 43 ng/L, a conservative safe water concentration estimated to be protective of avian life. In addition, a total of 26 sites (32%) had PFOA concentrations above 40 ng/L.     

Field evaluation of in situ source reduction of trichloroethylene in groundwater using bioenhanced in-well vapor stripping

Two technologies in combination, cometabolic bioremediation and in-well vapor stripping, were applied to reduce trichloroethylene (TCE) concentrations in groundwater at a contaminant source area without the need to pump contaminated groundwater to the surface for treatment. The vapor-stripping well reduced source TCE concentrations (as high as 6-9 mg/L) by over 95%. Effluent from the well then flowed to two bioremediation wells, where additional reductions of approximately 60% were achieved. TCE removal was extensively monitored (for research and not regulatory purposes) using an automated system that collected samples about every 45 min at 55 locations over an area of approximately 50 x 60 m2. During 4.5 months of system operation, total TCE mass removal was 8.1 kg, 7.1 kg of which resulted from in-well vapor stripping and 1.0 kg from biotreatment. The system reduced the average TCE concentration of about 3000 microg/L in the source-zone groundwater to about 250 microg/L in water leaving the treatment zone, effecting greater than 92% TCE removal. A 6 month rebound study after system operation ceased found TCE concentrations then increased significantly in the treatment zone due to diffusion from the fractured rock below and perhaps other processes, with mass increases of about 1.5 kg in the lower aquifer and 0.3 kg in the upper aquifer.     

Potentiostatic electrodeposition of cuprous oxide thin films for photovoltaic applications

Potentiostatic deposition of Cu₂O thin films on glass substrates coated with F-doped SnO₂ from an alkaline electrolyte solution (pH 12.5) containing copper (II) sulfate and lactic acid was studied for fabrication of a Cu₂O/Al-doped ZnO (AZO) heterojunction solar cell. The band gap of the electrodeposited Cu₂O films was determined by photoelectrochemical measurements to be around 1.9 eV irrespective of the applied potentials. The solar cells with a glass/FTO/Cu₂O/AZO structure were fabricated by sputtering an AZO film onto the Cu₂O film followed by deposition of an Al contact by vacuum evaporation. The highest efficiency of 0.603% was obtained with a Cu₂O film deposited at −0.6 V (vs. Ag/AgCl). This was attributed to better compactness and purity of the Cu₂O film than those of the Cu₂O films deposited at other potentials.     

Synthesis of pH-sensitive micelles from linseed oil using atom transfer radical polymerisation (ATRP)

This paper reports the synthesis of an amphiphilic copolymer from linseed oils and its successive auto-association in water into pH-sensitive micelles. An original ATRP lipoinitiator is first designed from linseed oil in two steps. tert-butyl acrylate (tBA) polymerization is consequently initiated from this original initiator and amphiphilic copolymers are obtained after subsequent acidolysis of the PtBA block into poly(acrylic acid) (PAA). The ability of a lipid-b-PAA copolymer to auto-associate in water is finally investigated through different techniques (Fluorescence, Surface Tension, QELS). This copolymer forms well-defined micelles in acidic media with a low critical micellar concentration (cmc) of 7.6 mg L^?1 and dissociates when the pH is raised above 7.     

Monoammonium glycyrrhizinate stability in aqueous buffer solutions

The objective of this research is to evaluate the thermal stability of monoammonium glycyrrhizinate. Thermodegradation of solutions of monoammonium glycyrrhizinate at various temperatures (50, 70 and 90°C) was studied. This degradation appeared to follow first-order kinetics independently of temperature and was found to be pH dependent. The experiments revealed an activation energy (E_a) of about 33 kJ mol⁻¹ and a t_90% of about 3 years at 20°C in a pH range from 7 to 9. So it can be concluded that monoammonium glycyrrhizinate is stable in a pH range from 7 to 9. It can be interesting for use in oral care or in food industry. © 1998 SCI.     

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