Improved power density and Cr/Pb removal using ozone in a microbial desalination cell

Environmental Chemistry Letters - Microbial desalination cells are promising bio-electrochemical technologies for water desalination, treating wastewater and bioelectricity production. In this...     

The mechanism of crustacean salinity tolerance: Cell volume regulation by K+ and glycine effluxes

The regulation of muscle fiber K⁺ and free amino acid (FAA) concentrations during hypoosmotic stress was investigated in the moderately euryhaline crab Cancer irroratus. After 6 h of exposure to 60% ASW, muscle fiber K⁺ concentration declined from 185 mM to 140 mM. Following this, the blood glycine levels began to increase, indicating an FAA efflux from the cells. These data indicate that both muscle fiber K⁺ and FAA contribute to cell volume regulation in C. irroratus. The early release of K⁺ limits the initial rate of cell hydration. The subsequent efflux of glycine accounts for the volume regulation response of the muscle fibers. The cell volume regulatory system of C. irroratus is a coordinated use of both inorganic ions and FAA.     

Improved soil carbonate determination by FT-IR and X-ray analysis

In forest soils on calcareous parent material, carbonate is a key component that influences both chemical and physical soil properties and thus fertility and productivity. At low organic carbon contents, it is difficult to distinguish between organic and inorganic carbon, e.g. carbonates, in soils. The common gas-volumetric method to determine carbonate has a number of disadvantages. We hypothesize that a combination of two spectroscopic methods, which account for different forms of carbonate, can be used to model soil carbonate in our region. Fourier transform mid-infrared spectroscopy was combined with X-ray diffraction to develop a model based on partial least squares regression. Results of the gas-volumetric Scheibler method were corrected for the calcite/dolomite ratio. The best model performance was achieved when we combined the two analytical methods using four principal components. The root mean squared error of prediction decreased from 13.07 to 11.57, while full cross-validation explained 94.5 % of the variance of the carbonate content. This is the first time that a combination of the proposed methods has been used to predict carbonate in forest soils, offering a simple method to precisely estimate soil carbonate contents while increasing accuracy in comparison with spectroscopic approaches proposed earlier. This approach has the potential to complement or substitute gas-volumetric methods, specifically in study areas with low soil heterogeneity and similar parent material or in long-term monitoring by consecutive sampling.     

Isolation and characterization of hydrophilic dissolved organic matter in waters by ion exchange solid phase extraction followed by high resolution mass spectrometry

Environmental Chemistry Letters - Dissolved organic matter (DOM) is a complex substance occurring in marine and freshwater environments. DOM has many functions that modify physical, chemical and...     

Antibiofouling hollow-fiber membranes for dye rejection by embedding chitosan and silver-loaded chitosan nanoparticles

Environmental Chemistry Letters - The removal of toxic dyes from the wastewater and industrial effluents is a major environmental challenge. Various techniques have been employed for the removal of...     

Influence of pore size and membrane surface properties on arsenic removal by nanofiltration membranes

Four NF membranes were compared regarding arsenate rejection and their properties. Rejection of arsenate had no relationship with membrane pore size. A more negative surface charge was favorable for arsenate rejection at neutral pH. A severe membrane fouling could lead to a great reduction of arsenic rejection. Nanofiltration (NF) has a great potential in removing arsenate from contaminated water. The performance including arsenate rejection, water permeability and resistance to fouling could however differ substantially among NF membranes. This study was conducted to investigate the influence of membrane pore size and surface properties on these aspects of membrane performance. Four fully-aromatic NF membranes with different physicochemical properties were adopted for this study. The results showed that surface charge, hydrophobicity, roughness and pore size could affect water permeability and/or arsenate rejection considerably. A more negative surface charge was desirable to enhance arsenate rejection rates. NF90 and a non-commercialized membrane (M#1) demonstrated the best performance in terms of arsenate rejection and water permeability. The M#1 membrane showed less membrane fouling than NF90 when used for filtration of real arsenic-containing groundwater. This was mainly due to its distinct chemical composition and surface properties. A severe membrane fouling could lead to a substantial reduction of arsenic rejection. The M#1 membrane showed the best performance, which indicated that membrane modification could indeed enhance the overall membrane performance for water treatment.     

Role of membrane and compound properties in affecting the rejection of pharmaceuticals by different RO/NF membranes

This study was conducted to assess the merits and limitations of various high-pressure membranes, tight nanofiltration (NF) membranes in particular, for the removal of trace organic compounds (TrOCs). The performance of a low-pressure reverse osmosis (LPRO) membrane (ESPA1), a tight NF membrane (NF90) and two loose NF membranes (HL and NF270) was compared for the rejection of 23 different pharmaceuticals (PhACs). Efforts were also devoted to understand the effect of adsorption on the rejection performance of each membrane. Difference in hydrogen bond formation potential (HFP) was taken into consideration. Results showed that NF90 performed similarly to ESPA1 with mean rejection higher than 95%. NF270 outperformed HL in terms of both water permeability and PhAC rejection higher than 90%. Electrostatic effects were more significant in PhAC rejection by loose NF membranes than tight NF and LPRO membranes. The adverse effect of adsorption on rejection by HL and ESPA1 was more substantial than NF270 and NF90, which could not be simply explained by the difference in membrane surface hydrophobicity, selective layer thickness or pore size. The HL membrane had a lower rejection of PhACs of higher hydrophobicity (log D>0) and higher HFP (>0.02). Nevertheless, the effects of PhAC hydrophobicity and HFP on rejection by ESPA1 could not be discerned. Poor rejection of certain PhACs could generally be explained by aspects of steric hindrance, electrostatic interactions and adsorption. High-pressure membranes like NF90 and NF270 have a high promise in TrOC removal from contaminated water.

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Removal and recovery of uranium(VI) by adsorption onto a lignocellulosic-based polymeric adsorbent containing amidoxime chelating functional group

A new adsorbent (ABS) with amidoxime functional group was prepared through graft polymerization of acrylonitrile onto banana stem (BS) using ceric ammonium nitrate (CAN)/HNO₃ initiator system, followed by treatment with hydroxylamine hydrochloride in alkaline solution. Infrared spectroscopy, surface area analyzer, thermogravimetry, and potentiometric titration were used for the characterization of the adsorbent. Effective removal of U(VI) ions was demonstrated at the pH range 4.0–6.0. The mechanism for the removal of U(VI) ions by ABS was based on complexation adsorption model. Equilibrium was achieved in approximately 3 h. The experimental kinetic data were analyzed using first-order, second-order, and Elovich kinetic models, and are well fitted with second-order kinetics. The temperature dependence indicates an exothermic process. U(VI) adsorption was found to decrease with increase of ionic strength. The Freundlich isotherm model fitted the experimental equilibrium data well. The adsorption efficiency was tested using synthetic nuclear industry effluents. The maximum adsorption capacity for U(VI) removal was found to be 80 mg g^-1 at 20°C. Adsorbed U(VI) ions were desorbed effectively, about 99% by 0.2 M HCl. Repeated adsorption/desorption cycles show the feasibility of the ABS for the removal of U(VI) ions from water and nuclear industry effluents.     

Ammonium and free amino acid uptake by a deep-sea mussel (Bathymodiolus sp., undescribed) containing methanotrophic bacterial symbionts

The morphology of the lophophore and mouth was measured for freshly collected colonies of seven common bryozoan reef species at three sites along the central Caribbean coast of Panamá during the dry season, from the end of December 1988 through May 1989. Characters measured or scored include the number of tentacles, circumference of the lophophore, abanal and anal tentacle length, abanal and anal tentacle spacing, and perimeter of the mouth. Taxa studied include three species each of Stylophoma Levinsen, and Steginoporella (Smitt), and one species of Trematooecia Osburn. Individuals were collected from both continental and offshore fringing reefs from depths of 1 to>30 m. Terrestrial runoff from heavy tropical rains, sedimentation, and sea exposure vary greatly between sites. Congeneric species showed small but consistent differences in lophophore size, but little or no difference in spacing of tentacles or perimeter of the mouth. This suggests that closely related species feed on similarly sized particles despite their overall differences in zooidal size. Lopophore morphology also varied intraspecifically between reefs, particularly in the length of the tentacles and spacing between tentacles. Patterns of variation were similar for all species, which implies that species shift their diets in similar directions between the different reefs. The combination of these patterns suggests that niche diversification in feeding does not occur among congeneric species in the cheilostomes examined.     

Improved degradation of azo dyes by lignin peroxidase following mutagenesis at two sites near the catalytic pocket and the application of peroxidase-coated yeast cell walls

• Mutations in Lignin peroxidase Trp171 environment improved azo dyes degradation. • Expression on yeast cell surface and cell lysis allowed reusability of biocatalyst. • Aga2-LiP chimeric variants were characterized. The enzymatic degradation of azo dyes is a promising alternative to ineffective chemical and physical remediation methods. Lignin peroxidase (LiP) from Phanerochaete chrysosporium is a heme-containing lignin-degrading oxidoreductase that catalyzes the peroxide-dependent oxidation of diverse molecules, including industrial dyes. This enzyme is therefore ideal as a starting point for protein engineering. Accordingly, we subjected two positions (165 and 264) in the environment of the catalytic Trp171 residue to saturation mutagenesis, and the resulting library of 10⁴ independent clones was expressed on the surface of yeast cells. This yeast display library was used for the selection of variants with the ability to break down structurally-distinct azo dyes more efficiently. We identified mutants with up to 10-fold greater affinity than wild-type LiP for three diverse azo dyes (Evans blue, amido black 10B and Guinea green) and up to 13-fold higher catalytic activity. Additionally, cell wall fragments displaying mutant LiP enzymes were prepared by toluene-induced cell lysis, achieving significant increases in both enzyme activity and stability compared to a whole-cell biocatalyst. LiP-coated cell wall fragments retained their initial dye degradation activity after 10 reaction cycles each lasting 8 h. The best-performing mutants removed up to 2.5-fold more of each dye than the wild-type LiP in multiple reaction cycles.