Equilibrium sorption isotherm for metal ions on tree fern

A new sorbent system for removing heavy metal ions, such as Zn(II), Cu(II) and Pb(II), from aqueous solutions has been investigated. This new sorbent is tree fern, an agriculture product. Variables of the system include solution temperature and sorbent particle size. The experimental results were fitted to the Langmuir, Freundlich and Redlich–Peterson isotherms to obtain the characteristic parameters of each model. Both the Langmuir and Redlich–Peterson isotherms were found to well represent the measured sorption data. According to the evaluation using the Langmuir equation, the maximum sorption capacities of metal ions onto tree fern were 7.58 mg/g for Zn(II), 10.6 mg/g for Cu(II) and 39.8 mg/g for Pb(II). It was noted that an increase in temperature resulted in a higher metal loading per unit weight of the sorbent. Decreasing the particle sizes of tree fern led in an increase in the metal uptake per unit weight of the sorbent.     

Modeling of DNAPL-Dissolution,Rate-Limited Sorption and Biodegradation Reactions in Groundwater Systems

This article presents an approach for modeling the dissolution process of single component dense non-aqueous phase liquids (DNAPL), such as tetrachloroethene and trichloroethene, in a biologically reactive porous medium. In the proposed approach, the overall transport processes are conceptualized as three distinct reactions. Firstly, the dissolution (or dissolving) process of a residual DNAPL source zone is conceptualized as a mass-transfer limited reaction. Secondly, the contaminants dissolved from the DNAPL source are allowed to partition between sediment and water phases through a rate-limited sorption reaction. Finally, the contaminants in the solid and liquid phases are allowed to degrade by a set of kinetic-limited biological reactions. Although all of these three reaction processes have been researched in the past, little progress has been made towards understanding the combined effects of these processes. This work provides a rigorous mathematical model for describing the coupled effects of these three fundamental reactive transport mechanisms. The model equations are then solved using the general-purpose reactive transport code RT3D (Clement, 1997).     

Treatment of chlorinated volatile organic compounds in upflow wetland mesocosms

Sorption, biodegradation and hydraulic parameters were determined in the laboratory for two candidate soil substrate mixtures for construction of an upflow treatment wetland for volatile organic compounds (VOCs) at a Superfund site. The major parent contaminants in the groundwater at the Superfund site were cis-1,2-dichloroethene (cis-1,2-DCE) and 1,1,1-trichloroethane (1,1,1-TCA). The two mixtures; one a mixture of sand and peat, the other a mixture of sand, peat and Bion Soil, a product derived from agricultural wastes; were selected from ten possible mixtures based on the results of hydraulic and geotechnical testing. The sand and peat mixture had an average hydraulic conductivity of 4.95×10⁻⁴ cm/s with a critical flow of 39.5 gpm/acre (368 l/min/ha) without fluidization of the bed. The sand, peat and Bion Soil mixture had an average hydraulic conductivity of 3.02×10⁻⁴ cm/s with a critical flow of 36.8 gpm/acre (344 l/min/ha) without fluidization of the bed. Retardation coefficients ranged from 1 to 7.3 for target VOCs with higher coefficients observed in the mixture containing the Bion Soil. Consistently higher spatial and temporal first-order removal rate constants were observed in the sand, peat and Bion Soil mixture (cis-1,2-DCE, 0.84±0.36/day; 1,1,1-TCA, 6.52±3.12/day) than in the sand and peat mixture (cis-1,2-DCE, 0.37±0.13/day; 1,1,1-TCA, 1.48±0.42/day). Results from anaerobic microcosm studies confirmed that biodegradation was occurring in the columns and that the sand, peat and Bion Soil mixture had higher degradation rate than the sand and peat mixture. Vinyl chloride (VC) was identified as a ‘design’ contaminant since it is a proven carcinogen and had the lowest removal rate constant for both substrate mixtures. Effective wetland bed depths for VC removal of 900 and 210 cm will be required for peat and sand alone and sand, peat and Bion Soil mixtures, respectively.     

Uranium sorption onto natural sediments within a small stream in central Japan

In this study, we surveyed the uranium (U) load in stream water within a humid forest in Japan, and clarified the fact that changes in U load depended on the amount of sediment accumulated behind dams constructed along the stream. To elucidate the relationship between U and the accumulated sediments, we conducted U sorption experiments in the laboratory using stream water and sampled sediments. The chemistry of the stream water was analyzed in the field for pH, electrical conductivity (EC), and temperature, as well as laboratory analyses via inductively coupled plasma mass spectrometry (ICP-MS). We determined the amount of organic material, amorphous material, and total U contents in the sediments. Following the sorption experiments, we analyzed the pH and U concentrations in experimental solutions and determined the distribution coefficients of U for the sediments. The logarithm value of the distribution coefficients of U for amorphous material shows a positive correlation with pH, while the logarithm value of the distribution coefficients of U for organic material is independent of pH (4.7–6.9). Although the logarithm value of the distribution coefficient of U for amorphous material was 0.1–0.5 units larger than the value for organic material, U was effectively removed from the stream water by sorption onto organic material (humic substances and decomposing leaves), because the amount of organic material exceeded that of amorphous material.     

Methodological aspects of microcalorimetry used to assess the dynamics of microbial activity during composting

Isothermal microcalorimetry is a sensitive non-invasive analytical tool that can become useful in research on compost and other biosolids. The aim of the present study was to address several methodological aspects that are critical to the use of microcalorimetry to assess the dynamics of microbial activity in such systems. The results show that: (1) The calorimetric baseline is strongly influenced by the run temperature in the range relevant to composting systems (20–60 °C), and is also affected by addition of the water that is required to maintain or optimize microbial activity, presumably because some water evaporates through ampoule gaskets. (2) Amending mature compost with readily available substrates requires additional careful baseline treatment. (3) Sample heterogeneity can be successfully minimized by passing through a 2-mm sieve. Additional size separation can be useful to enable focusing on the more active fractions. (4) Oxygen depletion is a key feature in batch calorimetric analysis; for samples of highly active composts or manure, the total amount of heat released relative to the oxygen available in the ampoule may indicate the co-existence of anaerobic and aerobic metabolic pathways. Finally, practical recommendations for microcalorimetry analyses of pre-mature and mature composts are outlined.     

Imbibitional damage in conidia of the entomopathogenic fungi Beauveria bassiana, Metarhizium acridum, and Metarhizium anisopliae

When dried organisms are immersed in water, rapid imbibition may cause severe damage to plasma membranes; in unicellular organisms, such damage is usually lethal. This study investigated effects of water activity (dryness) of organisms and immersion temperature on imbibitional damage in three insect pathogenic fungi. Conidial powders of Beauveria bassiana (Bb), Metarhizium anisopliae (Ma) and Metarhizium acridum (Mac) were dried/hydrated to a broad range of water activities (a_w) (0.023–0.961) prior to immersion in water at 0.5–33 °C. Imbibitional damage in conidia of each fungus occurred rapidly, with no differences in viabilities observed following immersion for 2 vs. 60 min. Damage increased with decreasing water activity of the conidia and decreasing temperature of the immersion water. Dry (a_w  0.333) Metarhizium spp. conidia were highly susceptible to imbibitional damage, with viability declining to 5% after immersion at 0.5 °C and 63% following immersion at 15 °C. Germination of the driest Ma conidia was reduced to 66% after treatment at 25 °C. In contrast, Bb was highly tolerant to damage, with significant reductions in viability (to levels as low as 43–65%) occurring only when dry conidia were immersed at 0.5 °C. Damage was prevented when conidia were slowly rehydrated by humidification prior to immersion and immersion temperature was increased to 33–34 °C; germination of all fungi was 94% under these optimal conditions. However, immersion of the driest Bb, Ma, and Mac powders in warm water (33 °C) also resulted in high viabilities (95%, 89%, and 94%, respectively), and slow-rehydrated conidia also retained high viability (87%, 92%, and 83%, respectively) after immersion in ice-cold water (0.5 °C). Formulation of conidia in pure (non-emulsifiable) paraffinic oil provided considerable protection from imbibitional damage. This study underscores a need for establishing standard protocols for preparing aqueous suspensions of sensitive fungi for both research and commercial applications.     

Siderophore sorption to clays

Siderophores are low molecular weight organic ligands exuded by some aerobic organisms and plants to acquire Fe under Fe-limited conditions. The hydroxamate siderophores may sorb to aluminosilicate clays through a variety of mechanisms depending upon the nature of the clay and of the siderophore along with solution conditions such as pH, ionic strength, and presence of metal cations. They may also affect metal binding to clays. Here, we review previous studies of siderophore sorption to aluminosilicate clays; briefly discuss how the techniques of X-ray diffractometry, Fourier-transform infrared spectroscopy, and X-ray absorption spectroscopy may be applied to such studies; review effects of siderophores on metal sorption to clays; and highlight some areas for future research.     

Reversible structural change of host framework triggered by desorption and adsorption of guest benzene molecules in Fe(NCS)2(bpp)2·2(benzene) (bpp = 1,3-bis(4-pyridyl)propane)

Assembled iron complex Fe(NCS)₂(bpp)₂·2(benzene) (bpp = 1,3-bis(4-pyridyl)propane), enclathrating benzene molecules, has been synthesized and its host framework was 1D chain structure. By releasing benzene molecules, the host framework changed to 2D interpenetrated structure. The desorbed complex enclathrated benzene molecules again and the host framework returned to 1D structure. Although the spin state remained in the high spin upon the desorption and adsorption of the benzene molecules, ⁵⁷Fe Mössbauer spectra revealed that the symmetry around iron atom changed depending on the sorption. The reversible structural change of host framework was tried to explain by two factors: the crystal stability by making up the interstitial space and the conformer stability in coordinated bridging ligand bpp.     

消杀型纳米催化剂抗病毒作用的研究

本文探讨112种消杀型纳米催化剂吸附与灭活病毒的功效,为开发新型抗病毒纳米材料提供理论依据。我们将各种纳米催化剂与副流感病毒、人疱疹病毒Ⅰ型、腺病毒1型及5型作用一定时间后,分别以血凝试验及观察CPE变化的方法判断纳米材料对各种病毒的吸附与灭活作用,并在电子显微镜下观察纳米材料对病毒的吸附情况。结果在所检测的112种纳米催化剂中,用血凝试验分别筛选出强吸附力催化剂 29 种、中吸附力催化剂 36 种、弱吸附力催化剂47种。其中,13 种强吸附力催化剂对副流感病毒的吸附率在 87.5%~93.75%之间,并以 AB 24的抗病毒效果最好。     

Fast stopped-flow microcalorimeter

A fast stopped-flow microcalorimeter using a thermistor and an a.c. bridge is described. Time resolution, limited by the response of the thermistor, is 3 ms for t 1/2 while sensitivity is 100 mu degree C in this bandpass. A reaction requires 0.3 ml of each reactant. The microcalorimeter is adiabatic to within 2% for 2 s and mixing may be repeated every 5 min. Computer finite element simulation techniques (FEST) are used to correct for the thermistor response time and heat losses. Results of tests with reactions of NaOH and HCl, NaHCO3, and HCl, and glyclyglycine and CO2 agree with published kinetic and thermodynamic values to within an experimental error of less than 2%.