Adsorption of anionic dye on magnesium hydroxide-coated pyrolytic bio-char and reuse by microwave irradiation

Magnesium hydroxide-coated pyrolytic bio-char composite was prepared by chemical precipitation, and the adsorption behavior of anionic dye (directly frozen yellow) onto magnesium hydroxide-coated pyrolytic bio-char was investigated in the batch mode. The Fourier transform infrared spectroscopy, X-ray diffraction spectroscopy and X-ray fluorescence spectroscopy of adsorbents were characterized. Adsorption studies were performed at different pH, salt concentration, contacting time and dye concentration. The pH value of the solution influenced the adsorption capacity significantly, and adsorption is favored of pH 6–8. Salt coexisted in solution increased slightly directly frozen yellow adsorption capacity. The isotherm data were analyzed by Langmuir and Freundlich isotherm model, and Langmuir model was better to predict the equilibrium data. Thermodynamic calculations showed that the adsorption was a spontaneous and endothermic process. Exhausted magnesium hydroxide-coated pyrolytic bio-char was treated by microwave irradiation, and yield of regeneration was 98 % in the case of microwave irradiated time 5 min at 320 W. The magnesium hydroxide-coated pyrolytic bio-char can be reused.     

The effect of iron on montmorillonite stability. (I) Background and thermodynamic considerations

It is envisaged that high-level nuclear waste (HLW) will be disposed of in underground repositories. Many proposed repository designs include steel waste canisters and bentonite backfill. Natural analogues and experimental data indicate that the montmorillonite component of the backfill could react with steel corrosion products to produce non-swelling Fe-rich phyllosilicates such as chamosite, berthierine, or Fe-rich smectite. In K-bearing systems, the alteration of montmorillonite to illite/glauconite could also be envisaged. If montmorillonite were altered to non-swelling minerals, the swelling capacity and self-healing properties of the bentonite backfill could be reduced, thereby diminishing backfill performance. The main aim of this paper was to investigate Fe-rich phyllosilicate mineral stability at the canister-backfill interface using thermodynamic modelling. Estimates of thermodynamic properties were made for Fe-rich clay minerals in order to construct approximate phase-relations for end-member/simplified mineral compositions in logarithmic activity space. Logarithmic activity diagrams (for the system Al₂O₃-FeO-Fe₂O₃-MgO-Na₂O-SiO₂-H₂O) suggest that if pore waters are supersaturated with respect to magnetite in HLW repositories, Fe(II)-rich saponite is the most likely montmorillonite alteration product (if f_O2(g) values are significantly lower than magnetite-hematite equilibrium). Therefore, the alteration of montmorillonite may not be detrimental to nuclear waste repositories that include Fe, as long as the swelling behaviour of the Fe-rich smectite produced is maintained. If f_O2(g) exceeds magnetite-hematite equilibrium, and solutions are saturated with respect to magnetite in HLW repositories, berthierine is likely to be more stable than smectite minerals. The alteration of montmorillonite to berthierine could be detrimental to the performance of HLW repositories.     

Structural and petrological evidence for the continuation of the Isfahan fault system across the Urumieh-Dokhtar zone of central Iran

The Isfahan fault system, a north-trending, dextral strike-slip fault across the Sanandaj-Sirjan zone, represents the boundary between the northwestern and the southeastern parts of the Sanandaj-Sirjan zone and it terminates in the north at the southern boundary of the Urumieh-Dokhtar zone. This paper focuses on the continuation of the Isfahan fault system across the Urumieh-Dokhtar zone north of Isfahan city. The Urumieh-Dokhtar magmatic assemblage belt is located along the active margin of the Iranian plate and the Arabian plate. The Karkas fault strikes nearly north-south, has a length of about 40 km, a normal component of movement, and it truncates the Urumieh-Dokhtar zone. Due to the location of this fault and the mechanism similar to the Isfahan fault system, the Karkas fault can be considered a continuation of the Isfahan fault system that has been displaced dextrally by the southwestern bordering faults of the Urumieh-Dokhtar zone. The unique juxtaposition association of the Silurian volcanic rocks in the Urumieh-Dokhtar zone, near the Karkas fault, provides an important evidence regarding the major role of this fault in the geological evolution of the region. The Silurian volcanic rocks outcrop in two districts of the study area and generally are composed of basalts. The alkaline basalt composition is determined from mineralogy and immobile elements geochemistry. The geotectonic setting diagrams classified the Silurian volcanic rocks as the within plate basalts. Thus, an intracontinental rifting under extensional tectonic regime can be inferred as the setting that controlled formation of these volcanic rocks. They were created by an alkaline to transitional magmas generated due to low partial melting at depth. The alkaline basalts were most likely derived from an asthenosphere-dominated mantle source due to extension and partial melting. The north trending extensional faults affected thinned overlying continental lithosphere in the Paleozoic era, facilitating magma penetration and eruption.     

Removal of cadmium (II) from aqueous solution and natural water samples using polyurethane foam/organobentonite/iron oxide nanocomposite adsorbent

A novel polyurethane foam/organobentonite/iron oxide nanocomposite adsorbent was successfully prepared via in situ polymerization of toluene diisocyanate and polyol in presence of 5 wt% organobentonite/iron oxide. The obtained nanocomposite was characterized in detail, and the results revealed that the clay layers are exfoliated and/or intercalated in the polymer matrix forming a nanocomposite structure. The application of the prepared nanocomposite for adsorption of cadmium ions from aqueous solution was tested as a function of various experimental parameters using batch procedures. Adsorptive removal of Cd(II) onto the nanocomposite attained maximum at adsorbent content 1.5 g/L, pH 6, and the equilibrium was established within 60 min. Kinetic studies showed that the experimental data fit very well to pseudo-second-order model, and the adsorption process proceeds through three steps. It was found that external liquid film and intraparticle diffusion steps deeply affect the rate of Cd²⁺ ions adsorption onto the synthesized nanocomposite. Langmuir isotherm model fitted the adsorption data better than Freundlich with a maximum adsorption capacity (q _m) for Cd(II) equal to 78 mg/g under the specified experimental conditions. The synthesized nanocomposite afforded effective extraction for Cd²⁺ ions from natural water samples and excellent reusability feature. This study declares the potential efficiency of a new clay/polymer nanocomposite as alternative for wastewater remediation.     

First record of 1.2 Ga quartz dioritic magmatism in the Archaean Yilgarn Craton,Western Australia,and its significance

Farming of southern bluefin tuna in South Australia currently contributes to more than 30% of the value of the aquaculture production in Australia. This study investigated the natural sedimentary setting of the area designated for this important industry in coastal waters off Port Lincoln, and explored the links between the natural distribution of sediments and potential environmental effects and risks to the industry. Sediments were mostly composed of poorly sorted silts and fine sands, predominantly skeletal remains of carbonate-secreting organisms. The contribution of plankton to the organic matter remaining in the sediments was calculated to be in excess of 80% using concentration-dependent stable-isotope mixing models. An erosional area was identified south of Rabbit Island where sediments contained up to 50% siliciclastic material, grainsize distributions were better sorted and coarser, and organic carbon and total nitrogen contents were very low. In contrast, deeper waters north of Cape Donington were identified as a depocentre for fine sediments, which contained organic matter levels twice those elsewhere in the region despite the extremely high carbonate contents (>80%). The heavier stable isotopic signature of nitrogen suggested that this organic matter comprised a greater fraction of weathered components, probably advected to the area by suspended and bedload transport. This local variability of sediment characteristics in the farming zone suggests that the benthic assimilative capacity of farmed sites will depend on their location. Wastes from pens located south of Rabbit Island in particular are likely to be quickly winnowed out by wave and tidal action. These pens are also less likely to be affected by resuspension of fine sediments that might be associated with unusually severe storms.     

Secondary geochemical dispersion in the Precambrian auriferous Hutti-Maski schist belt, Raichur district, Karnataka, India. Part I: anomalies of As, Sb, Hg and Bi in soil and groundwater

The nature of secondary geochemical dispersion of As, Sb, Hg and Bi in soil and ground water of the semi-arid, tropical, Archaean, auriferous, Hutti-Maski greenstone belt has been investigated for identification of appropriate geochemical techniques for Au exploration in similar terrains.Results indicate that the <180 μm size-fraction of C-horizon soil is an appropriate sampling medium for delineating pedogeochemical anomalies of As, Sb, Hg and Bi related to gold mineralisation. These pedogeochemical anomalies along with anomalous values of alkalinity, chloride, sulphate, As and Sb in groundwater are controlled significantly by primary mineralisation located along shear zones in the greenstone belt. Arsenic anomalies in soil are broad, whereas, those of Sb and Bi are restricted to narrow zones directly over mineralised areas. In contrast, Hg anomalies around known mineralised areas are irregular and do not clearly demarcate the mineralised areas. The study indicates that anomalies of As, Sb and Hg in soil are principally hydromorphic, whereas those of Bi are clastic.The study recommends use of groundwater sampling at 2–3 km spacing with routine analysis of chloride, sulphate and alkalinity along with As and Sb in the first phase. This may be followed up with sampling of C-horizon of soils on a 1 km square grid for As-anomalies. Arsenic-anomalous areas may be sampled for As, Sb, Hg and Bi on a 500 m square grid for detailed exploration.     

pH influence on sorption characteristics of heavy metal in the vadose zone

Sorption is an important process in the modelling and prediction of the movement of heavy metals in unsaturated clay barriers. This experimental study investigates the effect of pH changes in the acidic range on the sorption characteristics of heavy metals such as: lead, copper and zinc in an unsaturated soil. A series of one-dimensional coupled solute and moisture leaching column tests, using different heavy metal solutions, were conducted on an unsaturated illitic soil at varying pH values. Variations of volumetric water content (VWC) with distance were measured for different time durations, and concentrations of heavy metals in the liquid and solid phases were analysed. Partitioning coefficient profiles of contaminants along the soil column were determined for each individual layer in the soil.

Results from column leaching tests showed that the sorption characteristics of heavy metals are controlled by many factors which should be taken into consideration, i.e. the VWC, time of wetting, soil pH, and the influent heavy metal concentrations. Simplification of K_d as a constant and of the VWC as a linear function cannot be considered a good assumption and may lead to an improper evaluation of the sorption phenomena and also to serious errors in predicting contaminant transport through unsaturated soils.     

Experimental silicate mineral/melt partition coefficients for beryllium and the crustal Be cycle from migmatite to pegmatite

Partition coefficients (D_Be^mineral/melt) for beryllium between hydrous granitic melt and alkali feldspars, plagioclase feldspars, quartz, dark mica, and white mica were determined by experiment at 200 MPa H₂O as a function of temperature (650-900°C), activity of Be in melt (trace levels to beryl saturation), bulk composition, and thermal run direction. At trace levels, Be is compatible in plagioclase of An₃₁ (1.84 at 700°C) and muscovite (1.35 at 700°C) but incompatible in biotite (0.39-0.54 from 650-800°C), alkali feldspar (0.38-0.19 from 680-850°C), quartz (0.24 at 800°C), and albite (0.10 at 750°C). The partition coefficients are different at saturation of the melt in beryl: lower in the case of plagioclase of An₃₁ (0.89 at 700°C), muscovite (0.87 at 700°C), biotite (0.18-0.08 from 675-800°C), alkali feldspar (0.18-0.14 from 680-700°C), and quartz (0.17-0.08 from 750-800°C), but higher in the case of albite (0.37 at 750°C).With other data sources, these new partition coefficients were utilized to track, first, the distribution of Be between aluminous quartzofeldspathic source rocks and their anatectic melts, and second, the dispersion or concentration of Be in melt through igneous crystal fractionation of different magma types (e.g., S-type, I-type) up to beryl-saturated granitic pegmatites and, finally, into their hydrothermal aureoles. Among the rock-forming minerals, cordierite, calcic oligoclase, and muscovite (in this order) control the fate of Be because of the compatibility of Be in these phases. In general, beryl-bearing pegmatites can arise only after extended crystal fractionation of large magma batches (to F, fraction of melt remaining, ≤0.05); granitic magmas that originate from cordierite-bearing protoliths or that contain large modal quantities of calcic oligoclase will not achieve beryl saturation at any point in their evolution.     

Formation of intrathermocline eddies at ocean fronts by wind-driven destruction of potential vorticity

A mechanism for the generation of intrathermocline eddies (ITEs) at wind-forced fronts is examined using a high resolution numerical simulation. Favorable conditions for ITE formation result at fronts forced by “down-front” winds, i.e. winds blowing in the direction of the frontal jet. Down-front winds exert frictional forces that reduce the potential vorticity (PV) within the surface boundary in the frontal outcrop, providing a source for the low-PV water that is the materia prima of ITEs. Meandering of the front drives vertical motions that subduct the low-PV water into the pycnocline, pooling it into the coherent anticyclonic vortex of a submesoscale ITE. As the fluid is subducted along the outcropping frontal isopycnal, the low-PV water, which at the surface is associated with strongly baroclinic flow, re-expresses itself as water with nearly zero absolute vorticity. This generation of strong anticyclonic vorticity results from the tilting of the horizontal vorticity of the frontal jet, not from vortex squashing. During the formation of the ITE, high-PV water from the pycnocline is upwelled alongside the subducting low-PV surface water. The positive correlation between the ITE’s velocity and PV fields results in an upward, along-isopycnal eddy PV flux that scales with the surface frictional PV flux driven by the wind. The relationship between the eddy and wind-induced frictional PV flux is nonlocal in time, as the eddy PV flux persists long after the wind forcing is shut off. The ITE’s PV flux affects the large-scale flow by driving an eddy-induced transport or bolus velocity down the outcropping isopycnal layer with a magnitude that scales with the Ekman velocity.     

Parameterization of the Absorption of the H_2O Continuum,CO_2,O_2,and Other Trace Gases in the Fu-Liou Solar Radiation Program

The absorption properties of the water vapor continuum and a number of weak bands for H2O, O2, CO2, CO, N2O, CH4, and O3 in the solar spectrum are incorporated into the Fu-Liou radiation parameterization program by using the correlated k-distribution method (CKD) for the sorting of absorption lines. The overlap absorption of the H2O lines and the H2O continuum (2500-14500 cm-1) are treated by taking the two gases as a single-mixture gas in transmittance calculations. Furthermore, in order to optimize the computation efforts, CO2 and CH4 in the spectral region 2850-5250 cm-1 are taken as a new single-mixture gas as well. For overlap involving other absorption lines in the Fu-Liou spectral bands, the authors adopt the multiplication rule for transmittance computations under which the absorption spectra for two gases are assumed to be uncorrelated. Compared to the line-by-line (LBL) computation, it is shown that the errors in fluxes introduced by these two approaches within the context of the CKD method are small and less than 0.48% for the H2O line and continuum in the 2500-14500 cm-1 solar spectral region, -1% for H2O (line) H2O (continuum) CO2 CH4 in the spectral region 2850-5250 cm-1, and -1.5% for H2O (line) H2O (continuum) O2 in the 7700-14500 cm-1 spectral region. Analysis also demonstrates that the multiplication rule over a spectral interval as wide as 6800 cm-1 can produce acceptable errors with a maximum percentage value of about 2% in reference to the LBL calculation. Addition of the preceding gases increases the absorption of solar radiation under all sky conditions. For clear sky, the increase in instantaneous solar absorption is about 9%-13% (~12 W m~2) among which the H2O continuum produces the largest increase, while the contributions from O2 and CO2 rank second and third, respectively. In cloudy sky, the addition of absorption amounts to about 6-9 W m-2. The new, improved program with the incorporation of the preceding gases produces a smaller solar absorption in clouds due to the reduced solar flux reaching the cloud top.