Hydrogen Sorption Behavior of Cast Ag-Mg Alloys

In this paper, the hydrogen sorption properties of casted Ag-Mg alloys were investigated. The obtained alloys were structurally analyzed by X-ray diffraction (XRD) and observed by scanning electron microscopy (SEM). The study was carried out for four alloys from the two-phase region (Mg) + γ′ (AgMg4) with nominal concentrations of 5 wt. %, 10 wt. %, 15 wt. %, and 20 wt. % Ag, four alloys with nominal compositions equivalent to intermetallic phases: AgMg4, AgMg3, AgMg, and Ag3Mg, one alloy from the two-phase region AgMg + Ag3Mg (Ag60Mg40), and one alloy from the two-phase region AgMg + AgMg3 (Ag40Mg60). The hydrogenation process was performed using a Sievert-type sorption analyzer. The hydride decomposition temperature and kinetic properties of the synthesized hydrides were investigated by differential scanning calorimetry (DSC) coupled with thermogravimetric analysis (TGA). Samples with high magnesium content were found to readily absorb significant amounts of hydrogen, while hydrogen absorption was not observed for samples with silver concentrations higher than 50 at. % (AgMg intermetallic phase).

Effectiveness of Zr(IV)-Loaded Banana Peels Biomass for the Uptake of Fluoride Anion from Water

The present study reports the fluoride uptake potential of Zr(IV)-loaded saponified banana peels (Zr(IV)-SBP) from water. Zr(IV)-SBP was synthesized by loading Zr(IV) onto banana peel biomass after saponification and sorbent characterization was performed by using different techniques including FE-SEM (Field Emission Scanning Electron Microscopy), FTIR (Fourier Transform Infra-Red) spectroscopy and zeta potential analysis. Batch experiments were carried out to examine the monitoring factors for the uptake of fluoride onto the investigated adsorbent. The optimal pH and contact time were found to be 2.94 and 300 minutes, respectively. The results from characterization techniques concurred that Zr(IV)-SBP have prominent adsorption sites favorable for the sorption of fluoride ions. The sorption behavior of fluoride onto Zr(IV)-SBP was best fitted with the Langmuir adsorption isotherm and pseudo-second-order kinetics model. The maximum adsorption capacity of Zr(IV)-SBP was 36.02 mg/g using the Langmuir isotherm model. The coexisting ions like chloride and nitrate caused very small interference, elevated concentration of sulphate notably lowers the fluoride adsorption percentage in the binary system, and the sorption using multiple systems was lowered significantly which is due to the synergistic effect of co-existing interfering ion. The adsorbed fluoride was completely desorbed using 2M NaOH solution. Fluoride sorption performance of Zr(IV)-SBP demonstrated that it can be a low cost, environmentally benign and one of the highly potent alternatives for the remediation of fluoride ions to avoid ablation on the water.

Sorption behavior of natural uranium from aqueous solutions using modified activated carbon with quinoline

The activated carbon (AC) was modified by molecules of quinoline (Q) and the new prepared AC impregnated by Q was characterized using Fourier transform infrared (FTIR), Raman spectroscopy, surface measurements, scanning electron microscope (SEM) and transmission electron microscope (TEM). These analytical techniques demonstrated a successful preparation of AC-Q as a new material which was examined for its sorption behavior for natural uranium. The sorption results by batch mode indicated the optimum conditions for 94.5% removal of U(VI) ions at pH 4.7 and an equilibrium contact time of 90 min. The analysis of sorption data revealed that the pseudo-second-order and Langmuir were more fitted than other estimated models. The sorption capacity of U(VI) was ∼63 mg/g onto AC-Q as adsorbent martial. The thermodynamic data demonstrated that the sorption of uranium is endothermic and spontaneous. New mechanism was supposed based on the role of the abrasive material quinoline on the mechanical removal of uranium from aqueous solution.

Insight into the Sorption and Activation Energy Phenomenon of Kenaf Shive Sorbents in Crude Oil/Water Mixture

The secondary effect discovery of synthetic sorbents opened another research direction for many field of studies. However, the sorption parameters of lignocellulosic sorbents are rarely reported most importantly, kenaf shive. This paper centered at the sorption behavior of optimized kenaf shive sorbents using Response Surface Methodology (RSM) via surface deposit technique. Five-level Central Composite Design (CCD) experimental matrix was used to analyze the effect of particle sizes (125-1000 µm), stirring time (5-30min) and methyltrimethoxysilane (MTMS) concentration (5-20% v/v) as individual and combined variables process in the developed sorbents. The unmodified shive was compared with the modified, and it reveals a positive shift in the sorption capability. Instrumental analysis such as FTIR (Fourier Transform Infra-Red), DT-TGA (Differential Thermal-Thermogravimetric analysis) and BET (Brunaure-Emmett-Teller) were carried out on the optimized sorbent and the results were in conformity with the sorption results. The sorption behavior deployed fits the pseudo-first-order and Langmuir isotherm with regression coefficient R2=0.9496 and R2=0.9400. The sorption property was found to be spontaneous and exothermic, however, the activation energy studies shows physic-sorption phenomenon with 25.3 kJmol-1 and R2=0.9360.

Effect of Soil Solution Properties and Cu2+ Co-Existence on the Adsorption of Sulfadiazine onto Paddy Soil

Paddy soils are globally distributed and saturated with water long term, which is different from most terrestrial ecosystems. To better understand the environmental risks of antibiotics in paddy soils, this study chose sulfadiazine (SDZ) as a typical antibiotic. We investigated its adsorption behavior and the influence of soil solution properties, such as pH conditions, dissolved organic carbon (DOC), ionic concentrations (IC), and the co-existence of Cu2+. The results indicated that (1) changes in soil solution pH and IC lower the adsorption of SDZ in paddy soils. (2) Increase of DOC facilitated the adsorption of SDZ in paddy soils. (3) Cu2+ co-existence increased the adsorption of SDZ on organic components, but decreased the adsorption capacity of clay soil for SDZ. (4) Further FTIR and SEM analyses indicated that complexation may not be the only form of Cu2+ and SDZ co-adsorption in paddy soils. Based on the above results, it can be concluded that soil solution properties and co-existent cations determine the sorption behavior of SDZ in paddy soils.

Comparative Studies on Sorption Recovery and Molecular Selectivity of Bondesil PPL versus Bond Elut PPL Sorbents with Regard to Fulvic Acids

Large scale isolation—in gram quantities—of dissolved organic matter (DOM) from natural waters is necessary for detailed investigation of its role in chemical and microbial processes driving carbon cycling under conditions of global climate change. The best candidate for a use in these large-scale experiments is a bulk sorbent Bondesil PPL, which has the same modification as the widely used Bond Elut PPL sorbent. There have been no studies so far reported on interchangeability of these sorbents with regard to DOM isolation. This work was devoted to comparative studies on sorption efficiency and molecular selectivity of these two sorbents—Bond Elut PPL and Bondesil PPL with regard to DOM components. Fulvic acids (FA) from peat water leachate were used as a model DOM. Laboratory solid phase extraction (SPE) setup was used for monitoring sorption recovery and extraction yield. It included three parallel experiments on pre-packed Bond Elut PPL cartridges (500 mg/3 mL) and three self-packed Bondesil PPL cartridges (500 mg/3 mL). Fourier transform ion cyclotron resonance mass spectrometry (FT ICR MS) and 13C/1H nuclear magnetic resonance (NMR) spectroscopy were used for determination of molecular and structural group compositions of the FA isolates obtained with a use of two different sorbents. The results of this study allowed a conclusion on interchangeability of the two sorbents used in this study for the purposes of DOM isolation from natural waters. This conclusion was backed up by similarity of sorption behavior of the peat FA components on both sorbents and by high similarity of molecular compositions and carbon distribution among the main structural groups.

Molecular Simulation of Methane Sorption onto Kerogen Surface of Shale in Presence of Surfactant

Shale reservoirs, despite having abundance in hydrocarbon storage, offer significant challenges in terms of understanding the pore-scale and reservoir-scale phenomenon. Typically, hydraulic fracturing treatment is implemented to improve hydrocarbon productivity through the injection of fracturing fluid to induce the breakdown of the formation to create fractures, hence allowing a flow conduit for hydrocarbon to be produced at a higher flow rate of oil and/or gas. In this work, molecular dynamics (MD) simulation using GROMACS were utilized to create a 3D model comprised of methane (CH4), surfactant and graphite. Surfactant, as represented by the cationic cetyl trimethyl ammonium bromide (CTAB) was added along with water to represent water-based visco-elastic surfactant (VES) as an additive to reduce the surface tension of hydrocarbon to shale (represented by graphene). A realistic molecular model was created to examine the interaction of CTAB towards the adsorption pattern of methane onto graphene, in order to reveal the displacement efficiency of methane after wettability modification due to the effect of surfactant on the graphene on a nanoscale. The findings suggest that addition of CTAB as surfactant may enhance the production of methane though the reduction of IFT and adsorption capability of methane to the wall of shale. The result yielded consistent trends, where methane's tendency to stick to the adsorption site (at approximately 1.5 nm from the center of the system) was reduced and more methane molecules were accumulated at the center of the pore space. This study has uncovered the adsorption process and the effect of CTAB in altering the sorption behavior of methane towards shale. This would contribute to the enhancement of long-term shale gas production by providing more information on salinity and pressure sensitivity, enabling extraction to be done at a lower cost.

Sorption Behavior of Lead (Pb) onto Agricultural Soils of Khyber Pakhtunkhwa, ‎Pakistan: Potentials for Leaching

Lead (Pb) contamination in soil and subsequent transport in groundwater poses severe threats to the food safety and human health. In current study, the effects of soil organic matter on sorption behavior of Pb onto six agricultural soils were investigated by batch sorption experiments and microscopic characterization. Results indicated that Pb sorption onto agricultural soils was dominated by the soil organic matter content and soil texture. The decrease of organic matter content reduced the sorption capacity of Pb onto agricultural soils. Based on soil texture, the Pb sorption was highest in clay soil and lowest in silt type of soil. The overall Pb sorption was in the order of clay > clay loam > silty clay loam ≈ loam > silt loam > silt. The sorption isotherms of measured aqueous and soil phase Pb concentrations were fit well with the linear sorption model. The organic carbon normalized partition coefficients (Log KOC) ranged from 2.90 to 2.99. Linear partition coefficient (Kd) values were positively correlated with the soil properties, such as clay (R2 =0.90), OC (R2 =0.94) and pH (R2 = 0.45); however, weak correlation was found between Kd and soil sand contents (R2 = 0.12). The leachability model showed potential risk of Pb leaching from silt soil with lowest organic matter content. The findings are of significant importance for understanding potential threats of Pb to the soil ecosystem, groundwater, plants, and humans.