STM observation of Ag adatom interactions on the Si(1 1 1)-(7×7) surface

STM imaging of Ag atoms adsorbed on the Si(1 1 1)-(7×7) surface is studied. Appearance of a single Ag adatom on perfect surface is compared with images of adatoms interacting with surface defects and adsorbates. Importance of real-time observation of surface processes for image interpretation is demonstrated on imaging Ag adatoms at various situations. Influence of tunnelling conditions (voltage between a tip and surface) on imaging surface objects is studied and visibility of single Ag adatoms and clusters is discussed.     

Mass recovery adsorption refrigeration cycle—improving cooling capacity

The study investigates the performance of two-bed, silica gel-water adsorption refrigeration cycle with mass recovery process. The cycle with mass recovery can be driven by the relatively low temperature heat source. In an adsorption refrigeration cycle, the pressures in adsorber and desorber are different. The chiller with mass recovery process utilizes the pressure difference to enhance the refrigerant mass circulation. Cooling capacity and coefficient of performance (COP) were calculated by cycle simulation computer program to analyze the influences of operating conditions. The mass recovery cycle was compared with conventional cycle such as the single stage adsorption cycle in terms of cooling capacity and COP. The results show that the cooling capacity of mass recovery cycle is superior to that of conventional cycle and the mass recovery process is more effective for low regenerating temperature.     

Growth of aluminum nitride thin films prepared by plasma-enhanced atomic layer deposition

Aluminum nitride (AlN) thin films were deposited by atomic layer deposition from aluminum chloride (AlCl₃) and an ammonia/hydrogen plasma. The most important role of the ammonia/hydrogen plasma was to act as a reducing agent to extract Cl from AlCl₃, and to form AlN subsequently. The growth rate was saturated at ∼0.042 nm/cycle, and the thickness was proportional to the number of reaction cycles. Repeating this reaction cycle led to precisely controlled growth. The film properties were analyzed using Auger electron spectroscopy, X-ray photoelectron spectroscopy, Rutherford backscattering spectroscopy and time-of-flight elastic recoil detection analysis. The concentration of chlorine and hydrogen impurities was 0.23 and 2.01 at.%, respectively. AlN films showed good anti-oxidation properties when O₂ was annealed at 650 °C for 30 min.     

Characterization of Clay Particle Surfaces for Contaminant Sorption in Soil Barriers Using Flow Microcalorimetry

Clays such as kaolinite and bentonite are widely used in various industries as sorbents. The sorptive characteristics of clays are exploited when they are used in contaminant barrier systems. To use clays effectively, their surface characteristics need to be known; especially, when they are used for contaminant sorption. Available surface area of clay minerals and the characteristics that depend on it are very sensitive to environmental changes such as those that can be induced by changes in the composition of pore fluid. Flow microcalorimetry with a down-stream concentration was used to determine the heats and amounts of adsorption of acids and bases on the clays. Test results presented herein revealed that both kaolinite and bentonite exhibit significantly different adsorption isotherms and heat of wetting under high pH and low pH conditions. Kaolinite has the capacity to adsorb both acidic and basic molecules almost equally. However, it has a tendency to adsorb more base than acid because of its stronger complexation capacity with acids than with bases. On the other hand, bentonite has a tendency to adsorb more acidic than basic molecules per gram. These results also indicate that both kaolinite and bentonite have different heats of wetting characteristics. As the concentrations of the acids and bases increase, the heat of wetting of kaolinite decreases while that of bentonite increases.     

Adsorption Characteristics of Oxide Coated Buoyant Media (ρs<1.0) for Storm Water Treatment. I: Batch Equilibria and Kinetics

Urban rainfall-runoff mobilizes and transports significant loads of metal species. Promulgation of National Pollutant Discharge Elimination System Phase II regulations has spurred development of Unit Operations and Processes (UOPs) Best Management Practices (BMPs) for control of metal species. Recent UOP designs provide both adsorption and filtration using engineered media such as manganese oxide coated polymeric media (MOPM). Divalent metal species adsorption onto a manganese oxide coated polymeric medium was evaluated through batch adsorption experiments using a flowthrough batch reactor. Freundlich isotherms were utilized to fit the experiment data. For the media examined, MOPM, adsorption is pH dependent and results indicate a favorable solute pH range of >6 for metal species adsorption. The relative adsorption affinity of MOPM for four divalent metal species typically found in storm water is Pb(II)>Cu(II)>Cd(II)>Zn(II). Adsorption rates were rapid for this flowthrough batch system with over 50% removal in the first 30 min and over 90% removal within 5 h at a surface loading rate of 500 mL/cm2?min. The pH drift patterns, due to surface complexation, during each experiment, coincided with the metal species removal rate curve. Study results indicated that the inclusion of a thin manganese coating can significantly increase media adsorption capacity. MOPM has a comparable adsorption capacity for the divalent metal species compared to other commercial and research media.     

Selective adsorption of uranyl ion on ion-imprinted chitosan/PVA cross-linked hydrogel

An interpenetration network (IPN) ion-imprinting hydrogel (IIH) was synthesized using uranyl ions as template for adsorption and removal of uranyl ions from aqueous solutions. The IIH was obtained via cross-linking of blended chitosan/polyvinyl alcohol (PVA) using ethylene glycol diglycidyl ether (EGDE). The ability of the IIH to adsorb and remove uranyl ions from aqueous solutions was assessed using a batch adsorption technique. The maximum adsorption capacity was observed in the pH range of 5.0-6.0. The adsorption process could be well described by both the Langmuir and Freundlich isotherms and the maximum adsorption capacity calculated from Langmuir equation was 156 mg/g. Equilibrium was achieved within 2 h. The kinetic data, obtained at optimum pH 5.0 could be fitted with to a pseudo-second order equation. The selectivity coefficient of uranyl ion and other metal cations on IIH indicated an overall preference for uranyl ions which was much higher compared with the non-imprinted hydrogel. This suggests that the IIH is a promising sorbent material for the selective removal of uranyl ions from aqueous solutions.     

Adsorption of dyes from aqueous solutions on activated charcoal

Adsorption of industrially important dyes namely bromophenol blue, alizarine red-S, methyl blue, methylene blue, eriochrome black-T, malachite green, phenol red and methyl violet from aqueous media on activated charcoal has been investigated. The effect of shaking time, pH and temperature on the adsorption behaviour of these dyes has been studied. It was noted that adsorption of all the dyes on activated charcoal decreases with an increase in the pH and the temperature. The adsorption isotherms at different temperatures were found to be of L-type. Adsorption data was fitted to Freundlich, BET and Langmuir isotherms and various adsorption parameters have been calculated. The thermodynamic parameters such as DeltaG, DeltaH and DeltaS were calculated from the slopes and intercepts of the linear variation of lnK against 1/T, where K is the adsorption coefficient obtained from Langmuir equation, was used. The calculated values for the heat of adsorption and the free energy indicate that adsorption of dyes is favored at low temperatures and the dyes are chemisorbed on activated charcoal.     

Uniform α-Fe2O3 nanotubes fabricated for adsorption and photocatalytic oxidation of naphthalene

Uniform α-Fe₂O₃ nanotubes with small aspect ratio were successfully fabricated by a hydrothermal method. In situ Fourier-transform infrared spectroscopy was used to study the mechanistic details of adsorption and photocatalytic oxidation of naphthalene over theα-Fe₂O₃ nanotubes. A possible degradation mechanism of naphthalene was proposed.     

Kinetic investigation of zinc electrodeposition from sulfate electrolytes in the presence of impurities and ionic liquid additive [BMIM]HSO4

The effects of some common impurities such as copper, iron, nickel, cobalt, lead and their interaction with an ionic liquid additive 1-butyl-3-methylimidazolium hydrogen sulfate-[BMIM]HSO₄ on zinc electrodeposition from acidic sulfate electrolyte were characterized in terms of the polarization behavior and the kinetics of zinc deposition using cyclic voltammetry and potentiodynamic polarization measurements. The results showed that these metallic impurities studied exerted some different changes in cyclic and cathodic polarization voltammograms. The addition of [BMIM]HSO₄ was observed to counteract the detrimental effects of these impurities and induced a blocking effect on the zinc electrodeposition process through its cathodic adsorption on the electrode surface. The adsorption of this additive shifted the electroreduction potential of zinc ions towards more negative values, restricted impurities ions from being electroreduced, and inhibited hydrogen evolution. Moreover, the kinetics analysis of cathodic polarization suggested that the presence of these impurities alone and in combination with [BMIM]HSO₄ had no effect on the Tafel slope and transfer coefficient but affected the exchange current density for the zinc deposition.     

Simulation of methylene blue adsorption by salts-treated beech sawdust in batch and fixed-bed systems

Batch and column kinetics of methylene blue adsorption on calcium chloride, zinc chloride, magnesium chloride and sodium chloride treated beech sawdust were simulated, using untreated beech sawdust as control, in order to explore its potential use as a low-cost adsorbent for wastewater dye removal. The adsorption capacity, estimated according to Freundlich's model, the Langmuir constant K(L) and the adsorption capacity coefficient values, determined using the Bohart and Adams' bed depth service model indicate that salts treatment enhanced the adsorption properties of the original material. Since sawdust is an industrial waste/byproduct and the salts used can be recovered as spent liquids from various chemical operations, this process of adsorbent upgrading/modification might be considered to take place within an 'Industrial Ecology' framework.