Influence of chitosan characteristics on polymer properties: II. Platinum sorption properties

The sorption of platinum on glutaraldehyde cross‐linked chitosan was investigated at pH 2, using several chitosan samples prepared from different origins and characterized by different mol fractions of N‐acetylation (F_A). The influence of material conditioning was also tested: chitosan was dissolved and then re‐precipitated and/or dried (using either oven‐drying or freeze‐drying). The influence of the different characteristics and treatments on both sorption isotherms and uptake kinetics was checked. Part I has studied the effect of preparation and source on sample crystallinity. Shrimp chitosan has a greater sorption affinity for platinum than fungal chitosan and squid chitosan respectively. Sorption kinetics were found comparable for fungal chitosan and shrimp chitosan, while diffusion was more restricted in squid chitosan due to the higher crystallinity. Decreasing the F_A increased sorption capacity for shrimp chitosan but decreased sorption levels for squid material. While F_A did not influence sorption kinetics for shrimp material it strongly decreased kinetics for squid chitosan. The type of drying procedure hardly affected sorption kinetics and isotherms but when a re‐precipitation step was included in the preparation procedure, the material had to be freeze‐dried to maintain high sorption properties. The freeze‐drying did not control sorption performance, except in the case of re‐precipitated material. © 2003 Society of Chemical Industry     

Cysteine-Functionalized Chitosan Magnetic Nano-Based Particles for the Recovery of Uranium(VI): Uptake Kinetics and Sorption Isotherms

Magnetic-chitosan nanoparticles, functionalized with cysteine, were synthesized and characterized by element analysis, FT-IR, XRD, TEM, and vibrating sample magnetometry. The sorbent was tested for U(VI) recovery, considering:

• a. pH effect,

• b. sorption isotherms (fitted by Langmuir equation), and

• c. uptake kinetics (modeled using the PSORE).

Maximum sorption capacity approached 100 mg U g^?1. The nanometric size of sorbent reduces the impact of resistance to intraparticle diffusion; this may explain the fast kinetics (equilibrium within 50 min). The reaction is exothermic, spontaneous. The metal could be desorbed using acidified urea solution and the sorbent could be recycled for 5 cycles.     

Nickel and cobalt sorption on anaerobic granular sludges: kinetic and equilibrium studies

The kinetics and equilibria of sorption of the divalent metal ions cobalt and nickel onto anaerobic granular sludge are described. Single component and binary equimolar systems were studied at different pH values (pH 6, 7 and 8). The kinetic modelling of metal sorption by anaerobic granular sludge has been carried out using Lagergren equations. On fitting the experimental kinetic data both in first‐ and pseudo‐second‐order equations, the regression analysis of a pseudo‐second‐order equation gave a higher r² value, indicating that both external mass transfer and intra‐particle diffusion are involved in the sorption process. The experimental isotherm data were analysed using the Langmuir, Freundlich and Redlich–Peterson equations. The Redlich isotherm, a combination of the Langmuir and Freundlich equations, was found to have the highest regression correlation coefficients at pH 7. At pH 8, the Langmuir mechanism dominated for cobalt and nickel adsorption. In contrast, at pH 6, the Freundlich equation gave a better correlation coefficient which suggests a more heterogeneous adsorption at that pH. The maximal adsorption capacity of the granular sludge, as determined by the Langmuir equation, for cobalt or nickel in single systems (8.92 mg g^?1 Co TSS; 9.41 mg g^?1 Ni TSS, pH 7) compared with binary systems (8.06 mg g^?1 Co TSS; 8.43 mg g^?1 Ni TSS, pH 7) showed no great difference in the accumulation of these metals onto granular sludge. Copyright © 2004 Society of Chemical Industry     

Palladium and platinum sorption on a thiocarbamoyl‐derivative of chitosan

Novel proton exchange membranes are solvent‐cast from N,N‐dimethylacetamide (DMAc) solutions of the crosslinked poly(arylene ether ketone) copolymer with pendant carboxylic acid group (C‐SPAEK) via poly(ethylene glycol) (PEG) with different amounts. These membranes are formed as a result of physical and chemical crosslinking. In this study, ¹H‐NMR and FTIR have been used to confirm the chemical structures of the copolymers. Mechanical and thermal properties, swelling and proton conductivity are affected by the crosslinker (PEG) content in the copolymers. Compared to the noncrosslinked C‐SPAEK membrane, the crosslinked membranes become more flexible and greatly reduced water uptake and swelling ratio with only slight sacrifice in proton conductivities. And the crosslinked membranes keep higher proton conductivities without a sharply decrease at higher temperature. These results show that the crosslinked membranes have potential applications as proton exchange membranes for fuel cell. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Influence of humectants on the drying kinetics,water mobility,and moisture sorption isotherm of osmosed air-dried papaya

Papaya slices were sequentially soaked in 40, 50, and 60° Brix sucrose solutions. There was a higher water loss and solids gain when 60° Brix sucrose solution was partially substituted with 10% (w/v) sorbitol, 10% (v/v) glycerol, or invert sugar. The modified Henderson and Pabis model provided the best fit to experimental drying kinetics. Moisture sorption isotherm of all dried papaya, at 30 ± 2°C, was a type III with different curvature, revealing different sugar-binding ability towards water molecules. The Henderson model showed suitable fit to experimental desorption isotherm data. NMR water mobility revealed the better ability of glycerol to bind water than sucrose.     

Acid Precipitation of Kraft Lignin from Aqueous Solutions: The Influence of pH,Temperature, and Xylan

In this study, the manners in which temperature (45–77?°C) and the addition of xylan (5?g/95?g lignin) influence the onset of precipitation and evolution of the particle size distribution during acid precipitation of softwood kraft lignin were investigated in situ. No systematic trend between the onset pH of precipitation and the temperature or the addition of xylan could be observed at these conditions: the average onset pH was found to be 9.3. However, the size of the agglomerates increased as the temperature was increased, but added xylan rendered a decrease in agglomerate size. A higher onset pH was measured at increased Na ion concentration. The results indicate that the ionization degree of the phenolic groups influences the precipitation at 1?M Na ions but it is also probable that the degree of ionization of the carboxylic groups (on kraft lignin and xylan) influences precipitation (particle numbers and sizes).     

An experimental investigation of poly(vinyl chloride) emulsion polymerization: Effect of initiator and emulsifier concentrations on polymerization kinetics and product particle size

Effects of concentration changes in initiator species Na₂SO₃, (NH₄)₂S₂O₈ and CuSO₄, and emulsifier, ammonium stearate, on poly(vinyl chloride) (PVC) emulsion polymerization kinetics and on product particle size were experimentally investigated. It was observed that to obtain industrially significant rates and overall conversions, not only an optimum concentration ratio of Na₂SO₃/(NH₄)₂S₂O₈/CuSO ₄ must be used, but also the concentrations of these species must be above certain limits. Increasing the concentration of the emulsifier used did not influence the rate of polymerization, but led to increases in limiting conversions. Product particle size analyses indicate that average particle size is independent of initiator concentration and rate of initiation. An increase in the emulsifier concentration on the other hand appears to lead to an increase in number of particles in the system and thus promotes smaller particle sizes.     

Influence of 2-hydroxypropyltrimethyl ammonium chloride chitosan on sedimentation and volume change behavior of cohesive soil sediments

The 2-hydroxypropyltrimethyl ammonium chloride chitosan (HACC), introducing the functional quaternary ammonium group to the structure of Chitosan, has greatly broadened the application prospect. The influence on natural cohesive soil has rarely been considered. The sedimentation tests for the natural soil in HACC solutions and the HACC-treated soils in distilled water are considered to analyze the change of sedimentation behaviors in this paper. Moreover, the potential change on the surface of soil particles, the change in particle size distribution, X-ray diffraction of Ca-montmorillonite/HACC, and scanning electron microscopy images are investigated to explain the reasons for the results. Results indicate that the surface potential of soil particles achieved reversal, and the particle size had significant agglomeration. The adsorption of HACC results in the rapid sedimentation of the treated soils in water. HACC has a significant influence on setting time and final volume. HACC cannot inhibit the interlayer swelling of Ca-montmorillonite. The dehydration process can promote the aggregation effect of the treated soils. The specific effects provided an essential train of thought to solve soil problems.     

Green catalysts for Fenton-like oxidation of Procion Red MX-5B: Influence of the activation method and the reaction parameters on dye removal

The catalytic activities of the iron catalysts over activated carbon supports prepared by different activation methods in the heterogeneous Fenton-like oxidation of Procion Red MX-5B were investigated. The activated carbons were prepared from walnut shells by applying physical and three chemical activation methods, including HNO₃, ZnCl₂, and KOH activations to obtain various catalyst supports. KOH-activated carbon catalyst was assessed to be the most efficient one. Under the optimum reaction conditions, 47.5% COD removal, 51.6% degradation, and 91.6% decolorization efficiencies were achieved in the presence of this catalyst. In the kinetic study, the activation energy was evaluated as 47.36 kJ/mol.