Influence of pH and Metal-Ion Concentration on the Kinetics of Nonenzymic Browning

Author(s):  
John O'Brien
2020 ◽  
Vol 32 (4) ◽  
pp. 727-732
Author(s):  
Harish Sharma ◽  
Rajesh Kumar ◽  
Mahesh Chandra Vishwakarma ◽  
Sushil Kumar Joshi ◽  
Narender Singh Bhandari

In present study, Pyras pashia leaves were used as low cost biosorbent to study biosorption of Cu(II), Pb(II) and Cd(II) ions from contaminated wastewater. In the employed batch methods pH, contact time, metal ion concentration, temperature, biosorbent doses were taken as study parameters. The pH was varied from pH 1-9 to study the influence of pH on biosorption of metal ions by Pyras pashia. The optimum pH for the removal of Cu(II), Pb(II) and Cd(II) is observed at pH 5. The biosorption equilibrium time was varied between 15-75 min. Langmuir, Freundlich and Temkin isotherms were employed to study the biosorption. The biosorption parameter fits well with Langmuir isotherm. The biosorption of metal ions was increased with increasing biosorbent dose and contact time while increase in pH, metal ion concentration and temperature decrease the biosorption. Thermodynamic data suggest that the bisorption process was spontaneous, feasible and endothermic.


2018 ◽  
Vol 16 (1) ◽  
pp. 45 ◽  
Author(s):  
F. Widhi Mahatmanti ◽  
Nuryono Nuryono ◽  
Narsito Narsito

In this research, chitosan based membrane blended with rice hull ash (RHA) silica and polyethylene glycol (PEG) has been applied as adsorbent of Ca(II), Mg(II), Zn(II) and Cd(II) in an aqueous solution. Membrane was synthesized by blending RHA silica and polyethylene glycol into chitosan. Silica and polyethylene glycol blended into the chitosan to improve the mechanical properties and the membrane porous. The membrane was characterized using Fourier Transform infrared (FTIR) spectroscopy, X-Ray Diffraction (XRD), Scanning Electron Microscopy (SEM), and swelling degree analyzer. Adsorption of metal ions investigated was conducted in a batch system with variation of pH, initial ion concentration and contact time. Thermodynamics and kinetics of adsorption were evaluated based on the adsorption data at initial metal ion concentration and contact time variations, respectively. Results showed that the optimum condition of adsorption was at pH 9.0 for Ca(II), 6.0 for both Mg(II) and Zn(II) and 5.5 for Cd(II), and contact time of 24 h for all ions investigated. Kinetics of all investigated metal ion adsorption followed a kinetic model of pseudo-second-order. Adsorption of Ca(II) and Mg(II) on the membrane fitted to Freundlich model with the affinity of 1.266 and 1.099, respectively; and Zn(II) and Cd(II) fitted to Langmuir one with the capacity of 182 and 106 µmol/g, respectively.


Author(s):  
Neetu Tewari ◽  
P Vasudevan

The adsorption of Hexavalent chromium [Cr (VI)] from aqueous solution by raw baggase was studied as a function of initial pH, contact time, dose, concentration and temperature. The optimum initial pH for Cr (VI) uptake was 2.0. At the optimal conditions, Cr (VI) uptake was increased as the dose of adsorbent; the initial metal ion concentration and temperature were increased. Adsorption was fast initially and within the first 30 minutes of contact, the adsorption of Cr (VI) on baggase showed a total uptake of 84.4%. The adsorption data fitted well to Langmuir isotherm model. The maximum adsorption of baggase was found to be 9.4 mg/g. The kinetics of the adsorption was found to be pseudo-second-order. Thermodynamic parameters like activation energy, Gibbs free energy change, enthalpy and entropy were also evaluated. The values for activation energy and enthalpy were found to be 13.4 and 10.7 kJ/mol. Adsorption was found to be endothermic.


2010 ◽  
Vol 10 (1) ◽  
pp. 80-87
Author(s):  
Dewi Umaningrum ◽  
Uripto Trisno Santoso ◽  
Radna Nurmasari ◽  
Rahmat Yunus

Study on adsorption kinetics of of Pb(II), Cd(II) and Cr(III) on adsorbent which was produced by protected-crosslinking of humic acid-chitosan has been done. The Langmuir-Hinshelwood, pseudo first- and second-order kinetics models were used to describe the kinetic data, and the rate constants of adsorption were also evaluated. The experimental data fitted well the second-order kinetics model, indicating that the chemical sorption is the rate-limiting step, instead of mass transfer. The initial metal ion concentration significantly affects the adsorption rate. An increase in initial metal ion concentration results in the decrease in adsorption rate of the metals.   Keywords: kinetics, adsorption, crosslinking, humic acid, chitosan


2019 ◽  
Author(s):  
Chem Int

A study of removal of heavy metal ions from heavy metal contaminated water using agro-waste was carried out with Musa paradisiaca peels as test adsorbent. The study was carried by adding known quantities of lead (II) ions and cadmium (II) ions each and respectively into specific volume of water and adding specific dose of the test adsorbent into the heavy metal ion solution, and the mixture was agitated for a specific period of time and then the concentration of the metal ion remaining in the solution was determined with Perkin Elmer Atomic absorption spectrophotometer model 2380. The effect of contact time, initial adsorbate concentration, adsorbent dose, pH and temperature were considered. From the effect of contact time results equilibrium concentration was established at 60minutes. The percentage removal of these metal ions studied, were all above 90%. Adsorption and percentage removal of Pb2+ and Cd2+ from their aqueous solutions were affected by change in initial metal ion concentration, adsorbent dose pH and temperature. Adsorption isotherm studies confirmed the adsorption of the metal ions on the test adsorbent with good mathematical fits into Langmuir and Freundlich adsorption isotherms. Regression correlation (R2) values of the isotherm plots are all positive (>0.9), which suggests too, that the adsorption fitted into the isotherms considered.


1990 ◽  
Vol 55 (8) ◽  
pp. 1984-1990 ◽  
Author(s):  
José M. Hernando ◽  
Olimpio Montero ◽  
Carlos Blanco

The kinetics of the reactions of iron(III) with 6-methyl-2,4-heptanedione and 3,5-heptanedione to form the corresponding monocomplexes have been studied spectrophotometrically in the range 5 °C to 16 °C at I 25 mol l-1 in aqueous solution. In the proposed mechanism for the two complexes, the enol form reacts with the metal ion by parallel acid-independent and inverse-acid paths. The kinetic constants for both pathways have been calculated at five temperatures. Activation parameters have also been calculated. The results are consistent with an associative activation for Fe(H2O)63+ and dissociative activation for Fe(H2O)5(OH)2+. The differences in the results for the complexes of heptanediones studied are interpreted in terms of steric factors.


Coatings ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 820
Author(s):  
Beibei Han ◽  
Mengyuan Yan ◽  
Dongying Ju ◽  
Maorong Chai ◽  
Susumu Sato

The amorphous hydrogenated (a-C:H) film-coated titanium, using different CH4/H2 and deposition times, was prepared by the ion beam deposition (IBD) method, which has the advantage of high adhesion because of the graded interface mixes at the atomic level. The chemical characterizations and corrosion behaviors of a-C:H film were investigated and evaluated by SEM, AFM, Raman spectroscopy, EPMA, TEM and XPS. An a-C:H film-coated titanium was corroded at 0.8 V, 90 °C in a 0.5 mol/L H2SO4 solution for 168 h. The metal ion concentration in the H2SO4 corrosion solution and the potentiodynamic polarization behavior were evaluated. Results indicate that a higher CH4/H2 of 1:0 and a deposition time of 12 h can result in a minimum ID/IG ratio of 0.827, Ra of 5.76 nm, metal ion concentration of 0.34 ppm in the corrosion solution and a corrosion current of 0.23 µA/cm2. The current density in this work meets the DOE’s 2020 target of 1 µA/cm2. Electrical conductivity is inversely proportional to the corrosion resistance. The significant improvement in the corrosion resistance of the a-C:H film was mainly attributed to the increased sp3 element and nanocrystalline TiC phase in the penetration layer. As a result, the a-C:H film-coated titanium at CH4/H2 = 1:0 with improved anti-corrosion behavior creates a great potential for PEMFC bipolar plates.


Author(s):  
David C. Cowell

An automated method is described, using standard continuous flow techniques, for the determination of urine fluoride ion concentration using a fluoride ion selective electrode. It is shown that the kinetics of the electrode response to changes in fluoride ion can be used for the accurate measurement of fluoride ion concentration in urine, and that equilibration of the electrode response is not a prerequisite for the measurement of fluoride ion. Recovery experiments are in the range 83 to 90%; in-batch precision is between 0·9 and 1·6% and carryover 2·5% or less.


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