Full Journal Title: Transactions of the Indian Institute of Metals
ISO Abbreviated Title: Trans. Indian Inst. Met.
JCR Abbreviated Title: T Indian I Metals
ISSN: 0019-493X
Issues/Year: 6
Journal Country/Territory: India
Language: English
Publisher: Indian Inst Metals
Publisher Address: Metal House, Plot 13/4, Block AQ, Sector V, Salt Lake, Calcutta 700 091, IN
Subject Categories:
Metallurgy & Metallurgical Engineering: Impact Factor
? Nath, S.K., Jena, A. and Mishra, S.P. (1997), Removal of cadmium by wood charcoal. Transactions of the Indian Institute of Metals, 50 (4), 235-239.
Abstract: Wood charcoal was used to remove Cd from acidic waste water. The adsorption of Cd depends on various adsorption parameters such as pH, temperature, metal ion concentration and amount of adsorbent. Adsorption kinetics were fast initially followed by slower kinetics and attained a stationery phase within one hour. The activation energy was found to be 64.844 kJ/mole. From the enthalpy change the adsorption reaction was found to be endothermic. Various other thermodynamic parameters such as free energy change and entropy change were also calculated.
Keywords: Activation, Adsorbent, Adsorption, Cadmium, Cd, Charcoal, Kinetics, Metal, pH, Waste, Waste Water, Water, Wood
Title: Transactions of the Institute of British Geographers
Full Journal Title: Transactions of the Institute of British Geographers
ISO Abbreviated Title:
JCR Abbreviated Title:
ISSN:
Issues/Year:
Journal Country/Territory:
Language:
Publisher:
Publisher Address:
Subject Categories:
: Impact Factor
? Levins, D.M. and Glastonburg, J.R. (2003), Mark Melton’s geomorphology and geography’s quantitative revolution Christopher J Keylock. Transactions of the Institute of British Geographers, 28 (2), 142-157.
Full Text: Tra Ins Bri Geo28, 142
Abstract: Mark Melton published some important papers in the late 1950s that have had a significant influence upon the subsequent development of geomorphology. Two of these papers were published in the same journal in the same year, and have a similar number of total citations, and these are compared in this study. Although both papers present novel empirical findings and discuss innovative conceptual frameworks, the extent and manner to which they have been used within geography and geology differs quite markedly. This reveals marked differences in the conceptual frameworks and research priorities of the two groups of scientists, which may help explain why geomorphology has proceeded differently on the two sides of the Atlantic since the quantitative revolution.
Title: Transactions of the Institution of Chemical Engineers and the Chemical Engineer
Full Journal Title: Transactions of the Institution of Chemical Engineers and the Chemical Engineer
ISO Abbreviated Title: Trans. Instn. Chem. Enger. (London)
JCR Abbreviated Title:
ISSN:
IDS Number: N0120
Issues/Year:
Journal Country/Territory:
Language:
Publisher:
Publisher Address:
Subject Categories:
: Impact Factor
? Levins, D.M. and Glastonburg, J.R. (1972), Particle-liquid hydrodynamics and mass-transfer in a stirred vessel. 2. Mass-transfer. Transactions of the Institution of Chemical Engineers and the Chemical Engineer, 50 (2), 132-??.
Title: Transactions of the Institute of Metal Finishing
Full Journal Title: Transactions of the Institute of Metal Finishing
ISO Abbreviated Title: Trans. Inst. Metal Finish.
JCR Abbreviated Title: T I Met Finish
ISSN: 0020-2967
Issues/Year: 6
Journal Country/Territory: England
Language: English
Publisher: Inst Metal Finishing
Publisher Address: Exeter House 48 Holloway Head, Birmingham B1 1NQ, England
Subject Categories:
Metallurgy & Metallurgical Engineering: Impact Factor 0.248, / (2003)
Materials Science, Coatings & Films: Impact Factor 0.248, / (2003)
? Gyliene, O., Tarozaite, R. and Nivinskiene, O. (2004), Sorption of Ni(II)-citrate complex from electroless nickel plating solutions onto chitosan. Transactions of the Institute of Metal Finishing, 82 (1-2), 38-42.
Abstract: Spent electroless nickel plating solutions contain Ni(II)-citrate complexes which are hazardous to the environment. These, complexes can be removed by using chitosan as a sorbent. Kinetic investigations indicate that Ni(II) sorption front complex solutions onto chitosan can be described by a pseudo-second order rate model. The experimental data of the adsorption under equilibrium conditions for both Ni(II) and citrate correlate well with the Freundlich isotherm equation. During the sorption of Ni(II)-citrate complex on chitosan competition between Ni(H) and citrate ions takes place. The citrate sorption prevails.
Adipate, the additive used in electroless nickel plating solutions, is not sorbed by chitosan, but its presence in solutions has an increasing effect on citrate sorption from citrate solutions without Ni(II) and the increasing effect on Ni(II) sorption from Ni(II)-citrate complex solutions. The other components of electroless nickel plating solution, i.e. hypophosphite, sulphate, phosphite have no influence on sorption.
Keywords: Electroless Nickel Plating, Ni(II)-Citrate Adipate, Chitosan, Adsorption, Freundlich Isotherm, Pseudo-Second Order Kinetic Model, FT-IR Investigations, Heavy-Metal Ions, Aqueous-Solutions, Removal, Chitin, Equilibrium, Sorbents
Title: Transactions of Nonferrous Metals Society of China
Full Journal Title: Transactions of Nonferrous Metals Society of China
ISO Abbreviated Title: Trans. Nonferrous Met. Soc. China
JCR Abbreviated Title: T Nonferr Metal Soc
ISSN: 1003-6326
Issues/Year: 4
Journal Country/Territory: Peoples R China
Language: English
Publisher: Allerton Press Inc
Publisher Address: 150 Fifth Ave, New York, NY 10011
Subject Categories:
Metallurgy & Metallurgical Engineering: Impact Factor
? Xia, H.P. and Ke, J.J. (1996), Adsorption mechanism of some bivalent heavy metal cations in solutions using montmorillonite. Transactions of Nonferrous Metals Society of China, 6 (1), 32-34.
Full Text: Tra Non Met Soc Chi6, 32.pdf
Abstract: The frontier orbital energies of montmorillonite molecule and [Me (H2O)6]2+ (Me = Cu2+, Zn2+, Co2+ and Ni2+) were calculated by INDO method. Results showed that the chemical interaction between montmorillonite molecule and [CU (H2O)6]2+ or [Zn (H2O)6]2+ was possible. The experimental results of powder X-ray diffraction and isothermal adsorption supported the above-mentioned calculation results.
? Dong, H.J. and Jin, C. (1996), Adsorption and activation of metal ions on kyanite. Transactions of Nonferrous Metals Society of China, 6 (3), 22-24.
Full Text: 1996\Tra Non Met Soc Chi6, 22.pdf
Abstract: It was discovered that the adsorption of metal ions on mineral surface had much to do with their activation for mineral in flotation. The authors proposed a percentage of adsorptive precipitation (PAP) to represent activation power of metal ions. The greater the PAP of the metal ion, the stronger its activation power. When the PAP was small to a certain extent, the metal ion showed a depression effect on mineral in flotation.
? Liu, Y.G., Li, C.F., Zhao, X., Tang, C.F., Xu, W.H., Li, X. and Nakanishi, A. (2004), Effect of pH on cadmium adsorption by red soil. Transactions of Nonferrous Metals Society of China, 14 (1), 60-65.
Full Text: Tra Non Met Soc Chi14, 60.pdf
Abstract: To study the effect of pH on Cd adsorption and species, the red soil was taken as adsorbent. The curve of Cd adsorbed vs pH shows three stages, namely, the adsorption amount increasing slowly at low pH, then increasing quickly with the rise of pH, and reaching the maximum amount at high pH. The result of theoretical analysis on precipitation reactions indicates that the precipitation reaction is controlled by carbonate until pH is a bit higher than 11. The adsorption data at different pH values and initial Cd(R) concentrations were fitted by a linear least squares technique, to the Langmuir, Frundlich and Temkin adsorption isotherms, and the results show that Langmuir isotherm is the best which can well describe the adsorption behavior of Cd in red soil. At last, a pH-dependent model of adsorption isotherms of Cd was established by substituting the fitting results obtained from experimental data for the parameters in Langmuir equation.
Keywords: Cd, Mineral Adsorbent, Coordination, Red Soil, Organic-Matter, Solubility, Speciation, Water
? Liu, Y.G., Fan, T., Zeng, G.M., Li, X., Tong, Q., Ye, F., Zhou, M., Xu, W.H. and Huang, Y.E. (2006), Removal of cadmium and zinc ions from aqueous solution by living Aspergillus niger. Transactions of Nonferrous Metals Society of China, 16 (3), 681-686.
Full Text: 2006\Tra Non Met Soc Chi16, 681.pdf
Abstract: The potential of living Aspergillus niger to remove cadmium and zinc from aqueous solution was investigated. Effects of pH, initial concentration, contact time, temperature and agitation rate on the biosorption of Cd(II) and Zn(II) ions were studied. The optimum adsorption pH value for Cd(II) and Zn(II) were 4.0 and 6.0. The best temperature and agitation rate were in the range of 25-30°C and 120 r/min for all metal ions. Under the optimal conditions, the maximum uptake capacities of Cd(II) and Zn(II) ions are 15.50 mg/g and 23.70 mg/g at initial concentrations of 75 mg/L and 150 mg/L, respectively. Biosorption equilibrium is established within 24 h for cadmium and zinc ions. The adsorption data provide an excellent fit to Langmuir isotherm model. The results of the kinetic studies show that the rate of adsorption follows the pseudo-second order kinetics.
Keywords: Aspergillus Niger, Biosorption, Cadmium, Zinc, Biosorption Isotherm, Kinetic Model, Biosorption, Lead, Bioaccumulation, Chromium(VI), Copper(II), Biomass, Metals, Strain, Zn2+, Cd2+
? Chai, L.Y., Wei, S.W., Peng, B. and Li, Z.Y. (2007), Adsorption of Ag(I) on H2TiO3 from aqueous solutions. Transactions of Nonferrous Metals Society of China, 17 (4), 832-835.
Full Text: 2007\Tra Non Met Soc Chi17, 832.pdf
Abstract: Adsorption of silver ions from aqueous solution onto H2TiO3 was studied. Equilibrium experimental studies were performed to determine the adsorption capacity of H2TiO3 for silver ion at various pH values. Batch experiments were conducted in the range of pH value 3-7 and silver ions concentration 10-200 mg/L. The results show that the adsorption is strongly dependent on pH value. The equilibrium absorption capacity of H2TiO3 increases significantly with the increase of pH value from 3 to 7. The adsorption of silver ion obeys the Langmuir isothermal equation well in the concentration range studied, the adsorption constant is 0.054 7, 0.052 4, 0.088 1 at pH 5, 6 and 7, respectively, and the maximum adsorption capacities are 23.64, 29.76 and 40.82 mg/g.
Keywords: Silver Ions, Adsorption, Hydrous Titania, Photocatalytic Activity, Antibacterial Activity, Thin-Films, Silver, Fibers, Metal, TiO2, Ions, Zinc
? Chai, L.Y., Chen, Y.N., Shu, Y.D., Chang, H. and Li, Q.Z. (2007), Adsorption and removal of cadmium(II) from aqueous solutions by bio-formulation. Transactions of Nonferrous Metals Society of China, 17 (5), 1057-1062.
Full Text: 2007\Tra Non Met Soc Chi17, 1057.pdf
Abstract: A novel sorbent, bio-formulation(BF), was prepared and employed for the adsorption of cadmium(Cd) ion from. aqueous system. The process of adsorption follows the pseudo second-order kinetic equation and the adsorption behavior is fitted with a Freundlich isotherm. The removal rate of Cd is slightly dependent on the initial pH value over a wide range of 4-11. The addition of Zn2+ and Cu2+ ions hardly affects the Cd adsorption, whereas the coexisting Pb2+ ion greatly interferes with the adsorption. The adsorption mechanism is supposed as a cation-exchange process between Cd2+ and calcium and Mg2+ present on the surface of BF, and somewhat as adsorption in a hydrolyzed form. The adsorbed Cd ions are desorbed effectively by a 0. 1 mol/L HCl solution.
Keywords: Adsorption, Adsorption Behavior, Adsorption Mechanism, Aqueous Solutions, Behavior, Bio-Formulation(BF), Biomass, Biosorption, Cadmium, Calcium, Cation Exchange, Cation-Exchange, Cd, Cd2+, Cu2+, Desorption, Freundlich, Freundlich Isotherm, HCl, HCl Solution, Ion, Ions, Isotherm, Kinetic, Kinetic Equation, Mechanism, Metal-Cations, Mg2+, Pb2+, pH, Process, Pseudo Second Order, Pseudo Second Order Kinetic, Pseudo Second-Order, Pseudo-Second-Order, Range, Rate, Removal, Removal Rate, Second Order, Solutions, Sorbent, Sorption, Surface, Value, Zn2+
? Liu, Y.G., Feng, B.Y., Fan, T., Zhou, H.Z. and Li, X. (2008), Tolerance and removal of chromium(VI) by Bacillus sp strain YB-1 isolated from electroplating sludge. Transactions of Nonferrous Metals Society of China, 18 (2), 480-487.
Full Text: 2008\Tra Non Met Soc Chi18, 480.pdf
Abstract: Four chromium(VI)-resistant bacteria named YB-1, YB-2, YB-3 and YB-4 were isolated from Cr-electroplating sludge. YB-1 and YB-2 were identified as a member of Bacillus sp. based on morphology and Biolog Microstation System. The strain of YB-1 was selected to test for its resistance and ability to remove Cr(VI) from aqueous solution. The results indicate that YB-1 exhibits high MIC value which can almost reach 140 mg/L and the growth of YB-1 in liquid medium containing 60 mg/L Cr(VI) is affected especially in the late exponential phase and stationary phase. Furthermore, the potential of living and freeze-dried YB-1 biomass to remove Cr(VI) was studied in different pH, biosorbent dose, contact time and initial concentration using the batch method. At the optimal conditions, living and freeze-dried biomass are capable of absorbing 34.5 mg/g and 17.8 mg/g chromium(VI) at initial concentration of 60 mg/L, respectively. The adsorption data were fitted to Langmuir isotherm model for these two sorbents. Kinetic studies show that the rates of sorption all follow the pseudo-second order kinetics.
Keywords: Adsorption, Aqueous Solution, Aqueous-Solution, Aspergillus-Niger, Bacillus, Bacillus sp., Bacteria, Biomass, Biosorbent, Biosorption, Biosorption, Cadmium, Chromium(VI), Cr(VI), Cr(VI), Growth, Ions, Isotherm, Kinetic, Kinetic Model, Kinetics, Langmuir, Langmuir Isotherm, Minimal Inhibitory Concentration, Model, Morphology, pH, Potential, Pseudo-Second Order, Removal, Resistance, Sludge, Solution, Sorption
? Feng, N.C., Guo, X.Y. and Liang, S. (2009), Kinetic and thermodynamic studies on biosorption of Cu(II) by chemically modified orange peel. Transactions of Nonferrous Metals Society of China, 19 (5), 1365-1370.
Full Text: 2009\Tra Non Met Soc Chi19, 1365.pdf
Abstract: Cu(II) biosorption by orange peel that was chemically modified with sodium hydroxide and calcium chloride was investigated. The effects of temperature, contact time, initial concentration of metal ions and pH on the biosorption of Cu(II) ions were assessed. Thermodynamic parameters including change of free energy (ΔG°), enthalpy (ΔH°) and entropy (ΔS°) during the biosorption were determined. The results show that the biosorption process of Cu(II) ions by chemically treated orange peel is feasible, spontaneous and exothermic under studied conditions. Equilibrium is well described by Langmuir equation with the maximum biosorption capacity(qm) for Cu(II) as 72.73 mg/g and kinetics is found to fit pseudo-second order type biosorption kinetics. As the temperature increases from 16ºC to 60ºC, copper biosorption decreases. The loaded biosorbent is regenerated using HCl solution for repeatedly use for five times with little loss of biosorption capacity.
Keywords: Adsorption, Aqueous-Solutions, Biosorbent, Biosorption, Biosorption Kinetics, Calcium, Calcium Chloride, Capacity, Chloride, Concentration, Copper, Copper, Copper Biosorption, Cu(II), Cu(II) Biosorption, Cu(II) Ions, Energy, Equilibrium, Exothermic, Hydroxide, Ions, Isotherms, Kinetic, Kinetics, Langmuir, Langmuir Equation, Metal, Metal Ions, Modified, Orange Peel, pH, Pretreated Biomass, Pseudo Second Order, Pseudo-Second Order, Pseudo-Second-Order, Removal, Sodium, Solution, Sorption, Temperature, Thermodynamic, Thermodynamic Parameters, Thermodynamic Studies, Thermodynamics, Waste-Water
? Gu, W., Sun, C.J., Liu, Q. and Cui, H.X. (2009), Adsorption of avermectins on activated carbon: Equilibrium, kinetics, and UV-shielding. Transactions of Nonferrous Metals Society of China, 19, S845-S850.
Full Text: 2009\Tra Non Met Soc Chi19, S845.pdf
Abstract: The adsorption of biopesticide avermectins onto activated carbon from ethanol solution with different initial concentrations at 303.15 K was performed. The obtained equilibrium and kinetic data of the adsorption process were assayed to evaluate the adsorption potential of activated carbon for avermectins. The results show that the activated carbon is effective for the adsorption of avermectins. Moreover, the adsorption of avermectins onto activated carbon agrees with Langmuir isotherm model, while pseudo-second-order kinetics model is better fitable for such adsorption process. In addition, activated carbon can efficiently protect adsorbed avermectins from photodegradation.
Keywords: Activated Carbon, Adsorption, Aqueous-Solution, Avermectins, Carbon, Constitution, Data, Equilibrium, Ethanol, Fundamental Properties, Isotherm, Isotherm Model, Kinetic, Kinetics, Kinetics Model, Langmuir, Langmuir Isotherm, Langmuir Isotherm Model, Liquids, Model, Photodegradation, Potential, Pseudo Second Order, Pseudo Second Order Kinetics, Pseudo-Second-Order, Pseudo-Second-Order Kinetics, Solids, Solution, UV-Shielding, Waste
? Feng, N.C., Guo, X.Y. and Liang, S. (2010), Enhanced Cu(II) adsorption by orange peel modified with sodium hydroxide. Transactions of Nonferrous Metals Society of China, 20, S146-S152.
Full Text: 2010\Tra Non Met Soc Chi20, S146.pdf
Abstract: Copper adsorption by orange peel, which was chemically modified with sodium hydroxide, was investigated. The adsorbent was characterized using surface area analyzer, infrared spectroscopy and scanning electron microscopy. Total negative charge and zeta potentials on the adsorbent surface were determined. Equilibrium isotherms and kinetics were obtained and the effects of solution pH value, adsorbent concentration and temperature were studied in batch experiments. Column experiments were performed to study practical applicability, and breakthrough curves were obtained. Equilibrium is well described by Langmuir and Freundlich isotherms, and kinetics is found to fit pseudo-second order type adsorption kinetics. According to Langmuir equation, the maximum adsorption capacity for Cu(II) is 50.25 mg/g at pH value of 5.3. The results show additional chemical modification of the adsorbent by NaOH and the increased adsorption capacity.
Keywords: Acid, Adsorbent, Adsorption, Adsorption Kinetics, Aqueous-Solutions, Biosorption, Cadmium(II), Copper, Equilibrium, Isotherms, Kinetic, Kinetics, Langmuir, Maximum Adsorption Capacity, Orange Peel, Recovery, Removal, Vulgaris, Waste-Water
? Xu, Z.G., Wu, Y.K., Zhang, J.D., Zhang, L. and Wang, L.J. (2010), Equilibrium and kinetic data of adsorption and separation for zirconium and hafnium onto MIBK extraction resin. Transactions of Nonferrous Metals Society of China, 20 (8), 1527-1533.
Full Text: 2010\Tra Non Met Soc Chi20, 1527.pdf
Abstract: The equilibrium and kinetics of methyl isobutyl ketone (MIBK) extraction resin for adsorption and separation of zirconium and hafnium were studied under the different conditions of acidity, initial total concentrations of zirconium and hafnium and temperature. The equilibrium data of both zirconium and hafnium are found to follow the Freundlich adsorption isotherm, and the Freundlich isotherm constants (K-F) are 3.53 and 0.64 mg/g, respectively. The equilibrium data of zirconium also fit the Langmuir adsorption isotherm, and the saturation adsorption capacity (Qmax) and the Langmuir isotherm constant (K-L) are 75.93 mg/g and -0.012 7 L/g, respectively. The obtained kinetic data of both zirconium and hafnium are found to fit the HO pseudo-second-order kinetic model, and the rate constants of pseudo-second-order equation (k(2)) are -0.019 and 0.41 g/(mg.min), respectively. Column tests show that the MIBK extraction resin could be used as efficient adsorbent material for separating hafnium from zirconium.
Keywords: Acid, Acidity, Adsorbent, Adsorption, Adsorption Capacity, Adsorption Isotherm, Aqueous-Solutions, Capacity, Column, Data, Equilibrium, Extraction, Extraction Resin, Freundlich, Freundlich Adsorption Isotherm, Freundlich Isotherm, Hafnium, Isotherm, Kinetic, Kinetic Model, Kinetics, Langmuir, Langmuir Adsorption Isotherm, Langmuir Isotherm, Methyl Isobutyl Ketone, Model, Pseudo Second Order, Pseudo-Second-Order, Pseudo-Second-Order Equation, Pseudo-Second-Order Kinetic Model, Rate Constants, Removal, Resin, Saturation, Separation, Sorption, Temperature, XAD-4, Zirconium
? Wen, J.J., Zhang, Q.X., Zhang, G.Q. and Cao, Z.Y. (2010), Deep removal of copper from cobalt sulfate electrolyte by ion-exchange. Transactions of Nonferrous Metals Society of China, 20 (8), 1534-1540.
Full Text: 2010\Tra Non Met Soc Chi20, 1534.pdf
Abstract: SP-C was applied for the removal of Cu2+ from simulated cobalt sulfate electrolyte containing Co2+ 50 g/L and Cu2+ 0.5-2.0 g/L. Experimental conditions included pH of 2-4, temperature of 20-60ºC and contact time of 10-40 min. The investigation demonstrated that SP-C had recommendable efficiency in adsorbing Cu2+ from the electrolyte with 25- to 100-fold of Co2+. The optimal adsorption conditions of SP-C were pH of 4, contact time of 30 min and ambient temperature. The study also showed that the loaded resin could be effectively eluted with 2.0 mol/L H2SO4 solution at a contact time of 40 min; the peak concentration of Cu2+ in the eluate was about 35 g/L. The sorption characteristics of Cu2+ by SP-C could be described by Langmuir isotherm and the pseudo second-order kinetic equation. Infrared spectra showed that nitrogen atoms in the functional group coordinated with Cu2+ to form coordination bands.
Keywords: Adsorption, Characteristics, Chelating Resin, Co2+, Cobalt, Cobalt Sulfate Electrolyte, Concentration, Coordination, Copper, Cu2+, Efficiency, Equilibrium, Functional Group, Investigation, Ion Exchange, Ion-Exchange, Ionexchange, Isotherm, Kinetic, Kinetic Equation, Langmuir, Langmuir Isotherm, Loaded Resin, Nickel, Nitrogen, Pb2+, pH, Pseudo Second Order, Pseudo Second-Order, Pseudo-Second-Order, Recovery, Removal, Removal of Copper, Resin, Second Order, Second-Order, Solution, Sorption, Sulfate, Temperature
? Xiong, C.H., Wang, G.T. and Yao, C.P. (2011), Adsorption of ytterbium(III) from aqueous solution by SQD-85 resin. Transactions of Nonferrous Metals Society of China, 21 (12), 2764-2771.
Full Text: 2011\Tra Non Met Soc Chi21, 2764.pdf
Abstract: Adsorption and desorption behavior of Yb(III) by SQD-85 resin was investigated by various chemical methods and IR spectrometry. The adsorption capacity of SQD-85 resin for Yb(III) was studied as a function of solution pH, initial concentration of Yb(III), temperature and contact time. The optimal pH for the adsorption was 5.50 in the HAc-NaAc system, and the maximum adsorption capacity was estimated to be 347.6 mg/g at 308 K. The isotherms adsorption data fit well with Langmuir model. The adsorption kinetics data are in agreement with pseudo-second-order model. Thermodynamic parameters indicate that Yb(III) adsorption by SQD-85 resin is endothermic and spontaneous in nature. Thomas model is reasonably accurate in predicting experimental column results. The dynamic desorption rate of Yb(III) can increase to 97.3% when the elution agent is 1.0 mol/L HCl. These results suggest that Yb(III) in aqueous solution can be removed and recovered by SQD-85 resin efficiently.
Keywords: Activation, Adsorption, Adsorption Kinetics, Concentration, Desorption, Elution, Ions, Ir, Isotherms, Kinetics, Langmuir, Lead, Mechanism, Metals, pH, Rare-Earth-Elements, Removal, Resin, Samples, Separation, SQD-85 Resin, Temperature, Thermodynamic, Thermodynamic Parameters, Thermodynamics, Thomas Model, Water, Yb(III)
Share with your friends: |