Studies of Adsorption of Cadmium Ions by Biowaste Adsorbent from Aqueous Solutions with Ion-Selective Electrodes and ICP-OES

Using environment-friendly and low-cost biowaste adsorbents as toxic metal ion removal substrates from aqueous solutions has a great economic advantage. This work evaluated pumpkin and potato peel biowastes for the adsorption of cadmium ions. The biowastes were treated with acid or base. Batch experiments were carried out by introducing a known concentration of metal ion solution into the biowaste sorbent at various pH levels. The pH and metal ion concentration was monitored with pH and cadmium ion-selective electrode continuously for two hours, and the final concentration for the metal ion after 24 hours was measured with the cadmium electrode and then confirmed with ICP-OES. L-type isotherms were obtained that fit to Freundlich model. Adsorption isotherms showed chemical adsorption and the kinetics following the second order model. Equilibrium adsorption capacity is higher than 29 mg/g at pH 5.6 when the initial concentration is 220 ppm. Dynamic cadmium adsorption capacity is 17 mg/g from aqueous solution when the feed solution is 220 ppm with pumpkin peel biowaste sorbent. The biowaste materials can be regenerated with acid washing.

Highly Efficient and Selective Removal of Pb（II） ions by Sulfur-Containing Calcium Phosphate Nanoparticles

A facile one-step co-precipitation method was demonstrated to fabricate amorphous sulfurcontaining calcium phosphate （SCP） nanoparticles, in which the sulfur group was in-situ introduced into calcium phosphate. The resulting SCP exhibited a noticeable enhanced performance for Pb（II） removal in comparison with hydroxyapatite （HAP）, being capable of easily reducing 20 ppm of Pb（II） to below the acceptable standard for drinking water within less than 10 min. Remarkably, the saturated removal capacities of Pb（II） on SCP were as high as 1720.57 mg/g calculated by the Langmuir isotherm model, exceeding largely that of the previously reported absorbents. Significantly, SCP displayed highly selective removal ability toward Pb（II） ions in the presence of the competing metal ions （Ni（II）, Co（II）, Zn（II）, and Cd（II））. Further investigations indicated that such ultra-high removal efficiency and preferable affinity of Pb（II） ions on SCP may be reasonably ascribed to the formation of rodlike hydroxypyromorphite crystals on the surface of SCP via dissolution-precipitation and ion exchange reactions, accompanied by the presence of lead sulfide precipitates. High removal efficiency, fast removal kinetics and excellent selectivity toward Pb（II） made the obtained SCP material an ideal candidate for Pb（II） ions decontamination in practical application.

Adsorption characteristics of Pb(Ⅱ)ions on sulfidized hemimorphite surface under ammonium sulfate system

In this work,the effect of ammonium sulfate on the adsorption characteristics of low-concentration Pb(Ⅱ)ions on the sulfidized hemimorphite surface was comprehensively investigated.The results showed that ammonium sulfate could increase the maximum recovery of hemimorphite from 69.42%to 88.24%under a low concentration of Pb(Ⅱ)ions.On the hemimorphite surface pretreated with ammonium sulfate,the adsorption of Pb(Ⅱ)ions was enhanced and the main species of Pb adsorbed was changed from Pb―O/OH to PbS.This was due to the larger amount of ZnS providing more effective adsorption sites for Pb components to generate Pb S.Meanwhile,the intensity of ZnS decreased with the formation of PbS,demonstrating that ZnS was covered by PbS which formed later on the mineral surface.It was beneficial for the adsorption of butyl xanthate on the hemimorphite surface to form more hydrophobic substances.As a result,ammonium sulfate played a crucial role in realizing the efficient recovery of hemimorphite.

Removal of lead and cadmium ions by single and binary systems using phytogenic magnetic nanoparticles functionalized by 3-marcaptopropanic acid

The present research study is focused on green fabrication of superparamagnetic Phytogenic Magnetic Nanoparticles(PMNPs), and then its surface functionalization with 3-Mercaptopropionic acid(3-MPA). The resulting material(i.e. 3-MPA@PMNPs) characterized by FTIR, powder XRD, SEM, TEM, EDX, VSM, BET and TGA techniques and then further employed for the investigation of the adsorptive removal of lead(Pb^2+) and cadmium(Cd^2+) ions from aqueous solutions in single and binary systems. The material showed fastest adsorptive rate(98.23%) for Pb^2+ and(96.5%) Cd2+within the contact time of 60 min at pH 6.5 in the single system. The experimental data were fitted well to Langmuir isotherm, indicated monolayer adsorption of both metal ions onto 3-MPA@PMNPs and an estimated comparable adsorptive capacity of 68.41 mg·g^-1(Pb2+) and 79.8 mg·g^-1(Cd2+) at p H 6.5. However, kinetic data agreed well with pseudo-second-order model, and indicated that the removal mainly supported chemisorption and/or ion-exchange mechanism. Thermodynamic parameters such asΔGo,ΔHo, and ΔSo, were-3259.20, 119.35 and 20.73 for Pb^2+, and-1491.10, 45.441 and 7.87 for Cd^2+ at temperature 298.15 K, confirmed that adsorption was endothermic, spontaneous and favorable. The material demonstrated higher selectivity of Pb2+ and its removal efficiency was(98.20 ± 0.3)% in binary system experiments. The material persisted performance up-to seven(07) consecutive treatment cycles without losing their stability and offered comparable fastest magnetic separation(35 s) from aqueous solutions. Therefore, it is recommended that the prepared material can be employed to remove toxic heavy metal ions from water/wastewaters and this "green" method can easily be implemented at large scale in low economy countries.

Removal of Cadmium Ions from Aqueous Solution by Silicate-incorporated Hydroxyapatite

This article reports a preliminary research on silicate-incorporated hydroxyapatite as a new environmental mineral used to remove cadmium ions from aqueous solutions. The silicate-incorporated hydroxyapatite was prepared by coprecipitation and calcining, and silicate was incorporated into the crystal lattice of hydroxyapatite by partial substitution of phosphate. The amount of cadmium ions removed by silicate-incorporated hydroxyapatite was significantly elevated, which was 76% higher than that of pure hydroxyapatite. But the sorption behavior of cadmium ions on silicate-incorporated hydroxyapatite was similar to that of pure hydroxyapatite. Morphological study revealed that silicate incorporation confined the crystal growth and increased the specific surface area of hydroxyapatite, which were in favor of enhancing the cadmium ion sorption capacity of the samples. Incorporation of silicate into hydroxyapatite seems to be an effective approach to improve the environmental property of hydroxyapatite on removal of aqueous cadmium ions.

Syntheses, Crystal Structures and Characterization of Two New Cadmium(II) Arsonates

Two cadmium arsonate coordination polymers, Cd（HL1）2 （1, H2L1 = 4-aminophenylarsonatic acid） and Cd（H2L2）2·2H2O （2, H3L2 = 2-（4-arsonphenylamino）acetic acid）, have been synthesized and characterized by IR and single-crystal X-ray diffraction. Crystal data for 1： triclinic, space group P1 with a = 5.7559（12）, b = 7.0903（14）, c = 8.9925（18）, α = 89.04（3）, β = 80.79（3）, γ = 85.09（3）o, Dc = 2.496 g·cm-3, μ = 6.095 mm-1, F（000） = 260, Z = 1, the final R = 0.0574 and wR = 0.1376 for 1489 observed reflections with I 〉 2σ（I）. And those for 2： monoclinic, space group P21/c with a = 4.7595（10）, b = 9.925（2）, c = 22.609（5）, β = 91.81（3）°, Dc = 2.167 g·cm-3, μ = 4.168 mm-1, F（000） = 684, Z = 2, the final R = 0.0335 and wR = 0.0815 for 2340 observed reflections with I 〉 2σ（I）. The structure of 1 shows a two-dimensional layer consisting of inorganic chains of {CdN2（AsO3）2} along the a axis linking with the phenyl groups. These layers are further linked through strong interlayer hydrogen bonding interaction to form a three-dimensional hydrogen bond supramolecular architecture. Compound 2 has inorganic chains of {CdO2（AsO3）2} similar to 1, which connect with four adjacent inorganic chains forming a three-dimensional framework.

Synthesis and Characterization of Chiral Mercury(II) and Cadmium(II) Complexes with 3,3'-Bipyridine-5,5',6,6'-tetramethyl-2,2'-dimethoxy-1,1'-biphenyl

Two homochiral mercury （1） and cadmium （2） complexes derived from chiral twisted biphenyl pyridine ligand （3,3＇-bipyridine-5,5＇,6,6＇-tetramethyl-2,2＇-dimethoxy-1,1＇-biphenyl） have been synthesized and characterized by IR, microanalysis, TGA, UV-Vis, powder and single-crystal X-ray crystallography. Both 1 and 2 crystallize in orthorhombic space group P21212 with Z = 2. For 1, a = 14.2038（16）, b = 14.3630（17）, c = 7.0257（8）, V = 1433.3（3）3, Mr = 878.91, Dc = 2.037 g/cm3, μ = 7.549 mm-1, F（000） = 824, the final GOF = 1.017, R = 0.0296 and wR = 0.0645 for 2925 observed reflections with I 2σ（I）. For 2, a = 14.212（3）, b = 14.392（3）, c = 7.0498（14）, V = 1442.0（5）3, Mr = 790.72, Dc = 1.821 g/cm3, μ = 2.924 mm–1, F（000） = 760, the final GOF = 1.075, R = 0.0340 and wR = 0.0834 for 3144 observed reflections with I 2σ（I）. The crystal structures of 1 and 2 are isostructural and each adopts a two-dimensional supramolecular network which contains the C–H···π interactions.

Modeling Date Palm Trunk Fibers (DPTF) Packed Bed Adsorption Performances for Cadmium Removal from Aqueous Wastewater

In this study,the potential of a low-cost bio-adsorbent,taken directly from Date Palm Trunk Fibers(DPTF)agricultural wastes,for cadmium ions removal from wastewaters is examined.The performances of this adsorbent are evaluated by building breakthrough curves at different bed heights and flow rates while keeping other parameters,such as the initial feed concentration,pH,and particle size,constant.The results indicate that the maximum cadmium adsorption capacity of DTPF can be obtained from the Thomas model as 51.5 mg/g with the most extended mass transfer zone of 83 min at the lowest flow rate at 5 ml/min.The saturation concentrations(NO)and the rate constant(kab)obtained from the BDST(bed depth service time)model are 7022.16 mg/l and 0.0536 l/mg.min,respectively.Using the Yon-Nelsen Model,it is found that operating at a lower flow rate leads to a larger value of the elapsed needed time to reach a 50%breakthrough.The Wolborska model indicates that the bed capacity increases with decreasing the flow rate,and the adsorbent can achieve a greater external mass transfer kinetic coefficient(2.271/min)at a higher flow rate.

Alumina/Iron Oxide Nano Composite for Cadmium Ions Removal from Aqueous Solutions

Magnetic alumina nano composite (MANC) was prepared for combination of the adsorption features of nano activated alumina with the magnetic properties of iron oxides to produce a nano magnetic adsorbent, which can be separated from the medium by a simple magnetic process after adsorption. MANC was characterized using XRD, SEM, TEM, EDX and surface area (BET). Quantum design SQUID magnetometer was used to study the magnetic measurement. The present study was conducted to evaluate the feasibility of MANC for the removal of cadmium ions from aqueous solutions through batch adsorption technique. The effects of pH, adsorbent dose, temperature, contact time and initial Cd2+ concentration on cadmium ions adsorption were studied. Equilibrium data were fitted to Langmuir, Freundlich and Temkin isotherms. The equilibrium data were best represented by the Langmuir isotherm. The kinetic data were fitted to pseudo-first-order, pseudo-second-order, Elovich and intraparticle diffusion models, and it was found to follow closely the pseudo-second-order model. Thermodynamic parameters were calculated for the Cd2+ ion-MANC system and the positive value of ΔH° showed that the adsorption was endothermic in nature. Furthermore, a single-stage batch adsorber was designed for the removal of Cd2+ ions by MANC based on the equilibrium data obtained.

Removal of cadmium ions from aqueous solution via micellar-enhanced ultrafiltration

To separate cadmium ions from aqueous solution efficiently, micellar-enhanced ultrafiltration(MEUF) of hollow ultrafiltration membrane was used, with sodium dodecyl benzene sulfonate (SDBS) and sodium dodecyl (sulfate) (SDS) as surfactants. The important parameters affecting the rejection of cadmium, the permeate flux and the secondary resistance were investigated, including surfactant species, surfactant concentration, operating time, trans-membrane pressure, the addition of electrolyte and solution pH. The results show that the rejection rate of cadmium reaches 97.8%. Trans-membrane pressure and the addition of electrolyte (NaCl) are less influential while surfactant species, surfactant concentration and pH value are important for micellar-enhanced ultrafiltration. The optimum concentration of surfactant is the critical micelle concentration, and SDBS is better than SDS. (Micellar-)(enhanced) ultrafiltration with SDBS can separate cadmium ions from aqueous solution efficiently.

Sesame Husk as Adsorbent for Copper(II) Ions Removal from Aqueous Solution

In this study, the adsorption behavior of copper(II) ions from aqueous solutions onto sesame husk (SH) was investigated. The effect of different parameters such as pH, contact time, adsorbent dosage, adsorbate concentration, temperature and agitation speed was studied. Thermodynamic parameters, equilibrium isotherms and kinetic data have been evaluated. The functional groups and surface morphology of SH adsorbent were characterized by FTIR and SEM. Adsorption equilibrium isotherms were expressed by Langmuir, Freundlich and Dubinin-Radushkevich (D-R) adsorption models and it was found that Langmuir adsorption model fits the experimental data better than Freundlich and D-R models. The adsorption can be best described by the pseudo second-order kinetic model.

Atomic Absorption and Vibrational Spectral Magnetic Studies on the Removal of Cu(II) and Co(II) Ions Using Synthetic Nano Adsorbent Fe₃O₄

Adsorption of Cu(II) and Co(II) from aqueous solutions on synthetic nano Fe3O4 has been studied. The effect of experimental parameters such as initial concentration of the metal ions, adsorbent dosage, contact time and pH has been investigated. Optimum removal efficiency of Cu(II) ion was found to be 97.8% with the dose rate of 1.07 g/L in 60 minutes at pH = 5.5 and for Co(II) ion, it was found to be 99.2% with the dose rate of2.57 g/L in 10 minutes at pH = 5.4. The removal of Co(II) ions require only 10 minutes with the efficient removal of 99.2%, whereas Cu(II) ions require 60 minutes with the maximum removal of 97.8%. In order to understand the effective removal of Cu(II) and Co(II) ions on Fe3O4, room temperature magnetic measurement was carried out using Vibrational Spectrum Magnetometer (VSM), before and after adsorption with a maximum applied magnetic field of 20,000 G.

Demineralised Lignite Fly Ash for the Removal of Zn(II) Ions from Aqueous Solution

Among the various possibilities of limiting the disposal of fly ashes (lignite), their reutilization as adsorbent materials is worthy of consideration. To this end, proper ashes beneficiation techniques can be put into practice. The adsorption of toxic compounds from industrial wastewater is an effective method for both treating these effluents and recycling lignite fly ash. The aim of this paper is to give a contribution for understanding the relationships among beneficiation treatments, adsorbent properties and adsorption mechanism and efficiency. In this context, the lignite fly ash was demineralised using concentrated HCl and HF (FA-DEM) and was used as adsorbent for Zn(II) ions from aqueous solutions. Batch experiments were carried out under various adsorbent dosages, pH, contact time and different metal ion concentrations. For FA-DEM, the 57.7% removal of Zn(II) ion was achieved under the optimum conditions of adsorbent dosages of 4 g/L, pH at 6, temperature at 303 K and the contact time of 1.15 h. The adsorption of Zn(II) ions onto FA-DEM followed the pseudo second order kinetics. The Langmuir isotherm model best represented the equilibrium data.

Preparation, Characterization, and Application of Manganese Oxide Coated Zeolite as Adsorbent for Removal of Copper(II) Ions from Seawater

The present study is aimed to examine the adsorption characteristics of Cu(II) by using the novel cellulose acetate composite and to apply it for the removal of Cu(II) from real wastewater samples. In order to achieve this objective, ethylenediamine, diethylenetriamine, triethylenetetramine and te-traethylenepentanene were used for immobilization of grafted cellulose acetate-nanoscale manganese dioxide. Cellulose was extracted from mangrove species Avicennia marina and converted to cellulose acetate then it was formed composite with nano-manganese dioxide via precipitation of nano-manganese dioxide on it. The composite was grafted with acrylamide monomer before immobilization. The synthesized compounds were used for adsorption of Cu(II) and characterized by FT-IR, TGA and SEM. The adsorption characteristics of synthesized sorbents were optimized. Langmuir and Freundlich models were used to establish sorption equilibria. The analytical applications of these modified materials were applied successfully for the removal of Cu(II).

Cadmium-containing Wastewater Induced by SRB:Effect of Multiple Ions and Mineralization Process

The effects of various general and heavy metal ions in acidic cadmium-containing wastewater on SBR desulfurization and cadmium removal under different concentrations were studied.CrO_(4)^(2-) and S^(2-) inhibited SRB mineralization,and Mg^(2+),Ca^(2+),Fe^(2+),and Fe^(3+) promoted SRB mineralization at low concentration(<50 mg/L).The inhibitory concentrations of Cu^(2+),Mn^(2+),Co^(2+),Zn^(2+),Pb^(2+),Hg^(2+),Cr^(3+),and Ni^(2+) were 10,30,2,20,25,5,30 mg/L,respectively.The inhibition order was Co^(2+)>Hg^(2+)>Cu^(2+)>Ni^(2+)>Zn^(2+)>Pb^(2+)>Mn^(2+)>Cr^(3+).Furthermore,the inverted microscopy and scanning electron microscopy(SEM)were used to observe the sediment crystallization process from macroscopic and microscopic viewpoints in the optimized ion environment.The experimental results show that under the mineralization of SRB,cadmium sediment crystallization is mainly divided into the rapid growth of bacteria,crystal nucleus production,block formation,and crystallization occuration.At the same time,X-ray diffraction(XRD)and energy-dispersive spectra(EDS)have also confirmed the sediment and crystallization.

Effect of Hg(II) and Pb(II) Ions on C-Phycocyanin (<i>Spirulina</i><i>platensis</i>)

Influence of Hg(II) and Pb(II) ions on C-Phycocyanin (C-PC) from cyanobacteria Spirulina platensis was investigated using Fluorescence spectroscopy. Fluorescence measurements demonstrate quenching of C-PC emission by Hg(II) and Pb(II), and blue shifts in the fluorescence spectra. The effect of DNA on the fluorescence of Hg(II)-and Pb(II)-C-PC (from Spirulina platensis) complexes was also studied. It was shown that the fluorescence intensity of Hg-C-PC after addition of DNA gave rise to the fluorescence buildup. At the same time, addition of DNA to the Pb(II)-C-PC complexes showed no such effect. In the case of Hg(II)-C-PC, fluorescence intensity significantly decreases in time, while for Pb(II)-C-PC, decrease of the fluorescence intensity is not significant, but blue shift of the peak takes place.

Biochemical and Immunochemical Characterization of Caenorhabditis elegans Metallothioneins I and II Induced by Cadmium

Metallothioneins in Caenorhahditis elegans (CeMT-Ⅰ and Ⅱ) were punned by the combination of gel filtration ion-exchange chromatography.and high-performance liquid chromatography.Amino acid compositions and amino-terminal sequences of CeMT-Ⅰ and Ⅱ were slightly different from those of vertebrate MTs previously reported, although cysteine residue contents were relatively high.Enzyme immunoassay using anti-CeMT-Ⅱ antibody showed the difference of antigenicity to rat MT-Ⅰ and Ⅱ and even to CeMT-Ⅰ. Immunohistochemical staining revealed the existence of CeMT-Ⅱ in the intestine and the eggs, suggesting the role of MT in detoxification and homeostasis of heavv metals. 1990 Academic Press.Inc.

The Uptake of Copper(II) Ions by Chelating Schiff Base Derived from 4-Aminoantipyrine and 2-Methoxybenzaldehyde

The Schiff base, 4-[(2-methoxybenzylidene)amino]-1,5-dimethyl-2-phenyl-1H-pyrizol-3(2H)-one (SB), was used for the first time to adsorb copper(II) ions in aqueous solution. Various parameters such as initial pH, agitation period and different initial concentration of copper(II) ions which influenced the adsorption capacity were investigated. The equilibrium adsorption data for copper(II) ions were fitted to Langmuir, Freundlich and Dubinin-Radushkevish isotherm models. The maximum monolayer adsorption capacity of SB as obtained from Langmuir isotherm was 5.64 mg/g. Kinetic data correlated well with the pseudo second-order kinetic model indicating that chemical adsorption was the rate limiting step.

CdI₂Extraction with 18-Crown-6 Ether into Various Diluents: Classification of Extracted Cd(II) Complex Ions Based on the HSAB Principle

CdI2 in water was extracted with 18-crown-6 ether (L) into 10 diluents at 298 K. The following equilibrium constants were determined or evaluated: some extraction constants (Kex/mol-3·dm9 & Kex,ip/mol-2·dm6 for CdLI2, Kex±/mol-2·dm6 for CdLI+ with I-, & Kex2±/mol-1·dm3 for CdL2+ with 2I-), conditional distribution constants (KD,I for I-, KD,CdLI for CdLI+, & KD,CdL for CdL2+) between the two phases, and an ion-pair formation constant (K1,org/mol-1·dm3) for CdLI+ and that (K2,org/mol-1·dm3) for CdLI2 in the organic (org) phases. Using the K1,org and K2,org values, acidities of the complex ions, CdL2+ and CdLA+ (A- = I-, Br-, & Cl-), in the 11 diluents were classified by applying the HSAB rule. Especially, the CdLA+ ions were classified as the soft acids in 9 diluents. Also, molar volumes (Vj/cm3·mol-1) of j = CdLI2 and CdL2+ were determined with the regular-solution-theory plot of logKex,ip vs. logKD,L and its pseudo-plot of logKD,CdL, respectively. Here, KD,L denotes the distribution constant of L between the two phases. So, sizes among CdLA2 and CdL2+ were compared by using the Vj values. Additionally, some distribution equilibrium potentials (dep/V) between the water and org bulk phases were topically calculated from an equation of KD,I with KSD,I, where the symbol KSD,I shows a standard distribution constant of I- at dep = 0 V for a given diluent.

Quantitative analysis of cefixime via complexation with palladium(Ⅱ) in pharmaceutical formulations by spectrophotometry

An optimized and validated spectrophotometric method has been developed for the determination of cefixime in pharmaceutical formulations. The method is based on the complexa- tion reaction between cefixime and palladium ion in the presence of acidic buffer solution （pH 3） in ethanol-distilled water medium at room temperature. The complex absorbed maximally at 352 nm. Beer＇s law is obeyed in the working concentration range of 2.5-35 μg/mL with apparent molar absorptivity of 1.015×104 L/mol cm and Sandell＇s sensitivity of 0.001 μg/cm2/0.001 absorbance unit. The limits of detection and quantitation for the proposed method are 0.175 and 0.583μg/mL, respectively. The effect of common excipients used as additives has been studied in the determination of cefixime. The proposed method has been successfully applied for the determina- tion of cefixime in pharmaceutical formulations. The results obtained by the proposed method were statistically compared with the reference method using t and F values and found no significant difference between the two methods.