Sorption of strontium ions from aqueous solutions by oxidized multiwall carbon nanotubes

Multiwall carbon nanotubes (MWCNTs) oxidized by nitric acid solution were used to investigate the adsorption behavior of strontium from aqueous solutions similar to the nuclear waste media. The physical properties of both as produced and oxidized MWCNTs were studied by Boehm’s titration method and nitrogen adsorption/desorption. The results showed that the surface properties of MWCNTs such as specific surface area, functional groups and the total number of acid sites were improved after oxidation. Furthermore, the effect of solution conditions such as initial concentration of strontium(II), pH, ionic strength, MWCNT concentration and contact time were studied at room temperature. The results of this study showed that the adsorption of strontium(II) was significantly influenced by the pH value and the solution ionic strength. According to the Langmuir model, the maximum adsorption capacities of strontium(II) onto the as produced and oxidized MWCNTs were obtained as 1.62 and 6.62 mg g^?1, respectively. The contact time to reach equilibrium was 100 min. The good adsorption of strontium(II) on oxidized MWCNTs at the lower ionic strength, the relatively high pH and the short equilibrium time indicate that the oxidized MWCNTs have great potential applications in the field of the environmental protection.     

Adsorption of cesium (I) from aqueous solution using oxidized multiwall carbon nanotubes

Multiwall carbon nanotubes (MWCNTs) were modified by nitric acid solution and then used to study the adsorption of cesium from aqueous solution using a batch technique under ambient conditions. As produced and oxidized MWCNTs were characterized by nitrogen adsorption/desorption, Boehm’s titration method and Fourier transform infrared spectroscopy. The physical properties of MWCNTs such as functional groups, total number of acid sites and specific surface area were greatly improved after oxidation, and these were responsible for more sorption of cesium from aqueous solution and made them more dispersible in water. The adsorption of cesium ions as a function of contact time, initial concentration of cesium, pH, ionic strength and oxidized MWCNT concentrations was also investigated. The results showed that cesium adsorption percentage strongly depended on the pH value, oxidized MWCNT content and on the solution ionic strength. Kinetic data indicated that the adsorption process achieved equilibrium within 80 min. Equilibrium data for as produced and oxidized MWCNTs was well described by both Freundlich and Langmuir isotherms. The dominant mechanism of cesium adsorption on oxidized MWCNTs may be mainly attributed to ion exchange. This study suggests that oxidized MWCNTs can be a promising candidate for the removal of cesium from nuclear waste solution.     

Adsorption and desorption behavior of tetravalent zirconium onto a silica-based macroporous TODGA adsorbent in HNO3 solution

To understand the separation behavior of Zr(IV) in the partitioning process for high level liquid waste, a silica-based macroporous adsorbent (TODGA/SiO₂-P) was prepared by impregnating N,N,N′,N′-tetraoctyl-3-oxapentane-1,5-diamide (TODGA) into a macroporous silica/polymer composite particles support (SiO₂-P). Adsorption and desorption behavior of Zr(IV) from nitric acid solution onto silica-based TODGA/SiO₂-P adsorbent were investigated by batch experiment. It was found that TODGA/SiO₂-P showed strong adsorption affinity to Zr(IV) and this adsorption process reached equilibrium state around 6 h at 298 K. Meanwhile, HNO₃ concentration had no significant effect on the adsorption of Zr(IV) above 1 M. From calculated thermodynamic parameters, this adsorption process could occur spontaneously at the given temperature and was confirmed to be an exothermic reaction. This adsorption process could be expressed by Langmuir monomolecular layer adsorption mode and the maximum adsorption capacity were determined to be 0.283 and 0.512 mmol/g for Zr(IV) at 298 and 323 K, respectively. In addition, more than 90 % of Zr(IV) adsorbed onto adsorbent could be desorbed with 0.01 M diethylenetriamine pentaacetic acid solution within 24 h at 298 K.     

Effect of oxidation treatment of multi-walled carbon nanotubes on the adsorption of pentachlorophenol from aqueous solution: Kinetics study

Multi-walled carbon nanotubes (MWCNTs) were oxidized using different oxidizing agents and the produced oxidized MWCNTs were characterized using different techniques. IR measurements showed the presence of carboxylic acid function groups especially for the MWCNTs oxidized with nitric acid and hydrogen peroxide. The adsorption of pentachlorophenol (PCP) to pristine and oxidized multi-walled carbon nanotubes (MWCNTs) has been studied. The results showed that the oxidation of the MWCNTs decreased their abilities to adsorb PCP compared with the pristine MWCNTs. The adsorption was studied kinetically and the results showed that the adsorption process occurs in two different steps. The first step involves the transfer of PCP to the surface of the oxidized MWCNTs, which was very fast due to the diffusion of PCP from the liquid phase to the solid phase. This step followed by a second slower step of adsorption could be due to intra-particle diffusion.     

Competitive adsorption of uranium(VI) and thorium(IV) ions from aqueous solution using triphosphate-crosslinked magnetic chitosan resins

The triphosphate-crosslinked magnetic chitosan resins (TPP-MCR) with a diameter range of 200–350 nm were synthesized for the adsorption of U(VI) and Th(IV) ions from aqueous solutions. The adsorption experiments were conducted in both mono-component systems with pure actinide solution and bi-component systems with different U/Th mass ratios. The maximum adsorption capacities in mono-component systems determined by Langmuir model were 169.5 and 146.8 mg g^?1 for U(VI) and Th(IV), respectively. In bi-component systems, U(VI) and Th(IV) adsorption capacities were reduced significantly, and the combined sorption capacities were substantially lower (almost halved) compared to those obtained by the addition of sorption capacities using mono-component solutions, indicating that U(VI) and Th(IV) compete for the same sorption sites. Adsorption–desorption experiments for five cycles illustrated the feasibility of the repeated use of TPP-MCR for the adsorption of U(VI) and Th(IV) ions.     

Zr-TUD-1: a Lewis acidic, three-dimensional, mesoporous, zirconium-containing catalyst

A three-dimensional, mesoporous, silicate containing zirconium, Zr-TUD-1, was synthesized by a direct hydrothermal treatment method with triethanolamine as a complexing and templating reagent to ensure that zirconium was incorporated as isolated atoms. The mesoporosity of Zr-TUD-1 was confirmed by X-ray diffraction (XRD), N(2) sorption and high-resolution transmission electron micrograph (HR-TEM) studies. The nature and strength of the Lewis acid sites present in Zr-TUD-1 were evaluated by FTIR studies of pyridine adsorption and temperature-programmed desorption of ammonia. FTIR, X-ray photoelectron spectroscopic (XPS) and UV/Vis spectroscopic studies showed that, at Si/Zr ratios of 25 and higher, all the zirconium was tetrahedrally incorporated into the mesoporous framework, while at low Si/Zr ratios, a small part of the zirconium was present as ZrO(2) nanoparticles. Zr-TUD-1 is a Lewis acidic, stable and recyclable catalyst for the Meerwein-Ponndorf-Verley (MPV) reaction and for the Prins reaction.     

Effect of pH and ionic strength on U(IV) sorption to oxidized multiwalled carbon nanotubes

Multiwalled carbon nanotubes (MWCNTs) have attracted multidisciplinary study because of their unique physicochemical properties. Herein, the sorption of U(VI) from aqueous solution to oxidized MWCNTs was investigated as a function of contact time, pH and ionic strength. The results indicate that U(VI) sorption on oxidized MWCNTs is strongly dependent on pH and ionic strength. The sorption of U(VI) is mainly dominated by surface complexation and cation exchange. The sorption of U(VI) on oxidized MWCNTs is quickly to achieve the sorption equilibrium. The sorption capacity calculated from sorption isotherms suggests that oxidized MWCNTs are suitable material in the preconcentration and solidification of U(VI) from large volumes of aqueous solutions.     

Light scattering studies to determine molecular weight of freshly prepared Zr(IV) hydrous polymer

In the present work, Zr(IV) has been taken as a homologue for Pu(IV) in order to study the behaviour of Pu in aqueous systems. The direct detection of polymerization of tetravalent zirconium and determination of molecular weight of freshly prepared Zr(IV) polymer was performed by using dynamic light scattering device. Experiments were conducted at 4 different concentrations of zirconium prepared in 1 M nitric acid at 298 K. Particle diameter d ₅₀ was estimated as 255 nm. Differential refractive index increment was also measured. The molecular weight of freshly prepared Zr(IV) polymer was determined as 1,610 Da and second virial coefficient A ₂ = ?0.0106 ml g^?1 Da by using Debye plot showing that Zr(IV) can undergo hydrolysis even under strongly acidic conditions leading to the formation of high molecular weight hydrated polymers.     

Effects of solution chemistry on the adsorption of ibuprofen and triclosan onto carbon nanotubes

Single-walled carbon nanotubes (SWCNTs), multiwalled carbon nanotubes (MWCNTs), and oxidized MWCNTs (O-MWCNTs) were studied for the adsorption of ibuprofen (IBU) and triclosan (TCS) as representative types of pharmaceutical and personal care products (PPCPs) under different chemical solution conditions. A good fitting of sorption isotherms was obtained using a Polanyi-Manes model (PMM). IBU and TCS sorption was stronger for SWCNTs than for MWCNTs due to higher specific surface area. The high oxygen content of O-MWCNT further depressed PPCP sorption. The sorption capacity of PPCPs was found to be pH-dependent, and more adsorption was observed at pHs below their pK(a) values. Ionic strength was also found to substantially affect TCS adsorption, with higher adsorption capacity observed for TCS at lower ionic strength. In the presence of a reference aquatic fulvic acid (FA), sorption of IBU and TCS was reduced due to the competitive sorption of FA on carbon nanotubes (CNTs). Sorption isotherm results with SWCNTs, MWCNTs and O-MWCNTs confirmed that the surface chemistry of CNTs, the chemical properties of PPCPs, and aqueous solution chemistry (pH, ionic strength, fulvic acid) all play an important role in PPCP adsorption onto CNTs.     

Effect of pH, ionic strength and temperature on sorption characteristics of Th(IV) on oxidized multiwalled carbon nanotubes

Oxidized multiwalled carbon nanotubes (MWCNTs) were characterized by SEM and FTIR. The sorption of Th(IV) on MWCNTs was studied as a function of contact time, pH, ionic strength, Th(IV) concentration and temperature. The results indicate that the sorption of Th(IV) on MWCNTs is strongly dependent on pH and weakly dependent on ionic strength. The sorption thermodynamics of Th(IV) on MWCNTs was carried out at 293.15, 313.15 and 333.15 K, respectively, and the thermodynamic parameters (standard free energy changes (??G ⁰), standard enthalpy change (??H ⁰) and standard entropy change (??S ⁰)) were calculated from the temperature dependent sorption isotherms. The sorption of Th(IV) on MWCNTs is a spontaneous and endothermic process. The oxidized MWCNTs may be a promising candidate for the preconcentration and solidification of Th(IV), or its analogue actinides from large volumes of aqueous solutions.     

Adsorptive removal of thorium from aqueous solution using diglycolamide functionalized multi-walled carbon nanotubes

Multi-walled carbon nanotubes (MWCNTs) were functionalized with diglycolamide (DGA) through chemical covalent route. The adsorption behavior of the DGA-functionalized-MWCNTs (DGA-MWCNTs) towards thorium from aqueous solution was studied under varying operating conditions of pH, concentration of thorium, DGA-MWCNTs dosages, contact time, and temperature. The effective range of pH for the removal of Th(IV) is 3.0–4.0. Kinetic data followed a pseudo-second-order model. The equilibrium data were correlated with the Langmuir, Freundlich, Dubinin-Radushkevich and Temkin models. The equilibrium data are best fitted with Langmuir model. The equilibrium Th(IV) sorption capacity was estimated to be 10.58 mg g^?1 at 298 K. The standard enthalpy, entropy, and free energy of adsorption of the thorium with DGA-MWCNTs were calculated to be 8.952 kJ mol^?1, 0.093 kJ mol^?1 K^?1 and -18.521 kJ mol^?1 respectively at 298 K. The determined value of sticking probability (0.072) and observed kinetic and isotherm models reveal the chemical adsorption of thorium on DGA-MWCNTs.     

Kinetics and thermodynamics of sorption of nitroaromatic compounds to as-grown and oxidized multiwalled carbon nanotubes

The sorption kinetics and thermodynamics of 1,3-dinitrobenzene (DNB), m-nitrotoluene (mNT), p-nitrophenol (pNP), and nitrobenzene (NB) on as-grown and nitric acid-oxidized multiwalled carbon nanotubes (MWCNTs) were investigated. The sorption kinetics was well described by a pseudo-second-order rate model, while both Langmuir and Freundlich models described the sorption isotherms well and the sorption thermodynamic parameters of equilibrium constant (K(0)), standard free energy (DeltaG), standard enthalpy (DeltaH), and standard entropy changes (DeltaS) were measured. The values of DeltaH and DeltaG suggested that the sorption of nitroaromatics (NACs) onto MWCNTs was exothermic and spontaneous. The structure, number, and position of nitro groups of NACs were the main factors affecting the sorption rate and capacity. Treatment of the MWCNTs with nitric acid increased both the surface area and the pore volume and introduced oxygen-containing functional groups to the MWCNTs, which depressed the sorption of NACs onto MWCNTs.     

Zr改性MnO_x/MWCNTs催化剂的结构特征与低温SCR活性

以ZrO(NO3)2·2H2O为前驱体对多壁碳纳米管(MWCNTs)进行了改性并负载MnOx制备了MnOx/ZrO2/MWCNTs催化剂.考察了Zr对催化剂低温选择性催化还原(SCR)反应活性的影响,并通过多种分析手段对催化剂的结构进行了表征.结果表明Zr的添加对催化剂的低温SCR活性具有显著的促进作用,当Zr负载量为30%时,催化剂活性最佳.X射线衍射(XRD)、拉曼(Raman)光谱、透射电镜(TEM)、N2吸附-脱附的表征结果分析表明,适量的Zr改性促进了MnOx在载体表面的分散,增强金属氧化物与MWCNTs之间的作用,也能增加催化剂的比表面积、孔容和孔径.X射线光电子能谱(XPS)、H2程序升温还原(H2-TPR)和NH3程序升温脱附(NH3-TPD)的分析结果则显示,Zr能提高催化剂表面化学吸附氧浓度,促进Mn3+转化为Mn4+,从而使催化剂表面的活性位点增多,氧化还原能力增强,同时还提高了催化剂表面酸性位点的数量和强度,促进了NH3的吸附,是MnOx/ZrO2/MWCNTs催化剂低温SCR活性提高的主要原因.     

Adsorption characteristics of various organic substances on the surfaces of tantalum, titanium, and zirconium

Adsorption characteristics of carboxylic acids, amines, an octapeptide composed of four L-alanine and four L-aspartic acid residues (Peptide-A4D4), and beta-lactoglobulin (beta-Lg) on tantalum (Ta), titanium (Ti), and zirconium (Zr) particles were examined at 30 degrees C and in some case, were compared with their adsorption onto SUS316L stainless steel particles (S6L). The adsorption isotherms on the Ta, Ti, and Zr particles could usually be expressed either by a Langmuir-type equation for reversible adsorption or by a modified Langmuir-type adsorption equation including terms for both reversible and irreversible adsorption. The adsorption equilibrium of benzoic acid, benzylamine, and m-xylylenediamine on all the metal surfaces followed a Langmuir-type equation, while those of phthalic acid, mellitic acid, and Peptide-A4D4 could be fitted to the modified Langmuir-type adsorption equation. The adsorption characteristics of different adsorbates on the different surfaces were discussed particularly with reference to the pH dependencies of the q(irrev), q(rev), and K values and the electrostatic properties of the oxidized surface of the metal particles. Fourier transform infrared spectroscopic analyses using a reflection/absorption technique (RA-IR) indicated that phthalic acid and mellitic acid are adsorbed in similar adsorption states irrespective of the type of metal. beta-Lg was adsorbed onto the surfaces principally in an irreversible manner. The desorption behavior of beta-Lg from Ta, Ti, and S6L surfaces was examined, in order to evaluate the extent of interaction between beta-Lg and the metals.     

Critical Evaluation of Adsorption–Desorption Hysteresis of Heavy Metal Ions from Carbon Nanotubes: Influence of Wall Number and Surface Functionalization

Single‐, double‐, and multi‐walled carbon nanotubes (SWCNTs, DWCNTs, and MWCNTs), and two oxidized MWCNTs with different oxygen contents (2.51 wt % and 3.5 wt %) were used to study the effect of the wall number and surface functionalization of CNTs on their adsorption capacity and adsorption–desorption hysteresis for heavy metal ions (Ni^II, Cd^II, and Pb^II). Metal ions adsorbed on CNTs could be desorbed by lowering the solution pH. Adsoprtion of heavy metal ions was not completely reversible when the supernatant was replaced with metal ion‐free electrolyte solution. With increasing wall number and amount of surface functional groups, CNTs had more surface defects and exhibited higher adsorption capacity and higher adsorption–desorption hysteresis index (HI) values. The coverage of heavy metal ions on the surface of CNTs, solution pH, and temperature affect the metal ion adsorption–desorption hysteresis. A possible shift in the adsorption mechanism from mainly irreversible to largely reversible processes may take place, as the amount of metal ions adsorbed on CNTs increases. Heavy metal ions may be irreversibly adsorbed on defect sites.     

Adsorption of thorium(IV) from aqueous solution by non-living biomass of mangrove endophytic fungus Fusarium sp. #ZZF51

The adsorption of thorium(IV) from aqueous solution by mangrove endophytic fungus Fusarium sp. #ZZF51 is studied by using a batch experiments. The parameters that affect the thorium(IV) sorption, such as solution pH, initial thorium(IV) concentration, contact time, and biomass dose, are discussed in detail. The maximum biosorption of thorium(IV) and the equilibrium sorption capacity are found to be 91 ± 1 % and 11.35 mg g^?1 respectively at pH 3.0, contact time 20 min, initial thorium(IV) concentration 50 mg L^?1 and non-living biomass dose 4.0 g L^?1. Kinetics data follow the pseudo-second-order model and equilibrium data agree with the Temkin isotherm model very well. FT-IR analysis indicates that hydroxyl and carbonyl groups play an important role in the biosorption process.     

Removal of 2.4-dichloro phenoxyacetic acid from aqueous solution by adsorption on activated carbon. A kinetic study

The sorption of 2.4-dichloro phenoxyacetic acid (2.4-D) on two different activated carbons was determined using the batch equilibration technique. The calculated slopes of the Freundlich sorption isotherms were significantly less than 1. The (K) values were higher for the activated carbon which has the higher specific surface, and increased with NaCl concentration. The rate of attaining equilibrium of 2.4-D increased with a decrease in absorbent concentration. Dynamic modelling of the adsorption showed that a first order reversible kinetic model was followed for the adsorption process. The overall rate constant K′, the adsorption rate K₁, the desorption rate constant K₂, and the equilibrium constant K_c for the adsorption process were calculated.     

Removal of cationic dyes: basic magenta and methylene blue from aqueous solution by adsorption on modified loofah

Modified loofah was prepared by a simple chemical graft method to improve its adsorption for cationic dyes. Experimental results showed that the maximum amounts of basic magenta and methylene blue loaded on the modified loofah were 83.5 and 85.5 mg g^?1, and that on the unmodified loofah were 22.2 and 33.7 mg g^?1, respectively. The adsorption for both dyes could reach equilibrium after 300 min. A pseudo-second-order model is suitable for describing the adsorption and desorption kinetics of both dyes on the modified sorbent. According to the intra-particle diffusion model, sorption and desorption processes for the two dyes both presented two distinct phases and were mainly controlled by intra-particle diffusion. The dye-loaded modified loofah could be regenerated by using the mixture solution of HCl and ethanol (V_HCl:V_ethanol = 3:2) as eluent. Adsorption in the binary system showed that adsorption of the dyes was depressed by the presence of the other dye, and the two dyes could be removed efficiently when the initial concentrations were lower than 5.0 × 10^?5 mol L^?1. The Langmuir competitive model was suitable to predict the sorption isotherm in the binary system.     

Zr 改性MnOx/MWCNTs催化剂的结构特征与低温SCR活性

以ZrO（NO₃）₂·2H₂O为前驱体对多壁碳纳米管（MWCNTs）进行了改性并负载MnO_x制备了MnO_x/ZrO₂/MWCNTs 催化剂. 考察了Zr 对催化剂低温选择性催化还原（SCR）反应活性的影响,并通过多种分析手段对催化剂的结构进行了表征. 结果表明Zr 的添加对催化剂的低温SCR活性具有显著的促进作用,当Zr 负载量为30%时,催化剂活性最佳. X射线衍射（XRD）、拉曼（Raman）光谱、透射电镜（TEM）、N₂吸附-脱附的表征结果分析表明,适量的Zr 改性促进了MnO_x在载体表面的分散,增强金属氧化物与MWCNTs 之间的作用,也能增加催化剂的比表面积、孔容和孔径. X 射线光电子能谱（XPS）、H₂程序升温还原（H₂-TPR）和NH₃程序升温脱附（NH₃-TPD）的分析结果则显示,Zr 能提高催化剂表面化学吸附氧浓度,促进Mn³⁺转化为Mn⁴⁺,从而使催化剂表面的活性位点增多,氧化还原能力增强,同时还提高了催化剂表面酸性位点的数量和强度,促进了NH₃的吸附,是MnO_x/ZrO₂/MWCNTs 催化剂低温SCR活性提高的主要原因.     

Adsorption of uranium (VI) from aqueous solution by tetraphenylimidodiphosphinate

The adsorption of uranium (VI) using tetraphenylimidodiphosphinate (Htpip) was studied. Factors of affecting sorption efficiency have been investigated and results showed the adsorption of uranium (VI) was equilibrium at pH 4.5, time 20 min, adsorbent dosage 0.005 g and initial concentration 50 mg L^?1 reaching 99.86 mg g^?1 of adsorption capacity and 99.86% of removal efficiency. Additionally, the interfering ions studies showed that the adsorbent possessed excellent adsorption selectivity of uranium (VI). The surface morphology of Htpip was investigated by SEM. The adsorption process of uranium (VI) onto Htpip fit the pseudo-second-order kinetic model and the Freundlich isotherm model very well.