共查询到20条相似文献,搜索用时 31 毫秒
1.
Gui-Yin Li Yu-Ren Jiang Ke-Long Huang Ping Ding Li-Li Yao 《Colloids and surfaces. A, Physicochemical and engineering aspects》2008,320(1-3):11-18
The adsorption of Saccharomyces cerevisiae mandelated dehydrogenase (SCMD) protein on the surface-modified magnetic nanoparticles coated with chitosan was studied in a batch adsorption system. Functionalization of surface-modified magnetic particles was performed by the covalent binding of chitosan onto the surface of magnetic Fe3O4 nanoparticles. Characterization of these particles was carried out using FTIR spectra, transmission electron micrography (TEM), X-ray diffraction (XRD) and vibrating sample magnetometry (VSM). Magnetic measurement revealed that the magnetic Fe3O4–chitosan nanoparticles were superparamagnetic and the saturation magnetization was about 37.3 emu g−1. The adsorption capacities and rates of SCMD protein onto the magnetic Fe3O4–chitosan nanoparticles were evaluated. The adsorption capacity was influenced by pH, and it reached a maximum value around pH 8.0. The adsorption capacity increased with the increase in temperature. The adsorption isothermal data could be well interpreted by the Freundlich isotherm model. The kinetic experimental data properly correlated with the first-order kinetic model, which indicated that the reaction is the adsorption control step. The apparent adsorption activation energy was 27.62 kJ mol−1 and the first-order constant for SCMD protein was 0.01254 min−1 at 293 K. 相似文献
2.
Juan Mou Chengjuan Li Guoju Wang Wenxian Shi 《Journal of Radioanalytical and Nuclear Chemistry》2012,292(3):1099-1104
The removal of heavy metal ion Co(II) from aqueous solution is studied using γ-Al2O3 by batch technique. The experiments are performed at T = 20 ± 2 °C, in 0.01 M NaNO3 solutions and under aerobic conditions. The effect of pH, ionic strength, fulvic acid (FA) and alumina concentration on the
sorption of Co(II) on alumina are also respectively investigated. The pH affects the sorption of Co(II) significantly as compared
with the effect of FA and ionic strength. The results indicate that strong chemical bonds are formed between Co(II) and the
bare or FA coated alumina surface, and a transition from the adsorption to surface-induced precipitation of Co(II) on alumina
surface takes place. The addition sequences of Co/FA on Co(II) sorption is also studied and the results indicate that the
sorption of Co(II) in ternary system is independent of addition sequences. The results also suggest that the sorption of metal
ions on mineral surface depends on the nature of mineral, nature of organic ligand and nature of metal ion. 相似文献
3.
Amit Bansiwal Dilip Thakre Nitin Labhshetwar Siddharth Meshram Sadhana Rayalu 《Colloids and surfaces. B, Biointerfaces》2009,74(1):216-224
Highly selective material based on naturally occurring biomaterial namely chitosan has been designed for the defluoridation of water. Lanthanum incorporated chitosan beads (LCB) were prepared using precipitation method. The synthesis was optimized by varying different synthesis parameters namely lanthanum loading, complexation and precipitation time, strength of ammonia solution used for precipitation, drying time, etc. Lanthanum incorporated chitosan beads were characterized using SEM, FTIR, XRD and EDX. Surface area of LCB was observed to be 2.76 m2 g−1. The equilibrium adsorption data fitted well to Langmuir adsorption isotherm and showing maximum fluoride adsorption capacity of 4.7 mg g−1 with negligible lanthanum release. Kinetic study reveals that adsorption of fluoride is fast and follows pseudo-first-order kinetics. The effect of pH was also studied and the best efficiency was observed at pH 5. Presence of sulphate, nitrate and chloride marginally affected the removal efficiency, however drastic reduction in fluoride uptake was observed in the presence of carbonate and bicarbonate. Negative value of change in free energy (ΔG°) and positive value of change in entropy (ΔS°) suggest the adsorption of fluoride by LCB is feasible and spontaneous process. Positive value of change in enthalpy (ΔH°) suggests the process of fluoride adsorption is endothermic in nature. Regeneration study reveals that 1 M ammonium chloride solution appears to be the promising regeneration media showing 81.22% regeneration. The adsorption capacity of LCB was similar in fluoride-contaminated ground water collected from Dhar district of Madhya Pradesh, India, as compared to simulated water. 相似文献
4.
Lipeng Zhang Hui Zhang Zhiwei Ge Xianjin Yu 《Journal of Radioanalytical and Nuclear Chemistry》2011,288(2):537-546
The fate and transport of toxic metal ions and radionuclides in the environment is generally controlled by sorption reactions.
The removal of 60Co(II) from wastewaters by MnO2 was studied as a function of various environmental parameters such as shaking time, pH, ionic strength, foreign ions, and
humic substances under ambient conditions. The results indicated that the sorption of 60Co(II) on MnO2 was strongly dependent on pH and ionic strength. At low pH, the sorption of 60Co(II) was dominated by outer-sphere surface complexation and ion exchange with Na+/H+ on MnO2 surfaces, whereas inner-sphere surface complexation was the main sorption mechanism at high pH. The presence of HA/FA enhances
60Co(II) sorption at low pH values, whereas reduces 60Co(II) sorption at high pH values. The Langmuir and Freundlich models were used to simulate the sorption isotherms of 60Co(II) at three different temperatures of 298.15, 318.15 and 338.15 K. The thermodynamic parameters (ΔH
0, ΔS
0 and ΔG
0) calculated from the temperature dependent sorption isotherms indicated that the sorption process of 60Co(II) on MnO2 was endothermic and spontaneous. 相似文献
5.
Hui Zhang Xianjin Yu Lei Chen Jiaqiang Geng 《Journal of Radioanalytical and Nuclear Chemistry》2010,286(1):249-258
The sorption of 63Ni(II) from aqueous solution using ZSM-5 zeolite was investigated by batch technique under ambient conditions. ZSM-5 zeolite
was characterized by point of zero net proton charge (PZNPC) titration. The sorption was investigated as a function of shaking
time, pH, ionic strength, foreign ions, humic acid (HA), fulvic acid (FA) and temperature. The results indicate that the sorption
of 63Ni(II) on ZSM-5 zeolite is strongly dependent on pH. The sorption is dependent on ionic strength at low pH, but independent
of ionic strength at high pH values. The presence of HA/FA enhances 63Ni(II) sorption at low pH values, whereas reduces 63Ni(II) sorption at high pH values. The sorption isotherms are simulated by Langmuir model very well. The thermodynamic parameters
(i.e., ∆H
0, ∆S
0 and ∆G
0) for the sorption of 63Ni(II) are determined from the temperature dependent sorption isotherms at 293.15, 313.15 and 333.15 K, respectively, and
the results indicate that the sorption process of 63Ni(II) on ZSM-5 zeolite is spontaneous and endothermic. 相似文献
6.
Yolda Seki Kadir Yurdako 《Colloids and surfaces. A, Physicochemical and engineering aspects》2009,340(1-3):143-148
Equilibrium, kinetics and thermodynamic aspects of sorption of Promethazine hydrochloride (PHCl) onto iron rich smectite (IRS) from aqueous solution were investigated. The effect of pH on sorption of PHCl onto IRS was also found out. Experimental data were evaluated by using Langmuir, Freundlich and Dubinin–Raduschkevich (DR) isotherm equations. Freundlich and DR equations provided better compatibility than Langmuir equation. Besides, it was determined that the maximum sorption of PHCl takes place at about pH 5. From kinetic studies, it was obtained that sorption kinetics follow pseudo-second-order kinetic model for PHCl sorption onto IRS. When thermodynamic studies are concerned, the values of activation energy (Ea), ΔG°, ΔH° and ΔS° were obtained. ΔG° values are in the range of −8.84 and −9.45 kJ mol−1 indicating spontaneous nature of physisorption. The negative value of the ΔH° (−3.20 kJ mol−1) indicates exothermic nature of adsorption. FTIR analysis and SEM observations of IRS and PHCl adsorbed IRS were also carried out. Sorption experiments indicate that IRS may be used effectively for the adsorption of PHCl. 相似文献
7.
Tanveer Hussain Bokhari A. Mushtaq Islam Ullah Khan 《Journal of Radioanalytical and Nuclear Chemistry》2010,285(2):389-398
In this work, sorption of Ni(II) from aqueous solution to goethite as a function of various water quality parameters and temperature
was investigated. The results indicated that the pseudo-second-order rate equation fitted the kinetic sorption well. The sorption
of Ni(II) to goethite was strongly dependent on pH and ionic strength. A positive effect of HA/FA on Ni(II) sorption was found
at pH < 8.0, whereas a negative effect was observed at pH > 8.0. The Langmuir, Freundlich, and D-R models were applied to
simulate the sorption isotherms at three different temperatures of 293.15 K, 313.15 K and 333.15 K. The thermodynamic parameters
(ΔH
0, ΔS
0 and ΔG
0) were calculated from the temperature dependent sorption, and the results indicated that the sorption was endothermic and
spontaneous. At low pH, the sorption of Ni(II) was dominated by outer-sphere surface complexation or ion exchange with Na+/H+ on goethite surfaces, whereas inner-sphere surface complexation was the main sorption mechanism at high pH. 相似文献
8.
Sh. Yu X. Li A. Ren D. Shao Ch. Chen X. Wang 《Journal of Radioanalytical and Nuclear Chemistry》2006,268(2):387-392
Summary The
removal of heavy metal ion Co(II) from aqueous solution was studied usingg-Al2O3
by batch technique. The experiments were performed at T=20±2 °C, in 0.01M
NaNO3 solutions and under aerobic conditions. The effect of pH,
ionic strength, fulvic acid (FA) and alumina amount on the sorption of Co(II)
on alumina were also investigated. The pH affected the sorption of Co(II)
significantly as compared with the effect of FA and ionic strength. The results
indicated that strong chemical bonds are formed between Co(II) and functional
groups of the bare or FA coated alumina, and a precipitation of Co(II) takes
place on the alumina surface, induced by a transition from the adsorption to
surface. The addition sequences of Co/FA on Co(II) sorption were also studied:
the sorption of Co(II) in the ternary system was found independent of addition
sequences.</p>
</p> 相似文献
9.
Mini Namdeo S.K. Bajpai 《Colloids and surfaces. A, Physicochemical and engineering aspects》2008,320(1-3):161-168
This research focuses on removal of Fe(III) from aqueous solution using chitosan–magnetite nanocomposites as potential sorbent. The presence of nanosized magnetic particles within the nanocomposites was confirmed by TEM and SAED analysis. The particles with diameter 508 μm and 84 μm, follow Frendlich sorption isotherm at 30 °C, and the Frendlich constants (KF, 1/n) have been found to be 5.974 mg g−1, 2.66 and 35.98 mg g−1, 1.385, respectively. Out of various kinetic models, the experimental data for dynamic uptake of Fe(III) is best fitted on ‘pseudo-second order’ kinetic model. The linear nature of plots between log (% sorption) and log (time) is indicative of intra-particle diffusion. For the particles with diameters 508 μm and 84 μm, the value of kid was found to be 1.78 mg l−1 min−0.5 and 2.13 mg l−1 min−0.5. The sorption mean free energy from the Dubinin–Radushkevic isotherm was found to be 7.04 kJ mol−1 indicating chemical nature of sorption. The increase in chitosan content in sorbent particles is found to enhance the Fe(III) uptake. The various thermodynamic parameters have also been evaluated. Finally, the presence of Cu2+ ions in the sorbate is found to decrease the uptake of Fe(III). 相似文献
10.
Zhiqiang Guo Dapeng Xu Donglin Zhao Shouwei Zhang Jinzhang Xu 《Journal of Radioanalytical and Nuclear Chemistry》2011,287(2):505-512
This work contributed to the adsorption of radiocobalt on goethite as a function of contact time, pH, ionic strength and foreign
ions in the absence and presence of fulvic acid (FA) under ambient conditions. The results indicated that adsorption of Co(II)
was dependent on ionic strength and foreign ions at low pH values (pH < 7.8), and independent of ionic strength and foreign
ions at high pH values (pH > 7.8). Outer-sphere surface complexation and/or ion exchange were the main mechanisms of Co(II)
adsorption on goethite at low pH values, whereas inner-sphere surface complexation was the main adsorption mechanism at high
pH values. The presence of FA enhanced Co(II) adsorption at low pH values, but reduced Co(II) adsorption at high pH values.
The thermodynamic data (ΔH
0, ΔS
0, ΔG
0) were calculated from the temperature dependent adsorption isotherms, and the results suggested that adsorption process of
Co(II) on goethite was spontaneous and endothermic. The results are crucial to understand the physicochemical behavior of
Co(II) in the nature environment. 相似文献
11.
Saulius Martusevi
ius Gediminas Niaura Zita Talaikyt Valdemaras Razumas 《Vibrational Spectroscopy》1996,10(2)
The adsorption of
-histidine on a copper electrode from H2O- and D2O-based solutions is studied by means of surface-enhanced Raman scattering (SERS) spectroscopy. Different adsorption states of histidine are observed depending upon pH, potential, and the presence of the SO2−4 and Cl− ions. In acidic solutions of pH 1.2 the imidazole ring of the adsorbed histidine remains protonated and is not involved in the chemical coordination with the surface. The SO2−4 and Cl− ions compete with histidine for the adsorption sites. In solutions of pH 3.1 three different adsorption states of histidine are observed depending on the potential. Histidine adsorbs with the protonated imidazole ring oriented mainly perpendicularly to the surface at potentials more positive than −0.2 V. Transformation of that adsorption state occurs at more negative potentials. As this takes place, histidine adsorbs through the α-NH2 group and the neutral imidazole ring. The Cl− ions cause the protonation and detachment of the α-NH2 group from the surface and the formation of the ion pair NH+3 … Cl− can be observed. In the neutral solution of pH 7.0 histidine adsorbs through the deprotonated nitrogen atom of the imidazole ring and the α-COO− group at E ≥ −0.2 V. However, this adsorption state is transformed into the adsorption state in which the α-NH2 group and/or neutral imidazole ring participate in the anchoring of histidine to the surface, once the potential becomes more negative. In alkaline solutions of pH 11.9 histidine is adsorbed on the copper surface through the neutral imidazole ring. 相似文献
12.
Zhang Hongxia Wen Chuanxi Tao Zuyi Wu Wangsuo 《Journal of Radioanalytical and Nuclear Chemistry》2011,287(1):13-20
We have performed a large number of batch sorption experiments of uranyl onto SiO2 and examined the effects of nitrate or ionic strength, phosphate, fulvic acid(FA), phthalic acid (PH), salicylic acid (SA),
and catechol (CA) on the uranyl sorption onto SiO2. Three sorption edges and three sorption isotherms at ionic strengths 0.05, 0.1, and 0.5 mol/L KNO3 were used to investigate the effect of ionic strength or nitrate on the sorption and the Langmuir, Freundlich, and Dubinin-Radushkevich
models are used to simulate the sorption isotherms, respectively. Five sorption edges in the presence of phosphate, FA, PH,
SA, and CA were compared with that in the absence of complexing ligand. The results suggest that the effect of complexation
of uranyl with nitrate on the uranyl sorption can be negligible and the sorption can be described Freundlich and D-R model
very well. The positive effect of phosphate on the uranyl sorption was found, though the extent of effect was decreased with
increasing pH. The positive effect and the negative effect of FA on the uranyl sorption were found at low pH and high pH ranges,
respectively. The sorption edge of uranyl sorption remained unaffected in the presence of PH in the pH 2–10. In the presence
of SA, the no effect and the negative effect on the uranyl sorption were, respectively, found at low pH and high pH ranges.
The negative effect of CA on the uranyl sorption was found in the pH 2–10. 相似文献
13.
Dong Lijia Yang Jianxia Mou Yinyan Sheng Guodong Wang Linxia Linghu Wensheng Asiri Abdullah M. Alamry Khalid A. 《Journal of Radioanalytical and Nuclear Chemistry》2017,314(1):377-386
Herein, we used biochar pyrolyzed from rice straw to adsorb uranium (U) from aqueous solutions. The adsorption of U(VI) on biochar was strongly dependent on pH but independent on ionic strength. HA/FA enhanced the sorption at pH <6.8 while inhibited the sorption at pH >6.8. The sorption reached equilibrium within 3 h, which was not mediated by pH. The adsorption process was spontaneous and endothermic, and enhanced at higher temperature. However, the influence of temperature was negligible at low initial U(VI) concentrations. Therefore, biochar derived from rice straw may be a promising adsorbent for the removal of U(VI).
相似文献14.
Yunhui Dong Zhengjie Liu Yueyun Li Lei Chen Zengchao Zhang 《Journal of Radioanalytical and Nuclear Chemistry》2012,292(2):619-627
The sorption of Cd(II) from aqueous solution on γ-Al2O3 was investigated under ambient conditions. Experiments were carried out as a function of contact time, solid content, pH,
ionic strength, foreign ions, fulvic acid and temperature. The results indicated that the sorption of Cd(II) was strongly
dependent on pH and ionic strength. At low pH, the sorption of Cd(II) was dominated by outer-sphere surface complexation and
ion exchange with Na+/H+ on γ-Al2O3 surfaces, whereas inner-sphere surface complexation was the main sorption mechanism at high pH. The Langmuir, Freundlich
and Dubinin–Radushkevich (D–R) models were used to simulate the sorption isotherms at three different temperatures. The thermodynamic
data (ΔG
0, ΔS
0, ΔH
0) calculated from the temperature dependent sorption isotherms suggested that the sorption of Cd(II) on γ-Al2O3 was an spontaneous and endothermic process. 相似文献
15.
Zhiqiang Guo Donglin Zhao Yuan Li Zhesheng Chen Haihong Niu Jinzhang Xu 《Journal of Radioanalytical and Nuclear Chemistry》2011,288(3):829-837
The sorption of radiocadmium on Ca-montmorillonite as a function of contact time, pH, ionic strength, foreign ions, humic acid (HA) and fulvic acid (FA) was studied using batch technique. The results demonstrated that the sorption of Cd(II) was dependent on ionic strength at pH < 9, and was independent of ionic strength at pH > 9. Outer-sphere surface complexation and/or ion exchange were the main mechanism of Cd(II) sorption on Ca-montmorillonite at low pH, whereas the sorption at high pH was mainly dominated via inner-sphere surface complexation. The sorption of Cd(II) on Ca-montmorillonite was dependent on foreign ions at low pH values, but was independent of foreign ions at high pH values. A positive effect of HA/FA on Cd(II) sorption was found at low pH values, whereas a negative effect was observed at high pH values. The thermodynamic parameters (i.e., ??H 0, ??S 0, ??G 0) were calculated from the temperature dependent sorption isotherms, and the results indicated that the sorption process of Cd(II) on Ca-montmorillonite was spontaneous and endothermic. 相似文献
16.
Novel drug‐loaded hydrogel beads for intestine‐targeted controlled release were developed by using pH‐ and temperature‐sensitive carboxymethyl chitosan‐graft‐poly(N,N‐diethylacrylamide) (CMCTS‐g‐PDEA) hydrogel as carriers and vitamin B2 (VB2) as a model drug. The hydrogel beads were prepared based on Ca2+ ionic crosslinking in acidic solution and formed dual crosslinked network structure. The structure of hydrogel and morphology of drug‐loaded beads were characterized by Fourier transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), and scanning electron microscopy (SEM). The study about swelling characteristics of hydrogel beads indicated that the beads had obvious pH‐ and temperature‐sensitivity. In vitro release studies of drug‐loaded beads were carried out in pH 1.2 HCl buffer solution and pH 7.4 phosphate buffer solution at 37°C, respectively. The results indicated that the dual crosslinked method could effectively control the drug release rate under gastrointestinal tract (GIT) conditions, which was superior to traditional single crosslinked beads. In addition, the effects of grafting percentage, pH value, and temperature on the release behavior of the VB2 were investigated. The drug release mechanism of CMCTS‐g‐PDEA drug‐loaded beads was analyzed by Peppa's potential equation. According to this study, the dual crosslinked hydrogel beads based on CMCTS‐g‐PDEA could serve as suitable candidate for drug site‐specific carrier in intestine. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献
17.
Thayyath Sreenivasan Anirudhan Sreenivasan Rijith 《Colloids and surfaces. A, Physicochemical and engineering aspects》2009,351(1-3):52-59
A novel glutaraldehyde cross-linked epoxyaminated chitosan (GA-C-ENCS) prepared through chemical modification was used as an adsorbent for the removal and recovery of Cu(II) from aqueous media. The adsorbent was characterized by FTIR, SEM-EDS, ESR, TG/DTG, BET-surface area and potentiometric titration. The Cu(II) adsorption process, which was pH dependent showed maximum removal at pH 6.0. Adsorption equilibrium was achieved within 3 h. The adsorption of Cu(II) followed a reversible-first-order kinetics. The equilibrium data were evaluated using the Langmuir, Freundlich and Dubinin–Radushkevich isotherm models. The best interpretation for the equilibrium data was given by the Dubinin–Radushkevich isotherm. The adsorption capacity of the adsorbent increased from 3.11 to 3.71 mmol g−1 when the temperature was increased from 20 to 50 °C. The complete removal of 20.7 mg L−1 Cu(II) from electroplating industry wastewater was achieved by 0.4 g L−1 GA-C-ENCS. Regeneration experiments were tried for four cycles and the results indicate a capacity loss of <7.0%. 相似文献
18.
D. K. Das P. N. Pathak S. Kumar V. K. Manchanda 《Journal of Radioanalytical and Nuclear Chemistry》2009,281(3):449-455
Sorption behavior of 241Am (~10−9 M) on naturally occurring mineral pyrite (particle size: ≤70 μm) has been studied under varying conditions of pH (2–11),
and ionic strength (0.01–1.0 M (NaClO4)). The effects of humic acid (2 mg/L), other complexing anions (1 × 10−4 M CO3
2−, SO4
2−, C2O4
2− and PO4
3−), di- and trivalent metal ions (1 × 10−3 M Mg2+, Ca2+ and Nd3+) on sorption behavior of Am3+ at a fixed ionic strength (I = 0.10 M (NaClO4)) have been studied. The sorption of 241Am on pyrite increased with pH from 2.8 (84%) to 8.1 (97%). The sorption of 241Am decreased with ionic strength at low pH values (2 ≤ pH ≤ 4), but was insensitive in the pH range of 4–10, suggesting the
formation of outer-sphere complexes on pyrite surface at lower pH, and inner-sphere complexes at higher pH values. The sorption
of 241Am increased in the presence of (i) humic acid (5 < pH < 7.5), and (ii) C2O4
2− (2 < pH < 3). By contrast, other complexing anions such as (carbonate, phosphate, and sulphate) showed negligible influence
on 241Am sorption. The presence of Mg2+, Ca2+ ions showed marginal effect on the sorption profile of 241Am; while the presence of Nd3+ ion suppressed its sorption significantly under the conditions of present study. The sorption of 241Am on pyrite decreased with increased temperature indicating an exothermic process. 相似文献
19.
Interactions in the WO
2
2−
-H+-H2O system was studied by pH-potentiometric titration at 25 ± 0.1°C for c
w
0
= 8 × 10−3 to 2 × 10−2 mol/l. An accurate mathematical model for polycondensation of tungsten(VI) anions in aqueous solution was proposed. The concentration constants of formation were calculated and the diagrams of distribution of isopolyanions of tungsten(VI) were plotted for pH from 1 to 8 with nitrate ions as a supporting electrolyte at different ionic strengths of the solution (I = 0.10 to 0.50). The dependences of the concentration equilibrium constants in solutions on the ionic strength were approximated by Pitzer’s method. The thermodynamic constants of formation and standard Gibbs energies of formation of isopolytungstates from WO
4
2−
were calculated. The most probable scheme of interconversions of isopolyanions in solution at different pH values was proposed.__________Translated from Koordinatsionnaya Khimiya, Vol. 31, No. 8, 2005, pp. 583–589.Original Russian Text Copyright © 2005 by Rozantsev, Sazonova. 相似文献
20.
Titanate nanotubes (TNTs) have attracted great interest in multidisciplinary study since their discovery. The adsorption of thorium [Th(IV)] onto TNTs in the absence and presence of humic acid (HA)/fulvic acid (FA) was studied by batch technique. The influence of pH from 2.0 to 10.0, ionic strength from 0.001 to 0.1 mol L?1 NaClO4, and coexisting electrolyte cations (Li+, Na+, K+) and antions (ClO4 ?, NO3 ?, Cl?) on the adsorption of Th(IV) onto TNTs was tested. The adsorption isotherms of Th(IV) was determined at pH 3.0 and analyzed with Langmuir and Freundlich adsorption models, respectively. The results demonstrated that the adsorption of Th(IV) onto TNTs increases steeply with increasing pH from 2.0 to 4.0. Generally, HA/FA was showed to enhance Th(IV) adsorption onto TNTs at low pH values, but to reduce Th(IV) adsorption onto TNTs at high pH values. The adsorption of Th(IV) onto TNTs was also dependent on coexisting electrolyte ions in aqueous solution under our experimental conditions. The adsorption of Th(IV) onto TNTs is exothermic and spontaneous. The findings indicating that TNTs can be used as a promising candidate for the enrichment and solidification of Th(IV) or its analogue actinides from large volume solution in real work. 相似文献