scholarly journals Selective adsorption behavior of Cd2+ imprinted acrylamide-crosslinked-poly(alginic acid) magnetic polymers: fabrication, characterization, adsorption performance and mechanism

2020 ◽  
Author(s):  
Zuyu Li ◽  
Shuangzhen Guo ◽  
Da Li ◽  
Lihua Zang
Keyword(s):  
Metal Ions ◽  
Adsorption Capacity ◽  
Alginic Acid ◽  
Selective Adsorption ◽  
Physical Adsorption ◽  
Maximum Adsorption Capacity ◽  
Magnetic Adsorbent ◽  
Langmuir Isotherm Model ◽  
Pseudo Second Order ◽  
The Impact

Abstract Poly(acrylamide) grafted and glutaraldehyde-crosslinked alginic acid nano-magnetic adsorbent (AAMA) was prepared by selecting Cd2+ as a template ion. Scanning electron microscope (SEM), Thermo-gravimetric analyzer (TGA), Vibrating sample magnetometer (VSM) and Infrared Spectroscopy (IR)were used to characterize the morphology and structure of AAMA. The adsorption of AAMA for different metal ions was compared and the impact of various factors for adsorption of Cd2+ was systematically investigated. These results suggested that the AAMA was the aggregates of Fe3O4 nanoparticles with a diameter of about 50–100 nm. and had selectivity for Cd2+ adsorption. The maximum adsorption capacity for Cd2+ is 175 mg/g at pH 5.0 and 303 K. The experimental data were well described by the Langmuir isotherm model and pseudo-second-order model. The parameters of adsorption thermodynamics concluded that the adsorption progress is spontaneous and endothermic in nature. The parameters of adsorption activation energy suggested that there is physical adsorption and chemisorption on the adsorption of metal ions. AAMA could be regenerated by EDTA and still keep 71% adsorption capacity in the fifth consecutive adsorption-regeneration cycle. Therefore, AAMA would be useful as a selective and high adsorption capacity nano-magnetic adsorbent in the removal of Cd2+ from wastewater.

scholarly journals Adsorption of Tea Polyphenols using Microporous Starch: A Study of Kinetics, Equilibrium and Thermodynamics

Molecules ◽  
2019 ◽  
Vol 24 (8) ◽  
pp. 1449 ◽  
Author(s):  
Xianchun Hu ◽  
Xianfeng Du
Keyword(s):  
Physical Adsorption ◽  
Tea Polyphenols ◽  
Adsorptive Capacity ◽  
Partial Hydrolysis ◽  
Maximum Adsorption Capacity ◽  
Solution Ph ◽  
Long Term Storage ◽  
Langmuir Isotherm Model ◽  
Pseudo Second Order ◽  
Ft Ir

Microporous starch (MPS) granules were formed by the partial hydrolysis of starch using α–amylase and glucoamylase. Due to its biodegradability and safety, MPS was employed to adsorb tea polyphenols (TPS) based on their microporous characteristics. The influences of solution pH, time, initial concentration and temperature on the adsorptive capacity were investigated. The adsorption kinetics data conformed to the pseudo second–order kinetics model, and the equilibrium adsorption data were well described by the Langmuir isotherm model. According to the fitting of the adsorption isotherm formula, the maximum adsorption capacity of TPS onto MPS at pH 6.7 and T = 293 K was approximately 63.1 mg/g. The thermodynamic parameters suggested that the adsorption of TPS onto MPS was spontaneous and exothermic. Fourier transform infrared (FT–IR) analysis and the thermodynamics data were consistent with a physical adsorption mechanism. In addition, MPS-loaded TPS had better stability during long-term storage at ambient temperature.

Adsorption kinetics and thermodynamics of acid Bordeaux B from aqueous solution by graphene oxide/PAMAMs

2015 ◽  
Vol 72 (7) ◽  
pp. 1217-1225 ◽  
Author(s):  
Fan Zhang ◽  
Shengfu He ◽  
Chen Zhang ◽  
Zhiyuan Peng
Keyword(s):  
Graphene Oxide ◽  
Adsorption Capacity ◽  
Ph Value ◽  
Maximum Adsorption Capacity ◽  
Freundlich Model ◽  
Equilibrium Data ◽  
Langmuir Isotherm Model ◽  
Pseudo Second Order ◽  
Effects Of Media ◽  
Better Than

Graphene oxide/polyamidoamines dendrimers (GO/PAMAMs) composites were synthesized via modifying GO with 2.0 G PAMAM. The adsorption behavior of the GO/PAMAMs for acid Bordeaux B (ABB) was studied and the effects of media pH, adsorption time and initial ABB concentration on adsorption capacity of the adsorbent were investigated. The optimum pH value of the adsorption of ABB onto GO/PAMAMs was 2.5. The maximum adsorption capacity increased from 325.78 to 520.83 mg/g with the increase in temperature from 298 to 328 K. The equilibrium data followed the Langmuir isotherm model better than the Freundlich model. The kinetic study illustrated that the adsorption of ABB onto GO/PAMAMs fit the pseudo-second-order model. The thermodynamic parameters indicated that the adsorption process was physisorption, and also an endothermic and spontaneous process.

scholarly journals Adsorption of Cu(II) by Poly-γ-glutamate/Apatite Nanoparticles

Polymers ◽  
2021 ◽  
Vol 13 (6) ◽  
pp. 962
Author(s):  
Kuo-Yu Chen ◽  
Wei-Yu Zeng
Keyword(s):  
Adsorption Capacity ◽  
Kinetic Studies ◽  
Maximum Adsorption Capacity ◽  
Gravimetric Analysis ◽  
Solution Ph ◽  
Equilibrium Data ◽  
Langmuir Isotherm Model ◽  
Pseudo Second Order ◽  
Initial Adsorption ◽  
Adsorption Equilibrium Data

Poly-γ-glutamate/apatite (PGA-AP) nanoparticles were prepared by chemical coprecipitation method in the presence of various concentrations of poly-γ-glutamate (γ-PGA). Powder X-ray diffraction pattern and energy-dispersive spectroscopy revealed that the main crystal phase of PGA-AP was hydroxyapatite. The immobilization of γ-PGA on PGA-AP was confirmed by Fourier transform infrared spectroscopy and the relative amount of γ-PGA incorporation into PGA-AP was determined by thermal gravimetric analysis. Dynamic light scattering measurements indicated that the particle size of PGA-AP nanoparticles increased remarkably with the decrease of γ-PGA content. The adsorption of aqueous Cu(II) onto the PGA-AP nanoparticles was investigated in batch experiments with varying contact time, solution pH and temperature. Results illustrated that the adsorption of Cu(II) was very rapid during the initial adsorption period. The adsorption capacity of PGA-AP nanoparticles for Cu(II) was increased with the increase in the γ-PGA content, solution pH and temperature. At a pH of 6 and 60 °C, a higher equilibrium adsorption capacity of about 74.80 mg/g was obtained. The kinetic studies indicated that Cu(II) adsorption onto PGA-AP nanoparticles obeyed well the pseudo-second order model. The Langmuir isotherm model was fitted well to the adsorption equilibrium data. The results indicated that the adsorption behavior of PGA-AP nanoparticles for Cu(II) was mainly a monolayer chemical adsorption process. The maximum adsorption capacity of PGA-AP nanoparticles was estimated to be 78.99 mg/g.

Pyridinium-functionalized magnetic mesoporous silica nanoparticles as a reusable adsorbent for phosphate removal from aqueous solution

2016 ◽  
Vol 74 (5) ◽  
pp. 1127-1135 ◽  
Author(s):  
Fang Ma ◽  
Hongtao Du ◽  
Ronghua Li ◽  
Zengqiang Zhang
Keyword(s):  
Aqueous Solution ◽  
Silica Nanoparticles ◽  
Adsorption Capacity ◽  
Mesoporous Silica Nanoparticles ◽  
Phosphate Removal ◽  
Maximum Adsorption Capacity ◽  
Intra Particle Diffusion ◽  
Langmuir Isotherm Model ◽  
Pseudo Second Order ◽  
Magnetic Mesoporous Silica

In this work, pyridinium-functionalized silica nanoparticles adsorbent (PC/SiO2/Fe3O4) was synthesized for phosphate removal from aqueous solutions. The removal efficiency of phosphate on the PC/SiO2/Fe3O4 was carried out and investigated under various conditions such as pH, contact temperature and initial concentration. The results showed that the adsorption equilibrium could be reached within 10 min, which fitted a Langmuir isotherm model, with maximum adsorption capacity of 94.16 mg/g, and the kinetic data were fitted well by pseudo-second-order and intra-particle diffusion models. Phosphate loaded on the adsorbents could be easily desorbed with 0.2 mol/L of NaOH, and the adsorbents showed good reusability. The adsorption capacity was still around 50 mg/g after 10 times of reuse. All the results demonstrated that this pyridinium-functionalized mesoporous material could be used for the phosphate removal from aqueous solution and it was easy to collect due to its magnetic properties.

scholarly journals Hydrazinolyzed cellulose-g-polymethyl acrylate as adsorbent for efficient removal of Cd(II) and Pb(II) ions from aqueous solution

2016 ◽  
Vol 75 (5) ◽  
pp. 1051-1058 ◽  
Author(s):  
Qiujin Jia ◽  
Wanting Zhang ◽  
Dongping Li ◽  
Yulong Liu ◽  
Yuju Che ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Adsorption Capacity ◽  
Physical Adsorption ◽  
Freundlich Isotherm ◽  
Isotherm Model ◽  
Initial Ph ◽  
Langmuir Isotherm Model ◽  
Pseudo Second Order ◽  
Adsorption Desorption ◽  
Efficient Adsorbent

Hydrazinolyzed cellulose-graft-polymethyl acrylate (Cell-g-PMA-HZ), an efficient adsorbent for removal of Cd(II) and Pb(II) from aqueous solution, has been prepared by ceric salt-initiated graft polymerization of methyl acrylate from microcrystalline cellulose surface and subsequent hydrazinolysis. The influences of initial pH, contact time, and temperature on adsorption capacity of Cell-g-PMA-HZ as well as adsorption equilibrium, kinetic and thermodynamic properties were examined in detail. As for Cd(II) adsorption, kinetic adsorption can be explained by pseudo-second-order, while adsorption isotherm fits well with Langmuir isotherm model, from which maximum equilibrium adsorption capacity can be derived as 235.85 mg g−1 at 28 °C. Further thermodynamic investigation indicated that adsorption of Cd(II) by adsorbent Cell-g-PMA-HZ is endothermic and spontaneous under studied conditions. On the other hand, isotherm of Pb(II) adsorption fits well with Freundlich isotherm model and is more likely to be a physical-adsorption-dominated process. Consecutive adsorption–desorption experiments showed that Cell-g-PMA-HZ is reusable with satisfactory adsorption capacity.

scholarly journals Adsorptive removal of Ni2+ and Cd2+ from wastewater using a green longan hull adsorbent

2017 ◽  
Vol 36 (1-2) ◽  
pp. 762-773 ◽  
Author(s):  
Xingmei Guo ◽  
Sihan Tang ◽  
Yan Song ◽  
Junmin Nan
Keyword(s):  
Metal Ions ◽  
Adsorption Capacity ◽  
Adsorption Mechanism ◽  
Maximum Adsorption Capacity ◽  
Adsorptive Removal ◽  
Langmuir Adsorption ◽  
Monolayer Adsorption ◽  
Pseudo Second Order ◽  
Adsorptive Mechanism ◽  
Optimized Conditions

The adsorptive removal of Ni2+ and Cd2+ at concentrations of approximately 50 mg L−1 in wastewater is investigated using an agricultural adsorbent, longan hull, and the adsorptive mechanism is characterized. The maximum adsorption capacity of approximately 4.19 mg g−1 Cd2+ was obtained under the optimized conditions of room temperature, pH 5.0, and a solid-to-liquid ratio of 1:30 in approximately 15 min. For Ni2+, the maximum adsorption capacity of approximately 3.96 mg g−1 was obtained at pH 4.7 in approximately 20 min. The adsorption kinetics for both metal ions on the longan hull can be described by a pseudo second-order rate model and are well fitted to the Langmuir adsorption isotherm. The adsorption mechanism of the longan hull to Ni2+ and Cd2+ ions is shown to be a monolayer adsorption of metal ions onto the absorbent surface. Thereinto, the longan hull adsorbent contains N–H, C–H, C=O, and C=C functional groups that can form ligands when loaded with Ni2+ and Cd2+, which reduces the fluorescence of the dried longan hull material.

scholarly journals Synthesis of Large Pore LTL and MOR Zeolites and Use as Adsorbent for The Removal of Heavy Metal and Radioactive Metal Ions in Aqueous Solution

2021 ◽  
Author(s):  
Duy Hoai-Phuong Nguyen ◽  
Quang Thanh Le ◽  
Tung Cao Thanh Pham ◽  
Thanh Tu Le
Keyword(s):  
Aqueous Solution ◽  
Heavy Metal ◽  
Metal Ions ◽  
Adsorption Capacity ◽  
Order Kinetic ◽  
Experiment Data ◽  
Large Pore ◽  
Order Kinetic Model ◽  
Langmuir Isotherm Model ◽  
Pseudo Second Order

Abstract Heavy metal and radioactive ions can cause serious environmental problems if they are not completely removed from wastewater as well as in groundwater. In this study, large pore LTL and MOR zeolites were successfully synthesized and used as adsorbent to remove Pb2+, Cu2+, Zn2+, Cd2+, Cs+ and Sr2+ ions in aqueous solution. At low initial concentration (10 ppm), LTL and MOR zeolites effectively removed above metal ions with removal efficiency in the range of 95–99%. Both zeolites showed high affinity to Cs+ and Pb2+ ions with the adsorption capacity of LTL zeolite to Cs+ and Pb2+ were 278.8 mg/g and 141.4 mg/g, and that of MOR zeolite were 238.8 mg/g and 178.9 mg/g, respectively. The EDS results showed that Pb2+ ions from the aqueous solution were exchanged with exchangeable Na+ ions in MOR zeolite and K+ ions in LTL zeolite. The pseudo-second-order kinetic model and Langmuir isotherm model fitted better to experiment data on the adsorption of metal ions on both LTL and MOR zeolite. This result revealed that the adsorption of these metal ions on LTL and MOR zeolite was monolayer chemisorption. The equilibrium adsorption results showed that the microstructure of zeolite significantly affected the adsorption capacity of LTL and MOR zeolite on removal of tested metal ions.

scholarly journals Hg selective adsorption on polypropylene-based hollow fiber grafted with polyacrylamide

2017 ◽  
Vol 36 (1-2) ◽  
pp. 287-299 ◽  
Author(s):  
Changkun Liu ◽  
Jizhen Jia ◽  
Ji’an Liu ◽  
Xiaoyan Liang
Keyword(s):  
Heavy Metal ◽  
Metal Ions ◽  
Adsorption Capacity ◽  
Hollow Fiber ◽  
Heavy Metal Ions ◽  
Hollow Fiber Membrane ◽  
Selective Adsorption ◽  
Maximum Adsorption Capacity ◽  
Order Kinetic ◽  
Fiber Membrane

A novel polypropylene hollow fiber membrane with a new function of selective adsorption of mercury ions in aqueous solutions was successfully prepared. The surface of the polypropylene hollow fiber membrane was initially modified with polydopamine by surface polymerization, and subsequently grafted with polyacrylamide (PAM) polymer brush via the surface initiated atom transfer radical polymerization (SI-ATRP) technique (thereafter named as PP-PAM). This study investigated the adsorption performance of Hg(II) ions by PP-PAM and the effect of various influencing factors on Hg(II) ion adsorption. The experiment indicated that the Hg(II) adsorption capacity of the PP-PAM increased with the increase of the pH, and the Hg(II) adsorption kinetics was consistent with the pseudo-second-order kinetic model. The adsorption isotherm followed the Langmuir model, with the maximum adsorption capacity calculated to be 0.854 mmol/g for Hg(II) ions. The adsorption study in multi-component system indicated that PP-PAM preferentially adsorbs Hg(II) over Pb(II) ions, with significant adsorption capacity difference of the two heavy metal ions. This study provided an efficient method for the preparation of the adsorptive polypropylene hollow fiber membrane, which expands its application for the selective removal of heavy metal ions.

scholarly journals Preparation of Calixarene-PI Nanofibers and Application as a Selective Adsorbent for Heavy Metal Ions

2018 ◽  
Vol 13 (1) ◽  
pp. 155892501801300
Author(s):  
Xuchen Tao ◽  
Quan Feng ◽  
Hui He
Keyword(s):  
Heavy Metal ◽  
Metal Ions ◽  
Adsorption Kinetics ◽  
Heavy Metal Ions ◽  
Selective Adsorption ◽  
Physical Adsorption ◽  
Second Order ◽  
Kinetics Model ◽  
Isothermal Model ◽  
Pseudo Second Order

In order to utilize the adsorption selectivity of calixarenes towards heavy metal ions, calixarene functionalized polyimide (Calix-PI) fibers were prepared by three main synthesis procedures including preparation of the calixarene polyamide acid (Calix-PAA) spinning solution via amidation, fabrication of the Calix-PAA fibers by electrospinning, and preparation of the Calix-PI fibers via thermal imidization on the Calix-PAA fibers. The Calix-PI fibers were characterized by Fourier transform infrared spectroscopy, scanning electronic microscopy and thermogravimetric analysis. The Calix-PI fibers display selective adsorption on Pb(II), which is fit with the pseudo-second-order adsorption kinetics model and the Freundlich adsorption isothermal model. The rate constant of the pseudo-second-order adsorption kinetics model and the maximum Pb(II) uptake have all been calculated. The practical adsorption of Pb(II) on the Calix-PI fibers is mainly attributed to the monolayer chemical adsorption and slightly depended on the physical adsorption.

scholarly journals Pectin/Activated Carbon-Based Porous Microsphere for Pb2+ Adsorption: Characterization and Adsorption Behaviour

Polymers ◽  
2021 ◽  
Vol 13 (15) ◽  
pp. 2453
Author(s):  
Ri-si Wang ◽  
Ya Li ◽  
Xi-xiang Shuai ◽  
Rui-hong Liang ◽  
Jun Chen ◽  
...  
Keyword(s):  
Activated Carbon ◽  
Profile Analysis ◽  
Removal Rate ◽  
Physical Adsorption ◽  
Kinetic Studies ◽  
Maximum Adsorption Capacity ◽  
Texture Profile ◽  
Langmuir Isotherm Model ◽  
Pseudo Second Order ◽  
Adsorption Desorption

The development of effective heavy metal adsorbents has always been the goal of environmentalists. Pectin/activated carbon microspheres (P/ACs) were prepared through simple gelation without chemical crosslinking and utilized for adsorption of Pb2+. Scanning electron microscopy (SEM) revealed that the addition of activated carbon increased the porosity of the microsphere. Texture profile analysis showed good mechanical strength of P/ACs compared with original pectin microspheres. Kinetic studies found that the adsorption process followed a pseudo-second-order model, and the adsorption rate was controlled by film diffusion. Adsorption isotherms were described well by a Langmuir isotherm model, and the maximum adsorption capacity was estimated to be 279.33 mg/g. The P/ACs with the highest activated carbon (P/AC2:3) maintained a removal rate over 95.5% after 10 adsorption/desorption cycles. SEM-energy-dispersive X-ray spectrum and XPS analysis suggested a potential mechanism of adsorption are ion exchange between Pb2+ and Ca2+, electronic adsorption, formation of complexes, and physical adsorption of P/ACs. All the above results indicated the P/ACs may be a good candidate for the adsorption of Pb2+.

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