scholarly journals The New Approach to the Preparation of Polyacrylamide-Based Hydrogels: Initiation of Polymerization of Acrylamide with 1,3-Dimethylimidazolium (Phosphonooxy-)Oligosulphanide under Drying Aqueous Solutions

Polymers ◽  
2021 ◽  
Vol 13 (11) ◽  
pp. 1806
Author(s):  
Natalia Tarasova ◽  
Alexey Zanin ◽  
Efrem Krivoborodov ◽  
Ilya Toropygin ◽  
Ekaterina Pascal ◽  
...  
Keyword(s):  
Aqueous Solutions ◽  
Polymer Network ◽  
Crosslinking Density ◽  
Polyacrylamide Gel ◽  
Order Kinetic ◽  
New Approach ◽  
Equilibrium Degree ◽  
Swelling Rate ◽  
Acrylamide Polymerization ◽  
High Equilibrium

The new initiator of the polymerization of acrylamide, leading to the formation of crosslinked polyacrylamide, was discovered. The structure of the synthesized polyacrylamide was characterized by XRD, 1Н NMR, and 13С NMR spectroscopy. It was shown that 1,3-dimethylimidazolium (phosphonooxy-)oligosulphanide is able to initiate radical polymerization under drying aqueous solutions of acrylamide, even at room temperature. According to XRF data, the synthesized polyacrylamide gel contains 0.28 wt% of sulphur. The formed polymer network has a low crosslinking density and a high equilibrium degree of swelling. The swelling rate of polyacrylamide gel in water corresponds to the first order kinetic equation with the rate constant 6.2 × 10−2 min−1. The initiator is promising for combining acrylamide polymerization with the processes of gel molding and drying.

Chitosan-based Magnetic Composites - Efficient Adsorbents for Removal of Pb(II) and Cu(II) from Aqueous Mono and Bicomponent Solutions

2018 ◽  
Vol 69 (9) ◽  
pp. 2323-2330 ◽  
Author(s):  
Daniela C. Culita ◽  
Claudia Maria Simonescu ◽  
Rodica Elena Patescu ◽  
Nicolae Stanica
Keyword(s):  
Aqueous Solutions ◽  
Metal Ions ◽  
Chemical Properties ◽  
Order Kinetic ◽  
Mass Ratio ◽  
Magnetic Adsorbent ◽  
Magnetic Composites ◽  
Initial Ph ◽  
Order Kinetic Model ◽  
Physical And Chemical

A series of three chitosan-based magnetic composites was prepared through a simple coprecipitation method. It was investigated the influence of mass ratio between chitosan and magnetite on the physical and chemical properties of the composites in order to establish the optimum conditions for obtaining a composite with good adsorption capacity for Pb(II) and Cu(II) from mono and bicomponent aqueous solutions. It was found that the microspheres prepared using mass ratio chitosan / magnetite 1.25/1, having a saturation magnetization of 15 emu g--1, are the best to be used as adsorbent for the metal ions. The influence of different parameters such as initial pH values, contact time, initial concentration of metal ions, on the adsorption of Pb(II) and Cu(II) onto the chitosan-based magnetic adsorbent was investigated in details. The adsorption process fits the pseudo-second-order kinetic model in both mono and bicomponent systems, and the maximum adsorption capacities calculated on the basis of the Langmuir model were 79.4 mg g--1 for Pb(II) and 48.5 mg g--1 for Cu(II) in monocomponent systems, while in bicomponent systems were 88.3 and 49.5 mg g--1, respectively. The results revealed that the as prepared chitosan-based magnetic adsorbent can be an effective and promising adsorbent for Pb(II) and Cu(II) from mono and bicomponent aqueous solutions.

Comparison of the fixation of several metal ions onto a low-cost biopolymer

2002 ◽  
Vol 2 (5-6) ◽  
pp. 217-224 ◽  
Author(s):  
Z. Reddad ◽  
C. Gérente ◽  
Y. Andrès ◽  
P. Le Cloirec
Keyword(s):  
Aqueous Solutions ◽  
Metal Ions ◽  
Low Cost ◽  
Operating Conditions ◽  
Order Kinetic ◽  
Adsorption Mechanisms ◽  
Equilibrium Data ◽  
Order Kinetic Model ◽  
Beet Pulp ◽  
Removal Of Metal Ions

In the present work, sugar beet pulp, a common waste from the sugar refining industry, was studied in the removal of metal ions from aqueous solutions. The ability of this cheap biopolymer to sorb several metals namely Pb2+, Cu2+, Zn2+, Cd2+ and Ni2+ in aqueous solutions was investigated. The metal fixation capacities of the sorbent were determined according to operating conditions and the fixation mechanisms were identified. The biopolymer has shown high elimination rates and interesting metal fixation capacities. A pseudo-second-order kinetic model was tested to investigate the adsorption mechanisms. The kinetic parameters of the model were calculated and discussed. For 8 × 10-4 M initial metal concentration, the initial sorption rates (v0) ranged from 0.063 mmol.g-1.min-1 for Pb2+ to 0.275 mmol.g-1.min-1 for Ni2+ ions, with the order: Ni2+ > Cd2+ > Zn2+ > Cu2+ > Pb2+. The equilibrium data fitted well with the Langmuir model and showed the following affinity order of the material: Pb2+ > Cu2+ > Zn2+ > Cd2+ > Ni2+. Then, the kinetic and equilibrium parameters calculated qm and v0 were tentatively correlated to the properties of the metals. Finally, equilibrium experiments in multimetallic systems were performed to study the competition of the fixation of Pb2+, Zn2+ and Ni2+ cations. In all cases, the metal fixation onto the biopolymer was found to be favourable in multicomponent systems. Based on these results, it is demonstrated that this biosorbent represents a low-cost solution for the treatment of metal-polluted wastewaters.

Synthesis and Characterization of Chitosan templated Mesoporous Silica: Efficient use of Mesoporous Silica in the removal of Cu(II) from Aqueous Solutions

2016 ◽  
Vol 4 (2) ◽  
pp. 105-112
Author(s):  
Lalchhing puii ◽  
◽  
Seung-Mok Lee ◽  
Diwakar Tiwari ◽  
◽  
...  
Keyword(s):  
Mesoporous Silica ◽  
Aqueous Solutions ◽  
Background Electrolyte ◽  
Second Order ◽  
Order Kinetic ◽  
Sorption Data ◽  
Column Reactor ◽  
Wide Ph Range ◽  
Freundlich Adsorption Isotherm ◽  
Pseudo Second Order

A mesoporous silica was synthesized by annealing (3-Aminopropyl) triethoxysilane grafted chitosan at 800˚C. The mesoporous silica was characterized by the XRD (X-ray diffraction) analysis. The BET specific surface area and pore size of silica was found to be 178.42 m2/g and 4.13 nm. The mesoporous silica was then employed for the efficient remediation of aqueous solutions contaminated with Cu(II) under batch and column reactor operations. The mesoporous silica showed extremely high per cent removal of Cu(II) at wide pH range i.e., pH ~2.0 to 7.0. Relatively a fast uptake of Cu(II) was occurred and high percentage removal was obtained at initial concentrations studied from 1.0 to 15.0 mg/L. The equilibrium state sorption data were utilized for the Langmuir and Freundlich adsorption isotherm studies. Moreover, the effect of an increase in background electrolyte concentrations from 0.0001 to 0.1 mol/L NaNO3 was assessed for the uptake of Cu(II) by mesoporous silica. The equilibrium sorption was achieved within 240 min of contact and the kinetic data is best fitted to the pseudo-second-order and fractal like pseudo-second-order kinetic models. In addition, the mesoporous silica was used for dynamic studies under column reactor operations. The breakthrough curve was then used for the non-linear fitting of the Thomas equation and the loading capacity of the column for Cu(II) was estimated.

scholarly journals Acid red G dye removal from aqueous solutions by porous ceramsite produced from solid wastes: Batch and fixed-bed studies

2020 ◽  
Vol 9 (1) ◽  
pp. 770-782
Author(s):  
Tianpeng Li ◽  
Jing Fan ◽  
Tingting Sun
Keyword(s):  
Aqueous Solutions ◽  
Dye Removal ◽  
Coal Fly Ash ◽  
Exothermic Reaction ◽  
Fixed Bed ◽  
Column Experiment ◽  
Solid Wastes ◽  
Order Kinetic ◽  
Cost Effective Treatment ◽  
Acid Red G

AbstractA novel porous ceramsite was made of municipal sludge, coal fly ash, and river sediment by sintering process, and the performance of batch and fixed-bed column systems containing this material in the removal of acid red G (ARG) dye from aqueous solutions was assessed in this study. The results of orthogonal test showed that sintering temperature was the most important determinant in the preparation of porous ceramsite, and it possesses developed pore structure and high specific surface area. Batch experiment results indicated that the adsorption process of ARG dye toward porous ceramsite was a spontaneous exothermic reaction, which could be better described with Freundlich–Langmuir isotherm model (R2 > 0.992) and basically followed the pseudo-first-order kinetic equation (R2 > 0.993). Column experiment results showed that when the porous ceramsite was used as packing material, its adsorption capacity was roughly improved by 3.5 times compared with that in batch system, and the breakthrough behavior was simulated well with Yoon–Nelson model, with R2 > 0.954. This study suggested that the novelty man-made porous ceramsite obtained from solid wastes might be processed as a certain cost-effective treatment material fit for the dye removal in aqueous solutions.

scholarly journals Adsorptive Removal of Phosphate from Aqueous Solutions Using Low-Cost Volcanic Rocks: Kinetics and Equilibrium Approaches

Materials ◽  
2021 ◽  
Vol 14 (5) ◽  
pp. 1312
Author(s):  
Dereje Tadesse Mekonnen ◽  
Esayas Alemayehu ◽  
Bernd Lennartz
Keyword(s):  
Aqueous Solutions ◽  
Low Income ◽  
Low Cost ◽  
Volcanic Rocks ◽  
Phosphate Removal ◽  
Phosphate Adsorption ◽  
Adsorptive Capacity ◽  
Batch Adsorption ◽  
Order Kinetic ◽  
Adsorptive Removal

The contamination of surface and groundwater with phosphate originating from industrial and household wastewater remains a serious environmental issue in low-income countries. Herein, phosphate removal from aqueous solutions was studied using low-cost volcanic rocks such as pumice (VPum) and scoria (VSco), obtained from the Ethiopian Great Rift Valley. Batch adsorption experiments were conducted using phosphate solutions with concentrations of 0.5 to 25 mg·L−1 to examine the adsorption kinetic as well as equilibrium conditions. The experimental adsorption data were tested by employing various equilibrium adsorption models, and the Freundlich and Dubinin-Radushkevich (D-R) isotherms best depicted the observations. The maximum phosphate adsorption capacities of VPum and VSco were calculated and found to be 294 mg·kg−1 and 169 mg·kg−1, respectively. A pseudo-second-order kinetic model best described the experimental data with a coefficient of correlation of R2 > 0.99 for both VPum and VSco; however, VPum showed a slightly better selectivity for phosphate removal than VSco. The presence of competitive anions markedly reduced the removal efficiency of phosphate from the aqueous solution. The adsorptive removal of phosphate was affected by competitive anions in the order: HCO3− >F− > SO4−2 > NO3− > Cl− for VPum and HCO3− > F− > Cl− > SO4−2 > NO3− for VSco. The results indicate that the readily available volcanic rocks have a good adsorptive capacity for phosphate and shall be considered in future studies as test materials for phosphate removal from water in technical-scale experiments.

scholarly journals Kinetic, isotherm and thermodynamic studies with linear and non-linear fitting for cadmium(II) removal by black carbon of pine cone

2017 ◽  
Vol 76 (8) ◽  
pp. 2242-2253 ◽  
Author(s):  
Z. Yavari ◽  
M. Noroozifar
Keyword(s):  
Aqueous Solutions ◽  
Black Carbon ◽  
Adsorption Process ◽  
Order Kinetic ◽  
Cadmium Removal ◽  
Thermodynamic Studies ◽  
Linear Fitting ◽  
Pine Cone ◽  
Fitting Method ◽  
Non Linear

In this study, black carbon from pine cone (BCPC) and acidic-modified BCPC (MBCPC) powder as a popular agricultural waste in the southeast of Iran were used for cadmium removal from aqueous solutions. The effect of various factors, such as surface chemistry and dosage of adsorbent, contact time, size of particles, initial concentration of cadmium, temperature, and pH of aqueous solutions, was investigated. The results show cadmium removal with usage of the mentioned adsorbents increased after acidic modification. It was noteworthy in this work that the removal percentage of pollutant was above 90% for suggested biosorbents. The obtained experimental data for optimum conditions were selected to model the adsorption behavior of the materials with usage of six isotherm equations via non-linear fitting method and the residual root mean square error estimation for each model. The adsorption of cadmium preferably fitted Khan and Langmuir–Freundlich isotherms for BCPC and MBCPC adsorbents, respectively. The kinetic studies via linear fitting method proved the second-order kinetic was the applicable model for the adsorption process. Thermodynamic studies show the adsorption process of cadmium onto BCPC and MBCPC was spontaneous and endothermic.

scholarly journals Multi-Component Adsorption of Benzene, Toluene, Ethylbenzene, and Xylene from Aqueous Solutions by Montmorillonite Modified with Tetradecyl Trimethyl Ammonium Bromide

2013 ◽  
Vol 2013 ◽  
pp. 1-10 ◽  
Author(s):  
H. Nourmoradi ◽  
Mehdi Khiadani ◽  
M. Nikaeen
Keyword(s):  
Experimental Data ◽  
Aqueous Solutions ◽  
Structural Changes ◽  
Freundlich Isotherm ◽  
Isotherm Models ◽  
Ammonium Bromide ◽  
Order Kinetic ◽  
Multicomponent Adsorption ◽  
Benzene Toluene ◽  
Kinetic And Isotherm Models

Multicomponent adsorption of benzene, toluene, ethylbenzene, and xylene (BTEX) was assessed in aqueous solutions by montmorillonite modified with tetradecyl trimethyl ammonium bromide (TTAB-Mt). Batch experiments were conducted to determine the influences of parameters including loading rates of surfactant, contact time, pH, adsorbate concentration, and temperature on the adsorption efficiency. Scanning electron microscope (SEM) and X-ray diffractometer (XRD) were used to determine the adsorbent properties. Results showed that the modification of the adsorbent via the surfactant causes structural changes of the adsorbent. It was found that the optimum adsorption condition achieves with the surfactant loading rate of 200% of the cation exchange capacity (CEC) of the adsorbent for a period of 24 h. The sorption of BTEX by TTAB-Mt was in the order ofB<T<E<X. The experimental data were fitted by many kinetic and isotherm models. The results also showed that the pseudo-second-order kinetic model and Freundlich isotherm model could, respectively, be fitted to the experimental data better than other available kinetic and isotherm models. The thermodynamic study indicated that the sorption of BTEX with TTAB-Mt was achieved spontaneously and the adsorption process was endothermic as well as physical in nature. The regeneration results of the adsorbent also showed that the adsorption capacity of adsorbent after one use was 51% to 70% of original TTAB-Mt.

Highly efficient carbonaceous nanofiber/layered double hydroxide nanocomposites for removal of U(VI) from aqueous solutions

2019 ◽  
Vol 107 (4) ◽  
pp. 299-309
Author(s):  
Shuqi Yu ◽  
Xiangxue Wang ◽  
Shunyan Ning ◽  
Zhongshan Chen ◽  
Xiangke Wang
Keyword(s):  
Ionic Strength ◽  
Aqueous Solutions ◽  
Layered Double Hydroxide ◽  
Photoelectron Spectroscopy ◽  
Environmental Remediation ◽  
Three Dimensional ◽  
Order Kinetic ◽  
Surface Bonding ◽  
Double Hydroxide ◽  
Shed Light

Abstract The three-dimensional (3D) carbonaceous nanofiber and Ni-Al layered double hydroxide (CNF/LDH) nanocomposite was successfully prepared by a facile one-step hydrothermal methodology. Characterization of scanning electron microscope (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), XRD, and Fourier transformed infrared spectroscopy (FTIR) provided a demonstration that the modified CNF/LDH nanocomposite possessed abundant functional groups, for instance, metal-oxygen surface bonding sites (Ni–O as well as Al–O) and free-metal surface bonding sites (C–O, C–O–C, as well as O–C=O). The elimination of representative radionuclide (i.e. U(VI)) on the CNF/LDH nanocomposite from aqueous solutions was explored as a key function of pH, ionic strength, contact time, reaction temperature as well as radionuclide preliminary concentrations with the use of the batch methodology. As revealed by the findings, the sorption of radionuclides on CNF/LDH nanocomposite adhered to the pseudo-second-order kinetic model as well as Langmuir model. The maximum elimination capacity of U(VI) amounted to be 0.7 mmol/g. The independent of ionic strength shed light on the fact that inner-sphere surface complexation mainly overpowered radionuclide uptake by the CNF/LDH nanocomposite, which was further verified through the combination of FTIR and XPS spectral analyses. The abovementioned analyses shed light on the fact that the CNF/LDH nanocomposite can be regarded as a latent material to preconcentration radionuclides for environmental remediation.

scholarly journals Photoreduction of Cr(VI) Ions in Aqueous Solutions by UV/ Photocatalytic Processes

2012 ◽  
Vol 2012 ◽  
pp. 1-7 ◽  
Author(s):  
Chih Ming Ma ◽  
Yung Shuen Shen ◽  
Po Hsiang Lin
Keyword(s):  
Aqueous Solutions ◽  
Reaction Rate ◽  
Removal Rate ◽  
Experimental Results ◽  
Order Kinetic ◽  
Solution Ph ◽  
Relationship Of ◽  
The Relationship ◽  
Photocatalytic Processes ◽  
Order Kinetic Equation

This study discussed the photoreduction of Cr(VI) ions in aqueous solutions by UV/TiO2photocatalytic processes under various operational factors. Experimental results showed that the removal rate of Cr(VI) increased with decreasing solution pH values and with increasing dosages of organic compounds, indicating that the recombination rate of electrons and h+can be retarded in the reaction systems by the addition of the scavenger, thus raising the reaction rate of Cr(VI). The relationship of the chemical reaction rate of Cr(VI), TiO2dosage, and changes of Cr(VI) concentration was expressed by the pseudo-first-order kinetic equation. Comparing the experimental results of two different doping metals in modified TiO2photoreduction systems, the removal rate of Cr(VI) by the Ag/TiO2process is larger, possibly because the electron transferring ability of Ag is superior to that of Cu. However, the photoreduction rates of Cr(VI) by modified UV/TiO2processes are worse than those by a nonmodified commercial UV/TiO2process.

scholarly journals KINETICS OF OZONE REACTIONS WITH ADENINE AND CYTOSINE IN AQUEOUS SOLUTIONS

2020 ◽  
Vol 63 (10) ◽  
pp. 17-22
Author(s):  
Aigul A. Maksyutova ◽  
Elvina R. Khaynasova ◽  
Yuriy S. Zimin
Keyword(s):  
Aqueous Solutions ◽  
Rate Constants ◽  
Correlation Coefficients ◽  
Activation Parameters ◽  
Second Order ◽  
Order Kinetic ◽  
Temperature Dependences ◽  
Ozone Reactivity ◽  
Kinetics Of ◽  
Ozone Reactions

The ultraviolet spectroscopy method has been applied to study the kinetics of the ozone reactions with nitrogenous bases (NB), namely adenine and cytosine in aqueous solutions. At the first research stage, the range of NB working concentrations has been determined. It was found that linear dependences between optical densities and concentrations of nitrogenous bases aqueous solutions are quite reliable, with correlation coefficients r ≥ 0.998, are satisfied up to [NB] = 2.3 ∙ 10–4 mol/l. According to the Bouguer-Lambert-Beer law, adenine and cytosine extinction coefficients in aqueous solutions were determined and subsequently used to calculate their residual concentrations. At the next stage, the kinetics of nitrogenous bases ozonized oxidation was studied with equal initial concentrations of the starting substances ([NB]0 = [О3]0). The results revealed that the kinetic consumption curves of the starting reagents are fairly well linearized (r ≥ 0.996) in the second-order reaction equation coordinates. As found with the bubbling installation, 1 mol of the absorbed ozone falls on 1 mol of the used NB. Thus, the reactions of ozone with adenine and cytosine explicitly proceed according to the second-order kinetic laws (the first – according to О3 and the first – according to NB). The rate constants were calculated by the integral reaction equations, the values of which indicate a higher ozone reactivity in relation to nitrogen bases. The temperature dependences of the second-order rate constants was studied ranging 285-309 K, and the activation parameters (pre-exponential factors and activation energies) of the ozone reactions with adenine and cytosine in aqueous solutions were determined.

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