Mechanisms of Lead Adsorption on Chitosan/PVA Hydrogel Beads

Langmuir ◽  
2002 ◽  
Vol 18 (25) ◽  
pp. 9765-9770 ◽  
Author(s):  
Li Jin ◽  
Renbi Bai
RSC Advances ◽  
2015 ◽  
Vol 5 (111) ◽  
pp. 91414-91422 ◽  
Author(s):  
Yi Zhang ◽  
Bing Hui ◽  
Lin Ye

Toughened PVA hydrogel beads were prepared by co-crosslinking with glycerol, resulting in the formation of a uniform and dense network gel structure, and the tensile property and hydraulic impact resistance were efficiently improved.


2021 ◽  
Vol 6 (1) ◽  
pp. 115-123
Author(s):  
Luísa P. Cruz-Lopes ◽  
Morgana Macena ◽  
Bruno Esteves ◽  
Raquel P. F. Guiné

Abstract Industrialization increases the number of heavy metals released into the environment. Lead (Pb2+), nickel (Ni2+) and chromium (Cr6+) are among these toxic metals and cause irreversible effects on ecosystems and human health due to their bio-accumulative potential. The decontamination through adsorption processes using lignocellulosic wastes from agricultural and/or forestry processes is a viable solution. Hence, this work aimed at studying the effect of pH on the biosorption of the metal ions using four different by-product materials: walnut shell, chestnut shell, pinewood and burnt pinewood. These experiments were conducted with solutions of the three heavy metals in which the adsorbents were immersed to measure the rate of adsorption. A range of pH values from 3.0 to 7.5 was used in the experiments, and the concentrations were determined by atomic absorption. The results showed different behaviour of the biosorbent materials when applied to the different metals. The lead adsorption had an ideal pH in the range of 5.5–7.5 when the walnut shell was used as an adsorbent, corresponding to values of adsorption greater than 90%, but for the other materials, maximum adsorption occurred for a pH of 7.5. For the adsorption of chromium, the pH was very heterogeneous with all adsorbents, with optimal values of pH varying from 3.0 (for chestnut shell) to 6.5 (for walnut shell and wood). For nickel, the best pH range was around pH 5, with different values according to the lignocellulosic material used. These results indicate that the tested biosorbents have the potential to decontaminate wastewater in variable extensions and that by controlling the pH of the solution; a more efficient removal of the heavy metals can be achieved.


Author(s):  
Shaoyi Wang ◽  
Jiawei Wu ◽  
Jianqun Jiang ◽  
Shakil Masum ◽  
Haijian Xie
Keyword(s):  

Polymers ◽  
2021 ◽  
Vol 13 (9) ◽  
pp. 1513
Author(s):  
Yuezhou Wei ◽  
Khalid A. M. Salih ◽  
Mohammed F. Hamza ◽  
Toyohisa Fujita ◽  
Enrique Rodríguez-Castellón ◽  
...  

High-tech applications require increasing amounts of rare earth elements (REE). Their recovery from low-grade minerals and their recycling from secondary sources (as waste materials) are of critical importance. There is increasing attention paid to the development of new sorbents for REE recovery from dilute solutions. A new generation of composite sorbents based on brown algal biomass (alginate) and polyethylenimine (PEI) was recently developed (ALPEI hydrogel beads). The phosphorylation of the beads strongly improves the affinity of the sorbents for REEs (such as La and Tb): by 4.5 to 6.9 times compared with raw beads. The synthesis procedure (epicholorhydrin-activation, phosphorylation and de-esterification) is investigated by XPS and FTIR for characterizing the grafting route but also for interpreting the binding mechanism (contribution of N-bearing from PEI, O-bearing from alginate and P-bearing groups). Metal ions can be readily eluted using an acidic calcium chloride solution, which regenerates the sorbent: the FTIR spectra are hardly changed after five successive cycles of sorption and desorption. The materials are also characterized by elemental, textural and thermogravimetric analyses. The phosphorylation of ALPEI beads by this new method opens promising perspectives for the recovery of these strategic metals from mild acid solutions (i.e., pH ~ 4).


2021 ◽  
Vol 213 (1) ◽  
pp. 53-66
Author(s):  
Qing Zhang ◽  
Meina Liang ◽  
Xiaozhang Yuan ◽  
Shuiping Xu ◽  
Lili Huang

2021 ◽  
Vol 9 (4) ◽  
pp. 105269
Author(s):  
Elias Reinoso-Guerra ◽  
Juliet Aristizabal ◽  
Bárbara Arce ◽  
Elsie Zurob ◽  
Geraldine Dennett ◽  
...  

Gels ◽  
2021 ◽  
Vol 7 (2) ◽  
pp. 71
Author(s):  
Takuro Taniguchi ◽  
Kenji Urayama

We investigated the linear dynamic viscoelasticity of dual cross-link (DC) poly(vinyl alcohol) (PVA) (DC-PVA) hydrogels with permanent and transient cross-links. The concentrations of incorporated borate ions to form transient cross-links in the DC-PVA hydrogels (CBIN) were determined by the azomethine-H method. The dynamic viscoelasticity of the DC-PVA hydrogel cannot be described by a simple sum of the dynamic viscoelasticity of the PVA gel with the same permanent cross-link concentration and the PVA aqueous solution with the same borate ion concentration (CB = CBIN) as in the DC-PVA gel. The DC-PVA hydrogel exhibited a considerably higher relaxation strength, indicating that the introduction of permanent cross-links into temporary networks increases the number of viscoelastic chains with finite relaxation times. In contrast, the relaxation frequency (ωc) (given by the frequency at the maximum of loss modulus) for the DC-PVA hydrogel was slightly lower but comparable to that for a dilute PVA solution with the same CB. This signifies that the relaxation dynamics of the DC-PVA hydrogels is essentially governed by the lifetime of an interchain transient cross-link (di-diol complex of boron). The effect of permanent cross-linking on the relaxation dynamics was observed in the finite broadening of the relaxation-time distribution in the long time region.


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