Experimental and DFT studies on the selective adsorption of Pd(II) from wastewater by pyromellitic-functionalized poly(glycidyl methacrylate) microsphere

2020 ◽  
Vol 300 ◽  
pp. 112296 ◽  
Author(s):  
Jiling Zhao ◽  
Chen Wang ◽  
Shixing Wang ◽  
Yang Zhou ◽  
Bing Zhang
2018 ◽  
Vol 5 (6) ◽  
pp. 180281 ◽  
Author(s):  
Youning Chen ◽  
Wei Zhao ◽  
Huan Wang ◽  
Xiaohua Meng ◽  
Linjie Zhang

A novel polyamine-type starch/glycidyl methacrylate (GMA) copolymer with a high capacity for the adsorption of heavy metal ions was prepared via graft copolymerization of GMA and corn starch and a subsequent amination reaction between amino group of diethylenetriamine and epoxy group in GMA. The copolymers were characterized by Fourier transform infrared spectrometry, X-ray diffraction and scanning electron microscopy, and adsorption properties on modified starch of Cu(II), Pb(II), Cd(II) and Cr(III) were studied. By analysing the relationship between adsorption capacity and pH, adsorption isotherms and adsorption kinetics, it is proved that the adsorption of the four metal ions is mainly based on the chemical adsorption of coordination. The maximum adsorption capacities of the copolymer were up to 2.33, 1.25, 0.83 and 0.56 mmol g −1 for Cu(II), Pb(II), Cd(II) and Cr(III), respectively. The adsorption of the four concerned metal ions was hardly affected by common coexisting ions such as Na(I), K(I), Ca(II) and Mg(II), whereas it was slightly decreased when Fe(II) and Zn(II) coexisted in the solution, which illustrates the selective adsorption of Cu(II), Pb(II), Cd(II) and Cr(III) from wastewater. After 10 cycles of adsorption–desorption experiments, there was no significant change in the adsorption capacity, indicating that the polyamine-type starch/GMA copolymer has high adsorption capacity and good reusability.


2021 ◽  
Vol 404 ◽  
pp. 124140
Author(s):  
Lei Xu ◽  
Yani Liu ◽  
Jingang Wang ◽  
Ying Tang ◽  
Zhe Zhang

RSC Advances ◽  
2014 ◽  
Vol 4 (39) ◽  
pp. 20323-20333 ◽  
Author(s):  
Rupa Shantamal Madyal ◽  
Jyotsna Sudhir Arora

The current study provides molecular-level insights into the CO2–amine functionalized polystyrene complexes, enabling design of newer CO2 selective adsorbents.


Author(s):  
Ali Ekramipooya ◽  
Farshad Mirzaee Valadi ◽  
Mostafa Latifi pour ◽  
Davood Rashtchian ◽  
Mohammad Reza Gholami

2018 ◽  
Vol 743 ◽  
pp. 17-25 ◽  
Author(s):  
Xuanwen Liu ◽  
Renchao Wang ◽  
Zhiyuan Ni ◽  
Wanlin Zhou ◽  
Yuchen Du ◽  
...  

Author(s):  
J.A. Panitz

The first few atomic layers of a solid can form a barrier between its interior and an often hostile environment. Although adsorption at the vacuum-solid interface has been studied in great detail, little is known about adsorption at the liquid-solid interface. Adsorption at a liquid-solid interface is of intrinsic interest, and is of technological importance because it provides a way to coat a surface with monolayer or multilayer structures. A pinhole free monolayer (with a reasonable dielectric constant) could lead to the development of nanoscale capacitors with unique characteristics and lithographic resists that surpass the resolution of their conventional counterparts. Chemically selective adsorption is of particular interest because it can be used to passivate a surface from external modification or change the wear and the lubrication properties of a surface to reflect new and useful properties. Immunochemical adsorption could be used to fabricate novel molecular electronic devices or to construct small, “smart”, unobtrusive sensors with the potential to detect a wide variety of preselected species at the molecular level. These might include a particular carcinogen in the environment, a specific type of explosive, a chemical agent, a virus, or even a tumor in the human body.


2020 ◽  
Author(s):  
Rui Guo ◽  
Xiaotian Qi ◽  
Hengye Xiang ◽  
Paul Geaneoates ◽  
Ruihan Wang ◽  
...  

Vinyl fluorides play an important role in drug development as they serve as bioisosteres for peptide bonds and are found in a range of biologically active molecules. The discovery of safe, general and practical procedures to prepare vinyl fluorides remains an important goal and challenge for synthetic chemistry. Here we introduce an inexpensive and easily-handled reagent and report simple, scalable, and metal-free protocols for the regioselective and stereodivergent hydrofluorination of alkynes to access both the E and Z isomers of vinyl fluorides. These conditions were suitable for a diverse collection of alkynes, including several highly-functionalized pharmaceutical derivatives. Mechanistic and DFT studies support C–F bond formation through a vinyl cation intermediate, with the (E)- and (Z)-hydrofluorination products forming under kinetic and thermodynamic control, respectively.<br>


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