scholarly journals Functionalized Poly(arylene ether nitrile) Porous Membrane with High Pb(II) Adsorption Performance

Polymers ◽  
2019 ◽  
Vol 11 (9) ◽  
pp. 1412 ◽  
Author(s):  
Xiaocan Liu ◽  
Meirong Zhou ◽  
Xuefei Zhou ◽  
Lingling Wang ◽  
Xiaobo Liu

Porous materials with high specific surface area possess a broad application prospect in the treatment of wastewater. In this work, sulfonated poly(arylene ether nitrile) (SPEN) functionalized with a carboxylic acid group was successfully synthesized, which was subsequently transformed into SPEN porous membranes with cetyltrimethyl ammonium bromide (CTAB) as pore-forming agents to study the adsorption performance for lead ions in aqueous solution. Then, experiments were conducted to investigate the effect of pH, contact time and initial solution concentration on the adsorption performance of porous membranes, and the adsorption capacities of porous membranes with different content (0, 5 and 15 wt %) of CTAB were 183.60, 161.73 and 127.43 mg/g, respectively, which manifested that the adsorption capacity decreased with the increase of CTAB. The adsorption capacities of porous membranes increased with the increase of the initial concentration of lead ions, and the maximum reached was 246.96 mg/g. The simulation of adsorption kinetics revealed that the adsorption was accorded with the pseudo-second-order kinetic model and Langmuir equation, indicating that the adsorption process followed Langmuir monolayer adsorption. Thermogravimetric analysis demonstrated that the porous membranes had excellent thermodynamic properties both before and after adsorption. In addition, the change of adsorption peak in the Attenuated Total Reflectance Fourier Transform Infrared Spectroscopy (ATR-FTIR) spectrum indicated that the absorption performance of porous membranes for lead ions benefited from the chelation between lead ions and the carboxylic acid group on SPEN. Moreover, the porous membranes maintained excellent adsorption properties after circulating five times under the conditions of acidic or alkaline, and the cycle regeneration effect was outstanding.

2006 ◽  
Vol 62 (7) ◽  
pp. o2751-o2752 ◽  
Author(s):  
Ting Sun ◽  
Jian-Ping Ma ◽  
Ru-Qi Huang ◽  
Yu-Bin Dong

In the title compound, C10H7N3O4·H2O, one carboxyl group is deprotonated and the pyridyl group is protonated. The inner salt molecule has a planar structure, apart from the carboxylic acid group, which is tilted from the imidazole plane by a small dihedral angle of 7.3 (3)°.


2014 ◽  
Vol 70 (12) ◽  
pp. o1242-o1243 ◽  
Author(s):  
Wei Tang ◽  
Neng-Hua Chen ◽  
Guo-Qiang Li ◽  
Guo-Cai Wang ◽  
Yao-Lan Li

The title compound [systematic name: 3β-hydroxylup-20(29)-en-28-oic acid methanol monosolvate], C30H48O3·CH3OH, is a solvent pseudopolymorph of a naturally occurring plant-derived lupane-type pentacyclic triterpenoid, which was isolated from the traditional Chinese medicinal plantSyzygium jambos(L.) Alston. The dihedral angle between the planes of the carboxylic acid group and the olefinic group is 12.17 (18)°. TheA/B,B/C,C/DandD/Ering junctions are alltrans-fused. In the crystal, O—H...O hydrogen bonds involving the hydroxy and carboxylic acid groups and the methanol solvent molecule give rise to a two-dimensional network structure lying parallel to (001).


2012 ◽  
Vol 13 (1) ◽  
pp. 1-8 ◽  
Author(s):  
Dongho Kim ◽  
Yoomi Yoon ◽  
Ildoo Chung ◽  
Chanyoung Park ◽  
Jongwoo Bae ◽  
...  

2017 ◽  
Vol 19 (46) ◽  
pp. 31345-31351 ◽  
Author(s):  
Juan Ramón Avilés-Moreno ◽  
Giel Berden ◽  
Jos Oomens ◽  
Bruno Martínez-Haya

Protonated arginine interacts with 12-crown-4 through the guanidinium side group. In the complex with the N-substituted analog cyclen, the dominant conformation is the result of the proton transfer from the carboxylic acid group of the amino acid to the macrocycle.


2011 ◽  
Vol 100B (2) ◽  
pp. 569-576 ◽  
Author(s):  
Jonggu Park ◽  
Qiang Ye ◽  
Viraj Singh ◽  
Sarah L. Kieweg ◽  
Anil Misra ◽  
...  

1965 ◽  
Vol 20 (7) ◽  
pp. 883-887 ◽  
Author(s):  
J. H. Beynon ◽  
B. E. Job ◽  
A. E. Williams

The mass spectra of benzoic acid, phthalic acid, isophthalic acid and terephthalic acid, together with the analogues deuterated on the carboxylic acid group have been studied. Exchange of the deuterium atom with hydrogen atoms on the positions ortho to a carboxylic acid group on the aromatic ring has been studied using meta-stable peaks.


Sign in / Sign up

Export Citation Format

Share Document