Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractPhytohormones mediate volatile emissions during the interaction of compatible and incompatible pathogens: the role of ethylene in Pseudomonas syringae infected tobacco    Next AbstractSelected ion flow tube mass spectrometry analysis of volatile metabolites in urine headspace for the profiling of gastro-esophageal cancer »

J Hazard Mater


Title:"Synthesis, characterization and adsorption properties of diethylenetriamine-modified hypercrosslinked resins for efficient removal of salicylic acid from aqueous solution"
Author(s):Huang J; Jin X; Mao J; Yuan B; Deng R; Deng S;
Address:"School of Chemistry and Chemical Engineering, Central South University, Changsha, Hunan 410083, China. jianhanhuang@csu.edu.cn"
Journal Title:J Hazard Mater
Year:2012
Volume:20120326
Issue:
Page Number:406 - 415
DOI: 10.1016/j.jhazmat.2012.03.053
ISSN/ISBN:1873-3336 (Electronic) 0304-3894 (Linking)
Abstract:"We report an effective approach for tailoring the pore textural properties and surface polarity of a hypercrosslinked resin to enhance its adsorption capacity and selectivity for removing salicylic acid from aqueous solution. Four hypercrosslinked resins were synthesized by controlling the reaction time of the self Friedel-Crafts reaction of chloromethylated polystyrene-co-divinylbenzene, and then modified with diethylenetriamine to adjust their surface polarity. The resins were characterized with N(2) adsorption for pore textural properties, Fourier transform infrared spectroscopy (FT-IR) for surface functional groups, chemical analysis for residual chlorine content and weak basic exchange capacity. Adsorption equilibrium, kinetics and breakthrough performance were determined for the removal of salicylic acid from aqueous solution on a selected resin HJ-M01. The equilibrium adsorption capacity of salicylic acid on HJ-M01 is significantly higher than that on its precursor HJ-11 and a few commercial adsorbents including AB-8, XAD-4 and XAD-7. The dynamic adsorption capacity of salicylic acid on HJ-M01 was found to be 456.4 mg/L at a feed concentration of 1000 mg/L and 294 K. The used resin could be fully regenerated with 1% sodium hydroxide solution. The hypercrosslinked resins being developed were promising alternatives to commercial adsorbents for removing salicylic acid and other volatile organic compounds (VOCs) from aqueous solution"
Keywords:"Adsorption Hydrogen-Ion Concentration Microscopy, Electron, Scanning Polyamines/*chemistry Salicylic Acid/*chemistry Solutions Spectroscopy, Fourier Transform Infrared Water;"
Notes:"MedlineHuang, Jianhan Jin, Xiaoying Mao, Jinglin Yuan, Bin Deng, Rujie Deng, Shuguang eng Research Support, Non-U.S. Gov't Netherlands 2012/04/10 J Hazard Mater. 2012 May 30; 217-218:406-15. doi: 10.1016/j.jhazmat.2012.03.053. Epub 2012 Mar 26"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 29-06-2024