Piperidine-functionalized supports sequester atrazine from solution

被引:12
作者
Hollink, E [1 ]
Tichy, SE [1 ]
Simanek, EE [1 ]
机构
[1] Texas A&M Univ, Dept Chem, College Stn, TX 77843 USA
关键词
D O I
10.1021/ie0494566
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
To achieve irreversible (covalent) capture of monochlorotriazine herbicides such as atrazine, three commercially available poly(styrene) resins (Janda Jels) that vary in size were modified with reactive isonipecotic acid groups. The materials were characterized using the Kaiser test, infrared (IR) spectroscopy, and titration experiments that indicated the relative number of accessible nucleophiles. Sequestration of atrazine from aqueous solutions using these polymers was monitored using liquid chromatography-mass spectrometry. Large (50-100 mesh) and medium (100-200 mesh) resins remove all detectable traces of atrazine from water at similar rates, whereas the smallest resin (200-400 mesh) removes the herbicide at a slower rate. Generally, the sequestration of atrazine by reactive, nucleophilic resins seems to be a suitable strategy for additional inquiry, particularly as an alternative to the current method of wastewater treatment-activated charcoal.
引用
收藏
页码:1634 / 1639
页数:6
相关论文
共 40 条
[1]   Removal of atrazine from water using covalent sequestration [J].
Acosta, EJ ;
Steffensen, MB ;
Tichy, SE ;
Simanek, EE .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2004, 52 (03) :545-549
[2]   Design, synthesis, and modeling of novel cyclic thrombin receptor-derived peptide analogues of the Ser42-Phe-Leu-Leu-Arg46 motif sequence with fixed conformations of pharmacophoric groups:: Importance of a Phe/Arg/NH2 cluster for receptor activation and implications in the design of nonpeptide thrombin receptor mimetics [J].
Alexopoulos, K ;
Panagiotopoulos, D ;
Mavromoustakos, T ;
Fatseas, P ;
Paredes-Carbajal, MC ;
Mascher, D ;
Mihailescu, S ;
Matsoukas, J .
JOURNAL OF MEDICINAL CHEMISTRY, 2001, 44 (03) :328-339
[3]   Characterization of monoclonal antibodies raised against different structures belonging to the s-triazine group of herbicides [J].
Bruun, L ;
Koch, C ;
Jakobsen, MH ;
Pedersen, B ;
Christiansen, M ;
Aamand, J .
ANALYTICA CHIMICA ACTA, 2001, 436 (01) :87-101
[4]   PYBOP - A NEW PEPTIDE COUPLING REAGENT DEVOID OF TOXIC BY-PRODUCT [J].
COSTE, J ;
LENGUYEN, D ;
CASTRO, B .
TETRAHEDRON LETTERS, 1990, 31 (02) :205-208
[5]   The adsorption of herbicides and pesticides on clay minerals and soils. Part 2. Atrazine [J].
Davies, JED ;
Jabeen, N .
JOURNAL OF INCLUSION PHENOMENA AND MACROCYCLIC CHEMISTRY, 2003, 46 (1-2) :57-64
[6]  
DeSutter TM, 2003, WEED SCI, V51, P456, DOI 10.1614/0043-1745(2003)051[0456:ASADAA]2.0.CO
[7]  
2
[8]   Pesticides and cancer [J].
Dich, J ;
Zahm, SH ;
Hanberg, A ;
Adami, HO .
CANCER CAUSES & CONTROL, 1997, 8 (03) :420-443
[9]  
DILLON AP, 1981, PESTICIDE DISPOSAL D
[10]   Selective trace enrichment of chlorotriazine pesticides from natural waters and sediment samples using terbuthylazine molecularly imprinted polymers [J].
Ferrer, I ;
Lanza, F ;
Tolokan, A ;
Horvath, V ;
Sellergren, B ;
Horvai, G ;
Barceló, D .
ANALYTICAL CHEMISTRY, 2000, 72 (16) :3934-3941