Photodegradation of phosphonates in water

被引:82
作者
Lesueur, C
Pfeffer, M
Fuerhacker, M
机构
[1] Univ Nat Resources & Appl Life Sci, BOKU, Dept Water Atmosphere & Environm, Inst Sanit Engn & Water Pollut Control, A-1190 Vienna, Austria
[2] Dept Forest Ecol, Unit Agr Pedol, A-1131 Vienna, Austria
关键词
photodegradation; iron; pH; phosphonates; AMPA;
D O I
10.1016/j.chemosphere.2004.10.049
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Phosphonates are widely used as chelating agents, e.g., in water cooling systems, in bleaching baths or as scale inhibitors in deflocculation agents. They are considered to be difficult to degrade and produce aminomethylphosphonic acid (AMPA) as a metabolite. As the fate of phosphonates in the environment is not very well known the present work aims at simulating the time dependent photodegradation of four selected phosphonates: nitrilotris-methylenephosphonic acid (NTMP), ethylenediamine-tetra-methylenephosphonic acid (EDTMP), diethylenetriaminepenta-methylenephosphonic acid (DTPMP) and hexaethylenediamine-tetra-methylenephosphonic acid (HDTMP), at concentrations of 1mg/l (i.e. 3.2 mu M NTMP, 2.3 mu M EDTMP, 1.7 mu M DTPMP and 2.0 mu M HDTMP) irradiated by a middle pressure mercury lamp emitting between 190 and 600 nm. The influence of iron under different pH ranges (3, 5-6 and 10) are tested. The degradation of phosphonates is measured by the release of orthophosphates (PO4-P) and aminornethylphosphonic acid (AMPA). This study shows that phosphonates are substances that undergo UV light conversion, which is enhanced in the presence of iron. The half-life without iron is between 15 and 35min at pH 3, between 10 and 35min at pH 5-6 and between 50 and 75min at pH 10. The half-life in the presence of 3.6 mu M iron is between 5 and 10min at pH 3, between 5 and 15min at pH 5-6 and between 35 and 60min at pH 10. The individual substances do not significantly influence the reaction rates whereas the presence of iron and the pH have significant effects. The total conversion of phosphonates after 90min is 75-100% for pH values of 3 and 5-6 and 55-75% for a pH of 10 dependent on the presence of iron. In the environment longer degradation times are to be expected since natural light is weaker by a factor between 125 and 300 in the UVB, a factor between 3 and 8 in the UVA and of the same intensity in the visible range than the light in our study. Although orthophosphates are the major products, AMPA is also shown to be a by-product of the photodegradation of phosphonates that is later converted into orthophosphate. (c) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:685 / 691
页数:7
相关论文
共 20 条
[1]   PHOTODECOMPOSITION OF FE(III) AMINOPOLYCARBOXYLATES [J].
CAREY, JH ;
LANGFORD, CH .
CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1973, 51 (22) :3665-3670
[2]  
Gledhill William E., 1992, HDB ENV CHEM F, P261
[3]  
HUEBERS HA, 1990, METALS THEIRY COMP 2, V1, P945
[4]   Environmental risk assessment of phosphonates, used in domestic laundry and cleaning agents in the Netherlands [J].
Jaworska, J ;
Van Genderen-Takken, H ;
Hanstveit, A ;
van de Plassehe, E ;
Feijtel, T .
CHEMOSPHERE, 2002, 47 (06) :655-665
[5]   MODELING THE PHOTOCHEMICAL DEGRADATION OF ETHYLENEDIAMINETETRAACETATE IN THE RIVER GLATT [J].
KARI, FG ;
GIGER, W .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1995, 29 (11) :2814-2827
[6]  
Klinger J., 1998, Vom Wasser, V91, P15
[7]   AEROBIC PHOTODEGRADATION OF FE(III)-(ETHYLENEDINITRILO)-TETRAACETATE (FERRIC EDTA) - IMPLICATIONS FOR NATURAL-WATERS [J].
LOCKHART, HB ;
BLAKELEY, RV .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1975, 9 (12) :1035-1038
[8]   PHOTODEGRADATION OF FERRIC ETHYLENEDIAMINETETRA(METHYLENEPHOSPHONIC ACID) (EDTMP) IN AQUEOUS-SOLUTION [J].
MATTHIJS, E ;
DEOUDE, NT ;
BOLTE, M ;
LEMAIRE, J .
WATER RESEARCH, 1989, 23 (07) :845-851
[9]   Determination of phosphonates in natural waters by ion-pair high-performance liquid chromatography [J].
Nowack, B .
JOURNAL OF CHROMATOGRAPHY A, 1997, 773 (1-2) :139-146
[10]   Degradation of nitrilotris(methylenephosphonic acid) and related (amino)phosphonate chelating agents in the presence of manganese and molecular oxygen [J].
Nowack, B ;
Stone, AT .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2000, 34 (22) :4759-4765