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| Content Provider | World Health Organization (WHO)-Global Index Medicus |
|---|---|
| Author | Huang, Jianyin Bennett, William W. Teasdale, Peter R. Gardiner, Sean Welsh, David T. |
| Description | Country affiliation: Australia Author Affiliation: Huang J ( Environmental Futures Research Institute, Griffith University, Gold Coast Campus, QLD 4222, Australia.); Bennett WW ( Environmental Futures Research Institute, Griffith University, Gold Coast Campus, QLD 4222, Australia.); Teasdale PR ( Environmental Futures Research Institute, Griffith University, Gold Coast Campus, QLD 4222, Australia. Electronic address: p.teasdale@griffith.edu.au.); Gardiner S ( Environmental Futures Research Institute, Griffith University, Gold Coast Campus, QLD 4222, Australia.); Welsh DT ( Environmental Futures Research Institute, Griffith University, Gold Coast Campus, QLD 4222, Australia.) |
| Abstract | A new diffusive gradients in thin films (DGT) technique, using Purolite A520E anion exchange resin, was developed and evaluated for the measurement of NO3N in freshwaters. Purolite A520E had a very high uptake efficiency (>98%) and elution efficiency (82.7% with 2 mol L(-1) NaCl as eluent) for NO3N. The 24 h mass vs. time validation experiments had excellent linearity (R(2) ≥ 0.997) and the intrinsic capacity of the binding layer for NO3N was 849 ± 24 µg. NO3N uptake was quantitative over a pH (3.5-8.5) range typical of most natural freshwaters. Several anions competed with NO3N to produce a lower effective binding capacity for NO3N in the following order of selectivity, Cl(-) > HCO3(-) > SO4(2-) > H2PO4(-), although NO3N measurements were quantitative at ionic strengths 0.0001-0.008 mol L(-1) as NaCl. NO2N did not adversely affect determination of NO3N at typical concentrations. Field deployments of DGT samplers with varying diffusive layer thicknesses validated the use of the technique in situ, allowed calculation of the diffusive boundary layer and accurate measurement of NO3N (CDGT/CSOLN 1.03-1.04). Reproducibility of the technique during field deployments was good (relative standard deviation < 3.2%). Limits of detection of A520E-DGT for NO3N were 13.15 µg L(-1) and 7.52 µg L(-1) (equivalent to 0.94 and 0.54 µmol L(-1)) based on 24 h and 48 h deployments, respectively. A520E-DGT determined NO3N concentrations during field deployments were very similar to the average values obtained from 0.45 µm filtered grab samples, which confirmed that the new DGT technique produced highly representative results. |
| File Format | HTM / HTML |
| ISSN | 00032670 |
| Journal | Analytica Chimica Acta |
| Volume Number | 923 |
| e-ISSN | 18734324 |
| Language | English |
| Publisher | Elsevier |
| Publisher Date | 2016-06-07 |
| Publisher Place | Netherlands |
| Access Restriction | One Nation One Subscription (ONOS) |
| Content Type | Text |
| Resource Type | Article |
| Subject | Spectroscopy Environmental Chemistry Analytical Chemistry Biochemistry |
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