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1.
A comparative study of three methods for the determination of iodate-iodine in seawater is described. In one method the iodate is determined polarographically while in the others the iodate is determined colorimetrically as iodonium ions. In one of the colorimetric methods each sample is pre-treated with excess iodine-water in an attempt to eliminate suspected interference from naturally occurring reducing agents. The tests were conducted on a selection of open-ocean and near-shore waters with iodate concentrations ranging from 0 to 60 μg 1?1-I. The tests indicated that the polarographic method and the colorimetric method without iodine-water give the more reliable measurement of iodate concentration. Also, the method with iodine water was found to be in error especially at low iodate concentrations. Reducing agents, if present, were found not to interfere significantly. 相似文献
2.
A method is described for the detection of free α-amino acids in the picomole range in seawater samples of less than 100 ml volume. The modifications made to a standard amino acid analyser to incorporate a fluorimetric detection system are described in detail, together with the methods for desalting the seawater samples on cation exchange resin and the concentration procedures prior to analysis. A complete analysis of up to 30 amino acids requires around 3 h with a detection limit of around 0.05 μg of an individual acid per litre. Twenty samples of seawater from different depths in the open Baltic have been analysed for their FAA contents together with 3 samples taken from the Kiel Fjord. The total FAA content of the samples ranges from 4.5 to 84 μg/l with a mean of around 25 μg/l. Five samples were hydrolysed prior to analysis in order to estimate the CAA content of the seawater. The values lay in the range 438–805 μg/l. 相似文献
3.
离子色谱-电感耦合等离子体质谱联用测定海水中的IO3^-和I^- 总被引：1，自引：0，他引：1
研究了离子色谱-电感耦合等离子体质谱（IC-ICPMS）联用技术直接进样测定海水中IO3^-和I^-的方法．采用IonPacAG23离子色谱保护柱分离IO3^-和I^-，以浓度4．0mmol／dm3的KOH为流动相，流量为1．0cm3／min，每个样品的分析时间为2．5min．采用2．5×10^-3cm^3的进样量，IO3^-和I^-的检出限分别达到0．6和0．4nmol／dm2，可满足海水中碘形态的定量分析．该方法的IO3^-和I^-浓度范围在2．0nmol／dm3～2．0μmol／dm3． 相似文献
4.
Victor W. Truesdale 《Marine Chemistry》1978,6(3):253-273
The development of procedures for the determination of iodate- and total-iodine content of seawater, which use a Technicon Auto-Analyser, is described. In both procedures the appropriate iodine species is first converted to iodate-iodine. Then, this is reacted with acid and excess iodide to give the iodonium ion, I3?, which is detected spectrophotometrically. In the total-iodine procedure the pre-oxidation is accomplished using bromine water. In the iodate procedure a pre-oxidation step using iodine-water can be included. It is anticipated that this will be used to test for the presence of naturally occurring reducing agents in seawaters, which by their action on iodonium ions could lead to an underestimate in iodate concentration. Seawaters, particularly coastal and surface oceanic ones, are known to contain iodine-reducing substances. Therefore, the validity of results obtained through the iodometric method for iodate must remain in some doubt until these tests have been made. The use of this method on anoxic waters which contain sulphides appears to be a prime example of where caution should be observed. The iodate procedure, both with and without pre-oxidation, has been tested on approximately 50 samples of waters from the Eastern Pacific Ocean; these waters did not appear to contain significant amounts of reducing agents. In a similar study, it was found that there was no significant difference between the results obtained by the new total-iodine procedure and an earlier automatic catalytic one. 相似文献
5.
《African Journal of Marine Science》2013,35(1):189-198
Analytical methods for the automatic determination of micronutrients in seawater based on the TECHNICON Auto Analyzer (AAII) principles are described. The methods are adaptations and modifications of existing photometric methods already described in the literature. Automated methods are presented for the determination of the different forms of nitrogen available to plant life, namely nitrite, nitrate, ammonia and total nitrogen, as well as for phosphate-phosphorus and silicate-silicon. All these methods are in routine use by the Sea Fisheries Research Institute. 相似文献
6.
Dissolved iodine species and the relationship between its distribution and salinity in Jiulong River estuarine water have been determined. It has been found that the total iodine, iodate and iodide are positive linear with salinity. This indicates that dissolved iodine species (IO-3 and I- ) in estuarine water .how conservative behaviour. The river water contains 2. 40μg/1 as iodide and less than 1. 0μg/1 as iodate, and iodide is the predominant species. Whereas the sea water contains 39. 4μg/1 as iodate and 4. 00μg/1 as iodide, and iodate is the dominant form. The distribution of dissolved iodine in pore water, as a function of depth, has been studied. Iodine in pore water occurs as iodide. The apparent fluxes of soluble iodine from the sediment to the overlying water in the estuary have been determined. The values are 2. 4 (15℃) and 27μmol/(m2·d) (30℃) respectively. 相似文献
7.
A precise method for the determination of total iodine in seawater, which uses a Technicon Auto-Analyser II system and is based on Truesdale and Spencer's (1974) and Truesdale and Smith's (1975) earlier works with a catalytic procedure, is described. The procedure operates over a range of 30–80 μg1?1 of iodine. As requested by Mark (1973), the way in which the procedure can be varied to suit other applications, and therefore ranges, is explained in detail. The standard deviation at the 50 μg1?1 level was found to be 0.12 μ1?1 showing that the method's precision exceeds most, if not all, previously published procedures for this variable. This high degree of resolution makes the procedure suitable for oceanic investigations. The effects of varying the reaction time, the temperature at which the reaction proceeds and the salinity of samples and standards are described. The advantages of using a Technicon Auto-Analyser II system rather than an Auto-Analyser I system are discussed. With slight modification the procedure can also be used in the measurement of river flow where sodium iodide is used as tracer in the dilution method. 相似文献
8.
本文介绍了低盐度海水中5种重金属元素混合溶液标准物质的研究和制备过程。以稀释的大洋海水为基体,用容量法以加标方式制备了低盐度海水中重金属标准物质。各元素统计结果表明样品的均匀性和稳定性良好。经9家具有中国计量认定(CMA)资质的实验室分别采用原子吸收分光光度法、电感耦合等离子体质谱法和阳极溶出伏安法对标准溶液进行分析定值,并用国家标准物质作量值溯源,以分析结果的总平均值作为标准值,标准值及不确定度的结果分别为铜15.2±0.7 μg/L、铅15.3±0.7 μg/L、锌98.9±4.7 μg/L、镉2.02±0.10 μg/L以及铬15.3±0.6 μg/L。该标准物质可用于近岸、河口区低盐度海水重金属分析过程的量值传递和质量控制。 相似文献
9.
A modified procedure has been proposed for the colorimetric determination of dissolved oxygen in seawater to improve its precision and accuracy. When a pickled sample is acidified, iodine liberated in the iodometric reaction is measured by direct spectrophotometry at 456 nm. Loss of molecular iodine by volatilization is eliminated by transferring the sample to a flow cuvette without contact with air. The method was calibrated for oxygen by spiking known amounts of potassium iodate. Precision was found at better than 0.2% r.s.d. (full scale). Evaluation of accuracy was made by comparison with calculated oxygen solubilities, which shows a relative bias of no more than 0.5% for oxic waters. The analytical throughput was much faster than that of the standard titration procedure. 相似文献
10.
George T.F Wong 《Marine Chemistry》1980,9(1):13-24
An oxidation state diagram was used to study the relative stability of inorganic iodine species in an aqueous system. It is shown that although iodate is the most stable form, iodide may exist as a metastable form in a basic solution. Molecular iodine may undergo disproportionation to form iodide and iodate. Results from laboratory studies suggest that molecular iodine is rapidly taken up by seawater, and hypoiodite is probably formed. Hypoiodite is also unstable in seawater, and may react with organic matter or undergo autodecomposition. Direct reactions between molecular iodine and organic matter were not observed. 相似文献
11.
The distribution and speciation of iodine, a biophilic redox-sensitive trace element, in waters overlying and in the Orca Basin, Gulf of Mexico, which contains hypersaline, anoxic and yet non-sulfide-bearing brine have been determined. The distribution of iodate and iodide in the oxic waters overlying the anoxic brine are similar to those reported in other oceans. However, in the oxic-anoxic mixing zone, iodate disappears while the concentration of iodide reaches a maximum of 8.1 μM, the highest concentration ever reported in open oceans. There is also a maximum in specific iodine of 30.7 nM‰?1 at this depth. Specific iodine in oxic seawater is only about 10–14 nM ‰?1. These features may be explained by the preferential dissolution of biogenic particles that have accumulated in a strong pycnocline. In the anoxic brine proper, the concentration of iodide is 3.8 μM and can be explained almost entirely by the simultaneous mobilization of chloride and iodide during the dissolution of evaporite beds as the specific iodine of 14.5 nM‰?1 is only slightly higher than those observed in the oxic waters. 相似文献
12.
Toward assessing the biogeochemical significance of seaweeds in relation to dissolved iodine in seawater, the effect of whole seaweeds (Laminaria digitata and Fucus serratus) upon iodide and iodate, at essentially natural concentrations, has been studied. The weeds were carefully removed from the sub-littoral zone of the Menai Straits and exposed to iodide and iodate at their natural temperature (6 °C), but under continuous illumination. Laminaria digitata was found to decrease the concentration of iodate with an exponential rate constant of 0.008–0.24 h−1. This is a newly discovered process which, if substantiated, will require an entirely new mechanism. Generally, apparent iodide concentration increased except in a run with seawater augmented with iodide, where it first decreased. The rate constant for loss of iodide was 0.014–0.16 h−1. Meanwhile, F. serratus was found not to decrease iodate concentrations, as did L. digitata. Indeed, after ∼30 h iodate concentrations increased, suggesting that the weed may take in iodide before oxidising and releasing it. If substantiated, this finding may offer a way into one of the most elusive of processes within the iodine cycle – iodide oxidation. With both seaweeds sustained long-term increases of apparent iodide concentration are most easily explained as a secretion by the weeds of organic matter which is capable of reducing the Ce(IV) reagent used in determination of total iodine. Modelling of the catalytic method used is provided to support this contention. The possibility of developing this to measure the strain that seaweeds endure in this kind of biogeochemical flux experiment is discussed. A Chemical Oxygen Demand type of approach is applied using Ce(IV) as oxidant. The results of the iodine experiments are contrasted with the several investigations of 131I interaction with seaweeds, which have routinely used discs of weed cut from the frond. It is argued that experiments conducted with stable iodine may measure a different variable to that measured in radio-iodine experiments. 相似文献
13.
Aerated solutions of potassium iodide in de-ionised water, of between 5–20% (w/v), were exposed to ambient spring sunlight to estimate the rate of photochemical production of molecular iodine from iodide and oxygen in seawater. This rate cannot be measured directly as other reactions, for example the reduction of molecular iodine by organic matter, interfere. Also, a parallel photo-oxidation, initiated by organic matter in real seawater, may also occur. The experiments yield a half-life for iodide in tropical surface waters of about 29 months suggesting that the reaction is insignificant. At this rate it will not compete effectively against the reduction of molecular iodine by organic matter, and hence molecular iodine should not appear. The experiments also consider the photo-oxidation by nitrate, and iodate, a combination of nitrite and oxygen, and eliminate significant interference by chloride, bromide and the phosphate buffer. The rate of photo-oxidation with each of the first three oxidations is found to be first order with respect to oxidant concentration. The variation of photo-oxidation rate with pH is also studied, with a brief investigation without conventional oxidant, where electron cage complexes still promote photo-oxidation. The photochemical action spectrum for these reactions in sunlight is shown to extend between 300 and 425 nm. The photo-oxidation of iodide by iodate is more interesting to marine chemistry as the photo-reduction of iodate. Nevertheless, the reduction-rate is judged to be several orders too low to be significant in seawater. The mechanism of the reactions are discussed and lessons drawn on the stability of potassium iodide solutions used in iodate analysis. The KI actinometer is recommended to those studying other photochemical systems activated by UV-A light as it is linear and very simple and reliable. 相似文献
14.
A low-absorbance differential cold vapor atomic absorption method is developed for direct determination of trace mercury in seawater. The sensitivity of the method is good at 1 ng mercury per liter and precision is excellent with a relative standard deviation of 13.9% at 12 ng Hg/1 level and 3.2% at 39 ng Hg/1 level respectively. The method is proved to be rapid and simple, and has been applied to the analysis of mercury in seawater from Xiamen Harbor and the Central Pacific Ocean. 相似文献
15.
Anna M. Farrenkopf Michael E. Dollhopf Sinad Ní Chadhain George W. Luther III Kenneth H. Nealson 《Marine Chemistry》1997,57(3-4)
Shipboard incubations from the US JGOFS cruise to the Arabian Sea (TN045) March, 1995 showed evidence of iodate reduction in 0.45 μ (Gelman Supor membrane) filtered seawater samples collected from intermediate depths (200–600 m) within the oxygen minimum zone (OMZ). Inorganic chemical reduction of iodate in these samples was ruled out as no free sulfide was measurable and concentrations of ammonia and nitrite were found to be less than 5 μM. To examine whether the reduction of iodate observed at sea could have been the result of bacterial metabolism, reduction of iodate (IO3−) to iodide (I−) by Shewanella putrefaciens strain MR-4 was studied in artificial seawater using electrochemical methods. MR-4 is a ubiquitous marine bacterium which may be of considerable importance when considering redox zonation in the water column because it is a facultative anaerobe and may switch amongst a suite of electron acceptors to support metabolism. In all experiments MR-4 reduced all iodate to iodide. The rate of formation of [I−]in the culture followed pseudo-first order kinetics. This is the first report of the marine bacterial reduction of iodate where the concentrations of iodide and iodate were measured directly. Our results may help to explain the depth distribution of iodine speciation reported in productive waters like the Arabian Sea and for the first time couple iodine speciation with bacterial productivity in the ocean. 相似文献
16.
A laser-induced fluorometric method for the rapid determination of trace level? of uranium in seawater with the Modified Anti-interference Fluorometric Reagent for uranium (MAFG) is described. Only a sample volume of 1.5-2.5 ml is used in each determination and no pre-scparation and concentration steps are required. The analysis rate is a sample per 5 min. The relative standard deviation of ten replicate determinations on 3.44 ppb U of the natural seawater is 4.7%. 相似文献
17.
Victor W. Truesdale 《Marine Chemistry》1975,3(2):111-119
An iodine component in seawater, which is ‘unreactive’ to the total inorganic method described by Truesdale and Spencer (1974), has been discovered. The component is measured as the increase in ‘reactive’ iodine that accompanies irradiation of seawater with high-intensity UV light. The highest concentration recorded for an inshore water was . As some known organic-iodine compounds behave in a similar manner to UV irradiation, it is suggested that the ‘unreactive’ iodine is organically bound iodine. 相似文献
18.
An analytical method is proposed for the direct determination of Cd in seawater by differential pulse anodic stripping voltammetry and the derivative technique with a hanging mercury drop electrode. The process of determination is quick, simple and convenient. The concentration of Cd in seawater is only determined by adjusting the acidity of seawater to pH 2 and by taking three minutes' plating time. Sensitivity of the method is about 1×10-10M, and accuracy of that satisfactory. Relative standard deviation is about 12% when the concentration of Cd in seawater is approximately 0.04 ppb. A good agreement was obtained by a standard curve and a standard addition technique respectively from determining Cd in the same seawater. Actual measurement time per sample is about 10 min. 相似文献
19.
The concentrations of dissolved chromium in seawater of the Bohai Gulf vary from trace to 1.6 μg /1 while those of particulate chromium from trace to 8.66 μg/1, indicating that the concentration of chromium in seawater of nearshore and estuary in the Bohai Gulf is higher than that of offshore, and reflecting the effects of estuarine and terrestrial pollutions. Observation data indicate that there is a positive correlation between particulate chromium and COD.The result shows that organic matter in seawater has a strong ability to combine chromium. When particulate chromium meets with seawater in estuary, it gradually settles down to sea-bottom sediments. Ratio of particulate chromium to total chromium in the Bohai Gulf yields a higher value, exceeding 90% in estuarine area, i.e. particulate chromium is a predominant form in seawater of the Bohai Gulf. 相似文献
20.
A study of inorganic iodine speciation in the waters of seven Croatian coastal caves is described. These are anchialine caves as they are connected hydraulically with Adriatic Sea surface water, with the tide inside the cave rising and falling with that outside, but replenishment of the water is restricted by the karst rock. In effect, the water in the cave probably acts more like a piston, and although moving slightly vertically, has a long residence time compared to a fully-flushing cave. Anchialine environments display a number of unusual features, e.g., a well-developed pycnocline, hypoxia and endemic fauna. Iodate and iodide were determined by differential pulse voltammetry and cathodic stripping square wave voltammetry, respectively. Low iodide concentrations (< 10 nM) have been consistently identified in the bottom water of the caves where concentrations of 90–100 nM would ordinarily be expected from intrusion of Eastern Adriatic surface seawater. Where total inorganic iodine concentrations behave conservatively with salinity the loss of the iodide implies oxidation to iodate. As iodide oxidation remains one of the enduring academic problems of the marine iodine system the study of iodine in anchialine caves may help unravel it. Iodate reduction was observed in mid-water, at the halocline, and mechanisms for the reduction involving either respiration or chemolitho-autotrophic bacteria are considered. The respiration mechanism is favoured because of enhanced alkalinity found in the near surface waters of the caves. 相似文献