环境水体中碘的存在形态及其影响因素研究
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摘要
碘是人体合成甲状腺激素必不可少的微量元素,在人体的新陈代谢、生长发育过程中发挥着举足轻重的作用。环境水体是地球化学循环中进行元素转化和迁移的媒介,是人体摄取碘的重要来源。因此研究环境水体中碘元素的存在形态可为进一步研究碘在自然环境中的迁移转化条件和规律提供理论依据,而且还能够准确地评价碘对环境和生态体系的影响。研究碘的分析方法有很多种,其中,电感耦合等离子体质谱技术由于具有较低的检出限、较少的干扰、较高的灵敏度和精密度、较宽的线性范围,而成为环境地球化学中同时检测多个元素的首选技术。将它与其它分离技术联用已成为碘元素形态分析的最有效研究方法。
     本文以环境水体中碘的存在形态为研究目标,建立了电感耦合等离子体质谱测定碘总量的分析方法和电感耦合等离子体质谱与离子色谱联用测定碘形态的新方法,以此为基础,研究了海水、湖水、地下水和大气降水等环境水体中碘的总量和存在形态,并分析探讨了水体中碘存在形态的影响因素,进而分析不同水体中碘形态转化的原因及其环境地球化学行为。
     主要研究成果如下:
     (1)在系统总结环境水体中碘的来源、分布、地球化学循环、碘与人体健康关系的基础上,详细综述了碘总量和形态分析方法的研究进展。
     (2)研究建立了电感耦合等离子体质谱技术测定碘总量的分析方法。以Lu作内标,仪器经混合标准调谐液优化后建立的测定碘总量的标准曲线线性范围宽达5个数量级,碘的检出限低至0.0218μg/L,精确度高(RSD=3.85%),准确性好(国家标准碘盐的测定结果与标准值相符)。
     (3)研究建立了一种新的短柱分离离子色谱-电感耦合等离子体质谱联用技术测定碘形态的分析方法。经优化得出最佳的分离条件:Dionex IonPacAG11(4×50mm)作分离柱,8mmol/L的(NH_4)_2CO_3溶液作流动相,流速1.5mL/min、进样量20μL。在该分离条件下以电感耦合等离子体质谱作检测器得到的IO_3~-和I-的线性范围宽(0.1-100μg/L),线性关系良好(相关系数r~2均大于0.9996),IO_3~-和I-的检出限低(分别为0.015μg/L和0.081μg/L),精确度高(RSD<4.3%),IO_3~-和I-的分离时间短(170s左右)。
     (4)采用建立的短柱分离离子色谱-电感耦合等离子体质谱联用技术对市面零售的加碘食盐中碘的形态进行了研究,并分析了经人体循环代谢后尿液中碘的形态。结果表明:市售食盐中的碘均以IO_3~-形态存在,经过人体循环代谢,最终以I-形态随尿排出。为进一步研究IO_3~-在生物体(人体)中的代谢机理提供了基础。从尿碘总量来看长春市民没有碘缺乏病的危险。
     (5)采用建立的新方法对不同环境水样中碘的含量、形态、形态赋存的原因及其环境地球化学行为进行了研究。结果表明:不同水体中碘的总量和存在形态不尽相同。总体来说海水中碘的含量比陆地水中碘的含量要高。海水和长春南湖水中碘主要以IO_3~-和I-两种形态存在,且含量适中。从长春大气降水判断长春属缺碘区,其中IO_3~-和I-的含量之和还不足碘总量的一半。从长春自来水和地下水中碘含量判断长春属于适碘区,但自来水中碘主要以IO_3~-形态存在而地下水中主要以I-存在,且所占比例都接近100%。
     (6)研究pH、氧化还原环境、盐度和有机质含量等主要影响因素对碘形态转化的影响。结果表明:IO_3~-形态与氧化剂含量、盐度和有机质含量呈显著相关,与0-50℃的环境水温和4-10的环境水pH值没有明显的相关性。而I-与所有考察的因素均具有较好的相关性,尤其与氧化剂的含量、盐度和有机质含量相关性显著。根据理论Eh-pH图分析的环境水体中碘的存在形态与实际水体中的存在形态有差别,说明环境水体中碘形态受地理位置、环境条件影响较大。
Iodine is an essential microelement which can composes hormone of thyroidgland, and it is very important for metabolism and human body’s growth development.Environmental water system is a medium of elementary transformation andtransference in circle of geochemistry, and it is an important source of iodine forhuman body. Therefor, the study on speciation of iodine in environmental watersystem can offer theoretic basis for transferred conditions and rules of iodine inentironment. And it can truly evaluate the influence of iodine on surroundings andecosystem. There are many analytical methods for study of iodine. Inductivelycoupled plasma mass spectrometry (ICP-MS) has been a preferred technique foranalysis of various trace elements in environmental geochemistry owing to its lowlimits of detection, few interferences, high sensitivity and precision, widely dynamiclinearity. The combination of other separation technique with its specific detectiontechniques has become most effective methods for iodine speciation of some specialsamples.
     The speciation of iodine in environmental water system was selected as target inthis dissertation. Two new methods had been established, one was inductively coupledplasma mass spectrometry technique for determination of total iodine, the other wasion chromatography coupled with inductively coupled plasma mass spectrometrytechnique for speciation analysis of iodine. On the basis of these methods, thecontents of total iodine and its speciation in environmental water system includingseawater, lake water, groundwater and atmosphere precipitation etc had been studied.Finally, the influencing factors which could affect the speciation of iodine, the reasonsof speciation tansform and behaviors in environmental geochemistry of iodine hadbeen discussed.
     The major results are described as follows:
     (1) On the basis of summarization on the source, distributing, circle of geochemistry of iodine and the relation of iodine to the human health, progress in thestudy of analytical methods for total iodine and its speciation had been summarized inditail.
     (2) An analytical method was established for total iodine by ICP-MS with Lu asinternal standard. The stadard curve of total iodine, established on the optimalinstrumental operating parameters which were adjusted by mixed criterion solution,had wide linear ranges which reached to five magnitude, the detection limit of iodinewas0.0218μg/L, the precision was high wih RSD=3.85%, the method was alsovalidated using certified reference materials, and the results were in good agreementwith the certified values, which showed the veracity of method was good.
     (3) A fast analytical method was developed for speciation of iodine by shortcolumn ion chromatography (IC) coupled with inductively plasma mass spectrometry(ICP-MS). The optimal separation conditions were obtained after optimization whichwere separation column, Dionex Ion PacAG11(4×50mm); mobile phase,8mmol/L(NH4)2CO3solution; flow rate,1.5mL/min; injection volume,20μL. Under theoptimal separation conditions and ICP-MS detector, IO_3~-and I-both had wide linearranges (0.1-100μg/L), good linearity (r2>0.9996), low detection limits (0.015μg/Land0.081μg/L for IO_3~-and I-, respectively), high precision (RSD<4.3%), shortseparation time (nearly170s).
     (4) The established short column IC coupled with ICP-MS for Speciation ofiodide and iodate was applied to determination of iodized salts collected from localmarkets and human urine samples collected from volunteers. The results showed thatiodine in the iodized salts firstly existed as IO_3~-and was all transformed to I-after themetabolizing cycle in the human body, which would supply basis to further study onmetabolizing mechanism of IO_3~-in organism (human). The dangers of IDD inChangchun City was inexistent from the contents of urine iodine.
     (5) The contents, speciation, reasons of speciation and their behaviors inenvironmental geochemistry of iodine in different environmental water system hadbeen studied by the proposed method in this work. As the results revealed, thecontents and speciation of iodine in different environmental water system weredifferent from each other. In a word, the content of iodine in seawater was higher thanthat in land water. The iodine were existed as IO_3~-and I-in seawater and ChangchunSouth lake water, and the contents were moderate. Changchun was section of iodine deficiency which judged by atmospheric precipitation, the total content of IO_3~-and I-was fewer than half of total iodine. Changchun was section of moderate iodine whichjudged by tap water and groundwater, however, the existent speciations of iodine inthese two waters were IO_3~-for tap water and I-for groundwater, respectively, nealyboth were100%.
     (6) The infulence of pH value, oxidation-reduction surroundings, salinity andcontent of organic substance on the speciation tansform of iodine had been studied.The results showed that speciation of IO_3~-had remarkable relativity with the contentsof oxidant, salinity and organic substance, by contraries, it had no relativity withwater temperature between0-50oC and pH value between4-10. However, thespeciation of I-had good relativity with all factors, especially with content of oxidant,salinity and content of organic substance. The theoretic species of iodine according tothe diagram of Eh-pH were different to the real species of iodine in environmentalwater system, which revealed that the speciation of iodine in environmental watersystem had been significantly affected by geographical position and environmentalconditions.
引文
-:未检出;a:仪器的测量误差引起超过最大百分含量或低于最小百分含量
    [1]傅永怀.微量元素与临床[M].北京:中国医药科技出版社,1997.
    [2]柴巍中,王京宇,欧阳荔,等.从生命元素的发展历史和互作关系看当前生命元素研究的现状和局限以及开展全元素研究的重要意义[J].微量元素与健康研究,2003,20(5):54-58.
    [3]郝立波,戚长谋主编.地球化学原理[M].第三版,北京:地质出版社,2004.
    [4]徐鹏,孙建民,孙汉文.化学浸提法研究中药赤石脂中活性铝的溶出及形态分布[J].光谱学与光谱分析,2003,23(6):1203-1205.
    [5] Lamy I, Bourgeois S, Bermond A. Soil Cadmium Mobility as a Consequence ofSewage Sludge Disposal[J]. J. Environ. Quality,1993,22(4):731-737.
    [6] Graeme E B, Simon C A, Jennifer L S. Speciation and bioavailability of tracemetals in water: progress since1982[J]. Australian Journal of Chemistry,2004,57:903-919.
    [7]赵艳慧,黄荣清,李科研,等. HPLC/ICP-MS联用技术在微量元素形态研究中的应用[J].现代仪器,2009,3:1-5.
    [8]刘虎生,邵宏翔.电感耦合等离子体质谱技术与应用[M].北京:化学工业出版社,2005.
    [9] Amr M A, Mohsen H T, Zahran N F, et al. Quantification of heavy metals in claysby dry plasma laser ablation-ICP-MS[J]. International Journal of MassSpectrometry,2007,278:66-72.
    [10] Banat K M, Howari F M, Al-Hama A A. Heavy metals in urban soils of centralJordan: Should we worry about their environmental risks?[J]. EnvironmentalResearch,2005,97(3):258-273.
    [11] Yosllida S, Muramatsu Y, Tayami K, et al. Determimtion of major and traceelements in Japanese rock reference sainples by ICP-MS[J]. International Journalof Environmental Analytical Chemistry,1996,63(l):195-206.
    [12] Jolyon M D, John C H, Malcolm T M. Rapid trace element analysis ofspeleothems by ELA-ICP-MS[J]. Chemical Geology,2006,231:102-117.
    [13] Zheng Y, Weinman B, Cronin T, et al. A rapid procedure for the determinationof thorium, uranium, cadmium and molybdenum in small sediment samples byinductively coupled plasma-mass spectrometry: application in ChesapeakeBay[J]. Applied Geochemistry,2003,18:539-549.
    [14] Hou X L, Roos P. Critical comparison of radiometric and mass spectrometricmethods for the determination of radionuclides in environmental, biological andnuclear waste samples[J]. Analytica Chimica Acta,2008,608:105-139.
    [15]程先豪.海洋沉积物中碘的早期成岩再迁移[J].海洋学报,1993,15(4):56-63.
    [16] Truesdale V W, Simon F, Watts A R. On the Possibility of iodide oxidation inthe near-surface of the Black Sea and its implications to iodine in the generalocean[J]. Deep-Sea Research I,2001,48:2397-2412.
    [17] Maetaylor R S, Gilligan J J, Castleman A W Jr. Reactions of iodine oxide andiodine oxoaeid anion species with nitric acid[J]. International Joumal of MassSpectrometry,1998,179-180:327-335.
    [18] Cook P L M, Carpenter P D, Butler E C V. Speciation of dissolve diodine in thewaters of a humic-rich estuary[J]. Marine Chemistry,2000,69(3):179-192.
    [19] Yasuyuki Muramatsu, Udo Fehn, Satoshi Yoshida. Recycling of iodine infore-are areas:evidence from the iodine brines in Chiba, JaPan[J]. Earth andplanetary science letters,2001,192:583-593.
    [20]李洪伟.黄河下游流域地下水和土壤中不同形态碘的分离测定及应用研究
    [D].北京:北京化工大学,2009.
    [21]陈祖培,刘德润,杨英奎.高碘地区与地方性高碘甲状腺肿[J].中国地方病学杂志,1998,17(6):385-388.
    [22]白耀.甲状腺病学——基础与临床[M].北京:科学技术出版社,2003.
    [23]王夔.生命科学中的微量元素[M].第2版,北京:中国计量出版社,1996,758-783.
    [24]唐肇礼,姜祥坤,梁伟,等.聊城市水源性高碘地区分布与居民碘营养调查[J].中国地方病学杂志,2006,25(6):683-685.
    [25]何金生,徐小华,周慧敏,等.北京市城区368例健康人血清碘的水平[J].微量元素与健康研究,2001,18(3):55-58.
    [26]徐志鑫,王瑞琴,蔡旭,等.不同人群尿碘水平监测结果分析[J].中国地方病防治杂志,2006,21(6):366-367.
    [27]张建勤.2005年安徽省碘缺乏病病情监测结果分析[J].安徽预防医学杂志,2007,13(1):20-22.
    [28]孙翠琴,范洪宾.孕产妇及儿童体内碘含量的调查[J].中国妇幼保健,2007,22(3):392-393.
    [29]严爱兰.碘生物地球化学行为的125I示踪与植物中生物碘的稳定性研究[D].浙江:浙江大学,2008.
    [30]苗键,高琦,许思来.微量元素与相关疾病[M].郑州:河南医科大学出版社,1997.
    [31]赵振华.微量元素地球化学原理[M].北京:科学出版社,1997.
    [32] Nath S K, Moinier B, Thuillier F, et al. Urinary excretion of iodide and fluoridefrom supplemented food grade salt[J]. Int. J. Vitam. Nutr. Res.1992,62(1):66-72.
    [33]王夔.生命科学中的微量元素(下卷)[M].北京:中国计量出版社,1992.
    [34] Chamberlain A C. Interception and retention of radioactive aerosols byvegetation[J]. Atmosphere Environment,1970,4:57-78.
    [35] Whitehead D C. The distribution and transformations of iodine in theenvironment[J]. Environment international,1984,10:321-339.
    [36] Whitehead D C. Iodine in British soils[J]. Journal of science on food agriculture,1973,24:43-50.
    [37] Atkins D H F, Chadwick R C, Chamberlain A C. Deposition of radioactivemethyl iodide to vegetation[J]. Health physiology,1967,13:91-92.
    [38] Moyers J L, Duce R A. Gaseous and particulate iodine in the marineatmosphere[J]. Journal of geophysical research,1972,77:5229-5238.
    [39] Luten J B, Woittiez J R W, Das H A, et al. Determination of iodine in rainwater[J]. Journal of Radioanalytical and Nuclear Chemistry,1978,43:175-185.
    [40] Cicerone R J. Halogens in the atmosphere[J]. Review of geophysics spacephysiology,1981,19:123-139.
    [41] Bewers J M, Haysorn H H. Terrigenous dust contribution of fluoride and iodinein atmospheric precipitation[J]. Journal derecherches atmosphere,1974,8:689-697.
    [42] Moyers J L, Zoller W H, Duce R A. Gaseous bromine and particulate leadvanadium, and bromine in polluted atmosphere[J]. Journal of atmosphere science,1971,28:95-98.
    [43] Duce R A, Zoller W H, Moyers J L. Paticulate and gaseous halogens in theAntarctic atmosphere[J]. Journal of geophysical research,1973,78:7802-7811.
    [44] Bertine K K, Geldberg E D. Trace elements in clams, mussels and shrimp[J].Science,1971,173:233-235.
    [45] Delange F, Burgi H, Chen Z P, et al. World status of monitoring iodinedeficiency disorders control programs[J]. Thyroid,2002,12:915-924.
    [46] WHO, UNICEF, ICCIDD. Assessment of iodine deficiency disorders andmonitoring their elimination: a guide for programme managers.2nd ed. Geneva:World Health Organization,2001.
    [47] Soldin O P. Controversies in urinary iodine determinations[J]. ClinicalBiochemistry,2002,35(8):575-579.
    [48] Andersson M, Takkouche B, Egli I, et al. Current global iodine status andprogress over the last decade towards the elimination of iodine deficiency[J].Bulletin of the World Health Organization,2005,83:518-525.
    [49] Mazzarell C, Terracciano D, Di Carlo A, et al. Iodine status assessment inCampania (Italy) as determined by urinary iodine excretion[J]. Appliednutritional investigation,2009,25:926-929.
    [50] Andó S, Maggiolini M, Di Carlo A, et al. Endemic goiter in Calabria:etiopathogenesis and thyroid function[J]. Journal of EndocrinologicalInvestigation,1994,17:329-333.
    [51] Aghini-Lombardi F A L, Martino E, Vitti P, et al. The spectrum of thyroiddisorders in an iodine-deficient community: the Pescopagano survey[J]. Journalof Clinical Endocrinology and Metabolism,1999,84:561-566.
    [52] Vermiglio F, Finocchiaro M D, Lo Presti V P, et al. Partial beneficial effects ofthe so called “silent iodine prophylaxis” on iodine deficiency disorders (IDD) innortheastern Sicily endemia[J]. Journal of Endocrinological Investigation,1989,12:123-126.
    [53] Soldin O P, Soldin S J, Pezzullo J C. Urinary iodine percentile ranges in theUnited States[J]. Clinica Chimica Acta,2003,328:185-190.
    [54]符燕,张小磊,马建华.碘与地方性甲状腺肿[J].微量元素与健康研究,2006,23(5):64-66.
    [55]陈志辉.近年来国内外碘缺乏病防治研究进展[J].海峡预防医学杂志,2001,7(2):27-29.
    [56] Hetzel B S. Iodine deficiency disorders (IDD) and their eradication[J]. TheLancet,1983,2:1126-1129.
    [57]洪春来.土壤-蔬菜系统中碘的生物地球化学行为与蔬菜对外源碘的吸收机制研究[D].浙江:浙江大学,2007.
    [58]王柯,侯小琳,张永保.碘的微堆超热中子活化法测定[J].核化学与放射化学,18(4):243-246.
    [59] Fuge R. Iodine in water, Possible links with endemic goiter[J]. AppliedGeochemistry,1989,4:203-208.
    [60]朱宪彝.地方性甲状腺肿流行病学[A].中国医学百科全书地方病学[M].上海:上海科学技术出版社,1985,29-30.
    [61]谭见安.中华人民共和国地方病与环境图集[M].北京:科学出版社,1989.
    [62]但德忠,李平.环境地球化学中的碘与我国的碘缺乏病[J].矿物岩石,1994,14(4):69-75.
    [63] Stárka, La kol. Aktuální endokrinologie[M]. Praha: Maxdorf Jesenius,1999.
    [64] Pantuckova P, Krivankova L. Fast and simple method for determination ofiodidein human urine, serum, sea water, and cooking salt by capillary zoneelectrophoresis[J]. Electrophoresis,2004,25:1102-1111.
    [65] Ortner D J, Hotz G. Skeletal manifestations of hypothyroidism fromSwitzerland[J]. American Journal of Physical Anthropology,2005,127:1-6.
    [66]刘占广.碘盐含碘量分析综述[J].海湖盐与化工,1999,28(6):33-35.
    [67] Delong G R, Paul W L. Effect on infant mortality of iodination of irrigation waterin a severely iodine-deficient area of China[J]. The Lancet,1997,1350(13):771-773.
    [68]刘会媛,白鹤英.加碘食盐中碘损失的实验研究[J].中国井矿盐,2004,5:43-45.
    [69]石磊,周瑞华,王光亚.食物烹调方法对含碘食盐中碘含量的影响[J].卫生研究,1998,27(6):412-414.
    [70]李洋,刘鑫.碘与人体健康[J].微量元素与健康研究,2004,2l(1):56-60.
    [71] Passos M C E, Ramos C F, Dutra S C P, et al. Transfer of iodine through the milkin protein-restricted lacating rats[J]. Joumal of Nutritional Biochemistry,2001,12:300-303.
    [72] Shibata S, Kamata E, Nakashima R.2-[2-(5-Bromopyridyl)azo]-5-dimethyIaminoPhenol: a new sensitive reagent for cadmium[J]. Analytical Chimiea Acta,1976,82:169-174.
    [73] Johnson D, Florence T. A study of some pyridylazo dyestuffs as chromogenicreagents and the elucidation of the nature of their metal complex spectra[J].Talanta,1975,22:253-265.
    [74]李慧霞.荧光/分光光度法检测环境水样中痕量金属离子的研究[D].长沙:湖南大学,2009.
    [75]张军,毛丽莉,杨桂朋,等.固载化离子液体富集-流动注射分光光度法测定废水中痕量汞[J].光谱学与光谱分析,2010,30(7):1979-1982.
    [76]代仕均,张新申.流动注射-分光光度法分析水体中的痕量铜[J].皮革科学与工程,2011,2l(1):62-67.
    [77] Silva M, Fernandez L, Olsina R, et al. Cloud point extraction, preconeentrationand spectrophotometric determination of erbium(III)-2-(3,5-dichloro-2-pyridylazo)-5-dimethylaminophenol[J]. Analytica Chimica Acta,1997.342:229-238.
    [78] Endo M, Ishihara M, Yotsuyanagi T. Autoeatalytic decomposition of cobaltcomplexes as an indicator system for the determination of trace amounts ofcobalt and effectors[J]. Analyst,1996,12l:39l-394.
    [79] Mizgunova U, Zolotova G, Dolmanova I. Enzymic method for the determinationof ethanol and methanol with spectrophotometric detection of the rate of theprocess[J]. Analyst,1996.12l:43l-433.
    [80] Dol I, Knochen M, Altesor C. Enhancement of precision and accuracy inderivative spectrophotometry of highly absorbing samples[J]. Analyst,1991,116:69-75.
    [81] Wang N, Liang W, Qi P. Determination of neodymium in rare earth mixtures byfounh-derivative spectrophotometry[J]. Analytica Chimica Acta,199l,254:153-157.
    [82] Oehrle S. Controlled changes in selectivity of cation separations by capillaryelectrophoresis using various crown-ether additives[J]. Journal ofChromatography A,1996,745:87-92.
    [83] Macka M. Haddad P. Determination of metal ions by capillary electrophoresis[J].Electrophoresis,1997,18:2482-2501.
    [84] Alexander J N, Poli J B, Markides K E. Evaluation of automated isocratic andgradient nano-liquid chromatography and capillary electrochmmatography[J].Analytical Chemistry.1999,7l:2398-2409.
    [85] Bourguiguon B, Aguiar P F D, Khots M S, et al. Optimization in irregularlyshaped regions: pH and solvent strength in reversed phase high-performanceliquid chromatography[J]. Analytical Chemistry,1994,66:893-904.
    [86] Kumar K, Sukumaran K V, Tweedle M F. Determination of free gadolinium(3+)as a cyclohexanediaminetetraacetie acid complex by reversed-phase HPLC inionic gadolinium(III)chelates[J]. Analytical Chemistry,1994,66:295-299.
    [87] Sultan S M, Walmsley A D. Chemometrical optimization FIA of perpbenazimassay[J]. Talanta,1998,46:897-906.
    [88] Mayer C, Schalkhammer T, Pittner F. Enzyme-based flow injection analysissystem for glutamine and glutamate in mammalian cell culture media[J].Analytical Biochemistry,1999,268:110-116.
    [89]李俊锋,杨兵,王洪艳.流动注射催化动力学光度法测定碘的研究[J].分析科学学报,2004,20(5):513-515.
    [90]崔鑫,宋雅东,齐建立,等.血液中铅镉分析方法的研究[J].现代仪器,2006,2:50-51.
    [91]肖珊美,陈建荣弘,沈玉勤.双硫腙浊点萃取-石墨炉原子吸收光谱法测定环境水样中痕量铅的研究[J].光谱学与光谱分析,2006,26(5):955-958.
    [92]朱霞石,朱小红,封克,等.浊点萃取-石墨炉原子吸收光谱法测定环境样品中的痕量镉[J].分析化学,2006,34(7):951-954.
    [93]蒋晓凤,赵一先.石墨炉原子吸收光谱法测定大气降水中镉镍铅[J].环境监测管理与技术,2008,20(6):47-48.
    [94]朱霞石,江祖成,李杉,等.以8-羟基喹啉为化学改进剂石墨炉原子吸收光谱测定水和空气尘粒物中铬的研究[J].分析试验室,2002,21(4):13-15.
    [95] Correia P R M. de Oliveira E, Oliveira P V. Elisabeth Simultaneousdetermination of manganese and seleniumin serum by electrothermalatomicabsorption spectrometry[J]. Talanta,2001,57(3):527-531.
    [96] Walsh A. The application of atomic absorption spectra to chemical analysis[J].spectrochimica Acta,1955,7:108-117.
    [97] Koizumi H, Yasuda K. Determination of lead, cadmium and zinc using theZeeman effect in atomic absorption spectrometry[J]. Analitical Chemistry,1976,48:1178-1182.
    [98]石金辉,焦奎,刘天伟.火焰原子吸收光谱法间接测定碘[J].分析化学,1998,26(1):122-122.
    [99] Kirkbright G F, Ward A F, West T S. Atomic emission spectrometry with aninduction-coupled high frequency plasma source. The determination of iodine,mercury, arsenic, and selenium[J]. Analytica Chimica Acta,1973,64(3):353-362.
    [100]王化南,陈瑶,刘志宏,等.提高碘的ICP-AES测定灵敏度的一种进样方法[J].分析测试学报,1994,13(4):71-73.
    [101] Gray A L. Mass spectrometric analysis of solutions using anatmospheric-pressure ion-source[J]. Analyst,1975,100(1190):289-299.
    [102] Houk R S, Fassel V A, Flesch G D, et al. Inductively coupled argon plasma asan ion source for mass spectrometric determination of trace elements[J].Analytical Chemistry,1980,52(14):2283-2289.
    [103] Date A R, Gray A L. Plasma source mass spectrometry using an inductivelycoupled plasma and a high resolution quadrujpole mass filter[J]. Analyst,1981,106:1255-1267.
    [104] Houk R S, Montaser A, Fassel V A. Mass spectra and ionization temperature inan argon inductively coupled plasma[J]. Applied Spectroscopy,1983,37(5):425-428.
    [105] Gray A L, Date A R. Inductively coupled plasma-source mass spectrometryusing continuum-flow ion extraction [J]. Analyst,1983,108(1290):1033-1050.
    [106] Date A R, Gray A L. Development progress in plasma source-massspectrometry[J]. Analyst,1983,108(1283):159-165.
    [107] Date A R, Gray A L. Progress in plasma source-mass spectrometry[J].Spectrochimica Acta Part B-atomic spectroscopy,1983,38(1-2):29-37.
    [108] Houk R S, Fassel V A, Flesh G D, et al. Inductively coupled argon plasma as anion source for mass spectrometric determination of trace elements[J]. AnaliticalChemistry,1980,52(14):2283-2289.
    [109]邵友斌.等离子质谱法在元素分析中的应用[J].岩矿测试,1992,11(1-2):24-26.
    [110] Daniels S L, Arslan Z. Coprecipitation with calcium hydroxide fordetermination of iron in fish otoliths by collision cell ICP-MS[J]. Journal ofMass Spectrometry,2007,5:584-590.
    [111] Dufailly V, Noel L, Guerin T. Optimisation and critical evaluation of a collisioncell technology ICP-MS system for the determination of arsenic in foodstuffs ofanimal origin[J]. Analytica Chimica Acta,2008,2:134-142.
    [112] Wrobel K, Wrobel K, Figueroa J A L, et al. Analytical speciation of mercury infish tissues by reversed phase liquid chromatography-inductively coupledplasma mass spectrometry with Bi3+as internal standard[J]. Talanta,2009,3:706-711.
    [113] Navaza A P, Encinar J R, Ballesteros A, et al. Capillary HPLC-ICPMS andtyrosine iodination for the absolute quantification of peptides using genericstandards[J]. Analytical Chemistry,2009,13:5390-5399.
    [114] Kipphardt H, Matschat R. Purity assessment for providing primary standards forelemental determination-a snap shot of international comparability[J].Microchimica Acta,2008,1-2:269-275.
    [115] Lemes M, Wang F. Methylmercury speciation in fish muscle by HPLC-ICP-MSfollowing enzymatic hydrolysis[J]. Journal of Analytical Atomic Spectrometry,2009,5:663-668.
    [116] Kagawa T, Ohno M, Seki T, et al.Online determination of copper in aluminumalloy by microchip solvent extraction using isotope dilution ICP-MS method[J].Talanta,2009,4:1001-1005.
    [117] Jakubowski N, Dorka R, Steers E, et al. Trends in glow dischargespectroscopy[J]. Journal of Analytical Atomic Spectrometry,2007,7:722-735.
    [118] Matschat R, Hinrichs J, Kipphardt H. Application of glow discharge massspectrometry to multielement ultra-trace determination in ultrahigh-puritycopper and iron: a calibration approach achieving quantification andtraceability[J]. Analytical and Bioanalytical Chemistry,2006,1:125-141.
    [119] Pisonero J, Fernandez B, Gunther D. Critical revision of GD-MS, LA-ICP-MSand SIMS as inorganic mass spectrometric techniques for direct solidanalysis[J]. Journal of Analytical Atomic Spectrometry,2009,9:1145-1160.
    [120] Walke A V. Why is SIMS underused in chemical and biological analysis?[J].Challenges and opportunities Analytical Chemistry,2008,23:8865-8870.
    [121] Pennebaker F M, Jones D A, Gresham C A, et al. Spectroscopic instrumentationin the2lst Century: excitement at the horizon[J]. Journal of Analytical AtomicSpectrometry,1999,13:821-843.
    [122] Olney T N, Chen W, Douglas D J. Gas dynamics of the ICP-MS interface:impact Perssuer porbe measurements of gas flow porfiles[J]. Journal ofAnalytical Atomic Spectrometry,1999,14:9-18.
    [123] Duersch B S, Pattesron J E, Farnsworth P B. The effects of a torch shield onperformance of the vacuum interface of an inductively coupled plasma massspectrometer[J]. Journal of Analytical Atomic Spectrometry,1999,14:615-621.
    [124] Javris K E, Mason P, Platzner T, et al. Critical assessment of the effects ofskimmer cone geometry on spectroscopic and non-spectroscopic interference ininductively coupled Plasma masss spectrometry[J]. Journal of AnalyticalAtomic Spectrometry,1998,13:689-697.
    [125] Vanhaecke F, Wannemacker G, Moens L, et al. Dependence of detector deadtime on analyte mass number in inductively coupled plasma masssspectrometry[J]. Journal of Analytical Atomic Spectrometry,1998,13:567-573.
    [126] Chen Y, Farnsworth P B. Ion deposition experiments as a tool for the study ofthe spatial distribution of analyte ions in the second vacuum stage of aninductively coupled Plasma masss spectrometry[J]. Spectrochim Acta Part B,1997,52:231-239.
    [127] Duersch B S, Chen Y, Ciocan A, et al. Optical measurements of ion density inthe second vacuum stage of an inductively coupled Plasma masssspectrometry[J]. Spectrochim Acta Part B,1998,53:569-579.
    [128] Vanhoe H, Allemeersch F V, Versieck J, et al. Effect of solvent type on thedetermination of total iodine in milk powder and human serum by inductivelycoupled plasma mass spectrometry[J]. Analyst,1993,118(8):1015-1019.
    [129] Stürup S, Bchert A. Direct determination of copper and iodine in milk andpowder in alkaline solution by flow injection inductively coupled plasma massspectrometry[J]. Fresenius Journal of Analytical Chemistry,1996,354(3):323-326.
    [130] Baumann H. Rapid and sensitive determination of iodine in fresh milk and milkpowder by inductively coupled plasma mass spectrometry[J]. Fresenius Journalof Analytical Chemistry,1990,338(7):809-812.
    [131] Allain P, MaurasY, Douge C, et al. Determination of iodine and bromine inplasma and urine byinductively coupled plasma mass spectrometry[J]. Analyst,1990,115(6):813-815.
    [132] Larsen E H, Ludwigsen M B. Determination of iodine in food-related certifiedreference materials using wet ashing and determination by inductively coupledplasmamass spectrometry[J]. Journal of Analytical Atomic Spectrometry,1997,12(6):459-464.
    [133] Cox R J, Pickford C J. Determination of iodine-129in vegetable samples byinductively coupled plasmamass spectrometry[J]. Journal of Analytical AtomicSpectrometry,1992,4:635-640.
    [134] Larsen E H, Ludwigsen M B. Determination of iodine in food-related certifiedreference materials using wet ashing and detection by inductively coupledplasma mass spectrometry[J]. Journal of Analytical Atomic Spectrometry,1997,12(4):435-439.
    [135]李冰,何红蓼,史世云,等.电感耦合等离子体质谱法同时测定地质样品中痕量碘溴硒砷的研究Ⅰ.不同介质及不同阴离子形态对测定信号的影响[J].岩矿测试,2001,20(3):161-166.
    [136]马新荣,李冰,韩丽荣,等.稀氨水密封溶解-电感耦合等离子体质谱测定土壤沉积物及生物样品中的碘、溴[J].岩矿测试,2003,22(3):174-178.
    [137]李杰,钟立峰,崔学军,等. Carius管溶样-标准加入电感藕合等离子体质谱法测定土壤中碘[J].岩矿测试,2006,25(l):19-21.
    [138]黄光明,窦银萍,张静梅,等.电感耦合等离子体质谱法同时测定地下水中硼溴碘[J].岩矿测试,2008,27(1):25-28.
    [139]赵志飞,储溱,方金东,等.电感耦合等离子体质谱法测定湖泊水中痕量溴、碘[J].资源环境与工程,2009,23(3):324-326.
    [140]莫曦明,梁旭霞,陈砚朦,等.电感耦合等离子体质谱法(ICP-MS)测定饮用水中碘元素[J].中国卫生检验杂志,2006,16(10):1179-1180.
    [141] Macours P, Aubry J C, Hauquier B, et al. Determination of urinary iodine byductively coupled plasma mass spectrometry[J]. Journal of Trace Elements inMedicine and Biology,2008,22:162-165.
    [142]牟世芬,刘克纳.离子色谱方法及应用[M].北京:化学工业出版社,2000.
    [143] Liu Y J, Mou S F. Simultaneous determination of trace level bromate andchlorinated haloacetic acids in bottled drinking water by ion chromatography[J].Microchemical Journal,2003,75(2):79-86.
    [144] Willy M, Nico R, Wang W. Analysis of atmospheric aerosols byparticle-induced X-ray emission, instrumental neutron activation analysis, andion chromatography[J]. Nuclear instruments&methods in physics researchsection B-beam interactions with materials and atoms,2011,269(22):2693-2698.
    [145]裴翠锦,姚国光.离子色谱法同时测定地下水中5种阴离子的研究[J].湖北农业科学,2011,50(4):831-832.
    [146]张琢,邵超英,温晓华,等.地下水中钙和镁的离子色谱法同时测定[J].岩矿测试,2010,29(5):621-624.
    [147]杨春英,杭义萍,钟新林.离子色谱法同时测定饮用水中5种消毒剂副产物[J].分析化学,2007,35(11):1647-1650.
    [148] Liu Y J, Mou S F, Chen D Y. Determination of trace-level haloacetic acids indrinking water by ion chromatography-inductively coupled plasma massspectrometry[J]. Journal of Chromatography A,2004,1039:89-95.
    [149]刘勇建,牟世芬,杜兵,等.微波浓缩-离子色谱法测定饮用水中的痕量溴酸根和高氯酸根[J].色谱,2002,20(2):129-132
    [150]张萍,史亚利,蔡亚岐,等.改进的离子色谱法测定环境水样中的高氯酸盐[J].高等学校化学学报,2007,28(7):1246-1250.
    [151]张萍,史亚利,蔡亚岐,等.大体积进样离子色谱法测定环境水样中高氯酸根[J].分析化学,2006,34(11):1575-1578.
    [152]沈敏,冯睿,陈浩,等.离子色谱法同时测定降水中的9种阴离子[J].分析科学学报,2007,23(3):334-336.
    [153]袁东.离子色谱法同时测定雨水中5种阴离子研究[J].安徽农业科学,2010,38(14):7412-7413.
    [154]戴九兰,朱永官,张民.安培检测-离子色谱法测定菠菜伤流液中的碘含量[J].环境化学,2004,2(3):351-352.
    [155]佘小林.离子色谱法快速测定土壤中碘量[J].岩矿测试,2005,24(2):145-147.
    [156]柴成文,刘克纳,牟世芬.安培检测-离子色谱法测定乳品中的微量碘[J].色谱,2001,19(1):94-96.
    [157] Zou H F, Li X L, Zhang Y K, et al. Determination of iodine anion in dried kelpand iodized throat tablets by reversed-phase ion-pair liquid chromatography withdirect UV detection[J]. Chromatographia,1990,30(3-4):228-230.
    [158]潘峰,路菊,孙玮,等.反相离子对色谱法分析交联淀粉碘的碘[J].理化检验-化学分册,2004,40(4):210-212.
    [159] Xu X R, Li H B, Gu J D, et al. Determination of iodate in iodized salt byreversed-phase high performance liquid chromatography with UV detection [J].Chromatographia,2004,60(11-12):721-723.
    [160]吴晓芳,鲁杰.离子色谱法测定矿泉水中的溴和碘[J].中国公共卫生,2000,16(7):598-598.
    [161]林奇,陈立奇,林红梅,等.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-[J].台湾海峡,2010,29(1):135-139.
    [162] Shi H L, Adams C. Rapid IC-ICP/MS method for simultaneous analysis ofiodoacetic acids, bromoacetic acids, bromate, and other related halogenatedcompounds in water[J]. Talanta,2009,79:523-527.
    [163] Luther G W, Swartz C B, Uliman W J. Directdetermination of iodine inseawater by cathodic stripping square wave voltammetry[J]. AnalyticalChemistry,1988,60:1721-1724.
    [164]李吉学,卢洁,骆望美,等.微波消化-阴极溶出伏安法测定尿碘[J].南京军医学院学报,2000,22(1):50-51.
    [165]倪宏刚,郑建斌.示波伏安法测定碘酸钾碘盐中碘[J].理化检验-化学分册,2006,42(7):569-571.
    [166]秦汉明.离子选择性电极测定海带、菜中碘及碘的浸出率[J].化学世界,2002,43(ll):572-573.
    [167]雷艳秋,姚伟东.离子选择电极法测定尿中碘的干扰实验[J].黑龙江环境通报,2005,29(2):41-43.
    [168]蒋文强,吕霞,李关宾.高效毛细管电泳法测定药物中的碘[J].中国医药工业杂志,2000,31(7):314-316.
    [169] Yip Y C, Lam J C W, Tong W F. Commonly used methodologies for inorganicanalysis in international key comparisons[J]. Trends in Analytical Chemistry,2009,2:214-236
    [170] Zeisler R, James W D, Mackey E A, et al. NAA characterization of the newbovine liver SRM[J]. Journal of Radioanalytical and Nuclear Chemistry,2008,3:783-787.
    [171] Nayak P K, Wierczinski B, Lahiri S. Rare-earth elemental analysis of bandediron-formations by instrumental neutron activation analysis[J]. Journal ofRadioanalytical and Nuclear Chemistry,2008,1:179-184.
    [172] Byrne A R, Dermelj M, Tusek-Znidarie M. A study of the iodinated resincolumn for the determination of iodine in biological fluids by radiochemicalneutron activation analysis[J]. Journal of Radioanalytical and NuclearChemistry,1985,91(2):315-322.
    [173] Rao R R, Holzbecher J, Chatl A. Epithermal instrumental neutron activationanalysis of biological reference materials for iodine[J]. Fresenius Journal ofAnalytical Chemistry,1995,352:53-57.
    [174] Dermelj M, Slejkovec Z, Byme A R, et al. Investigation of the quenching ofperoxyoxalate chemiluminescence by amine substituted compounds [J]. Analyst,1992,117(3):443-447.
    [175]刘虎威.气相色谱方法及应用[M].北京:化学工业出版社,2007.
    [176]杨海鹰.气相色谱在石油化工中的应用[M].北京:化学工业出版社,2004.
    [177] Buhberger W, Heubauer U. Selective determination of bromide and iodide inserum and urine by gas chromatography[J]. Microchimica Acta,1989,111(1/2):137-142.
    [178] Wuilloud R G, de Wuilloud J C A, Vonderheide A P, et al. Determination ofiodinated phenol species at parts-per-trillion concentration levels in differentwater samples by solid-phase microextraction/offline GC-ICP-MS[J]. Journalof Analytical Atomic Spectrometry,2003,18:1119-1124.
    [179] Shinonaga T, Gerzabek M H, Strebl F, et al. Transfer of iodine from soil tocereal grains iagricultrual areas of Austria[J]. The Science of the TotalEnvironment,2001,267(1-3):33-40.
    [180] Schwehr K A, Santschi P H. Sensitive determination of iodine species,including organo-iodine, for fresh water and sea water samples using highperformance liquid chromatography and spectrophotometric detection[J].Analytica Chimica Acta,2003,482(1):59-71.
    [181]何红蓼,李冰,杨红霞,等.环境样品中痕量元素的化学形态分析Ⅰ.分析技术在化学形态分析中的应用[J].岩矿测试,2005,24(1):51-58.
    [182]杨景芝,杨世钺.用离子选择性电极法测定尿碘[J].中华预防医学杂志,1992,26(3):176-178.
    [183] Pantsar-Kallio M, Manninen P K G. Speciation of halogenides and oxyhalogensby ion chromatography inductively coupled plasma mass spectrometry[J].Analytica Chimica Acta,1998,360(1-3):161-166.
    [181] Bernhard M, Peter S, Heidi W. Method developments for iodine speciation byreversed-pase liquid chromatography-ICP-MS spectrometry[J]. BiologicalTrace Element Reserch,2000,78(1-3):67-79.
    [182] Bernhard M, Peter S, Heidi W. Iodine speciation in human serum byreversed-phase liquid chromatography-ICP-MS spectrometry[J]. BiologicalTrace Element Reserch,2000,78(1-3):81-91.
    [183]刘崴,杨红霞,李冰,等.高效液相色谱-电感耦合等离子体质谱测定地下水中碘形态稳定性[J].分析化学,2007,35(4):571-574.
    [184] Shah M, Wuilloud R G, Kannamkumarath S S, et al. Iodine speciation studies incommercially available seaweed by coupling different chromatographictechniques with UV and ICP-MS detection[J]. Journal of Analytical AtomicSpectrometry,2005,20:176-182.
    [185] Bhagat P R, Acharya R, Nair A G C, et al. Estimation of iodine in food, foodproducts and salt using ENAA[J]. Food Chemistry,2009,115:706-710.
    [186] Manion B, Ye M, Holbein B E, et al. Quantification of total iodine in intactgranular starches of different botanical origin exposed to iodine vapor at variouswater activities[J]. Carbohydrate Research,2011,346(15):2482-2490.
    [187] Gelinas Y, Krushevska A, Barnes R M. Determination of total iodine innutritional and biological samples by ICP-MS following their combustionwithin an oxygen stream[J]. Analytical Chemistry,1998,70(5):1021-1025.
    [188] Netten C V, Cann S A H, Morley D R, et al. Elemental and radioactive analysisof commercially available seaweed[J]. Science of the Total Environment,2000,255(1-3):169-175.
    [189] Fecher P A, Goldmann I, Nagengast A. Determination of iodine in food samplesby inductively coupled plasma mass spectrometry after alkaline extraction[J].Journal of Analytical Atomic Spectrometry,1998,13(9):977-982.
    [190] Sayuri Kodama, Yoshio Takahashi, Kazu Okumura, et al. Speciation of iodinein solid environmental samples by iodine K-edge XANES: Application to soilsand ferromanganese oxides[J]. Science of the Total Environment,2006,363:275-284.
    [191] Wu D S, Deng H W, Zheng B S, et al. Iodine in Chinese coals and itsgeochemistry during coalification[J]. Applied Geochemistry,2008,23:2082-2090.
    [192] Brown C F, Geiszler K N, Vickerman T S. Extraction and Quantitative Analysisof Iodine in Solid and Solution Matrixes[J]. Anal. Chem.,2005,77:7062-7066.
    [193]金瑞娣.食盐中碘含量的分析测定[J].中国井矿盐,2005,35(1):38-41.
    [194]王彦,薛斌.分光光度法测定食盐中的碘含量[J].辽宁化工,1996,15(1):57-58.
    [195]刘翠格,默丽萍,魏永巨.加碘酸钾食盐中碘含量的紫外分光光度法测定[J].河北师范大学学报(自然科学版),2003,27(5):497-530.
    [196]傅厚暾,赵俐敏,张艳丽.离子色谱分析加碘食盐中的微量碘[J].分析化学,1999,27(6):684-687.
    [197]陈朝晖,董晓莉.离子色谱法测定食盐中的碘含量[J].现代科学仪器,2004,5:65-66.
    [198]范文秀,王泽云.2′,7′-二氯荧光素荧光光谱法测定食盐中的IO3-含量[J].广东微量元素科学,2006,13(3):58-61.
    [199]黄会秋.气相色谱法测定加碘食盐中碘[J].分析检验-食品科学,2002,23(1):122-123.
    [200] Cripps R, Venuat L, Bruchertseifer H. Quick analytical method for thedetermination of iodide and iodate ions in aqueous solutions[J]. Journal ofRadioanalytical and Nuclear Chemistry,2003,256(2):357-360
    [201] Huang Z, Ito K, Andrei R, et al. Speciation studies by capillaryelectrophoresis-simultaneous determination of iodide and iodate in seawater[J].Analytical and Bioanalytical Chemistry,2004,378:1836-1841.
    [202] Huang Z, Ito K, Hirokawa T. Further research on iodine speciation in seawaterby capillary zone electrophoresis with isotachophoresis preconcentration[J].Journal of Chromatography A,2004,1055:229-234.
    [203] Leiterer M, Truckenbrodt D, Franke K. Determination of iodine species in milkusing ion chromatographic separation and ICP-MS detection[J]. European FoodResearch and Technology,2001,213:150-153.
    [204] Chen Z L, Megharaj M, Naidu R. Speciation of iodate and iodide in seawater bynon-suppressed ion chromatography with inductively coupled plasma massspectrometry[J]. Talanta,2007,72:1842-1846.
    [205] Stark H J, Mattusch J, Wennrich R, et al. Investigation of the IC-ICP-MSdetermination of iodine species with reference to sample digestionprocedures[J]. Fresenius Journal of Analitical Chemistry,1997,359(4-5):371-374.
    [206] Leiterer M, Truckenbrodt D, Franke K. Determination of iodine species in milkusing ion chromatographic separation and ICP-MS detection[J]. European FoodResearch and Technology,2001,213(2):150-153.
    [207] Sanchez L F, Szpunar J. Speciation analysis for iodine in milk by size-exclusionchromatography with inductively coupled plasma mass spectrometric detection(SEC-ICP MS)[J]. Journal of Analytical Atomic Spectrometry,1999,14:1697-1702.
    [208] Michalke B, Schramel P. Iodine speciation in biological samples by capillaryelectrophoresis-inductively coupled plasma mass spectrometry[J].Electrophoresis,1999,20(12):2547-2553.
    [209]苏宇亮,吴杰,方黎.离子色谱-电感耦合等离子体质谱联用法同时分析水中碘酸根和碘离子[J].给水排水,2008,34(7):29-31.
    [210] Gammelgaard B, Jùns O. Determination of selenite and selenate in human urineby ion chromatography and inductively coupled plasma mass spectrometry[J].Journal of Analytical Atomic Spectrometry,2000,15:945-949.
    [211] Vanhoe H, Van A F, Versieck J, et al. Effect of solvent type on thedetermination of total iodine in milk powder and human serum by inductivelycoupled plasma mass spectrometry[J]. Analyst,1993,118(8):1015-1019
    [212] Cripps R, Venuat L, Bruchertseifer H. Quick analytical method for thedetermination of iodide and iodate ions in aqueous solutions[J]. Journal ofRadioanalytical and Nuclear Chemistry,2003,562(2):357-360.
    [213] Liebhafsky H A, Roe G M. Detailed mechanism of the dushman reactionexplored by computer[J]. International Journal of Chemical Kinetics,1979,11(7):693-703.
    [214] B’Hymer C, Caruso J A. Evaluation of HPLC systems for the separation andquantification of arsenic compounds from apple extracts[J]. Journal of LiquidChromatography&Related Technologies,2002,25(4):639-653.
    [215] Brandao A C M, Buchberger W W, Butler E C V, et al. Matrix-elimination ionchromatography with postcolumn reaction detection for the determination ofiodide in saline waters[J]. Journal of Chromatography A,1995,706(1-2):271-275.
    [216]向仲朝,廖成华. SE-30弹性石英毛细管色谱柱测定水和食盐中微量碘化物[J].中国地方病防治杂志,1991,6(4):233-234.
    [217]刘颖,于钧,付可为,等.食盐中总碘含量测定方法——溴氧化滴定法[J].中国地方病防治杂志,1999,14(6):329-330.
    [218]郭宇晖,陈希中.气相色谱法测定加碘食盐中的碘[J].福建分析测试,1998,7(4):947-949.
    [219]杨景芝,孙衍华,刘连伟,等.标准加入法快速测定精制食盐中加入的碘[J].山东农业大学学报(自然科学版),2005,36(2):255-257.
    [220]彭寨玉,莫曦明,杨挺立,等.电感耦合等离子体质谱法(ICP-MS)测定尿中碘[J].中国卫生检验杂志,2007,17(11):1946-1949.
    [221]中华人民共和国卫生行业标准. WS/T107-1999尿碘的砷铈催化分光光度测定法[S].中华人民共和国卫生部发布,1999.
    [222]陈清,卢国呈.微量元素与健康[M].北京:北京大学出版社,1989.
    [223]阎玉芹.碘的砷铈催化分光光度测定方法[J].中国地方病防治杂志,1997,16(1):37.
    [224]刘颖,张榕,布伟静,等.顺序注射尿碘测定仪的研制及应用[J].分析化学,2009,37(11):1706-1710.
    [225] Dexter K S, Ward N I. Mobility of heavy metals within freshwater sedimentsaffected by motorway stormwater[J]. Science of the Total Envimnment,2004,334-335:271-277.
    [226]中华人民共和国国家标准. GB/T5750.2-2006生活饮用水标准检验方法水样的采集与保存[S].中华人民共和国卫生部,中国国家标准化管理委员会发布,2007.
    [227]江贵斌.环境样品前处理技术[M].北京:化学工业出版社,2004.
    [228]国家环境保护总局《水和废水监测分析方法》编委会.水和废水监测分析方法[M].第四版,北京:中国环境科学出版社,2002.
    [229]中华人民共和国国家标准. GB/T14581-93水质湖泊和水库采样技术指导
    [S].国家环境保护总局批准,1994.
    [230]中华人民共和国国家标准. GB13580.2-92大气降水样品的采集与保存[S].国家环境保护总局批准,1993.
    [231] Gilfedder B S, Biester H, Petri M. Iodine speciation in rain and snow:Implications for the atmospheric iodine sink[J]. Journal of GeophysicalResearch,2007,112(D7):1-7.
    [232] Gilfedder B S, Petri M, Biester H. Iodine and bromine speciation in snow andthe effect of orographically induced precipitation[J]. Atmospheric Chemistryand Physics,2007,7(10):2661-2669.
    [233] Liebhafsky H A, Roe G M. The detailed mechanism of the Dushman reactionexplored by computer[J]. International Journal of Chemical Kinetics,1979,11(7):693-703.
    [234] Vanloon G W, Duffy S J. Environmental Chemistry[M]. New York: OxfordUniversity Press Inc,2000,239-257.
    [235] Fu P Q, Wu F C, Liu C Q, et al. Spectroscopic characterization and molecularweight distribution of dissolved organic matter in sediment porewaters fromLake Erhai, Southwest China[J]. Biogeochemistry,2006,81:179-189.
    [236] Wu F C, Evans R D, Dillon P J. Rapid quantification of humic and fulvic acidsbu HPLC in natural waters[J]. Applied Geochemistry,2007,22:1598-1605.
    [237] Wu F C, Kothawala D N, Evans R D, et al. Relationships between DOCconcentration, molecular size and fluorescence properties of DOM in astream[J]. Applied Geochemistry,2007,22:1659-1667.
    [238] Wetzel R G. Limnology[M].2nd ed., Philadelphia: Saunders CollegePublishing,1983.
    [239] Hwang S J. Carbon dynamics of plankton communities in nearshore andoffshore Lake Erie: The significance of the microbial loop for higher trophiclevels[D]. Kent: Kent State University,1995.
    [240] Hopkinson C, Cifuentes L. DON subgroup report[J]. Marine Chemistry,1993,41:23-36.
    [241] Kitis M, Kilduff J E, Karanfil T. Isolation of dissolved organic matter(DOM)from surface waters using reverse osmosis and its impact on the reactivity ofDOM to formation and speciation of disinfection by-products[J]. WaterResearch,2001,35:2225-2234.
    [242] Donat J R, Bruland K W. Trace elements in the oceans. In: Salbu B, Steinnes Eeds. Trace elements in natural waters[M]. Boca Raton, FL: CRC Press,1995,247-281.
    [243] Yin Y J, Allen H E, Huang C P, et al. Kinetics of mercury(II) adsorption anddesorption on soil[J]. Environmental Science&Technology,1997,31(2):496-503.
    [244] Gledhill M, Van den berg C M G. Determination of complexation of iron(iii)with natural organic complexing ligands in seawater using cathodic strippingvoltammetry[J]. Marine Chemistry,1994,47(1):41-54.
    [245] Schall C, Heumann K G, Kirst G O. Biogenic volatile organoiodine andorganobromine hydrocarbons in the Atlantic Ocean from42°N to72°S[J].Fresenius Journal of Analytical Chemistry,1997,359:298-305.
    [246] Moore R M, Graszko W. Methyl iodide distribution in the ocean and fluxes tothe atmosphere[J]. Geophysical Research,1999,104(C5):11163-11171.
    [247] Hou X L, Chai C F, Qian Q F, et al. Study on the chemical species of iodine insame seaweeds(I)[J]. Science of the Total Environment,1997,204(3):215-221.
    [248] Hou X L, Yan X J, Chai C F. Study on chemical species of iodine in someseaweed (II) Iodine-bound biological maro-molecules[J]. Journal ofRadioanalytical and Nuclear Chemistry,2000,245(3):461-467.
    [249] Liu Y, Gunten H R. Migration chemistry and behaviour of iodine relevent togeological disposal of radioactive wastes, A literature review with acompilation of sorption data, Paul Scherrer Institute, Switzerland, PSI-16,1988.
    [250] Yasuyuki Muramatsu, Udo Fehn, Satoshi Yoshida. Recycling of iodine infore-arc areas: evidence from the iodine brines in Chiba, Japan[J]. Earth andplanetary science letters,2001,192:583-593.
    [251] Spencer M. Steinberg, Brenda Buck, et al. The speciation of iodine in the saltimpacted Black Butte soil series along the Virgin river, Nevada, USA[J].Applied Geochemistry,2008,23:3589-3596.
    [252]彭永梅.碘与甲状腺疾病[J].现代医药卫生,2002,18(10):864-865.
    [253] Tlruesdale V W, Watts S F, Rendell A R. On the Possibility of iodide oxidationin the near-surface of the Black Sea and its implications to iodine in the generalocean[J]. Deep-Sea Research I,2001,48:2397-2412.

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