共查询到19条相似文献，搜索用时 250 毫秒
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为科学评价测量结果的可靠性,对海水中137Cs γ能谱分析方法的不确定度进行了评估。根据《化学分析中不确定度的评估指南》,分析不确定度的来源并逐一对各不确定度分量进行了量化,最终计算了合成相对标准不确定度。结果表明,影响海水中137Cs γ能谱测量不确定度的因素分别为样品源137Cs峰区计数、标准源活度、取样体积、化学回收率、本底137Cs峰区计数及标准源137Cs峰区计数,其中样品源137Cs峰区计数的不确定度贡献最为突出。对于137Cs活度浓度为1.28 mBq/L的海水样品,其合成相对标准不确定度为9.78%。 相似文献
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2011-03-11日本福岛核电站放射性物质发生泄漏事件,本研究基于MASNUM(Laboratory of Marine Science and Numerical Modeling)海洋环流模式,建立了西北太平洋海洋放射性物质输运扩散模式,对事故释放的~(137)Cs在海洋中的输运和扩散过程进行了20a的模拟与预测。根据与观测资料的比较,验证了所建立的模式具备模拟放射性物质在海洋中的输运扩散过程的能力。结果显示:至2015年,~(137)Cs表层活度浓度已经扩散至整个中国海域,活度浓度值在0.01Bq/m~3左右;事故发生10a后,研究海域~(137)Cs表层活度浓度趋于均匀,为0.20~0.60Bq/m~3左右;20a后,~(137)Cs在海洋表层的活度浓度要小于0.15Bq/m~3。垂向扩散的结果显示:事故发生10a后,黄海海域~(137)Cs垂向分布较为均匀,东海东部陆架海域活度浓度高于西部海域,且上层海水中~(137)Cs活度浓度高于底层海水,南海北部海域~(137)Cs活度浓度高于南部海域,且略小于黄海和东海;至2030年,中国近海~(137)Cs的活度浓度的垂向分布趋于均匀,南海略高于黄海和东海;日本海~(137)Cs活度浓度主要集中在表层,最大活度浓度出现在2016年,约为0.20Bq/m~3;西北太平洋海域~(137)Cs活度浓度要高于其他4个海域;2030年以后,整个海域~(137)Cs活度浓度在水平和垂向分布均趋于均匀,均小于0.15Bq/m~3。 相似文献
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离线固相萃取螯合富集分离-ICP-MS测定海水中的稀土元素 总被引：1，自引：0，他引：1
通过测定条件优化、方法比对等实验建立了一种固相萃取小柱离线螯合富集分离电感耦合等离子体质谱仪测定海水中稀土元素的方法。海水样品通过调节p H后,进入VAC ELUT SPS24 Agilent圆形固相萃取装置,其主要基体物质的去除率高于97%;萃取富集的优化条件是海水样品p H 4.0~7.0,海水进入萃取柱速率2 m L/min,硝酸洗脱液浓度为1 mol/L;方法对稀土元素的加标回收率为83%~108%,14种稀土元素的检出限为0.057~0.613 ng/L,RSD10%;该方法与氢氧化铁共沉淀法富集稀土元素比对测定结果一致,方法具有准确度与精密度高、操作简便快速等优点,可用于海水样品中稀土元素的定量精确测量。 相似文献
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根据2000年6月10～14日在浙江省西沪港采集的海水样品,利用AA-800石墨炉原子吸收分光光度技术和阳极溶出伏安法测定样品中重金属铜的含量,获得铜在海水中受不同的有机配体控制.不同粒级的铜表观配位容量表明西沪港海水过孔径1.00μm微孔膜的(ACuCC)较高,为144.4nmol/dm3;过0.40和0.20μm滤膜的(ACuCC)分别为103.0和102nmol/dm3;铜的有机配体条件稳定常数的对数值在7.25～9.14之间.铜的总量为21.72nmol/dm3.铜全部为稳定溶解态,其中pH2酸溶态占95.0%,强有机结合态占5.0%.溶解态铜中有机结合态占过滤海水中总铜的61.6%. 相似文献
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海水中丙烯酸的高效液相色谱法建立及应用 总被引：2，自引：0，他引：2
建立了一种测定海水介质中丙烯酸的高效液相色谱法。采用耐纯水相和较低pH的Agilent SB-Aq-C18柱(100 mm×4.6 mm i.d.,5 μm), 0.35%磷酸溶液(pH=2)为流动相,使用紫外检测器,检测波长为210 nm,外标法定量测定。丙烯酸的保留时间在14.2~ 14.9 min,方法的检出限为4 nmol/dm3(S/N=3),在0.01~10 μmol/dm3的范围内均有良好的线性关系,相关系数可达0.999 6,加标回收率为95.4%~98.1%,相对标准偏差为1.3%~1.6%(1.04~2.32 μmol/dm3)。采用0.2 μm滤膜重力过滤冷藏的办法来保存海水丙烯酸样品。检测出2011年5月份青岛近海海水中丙烯酸的平均浓度为(0.101±0.069) μmol/dm3;海洋微藻球形棕囊藻在整个生长周期内培养体系中丙烯酸的浓度为0.339~2.219 μmol/dm3。 相似文献
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若干南极环境样品的放射性 总被引：2，自引：0，他引：2
本文观测比较了第六次南极考察采集的样品和190年采集的中国近海样品的放射性。结果表明,南极海洋沉积物的天然核素、~(137)Cs与中国近海沉积物一样均处于正常的波动范围,并有明显的沉积现象;南大洋表层海水的总β放射性比中国近海海水的少17%～52%;南极地衣对总β放射性的浓集系数达1.3×10~3～2.3×10~3,茎、果实是浓集放射性的关键器官,对~(137)Cs的浓集量达17.5Bq/kg(干),为中国近海海洋植物的8～14倍。 相似文献
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利用螺旋藻富集碘的实验 总被引：5，自引：0，他引：5
本文研究了碘化钾 (KI)对极大螺旋藻 (Spirulinamaxima)生长的影响以及碘在细胞中的富集作用 .结果表明 :在 0～ 40 0mg/dm3范围内 ,KI对螺旋藻的生长没有明显的抑制作用 ,在较低的含量内甚至有一定的促进作用 .极大螺旋藻的最高KI耐受范围在 40 0 0～ 50 0 0mg/dm3之间 .螺旋藻细胞中的碘含量与培养液中外加的KI含量有一定的关系 ,在KI添加含量为 90 0mg/dm3时 ,螺旋藻的收获量 (2 77.1 7mg/dm3)比对照组 (1 0 4.47mg/dm3)增加 1 65%,藻细胞碘含量[0 .3 3 1× 1 0 -2 (m/m) ]比对照组 [0 .0 2 5× 1 0 -2 (m/m) ]增加约 1 2倍 . 相似文献
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A novel approach to in situ extraction of Cs radionuclides from seawater is described which offers many advantages over previous methods. Cesium (stable and radioactive) is partially stripped from seawater as it passes in series through a tandem cartridge consisting of twin beds of ion exchange resin impregnated with cupric ferrocyanide. It is demonstrated that, when seawater passes through this cartridge at a constant flow-rate, collection efficiencies of each bed are the same, allowing the calculation of the seawater Cs nuclide concentration. The cartridge is made of inexpensive, readily available, PVC pipe fittings and is easily deployed under various field conditions. Procedures are described for resin preparation and desorption and radiochemical purification of the collected Cs. Thousands of liters of seawater can be stripped of Cs in this way, permitting substantial improvement in the sensitivity of measurement of 134Cs and 137Cs. 相似文献
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良好的环境质量是厦门成为一个宜居和滨海旅游城市的重要基石。自日本福岛核事故发生和福建省核电站陆续运行之后,厦门邻近海域潜在的核污染风险受到公众和管理部门的关注。本研究测定了2015年2月和8月厦门邻近海域海水和海洋沉积物中主要放射性核素的含量水平,并据此评价了该海域的环境放射性质量状况。结果表明海水中总铀、90Sr、226Ra、137Cs处于我国海洋放射性水平变化范围以内,无明显季节差异,其他放射性核素58Co、60Co、134Cs、110mAg、59Fe、54Mn、65Zn均未检出,海水中90Sr和137Cs的活度最大值远低于国家海水水质标准限值,海洋沉积物中放射性核素活度水平亦在我国海洋放射性水平变化范围以内。利用我国现有的海洋放射性环境质量评价方法对厦门邻近海域放射性质量状况进行分级评价得出其海水放射性质量为2级,海洋沉积物放射性环境质量为1级,均属于安全级别。研究结果表明2015年在厦门附近海域未观测到放射性污染现象。 相似文献
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历次核试验进入海洋的~(137)Cs对中国近海影响的模拟研究 总被引：1，自引：0，他引：1
1945年以来,世界各主要核国家进行了数千次核试验,这些核试验产生的绝大部分放射性物质通过多种途径进入海洋,对海洋环境造成放射性污染。本文建立了一个准全球海洋的放射性物质输运和扩散数值模式,通过数值模拟手段评估了历史核试验释放的放射性物质137 Cs对中国近海海洋环境的影响。本文借助前人工作评估了核试验释放137Cs进入海洋的途径和总量;通过比较模拟结果与观测资料,表明本文建立的放射性物质模式能够较好地模拟出137Cs在中国近海及其邻近海域的分布情况和随时间演变特征;模拟结果表明中国近海里的137Cs浓度在20世纪50年代中期达到最大,其中吕宋海峡海域137Cs浓度最高,达80.99Bq/m3;进一步分析了2011年3月份日本福岛核事故前中国近海137Cs浓度分布状况,2011年整个中国近海137Cs浓度介于1.0~1.6Bq/m3间,且其浓度垂向分布较均匀,相对封闭的南海浓度略高于其他海域。 相似文献
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The transfer of 137C3, 60Co along Platymonas sp., Brachionus plieatilis Muller and Tilapia mos-sambica Peters was studied by using the tracer methods of both 137C3 and 60Co with Ge (Li) Gamma ray detector and S-80 type multichannel-analyser for measuring the radioactivity of the sample. The experiment was carried out in four groups and the period of the experiment was fifteen days. It was found that 60Co could be transferred along seawater→Platymonas→Brackionus→Tilapia, and that 137C3 could only be transferred from seawater to Platymonas. 137C3 was not accumulated by Brachionus in any group of the experiment. Brachionus ingested 60Co mainly from Platymonas, when 60Co was ingested by Tilapia; Brachionus played an important role in the transfer and the Tilapia ingested 137C3 mainly from seawater. 相似文献
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Transfer rule of 137C3 and 60Co in seawater and an arrificial food web which made up of Platy-monas, Arca, tenaeus and Tilapia were studied.The results showed that the transfer of nuclide could be realized in a longer food chain in which seawater contained radioactivity, the transfer along food chain alone was slight, the pathway of nuclide uptaken by organism was mainly from seawater,but the pressnce of the food was helpful to the transfer of the nuclide, the transfer efficiency of 60Co by every member in the marine food chain was greater than that of 137C3. 相似文献
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A method for the determination of nanomolar concentrations of orthophosphate in oligotrophic seawater developed by Liang et al. (2007) has been modified to make it fully feasible for shipboard application and for faster sample throughput with minimized
sample volume. The technique is based on the flow injection method with solid phase extraction on a Sep-Pak C18 cartridge
and colorimetric detector. The Schlieren effect was minimized by rinsing the cartridge sequentially with 5 mL water and 2
mL 95% ethanol solution. With three micro pumps in parallel, savings of up to 80% in amount of reagents and 25% volume of
seawater samples could be achieved in comparison to the previous method. Variation of stopped flow time and sample loading
time gave 3 different standard curves, which corresponded to 3 linear ranges within 3.4 and 515 nM. The modified method permits
the analysis of samples over a wide range of concentrations, and has been successfully applied to shipboard determination
of trace orthophosphate in more than 200 seawater samples during a one-month cruise in the South China Sea. For seawater at
concentrations of 20.6, 82.5, 206.2 nM orthophosphate, the relative standard deviations (RSD) (n = 6), determined daily for 6 days on board ship were 4.45%, 4.73% and 6.75%, respectively. Five seawater samples collected
in the Station SEATS (South East Asia Time Series Station at 18°N, 116°E) were analyzed using the present method both on board
and in a land-based laboratory, as well as with the magnesium hydroxide-induced coprecipitation (MAGIC) method, and showed
no significant difference according to the statistical t-test. 相似文献
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Arrigo A. Cigna 《Ocean Science Journal》2006,41(4):261-290
The concentrations of man made radionuclides in surface seawater since early ′60s are here reported as measured in Italy and
Japan. Most of the data refers to90Sr and137Cs, but occasionally the concentrations of89Sr and134Cs in some Italian samples are also given. The main sources of man made radionuclides were the global fallout produced by
the nuclear weapon tests and the Chernobyl accident. The respective contributions to the contamination of surface seawater
around both countries are discussed. 相似文献
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The influence of several operational parameters, including pH, flow rate, total volume of water passed, and choice of eluants, upon the efficiency of extraction of organic matter from seawater by two forms of commercially-available resin, XAD-2 and XAD-8, is considered. The overall efficiency of adsorption is at best 40%. The main factor determining the adsorption efficiency of XAD resin for natural organic matter is pH. The efficiency at normal seawater pH is only half that at pH 2.0. Although the efficiency decreases with increasing flow rate, the decrease is not great up to 3 bed vol./min. With increasing volume of water passed, the adsorption capacity of the resin initially drops, but reaches an approximately constant level after 1000 bed volumes. Alkaline solutions, either NH4OH or NaOH, followed by methanol, completely recover adsorbed organic material from the resin. There is no significant advantage of XAD-8 over XAD-2 for seawater extractions, and the materials adsorbed by the two forms of resin are not substantially different.A new separation method combining XAD-2 resin and activated carbon as adsorbents in series in a column has been developed. Efficiencies of up to 90% were obtained in the extraction of acidified seawater. When the volume of water passed was less than 500 bed volumes, the adsorption as measured by UV-oxidation was quantitative. Elution of 90–100% of the adsorbed organic carbon was possible when ammonium hydroxide (7 M), methanol and an ammonium hydroxide—methanol mixture were used sequentially. 相似文献