Cesium-137 concentrations, trends, and sources observed in Kuwait City, Kuwait

As part of the development support for the Comprehensive Nuclear-Test-Ban Treaty (CTBT), the Prototype International Data Center (PIDC) has been processing radionuclide data since 1995. Radionuclide data received from field stations includes gamma-ray spectra, meteorological data, and state of health (SOH) information. To date over 20 radionuclide monitoring stations have transmitted data to the PIDC. The radionuclide monitoring system collects both aerosol and gas samples. Gamma-ray spectral analysis is performed on the samples to determine if they contain anthropogenic radionuclides indicative of nuclear debris. A key radionuclide monitored by this system is ¹³⁷Cs. Due to the half-life of ¹³⁷Cs (30.17 y), amounts of this radionuclide releases are still present in the soil and atmosphere as a result of past nuclear tests and reactor releases. ¹³⁷Cs from these sources are routinely detected in the prototype CTBT radionuclide monitoring system. Out of the multiple stations that contribute data to the PIDC, the highest ¹³⁷Cs activity concentrations and largest range of concentrations are observed at the Kuwait City, Kuwait station. A special study was conducted to investigate the concentrations, trends, and origin of ¹³⁷Cs in the Kuwait aerosol. This study combines over four years worth of aerosol data, meteorological data and soil sample analysis to explore this matter.     

Temporal evolution of lead isotope ratios and metal concentrations in sediments of the north Aegean Sea,in Turkish coast

In present research, fifteen surficial and two profile sediment samples were studied in terms of sediment chronology and pollution degree on the ground of pollution indexes such as enrichment factor (EF), contamination factor (CF), Pollution Load Index (PLI) and lead isotope ratios (²⁰⁶Pb/²⁰⁷Pb, ²⁰⁸Pb/²⁰⁶Pb). Lead-210 (polonium-210) activity concentrations were measured by utilizing alpha spectrometry. Sediment chronology was determined via modified CRS mathematical model. Average mass accumulation rates are 0.301 and 0.227 g cm^?2 year^?1 in Bak?rçay River mouth and Ayval?k offshore stations respectively. Mass accumulation rates do not display the systematic increases along the cores from bottom layers to top layers. In Bak?rçay River mouth station ²¹⁰Pb flux is higher than the range of global atmospheric ²¹⁰Pb flux value. Due to the high CF and EF values of Sr both of stations have hydrothermal features. Ayval?k offshore station has displayed Na, Cd pollution since 1945, but Na, Cd, As, Mo, Ag pollutions have existed in Bak?rçay River mouth station since 1983 in terms of CF and EF values. According to PLI index, Bak?rçay River mouth station has “starting level pollution” degree and it displayed an “acute corruption” in 1981. ²⁰⁶Pb/²⁰⁷Pb ratios range from 1.17 to 1.25, ²⁰⁸Pb/²⁰⁶Pb ratios range from 1.99 to 2.16 in study area. When ²⁰⁶Pb/²⁰⁷Pb and ²⁰⁸Pb/²⁰⁶Pb ratios are evaluated with together, it is seen that both of the stations have had the natural (geologic) sediments since 2011.     

Design of air quality monitoring networks and its application to NO2 and O3 in Cordova, Spain

Air monitoring networks are necessary to assess air quality in order to reduce pollution to levels which minimise harmful effects on human health and the environment. This paper describes a method to design air quality monitoring networks for nitrogen dioxide and ozone and its application in Cordova, Andalusia, southern Spain. The city has a population of 325,453 inhabitants and traffic is its main source of air pollution. The first step of this method made it possible to determine from historical data that two control stations for NO₂ and one control stations for O₃ are necessary according to the legislation. Sampling campaigns with passive diffusion samplers at 81 sites were then carried out to obtain information on the pollution distribution in Cordova. The sampling campaigns in 2001–2002 revealed an average concentration of 19.5 μg/m³ for NO₂ with maximum values up to 28.6 μg/m³ in Cordova city centre. The average ozone concentrations were recorded downwind from the emission source, reaching 91.8 μg/m³; the average ozone value in Cordova was 65.3 μg/m³. After spatial interpolation of the obtained values with Geographical Information Systems, a selection of the best locations for the monitoring stations was made, in line with the macro- and microscale siting requirements of the European Directive 2008/50/EC on ambient air quality and cleaner air for Europe. A second sampling campaign with diffusive samplers was carried out in 2007 to control if the locations of the air quality assessment stations were still representative for their zone.     

Variation of <Superscript>231</Superscript>Pa, <Superscript>230</Superscript>Th and <Superscript>231</Superscript>Pa<Subscript>ex</Subscript>/<Superscript>230</Superscript>Th<Subscript>ex</Subscript> in surface sediments of the Sabah–Sarawak coastal waters

Protactinium and thorium activities were measured in eight surface sediment taken in 2004 to determine effectiveness scavenging of ²³¹Pa at Sabah–Sarawak coastal waters. The result found that activity ratios of ²³¹Pa_ex/²³⁰Th_ex were ranged from 0.07 to 0.13 at all sampling stations. The high ²³¹Pa_ex/²³⁰Th_ex activity ratio than the production ratio of 0.093 in seawater at station SR 01, SR 02, SR 04, SB 02 and SB 05, revealed that ²³¹Pa is effectively removed from the water column into the sediment in comparison with ²³⁰Th at those stations. Low percentage of ²³⁰Th_ex (90–95%) in comparison with ²³¹Pa_ex at all stations can be attributed to less efficiently scavenged of ²³⁰Th onto particles prior deposited at the marine sediment bed.     

Naphthalene dianhydride based selective detection targetable fluorescent probe for monitoring exogenous Iron in living cells

A green emissive PET operating fluorescent turn-on cell permeable novel probe R1 has been successfully developed and utilized for the detection of Fe⁺³ in the pure aqueous system at sub-nanomolar level. Moreover, probe R1 demonstrate highly sensitive and selective towards Fe⁺³ over the other divalent and trivalent metal ions and was established by using fluorescence spectroscopy. The efficiency and aid of R1 was demonstrated by the fluorescence imaging of captured Fe⁺³ within Pollen grains by using fluorescence microscopy. These results indicate that, this is the first fluorescent turn-on PET probe to detect sub-nanomolar Fe⁺³ in the pure aqueous system and in cellular level.     

Source term estimation using air concentration measurements during nuclear accident

The focus of this paper is locating and quantifying the diffusion source of ¹³⁷Cs by using observation data collected from monitoring stations. The estimation method is firstly tested in synthetic experiments and then verified with real ¹³⁷Cs concentration data of Fukushima accident. An atmospheric dispersion simulation system is used to support particle diffusion model. Besides, ridge regression is applied to calculate release rate. In terms of location estimation, posterior function of the source location can be deduced according to Bayesian inference. particle swarm optimization (PSO) method is implemented to locate diffusion source.     

Electrochemical evaluation of avidin-biotin interaction using N-iodoacetyl-N-biotinylhexylenediamine

The avidin-biotin assay was investigated by an electrochemical procedure based on the chemical reaction between cysteine containing a thiol group and N-iodoacetyl-N-biotinylhexylenediamine (IB). In the presence of avidin and biotin this reaction, whereby the thiol group combines with IB, is controlled because IB has a biotin part; that is, avidin and biotin are detected indirectly by measurement of iodide ion or cysteine. To achieve a high sensitivity of detection, Hg(II) was introduced as a marker that interacts with cysteine and the oxidation peak from Hg(0) to Hg(II) was measured. The sensitivity of detection of avidin was at the level of 10⁻⁹ M. The relative standard deviation at 1 × 10⁻⁸ M avidin was 4.8% (n = 5). On the other hand, a response curve to detect biotin was obtained by the competitive reaction between IB and biotin for the limited binding sites of avidin. The change in peak current enables the detection of biotin at the level of 10⁻⁹ M. This method has the advantage that it is not necessary to separate free IB from bound IB.     

BeF-Emissionsbanden im induktiv gekoppelten plasma

In this study we try to detect metal fluoride bands in the inductively coupled plasma. BeF¹ provided the most intense spectra with a head at 300.99 nm. Maximum intensity of BeF¹ was found under the following conditions: high carrier gas flow, low power level and low observation height above the load coil. The detection limit of fluoride by means of molecular emission was 400 mg l^?1.     

A colorimetric squaraine-based probe and test paper for rapid naked eyes detection of copper ion (II)

A colorimetric probe N,N’-bis(2-methoxy-ethyl)-2,3,3-trimethyl-3H-squaraine (MOESQ) with H₂O solubility was synthesized to detect Cu²⁺. MOESQ exhibits good selectivity, high sensitivity and fast UV-Vis response toward Cu²⁺ over other competing ions in CH₃CN. The detection limit of MOESQ for Cu²⁺ in CH₃CN can reach 1.88?×?10^?7?molL^?1. By adsorbing MOESQ on the chromatography paper, a colorimetric test paper for Cu²⁺ was prepared, which could detect Cu²⁺ with the color change from blue to faint yellow even in the limit of detection concentration of 10^?6?molL^?1.     

Radioactivity distribution of thorium in sediment core of the Sabah-Sarawak coast

Thorium activity concentrations were measured in seven marine sediment cores taken from Sabah-Sarawak coast on 2004 by using a gravity box corer. Collected sediments were generally homogenous mud which contained much more mixture of silt and clay compared to sand and relatively low content of organic carbon (i.e. less than 5% at all sampling stations). The results found that activity concentrations of ²³⁰Th, ²³²Th and ratios of ²³⁰Th/²³²Th were ranged from 6.5–20.4 Bq/kg dry wt., 6.8–27.8 Bq/kg dry wt. and 0.69–0.92, respectively. It seem that, ²³²Th activity concentrations are slightly higher than ²³⁰Th at all sampling stations and both radionuclides were generally high at Sabah compared to Sarawak coastal waters. ²³⁰Th activity concentrations in sediment core appear to be correlated with the activity concentrations of ²³²Th at some sampling station. These indicating both radionuclides were supplied from the same of environment and source origin of detrital from terrestrial and shallower water. The low ²³⁰Th/²³²Th activity ratio which is less than unity suggesting that ²³²Th was actively and rapidly regenerated compared to ²³⁰Th from ²³⁴U. It also can be attributed to less efficiently scavenge of ²³⁰Th onto particles prior deposited at the marine sediment bed.     

Analysis of Nascent Rotational Energy Distributions and Reaction Mechanisms of the Gas‐Phase Radical–Radical Reaction O(3P)+(CH3)2CH→C3H6+OH

This paper reports on the gas‐phase radical–radical dynamics of the reaction of ground‐state atomic oxygen [O(³P), from the photodissociation of NO₂] with secondary isopropyl radicals [(CH₃)₂CH, from the supersonic flash pyrolysis of isopropyl bromide]. The major reaction channel, O(³P)+(CH₃)₂CH→C₃H₆ (propene)+OH, is examined by high‐resolution laser‐induced fluorescence spectroscopy in crossed‐beam configuration. Population analysis shows bimodal nascent rotational distributions of OH (X²Π) products with low‐ and high‐N′′ components in a ratio of 1.25:1. No significant spin–orbit or Λ‐doublet propensities are exhibited in the ground vibrational state. Ab initio computations at the CBS‐QB3 theory level and comparison with prior theory show that the statistical method is not suitable for describing the main reaction channel at the molecular level. Two competing mechanisms are predicted to exist on the lowest doublet potential‐energy surface: direct abstraction, giving the dominant low‐N′′ components, and formation of short‐lived addition complexes that result in hot rotational distributions, giving the high‐N′′ components. The observed competing mechanisms contrast with previous bulk kinetic experiments conducted in a fast‐flow system with photoionization mass spectrometry, which suggested a single abstraction pathway. In addition, comparison of the reactions of O(³P) with primary and tertiary hydrocarbon radicals allows molecular‐level discussion of the reactivity and mechanism of the title reaction.     

Radiometric dating of sediment records in Kuwait’s marine area

Six sediment cores collected from the Northwestern Arabian/Persian Gulf have been radiometrically dated by ²¹⁰Pb. Three cores were collected from stations within the Kuwait Bay, and three others were collected from stations outside the bay. Two models have been used for ²¹⁰Pb dating of sediment cores, i.e. Constant Flux: Constant Sedimentation (CF:CS) Model and the Constant Rate of Supply (CRS) Model. The average rates were found to vary significantly between 0.16 and 1.00 cm y^?1 for stations outside and within the bay respectively. The variability of the sedimentation rate was essentially physiographic characteristics and variable hydrodynamic condition. In this study, ¹³⁷Cs fallout radiotracer was also used to construct a realistic chronology. It was observed that the ¹³⁷Cs in the entire vertical profile has been continuously contributed by fluvial and atmospheric deposition.     

Air quality monitoring network design to control nitrogen dioxide and ozone, applied in Malaga, Spain

Air monitoring networks are necessary to assess air quality in order to reduce pollution to levels which minimize harmful effects on human health and the environment. This paper describes a method to design or optimize air quality monitoring networks for nitrogen dioxide and ozone and its application in Malaga, a medium large city located in Andalusia, southern Spain, with traffic being the main source of air pollution. The completion of this method revealed that the old assessment network in Malaga was badly designed and made it possible to determine that one traffic-orientated and one background control station were necessary for NO₂ assessment in Malaga, as well as two control stations for O₃. First the number of stations necessary is obtained from historical data. Sampling campaigns with passive diffusion samplers at 74 sites were then carried out to obtain information on the pollution distribution in Malaga. The average concentrations found for NO₂ and O₃ were 22.8 μg/m³ and 64.3 μg/m³ respectively. Maximum values of up to 42.2 μg/m³ NO₂ were found in Malaga city centre and O₃ reached 91.5 μg/m³ downwind from the emission source. After spatial interpolation of the obtained values with Geographical Information Systems, a selection of the best locations for the monitoring stations was made, in line with the macro- and microscale siting requirements of the European Directive 2008/50/EC on ambient air quality and cleaner air for Europe.     

Spectra edited by relative signs of homonuclear couplings of low abundance nuclei

The proposed homonuclear coupling sign edited (HCSE) experiment can detect signed homonuclear couplings between low abundant nuclei like ¹³C, ²⁹Si and ¹⁵N in linear spin systems, that is, in systems where two nuclei are coupled by the measured coupling, and one of them is coupled by a second coupling to a nucleus of different kind. The third nucleus is usually high abundant hydrogen. Two spectra are measured during the HCSE experiment. Their weighed sum and difference yield two other spectra, one containing peaks coupled only by positive measured couplings and the other having peaks coupled by negative measured couplings. The usual E.COSY‐type experiment requires all three couplings in the three spin system (triangular spin system) and not only two couplings as the HCSE experiment. The experiment was successfully tested on known carbon–carbon and silicon–silicon two bond couplings. A set of six simple siloxanes with |²J(Si‐O‐Si)| couplings ranging from 0.5 to 9.0 Hz was measured for the first time, and all the couplings were found to be positive. Copyright © 2012 John Wiley & Sons, Ltd.     

226Ra, 228Ra and 228Ra/226Ra in surface marine sediment of Malaysia

Surface sediment samples were collected at the West (east coast and west coast of Peninsular Malaysia) and East (Sabah and Sarawak) Malaysia in several expeditions within August 2003 until June 2008 for determining the level of natural radium isotopes. Activity concentrations of ²²⁶Ra and ²²⁸Ra in surface marine sediment at 176 sampling stations were measured. The activity concentrations of both radionuclides in Malaysia (East and West Malaysia) display varied with the range from 9 to 158 Bq/kg dry wt. and 13 to 104 Bq/kg dry wt., respectively. Meanwhile, the ratio distributions of ²²⁸Ra/²²⁶Ra were ranged from 0.62 to 3.75. This indicated that the ratios were slightly high at west coast of Peninsular Malaysia compared to other regions (east coast of Peninsular Malaysia, Sabah and Sarawak). The variation of activity concentrations of ²²⁶Ra and ²²⁸Ra and its ratios were also supported by the statistical analyses of one-way ANOVA and t test at 95 % confidence level, whereby there were proved that the measured values were different between the regions. These different were strictly related to their half-life, potential input sources (included their parents, ²³⁸U and ²³²Th), parent’s characteristic, the geological setting/formation of the study area, environment origin and behavior.     

Innovative concept for a major breakthrough in atmospheric radioactive xenon detection for nuclear explosion monitoring

The verification regime of the comprehensive test ban treaty (CTBT) is based on a network of three different waveform technologies together with global monitoring of aerosols and noble gas in order to detect, locate and identify a nuclear weapon explosion down to 1 kt TNT equivalent. In case of a low intensity underground or underwater nuclear explosion, it appears that only radioactive gases, especially the noble gas which are difficult to contain, will allow identification of weak yield nuclear tests. Four radioactive xenon isotopes, ^131mXe, ^133mXe, ¹³³Xe and ¹³⁵Xe, are sufficiently produced in fission reactions and exhibit suitable half-lives and radiation emissions to be detected in atmosphere at low level far away from the release site. Four different monitoring CTBT systems, ARIX, ARSA, SAUNA, and SPALAX? have been developed in order to sample and to measure them with high sensitivity. The latest developed by the French Atomic Energy Commission (CEA) is likely to be drastically improved in detection sensitivity (especially for the metastable isotopes) through a higher sampling rate, when equipped with a new conversion electron (CE)/X-ray coincidence spectrometer. This new spectrometer is based on two combined detectors, both exhibiting very low radioactive background: a well-type NaI(Tl) detector for photon detection surrounding a gas cell equipped with two large passivated implanted planar silicon chips for electron detection. It is characterized by a low electron energy threshold and a much better energy resolution for the CE than those usually measured with the existing CTBT equipments. Furthermore, the compact geometry of the spectrometer provides high efficiency for X-ray and for CE associated to the decay modes of the four relevant radioxenons. The paper focus on the design of this new spectrometer and presents spectroscopic performances of a prototype based on recent results achieved from both radioactive xenon standards and air sample measurements. Major improvements in detection sensitivity have been reached and quantified, especially for metastable radioactive isotopes ^131mXe and ^133mXe with a gain in minimum detectable activity (about 2 × 10^?3 Bq) relative to current CTBT SPALAX? system (air sampling frequency normalized to 8 h) of about 70 and 30 respectively.     

Implementation and Characterization of a femto-Farad Capacitive Sensor for pico-Liter Liquid Monitoring

An fF-level capacitive sensor, intended for pL liquid measurements, has been fabricated with MEMS technology and successfully characterized. The sensor measures liquid level variations in a microfluidic channel. The sensor’s capacitance varies from 1.5 fF (channel empty) to 12.8fF (channel filled with 63 pL of water). To reliably detect such small capacitance changes, a low noise measurement system, based on a lock-in amplifier, was implemented. The measured sensitivity of the system is 14.1 mV/fF, and the capacitance detection limit is 0.057 aF/Hz^1/2, which corresponds to a volumetric resolution of about 0.22 fL/Hz^1/2.     

Separation and purification and beta liquid scintillation analysis of 151Sm in Savannah River Site and Hanford Site DOE high level waste

This paper describes development work to obtain a product phase of ¹⁵¹Sm pure of any other radioactive species so that it can be determined in US Department of Energy high level liquid waste and low level solid waste by liquid scintillation b-spectroscopy. The technique provides separation from mCi/ml levels of ¹³⁷Cs, Pu a- and ²⁴¹Pu b-decay activity, and ⁹⁰Sr/⁹⁰Y activity. The separation technique is also demonstrated to be useful for the determination of ¹⁴⁷Pm.     

Fast‐response Electrochemical Detection of Trinitrotoluene at Sub‐ppb Levels on Nitrogenized Porous Carbon Spheres

We present sub‐ppt level detection of explosive trinitrotoluene by constructing a fast‐response electrochemical sensor using nitrogenized porous carbon spheres (NPCS). NPCS with nitrogen doping and amino functionalization accelerates charge transfer and trinitrotoluene accumulation. A high sensitivity of 60.2 μA cm^?2 ppb^?1 and a detection limit of 0.15 ppb are achieved on NPCS, among the best of recently reported trinitrotoluene electrochemical sensors. Moreover, response time of NPCS is greatly reduced by two times comparing with nitrogen‐free sample. NPCS also offers high selectivity, repeatability and stability, rendering new opportunities to fast detect trinitrotoluene for home security and environment protection.     

The dynamics of a novel method coupling high-performance liquid chromatography with resonance Rayleigh scattering

The dynamics of a novel method coupling high‐performance liquid chromatography (HPLC) with resonance Rayleigh scattering (RRS) is presented in the paper. The method was employed in the detection of fluoroquinolones (FQs) of urine samples from healthy human beings, by forming ion‐association complexes between the components separated from HPLC and [Ce(OH)₃]⁺ as the molecular recognition probe. The RRS signal was measured at λ_ex=λ_em=365 nm. It was applied to detect three FQs and obtained satisfactory results. The RRS spectral characteristics of the analytes and the kinetics of flow rate, proportion of organic phase, reaction time and the aggregation level of ion‐association complexes were investigated, which provided a new basis for the development of the hyphenated techniques. It was established that the presence of HPLC‐RRS would open up a new field in the determination of analytes in the absence of UV or fluorescence.