Measuring (210) Pb by accelerator mass spectrometry: a study of isobaric interferences of (204,205,208) Pb and (210) Pb.

RATIONALE: The measurement of (210) Pb provides an assessment of the risk an individual faces of developing lung cancer as a result of their exposure to radon and radon decay products. Existing radiometric techniques are not sensitive enough to detect (210) Pb in many exposures. This report describes the further development of a method of measuring (210) Pb using Accelerator Mass Spectrometry (AMS). METHODS: (204,205,208,) (210) Pb measurements were performed by AMS. Samples were prepared from stock solutions of (204) Pb, (205) Pb, (208) Pb and (210) Pb and measured by making PbF3 (-) ions at the IsoTrace AMS facility using a SIMS-type Cs(+) sputter source. Potential interferences in Pb(3) (+) isotope measurement and the overall efficiency of Pb beam production were determined experimentally. RESULTS: (204) Pb and (205) Pb suffer from molecular and atomic isobaric interferences that cannot be removed without sacrificing the efficiency of (210) Pb measurements whereas (208) Pb suffers from no interferences. The abundance sensitivity of (210) Pb/(208) Pb was 1.3 × 10(-12) . Keeping the (210) Pb/(208) Pb spike below this level resulted in a detection limit of 4.4 mBq of (210) Pb using the IsoTrace AMS facility. CONCLUSIONS: This study identified key interferences in the measurement of PbF3 (-) → Pb(3) (+) ions and demonstrated a new AMS method to measure (210) Pb. This new AMS technique is about five times more sensitive than gamma and beta spectroscopy measurements of (210) Pb and the measurement time is much shorter. Copyright © 2016 John Wiley & Sons, Ltd.

Detection of (135) Cs by accelerator mass spectrometry.

RATIONALE: The ability to measure both (135) Cs and (137) Cs can provide an estimate of the age and source of Cs isotopes in an environmental sample. Accelerator mass spectrometry (AMS) consistently reports lower abundance sensitivities than other techniques and, with the addition of an on-line reaction cell, simpler isobaric suppression. Therefore, an AMS methodology was developed to measure Cs isotopes using CsF2- as the initial anion. METHODS: The ion beam is passed through the Isobar Separator for Anions (ISA) where it is captured by radiofrequency quadrupoles in a gas cell before injection into the tandem accelerator. In the ISA, the beam reacts with O2 gas, selectively removing the BaF2- and leaving the Cs analyte to be reaccelerated and sent through the remainder of the AMS system. RESULTS: The BaF2- signal was attenuated by a factor of 10(5) in the ISA while 25% of the original CsF2- current was transmitted into the accelerator. (135) Cs was measured without any interference from (133) Cs to an abundance sensitivity of 1.3 × 10(-10) . The abundances of four stable Ba isotopes (masses 133, 134, 135 and 137) were measured and no isotope-dependent bias was detected using the ISA in vacuum. CONCLUSIONS: The results demonstrate the feasibility of measuring long-lived Cs isotopes without Ba interference by AMS with on-line isobar separation and the ability to use shorter lived Cs isotopes for yield tracing.

Extraction of (129)I and (127)I via combustion from organic rich samples using (125)I as a quantitative tracer.

Iodine-129 ((129)I) is a biophilic, naturally occurring radioisotope (half-life: 1.57 × 10(7) years) that has been released in large quantities by nuclear fuel reprocessing. This iodine has cycled throughout the globe and chiefly the northern hemisphere and can be found in a wide variety of environmental materials, particularly organic rich soil and organic matter. Extracting iodine reliably from solid samples has been done by a variety of methods, however, pyrohydrolysis has been the most widely used. There is a wide variation between existing pyrohydrolysis techniques and this raises questions about the quantitative recovery of iodine from method to method. In order to quantify iodine recovery from pyrohydrolysis we have spiked samples with an iodine-125 radiotracer prior to combustion and trapping in an alkaline solution. Inorganic (125)I tracer was used as well as humic acid labeled with (125)I to simulate the behavior of (129)I and (127)I in complex organic substances and extract iodine regardless of how it is partitioned. Using these tracers we explored the effect on recovery of (125)I under a variety of combustion parameters. These include carrier gas flow rate and iodine volatilization temperature. We observed that the best recoveries of (125)I were at flow rates between 400 and 800 mL/min and most (125)I recoveries were above 85%. The experiment to determine the temperature at which iodine volatilizes from the sample showed two distinct trends for the release of iodine. One trend showed that most iodine is released at approximately 525 °C, while the other trend showed that the samples needed to reach 800 °C and remain there for at least an hour. These findings illustrate the usefulness and importance of using a quantitative recovery tracer for every iodine extraction. We then combusted and precipitated several Atlantic Ocean seaweed and standard reference materials for AMS analysis as AgI. The (129)I concentration of the seaweed ranged between 4.4-5.5 × 10(9) atoms/g and the (129)I/(127)I ratio was 2.3-2.9 × 10(-9), both of which compare well to published values for Atlantic seaweed. The results for the standard reference materials also agree with specified values indicating that this technique is reliable. By optimizing pyrohydrolysis conditions and testing the recovery of iodine with a (125)I tracer it is possible to quantify and maximize recovery from organic samples. This will allow for the investigation of variations in the (129)I concentration and (129)I/(127)I ratio with a high degree of precision in complex, organic rich samples.

On-line HfF5(-)/WF5(-) separation in an O2-filled radiofrequency quadrupole gas cell.

RATIONALE: An experimental Isobar Separator for Accelerator Mass Spectrometry (ISAMS) instrument has been used to demonstrate an on-line separation of HfF5(-) from its isobar WF5(-). This is necessary, in addition to sample preparation chemistry, for measuring (182)Hf at natural levels by Accelerator Mass Spectrometry (AMS). METHODS: The device utilizes a radiofrequency quadrupole (RFQ) controlled gas cell, wherein anion-gas reactions at eV energies attenuate the interfering isobars of the analyte molecular anions, leaving HfF5(-) for AMS analysis. The RFQ also helps to control the multiple scattering resulting from the ion-gas collisions. RESULTS: O2 gas was used in the HfF5(-)/WF5(-) separation and WF5(-) was attenuated by nearly 3 orders of magnitude while maintaining ~75% transmission of HfF5(-). It is expected that the transmission and attenuation can be increased by further research. CONCLUSIONS: This result advances the possibility of detecting natural (182)Hf when AMS is supplemented with an isobar separator in the injection system.

Mass spectrometry with accelerators.

As one in a series of articles on Canadian contributions to mass spectrometry, this review begins with an outline of the history of accelerator mass spectrometry (AMS), noting roles played by researchers at three Canadian AMS laboratories. After a description of the unique features of AMS, three examples, (14)C, (10)Be, and (129)I are given to illustrate the methods. The capabilities of mass spectrometry have been extended by the addition of atomic isobar selection, molecular isobar attenuation, further ion acceleration, followed by ion detection and ion identification at essentially zero dark current or ion flux. This has been accomplished by exploiting the techniques and accelerators of atomic and nuclear physics. In 1939, the first principles of AMS were established using a cyclotron. In 1977 the selection of isobars in the ion source was established when it was shown that the (14)N(-) ion was very unstable, or extremely difficult to create, making a tandem electrostatic accelerator highly suitable for assisting the mass spectrometric measurement of the rare long-lived radioactive isotope (14)C in the environment. This observation, together with the large attenuation of the molecular isobars (13)CH(-) and (12)CH 2(-) during tandem acceleration and the observed very low background contamination from the ion source, was found to facilitate the mass spectrometry of (14)C to at least a level of (14)C/C ~ 6 × 10(-16), the equivalent of a radiocarbon age of 60,000 years. Tandem Accelerator Mass Spectrometry, or AMS, has now made possible the accurate radiocarbon dating of milligram-sized carbon samples by ion counting as well as dating and tracing with many other long-lived radioactive isotopes such as (10)Be, (26)Al, (36)Cl, and (129)I. The difficulty of obtaining large anion currents with low electron affinities and the difficulties of isobar separation, especially for the heavier mass ions, has prompted the use of molecular anions and the search for alternative methods of isobar separation. These techniques are discussed in the latter part of the review.

[Therapy of monosymptomatic nocturnal enuresis in childhood and adolescence: what is the evidence?]. / Therapie der monosymptomatischen Enuresis im Kindes- und Jugendalter--Was ist gesichert?

Nocturnal enuresis (bedwetting) is one of the most frequent urological symptoms in children, affecting about 20% of five year olds. It is a heterogeneous disorder with a whole variety of etiologic factors (genetic, endocrinological, neurobiological), particularly a dysfunction of the lower urinary tract. Despite the prevalence of enuresis many questions regarding the complex pathophysiological mechanisms remain unanswered. While nocturnal enuresis per se is clearly not a disease, psychosocial problems have been reported in up to 40% of affected children. Management strategies comprise behavioural and pharmacological approaches, either in isolation or combined. Although expectations were high, especially with pharmacological interventions, the results are usually disappointing with high recurrence rates. Extensive analyses of the available literature on the efficacy of enuresis treatment modalities reveal a poor quality of many trials with a whole range of methodological flaws. Therefore, further comparative studies of adequate methodological quality are needed.

Characterization of the NIST seaweed Standard Reference Material.

The National Institute of Standards and Technology (NIST) Standard Reference Material (SRM) for seaweed was developed through an interlaboratory comparison with 24 participants from 16 countries. After evaluating different techniques to calculate certified values for the radionuclides, the median method was found to be the most representative technique. The certified values were provided for 13 radionuclides and information values were given for 15 more radionuclides. Results for the natural decay series showed disequilibrium in both the uranium and thorium series.

[Adrenalectomy within the scope of tumor nephrectomy--overtreatment?]. / Adrenalektomie im Rahmen der Tumornephrektomie--ein Overtreatment?

Metastatic spread to the ipsilateral adrenal gland occurs in 1.2-10% of patients with renal cell carcinoma (RCC). In the majority of these cases, the primary tumor is locally advanced with poor differentiation, venous invasion, and involvement of the regional lymph nodes. Adrenal metastases are usually detected preoperatively by CT scan or MRI. Adrenal metastases are indicators of systemic disease with poor prognosis quo ad vitam. Only 0.5-2.3% of patients with RCC and adrenal metastases are free of venous invasion or lymphatic disease. In this small subset of patients, cure is possible by surgical removal of the adrenal gland. In 97.7-99.5% of patients with RCC, ipsilateral adrenalectomy has no impact on their prognosis. We therefore conclude that this procedure should be performed only if there is radiological suspicion of an adrenal mass.