کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1683556 | 1518750 | 2010 | 4 صفحه PDF | دانلود رایگان |

36Cl AMS measurements at natural isotopic concentrations have yet been performed only at tandem accelerators with 5 MV terminal voltage or beyond. We have developed a method to detect 36Cl at natural terrestrial isotopic concentrations with a 3-MV system, operated above specifications at 3.5 MV.An effective separation was obtained with an optimized split-anode ionization chamber design (adopted from the ETH/PSI Zurich AMS group), providing a suppression factor of up to 30,000 for the interfering isobar 36S. Despite the good separation, a relatively high sulfur output from the ion source (36S−/35Cl− ≈ 4 × 10−10 for samples prepared from chemically pure reagents), and a possibly cross contamination resulted in a background corresponding to 36Cl/Cl ≈ 3 × 10−14. The method was applied to samples containing between 105 and 106 atoms 36Cl/g rock from sites in Italy and Iran, which were already investigated by other laboratories for surface exposure dating. The 36Cl/Cl ratios in the range from 2 × 10−13 to 5 × 10−12 show a generally good agreement with the previous results.These first measurements demonstrate that also 3-MV tandems, constituting the majority of dedicated AMS facilities, are capable of 36Cl exposure dating, which is presently the domain of larger facilities.
Journal: Nuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms - Volume 268, Issues 7–8, April 2010, Pages 744–747