The optimum operating conditions providing minimum run-time and running costs have been studied theoretically for a thermal diffusion plant to be used for the enrichment of the radiocarbon isotope from finite sample size.

The calculations are based on a simple approximate model of the enrichment process, regarding the isotope separation column as operating under quasi-stationary state conditions. The temporal variation of the isotope accumulation is given by a single exponential term. From comparison with the numerical solution of the separation tube equation, approximate models of this simple type appear hardly sufficient for analytical work but seem well suited for optimization calculations. For column operation not too close to the equilibrium state, the approximate run-times were found accurate within 0.2 d.

The approximate model has been applied to a column of the concentric type, operated on gaseous methane. Cross-section configuration and temperatures were not varied (hot and cold wall radii: 2.0 and 2.6cm, respectively; hot and cold wall temperatures: 400°C and 14°C, respectively). The column transport coefficients used were derived from measurements. Run-time was minimized by optimizing both the operating pressure and the sample collection mode for different total sample size (range studied: 24 to 100 g), mass of enriched sample (1.8, 2.4, and 3.0 g), enrichment factor (12, 15, and 20) and column length (8 to 18 m). Optimum working pressures are between 1 and 2 atm. Usually, about 90 percent of the enriched sample mass is extracted favorably from the column itself, the length of the sampling section being about 2.5 to 5 m. Typical runtimes are between 3 days and 2 weeks, and isotope yield may reach 90 percent.

Optimum operating conditions have also been calculated for other column configurations reported in literature and are compared with the experimental results.

Accelerator mass spectrometry radiocarbon (AMS 14C) dating was used for determining the age of wedge ice. It has been found that between 11,270 and 6420 cal BP, or the Greenlandian and Northgrippian stages of the Holocene, ice wedges grew syngenetically in sandy deposits with gravel in the Chara River valley. The variations of δ18O values in the ice wedges are about 8‰, from –25.5‰ to –18.8‰. Based on the stable isotope composition of ice wedges, paleotemperature reconstructions revealed that the mean January temperature was as low as –38°C during the coldest periods of the early half of the Holocene and as high as –28°C during the warmer periods.

We report on an initial long-term study of dissolved inorganic and organic carbon (DIC) from Sabino Creek, located in Sabino Canyon, Pima County, Arizona. The purpose of this study was to monitor changes in dissolved radiocarbon (14C) with time and to understand the processes contributing to these variations. Our results span the period 2009–2016 and show a mixing trend between dissolved inorganic and organic carbon modern end-members with an older component. This study provides preliminary information for more detailed research on recycling of organic components in this stream system.

The accelerator mass spectrometry (AMS) facility at Seoul National University (SNU-AMS) was accepted in December 1998 and results reported first at the Vienna AMS conference in October 1999 and at the 17th Radiocarbon Conference in Israel, June 2000. At the Vienna conference, we reported our accelerator system and sample preparation systems (Kim et al. 2000). Recent developments of the AMS facility have been regularly reported at AMS conferences (Kim et al. 2001, 2004, 2007). Meanwhile, about 1000 unknown archaeological, geological, and environmental samples have been measured every year. In this report, the archaeological and geological data carried out in 2002 are presented in terms of years BP (before present, AD 1950), following the SNU-AMS date lists I and II published in Radiocarbon (Kim et al. 2006a,b).

We present an overview of the beginning and early years of radiocarbon dating in Russia. Achievements of several major scholars in this field from Leningrad (St. Petersburg), Moscow and Novosibirsk are briefly described. The existing and closed Russian laboratories are also mentioned.

The understanding of the 14C behavior in waste packages could lead, in the Spanish context, to a revision of the management strategies for radioactive waste and a revaluation of the near surface repository devoted to the disposal of waste containing this radionuclide in high concentrations. To achieve this objective, and in the context of the EU project Carbon-14 Source Term (CAST), the authors of the work presented in this paper have performed leaching experiments with irradiated graphite considering two different scenarios. One, in which the leaching solution simulates some of the expected conditions in a repository where a granite/bentonite mixture has been used as backfill material, and the other, using deionized water as a high efficiency chemical removal agent and for comparison purposes. The analytical approach to measure the release rate and speciation of 14C from irradiated graphite samples in the aqueous and gaseous phase is also described. The main results obtained shows that, after 359 days of leaching, no 14C activity was detected above the detection limits, and only leaching rates regarding beta-gamma emitters were observed: 2×10–6 cm/day for 137Cs and 1×10–5 cm/day for 60Co in granite/bentonite water media and 4×10–6 cm/day for 137Cs in pure water.

The radiocarbon concentration of dissolved inorganic carbon in groundwater is most logically and completely represented as the product of 5 time-variable factors; these are mutually independent, and all must be considered and evaluated to determine a groundwater residence time. In the case of one factor, the 14C/(12C+13C) ratio of atmospheric CO2, its time variability can be side-stepped by assuming it to be constant at the pre-bomb 1950 value, and assigning an apparent half-life in the radioactive decay term. Apparent half-lives are calculated here for 5 separate periods extending back to 24,000 BP, working from the INTCAL98 atmospheric calibration. This approach can be extended further back in time when the necessary atmospheric calibrations are updated with greater certainty. The procedure is applied to the recently-explored Wairau Deep Aquifer, underlying central areas of the coastal Wairau Plain, Marlborough. The evolution of dissolved inorganic carbon concentration for this river-recharged groundwater is apparent from distinct trends in 13C, and is confirmed by hydrochemical modelling. Extension to the 14C concentrations yields minimum/maximum limits for groundwater residence times to 3 wells. In all 3 cases, the maximum is uncertain due to present uncertainty of the apparent half-life applicable before 24,000 BP. Residence times for the 2 wells closest to the recharge area are at least 17,400 yr, while that for a well further down the aquifer is at least 38,500 yr. Recharge, therefore, occurred during the Otiran glaciation, while the present-day near-surface fluvioglacial deposits of the Wairau Plain were accumulating. Drawdown-recovery records over 3 yr indicate a permeable connection to compensating recharge, enabling limited exploitation for vineyard irrigation.

The chemical form of 14C released from irradiated stainless steel is a key parameter in the safety assessment of the subsurface disposal system in Japan. In this study, to identify the chemical form of the released carbon, unirradiated stainless-steel powders, which were found to be water-atomized powders with a silicon oxide film, were immersed in NaOH and HCl solutions under low-oxygen conditions for approximately 25 days. The results showed that the main chemical forms of the carbon were colloidal carbon in the NaOH solution and colloidal carbon and formic and acetic acids in the HCl solution. Almost no hydrocarbons were detected in both solution systems. Concerning the source of the colloidal carbon and carboxylic acids, the hypothesis that carbon in the oxide layer is released is considered to be reasonable. The very small amounts of hydrocarbons generated prevented us from discussing the source of the hydrocarbons. To validate the hypothesis and obtain further information on the hydrocarbons, additional experiments are necessary. In particular, for long-term safety assessment, it is important to determine whether the colloidal carbon, carboxylic acids and hydrocarbons are continuously released during the corrosion process. Therefore, information on the temporal evolution of the carbon should be obtained.

This article discusses radiocarbon dating results of documents preserved at the Central Library of the University of Tehran (hereafter, CLUT) as part of the project “Irankoran.” The paper adds new evidence to an ongoing campaign of dating Qurʾāns and Oriental manuscripts by the Corpus Coranicum Project. The dated manuscripts include one kūfī fragment of the Qurʾān on parchment (no. 10950) and a selection of Islamic and Persian manuscripts, all from the second millennium: the Arabic dictionary Muǧmal al-Luġah (Meškāt no. 203), the medical encyclopedia Ḏaḫīrah-ye Kh w ārazmšāhī (no. 5156), the epic Panǧ Ganǧ of Neẓāmī (no. 5179), the book of wisdom Ādāb al-Falāsifah (no. 2165) attributed to Ḥunayn b. Isḥāq (d. 873 CE), and one of the oldest extant manuscripts of the Avesta Wīdēwdād (no. 11263). Although the authenticity of their colophons is disputed, radiocarbon dating supports the dates of the colophons; even in cases where they were suspected of being tampered with, they most likely present the accurate original dates of the corresponding manuscripts. Only in the case of Ādāb al-Falāsifah (no. 2165), radiocarbon dating of the parchment has identified the manuscript as non-authentic. Inconsistent carbon dating results of two samples taken from Ḏaḫīrah-ye Khwārazmšāhī (no. 5156) and Panǧ Ganǧ (no. 5179) provide evidence of later replaced/added leaves.

The Chair, Renee Kra, opened the Workshop with the announcement that the IRDB will be officially located at the Geosciences Department, University of Arizona, Tucson, and will begin operating on January 2, 1989.

Museum collections are extremely valuable sources of material for ongoing research, although the conservation history of some objects is not always recorded, which can be problematic for chemical analyses. While most contamination is removed using the acid-base-acid treatment, this may not be the case for cross-linked contamination. The XAD resin protocol was implemented at the radiocarbon (14C) laboratory in the Muséum national d’Histoire naturelle, and the setup was tested using known age bone samples and a consolidated Palaeolithic bone. Known age samples were consolidated with shellac or Paraloid, aged for a month, treated with or without the XAD resin and 14C dated. Bone blank results showed that XAD resin was able to remove shellac, which was not the case for the ABA-only method. Results from VIRI I were more variable and VIRI F was possibly too young to show the effects of the consolidants. Two 14C dates on the Palaeolithic bone after XAD treatment are statistically the same, while a sample without XAD treatment was significantly older, suggesting that the contaminant was not fully removed by the ABA-only treatment. This study demonstrates the potential of the XAD treatment to clean heritage bone samples stored in museums prior to geochemical analyses.

The accelerator mass spectrometry facility at Seoul National University (SNU-AMS) began functioning in December 1998 and was first reported at the Vienna AMS conference in October 1999 and at the 17th Radiocarbon Conference in Israel in June 2000. At the Vienna conference, we reported our accelerator system (Kim et al. 2000) and the basic sample preparation system (Lee et al. 2000), including the combustion line to produce CO2; the catalytic reduction line for the graphitization of CO2; and also pretreatment procedures for wood, charcoal, and peat samples. Recent progress of the AMS facility (Kim et al. 2001) and extension of the sample pretreatment system to iron and bone samples were reported at the 17th Radiocarbon Conference (Cheoun et al. 2001). In the meantime, extensive testing of accuracy and reproducibility has been carried out, and ∼1000 unknown archaeological and geological samples have been measured every year. A report of data carried out in 1999 is presented by Kim et al. (this issue). In this report, the archaeological, geological, and environmental data carried out in 2000 are presented in terms of yr BP.

In this paper, we discuss how the radiocarbon dating of soot on oil lamps can help determine the chronology of the Jewish catacombs of Rome. We also explore the ramifications of our work for the typological study of Roman period terracotta lamps.