TY - JOUR
T1 - Direct analysis of cotton swipes for plutonium isotope determination by microextraction-ICP-MS
AU - Manard, Benjamin T.
AU - Metzger, Shalina C.
AU - Rogers, Kayron T.
AU - Ticknor, Brian W.
AU - Zirakparvar, N. Alex
AU - Roach, Benjamin D.
AU - Bostick, Debra A.
AU - Hexel, Cole R.
N1 - Publisher Copyright:
© The Royal Society of Chemistry.
PY - 2021/10
Y1 - 2021/10
N2 - This study demonstrates a method for determining the isotopic composition of low-level (sub-pg) plutonium (Pu) directly from a cotton swipe. Environmental sample (ES) swipes are routinely employed as a tool for monitoring activities in nuclear facilities. Traditional ES swipe analysis, as employed in nuclear safeguards, utilizes laborious ashing, digestion, and chemical separation procedures prior to mass spectrometric (MS) analysis. Here, an innovative sample introduction technique employing a microextraction probe to extract Pu directly from the swipe surface is described. The microextraction probe lowers onto the swipe surface, seals on a small area (8 mm2), and delivers solvent (2% HNO3) to extract actinide material that may be present. The extracted analyte is subsequently directed into a sector field inductively coupled plasma (ICP)-MS for isotope ratio determination. This microextraction-ICP-MS method successfully determined the isotopic composition (240Pu/239Pu and 242Pu/239Pu) of three Pu certified reference materials (CRM 136, 137, and 138) that were deposited (1 pg) onto ES swipes. The percent relative difference from the certified value, uncorrected for instrumental fractionation, was <2% for the 240Pu/239Pu ratio on all three CRMs and <10% for the 242Pu/239Pu ratio on CRM 136 and 138. The percent relative standard deviation, an estimate of the sample-to-sample isotopic precision, was <4% for the 240Pu/239Pu and <15% for the 242Pu/239Pu. Method limits of detection were determined, based on measurements of an enriched 244Pu material, to be ∼7 fg. Additionally, a mixed uranium (U) and Pu deposition was made to determine the method's ability to simultaneously extract U and Pu and determine the isotopic composition of both analytes.
AB - This study demonstrates a method for determining the isotopic composition of low-level (sub-pg) plutonium (Pu) directly from a cotton swipe. Environmental sample (ES) swipes are routinely employed as a tool for monitoring activities in nuclear facilities. Traditional ES swipe analysis, as employed in nuclear safeguards, utilizes laborious ashing, digestion, and chemical separation procedures prior to mass spectrometric (MS) analysis. Here, an innovative sample introduction technique employing a microextraction probe to extract Pu directly from the swipe surface is described. The microextraction probe lowers onto the swipe surface, seals on a small area (8 mm2), and delivers solvent (2% HNO3) to extract actinide material that may be present. The extracted analyte is subsequently directed into a sector field inductively coupled plasma (ICP)-MS for isotope ratio determination. This microextraction-ICP-MS method successfully determined the isotopic composition (240Pu/239Pu and 242Pu/239Pu) of three Pu certified reference materials (CRM 136, 137, and 138) that were deposited (1 pg) onto ES swipes. The percent relative difference from the certified value, uncorrected for instrumental fractionation, was <2% for the 240Pu/239Pu ratio on all three CRMs and <10% for the 242Pu/239Pu ratio on CRM 136 and 138. The percent relative standard deviation, an estimate of the sample-to-sample isotopic precision, was <4% for the 240Pu/239Pu and <15% for the 242Pu/239Pu. Method limits of detection were determined, based on measurements of an enriched 244Pu material, to be ∼7 fg. Additionally, a mixed uranium (U) and Pu deposition was made to determine the method's ability to simultaneously extract U and Pu and determine the isotopic composition of both analytes.
UR - http://www.scopus.com/inward/record.url?scp=85116913391&partnerID=8YFLogxK
U2 - 10.1039/d1ja00255d
DO - 10.1039/d1ja00255d
M3 - Article
AN - SCOPUS:85116913391
SN - 0267-9477
VL - 36
SP - 2202
EP - 2209
JO - Journal of Analytical Atomic Spectrometry
JF - Journal of Analytical Atomic Spectrometry
IS - 10
ER -