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May 31, 2012 - ACS Software. Anal. Chem. , 1993, 65 (17), pp 758A–758A. DOI: 10.1021/ac00065a735. Publication Date: September 1993. ACS Legacy ...
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FOCUS on surfaces. Other uses include the determination of atmospheric com­ p o s i t i o n c h a n g e s t h a t took place thousands of years ago as well as the a b i l i t y to t r a c k t h e m o v e m e n t of ocean currents and the effects of glo­ bal warming. These applications were p r e s e n t e d in a n oral session t h a t followed Davis' plenary lecture. "It's as though you h a d reinvented scintillation counting," Davis said. W h y is t h e i n s t r u m e n t a t i o n so large? "You can think of an accelera­ tor m a s s spectrometer as a tandem mass spectrometer, in the center of which someone has inserted a 1000fold gain in energy," Davis said. A Cs sputtering ion source produces nega­ tive ions, a n d a l o w - e n e r g y m a s s s p e c t r o m e t e r deflects t h e d e s i r e d m a s s fraction into t h e accelerator. The ions are accelerated to 7 χ 10 6 eV in the center of the machine, stripped to remove m o l e c u l a r i s o b a r s , a n d passed through a high-energy mass spectrometer. The negative ion beam mass fraction t h a t is selected alter­ n a t e s between m a s s e s for the r a r e and the stable isotopes before accel­ eration. After p a s s i n g t h r o u g h t h e high-energy mass spectrometer, the stable isotope ions are integrated as a current, whereas ions for the rare i s o t o p e — w i t h energies o f - 1 9 - 8 1 MeV, d e p e n d i n g on t h e i s o t o p e — pass through a magnetic filter to a gas ionization counter w h e r e they are determined redundantly. AMS h a s been developed most completely to date for 10 Be, 1 4 C, 26 A1, 36 C1, 4 1 Ca, and 1 2 9 I. The gargantuan i n s t r u m e n t a t i o n used at Livermore can determine rare-to-stable isotope ratios for all of these, but this kind of flexibility d e m a n d s changes in Cs s p u t t e r i n g source p a r a m e t e r s , ion optics, and chemical suppression of isobars for each isotope. This much instrumentation is neither practical n o r n e c e s s a r y for m o s t r o u t i n e analyses in a r e a s such as biomedicine, where perhaps only 14 C or 4 1 Ca m i g h t be used. Davis said p r i v a t e c o m p a n i e s a r e developing a d e d i ­ cated 14 C tandem accelerator for bio­ medical experiments that has a foot­ print of ~ 8 χ 12 ft. and a projected cost o f - $ 7 5 0 , 0 0 0 . Most of Wednesday was devoted to the ASMS business meeting. But to start things off, Ron Hites of Indiana University at Bloomington presented an e n t e r t a i n i n g plenary lecture on applications of MS to environmental science, followed by Christie Enke's 1993 ASMS Award lecture. Hites described the use of continu­ ous-flow fast a t o m b o m b a r d m e n t M S / M S to d e t e r m i n e w h e t h e r t h e

758 A • ANALYTICAL CHEMISTRY, VOL. 65, NO. 17, SEPTEMBER 1, 1993

process a t a w a s t e w a t e r t r e a t m e n t plant was breaking down and remov­ ing alkylbenzenesulfonate detergents effectively. "It's the first FAB spec­ trum of 'Fab', " he quipped. Although some of the detergents were removed in the first stage of t r e a t m e n t , t h e quantity of longer chain detergents rose in the second stage because they were adsorbed onto solids and recy­ cled. Other examples of MS for envi­ r o n m e n t a l i n v e s t i g a t i o n s included electron capture negative ionization MS, used to determine the temporal trends of dioxin deposition from the atmosphere to lake sediments, and the detection of Triton nonionic de­ t e r g e n t s in P h i l a d e l p h i a d r i n k i n g water. This study helped to convince t h e city's w a t e r a u t h o r i t y to stop t a k i n g water into the system when the Delaware River tide was coming in from downstream, where a sewage plant was located. This year's 1993 ASMS Award for a Distinguished Contribution in Mass S p e c t r o m e t r y was p r e s e n t e d jointly to Christie Enke of Michigan S t a t e U n i v e r s i t y in E a s t L a n s i n g a n d Rick Yost of the U n i v e r s i t y of Florida in Gainesville for the devel­ o p m e n t of t h e t r i p l e q u a d r u p o l e mass spectrometer. Enke and Yost announced their in­ vention in a short communication in the Journal of the American Chemical Society in 1978. Prior to that, the only tandem mass spectrometers had been electrostatic and magnetic sec­ tor instruments. The new spectrome­ t e r u s e s two quadrupoles for m a s s a n a l y s i s of p r e c u r s o r a n d product ions, respectively, with a third qua­ drupole between t h e m for collision» ally induced dissociation of selected precursors from the ionization source (see Anal. Chem. 1979, 51, 1251 A 1264 A). In his award lecture, Enke described the process of developing t h e triple quadrupole t a n d e m m a s s spectrometer with Yost at Michigan State University and stressed the importance of selecting an interme­ d i a t e process t h a t would m a k e t h e two mass separations truly orthogo­ nal. Research a w a r d s w e n t to S u s a n Graul of C a r n e g i e - M e l l o n Univer­ sity and Robert Levis of Wayne State University. Nominations are being sought for t h e 1994 ASMS Award, which will be presented at the 42nd Conference, May 2 9 - J u n e 3, 1994, at the Hyatt Regency Hotel in Chicago. Those interested in making a nomi­ nation for the award may contact J u ­ dith Sjoberg, ASMS, 815 Don Gaspar Ave., Santa Fe, NM 87501; 505-9894517. Deborah Noble