Jd. Romick et al., AUTOMATION OF THE GAMMA-RAY SPECTROSCOPY COUNTING SYSTEM AT THE DOW-CHEMICAL-COMPANY ANALYTICAL-SCIENCES-LABORATORY, Nuclear instruments & methods in physics research. Section A, Accelerators, spectrometers, detectors and associated equipment, 353(1-3), 1994, pp. 393-396
The neutron activation analysis group within the Analytical Sciences L
aboratory analyzes 3000-5000 samples annually for a wide variety of an
alytes. Due to the high sample load, it is imperative that the gamma s
pectroscopy counting system be automated to maximize the efficiency of
the system while ensuring the accuracy of the analyses. Using a Zymar
k robotic system, Compumotor drives, and DEC-based Canberra/Nuclear Da
ta software we have automated sample changing, detector positioning, a
nd data acquisition. Automation of these functions has resulted in a m
ore consistent counting geometry, minimized crosstalk between samples,
and accurate repositioning of the detectors for standardless quantita
tive analysis. The Zymark robotic system currently controls two detect
or systems, but is designed to control up to three independent detecto
r systems. Canberra/Nuclear Data software, operating on a Microvax 310
0, issues commands to the Zymark controller to change samples when spe
ctral acquisition is complete. Once a new sample is in place, the robo
t sends a signal to the Microvax to begin data acquisition. Up to 40 s
amples, with sizes between 1 and 20 mi, can be accommodated using cust
omized sample racks and sample holders. The location of the sample rac
ks relative to the detectors has eliminated noticeable crosstalk betwe
en samples in the racks and samples being counted. The two HPGe detect
ors for each detector system sit on motorized platforms controlled by
programmable Compumotor drives. Programmed function keys move the dete
ctors in or out at fixed increments to optimize sample/detector geomet
ry. The high resolution of the stepper motors enables accurate reposit
ioning of detectors so that previously acquired standard spectra can b
e compared with samples activated and counted under identical conditio
ns but at different times.