Metals suitable for fluorine gas target bodies: First use of aluminum for the production of [F-18]F-2

被引:8
作者
Bishop, A
Satyamurthy, N
Bida, G
Phelps, M
Barrio, JR
机构
[1] UNIV CALIF LOS ANGELES,SCH MED,DIV NUCL MED,DEPT MOL & MED PHARMACOL,LOS ANGELES,CA 90095
[2] US DOE,LAB STRUCT BIOL & MOL MED,LOS ANGELES,CA 90095
[3] BIOMED RES FDN NW LOUISIANA,SHREVEPORT,LA 71103
来源
NUCLEAR MEDICINE AND BIOLOGY | 1996年 / 23卷 / 03期
关键词
F-18]F-2 target; aluminum; silver; electroformed nickel; Langmuir-Rideal mechanism;
D O I
10.1016/0969-8051(95)02038-1
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
A comprehensive evaluation of different metals (aluminum, silver, copper, nickel, and gold plated copper) was undertaken for the fabrication of target bodies with straight and conical bore shapes for the production of [F-18]F-2 via the Ne-20(d,alpha)F-18 nuclear reaction. Of these metals, aluminum, silver and copper have never been used for the production of [F-18]F-2. All these target bodies were easily passivated using a mild beam-induced plasma technique in the presence of 1% F-2 in neon or argon. The recovery of F-18 activity was higher with electroformed nickel and silver bodies, probably due to favorable thermal conductivities. Aluminum proved to be a useful material for fluorine gas targets. The consistent recovery of F-18 activities, ease and low cost of manufacturing and low nuclear activation properties all make aluminum an ideal choice for fluorine gas targetry. To our knowledge, this investigation is the first to highlight the use of aluminum as a target body material for the routine production of [F-18]F-2. A reasonable mechanism based on the Langmuir-Rideal surface atom recombination is also proposed for the behavior of [F-18]F-2 recovery from a nickel target body.
引用
收藏
页码:181 / 188
页数:8
相关论文
共 56 条
[1]  
ARUTYUNOV VS, 1977, KINET CATAL, V18, P267
[2]   HALIDES OF TRANSITION ELEMENTS OF FIRST LONG PERIOD [J].
BARBER, M ;
TAYLOR, NH ;
LINNETT, JW .
JOURNAL OF THE CHEMICAL SOCIETY, 1961, (AUG) :3323-&
[3]  
BIDA GT, 1980, J NUCL MED, V21, P758
[4]  
BIDA GT, 1991, P 4 INT WORKSH TARG, P130
[5]  
BISHOP AJ, 1994, THESIS U CALIFORNIA
[6]  
BLESSING G, 1986, APPL RADIAT ISOTOPES, V37, P1133
[7]  
BOND DL, 1979, 7964 JPL CALTECH
[8]   HALOGEN RECOMBINATION-DISSOCIATION REACTIONS - CURRENT STATUS [J].
BOYD, RK ;
BURNS, G .
JOURNAL OF PHYSICAL CHEMISTRY, 1979, 83 (01) :88-92
[9]  
CANNON WA, 1968, T METALL SOC AIME, V242, P1635
[10]  
CASELLA V, 1980, J NUCL MED, V21, P750