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On moving fast and breaking things
Craig Piercycpiercy@ans.org
So much of what is happening in federal nuclear policy these days seems driven by a common approach popularized in the technology sector. Silicon Valley calls it “move fast and break things,” a phrase originally associated with Facebook’s early culture under Mark Zuckerberg. The idea emerged in the early 2000s as software companies discovered that rapid iteration, frequent experimentation, and a willingness to tolerate failure could dramatically accelerate innovation. This philosophy helped drive the growth of the social media, smartphones, cloud computing, and digital platforms that now underpin modern economic and social life.
Today, that mindset is also influencing federal nuclear policy. The Trump administration views accelerated nuclear deployment as part of a broader competition with China for technological and AI leadership. In that context, it seems willing to accept greater operational risk in pursuit of strategic advantage and long-term economic and security objectives.
Henry H. Kramer and Werner H. Wahl
Nuclear Science and Engineering | Volume 22 | Number 3 | July 1965 | Pages 373-382
Technical Paper | doi.org/10.13182/NSE65-A20941
Articles are hosted by Taylor and Francis Online.
Metastable isomers of stable isotopes may be formed in a nuclear reactor by inelastic neutron scattering and photoexcitation of the stable isotopes, and by radiative neutron capture and (n,2n) reactions on neighboring stable isotopes. The relative importance of these reactions for the production of Ba137m, Cd111m, Se77m, and Sr87m was evaluated by the irradiation of normal and isotopically enriched samples of the elements in the mixed radiation field of the Union Carbide Research Reactor. Radiative neutron capture is the most important source of Cd111m, Se77m and Sr87m in samples of normal isotopic abundance. Inelastic neutron scattering is the prime contributor to the production of Ba137m and is of considerable importance in the production of Cd111m. The (n,2n) reaction appears to be significant only in the production of Ba137m. The formation of these isomers by photoexcitation by the gamma-ray flux associated with the reactor appears to be insignificant when compared with the production by the other three processes. The cross sections determined in these investigations are generally in good agreement with available published values. Reactions for which cross sections were determined and not found in the literature include: Ba137(n,n′)Ba137m, = 0.22b; Cd111 (n,n′) Cd111m, = 0.14b; Se77(n,n′)Se77m, = 0.60b;Sr87(n,n′)Sr87m, = 0.12b; Ba138(n,2n)Ba137m, = 2.0mb; and Cd112 (n,2n)Cd111m, = 0.35mb. The data indicate that, for short irradiation periods in the fluxes employed in these studies, the metastable isomers Ba137m, Cd111m, Se77m and Sr87m are the most sensitive activation-analysis indicators for these elements and give detection sensitivities in the low nanogram range.