The isotope separation factor for adsorption of tracer-HTO/bulk-H2Oon tris (ethylenediamine) cobalt complex [Co (en) 3] Cl3is analyzed in accordance with the ideal adsorbed solution theory by using the isotherms for pure-component adsorption ofH2OandD2O.It has been studied that the isotherms are composite which result from two types of adsorption of water molecules on primary and secondary coordination sites in the complex crystal. The separation factorβshows two of high and low plateaus which respectively correspond to the primary adsorption where the equilibrium pressure exhibits a plateau and the secondary adsorption where the pressure rises up to the saturated vapor pressure. The high plateauβis larger thanα, the relative volatility ofH2OtoHTO.On the other hand, the low plateauβis smaller thanα.In this paper, approximate equations are presented for estimating the plateausβwith respect to temperature.
A new equation is proposed which correlates ortho-positronium (o-Ps) lifetime (τ) to the pore radius bigger than -l nm, by introducing quantum radius of positronium (Rps) .We assume that the annihilation rate of o-Ps in nano-pores is dependent on the fraction of the two different annihilation processes; o-Ps annihilated in free space (-140 ns) and by pick-off reaction with anti parallel spin electron extruded from spherical wall. The annihilation late, λhole (=1/τhole), in nano-pores is assumed to be expressed by the following equation. λholo= {λR2γ=2 [1-R/R+ΔR+1/2πsin (2πR/R+ΔR) ] (f (R≤0) λ3γf (R) +λRα2γ (1-f (R) ) (f (R>0) where λ3γ=1/140, Ra=RPs-ΔR, f (R) = (R-Ra/R+ΔR) b.
In14Cdating by LSC system, benzene is usually synthesized from collected samples via several chemical reactions such as pretreatment, carbonization, combustion, carbonating, carbide production, acetylene generation and polymerization. Since a great deal of efforts is required to the sample preparation, we proposed an another rapid process where the carbonized samples reacted to melted lithium metal directly to produce lithium carbide. Although the yield generating acetylene gas from carbonized samples was low, 52.5±1.5% on average, the yield synthesizing benzene from acetylene was 90% or more in the successive process. Some impurity atoms contained in carbonized samples deteriorate apparently the yield generating acetylene but they did not influence the yield synthesizing benzene from acetylene. This shows that combustion is not indispensable process in14Csample preparation. 14Cages for the samples prepared by the proposed method were agreed to those for the same samples prepared by the conventional method within the age variation corresponding to the statistical error of 1σ.Therefore the fractionation effect of carbon isotopes may be low, if any, in the proposed process. Since this method does not contain combustion and the following carbonating process, the sample preparation is fairly shortened.
We studied the performance of“Ready Cap”solid scintillator developed for the liquid scintillation counter, by using45Ca which is usually employed to deduce intracellular signaling by the tracer method. The liquid scintillators“AQUASOL-2”and“ATOMLIGHT”were used for comparison. Our findings were as follows: (1) A high counting efficiency of over 90% was achieved with the wide range of 200 to 106dpm, (2) measurement errors due to the uneven resolution of the solid scintillator and/or due to contents such as biological high polymers causing a hindrance in scintillation process were revealed to be low at below 5.3%, and (3) minimal effects were observed on (1) and (2) above even when actual samples containing biological high polymers and cell extracts with biopolymers detergent agent were used. We conclude that the solid scintillator studied here is practically enough useful for liquid scintillation measurement required in biological experiments.