THE DETERMINATION OF HEAVY WATER

1949 ◽  
Vol 27b (1) ◽  
pp. 1-5 ◽  
Author(s):  
I. E. Puddington

A reasonably simple procedure for determining the concentration of heavy water solutions, based on the comparison of the vapor pressures of these solutions with pure water, has been developed. The method is useful for samples as small as 0.5 mgm. and the sample may be recovered. Individual determinations require about two hours. In the work reported, mean determinations did not vary from the best curve through the experimental points by more than 0.2 mole % of D2O, while the spread in any group of readings was about ±0.25 mole %.

2019 ◽  
Vol 4 (65) ◽  
Author(s):  
V.G Zinovyev. ◽  
V.T. Lebedev ◽  
I.A. Mitropolsky ◽  
G.I. Shulyak ◽  
P.A. Sushkov ◽  
...  

Author(s):  
V A Tikhomirov ◽  
D I Mendeleev ◽  
V V Kurenkov ◽  
M R Menyashev ◽  
N A Sivov ◽  
...  

1958 ◽  
Vol 7 (5) ◽  
pp. 301-304 ◽  
Author(s):  
Saburo YANAGISAWA ◽  
Michiharu SEKI ◽  
Yoshikazu WATANABE ◽  
Shigeru NAKAMURA ◽  
Fumio MORIYA

1982 ◽  
Vol 60 (1) ◽  
pp. 14-20 ◽  
Author(s):  
J. Szewczyk ◽  
J. Karniewicz ◽  
W. Kolasiński

2006 ◽  
Vol 61 (5-6) ◽  
pp. 341-346 ◽  
Author(s):  
Jae-Woo Park ◽  
A. M. Abd El-Aty ◽  
Myoung-Heon Lee ◽  
Sung-Ok Song ◽  
Jae-Han Shim

A multiresidue method for the simultaneous determination of 22 organochlorine (OCs) and organophosphorus (Ops) pesticides (including isomers and metabolites), representing a wide range of physicochemical properties, was developed in fatty matrices extracted from meat. Pesticides were extracted from samples with acetonitrile/n-hexane (v :v, 1:1). The analytical screening was performed by gas chromatography coupled with electron-capture detection (ECD). The identification of compounds was based on their retention time and on comparison of the primary and secondary ions. The optimized method was validated by determining accuracy (recovery percentages), precision (repeatability and reproducibility), and sensitivity (detection and quantitation limits) from analyses of samples fortified at 38 to 300 ng/g levels. Correlation coefficients for the 22 extracted pesticide standard curves (linear regression analysis, n = 3) ranged from 0.998 to 1.000. Recovery studies from 2 g samples fortified at 3 levels demonstrated that the GC-ECD method provides 64.4-96.0% recovery for all pesticides except 2,4′-DDE (44.6-50.4%), 4,4′-DDE (51.1-57.5%) and 2,4′-DDT (50.0-51.2%). Both repeatability and reproducibility relative standard deviation values were < 20% for all residues. Detection limits ranged from 0.31 to 1.27 ng/g and quantification limits were between 1.04 and 4.25 ng/g. The proposed analytical method may be used as a simple procedure in routine determinations of OCs and Ops in meat. It can also be applied to the determination of pesticide multi-residues in other animal products such as butter and milk.


2005 ◽  
Vol 60 (3) ◽  
pp. 787-796 ◽  
Author(s):  
Shawn P. Ryan ◽  
Brian K. Gullett ◽  
Dennis Tabor ◽  
Lukas Oudejans ◽  
Abderrahmane Touati
Keyword(s):  

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