On Risk Assessment for Determination of in-Situ Data Requirements

1981 ◽  
Vol 28 (1) ◽  
pp. 242-243
Author(s):  
D. E. Wood
1991 ◽  
Vol 222 ◽  
Author(s):  
B. Johs ◽  
J. L. Edwards ◽  
K. T. Shiralagi ◽  
R. Droopad ◽  
K. Y. Choi ◽  
...  

ABSTRACTA modular spectroscopic ellipsometer, capable of both in-situ and ex-situ operation, has been used to measure important growth parameters of GaAs/AIGaAs structures. The ex-situ measurements provided layer thicknesses and compositions of the grown structures. In-situ ellipsometric measurements allowed the determination of growth rates, layer thicknesses, and high temperature optical constants. By performing a regression analysis of the in-situ data in real-time, the thickness and composition of an AIGaAs layer were extracted during the MBE growth of the structure.


2017 ◽  
Vol 26 (3) ◽  
pp. 317-325
Author(s):  
Mohsen Rezaei ◽  
Rasoul Ajalloeian ◽  
Mohammad Ghafoori

For determination of the in-situ deformation modulus of rock mass at Bakhtiari Dam site, located in south-west of Iran, plate jacking tests (PJT) and dilatometer tests (DLT) carried out during the geotechnical investigations. In this study, the results of PJTs and DLTs were compared. This comparison involves 89 vertical and horizontal PJTs and 83 DLTs carried out in 6 rock units of Sarvak formation. Although, both PJTs and DLTs in the Bakhtiari Dam site were performed in same geological and geotechnical conditions, but there are not sufficient side by side data to make a paired two samples correlation. Therefore, the mean of in-situ data was compared at each rock unit. Besides Mann–Whitney U tests were performed to compare in-situ test results. The comparison shows that the deformation modulus measured by both methods has no significant differences. However, in low quality rock masses the moduli measured by the use of DLTs were greater than the modulus measured by PJTs. Conversely, in high quality rock masses the results of PJTs were greater than DLT’s.


1988 ◽  
Author(s):  
D. T. Decker ◽  
J. M. Retterer ◽  
J. R. Jasperse ◽  
D. N. Anderson ◽  
R. W. Eastes ◽  
...  

Author(s):  
Jonathan Richetti ◽  
Kenneth J. Boote ◽  
Gerrit Hoogenboom ◽  
Jasmeet Judge ◽  
Jerry A. Johann ◽  
...  

1961 ◽  
Vol 38 (4) ◽  
pp. 545-562 ◽  
Author(s):  
L. Kecskés ◽  
F. Mutschler ◽  
I. Glós ◽  
E. Thán ◽  
I. Farkas ◽  
...  

ABSTRACT 1. An indirect paperchromatographic method is described for separating urinary oestrogens; this consists of the following steps: acidic hydrolysis, extraction with ether, dissociation of phenol-fractions with partition between the solvents. Previous purification of phenol fraction with the aid of paperchromatography. The elution of oestrogen containing fractions is followed by acetylation. Oestrogen acetate is isolated by re-chromatography. The chromatogram was developed after hydrolysis of the oestrogens 'in situ' on the paper. The quantity of oestrogens was determined indirectly, by means of an iron-reaction, after the elution of the iron content of the oestrogen spot, which was developed by the Jellinek-reaction. 2. The method described above is satisfactory for determining urinary oestrogen, 17β-oestradiol and oestriol, but could include 16-epioestriol and other oestrogenic metabolites. 3. The sensitivity of the method is 1.3–1.6 μg/24 hours. 4. The quantitative and qualitative determination of urinary oestrogens with the above mentioned method was performed in 50 pregnant and 9 non pregnant women, and also in 2 patients with granulosa cell tumour.


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