A Semi-Linear Method for Particle Kinematics Under Steep Random-Wave Crests

Author(s):  
Nwaka Chuks Ojieh ◽  
Nigel Barltrop

The determination of random wave kinematics in high sea-states especially in the region above mean water surface has been a major challenge and most proposed methods are not robust. In this work, a method which is similar to stretching and extrapolation in its simplicity is developed based on a simplified form of wave-wave interaction which is robust to 2nd order. To check the usefulness of the new method, horizontal particle velocity results are compared with Zhang’s HWM, Wheeler stretching, linear extrapolation above MWL, experimental measurements and theoretical computations of Longridge et al (1996), Skjelbriea et al (1991) and Stansberg et al (2006). Results of the new method show good agreement with the results of Skjelbriea et al (1991) and are closer to experiment than 2nd order results of Stansberg et al (2006) while only showing a qualitative agreement with Longridge et al (1996). The poorer comparison with Longridge et al (1996) is probably because it was not possible to reproduce the exact time series used by Longridge et al as the exact amplitudes and phases were not available. The improved capability of the new method over existing methods has thus been demonstrated and its advantage over the HWM lies in being simpler to implement.

1994 ◽  
Vol 04 (02n03) ◽  
pp. 165-179 ◽  
Author(s):  
K. SERA ◽  
S. FUTATSUGAWA ◽  
S. HATAKEYAMA ◽  
S. SAITOU

A new method has been developed to determine absorption curves which are needed to derive quantitative values in PIXE analysis. In this method two spectra obtained with absorbers of different thickness are divided by each other after background subtraction and the absorption curve can be obtained immediately. Absorption curves for a 50 and a 200 µm-thick Mylar films and that for a Cr foil of 2500 µg/cm2 were determined experimentally. These curves are in good agreement with the absorption values derived from peak areas of characteristic x-rays. This method enables one to obtain absorption curves for any kind of absorber accurately and quickly.


1961 ◽  
Vol 22 (1) ◽  
pp. 47-58 ◽  
Author(s):  
R. A. A. SALOKANGAS ◽  
R. D. BULBROOK

SUMMARY 1. The purification step described by Ittrich (1958) has been incorporated in the method of Brown, Bulbrook & Greenwood (1957b) for estimating urinary oestrogens. 2. When the Kober colours given by urinary oestrone, oestradiol-17β and oestriol are extracted with tetrachloroethane containing p-nitrophenol, the decrease in the absorption due to impurities is such that the Kober reaction can be scaled down and micro-cells used in the measurement of the final colours. 3. Amounts of urinary oestrogens as low as 0·5 μg./24 hr. specimen can be measured with a reasonable degree of accuracy and precision. 4. The results with the new method show that the method of Brown et al. (1957b) gives over-estimates of approx. 1 μg. oestrone and 1 μg. oestriol/24 hr. urine specimen when used for the estimation of urinary oestrogens of low titre.


2014 ◽  
Vol 941-944 ◽  
pp. 2209-2218
Author(s):  
Muhammad Ilyas Khan ◽  
Shu Yuan Ma ◽  
Saifullah Samo

Measurement of parallelism error is one of important icon in the measurement of orientation tolerances. This paper presents new method of parallelism error measurement and is based on the flatness plane using minimum zone technique. Real coded genetic algorithm has been proposed to determine the flatness plane coefficients and flatness error. Flatness plane has been developed using plane coefficients and then parallelism error has been determined from the flatness plane. One example has been presented to show the effectiveness of the proposed parallelism error measurement method. The result of the proposed method has been compared to co-ordinate measuring machine (CMM) built-in function for parallelism error measurement and the results are in good agreement. In addition to determination of parallelism error measurement, the proposed algorithms also calculate flatness error and can also be extended to measurement of other types of geometrical tolerances with slight modifications.


Author(s):  
Paul Trinder

Two hundred microlitres of plasma is deproteinised, and chloride is removed with TCA/silver iodate. After centrifugation the phenylalanine in the protein-free extract is oxidised to benzaldehyde with buffered sodium metaperiodate. The benzaldehyde is extracted into iso-octane, and the absorbance of the organic layer is measured at 240 nm. The method gives good agreement with a paper chromatographic method at normal and elevated levels of phenylalanine. All the reagents are stable indefinitely, and a single determination can be completed in 15 minutes.


1963 ◽  
Vol 46 (6) ◽  
pp. 1060-1062
Author(s):  
R B Maybury ◽  
R Payfer

Abstract A new method is presented for the nonaqueous titration of piperazine in formulations in which the piperazine base is first brought into aqueous solution, and the solution is made strongly alkaline and extracted with chloroform. The chloroform solution of piperazine is then titrated with acetous perchloric acid to alpha-naphthol benzein indicator. The procedure is rapid, shows good agreement with other methods, and is applicable to most kinds of piperazine formulations. An alternative procedure for piperazine adipate, citrate, or tartrate in powders is given, in which the compound is dissolved and titrated directly in glacial acetic acid.


1966 ◽  
Vol 49 (2) ◽  
pp. 257-260
Author(s):  
Richard Stein ◽  
Robert S Ferrera ◽  
Robert F Brown

Abstract A rapid screening method for determining insect fragments in cocoa uses a 5 g sample of cocoa and requires only 10 minutes for extraction, as compared with the 50 g samples in the official method. The new method shows approximately eqvial recoveries and good agreement between determinations and analysts.


2007 ◽  
Vol 5 ◽  
pp. 115-118 ◽  
Author(s):  
M. Camp ◽  
R. Herschmann ◽  
T. Zelder ◽  
H. Eul

Abstract. This paper shows a new method to determine the input impedance of RFID transponder antennas with a combination of on-wafer-prober and network analyzer. It is shown that the results are in a good agreement with FEM simulations (HFSS) for a large part of the examined antenna structures.


1960 ◽  
Vol 23 ◽  
pp. 227-232 ◽  
Author(s):  
P WEST ◽  
G LYLES
Keyword(s):  

1977 ◽  
Vol 37 (02) ◽  
pp. 210-215 ◽  
Author(s):  
R Margalit ◽  
E Gidron ◽  
Y Shalitin

SummaryThe term “effective activator” of plasminogen is proposed, to denote the resultant of activator-antiactivator interaction, and a method for the determination of the level of these activators is described. By adding axcess plasminogen to the euglobulin fraction of plasma the influence of the level of endogenous plasminogen and of the antiplasmin is eliminated. It is shown that the level of fibrinogen has very little bearing on the results. An effective activator unit is defined as equal to 1 CTA unit of urokinase activity on a fibrinogen-plasminogen substrate.


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