Cooley

Cooley J W and ] W Tukey 1965. An Algorithm for the Machine Calculation of Complex Fourier Series Aiathemalics of Computation 19 297-301. 

S. D. Cooley and. W. Walker, Celanese Chemical Co. Technical Center, Corpus Christi, Tex., unpublished data. 

S. D. Cooley andj. D. Powers, "Maleic Acid and Anhydride," iu Enyclopedia of Chemical Processing and Design, Vol. 29, Marcel Dekker, Inc., New York, 1988,... 

In the treatment of poisoning by lead or other metal ions, higher concentrations of chelant can be safely obtained in humans by administering Na2CaEDTA rather than Na EDTA. The metal ion is bound by displacing small amounts of Ca " that the body can tolerate. Use of Na EDTA would result in calcium chelation and thus serious depletion of calcium in the body fluids (44). Removal of iron in Cooley s anemia is accompHshed by using chelants that are relatively specific for iron (45). 

From the time function F t) and the calculation of [IT], the values of G may be found. One way to calculate the G matrix is by a fast Fourier technique called the Cooley-Tukey method. It is based on an expression of the matrix as a product of q square matrices, where q is again related to N by = 2 . For large N, the number of matrix operations is greatly reduced by this procedure. In recent years, more advanced high-speed processors have been developed to carry out the fast Fourier transform. The calculation method is basically the same for both the discrete Fourier transform and the fast Fourier transform. The difference in the two methods lies in the use of certain relationships to minimize calculation time prior to performing a discrete Fourier transform. 

Cooley. Specify twin coolers with non-interrupting transfer valve. Spevily materials of construction, utilities, and fouling factor,... 

Garrison, G. W., Cooley, B. L., and El-Halwagi, M. M. (1995). Synthesis of mass exchange networks with multiple target mass separating agents. Dev. Chem. Eng. Miner. Proc. 3(1), 31-19. 

Spero and Cooley have reported an alternate route to 6-methyl-A -3-keto steroids by using 3,3-ethyIenedioxy-5a,6a-epoxides (6). In contrast... 

Ellis, B., Petrow, V., Stansfield, M. and Stuart-Webb, I.A. U.S. Patent 2,927,119 Mar. 1, 1960 assigned to The British Drug Houses Limited, England Barton, S.P., Burn, D., Cooley, G., Ellis, B., Petrow, V. and Stuart-Webb, I.A. U.S. Patent 2,939,819 June 7, 1960 assigned to The British Drug Houses Limited, England... 

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