Finches

Finch D. Cone-beam reconstruction with sources on a curve., SIAM J. Appl. Math., V. 45(4), 1985,p.665-673. 

C. A. Finch, ed.. Polyvinyl Alcohol Properties and Application, John Wiley Sons, Ltd., Chichester, U.K., 1973, Chapt. 9. 

Monographs bv Sastiw (1988), Finch and Dobbv (1990), and Rubinstein (1994) provide an oveniew of the design and operational aspects of Rotation columns,... 

The hberation of a valuable constituent does not necessarily translate direclly into recoveiy in downstream processes. For example, flotation tends to be more efficient in intermediate sizes than at coarse or fine sizes [Mclvor and Finch, Minerals Engineeiing, 4(1), 9-23 (1991)]. For coarser sizes, failure to liberate may be the hmitation finer sizes that are liberated may still be carried through by the water flow. A conclusion is that overgrinding should be avoided by judicious use of size classifiers with recycle grinding. 

Figure 3.14 Sickle-cell hemoglobin molecules polymerize due to the hydrophobic patch introduced by the mutation Glu 6 to Val in the P chain. The diagram (a) illustrates how this hydrophobic patch (green interacts with a hydrophobic pocket (red) in a second hemoglobin molecule, whose hydrophobic patch interacts with the pocket in a third molecule, and so on. Electron micrographs of sickle-cell hemoglobin fibers are shown in cross-section in (b) and along the fibers in (c). [(b) and (c) from J.T. Finch et al., Proc. Natl. Acad. Set. USA 70 718-722, 1973.)...

Finch, J.T., et al. Stmcture of sickled erythrocytes and of sickle-cell hemoglobin fibers. Proc. Natl. Acad. Sci. USA 70 718-722, 1973. 

FINCH, c.A. (Ed.), Polyvinyl alcohol Properties and Applications, Wiley New York (1973) PRITCHARD, J.G., Poly(Vinyl alcohol) Basic Properties and Uses, Macdonald, London (1970) Properties and Applications of Polyvinyl Alcohol (SCI Monograph No. 30), Society of the Chemical Industry, London (1968)... 

Work also prepared a series of carbinolamines and polyamines without a quinoline nucleus but, in other respects, conforming in type and range of molecular weight, with quinoline compounds known to possess plasmocidal activity. As none of these were active, it seems clear that the quinoline nucleus in the cinchona alkaloids and in certain synthetic anti-malarials is a potent factor in the production of plasmocidal action. Later the same author made (1942) a series of lepidylamine derivatives of the form R. Q. CHj. NH[CH2] . NEtj, which were found to be inactive, in spite of their similarity to the active examples of the type R. Q. NH[CH2] . NEt2 prepared by Magidson and Rubtzow. Rubtzow (1939) has also shown that an isomeride of dihydroquinine (II) with the quinuclidine nucleus attached via the carbinol group at C in the quinoline nucleus was inactive in an infection of Plasmodium prcecox in finches. 

A. Finch, P. N. Gates and T. H. Page, Inorg. Chim. Acta... 

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