Condensers Wiley

Kakac, S. Ed., Boilers, Evaporators, and Condensers Wiley Interscience New York, 1991. 

Fusco, R. 1967, in Wiley, R. H. (ed.), Pyrazoles, Pyrazolines, Pyraiolidines, Indaioles. and Condensed Rings, p. 3, Interscience New York... 

These various considerations led Pierce, Wiley and Smith in 1949, and independently, Dubinin, to postulate that in very fine pores the mechanism of adsorption is pore filling rather than surface coverage. Thus the plateau of the Type 1 isotherm represents the filling up of the pores with adsorbate by a process similar to but not identical with capillary condensation, rather than a layer-by-layer building up of a film on the pore walls. 

P. W. Morgan, Condensation Polymers by Interfacial and Solution Methods olm. Wiley Sons, Inc., New York, 1965. 

L. C. Behr, R. Fusco, and C. H. Jarboe, iu R. H. Wiley, ed., "Pyrazoles, Pyrazolines, PyrazoUdines, Indazoles and Condensed Rings," Vol. 22 of A. Weissberger, ed.. The Chemistry of ELetero( clic Compounds Wiley-lnterscience, New York, 1967. 

L. Holland. Vacuum Deposition of Thin Films, Chapman and Hall, London (1966) TS 695 H6. J.P. Hii th and M. Pound. Condensation and Evaporation, Pergamon Piess New York (1963). J.M. Howe. Intetfaces in Materials, J. Wiley and Sons, New York (1997) QC 173.4.157 H68. A.V. Goldstein (ed.). Handbook of Nanomaterials, Marcel Dekker, New York (1997) TA418.9. 

Schatz, G. and Weidinger, A. (1996) Nuclear Condensed Matter Physics Nuclear Methods and Applications (Wiley, Chichester). 

Electronic version of Sax s Dangerous Properties of Industrial Materials, 9th ed., Hawley s Condensed Chemical Dictionaiy Prager s Environmental Contaminant Reference Databook, Vols, I, II III Verschueren s Handbook of Environmental Data on Organic Chemicals, 3rd ed. and Pohan-ish and Greene s Hazardous Materials Handbook, on CD-ROM, John Wiley and Sons, New York, NY, 1998. 

R] Singerman, G. M. Cinnolines. In Heterocyclic Compounds. Condensed Pyridazines Including Cinnolines and Phthalazines-, Weissberger, A., Taylor, E. C. Eds. John Wiley Sons New York-London, 1973 pi. 

Holden, G., Condensed Encyclopedia of Polymer Science and Engineering, John Wiley and Sons, 1990, pp. 296-291. 

Various reviews dealing with the 1,2.4-triazines have been published. The most recent is that published by Neunhoeffer and Wiley (78HC749) covering the literature through 1974. Owing to the increase of the number of publications on the 1,2,4-triazines, a survey of the literature on their condensed ring systems with three- to five-membered heterocycles, from 1974 through 1992, constitutes the subject of this review. 

R. N. Castle, Condensed Pyridazines, including Cinnolines and Phthalazines. Wiley (Interscience), New York, 1973. 

H. R. Kricheldorf and Z. Denchev, in Transreactions in Condensation Polymers, S. Fakirov (Ed.), Wiley-VCH Verlag GmbH, Weinheim, Germany, 1999, p. 1. 

The hydrogel is allowed to stand for a few days during which time a process called sinerisis takes place. During sinerisis the condensation of the primary particles, one with another, continues and the gel shrinks further, accompanied by the elimination of more saline solution that exudes from the gel. After three or four days, sinerisis is complete and the gel becomes firm and can now be washed free of residual electrolytes with water. The washed product is finally heated to 120°C to complete the condensation of the surface silanol groups between the particles, and a hard xerogel is formed. It is this xerogel that is used as the LC stationary phase and for bonded phase synthesis. It is not intended to discuss the production of silica gel in detail and those interested are referred to "Silica Gel and Bonded Phases", published by Wiley (1). 

Lewis, R.J. (Ed.), Hawley s Condensed Chemical Dictionary, 13th ed., John Wiley Sons, 1997. (E,F,H,J)... 

J. Bezemer and W. G. J. H. M. van Sark, Electronic, Optoelectronic and Magnetic Thin Films, Proceedings of the 8th International School on Condensed Matter Physics (ISCMP), Varna, Bulgaria, 1994, p. 219. Wiley, New York, 1995. 

Jones G. The Knoevenagel Condensation. Vol. 15. Organic Reactions. New York Wiley, 1967 204-599. 

Fakirov, S, (ed) Transreactions in Condensation Polymers, (1999) Wiley-VCH, New York. 

Figure 7.1 The overall pathway of haem biosynthesis. 5-AminolaevuIinate (ALA) is synthesized in the mitochondrion, and is transferred to the cytosol where it is converted to porphobilinogen, four molecules of which condense to form a porphyrin ring. The next three steps involve oxidation of the pyrrole ring substituents to give protoporphyrinogen fX, whose formation is accompanied by its transport back into the mitochondrion. After oxidation to protoporphyrin IX, ferrochelatase inserts Fe2+ to yield haem. A, P, M and V represent, respectively acetyl, propionyl, methyl and vinyl (—CH2=CH2) groups. From Voet and Voet, 1995. Reproduced by permission of John Wiley Sons, Inc.

Figure 5.8 Examples of formation and cleavage of carbon-carbon bonds (a) aldol condensation, (b) Claisen ester condensation and (c) decarboxylation of a P-keto acid. (From Voet and Voet, 2004. Reproduced with permission from John Wiley Sons., Inc.)...

Figure 4.17 Schematic view of the chemical healing process in semi-crystalline linear polycondensates TR, transreactions AC, additional (post)condensation D, diffusion [87]. From Fakirov, S., J. Polym. Sci., Polym. Phys. Ed., 22,2095-2104 (1984), Copyright John Wiley Sons, Inc., 1984. Reprinted by permission of John Wiley Sons, Inc...

Myers, B. J. Darzens Glycidic Ester Condensation In Name Reactions in Heterocyclic Chemistry, Li, J. J. Corey, E. J., Eds. Wiley Sons Hoboken, NJ, 2005, 15—21. (Review). 

---