Thesis(M.S.)--Auburn University, 2007. / Abstract. Vita. Includes bibliographic references.

Thesis (Ph.D.)--Texas Tech University, 2004. / Adviser: Mario G. Beruvides. Includes bibliographical references.

Thesis (M.A.Sc.)--Dalhousie University (Canada), 2007. / Includes bibliographical references.

Thesis (M.S.)--West Virginia University, 2000. / Title from document title page. Document formatted into pages; contains xi, 65 p. : ill. (some col.). Includes abstract. Includes bibliographical references (p. 63-65).

Thesis (Ph. D.)--Institute of Paper Science and Technology, 1986. / Includes diagram of a drying apparatus, p. 14. Bibliography: leaves 102-103.

No abstract available. / Thesis (Ph.D.)-University of Natal, Durban, 1991.

Drying procedures, like other important unit operations in pharmacy, have received little attention in pharmaceutical literature. Within recent years, however, growing interest in these pharmaceutical engineering areas has become apparent. Fluidization operations, although relatively unexplored in pharmacy, have been firmly established on a broad scale in other industries. Fluidization may be defined as the suspension and agitation of a bed of particulate solids by a vertically rising stream of gas. Each suspended particle is surrounded by the gas. This relative velocity of the gas and solid particles is high, although the gas velocity itself is relatively low. Heat is transferred by by a combination of conduction and convection and by the movement of the solid particles (1). Fluidized bed drying of moist phosphate rock, coal, and many other materials has been discussed in technical literature (1, 2). However, relatively few reports have appeared on the applications of fluidized beds to materials of pharmaceutical interest. These technical studies show that uniform bed temperatures with high heat and mass transfer rates are obtainable in fluidization system. Product temperatures are controllable over narrow limits within the fluidized bed. These reported advantages would appear to have particular importance in processing pharmaceuticals. It is difficult to understand, therefore, why only a few studies on fluidized bed drying have appeared in pharmaceutical literature. Apparently no comprehensive studies dealing with finished tablets, compressed from granulations dried by the fluidization technique, have appeared in pharmaceutical literature. Accordingly, it would seem appropriate that more studies be conducted, in pharmaceutical fields, concerning drying procedures, especially the fluidization process. The present project will consist of conducting a series of tests on identical granule formulations dried by the conventional air drying and oven drying processes as well as the fluidized bed drying technique. The present work will also include the performance of tests on specific physical properties of tablets compressed from the test granulations.

Thesis (Ph. D.)--University of Missouri-Columbia, 1997. / Typescript. Vita. Includes bibliographical references (leaves 115-119). Also available on the Internet.

Thesis (Ph. D.)--University of Missouri-Columbia, 1997. / Typescript. Vita. Includes bibliographical references (leaves 115-119). Also available on the Internet.

Thesis (Ph. D. in Chemical Engineering)--Vanderbilt University, Dec. 2009. / Title from title screen. Includes bibliographical references.