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Fluidized bed drying of pharmaceutical materials: batch and continuous manufacturing

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TitleInfo
Title
Fluidized bed drying of pharmaceutical materials: batch and continuous manufacturing
Name (type = personal)
NamePart (type = family)
Chen
NamePart (type = given)
Hao
NamePart (type = date)
1992-
DisplayForm
Hao Chen
Role
RoleTerm (authority = RULIB)
author
Name (type = personal)
NamePart (type = family)
Glasser
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Benjamin J
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Benjamin J Glasser
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Advisory Committee
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chair
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NamePart (type = family)
Hara
NamePart (type = given)
Masanori
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Masanori Hara
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Advisory Committee
Role
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internal member
Name (type = personal)
NamePart (type = family)
Ramachandran
NamePart (type = given)
Rohit
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Rohit Ramachandran
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Advisory Committee
Role
RoleTerm (authority = RULIB)
internal member
Name (type = personal)
NamePart (type = family)
Metzger
NamePart (type = given)
Matthew
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Matthew Metzger
Affiliation
Advisory Committee
Role
RoleTerm (authority = RULIB)
outside member
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NamePart
Rutgers University
Role
RoleTerm (authority = RULIB)
degree grantor
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NamePart
School of Graduate Studies
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school
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Text
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theses
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2019
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2019-05
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2019
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English
Abstract (type = abstract)
Drying processes are common in the chemical, pharmaceutical and food industries. It is one of the traditional methods that removes moisture or solvents to provide stable products and/or semi-finished products. It is also known that the drying process is energy intensive. It has been reported that an average of 12 % of all energy consumed in the world is used for drying, and the cost of drying could reach up to 60 % - 70 % of total cost of investments. Therefore, the optimal operation of the drying process is sought to meet the requirements for cost-effective manufacturing.
In the pharmaceutical industry, the particulate ingredients are often granulated to improve their flowability and uniformity. A fluidized bed gas-solid drying is usually followed to remove the moisture that is introduced during the granulation. Before a new formulation is launched into commercial size units, it is prevalent to do lab-scale tests to understand its characteristics. Although a number of studies have been done on fluidized bed scale-up, practical scale-up rules for fluidized bed drying still remain unclear. This work will start with understanding several important operational parameters for fluidized beds. Then, a practical scaling rule will be introduced to predict the drying behavior of a pharmaceutical excipient in large scale units based on lab-scale results.
Another part of the work will be to try and use the knowledge gained from the batch mode fluidized bed dryers to predict the behavior of a continuous mode fluidized bed dryer. Several pharmaceutical manufacturers are moving towards continuous manufacturing due to its potential to improve agility, flexibility, and robustness.The fluidized bed unit operation can be easily implemented as a continuous process for drying. One of the most important tools to characterize a continuous unit is the residence time distribution (RTD). It describes the probability distribution of the material staying in the unit. The RTD will be investigated in this work via a tracer study. With the RTD model for flow in the continuous fluidized bed and drying kinetic models constructed with data from lab-scale experiments, we will develop an approach to predict the final moisture content of the product. The final moisture content variations caused by changes in the operating condition or changes in the feed material will also be evaluated.
Subject (authority = local)
Topic
Fluidized bed
Subject (authority = RUETD)
Topic
Chemical and Biochemical Engineering
Subject (authority = LCSH)
Topic
Drugs -- Drying
RelatedItem (type = host)
TitleInfo
Title
Rutgers University Electronic Theses and Dissertations
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ETD
Identifier
ETD_9712
PhysicalDescription
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application/pdf
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text/xml
Extent
1 online resource (xiii, 191 pages) : illustration
Note (type = degree)
Ph.D.
Note (type = bibliography)
Includes bibliographical references
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Title
School of Graduate Studies Electronic Theses and Dissertations
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rucore10001600001
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NjNbRU
Identifier (type = doi)
doi:10.7282/t3-5bsf-9314
Genre (authority = ExL-Esploro)
ETD doctoral
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Rights

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The author owns the copyright to this work.
RightsHolder (type = personal)
Name
FamilyName
Chen
GivenName
Hao
Role
Copyright Holder
RightsEvent
Type
Permission or license
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2019-04-08 10:06:41
AssociatedEntity
Name
Hao Chen
Role
Copyright holder
Affiliation
Rutgers University. School of Graduate Studies
AssociatedObject
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Name
Author Agreement License
Detail
I hereby grant to the Rutgers University Libraries and to my school the non-exclusive right to archive, reproduce and distribute my thesis or dissertation, in whole or in part, and/or my abstract, in whole or in part, in and from an electronic format, subject to the release date subsequently stipulated in this submittal form and approved by my school. I represent and stipulate that the thesis or dissertation and its abstract are my original work, that they do not infringe or violate any rights of others, and that I make these grants as the sole owner of the rights to my thesis or dissertation and its abstract. I represent that I have obtained written permissions, when necessary, from the owner(s) of each third party copyrighted matter to be included in my thesis or dissertation and will supply copies of such upon request by my school. I acknowledge that RU ETD and my school will not distribute my thesis or dissertation or its abstract if, in their reasonable judgment, they believe all such rights have not been secured. I acknowledge that I retain ownership rights to the copyright of my work. I also retain the right to use all or part of this thesis or dissertation in future works, such as articles or books.
Copyright
Status
Copyright protected
Availability
Status
Open
Reason
Permission or license
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