This study was conducted to determine the effect, if any, on the PCT responses of glasses cooled at different rates. Two bounding cooling profiles were used in this study: rapidly quenched and a canister centerline cooling curve. Glasses were selected based on a number of criteria, but mainly to challenge the regions where amorphous phase separation is expected based upon current model predictions. The current DWPF homogeneity constraint, imposed to preclude regions of phase separation, predicted that most of the glasses selected would be phase separated. It was, therefore, important to ensure that deleterious phase separation does not occur at either cooling profile. In this case, deleterious phase separation is defined as the formation of an amorphous phase in the glass that significantly decreases the glass durability as measured by the PCT response.
This report is a modified version of WSRC-TR-2001-00124, Revision 0. Information related to the chemical compositions of the study glasses has been removed from this version. WSRC has submitted a patent application for the frit (designated as BD1) utilized in the study and is limiting the distribution of the details of the compositions of the study glasses to protect its intellectual property rights pending patent clearance.
The results presented in this report are for nine Precipitate Hydrolysis Aqueous (PHA) Phase 4 glasses. Three of the glasses contained HM sludge at 22, 26, and 30 wt% respectively, 10 wt% PHA and 1.25 wt% monosodium titanate (MST), all on an oxide basis. The remaining six glasses were selected from the Phase 1 and Phase 2 studies (Purex sludge) but with an increased amount of MST. The high-end target for MST of 2.5 wt% oxide was missed in Phases 1 and 2 due to (approximately)30 wt% water content of the MST. A goal of this Phase 4 study was to determine whether this increase in titanium concentration from the MST had any impact on glass quality or processibility. Two of the glasses, pha14c and pha15c, were rebatched and melted due to apparent batching errors with pha14 and pha15. The models currently in the Defense Waste Processing Facility's (DWPF) Product Composition Control System (PCCS) were used to predict durability, homogeneity, liquidus, and viscosity for these nine glasses. All of the HM glasses and half of the Purex glasses were predicted to be phase separated, and consequently prediction of glass durability is precluded with the cument models for those glasses that failed the homogeneity constraint. If one may ignore the homogeneity constraint, the measured durabilities were within the 95% prediction limits of the model. Further efforts will be required to resolve this issue on phase separation (inhomogeneity). The liquidus model predicted unacceptable liquidus temperatures for four of the nine glasses. The approximate, bounding liquidus temperatures measured for all had upper limits of 1,000 C or less. Given the fact that liquidus temperatures were only approximated, the 30 wt% loading of Purex may be near or at the edge of acceptability for liquidus. The measured viscosities were close to the predictions of the model. For the Purex glasses, pha12c and pha15c, the measured viscosities of 28 and 23 poise, respectively, indicate that DWPF processing may be compromised at the low end of the viscosity range (20 poise). Although the HM sludge glass examined (10 wt% PHA) had a measured viscosity of (approximately)90 poise, the HM glasses at 7wt% PHA are predicted to be higher than the 100 poise limit for DWPF. Further work will be required to resolve these issues.
This is the first book to present a topical overview of the research and development of microbial polyesters. Comprehensive and amply illustrated, it covers the * biosynthesis * structure * properties * applications of these biodegradable and biocompatible thermoplastics. The book provides the reader with the necessary background to understand the nature and mechanism of biological polymerization. It unites aspects from both the biological and polymer sciences and is a typical modern example of the analysis of biological macromolecules.
A guide to the development and manufacturing of pharmaceutical products written for professionals in the industry, revised second edition The revised and updated second edition of Chemical Engineering in the Pharmaceutical Industry is a practical book that highlights chemistry and chemical engineering. The book’s regulatory quality strategies target the development and manufacturing of pharmaceutically active ingredients of pharmaceutical products. The expanded second edition contains revised content with many new case studies and additional example calculations that are of interest to chemical engineers. The 2nd Edition is divided into two separate books: 1) Active Pharmaceutical Ingredients (API’s) and 2) Drug Product Design, Development and Modeling. The active pharmaceutical ingredients book puts the focus on the chemistry, chemical engineering, and unit operations specific to development and manufacturing of the active ingredients of the pharmaceutical product. The drug substance operations section includes information on chemical reactions, mixing, distillations, extractions, crystallizations, filtration, drying, and wet and dry milling. In addition, the book includes many applications of process modeling and modern software tools that are geared toward batch-scale and continuous drug substance pharmaceutical operations. This updated second edition: Contains 30new chapters or revised chapters specific to API, covering topics including: manufacturing quality by design, computational approaches, continuous manufacturing, crystallization and final form, process safety Expanded topics of scale-up, continuous processing, applications of thermodynamics and thermodynamic modeling, filtration and drying Presents updated and expanded example calculations Includes contributions from noted experts in the field Written for pharmaceutical engineers, chemical engineers, undergraduate and graduate students, and professionals in the field of pharmaceutical sciences and manufacturing, the second edition of Chemical Engineering in the Pharmaceutical Industryf ocuses on the development and chemical engineering as well as operations specific to the design, formulation, and manufacture of drug substance and products.
Encyclopedia of Renewable and Sustainable Materials, Five Volume Set provides a comprehensive overview, covering research and development on all aspects of renewable, recyclable and sustainable materials. The use of renewable and sustainable materials in building construction, the automotive sector, energy, textiles and others can create markets for agricultural products and additional revenue streams for farmers, as well as significantly reduce carbon dioxide (CO2) emissions, manufacturing energy requirements, manufacturing costs and waste. This book provides researchers, students and professionals in materials science and engineering with tactics and information as they face increasingly complex challenges around the development, selection and use of construction and manufacturing materials. Covers a broad range of topics not available elsewhere in one resource Arranged thematically for ease of navigation Discusses key features on processing, use, application and the environmental benefits of renewable and sustainable materials Contains a special focus on sustainability that will lead to the reduction of carbon emissions and enhance protection of the natural environment with regard to sustainable materials
