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Drying overview

Overview. Three approaches are used to make most sol—gel products method 1 involves gelation of a dispersion of colloidal particles method 2 employs hydrolysis and polycondensation of alkoxide or metal salts precursors followed by supercritical drying of gels and method 3 involves hydrolysis and polycondensation of alkoxide precursors followed by aging and drying under ambient atmospheres. [Pg.249]

Applications Identification of polymer additives by TLC-IR is labour intensive and comprises extraction, concentration of extracts, component separation by TLC on silica, drying, removal of spots, preparation of KBr pellets and IR analysis. The method was illustrated with natural rubber formulations, where N-cyclohexyl-2-benzothiazyl sulfenamide, IPPD and 6PPD antioxidants, and a naphthenic plasticiser were readily quantified [765]. An overview of polymer/additive type compounds analysed by transfer TLC-FTIR is given in Table 7.80. [Pg.534]

Gharsallaoui, A., G. Roudaut, O. Chambin et al. 2007. Applications of spray-drying in microencapsulation of food ingredients An overview. Food Res. Int. 40 1107-1121. [Pg.251]

Figure 8.7 Overview of the manufacture of Betaferon, a recombinant human IFN-(3 produced in E. coli. The product differs from native human IFN-(3 in that it is unglycosylated and cysteine residue 17 had been replaced by a serine residue. E. coli fermentation is achieved using minimal salts/glucose media and product accumulates intracellularly in inclusion body (IB) form. During downstream processing, the lbs are solubilized in butanol, with subseguent removal of this denaturant to facilitate product refolding. After two consecutive gel-filtration steps, excipients are added, the product is filled into glass vials and freeze-dried. It exhibits a shelf life of 18 months when stored at 2-8 °C... Figure 8.7 Overview of the manufacture of Betaferon, a recombinant human IFN-(3 produced in E. coli. The product differs from native human IFN-(3 in that it is unglycosylated and cysteine residue 17 had been replaced by a serine residue. E. coli fermentation is achieved using minimal salts/glucose media and product accumulates intracellularly in inclusion body (IB) form. During downstream processing, the lbs are solubilized in butanol, with subseguent removal of this denaturant to facilitate product refolding. After two consecutive gel-filtration steps, excipients are added, the product is filled into glass vials and freeze-dried. It exhibits a shelf life of 18 months when stored at 2-8 °C...
Table 8.1 gives an overview of structural and operational measures that affect the type and course of the in-sewer dry-weather processes. The table exemplifies how process design and operation of sewer networks can be implemented. In other words, it is an overview of methods for wastewater design. ... [Pg.207]

Both wet-ceramic techniques and direct-deposition techniques require preparation of the feedstock, which can consist of dry powders, suspensions of powders in liquid, or solution precursors for the desired phases, such as nitrates of the cations from which the oxides are formed. Section 6.1.3 presented some processing methods utilized to prepare the powder precursors for use in SOFC fabrication. The component fabrication methods are presented here. An overview of the major wet-ceramic and direct-deposition techniques utilized to deposit the thinner fuel cell components onto the thicker structural support layer are presented below. [Pg.256]

Practically all available iodinated extracellular X-ray contrast agents have been encapsulated into liposomes using different lipids and methods of preparation. Table 1 gives a short and intentionally incomplete overview of some of the approaches. The first liposomal contrast agent preparation that was tested in humans contained diatrizoate [48]. The injected dose was up to 0.5 ml kg k The preparation was effective even in plain radiography where lesions down to 0.8-1.0 cm could be detected in patients. However, adverse events such as fever and hyperthermia, which occurred in 30% of the patients, limited further use. We have incorporated iopromide into MLVs that were prepared from phosphatidyl choline (PC), cholesterol and stearic acid at a molar ratio of 4 5 1 using the ethanol-evaporation technique [44]. The liposomes can be stored freeze-dried and they are reconstituted before use by... [Pg.182]

Keey, R.B., The industrial drying of foods an overview, in Baker, C.G.J., (ed.). Industrial drying of foods, Blackie, London, 1997. [Pg.136]

Neorecormon is one such product. Produced in an engineered CHO cell line constitutively expressing the EPO gene, the product displays an amino acid sequence identical to the native human molecule. An overview of its manufacturing process is presented in Figure 6.7. The final freeze-dried product contains urea, sodium chloride, polysorbate, phosphate buffer and several amino acids as excipients. It displays a shelf-life of 3 years when stored at 2-8 °C. A pre-filled syrine form of the product (in solution) is also available, which is assigned a 2 year shelf-life at 2-8 °C. [Pg.268]

An overview of potential excipient physicochemical factors that influence dry powder dispersion are summarized here. [Pg.240]

The submicron particle number size distribution controls many of the main climate effects of submicron aerosol populations. The data from harmonized particle number size distribution measurements from European field monitoring stations are presented and discussed. The results give a comprehensive overview of the European near surface aerosol particle number concentrations and number size distributions between 30 and 500 nm of dry particle diameter. Spatial and temporal distributions of aerosols in the particle sizes most important for climate applications are presented. Annual, weekly, and diurnal cycles of the aerosol number concentrations are shown and discussed. Emphasis is placed on the usability of results within the aerosol modeling community and several key points of model-measurement comparison of submicron aerosol particles are discussed along with typical concentration levels around European background. [Pg.297]

The analytical method for moisture determination must be validated before use during process validation studies. There are numerous techniques for moisture analysis that range from physical methods, such as loss on drying, to chemical methods, such as Karl Fisher titration. A comparative review of the conventional techniques are presented in an overview [32], The measurement of residual moisture is lyophilized pharmaceuticals by near-infrared (NIR) spectroscopy has recently been expanded [33]. [Pg.360]

The purpose of this chapter is to present a description of the freeze drying process, an overview of the physical chemistry of freezing and freeze drying, as well as a discussion of the influence of physical state of... [Pg.261]

III. AN OVERVIEW OF THE PHYSICAL CHEMISTRY OF FREEZING AND FREEZE DRYING... [Pg.264]


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Overview of Dry Granulation Processes and Equipment Design

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