Spectroscopy, particle size distribution

Several properties of the filler are important to the compounder (279). Properties that are frequentiy reported by fumed sihca manufacturers include the acidity of the filler, nitrogen adsorption, oil absorption, and particle size distribution (280,281). The adsorption techniques provide a measure of the surface area of the filler, whereas oil absorption is an indication of the stmcture of the filler (282). Measurement of the sdanol concentration is critical, and some techniques that are commonly used in the industry to estimate this parameter are the methyl red absorption and methanol wettabihty (273,274,277) tests. Other techniques include various spectroscopies, such as diffuse reflectance infrared spectroscopy (drift), inverse gas chromatography (igc), photoacoustic ir, nmr, Raman, and surface forces apparatus (277,283—290). 

Suhtnicion nickel powders luive been synthesized successfully from aqueous NiCh at various tempmatuTKi and times with ethanol-water solvent by using the conventional and ultrasonic chemical reduction method. The reductive condition was prepared by flie dissolution of hydrazine hydrate into basic solution. The samples synthesized in various conditions weae claractsiz by the m ins of an X-ray diffractometry (XRD), a scanning electron microscopy (SEM), a thermo-gravimetry (TG) and an X-ray photoelectron spectroscopy (XPS). It was found that the samples obtained by the ultrasonic method were more smoothly spherical in shape, smaller in size and narrower in particle size distribution, compared to the conventional one. 

Covering monometallic (Pd, Sn) and multimetallic (Pd-Sn, Pd-Ag) systems, several examples are presented in this chapter to illustrate the possibility offered by this chemistry to control the particle size distribution and the bimetallic interaction at a molecular level. This work is supported by a multitechnique characterization approachusing SnM6ssbauerspectroscopy,X-rayphotoelectron spectroscopy (XPS), low-energy ion spectroscopy (LEIS), and transmission electron microscopy (TEM). Catalytic performances in hydrogenation of different unsaturated hydrocarbons (phenylacetylene, butadiene) are finally discussed in order to establish structure-reactivity relationships. 

Raman spectroscopy s sensitivity to the local molecular enviromnent means that it can be correlated to other material properties besides concentration, such as polymorph form, particle size, or polymer crystallinity. This is a powerful advantage, but it can complicate the development and interpretation of calibration models. For example, if a model is built to predict composition, it can appear to fail if the sample particle size distribution does not match what was used in the calibration set. Some models that appear to fail in the field may actually reflect a change in some aspect of the sample that was not sufficiently varied or represented in the calibration set. It is important to identify any differences between laboratory and plant conditions and perform a series of experiments to test the impact of those factors on the spectra and thus the field robustness of any models. This applies not only to physical parameters like flow rate, turbulence, particulates, temperature, crystal size and shape, and pressure, but also to the presence and concentration of minor constituents and expected contaminants. The significance of some of these parameters may be related to the volume of material probed, so factors that are significant in a microspectroscopy mode may not be when using a WAl probe or transmission mode. Regardless, the large calibration data sets required to address these variables can be burdensome. 

A. Gupta, G.E. Peck, R.W. Miller and K.R. Morris, Nondestructive measurements of the compact strength and the particle-size distribution after milling of roller compacted powders by near-infrared spectroscopy, J. Pharm. Sci., 93(4), 1047-1053 (2004). 

A.J. O Neil, R.D. Jee and A.C. Moffat, Measurement of the cumulative particle size distribution of microcrystalline cellulose using near infrared reflectance spectroscopy. Analyst, 124, 33-36 (1999). 

M. Blanco and A. Peguero, An expeditious method for determining particle size distribution by near infrared spectroscopy comparison of PLS2 and ANN models, Talanta, 77(2), 647-651 (2008). 

Methods for analysis of the particle size distribution in the aerosol cloud include techniques such as time of flight measurement (TOE), inertial impaction and laser diffraction. Dynamic light scattering (photon correlation spectroscopy) is confined to particles (in suspension) in the submicron range. In addition to the size distribution, the particle velocity distribution can be measured with the Phase Doppler technique. 

Chem. Geol. 157 275-284 Meisel.W. (1989) Corrosion processes and their inhibition as studied by Mdssbauer conversion and other electron spectroscopies. Hy-perfine Interactions 45 73-90 Meisen, U. Kathrein, H. (2000) The influence of particle size, shape and particle size distribution on properties of magnetites for the production of toners. J. Imag. Sci. Techn. 44 508-513... 

Chu 1991 Schmitz 1990). For example, the dynamic version of the diffusing wave spectroscopy described in Vignette V is a form of DLS, although in diffusing wave spectroscopy the method of analysis is different in view of multiple scattering. Most of the advanced developments are beyond the scope of this book. However, DLS is currently a routine laboratory technique for measuring diffusion coefficients, particle size, and particle size distributions in colloidal dispersions, and our objective in this section is to present the most essential ideas behind the method and show how they are used for particle size and size distribution measurements. 

Abstract We review the preparation, characterization, and properties of dendrimer-templated bimetallic nanoparticles. Polyamidoamine (PAMAM) dendrimers can be used to template and stabilize a wide variety of mono- and bimetallic nanoparticles. Depending on the specific requirements of the metal system, a variety of synthetic methodologies are available for preparing nanoparticles with diameters on the order of 1-3 nm with narrow particle size distributions. The resulting dendrimer-encapsulated nanoparticles, or DENs, have been physically characterized with electron microscopy techniques, as well as UV-visible and X-ray photoelectron spectroscopies. 

Each of the aforementioned techniques is capable of measuring powder that would be used in low-dose, solid oral dosage formulations. The technique must be compatible with the drug substance, and must be capable of producing the information that is needed. For example, if the particle size distribution is needed to ensure dose content uniformity, photon correlation spectroscopy can only provide an average particle size. In this instance, laser diffraction or image analysis would be more suitable techniques. Table 13.1 contains a comparison of the techniques that have been discussed. 

In essence, the test battery should include XRPD to characterize crystallinity of excipients, moisture analysis to confirm crystallinity and hydration state of excipients, bulk density to ensure reproducibility in the blending process, and particle size distribution to ensure consistent mixing and compaction of powder blends. Often three-point PSD limits are needed for excipients. Also, morphic forms of excipients should be clearly specified and controlled as changes may impact powder flow and compactibility of blends. XRPD, DSC, SEM, and FTIR spectroscopy techniques may often be applied to characterize and control polymorphic and hydrate composition critical to the function of the excipients. Additionally, moisture sorption studies, Raman mapping, surface area analysis, particle size analysis, and KF analysis may show whether excipients possess the desired polymorphic state and whether significant amounts of amorphous components are present. Together, these studies will ensure lotto-lot consistency in the physical properties that assure flow, compaction, minimal segregation, and compunction ability of excipients used in low-dose formulations. 

During these temperature and gas treatments, processes like reduction, oxidation and sintering take place. In Chapter 2 it is clarified what processes are responsible for the final metal particle size and particle size distribution. This is done using a combination time resolved extended X-ray absorption fine structure spectroscopy (quick EXAFS) and mass spectrometry. 

Photon correlation spectroscopy (PCS) has become a method of choice for sizing particles in the 3-3000nm range. Advances in the analysis of PCS data permit extraction of the particle size distribution as well as the mean diameter. 

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