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Composition, critical

Alloy Composition Critical velocity in 25 mm dia. tube ms Critical shear stress Nm ... [Pg.295]

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. [Pg.439]

Figure 3.2. Fick diffusion coefficient D as a function of temperature for the system water-triethyl-amine. Measured data for Fick diffusivity D at constant composition = critical composition X2 = 0.0874. Critical temperature = 18.3°C. Data from Haase and Siry (1968). Figure 3.2. Fick diffusion coefficient D as a function of temperature for the system water-triethyl-amine. Measured data for Fick diffusivity D at constant composition = critical composition X2 = 0.0874. Critical temperature = 18.3°C. Data from Haase and Siry (1968).
Due to unsaturation or strain, equilibrium of the interatomic forces on a sur ce is reached by adsorption of surrounding molecules. Therefore, the chemical composition of the fost atomic layer may be different from that of the bulk. The importance of the sur ce with respect to the bulk in nanostructured powders makes the exact knowledge of the sur ce composition critical. Fourier transform infrared (FT-IR) spectrometry is a powerful tool to determine the nature of the chemical sur ce species as well as the reactive sites. As an example of an FT-IR sur ce study, a nanostructured aluminum nitride powder was analyzed and its sur ce was coiiq)ared with the y-alumina sur ce. [Pg.312]

Figure 1 Variation of tensile strength in an axially stressed fibre and shear stress at the interface in a short fibre-reinforced composite critical length of fibre = Z,. (Cox, H.L. (1952) Brit. J. Appl. Phys., 3, 72). Figure 1 Variation of tensile strength in an axially stressed fibre and shear stress at the interface in a short fibre-reinforced composite critical length of fibre = Z,. (Cox, H.L. (1952) Brit. J. Appl. Phys., 3, 72).
An investigation of several methodological aspects of obtaining urinary protein profiles by SELDI-TOF-MS revealed that among the extrinsic factors instrument settings and matrix composition critically influenced peak detection and reproducibility, while freeze-thaw cycles had minimal effects. Intrinsic factors of significance included blood in urine, dilution, and first-void vs. midstream urine [100]. [Pg.391]

Intramolecular [80] and intermolecular [81,82] trapping of acylpalladium intermediates with enolates has been studied. Intermolecular versions can involve trapping with both C- and 0-enolates. The Pd-catalyzed carbonylation reactions of alkenyl iodides in the presence of various ketone enolate precursors displayed an interesting dichotomy the expected 0-enolate trapping product 47 may undergo cyclization to give six-membered lactone 48, and the product s composition critically depends on the amount of a base and the structure of ketones (Scheme 9.19). [Pg.235]

The flow properties of adhesives and sealants depend on their composition. Critical flow properties are listed in Table 2. [Pg.279]

When the two components are mixed together (say in a mixture of 10% ethane, 90% n-heptane) the bubble point curve and the dew point curve no longer coincide, and a two-phase envelope appears. Within this two-phase region, a mixture of liquid and gas exist, with both components being present in each phase in proportions dictated by the exact temperature and pressure, i.e. the composition of the liquid and gas phases within the two-phase envelope are not constant. The mixture has its own critical point C g. [Pg.100]

The initial condition for the dry gas is outside the two-phase envelope, and is to the right of the critical point, confirming that the fluid initially exists as a single phase gas. As the reservoir is produced, the pressure drops under isothermal conditions, as indicated by the vertical line. Since the initial temperature is higher than the maximum temperature of the two-phase envelope (the cricondotherm - typically less than 0°C for a dry gas) the reservoir conditions of temperature and pressure never fall inside the two phase region, indicating that the composition and phase of the fluid in the reservoir remains constant. [Pg.102]

For both volatile oil and blaok oil the initial reservoir temperature is below the critical point, and the fluid is therefore a liquid in the reservoir. As the pressure drops the bubble point is eventually reached, and the first bubble of gas is released from the liquid. The composition of this gas will be made up of the more volatile components of the mixture. Both volatile oils and black oils will liberate gas in the separators, whose conditions of pressure and temperature are well inside the two-phase envelope. [Pg.104]

Classic nucleation theory must be modified for nucleation near a critical point. Observed supercooling and superheating far exceeds that predicted by conventional theory and McGraw and Reiss [36] pointed out that if a usually neglected excluded volume term is retained the free energy of the critical nucleus increases considerably. As noted by Derjaguin [37], a similar problem occurs in the theory of cavitation. In binary systems the composition of the nuclei will differ from that of the bulk... [Pg.335]

Fluctuations in density and composition produce opalescence, a recognized feature of the critical region. [Pg.648]

The field-density concept is especially usefiil in recognizing the parallelism of path in different physical situations. The criterion is the number of densities held constant the number of fields is irrelevant. A path to the critical point that holds only fields constant produces a strong divergence a path with one density held constant yields a weak divergence a path with two or more densities held constant is nondivergent. Thus the compressibility Kj,oi a one-component fluid shows a strong divergence, while Cj in the one-component fluid is comparable to (constant pressure and composition) in the two-component fluid and shows a weak... [Pg.649]

Figure A2.5.31. Calculated TIT, 0 2 phase diagram in the vicmity of the tricritical point for binary mixtures of ethane n = 2) witii a higher hydrocarbon of contmuous n. The system is in a sealed tube at fixed tricritical density and composition. The tricritical point is at the confluence of the four lines. Because of the fixing of the density and the composition, the system does not pass tiirough critical end points if the critical end-point lines were shown, the three-phase region would be larger. An experiment increasing the temperature in a closed tube would be represented by a vertical line on this diagram. Reproduced from [40], figure 8, by pennission of the American Institute of Physics. Figure A2.5.31. Calculated TIT, 0 2 phase diagram in the vicmity of the tricritical point for binary mixtures of ethane n = 2) witii a higher hydrocarbon of contmuous n. The system is in a sealed tube at fixed tricritical density and composition. The tricritical point is at the confluence of the four lines. Because of the fixing of the density and the composition, the system does not pass tiirough critical end points if the critical end-point lines were shown, the three-phase region would be larger. An experiment increasing the temperature in a closed tube would be represented by a vertical line on this diagram. Reproduced from [40], figure 8, by pennission of the American Institute of Physics.
Other pairs of liquids which exhibit an upper consolute temperature are methyl alcohol - cyclohexane (C.S.T. 49 -1° critical composition 29 per cent, by weight of methyl alcohol) isopentane - phenol (63 5° 51 per cent, of isopentane) and carbon disulphide - methyl alcohol (40-5° 80 per cent, of carbon disulphide). [Pg.18]

Many pairs of partially miscible liquids possess neither a lower nor an upper C.S.T. for reasons outlined in the previous paragraph. Thus consider the two liquid phases from the two components water and diethyl ether. Upon cooling the system at constant pressure, a point will be reached when a third phase, ice, will form, thus rendering the production of a lower C.S.T. impossible, likewise, if the temperature of the two layers is raised, the critical point for the ether rich layer will be reached while the two liquid phases have different compositions. Above the critical point the ether-rich layer will be converted into vapour, and hence the system will be convert into a water rich liquid and an ether rich vapour the upper C.S.T. cannot therefore be attained. [Pg.19]

Still assuming terminal control, evaluate r and T2 from these data. Criticize or defend the following proposition The copolymer composition equation does not provide a very sensitive test for the terminal control mechanism. [Pg.499]

Fig. 3. Typical nonionic amphiphile—oil—water—temperature phase diagram, illustrating (a) the S-shaped curve of T, M, and B compositions, (b) the lines of plait points, (c) the lower and upper critical end points (at and respectively), and (d) the lower and upper critical tielines. Fig. 3. Typical nonionic amphiphile—oil—water—temperature phase diagram, illustrating (a) the S-shaped curve of T, M, and B compositions, (b) the lines of plait points, (c) the lower and upper critical end points (at and respectively), and (d) the lower and upper critical tielines.
Modem scaling theory is a quite powerful theoretical tool (appHcable to Hquid crystals, magnets, etc) that has been well estabUshed for several decades and has proven to be particularly useful for multiphase microemulsion systems (46). It describes not just iuterfacial tensions, but virtually any thermodynamic or physical property of a microemulsion system that is reasonably close to a critical poiat. For example, the compositions of a microemulsion and its conjugate phase are described by equations of the foUowiug form ... [Pg.152]


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See also in sourсe #XX -- [ Pg.536 ]




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