Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Temperature conversion chart

TABLE 5 Film Development Temperature Conversion Chart... [Pg.335]

A-l Alphabetical Conversion Factors, 416 A-2 Physical Property Conversion Factors, 423 A-3 Synchronous Speeds, 426 A-4 Conversion Factors, 427 A-5 Temperature Conversion, 429 A-6 Altitude and Atmospheric Pressures, 430 A-7 Vapor Pressure Curves, 431 A-8 Pressure Conversion Chart, 432 A-9 Vacuum Conversion, 433 A-10 Decimal and Millimeter Equivalents of Fractions,... [Pg.499]

Figure 3.18 is a conversion chart for the reactant mixture and shows rate curves in the conversion-temperature plane. The line AA is plotted on the chart from the linear T—x relation. The rate of reaction at any conversion level within the reactor may therefore be obtained by reading the rate corresponding to the intersection of the line with various conversion ordinates. [Pg.159]

This conversion chart can be used to easily determine changes in development time at different temperatures. Find the recommended time/temperature then use the time to the left or right for changes in temperature. [Pg.335]

The best current 100% solids epoxy adhesives contain about 70% aluminum oxide by weight and give thermal conductivities in the range of 0.8-1 in the English units shown in Table 2. For convenience, a conversion chart is included in Table 2 to permit conversion to any other set of units. The k values for the best alumina-filled epoxies are 10-12 times greater than for unfilled epoxy resins, but are still much lower than for pure metals or solders. Nevertheless, heat flow is adequate for bonding most components. For example, an adhesive with a thermal conductivity of 0.91 and a bond thickness of 3 mils would be able to transfer about 20 W/cm of surface area, with a AT only about 10 C above the heat sink temperatures ... [Pg.709]

Pressure/vacuum, 435, 466 Vacuum systems, 343 Absolute pressure conversions, 363 Air inleakage, 366 Calculations, 366-375 Dissolved gases release, 368 Estimated air inleakage, table, 366 Evacuation time, 371 Maximum air leakage, chart, 367 Specific air inleakage rates, 368 Temperature approach, 375 Classifications, 343 Diagrams, 380 Pressure drop, 353 Pressure levels, 343, 352 Pressure terminology, 348 Pump down example, 381 Pump down time, 380 Thermal efficiency, 384 Valve codes, 26... [Pg.630]

The friction factor may be calculated from a knowledge of the fluid Reynolds number using the chart shown as Figure 13.2. Table 13.1 indicates the friction factors that correspond to zero and 80% conversion for the three pipe sizes of interest at two temperature levels. Examination... [Pg.545]

Energy conversion table. Values of photon (vacuum) wavelength (nm), wavenumber (1 cm-1), frequency (THz) and energy (eV, J), as well as the energy per mole (J mol-1) of a chemical reaction can be easily converted if a ruler is placed horizontally over the chart. The bandgaps of different semiconductors are also indicated, as well as the wavelength of the intensity peak of a blackbody radiation for different temperatures. [Pg.272]

Suitable conversion tables are available (ASTM D341), and each table or chart is constructed such that for any given petroleum or petroleum product, the viscosity-temperature points result in a straight line over the applicable temperature range. Thus, only two viscosity measurements need be made at temperatures far enough apart to determine a line on the appropriate chart from which the approximate viscosity at any other temperature can be read. [Pg.50]

Besides proving the formation of p-chelates [Pd(CH7CH7C(0)Me)(P-P)] at room temperature, the spectra showed the occurrence of chain-transfer by protonolysis with adventitious water to give the p-hydroxo compounds cis/trans [Pd(p-OH)(P-P)]2 as well as the conversion of the latter compounds into cis/trans bis-chelates [Pd(P-P)2] (Chart 7.2) [5f]. Independent experiments with isolated compounds showed that the p-OH and bis-chelate complexes are not dead ends, and can reenter the catalysis cycle to give alternating polyketones. [Pg.283]

CONSTRUCTION OF THE RATE CONVERSION-TEMPERATURE CHART FROM KINETIC DATA... [Pg.217]

With the system of Example 9.2 and starting with an R-free solution, kinetic experiments in a batch reactor give 58.1% conversion in 1 min at 65°C, 60% conversion in 10 min at 25°C. Assuming reversible first-order kinetics, find the rate expression for this reaction and prepare the conversion-temperature chart with reaction rate as parameter. [Pg.217]

Chart / shows a plot of gross conversion of raw material as a function of temperature and recycle of product. The lines are contours of percentage of conversion and show that the increase in the percentage of conversion with percentage of product depends on the reaction temperature. [Pg.102]

Chart II shows the same response at a higher level of activator. Comparison with Chart I shows that activator gives higher conversion at high temperatures but lower conversion at low temperatures. [Pg.102]

Chart 17. Linear Polymer — 2D Grid Structure Conversion at Room Temperature... [Pg.364]

Psychrometric Software and Tables As an alternative to using charts or individual calculations, lookup tables have been published for many years for common psychrometric conversions, e.g., to find relative humidity given the dry-bulb and wet-bulb temperatures. These were often very extensive. To give precise coverage of in 1°C or 0.1°C steps, a complete table woul(3 be needed for each individual dry-bulb temperature. [Pg.1334]

Sterically Restricted Poly (methacrylate ester)s. It was recognized by Okamoto and coworkers150 that the anionic polymerization of tri-phenylmethyl methacrylate (TrMA, 41) (Chart 8) at low temperature in the presence of an optically active initiator results in the formation of an isotactic, optically active polymer. The helical conformation of the backbone in these macromolecules is the result of steric interactions between the bulky trityl groups, as was shown by the loss of optical activity upon their conversion to methyl ester groups. This class of bulky... [Pg.349]

A 5% increase in reactor feed temperature was introduced and maintained for 60 min before returning the feed stream to normal operating conditions. The multivariate charts (Figure 5.2) are the first to detect the disturbance to the reactor operation. The statistic exceeds the 99% confidence interval 25 min after the disturbance was introduced, and the SPE statistic 20 min after the disturbance, a few minutes earlier than the chart. The initiator concentration in the reactor exceeds the statistical limits of the Shewhart chart (Figure 5.3) after 35 min. Reactor temperature and conversion readings exceed the statistical limits after approximately 40 min and the polydispersity measurement exceeds the univariate limit after 44 min. [Pg.105]

For the l,5-dimethyl-3,7-di-tert-butyl-3,7-diazybicyclo[3.3.1]nonan-9-one (96) the cb conformation is observed in the solid state (see Chart 14). However, it is not clear whether this conformation is a result of the bulky N-substiments or an effect of the hindered flattening of the wings due to the 1,5-methyl substituents (157). Interestingly, the 1,5-dinitro derivative 97, which has no sterically demanding substiments, shows a cb conformation in the solid state and an interconversion between the degenerate cb and be forms in solution. The activation barrier was found by low temperature C-NMR experiments to be 27.2 kj moP (158). Direct conversion of 97 yields the 1,5-diamino derivative 98, from which the 1,5-dibromo- (99) and the 1,5-dUiydroxo-derivatives (100) are obtained (see Scheme 11). These all adopt the twin-chair conformation in the solid state (144). [Pg.632]


See other pages where Temperature conversion chart is mentioned: [Pg.30]    [Pg.186]    [Pg.560]    [Pg.30]    [Pg.186]    [Pg.560]    [Pg.341]    [Pg.518]    [Pg.104]    [Pg.214]    [Pg.232]    [Pg.452]    [Pg.67]    [Pg.122]    [Pg.354]    [Pg.643]    [Pg.499]    [Pg.278]    [Pg.55]    [Pg.173]    [Pg.59]    [Pg.128]    [Pg.6]    [Pg.109]    [Pg.59]    [Pg.509]    [Pg.571]    [Pg.173]   
See also in sourсe #XX -- [ Pg.335 ]




SEARCH



Temperature conversions

© 2024 chempedia.info