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Peaking units

SERVICE ouantity SUSTAINED - - PEAK UNIT KVA OPERATING PRESSURE TEMPERATURE REMARKS... [Pg.34]

Therefore we now focus on the hour 3-4 p.m., for which intertemporal effects and the gas-price impact from peaking units running at maximum a few hours a day is least prevalent, as indicated... [Pg.58]

Methylene Carbon Peaks Unit Sequence not resolvable 39.0 - 34.0 (rrr - mmm) ... [Pg.273]

The surface profilometer software calculates numerous parameters from the surface roughness profile. As the Advanced Processing Program continues, the research effort will be focused on detennining which of these roughness parameters or additional spectral analysis (max peak/unit distance, fractal dimension, etc.) are predictive of mechanical behavior, and relating them to fabrication variables. [Pg.88]

Table 2.3. Abundances of isotopic peaks (unit resolution) from element combinations. ... [Pg.3]

Measure the area of the benzene peak. Units must be consistent with 9.4. [Pg.706]

For liquid and gaseous fuel For nonpeaking imits, 800 g/GJ of output, and for peaking units, 970 g/GJ of output, all based on the lower heating value of the fuel. [Pg.280]

Photodissociation cross sections tend to peak in the 10 cm range and hence are often given in Mb (megabam) units. [Pg.800]

Furthennore, the magnetic diffraction and the nuclear diffraction do not interfere with one another, and the nuclear and magnetic intensities simply add together, although in many cases the magnetic unit cell is larger than the nuclear unit cell, which produces additional diffraction peaks. [Pg.1367]

These are the same states as in Figure Bl.l 1.8, but attention is now drawn to the populations of the four spin states, each reduced by subtracting the 25% population that would exist at very low field, or alternatively at infinite temperature. The figures above each level are these relative differences, in convenient units. The intensity of any one transition, i.e. of the relevant peak in the doublet, is proportional to the difference of these differences, and is therefore proportionally relative to unity for any transition at Boltzmaim equilibrium, and 4 for any transition. [Pg.1456]

The use of larger particles in the cyclotron, for example carbon, nitrogen or oxygen ions, enabled elements of several units of atomic number beyond uranium to be synthesised. Einsteinium and fermium were obtained by this method and separated by ion-exchange. and indeed first identified by the appearance of their concentration peaks on the elution graph at the places expected for atomic numbers 99 and 100. The concentrations available when this was done were measured not in gcm but in atoms cm. The same elements became available in greater quantity when the first hydrogen bomb was exploded, when they were found in the fission products. Element 101, mendelevium, was made by a-particle bombardment of einsteinium, and nobelium (102) by fusion of curium and the carbon-13 isotope. [Pg.443]

Likewise, a basis set can be improved by uncontracting some of the outer basis function primitives (individual GTO orbitals). This will always lower the total energy slightly. It will improve the accuracy of chemical predictions if the primitives being uncontracted are those describing the wave function in the middle of a chemical bond. The distance from the nucleus at which a basis function has the most significant effect on the wave function is the distance at which there is a peak in the radial distribution function for that GTO primitive. The formula for a normalized radial GTO primitive in atomic units is... [Pg.234]

Chemical shifts are expressed in S units ppm of applied magnetic field with internal TMS peak as reference. [Pg.67]

All the chemical shifts are expressed in 5 units ppm of applied field and TMS as reference peak. [Pg.76]

The most obvious feature of these C chemical shifts is that the closer the carbon is to the electronegative chlorine the more deshielded it is Peak assignments will not always be this easy but the correspondence with electronegativity is so pronounced that spec trum simulators are available that allow reliable prediction of chemical shifts from structural formulas These simulators are based on arithmetic formulas that combine experimentally derived chemical shift increments for the various structural units within a molecule... [Pg.550]

There is a small peak one mass unit higher than M m the mass spectrum of ben zene What is the origin of this peak d What we see m Figure 13 40 as a single mass spectrum is actually a superposition of the spectra of three isotopically distinct benzenes Most of the benzene molecules contain only and H and have a molecular mass of 78 Smaller proportions of benzene molecules contain m place of one of the atoms or m place of one of the protons Both these species have a molecular mass of 79... [Pg.569]

Not only the molecular ion peak but all the peaks m the mass spectrum of benzene are accompanied by a smaller peak one mass unit higher Indeed because all organic com pounds contain carbon and most contain hydrogen similar isotopic clusters will appear m the mass spectra of all organic compounds... [Pg.569]

The peak at m/z 77 m the mass spectrum of chlorobenzene m Figure 13 41 is attributed to this fragmentation Because there is no peak of significant intensity two atomic mass units higher we know that the cation responsible for the peak at m/z 77 cannot contain chlorine... [Pg.570]

Section 13 20 IR spectroscopy probes molecular structure by examining transitions between vibrational energy levels using electromagnetic radiation m the 625-4000 cm range The presence or absence of a peak at a charac tenstic frequency tells us whether a certain functional group is present Table 13 4 lists IR absorption frequencies for common structural units... [Pg.577]

Natural Isotopic Abundances. The relative abundances of natural isotopes produce peaks one or more mass units larger than the parent ion (Table 7.75a). For a compound C H O N, a formula allows one to calculate the percent of the heavy isotope contributions from a monoisotopic peak, Pto the Pm + 1 peak ... [Pg.812]

Compounds that contain chlorine, bromine, sulfur, or silicon are usually apparent from prominent peaks at masses 2, 4, 6, and so on, units larger than the nominal mass of the parent or fragment ion. Eor example, when one chlorine atom is present, the P + 2 mass peak will be about one-third the intensity of the parent peak. When one bromine atom is present, the P + 2 mass peak will be about the same intensity as the parent peak. The abundance of heavy isotopes is treated in terms of the binomial expansion (a -I- h) , where a is the relative abundance of the light isotope, b is the relative abundance of the heavy isotope, and m is the number of atoms of the particular element present in the molecule. If two bromine atoms are present, the binomial expansion is... [Pg.812]

For example, a metastable peak appeared at 147.9 mass units in a mass spectrum with prominent peaks at 65, 91, 92, 107, 108, 155, 172, and 200 mass units. Try all possible combinations in the above expression. The fit is given by... [Pg.814]

Retention Behavior. On a chromatogram the distance on the time axis from the point of sample injection to the peak of an eluted component is called the uncorrected retention time The corresponding retention volume is the product of retention time and flow rate, expressed as volume of mobile phase per unit time ... [Pg.1104]


See other pages where Peaking units is mentioned: [Pg.406]    [Pg.407]    [Pg.648]    [Pg.294]    [Pg.208]    [Pg.79]    [Pg.80]    [Pg.258]    [Pg.280]    [Pg.41]    [Pg.225]    [Pg.272]    [Pg.9]    [Pg.406]    [Pg.407]    [Pg.648]    [Pg.294]    [Pg.208]    [Pg.79]    [Pg.80]    [Pg.258]    [Pg.280]    [Pg.41]    [Pg.225]    [Pg.272]    [Pg.9]    [Pg.11]    [Pg.450]    [Pg.1373]    [Pg.1381]    [Pg.1454]    [Pg.1458]    [Pg.1866]    [Pg.563]    [Pg.739]    [Pg.523]    [Pg.539]    [Pg.540]   
See also in sourсe #XX -- [ Pg.79 ]




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Measurement units molecular peaks

Peak positions as a function of unit cell dimensions

Unit-Mass Molecular Ion and Isotope Peaks

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