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Elemental shifts

For the case of a double-D coil we multiply each matrix element with an element shifted by a constant distance of the same line. This is done in x- and y-direction. The distance between the two elements is the correlation length X for filtering in x-direction and a second correlation length for the movement in y-direction. Thus one gets two new matrices Ax and Ax for the filtering from the left to the right (positiv x-direction) and vice versa (negativ x-direction). [Pg.261]

Titanium is susceptible to pitting and crevice corrosion in aqueous chloride environments. The area of susceptibiUty for several alloys is shown in Figure 7 as a function of temperature and pH. The susceptibiUty depends on pH. The susceptibiUty temperature increases paraboHcaHy from 65°C as pH is increased from 2ero. After the incorporation of noble-metal additions such as in ASTM Grades 7 or 12, crevice corrosion attack is not observed above pH 2 until ca 270°C. Noble alloying elements shift the equiUbrium potential into the passive region where a protective film is formed and maintained. [Pg.104]

Scientific chemistry has its roots in the European Enlightenment. All 92 naturally occurring elements were discovered and identified here. The map shows that England, France, and Sweden played central roles, whereas in Germany research was carried out in the various regional centers. With the advent of atomic research, the emphasis on the discovery of the artificial elements shifted to the USA. They were later joined by Russia (Dubna) and Germany (Institute for Heavy-Ion Research). [Pg.103]

At this stage of the synthesis, it was necessary to resort to a second conformational control element (shifting the B ring from a chair-chair to a boat-chair conformation), which ensures the generation of the C(l)-C(2) enolate of a C(2) ketone and allows the epimerisation of the substituent at C(3)a (which will return the B ring to the chair-chair conformation). [Pg.402]

Since the nucleus undergoing (i decay is usually contained in an atom or a molecule, the /J decay is accompanied by rearrangement of the corresponding electron shell. The f decay results in the formation of a positive molecular ion in which the initial radioactive nucleus has transformed into a nucleus of the element shifted one square to the right in the periodic table. In the case of fi+ decay, the daughter ion is charged negatively, and the radioactive nucleus is replaced by a nucleus of the element shifted one square to the left in the periodic table.1 Namely... [Pg.289]

The percolation model suggests that it may not be necessary to have a rigid geometry and definite pathway for conduction, as implied by the proton-wire model of membrane transport (Nagle and Mille, 1981). For proton pumps the fluctuating random percolation networks would serve for diffusion of the ion across the water-poor protein surface, to where the active site would apply a vectorial kick. In this view the special nonrandom structure of the active site would be limited in size to a dimension commensurate with that found for active sites of proteins such as enzymes. Control is possible conduction could be switched on or off by the addition or subtraction of a few elements, shifting the fractional occupancy up or down across the percolation threshold. Statistical assemblies of conducting elements need only partially fill a surface or volume to obtain conduction. For a surface the percolation threshold is at half-saturation of the sites. For a three-dimensional pore only one-sixth of the sites need be filled. [Pg.150]

As electro positivity increases, the azides of the heavier IV A elements shift toward a more hydrophile behavior. This pattern is qualitatively noticeable in the triorganyl element azides (see Table XFV for trimethyl compounds). The triphenyl compounds display a similar behavior [9,261,272]. Basically, all R3E1(N3) compounds are accessible from the respective chloro compounds and sodium azide in ether/water media [273]. [Pg.68]

Becently the flow-pressure drop characteristics of the stainless steel element shifted abruptly and the cause of this shift must be determined and steps taken to prevent Its recurrence. Plugging of the pores In the restrictor Is a likely cause, but some effort must be expended to verify this. [Pg.48]

If a diode s source of power is an alternating emf, electrons can flow during only half the cycle. A simple diode with a single-phase AC supply voltage produces a series of half-waves separated by half-cycle intervals. A three-phase signal has no periods without current flow but is still extremely choppy. Adding a second element shifted 180° in phase from the first, for example in a second wye connection with reversed polarity, fills the gaps and produces full-wave rectification. [Pg.717]

Stream. The volume element shifted can be determined by calibration. This principle is applied with all existing modern micro flow systems. [Pg.262]

Electronegative elements shift absorptions downfield. The carbons of alkenes and benzene rings, and carbonyl carbons are also shifted downfield. [Pg.359]


See other pages where Elemental shifts is mentioned: [Pg.125]    [Pg.135]    [Pg.154]    [Pg.428]    [Pg.281]    [Pg.94]    [Pg.527]    [Pg.154]    [Pg.270]    [Pg.344]    [Pg.453]    [Pg.467]    [Pg.57]    [Pg.2639]    [Pg.281]    [Pg.121]    [Pg.181]    [Pg.527]    [Pg.440]    [Pg.37]    [Pg.145]   
See also in sourсe #XX -- [ Pg.121 , Pg.122 , Pg.123 ]




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Chemical Shifts of Other Elements

Chemical isomer shift elements)

HEMICAL SHIFT CORRELATIONS FOR 13C AND OTHER ELEMENTS

Principal elements chemical shift tensors

Sampling element, phase shift

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