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Structural changes during adsorption

The structural parameters of the complexes were studied in the dry and swollen states by WAXS, SAXS, DSC, nitrogen BET adsorption, ISEC and pycnometry. The original polymer structure changed during complex formation to materials of higher porosity. The relationship between the support structure and catalyst activity and selectivity was studied in model reactions, namely, hydrosilylation of alkenes, dienes and alkynes (Scheme 11.6). [Pg.320]

Figure 8 Simulated adsorption by molecular dynamics of (A) poly (p-phenylene) oxide (PRO), (B) poly(methyl-l,4-phenylene) (PMP) and (C) poly(iso-propyl-l,4-phenylene) (PIPP) on an alumina surface showing substantial structural changes during the adsorption process (upper figure initial conformation lower figure = adsorbed conformation) (From Ref. 71.) Note the formation or absence of adsorption loops in the polymer chains for the different cases. Figure 8 Simulated adsorption by molecular dynamics of (A) poly (p-phenylene) oxide (PRO), (B) poly(methyl-l,4-phenylene) (PMP) and (C) poly(iso-propyl-l,4-phenylene) (PIPP) on an alumina surface showing substantial structural changes during the adsorption process (upper figure initial conformation lower figure = adsorbed conformation) (From Ref. 71.) Note the formation or absence of adsorption loops in the polymer chains for the different cases.
X-ray powder diffraction (XRPD), thermo gravimetric (TGA) analysis, solid-state nuclear magnetic resonance (NMR), and measurements of adsorption isotherms are key methods for characterizing zeolite-like behavior. However, a simple proof for observing structural changes during the sorption processes is XRPD. [Pg.1002]

While the densely packed Pt(lll) surface does not undergo a structural change during these processes, the (100) and (110) oriented surfaces exhibit phase transitions upon CO adsorption [98, 99]. The respective uncovered surfaces are reconstructed (i.e., the topmost layer has an atomic configuration... [Pg.463]

INFLUENCE OF PORE STRUCTURE PARAMETERS ON THE INTRAPARTICLE PRESSURE CHANGE DURING ADSORPTION... [Pg.225]

In genercil, cill structural changes vhich occur during a surface reaction (reconstruction, or removal of reconstruction) can have a marked effect on both the rate of adsorption and desorption. Possible candidates for these phenomena bo occur are all metal surfaces vhich can undergo reconstruction upon interaction with a chemicedly active ad-soj ate. Interesting systems here are (besides the cilready known Pt (100) orNi(IIO) faces) Ir(100)/0,00 or W(100)Al and Mo(100)/H. [Pg.235]

A large portion of the calculated entropy change (+ or -) results from the relative ordering or disrupting of water structure during adsorption. [Pg.144]

Changes in the protein ternary structure during adsorption. There is a difference in softness between different proteins and the ternary structure may change when it adsorbs. [Pg.443]

Unfortunately these data do not permit of calculation of the change in adsorption per sq. cm. caused by the gradual readjustment of the atomic positions into the stable configurations, since during the process of sintering the superficial surface undergoes contraction as well as a modification in the structure. Some measure... [Pg.128]

Physical adsorption is accompanied by low heats of adsorption with no violent or disruptive structural changes occurring to the surface during the adsorption measurement. [Pg.8]

We should note that this article by Ya.B. apparently remained little noticed in its time. In any case, we are unaware of any reference to it in the works of other authors. This is explained by the fact that its ideas were far ahead of their time. Only in recent years, due to the wide application of physical methods in studies of adsorption and catalysis, have the changes in the surface (and volume) structure of a solid body during adsorption and catalysis been proved. Critical phenomena have been discovered, phenomena of hysteresis and auto-oscillation related to the slowness of restructuring processes in a solid body compared to processes on its surface. Relaxation times of processes in adsorbents and catalysts and comparison with chemical process times on a surface were considered in papers by O. V. Krylov in 1981 and 1982 [1] (see references at end of Introduction). [Pg.9]

When the composite-matrix is formed with a polystyrene solution as a dispersion medium, the self-assembly of silica particles is influenced by the adsorption of macromolecules on their surface. During adsorption, both solitary macromolecules and their aggregates transfer simultaneously onto the adsorbent surface. Depending on solution concentration, not only the conformation of adsorbed molecules but also the number and size of macromolecular aggregates in the solution change on adsorption. This leads to the formation of complex-shaped structures, which are linked by a system of nonvalent interactions and consist of polymeric-inorganic blocks[8,14] this is of interest in the preparation of a nanostructured medium (polystyrene-silica gel) as a precomposite for the fabrication of carbon structures in a matrix of silica particles. [Pg.523]


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See also in sourсe #XX -- [ Pg.8 , Pg.83 , Pg.393 ]




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Adsorption changes

Changes during

Structural change

Structural changes during

Structure change

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