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Metallic pillars

Figure 3 shows trapezoidal metallic features embedded in the regions of porous AI2O3 (Fig. 3a), which are obtained after localized anodization, and metallic pillars, which are obtained after chemical etching of porous AI2O3 (Fig. 3b). Being qualitative, Figs. 2 and 3 provide a framework for the analysis of the technological issues associated with localized anodization of A1 films. Figure 3 shows trapezoidal metallic features embedded in the regions of porous AI2O3 (Fig. 3a), which are obtained after localized anodization, and metallic pillars, which are obtained after chemical etching of porous AI2O3 (Fig. 3b). Being qualitative, Figs. 2 and 3 provide a framework for the analysis of the technological issues associated with localized anodization of A1 films.
Figure 6. Cross-sectional SEM micrographs showing metallic pillars of 3-pm-thick Al-0.5%Cu preserved under the anodization mask of barrier AI2O3. Porous-type anodization voltage is 20 V. Reproduced from Ref.32 with permission from... Figure 6. Cross-sectional SEM micrographs showing metallic pillars of 3-pm-thick Al-0.5%Cu preserved under the anodization mask of barrier AI2O3. Porous-type anodization voltage is 20 V. Reproduced from Ref.32 with permission from...
Pillared layered clays (PILC) containing different hydrated cations in the interlayer space are also selective catalysts. Pinacol and 2,3-diphenyl-2,3-butanediol have been studied in the presence of Al-PILC, Zr-PILC, and Cr-PILC [38], Zr-PILC, with the lowest acidity, gave rise to the largest amount of diene from pinacol (32 % and 22 %, depending on the method of preparation). The rearrangement was selective in the presence of a mixed-metal pillared layered clay (Fe Aln-PILC, sealed tube, 398 K, 1 h, catalyst/diol = 5) [40],... [Pg.238]

JD Wang, RA CahiU, G Serrette, WL Shes, A Clearfield. Catalytic study of polyoxo-metalate-pillared layered double hydroxides, American Chemical Society Southwest Regional Meeting, Austin, TX, 1993. [Pg.457]

There are many other techniques to modify the Mt, although some of them are more complex or expensive than ionic exchange. The most popular are ionic exchange in other solvents rather than water [22, 23], ionic exchange using chromatography technique [24], metal pillaring, etc. [Pg.260]

At that time, fire, water, soil, and air represented the pillars of the four-element apprenticeship. Metals were extracted as pure elements in the present sense), even if they were not yet recognized as such. They were designated by astronomical and astrological symbols. [Pg.19]

To obtain the necessary pressure on the lid, and for general protection when the bomb is being heated, the bomb is placed in a hea y metal case G, in which the collar E of the bomb rests in a circular recess at the top of G, and the base of A just appears through the bottom of G. The lid H of the case screws down over G, and has an orifice through which the pillar F of the bomb projects when H is screwed firmly down onto G. The bottom portion of G and the sides of H are made of hexagonal cross-section so that both can be firmly held with suitable tools whilst H is being screwed down and is thus thrusting the lid C of the bomb firmly down onto the base A. [Pg.506]

Suspend the bomb by a wire or a metal rod through F. Fill with water the annular space between the pillar F and the hole in the top of H. Now heat the base of A with a pointed flame, e.., from a blowpipe pointing upwards. The time required for heating in this way is usually about i minute, but an ordinary Bunsen flame, used without concentration on the bottom of A, may require about 4 minutes. The... [Pg.506]

Pillared clays are smectite minerals or iUite-smectite minerals that have been stmcturaHy modified to contain pillars of stable inorganic oxide. The pillars prop open the smectite stmcture so they have a basal space of approximately 3.0 nm. Typical metals in the pillars include Al, Zr, Ti, Ce, and Fe, and these materials are used in catalytic processes to crack heavy cmde oils (110—112). [Pg.198]

The original pillared clays were made by (/) mixing smectite with a polymeric cationic hydroxy metal complex such as aluminum chlorhydrol (2) allowing a minimal amount of time for the cationic hydroxy metal complex to exchange with the interlayer cations and (7) calcining the resulting material to decompose the hydroxy metal complex (110). A number of newer methods have been developed to make pillared clays (111—117). [Pg.198]

Ancient iron structures sometimes show no sign of corrosion or at most, very little. The clean atmosphere of past centuries may be responsible in that it allowed a very thin adherent layer of oxide to develop on the surface [22], This layer very often protects against even today s increasingly aggressive industrial pollutants Very often the conditions of the initial corrosion are the ones that determine the lifespan of metals [23], A well-known example is the sacred pillar of Kutub in Delhi, which was hand forged from large iron blooms in 410 a.d. In the pure dry air, the pillar remains free of rust traces but shows pitting corrosion of the iron... [Pg.8]

Alberti G (1996) Layered metal phosphonates and covalently pillared diphosphonates. In Comprehensive supramolecular chemistry, vol 7. Pergamon, New York, p 151... [Pg.160]

Figure 4.1 clearly illustrates the modular construction of MOFs, with ligands used as pillars and metal clusters as node points. One unique feature of MOFs seems to be the possibihty to systematically modify their lattice. For instance, by replacing the terephthalate ligands of MOF-5 (Figure 4.1) with different dicarboxylate ligands, a family of isoreticular metal-organic frameworks (known in literature as the... [Pg.76]

Figure 18.13 Chemical structures of selected cofacial strapped diporphyrins (a), pillared diporphyrins (h), and pillared porphyrin/corrole, dicorrole, and diphthalocyanine derivatives (c) whose metal complexes have heen studied as ORR catalysts. Conventional notations for the structures are also hsted (in bold). Other molecular architectures of cofacial porphyrins are known, hut the corresponding complexes have not yet been studied as ORR catalysts. Figure 18.13 Chemical structures of selected cofacial strapped diporphyrins (a), pillared diporphyrins (h), and pillared porphyrin/corrole, dicorrole, and diphthalocyanine derivatives (c) whose metal complexes have heen studied as ORR catalysts. Conventional notations for the structures are also hsted (in bold). Other molecular architectures of cofacial porphyrins are known, hut the corresponding complexes have not yet been studied as ORR catalysts.
Other metal oxide catalysts studied for the SCR-NH3 reaction include iron, copper, chromium and manganese oxides supported on various oxides, introduced into zeolite cavities or added to pillared-type clays. Copper catalysts and copper-nickel catalysts, in particular, show some advantages when NO—N02 mixtures are present in the feed and S02 is absent [31b], such as in the case of nitric acid plant tail emissions. The mechanism of NO reduction over copper- and manganese-based catalysts is different from that over vanadia—titania based catalysts. Scheme 1.1 reports the proposed mechanism of SCR-NH3 over Cu-alumina catalysts [31b],... [Pg.13]

By considering the results of previous experiment, they synthesized cobalt-, nickel-, copper-, and zinc-based, new pillared MOFs of similar topologies which exhibited good water stability [233]. The grafted methyl group on the benzene dicarboxlate (BDC) ligand introduced steric factors around the metal centers consequently, water stability of MOF drastically improved. [Pg.141]


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See also in sourсe #XX -- [ Pg.218 , Pg.219 , Pg.226 , Pg.227 , Pg.228 ]

See also in sourсe #XX -- [ Pg.191 ]




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