Platinum catalyst alternative

R SiH and CH2= CHR interact with both PtL and PtL 1. Complexing or chelating ligands such as phosphines and sulfur complexes are exceUent inhibitors, but often form such stable complexes that they act as poisons and prevent cute even at elevated temperatures. Unsaturated organic compounds are preferred, such as acetylenic alcohols, acetylene dicarboxylates, maleates, fumarates, eneynes, and azo compounds (178—189). An alternative concept has been the encapsulation of the platinum catalysts with either cyclodextrin or in thermoplastics or siUcones (190—192). 

An alternative approach to increase the oxidation rate is the use of alkaline solutions, because bases enhance the reactivity of L-sorbose and weaken the adsorption strength of 2-KLG. Unfortunately, the rate enhancement at higher pH is accompanied by a drop in selectivity due to the poor stability of 2-KLG in alkaline solutions. To circumvent this problem, we have modified the platinum catalysts by adsorbed tertiary amines and carried out the oxidation in neutral aqueous solution [57], This allowed to enhance the rate without increasing the pH of the bulk liquid, which leads to detrimental product decomposition. Small quantities of amines (molar ratio of amine sorbose = 1 1700, and amine Pts = 0.1) are sufficient for modification. Using amines of pKa a 10 for modification, resulted in a considerable rate enhancement (up to a factor of 4.6) with only a moderate loss of selectivity to 2-KLG. The rate enhancement caused by the adsorbed amines is mainly determined by their basicity (pKa). In contrast, the selectivity of the oxidation was found to depend strongly on the structure of the amine. 

The PEMFCs require expensive polymer membrane (e.g., Nation ), and operate at a low temperature (e.g., 80°C). Although low temperature reduced the cost of material, the heat generated at low temperatures is more difficult to remove. Alternate proton conducting membranes (e.g., inorganic polymer composites) that will operate at a high temperature (e.g., 200°C) are required. The expensive platinum catalyst used for electrochemical reactions can be poisoned by even trace amounts of carbon monoxide in the hydrogen fuel stream. Hence, a more tolerant catalyst material needs to be developed. 

The feasibility of carbon-supported nickel-based catalysts as the alternative to the platinum catalyst is studied in this chapter. Carbon-supported nickel (Ni/C, 10 wt-metal% [12]), ruthenium (Ru/C, 10 wt-metal% [12]), and nickel-ruthenium composite (Ni-Ru/C, 10 wt-metal%, mixed molar ratio of Ni/Ru 0.25,1,4, 8, and 16 [12]) catalysts were prepared similarly by the impregnation method. Granular powders of the activated carbon without the base pretreatment were stirred with the NiCl2, RuC13, and NiCl2-RuCl3 aqueous solutions at room temperature for 24 h, respectively. Reduction and washing were carried out in the same way as done for the Pt/C catalyst. Finally, these nickel-based catalysts were evacuated at 70°C for 10 h. 

We have described a new system of polymeric snpports based on multifunctional, exceptionally sterically hindered carbosilane moieties, grafted with block poly(vinylmethyl-co-dimethyl)siloxane arms. They offer uniformly periphery-distribnted active sites (-CH = CH moieties) and can be used for preparation of novel catalysts. Platinum was thus attached to the polymers via coordination to vinyl gronps. The materials used in hydrosilylation of vinylsilanes can be considered as an alternative for traditional platinum catalysts. The utility of the catalysts seems to be dependent on the ratio [D]/[V] in the copolysiloxane arm. Those with too high amonnt of vinyl groups suffer from poor solubility and catalytic performance dne to excessive inter/intra-chain coordinative cross-linking. 

Figure 7 Simplified schematic diagram of a continuously regenerating trap (CRT). The platinum catalyst oxidizes hydrocarbons and carbon monoxide, and also nitric oxide to nitrogen dioxide, which is used to oxidize soot retained in the filter. In the illustration this is a ceramic-wall flow filter, which has alternate channels blocked at the front inlet and rear outlet faces.

An alternative means of technical-scale access to fluoroarenes is the fluoroformate method. Starting from the corresponding phenol a fluoroformate is generated by reaction with carbonyl chloride fluoride and subsequently catalytically decarboxy-lated to the aryl fluoride, in the gas phase, by contact with hot platinum [80] (Scheme 2.30). A newer, greener variant of the fluoroformate process has recently been introduced by Rhodia. In this the fluoroformate is formed by the (catalyzed) reaction of the phenol with COj in HF, and the expensive platinum catalyst is replaced by an aluminum-based material. 

It has already been pointed out that hydrazine is probably subject to attack by atomic hydrogen and in this connection it is interesting to note that an alternative technique in which atomic hydrogen is converted to the less reactive molecular form through the agency of a platinum catalyst has also shown increased yields of hydrazine (7). 

Sodium borohydride-acetic acid treatment of 5- and 6-substituted quinoxalines yields 1,2,3,4-tetrahydroquinoxalines. Alternatively, reduction is effected with hydrogen and a platinum catalyst.The acetic acid-borohydride technique gives excellent yields of 5- and 6-amino-... 

Cyclization to the pentacyclic Aspidosperma series could be accomplished by two alternative routes reaction with mercuric acetate or oxygen in the presence of a platinum catalyst in this way, vincadifformine (2) and minovine (506) were produced (Scheme 30). 

Other approaches have focused upon using non-precious metals and their oxides as alternatives to the platinum catalysts. For example, the mixed oxide catalysts of the binary and ternary alloys of noble metals and transition metals have been investigated for the oxygen evolution reaction in solid polymer electrolyte water electrolyzers. Binary, ternary, and quaternary platinum alloys with base metals of Cu, Ni, and Co have been used as electrocatalysts in liquid acid electrolyte cells. It was also reported that a R-Cu-Cr alloy displayed better activity to oxygen reduction than R and Pt-Cr in liquid electrolyte.The enhanced electrocatalytic activity of these types of alloys has been attributed to various factors, including the decrease of the nearest neighbor distance of platinum,the formation of Raney type... 

The availability of microprocessor control of the reactor system greatly improves the speed and accuracy with kinetic measurements can be made, and the number of levels of the variables that can be used. The better quality permits a more rigorous comparison between alternate rate expressions, and increases the reliability of the derived constants for that selected. These advantages have been exploited in extensive studies (see Further Reading list) of the hydrogenolysis of the lower alkanes on standard platinum catalysts,as the following examples will illustrate. 

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