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Poisoning neutralization

Figure 3a is a schematic of the functionalized zeolite beta. Figure 3b plotted the catalytic conversion of HEX and PYC over 6 A zeolites as a function of time. For sulfonated zeolite (Z-S03H), more than 60 % HEX was converted in 4 hours, and nearly complete conversion was observed over 12 hours. On the other hand, PYC, which has a large molecular size and cannot enter the microporosity, showed less than 8 % conversion over extended reaction time with same Z-S03H as catalyst. Both HEX and PYC were also reacted over pure zeolite beta (Z), and the TMMPS functionalized zeolite (Z-SH) before it was treated with H202. Pure zeolite and Z-SH showed low catalytic activity, and only a small fraction of either HEX or PYC was converted. Further evidence of the size selectivity is provided when amines of different sizes are used to poison (neutralize) the acid sites (19). As shown in Figure 3c, the... [Pg.733]

Arsenic (atomic number 33, atomic mass 74.9216) is the 20th most abundant element in the earth s crust. It belongs to the elements of the P block of the Periodic System where it is placed below phosphorus and above antimony. The mass numbers of its isotopes range from 68 to 80 however, only the natural isotope 75 is stable. The gamma-emitting radioisotopes As (half-life 26.4 h), As (half-life 17.77 d), and As ( half-life 80.3 d) are commercially available and often used for method development and control (Krivan, 1987 Krivan and Arpadjan, 1989). Elemental arsenic exists at room temperature as metallic or gray arsenic, and yellow arsenic. As a center element of the P block it can be found both in metallic and covalent compounds. The oxidation states are -III, 0, -i-lll, and -I- V. Arsenic trihydride (arsine, AsHa) is a colourless, very poisonous, neutral gas with a characteristic garlic odour. [Pg.291]

The advent of a large international trade in methanol as a chemical feedstock has prompted additional purchase specifications, depending on the end user. Chlorides, which would be potential contaminants from seawater during ocean transport, are common downstream catalyst poisons likely to be excluded. Limitations on iron and sulfur can similarly be expected. Some users are sensitive to specific by-products for a variety of reasons. Eor example, alkaline compounds neutralize MTBE catalysts, and ethanol causes objectionable propionic acid formation in the carbonylation of methanol to acetic acid. Very high purity methanol is available from reagent vendors for small-scale electronic and pharmaceutical appHcations. [Pg.282]

The common impurities found in amines are nitro compounds (if prepared by reduction), the corresponding halides (if prepared from them) and the corresponding carbamate salts. Amines are dissolved in aqueous acid, the pH of the solution being at least three units below the pKg value of the base to ensure almost complete formation of the cation. They are extracted with diethyl ether to remove neutral impurities and to decompose the carbamate salts. The solution is then made strongly alkaline and the amines that separate are extracted into a suitable solvent (ether or toluene) or steam distilled. The latter process removes coloured impurities. Note that chloroform cannot be used as a solvent for primary amines because, in the presence of alkali, poisonous carbylamines (isocyanides) are formed. However, chloroform is a useful solvent for the extraction of heterocyclic bases. In this case it has the added advantage that while the extract is being freed from the chloroform most of the moisture is removed with the solvent. [Pg.63]

Chemical Reactivity - Reactivity with Water Reacts vigorously with water, generating phosphine, which is a poisonous and spontaneously flammable gas Reactivity with Common Materials Can react with surface moisture to generate phosphine, which is toxic and spontaneously flammable Stability During Transport Stable if kept dry Neutralizing Agents for Acids and Caustics Not pertinent Polymerization Not pertinent Inhibitor of Polymerization Not pertinent. [Pg.78]

As well as viscosity, other factors to be aware of include the purity of the ionic liquids. The presence of residual halide ions in neutral ionic liquids can poison transition metal catalysts, while different levels of proton impurities in chloroalumi-... [Pg.332]

Ionic compounds have chemical properties very different from those of the neutral atoms from which they form. Sodium metal reacts very violently with water, and chlorine gas is poisonous and highly corrosive. In contrast, sodium chloride simply dissolves in water and is a substance that most people use to season their food. [Pg.104]

As evidenced by experiments carried out on partially poisoned catalysts with 2,6-di-tert-butylpyridine, a significant decrease in the catalytic activity (of about 65-70 %) occurs because of a partial neutralization of the external acid sites. This means that the alkylation takes place predominantly on the external surface. [Pg.360]

Antitoxin An antibody formed in response to and capable of neutralizing a biological poison, an animal serum containing antitoxins, or a solution of antibodies (e.g., diphtheria antitoxin and botulinum antitoxin) derived from the serum of animal immunized with specific antigens. Antitoxins are used to confer passive immunity and for treatment. [Pg.296]

The neutral esters of sulphuric add and especially the dimethyl ester are very poisonous. All experiments in which they are used must therefore he carried out very cautiously in the fume chamber. [Pg.244]


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See also in sourсe #XX -- [ Pg.191 ]




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