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Hydrogen purpose

Ultrasonics can activate inactive catalysts, as illustrated by the activation of extremely inactive Ni powder for hydrogenation purposes. Surface studies of the metal after sonication... [Pg.164]

Note. (1) This treatment removes a substantial proportion of the excess of copper(u) oxide and renders the catalyst more active for hydrogenation purposes. [Pg.427]

For many purposes the hydrogen electrode is not convenient and it can be replaced by another cell of known standard electrode potential. A well-known example is the calomel cell shown in Figure 4.5. [Pg.99]

For XH bonds, where X isany heavy atom, the hydrogen electron den sity is ri ot th ough t to be cen tered at th e position of th e hydrogen n ueleus but displaced alon g th e bon d sorn ewhat, towards X. The MM+ force field reduces the XH bond length by a factor of 0.9 I 5 strictly for th e purposes of calculatin g van der Waals in teraction s with hydrogen atoms. [Pg.188]

Lead formate separates from aqueous solution without water of crystallisation. It can therefore be used for the preparation of anhydrous formic acid. For this purpose, the powdered lead formate is placed in the inner tube of an ordinary jacketed cond ser, and there held loosely in position by plugs of glass-wool. The condenser is then clamped in an oblique position and the lower end fitted into a receiver closed with a calcium chloride tube. A current of dry hydrogen sulphide is passed down the inner tube of the condenser, whilst steam is passed through the jacket. The formic acid which is liberated... [Pg.114]

Preparation of REAOENTS.t It is essential for this preparation that the zinc powder should be in an active condition. For this purpose, it is usually sufficient if a sample of ordinary technical zinc powder is vigorously shaken in a flask with pure ether, and then filtered off at the pump, washed once with ether, quickly drained and without delay transferred to a vacuum desiccator. If, however, an impure sample of zinc dust fails to respond to this treatment, it should be vigorously stirred in a beaker with 5% aqueous sodium hydroxide solution until an effervescence of hydrogen occurs, and then filtered at the pump, washed thoroughly with distilled water, and then rapidly with ethanol and ether, and dried as before in a vacuum desiccator. The ethyl bromoacetate (b.p. 159 ) and the benzaldehyde (b.p. 179 ) should be dried and distilled before use. [Pg.287]

Assemble an apparatus similar to that used in the prenous experiment, i.e., a 500 ml. conical flask fitted at the neck with a freshly-charged calcium chloride tube, a dropping-funnel, and in addition an outlet-tube joined to the water-pump so that dry air can be drawn through the calcium chloride tube and thence through the conical flask. The purpose of the air-stream is to remove as much as possible of the excess of hydrogen chloride. [Pg.310]

Vinyl compounds. Vinyl chloride (prepared from acetylene and hydrogen chloride) 3 ields polyvinyl chloride (P.V.C.), which is employed as a rubber substitute and for other purposes. Vinyl acetate (from... [Pg.1015]

Single-bond cleavage with molecular hydrogen is termed hydrogenolysis. Palladium is the best catalyst for this purpose, platinum is not useful. Desulfurizations are most efficiently per-formed with Raney nickel (with or without hydrogen G.R. Pettit, 1962 A or with alkali metals in liquid ammonia or amines. The scheme below summarizes some classes of compounds most susceptible to hydrogenolysis. [Pg.113]

The heats of formation of most organic com pounds are derived from heats of reaction by arith metic manipulations similar to that shown Chemists find a table of AH values to be convenient because it replaces many separate tables of AH° values for indi vidual reaction types and permits AH° to be calcu lated for any reaction real or imaginary for which the heats of formation of reactants and products are available It is more appropriate for our purposes however to connect thermochemical data to chemi cal processes as directly as possible and therefore we will cite heats of particular reactions such as heats of combustion and heats of hydrogenation rather than heats of formation... [Pg.86]

A halogen substituent Irke hydrogen rs monovalent and when present rn a molec ular formula rs treated as rf rt were hydrogen for counting purposes... [Pg.574]

Acyl chlorides react with carboxylic acids to yield acid anhydrides When this reaction is used for preparative purposes a weak organic base such as pyridine is normally added Pyridine is a catalyst for the reaction and also acts as a base to neutralize the hydrogen chloride that is formed... [Pg.839]

A schematic illustration of a typical inlet apparatus for separating volatile hydrides from the analyte solution, in which they are generated upon reduction with sodium tetrahydroborate. When the mixed analyte solution containing volatile hydrides enters the main part of the gas/liquid separator, the volatiles are released and mix with argon sweep and makeup gas, with which they are transported to the center of the plasma. The unwanted analyte solution drains from the end of the gas/liquid separator. The actual construction details of these gas/liquid separators can vary considerably, but all serve the same purpose. In some of them, there can be an intermediate stage for removal of air and hydrogen from the hydrides before the latter are sent to the plasma. [Pg.100]

The three isotopes of hydrogen are almost indistinguishable for most chemical purposes, but a mass Spectrometer can see them as three different entities of mass 1, 2, and 3 Da. Isotopes of other elements can also be distinguished. Mass spectrometry is important for its ability to separate the isotopes of elements. [Pg.423]


See other pages where Hydrogen purpose is mentioned: [Pg.868]    [Pg.868]    [Pg.96]    [Pg.96]    [Pg.868]    [Pg.868]    [Pg.868]    [Pg.868]    [Pg.96]    [Pg.96]    [Pg.868]    [Pg.868]    [Pg.95]    [Pg.165]    [Pg.169]    [Pg.210]    [Pg.601]    [Pg.385]    [Pg.347]    [Pg.409]    [Pg.181]    [Pg.249]    [Pg.126]    [Pg.702]    [Pg.100]    [Pg.144]    [Pg.168]    [Pg.256]    [Pg.472]    [Pg.23]    [Pg.368]    [Pg.8]    [Pg.409]    [Pg.249]    [Pg.339]    [Pg.158]    [Pg.202]    [Pg.247]    [Pg.339]    [Pg.24]    [Pg.42]   


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