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With steam

Reducing wastewater associated with steam generation by both reducing steam use through improved heat recovery and by making the steam system itself more efficient. [Pg.297]

When the bed is saturated, regeneration of the adsorbent is necessary. Carbon beds are typically regenerated with steam, hot air, or a combination of vacuum and hot gas. [Pg.305]

The Fischer-Tropsch reaction is essentially that of Eq. XVIII-54 and is of great importance partly by itself and also as part of a coupled set of processes whereby steam or oxygen plus coal or coke is transformed into methane, olefins, alcohols, and gasolines. The first step is to produce a mixture of CO and H2 (called water-gas or synthesis gas ) by the high-temperature treatment of coal or coke with steam. The water-gas shift reaction CO + H2O = CO2 + H2 is then used to adjust the CO/H2 ratio for the feed to the Fischer-Tropsch or synthesis reactor. This last process was disclosed in 1913 and was extensively developed around 1925 by Fischer and Tropsch [268]. [Pg.730]

Reaction conditions Does not react with water Very slowly with water, readily with steam React with cold water, vigour of reaction increasing. [Pg.125]

Neither boron nor aluminium reacts with water at room temperature but both react with steam at red heat liberating hydrogen ... [Pg.144]

In the absence of oxygen, gallium and indium are unaffected by water. Thallium, the most metallic element in Group III, reacts slowly with hot water and readily with steam to produce thallium(I) oxide, TI2O. [Pg.144]

Evidence for the solvated electron e (aq) can be obtained reaction of sodium vapour with ice in the complete absence of air at 273 K gives a blue colour (cf. the reaction of sodium with liquid ammonia, p. 126). Magnesium, zinc and iron react with steam at elevated temperatures to yield hydrogen, and a few metals, in the presence of air, form a surface layer of oxide or hydroxide, for example iron, lead and aluminium. These reactions are more fully considered under the respective metals. Water is not easily oxidised but fluorine and chlorine are both capable of liberating oxygen ... [Pg.271]

It is a gas at room temperature with a boiling point of 128 K. It is a strong oxidising agent, some reactions occurring with explosive violence. Water hydrolyses it slowly at room temperature, but the reaction evolving oxygen is rapid in the presence of a base, and explosive with steam ... [Pg.334]

The material to be steam-distilled (mixed with some water if a solid compound, but not otherwise) is placed in C, and a vigorous current of steam blown in from D. The mixture in C is thus rapidly heated, and the vapour of the organic compound mixed with steam passes over and is condensed in E. For distillations on a small scale it is not necessary to heat C if, however, the flask C contains a large volume of material or material which requires prolonged distillation, it should be heated by a Bunsen burner, otherwise the steady condensation of steam in C will produce too great a volume of liquid. [Pg.33]

The effect of superheated steam may be illustrated by reference to baizaldehyde, which boils at 178° at 760 mm. It distils with steam at 97-9° (Pj = 703-5 mm. and pg = 56-5 mm.) and the distillate contains 32-1 per cent, of benzaldehyde by weight. If one employs steam superheated to 133°, the vapour pressure of benzaldehyde (extrapolated from the boUing point - pressure curve) is 220 mm. hence pj = 540 (water), Pg = 220 (benzaldehyde), and... [Pg.15]

From nitriles by treatment with anhydrous Stannous chloride dissolved in ether saturated with hydrogen chloride the resulting crystaUine aldimine stannichloride, [(RCH=NHj)2] SnCl, or (RCH=NH,HCl)2SnCl4, is hydrolysed by warm water, and the aldehyde is isolated by distillation with steam or by extraction with a solvent (Stephen reaction), for example, for R = CH3(CH2)4, i.e., n-amyl ... [Pg.318]

Oximes, hydrazines and semicarbazones. The hydrolysis products of these compounds, t.e., aldehydes and ketones, may be sensitive to alkali (this is particularly so for aldehydes) it is best, therefore, to conduct the hydrolysis with strong mineral acid. After hydrolysis the aldehyde or ketone may be isolated by distillation with steam, extraction with ether or, if a solid, by filtration, and then identified. The acid solution may be examined for hydroxylamine or hydrazine or semicarbazide substituted hydrazines of the aromatic series are precipitated as oils or solids upon the addition of alkali. [Pg.1075]

Ammonia (NH3) is the most important commercial compound of nitrogen. It is produced by the Haber Process. Natural gas (methane, CH4) is reacted with steam to produce carbon dioxide and hydrogen gas (H2) in a two step... [Pg.19]

Oxidation Step. A review of mechanistic studies of partial oxidation of propylene has appeared (58). The oxidation process flow sheet (Fig. 2) shows equipment and typical operating conditions. The reactors are of the fixed-bed shell-and-tube type (about 3—5 mlong and 2.5 cm in diameter) with a molten salt coolant on the shell side. The tubes are packed with catalyst, a small amount of inert material at the top serving as a preheater section for the feed gases. Vaporized propylene is mixed with steam and ak and fed to the first-stage reactor. The feed composition is typically 5—7% propylene, 10—30%... [Pg.152]

Steps. Thermal-swing cycles have at least two steps, adsorption and heating. A cooling step is also normally used after the heating step. A portion of the feed or product stream can be utilized for heating, or an independent fluid can be used. Easily condensable contaminants may be regenerated with noncondensable gases and recovered by condensation. Water-iminiscible solvents are stripped with steam, which may be condensed and separated from the solvent by decantation. Fuel and/or air may be used when the impurities are to be burned or incinerated. [Pg.279]

SO2 absorbed with buffered citric acid solution. SO2 reduced with H2S to S. H2S produced on site by reduction of S with steam and methane. [Pg.390]

SO2 absorbed with buffered citric acid solution. SO2 stripped from solution with steam. [Pg.390]

Secunda discharges no process water effluents. AU. water streams produced are cleaned and reused in the plant. The methane and light hydrocarbons in the product are reformed with steam to generate synthesis gas for recycle (14). Even at this large scale, the cost of producing fuels and chemicals by the Fischer-Tropsch process is dominated by the cost of synthesis gas production. Sasol has estimated that gas production accounts for 58% of total production costs (39). [Pg.168]

Another hydrogenation process utilizes internally generated hydrogen for hydroconversion in a single-stage, noncatalytic, fluidized-bed reactor (41). Biomass is converted in the reactor, which is operated at about 2.1 kPa, 800°C, and residence times of a few minutes with steam-oxygen injection. About 95% carbon conversion is anticipated to produce a medium heat value (MHV) gas which is subjected to the shift reaction, scmbbing, and methanation to form SNG. The cold gas thermal efficiencies are estimated to be about 60%. [Pg.25]

Chemical Use. Both natural gas and natural gas Hquids are used as feedstocks in the chemical industry. The largest chemical use of methane is through its reactions with steam to produce mixtures of carbon monoxide and hydrogen (qv). This overall endothermic reaction is represented as... [Pg.174]

In the presence of catalysts, the CO reacts with steam through the shift reaction to produce additional hydrogen and CO2 as represented by... [Pg.174]

Steam Reforming. In steam reforming, light hydrocarbon feeds ranging from natural gas to straight mn naphthas are converted to synthesis gas (H2, CO, CO2) by reaction with steam (qv) over a catalyst in a primary reformer furnace. This process is usually operated at 800—870°C and 2.17—2.86... [Pg.418]


See other pages where With steam is mentioned: [Pg.14]    [Pg.184]    [Pg.327]    [Pg.357]    [Pg.432]    [Pg.237]    [Pg.15]    [Pg.178]    [Pg.734]    [Pg.524]    [Pg.924]    [Pg.75]    [Pg.282]    [Pg.17]    [Pg.418]    [Pg.419]    [Pg.469]    [Pg.493]    [Pg.573]    [Pg.573]    [Pg.26]    [Pg.74]    [Pg.80]    [Pg.84]    [Pg.445]    [Pg.282]    [Pg.390]    [Pg.421]    [Pg.421]   


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Apparatus, adapter for steam distillations Claisen flask modified with column

Available energy with steam

Basic arrangement of adsorptive solvent recovery with steam desorption

Carbon monoxide reaction with steam

Determination of organic acids which are volatile with steam

Distillation with steam

Distillation with superheated steam

Evacuation with Steam Jets

Heating with Steam

Hydrocracking with steam

Hydrogen separation steam reforming with membranes

Integrating production with steam

Magnesium reaction with steam

Methane reaction with steam

Methane, reaction with steam, heterogeneous

Phenol index with 4-aminoantipyrine without extraction after steam distillation

Plants with conventional steam reforming

Power supply generation with steam

Reaction of Methane with Steam

Reforming with steam

Rug Steam Cleaners—Powder with Phosphate

Shell and Tube Heat Exchanger with Condensing Steam

Spectrophotometric determination with lanthanum alizarin complexone, directly or following steam acid distillation

Steam engines cogeneration with

Steam reaction with coke

Steam transport with

Steam, reaction with carbon

Steam, reaction with hair

Surface condensers with multiple condensing steam

System Designs for Natural Gas Fed PEMFC and PAFC Plants with Steam Reformers

Temperature Control with Boilup (Steam Flow Rate)

With Superheated Steam

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