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Vapour production

Vapours can be produced in landfills but probably the most common cause of vapours in the groimd is the presence of hydrocarbon contamination from fuel and chemical spills or leaks in locations such as petrol filling stations or industrial sites. In these cases the vapours are present as a result of volatilisation from contamination of the soil or groxmdwater. [Pg.41]

In landfill gas generated from landfill sites there are several hundred trace volatile hydrocarbon gases that can be present, for example volatile organic compounds (VOCs). Their total presence is typically about 1% of the total volume of landfill gas. There are many household chemical products that will [Pg.41]

Volatile organic compoxmds may be released from waste by the following physical processes  [Pg.42]

The source of vapours (hydrocarbon contamination) can also migrate significant distances in groxmdwater. However, this type of migration is beyond the scope of this handbook and readers should refer to the wealth of other books [Pg.42]


Examples of preservatives are phenylmercuric nitrate or acetate (0.002% w/v), chlorhexidine acetate (0.01 % w/v), thiomersal (0.01 % w/v) and benzalkorrium chloride (0.01 % w/v). Chlorocresol is too toxic to the comeal epithehum, but 8-hydroxyquinoline and thiomersal may be used in specific instances. The principal considerahon in relation to antimicrobial properties is the activity of the bactericide against Pseudomonas aeruginosa, a major source of serious nosocomial eye infections. Although benzal-konium chloride is probably the most active of the recommended preservatives, it cannot always be used because of its incompatibility with many compounds commonly used to treat eye diseases, nor should it be used to preserve eye-drops containing anaesthetics. Since benzalkonium chloride reacts with natural mbber, silicone or butyl rabber teats should be substituted. Since silicone mbber is permeable to water vapour, products should not be stored for more than 3 months after manufacture. As with all mbber components, the mbber teat should be pre-equilibrated with the preservative prior to... [Pg.417]

Yields for the reactor system should be calculated on the basis of equal liquid residence times in the two reactors, with a negligible amount of unreacted chlorine in the vapour product streams. It may be assumed that the liquid product stream contains 1.5 wt per cent of hydrogen chloride ... [Pg.970]

Vapour production by flash vaporisation — approximate evaluation... [Pg.784]

As the gas or vapour production rate increases, the flow regime may change from churn-turbulent to droplet flow, in which a fluidised bed of liquid droplets is present in the reactor (see Figure A3.1). This is of less practical interest for relief system sizing because if the gas or vapour rate is so high as to give droplet flow, the relief system size is likely to be impractically large. [Pg.27]

Leung s method is given in 6.3.2 below. The method.is an approximate solution to the differential mass and energy balances for the reactor during relief and takes account of both emptying via the relief system and the tempering effect of vapour production due to relief. The method makes use of adiabatic experimental data for the rate of heat release from the runaway reaction (see Annex 2). Nomenclature is given in Annex 10. [Pg.41]

The basis of the method is to relieve the same volumetric flow of two-phase mixture as the volumetric rate of gas/ vapour production by the reaction, i.e. [Pg.187]

As a result of the thermal cracking, solid coke and pyrolytic vapours are produced. The coke is removed from the reactor and utilized further, while the vapour products are passed into a two-step condensation system. Wenning [8] states that, in order to prevent... [Pg.534]

The vapour product from fluid bed and transported bed reactors has a low partial pressure of collectible products due to the large volumes of fluidising gas, and this is an important design consideration in liquid collection. [Pg.987]

The exothermic process is a slow process, therefore the extended thermolysis gas-vapour production will not result in an explosive production of gas vapours. The thermolysis gas-vapour production is promptly removed from the reaction space by the master fan. [Pg.1655]

Ampoule sample, taken from the hot (220 °C) gas/vapour product stream after a hot trap at 200°C and after depressurizing. The ampoule is sealed and stored for later analysis. Sampling duration is less than 0.1 second. [Pg.178]

Perform LORA for the scenario of liquid carry over to vapour product line resulting in fire and explosion downstream , for the system shown in Figure 3.12. Assume the probability of occurrence is of medium category (likelihood 0.001/yr) and severity is category 2 as per Risk Matrix Table 3.2. Propose the minimum IPLs required in the... [Pg.94]

Part 1 Research paper - Liquid dispersal and vapour production during overfilling incidents... [Pg.67]

While split-ranging is common in industry it does have some limitations. Figure 5.31 shows another method of controlling pressure in a distillation column, often used when vapour production is intermittent. In the absence of sufficient vapour the scheme is designed to allow a noncondensible gas into the column. So, on increasing pressure, the controller will first begin to close valve A until it is fully closed. If the pressure does not fall sufficiently, it will then begin to open valve B. [Pg.140]

The vapour sample would only be representative of distillate composition if the condenser is total. However, if a vapour product is only produced intermittently then it may be practical to detect production and temporarily disable the use of the analyser measurement in any control scheme. [Pg.360]

Parts of the unit may have hydraulic limits. These might apply to any vapour product and to pumps on feed, products and reflux. They can also apply to the flow of coolant through the condenser and heating fluid through the reboiler. As we saw at the beginning of this chapter the column may blow, weep or flood. [Pg.365]

Figure 8.6 shows a scheme where column pressure is controlled by regulating the flow of the vapour product from the accumulator. The reflux is on flow control. A level controller is required to control the coolant flow in order to maintain accumulator liquid inventory. This method provides a smooth, rapidly responding column pressure control. [Pg.193]

Occasionally, much larger flow rate spikes were observed. Tapping or shaking a dewar of LIN also induced large flow rate spikes. These spikes were the first indication of what are now called vapour explosions , when the rate of vapour production could exceed the limiting, choked flow capability of the vent to the atmosphere or the narrow 20 mm necks of the dewars in use. The solution to the problem was therefore to use 50 mm wide-necked dewars, so that choked flow was never reached under the vapour explosions being experienced. [Pg.7]

Historically, the LPG industry had, in 1969, recognised the rollover sequence and acted upon the perceived hazard of stratification and excessive vapour production from uncontrolled convective mixing. [Pg.65]

Accurate humidity measurements are very expensive, compared with their significance for indirect calorimetry. So some experimentors just do not perform these measurements and precondition the air in case of temperature and humidity. The humidity in the chamber is, as stated before, not easy to measure and even harder to control. This is caused by the large variations of the water vapour production of the subject, especially during different phases of locomotor activity (increased breathing, sweating) and the water storage within the chamber. The water vapour tends to adhere to (and even diffuse into) the inner surface of the chamber and furniture and can not be measured exactly and quickly enough. [Pg.526]


See other pages where Vapour production is mentioned: [Pg.146]    [Pg.123]    [Pg.175]    [Pg.198]    [Pg.282]    [Pg.26]    [Pg.190]    [Pg.132]    [Pg.550]    [Pg.1272]    [Pg.1309]    [Pg.265]    [Pg.356]    [Pg.13]    [Pg.148]    [Pg.44]    [Pg.98]    [Pg.230]    [Pg.292]    [Pg.298]    [Pg.292]    [Pg.292]    [Pg.41]   


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Product Temperature and Vapour Removal

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