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Carbon dioxide disposal

The control of carbon dioxide emission from burning fossil fuels in power plants or other industries has been suggested as being possible with different methods, of which sequestration (i.e., collecting CO2 and injecting it to the depth of the seas) has been much talked about recently. Besides of the obvious cost and technical difficulties, this would only store, not dispose of, CO2 (although natural processes in the seas eventually can form carbonates, albeit only over very long periods of time). [Pg.217]

The aqueous sodium naphthenate phase is decanted from the hydrocarbon phase and treated with acid to regenerate the cmde naphthenic acids. Sulfuric acid is used almost exclusively, for economic reasons. The wet cmde naphthenic acid phase separates and is decanted from the sodium sulfate brine. The volume of sodium sulfate brine produced from dilute sodium naphthenate solutions is significant, on the order of 10 L per L of cmde naphthenic acid. The brine contains some phenolic compounds and must be treated or disposed of in an environmentally sound manner. Sodium phenolates can be selectively neutralized using carbon dioxide and recovered before the sodium naphthenate is finally acidified with mineral acid (29). Recovery of naphthenic acid from aqueous sodium naphthenate solutions using ion-exchange resins has also been reported (30). [Pg.511]

The common treatment methods are acidification, neutralization, and incineration. When oxahc acid is heated slightly in sulfuric acid, it is converted to carbon monoxide, carbon dioxide, and water. Reaction with acid potassium permanganate converts it to carbon dioxide. Neutralization with alkahes, such as caustic soda, yields soluble oxalates. Neutralization with lime gives practically insoluble calcium oxalate, which can be safely disposed of, for instance, by incineration. [Pg.461]

Emissions During Disposal and Incineration. The increasing use of modem incinerators to dispose of domestic waste results in complete combustion of plasticizers to carbon dioxide and water. The preponderance of plasticizer going into landfiUs is as plasticized PVC. Once a landfiU has been capped anaerobic conditions prevail and it is biologically relatively inactive. Under these conditions the main route by which organic components are removed from the landfiU contents is by ingress of water, extraction, and subsequent loss of water from the site to the environment. [Pg.132]

Essentially no waste products are formed ia the USP process if hydriodic acid and either sodium hydroxide or sodium carbonate are used as reactants. Water results from use of the former a mole equivalent quantity of carbon dioxide is produced from the latter reagents. Higher quaUty grades may require some purification steps which may result ia wastes from the treatment. Disposal of these impurities must then be carried out. [Pg.190]

The increasing number of atomic reactors used for power generation has been questioned from several environmental points of view. A modern atomic plant, as shown in Fig. 28-3, appears to be relatively pollution free compared to the more familiar fossil fuel-fired plant, which emits carbon monoxide and carbon dioxide, oxides of nitrogen and sulfur, hydrocarbons, and fly ash. However, waste and spent-fuel disposal problems may offset the apparent advantages. These problems (along with steam generator leaks) caused the plant shown in Fig. 28-3 to close permanently in 199T. [Pg.451]

The catalyst dust is then separated from the resulting carbon dioxide stream via cyclones and/or electrostatic precipitators and is sent off-site for disposal or treatment. Generated wastewater is typically sour water from the fractionator containing some oil and phenols. Wastewater containing metal impurities from the feed oil can also be generated from the steam used to purge and regenerate catalysts. [Pg.90]

Lung function Relating to the transfer of oxygen from air into the blood and the disposal of carbon dioxide from the blood to the air. [Pg.1456]

Obviously the availability of a non-carbon fuel, usually hydrogen, would obviate the need for carbon dioxide extraction and disposal, and a plant with combustion of such a fuel becomes a simple solution (Cycle Cl, a hydrogen burning CBT plant, and Cycles C2 and C3, hydrogen burning CCGT plants). [Pg.133]

We consider first Cycles A of Table 8.1 A and the a.ssociated Figs. 8.6-8.8. These are cycles in which the major objective is to separate or sequestrate some or all of the carbon dioxide produced, and to store or dispose it. This can be achieved either by direct removal of the CO2 from the combustion ga.ses with little or no modification to the existing plant or by modest restructuring or alteration of the conventional power cycle so that the carbon dioxide can be removed more easily. [Pg.144]

Obviously, u.se of a non-carbon fuel—usually containing hydrogen—obviates the need for any carbon dioxide extraction and disposal. These cycles are listed in Table 8.1C, and the associated Figs. 8.15-8.17. [Pg.152]

Butane, C4H10, is widely used as a fuel for disposable lighters. When one mole of butane is burned in oxygen, carbon dioxide and steam are formed and 2658.3 kj of heat is evolved. [Pg.222]

A number of environmental issues have received widespread publicity (Table 7.1), from major accidents at plants (e.g., Seveso and Bhopal) to the global and regional impacts associated with energy utilization (e.g., carbon dioxide, acid rain, and photochemical oxidants), the improper disposal of chemical waste (e.g., Love Canal and Times Beach), and chemicals that have dispersed and bioaccumulated affecting wildlife (e.g., PCBs and DDT) and human health (e.g., cadmium, mercury, and asbestos). [Pg.120]

The major functions of the red blood ceil are relatively simple, consisting of dehvering oxygen to the tissues and of helping in the disposal of carbon dioxide and protons formed by tissue metabolism. Thus, it has a much simpler structure than most human cells, being essentially composed of a membrane surrounding a solution of hemoglobin (this protein forms about 95% of the intracellular protein of the red cell). There are no... [Pg.609]

Methods used to control presumptive corrosion include deaeration and dehydration. Carbon dioxide and hydrogen sulfide are the main corrosives in pipelines for natural gas, but they are only aggressive in the presence of water. Therefore sweetening and drying the gas are useful to prevent corrosion. In oil pipelines, water emulsified in crude oil can cause corrosion problems [251]. Emulsified crude oil in separated produced water is also an environmental and disposal problem. [Pg.152]

Holloway S. and Van Der Straaten R. The joul II project-The underground disposal of carbon dioxide. 1995 Energy Conversion and Management 36(6-9) 519-522. [Pg.167]

PagnierH.J.M., et al. C02-sequestration in the Netherlands inventory of the potential for the combination of subsurface carbon dioxide disposal with enhanced coalbed methane production. In Proceedings of Fifth International Conference on Greenhouse Gas Control Technologies, CSIRO Publishing, Collingwood, Australia. 2001 555-560. [Pg.171]

Interaction is exothermic, and if air is present, incandescence may occur with freshly prepared granular material. Admixture with oxygen causes a violent explosion [1], Soda-lime, used to absorb hydrogen sulfide, will subsequently react with atmospheric oxygen and especially carbon dioxide (from the solid coolant) with a sufficient exotherm in contact with moist paper wipes (in a laboratory waste bin) to cause ignition [2], Spent material should be saturated with water before separate disposal. Mixture analogous to soda-lime, such as barium hydroxide with potassium or sodium hydroxides, also behave similarly [1],... [Pg.1654]

Also, by the very nature of chemical transformations, there are almost always unused chemicals remaining. These chemical leftovers include contaminants in the raw materials, incompletely converted raw materials, unavoidable coproducts, unselective reaction by-products, spent catalysts, and solvents. There have long been efforts to minimize the production of such waste products, and to recover and reuse those that cannot be eliminated. For those that cannot be reused, some different use has been sought, and as a last resort, efforts have been made to safely dispose of whatever remains. The same efforts apply to any leftovers from the production of the energy from the fuels produced or consumed by the processing industries. Of particular immediate and increasing concern are the potential detrimental effects of carbon dioxide emissions to the atmosphere from fossil fuel combustion, as discussed further in Chapters 9 and 10. [Pg.34]


See other pages where Carbon dioxide disposal is mentioned: [Pg.472]    [Pg.472]    [Pg.217]    [Pg.25]    [Pg.222]    [Pg.230]    [Pg.354]    [Pg.35]    [Pg.175]    [Pg.240]    [Pg.473]    [Pg.178]    [Pg.369]    [Pg.280]    [Pg.532]    [Pg.31]    [Pg.409]    [Pg.242]    [Pg.576]    [Pg.132]    [Pg.216]    [Pg.475]    [Pg.149]    [Pg.492]    [Pg.27]    [Pg.264]    [Pg.214]    [Pg.10]    [Pg.742]    [Pg.170]    [Pg.37]    [Pg.552]    [Pg.1722]   
See also in sourсe #XX -- [ Pg.132 ]




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