Carbon dioxide ratios

Fig. 1. A new process (Urea Technologies) developed for the Tennessee Valley Authority operates at considerable energy savings. Urea is produced in an overall exothermic reaction of ammonia and carbon dioxide at elevated pressure and temperature. In a highly exothermic reaction, ammonium carbamate is first formed as an intermediate compound, followed by its dehydration to urea and water, which is a slightly endothermic reaction. The conversion of CO2 and NH3 to urea depends oil the ammonia-to-caibon dioxide ratio, temperature, and water-to-carbon dioxide ratio, among other factors. The new process makes maximum use of the heat created in the initial reaction, including heat recycling. 1 Urea Technologies and Tennessee Valley Authority)...

It is concluded that carbon dioxide foam or emulsion flooding has great promise. The oil recovery is significantly higher than with the use of WAG at the same water - carbon dioxide ratio. 

Madsen, J., B.S. Bjerg, T. Hvelplund, M.R. Weisbjerg and P. Lund, 2010. Methane and carbon dioxide ratio in excreted air for quantification of the methane production from ruminants. Livestock Sci. 129, 223-227. 

The use of accurate isotope ratio measurement is exemplified here by a method used to determine the temperature of the Mediterranean Sea 10,000 years ago. It is known that the relative solubility of the two isotopic forms of carbon dioxide COj) in sea water depends on temperature... 

One method for measuring the temperature of the sea is to measure this ratio. Of course, if you were to do it now, you would take a thermometer and not a mass spectrometer. But how do you determine the temperature of the sea as it was 10,000 years ago The answer lies with tiny sea creatures called diatoms. These have shells made from calcium carbonate, itself derived from carbon dioxide in sea water. As the diatoms die, they fall to the sea floor and build a sediment of calcium carbonate. If a sample is taken from a layer of sediment 10,000 years old, the carbon dioxide can be released by addition of acid. If this carbon dioxide is put into a suitable mass spectrometer, the ratio of carbon isotopes can be measured accurately. From this value and the graph of solubilities of isotopic forms of carbon dioxide with temperature (Figure 46.5), a temperature can be extrapolated. This is the temperature of the sea during the time the diatoms were alive. To conduct such experiments in a significant manner, it is essential that the isotope abundance ratios be measured very accurately. 

In a similar vein, mean seawater temperatures can be estimated from the ratio of 0 to 0 in limestone. The latter rock is composed of calcium carbonate, laid down from shells of countless small sea creatures as they die and fall to the bottom of the ocean. The ratio of the oxygen isotopes locked up as carbon dioxide varies with the temperature of sea water. Any organisms building shells will fix the ratio in the calcium carbonate of their shells. As the limestone deposits form, the layers represent a chronological description of the mean sea temperature. To assess mean sea temperatures from thousands or millions of years ago, it is necessary only to measure accurately the ratio and use a precalibrated graph that relates temperatures to isotope ratios in sea water. 

The concentration of is determined by measurement of the specific P-activity. Usually, the carbon from the sample is converted into a gas, eg, carbon dioxide, methane, or acetylene, and introduced into a gas-proportional counter. Alternatively, Hquid-scintiHation counting is used after a benzene synthesis. The limit of the technique, ca 50,000 yr, is determined largely by the signal to background ratio and counting statistics. 

The ratio of hydrogen to carbon monoxide is controlled by shifting only part of the gas stream. After the shift, the carbon dioxide, which is formed in the gasifier and in the water gas reaction, and the sulfur compounds formed during gasification, are removed from the gas. 

Gas Reduction. The use of a gaseous reduciag agent is attractive because the metal is produced as a powder that can easily be separated from the solution. Carbon dioxide, sulfur dioxide, and hydrogen can be used to precipitate copper, nickel, and cobalt, but only hydrogen reduction is appHed on an iadustrial scale. In the Sherritt-Gordon process, the excess ammonia is removed duting the purification to achieve a 2 1 ratio of NH iNi ia solution. Nickel powder is then precipitated by... 

Synthesis gas, a mixture of CO and o known as syngas, is produced for the oxo process by partial oxidation (eq. 2) or steam reforming (eq. 3) of a carbonaceous feedstock, typically methane or naphtha. The ratio of CO to may be adjusted by cofeeding carbon dioxide (qv), CO2, as illustrated in equation 4, the water gas shift reaction. 

Gas purification processes fall into three categories the removal of gaseous impurities, the removal of particulate impurities, and ultrafine cleaning. The extra expense of the last process is only justified by the nature of the subsequent operations or the need to produce a pure gas stream. Because there are many variables in gas treating, several factors must be considered (/) the types and concentrations of contaminants in the gas (2) the degree of contaminant removal desired (J) the selectivity of acid gas removal required (4) the temperature, pressure, volume, and composition of the gas to be processed (5) the carbon dioxide-to-hydrogen sulfide ratio in the gas and (6) the desirabiUty of sulfur recovery on account of process economics or environmental issues. 

Process selectivity indicates the preference with which the process removes one acid gas component relative to or in preference to another. For example, some processes remove both hydrogen sulfide and carbon dioxide, whereas other processes are designed to remove hydrogen sulfide only. Thus it is important to consider the process selectivity for hydrogen sulfide removal compared to carbon dioxide removal, ie, the carbon dioxide-to-hydrogen sulfide ratio in the natural gas, in order to ensure minimal concentrations of these components in the product. 

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