Carbon dioxide CAS

CARBON DIOXIDE. (CAS 124-38-91. CO., formula weight 44.01. colorless, odorless, nonloxic gas at standard conditions. High concentrations of the gas do cause stupefaction and suffocation because of the displacement of ample oxygen for breathing. Density 1.9769 g/l (O C. 760 ton). sp gr 1.53 tair — 1.00). mp -56.6"C (5.2 atmospheresl. solid CO sublimes at -79°C (760 torr). critical pressure 73 atmospheres, critical temperalure 3I C. Carbon dioxide is soluble in HiO (approximately I volume CO. in I volume H.O at 15 C. 760 tom. soluble in alcohol, and is rapidly absorbed by most alkaline solutions. The solubility of CO in H 0 for various pressures and temperatures is given in Table I. 

An aqueous solution of Ca(OH)2, which is only slightly soluble in water, is called lime water, which is used as a test for carbon dioxide Ca(OH)2(aq) + C02(g) — CaCOsCs) + H20(l). 

LB Number 4 005 Substance 1 poly(/ert-butyl acrylate) CAS Number 1 25232-27-3 Substance 2 carbon dioxide CAS Number 2 124-38-9 Substance 3 tert-butyl acrylate CAS Number 1663-39-4 ... 

Reaction of potassium phenoxide with carbon dioxide (ca 6MPa) at room temperature and subsequent treatment with wet solvent gave both o- and p-hydroxybenzoic acids, although the former predominated. Differences from the Kolbe-Schmitt reaction are that the o-hydroxybenzoic acid is formed at much lower temperatures and the formation of the para-isomer is not ascribable to thermal rearrangement of the ortho-isomer. 

Quantitative analysis of the products of oxidation of l-[1- and 6- C]ascorbic acid with periodate at pH 7.5 showed that 2 moles of formate (from C-4 and C-5) and 1 mole each of carbon dioxide (from C-3), oxalate (from C-1 and C-2), and formaldehyde (from C-6) are formed, together with carbon dioxide (ca. 17%) liberated from a side-reaction at... 

If the hydrogencarbonate is in solution and the cation is Ca or Mg. the insoluble carbonate is precipitated this reaction may be used, therefore, to remove hardness in water by precipitation of Ca or Mg ions.) The ease of decomposition of hydrogencar-bonates affords a test to distinguish between a hydrogencarbonate and a carbonate carbon dioxide is evolved by a hydrogencarbonate, but not by a carbonate, if it is heated, either as the solid or in solution, on a boiling water bath. 

Prepare a mixture of 30 ml, of aniline, 8 g. of o-chloro-benzoic acid, 8 g. of anhydrous potassium carbonate and 0 4 g. of copper oxide in a 500 ml. round-bottomed flask fitted with an air-condenser, and then boil the mixture under reflux for 1 5 hours the mixture tends to foam during the earlier part of the heating owing to the evolution of carbon dioxide, and hence the large flask is used. When the heating has been completed, fit the flask with a steam-distillation head, and stcam-distil the crude product until all the excess of aniline has been removed. The residual solution now contains the potassium. V-phenylanthrani-late add ca. 2 g. of animal charcoal to this solution, boil for about 5 minutes, and filter hot. Add dilute hydrochloric acid (1 1 by volume) to the filtrate until no further precipitation occurs, and then cool in ice-water with stirring. Filter otT the. V-phcnylanthranilic acid at the pump, wash with water, drain and dry. Yield, 9-9 5 g. I he acid may be recrystallised from aqueous ethanol, or methylated spirit, with addition of charcoal if necessary, and is obtained as colourless crystals, m.p. 185-186°. 

Blank on tube. It Is advisable with a newly packed tube to carry out a determination on A.R. glucose (ca. 25 mg.) this serves to burn out the tube by removing occluded air from the permanent filling and also as an additional check on the quality of the carbon dioxide supply. 

Mix 100 g. of ammonium chloride and 266 g. of paraformaldehyde in a 1-litre rovmd-bottomed flask fitted with a long reflux condenser containing a wide inner tube (ca. 2 cm. diameter) the last-named is to avoid clogging the condenser by paraformaldehyde which may sublime. Immerse the flask in an oil bath and gradually raise the temperature. The mixture at the bottom of the flask liquefies between 85° and 105° and a vigorous evolution of carbon dioxide commences at once remove the burner beneath the oil bath and if the reaction becomes too violent remove... 

Mix together in a 250 ml. flask carrying a reflux condenser and a calcium chloride drying tube 25 g. (32 ml.) of freshly-distilled acetaldehyde with a solution of 59-5 g. of dry, powdered malonic acid (Section 111,157) in 67 g. (68-5 ml.) of dry pyridine to which 0-5 ml. of piperidine has been added. Leave in an ice chest or refrigerator for 24 hours. Warm the mixture on a steam bath until the evolution of carbon dioxide ceases. Cool in ice, add 60 ml. of 1 1 sulphuric acid (by volume) and leave in the ice bath for 3-4 hours. Collect the crude crotonic acid (ca. 27 g.) which has separated by suction filtration. Extract the mother liquor with three 25 ml. portions of ether, dry the ethereal extract, and evaporate the ether the residual crude acid weighs 6 g. Recrystallise from light petroleum, b.p. 60-80° the yield of erude crotonic acid, m.p. 72°, is 20 g. 

Add 40 ml. of ethyl alcohol to 21 -5 g. of 70 per cent, ethylenediamine solution (0 -25 mol) dissolve 36 -5 g. of adipic acid (0 -25 mol) in 50 ml. of a 6 1 mixture of ethyl alcohol and water. Mix the two solutions, stir and cool. Filter off the resulting salt and recrystalliae it from 60 ml. of a 6 1 ethyl alcohol - water mixture, and dry the salt in the air. Heat the salt in an atmosphere of oxygen-free nitrogen or of carbon dioxide in an oil bath until it melts (ca. 160°) the product will sohdify after a short time. Reduce the pressure to 15 mm. of mercury or less and raise the temperature of the oil bath until the product remelts (about 290°) and continue the heating for 4r-5 hours. Upon coohng, a nylon type polymer is obtained. 

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. 

Anhydrous, monomeric formaldehyde is not available commercially. The pure, dry gas is relatively stable at 80—100°C but slowly polymerizes at lower temperatures. Traces of polar impurities such as acids, alkahes, and water greatly accelerate the polymerization. When Hquid formaldehyde is warmed to room temperature in a sealed ampul, it polymerizes rapidly with evolution of heat (63 kj /mol or 15.05 kcal/mol). Uncatalyzed decomposition is very slow below 300°C extrapolation of kinetic data (32) to 400°C indicates that the rate of decomposition is ca 0.44%/min at 101 kPa (1 atm). The main products ate CO and H2. Metals such as platinum (33), copper (34), and chromia and alumina (35) also catalyze the formation of methanol, methyl formate, formic acid, carbon dioxide, and methane. Trace levels of formaldehyde found in urban atmospheres are readily photo-oxidized to carbon dioxide the half-life ranges from 35—50 minutes (36). 

Significant differences in net photosynthetic assimilation of carbon dioxide are apparent between C, C, and CAM biomass species. One of the principal reasons for the generally lower yields of C biomass is its higher rate of photorespiration if the photorespiration rate could be reduced, the net yield of biomass would increase. Considerable research is in progress (ca 1992) to achieve this rate reduction by chemical and genetic methods, but as yet, only limited yield improvements have been made. Such an achievement with C biomass would be expected to be very beneficial for foodstuff production and biomass energy appHcations. 

The conversion of coal to gas on an industrial scale dates to the early nineteenth century (14). The gas, often referred to as manufactured gas, was produced in coke ovens or similar types of retorts by simply heating coal to vaporize the volatile constituents. Estimates based on modem data indicate that the gas mixture probably contained hydrogen (qv) (ca 50%), methane (ca 30%), carbon monoxide (qv) and carbon dioxide (qv) (ca 15%), and some inert material, such as nitrogen (qv), from which a heating value of approximately 20.5 MJ/m (550 Btu/fT) can be estimated (6). 

Ca.rhona.tlon, GalHum can be extracted by fractional carbonation which consists of treating the aluminate solution with carbon dioxide in several controlled stages. This process is no longer under industrial operation (6). 

The quantity of breathing gas consumed in deep dives is of both economical and logistical concern at depths of 300 m, a reasonably active diver requites ca 1.8 m (64 fT at STP) of breathing gas per minute. In closed-cycle breathing systems, of both the self-contained and umbiHcal types, the helium is recitculated after carbon dioxide is removed and the oxygen replenished (147). 

In 1974 a 1000 t/d ammonia plant went into operation near Johaimesburg, South Africa. The lignitic (subbituminous) coal used there contains about 14% ash, 36% volatile matter, and 1% sulfur. The plant has six Koppers-Totzek low pressure, high temperature gasifiers. Refrigerated methanol (—38° C, 3.0 MPa (30 atm)) is used to remove H2S. A 58% CO mixture reacts with steam over an iron catalyst to produce H2. The carbon dioxide is removed with methanol (at —58° C and 5.2 MPa (51 atm)). Ammonia synthesis is carried out at ca 22 MPa (220 atm) (53) (see Ammonia). 

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