Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Atmospheric pressure tests

Some other results of other TPH experiments can be seen in Table 1. In atmospheric-pressure tests at 900°C with 500 ppm HjS in the gas phase, sulfur was not desorbed from Catalyst Al. The same phenomenon was noticed in the tests performed at 900°C under 5 bar pressure with Catalysts A2 and C. In addition, when the sulfur content of the catalyst beds was analyzed after TPH experiments, it was observed that only a small amount of sulfur was present on the catalyst. This observation indicates that sulfur adsorption is not completely reversible, but that part of the adsorbed sulfur remains on the catalyst. The effect of this phenomenon was also observed when a catalyst was regenerated by removal of HjS to the gas mixture in fixed-bed poisoning tests. The catalyst activity did not reach the original level (with no HjS in the gas) especially in ammonia decomposition. The analysis of the sulfur content of the bed showed that a small amount of sulfur was still present on the catalyst. [Pg.476]

This is the most common method. It is used for gasolines, kerosenes, gas oiis and similar products. The test is conducted at atmospheric pressure and is not recommended for gasolines having high dissolved gas contents or solvents whose cut points are close together. [Pg.100]

Place 35 ml. of a M solution of aluminium tsopropoxide or 7 g. of solid aluminium tsopropoxide, 450 ml. of dry isopropyl alcohol and 21 g. of purified benzaldehyde (Section IV,115) in a 1 litre round-bottomed flask. Fit a short reflux condenser (no water in the cooling jacket) or better a Hahn condenser (2) (containing a 1 cm. layer of ethyl alcohol in the iimer tube) to the flask and arrange for slow distillation from a water bath at the rate of 3-6 drops per minute. Continue the heating until a negative test for acetone is obtained after 5 minutes of total reflux (6-9 hours) if the volume of the mixture falls below 200 ml. during the reduction, add more isopropyl alcohol. Remove the reflux or Hahn condenser and distil off (Fig. II, 13, 3) most of the isopropyl alcohol under atmospheric pressure from a suitable oil bath. Hydrolyse the... [Pg.884]

A report on the continuous flash pyrolysis of biomass at atmospheric pressure to produce Hquids iadicates that pyrolysis temperatures must be optimized to maximize Hquid yields (36). It has been found that a sharp maximum ia the Hquid yields vs temperature curves exist and that the yields drop off sharply on both sides of this maximum. Pure ceUulose has been found to have an optimum temperature for Hquids at 500°C, while the wheat straw and wood species tested have optimum temperatures at 600°C and 500°C, respectively. Organic Hquid yields were of the order of 65 wt % of the dry biomass fed, but contained relatively large quantities of organic acids. [Pg.23]

The vapor/hquid ratio tests measure the amount of vapor formed from a given volume of Hquid at a given temperature at atmospheric pressure. A common measure used in specifying gasoline is the temperature at which the vapor/Hquid ratio is 20 (fV/L=2o ) Although V/L can be measured experimentally, it is a difficult and time consuming test to carry out, and techniques have been developed to calculate it from RVP and D86 values. [Pg.182]

The narcotic potency and solubiUty in oHve oil of several metabohcaHy inert gases are Hsted in Table 10. The narcotic potency, ED q, is expressed as the partial pressure of the gas in breathing mixtures requited to produce a certain degree of anesthesia in 50% of the test animals. The solubiUties are expressed as Bunsen coefficients, the volume of atmospheric pressure gas dissolved by an equal volume of Hquid. The Hpid solubiHty of xenon is about the same as that of nitrous oxide, a commonly used light anesthetic, and its narcotic potency is also about the same. As an anesthetic, xenon has the virtues of reasonable potency, nonflammability, chemical inertness, and easy elimination by the body, but its scarcity and great cost preclude its wide use for this purpose (see Anesthetics). [Pg.17]

Feed analyses in terms of component concentrations are usually not available for complex hydrocarbon mixtures with a final normal boihng point above about 38°C (100°F) (/i-pentane). One method of haudhug such a feed is to break it down into pseudo components (narrow-boihng fractions) and then estimate the mole fraction and value for each such component. Edmister [2nd. Eng. Chem., 47,1685 (1955)] and Maxwell (Data Book on Hydrocarbons, Van Nostrand, Princeton, N.J., 1958) give charts that are useful for this estimation. Once values are available, the calculation proceeds as described above for multicomponent mixtures. Another approach to complex mixtures is to obtain an American Society for Testing and Materials (ASTM) or true-boihng point (TBP) cui ve for the mixture and then use empirical correlations to con-strucl the atmospheric-pressure eqiiihbrium-flash cui ve (EF 0, which can then be corrected to the desired operating pressure. A discussion of this method and the necessary charts are presented in a later subsection entitled Tetroleum and Complex-Mixture Distillation. ... [Pg.1264]

Carbon should be prewetted prior to being placed in the test columns. Backwashing the carbon at low rates (2.5 m/hr) does not remove the air. Rates that would expand the bed 50 percent or 15-30 m/hr, are required. The liquid used for prewetting can either be water, if it is compatible with the liquid to be treated, or a batch of the liquid to be treated which has been purified previously. There are three types of carbon systems (1) fixed beds, (2) pulse beds, and (3) fluidized beds, and these can be used singly, in parallel, or in combination. The majority of systems are either fixed or pulse beds. The two basic types of adsorbers which can be designed to operate under pressure or at atmospheric pressure are the moving or pulse bed and the fixed bed. Either can be operated as packed or expanded beds. [Pg.308]

A workman, pressure testing pipe work with a hand-operated hydraulic pump, told his foreman ih.n he could i ]( ct llic uauuc reading above 200 psi. The foreman told him to pump harder. He did so bursting the pipeline Hie uiue wus calibrated in atmospheres and not psi. The abbreviation "atm." in small letters was not under,in nl... [Pg.170]

The basic alloy at atmospheric pressure and T = 20°C demonstrated the per cent elongation <5 = 31% and the per cent reduction ip = 65% while plastic properties of the hydrogenated alloy were close to zero. But an opposite relation was observed in tensile tests under a pressure of 6.5 kbar. The plastic properties of the hydrogenated alloy increased to <5 = 33% and /> = 83% at P = 6.5 kbar and T = 20°C while those of the basic alloy changed only slightly (Fig. 11). [Pg.434]

Pressure losses through the shell side of exchangers are subject to much more uncertainty in evaluation than for tube side. In many instances, they should be considered as approximations or orders of magnitude. This is especially true for units operating under vacuum less than 7 psia. Very little data has been published to test the above-atmospheric pressure correlations at below-atmospheric pressures. The losses due to differences in construction, baffle clearances, tube clearances, etc., create indeterminate values for exact correlation. Also see the short-cut method of reference 279. [Pg.211]

Plastic Viscosity and Yield Point. Plastic viscosity and yield point measurements are obtained from a direct indicating viscometer. Due to the temperature effect on the flow properties of oil-base mud, the testing procedure is modified. The mud sample in the container is placed into a cup heater [23]. The heated viscometer cup provides flow property data under atmospheric pressure and bottomhole temperature. [Pg.657]

D-86 is a common ASTM test method that measures the boiling point of light liquid hydrocarbons at various volume percent fractions. The sample is distilled at atmospheric pressure, provided its final boiling point (end point) is less than 750°F. [Pg.359]

Beyer (B8) has recently reported experimental data obtained in small test motors under atmospheric and altitude conditions. At atmospheric pressure, his results showed the observed ignition delay to be a function of the delivery rate, as shown in Fig. 10. Additional data obtained in small test motors by Fullman and Nielsen (F6) are shown for comparison. These latter investigators conducted studies on the effects of various injectors, with delivery from both the head end and the aft end. Their results indicate that the hollow-cone injector is the most efficient. This subject has been treated in more detail by Miller (M7). [Pg.24]

Self-Test 4.1A What is the atmospheric pressure when the height of the mercury column in a barometer is 756 mm ... [Pg.264]

Self-Test 4.1B The density of water at 20°C is 0.998 g-cm-3. What height would the column of liquid be in a water barometer when the atmospheric pressure corresponds to 760. mm of mercury ... [Pg.264]

Sfi.F-TeST 4.2A What is the pressure in a system when the mercury level in the system-side column in an open-tube mercury manometer is 25 mm lower than the mercury level in the atmosphere-side column and the atmospheric pressure corresponds to 760. mmHg at 15°C ... [Pg.265]

Self-Test 4.3B The atmospheric pressure in Denver, Colorado, on a certain day was 630. Torr. Express this pressure in pascals. [Pg.266]

Sf.ef-Test 4.14A A baby with a severe bronchial infection is in respiratory distress. The anesthetist administers heliox, a mixture of helium and oxygen with 92.3% by mass 02. What is the partial pressure of oxygen being administered to the baby if atmospheric pressure is 730 Torr ... [Pg.280]

The reaction test was carried out at atmospheric pressure using a vertical continuous flow fixed bed reactor. The content of effluent gas was analyzed by a gas chromatograph (HP 5890). [Pg.226]


See other pages where Atmospheric pressure tests is mentioned: [Pg.377]    [Pg.622]    [Pg.192]    [Pg.149]    [Pg.622]    [Pg.345]    [Pg.75]    [Pg.622]    [Pg.17]    [Pg.65]    [Pg.377]    [Pg.622]    [Pg.192]    [Pg.149]    [Pg.622]    [Pg.345]    [Pg.75]    [Pg.622]    [Pg.17]    [Pg.65]    [Pg.105]    [Pg.96]    [Pg.131]    [Pg.113]    [Pg.215]    [Pg.24]    [Pg.415]    [Pg.427]    [Pg.189]    [Pg.200]    [Pg.1232]    [Pg.251]    [Pg.251]    [Pg.163]    [Pg.41]    [Pg.40]    [Pg.44]    [Pg.281]    [Pg.258]   
See also in sourсe #XX -- [ Pg.75 ]




SEARCH



Pressure test

Test in argon at atmospheric pressure

Testing pressure

© 2024 chempedia.info