Hourly space velocity

The MTDP process, which is similar to the Tatoray process, produces an equilibrium composition of xylene isomers. A -xylene yield of 24% in the xylene product is formed at 42—48 wt % toluene conversion over the heterogeneous catalyst at 390—495°C, 4.2 MPa (600 psig), 1 2 Hquid hourly space velocity, and 4 H2/hydrocarbon molar feed ratio. A new ZSM-5 catalyst, which has higher activity and stability than the current catalyst, has been reported (93). 

To manufacture the lower aLkylamines by Method 1, ammonia and alcohol are passed continuously over a fixed bed containing the catalyst in a gas—soHd heterogeneous reaction. The ammonia to alcohol mole ratio varies from 2 1 to 6 1 depending on the amine desired as shown in Figure 1. Operating conditions are maintained in the range from 300—500°C and 790—3550 kPa (100—500 psig) at a gas hourly space velocity between 500—1500 vol/vol per hour. Yields are typically in excess of 90%. 

C and 6.9 MPa (70.3 kg/cm ) in 100% selectivity (113). The neoalcohol was also produced in selectivities of 99% by employing zirconium hydroxide catalysts (114,115). The rates of the latter process, however, are reportedly low at Hquid hourly space velocity (LHSV) of <1 kg/catalyst-h. A catalyst from... 

The quantity of catalyst used for a given plant capacity is related to the Hquid hourly space velocity (LHSV), ie, the volume of Hquid hydrocarbon feed per hour per volume of catalyst. To determine the optimal LHSV for a given design, several factors are considered ethylene conversion, styrene selectivity, temperature, pressure, pressure drop, SHR, and catalyst life and cost. In most cases, the LHSV is ia the range of 0.4—0.5 h/L. It corresponds to a large quantity of catalyst, approximately 120 m or 120—160 t depending on the density of the catalyst, for a plant of 300,000 t/yr capacity. 

Both catalyst space velocity and bed geometry play a role. The gas hourly space velocity (GHSV) is used to relate the volumetric flow rate to the catalyst volume. GHSV has units of inverse hour and is defined as the volume flow rate per catalyst volume. 

GHSV (gas hourly space velocity) = (volumes of feed as gas at STP/h)/(vohime of reactor or its content of catalyst) = SCFH gas feed/fF. 

LHSV (liquid hourly space velocity) = (volume of liquid feed at 60°F/h)/(fF of reactor) = SCFH hquid feed/fF. 

WHSV (weight hourly space velocity) = (lb feed/h)/(lb catalyst). 

The reactor feed may be preheated and the feed pressure may alter. The volumetric flowrate of gases depends on the reactor temperature and pressure at fixed mass flowrate. In many cases, the feed is liquid at room temperature, while the reaction mixture is a gas at the higher temperature in the reactor. In these instances, the performance of the reactor is represented as conversion and selectivity against the liquid hourly space velocity (LHSV). This is defined as... 

Another commonly used term is the gas hourly space velocity (GHSV), which is defined as... 

Normally, catalytic reformers operate at approximately 500-525°C and 100-300 psig, and a liquid hourly space velocity range of 2-4 hr" Liquid hourly space velocity (LHSV) is an important operation parameter expressed as the volume of hydrocarbon feed per hour per unit volume of the catalyst. Operating at lower LHSV gives the feed more contact with the catalyst. 

Figure 9-5. Effect of temperature and liquid hourly space velocity on conversion. ...

Catalyst system Temperature (K) Conditions Pressure (10s Nm-2) Weight hourly space velocity (hr-1) Conversion" (%) Selectivity6 (%) Ethene/butene molar ratio" Reference... 

A vapor phase process for deparaffmization of light gas oils performed by the BP works in this way The gas oil, boiling range 230-320°C, is passed over a 5-A molecular sieve at 320°C and a pressure of 3.6 bar. The space velocity is 0.63 vol liquid gas oil per vol molecular sieve and per hour, [liquid hourly space velocity (lhsv) = 0.63] the adsorption period takes 6 min. Together with the gas oil vapor 120 vol N2 per vol liquid gas oil is led over the sieve as carrier and purge gas. After the adsorption period the loaded molecular sieve is purged at the same temperature with pure N2 for 6 min. Subsequently, the adsorbed /z-alkanes are desorbed by 1 vol liquid /z-pentane per vol molecular sieve and per hour. The /z-pentane is recovered from the /z-alkane//z-pentane mixture by simple distillation [15]. The IsoSiv process of the Union Carbide Corporation works in a similar way [16]. The purity of the isolated /z-alkanes is >98%. 

The catalytic experiments were performed at the stationnary state and at atmospheric pressure, in a gas flow microreactor. The gas composition (NO, CO, O2, C3H, CO2 and H2O diluted with He) is representative of the composition of exhaust gases. The analysis, performed by gas chromatography (TCD detector for CO2, N2O, O2, N2, CO and flame ionisation detector for C3H6) and by on line IR spectrometry (NO and NO2) has been previously described (1). A small amount of the sample (10 mg diluted with 40 mg of inactive a AI2O3 ) was used in order to prevent mass and heat transfer limitations, at least at low conversion. The hourly space velocity varied between 120 000 and 220 000 h T The reaction was studied at increasing and decreasing temperatures (2 K/min) between 423 and 773 K. The redox character of the feedstream is defined by the number "s" equal to 2[02]+[N0] / [C0]+9[C3H6]. ... 

Room temperature CO oxidation has been investigated on a series of Au/metal oxide catalysts at conditions typical of spacecraft atmospheres CO = 50 ppm, COj = 7,000 ppm, H2O = 40% (RH) at 25 C, balance = air, and gas hourly space velocities of 7,000- 60,000 hr . The addition of Au increases the room temperature CO oxidation activity of the metal oxides dramatically. All the Au/metal oxides deactivate during the CO oxidation reaction, especially in the presence of CO in the feed. The stability of the Au/metal oxide catalysts decreases in the following order TiOj > FejO, > NiO > CO3O4. The stability appears to decrease with an increase in the basicity of the metal oxides. In situ FTIR of CO adsorption on Au/Ti02 at 25 C indicates the formation of adsorbed CO, carboxylate, and carbonate species on the catalyst surface. 

For the n-Cq reforming and n-C[2 isomerization reactions the catalysts were run in a fixed bed micro reactor equipped with on-line GC analysis. The catalyst, together with a quartz powder diluent, was added to a 6 inch reactor bed. A thermocouple was inserted into the center of the bed. The catalysts were calcined at 350-500°C immediately prior to use and reduced in H2 at 350-500°C for 1 hour. n-Heptane or dodecane (Fluka, puriss grade) were introduced via a liquid feed pump. The mns were made at 100-175 psi with a H2/n-heptane (or n-Ci2) feed ratio of 7 and a weight hourly space velocity of 6-11. 

Benzene hydrogenation was used to probe metal site activity. A 12/1 H2/benzene feed was passed over the catalysts at 700 kPa with a weight hourly space velocity of 25. The temperature was set to 100°C and the conversion of benzene to cyclohexane was measured after 2 hours at temperature. The temperature was then increased at 10°C increments and after two hours, the conversion remeasured. 

The reactions were carried out in the steady state flow mode as described previously [11]. Differential kinetics were determined from plots of conversion vs. W/F. Three catalysts CoZSM-5, HZSM-5 and NaZSM-5 (Si/AI = 11) were studied in this work. The catalyst preparation and the standard pretreatment used prior to reaction have been described previously [11]. It involved dehydration in flowing dried 0 as the temperature was raised slowly to 500°C. The feed comprised CH4 (0.28%), NO (0.21 %) or NOj (0.21 %). and/or Oj (2.6%) in He. The flow rate was 75 ml/min and the gas hour space velocity (GHSV) was varied between 4,500 and 250,000 h by changing the weight of catalyst samples. 

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