Hydrocarbons light olefinic

More precisely, the rate of ozone formation depends closely on the chemical nature of the hydrocarbons present in the atmosphere. A reactivity scale has been proposed by Lowi and Carter (1990) and is largely utilized today in ozone prediction models. Thus the values indicated in Table 5.26 express the potential ozone formation as O3 formed per gram of organic material initially present. The most reactive compounds are light olefins, cycloparaffins, substituted aromatic hydrocarbons notably the xylenes, formaldehyde and acetaldehyde. Inversely, normal or substituted paraffins. 

Mobil MTG and MTO Process. Methanol from any source can be converted to gasoline range hydrocarbons using the Mobil MTG process. This process takes advantage of the shape selective activity of ZSM-5 zeoHte catalyst to limit the size of hydrocarbons in the product. The pore size and cavity dimensions favor the production of C-5—C-10 hydrocarbons. The first step in the conversion is the acid-catalyzed dehydration of methanol to form dimethyl ether. The ether subsequendy is converted to light olefins, then heavier olefins, paraffins, and aromatics. In practice the ether formation and hydrocarbon formation reactions may be performed in separate stages to faciHtate heat removal. 

Flowever, information concerning the characteristics of these systems under the conditions of a continuous process is still very limited. From a practical point of view, the concept of ionic liquid multiphasic catalysis can be applicable only if the resultant catalytic lifetimes and the elution losses of catalytic components into the organic or extractant layer containing products are within commercially acceptable ranges. To illustrate these points, two examples of applications mn on continuous pilot operation are described (i) biphasic dimerization of olefins catalyzed by nickel complexes in chloroaluminates, and (ii) biphasic alkylation of aromatic hydrocarbons with olefins and light olefin alkylation with isobutane, catalyzed by acidic chloroaluminates. 

The main route for producing light olefins, especially ethylene, is the steam cracking of hydrocarbons. The feedstocks for steam cracking units range from light paraffinic hydrocarbon gases to various petroleum fractions and residues. The properties of these feedstocks are discussed in Chapter 2. 

In Europe naphtha is the preferred feedstock for the production of synthesis gas, which is used to synthesize methanol and ammonia (Chapter 4). Another important role for naphtha is its use as a feedstock for steam cracking units for light olefins production (Chapter 3). Heavy naphtha, on the other hand, is a major feedstock for catalytic reforming. The product reformate containing a high percentage of Ce-Cg aromatic hydrocarbons is used to make gasoline. Reformates are also extracted to separate the aromatics as intermediates for petrochemicals. 

In general, crude oils and natural gases are composed of a mixture of relatively unreactive hydrocarbons with variable amounts of nonhydrocarbon compounds. This mixture is essentially free from olefins. However, the C2 and heavier hydrocarbons from these two sources (natural gas and crude oil) can be converted to light olefins suitable as starting materials for petrochemicals production. 

Yao, J., Kimble, J.B., and Drake, C.A. (2000) A method of making such improved zeolite material and the use thereof the conversion of non-aromatic hydrocarbon to aromatics and light olefins. U.S. Patent 6, 048,815. 

Dharia, D., et al. Increase Light Olefins Production. Hydrocarbon Processing, April 2004. 

The effect of the Si/Al ratio of H-ZSM5 zeolite-based catalysts on surface acidity and on selectivity in the transformation of methanol into hydrocarbons has been studied using adsorption microcalorimetry of ammonia and tert-butylamine. The observed increase in light olefins selectivity and decrease in methanol conversion with increasing Si/Al ratio was explained by a decrease in total acidity [237]. 

Studies at Mobil Research have shown that light olefins instead of gasoline can be made from methanol by modifying both the ZSM-5-type MTG (Methanol-to-Gasoline) catalyst and the operating conditions. Work carried out in micro-scale fluidized-bed reactors show that methanol can be completely converted to a mixture of hydrocarbons containing about 76 wt% C2-C5 olefins. The remaining hydrocarbons are 9% C1-C5 paraffins, of which the major component is isobutane, and 15% C6+, half of which is aromatic. 

The 100 BPD MTG project was extended recently to demonstrate a related fluid bed process for selective conversion of methanol to light olefins (MTO). The products of the MTO reaction make an excellent feed to the commercially available Mobil Olefins to Gasoline and Distillate process (MOGD) which selectively converts olefins to premium transportation fuels ( 1). A schematic of the combined processes is shown in Figure 1. Total liquid fuels production is typically greater than 90 wt% of hydrocarbon in the feed. Distillate/gasoline product ratios from the plant can be adjusted over a wide range to meet seasonal demands. 

The conversion of methanol to hydrocarbons (MTHC) on acidic zeolites is of industrial interest for the production of gasoline or light olefins (see also Section X). Upon adsorption and conversion of methanol on calcined zeolites in the H-form, various adsorbate complexes are formed on the catalyst surface. Identification of these surface complexes significantly improves the understanding of the reaction mechanism. As demonstrated in Table 3, methanol, dimethyl ether (DME), and methoxy groups influence in a characteristic manner the quadrupole parameters of the framework Al atoms in the local structure of bridging OH groups. NMR spectroscopy of these framework atoms under reaction conditions, therefore, helps to identify the nature of surface complexes formed. 

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