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Naphtha treating

Two undesirable aspects of FCC naphtha quaUty are that it may contain unacceptably high amounts of foul smelling mercaptans, and that its thermal stabiUty may be too low. Mercaptans are usually found in the light FCC naphtha and may be removed or converted to sulfides and disulfides by a sweetening process such as Merox, developed by UOP. Thermal stabiUty is improved in sweetening processes through removal of cresyUc and naphthenic acids. It may be further improved by clay treating and by addition of oxidation inhibitors such as phenylene diamine. [Pg.184]

Virgin naphtha hydrofining processing conditions have been standardized at 550°F, 4 V/hr/V, 300-400 psig and 400-500 SCF/B of 70% H treat gas. Such conditions will make a 4 ppm sulfur product of most stocks of interest. [Pg.67]

In treating cracked stocks such as steam cracked naphtha or visbreaker naphtha, which are highly olefinic in nature, nickel molybdate or nickel tungstate catalysts are generally employed. These catalysts have much higher activity for olefin samration reactions than does cobalt molybdate. [Pg.68]

Rerunning is a second distillation step applied to distillate stocks in order to remove undesirable higher boiling materials from the product. These materials may be present because of poor fractionation in the primary distillation step more frequently they are heavy polymers formed in treating operations. Rerunning may be combined with solvent removal, as in the case of heavy lube distillates which are diluted with naphtha to lower their viscosity before being chemically treated. [Pg.84]

Depending upon the refinery needs, the raw C5 plus steam cracked naphtha may be sent to isoprene extraction, treated to remove gum forming diolefins and sent to the refinery gasoline pool, or else completely hydrogenated and then fed to an aromatics extraction unit. [Pg.103]

The liquefied plastic fraction is heated to over 400 °C. This leads to cracking of the plastic into components of different chain lengths. Gases count for 20%-30% and oils for 60%-70% they are separated by distillation. Any naphtha produced is treated in a steam cracker, resulting in monomers like ethylene and propylene that are recovered. Such monomers can be used to produce plastics again. The heavy fractions can be processed into synthesis gas or conversion coke and then be transferred for further use. At most 5% of the input is converted into a mineral fraction. It is likely that this consists mainly of the inorganic additives in plastics. [Pg.8]

Mercaptans are the main sulfur compounds in LCN, thiophenes and substituted-thiophenes are present in MCN and benzothiophene (BT) and substituted-BT in the heavy naphthas. A caustic treatment would work for the removal of mercaptans from LCN, and take the total sulfur content below 20 ppm. However, MCN and HCN have to be treated in a more severe way. [Pg.25]

The new commercially available technologies concern the removal of sulfur with a minimum lost of octane rating. SCANfming and Prime G+ are the process technologies licensed by ExxonMobil and IFP, respectively. In SCANfining (Fig. 4), the complete naphtha (full range naphtha) is treated, with a proprietary catalyst. [Pg.26]

After bauxite treatment the product was fractionated to produce C3-C4 and naphtha (C5-204°C) fractions. The C3-C4 olefin-rich gas was oligomerized over a solid phosphoric acid (SPA) catalyst to produce an unhydrogenated polymer gasoline with a research octane number (RON) of 95 and MON of 82.21 The bauxite-treated FT motor gasoline (RON of 87, MON of 76) was mixed with the polymer gasoline and some natural gas condensates (and crude-oil-derived naphtha) to produce the final motor gasoline product. In this respect it is noteworthy that the Fe-HTFT-derived material was the high-octane-blend stock. [Pg.339]

In the HTFT oil refinery the light oil and <345°C fraction of the decanted oil (obtained by passing the decanted oil through a vacuum flash drum) were clay treated. Clay treatment is similar to Bauxite treatment and is used to increase the octane number of the naphtha by acidic isomerization and to reduce the oxygenate content of the oil. Processing the LTFT and HTFT in separate (and different)... [Pg.342]

Benzoraffln A hydrofining process for treating naphtha fractions derived from coal. It is a fixed-bed, gas-phase process using a cobalt/molybdenum oxide catalyst. Developed jointly by BASF, Veba-Chemie, and Lurgi, Ground 1960. [Pg.36]

Sulfur compounds are most commonly removed or converted to a harmless form by chemical treatment with lye. Doctor solution, copper chloride, or similar treating agents (Speight, 1999). Hydrorefining processes (Speight, 1999) are also often used in place of chemical treatments. When used as a solvent, naphtha is selected for its low sulfur content and the usual treatment processes remove only sulfur compounds. Naphtha, with its small aromatic content, has a slight odor, but the aromatics increase the solvent power of the naphtha and there is no need to remove aromatics unless odor-free naphtha is specified. [Pg.259]


See other pages where Naphtha treating is mentioned: [Pg.492]    [Pg.492]    [Pg.114]    [Pg.133]    [Pg.184]    [Pg.185]    [Pg.123]    [Pg.339]    [Pg.361]    [Pg.440]    [Pg.2518]    [Pg.436]    [Pg.442]    [Pg.249]    [Pg.93]    [Pg.95]    [Pg.213]    [Pg.218]    [Pg.221]    [Pg.64]    [Pg.97]    [Pg.21]    [Pg.37]    [Pg.8]    [Pg.10]    [Pg.361]    [Pg.1823]    [Pg.24]    [Pg.335]    [Pg.339]    [Pg.339]    [Pg.339]    [Pg.342]    [Pg.1354]    [Pg.13]    [Pg.109]    [Pg.58]    [Pg.233]    [Pg.512]   
See also in sourсe #XX -- [ Pg.347 , Pg.348 , Pg.349 , Pg.350 , Pg.351 , Pg.352 , Pg.353 , Pg.354 , Pg.355 , Pg.356 , Pg.357 , Pg.358 , Pg.359 ]




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Naphtha

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