Big Chemical Encyclopedia

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

Articles Figures Tables About

Heavy liquid product

Hydrotreating reduces the sulfur content of all the products. With hydrotreated feeds, more of the feed sulfur goes to coke and heavy liquid products. The same sulfur atoms that were converted to H S in the FCC process are also being removed first in the hydrotreating process. The remaining sulfur compounds are harder to remove. The heavier and more aromatic the feedstock, the greater the level of sulfur in the coke (Table 2-7). [Pg.59]

In long contact time thermal processes, essentially no net hydrogen is introduced into the heavy liquid products and the major product (SRC) continually dehydrogenates with increasing time (4,11). These last two points are illustrated in Table I and Figure 4. [Pg.138]

Preasphaltene, a heavy liquid product, is usually rich in polar functional groups, as they are sometimes called preasphaltol (76). Such groups still contain cations that limit their solubility and their removal from the catalyst surface. [Pg.76]

Because the formation of heavy liquid products is low, LPG is cracked in a very similar process to ethane cracking. Often LPG can be co-fed to the pyrolysis furnace with ethane and there is no need for an additional process plant. [Pg.146]

G.c. - m.s. analyses of light liquid products was carried out using 40 m x 0,3 mm silica phased capillary column coated with SE 30 and connected with VQ-70HS mass spectrometer. Heavy liquid products (b.p, > 180 C) were analysed by n.m.r. spectroscopy ( Bruker MSL-400). For characterization of the heavy liquid products, their were separated on a particular families of compounds by a colume chromatography technique. Educed fractions were analysed by g.c. - m.s. technique. [Pg.1390]

Furthermore, it was shown that for most feedstocks, as the H2S yield increased for a given feedstock, the sulfur in the gasoline increased. They also found that mild hydrotreating of the feed tended to remove H2S precursors, so that the H2S yield was decreased, as well as the sulfur in the gasoline, but that the sulfur in the heavy liquid products remained constant. From a commercial point of view it is important that hydrotreating or desulfiirisation technologies involve high capital investments [2]. [Pg.303]

Main fractionation column. Reactor effluent is separated into various products. The overhead includes gasoline and lighter material. The heavy liquid products, heavier naphtha, and cycle oils are separated as side cuts and slurry oil is separated as a bottom product. [Pg.2573]

Once we finish entering the heavy liquids product measurements in Figure 4.83, the status button of the calibration will turn yellow and indicate that the model is Not Solved . At this point we begin step 3 of the calibration process. [Pg.226]

Sulfur and nitrogen contents. Sulfur is concentrated in coke and heavy liquid products. Sulfur and nitrogen compounds form a variety of compounds that distribute throughout the product slate and in the offgas. [Pg.143]

The preparation of these compounds in the laboratory is not recommended and is rarely worth while because of the cheapness of the commercial products. Dimethyl sulphate is a heavy liquid, boiling at 188-6°, and is practically without odour. The vapour is highly poisonous and the substance should only be used in a fume cupboard with a good draught. The liquid itself is readily absorbed through the skin, with toxic results. [Pg.303]

The first step in a gas processing plant is to separate the components that are to be recovered from the gas into an NGL stream. It may then be desirable to fractionate the NGL stream into various liquefied petroleum gas (LPG) components of ethane, propane, iso-butane, or normal-butane. The LPG products are defined by their vapor pressure and must meet certain criteria as shown in Table 9-1. The unfractionated natural gas liquids product (NGL) is defined by the properties in Table 9-2. NGL is made up principally of pentanes and heavier hydrocarbons although it may contain some butanes and very small amounts of propane. It cannot contain heavy components that boil at more than 375°F. [Pg.241]

Hot splitless Liquid sample passes from syringe into hot inlet initial oven temperature critical (ca. 10 °C lower than b.p. of solvent) bulk of sample enters column (splitless time of 10-40 s) Dilute samples, containing heavy by-products Very broad, focusing required 0.1-2 80-95... [Pg.188]

In the reverse flow type, the hydrotreater reactor is fed with fresh and recycled feeds, and is operated to accomplish partial conversion of that combined feed in the first stage. A graded HDT-HCK bed or a multi-functional catalyst can be used in the first stage. A very effective H2 separation is used for the first-stage effluent gas. A bottoms fractionator or an adsorption unit is used for removal of heavy PAHs. Carbon adsorption extends the catalyst life. The liquid product of the first reactor is mixed with a mixture of fresh and recycled H2. The whole second stage effluent is hydrotreated in the first stage. [Pg.46]

Figure 21.2 shows the entire low-temperature process in block flow format. Following the reactor and cooler, the liquid EDC is washed, removing unreacted chlorine and catalyst. Product EDC is obtained in two distillation steps drying, where water and a small amount of light by-products are removed and purification, which removes a small amount of heavy by-products. Both of these distillation steps use steam-heated reboilers. [Pg.281]

Consecutively, the heavy paraffins are cracked into lighter hydrocarbon fractions by hydro-cracking. For example, for the Shell Middle Distillate Synthesis (SMDS) process, the liquid product stream is composed of 60% gasoil (diesel), 25% kerosene and 15% naphtha. The gaseous product mainly consists of LPG (a mixture of propane and butane) (Eilers et al., 1990). Figure 7.3 shows a simplified diagram comprising all process steps to produce synthetic hydrocarbons from biomass, natural gas and coal. [Pg.214]

The dominant share of styrene production comes from dehydrogenation of EB in plants like that shown in Figure 8-5. Some comes as a coproduct in propylene oxide/styrene plants. An even smaller amount is recovered from the gasoline fraction of olefins plants cracking heavy liquids. [Pg.125]

So not much else is formed. Thats a contrast to ethylene manufacture, especially cracking the heavy liquids, where the by-products are abundant. [Pg.138]

The process achieves about 90% conversion of ethane to VC. With the elimination of so many intermediate steps compared to the traditional EDC route, this process could achieve VC production cost savings of up to 35% anywhere an adequate supply of ethane can be found. That could even include the recycle stream from a heavy liquids olefins plant. If these killer economics persevere, this technology could grab all the growth in VC capacity and even replace most of the conventional VC capacity in a couple of decades. That s what happened to the acetylene-based route to VC when the ethylene-based route came on stream in the mid-20th century. [Pg.140]

FAU 5.5 NiO(1.7) M0O3 (6.7) Arabian heavy atmospheric residue Autoclave 410°G 9.8MPa 74.9% liquid product, 52% HDS activity, 26.8% HDN activity Contains mesopores [123]... [Pg.388]

The performance analysis and product analysis results confirm previous findings (3,8) that hydrotreating improves the quality of catalytic cracker feedstock and the resultant products. In addition, it was shown that the quality of the liquid products and the yields of the coke and the heavy cycle oil (HCO) from cracking of the severely hydrotreated feedstock (WM-2-9) were independent of the conditions of the cracking process. These results imply that there exists a degree of pretreatment hydrotreating above which... [Pg.304]

A similar chain-growth mechanism was said to occur with the first molybdenum-sulfur-potassium based catalysts of table I (15). For such a chain-growth mechanism, the heavier the average molecular weight of alcohols, the greater the formation of heavy compounds and, more often than not, the lower the alcohols selectivity. Furthermore, in Fischer-Tropsch type catalysts (24,25) diffusion limitations, mostly due to the presence of liquid products condensed in the micro porosity, increase with the size of diffusing molecules. These molecules are capable of... [Pg.43]


See other pages where Heavy liquid product is mentioned: [Pg.26]    [Pg.223]    [Pg.399]    [Pg.1395]    [Pg.357]    [Pg.396]    [Pg.397]    [Pg.26]    [Pg.223]    [Pg.399]    [Pg.1395]    [Pg.357]    [Pg.396]    [Pg.397]    [Pg.2]    [Pg.74]    [Pg.983]    [Pg.990]    [Pg.86]    [Pg.66]    [Pg.104]    [Pg.93]    [Pg.157]    [Pg.44]    [Pg.301]    [Pg.115]    [Pg.67]    [Pg.69]    [Pg.388]    [Pg.519]    [Pg.97]    [Pg.175]    [Pg.279]    [Pg.287]   
See also in sourсe #XX -- [ Pg.225 ]




SEARCH



Liquid heavy

Liquid production

© 2024 chempedia.info