Abstract:
A process for treating a hydrocarbon liquid composition to improve its storage and/or transportation stability, comprises contacting the hydrocarbon liquid composition with a polar trap, wherein the conductivity of the hydrocarbon liquid composition is not reduced by said contacting with a polar trap. The polar trap may be a clay treater containing attapulgus clay. The process may include sequentially passing the hydrocarbon liquid composition through a dehydrator and a clay treater at a flow rate of between about 100 and about 1000 m3 per hour. Advantageously, the hydrocarbon liquid composition is refined and in particular, may be a Merox™-treated jet fuel.
Abstract:
A desulfurizing device for a fuel cell includes a dehydrating element for absorbing moisture in a hydrocarbon fuel, and a desulfurizing element for absorbing a sulfur compound included in the hydrocarbon fuel that flows out of the dehydrating element. In another embodiment, the desulfurizing device for a fuel cell includes a dehydrating element for absorbing moisture included in a fuel, and a desulfurizing element. The desulfurizing element absorbs a sulfur compound included in the fuel flowing out of the dehydrating element if temperature of the desulfurizing element is below a predetermined temperature, and the desulfurizing element desorbs a sulfur compound included in the desulfurizing element whenever the desulfurizing element is heated above the predetermined temperature.
Abstract:
The invention relates to a treatment process of a sulphur-containing hydrocarbon fraction, comprising the following steps: a) a hydrodesulphurization step of said hydrocarbon fraction to produce a sulphur-depleted effluent, consisting of passing said hydrocarbon fraction mixed with hydrogen over at least one hydrodesulphurization catalyst. b) a step of separation of the partially desulphurized hydrocarbon fraction from the hydrogen introduced in excess, as well as the H2S formed in step a). c) a step of collecting the sulphurous compounds, consisting of placing the partially desulphurized hydrocarbon fraction originating in step b) in contact with an adsorbent comprising at least one element chosen from the group constituted by the elements of groups VIII, IB, IIB and IVA, the adsorbent being used in reduced form in the absence of hydrogen at a temperature above 40° C., the metal content in the reduced form of the adsorbent being above 25% by weight.
Abstract:
Abstract Described is a desorption process and a process for producing a catalytically deactivated formed zeolitic adsorbent, whereby both processes are suitable to improve the lifetime of a formed zeolithic adsorbant in the removal of sulfur compounds from sulfur contaminated gas and liquid feed streams. The adsorbent is in particular a synthetic 13X or LSX faujasite with a silica to alumina ratio from 1.9:1.0 to about 3.0:1.0. The cations of the faujasite include alkali and alkaline earth metals. The formed zeolite mixture is preferably catalytically deactivated due to a phosphate treatment. The desorption is carried out thermally, wherein the heat treatment is done at different temperature stages to avoid decomposition of the organic sulfur compounds.
Abstract:
A process for the cyclical regeneration of an adsorbent bed containing sulfur-oxidated compounds. The adsorbent bed is used to adsorb and separate sulfur-oxidated compounds from a hydrocarbonaceous stream to produce an adsorbent having adsorbed sulfur-oxidated compounds.
Abstract:
This invention provides a resid cracking apparatus comprising a riser, reactor, stripper cum separator with adjustable outlets in flow communication with adsorbent and catalyst regenerators for converting hydrocarbon residues containing higher concentration of conradson carbon content, poisonous metals such as nickel & vanadium and basic nitrogen etc., into lighter and valuable products and a process thereof.
Abstract:
A process for the removal of sulfur-oxidated compounds from a hydrocarbonaceous stream containing sulfur-oxidated compounds wherein the hydrocarbonaceous stream containing sulfur-oxidated compounds is contacted with an adsorbent which selectively adsorbs sulfur-oxidated compounds from the hydrocarbonaceous stream to produce an adsorbent having adsorbed sulfur-oxidated compounds. The loaded adsorbent containing sulfur-oxidated compounds is contacted with a desorbent to produce a desorbent containing sulfur-oxidated compounds and an adsorbent having a reduced content of sulfur-oxidated compounds. The regenerated adsorbent is then used to remove additional sulfur-oxidated compounds.
Abstract:
The invention comprises a process for removal of carbonyl sulfide from a hydrocarbon, which comprises contacting a hydrocarbon stream containing carbonyl sulfide with an adsorbent and then regenerating the adsorbent by passing a heated gas, containing a hydrolyzing agent. The adsorbent that is regenerated by using this process retains at least 70% of its capacity for adsorption of sulfur as compared to fresh adsorbent.
Abstract:
Disclosed is a liquid phase adsorption process for removing and concentrating heteroatom compounds in hydrocarbons (HCH), comprising the steps of adsorption, copurging and regeneration. In the adsorption step, a liquid hydrocarbon stream is fed to an adsorber, which adsorbs HCH and returns adsorption effluent. In the copurging step, HCH, which are extracted from the previous regeneration, are applied to the adsorber, displacing the copurging effluent. In the regeneration step, a polar solvent is flowed through the adsorber, purging HCH. Most of the HCH are then set aside for use in the next copuring step, while a small amount of the HCH are taken out from the process as HCH product. The present invention is economically advantageous in effectively removing HCH from hydrocarbon streams and increasing the concentration of HCH within an HCH product.
Abstract:
CuY and AgY zeolites as selective sorbents for desulfurization of liquid fuels. Thiophene and benzene were used as the model system, and vapor phase isotherms were measured. Compared with NaY, CuY and AgY adsorbed significantly larger amounts of both thiophene and benzene at low pressures. It is hypothesized that this is due to null-complexation with Cunull and Agnull. On a per-cation basis, more thiophene was adsorbed by Cunull than by Agnull, eg. 0.92 molecule/Cunull versus 0.42 molecule/Agnull at 2null10null5 atm and 120null C. Molecular orbital calculations confirmed the relative strengths of null-complexation: thiophene>benzene and Cunull>Agnull. The experimental heats of adsorption for null-complexation are in qualitative agreement with theoretical predictions. The invention further comprises a process and sorbents for removal of aromatics from hydrocarbons.
Abstract translation:CuY和AgY沸石作为液体燃料脱硫的选择性吸附剂。 使用噻吩和苯作为模型系统,并测量气相等温线。 与NaY相比,CuY和AgY在低压下吸收显着较大量的噻吩和苯。 假设这是由于与Cu +和Ag +的π络合。 在阳离子基础上,更多的噻吩被Cu +吸附,而不是Ag +,例如。 分子轨道计算证实了π络合:噻吩>苯和Cu +> Ag +的相对强度,分子/ Cu +与0.42分子/ Ag +在2x10-5atm和120℃。 pi络合的吸附实验热量与理论预测的定性一致。 本发明还包括从烃中除去芳族化合物的方法和吸附剂。