A multi-stage process for the production of an ISO 8217 compliant Product Heavy Marine Fuel Oil from ISO 8217 compliant Feedstock Heavy Marine Fuel Oil involving a Reaction System composed of one or more reactor vessels selected from a group reactor wherein said one or more reactor vessels contains one or more reaction sections configured to promote the transformation of the Feedstock Heavy Marine Fuel Oil to the Product Heavy Marine Fuel Oil. The Product Heavy Marine Fuel Oil has a Environmental Contaminate level has a maximum sulfur content (ISO 14596 or ISO 8754) between the range of 0.05 mass % to 1.0 mass. A process plant for conducting the process for conducting the process is disclosed that can utilize a modular reactor vessel.

A process for reducing the environmental contaminants in a ISO8217 compliant Feedstock Heavy Marine Fuel Oil, the process involving: mixing a quantity of the Feedstock Heavy Marine Fuel Oil with a quantity of Activating Gas mixture to give a feedstock mixture; contacting the feedstock mixture with one or more catalysts to form a Process Mixture from the feedstock mixture; separating the Product Heavy Marine Fuel Oil liquid components of the Process Mixture from the gaseous components and by-product hydrocarbon components of the Process Mixture and, discharging the Product Heavy Marine Fuel Oil. The Product Heavy Marine Fuel Oil is compliant with ISO 8217 for residual marine fuel oils and the Environmental Contaminants, which are selected from the group consisting of: a sulfur; vanadium, nickel, iron, aluminum and silicon and combinations thereof, have concentration less than 0.5 wt %. The Product Heavy Marine Fuel Oil can be used as or as a blending stock for an ISO 8217 compliant, IMO MARPOL Annex VI (revised) compliant low sulfur or ultralow sulfur heavy marine fuel oil.

Systems and methods for implicit chemical resolution of vacuum gas oils and fit quality determination are disclosed. The systems and methods include utilizing an FT-IR spectrum of an unknown VGO composition, and a database of FT-IR spectra of known VGO compositions, to determine a model of composition for the unknown VGO composition. Additionally, the fit quality for the model of composition is determined by performing a partial least squares analysis on specific spectral regions of interest in the FT-IR spectrum of the unknown VGO composition.

The methods described herein produce a naphthenic process oil, as classified by ASTM D-2226, containing 35-65% saturates and 35-65% aromatics as determined by ASTM D-2007. The produced naphthenic process oil also contains polyaromatic hydrocarbons (PAH), more specifically the EU/US EPA 8-regulated PAHs, less than 10 ppm. The naphthenic process oil is produced by first feeding gas oil ranging in viscosities up to 20 cSt at 100° C. through counter-current liquid-liquid extraction towers with a solvent having a selective affinity for aromatics. The extract is then cooled and either continuously processed through a coalescing separator or batch processed in a tank or decanter to produce a second raffinate, which can be further distilled to produce the naphthenic process oil.

A method for producing chemicals from crude oil by double-tube parallel multi-zone catalytic conversion is provided. The method may include the following steps: feeding the crude oil directly or separating the crude oil into light and heavy components by flash evaporation or distillation after desalination and dehydration; strengthening the contact and reaction between oil gas and catalyst by using two parallel reaction tubes with novel structure, controlling the reaction by zones, carrying out optimal combination on feeding modes according to different properties of reaction materials, controlling suitable reaction conditions for different materials, and increasing the production of light olefins and aromatics.

The present invention is in the field of heterogeneous catalysis.

Particularly, the present invention relates to a process for preparing catalysts advantageously usable in the hydrotreatment processes, for example in hydrodesulphurization, hydrodenitrogenation, hydrodearomatization processes of hydrocarbons.

More in particular, the present invention relates to a process for obtaining said catalysts, which comprise mixed oxides of Nickel, Aluminum, Molybdenum and Tungsten and optionally a transition metal Me selected from the group consisting of Zn, Mn, Cd, and a mixture thereof, an organic component C, and possibly an inorganic binder B.

Said mixed oxides comprise an amorphous phase and a pseudo-crystalline phase isostructural to Wolframite.

The present invention further relates to said hydrotreatment catalysts and a hydrotreatment process wherein said catalysts are used.

Methods are provided for processing deasphalted gas oils derived from thermally cracked resid fractions to form Group I, Group II, and/or Group III lubricant base oils. The yield of lubricant base oils (optionally also referred to as base stocks) can be increased by thermally cracking a resid fraction at an intermediate level of single pass severity relative to conventional methods. By performing thermal cracking to a partial level of conversion, compounds within a resid fraction that are beneficial for increasing both the viscosity and the viscosity index of a lubricant base oil can be retained, thus allowing for an improved yield of higher viscosity lubricant base oils from a thermally cracked resid fraction.

Ionic liquid containing compositions may be used in the production, recovery and refining of oil and gas. In addition, they may be used to treat cooling water and/or to inhibit and/or prevent corrosion of metals.

The invention concerns a method for rejuvenating an at least partially used catalyst originating from a hydroprocessing and/or hydrocracking process, the at least partially used catalyst being derived from a fresh catalyst comprising at least one group VIII metal (in particular, Co), at least one group VIB metal (in particular, Mo), an oxide support, and optionally phosphorus, the method comprising the steps: a) regenerating the at least partially used catalyst in a gas stream containing oxygen at a temperature between 300° C. and 550° C. so as to obtain a regenerated catalyst, b) then placing the regenerated catalyst in contact with phosphoric acid and an organic acid, each having acidity constant pKa greater than 1.5, c) performing a drying step at a temperature less than 200° C. without subsequently calcining it, so as to obtain a rejuvenated catalyst.

The present invention relates to a device and to a process for the fluidized bed catalytic cracking of a hydrocarbon feedstock, in which: a first feedstock (2) is cracked in a dense fluidized bed reactor (1) in the presence of a catalyst (3) to produce a first effluent; and at least one second feedstock (10) is cracked in a transport fluidized bed reactor (4) in the presence of the catalyst (3) supplied by the dense fluidized bed reactor (1) to produce a second effluent, the second feedstock (10) being a heavier feedstock than the first feedstock (2).