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3533 results about "Liquid product" patented technology

Pre-passivation process for a continuous reforming apparatus, and passivation process for a continuous reforming apparatus during the initial reacation

The present invention relates to a pre-passivation process for a continuous reforming apparatus prior to the reaction, or a passivation process for a continuous reforming apparatus during the initial reaction, comprising loading a reforming catalyst into the continuous reforming apparatus, starting the gas circulation and raising the temperature of a reactor, injecting sulfide into the gas at a reactor temperature ranging from 100-650° C., controlling the sulfur amount in the recycle gas within a range of 0.5-100×10−6 L/L so as to passivate the apparatus.
The process of the present invention may also comprise the following steps:
    • (1) loading a reforming catalyst into the continuous reforming apparatus, starting the gas circulation and raising the temperature of a reactor, feeding the reforming feedstock into the reaction system when the temperature of the reactor is increased to 300-460° C., introducing sulfide into the reaction system while or after the reforming feedstock is fed, controlling the ratio of the total sulfur amount introduced into the system to the reforming feedstock within the range of 0.5 μg/g-50 μg/g, reducing the content of sulfide introduced into the system when hydrogen sulfide concentration in the recycle gas reaches to 2.0 μL/L˜30 μL/L; and
    • (2) maintaining the reforming reactor at a temperature of 460-490° C., controlling the ratio of the total sulfur amount introduced into the system to the reforming feedstock within the range of 0.2 μg/g-0.5 μg/g, adjusting the amount of the reforming feedstock to the design value of the apparatus, increasing the reforming reaction temperature to 490-545° C. according to the requirements on the octane number of the liquid product, and letting the reforming apparatus run under normal operating conditions.
Owner:CHINA PETROCHEMICAL CORP +1

Catalytic multi-stage process for hydroconversion and refining hydrocarbon feeds

A multi-stage catalytic hydrogenation and hydroconversion process for heavy hydrocarbon feed materials such as coal, heavy petroleum fractions, and plastic waste materials. In the process, the feedstock is reacted in a first-stage, back-mixed catalytic reactor with a highly dispersed iron-based catalyst having a powder, gel or liquid form. The reactor effluent is pressure-reduced, vapors and light distillate fractions are removed overhead, and the heavier liquid fraction is fed to a second stage back-mixed catalytic reactor. The first and second stage catalytic reactors are operated at 700-850.degree. F. temperature, 1000-3500 psig hydrogen partial pressure and 20-80 lb./hr per ft.sup.3 reactor space velocity. The vapor and light distillates liquid fractions removed from both the first and second stage reactor effluent streams are combined and passed to an in-line, fixed-bed catalytic hydrotreater for heteroatom removal and for producing high quality naphtha and mid-distillate or a full-range distillate product. The remaining separator bottoms liquid fractions are distilled at successive atmospheric and vacuum pressures, low and intermediate-boiling hydrocarbon liquid products are withdrawn, and heavier distillate fractions are recycled and further upgraded to provide additional low-boiling hydrocarbon liquid products. This catalytic multistage hydrogenation process provides improved flexibility for hydroprocessing the various carbonaceous feedstocks and adjusting to desired product structures and for improved economy of operations.
Owner:HEADWATERS CTL

Container closure with overlying needle penetrable and thermally resealable portion and underlying portion compatible with fat containing liquid product, and related method

InactiveUS20060231519A1Avoiding seal integrity problemGood product containmentCapsLiquid fillingLiquid productFormulary
A container and method are provided for storing fat containing liquid products, such as infant or baby formula, or other milk-based products. The container includes a body defining a storage chamber for receiving the aseptic fat containing liquid product, and a first aperture in fluid communication with the storage chamber. The body does not leach more than a predetermined amount of leachables into the fat containing liquid product and does not undesirably alter a taste profile of the fat containing liquid product. A container closure assembly includes a stopper receivable within the first aperture for hermetically sealing the storage chamber. The stopper includes a first material portion defining an internal surface in fluid communication with the storage chamber forming at least most of the surface area of the container closure that can contact any fat containing liquid product within the storage chamber and that does not leach more than a predetermined amount of leachables into the fat containing liquid product or undesirably alter a taste profile of the fat containing liquid product. A second material portion of the stopper either (i) overlies the first material portion and cannot contact any product within the storage chamber, or (ii) forms a substantially lesser surface area of the container closure that can contact any product within the storage chamber in comparison to the first material portion. The second material portion is needle penetrable for filling the storage chamber with product, and a resulting needle aperture formed in the second material portion is thermally resealable such as by the application of laser energy to seal the product within the storage chamber. A sealing portion of the container closure is engageable with the body prior to needle filling the storage chamber to thereby form a substantially dry hermetic seal between the container closure and body.
Owner:MEDINSTILL DEV

Modified thermal processing of heavy hydrocarbon feedstocks

The present invention is directed to the upgrading of heavy petroleum oils of high viscosity and low API gravity that are typically not suitable for pipelining without the use of diluents. It utilizes a short residence-time pyrolytic reactor operating under conditions that result in a rapid pyrolytic distillation with coke formation. Both physical and chemical changes taking place lead to an overall molecular weight reduction in the liquid product and rejection of certain components with the byproduct coke. The liquid product is upgraded primarily because of its substantially reduced viscosity, increased API gravity, and the content of middle and light distillate fractions. While maximizing the overall liquid yield, the improvements in viscosity and API gravity can render the liquid product suitable for pipelining without the use of diluents. This invention particularly relates to reducing sulfur emissions during the combustion of byproduct coke (or coke and gas), to reducing the total acid number (TAN) of the liquid product, and to reducing the hydrogen sulfide content of one, or more than one component of the product stream. The method comprises introducing a particulate heat carrier into an up-flow reactor, introducing the feedstock at a location above the entry of the particulate heat carrier, allowing the heavy hydrocarbon feedstock to interact with the heat carrier for a short time, separating the vapors of the product stream from the particulate heat carrier and liquid and byproduct solid matter, regenerating the particulate heat carrier in the presence of the calcium compound, and collecting a gaseous and liquid product from the product stream.
Owner:IVANHOE HTL GASOLINEEUM

Catalyst for preparing aromatic hydrocarbon through methanol conversion as well as preparation method and application thereof

The invention discloses a catalyst for preparing aromatic hydrocarbon through methanol conversion. The catalyst comprises a component A and components B, wherein the mass ratio of component A to components B is 0.25-4; the component A is a modified zeolite molecular sieve and comprises 80-99wt% of molecular sieves and 1-20wt% of molecular sieve modifiers; the components B are oxide loaded metallic elements and halogen and comprise 85-95wt% of oxide, 0.5-10wt% of total metallic elements and 0.1-5wt% of halogen; and the component A and the components B are formed through squashing or extruding after being mixed uniformly. The catalyst has the following characteristics that: (1) the total recovery of benzene, toluene and xylene is higher and selectivity is high; (2) the raw material treatment capacity is large; (3) the non-aromatic hydrocarbon liquid product can serve as the solvent oil or gasoline component; (4) C4 hydrocarbon and non-aromatic hydrocarbon liquid phase products in the gas phase product can circularly enter into the catalyst bed layer, thus not only balancing the reaction heat but also improving the total recovery of the aromatic hydrocarbon; and (5) the catalyst has high activity and long life.
Owner:NORTHWEST UNIV

Method for preparing propylene and aromatic hydrocarbon by virtue of conversion of methanol

The invention relates to a method for preparing propylene and aromatic hydrocarbon by virtue of conversion of methanol, and the method is mainly used for solving the problem that the methanol is just converted into propylene and the aromatic hydrocarbon can not be co-produced in the prior art. The method comprises the following steps: 1) converting above 80% of methanol into dimethyl ether by virtue of pre-reaction; 2) feeding the generated diamethyl ether and residual methanol into a device for producing propylene from the methanol for reaction so as to obtain a material flow I which mainly comprises the propylene, ethylene and C4, C5, C6 and over-C6 hydrocarbons; 3) after the material flow I is separated, returning the ethylene back to the device for producing the propylene from the methanol for cycling reaction, and feeding C4 and C5 hydrocarbons into an aromatizing device for reaction so as to obtain a material flow II containing aromatic hydrocarbon; and 4) cooling the material flow II, separating a gas-phase product low-carbon hydrocarbons from a liquid-phase product, and separating the liquid product from the material flow I so as to obtain C6 and over-C6 hydrocarbons, mixing, extracting and separating so as to obtain the aromatic hydrocarbon and non-aromatic hydrocarbon. By using the technical scheme, the problem is well solved; and the method can be used in industrialproduction for preparing the ethylene and the aromatic hydrocarbon by virtue of conversion of methanol.
Owner:CHINA PETROLEUM & CHEM CORP +1

Liquefied Natural Gas and Hydrocarbon Gas Processing

A process for the recovery of ethane, ethylene, propane, propylene, and heavier hydrocarbons from a liquefied natural gas (LNG) stream and a hydrocarbon gas stream is disclosed. The LNG feed stream is divided into two portions. The first portion is supplied to a fractionation column at a first upper mid-column feed point. The second portion is directed in heat exchange relation with a first portion of a warmer distillation stream rising from the fractionation stages of the column, whereby the LNG feed stream is partially heated and the distillation stream is totally condensed. The condensed distillation stream is divided into a “lean” LNG stream and a reflux stream, whereupon the reflux stream is supplied to the column at a top column feed position. The second portion of the LNG feed stream is heated further to partially or totally vaporize it and thereafter supplied to the column at a first lower mid-column feed position. The gas stream is divided into two portions. The second portion is expanded to the operating pressure of the column, then both portions are directed in heat exchange relation with the lean LNG stream and the second portion of the warmer distillation stream, whereby both portions of the gas stream are cooled, the lean LNG stream is vaporized, and the second portion of the distillation stream is heated. The first portion of the gas stream, which has been cooled to substantial condensation, is supplied to the column at a second upper mid-column feed point, and the second portion is supplied to the column at a second lower mid-column feed point. The quantities and temperatures of the feeds to the column are effective to maintain the column overhead temperature at a temperature whereby the major portion of the desired components is recovered in the bottom liquid product from the column.
Owner:ORTLOFF ENGINEERS

Catalytic hydroconversion of chemically digested organic municipal solid waste materials

A hydrocarbon liquid feedstock containing at least 50 wt. % chemically digested organic-MSW material is catalytically hydroconverted utilizing either a single stage or two-stage catalytic reaction process to produce desirable lower-boiling hydrocarbon liquid products. The catalyst can be either a particulate supported type catalyst such as containing cobalt and / or molybdenum and / or nickel on alumina support, or a dispersed slurry type catalyst containing mainly iron oxide with anions of molybdate, phosphate, sulfate or tungstate, and combinations thereof. Broad useful reaction conditions are 600-860° F. (315-460° C.) temperature, 1000-3000 psi hydrogen partial pressure, and fresh feed rate of 20-60 pounds / hr / ft3 reactor volume. Effluent material from the final stage catalytic reactor is phase separated and the resulting liquid portion is fractionated to produce the desired low-boiling hydrocarbon liquid products particularly useful as transportation fuels. If desired, the chemically digested organic-MSW feedstock can be blended with petroleum residua and / or particulate coal and / or mixed waste plastics and the blended feed material processed in catalytic two-stage reactors to produce similar desirable low-boiling hydrocarbon liquid products.
Owner:HYDROCARBON TECH
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