Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Process for oxidation reactions

a technology of oxidation reaction and process, which is applied in the direction of electrolytic organic production, multiple component coatings, electrolytic coatings, etc., can solve the problems of difficult one-pot direct conversion of paraffins to oxygenates or olefins, inability to activate methane and reaction with oxygen to directly produce methanol in a commercial-scale continuous process, and low single-pass conversion of methane to methanol

Inactive Publication Date: 2017-03-09
PHILLIPS 66 CO
View PDF2 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The patent describes two different processes for using an oxygen transport membrane to produce methanol. In the first process, an oxidant species is flowed over the reducing side of the membrane, with O2− anions being continuously transported from the reducing side to the oxidizing side where they react with methane and a catalyst layer to produce methanol. In the second process, air is flowed over the reducing side of a solid oxide cell to produce antioxidized air and O2− anions, which are then only continuously transported from the reducing side of the cell to the oxidizing side. On the oxidizing side, the O2− anions react with methane and a catalyst layer to produce methanol. These processes use the membrane to efficiently convert oxygen to methanol, which can be useful for industrial applications such as fuel production.

Problems solved by technology

One-pot direct conversion of paraffins to oxygenates or olefins is difficult to obtain.
For example, the activation of methane and reaction with oxygen to directly produce methanol in a commercial-scale continuous process is not currently feasible.
However, such a process faces significant hurdles, for example the pulsed nature of methane and the oxidant means that the process is not continuous and the low α-oxygen capacity of the catalyst material means that the single pass conversion of methane to methanol is very low.
Others have attempted to achieve this solution but have required the addition of steam to the anode feedstock thereby increasing the cost and complexity of the system.
Such a system would also require a low operating temperature (below 250° C.) which would cause CO poisoning and rapidly deactivate the anode catalyst.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Process for oxidation reactions
  • Process for oxidation reactions
  • Process for oxidation reactions

Examples

Experimental program
Comparison scheme
Effect test

example 1

[0042][NH4][ZSM-5] (SiO2 / Al2O3=50) catalyst was crushed to a size of 20-40 mesh. The catalyst was calcined in a muffle furnace at 550° C. to convert the ammonium form to the acidic form, H-ZSM-5. Samples were heated to 150° C. at 2° C. / min, maintained at 150° C. for 2 hours, heated to 450° C. at 4° C. / min, maintained at 450° C. for 12 hours, then heated to 550° C. at 4° C. / min and held 550° C. for 6 hours. Following calcination, the catalyst was cooled to ambient temperature.

[0043]The resulting H-ZSM-5 powder was sieved to a particle size of <140 mesh and suspended in terpineol such that the resulting suspension was 35% H-ZSM-5 by weight. The H-ZSM-5 / terpineol suspension was then mixed with an equal weight of lanthanum strontium manganite (LSM) electrode ink.

[0044]The experiment used an electrolyte-supported button cell with total active electrode area of 0.71 cm2. The electrolyte material was scandia-stabilized zirconia (ScSZ). The cathode side of the electrolyte was coated with LS...

example 2

[0053]Strontium chloride (267 mg), lanthanum nitrate (1300 mg), and manganese sulfate (845 mg) were dissolved in distilled water (2 mL). This solution was added dropwise to ZSM-5 (4 g) with mechanical stir bar mixing. This wet powder was calcined in air to generate the oxide (500 C, 30 minutes).

[0054]One gram of the resulting dark powder oxide was combined with one gram of terpineol. This slurry was combined with 2 grams of commercially available lanthanum strontium manganite (LSM). A portion of this mixture was then deposited uniformly in a 1 cm diameter circle onto a 1 inch diameter electrolyte disc. This deposition was carried out by screen printing. The cell was heated to 125° C. for 30 min to remove the terpineol solvent.

[0055]An identical screen-printed deposition, this time of the pure commercial LSM, was carried out on the opposite face of the electrolyte disc, overlapping as exactly as possible with the deposition on the original side, sandwiching the electrolyte disc in be...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

PropertyMeasurementUnit
operating temperatureaaaaaaaaaa
α-oxygen capacityaaaaaaaaaa
electricalaaaaaaaaaa
Login to View More

Abstract

The current embodiment describes a process of flowing an oxidant species over the reducing side of an oxygen transport membrane. O2− anions are then continuously transported from the reducing side through the oxygen transport membrane to the oxidizing side where an organic compound is converted to a partially oxidized organic compound on the oxidizing side.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS[0001]This application is a Non-Provisional application which claims the benefit of and priority to U.S. Provisional Application Ser. No. 62 / 213,396 filed Sep. 2, 2015, entitled “Process for Oxidation Reactions,” which is hereby incorporated by reference.STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT[0002]None.FIELD OF THE INVENTION[0003]A process for oxidation reactions.BACKGROUND OF THE INVENTION[0004]One-pot direct conversion of paraffins to oxygenates or olefins is difficult to obtain. For example, the activation of methane and reaction with oxygen to directly produce methanol in a commercial-scale continuous process is not currently feasible.[0005]For example, to obtain methanol from methane, one would typically convert methane to syngas (H2+CO) which is then converted to methanol in a separate reaction step. Others have attempted to utilize α-oxygen species to oxidize methane to methanol. However, such a process faces sig...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(United States)
IPC IPC(8): C25B3/02C25B15/08C25B13/04C25B9/08C25B11/04C25B3/23C25B9/19
CPCC25B3/02C25B9/08C25B15/08C25B13/04C25B11/0478C25B3/23C25B9/19C25B11/091
Inventor INGRAM, DAVID B.RANDOLPH, BRUCE B.LOESCHER, MITCHELL E.GUPTA, AALO K.PAUL, UCHENNA P.LAFRANCOIS, CHRIS J.MCDANIEL, NEAL D.SMITH, DANIELLE K.BIERSCHENK, DAVID M.HE, TING
Owner PHILLIPS 66 CO
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products