Device and method for enhanced collection and assay of chemicals with high surface area ceramic

US9259708B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9259708-B2
Application numberUS-201213546948-A
CountryUS
Kind codeB2
Filing dateJul 11, 2012
Priority dateJul 11, 2012
Publication dateFeb 16, 2016
Grant dateFeb 16, 2016

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

A method and device for enhanced capture of target analytes is disclosed. This invention relates to collection of chemicals for separations and analysis. More specifically, this invention relates to a solid phase microextraction (SPME) device having better capability for chemical collection and analysis. This includes better physical stability, capacity for chemical collection, flexible surface chemistry and high affinity for target analyte.

First claim

Opening claim text (preview).

We claim: 1. A device for enhanced capture of target analytes, comprising: a. a support surface; and b. a thin film containing a mixture of at least two nanomaterials bound to the support surface, the mixture of the at least two nanomaterials including a first plurality of nanoporous particles, and a second plurality of nanoparticles as a binder to the nanoporous particles and the support surface, wherein the nanomaterials include a polyfunctional chemistry installed therein for capture of a target analyte. 2. The device of claim 1 wherein the nanoporous particles are silica nanoporous particles. 3. The device of claim 1 wherein the support surface is a substrate. 4. The device of claim 3 wherein the substrate is one of the following: a fiber, a metal wire, a planar support, and a tubular structure. 5. The device of claim 1 wherein the support surface is porous. 6. The device of claim 1 wherein support surface is coated by the thin film containing the mixtures of the nanoporous particles and the nanoparticles. 7. The device of claim 1 wherein the thin film is coated on the outside of the support surface. 8. The device of claim 1 wherein the thin film is coated on the inside of the support surface. 9. The device of claim 1 wherein the polyfunctional chemistry forms a sorbent layer. 10. The device of claim 9 wherein the sorbent layer is a silane, and other surface chemistries are installed such as physisorbed low vapor pressure organics or covalently bound surface chemistries such as phosphonic acid with organic components. 11. The device of claim 9 wherein the sorbent layer comprises the polyfunctional chemistry, wherein the polyfunctional chemistry is at least one of the following: organics, organometallics, metals, nanoparticle, complex molecules, and combinations thereof. 12. The device of claim 1 wherein the target analyte is a gas-phase or a liquid-phase analyte. 13. The device of claim 12 wherein the gas or liquid-phase trace level analyte is at least one of the following: explosives, explosive variants, chemical weapons agents, pesticides, and volatile organic compounds (VOCs). 14. A method of selective and specific capturing of target analytes comprising: a. providing a support surface; b. coating the support surface with a thin film containing a mixture of at least two nanomaterials bound to the support surface, the mixture of the at least two nanomaterials including a first plurality of nanoporous particles, and a second plurality of nanoparticles as a binder to the nanoporous particles and the support surface; and c. installing polyfunctional chemistry on a surface of the thin film to capture target analytes. 15. The method of claim 14 wherein the nanoporous particles are silica nanoporous particles. 16. The method of claim 14 wherein the support surface is a substrate. 17. The method of claim 16 wherein the substrate is one of the following: a fiber, a metal wire, a planar support, and a tubular structure. 18. The method of claim 14 wherein the thin film is coated on the outside of the support surface. 19. The method of claim 14 wherein the thin film is coated on the inside of the support surface. 20. The method of claim 14 wherein the thin film is deposited on to the support surface by at least one of the following: dip coating, molding, and spray-on. 21. The method of claim 20 wherein the thin film is subsequently sintered to solidify film adhesion to the support surface. 22. The method of claim 14 wherein the support surface is porous. 23. The method of claim 14 wherein the polyfunctional chemistry forms a sorbent layer. 24. The method of claim 23 wherein the sorbent layer is a silane. 25. The method of claim 23 wherein the sorbent layer comprises the polyfunctional chemistry, wherein the polyfunctional chemistry is at least one of the following: organics, metal centers, complex molecules, and combinations thereof. 26. The method of claim 14 wherein the target analyte is a gas-phase or a liquid-phase analyte. 27. The method of claim 26 wherein the gas or liquid-phase analyte is at least one of the following: explosives, explosive variants, chemical weapons agents, pesticides, drug, or volatile organic compounds (VOCs). 28. A device for selective and specific capture of target analytes, comprising: a. a tubular support having an empty space; and b. a thin film containing a mixture of at least two nanomaterials including a first plurality of nanoporous particles, and a second plurality of nanoparticles as a binder to the nanoporous particles and the tubular support, the thin film coated inside the tubular support, wherein a surface of the nanoporous particles includes polyfunctional chemistry installed therein for selective and specific capture of a target analyte drawn into the empty space. 29. A method of selective and specific capture of target analytes comprising: a. providing a tubular support having an empty space; b. coating the inside of the tubular support with a thin film containing a mixture of a first plurality of nanoporous particles, and a second plurality of nanoparticles as a binder to the nanoporous particles and the tubular support; c. installing polyfunctional chemistry on a surface of the nanoporous particles; and d. drawing a target analyte into the empty space for specific capture of the analyte with the nanoporous particles containing the chemistry. 30. The method of claim 29 further comprising separating and analyzing the captured analytes. 31. The device of claim 1 wherein the thin film is calcined at less than approximately 550° C. 32. The method of claim 14 further comprising calcining the thin film at less than approximately 550° C.

Assignees

Inventors

Classifications

  • characterised by their surface properties or porosity · CPC title

  • including use of a solid sorbent, semipermeable membrane, or liquid extraction · CPC title

  • Sorbents comprising a binder, e.g. for forming aggregated, agglomerated or granulated products · CPC title

  • Use of binding agents; addition of materials ameliorating the mechanical properties of the produced sorbent · CPC title

  • based on silica · CPC title

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Frequently asked questions

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What does patent US9259708B2 cover?
A method and device for enhanced capture of target analytes is disclosed. This invention relates to collection of chemicals for separations and analysis. More specifically, this invention relates to a solid phase microextraction (SPME) device having better capability for chemical collection and analysis. This includes better physical stability, capacity for chemical collection, flexible surface…
Who is the assignee on this patent?
Addleman Raymond S, Li Xiaohong Shari, Chouyyok Wilaiwan, and 4 more
What technology area does this patent fall under?
Primary CPC classification B01J20/103. Mapped technology areas include Operations & Transport.
When was this patent published?
Publication date Tue Feb 16 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).