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Thin layer chromatography plates

a thin layer, chromatography technology, applied in the direction of instruments, other chemical processes, separation processes, etc., can solve the problems of affecting the amount of deposition of coating materials achieved, affecting the efficiency of ald process, and affecting the amount of deposition of coating materials, etc., to prevent unwanted secondary interactions, improve separation efficiency, and eliminate the use of any binder

Inactive Publication Date: 2015-12-03
US SYNTHETIC CORP +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The invention is about a new kind of TLC plate, which is used in chromatography. The plate has elongated structures called stationary phases that are fixed to a substrate, rather than using a separate binder. This eliminates secondary interactions and improves separation efficiency. The stationary phases are made of silica and have silanol groups that make them functional for enhanced separation performance. The invention also includes a method for making the plate. The technical effect of the invention is to provide a more efficient and effective TLC plate for separation applications.

Problems solved by technology

The amount of deposition of the coating material achieved may be affected by process time.
Such an ALD process may be significantly slower, providing only a ca.
In some cases, random growth of CNTs 106 followed by infiltration and optionally oxidation of coating 108 can pose a potential problem.
Even if delamination does not appear to have occurred initially, the material may easily buckle and flake away as a result of a slight bump or touch because of the expansion.
Such binding agents can interfere with the performance of the TLC plate as the result of secondary interactions resulting from the binding agent.

Method used

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  • Thin layer chromatography plates
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Examples

Experimental program
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working examples

III. WORKING EXAMPLES

[0105]The following working examples are for illustrative purposes only and are not meant to be limiting with regards to the scope of the specification or the appended claims. Example 1 is representative of how the CNT structures were grown for all examples carried out.

example 1

[0106]The masks for photolithography were all based on a zig-zag geometry with 90° angles. Silicon wafers (University Wafers, South Boston, Mass.), 4″ diameter, were used as the backing material. A thin film of photoresist, AZ-3312-F (AZ Electronic Materials USA Corp, Somerville, N.J.), was spin coated onto the wafer. The resulting wafer was patterned via photolithography (Karl Suss Mask Aligner, Vermont, USA), followed by e-beam evaporation (Benton Vacuum E-beam Evaporator, Moorestown, N.J.) of a thin barrier layer of alumina (35 nm), and thermal evaporation (custom-built apparatus) of a few nanometers of iron (6 nm). The iron deposition was monitored using a quartz crystal device. The photoresist was then lifted off with a resist stripper (Micropsoit 1165, MicroChem, Newton, Mass.), leaving a pattern of Al2O3 / Fe at the surface.

[0107]The photolithographically patterned wafer was loaded into a fused silica tube (22 mm ID), preheated at 200° C. in a Lindberg / Blue M tube furnace (Ther...

examples 3-6

[0109]The use of one or more adhesion promoters (FIGS. 13B-13D), such as the contemplated amorphous carbon and / or alumina priming layers discussed in more detail below was believed to increase the number of nucleation sites on the CNTs, thereby allowing more conformal growth to take place. It was thought that only a very thin layer, perhaps only a few nanometers, of one or more adhesion priming layers may be sufficient to increase the number of nucleation sites available for subsequent infiltration or coating (e.g., through ALD or similar process). Accordingly, a small amount of carbon was deposited onto CNTs using ethylene diluted in argon at 900° C. The resulting carbon layers showed good conformality and even some measure crystallinity, as suggested by the texture of the TEM images of FIGS. 14A and 14B.

[0110]To explore whether these few nanometers of carbon might improve ALD or pseudo-ALD on CNTs, and to show that these plates indeed exhibit the desired stability and chromatograp...

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Abstract

In an embodiment, a method for manufacturing a thin layer chromatography (“TLC”) plate is disclosed. The method includes forming a layer of elongated nanostructures (e.g., carbon nanotubes), priming the elongated nanostructures with one or more adhesion priming layers, and at least partially coating the elongated nanostructures with a coating. The coating includes a stationary phase and / or precursor of a stationary phase for use in chromatography. The stationary phase may be functionalized with hydroxyl groups by exposure to a base or acid. The stationary phase may further be treated with a silane (e.g., an amino silane) to improve the performance of the TLC plate. Embodiments for TLC plates and related methods are also disclosed.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS[0001]This application is a continuation of U.S. application Ser. No. 14 / 186,996 filed on 21 Feb. 2014, which is a continuation of U.S. application Ser. No. 13 / 368,869 filed on 8 Feb. 2012 (now U.S. Pat. No. 8,702,984 issued on 22 Apr. 2014), the disclosures of each of the foregoing application are incorporated herein, in their entirety, by this reference.BACKGROUND[0002]Chromatography and solid-phase extraction (“SPE”) are commonly-used separation techniques employed in a variety of analytical chemistry and biochemistry environments. Chromatography and SPE are often used for separation, extraction, and analysis of various constituents, or fractions, of a sample of interest. Chromatography and SPE may also be used for the preparation, purification, concentration, and clean-up of samples.[0003]Chromatography and SPE relate to any of a variety of techniques used to separate complex mixtures based on differential affinities of components of a samp...

Claims

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Application Information

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IPC IPC(8): B01D15/10B01J20/283C23C16/40C23C16/02C23C16/455G01N30/92B01J20/284
CPCB01D15/10G01N30/92B01J20/283B01J2220/82C23C16/0272C23C16/45555C23C16/402B01J20/284B01J20/3204B01J20/3223B01J20/3236B01J20/324B01J20/3259B01J20/3289B01J20/3297B05D5/00B82Y30/00C23C16/01C23C16/403G01N30/6095
Inventor LINFORD, MATTHEW R.JENSEN, DAVID SCOTTDADSON, ANDREW E.DAVIS, ROBERT C.
Owner US SYNTHETIC CORP