Using porous activated asphaltenes as effective adsorbents for the removal of heavy metals in water
US-11511258-B2 · Nov 29, 2022 · US
US10549255B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10549255-B2 |
| Application number | US-201313760497-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 6, 2013 |
| Priority date | Aug 6, 2010 |
| Publication date | Feb 4, 2020 |
| Grant date | Feb 4, 2020 |
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Methods, compositions, devices and kits having a novel chromatographic material are provided herein for separating and identifying organic molecules and compounds, for example molecules and compounds containing electron rich functional groups such as carbon-carbon double bonds. The methods, compositions, and kits include a metal-thiolate chromatographic medium (MTCM) with a sulfur-containing functional group or a metal-selenolate chromatographic medium (MSCM) comprising a selenium-containing functional group covalently attached to a support medium, such that the sulfur-containing functional group or selenium-containing functional group is bound to at least one metal atom. The MTCM and/or MSCM has affinity and specificity to compounds having one or more carbon-carbon double bonds, and performs a highly efficient and rapid separation of samples yielding non-overlapping peaks of purified materials compared to traditional media.
Opening claim text (preview).
What is claimed is: 1. A separation system comprising: a silver thiolate chromatographic medium present as a stationary phase in a pipette or column, wherein the chromatographic medium comprises a sulfur-containing functional group wherein the sulfur is covalently bound to a silver atom, and wherein the sulfur-containing functional group is linked to a support by at least one spacer selected from: a (C 1 -C 15 )alkyl, a (C 1 -C 15 )alkoxy, a (C 1 -C 15 )heteroalkyl, a (C 6 -C 10 )aryl, a (C 1 -C 9 )heteroaryl, and a (C 6 -C 10 )aryl(C 1 -C 6 )alkyl, and a sample source coupled to the pipette or column comprising a sample to be separated, wherein the sample includes a compound having a functional group selected from the group consisting of alkenyls, alkynyls, aromatics, and amines. 2. The chromatographic medium according to claim 1 , on a support selected from the group consisting of: silica gel, alumina, polystyrene, agarose, modified polymeric resin, cellulose, magnesium silicate, dextran, and starch. 3. The chromatographic medium according to claim 1 , configured as an analytical component of a chromatographic separation system selected from: normal phase chromatography, reversed-phase chromatography, liquid chromatography, planar chromatography, column chromatography, flush chromatography, flash chromatography, thin layer chromatography, high performance liquid chromatography, gas chromatography, and solid phase extraction chromatography.
Gel sorbents · CPC title
involving a particular spacer or linking group, e.g. for attaching an active group · CPC title
In a cartridge · CPC title
Polymeric carriers, supports or substrates · CPC title
bonded via a spacer · CPC title
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