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The Process Of Separating A Selected Ion From A Plurality Of Other Ions In A Multiple Ion Solution By Contacting The Solution With A Macrocyclic Ligand Bonded To Silica Which Selectively Complexes With The Desired Ion
Jerald S. Bradshaw - Provo UT Reed M. Izatt - Provo UT Ronald L. Bruening - Provo UT James J. Christensen - late of Provo UT
Assignee:
Brigham Young University - Provo UT
International Classification:
B01D 1500
US Classification:
210674
Abstract:
The invention has composition of matter and process aspects. The composition of matter aspect relates to the compounds selected from the class consisting of: ##STR1## in which Silica is sand or silica gel. The process aspect involves the use of any of these compounds packed in a column through which a solution of the multiple ions is flowed to complex with the compound and separate a desired selected ion from a multiple ion solution, breaking the complex by flowing a receiving liquid through the column to free the desired ion and recovering the freed desired ion from the receiving liquid.
Poly N-Cyclic Aromatic Ligands Bonded To Solid Supports For Removing And Concentrating Ions From Solutions
Ronald L. Bruening - American Fork UT Krzysztof E. Krakowiak - Provo UT Reed M. Izatt - Provo UT Jerald S. Bradshaw - Provo UT
Assignee:
IBC Advanced Technologies, Inc. - American Fork UT
International Classification:
C02F 142
US Classification:
210670
Abstract:
A method and composition for the concentration and removal of desired metal ions from a source solution by contacting the solution with an N-cyclic aromatic hydrocarbon-containing ligand covalently bonded to a solid support through a hydrophilic spacer of the formula SS--A--X--(L). sub. n where SS is a solid support, A is covalent linkage mechanism, X is a hydrophilic spacer grouping, L is an N-cyclic aromatic containing ligand group and n is an integer of 1 to 6. X or L combined will not contain more than two amine nitrogen atoms. There will preferably be at least four N-cyclic groups present of which pyridine, pyrimidine, pyraxine, imidazole, quinoline, isoquinoline, naphthyridine, pyridopyridine, phenanthroline are representative. The desired ions in the source solution are bound to the ligands and are subsequently separated by contacting the ligand containing compound with a smaller volume of a receiving solution that removes the bound ions for recovery in concentrated form in the smaller volume of the receiving solution.
Jerald S. Bradshaw - Provo UT Bryant E. Rossiter - Provo UT Bryon J. Tarbet - Provo UT Deborah F. Johnson - Provo UT Milton L. Lee - Pleasant Grove UT Karin E. Markides - Upsala, SE
Assignee:
Brigham Young University - Provo UT
International Classification:
C08G 7704
US Classification:
528 25
Abstract:
Chiral copolymers containing chiral molecular grooves or cavities and oligosiloxane spacers are disclosed. The chiral portion of the copolymer is an enantiomerically enriched organic grouping, having physical properties attributed to uniform and stereochemically possible molecular grooves or cavities, which is chemically and thermally stable to gas, liquid or supercritical s fluid chromatographic conditions and is configured such that one enantiomer of an enantiomeric mixture will be better able to preferentially enter such groove or cavity and interact more strongly than other enantiomers in said mixture. The chiral grouping will contain one Or more combinations of organic moieties selected from the group consisting of methylene, phenylene, naphthylene, biphenylene, binaphthylene, a cyclodextrin and cycloalkylydene and substituted derivatives thereof and also includes non-metal atoms and functional groups which act as linking agents for the organic chiral cavity-containing moieties which are selected from the group consisting of ethers, thioethers, amines, carbonyls, amides, esters, sulfoxides, sulfonates, thioamides, thioesters, ureas, thioureas, carbamates, thiocarbamates, phosphines and phosphine oxides. The use of such polymers as chiral stationary phases in analytical and preparative gas, supercritical fluid and liquid chromatographic separations, and particularly for analysis of enantiomeric and other stereoisomeric mixtures of various substances is shown.
Analysis Of Ions Present At Low Concentrations In Solutions Containing Other Ions
Jerald S. Bradshaw - Provo UT Reed M. Izatt - Provo UT Ronald L. Bruening - Provo UT Virginia B. Christensen - Provo UT Robert Alldredge - Westminster CO
Assignee:
Brigham Young University - Provo UT
International Classification:
G01N 3000 C02F 162
US Classification:
436 77
Abstract:
The invention is a process of selectively and quantitatively removing and concentrating at least one selected ion prosent in low concentration with other ions in higher concentration in a multiple ion solution. The method comprises bringing a complexing agent for the selected ion(s) into contact with a different determined quantity of said multiple ion solution to remove and concentrate the selected ion(s) from the multiple ion solution; removing the multiple ion solution, from which the complexing agent has been removed, the selected ions from the complexing agent having the selected ion(s) complexed therewith, bringing the complexing agent complexed with selected ion(s) into contact with a determined quantity of receiving liquid to break the complex and remove the selected and concentrated ion(s) from the complexing agent therein, and determining the concentration of selected ion(s) in said receiving liquid from which the concentration of selected ion(s) in the multiple ion solution can be calculated. The metal ions in low concentration are often heavy metal ions, such as lead ions, and the process finds particularly advantageous utility in the determination of lead content in ppb in drinking water. The preferred apparatus for carrying out the process is a column packed with silica gel or silica-bonded macrocycle as the complexing agent which is preferably carried out using as the complexing agent a macrocyclic compound having at least four --A--CH. sub. 2 --CH. sub.
Sulfur-Containing Hydrocarbon Compounds And Process Of Using Same In Recovering And Concentrating Desired Ions From Solutions Thereof
Jerald S. Bradshaw - Provo UT Reed M. Izatt - Provo UT Bryon J. Tarbet - Provo UT Krzysztof Krakowiak - Provo UT Jan F. Biernat - Provo UT Ronald L. Bruening - Provo UT
Assignee:
Brigham Young University - Provo UT
International Classification:
B01D 3900 B01D 1508
US Classification:
2105021
Abstract:
The invention has compositions of matter and process aspects. The compositions of matter aspect relate to two classes of new organic compounds, viz. , A. intermediates which are sulfur-containing hydrocarbons covalently bonded to trialkoxysilane and B. that class of intermediates covalently bonded to an inorganic matrix, e. g. , silica, silica gel, glass, glass fibers, alumina, nickel oxide, zirconia, and titania. The process aspect comprises two processes, viz. , (1) a process for making the two new classes of compounds A and B, and (2) the process of removing and concentrating certain ions, such as noble metal ions and other transition metal ions, from solution thereof admixed with other ions which may be present in much higher concentrations by forming a complex of the desired ion(s) with a compound of class B, e. g. , by flowing the solution through a chromatography column packed with the compound, breaking the complex, e. g. , by flowing a receiving liquid through the column in much smaller amount than the amount of solution passed through it to remove and concentrate the desired ion(s) in solution in the receiving liquid and recovering the desired ion(s) from the receiving liquid.
Process Of Removing Ions From Solutions By Forming A Complex With A Sulfur Containing Hydrocarbon Covalently Bonded To Silica
Jerald S. Bradshaw - Provo UT Byron J. Tarbet - Provo UT Krzysztof E. Krakowiak - Provo UT Jan F. Biernat - Provo UT Ronald L. Bruening - Provo UT Reed M. Izatt - Provo UT
Assignee:
Brigham Young University - Provo UT
International Classification:
B01D 1500
US Classification:
210670
Abstract:
The invention has compositions of matter and process aspects. The compositions of matter aspect relate to two classes of new organic compounds, viz. , A. intermediates which are sulfur-containing hydrocarbons covalently bonded to trialkoxysilane and B. that class of intermediates covalently bonded to silica, e. g. , sand and silica gel. The process aspect comprises two processes, viz. , (1) A process for making the two new classes of compounds A and B, and (2) the process of removing and concentrating certain ions, such as noble metal ions and other transition metal ions, from solutions thereof admixed with other ions which may be present in much higher concentrations by forming a complex of the desired ion(s) with a compound of class B, e. g. , by flowing the solution through a chromatography column packed with the compound, breaking the complex, e. g. , by flowing a receiving liquid through the column in much smaller amount than the amount of solution passed through it to remove and concentrate the desired ion(s) in solution in the receiving liquid and recovering the desired ion(s) from the receiving liquid.
Single Arm Attached Cyclodextrin Polysiloxanes And Use Thereof As Chiral Stationary Phases In Chromatographic Separation Of Enantiomers
Jerald S. Bradshaw - Provo UT Milton L. Lee - Pleasant Grove UT Bryant E. Rossiter - Provo UT
Assignee:
Brigham Young University - Provo UT
International Classification:
C08F28300
US Classification:
525474
Abstract:
Cyclodextrin containing polymeric siloxanes wherein the cyclodextrin is connected to the polymeric siloxane by a single linking member connected to the 2, 3 or 6-position of the cyclodextrin are disclosed. These polymers are chemically and thermally stable to gas, supercritical fluid chromatographic conditions. The single arm attachment provides cyclodextrin containing polysiloxane polymers having synthesis reproducibility from batch to batch resulting in consistent chromatographic performance of the resulting chiral phases. The use of such polymers as chiral stationary phases in analytical and preparative gas, supercritical fluid and liquid chromatographic separations, and particularly for analysis of enantiomeric and other stereoisomeric mixtures of various substances is shown.
Analysis Of Ions Present At Low Concentrations In Solutions Containing Other Ions
Jerald S. Bradshaw - Provo UT Reed M. Izatt - Provo UT Ronald L. Bruening - Provo UT James J. Christensen - late of Provo UT Robert Alldredge - Westminster CO
Assignee:
Brigham Young University - Provo UT
International Classification:
G01N 3000 C02F 102
US Classification:
436 77
Abstract:
A method of selectively and quantitatively removing and concentrating at least one selected ion from a multiple ion solution in which other ions are present is disclosed. The method comprises (a) bringing a complexing agent for the selected ion(s) into contact with the multiple ion solution to remove and concentrate selected ion(s) from the multiple ion solution, wherein the complexing agent is selected from the group of macrocyclic compounds having at least four --A--CH. sub. 2 --CH. sub. 2 -- groups in which A is selected from O, O--CH. sub. 2, S, S--CH. sub. 2, N--R and N--R--CH. sub. 2 in which R is selected from H, lower alkyl and benzyl, with the macrocyclic compounds further having a hydrocarbon side chain having an end group ##STR1## in which X is selected from the group consisting of lower alkyl, benzyl, phenyl, halogen, O--CH. sub. 3, O--C. sub. 2 H. sub. 5 and O--M, wherein M is selected from the group consisting of sand, silica gel, glass, glass fibers, alumina, zirconia, titania and nickel oxide; (b) removing the multiple ion solution from which the complexing agent has removed the selected ion(s) from the complexing agent having the selected ion(s) complexed therewith; (c) bringing the complexing agent complexed with selected ion(s) into contact with a receiving liquid to break the complex and remove the selected and concentrated ion(s) from the complexing agent; and (d) determining the concentration of selected ion(s) in the receiving liquid from which the concentration of selected ion(s) in the multiple ion solution can be calculated.
Brigham Young University Aug 1966 - Jan 2000
Professor
Brigham Young University Aug 1966 - Jan 2000
Retired at Brigham Young University
Education:
University of California, Los Angeles 1959 - 1963
Doctorates, Doctor of Philosophy, Philosophy, Organic Chemistry
Skills:
Data Analysis Research Higher Education Science Public Speaking University Teaching Strategic Planning Microsoft Office Organic Synthesis Teaching Microsoft Excel Chemistry