Patent US3987058A successfully refreshed from Google Patents.
US3987058A
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Preparation and uses of stable, bound stationary phases
Assignee: United States Department of Agriculture
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Filing: 1975-02-27
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Granted: 1976-10-19
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Expires: 1995-02-27
Abstract
Abstract Sulfobenzylsilicas in which the organic moiety is bound to silica surfaces through a carbon-silicon bond are prepared by treating silica with thionyl chloride to chlorinate reactive silanol groups, reacting the product with benzyllithium and sulfonating the resulting benzylsilica. The sulfobenzylsilicas and their salts of noble metals are useful as bound stationary phases in various chromatographic procedures for the separation of a wide variety of natural product mixtures composed of closely related chemical compounds. For example, separation of methyl cis 9-octadecenoate and methyl trans 9-octadecenoate was readily achieved by gas-liquid chromatography on a modified silver sulfobenzylsilica column.
Inventors
- 👤 Donald H. Saunders
- 👤 Robert A. Barford
- 👤 Paul Magidman
- 👤 Herbert L. Rothbart
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-31 20:56
CPC Classifications
B; B01; B01J; B01J20/00; B01J20/28; B01J20/28054; B01J20/28057; B01J20/28061; B01J20/02; B01J20/10; B01J20/103; B01J20/28002; B01J20/28004; B01J20/28014; B01J20/28016; B01J20/28019; B01J20/281; B01J20/286; B01J20/29; B01J20/30; B01J20/3078; B01J20/3092; B01J20/32; B01J20/3202; B01J20/3204; B01J20/3231; B01J20/3242; B01J20/3244; B01J20/3246; B01J20/3248; B01J20/3251; B01J20/3253; B01J20/3257; B01J20/3268; B01J20/3272; B01J2220/00; B01J2220/50; B01J2220/54; B01J2220/58
Claims Analysis
Total Claims: 22
Claim 1
Independent Claim
58 words
A process for preparing sulfobenzylsilica comprising preparing silica chloride by treating silica with thionyl chloride, reacting the silica chloride with benzyllithium and sulfonating the resulting bound benzylsilica with chlorosulfonic acid to obtain sulfobenzylsilica in which the organic moiety is bound to the silica through a carbon-silicon bond and which contains at least 0.2 milliequivalents of acid per gram.
Claim 2
Dependent Claim
58 words
A process for preparing sulfobenzylsilica comprising preparing silica chloride by treating silica with thionyl chloride, reacting the silica chloride with benzyllithium and sulfonating the resulting bound benzylsilica with chlorosulfonic acid to obtain sulfobenzylsilica in which the organic moiety is bound to the silica through a carbon-silicon bond and which contains at least 0.2 milliequivalents of acid per gram.
Claim 3
Dependent Claim
32 words
The process of claim 1 in which thionyl chloride, benzyllithium and chlorosulfonic acid are present in excess of the stoichiometric amount relative to the amount of reactive sites per gram of silica.
Claim 4
Dependent Claim
42 words
The process of claim 2 in which the silica had a particle diameter range of from about 0.01 micron to about 300 microns and a surface area of from about 50 square meters per gram to about 400 square meters per gram.
Claim 5
Dependent Claim
20 words
The product of claim 2 wherein the sulfobenzylsilica was made from silica having an average particle diameter of 12 microns.
Claim 6
Dependent Claim
31 words
The product of claim 2 wherein the sulfobenzylsilica was made from silica having a particle diameter range of 60 to 200 microns and a surface area of 340 m 2 /gram.
Claim 7
Dependent Claim
28 words
The product of claim 2 wherein the sulfobenzylsilica was made from silica having a particle diameter of 0.012 microns and a surface area of 198 m 2 /gram.
Claim 8
Dependent Claim
28 words
The product of claim 2 wherein the sulfobenzylsilica was made from silica having a particle diameter of 8.0 microns and a surface area of 320 m 2 /gram.
Claim 9
Independent Claim
98 words
A method of separating for assay purposes traces of nitrosoproline from proline and other components in cured meat samples, comprising treating silica with thionyl chloride, reacting the resultant silica chloride with benzyllithium to obtain benzylsilica, sulfonating the benzylsilica with chlorosulfonic acid to obtain sulfobenzylsilica, said thionyl chloride, benzyllithium, and chlorosulfonic acid being present in excess of the stoichiometric amount, converting the sulfobenzylsilica by standard procedures to the sodium form, packing a high-pressure liquid chromatography column with the sodium form of the sulfobenzylsilica, transferring the cured meat sample to the column, and eluting with aqueous methanol to obtain nitrosoproline.
Claim 10
Independent Claim
98 words
A method of separating for assay purposes traces of nitrosoproline from proline and other components in cured meat samples, comprising treating silica with thionyl chloride, reacting the resultant silica chloride with benzyllithium to obtain benzylsilica, sulfonating the benzylsilica with chlorosulfonic acid to obtain sulfobenzylsilica, said thionyl chloride, benzyllithium, and chlorosulfonic acid being present in excess of the stoichiometric amount, converting the sulfobenzylsilica by standard procedures to the sodium form, packing a high-pressure liquid chromatography column with the sodium form of the sulfobenzylsilica, transferring the cured meat sample to the column, and eluting with aqueous methanol to obtain nitrosoproline.
Claim 11
Dependent Claim
88 words
A process for preparing silver sulfobenzylsilica in which the silver benzylsulfonate is chemically bound to the silica and which is useful in thin-layer and gas-liquid chromatography for the separation of cis and trans alkene isomers, comprising chlorinating the reactive silanol groups of silica by treating it with thionyl chloride, reacting the chlorinated product with benzyllithium, sulfonating the resultant benzylsilica to obtain sulfobenzylsilica, said thionyl chloride, benzyllithium and chlorosulfonic acid being present in excess of the stoichiometric amount and reacting the sulfobenzylsilica with silver nitrate to produce silver sulfobenzylsilica.
Claim 12
Dependent Claim
88 words
A process for preparing silver sulfobenzylsilica in which the silver benzylsulfonate is chemically bound to the silica and which is useful in thin-layer and gas-liquid chromatography for the separation of cis and trans alkene isomers, comprising chlorinating the reactive silanol groups of silica by treating it with thionyl chloride, reacting the chlorinated product with benzyllithium, sulfonating the resultant benzylsilica to obtain sulfobenzylsilica, said thionyl chloride, benzyllithium and chlorosulfonic acid being present in excess of the stoichiometric amount and reacting the sulfobenzylsilica with silver nitrate to produce silver sulfobenzylsilica.
Claim 13
Dependent Claim
97 words
A process for preparing a bound stationary phase having the capacity to separate long chain cis and trans alkene isomers comprising treating silica with thionyl chloride to obtain silica chloride, reacting the silica chloride with benzyllithium and sulfonating the resultant benzylsilica with chlorosulfonic acid to obtain sulfobenzylsilica, said thionyl chloride, benzyllithium, and chlorosulfonic acid being present in excess of the stoichiometric amount, converting the sulfobenzylsilica to the silver salt by reacting it with silver nitrate, treating the silver sulfobenzylsilica with hexamethyldisilazane to deactivate surface hydroxyl groups, and coating the modified silica with 12% ethylene glycol succinate polyester.
Claim 14
Dependent Claim
97 words
A process for preparing a bound stationary phase having the capacity to separate long chain cis and trans alkene isomers comprising treating silica with thionyl chloride to obtain silica chloride, reacting the silica chloride with benzyllithium and sulfonating the resultant benzylsilica with chlorosulfonic acid to obtain sulfobenzylsilica, said thionyl chloride, benzyllithium, and chlorosulfonic acid being present in excess of the stoichiometric amount, converting the sulfobenzylsilica to the silver salt by reacting it with silver nitrate, treating the silver sulfobenzylsilica with hexamethyldisilazane to deactivate surface hydroxyl groups, and coating the modified silica with 12% ethylene glycol succinate polyester.
Claim 15
Dependent Claim
169 words
A process for modifying the acid form of sulfobenzylsilica so that it has the capacity as a bound, stationary phase of separating long chain cis and trans alkene isomers, comprising the steps of: a. inserting tubing containing the acid form of the sulfobenzylsilica into a gas-liquid chromatograph; b. allowing helium gas to flow through the column of sulfobenzylsilica; c. heating the column to about 200° C.; d. silanizing the sulfobenzylsilica by injecting hexamethyldisilazane into the column and then removing unreacted hexamethyldisilazane; e. removing the silanized sulfobenzylsilica from the steel tubing and treating it with dilute nitric acid; f. washing the product of step (f) until the wash is neutral; g. treating the product of step (g) with about 2% aqueous silver nitrate to convert the product to the silver form, the amount of silver nitrate solution being in excess of the stoichiometric amount and then removing unreacted silver nitrate; h. drying the silanized silver sulfobenzylsilica; i. coating the dried product of step (h) with 12% ethylene glycol succinate polyester.
Claim 16
Dependent Claim
169 words
A process for modifying the acid form of sulfobenzylsilica so that it has the capacity as a bound, stationary phase of separating long chain cis and trans alkene isomers, comprising the steps of: a. inserting tubing containing the acid form of the sulfobenzylsilica into a gas-liquid chromatograph; b. allowing helium gas to flow through the column of sulfobenzylsilica; c. heating the column to about 200° C.; d. silanizing the sulfobenzylsilica by injecting hexamethyldisilazane into the column and then removing unreacted hexamethyldisilazane; e. removing the silanized sulfobenzylsilica from the steel tubing and treating it with dilute nitric acid; f. washing the product of step (f) until the wash is neutral; g. treating the product of step (g) with about 2% aqueous silver nitrate to convert the product to the silver form, the amount of silver nitrate solution being in excess of the stoichiometric amount and then removing unreacted silver nitrate; h. drying the silanized silver sulfobenzylsilica; i. coating the dried product of step (h) with 12% ethylene glycol succinate polyester.
Claim 17
Dependent Claim
21 words
The process of claim 11 in which the helium gas was highly purified and contained not more than 1.14 ppm impurities.
Claim 18
Dependent Claim
10 words
The modified sulfobenzylsilica prepared by the process of claim 12.
Claim 19
Dependent Claim
59 words
A process for preparing a stationary phase for gas-liquid chromatography comprising mixing two parts of a silanized silica having an average particle size diameter of 160 to 170 microns and a surface area of 4 to 6 m 2 /grams with one part of a silanized silver sulfobenzylsilica and then coating the mixture with 10% ethylene glycol succinate polyester.
Claim 20
Dependent Claim
59 words
A process for preparing a stationary phase for gas-liquid chromatography comprising mixing two parts of a silanized silica having an average particle size diameter of 160 to 170 microns and a surface area of 4 to 6 m 2 /grams with one part of a silanized silver sulfobenzylsilica and then coating the mixture with 10% ethylene glycol succinate polyester.
Claim 21
Dependent Claim
6 words
The stationary phase of claim 14.
Claim 22
Dependent Claim
46 words
A process for separating cis and trans 9-heneicosenes and Z-4 and E-4 tetradecene-1-ol-acetates, comprising packing a gas-liquid chromatographic column with a stationary phase of claim 15, heating it to about 200° to 210° C., and injecting samples of the mixtures to be separated into the column.
References Cited (Backward Citations)
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1979-10-19 | 1980-04-19 | 1980-10-19 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1983-10-19 | 1984-04-19 | 1984-10-19 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1987-10-19 | 1988-04-19 | 1988-10-19 | $7700.00 | Window Closed / Lapsed |