RU2000113194A - HYBRID ORGANO-INORGANIC GELS FOR EXTRACTION OF CHEMICAL ELEMENTS, SUCH AS LANTANIDES AND ACTINIDES, AND METHODS FOR PRODUCING THESE GELS - Google Patents
HYBRID ORGANO-INORGANIC GELS FOR EXTRACTION OF CHEMICAL ELEMENTS, SUCH AS LANTANIDES AND ACTINIDES, AND METHODS FOR PRODUCING THESE GELSInfo
- Publication number
- RU2000113194A RU2000113194A RU2000113194/04A RU2000113194A RU2000113194A RU 2000113194 A RU2000113194 A RU 2000113194A RU 2000113194/04 A RU2000113194/04 A RU 2000113194/04A RU 2000113194 A RU2000113194 A RU 2000113194A RU 2000113194 A RU2000113194 A RU 2000113194A
- Authority
- RU
- Russia
- Prior art keywords
- gel
- organic
- paragraphs
- functional group
- group
- Prior art date
Links
- 239000000499 gel Substances 0.000 title claims 10
- 238000000605 extraction Methods 0.000 title claims 3
- 229910052768 actinide Inorganic materials 0.000 title claims 2
- 150000001255 actinides Chemical class 0.000 title claims 2
- 229910052729 chemical element Inorganic materials 0.000 title 1
- 229910052710 silicon Inorganic materials 0.000 claims 10
- 125000000524 functional group Chemical group 0.000 claims 7
- 150000004703 alkoxides Chemical class 0.000 claims 6
- 229910052751 metal Inorganic materials 0.000 claims 5
- 239000002184 metal Substances 0.000 claims 5
- 125000000217 alkyl group Chemical group 0.000 claims 4
- 230000000536 complexating Effects 0.000 claims 4
- 150000002500 ions Chemical class 0.000 claims 4
- 125000000962 organic group Chemical group 0.000 claims 4
- 125000004429 atoms Chemical group 0.000 claims 3
- 230000000875 corresponding Effects 0.000 claims 3
- 238000006116 polymerization reaction Methods 0.000 claims 3
- 239000007864 aqueous solution Substances 0.000 claims 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 2
- 239000010703 silicon Substances 0.000 claims 2
- -1 silicon alkoxide Chemical class 0.000 claims 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 2
- ROFVEXUMMXZLPA-UHFFFAOYSA-N 2,2'-bipyridyl Chemical group N1=CC=CC=C1C1=CC=CC=N1 ROFVEXUMMXZLPA-UHFFFAOYSA-N 0.000 claims 1
- LDDQLRUQCUTJBB-UHFFFAOYSA-N Ammonium fluoride Chemical compound [NH4+].[F-] LDDQLRUQCUTJBB-UHFFFAOYSA-N 0.000 claims 1
- SBOJXQVPLKSXOG-UHFFFAOYSA-N O-amino-Hydroxylamine Chemical compound NON SBOJXQVPLKSXOG-UHFFFAOYSA-N 0.000 claims 1
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 claims 1
- 150000001408 amides Chemical class 0.000 claims 1
- 230000000694 effects Effects 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 229910052747 lanthanoid Inorganic materials 0.000 claims 1
- 150000002602 lanthanoids Chemical class 0.000 claims 1
- 239000012528 membrane Substances 0.000 claims 1
- 238000006068 polycondensation reaction Methods 0.000 claims 1
- 239000000843 powder Substances 0.000 claims 1
- 239000000741 silica gel Substances 0.000 claims 1
- 229910002027 silica gel Inorganic materials 0.000 claims 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims 1
- 238000003980 solgel method Methods 0.000 claims 1
- 125000001424 substituent group Chemical group 0.000 claims 1
- 238000005406 washing Methods 0.000 claims 1
Claims (1)
где М обозначает Si, Ti, Zr или Аl, в которую интегрированы органические молекулы, образующие комплексы с экстрагируемыми ионами, причем каждая органическая молекула ковалентно связана с одним или несколькими атомами М сетки, и отделяют гель, связавший ионы.1. The method of extraction present in aqueous solutions of ions belonging to the group of ions of actinides and / or lanthanides, which consists in the fact that the aqueous solution is brought into contact with a hybrid organo-inorganic gel containing a network of inorganic units of the formula:
where M is Si, Ti, Zr or Al, into which organic molecules are integrated that form complexes with extractable ions, each organic molecule being covalently linked to one or more atoms of the M network, and the gel binding the ions is separated.
в которых (М) обозначает ковалентную связь молекулы с атомом М, представляющим собой Si, Ti, Zr и/или Аl в неорганических звеньях сетки.3. The method according to p. 1 or 2, in which the complexing organic gel molecules correspond to one of the following formulas:
in which (M) denotes a covalent bond of the molecule with the atom M, which is Si, Ti, Zr and / or Al in inorganic units of the network.
5. Способ по п. 4, в котором гель представляет собой гибридный силикагель, отвечающий одной из следующих формул:
6. Способ по любому из пп. 1-3, в котором гибридный гель получен по методике золь-гель, согласно которой полимеризация осуществляется путем поликонденсации в присутствии воды по меньшей мере одного алкоксида металла, имеющего функциональный заместитель (и), формулы:
LM(OR1)l (I) или (R1O)lMLM(OR1)l (II),
в которой М обозначает Si, Ti, Zr или Al;
L обозначает комплексообразующую органическую группу, отвечающую одной из следующих формул:
R1 обозначает органическую группу, преимущественно алкил;
l = 3, когда М обозначает Si, Ti, или Zr или l = 2, когда М обозначает Al.4. The method according to any one of paragraphs. 1-3, in which the inorganic links are links:
5. The method according to p. 4, in which the gel is a hybrid silica gel corresponding to one of the following formulas:
6. The method according to any one of paragraphs. 1-3, in which the hybrid gel is obtained by the sol-gel method, according to which the polymerization is carried out by polycondensation in the presence of water of at least one metal alkoxide having a functional substituent (s) of the formula:
LM (OR 1 ) l (I) or (R 1 O) lMLM (OR 1 ) l (II),
in which M represents Si, Ti, Zr or Al;
L denotes a complexing organic group corresponding to one of the following formulas:
R 1 is an organic group, preferably alkyl;
l = 3 when M is Si, Ti, or Zr, or l = 2 when M is Al.
в которых R обозначает органическую, преимущественно алкильную группу.7. The method according to claim 6, in which the metal alkoxide containing the functional group (s) corresponds to one of the following formulas:
in which R denotes an organic, mainly alkyl group.
M(OR2)m (III)
в которой М обозначает Si, Ti, Zr или Al;
R2 обозначает органическую, преимущественно алкильную группу;
m = 4, когда М является Si, Ti или Zr, или m = 3, когда М обозначает Al.8. The method according to any one of paragraphs. 6 and 7, in which the metal alkoxide containing functional group (s) is polymerized with a metal alkoxide of the formula:
M (OR 2 ) m (III)
in which M represents Si, Ti, Zr or Al;
R 2 denotes an organic, mainly alkyl group;
m = 4 when M is Si, Ti or Zr, or m = 3 when M is Al.
(R3O)lM-X-M(OR3)l (IV)
в которой М обозначает Si, Ti, Zr или Al;
R3 обозначает органическую, преимущественно алкильную группу;
Х обозначает не образующую комплекса органическую группу;
l= 3, когда М обозначает Si, Ti или Zr, или l= 2, когда М обозначает Аl.10. The method according to any one of paragraphs. 6-9, in which the metal alkoxide containing the functional group (s) is also polymerized with an alkoxide of the formula
(R 3 O) lM-XM (OR 3 ) l (IV)
in which M represents Si, Ti, Zr or Al;
R 3 denotes an organic, mainly alkyl group;
X is a non-complexing organic group;
l = 3 when M is Si, Ti or Zr, or l = 2 when M is Al.
13. Способ по п. 7, в котором содержащий функциональную группу(ы) алкоксисилан полимеризован с 1-5 эквивалентами тетраэтоксисилана.12. The method according to p. 7, in which polymerized only containing a functional group (s) silicon alkoxide, corresponding to one of the formulas
13. The method of claim 7, wherein the alkoxysilane containing functional group (s) is polymerized with 1-5 equivalents of tetraethoxysilane.
17. Silicon alkoxide containing a functional group (s) of one of the following formulas:
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9713565 | 1997-10-29 | ||
FR9713565A FR2770153B1 (en) | 1997-10-29 | 1997-10-29 | INORGANIC-ORGANIC HYBRID GELS FOR THE EXTRACTION OF CHEMICAL SPECIES SUCH AS LANTHANIDES AND ACTINIDES, AND THEIR PREPARATION |
Publications (2)
Publication Number | Publication Date |
---|---|
RU2000113194A true RU2000113194A (en) | 2002-05-10 |
RU2207190C2 RU2207190C2 (en) | 2003-06-27 |
Family
ID=9512784
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU2000113194/04A RU2207190C2 (en) | 1997-10-29 | 1998-10-28 | Organomineral hybrid gels for extraction of minerals such as lanthanides and actinides and methods for preparing these gels |
Country Status (7)
Country | Link |
---|---|
US (1) | US6667016B1 (en) |
JP (1) | JP2001520932A (en) |
KR (1) | KR100531108B1 (en) |
FR (1) | FR2770153B1 (en) |
GB (1) | GB2349347B (en) |
RU (1) | RU2207190C2 (en) |
WO (1) | WO1999021654A1 (en) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4540935B2 (en) * | 2003-01-31 | 2010-09-08 | 日本曹達株式会社 | Silane derivatives and organic thin film forming bodies |
FR2866341B1 (en) * | 2004-02-12 | 2006-04-28 | Commissariat Energie Atomique | ORGANIC-INORGANIC PRINTED HYBRID GEL COMPRISING AN ORGANIC COMPLEXENT INVOLVING PI-PI AND / OR PI-NU INTERACTIONS |
US7534510B2 (en) | 2004-09-03 | 2009-05-19 | The Gillette Company | Fuel compositions |
US7674864B2 (en) | 2005-12-23 | 2010-03-09 | Boston Scientific Scimed, Inc. | Polymeric hybrid precursors, polymeric hybrid precursor composite matrices, medical devices, and methods |
US8455088B2 (en) | 2005-12-23 | 2013-06-04 | Boston Scientific Scimed, Inc. | Spun nanofiber, medical devices, and methods |
FR2933703B1 (en) * | 2008-07-11 | 2012-08-17 | Commissariat Energie Atomique | NANOPOROUS DETECTORS OF MONOCYCLIC AROMATIC COMPOUNDS AND OTHER POLLUTANTS |
FR3013059B1 (en) * | 2013-11-08 | 2016-01-01 | Commissariat Energie Atomique | USE OF ORGANIC-INORGANIC HYBRID MATERIAL FOR EXTRACTING URANIUM (VI) FROM AQUEOUS SOLUTION OF SULFURIC ACID, IN PARTICULAR FROM THE SULFURIC LIXATION OF A URANIUM URANIUM |
Family Cites Families (20)
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GB956276A (en) * | 1960-07-06 | 1964-04-22 | Wolfen Filmfab Veb | Process for the manufacture of thermostable organo silicon anion exchangers |
DE2357184A1 (en) * | 1973-11-16 | 1975-05-22 | Merck Patent Gmbh | PROCESS FOR THE PRODUCTION OF ORGANICALLY MODIFIED SILICON DIOXIDES |
US4203952A (en) * | 1974-05-28 | 1980-05-20 | The British Petroleum Company Limited | Process for the removal of heavy metals and transition metals other than platinum from solution |
US4278803A (en) * | 1980-01-07 | 1981-07-14 | Polaroid Corporation | Preparation of 2-Methylene-1,3-propanediamide |
US4448694A (en) * | 1981-09-04 | 1984-05-15 | Dow Corning Corporation | Metal extraction from solution and immobilized chelating agents used therefor |
DE3616133A1 (en) * | 1985-09-25 | 1987-11-19 | Merck Patent Gmbh | SPHERICAL SIO (DOWN ARROW) 2 (DOWN ARROW) PARTICLES |
EP0486469B2 (en) * | 1986-10-03 | 2000-06-21 | PPG Industries Ohio, Inc. | Organic-inorganic hybrid polymer |
US4746572A (en) * | 1986-11-28 | 1988-05-24 | E. I. Dupont De Nemours And Company | Structures surface modified with bidentate silanes |
US4943375A (en) * | 1987-09-04 | 1990-07-24 | Brigham Young University | 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 |
US5039419A (en) * | 1988-07-13 | 1991-08-13 | Brigham Young University | Sulfur-containing hydrocarbon compounds and process of using same in recovering and concentrating desired ions from solutions thereof |
US5084430A (en) * | 1988-08-26 | 1992-01-28 | Brigham Young University | Sulfur and nitrogen containing hydrocarbons and process of using same in separating desired ions from solutions thereof |
US5071819A (en) * | 1988-08-26 | 1991-12-10 | Ibc Advanced Technologies | Sulfur and nitrogen-containing hydrocarbons and process of using same in recovering and concentrating desired ions from solutions thereof |
US5078978A (en) * | 1989-11-06 | 1992-01-07 | Brigham Young University | Pyridine-containing alkoxysilanes bonded to inorganic supports and processes of using the same for removing and concentrating desired ions from solutions |
JP2795379B2 (en) * | 1989-11-29 | 1998-09-10 | 科学技術振興事業団 | Method for producing metal coordinating organosilicon polymer |
DE4309660A1 (en) * | 1993-03-25 | 1994-09-29 | Studiengesellschaft Kohle Mbh | Selective inorganic catalysts in the form of molecular impressions in cavities |
JP3170529B2 (en) | 1993-03-25 | 2001-05-28 | 大日本印刷株式会社 | Toner container |
DE4319909C2 (en) * | 1993-06-16 | 1996-11-07 | Solvay Deutschland | Airgel supported catalyst comprising palladium, platinum, nickel, cobalt and / or copper, process for its production and use of a palladium airgel supported catalyst |
US5668079A (en) * | 1994-09-27 | 1997-09-16 | Syracuse University | Chemically active ceramic compositions with an hydroxyquinoline moiety |
FR2725552B1 (en) * | 1994-10-05 | 1996-10-31 | Commissariat Energie Atomique | PROCESS FOR THE ALPHA PARTIAL DECONTAMINATION OF AN AQUEOUS EFFLUENT |
US5637135A (en) * | 1995-06-26 | 1997-06-10 | Capillary Technology Corporation | Chromatographic stationary phases and adsorbents from hybrid organic-inorganic sol-gels |
-
1997
- 1997-10-29 FR FR9713565A patent/FR2770153B1/en not_active Expired - Lifetime
-
1998
- 1998-10-28 WO PCT/FR1998/002309 patent/WO1999021654A1/en active IP Right Grant
- 1998-10-28 US US09/530,133 patent/US6667016B1/en not_active Expired - Fee Related
- 1998-10-28 KR KR10-2000-7004656A patent/KR100531108B1/en not_active IP Right Cessation
- 1998-10-28 GB GB0009736A patent/GB2349347B/en not_active Expired - Fee Related
- 1998-10-28 JP JP2000517801A patent/JP2001520932A/en active Pending
- 1998-10-28 RU RU2000113194/04A patent/RU2207190C2/en not_active IP Right Cessation
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