RU2528396C2 - Тиолсодержащие соединения для удаления элементов из загрязненной окружающей среды и способы их применения - Google Patents
Тиолсодержащие соединения для удаления элементов из загрязненной окружающей среды и способы их применения Download PDFInfo
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- RU2528396C2 RU2528396C2 RU2012113419/04A RU2012113419A RU2528396C2 RU 2528396 C2 RU2528396 C2 RU 2528396C2 RU 2012113419/04 A RU2012113419/04 A RU 2012113419/04A RU 2012113419 A RU2012113419 A RU 2012113419A RU 2528396 C2 RU2528396 C2 RU 2528396C2
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- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
- C07F7/1804—Compounds having Si-O-C linkages
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2253/00—Adsorbents used in seperation treatment of gases and vapours
- B01D2253/10—Inorganic adsorbents
- B01D2253/106—Silica or silicates
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2253/00—Adsorbents used in seperation treatment of gases and vapours
- B01D2253/25—Coated, impregnated or composite adsorbents
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
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- B—PERFORMING OPERATIONS; TRANSPORTING
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- B01D—SEPARATION
- B01D2257/00—Components to be removed
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- B01D2257/602—Mercury or mercury compounds
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
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PCT/US2010/050512 WO2011038385A2 (en) | 2009-09-28 | 2010-09-28 | Thiol-containing compounds for the removal of elements from contaminated milieu and methods of use |
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8950583B2 (en) | 2008-12-06 | 2015-02-10 | Ermes Medical Company Limited | Method to remove heavy metals from a mammal |
US8575218B2 (en) * | 2009-09-28 | 2013-11-05 | The University Of Kentucky Research Foundation | Thiol-containing compounds for the removal of elements from tissues and formulations therefor |
US8257672B2 (en) * | 2009-10-22 | 2012-09-04 | Urs Corporation | Method for preventing re-emission of mercury from a flue gas desulfurization system |
CN104160048B (zh) | 2011-10-07 | 2017-06-06 | 东曹株式会社 | 钯分离剂、以及其制造方法和用途 |
CN102531138A (zh) * | 2012-01-04 | 2012-07-04 | 南京师范大学 | 一种硫化物重金属捕集剂及其制备方法 |
CN103801270B (zh) * | 2012-11-14 | 2016-03-30 | 长沙飞达矿冶技术有限公司 | 用于处理含复杂重金属废水的环保材料及其生产工艺 |
GB2524831A (en) | 2014-04-04 | 2015-10-07 | Ermes Medical Company Ltd | New pharmaceutical use |
GB2526623A (en) | 2014-05-30 | 2015-12-02 | Ermes Medical Company Ltd | New pharmaceutical use |
US9802889B2 (en) | 2014-12-02 | 2017-10-31 | Covalent Research Technologies, LLC | Solid supported trithiol compounds for removing heavy metals from solution, and filtration systems utilizing the compounds |
EP4029497A1 (en) | 2016-08-05 | 2022-07-20 | EmeraMed Limited | New use of n,n-bis-2-mercaptoethyl isophthalamide for treating or preventing paracetamol toxicity |
US11130918B2 (en) | 2019-09-17 | 2021-09-28 | Baker Hughes Holdings Llc | Metal removal from fluids |
GB202005057D0 (en) | 2020-04-06 | 2020-05-20 | Emeramed Ltd | New Use |
CN112090221B (zh) * | 2020-08-13 | 2022-03-22 | 河北正元氢能科技有限公司 | 一种合成氨原料气净化方法及基于其的合成氨工艺 |
WO2023011117A1 (zh) * | 2021-08-02 | 2023-02-09 | 江苏扬农化工集团有限公司 | 吸附剂及其制备方法、己二胺的提纯方法、有机二胺的制备方法及所用的装置 |
CN117019117B (zh) * | 2023-09-19 | 2024-03-15 | 山东大学 | 一种含磷酸基团的咪唑基MOFs铀吸附材料及其制备方法 |
CN117603380B (zh) * | 2023-11-27 | 2024-07-23 | 华谱科仪(北京)科技有限公司 | 一种阳离子交换模式聚合物分离介质及其制备方法和应用 |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SU1734577A3 (ru) * | 1981-02-03 | 1992-05-15 | Империал Кемикал Индастриз Лимитед (Фирма) | Способ извлечени меди из водных растворов, содержащих ион хлора |
RU2002100125A (ru) * | 1999-06-09 | 2003-10-27 | Гербе | Комплексы металлов с бициклическими полиаминокислотами, способ их получения и их применение в медицине для получения изображения |
Family Cites Families (39)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2159183A1 (en) * | 1971-11-09 | 1973-06-22 | Fabre Sa Pierre | Amides and salts of sulphur - contg amino acids with dicarboxylic acids-treatment of skin disorders |
US4039446A (en) * | 1972-06-28 | 1977-08-02 | Sumitomo Chemical Company, Limited | Heavy metal-binding agent process |
US4281086A (en) * | 1978-12-11 | 1981-07-28 | The University Of Illinois Foundation | Polymer bound multidentate complexes |
JPS57102852A (en) * | 1980-12-19 | 1982-06-26 | Shionogi & Co Ltd | Dicarboxylic acid diamide |
DE3231982A1 (de) * | 1982-08-27 | 1984-03-01 | Süd-Chemie AG, 8000 München | Thiolathaltiges mittel und verfahren zur entfernung von schwermetallionen aus verduennten waessrigen loesungen |
US4673562A (en) * | 1983-08-19 | 1987-06-16 | The Children's Medical Center Corporation | Bisamide bisthiol compounds useful for making technetium radiodiagnostic renal agents |
US4751286A (en) * | 1985-11-19 | 1988-06-14 | The Johns Hopkins University | Protein label and drug delivery system |
US5200473A (en) * | 1988-03-25 | 1993-04-06 | Jeanneret Gris Gilbert | Chelating resins and method for their use in the extraction of metal ions |
US5073575A (en) * | 1988-08-26 | 1991-12-17 | The Regents Of The University Of California | Cadmium ion-chelating synthetic polymers and process thereof |
US4969995A (en) * | 1988-08-26 | 1990-11-13 | The United States Of America As Represented By The United States Department Of Energy | Removal of metal ions from aqueous solution |
DE3930674A1 (de) * | 1989-09-11 | 1991-03-21 | Diagnostikforschung Inst | Bifunktionelle chelatbildner zur komplexierung von tc- und re-isotopen, verfahren zu ihrer herstellung und darstellung von konjugaten daraus sowie deren verwendung in diagnostik und therapie |
JPH04124170A (ja) * | 1990-09-13 | 1992-04-24 | Nippon Shokubai Co Ltd | 多官能チオール化合物及びその製法 |
DE4107570A1 (de) * | 1991-03-07 | 1992-11-19 | Diagnostikforschung Inst | Chelate, deren metallkomplexe sowie ihre verwendung in diagnostik und therapie |
US5173470A (en) * | 1991-08-09 | 1992-12-22 | Brigham Young University | Compositions and processes for removing, separating and concentrating desired ions from solutions using sulfur and aralkyl nitrogen containing ligands bonded to inorganic supports |
NZ244613A (en) * | 1991-10-29 | 1996-05-28 | Bracco International B V Subst | A ligand containing a hypoxia-localising moiety, preparation thereof; a kit (optionally multivial) for preparing a metal complex containing the ligand |
US5494935A (en) * | 1992-01-17 | 1996-02-27 | University Of Utah Research Foundation | Methods for oral decorporation of metals |
SE508881C2 (sv) * | 1994-03-02 | 1998-11-16 | Ctc Medical Ab | Preparat avsett att vid behandling av i tänder befintliga amalgamfyllningar och/eller vid inserering av nya amalgamfyllningar hämma frisättning av Hg från amalgamet och/eller oskadliggöra frisatt Hg |
US5615862A (en) * | 1995-02-02 | 1997-04-01 | Gaudette; Robert M. | Metal precipitation composition for treating spent dry film stripping solution |
US5766478A (en) * | 1995-05-30 | 1998-06-16 | The Regents Of The University Of California, Office Of Technology Transfer | Water-soluble polymers for recovery of metal ions from aqueous streams |
US6126964A (en) * | 1996-01-04 | 2000-10-03 | Mirus Corporation | Process of making a compound by forming a polymer from a template drug |
US6896899B2 (en) * | 1996-12-31 | 2005-05-24 | Antioxidant Pharmaceuticals Corp. | Pharmaceutical preparations of glutathione and methods of administration thereof |
AU7371998A (en) * | 1997-05-07 | 1998-11-27 | University Of Pittsburgh | Inhibitors of protein isoprenyl transferases |
WO1999005302A1 (en) * | 1997-07-24 | 1999-02-04 | The Perkin-Elmer Corporation | Conjugates of transporter peptides and nucleic acid analogs, and their use |
US7087770B2 (en) * | 1998-05-16 | 2006-08-08 | Mirus Bio Corporation | Compound containing a labile disulfide bond |
US6936729B2 (en) * | 1998-05-16 | 2005-08-30 | Mirus Bio Corporation | Compound containing a labile disulfide bond |
JP4307728B2 (ja) * | 1998-06-19 | 2009-08-05 | テレフオンアクチーボラゲット エル エム エリクソン(パブル) | 移動体通信システムの通信状態の動的適合方法及び装置 |
FR2794744B1 (fr) * | 1999-06-09 | 2001-09-21 | Guerbet Sa | Complexes metalliques de polyaminoacides bicycliques, leur procede de preparation et leur application en imagerie medicale |
US6586600B2 (en) * | 2000-12-06 | 2003-07-01 | University Of Kentucky Research Foundation | Multidentate sulfur-containing ligands |
RS20100077A (en) * | 2001-04-30 | 2010-10-31 | Trommsdorff Gmbh. & Co. Kg. Arzneimittel | Pharamceutically active uridine esters |
US20040132101A1 (en) * | 2002-09-27 | 2004-07-08 | Xencor | Optimized Fc variants and methods for their generation |
US20060099239A1 (en) * | 2002-04-15 | 2006-05-11 | Coleman Henry D | Dietary supplement for promoting removal of heavy metals from the body |
US6852369B1 (en) * | 2002-09-05 | 2005-02-08 | University Of Kentucky Research Foundation | Method for prevention of solid dissolution through covalent ligand bonding |
US7582623B2 (en) * | 2004-05-20 | 2009-09-01 | The Regents Of The University Of California | Photoactive metal nitrosyls for blood pressure regulation and cancer therapy |
US20060115555A1 (en) * | 2004-12-01 | 2006-06-01 | Foulger Sidney W | Nutritional supplements containing xanthone extracts |
US9226885B2 (en) * | 2005-05-24 | 2016-01-05 | Allium Vitalis Incorporated | Personal care and medicinal products incorporating bound organosulfur groups |
US9186376B2 (en) * | 2005-09-30 | 2015-11-17 | Patrick James Baggot | Maternal chelation for embryo, fetal, and infant benefit |
US8950583B2 (en) * | 2008-12-06 | 2015-02-10 | Ermes Medical Company Limited | Method to remove heavy metals from a mammal |
US8575218B2 (en) * | 2009-09-28 | 2013-11-05 | The University Of Kentucky Research Foundation | Thiol-containing compounds for the removal of elements from tissues and formulations therefor |
US8426368B2 (en) * | 2010-03-25 | 2013-04-23 | The University Of Kentucky Research Foundation | Method of ameliorating oxidative stress and supplementing the diet |
-
2010
- 2010-09-28 IN IN2586DEN2012 patent/IN2012DN02586A/en unknown
- 2010-09-28 AU AU2010297933A patent/AU2010297933A1/en not_active Abandoned
- 2010-09-28 CA CA2775397A patent/CA2775397A1/en not_active Abandoned
- 2010-09-28 EP EP10819637.9A patent/EP2483239A4/en not_active Withdrawn
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- 2010-09-28 CN CN2010800505595A patent/CN102612511A/zh active Pending
- 2010-09-28 RU RU2012113419/04A patent/RU2528396C2/ru not_active IP Right Cessation
- 2010-09-28 US US12/892,464 patent/US20110076246A1/en not_active Abandoned
- 2010-09-28 WO PCT/US2010/050512 patent/WO2011038385A2/en active Application Filing
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SU1734577A3 (ru) * | 1981-02-03 | 1992-05-15 | Империал Кемикал Индастриз Лимитед (Фирма) | Способ извлечени меди из водных растворов, содержащих ион хлора |
RU2002100125A (ru) * | 1999-06-09 | 2003-10-27 | Гербе | Комплексы металлов с бициклическими полиаминокислотами, способ их получения и их применение в медицине для получения изображения |
Non-Patent Citations (1)
Title |
---|
GELINSKY M. et al, Inorganic Chemistry, vol. 41, 2002, p.2560-2564. LUDLOW F.R. et al, J.Am.Chem.Soc., vol. 130, 2008, p. 12218-12219. WEST K.R. et al, Organic Letters, vol. 7, no.13, 2005, p.2615-2618. * |
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WO2011038385A9 (en) | 2011-11-24 |
CA2775397A1 (en) | 2011-03-31 |
WO2011038385A2 (en) | 2011-03-31 |
EP2483239A2 (en) | 2012-08-08 |
IN2012DN02586A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 2015-08-28 |
AU2010297933A1 (en) | 2012-04-19 |
JP2013505963A (ja) | 2013-02-21 |
EP2483239A4 (en) | 2014-09-03 |
US20110076246A1 (en) | 2011-03-31 |
CN102612511A (zh) | 2012-07-25 |
WO2011038385A3 (en) | 2011-08-11 |
RU2012113419A (ru) | 2013-11-10 |
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