BR112012005861B1 - Aparelho refrigerador, método para produzir resfriamento em um refrigerador e método para substituir refrigerante - Google Patents
Aparelho refrigerador, método para produzir resfriamento em um refrigerador e método para substituir refrigerante Download PDFInfo
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- BR112012005861B1 BR112012005861B1 BR112012005861-4A BR112012005861A BR112012005861B1 BR 112012005861 B1 BR112012005861 B1 BR 112012005861B1 BR 112012005861 A BR112012005861 A BR 112012005861A BR 112012005861 B1 BR112012005861 B1 BR 112012005861B1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K5/00—Heat-transfer, heat-exchange or heat-storage materials, e.g. refrigerants; Materials for the production of heat or cold by chemical reactions other than by combustion
- C09K5/02—Materials undergoing a change of physical state when used
- C09K5/04—Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa
- C09K5/041—Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa for compression-type refrigeration systems
- C09K5/044—Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa for compression-type refrigeration systems comprising halogenated compounds
- C09K5/045—Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa for compression-type refrigeration systems comprising halogenated compounds containing only fluorine as halogen
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2205/00—Aspects relating to compounds used in compression type refrigeration systems
- C09K2205/10—Components
- C09K2205/12—Hydrocarbons
- C09K2205/122—Halogenated hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2205/00—Aspects relating to compounds used in compression type refrigeration systems
- C09K2205/10—Components
- C09K2205/12—Hydrocarbons
- C09K2205/126—Unsaturated fluorinated hydrocarbons
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Combustion & Propulsion (AREA)
- Thermal Sciences (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
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| US24287509P | 2009-09-16 | 2009-09-16 | |
| US61/242,875 | 2009-09-16 | ||
| PCT/US2010/048944 WO2011034929A1 (en) | 2009-09-16 | 2010-09-15 | Composition comprising cis-1,1,1,4,4,4-hexafluoro-2-butene and trans-1,2-dichloroethylene, apparatus containing same and methods of producing cooling therein |
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| BR112012005861A2 BR112012005861A2 (pt) | 2017-06-06 |
| BR112012005861B1 true BR112012005861B1 (pt) | 2019-09-24 |
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| BR112012005861-4A BR112012005861B1 (pt) | 2009-09-16 | 2010-09-15 | Aparelho refrigerador, método para produzir resfriamento em um refrigerador e método para substituir refrigerante |
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| EP (1) | EP2521757B1 (https=) |
| JP (1) | JP6176923B2 (https=) |
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| CN (1) | CN102695771B (https=) |
| AU (1) | AU2010295712B2 (https=) |
| BR (1) | BR112012005861B1 (https=) |
| CA (1) | CA2774202C (https=) |
| ES (1) | ES2582406T3 (https=) |
| IN (1) | IN2012DN02188A (https=) |
| MX (1) | MX365490B (https=) |
| MY (1) | MY160233A (https=) |
| WO (1) | WO2011034929A1 (https=) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8463441B2 (en) | 2002-12-09 | 2013-06-11 | Hudson Technologies, Inc. | Method and apparatus for optimizing refrigeration systems |
| CN102459498B (zh) | 2009-06-03 | 2016-08-24 | 纳幕尔杜邦公司 | 含有顺式-1,1,1,4,4,4-六氟-2-丁烯的冷却器设备及其制冷方法 |
| US20110144216A1 (en) * | 2009-12-16 | 2011-06-16 | Honeywell International Inc. | Compositions and uses of cis-1,1,1,4,4,4-hexafluoro-2-butene |
| TWI573971B (zh) | 2011-01-31 | 2017-03-11 | 杜邦股份有限公司 | 使用包含z-1,1,1,4,4,4-六氟-2-丁烯之工作流體製熱 |
| JP5721480B2 (ja) * | 2011-03-10 | 2015-05-20 | 三菱電機株式会社 | 冷凍サイクル装置 |
| BR112014020279A8 (pt) * | 2012-02-17 | 2017-07-11 | Du Pont | Composição do tipo azeótropo, processos para preparar uma espuma termoplástica, para produzir refrigeração, para produzir um produto aerossol e para extinguir ou suprimir um incêndio, composição de formação de espuma, processo para produzir uma espuma e espuma |
| US20130283832A1 (en) * | 2012-04-30 | 2013-10-31 | Trane International Inc. | Refrigeration system with purge using enrivonmentally-suitable chiller refrigerant |
| TW201411068A (zh) * | 2012-08-01 | 2014-03-16 | Du Pont | 於級聯熱泵中在最終級聯階段使用包含z-1,1,1,4,4,4-六氟-2-丁烯之工作流體製造加熱 |
| TW201412966A (zh) * | 2012-08-30 | 2014-04-01 | Du Pont | 為二氟氯甲烷設計之設備的再充填方法 |
| CN113897181A (zh) | 2013-01-25 | 2022-01-07 | 特灵国际有限公司 | 制冷剂添加剂和组合物 |
| US10513666B2 (en) * | 2015-03-02 | 2019-12-24 | Jxtg Nippon Oil & Energy Corporation | Refrigerator oil and working fluid composition for refrigerators |
| EP3289293A4 (en) * | 2015-04-27 | 2018-08-08 | Trane International Inc. | Improving glide in refrigerant blends and/or azeotopic blends, alternatives to r123 refrigerant, and refrigerant compositions, methods, and systems thereof |
| CN107923663B (zh) | 2015-08-11 | 2021-05-11 | 开利公司 | 低容量、低gwp的hvac系统 |
| US10612825B2 (en) | 2016-05-10 | 2020-04-07 | Trane International Inc. | Lubricant blends to reduce refrigerant solubility |
| KR20190065384A (ko) * | 2016-10-10 | 2019-06-11 | 더루브리졸코오퍼레이션 | 낮은 지구 온난화 잠재성의 냉매 시스템용 윤활제 |
| US10407602B2 (en) * | 2017-11-30 | 2019-09-10 | Trane International Inc. | Low global warming potential refrigerants in liquid chillers |
Family Cites Families (20)
| Publication number | Priority date | Publication date | Assignee | Title |
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| JPH05179043A (ja) | 1991-11-18 | 1993-07-20 | Daikin Ind Ltd | フルオロブテンからなる発泡剤およびプラスチック発泡体の製造方法 |
| WO1996040834A1 (en) | 1995-06-07 | 1996-12-19 | E.I. Du Pont De Nemours And Company | Refrigerants based on hydrofluoroether of fluoroether |
| US6030934A (en) | 1997-02-19 | 2000-02-29 | 3M Innovative Properties Company | Azeotropic compositions of methoxy-perfluoropropane and their use |
| US5848538A (en) * | 1997-11-06 | 1998-12-15 | American Standard Inc. | Oil and refrigerant pump for centrifugal chiller |
| US7094356B2 (en) | 2004-05-26 | 2006-08-22 | E. I. Dupont Denemours And Company | 1,1,1,2,2,4,5,5,5-nonafluoro-4-(trifluoromethyl)-3-pentanone refrigerant compositions and uses thereof |
| US20050285079A1 (en) * | 2004-06-29 | 2005-12-29 | Minor Barbara H | 1-Ethoxy-1,1,2,2,3,3,4,4,4-nonafluorobutane refrigerant compositions comprising functionalized organic compounds and uses thereof |
| JP2008531975A (ja) * | 2005-03-04 | 2008-08-14 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | エンジン排ガス駆動タービンを動力源とする冷凍/空気調節装置 |
| US20060245944A1 (en) | 2005-03-21 | 2006-11-02 | Leck Thomas J | Cooling apparatus powered by a ratioed gear drive assembly |
| US20060266975A1 (en) * | 2005-05-27 | 2006-11-30 | Nappa Mario J | Compositions comprising 3,3,4,4,5,5,6,6,6-nonafluoro-1-hexene |
| US7708903B2 (en) | 2005-11-01 | 2010-05-04 | E.I. Du Pont De Nemours And Company | Compositions comprising fluoroolefins and uses thereof |
| KR101350620B1 (ko) * | 2005-11-01 | 2014-02-06 | 이 아이 듀폰 디 네모아 앤드 캄파니 | 플루오로올레핀을 포함하는 조성물 및 그의 용도 |
| ES2642570T3 (es) * | 2006-02-28 | 2017-11-16 | The Chemours Company Fc, Llc | Composiciones azeotrópicas que comprenden compuestos fluorados para aplicaciones de limpieza |
| SG183037A1 (en) * | 2007-04-27 | 2012-08-30 | Du Pont | Azeotropic and azeotrope-like compositions of z-1,1,1,4,4,4-hexafluoro-2-butene |
| CA2684290C (en) * | 2007-06-12 | 2016-09-06 | E. I. Du Pont De Nemours And Company | Azeotropic and azeotrope-like compositions of e-1,1,1,4,4,4-hexafluoro-2-butene |
| WO2008157757A1 (en) | 2007-06-21 | 2008-12-24 | E. I. Du Pont De Nemours And Company | Method for leak detection in heat transfer system |
| US7795482B2 (en) | 2007-07-03 | 2010-09-14 | E. I. Du Pont De Nemours And Company | Method of hydrodechlorination to produce dihydrofluorinated olefins |
| FR2921665A1 (fr) | 2007-09-28 | 2009-04-03 | Arkema France | Composition a base de trans-1,2 dichloroethylene. |
| TW200930801A (en) | 2007-10-31 | 2009-07-16 | Du Pont | Compositions comprising iodotrifluoromethane and uses thereof |
| CN105505323A (zh) | 2008-03-07 | 2016-04-20 | 阿科玛股份有限公司 | 具有改进的油返回的卤代烯热传输组合物 |
| US7442321B1 (en) * | 2008-03-07 | 2008-10-28 | Arkema Inc. | Azeotrope-like composition of 1,1,1-trifluoro-3-chloropropene and trans-1,2-dichloroethylene |
-
2010
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| AU2010295712B2 (en) | 2014-09-25 |
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| CN102695771A (zh) | 2012-09-26 |
| IN2012DN02188A (https=) | 2015-08-21 |
| MY160233A (en) | 2017-02-28 |
| CA2774202C (en) | 2017-11-28 |
| US9150770B2 (en) | 2015-10-06 |
| MX365490B (es) | 2019-06-05 |
| US20120167599A1 (en) | 2012-07-05 |
| BR112012005861A2 (pt) | 2017-06-06 |
| KR20120075469A (ko) | 2012-07-06 |
| MX2012003239A (es) | 2012-04-10 |
| JP6176923B2 (ja) | 2017-08-09 |
| CN102695771B (zh) | 2016-02-17 |
| EP2521757B1 (en) | 2016-05-04 |
| JP2013505424A (ja) | 2013-02-14 |
| KR101772715B1 (ko) | 2017-08-29 |
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