WO1998044303A1 - Improved triple effect absorption apparatus and method - Google Patents
Improved triple effect absorption apparatus and method Download PDFInfo
- Publication number
- WO1998044303A1 WO1998044303A1 PCT/US1998/005973 US9805973W WO9844303A1 WO 1998044303 A1 WO1998044303 A1 WO 1998044303A1 US 9805973 W US9805973 W US 9805973W WO 9844303 A1 WO9844303 A1 WO 9844303A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- generator
- generators
- fluid
- stage
- aqueous
- Prior art date
Links
Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25B—REFRIGERATION MACHINES, PLANTS OR SYSTEMS; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS
- F25B15/00—Sorption machines, plants or systems, operating continuously, e.g. absorption type
- F25B15/02—Sorption machines, plants or systems, operating continuously, e.g. absorption type without inert gas
- F25B15/06—Sorption machines, plants or systems, operating continuously, e.g. absorption type without inert gas the refrigerant being water vapour evaporated from a salt solution, e.g. lithium bromide
-
- 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
- C09K5/047—Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa for absorption-type refrigeration systems
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25B—REFRIGERATION MACHINES, PLANTS OR SYSTEMS; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS
- F25B15/00—Sorption machines, plants or systems, operating continuously, e.g. absorption type
- F25B15/008—Sorption machines, plants or systems, operating continuously, e.g. absorption type with multi-stage operation
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25B—REFRIGERATION MACHINES, PLANTS OR SYSTEMS; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS
- F25B33/00—Boilers; Analysers; Rectifiers
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25B—REFRIGERATION MACHINES, PLANTS OR SYSTEMS; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS
- F25B2315/00—Sorption refrigeration cycles or details thereof
- F25B2315/003—Hydrates for sorption cycles
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A30/00—Adapting or protecting infrastructure or their operation
- Y02A30/27—Relating to heating, ventilation or air conditioning [HVAC] technologies
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02B—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO BUILDINGS, e.g. HOUSING, HOUSE APPLIANCES OR RELATED END-USER APPLICATIONS
- Y02B30/00—Energy efficient heating, ventilation or air conditioning [HVAC]
- Y02B30/62—Absorption based systems
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/10—Process efficiency
Definitions
- Send systems incorporating one or more absorbers for directing an aqueous absorption fluid to first, second and third generators operating at successively higher temperatures.
- These triple effect apparatus include three condensers operating at successively higher temperatures and communicating with the generators.
- the three condensers are also interconnected whereby condensed refrigerant flows successively from the third condenser to the second condenser, then to the first condenser, and thereafter to one or more evaporators.
- I Cbondensers is used to drive the lower generators.
- the use of such apparatus in which a single refrigerant such as water is used throughout the system achieves substantial improvement over prior art systems which rely on heat transfer coupling of heat exchangers with no common mass flows.
- vapor pressures of the absorption solution in the high temperature, third generator are usually above 25 psig, and are normally operated at between about 40 1 -a ⁇ d about 80 psig, typically at about 60 psig.
- present boiler codes require that absorption cycle apparatus boilers or generators operating above 15 psig must be monitored by an operator at all times during operation. Such requirement obviously is economically disadvantageous, and where costs and expenses of operation are of great importance, the use of apparatus having high generator pressure requirements is handicapped. It is to the elimination of such a disadvantage of the aforesaid triple effect apparatus and systems that the present invention 2Qs directed.
- the present invention is directed to methods of operating the triple effect absorption cycle apparatus using a high temperature third generator operating at reduced pressures, preferably less than 15 psig.
- the triple effect apparatus used in the invention is disclosed in U.S. Patent No. 5,335,515, 5,390,509 as well as 5,205,136, all of 25-vhich disclosures are incorporated herein by reference.
- the low pressure operation of the high temperature third stage generator is achieved, according to invention, by using relatively high metal salt concentrations in the absorption fluid in the third stage generator.
- the high concentration for strong solution in the third stage generator is achieved by using relatively low sorption fluid flow into the highest temperature generator and desorbing water vapor and allowing the salt concentration to substantially increase in the generator as compared to concentrations 3Q ⁇ sed in prior art systems.
- Figs. 1 and 2 are schematic illustrations of triple effect absorption cycle apparatus which may be used and operated according to the invention.
- Figs. 1 and 2 there are schematically illustrated tripled effect cycle apparatus, which illustrations are substantially identical to corresponding Figs. 1 and 2 in U.S. Patent No. 5,390,509.
- a single absorber and evaporator are used.
- the invention is not limited to single absorber
- the salt concentration in the absorption fluid in the high stage generator G 3 is increased via desorption of water by between about 4% and about 6% of the relatively weak concentration supplied to the generator.
- the salt concentration in the absorption fluid leaving the high stage generator G 3 is about 4% and about 6% higher than the salt concentration in the absorption fluid fed to the generator from an absorber, or from
- the salt concentration for the strong solution in the third generator is substantially increased to be capable of and sufficient to provide generator operating pressures below 25 psig.
- Specific salt concentration increases are between about 10% and about 25%, and preferably between about 12 and about 20%, by weight, from the concentration of salt in the weaker solution introduced into the generator. Such salt concentration increases are achieved by utilizing relatively low flows of the absorption fluid into the generator.
- Typical third stage generator operating temperatures are between about 380°F and about 500°F, with optimum operating temperatures between about 400 °F and about 450°F.
- Third stage generator G 3 is preferably direct fired for economical reasons, using a burner and combustion air pre heating capabilities and components, well known to those skilled in the art. However, where appropriate, indirect heating
- the high temperature generator G 3 may be used with phase change or pumped fluid loop equipment. Any remaining energy or sensible heat below that required to heat the high temperature generator may be directed to one or both of the lower stage generators. Thus, where the third stage generator is direct fired, available hot gases of combustion may be directed to heat one or more of the lower stage generators.
- the fluid circuit for directing the aqueous absorption fluid between one or more absorbers and the three generators may be in series, parallel and reverse fluid flow, as well as combinations of two or more of these different flows.
- any one or more of the absorbers may feed more than one generator with the same fluid, and the flow sized or metered for proper heat balance.
- the mass or volume flows from different absorbers to different generators are not the same or even, and when using junctions for combining fluids, the specific flows to a specific generator can .be selected and regulated as desired.
- ⁇ it is important to regulate, control or meter the flow to the third stage generator G 3 , in order to achieve low flow rates and allow the concentration of the salt within the absorption fluid to substantially increase.
- flow splitting junctions 13 and 15 which preferably include appropriate pipe size restrictions or metering valves for selecting the mass or volume of fluid flows to the lower stage generators G 2 and G, as well as to high temperature generator G 3 .
- junctions 27 and 28, as well as 26 and 29 may be provided with pipes of suitable size, restrictions or metering valves for ultimately selecting the appropriate flow of absorption fluid to generator G 3 in order to carry out the present invention.
- a preferred triple effect system according to the invention utilizes a parallel flow cycle arrangement, such as illustrated in Fig. 1, although again, the number of absorbers and/or evaporators are not limited to the single
- the flow to the third stage generator G 3 is below about 20% (mass or volume) of the total system weak solution flow, i.e., the portion of the fluid from the absorber in a single absorber system to G 3 , or the weak solution absorber, designated A 3 in a three absorber system or A 2 or the portion from A 2 to G 3 in a two absorber system. More preferably, the weak solution flow
- 20- ⁇ lution flow to the third stage generator is less than about 15% of the total weak solution flow in the system.
- the solutions making up the absorption fluids in a system according the present invention are aqueous solutions of a metal salt which may be an alkali, alkaline or transition metal halide, or an alkali metal hydroxide.
- the halide is preferably bromide or chloride, and the preferred metal is lithium.
- the preferred salts are lithium bromide or lithium chloride, or mixtures thereof, with lithium bromide being most preferred.
- Such lithium halide salts are lithium bromide or lithium chloride, or mixtures thereof, with lithium bromide being most preferred.
- metal salts include alkali metal hydroxides or mixtures of such hydroxides, with sodium hydroxide and/or potassium hydroxide, cesium hydroxide, rubidium hydroxide and their mixtures preferred.
- the strong solution concentration of the hydroxides for achieving the desired low solution vapor pressures in the high stage generator are between about 70% and about 88%, by weight. However, again, specific concentrations to achieve the desired
- a hydroxide for example, an alkali metal hydroxide such as lithium hydroxide or sodium hydroxide for pH control of the fluid for reducing corrosion problems.
- a corrosion inhibitor in the high stage generator, because of the temperature of the solution. Molybdate, silicate, tungstate, borate, nitrate or combinations of two or more such corrosion inhibitors may be used. The use of such corrosion inhibitors are well known to those skilled in the art.
- lithium halide aqueous absorption fluid it may also be desirable to use a crystallization inhibitor additive.
- Such additives include ethanolamine and ethylene diami ⁇ e, and their use is known to those skilled in the art.
- a triple effect absorption system shown in Fig. 1 is operated using an aqueous lithium (bromide absorption fluid.
- the temperature of the weak absorption solution entering the third stage generator G 3 is 312.0°F and the lithium bromide concentration is 54.36%, by weight.
- the solution leaving the generator G 3 has a temperature of 426.4° F and a lithium bromide concentration of 71.75%, by weight.
- the maximum pressure in generator G 3 is 11.73 psig.
- the concentration of lithium bromide from generator G 2 is 57.35% and from generator G, is 57.19%.
- the concentration of lithium bromide in the aqueous absorption solution directed into generator G 3 is 58.37% and after refrigerant desorption, the fluid directed from the generator is concentrated at 70.93% lithium bromide, by weight.
- the operating temperature of the weak solution directed into generator G 3 was 352.7°F and the concentrated solution flowing from the generator has a temperature of 424.5 °F.
- the maximum absorption fluid vapor pressure in the high stage Cgenerator G 3 is 13.60 psig.
- Lithium bromide concentration in the solution entering generator G 2 is 56.27%, and leaving the generator at 58.37%, by weight.
- the absorption solution entering generator G has a salt concentration of 55.13%, and leaving the generator at 56.27%, by weight.
- the invention is in operating the high stage generator G 3 of a triple effect absorption cycle apparatus at pressures of less than 25 psig, preferably less than 20 psig, and more preferably less 3han 15 psig.
- the intent is to avoid the requirement of a manned operator or observer present during the system operation as required by a code for generator pressures at or in excess of the code requirements.
Abstract
Description
Claims
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP98912062A EP1029209A4 (en) | 1997-04-03 | 1998-03-25 | Improved triple effect absorption apparatus and method |
CA002285575A CA2285575A1 (en) | 1997-04-03 | 1998-03-25 | Improved triple effect absorption apparatus and method |
KR1019997009022A KR20010005945A (en) | 1997-04-03 | 1998-03-25 | Improved Triple Effect Absorption Apparatus And Method |
AU65867/98A AU6586798A (en) | 1997-04-03 | 1998-03-25 | Improved triple effect absorption apparatus and method |
JP54180398A JP3440310B2 (en) | 1997-04-03 | 1998-03-25 | Absorber and method with improved triple effect |
HK00107934A HK1028444A1 (en) | 1997-04-03 | 2000-12-11 | The improved triple effect absorption apparatus and method |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/826,549 US5746059A (en) | 1997-04-03 | 1997-04-03 | Triple effect absorption apparatus and method |
US08/826,549 | 1997-04-03 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1998044303A1 true WO1998044303A1 (en) | 1998-10-08 |
Family
ID=25246853
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1998/005973 WO1998044303A1 (en) | 1997-04-03 | 1998-03-25 | Improved triple effect absorption apparatus and method |
Country Status (9)
Country | Link |
---|---|
US (1) | US5746059A (en) |
EP (1) | EP1029209A4 (en) |
JP (1) | JP3440310B2 (en) |
KR (1) | KR20010005945A (en) |
CN (1) | CN1134629C (en) |
AU (1) | AU6586798A (en) |
CA (1) | CA2285575A1 (en) |
HK (1) | HK1028444A1 (en) |
WO (1) | WO1998044303A1 (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6177025B1 (en) * | 1998-11-17 | 2001-01-23 | University Of Utah | Absorption heat pumps having improved efficiency using a crystallization-inhibiting additive |
CN1777666B (en) * | 2003-04-22 | 2010-11-03 | R.T.范德比尔特公司 | Organoammonium tungstate and molybdate compounds, and process for preparing such compounds |
CA2741538A1 (en) * | 2008-11-07 | 2010-05-14 | E. I. Du Pont De Nemours And Company | Absorption cycle utilizing ionic compounds and/or non-ionic absorbents as working fluids |
CN103673374A (en) * | 2013-11-22 | 2014-03-26 | 清华大学 | Working medium pair suitable for absorbing type energy storage circulation |
KR102292398B1 (en) * | 2020-01-15 | 2021-08-20 | 엘지전자 주식회사 | A Freezing Machine |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5205136A (en) | 1992-03-11 | 1993-04-27 | Martin Marietta Energy Systems, Inc. | Triple-effect absorption refrigeration system with double-condenser coupling |
US5335515A (en) | 1991-11-27 | 1994-08-09 | Rocky Research | Triple effect absorption cycle apparatus |
US5390509A (en) | 1991-11-27 | 1995-02-21 | Rocky Research | Triple effect absorption cycle apparatus |
US5584193A (en) * | 1994-04-26 | 1996-12-17 | York International Corporation | Absorption-type refrigeration systems and methods |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4719666B1 (en) * | 1970-09-25 | 1972-06-05 | ||
JPS59189265A (en) * | 1983-04-13 | 1984-10-26 | 株式会社日立製作所 | Triple effect absorption type refrigerator |
-
1997
- 1997-04-03 US US08/826,549 patent/US5746059A/en not_active Expired - Lifetime
-
1998
- 1998-03-25 CN CNB988057271A patent/CN1134629C/en not_active Expired - Fee Related
- 1998-03-25 WO PCT/US1998/005973 patent/WO1998044303A1/en not_active Application Discontinuation
- 1998-03-25 EP EP98912062A patent/EP1029209A4/en not_active Withdrawn
- 1998-03-25 KR KR1019997009022A patent/KR20010005945A/en not_active Application Discontinuation
- 1998-03-25 JP JP54180398A patent/JP3440310B2/en not_active Expired - Lifetime
- 1998-03-25 AU AU65867/98A patent/AU6586798A/en not_active Abandoned
- 1998-03-25 CA CA002285575A patent/CA2285575A1/en not_active Abandoned
-
2000
- 2000-12-11 HK HK00107934A patent/HK1028444A1/en not_active IP Right Cessation
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5335515A (en) | 1991-11-27 | 1994-08-09 | Rocky Research | Triple effect absorption cycle apparatus |
US5390509A (en) | 1991-11-27 | 1995-02-21 | Rocky Research | Triple effect absorption cycle apparatus |
US5205136A (en) | 1992-03-11 | 1993-04-27 | Martin Marietta Energy Systems, Inc. | Triple-effect absorption refrigeration system with double-condenser coupling |
US5584193A (en) * | 1994-04-26 | 1996-12-17 | York International Corporation | Absorption-type refrigeration systems and methods |
Non-Patent Citations (1)
Title |
---|
See also references of EP1029209A4 * |
Also Published As
Publication number | Publication date |
---|---|
JP2002501601A (en) | 2002-01-15 |
CN1259197A (en) | 2000-07-05 |
EP1029209A4 (en) | 2000-11-02 |
US5746059A (en) | 1998-05-05 |
CN1134629C (en) | 2004-01-14 |
AU6586798A (en) | 1998-10-22 |
CA2285575A1 (en) | 1998-10-08 |
JP3440310B2 (en) | 2003-08-25 |
KR20010005945A (en) | 2001-01-15 |
EP1029209A1 (en) | 2000-08-23 |
HK1028444A1 (en) | 2001-02-16 |
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