The present application is the US national stage under 35 U.S.C. §371 of International Application No. PCT/FR2008/051562 which claims the priority of French application 0757841 filed on Sep. 25, 2007, the content of which (description, claims and drawings) is incorporated herein by reference.
This invention concerns a method of calculation and adjustment—also named “control process” in this text—of the absorbing fluid concentration, for example of lithium bromide, in an absorption air-conditioning device.
This invention also involves an absorption air-conditioning device for the implementation of the method.
Finally, this invention involves a vehicle, in particular an automotive vehicle, equipped with such an absorption air-conditioning device.
An absorption air-conditioning device consists diagrammatically of an element in which desorption takes place (denoted “desorber” in the following text), an absorber, a condenser and an evaporator. In order to operate, the desorber and absorber are filled with a mixture of at least two miscible substances formed by a coolant fluid and an absorbing fluid. This mixture is combined in the absorber, in which the absorption of the coolant fluid by the absorbing fluid takes place. The coolant fluid and the absorbing fluid have sufficiently different evaporation pressures so that, when the desorber is heated, the most volatile of the two, that is the coolant fluid, evaporates and changes into a liquid in the condenser.
The desorber receives heat, and this outside contribution permits the evaporation of the liquid coolant from the mixture. This coolant fluid is then condensed in the condenser by cooling. The liquid obtained is trapped and evaporated in the evaporator and thus produces the cold of the air-conditioning. The absorber allows the solution to fix the coolant fluid molecules and, in this way, to maintain a low pressure and, therefore, a low evaporation temperature. The solution/coolant fluid reaction is exothermic. The absorber solution, therefore, must be cooled so that it retains its absorbing power.
A first goal of this invention is to provide a method of calculating and adjusting the concentration of the solution, that means the concentration of absorbing fluid. This permits guaranteeing good control over the risk of crystallization of the aforesaid solution in the entire air conditioning circuit.
Another goal of this invention is to provide such a method, that is faster and as accurate as the known adjustment processes from the prior art.
Another goal of this invention is to provide such a method, that contributes a better reactivity to the air-conditioning device than the one offered by the existing technical solutions.
One goal of this invention is also to provide an absorption air-conditioning device for the implementation of such a method, in which the risk of crystallization of the absorbing fluid in the entire air-conditioning circuit is optimally managed.
Finally, it is also a goal of this invention to provide a vehicle, in particular an automotive vehicle, equipped with such an absorption air-conditioning device which can adjust the absorbing fluid concentration.
To reach these goals, this invention conceives of a new control method of the absorbing fluid concentration in an absorption air-conditioner by including a desorber, a condenser, an evaporator and an absorber. This new process is comprised of the following stages, taken in combination:
According to the preferred mode, the concentration of the absorbing fluid solution is calculated at the output of the desorber by measuring, on the one hand, the coolant vapor pressure in the desorber and simultaneously, on the other hand, the temperature of the absorbing fluid solution at the output of the desorber.
According to the equally preferred mode, the calculation of the concentration at the time t is obtained by using the concentration at the time t−1, and by calculating a corrector for concentration by determining the concentration variation between t−1 and t, the aforesaid calculation of the corrector uses the coolant pressure measurement values and solution temperature at time t.
The calculation of the concentration at the time t responds to the following formula:
in which:
And Ai, Bi (i going from 0 to 3) are the constants pertaining to the absorbing fluid used (lithium bromide, for example).
In a preferential manner, the head loss is increased or decreased in the duct connecting the desorber to the condenser by operating a valve, for example a butterfly valve, arranged inside the aforesaid duct.
By preference, but without restricting the object of this invention, the absorbing fluid is lithium bromide, and the constants Ai, Bi (i going from 0 to 3) have the values determined experimentally and pertaining to this type of fluid.
The coolant fluid is, by preference, water.
This invention also provides an absorption air-conditioning device for the implementation of the method in conformity with what is described above in outline. This device includes, in a classic manner, a desorber, a condenser, an evaporator and an absorber. But, the desorber of this new device includes a pressure sensor for the measurement of the vapor pressure of the coolant of the aforesaid desorber and a temperature sensor for measuring the temperature of the absorbing fluid solution at the output of the desorber. Further, this new device includes a means to vary the head loss in the duct conducting the coolant fluid vapor to the condenser.
By preference, the means to vary the head loss in the duct leading the coolant fluid vapor to the condenser is a regulating valve, of the butterfly type.
According to the preferred embodiment, the desorber of the device includes a main heat exchange system of the plates type system, located over the tank of absorbing fluid solution, and a plate exchanger to reheat the solution going into the main thermal exchange system with the solution coming down from the solution tank.
In addition, an additional heating system of the solution, of the electrical resistance type, can bathe in the solution tank.
Finally, the invention supplies a vehicle, by preference an automotive vehicle, characterized in that it includes a absorption air-conditioning device of the type, conforming to the one described above in outline.
Other goals, advantages and features of the invention shall appear in the description of a preferred mode of embodiment, unrestricted in the object and the scale of this patent application, accompanied by drawings in which:
In reference to the drawing of
Water as vapor is then conducted by the piping 20 into the condenser 200 to be condensed by the cooling action of the outside air (cooling contribution illustrated diagrammatically by the arrow B). Water in liquid phase is conducted by the piping 10 into the evaporator 300. The cold produced at the time of the evaporation is transmitted to the cabin of the vehicle (not represented), as illustrated diagrammatically by the arrow C. For this purpose, a pump 310 and a forced convection air cooler 320 are provided, that are joined to the evaporator 300 by the piping 11, 12 and 13. The piping assembly 10 to 13 forms the water circuit in the liquid phase. The water vapor that comes out of the evaporator 300 is brought into the absorber 400 by the piping 21. The solution is cooled by the outside air to absorb the water vapor (cooling contribution illustrated diagrammatically by the arrow D). For this purpose, a pump 410 and a radiator 420 are provided, that are connected to the absorber 400 by the piping 16, 17, 18 and 19. The absorber 400 is connected to the desorber 100 by the piping 14, 15 and 16. The piping assembly 14 to 19 forms the salt solution circuit.
The concentration of the solution S at the output of the desorber 100 is the highest in the entire circuit of the air-conditioning device.
By concentration of the solution, designated X, one understands the ratio between the mass of absorbing fluid (lithium bromide, for example) and the total mass of the absorbing fluid and cooling fluid mixture of the two fluids.
The concentration of absorbing fluid is determined to depend on the two following physical measurements:
Calculation of the Concentration
The concentration X is linked to the temperature of coolant (water) te and to the temperature of the solution ts by the following relationship, designated R1:
In which, the constants have the following values:
The coolant vapors extracted from the desorber 100 are in the saturated state. Consequently, it is possible to connect the measured pressure P to a coolant temperature te.
We use, for example, the following formula:
With P in kPa (kilo Pascals) and te in ° C., we have the following relationship, designated R2:
in which the constants have the following values:
From the relationship R1 stated previously, we draw:
Solution of the Equation.
The temperature te is calculated using the pressure measurement and the equation designated R2 stated previously. The temperature is is the temperature of the solution S at the output 15 of the desorber 100.
The resolution of the equation R1 normally takes place using an iterative method. In general, three iterations are required to converge on the solution sought. The interest of the method presented is to achieve only a single iteration by taking the starting concentration as determined at time t−1.
We have, therefore, only one equation to solve of the type:
Xt=f(Xt−1,P,ts) or Xt=f(Xt−1,te,ts)
If we use a Newton type formula, for example, we obtain a formula R1 equivalent to:
Xt−1 is the concentration at the acquisition time t−1
It should be noted that the calculation of f(X) and of f′(X) uses the concentration at time t−1 and the measurements of pressure P of the coolant and temperature ts of the solution at time t.
In reality, only a concentration corrector is calculated which determines the variation of concentration according to new measured values of pressure and temperature.
The concentration of the solution is fixed at time t=0 as desired. For example, we fix Xt=0=60%.
The concentration of the solution at time t=0 can also be fixed according to the shut-off strategy used. For example, if one envisages, at the time of the last shut-down, a target concentration of 58%, the concentration at t=0 will be fixed at 58%.
Adjustment of the Concentration.
The calculation of the concentration, as described above, permits controlling the risk of crystallization of the salt solution (LiBr).
According to this invention, the adjustment of the concentration is based on the control of the condensation.
If the calculated concentration approaches a predetermined critical value, the head loss is increased in the duct 20 leading to the condenser 200 by activating, for example, a butterfly valve 103, represented diagrammatically in
Design of the Desorber
In reference to the drawing of
The previously referenced regulating valve 103 of the desorber performance is used and situated in the piping 20 between the desorber 100 and the condenser 200.
In a preferential manner, and in reference to
A plate exchanger 160 is incorporated within the desorber 100. The exchanger 160 functions to heat the solution going into the main exchange zone ZET with the solution coming down from the solution tank 140. The solution tank 140 is completely separated from the principal heating system by the coolant liquid of the motor. We can therefore free ourselves from a “by-pass” of the hot water required to permit a fast rise in the motor temperature.
The solution circuit is represented by the arrowed lines of the input 110 at the output 111 of the solution.
An additional heating system of the solution, of an electrical resistance type, not shown in
The main exchange system ZET is a plate type system permitting sufficient compaction of the device.
Valve 103, situated in the piping 20 leading to the condenser, permits controlling the concentration more quickly than by adjustment of the power contributed to the desorber 100. Valve 103 also permits dispensing with an adjustment of the exchange capacity of the condenser 200.
If the pressure in the condenser 200 is very low, there is a risk that the coolant cannot circulate from the condenser 200 to the coolant reserve of the absorber 400. Effectively, on an automotive vehicle, an operating difference in level cannot be guaranteed in all cases compatible with a gravity flow between the condensation zone and the evaporation zone. With the solution of this invention, we can open the valve 103 briefly to increase the pressure in the condenser and, thereby, “push” the coolant into the absorber's circuit.
The invention described above presents many advantages, among which are the following advantages:
The calculation method of the absorbing solution concentration stated above is faster and as accurate as the concentration calculation methods of the solutions known from the prior art.
The calculation method of the invention permits managing the risk of crystallization of the absorbing fluid, the lithium bromide for example, in the entire air-conditioning circuit.
The adjustment of the concentration by the control of the condensation contributes a better reactivity to the system. Effectively, the technical solutions known from the prior art generally consist in reducing the energy contribution to the desorber by activation of a valve that regulates the incoming hot water flow. These solutions, because of the thermal inertia brought into play, are a lot less effective than the solution from the invention that proposes a shutdown of the condensation, which shutdown has an almost immediate effect. Further, for an automotive application, the performances of the front panel (and therefore the condenser) can vary widely. The installation of a regulating valve between the desorber and the condenser, in accordance with this invention, permits isolating the condenser from the rest of the air-conditioning circuit.
Of course, this invention is not limited to the mode of embodiment described above as an example; other modes of embodiment can be conceived by a person skilled in the art without leaving the scope and the range of this invention.
Number | Date | Country | Kind |
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07 57841 | Sep 2007 | FR | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/FR2008/051562 | 9/2/2008 | WO | 00 | 3/24/2010 |
Publishing Document | Publishing Date | Country | Kind |
---|---|---|---|
WO2009/044034 | 4/9/2009 | WO | A |
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4596122 | Kantner | Jun 1986 | A |
5477696 | Takahata | Dec 1995 | A |
5586447 | Sibik | Dec 1996 | A |
6192694 | Hiro et al. | Feb 2001 | B1 |
6694772 | Inoue et al. | Feb 2004 | B2 |
Number | Date | Country |
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54131160 | Oct 1979 | JP |
58096963 | Jun 1983 | JP |
59086876 | May 1984 | JP |
61143665 | Jul 1986 | JP |
62069074 | Mar 1987 | JP |
62155478 | Jul 1987 | JP |
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11230633 | Aug 1999 | JP |
Entry |
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Search Report from corresponding International Application No. PCT/FR2008/051562, mailed Jun. 2, 2009. |
Number | Date | Country | |
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20100192603 A1 | Aug 2010 | US |