BACKGROUND
[0001] This disclosure relates generally to chiller systems used in air conditioning systems,
and more particularly to a purge system for removing contaminants from a refrigeration
system.
[0002] Chiller systems such as those utilizing centrifugal compressors may include sections
that operate below atmospheric pressure. As a result, leaks in the chiller system
may draw air into the system, contaminating the refrigerant. This contamination degrades
the performance of the chiller system. To address this problem, existing low pressure
chillers include a purge unit to remove contamination. Existing purge units use a
vapor compression cycle to separate non-condensable gas from the refrigerant. Existing
purge units are complicated and lose refrigerant in the process of removing contamination.
BRIEF DESCRIPTION
[0003] Disclosed is a refrigeration system including a heat transfer fluid circulation loop
configured to allow a refrigerant to circulate therethrough. A purge gas outlet is
in operable communication with the heat transfer fluid circulation loop. The system
also includes at least one gas permeable membrane having a first side in operable
communication with the purge gas outlet and a second side. The membrane includes a
separation layer including a porous inorganic material with pores of a size to allow
passage of contaminants through the membrane and restrict passage of the refrigerant
through the membrane, and a polymer coating over the separation layer. A permeate
outlet is in operable communication with the second side of the membrane.
[0004] In some embodiments, the system further includes a prime mover operably coupled to
the permeate outlet, and the prime mover is configured to move gas from the second
side of the membrane to an exhaust port leading outside the fluid circulation loop.
[0005] In any one or combination of the foregoing embodiments, the heat transfer fluid circulation
loop includes a compressor, a heat rejection heat exchanger, an expansion device,
and a heat absorption heat exchanger, connected together in order by conduit, and
the purge gas outlet is in operable communication with at least one of the heat rejection
heat exchanger, the heat absorption heat exchanger, or the membrane.
[0006] In any one or combination of the foregoing embodiments, the system further includes
a retentate return conduit operably coupling the first side of the membrane to the
fluid circulation loop. In some embodiments, the prime mover is a vacuum pump.
[0007] In any one or combination of the foregoing embodiments, the system further includes
a purge gas collector operably coupled to the purge outlet and the membrane.
[0008] In some embodiments, the system further includes a prime mover operably coupled to
the permeate outlet, the prime mover configured to move gas from the second side of
the membrane to an exhaust port leading outside the fluid circulation loop. In some
embodiments, the prime mover includes a vacuum pump in operable communication with
the second side of the membrane.
[0009] In any one or combination of the foregoing embodiments, the system further includes
a filter in operable communication with the purge outlet and the first side of the
membrane.
[0010] In any one or combination of the foregoing embodiments, the separation layer includes
a ceramic material.
[0011] In any one or combination of the foregoing embodiments, wherein the membrane includes
zeolite.
[0012] In any one or combination of the foregoing embodiments, the at least one gas permeable
membrane includes a plurality of gas permeable membranes; wherein the plurality of
gas permeable membranes are arranged in serial or parallel communication.
[0013] In any one or combination of the foregoing embodiments, the polymer layer includes
a polymer selected from a silicone rubber, fluorosilicone or polyimide.
[0014] In any one or combination of the foregoing embodiments, the polymer layer has a thickness
of 0.05 µm to 50 µm.
[0015] In any one or combination of the foregoing embodiments, the system further includes
a controller configured to operate the fluid circulation loop in response to a cooling
demand signal and to operate the prime mover in response to a determination of contaminants
in the fluid circulation loop.
[0016] In any one or combination of the foregoing embodiments, the controller is configured
to activate a purge back-flush mode in which gas is transported from the second side
of the membrane to the first side of the membrane.
[0017] In any one or combination of the foregoing embodiments, the controller is configured
to activate a heat source to heat the membrane to a temperature to remove contaminants.
[0018] Also disclosed is a method of operating a refrigeration system, comprising circulating
a refrigerant through a heat transfer fluid circulation loop in response to a cooling
demand signal. Purge gas comprising contaminants is collected from a purge outlet
in the fluid circulation loop. The contaminants are transferred across a permeable
molecular sieve membrane with a prime mover, said membrane comprising a porous inorganic
or metal organic framework with pores of a size to allow passage of the contaminants
through the membrane and restrict passage of the refrigerant through the membrane.
The method also includes periodically back-flushing the membrane by transporting gas
from the second side of the membrane to the first side of the membrane, or periodically
heating the membrane to a temperature to remove contaminants, or both periodically
transporting gas from the second side of the membrane to the first side of the membrane
and periodically heating the membrane to a temperature to remove contaminants.
[0019] In any one or combination of the foregoing embodiments, the method includes periodically
back-flushing the membrane by transporting gas from the second side of the membrane
to the first side of the membrane.
[0020] In any one or combination of the foregoing embodiments, the method also includes
periodically heating the membrane to a temperature to remove contaminants.
[0021] In any one or combination of the foregoing embodiments, the method also includes
passing the purge gas through a filter before reaching the membrane.
[0022] In any one or combination of the foregoing embodiments, the method also includes
transporting the contaminants through a polymer coating on the inorganic or metal
organic framework membrane.
[0023] In any one or combination of the foregoing embodiments, the method also includes
collecting the purge gas in a purge gas collector between the purge outlet and the
membrane.
[0024] In any one or combination of the foregoing embodiments, the method also includes
returning refrigerant from the first side of the membrane to the fluid circulation
loop.
BRIEF DESCRIPTION OF THE DRAWINGS
[0025] The following descriptions should not be considered limiting in any way. With reference
to the accompanying drawings, like elements are numbered alike:
FIG. 1 is a schematic depiction of a refrigeration system including a vapor compression
heat transfer refrigerant fluid circulation loop;
FIG. 2 is a schematic depiction of an example embodiment of a membrane purge system
for a refrigeration system;
FIG. 3 is a schematic depiction of a separation membrane;
FIG. 4 is a schematic depiction of an example embodiment of a membrane purge system
with purge collector and relevant components of a vapor compression heat transfer
refrigerant fluid circulation loop; and
FIG. 5 is a schematic depiction of another example embodiment of a membrane purge
system with purge collector and relevant components of a vapor compression heat transfer
refrigerant fluid circulation loop.
DETAILED DESCRIPTION
[0026] A detailed description of one or more embodiments of the disclosed apparatus and
method are presented herein by way of exemplification and not limitation with reference
to the Figures.
[0027] With reference to FIG. 1, a heat transfer fluid circulation loop such as can be used
in a chiller is shown in block diagram form in FIG. 1. As shown in FIG. 1, a compressor
10 pressurizes heat transfer fluid in its gaseous state, which both heats the fluid
and provides pressure to circulate it throughout the system. In some embodiments,
the heat transfer fluid, or refrigerant, comprises an organic compound. In some embodiments,
the refrigerant comprises a hydrocarbon or substituted hydrocarbon. In some embodiments,
the refrigerant comprises a halogen-substituted hydrocarbon. In some embodiments,
the refrigerant comprises a fluoro-substituted or chloro-fluoro-substituted hydrocarbon.
The hot pressurized gaseous heat transfer fluid exiting from the compressor 10 flows
through conduit 15 to heat exchanger condenser 20, which functions as a heat exchanger
to transfer heat from the heat transfer fluid to the surrounding environment, resulting
in condensation of the hot gaseous heat transfer fluid to a pressurized moderate temperature
liquid. The liquid heat transfer fluid exiting from the condenser 20 flows through
conduit 25 to expansion valve 30, where the pressure is reduced. The reduced pressure
liquid heat transfer fluid exiting the expansion valve 30 flows through conduit 35
to heat exchanger evaporator 40, which functions as a heat exchanger to absorb heat
from the surrounding environment and boil the heat transfer fluid. Gaseous heat transfer
fluid exiting the evaporator 40 flows through conduit 45 to the compressor 10, thus
completing the heat transfer fluid loop. The heat transfer system has the effect of
transferring heat from the environment surrounding the evaporator 40 to the environment
surrounding the condenser 20. The thermodynamic properties of the heat transfer fluid
must allow it to reach a high enough temperature when compressed so that it is greater
than the environment surrounding the condenser 20, allowing heat to be transferred
to the surrounding environment. The thermodynamic properties of the heat transfer
fluid must also have a boiling point at its post-expansion pressure that allows the
temperature surrounding the evaporator 40 to provide heat to vaporize the liquid heat
transfer fluid.
[0028] With reference now to FIG. 2, there is shown an example embodiment of a purge system
that can be connected to a vapor compression heat transfer fluid circulation loop
such as FIG. 1. As shown in FIG. 2, the purge system receives gas comprising refrigerant
gas and contaminants (e.g., nitrogen, oxygen, water vapor) through a connection 52
to a membrane separator 54 on a first side of a membrane 56. A prime mover such as
a vacuum pump 58 connected to the membrane separator 54 through connection 60 provides
a driving force to pass the contaminants through the membrane 56 and exit the system
from a second side of the membrane 56 through an outlet 62. In some embodiments, the
prime mover can be in the fluid loop, e.g., a refrigerant pump or compressor. Refrigerant
gas remains on the first side of the membrane 56 and can return to the fluid circulation
loop through connection 64.
[0029] The membrane 56 comprises a porous inorganic material. Examples of porous inorganic
materials can include ceramics such as metal oxides or metal silicates, more specifically
aluminosilicates (e.g., Chabazite Framework (CHA) zeolite, Linde type A (LTA) zeolite,
porous carbon, porous glass, clays (e.g., Montmorillonite, Halloysite). Porous inorganic
materials can also include porous metals such as platinum and nickel. Hybrid inorganic-organic
materials such as a metal organic framework (MOF) can also be used. Other materials
can be present in the membrane such as a carrier in which a microporous material can
be dispersed, which can be included for structural or process considerations.
[0030] Metal organic framework materials comprise metal ions or clusters of metal ions coordinated
to organic ligands to form one-, two- or three-dimensional structures. A metal-organic
framework can be characterized as a coordination network with organic ligands containing
voids. The coordination network can be characterized as a coordination compound extending,
through repeating coordination entities, in one dimension, but with cross-links between
two or more individual chains, loops, or spiro-links, or a coordination compound extending
through repeating coordination entities in two or three dimensions. Coordination compounds
can include coordination polymers with repeating coordination entities extending in
one, two, or three dimensions. Examples of organic ligands include, but are not limited
to, bidentate carboxylates (e.g., oxalic acid, succinic acid, phthalic acid isomers,
etc.), tridentate carboxylates (e.g., citric acid, trimesic acid), azoles (e.g., 1,2,3-triazole),
as well as other known organic ligands. A wide variety of metals can be included in
a metal organic framework. Examples of specific metal organic framework materials
include but are not limited to zeolitic imidazole framework (ZIF), HKUST-1.
[0031] In some embodiments, pore sizes can be characterized by a pore size distribution
with an average pore size from 2.5 Å to 10.0 Å, and a pore size distribution of at
least 0.1 Å. In some embodiments, the average pore size for the porous material can
be in a range with a lower end of 2.5 Å to 4.0 Å and an upper end of 2.6 Å to 10.0
Å. Å. In some embodiments, the average pore size can be in a range having a lower
end of 2.5 Å, 3.0 Å, 3.5 Å, and an upper end of 3.5 Å, 5.0 Å, or 6.0 Å. These range
endpoints can be independently combined to form a number of different ranges, and
all ranges for each possible combination of range endpoints are hereby disclosed.
Porosity of the material can be in a range having a lower end of 5 %, 10 %, or 15
%, and an upper end of 85 %, 90 %, or 95 % (percentages by volume). These range endpoints
can be independently combined to form a number of different ranges, and all ranges
for each possible combination of range endpoints are hereby disclosed.
[0032] The above microporous materials can be can be synthesized by hydrothermal or solvothermal
techniques (e.g., sol-gel,) where crystals are slowly grown from a solution. Templating
for the microstructure can be provided by a secondary building unit (SBU) and the
organic ligands. Alternate synthesis techniques are also available, such as physical
vapor deposition or chemical vapor deposition, in which metal oxide precursor layers
are deposited, either as a primary microporous material, or as a precursor to an MOF
structure formed by exposure of the precursor layers to sublimed ligand molecules
to impart a phase transformation to an MOF crystal lattice.
[0033] In some embodiments, the above-described inorganic or MOF membrane materials can
provide a technical effect of promoting separation of contaminants (e.g., nitrogen,
oxygen, or water molecules) from refrigerant gas, and low refrigerant loss. Other
membrane materials, such as porous and non-porous polymers can be subject to solvent
interaction with the matrix material, which can interfere with effective separation.
In some embodiments, the capabilities of the materials described herein can provide
a technical effect of promoting the implementation of various example embodiments
of refrigeration systems with purge, as described in more detail with reference to
the example embodiments below. For example, non-porous polymers are typically used
as membranes in air separation, operating on a mechanism known as "solution-diffusion",
whereby molecules are separated by first dissolving into the polymer matrix and then
diffusing at different rates across the membrane layer. In most instances, separation
is accomplished based on differences in the size of the molecules. However, while
refrigerant molecules are much larger than non-condensable air and water vapor molecules,
they have been found to have very high solubility into such polymer films, which results
in lower separation factors than anticipated based on molecular size.
[0034] As mentioned above, the microporous molecular sieve material can be disposed on a
gas permeable inorganic porous support such as alumina or zirconia, or other porous
ceramic or metallic (e.g., Fe, Ni) material. Thickness of the support can range from
10 µm to 10 mm, more specifically from 100 nm to 750 nm, and even more specifically
from 250 nm to 500 nm. In the case of tubular membranes 70 as described in FIG. 3,
fiber diameters can range from 0.1 mm to 100 mm, and fiber lengths can range from
0.02 m to 2 m.
[0035] In some embodiments, the microporous material can be deposited on the support as
particles in a powder or dispersed in a liquid carrier using various techniques such
as spray coating, dip coating, solution casting, etc. The dispersion can contain various
additives, such as dispersing aids, rheology modifiers, etc. Polymeric additives can
be used; however, a polymer binder is not needed, although a polymer binder can be
included and in some embodiments is included. However, a polymer binder present in
an amount sufficient to form a contiguous polymer phase can provide passageways in
the membrane for larger molecules to bypass the molecular sieve particles. Accordingly,
in some embodiments a polymer binder is excluded. In other embodiments, a polymer
binder can be present in an amount below that needed to form a contiguous polymer
phase, such as embodiments in which the membrane is in series with other membranes
that may be more restrictive. In some embodiments, particles of the microporous material
(e.g., particles with effective diameter of 0.01 µm to 10 mm, or in some embodiments
from 0.5 µm to 10 µm, can be applied as a powder or dispersed in a liquid carrier
(e.g., an organic solvent or aqueous liquid carrier) and coated onto the support followed
by removal of the liquid. In some embodiments, the application of solid particles
of microporous material from a liquid composition to the support surface can be assisted
by application of a pressure differential across the support. For example a vacuum
can be applied from the opposite side of the support as the liquid composition comprising
the solid microporous particles to assist in application of the solid particles to
the surface of the support.
[0036] In some exemplary embodiments, the layer is applied with a vacuum enhanced dip coating
process where a surface of the support is contacted with a liquid dispersion of the
microporous material dispersion while a vacuum is applied from the opposite side of
the support (or in the case of hollow tube membrane configuration of FIG. 3, the tubular
support 72 can be immersed in the liquid except for the open ends). The vacuum will
draw solvent from the dispersion through the porous support, resulting in deposition
of the microporous particles onto the support. In the case of hollow fiber membranes
as shown in FIG. 3, this vacuum filtration technique can be particularly effective,
as the hollow core 76 provides an enclosed space from which to draw a vacuum without
the necessity of a vacuum frame or similar structure that would be needed for a flat
or planar membrane configuration.
[0037] After coating a layer of microporous particles onto the support, the layer can be
dried to remove residual solvent and optionally heated to fuse the microporous particles
together into a contiguous layer. Exemplary heating conditions can be in a range having
at temperatures of at least 50°C, 75°C, or 100°C, more specifically from 20°C to 75°C,
and even more specifically from 20°C to 50°C.
[0038] Various membrane structure configurations can be utilized, including but not limited
to, flat or planar configurations, tubular configurations, or spiral configurations.
An example embodiment of a tubular configuration is schematically depicted in FIG.
3. As shown in FIG. 3, a tubular membrane 70 comprises a porous support configured
as tubular shell 72 surrounded by a molecular sieve layer 74. Thickness of the molecular
sieve layer can range from 2 nm to 500 nm, more specifically from 2 nm to 100 nm,
and even more specifically from 2 nm to 50 nm. The shell 72 defines a hollow core
76 that is open at both ends. In some embodiments, multiple tubular membranes are
disposed together in a tube bank with a header (not shown) at each end in fluid communication
with the hollow cores 76. In use, purge gas comprising refrigerant gas and contaminants
is delivered to the exterior of the membrane 70 at a greater pressure than that inside
the hollow cores 76 (e.g., by drawing a vacuum on the hollow cores 76 through the
headers). This pressure differential provides a driving force for non-condensable
nitrogen, oxygen or water molecules to pass through the molecular sieve layer while
the larger refrigerant molecules are restricted from passage through the molecular
sieve layer 74.
[0039] In some embodiments, the microporous material can be configured as nanoplatelets
such as zeolite nanosheets. Zeolite nanosheet particles can have thicknesses ranging
from 2 to 50 nm, more specifically 2 to 20 nm, and even more specifically from 2 nm
to 10 nm. The mean diameter of the nanosheets can range from 50 nm to 5000 nm, more
specifically from 100 nm to 2500 nm, and even more specifically from 100 nm to 1000
nm. Mean diameter of an irregularly-shaped tabular particle can be determined by calculating
the diameter of a circular-shaped tabular particle having the same surface area in
the x-y direction (i.e., along the tabular planar surface) as the irregularly-shaped
particle. Zeolite such as zeolite nanosheets can be formed from any of various zeolite
structures, including but not limited to, framework type MFI, MWW, FER, LTA, FAU,
and mixtures of the preceding with each other or with other zeolite structures. In
a more specific group of exemplary embodiments, the zeolite such as zeolite nanosheets
can comprise zeolite structures selected from MFI, MWW, FER, LTA framework type. Zeolite
nanosheets can be prepared using known techniques such as exfoliation of zeolite crystal
structure precursors. For example, MFI and MWW zeolite nanosheets can be prepared
by sonicating the layered precursors (multilamellar silicalite-1 and ITQ-1, respectively)
in solvent. Prior to sonication, the zeolite layers can optionally be swollen, for
example with a combination of base and surfactant, and/or melt-blending with polystyrene.
The zeolite layered precursors are typically prepared using conventional techniques
for preparation of microporous materials such as sol-gel methods.
[0040] With reference again to FIG. 3, a polymer coating 78 is disposed over the molecular
sieve layer 74. The polymer can be virtually any type of polymer that is resistant
to erosion by the refrigerant as a solvent and is capable of being coated onto the
molecular sieve layer, including but not limited to silicone polymers (i.e., polysiloxanes),
fluorosilicones, or polyimides. The polymer coating can be applied by any technique
including but not limited to spray coating, dip coating, roll coating, or extrusion,
followed by curing of the polymer coating. In some embodiments, the polymer coating
78 can be permeable to both refrigerant gas and the contaminants, through either or
both of porosity sieving or polymer solvent effects. In some embodiments, the polymer
coating 78 can allow for passage of both types of gases via a solution-diffusion mechanism.
In some embodiments, the polymer coating can have a thickness in a range with a lower
end of 0.05 µm, 0.1 µm, 0.5 µm, and an upper end of 4 µm, 10 µm, or 50 µm. These range
endpoints can be independently combined to form a number of different ranges, and
all ranges for each possible combination of range endpoints are hereby disclosed.
In some embodiments, the polymer coating can provide a technical effect of protecting
the molecular sieve layer 74 from exposure to contaminants such as oils, or to physical
damage. In some embodiments, the polymer coating can provide a technical effect of
reducing leakage of refrigerant across the membrane through pinholes. Although the
polymer coating may not be impervious to refrigerant molecules, it can fill in any
pinholes and significantly reduce the rate of mass transfer through any such pinholes.
The inorganic layer 74 may also contain grain boundaries, through which larger refrigerant
molecules can pass, which reduces the layer's selectivity. The polymer coating can
mask such grain boundaries, thereby reducing refrigerant permeance through the membrane.
[0041] With reference now to FIG. 4, another purge system is shown along with selected components
of the refrigerant fluid circulation loop of FIG. 1. As shown in FIG. 4, a purge collector
66 receives gas vented from the condenser 20. In some embodiments, the connection
of the vent line to the condenser can be made at a high point of the condenser structure.
In some embodiments, the purge collector can provide a technical effect of promoting
higher concentrations of contaminants at the membrane, which can promote more effective
mass transfer and separation. This effect can occur through a stratification of gas
in the purge collector in which lighter contaminants concentrate toward the top of
the purge collector and heavier refrigerant gas concentrates toward the bottom of
the purge collector. In some embodiments, the purge collector 66 can be any kind of
vessel or chamber with a volume or cross-sectional open space to provide for collection
of purge gas and for a low gas velocity during operation of the purge system vacuum
pump 58 to promote stratification. Stratification can also occur at any time when
the purge system is not operating (including during operation of the refrigeration
system fluid circulation loop), as the purge collector 66 remains in fluid communication
with the condenser vent line with essentially stagnant gas in the purge collector.
Other embodiments can also be employed to promote higher concentrations of contaminants
at the membrane separator 54, as discussed in more detail below.
[0042] In some embodiments, refrigerant from the first side of membrane 56 can be returned
to the refrigerant fluid circulation loop. As shown in FIG. 4, a connection 67 returns
retentate gas from the first side of membrane 56 to the refrigerant fluid circulation
loop at the evaporator 40, through a control device such as expansion valve 68 utilized
to accommodate the pressure differential between the first side of the membrane 56
(which is close to the pressure at the condenser 20) and pressure at the evaporator
40. It should be noted that the control device can control either or both flow through
or pressure drop across the control device, and expansion valve 68 is shown as an
integrated control device unit that performs both functions for ease of illustration,
but could be separate components such as a control valve and an expansion orifice.
In some embodiments, utilization of a bypass refrigerant return can provide a technical
effect of promoting greater concentrations of contaminants at the first side of membrane
56 by removing gas at the membrane 56 that is concentrated with refrigerant after
removal of contaminant gas molecules through the membrane 56, so that refrigerant-concentrated
gas can be displaced with gas from the purge collector 66 that has a higher concentration
of contaminants. The connection 67 can also include a control or shut-off valve, which
can be integrated with an expansion device (i.e., an expansion valve), as described
in more detail in
US patent application Serial No. 62/584,012, the disclosure of which is incorporated herein by reference in its entirety. In
alternative embodiments (not shown), the bypass conduit 67 can return refrigerant-laden
gas to a colder side of the condenser 20 or inlet of the compressor 10, in which case
an expansion device may not be needed due to lower pressure differential compared
to that of a bypass return to the evaporator 40. In such as case, the connection 67
can utilize a control device such as a control or shut-off valve 68 that does not
provide gas expansion. Other system variations such as centrifugal separators or chilling
coils integrated with a purge chamber, pumped recycle of permeate back to the retentate
(upstream) side of the membrane, cascaded multiple membranes, or alternative prime
movers such as a thermal prime mover or a pump or compressor in the fluid circulation
loop, are described in more detail in US patent application Serial No._/_, entitled
"Refrigeration Purge System", filed on even date herewith under attorney docket number
98251US01 (U301399US), the disclosure of which is incorporated herein by reference
in its entirety.
[0043] Additional embodiments can also be employed to protect or promote durability of the
membrane. For example, in some embodiments a controller (not shown) in operative communication
with various sensing and control components of the system can be configured to periodically
activate a purge backflush in which gas is transported from the second (i.e., permeate)
side of the membrane to the first (i.e., retentate) side of the membrane. As used
herein, "periodically" means that activation can be based on any sort of criteria
including human operator activation, or predetermined criteria including but not limited
to the passage of time, accumulated system operating time, accumulated system purge
cycle time, or measured system criteria such as measured pressure differential across
the membrane during purge cycle operation of the prime mover. The backflush mode can
be activated by isolating the membrane separator 54 from the purge collector 66 and
reversing the direction of the driving force. For example, in the example embodiments
of FIGS. 4-5, this can be accomplished by switching a 3-way valve (not shown) in the
conduit between the purge collector 66 and the membrane separator 54 to simultaneously
connect a bypass line (not shown) from the three-way valve connecting the suction
side of the vacuum pump 58 and the first side of the membrane 56 while isolating the
first side of the membrane 56 from the purge collector 66. A similar 3-way valve connection
can be employed at the suction side of the vacuum pump 58 to redirect the vacuum pump
connection between the second side of the membrane 56 or to the bypass line to the
first side of the membrane 56. In some embodiments, the controller can be configured
to periodically expose the membrane 56 to heat to remove contaminants such as oil.
In some embodiments, the membrane can be heated to at least 200°C, or to at least
300°C, or to at least 400°C. Heating can generally be kept under 200°C in order to
prevent degradation of the polymer layer 78, save energy and simplify thermal management.
[0044] In some embodiments, durability and protection of the membrane 56 can be promoted
by a filter such as a coalescing filter, moisture filter, or particulate filter between
the purge outlet and the membrane 56. In the example embodiment shown in FIG. 5, a
coalescing filter 79 is disposed in the gas flow path between the purge collector
66 and the membrane separator 54. One type of coalescing filter can have a cylindrical
inner rigid open mesh core (e.g., stainless steel) around which a fiber coalescing
medium (e.g., borosilicate glass fiber) is disposed. In some embodiments, the coalescing
medium can have a gradient pore structure by using layers of increasing pore size.
The inlet gas first encounters the smallest pores, which increase with penetration
distance to allow more space as the coalesced droplets grow. The coalescing medium
can be supported by an outer mesh structure to provide mechanical strength which is
then followed by a coarse outer wrap that serves as a drainage zone. Gas flows into
the hollow core of the cylinder and then radially outward through the filter media.
Tiny liquid droplets are captured by the inner filter media and coalesce into larger
liquid droplets that are captured and removed in the radially outward drainage zone.
[0045] The term "about", if used, is intended to include the degree of error associated
with measurement of the particular quantity based upon the equipment available at
the time of filing the application. For example, "about" can include a range of ±
8% or 5%, or 2% of a given value.
[0046] The terminology used herein is for the purpose of describing particular embodiments
only and is not intended to be limiting of the present disclosure. As used herein,
the singular forms "a", "an" and "the" are intended to include the plural forms as
well, unless the context clearly indicates otherwise. It will be further understood
that the terms "comprises" and/or "comprising," when used in this specification, specify
the presence of stated features, integers, steps, operations, elements, and/or components,
but do not preclude the presence or addition of one or more other features, integers,
steps, operations, element components, and/or groups thereof.
[0047] While the present disclosure has been described with reference to an exemplary embodiment
or embodiments, it will be understood by those skilled in the art that various changes
may be made and equivalents may be substituted for elements thereof without departing
from the scope of the present disclosure. In addition, many modifications may be made
to adapt a particular situation or material to the teachings of the present disclosure
without departing from the essential scope thereof. Therefore, it is intended that
the present disclosure not be limited to the particular embodiment disclosed as the
best mode contemplated for carrying out this present disclosure, but that the present
disclosure will include all embodiments falling within the scope of the claims.
1. A refrigeration system comprising
a heat transfer fluid circulation loop configured to allow a refrigerant to circulate
therethrough;
a purge gas outlet in operable communication with the heat transfer fluid circulation
loop;
at least one gas permeable membrane having a first side in operable communication
with the purge gas outlet and a second side, said membrane comprising a separation
layer comprising a porous inorganic material with pores of a size to allow passage
of contaminants through the membrane and restrict passage of the refrigerant through
the membrane, and a polymer coating over said separation layer; and
a permeate outlet in operable communication with the second side of the membrane.
2. The refrigeration system of claim 1, further comprising a prime mover operably coupled
to the permeate outlet, the prime mover configured to move gas from the second side
of the membrane to an exhaust port leading outside the fluid circulation loop.
3. The refrigeration system of claim 1, wherein the heat transfer fluid circulation loop
comprises a compressor, a heat rejection heat exchanger, an expansion device, and
a heat absorption heat exchanger, connected together in order by conduit;
wherein the purge gas outlet is in operable communication with at least one of the
heat rejection heat exchanger, the heat absorption heat exchanger, or the membrane.
4. The refrigeration system of claim 2 wherein the prime mover comprises a vacuum pump
in operable communication with the second side of the membrane.
5. The refrigeration system of any of claims 1-4, further comprising a filter in operable
communication with the purge outlet and the first side of the membrane.
6. The refrigeration system of any preceding claim, wherein the separation layer comprises
a ceramic material, particularly zeolite.
7. The refrigeration system of any preceding claim, wherein the at least one gas permeable
membrane comprises a plurality of gas permeable membranes; wherein the plurality of
gas permeable membranes are arranged in serial or parallel communication.
8. The refrigeration system of any preceding claim, wherein the polymer layer comprises
a polymer selected from a silicone rubber, fluorosilicone or polyimide.
9. The refrigeration system of any preceding claim, wherein the polymer layer has a thickness
of 0.05 µm to 50 µm.
10. The refrigeration system of any preceding claim, further comprising a controller configured
to operate the fluid circulation loop in response to a cooling demand signal and to
operate the prime mover in response to a determination of contaminants in the fluid
circulation loop.
11. The refrigeration system of claim 10, wherein the controller is configured to activate
a purge back-flush mode in which gas is transported from the second side of the membrane
to the first side of the membrane.
12. The refrigeration system of claims 10 or 11, wherein the controller is configured
to activate a heat source to heat the membrane to a temperature to remove contaminants.
13. A method of operating a refrigeration system, comprising
circulating a refrigerant through a heat transfer fluid circulation loop in response
to a cooling demand signal;
collecting purge gas comprising contaminants from a purge outlet in the fluid circulation
loop;
transferring the contaminants across a permeable molecular sieve membrane with a prime
mover, said membrane comprising a porous inorganic or metal organic framework with
pores of a size to allow passage of the contaminants through the membrane and restrict
passage of the refrigerant through the membrane; and
periodically back-flushing the membrane by transporting gas from the second side of
the membrane to the first side of the membrane, or periodically heating the membrane
to a temperature to remove contaminants, or both periodically transporting gas from
the second side of the membrane to the first side of the membrane and periodically
heating the membrane to a temperature to remove contaminants.
14. The method of claim 13, comprising
periodically back-flushing the membrane by transporting gas from the second side of
the membrane to the first side of the membrane; and/or
periodically heating the membrane to a temperature to remove contaminants.
15. The method of claim 13 or 14, further comprising
passing the purge gas through a filter before reaching the membrane; and/or
transporting the contaminants through a polymer coating on the inorganic or metal
organic framework membrane; and/or
collecting the purge gas in a purge gas collector between the purge outlet and the
membrane; and/or
returning refrigerant from the first side of the membrane to the fluid circulation
loop.