US20120181004A1

US20120181004A1 - Surface coating layer and heat exchanger including the surface coating layer

Info

Publication number: US20120181004A1
Application number: US13/109,559
Authority: US
Inventors: Yoon Chul SON; Sang Eui LEE; Ha Jin Kim; Dong Ouk KIM; Dong Earn KIM; Kun Mo Chu
Original assignee: Samsung Electronics Co Ltd
Current assignee: Samsung Electronics Co Ltd
Priority date: 2011-01-13
Filing date: 2011-05-17
Publication date: 2012-07-19
Also published as: EP2476990A2; CN102615866A; KR20120082278A; EP2476990A3

Abstract

A surface coating layer, in contact with a surface of a base material of a heat exchanger, comprises a plurality of composite layers comprising a first layer contacting a surface of the base material, the first layer comprising a first matrix and a first nanobody, and a second layer contacting a surface of the first layer and having an interface with the air, where the first layer and the second layer each include a different amount by volume of the first nanobody and the second nanobody, respectively.

Description

CROSS-REFERENCE TO RELATED APPLICATION

This application claims priority to Korean Patent Application No. 10-2011-0003676, filed Jan. 13, 2011, and all the benefits accruing therefrom under 35 U.S.C. 119, the content of which in its entirety is herein incorporated by reference.

BACKGROUND OF THE INVENTION

(a) Field of the Invention
A surface coating layer and a heat exchanger including the surface coating layer are provided.
(b) Description of the Related Art
A cooling device such as a refrigerator or a freezer lowers the temperature by repetition of the cooling cycle of compression-condensation-expansion-evaporation of a coolant, such as a fluid refrigerant which may be a liquid, gas, or a combination of these in equilibrium. The cooling device operates by increasing the temperature and pressure of the coolant from a low temperature and low pressure to a high temperature and high pressure, condensing the coolant under high temperature and high pressure by air cooling, reducing the pressure of the condensed coolant, and evaporating the coolant at reduced pressure and low pressure to absorb heat.
The cooling device includes a heat exchanger. Since the surface temperature of the heat exchanger drops below the freezing point of water during operation, frost may form on the surface of the heat exchanger especially where hot moist air passes through the heat exchanger. The formation of frost on the heat exchanger may disturb air flow and heat transfer of the air in a cooling tube, thus decreasing heat exchange efficiency.

SUMMARY OF THE INVENTION

In an exemplary embodiment, a surface coating layer is provided that may reduce the formation rate of frost, or that may rapidly remove formed frost to improve heat exchange efficiency.
In another exemplary embodiment, a heat exchanger includes the surface coating layer.
In an exemplary embodiment, a surface coating layer for a heat exchanger formed from a base material is provided, the surface coating layer comprising a plurality of composite layers comprising a first layer contacting a surface of the base material, the first layer comprising a first composite of a first matrix and a first nanobody; and a second layer contacting a surface of the first layer and having an air interface, the second layer comprising a second composite of a second matrix and a second nanobody and, wherein the first layer and the second layer each comprise a different amount by volume of the first nanobody and the second nanobody, respectively.
The first layer may comprise the first nanobody in an amount of about 30 to about 45 volume % based on the total volume of the first composite, and the second layer may comprise the second nanobody in an amount of about 12 to about 25 volume % based on the total volume of the second composite.
The first layer may comprise the first nanobody in an amount of about 40 volume % based on the total volume of the first composite, and the second layer may comprise the second nanobody in an amount of about 20 volume % based on the total volume of the second composite.
The composite layer may further comprise a third layer positioned between surfaces of the first layer and the second layer, the third layer comprising a third composite comprising a third matrix and a third nanobody, the third layer having a third nanobody content by volume which gradually decreases from an interface with the first layer to an interface with the second layer along a thickness dimension of the third layer.
The first layer may be a heat transfer layer for heat exchange from the base material to the air interface of the second layer, and the second layer may be a water-repellent layer for suppressing adherence of moisture comprised in the air.
The first layer may have higher thermal conductivity than the second layer.
The first layer may have thermal conductivity of about 1 W/m·K or more.
The second layer may have a contact angle of about 145° or more and a sliding angle of about 8° or less.
The second layer may have a thickness of about 100 nm to about 1 μm.
The first, second, and third nanobodies may each comprise nanotubes, nanofibers, nanowire, nanoparticles, nanospheres, or a combination comprising at least one of the foregoing.
The first, second, and third matrices may each comprise a silicon-based polymer, a fluorine-based polymer, a fluorine-substituted silicon polymer, or a combination comprising at least one of the foregoing.
The first layer and the second layer may each have a plurality of pores.
The surface of the second layer at the air interface may have a protrusion structure formed by the second nanobody.
In another exemplary embodiment, a heat exchanger comprises a base material, and a surface coating layer comprising a plurality of composite layers formed on a surface of the base material, the plurality of composite layers comprising a first layer contacting a surface of the base material, the first layer comprising a first composite comprising a first matrix and a first nanobody, and a second layer contacting a surface of the first layer and having an air interface, the second layer comprising a second composite comprising a second matrix and a second nanobody, wherein the first layer and the second layer each comprise a different amount by volume of the first nanobody and the second nanobody, respectively.
The first layer may comprise the first nanobody in an amount of about 30 to about 45 volume % based on the total volume of the first composite, and the second layer may comprise the second nanobody in an amount of about 12 to about 25 volume % based on the total volume of the second composite.
The composite layer may further comprise a third layer positioned between surfaces of the first layer and the second layer, the third layer comprising a third composite comprising a third matrix and a third nanobody, the third layer having a third nanobody content by volume which gradually decreases from an interface with the first layer to an interface with the second layer along a thickness dimension of the third layer.
The first layer may have thermal conductivity of about 1 W/m·K or more, and the second layer may have a contact angle of about 145° or more and a sliding angle of about 8° or less.
The surface coating layer may have a thickness of about 0.5 μm to about 100 μm, and the second layer has a thickness of about 100 nm to about 1 μm.
The nanobody may comprise nanotubes, nanofibers, nanowires, nanoparticles, nanospheres, or a combination comprising at least one of the foregoing, and the matrix may comprise a silicon-based polymer, a fluorine-based polymer, a fluorine-substituted silicon polymer, or a combination comprising at least one of the foregoing.
In another exemplary embodiment, a heat exchanger is provided which comprises a base material and a surface coating layer comprising a plurality of composite layers formed on a surface of the base material, the plurality of composite layers comprising a first layer contacting the surface of the base material and having thermal conductivity of about 1 W/m·K or more, the first layer comprising a first composite comprising a first matrix and a first nanobody, and a second layer contacting a surface of the first layer and having an air interface, a contact angle of about 145° or more, and a sliding angle of about 8° or less, the second layer comprising a second composite comprising a second matrix and a second nanobody.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a schematic diagram showing a heat exchanger according to an exemplary embodiment.

FIG. 2 is a cross-sectional view showing the stacking structure of the heat exchanger of FIG. 1.

FIG. 3 is a schematic diagram showing the surface coating layer according to an exemplary embodiment.

FIG. 4 is a cross-sectional view showing one example of the stacking structure of the surface coating layer of FIG. 3.

FIG. 5 is a cross-sectional view showing another example of the stacking structure of the surface coating layer of FIG. 3.

FIG. 6A is a graph showing the contact angle according to the amount by volume of nanobody.

FIG. 6B is a graph showing the sliding angle according to the amount by volume of nanobody.

FIG. 7 is a graph showing thermal conductivity according to the amount by volume of nanobody.

DETAILED DESCRIPTION

This disclosure will be described more fully hereinafter with reference to the accompanying drawings, in which exemplary embodiments are shown. This disclosure may, however, be embodied in many different forms and should not be construed as limited to the exemplary embodiments set forth herein.
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, regions, integers, steps, operations, elements, and/or components, but do not preclude the presence or addition of one or more other features, regions, integers, steps, operations, elements, components, and/or groups thereof. All ranges and endpoints reciting the same feature are independently combinable.
Unless otherwise defined, all terms (including technical and scientific terms) used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. It will be further understood that terms, such as those defined in commonly used dictionaries, should be interpreted as having a meaning that is consistent with their meaning in the context of the relevant art and the present disclosure, and will not be interpreted in an idealized or overly formal sense unless expressly so defined herein.
In the drawings, the thickness of layers, films, panels, regions, etc., are exaggerated for clarity. Like reference numerals designate like elements throughout the specification. It will be understood that when an element such as a layer, film, region, or substrate is referred to as being “on” another element, it can be directly on the other element or intervening elements may also be present. In contrast, when an element is referred to as being “directly on” another element, there are no intervening elements present.
As used herein, “alkyl” refers to a straight or branched chain saturated aliphatic hydrocarbon having the specified number of carbon atoms. “Alkenyl” is a straight or branched chain hydrocarbon that comprises at least one carbon-carbon double bond. Similarly, “cycloalkyl” and “cycloalkenyl” refers to groups including a monovalent cyclic alkyl and monovalent cyclic alkenyl moiety, respectively. “Alkoxy” refers to an alkyl moiety that is linked via an oxygen (i.e., —O-alkyl). Non-limiting examples of C1 to C30 alkoxy groups include methoxy groups, ethoxy groups, propoxy groups, isobutyloxy groups, sec-butyloxy groups, pentyloxy groups, iso-amyloxy groups, hexyloxy groups, octyloxy groups, and the like. The term “alkylene” refers to a straight, branched or cyclic divalent aliphatic hydrocarbon group. The term “alkenylene” refers to a straight, branched or cyclic divalent aliphatic hydrocarbon group containing a double bond. Similarly, “cycloalkylene” and “cycloalkenylene” refers to groups including a divalent cyclic alkyl and divalent cyclic alkenyl moiety, respectively.
As used herein “aryl,” means a cyclic moiety in which all ring members are carbon and at least one ring is aromatic. More than one ring may be present, and any additional rings may be independently aromatic, saturated or partially unsaturated, and may be fused, pendant, spirocyclic or a combination thereof. As used herein, the term “arylene” refers to a divalent radical formed by the removal of two hydrogen atoms from one or more rings of an aromatic hydrocarbon, wherein the hydrogen atoms may be removed from the same or different rings (preferably different rings), each of which rings may be aromatic or nonaromatic. As used herein, “aralkyl” refers to an alkylene group in which one of the hydrogen atoms of the alkyl is replaced by an aryl group. Representative aralkyl groups include, for example, a benzyl group, a phenylethyl group, a diphenylenemethylene group, a dimethylenephenylene group, and the like. An “aralkylene” group is an aryl or arylene group linked via an alkyl or alkylene moiety. The specified number of carbon atoms (e.g., C7 to C30) refers to the total number of carbon atoms present in both the aryl and the alkylene moieties. “Aryloxy” refers to an aryl moiety that is linked via an oxygen (i.e., —O-aryl).
A “heteroalkyl” group is an alkyl group that comprises at least one heteroatom covalently bonded to one or more carbon atoms of the alkyl group. A “heterocycloalkyl” group is a cycloalkyl group that comprises at least one heteroatom covalently bonded to one or more carbon atoms in the cycloalkyl group. A “heteroaryl” group is a monovalent carbocyclic ring system that includes one or more aromatic rings, in which at least one ring member (e.g., one, two or three ring members) is a heteroatom. For example, in a C3 to C30 heteroaryl, the total number of ring carbon atoms ranges from 3 to 30, with remaining ring atoms being heteroatoms. Multiple rings, if present, may be pendant, spiro or fused. “Heteroarylene” refers to a divalent radical formed by the removal of two hydrogen atoms from one or more rings of a heteroaryl moiety, wherein the hydrogen atoms may be removed from the same or different rings (preferably the same ring), each of which rings may be aromatic or nonaromatic. A “heteroaralkyl” group is a heteroaryl group linked via an alkylene moiety; likewise, a “heteroaralkylene” group is a heteroarylene group linked via an alkylene moiety. The specified number of carbon atoms (e.g., C3 to C30) refers to the total number of carbon atoms present in both the aryl and the alkylene moieties, with remaining ring atoms being heteroatoms as discussed above. As used herein, “combination” is inclusive of blends, mixtures, alloys, reaction products, and the like.
As used herein, when a definition is not otherwise provided, the term “substituted” refers to one substituted with a substituent selected from a C1 to C30 alkyl group, a C2 to C30 alkynyl group, a C6 to C30 aryl group, a C7 to C30 alkylaryl group, a C1 to C4 oxyalkyl group, a C1 to C30 heteroalkyl group, a C3 to C30 heteroalkylaryl group, a C3 to C30 alicyclic group, a C3 to C15 cycloalkenyl group, a C6 to C30 cycloalkynyl group, a C2 to C30 heterocycloalkyl group, a halogen (F, Cl, Br, or I), a hydroxyl group, a C1 to C30 alkoxy group, a nitro group, a cyano group, an amino group, an azido group, an amidino group, a hydrazino group, a hydrazono group, a carbonyl group, a carbamyl group, a thiol group, an ester group, a carboxyl group or a salt thereof, a sulfonic acid or a salt thereof, phosphoric acid or a salt thereof, or a combination comprising at least one of the foregoing. Where “fluoro” is used to describe a group such as in “fluoroalkyl”, “fluoroaryl”, etc. it will be understood that the group contains at least one fluorine group, or may be completely fluorinated (i.e., perfluorinated). Also as used herein, where a substituent such as fluorine is disclosed or implied for a group, such as “fluoroalkyl”, and “substituted” is also indicated for the group, the group contains both the disclose or implied substituent and an additional substituent not identical to the specified substituent.
Hereinafter, a heat exchanger according to one exemplary embodiment will be described with reference to FIG. 1 and FIG. 2.
FIG. 1 is a schematic diagram showing the heat exchanger according to one exemplary embodiment, and FIG. 2 is a cross-sectional view showing the stacking structure of the heat exchanger of FIG. 1.
Referring to FIG. 1, the heat exchanger according to one exemplary embodiment includes a cooling tube 20 and a plurality of cooling fins 30, wherein a coolant passes through the cooling tube 20, and hot air, and in particular hot moist air, passes between the cooling fins 30 so that heat exchange may occur.
Referring to FIG. 2, the stacking structure of the heat exchanger including the cooling tube 20 and the cooling fins 30 includes a base material 100 and a surface coating layer 120 formed on the surface of the base material 100.
The base material 100 may be formed of a metal having high thermal conductivity. High thermal conductivity of a metal, as used herein, means having a thermal conductivity of about 100 Watts per meter per Kelvin (W/m·K) or more. Materials having high thermal conductivities include aluminum (Al), copper (Cu), alloys thereof, and the like, or a combination comprising at least one of the foregoing, where combinations may include structural combinations such as plated structures, laminated structures, assemblies of components made from two or more different thermally conductive materials such as where a tube of one material has a vane assembly made of a different material attached thereto, or the like, or a combination comprising these structures.
The surface coating layer 120 is coated on the surface of the base material 100. The surface coating layer 120 may prevent formation of frost on the surface of the base material 100, particularly when hot moist air passes through the heat exchanger. The surface coating layer 120, in addition to preventing the accumulation of frost, allows for frost which may accumulate to be readily removed. Removal of any frost which does accumulate may be accomplished by any known method, such as sublimation, or by mechanical removal of the frost.
The surface coating layer 120 is described referring to FIG. 3 and FIG. 4.
FIG. 3 is a schematic diagram showing the surface coating layer 120 of one exemplary embodiment, and FIG. 4 is a cross-sectional view showing one example of the stacking structure of the surface coating layer 120 of FIG. 3.
Stacking structure, as used herein, may be an ordered structure such as successive layers of the coated nanobody, an array of substructures such as regularly and irregularly shaped spheres, cylinders, plates, rods, cones, tubes, polyhedra including trigonal and tetragonal pyramids, cubes, bipyramidal structures, dodecahedrons, eicosahedrons, or the like, or any combination of these structures, arranged in a regular pattern in both the plane of the surface and perpendicular to the surface of the nanobody 50 b, or may be irregularly stacked in partially random (as where the substructures are regularly arrayed in an x-y, x-z, or y-z plane but irregularly stacked in the remaining dimension, or fully random agglomeration of any of the above substructures. Interstitial spaces (i.e., pores) may be present in the layer. Combinations comprising at least one of the above substructures may be used.
The surface coating layer 120 is formed of a composite 50 including a matrix 50 a and a nanobody 50 b.
The matrix 50 a may be formed of, for example, a silicon-based polymer, a fluorine-based polymer, a fluorine-substituted silicon polymer, or a combination comprising at least one of the foregoing polymers.
The matrix 50 a may be formed of a silicon-based polymer. Useful silicon-based polymers include polyorganosiloxanes including a siloxane repeating unit represented by the following Chemical Formula 1.
—SIR¹R²O— Chemical Formula 1
In Chemical Formula 1, R¹and R²are each independently a substituted or unsubstituted C1 to C10 alkyl group, a substituted or unsubstituted C1 to C10 heteroalkyl group, a substituted or unsubstituted C3 to C10 cycloalkyl group, a substituted or unsubstituted C2 to C10 heterocycloalkyl group, a substituted or unsubstituted C1 to C10 alkoxy group, a substituted or unsubstituted C1 to C10 heteroalkoxy group, a substituted or unsubstituted C3 to C10 cycloalkoxy group, a substituted or unsubstituted C2 to C10 heterocycloalkoxy group, a substituted or unsubstituted C2 to C10 alkenyl group, a substituted or unsubstituted C2 to C10 heteroalkenyl group, a substituted or unsubstituted C3 to C10 cycloalkenyl group, a substituted or unsubstituted C2 to C10 heterocycloalkenyl group, a substituted or unsubstituted C6 to C20 aryl group, a substituted or unsubstituted C3 to C10 heteroaryl group, a substituted or unsubstituted C6 to C20 aryloxy group, a substituted or unsubstituted C3 to C10 heteroaryloxy group, a substituted or unsubstituted C7 to C20 aralkyl group, a substituted or unsubstituted C4 to C10 heteroaralkyl group, or a combination comprising at least one of the foregoing groups.
The fluorine-substituted silicon polymer may include siloxane units of Chemical Formula 1 in which R¹and R²are each independently fluorine, a substituted or unsubstituted C1 to C10 fluoroalkyl group, a substituted or unsubstituted C1 to C10 heterofluoroalkyl group, a substituted or unsubstituted C3 to C10 fluorocycloalkyl group, a substituted or unsubstituted C2 to C10 heterofluorocycloalkyl group, a substituted or unsubstituted C1 to C10 fluoroalkoxy group, a substituted or unsubstituted C1 to C10 heterofluoroalkoxy group, a substituted or unsubstituted C3 to C10 fluorocycloalkoxy group, a substituted or unsubstituted C2 to C10 heterofluorocycloalkoxy group, a substituted or unsubstituted C2 to C10 fluoroalkenyl group, a substituted or unsubstituted C2 to C10 heterofluoroalkenyl group, a substituted or unsubstituted C3 to C10 fluorocycloalkenyl group, a substituted or unsubstituted C2 to C10 heterofluorocycloalkenyl group, a substituted or unsubstituted C6 to C20 fluoroaryl group, a substituted or unsubstituted C3 to C10 heterofluoroaryl group, a substituted or unsubstituted C6 to C20 fluoroaryloxy group, a substituted or unsubstituted C3 to C10 heterofluoroaryloxy group, a substituted or unsubstituted C7 to C20 fluoroaralkyl group, a substituted or unsubstituted C4 to C10 heterofluoroaralkyl group, or a combination comprising at least one of the foregoing groups.
The siloxane repeating unit may be combined in various ways to form a cyclic, linear, or side chain structure, and the polyorganosiloxane may be a homopolymer, a copolymer, or a mixture thereof. Combinations of fluorinated and non-fluorinated siloxane repeating units may be used.
The polyorganosiloxane may include two or more kinds of siloxane repeating units, wherein the substituent bonded to the silicon in the repeating unit represented by the above Chemical Formula 1 the same or different. The siloxane repeating unit may be additionally combined with mono, di, tri, tetra, penta-, hexa-, etc., alkoxy- or chlorosiloxane precursors to siloxane units to further increase the branching of the polyorganosiloxanes. Monomers such as, for example, tetraethylorthosilane, tetramethylorthosilane, trimethoxymethyl silane, triethoxysilane, 1.2-bis(trimethoxysilyl)ethane, and the like, or combinations thereof, may be integrated into the polysiloxane chain to form a crosslinked structure and thereby increase the mechanical stability of the polyorganosiloxanes.
The polyorganosiloxane may include, for example, polydimethyl siloxane, polymethylphenyl siloxane, polydiphenyl siloxane, polyfluorosiloxane, polyvinylsiloxane, polyperfluorophenyl siloxane, or a combination thereof.
The fluorine-based polymer may be any polymer having a fluorine substituent on the polymer backbone, as a substituent or pendant group, or a combination of these. Fluorine-based polymers may thus have repeating units of substituted or unsubstituted C2 to C30 fluoroalkylene groups, substituted or unsubstituted C3 to C30 fluorocycloalkylene groups, substituted or unsubstituted C6 to C30 fluoroarylene groups, substituted or unsubstituted C7 to C30 fluoroaralkylene groups, or a combination comprising at least one of the foregoing fluorinated units. The repeating units may be directly connected to one another by carbon-carbon bonds, carbonyl groups, or may be connected through heteroatoms such as oxygen, nitrogen, or sulfur, or combinations comprising at least one of the foregoing. Repeating units may, in some instances, be connected by functional groups such as ester linkages, sulfone linkages, ether linkages, sulfide linkages (thioethers), amine linkages, amide linkages, imide linkages, or the like, or combinations comprising at least one of the foregoing. The fluorine-based polymers may include, for example, poly(tetrafluoroethylene), poly(vinylidene fluoride), perfluoroalkoxy polymers, (perfluorodiphenyl ethers), copolymers thereof, or the like, or combinations comprising at least one of the foregoing polymers. The above polyorganosiloxanes and the aforementioned fluorine-based polymers may also be used to form fluorinated silicon-based polymers comprising blocks of silicon-based polymer and fluorine based polymer.
The nanobody 50 b may include, for example, nanotubes, nanofibers, nanowires, nanoparticles, nanospheres, or a combination comprising at least one of the foregoing nanobodies. More specifically, carbon nanotubes, carbon nanofibers, Si nanowire, ZnO nanowire, Cu nanowire, GaN nanowire, or a combination comprising at least one of the foregoing, may be used.
The nanobody 50 b may have at least one dimension in the nano-scale range, i.e., about 1 to less than about 1,000 nm. The nanobody 50 b may have a diameter of, for example, about 1 nm to about 1,000 nm, and where the nanobody 50 b is asymmetrical a second (length) dimension of about 0.01 μm to about 1,000 μm. When the nanobody 50 b has a diameter and a length within the above ranges, dispersibility of the nanobody 50 b within the matrix may be improved and a protrusion structure, i.e., a structure having protrusions from the coated surface, may be readily formed when forming the surface coating layer.
The composite 50 may include the nanobody 50 b dispersed in the matrix 50 a, and it may be formed by, for example, spray coating, dip coating, or the like, such that the matrix 50 a is coated on the surface of the nanobody 50 b as shown in FIG. 3, when coating on a surface of the base material 100.
Where the nanobody 50 b is included in a predetermined amount or more, the surface coating layer 120 may further have a mesh structure having a plurality of pores 60. By forming such a mesh structure, stress in the structure may be reduced and durability may be increased. The pores may have an average largest cross-sectional dimension (i.e., diameter) of about 1 nm to about 10 μm, where the pores are smaller than the thickness of the surface coating layer 120 or that of any sublayer.
Referring to FIG. 4, the surface coating layer 120 includes a lower composite layer 120 a contacting a surface of the base material (not shown), and an upper composite layer 120 b on, and in some exemplary embodiments, directly on and contacting, a surface of the lower composite layer 120 a. The lower composite layer 120 a and the upper composite layer 120 b each has a different content by volume of the nanobody 50 b. The nanobody 50 b may be the same or different in each composite layer 120 a and 120 b.
In the surface coating layer 120, thermal conductivity and water repellency of the composite 50 may be varied according to the amount of the nanobody 50 b. To reduce the formation rate of frost on the surface of the heat exchanger or to rapidly remove formed frost, thermal conductivity of the surface coating layer 120 should be high (e.g., about 1 W/m·K or more). Simultaneously, water repellency, as shown by water contact angle, where high water contact angles for the surface coating layer of about 145 degrees or more, more specifically about 150 degrees or more, and still more specifically about 152 degrees or more, indicate very low wettability. Similarly, a low sliding angle of about 8 degrees or less, specifically about 6 degrees or less, and still more specifically about 5 degrees or less, also indicate low wettability, and hence, excellent water repellency.
The thermal conductivity and water repellency of the surface coating layer 120 may be varied by adjusting the amount by volume of the nanobody 50 b included in the composite 50.
In an exemplary embodiment, thermal conductivity and water repellency may be simultaneously improved by forming the surface coating layer 120 with a plurality of composite layers, each having a different amount of the nanobody 50 b.
Specifically, the lower composite layer 120 a is a part contacting the base material 100 and includes the nanobody 50 b in a first amount so as to improve thermal conductivity of the surface coating layer 120. The lower composite layer 120 a may have higher thermal conductivity than the upper composite layer 120 b. Lower composite layer 120 a may have thermal conductivity of about 1 W/m·K or more, specifically about 10 W/m·K or more, and more specifically about 25 W/m·K or more.
The upper composite layer 120 b is a part contacting the lower composite layer 120 a with the opposite surface exposed to the air, and it may include the nanobody 50 b in a second amount so as to increase water repellency at the air-lower composite layer 120 b interface.
This is explained referring to FIG. 6A to FIG. 7.
FIG. 6A is a graph showing contact angle according to nanobody content by volume, FIG. 6B is a graph showing sliding angle according to nanobody content by volume, and FIG. 7 is a graph showing thermal conductivities according to nanobody content by volume.
Referring to FIG. 6A and FIG. 6B, it may be seen that contact angles and sliding angles may be varied according to nanobody content, based on volume of the composite. The contact angle and the sliding angle are indicative of wettability at the solid surface, wherein a higher contact angle indicates lower wettability, and hence high hydrophobicity and water repellency, and a lower sliding angle indicates lower wettability, and hence high hydrophobicity and water repellency.
Referring to FIG. 6A and FIG. 6B, the upper composite layer 120 b may include the nanobody 50 b in an amount of about 12 to about 25 volume %, specifically about 15 to about 25 volume %, and more specifically about 17 to about 22 volume %, based on the total volume of the composite 50. The contact angle is preferably about 150° or more and the sliding angle is about 5° or less. Within the above range, the upper composite layer 120 b may include the nanobody 50 b in an amount of about 20 volume % based on the total volume of the composite 50.
Referring to FIG. 7, it may be seen that as the nanobody content increases, thermal conductivity increases. The lower composite layer 120 a may thus include the nanobody 50 b in an amount of about 30 to about 45 volume %, and specifically about 35 to about 45 volume %, based on the total volume of the composite 50 so as to have higher thermal conductivity than the upper composite layer 120 b. Within the above range, the lower composite layer 120 a may include the nanobody 50 b in an amount of about 40 volume % based on the total volume of the composite 50.
As described, the lower composite layer 120 a of the surface coating layer 120, which contacts the base material 100, may therefore include about 30 to 45 volume % of the nanobody 50 b so as to improve thermal conductivity, and the upper composite layer 120 b that contacts the air may therefore include about 15 to 25 volume % of the nanobody 50 b so as to increase water repellency.
In this way, formation of frost on the surface (i.e., on the surface coating layer) may be reduced or prevented, or any formed frost may be removed, by simultaneously increasing thermal conductivity and water repellency of the heat exchanger.
Hereinafter, the stacking structure of the surface coating layer 120 according to another exemplary embodiment will be explained referring to FIG. 5 together with FIG. 2 and FIG. 3.
FIG. 5 is a cross-sectional view showing another example of the stacking structure of the surface coating layer 120 of FIG. 3.
Referring to FIG. 5, the surface coating layer 120 includes a lower composite layer 120 a and an upper composite layer 120 b each having different contents by volume of the nanobody 50 b, and a middle composite layer 120 ab that is positioned between surfaces of the lower composite layer 120 a and the upper composite layer 120 b and includes the nanobody 50 b with a gradually changing content, which decreases from an interface with the lower composite layer 120 a to an interface with the upper composite layer 120 b along a thickness dimension of the middle composite layer 120 ab. As used herein, “gradually changing content” means a concentration gradient of the nanobody based on the volume of the composite for the middle composite layer 120 ab from the interface with the lower composite layer 120 a to the interface with the upper composite layer 120 b, decreasing along the dimension of layer thickness from the lower composite layer 120 a, to the upper composite layer 120 b.
The lower composite layer 120 a and the upper composite layer 120 b are as explained above.
The middle composite layer 120 ab may include the nanobody 50 b with a gradually changing content by volume between the amount by volume of the nanobody 50 b included in the lower composite layer 120 a and the amount by volume of the nanobody 50 b included in the upper composite layer 120 b. In the drawing, for better comprehension and ease of description, the lower composite layer 120 a, the middle composite layer 120 ab, and the upper composite layer 120 b are separately explained, but the amount by volume of the nanobody 50 b may be continuously changed without a boundary where the amount by volume of nanobody 50 b changes sharply with no apparent gradient at the interface between the lower composite layer 120 a and the middle composite layer 120 ab, and between the middle composite layer 120 ab and the upper composite layer 120 b.
The composite 50 may further include an additive such as a cross-linking agent, a catalyst, and the like, in addition to the matrix 50 a and the nanobody 50 b.
The cross-linking agent may cure the surface coating layer through a cross-linking reaction with the polymer forming the matrix 50 a. The cross-linking agent may include, for example, a silane-based compound, a SiH bond-containing organohydrosiloxane-based compound, and the like, or a combination comprising at least one of the foregoing.
The silane-based compound may include an alkoxysilane, an aminosilane, a vinylsilane, an epoxysilane, a (meth)acrylsilane, an alkylsilane, a phenylsilane, a chlorosilane, and the like. It will be understood that, as used herein, “(meth)acryl” includes both methacryl and acryl and may represent either of these.
Examples of the SiH bond-containing organohydrogensiloxane-based compound may include pentamethyltrihydrogencyclotetrasiloxane, 1,1,3,3-tetramethyldisiloxane, 1,3,5,7-tetramethylcyclotetrasiloxane, tris(hydrogendimethylsiloxy)methylsilane, tris(hydrogendimethylsiloxy)phenylsilane, methylhydrogencyclopolysiloxane, a methylhydrogensiloxane.dimethylsiloxane cyclic copolymer, a methylhydrogenpolysiloxane including end-capping trimethylsiloxy groups at both terminal ends, a dimethylsiloxane.methylhydrogensiloxane copolymer including end-capping trimethylsiloxy groups at both terminal ends, dimethylpolysiloxane including end-capping dimethylhydrogensiloxy groups at both terminal ends, a dimethylsiloxane.methylhydrogensiloxane copolymer including end-capping dimethylhydrogensiloxy groups at both terminal ends, a methylhydrogensiloxane.diphenylsiloxane copolymer including end-capping trimethylsiloxy groups at both terminal ends, a methylhydrogensiloxane.diphenylsiloxane.dimethylsiloxane copolymer including end-capping trimethylsiloxy groups at both terminal ends, a methylhydrogensiloxane.methylphenylsiloxane.dimethylsiloxane copolymer including end-capping trimethylsiloxy groups at both terminal ends, a methylhydrogensiloxane.dimethylsiloxane.diphenylsiloxane copolymer including end-capping dimethylhydrogensiloxy groups at both terminal ends, a methylhydrogensiloxane.dimethylsiloxane.methylphenylsiloxane copolymer including end-capping dimethylhydrogensiloxy groups at both terminal ends, a copolymer including a (CH₃)₂HSiO_1/2unit, a (CH₃)₃SiO_1/2unit, and a SiO_4/2unit, a copolymer including a (CH₃)₂HSiO_1/2unit and a SiO_4/2unit, and a copolymer including a (CH₃)₂HSiO_1/2unit, a SiO_4/2unit, and a (C₆H₅)₃SiO_1/2unit. Combinations comprising at least one of the foregoing units may be included.
The cross-linking agent may be included in an amount of about 1 to 200 parts by weight, specifically 10 to 100 parts by weight, based on 100 parts by weight of the matrix.
The catalyst when included promotes a cross-linking reaction of the polymer forming the matrix 50 a. Various metal and non-metal catalysts may be used therefor.
As the catalyst, for example, tin, titanium, zirconium, lead, iron, cobalt, antimony, manganese, bismuth, zinc, alloys thereof, compounds thereof, or combinations comprising at least one of the foregoing may be used in the case that the cross-linking reaction of the polymer is a condensation type reaction. Similarly for example platinum, palladium, rhodium, alloys thereof, compounds thereof, or a combination comprising at least one of the foregoing may be used in the case that the cross-linking reaction of the polymer is an addition type reaction.
The composite may be coated on the surface of the base material 100 and cured to form the surface coating layer 120.
The coating may be performed, for example, by spin coating, spray coating, laminating, dip coating, flow coating, roll coating, screen printing, and the like. Since the surface coating layer 120 includes a plurality of composite layers, each having different contents by volume of the nanobody 50 b as explained above, a composite layer including a first content of the nanobody 50 b may be coated to a predetermined thickness, and then a composite layer including a second content of the nanobody 50 b may be coated thereon to a predetermined thickness.
The curing may be performed by thermal curing at a temperature below a deformation temperature of the base material 100, photo curing, or a combination thereof.
The thickness of the surface coating layer 120 may be varied according to the shape and dimensions of the base material 100. The surface coating layer may have a thickness of about 0.5 μm to 100 μm. Among them, the upper composite layer 120 b may have a thickness of about 100 nm to 1 μm, with the balance of the thickness of the surface coating layer met by the lower composite layer, or lower and middle composite layer combined.
The surface coating layer 120 may have a protrusion structure wherein one end of the randomly arranged nanobody 50 b protrudes outside (i.e., toward the air interface) and the shape of the surface is irregular. Such a protrusion structure may further decrease contact area of the surface coating layer 120 to water, in concert with the low slide angle and high contact angle, to further improve water repellency.
While this invention has been described in connection with what is presently considered to be practical exemplary embodiments, it is to be understood that the invention is not limited to the disclosed embodiments, but, on the contrary, is intended to cover various modifications and equivalent arrangements included within the spirit and scope of the appended claims.

Claims

1. A surface coating layer for a heat exchanger formed of a base material, the surface coating layer comprising:

a plurality of composite layers comprising;

a first layer contacting a surface of the base material, the first layer comprising:

a first composite, comprising:

a first matrix, and

a first nanobody; and

a second layer contacting a surface of the first layer and having an air interface, the second layer comprising:

a second composite, comprising:

a second matrix, and

a second nanobody;

wherein the first layer and the second layer each comprise a different amount by volume of the first nanobody and the second nanobody, respectively.

2. The surface coating layer of claim 1, wherein the first layer comprises the first nanobody in an amount of about 30 to about 45 volume %, based on the total volume of the first composite, and

the second layer comprises the second nanobody in an amount of about 12 to about 25 volume %, based on the total volume of the second composite.

3. The surface coating layer of claim 2, wherein the first layer comprises the first nanobody in an amount of about 40 volume %, based on the total volume of the first composite, and

the second layer comprises the second nanobody in an amount of about 20 volume %, based on the total volume of the second composite.

4. The surface coating layer of claim 1, wherein the composite layer further comprises:

a third layer positioned between surfaces of the first layer and the second layer, the third layer comprising;

a third composite, comprising

a third matrix, and

a third nanobody,

the third layer having a third nanobody content by volume which gradually decreases from an interface with the first layer to an interface with the second layer along a thickness dimension of the third layer.

5. The surface coating layer of claim 1, wherein the first layer is a heat transfer layer for heat exchange from the base material to the air interface of the second layer, and

the second layer is a water-repellent layer for suppressing adherence of moisture included in the air.

6. The surface coating layer of claim 1, wherein the first layer has higher thermal conductivity than the second layer.

7. The surface coating layer of claim 1, wherein the first layer has a thermal conductivity of about 1 W/m·K or more.

8. The surface coating layer of claim 1, wherein the second layer has a contact angle of about 145° or more and a sliding angle of about 8° or less.

9. The surface coating layer of claim 1, wherein the second layer has a thickness of about 100 nm to about 1 μm.

10. The surface coating layer of claim 1, wherein the first nanobody and second nanobody each comprise nanotubes, nanofibers, nanowire, nanoparticles, nanospheres, or a combination comprising at least one of the foregoing.

11. The surface coating layer of claim 1, wherein the first matrix and second matrix each comprise a silicon-based polymer, a fluorine-based polymer, a fluorine-substituted silicon polymer, or a combination comprising at least one of the foregoing.

12. The surface coating layer of claim 1, wherein the first layer and the second layer each have a plurality of pores.

13. The surface coating layer of claim 1, wherein a surface of the second layer at the air interface has a protrusion structure formed by the second nanobody.

14. A heat exchanger, comprising:

a base material; and

a surface coating layer, comprising:

a plurality of composite layers, formed on a surface of the base material, the plurality of composite layers comprising:

a first layer contacting the surface of the base material, the first layer comprising:

a first composite, comprising:

a first matrix, and

a first nanobody; and

a second composite, comprising:

a second matrix, and

a second nanobody;

15. The heat exchanger of claim 14, wherein the first layer comprises the first nanobody in an amount of about 30 to about 45 volume % based on the total volume of the first composite, and

the second layer comprises the second nanobody in an amount of about 12 to about 25 volume % based on the total volume of the second composite.

16. The heat exchanger of claim 15, wherein the composite layer further comprises:

a third layer positioned between surfaces of the first layer and the second layer, the third layer comprising:

a third composite, comprising:

a third matrix, and

a third nanobody,

17. The heat exchanger of claim 15, wherein the first layer has thermal conductivity of about 1 W/m·K or more, and

the second layer has a contact angle of about 145° or more and a sliding angle of about 8° or less.

18. The heat exchanger of claim 15, wherein the surface coating layer has a thickness of about 0.5 μm to about 100 μm, and the second layer has a thickness of about 100 nm to about 1 μm.

19. The heat exchanger of claim 14, wherein the first nanobody and the second nanobody each comprise a nanotube, nanofiber, nanowire, nanoparticle, nanosphere, or a combination comprising at least one of the foregoing, and

the first matrix and the second matrix each comprise a silicon-based polymer, a fluorine-based polymer, a fluorine-substituted silicon polymer, or a combination comprising at least one of the foregoing.

20. A heat exchanger, comprising:

a base material, and

a surface coating layer, comprising:

a plurality of composite layers formed on a surface of the base material, the plurality of composite layers comprising:

a first layer contacting the surface of the base material, and having thermal conductivity of about 1 W/m·K or more, the first layer comprising:

a first composite, comprising:

a first matrix, and

a first nanobody; and

a second layer contacting a surface of the first layer and having an air interface, a contact angle of about 145° or more, and a sliding angle of about 8° or less, the second layer comprising:

a second composite, comprising:

a second matrix, and

a second nanobody.