Patent Application
20210170667
This application claims priority to Singapore application number 10201710108W filed on 6 Dec. 2017, the disclosure of which is hereby incorporated by reference.
The present invention generally relates to a method of preparing a polymeric substrate having a plurality of imprints on its inner surface and a method of preparing a mold.
Micro- or nano-structures or -patterns or -imprints on the inner luminal surface of polymeric materials have attracted growing research interests as they may be used as an alternative to coatings, which are usually applied on tubings to achieve additional functionalities. Such micro or nano-structures may impart a wide spectrum of functionalities, which may include but not limited to superhydrophobicity, lubricity, improved passive mixing, reduced biofouling, reduced haemolysis, anti-bacterial and enhanced ultrasound visibility. More recently, the micro- or nano-structured tubings are used in flow lines in hydraulic systems for the medical applications such as in blood pump tubing and as catheters.
Despite their promising properties and potential applications as outlined above, current processes for fabricating the micro- or nano-structures or -patterns remain challenging primarily due to the complex fabricating process. The inherent process challenges such as alignment issues may result in the loss of design, high costs, low through-puts and material constraints. For instance, the fabrication of nano-structures in polymers via molding has seen limited commercial applications to date. Replication of sub 10-nm features remains difficult to obtain reproducibly due to the lateral collapse of the features in the polymeric replica as well as the defects densities.
The present invention therefore provides an alternative method to fabricate imprinted materials that overcomes, or at least ameliorates, one or more of the disadvantages described above.
In one aspect, there is provided a method of forming a plurality of imprints on an inner surface of a polymeric substrate comprising the steps of:
a) contacting a liquid polymeric mixture with a mold having an imprint forming surface thereon;
b) curing the liquid polymeric mixture of step a) to form said polymeric substrate having said plurality imprints on said inner surface, when cured; and
c) removing said mold from said polymeric substrate.
In another aspect, there is provided a method of forming a mold having an imprint forming surface thereon, wherein said method is a nanoimprinting method, a micromachining method or a self-assembly method.
Advantageously, the method disclosed herein may produce the plurality of imprints in the form of micro- or nano-structures having high-aspect ratio.
More advantageously, the method as defined herein may form isotropic and anisotropic micro- or nano-structures.
Still advantageously, the micro- or nano-structured tubings produced by the method defined herein may be relatively long (˜10 cm).
Further advantageously, the micro- or nano-structured tubings produced by the method defined above may typically be re-used whereby the tubings can be both elastic and non-elastic (stiff).
In another aspect, there is provided a polymeric substrate prepared by the method as defined herein.
In another aspect, there is provided a mold prepared by the method as defined above.
The following words and terms used herein shall have the meaning indicated:
The term ‘organosilicon’ is to be interpreted broadly to refer to any organometallic compounds containing carbon-silicon bonds, which may include monomeric, oligomeric or polymeric form thereof.
The term “polyurethane” as used herein refers to macromolecules in the form of polymers, co-polymers or segmented polymers or segmented co-polymers which contain at least one urethane linkage. The urethane group has the general structure (—O—(CO)—NR—) where (CO) defines a carbonyl group C═O, and R is hydrogen or an alkyl group.
The term “alkyl” as a group or part of a group used in the present disclosure refers to a straight or branched aliphatic hydrocarbon group to be interpreted broadly, having from 1 to 16 carbon atoms, e.g., 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15 or 16 carbon atoms, preferably a C1-C16 alkyl, C1-C12 alkyl, more preferably a C1-C10 alkyl, most preferably C1-C6 alkyl unless otherwise noted. Examples of suitable straight and branched alkyl substituents include but is not limited to, methyl, ethyl, 1-propyl, isopropyl, 1-butyl, 2-butyl, isobutyl, tert-butyl, amyl, 1,2-dimethylpropyl, 1,1-dimethylpropyl, pentyl, isopentyl, hexyl, 4-methylpentyl, 1-methylpentyl, 2-methylpentyl, 3-methylpentyl, 2,2-dimethylbutyl, 3,3-dimethylbutyl, 1,2-dimethylbutyl, 1,3-dimethylbutyl, 5-methylheptyl, 1-methylheptyl, octyl, nonyl, decyl, undecyl, 2,2,3-trimethyl-undecyl, dodecyl, 2,2-dimethyl-dodecyl, tridecyl, 2-methyl-tridecyl, 2-methyl-tridecyl, tetradecyl, 2-methyl-tetradecyl, pentadecyl, 2-methyl-pentadecyl, hexadecyl, 2-methyl-hexadecyl and the like. The alkyl may be optionally substituted with another functional group such as alkyl but not limited to it.
The term “curing” as used in the present disclosure refers to the toughening or hardening of a polymeric material, which may occur via cross-linking of polymer chains. Therefore, unless otherwise specified, the curing process refers to a solidification process of the polymeric material.
The unit “micron(s)” as used in the present disclosure may be used interchangeable with “micrometer(s)” or “μm”.
The word “substantially” does not exclude “completely” e.g. a composition which is “substantially free” from Y may be completely free from Y. Where necessary, the word “substantially” may be omitted from the definition of the invention.
Unless specified otherwise, the terms “comprising” and “comprise”, and grammatical variants thereof, are intended to represent “open” or “inclusive” language such that they include recited elements but also permit inclusion of additional, unrecited elements.
As used herein, the term “about”, in the context of concentrations of components of the formulations, typically means+/−5% of the stated value, more typically +/−4% of the stated value, more typically +/−3% of the stated value, more typically, +/−2% of the stated value, even more typically +/−1% of the stated value, and even more typically +/−0.5% of the stated value.
Throughout this disclosure, certain embodiments may be disclosed in a range format. It should be understood that the description in range format is merely for convenience and brevity and should not be construed as an inflexible limitation on the scope of the disclosed ranges. Accordingly, the description of a range should be considered to have specifically disclosed all the possible sub-ranges as well as individual numerical values within that range. For example, description of a range such as from 1 to 6 should be considered to have specifically disclosed sub-ranges such as from 1 to 3, from 1 to 4, from 1 to 5, from 2 to 4, from 2 to 6, from 3 to 6 etc., as well as individual numbers within that range, for example, 1, 2, 3, 4, 5, and 6. This applies regardless of the breadth of the range.
Certain embodiments may also be described broadly and generically herein. Each of the narrower species and subgeneric groupings falling within the generic disclosure also form part of the disclosure. This includes the generic description of the embodiments with a proviso or negative limitation removing any subject matter from the genus, regardless of whether or not the excised material is specifically recited herein.
Exemplary, non-limiting embodiments of a method of forming a plurality of imprints on an inner surface of a polymeric substrate will now be disclosed.
The method of forming said plurality of imprints on the inner surface of the polymeric substrate comprising the steps of:
a) contacting a liquid polymeric mixture with a mold having an imprint forming surface thereon;
b) curing the liquid polymeric mixture of step a) to form said polymeric substrate having said plurality imprints on said inner surface, when cured; and
c) removing said mold from said polymeric substrate.
It is to be noted that the liquid polymeric mixture above refers to a liquid mixture prior to a curing step as defined above. Hence, the liquid polymeric mixture may be in the form of a pre-polymer, which upon curing is converted into a polymer and subsequently into a network of cross-linked polymer. The above liquid polymeric mixture essentially may comprise polymeric organosilicon compounds or polyurethanes. The polymeric organosilicon compounds may be selected from the group consisting of polymethylhydrosiloxane (PMHS), polydimethylsiloxane (PDMS), polyethylmethylsiloxane (PEMS), polydiethylsiloxane (PDES) and blends thereof. The polymeric organosilicon compounds shown here are not limiting. It may therefore encompass other suitable polymeric organosilicon compounds. The polyurethane as used herein is to be understood to encompass polymers or co-polymers or segmented polymers or segmented co-polymers containing a plurality of urethane linkages as defined above.
For clarity purposes, prior to the curing step as will be discussed below, the aforesaid polymeric organosilicon compounds may be in the state whereby the polymeric organosilicon compounds are already in the polymeric form but not cross-linked. Only when subjected to the curing process, such polymeric organosilicon compounds form a cross-linked network of polymers. The existence of such crosslinking may be indicated by changes in the physical properties or state of the polymers such as from liquid to solid.
The curing step of the above polymeric organosilicon compounds may be undertaken in the presence of heat or UV irradiation. The curing step may be undertaken when the liquid polymeric mixture is in contact with the mold. The curing step, which occurs in the presence of heat may be referred as thermocuring. The thermocuring may be undertaken by subjecting the liquid polymeric mixture as defined above to a heat source, which then will undergo a hardening process. Alternatively, the curing process may be undertaken in the presence of an ultraviolet light and visible light (UV) to initiate a photochemical reaction that generates the cross-linked polymers. The curing process described here is not limiting. Hence, other suitable curing techniques such as microwave-assisted curing may also be used, when suitable.
For thermal curing, a suitable heating temperature may be selected in the range from about 40° C. to about 200° C. such as about 50° C., about 60° C., about 70° C., about 80° C., about 90° C., about 100° C., about 110° C., about 120° C., about 130° C., about 140° C., about 150° C., about 160° C., about 170° C., about 180° C. or about 190° C. Any other suitable temperatures within the range above may also be used. When suitable, a room temperature curing may also be undertaken that is the curing is performed at a room temperature from about 20° C. to about 30° C. In the room temperature and thermal curing, a constant or variable temperature may be used. When UV-curing is used, the curing process may be undertaken at a room temperature such as from about 20° C. to about 30° C.
For any of the curing process defined above, the curing step may be undertaken for a certain period of time such as from about 1 minute to about 24 hours, about 1 minute to about 5 minutes, about 1 minute to about 10 minutes, about 1 minute to about 20 minutes, about 1 minute to about 30 minutes (0.5 hours), about 30 minutes (0.5 hours) to about 24 hours, about 1 hour to about 24 hours, about 1 hour to about 2 hours, about 1 hour to about 5 hours, about 1 hour to about 10 hours, about 2 hours to about 5 hours, about 2 hours to about 10 hours, about 2 hours to about 24 hours, about 5 hours to about 10 hours, about 5 hours to about 18 hours, about 5 hours to about 24 hours, about 10 hours to about 18 hours, about 10 hours to about 24 hours or about 18 hours to about 24 hours. Exemplary embodiment of the thermal curing is as follow: when polydimethylsiloxane (PDMS) is used as the liquid polymeric mixture, the thermal curing process may be completed in about 5 minutes at curing temperature of about 120° C. or higher. Hence, when a lower temperature of curing is used, a longer curing time or period may be needed.
In the method as defined above, the mold having said imprint forming surface thereon may comprise a dissolvable material, temperature-dependent material or pressure-dependent material.
The dissolvable material is defined as any material that can be completely or essentially dissolved in a suitable solvent or a mixture of solvents. The dissolvable material may be a polymer or co-polymer or a blend of two or more polymers or co-polymers. Non-limiting examples of the dissolvable material may include acrylic-based polymer, acrylate-based polymer, polystyrene or mixtures thereof.
The examples of the acrylic-based polymer and the acrylate-based polymer include but not limited to poly(methacrylic acid), polyacrylic acid, poly(methyl methacrylate), poly(ethyl methacrylate), poly(propyl methacrylate), poly(propyl methacrylate), poly(isopropyl methacrylate), poly(butyl methacrylate), poly(isobutyl methacrylate), poly(hexyl methacrylate), poly(octyl methacrylate), poly(dodecylmethacrylate), poly(2-ethoxyethyl methacrylate), poly(2-hydroxyethyl methacrylate), poly(2-chloroethyl methacrylate) and poly(benzyl methacrylate).
The solvent used to dissolve the dissolvable material above is preferably an organic solvent. Non-limiting examples of the organic solvent may include acetic acid, acetone, acetonitrile, benzene, 1-butanol, 2-butanol, 2-butanone, t-butyl-alcohol, carbon tetrachloride, chloroform, cyclohexane, 1,2-dichloroethane, dimethyl formamide (DMF), dimethyl sulfoxide (DMSO), ethanol, ethyl acetate, hexane, methanol, methyl t-butyl ether (MTBE), N-methyl-2-pyrrolidinone (NMP), pentane, 1-propanol, 2-propanol, pyridine, tetrahydrofuran (THF), toluene, triethyl amine, o-xylene, m-xylene and p-xylene.
Therefore, the present disclosure also provides a method of forming the plurality of imprints on the inner surface of the polymeric substrate comprising the steps of:
a) contacting the liquid polymeric mixture with the mold having the imprint forming surface thereon, wherein the mold having the imprint forming surface thereon comprises the dissolvable material as defined above;
b) curing the liquid polymeric mixture of step a) to form said polymeric substrate having said plurality imprints on said inner surface, when cured; and
c) exposing said mold to a solvent to thereby remove said mold from said polymeric substrate.
For the above method, it is to be understood that the inner surface of the polymeric substrate may be the one in direct contact with the outer surface of the mold (such as the one represented as (109) in
When the mold having said imprint forming surface thereon is a temperature-dependent material, such material may be a hydrocarbon or a mixture of two or more hydrocarbons. Said hydrocarbons may be a branched, a linear or combinations thereof having twenty to forty carbon atoms. In an embodiment, said hydrocarbons may have 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39 or 40 carbons. The example of such temperature-dependent material is paraffin wax, which is a solid at room temperature (at about 20° C. to 30° C.) and turns into a liquid when heated. The melting point of the paraffin wax may be in the range of between about 35° C. to about 80° C. depending on the chain length of the hydrocarbon.
When subjected to heating, the wax melts into a liquid, after which it can then be casted into the inner spaces of the polymeric substrate having the plurality of imprints on its inner surface. Upon removal of the heat (i.e. decrease in the temperature), the wax may solidify back and its surface may essentially conform to the plurality of imprints of the inner surface of the polymeric substrate. The solidified wax may have the imprint forming surface thereon. Upon demolding, the solidified wax may advantageously be further used for forming the plurality of imprints on the inner surface of a new polymeric substrate.
In essence, when the mold having said imprint forming surface thereon is the temperature-dependent material, the step of removing the mold from the polymeric substrate may be achieved by adjusting the temperature that is by increasing the temperature. The increase in temperature may selectively cause the mold, in this instance wax, to melt but not the polymeric substrate having the plurality of imprints on the inner surface. When wax is used as the mold, the polymeric substrate may be selected from the polysiloxanes, which have much higher degradation temperature than wax. The degradation temperature of said polysiloxanes must be at least about 20° C. to about 200° C. higher than that of the wax, such as at least about 25° C., about 35° C., about 45° C., about 50° C., about 65° C., about 75° C., about 100° C., about 125° C., about 150° C. or about 175° C.
Hence, the above process may advantageously not require the presence of a solvent or a mixture of solvent as the mold can be removed by adjusting the temperature as described above and therefore it may be termed as solvent-less removal method.
Therefore, the present disclosure further provides a method of forming the plurality of imprints on the inner surface of the polymeric substrate comprising the steps of:
a) contacting the liquid polymeric mixture with the mold having the imprint forming surface thereon, wherein the mold having the imprint forming surface thereon comprises the temperature-dependent material as defined above;
b) curing the liquid polymeric mixture of step a) to form said polymeric substrate having said plurality imprints on said inner surface, when cured; and
c) subjecting the mold to a temperature that is about the melting point temperature of the mold to thereby remove said mold from said polymeric substrate.
The mold having said imprint forming surface thereon may also be a pressure-dependent material. Therefore, the shape or size of such material may be distorted when the material is subjected to a vacuum. The pressure-dependent material referred in the present disclosure may be an elastomer, which may typically have a high elastic nature. Non-limiting examples of the elastomer may include natural rubbers such as latex or synthetic rubbers, which may be nitrile rubbers, silicone rubbers, urethane rubbers, butadiene rubbers, styrene-butadiene rubbers, neoprene rubbers, chloroprene rubbers, polysulfide rubbers and Ethylene Vinyl Acetate (EVA rubbers).
The present disclosure therefore also provides a method of forming the plurality of imprints on the inner surface of the polymeric substrate comprising the steps of:
a) contacting the liquid polymeric mixture with the mold having the imprint forming surface thereon, wherein the mold having the imprint forming surface thereon comprises the pressure-dependent material as defined above;
b) curing the liquid polymeric mixture of step a) to form said polymeric substrate having said plurality imprints on said inner surface, when cured; and
c) subjecting said mold to a vacuum to thereby remove said mold from said polymeric substrate.
In some embodiments, the polymeric substrate obtained from the above method advantageously may be used as a further mold that is the polymeric substrate having the plurality of imprints on its inner surface formed by the method as defined above may serve as an external mold.
When the polymeric substrate above is used as the external mold, a pressure-dependent material, preferably in the form of hollow cylinder, may be then inserted into the external mold. In this assembly, there are two molds, that is, the “external mold” of the polymeric substrate having the plurality of imprints on its inner surface and “an internal mold”, which has been inserted as described above. The liquid polymeric mixture may be then deposited into the spaces formed between the inner and external molds followed by curing the liquid polymeric mixture. The external mold may be removed by peeling it away, whereas the internal mold may be removed by subjecting the above assembly to a vacuum.
Upon subjecting the above assembly to the vacuum, the shape and/or size of the internal mold may be distorted due to its elasticity of the internal mold. As the pressure of the air inside the internal mold is reduced relative to the atmospheric pressure, the hollow internal mold is distorted in the above assembly. The distortion or collapse of the internal mold may “demold” the internal mold from the inner wall of the cured polymeric substrate and this will allow the removal of the internal mold.
As the internal mold above has elastic nature, the internal mold may, partially or completely, return to its original shape or size (before being subjected to the vacuum) such that it may advantageously be re-used to cast another polymeric substrate after the vacuum is released. Therefore, the method above may be considered cost-effective since the internal mold may be re-used further.
The external mold as defined above may be made of various polymers, which include but not limited to polyethylene, polystyrene, polycarbonate, polymethylmethacrylate, polypropylene, and polytetrafluoroethylene. The external cylindrical mold may also be made of metal or glass or ceramics. The external mold may be in a cylindrical shape. Such external cylindrical molds may be coated with a layer of anti-stiction coatings such as PTFE (Teflon) or perfluorodecyltrichlorosilane (FDTS) to reduce adhesion between the tubings and the external mold, and facilitate demolding.
Exemplary, non-limiting embodiments of a method of forming a mold having an imprint forming surface thereon will now be disclosed.
The mold having said imprint forming surface thereon may be fabricated via an imprinting method, a machining technique or a self-assembly process. However, it is to be understood that the above methods are not limiting. Therefore, other suitable techniques capable of generating the mold having the imprint forming surface with desired topographies may also be used where appropriate. The three methods above will be discussed further as follow.
When the imprinting method is used, the desired topographies may be imprinted or embossed on a surface of the polymeric material as defined above. Hence, for this purpose such polymeric material may be considered as a pre-mold. The suitable polymeric material used as the pre-mold is preferably polymethymethacryalate (PMMA) or polystyrene (PS). Such polymeric material may be in the form of sheets of films.
The polymeric sheets used may be preferably a thin polymeric sheet having a thickness in the range of from about 10 μm to about 100 μm, such as from about 10 μm to about 20 μm, from about 10 μm to about 40 μm, from about 10 μm to about 50 μm, from about 10 μm to about 60 μm, from about 10 μm to about 80 μm, from about 20 μm to about 40 μm, from about 20 μm to about 50 μm, from about 20 μm to about 60 μm, from about 20 μm to about 80 μm, from about 40 μm to about 50 μm, from about 40 μm to about 60 μm, from about 40 μm to about 80 μm or from about 60 μm to about 100 μm. More preferably, the thickness of the polymeric sheets is about 40 μm, about 50 μm or about 60 μm.
The polymeric sheets may be dissolved completely or partially in a solvent or a mixture of two or more solvents. The solvent is preferably an organic solvent. Non-limiting examples of the organic solvent may include acetic acid, acetone, acetonitrile, benzene, 1-butanol, 2-butanol, 2-butanone, t-butyl-alcohol, carbon tetrachloride, chloroform, cyclohexane, 1,2-dichloroethane, dimethyl formamide (DMF), dimethyl sulfoxide (DMSO), ethanol, ethyl acetate, hexane, methanol, methyl t-butyl ether (MTBE), N-methyl-2-pyrrolidinone (NMP), pentane, 1-propanol, 2-propanol, pyridine, tetrahydrofuran (THF), toluene, triethyl amine, o-xylene, m-xylene and p-xylene. It is to be noted that when the polymeric sheets can be dissolved for example in acetone, the substrate prepared by the method described herein is chemically resistant to acetone. Therefore, it is preferred that the polymeric sheets are selected in such a way that they can be dissolved in a solvent or a mixture of two or more solvents in which the substrate is chemically resistant to.
The imprinting step on the polymeric sheets above may require a two-dimensional flat master mold used to create the plurality of imprints, which may be micro- or nano-topographies. The two-dimensional flat master molds may comprise a metallic material, silicon-based material or a polymeric-based material. When the two-dimensional flat master molds are metallic materials, preferably the metal is nickel. For the two-dimensional flat master molds comprising a silicon-based material or a polymeric-based material, such silicon-based material or polymeric-based material may be the polymeric organosilicon compounds or polyurethanes as defined herein.
The imprinting step may be undertaken using a batch, continuous, semi-continuous or high-throughput imprinter under a suitable temperature and pressure for a period of time. The imprinting parameters may be adjusted during the imprinting step as appropriate or may be held constant throughout the imprinting process. When a batch imprinter system is used, the imprinting temperature may be set between about 100° C. to about 160° C., such as about 110° C., about 120° C., about 130° C., about 140° C. or about 150° C. The imprinting pressure in the batch imprinter system may be set to about 30, 40 or 50 atm. The duration of the imprinting step using batch imprinter system may be from about 200 to about 1000 seconds, preferably from about 300 to 600 seconds.
The imprinting step above may also be undertaken using UV-irradiation and such step may therefore be termed as an UV-imprinting. When UV-imprinting step is carried out, the polymeric sheet is preferably made of an UV-curable resin, which is dissolvable in a solvent after the UV-curing.
The imprinted or embossed polymeric sheets may then be adhered or attached onto an outer surface of the pre-mold in such a way that the non-imprinted surface of the polymeric film is in contact with the pre-mold to thereby form said mold having an imprint forming surface thereon. The pre-mold used for this purpose may comprise a polymeric material as aforementioned. The pre-mold as defined above has a straight parallel sides and cross-section composed of straight or curved lines. The preferred mold used in the above method is of a tube or a rod shape that is its cross-section is circular. When a tube or a cylindrical or a rod is used, the imprinted polymeric sheets may be adhered or attached thereon using an adhesive. Such adhesive may be a solid adhesive in the form of a tape made of acrylic or a liquid adhesive such as but not limited to chloroform. Upon adhesion or attachment, the mold having an imprint forming surface thereon may be formed.
It is to be understood that the mold having an imprint forming surface thereon after the adhesion or attachment above essentially may adopt or maintain the original shape of the pre-mold. For clarity purposes, if the pre-mold has a tube or rod shape, the mold having an imprint forming surface thereon may follow this tube or rod shape.
Throughout the present disclosure, unless specified otherwise, the term “mold” in a tube or a rod shape may be used interchangeably with “polymer rod”.
Therefore the present disclosure provides a method for forming a mold having an imprint forming surface thereon via a nano-imprinting method comprising the steps of:
i) imprinting the surface of a polymeric film; and
ii) adhering the imprinted polymeric film onto the outer surface of a pre-mold,
wherein the non-imprinted surface of the polymeric film is in contact with the pre-mold to thereby form said mold having the imprint forming surface thereon.
The mold having an imprint forming surface thereon as defined above may also be fabricated directly via machining techniques such as but not limited to laser, micro-electrical discharge machining (micro-EDM) or micro-milling. Any one of these aforesaid methods may selectively remove the polymeric material from defined positions on the mold's external surface to create the desired imprint forming surface with micro- or nano-patterns. Such technique enables the fabrication of seamless patterning around the circumference of the rod.
Alternatively, the mold having an imprint forming surface thereon may be manufactured via a deposition of a plurality of particles selected from polystyrene (PS), polymethylmethacrylate (PMMA) or silica onto the polymeric mold. The deposition may be achieved via drawing a meniscus of particle suspension along the length of the polymeric mold. Hence, this process may be considered as a self-assembly as the deposition occurs spontaneously without an external driving force. The deposition may occur in the presence of a solvent and one or more surfactants.
Following the deposition step, closely packed or loosely packed particles with the desired micro- or nano-topographies may be formed on the outer surface of the mold. The pattern or structure of the imprint formed may depend on the type of solvents and/or surfactants used.
The mold having the imprint forming surface thereon manufactured by any one of the methods described above serves as a template for preparing the substrate having the plurality of imprints on its inner surface. As mentioned above, the substrate produced may be in the form of a tube. The tube may be prepared via a casting or a coating technique.
When a casting technique is used, a liquid polymeric mixture (the liquid polymeric mixture here refers to the mixture prior to the curing step) may be deposited into spaces between the mold and an external mold, wherein said mold is inserted into said external mold. The mold of a tube or rod shape may have an imprint forming surface thereon. Therefore, when the tube mold is inserted into the external tube mold, such a system refers to two concentric layers of mold. In this configuration, the external mold may be removed after the liquid polymeric mixture is cured thereby forming said plurality of imprints on an inner surface of the polymeric substrate.
Following the deposition of the liquid polymeric mixture into the spaces as described above, the deposited liquid polymeric mixture may be optionally degassed to remove bubbles formed during the depositing step. The degassed liquid polymeric mixture may then be cured to thereby forming a polymeric substrate having said plurality imprints on its inner surface. The curing step may be undertaken in the presence of heat or UV radiation. Without being bound by theory, other suitable curing techniques may also be used in this step.
Following the above, the external mold may be removed by dissolving it in a solvent or peeling it away, followed by removing the mold having the imprint forming surface thereon such as by dissolving it in a mixture comprising two or more solvents. Since said mold must be dissolvable, material selection for said mold is therefore crucial. For example, when the mold is a polymethylmethacrylate (PMMA) or polystyrene (PS) mold, upon curing of the polymeric substrate, PMMA or PS mold may be dissolved either via pumping acetone through the tube or immersing it in acetone bath with or without stirring.
Finally, to remove any residue of the solvent from the substrate having the plurality of imprints on its inner surface, said substrate may be subjected to a washing step, wherein the washing is undertaken in a mixture of solvents. For example, when acetone is used for removing the mold, ethanol or isopropanol may be used to remove traces of acetone.
The dimensions of the substrate formed via casting method may be defined by the dimensions and/or topographies of the mold and the external mold.
Therefore, the present disclosure provides a method of forming the plurality of imprints on the inner surface of the polymeric substrate comprising the steps of:
a) contacting the liquid polymeric mixture as defined above with the mold having the imprint forming surface thereon, wherein the contacting step is undertaken via a casting technique;
b) curing the liquid polymeric mixture of step a) to form said polymeric substrate having said plurality imprints on its inner surface, when cured; and
c) removing said mold from said polymeric substrate.
As aforementioned, for the method where the contacting step is undertaken via casting process, it is to be appreciated that the inner surface of the polymeric substrate may be the one in direct contact with the outer surface of the mold (such as the one represented as (109) in
As an alternative to the casting method described above, the plurality of imprints on the inner surface of the polymeric substrate may also be formed via a coating method. Non-limiting examples of the coating method may include spray coating, dip coating or vapour deposition. The preferred coating method of the present disclosure is a dip-coating technique. In this method, unlike the casting technique, an external mold may not be required that is the dimensions of the substrate is determined by the dimensions of the mold having the imprint forming surface thereon and the parameters used in the coating step.
When the dip coating method is selected, said method may involve partial or complete dipping of the mold into a reservoir containing the liquid polymeric mixture followed by curing the liquid polymeric mixture. The dipping and curing steps may be repeated to obtain the polymeric substrate having the plurality of imprints on the inner surface with different thickness.
In some embodiments, the mold of cylindrical shape (rod with negative structures) is dipped vertically into a reservoir that contains the liquid polydimethylsiloxane (PDMS). The cylindrical mold may then be removed from the reservoir and allow excess liquid polymeric to drain away leaving a layer of liquid PDMS of the surface of the mold followed by curing the liquid PDMS thermally or under UV exposure. The dipping and curing steps above may be repeated to achieve the required wall thickness of the tubing.
Based on the above, the present disclosure also provides a method of forming the plurality of imprints on the inner surface of the polymeric substrate comprising the steps of:
a) contacting the liquid polymeric mixture as defined above with the mold having the imprint forming surface thereon, wherein the contacting step is undertaken via a dip-coating method;
b) curing the liquid polymeric mixture of step a) to form said polymeric substrate having said plurality imprints on its inner surface, when cured; optionally repeating steps a) and b); and
c) removing said mold from said polymeric substrate.
For the method where the contacting step is undertaken via dip-coating process, the inner surface of the polymeric substrate may be the one in direct contact with the outer surface of the mold (such as the one represented as (109) in
In the above curing process, a curing agent may be added to facilitate the hardening or toughening process. The curing agent plays an important role in the curing kinetics, gel time, degree of curing, viscosity, curing cycle as well as the final properties of the cured polymer or polymeric mixture. The curing agents may include active hydrogen-containing compounds and their derivatives, anionic and cationic initiators and reactive cross-linkers.
When one or more curing agent is added, the curing agent may be mixed with the liquid polymeric mixture as defined above following a ratio of about 1:5 to about 1:50 of the curing agent:liquid polymeric mixture. The ratio may be about 1:10, about 1:20, about 1:25, about 1:30 or about 1:40.
The plurality of imprints aforementioned may be in the form of micro- or nano-structures or topographical features, which may be replicated on the inner luminal surface of tubings. Thus, the plurality of imprints above may be in the form of one-dimensional, two-dimensional or three-dimensional structure(s). Such structures may be continuous or discrete.
It is to be understood that the topographical features may be arranged in ordered arrays, non-ordered meta-surfaces or random.
The plurality of imprints on the inner surface of the polymeric substrate as defined above may have a lateral dimension in the range of about 20 nm to about 500 μm, about 20 nm to about 100 nm, about 20 nm to about 60 nm, about 60 nm to about 100 nm, about 100 nm to about 1 μm, about 100 nm to about 500 nm, about 500 nm to about 1 μm, about 1 μm to about 500 μm, about 1 μm to about 250 μm, about 250 μm to about 500 μm. More preferably, the lateral dimension above is in the range of about 20 nm to about 40 nm such as about 21 nm, about 22 nm, about 23 nm, about 24 nm, about 25 nm, about 26 nm, about 27 nm, about 28 nm, about 29 nm, about 30 nm, about 31 nm, about 32 nm, about 33 nm, about 34 nm, about 35 nm, about 36 nm, about 37 nm, about 38 nm, about 39 nm or about 40 nm.
The plurality of imprints on the inner surface of the polymeric substrate as defined herein may have a vertical dimension in the range of about 1 nm to about 500 μm, about 1 nm to about 100 nm, about 1 nm to about 50 nm, about 50 nm to about 100 nm, about 100 nm to about 1 μm, about 100 nm to about 500 nm, about 500 nm to about 1 μm, about 1 μm to about 500 μm, about 1 μm to about 250 μm, about 250 μm to about 500 μm. More preferably, the vertical dimension above is in the range of about 1 nm to about 5 nm such as about 1 nm, about 2 nm, about 3 nm, about 4 nm or about 5 nm.
The method disclosed in the present invention therefore provides micro- or nano-structures or the plurality of imprints that may impart various functionalities to the tubing such as an anti-bacterial, superhydrophobic surface to reduce frictional drag, turbulence promoting structures to enhance mixing in the tube or anisotropic wetting structures that can promote flow.
The accompanying drawings illustrate a disclosed embodiment and serves to explain the principles of the disclosed embodiment. It is to be understood, however, that the drawings are designed for purposes of illustration only, and not as a definition of the limits of the invention.
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Non-limiting examples of the invention will be further described in greater detail by reference to specific Examples, which should not be construed as in any way limiting the scope of the invention.
H: hour(s)
m.p.: melting point
min: minute(s)
FDTS: perfluorodecyltrichlorosilane
PDMS: polydimethylsiloxane
PMMA: polymethylmethacrylate
PTFE: polytetrafluoroethylene (Teflon)
PS: polystyrene
Rt: room temperature
UV: ultraviolet irradiation
Poly(dimethylsiloxane) or PDMS (under trademark Sylgard® 184) was provided by the Dow Chemical Company (Midland, Mich., United States). Acetone and chloroform were purchased from Merck (Kenilworth, N.J., United States of America) and used without further purification, unless specified otherwise. Polymethylmethacrylate (PMMA) free-standing films were obtained from Goodfellow Cambridge Ltd. (United Kingdom). Perfluorodecyltrichlorosilane (FDTS) was purchased from Gelest Inc. (Morrisville, Pa., United States of America). Other reagents or materials and/or solvent(s) than the above were purchased from Sigma-Aldrich Corp. (St. Louis, Mo., United States of America) and were used as received where otherwise noted in the experimental text below.
The method of imparting micro- or nano-topographies on the curved, inner surface of the tubing involves creating a negative of the desired topographies on the outer surface of a dissolvable cylinder or polymer rod which can be dissolved by a solvent in which the tubing is chemically resistant to. The tubing can be formed by cast molding or dip-coating, with the patterned cylinder serving as a template for the inner surface of the tubing. Discrete topographies in addition to continuous topographies (e.g. lines), can be created using this method.
The following describes the sequential process that must be followed for the creation of the tubing:
1. Method to Create a Negative Relief of the Desired Topographies onto a Cylindrical Mold
This step enables the fabrication of the negative micro- or nano-features onto the cylindrical inner mold. The cylindrical inner mold can be a rod or a hollow tube. The hollow tube version allows solvents to be pumped and circulated through the inner mold and enhanced dissolution rate of the mold. The entire dissolvable inner mold embodiment must be dissolvable in the solvent. The cylindrical mold can be fabricated by nano-imprint, micro-machining or self-assembly methods as indicated in
The imprinting method allows two-dimensional (2D) flat master molds (101) to be used to create micro- or nano-topographies (111) on curved inner luminal surfaces (103). The desired topographies were first imprinted onto a thin freestanding polymer film (113) that can be dissolved by a solvent in which the tubing material is chemically resistant to. Imprinting temperature is above the glass transition temperature of the polymer film (
Polymer cylinders (121) are directly machined by techniques such as but not limited to laser, micro-EDM or micro-milling to create micro- or nano-patterns (123 or 125) on the polymer rod surface (
Micro- or nano-topographies (135) can also be achieved via the deposition of particles (e.g. PS, PMMA, silica-137) onto the tubes or rods by drawing a meniscus of particle suspension from the solution with micro- or nano-particles (133) along the length of the rod (131) (
2. Methods of Fabricating Tubings with Patterned Inner Surface
The inner cylindrical mold serves as the template for the fabrication of tubings. The tubings can be fabricated via two processes: casting or dip-coating. The diameter of the inner cylindrical mold defines the inner diameter of the tubings. The tubings' wall thickness and external diameter can be controlled by the outer cylindrical mold (casting method—
In the cast molding method, the external cylindrical mold (203) defines the external diameter of the tubing (
I. Casting the liquid polymer (e.g. PDMS-205) forming the tubing into a mold which comprises of two concentric layers whereby the inner layer is the patterned inner cylindrical mold (201), and the outer layer (203) is a tube that can be easily removed after the liquid polymer has cured. This outer layer (203) can be peeled away or be dissolved by a solvent which the tubing is chemically resistant to. The inner layer of the mold determines the inner diameter and surface of the tubing while the outer layer defines the outer diameter and surface of the tubing.
II. Degassing the liquid polymer to remove bubbles (207).
III. Curing the liquid polymer either by heat or UV (209). Curing conditions vary according to the temperature used. However, the curing temperature of the tubing polymer should be less than the glass transition temperature of the inner and outer mold. If curing temperature is higher than the glass transition temperature of the inner mold, the micro- or nano-topographies may be deformed.
IV. Removing the outer layer (203) of the mold by dissolving it or peeling it away.
I. Dipping the cylindrical mold (rod with the negative structures) (221) vertically into liquid pre-polymer mix (e.g. PDMS) (223) (
II. Removing the cylindrical mold from the liquid polymer and allow excess liquid polymer to drain away leaving a thin layer of liquid polymer (227) on the mold surface.
III. Curing the liquid polymer either thermally or under UV exposure (225).
IV. Repeating the dipping and curing steps (I)-(III) to achieve the required wall thickness (233) of the tubing.
We disclose two processes which can be used to dissolve the inner cylindrical mold using a solvent such as acetone after the curing of the tubing material. After the inner mold was dissolved, the tubings can be rinsed with ethanol and IPA to remove the solvent.
The assembly was immersed in a container of solvent capable of dissolving the inner cylindrical mold completely. In the case of PMMA or PS material, acetone is used. The bath can be heated above room temperature and stirred constantly to accelerate dissolution of the inner mold (
In this method, a hollow cylindrical mold was used in the tubing fabrication to allow solvent flow-through. The assembly was connected to a peristatic pump (301) and solvent reservoir (303) via silicone tubings. Solvent was pumped through the mold assembly and circulated continuously till the inner mold (305) was dissolved (
For the current prototype, a nickel mold was used to imprint on polymethylmethacrylate (PMMA) films with thickness of 0.05 mm via a batch imprinter system at elevated temperature and pressure. The conditions used for imprinting is: 120 to 150° C., 40 bars, and 300 to 600 seconds. These films can also be fabricated in a high-throughput manner via other imprinter systems such as roll-to-roll imprinter and roll-to-plate imprinter. The imprinted sheet/film was then adhered around a cylinder (e.g. PMMA or PS) by tape adhesive (e.g. acrylic tape). The adhesive can also be liquid adhesive or a solvent adhesive for acrylics such as chloroform. The cylindrical mold and adhesive must be dissolvable by the solvent in which the tubing is chemically resistant to.
As mentioned above, micro or nano-topographies were transferred from a nickel or silicon master mold onto freestanding thin PMMA films (0.05 mm thick) by nanoimprinting lithography or hot embossing process. The nanoimprinting process was performed at 150° C., 40 bars, 600 seconds. The films were demolded at 30° C. The imprinted PMMA films were wrapped around the circumference of the PMMA hollow cylinder (6 mm in diameter) to form the inner dissolvable mold. The PMMA film was adhered to the cylinder by acrylic-based double-sided tape. The assembly of the mold for casting the tubings is formed by using an outer cylindrical mold (polystyrene drinking straw; 10 mm in diameter) which defines the external diameter of the tubing and an inner dissolvable mold which defines the inner diameter. The inner dissolvable mold is secured in the center of the outer hollow mold by blue-tack. The blue-tack holds the inner mold along the center axis relative to the external mold. The mold assembly was left upright. Sylgard 184 was prepared in the ratio of 1:10 (curing agent:pre-polymer mix) by weight. Silicone pre-polymer mixtures were then poured into the spaces between the inner and outer mold. The mixtures were degassed in a vacuum desiccator to remove bubbles in the mix for 1 to 2 hours with the assembly standing upright. The assembly with the silicone mix was then cured thermally at 80° C. curing temperature over a period of 18 hours. After curing, the outer mold was peeled away.
Selective surface patterning (403) or whole surface area (401) patterning can be achieved using the method disclosed herein as indicated in
The key feature of this method is the use of an inner mold material which melts or vaporizes after increasing the temperature to above the material's melting or sublimation temperature.
Using existing tubings (e.g. silicone) with micro- or nano-topographies (501) on the inner luminal surface, the inner cylindrical mold can be casted with a compound or solution. This compound or solution can be heated to melt into a liquid state and solidify back when the temperature is reduced. An example is paraffin wax. It is a solid at room temperature and has melting points ranging from about 48° C. to 70° C. depending on the chain length of the hydrocarbon. When heated, the wax melts into a liquid (503) and can be casted into the existing tubings to form the inner cylindrical mold. Upon reduction in the temperature, the wax solidifies (505) back and conforms to the shape of the tubing including the micro- or nano-topographies (509). After demolding, the wax inner cylindrical mold (507) can be further used for casting new tubings (
2. Methods of Fabricating Tubings with Patterned Inner Surface
With the inner cylindrical mold, tubings can be casted using similar methods described previously such as dip-coating and casting. UV-curable resins can be used in placed of thermally-cured resins in this case. An example is UV-curable polydimethylsiloxane (silicone-based) material.
The removal of the inner mold does not require any solvent. The whole assembly will be heated (6010) above the melting or vaporizing temperature of the inner mold material to melt or vaporize away the inner mold (605). In the case of paraffin wax, the assembly can be heated above 50° C. to melt away the wax. The temperature will not melt the silicone tubing material, which has a high degradation temperature (
This method is used to fabricate tubings with micro- or nano-topographies on the inner luminal surface. However, this method is independent from the other two methods described above. This method comprises of the following main processes:
1. Method to Create a Negative Relief of the Desired Topographies onto an Elastic and Hollow Cylindrical Mold
Negative relief structures of the desired micro- or nano-topographies can be fabricated onto an elastic and hollow cylindrical mold (e.g. silicone) (751) by nanoimprint lithography method (
2. Methods of Fabricating Tubings with Patterned Inner Surface
Processes for fabricating the tubings are similar to methods previously described which include casting and dip-coating methods.
The key process is the use of vacuum in conjunction with the elasticity of the inner cylindrical mold to demold from the formed tubings (801). After the tubings are cured around the inner and outer cylindrical molds, the outer mold can be peeled away physically. To remove the inner elastic mold, one end of the inner hollow mold is sealed and the other end of the inner hollow cylindrical mold is connected to a vacuum source (
The types of micro- or nano-topographical features which can be replicated on the inner luminal surface of tubings include continuous one-dimensional (1 D) patterns, discrete two-dimensional (2D) arrays, and three-dimensional (3D) hierarchical structures. Micro- or nano-topographical features which can be fabricated or replicated by nanoimprint lithography, micro-machining techniques or self-assembly can potentially be transferred to the inner luminal surface of the tubings via the method as defined above. The patterns can be ordered arrays, non-ordered meta-surfaces or random (e.g. random roughness). Lateral and vertical dimensions of the features can go down to 30 nm and 2 nm respectively depending on the formulation of the tubing polymer.
Continuous or line grating features can include the cross-sections such as square waveform (901), V-grooves (903) and U-grooves (905) as shown in
Two-dimensional (2D) micro- or nano-structures can include regular arrays of protrusions (posts/pillars) (1001) (
Hierarchical or multilevel three-dimensional (3D) structures can be replicated on the inner luminal surface. A two-steps imprinting process can be performed on flat free-standing polymer films to achieve hierarchical micro- or nano-structures. Some examples of hierarchical or multilevel three-dimensional mold structures include the following as shown in
Micro- or nano-protrusions or wells with high aspect ratio more than 1 can potentially be fabricated on the inner luminal surface. The method disclosed herein does not require physical demolding of the inner mold from the tubings. Therefore, this method is advantageous in minimizing physical damage and preserves the high aspect ratio structures.
The imprinted polymeric substrate prepared by the method as defined above may be used generally in hydraulic applications. Hence, the polymeric substrate may be used as superhydrophobic tubings with reduced friction, tubings with enhanced passive mixing or tubings with anisotropic wetting structures that promote flow. The polymeric substrate prepared by the method as defined above may be used in medical applications. Hence, the polymeric substrate may be used as blood-handling tubings with reduced hemolysis, catheters with reduced biofouling or ultrasound-guided catheters with enhanced ultrasound visibility.
It will be apparent that various other modifications and adaptations of the invention will be apparent to the person skilled in the art after reading the foregoing disclosure without departing from the spirit and scope of the invention and it is intended that all such modifications and adaptations come within the scope of the appended claims.
| Number | Date | Country | Kind |
|---|---|---|---|
| 10201710108W | Dec 2017 | SG | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/SG2018/050595 | 12/6/2018 | WO | 00 |
