The present disclosure relates to a method for manufacturing a body, such as a film, comprising a particle structure fixated in a matrix material, said method comprising the steps of:
The disclosure also relates to a body obtained by said method, and to the use of said method in various applications.
Consumers' needs and industrial trends prompt the development of materials in many diverse fields such as sensor technology, 3D printing, printed electronics, food packaging and technical textiles. There has been a dramatic increase and development in all of these fields leading to major improvements. For instance, the introduction of active and intelligent food packaging can extend the shelf life of food or improve its organoleptic properties and thus prevent food losses. In a further example, technical textiles provide benefits in a large number of applications. Technical textiles are a large and growing sector directed to textiles manufactured for non-aesthetic purposes, where function is the primary criterion. Technical textiles include textiles for automotive applications, medical textiles (e.g., implants), geotextiles (reinforcement of embankments), agrotextiles (textiles for crop protection), and protective clothing (e.g., heat and radiation protection for fire fighter clothing, molten metal protection for welders, stab protection and bulletproof vests, and spacesuits).
Frequently, the desired material properties are imparted by particles included in the materials produced for a particular application. However, the location of the particles within the material is also critical for the overall material performance.
For instance, anisotropic materials are used in a wide and increasing range of applications. Typically, such materials include conductive particles fixated in a non-conductive matrix material. The conductive particles are intended to form conductive materials in the matrix material, so as to enable the anisotropic material to be, at least under certain circumstances, electrically conductive. Depending on the selection of particles and matrix materials, the anisotropic materials may be formed to be suitable for various applications, such as sensors, in solar cell applications, in printed electronics etc.
WO2014/001334 discloses a method for forming a body comprising a particle structure fixated in a matrix material. The particles are arranged in the matrix material as a result of being subjected to an electric and a magnetic field.
Despite their usefulness, methods relying on the use of electric and/or magnetic fields are limited to particles susceptible thereto. Further, the particle structure will be determined by the electric and/or magnetic field direction.
In some applications, the particles may include or consist of non-metallic particles thereby necessitating methods allowing for movement of these particles into a desired location within the material being formed. Examples of such particles include non-metallic oxygen scavengers, such as ascorbic acid, in food packaging, and silica particles in technical textiles. Coating technology is sometimes an option, but it is not always suitable or appropriate.
Acoustophoresis means migration with sound, wherein sound waves are the executors of movement. Particles in suspension exposed to an acoustic standing wave field will be affected by a radiation force. The force will cause the particles to move in the sound field if the acoustic properties of the particles differ from that of the surrounding medium. The magnitude of the particle movement and the particle movement direction will be determined by factors such as particle size, acoustic pressure amplitude, frequency of the sound wave etc.
Acoustophoresis has been used for separation purposes. U.S. Pat. No. 5,147,562 discloses an acoustophoresis method and apparatus for separation of species. It is mentioned that the acoustophoresis concept can utilize bulk congressional waves, surface waves or boundary waves between a solid (or liquid) container wall and a liquid subject. Acoustophoresis has also been used in the context of Lab on a Chip, i.e. on vary small scale, for biological applications. In Lab Chip, 2012, 2766-2770, it is described how Surface Acoustic Wave (SAW) acoustophoresis may be used for micro-object manipulation.
Mitri, F. G., Sinha, D. N. (IEEE, International Ultrasonics Symposium Proceedings, Pages 1556-1558, 2011) describe a method for making a repeating periodic 3D structure using ultrasound methods. This method is a fabrication technique. However, unlike the invention presented here this technique makes a material in a small cavity of 12 mm times 12 mm times 44 mm rather than a large film prepared by roll-to-roll or extrusion processes.
Manipulation of particles in fluid channels, such as “Lab on a Chip” devices, has also utilized acoustophoresis techniques to separate out a variety of materials. Lin et. al. (Surface acoustic wave acoustophoresis: now and beyond, Lab Chip., 2012 Aug. 21, pp 2766-70 and Wood et al. Alignment of particles in microfluidic systems using standing surface acoustic waves, Applied Physics letters; Jan. 1, 2008, Vol 92, Issue 4, p 044104 describe acoustic methods in a “Lab on a Chip” device. Such a device is quite different from the Roll-to-roll manufacturing/process technology application described here.
Thus, there is a need for alternative methods for forming materials such as functional materials allowing for increasing the versatility of the materials formed, and to enable industrial production thereof.
It is an object of the present disclosure to provide a method fulfilling said need
The above-mentioned object is achieved by a method for manufacturing a body comprising a particle structure fixated in a matrix material, said method comprising the steps of:
As used herein, “particle structure” is meant any desired configuration or structure of particles which is or is to be fixated in the matrix material.
As used herein “fixate” and “fixation” refers to make fixed, stationary, or unchanging. Fixation of the matrix material may be achieved by any suitable method, such as, for example, curing, ceramisation, cross-linking, gelling, irradiating, drying, heating, sintering or firing.
As used herein, “film” or “sheet” is meant any desired configuration or structure of the matrix material, for example made of ceramic, metallic, polymeric and/or biomolecular materials preferably width: 0.01-100 m: thickness: 0.01-10 mm, Length: 0.0001-100 km.
The acoustic wave may be provided between a first support and a second support contacting the mixture of viscous material and particles. Thus, there is provided a method as described herein further comprising a step of:
The first support and/or the second support may independently be made of a material comprising or consisting of steel, silicon, glass or any other suitable material. The first support and second support may be arranged to be located opposite to each other.
An acoustic wave may also be provided between further supports, said further supports contacting the mixture of viscous material and particles. The further supports, such as a third support and a fourth support, may be arranged to be opposite to each other and/or perpendicular to said first and second supports.
The acoustic standing wave may be provided by an acoustic resonator as known in the art. For instance, the acoustic resonator may be an ultrasonic transducer. The acoustic wave pressure amplitude and frequency may be adjusted to achieve the desired particle movement. The acoustic standing wave will provide one or more pressure node(s) and one or more pressure antinode(s). In the method described herein, a pressure node may be formed at an interface between the mixture of viscous matrix material and particles, and the first support and/or second support. Additionally or alternatively, a pressure node may be formed within the mixture of viscous matrix material and particles. Similarly, a pressure antinode may be formed at an interface between the mixture of viscous matrix material and particles, and the first support and/or second support. An antinode may also be formed within the mixture of viscous matrix material and particles. As an example, pressure nodes may be formed at the interface between the mixture and the first support, between the interface between the mixture and the second support and optionally within the mixture. Additionally, one or more pressure antinodes may be formed within the mixture. In a further example, pressure antinodes may be formed at the interface between the mixture and the first support, between the interface between the mixture and the second support and optionally within the mixture. Additionally, one or more pressure nodes may be formed within the mixture.
It will be appreciated that in the method described herein, the acoustic standing wave may be applied in one or more steps using acoustic standing waves of different magnitudes.
Depending on the particle properties such as size and aggregation state, the particles may gather at pressure nodes and/or pressure antinodes of the acoustic standing wave. For instance, large and/or rigid particles may gather at nodes while liquid particles may gather at antinodes. Time may also influence the result, making both small and large particles gather at nodes as time evolves.
The particles of the mixture of the method described herein may be one kind of particles or a mixture of different kinds of particles. The particles may be metallic, i.e. comprise or consist of a metal, or non-metallic. Examples of non-metallic particles include particles comprising or consisting of ceramic materials, polymers, oils, gases etc. Further, the particles may be conductive particles or non-conductive particles. In still a further example, the particles may be displaceable by a magnetic field such as paramagnetic particles or ferromagnetic particles.
The particles of the mixture of the method described herein may be selected from the group consisting of metal particles, air bubbles, oil droplets, polymer particles, carbonaceous particles, ceramic particles, bioactive particles, bacteria, viruses, archaea, fungi, sand particles, glass particles, colloidal particles and any combinations thereof.
The particles may be homogenous particles, i.e. a particle consists of a single material or a material mixture throughout the particle. However, the particles may also be heterogeneous particles, i.e. a particle consists of several materials. For example, the particle may have a core of one material, and a sheath of another material.
The particles may have any suitable shape. For instance, the particles may be substantially spherical or have an elongate shape.
Depending on the application, the particle size and/or size distribution may vary. As used herein, the particle size is understood to mean the largest linear dimension of the particle. As an example, the particles may have substantially the same size and/or density. The particle size may be in the micrometer or nanometer range. For instance, the particle size may be within the range of from 10 nm to 100 μm. Additionally or alternatively, the particles may have different sizes and/or densities. Further, the specific application will determine the appropriate concentration of particles to be used. If conductive particles are used in the method described herein, the concentration of these particles may be below a percolation threshold.
As used herein, a percolation threshold is defined as the lowest concentration of conductive particles necessary to achieve long-range conductivity in a random system. Such a random system is nearly isotropic.
The matrix material should be a material having a viscous form which is capable of being fixed. Fixation may be achieved by any suitable methods such as, for example, curing, cooling, ceramisation, cross-linking, gelling, irradiating, drying, heating, sintering, or firing. As an example, fixating the viscous matrix material may take place by curing.
The viscous matrix material may comprise or consist of a polymer. Fixating such as curing may then involve cross-linking of the polymer. The viscous matrix material may be UV-curable, and fixating of the viscous matrix material may comprise UV-curing thereof. Additionally or alternatively, the viscous matrix material may undergo humidity-curing, and fixating of the viscous material may comprise exposure of the mixture described herein to moisture, such as in air and at room temperature.
Prior to fixating of the viscous material, the method described herein may comprise one or more additional steps comprising subjecting the mixture of viscous matrix material and particles to an electric field and/or a magnetic field. The mixture may be subjected to the electric field and/or magnetic field before, after and/or at the same time as the mixture is subjected to the acoustic standing wave. In this way, different kinds of particles may be moved to different parts of the material being formed. For instance, conductive particles may be aligned along the flux direction along an electric field while non-conductive particles may gather at nodes and/or antinodes of the acoustic standing wave. In a further example, ferromagnetic particles are aligned along a flux direction along a magnetic field while non-magnetic particles gather at nodes and/or antinodes of the acoustic standing wave.
Once the viscous matrix material has been fixated, it may be desired to remove the first support and/or the second support. Thus, the method described herein may comprise a step of removal of said first support and/or said second support. The removal may take place by e.g. tearing, etching or dissolution of the support with a solvent. Upon removal of the first support and/or the second support at least part of the particle structure at the interface between the first and/or second support and the mixture of viscous matrix material and particles may become exposed. Additionally or alternatively, at least part of the particle structure may be embedded within the fixated matrix material so that it is not exposed, or exposed to a very limited extent, upon removal of the first support and/or the second support.
The matrix material may be a cross-linked polymer material upon fixation. This enables creation of bodies being useful for applications where the polymer properties of the matrix material is used together with the properties with the particle structure to achieve a desired function.
The body formed in the method described herein may have any suitable shape. For instance, it may have the shape of a film. In a further example, the body may have the shape of a layer, a combination of layers, a coil, a ball etc.
The body formed in the method described herein, may be used in combination with bodies formed by other methods. For instance, the body formed in the method described herein may be a layer, said layer being combined with layers formed by other methods.
Advantageously, the method described herein may be used in combination with well-known industrial methods. For instance, the industrial method may be adapted to include the method described herein. For instance, the method described herein may be used in combination with roll-to-roll processing, extrusion processes, 3D printing, electric and/magnetic fields, optical trapping and manipulation and/or printed electronics technology.
It will be appreciated that the method described herein may in itself be used on an industrial scale. This is a significant advantage, since it allows for large scale production of various kinds of materials as described herein.
The present disclosure also provides a body comprising a particle structure fixated in a matrix material, wherein said body is obtainable by the method described herein. There is also provided an article comprising said body is obtainable by the method described herein. The article may be selected form the group consisting of packaging materials, printed electronics, laminated materials, textiles such as technical textiles, paper and containers.
There is also provided a use of the method described herein for creating packaging materials such as food packaging materials.
There is also provided a use of the method described herein for creating printed electronics.
There is also provided a use of the method described herein for creating laminated materials.
There is also provided a use of the method described herein for creating textiles such as technical textiles.
There is also provided a use of the method described herein for creating paper.
There is also provided a use of the method described herein for creating containers.
The disclosure will now be further illustrated with reference to exemplary embodiments, with reference to the enclosed drawings, wherein:
a,b,c shows the AFS process used on micro organisms.
It should be noted that the drawings have not been drawn to scale and that the dimensions of certain features have been exaggerated for the sake of clarity.
Nanometer is abbreviated nm.
Micrometer is abbreviated μm.
Node is used interchangeably with pressure node.
Antinode is used interchangeably with pressure antinode.
AFS is used as abbreviation for “acoustophoresis”.
The device for preparing an anisotropic and/or inhomogeneous polymer film using an acoustic wave may be referred to as an acoustic force applicator (piezo). The acoustic is force applicator may be utilized for this method in a continuous process. In one or more embodiments, a continuous process may include a roll to roll process, where a roll of polymer film is provided, the polymer film is unrolled and moved through the acoustic field application zone to induce orientation in the polymer film, and rerolled on a take-up roll down line from the acoustic field application zone. In some embodiments, a continuous process may be provided where the polymer film is prepared, for example by polymer film casting on one end of the acoustic field generator, the polymer film is then moved through the acoustic field application zone to induce structures in the polymer film, and rolled on take-up roll down line from the acoustic field application zone.
Suitable polymers that may be used to create anisotropic polymer films include UV curable polymers, thermally curable polymers, and polymers in solution. The polymers may be heteropolymers or copolymers.
In one or more embodiments, the polymer film may include a block copolymer. In one or embodiments, the block copolymer may be a di-block copolymer represented by the formula: A-B, where A represents a block of repeating units and B represents a second different block of repeating units. In one or embodiments, the block copolymer may be a tri-block copolymer represented by the formula: A-B-A or A-B-C, where A represents a block of repeating units, B represents a second different block of repeating units, and C represents a third different block of repeating units. In one or embodiments, the block copolymer may be a tetra-block copolymer represented by the formula: A-B-A-B, A-B-C-A, A-B-C-B, or A-B-C-D, where A represents a block of repeating units, B represents a second different block of repeating units, and C represents a third different block of repeating units, and D represents a fourth different block of repeating units.
In embodiment that use a polymer in solution useful solvents for dissolving the polymer include, N-methyl pyrrolidine (NMP), dimethylformamide (DMF). dimethylsulfide (DMS), dimethylsulfoxide (DMSO), dimethyl acetamide (DMAC), cyclohexane, pentane, cyclohexanone, acetone, methylene chloride, carbon to tetrachloride, ethylene dichloride, chloroform, ethanol, isopropyl alcohol (IPA), butanols, THF, MEK, MIBK, toluene, heptane, hexane, 1-pentanol, water, or suitable mixtures of two or more thereof. The solvents can be both aqueous or non-aqueous.
In one or more embodiments, the concentration of polymer in solvent in the polymer solution is from about 5 weight percent to about 50 weight percent, in other embodiments from about 10 weight percent to about 45 weight percent, in other embodiments from about 15 weight percent to about 40 weight percent, in other embodiments from about 20 weight percent to about 35 weight percent, in still other embodiments from about 25 weight percent to about 30 weight percent.
As noted above, the polymer film may include particles. Suitable particle for use in preparing anisotropic polymer films include conducting particles semiconducting particles or dielectric particles. It should be noted, that in certain embodiment, particularly where a semi-conducting or conducting particle is used, an insulating layer may be required between the polymer film and the electrodes.
Suitable conductive particles may be prepared from Co, Ni, CoPt, FePt, FeCo. Fe3O4, Fe2O3, and CoFe2O4. Suitable semiconductive particles may be prepared from ZnS, CdSe, CdS, CdTe, ZnO, Si, Go, GaN, GaP, GaAS, InP, and InAs. Additional particles that may be conductive or semiconductive include carbon based nanoparticles, carbon black, carbon nanotubes (single as well as multi-walled) as well as other inorganic and organic synthetic or natural nanoparticles.
In some of the various embodiments, the size of the particles are in the range of about 0.1 nm to about 500 micrometres. In some of the various embodiments, the body has the shape of a film with width in the range of: 0.01-100 m, preferably 0.1 to 10 m, thickness 0.01-10 mm, preferable 0.1 to 1 mm and length: 0.0001-100 km, preferable above 1 m. In a roll to roll production of film, the film could be continuous and as such have an indefinite length.
The embodiments are further illustrated by the figures discussed below:
Imaging of AFS process in film. An inverted microscope is used to image the system. Changes in height can be observed by the change in the diffraction pattern of the particle. The images in
a, b, c shows how the AFS process is used on micro-organisms. The frequencies (F) were
Number | Date | Country | Kind |
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20150824 | Jun 2015 | NO | national |
Filing Document | Filing Date | Country | Kind |
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PCT/NO2016/000019 | 6/17/2016 | WO | 00 |