Patent Application
20170296972
The present disclosure generally relates to graphene-based materials and other two-dimensional materials and to composite materials in which the two-dimensional materials are disposed, and, more specifically, to methods for occluding at least a portion of undesired apertures, defects or pores in such materials.
Graphene represents an atomically thin layer of carbon in which the carbon atoms reside at regular lattice positions. Synthesizing graphene in a regular lattice is difficult due to the irregular occurrence of defects in as-synthesized two-dimensional materials. Such defects will also be equivalently referred to herein as “apertures,” or “holes.” Of particular interest for practical applications, for example, involving filtration, separation or selective containment, is the ability to make defect-free material of practical dimension. Processing and handling, which in most instances is required to use these materials, can also induce further defects in as-synthesized graphene and other two-dimensional materials.
Graphene has garnered widespread interest for use in a number of applications due to its favorable mechanical and electronic properties. Applications that have been proposed for graphene include, for example, optical devices, mechanical structures, and electronic devices. In addition to the foregoing applications, there is increasing interest in graphene for filtration or separation applications. In such applications, the presence of defects above a cutoff size or outside of a selected size range can be undesirable. On the other hand, defects below a critical size required for application-specific separation may be useful from a permeability perspective, as long as such defects do not negatively impact the integrity of the graphene.
The term “perforated graphene” is used herein to denote a graphene sheet with defects in its basal plane, regardless of whether the defects are natively present (intrinsic) or intentionally produced. Such apertures can be present in both single-layer and few-layer graphene (e.g., less than 10 graphene layers), multiple sheets of single layer graphene, as well as multiple sheets of few-layer graphene stacked upon one another. Multiple layer graphene includes those that are formed by stacking of independently synthesized single layer graphene as well as graphene grown in the form of multiple layers. The term “size-selective perforated graphene” is used herein to denote a graphene sheet with perforations or defects in its basal plane within a selected size range. Size-selective perforations in graphene include perforations that are intentionally introduced as well as intrinsic or native defects within a selected size range. The term size is used herein to refer to the dimensions of the perforation with respect to what fluids, chemical or particle can pass through or not pass through the perforation. A perforation may have any geometry including irregular geometry. Passage of a fluid and/or chemical species and/or particle through perforations in graphene depends at least in part on the size (i.e., the dimensions) of the perforations, but also can depend upon the chemical functionalization of the graphene at the perforation and on application of a voltage bias to the graphene. In one aspect of the inventive concepts disclosed herein, undesirable larger defects in graphene are mitigated employing methods of the inventive concepts disclosed herein.
Composite materials, typically composite membranes, in which a graphene sheet or other two-dimensional material is disposed on a porous substrate are useful in a variety of applications and particularly in filtering, selective barrier, or separation applications. A graphene sheet is disposed on a surface of a porous substrate, such that pores in the substrate are covered by the graphene sheet. Non-perforated, defect-free graphene, or graphene with defects below a application specific critical size, disposed over substrate pores prevents passage of fluids and/or chemical species and/or particles into and through the substrate pores. Introduction of size-selected perforations in the graphene sheet disposed on such pores provides for size-selected passage of fluids and/or chemical species and/or particles into and through the substrate pores. As noted above, size of graphene perforations is one of several factors that affect passage through the perforations. Composite membranes where pores in the substrate are covered by graphene having size-selective perforations are useful in a variety of filtering, separation and selective containment, and barrier layer applications. Due to the presence of intrinsic or native defects in graphene which can be created during synthesis and defects that are introduced by processing and handling, it is difficult to obtain composite membranes in which all or even the majority of substrate pores are covered by defect-free graphene or size-selected perforated graphene. Methods for reducing or eliminating flow through membrane substrate pores not covered by defect-free graphene or size-selected perforated graphene, and which do not significantly reduce the function of the membrane for filtration or separation would be particularly useful for preparation of practical filtration and separation materials. There are a number of methods available in the art for intentionally introducing perforations of desired size into graphene and other two-dimensional materials. Methods include among others, ion beam and particle beam irradiation such as with nanoparticles, UV-ozone exposure and patterning defects during synthesis of the two-dimensional material. Several techniques have been described for reducing or healing holes in graphene or composite membranes. For example, Zan et al. reports a nanoscale etching and reknitting process for healing graphene holes. This process is conducted over nanoscale dimensions and has limited applicability to materials of macroscopic dimensions. Published US application 2015/0122727 reports methods employing various means of deposition of materials to heal holes in graphene or plug holes in composite membranes. Methods reported include atomic layer deposition (ALD), chemical vapor deposition (CVD), and interfacial reaction.
In view of the foregoing, simplified techniques that allow a plurality of perforations having a desired size and chemistry to be prepared in graphene-based materials and other two-dimensional materials and reduces or prevents non-selective passage through the materials would be of considerable benefit in the art. Additionally, simplified techniques for the preparation of composite membranes in which substrate pores are covered by size-selected graphene or other two-dimensional material in which non-selective flow is prevented and which are useful in filtering or separation applications would also be of considerable interest. The present disclosure provides such methods and in particular provides composite membranes in which passage through substrate pores is mediated and/or controlled by size-selective perforated graphene.
The present disclosure describes methods for at least partially occluding flow of fluid and/or chemical species and/or particles through apertures within sheets of graphene-based materials or other two-dimensional materials. The present disclosure also describes related methods for occluding pores in a composite membrane to generate membranes where flow through the pores is mediated through size-selected perforated graphene or other two-dimensional materials.
In one aspect, the methods involve reacting an occluding moiety with defects or apertures in sheets of graphene-based materials or other two dimensional materials or catalyzing a reaction in such defects or apertures to mitigate the defect or aperture, where mitigation includes closing or healing of the defect or aperture or decreasing the size of the defect or aperture. In healing the graphene-based material, perforations in the graphene-based material may or may not be healed. Fluorescently tagged moieties may be used to verify healing or failure of healing. In an embodiment, reacting or catalyzing a reaction is directed to defects or aperture having a certain size, geometry or functionality. The methods can involve flowing a chemical moiety through the perforations in a sheet of the two-dimensional material such that only the moiety passing through the sheet of the two-dimensional material is available to react or catalyze a reaction with the defect or aperture, i.e., with chemical moieties at the defect or aperture. By choosing the occlusion technique and the occluding moiety, larger apertures in a sheet of a two-dimensional material can become occluded, for example, in preference to smaller apertures, producing a sheet of two dimensional material with improved flow selectivity. In some cases it can be desirable to occlude substantially all the apertures in a sheet of a two-dimensional material, such that the treated sheet of two-dimensional material is substantially impervious to flow of fluids or chemical species there through. The sheets of a two-dimensional material having at least partially occluded apertures prepared according to the embodiments described herein can be used in separation techniques and systems, although they are also usable in other applications, such as selective barrier applications. In an embodiment, sheets of two-dimensional material having at least partially occluded apertures and particularly sheets where the majority (greater than about 50%) of the apertures or wherein substantially all of the apertures are occluded can be used as starting material for preparation of size-selective perforated graphene or other two-dimensional material, wherein perforations of a selected size range are introduced into the sheets in which apertures have been occluded.
In some embodiments, perforated graphene-based material having at least a portion of its apertures occluded with a chemical moiety is described herein.
In another aspect, the disclosure relates to methods of making composite membranes in which a sheet of graphene-based material or other two-dimensional material is disposed on a surface of a porous substrate wherein at least a portion of the pores of the substrate are covered by the sheet of two-dimensional material and in which pores in the substrate, that are not covered or are only partially covered, are occluded with one or more occluding moieties such that fluid or other chemical moieties cannot pass through the occluded pores. The size of the moiety provides a selectivity for which size of pores will be occluded. The methods herein in certain embodiments ensure that pores in the composite membrane that are covered by the two-dimensional material are not occluded which results in composite membranes with minimal reduction in membrane function. Composite membranes with occluded pores include those in which a portion of the uncovered substrate pores are occluded, those in which a majority (50% or more) of the uncovered substrate pores are occluded and those in which substantially all (95% or more) of the uncovered pores are occluded. The two-dimensional material covering the pores may be defect and aperture-free, or may be size-selective perforated. In an embodiment, the two-dimensional material of the composite membrane is perforated after treatment to occlude pores that are not covered by the two-dimensional material. Size-selective perforation after pore occlusion provides composite membranes useful for size-selective filtration. Composite membranes in which uncovered pores are occluded are useful, for example, as starting materials for preparation of size-selective filtration membranes.
The disclosure also relates to composite membranes prepared by the methods herein wherein at least a portion of the uncovered pores of the substrate are occluded.
In an embodiment, the method of occluding uncovered pores includes introducing an occluding moiety into an uncovered pore. In an embodiment, the occluding moiety is one or more particles sized for at least partial entrance into the uncovered pore, but which do not pass through the pore. In an embodiment, the one or more particles are deformable after introduction into the pore by application of energy, for example, application of pressure, heat, light, particularly light of selected wavelength, or an ion or particle beam. In an embodiment, the one or more particles carry one or more chemical reactive groups which react or can be activated to react with compatible reactive groups in the pores, on the surface of the substrate or on other particles to facilitate anchoring of the one or more particles to occlude a pore.
In an embodiment, the occluding particles are swellable after entry into a pore. For example, the material from which the particle is made is selected such that it swells when contacted by material which is absorbed into the particle. In an embodiment, the particle is swellable on contact with a selected absorbable fluid. In an embodiment, the absorbable fluid is water or an aqueous solution. In an embodiment, the absorbable fluid is an organic solvent. In an embodiment, the absorbable fluid is a polar organic solvent. In an embodiment, the absorbable fluid is a non-polar organic solvent. In an embodiment, the occluding particles are hydrogel particles which swell on absorption of water. In an embodiment, the occluding particles are polymer particles which swell on adsorption of an organic solvent, such as cross linked organic thermoset polymers, for example.
In an embodiment, the one or more occluding particles are monodisperse with respect to particle size. In an embodiment, the one or more occluding particles have a selected range of particles sizes. In an embodiment, after initial occlusion of a pore by one or more particles of a given first size, additional secondary particles of a size less than that of the initial particles can optionally be introduced into a pore to further facilitate occlusion of the pore or to facilitate anchoring. In this embodiment, the first and secondary particles optionally carry reactive groups to facilitate reaction with compatible reactive groups on the surface of pores or on other particles. In this embodiment, after particle introduction, energy is optionally applied, for example, in the form of heat, light or ion beam irradiation to facilitate anchoring in the pores. The use of particles of different sizes can result in higher packing densities which can provide better occlusion of pores. Particle compositions can, for example, be employed for occlusion, which have bimodal or trimodal particle size distributions.
In an embodiment, the pore occluding moiety is one or more monomers or oligomers which are introduced into an uncovered pore and polymerized therein to form a polymer and occlude the pore. Polymerization may be activated by any known means that is not detrimental to the two-dimensional material or to the substrate, including for example, activation by heating to a selected temperature, irradiation with light of selected wavelength, and/or introduction of a polymerization catalyst, or other methods (see, for example, US Patent Application filed herewith, entitled SELECTIVE INTERFACIAL MITIGATION OF GRAPHENE DEFECTS, Atty. Docket No. 111423-1097, incorporated herein in its entirety) In some embodiments, a polymerization catalyst may be activated by application of heat, light or other form of energy.
In an embodiment, the pores of the substrate can be shaped along their length to facilitate occlusion by one or more particles. For example, the pores may be tapered where the size of the opening into a pore (e.g., the pore diameter) is larger than the size of the exit from the pore. In an embodiment, the pores of the substrate can be shaped at one or both pore openings (entrance or exit openings) to facilitate occlusion by one or more particles. Substrate pores may be shaped to have a desired geometry, e.g., circular, oval, rectangular, slit, square mesh, or the like to facilitate occlusion by one or more particles. Pores may be provided with internal ridges or ledges to facilitate occlusion by one or more particles. The lip or ridge may be at the top of the pore. The size of the exit from the pore (e.g., the exit diameter) may be decreased with respect to the pore opening to facilitate occlusion by particles. Shaping of pores may be combined with use of deformable particles. Shaping of pores may be combined with the use of particles carrying one or more reactive groups and in this embodiment shaped pores or the entrance or exit of the pores can be provided with compatible reactive groups to facilitate anchoring in the shaped pores. Shaping of the pores may be combined with any particle occluding method described herein. Shaping of the pores may be combined with polymerization of monomer and/or oligomers in shaped pores to occlude the pores.
In another embodiment, pore occlusion is obtained without introduction of an occluding moiety. In this embodiment, uncovered pores are occluded by the deformation or swelling of the substrate material forming the pore. In this embodiment, uncovered pores are selectively contacted to induce deformation or swelling of the substrate forming the pore to occlude the pore. Contacting can, for example, be with energy such as heat, light or an ion beam. Contacting can, for example, be with an absorbable fluid, such as water, aqueous solution or organic solvent, such that the substrate material at the pore swells to occlude the pore. In a related embodiment, the pores are provided with a deformable or swellable coating distinct from the substrate material. In this embodiment, selective contacting of uncovered pores with energy in the form, for example, of heat, light or an ion beam deforms the pore coating to occlude the pore. In this embodiment, where the coating is swellable, selective contacting of an uncovered pore with an absorbable fluid results in swelling to occlude the pore. Swellable coatings can, for example, be formed from swellable hydrogels or swellable polymers.
In an embodiment, the particles or other substrate pore occluding moieties are themselves selectively permeable having permeability that is selected for a given application. Permeable materials could include hydrogels, polymers, proteins, zeolites, metal-organic framework materials, or thin film solution membranes. The particles could also be covered with a semipermeable layer. An example would be a silica particle covered with polyethylene glycol. In an embodiment, the occluding particles are made at least in part of hydroxycellulose which is semi-permeable.
In an embodiment, particles, other occluding moieties, monomers, oligomers and optional polymerization catalysts, are introduced selectively into substrate pores that are not covered by two-dimensional material (uncovered substrate pores) by a flow of fluid, including liquid or gas. The flow of fluid or gas carrying the occluding moieties will not enter covered substrate pores. In an embodiment, selective introduction employs application of a cross-flow of fluid along the membrane and application of pressure. The cross-flow carrying occluding moieties is applied along the surface of the composite membrane upon which the two-dimensional material is disposed. In an embodiment, a flow of particles is applied to the top surface of a composite membrane and particles enter uncovered pores. The introduction step is optionally followed by a step of application of energy, a curing step or other step to facilitate anchoring of particles. Thereafter a cleaning step may be applied to the top surface of the composite material to remove particles that have not entered uncovered pores. Cycles of a particle introduction step, optional anchoring steps and a cleaning step may be repeated to achieve a desired level of pore occlusion. The effectiveness of pore occlusion can be assessed by flow rate measurements through an occluded composite membrane. More specifically, flow rate of a selected moiety (fluid, chemical species or particle) of a given size can be used to assess the effectiveness of substrate pore occlusion. In an embodiment, two or more of such cycles are performed. In an embodiment, five or more of such cycles are performed. In an embodiment, 9 or more of such cycles are performed.
In an embodiment, a pore occlusion process includes introduction of occluding moieties, more specifically particles, into substrate pores that are not covered by two-dimensional material (uncovered substrate pores). In an embodiment, a pore occlusion process further includes a step of removing occluding moieties that are not within substrate pores from the composite membrane. Introduction and removal (cleaning) steps can be repeated until a desired level of occlusion is achieved. In an embodiment, as described herein, a step of application of energy or chemical reaction can be applied after introduction of occluding moieties into substrate pores to facilitate anchoring of the moieties in the substrate pore.
In an embodiment, the methods herein for occluding defects, apertures or uncovered substrate pores are combined with methods of detection of defects or apertures in the two-dimensional material, such that occlusion methods are selectively applied to those portions of a sheet of two-dimensional material or those portions of a composite membrane where occlusion is needed. Such detection methods can include localized application of a selected assay fluid, e.g., a detectible gas, such as SF6, to the two-dimensional material or to the composite membrane to detect the location (or approximate location) of defects, apertures or uncovered pores by passage of the assay fluid. Detection methods can also include localized resistance or capacitance measurement, where a change in resistance or capacitance is an indication of a defect or aperture. Detection methods can further include the localized detection of passage of analytes, particles, electrons or light, e.g., UV or visible light, through defects, apertures or through uncovered pores.
The foregoing has outlined rather broadly the features of the present disclosure in order that the detailed description that follows can be better understood. Additional features and advantages of the disclosure will be described hereinafter. These and other advantages and features will become more apparent from the following description.
For a more complete understanding of the present disclosure, and the advantages thereof, reference is now made to the following descriptions to be taken in conjunction with the accompanying drawings describing specific embodiments of the disclosure, wherein:
A variety of two-dimensional materials useful according to inventive concepts disclosed herein are known in the art. In various embodiments, the two-dimensional material comprises graphene, carbon nanomembranes (CNM), molybdenum disulfide, or boron nitride (specifically the hexagonal crystalline form of boron nitride). In an embodiment, the two-dimensional material is a graphene-based material. In more particular embodiments, the two-dimensional material is graphene. Graphene according to the embodiments of the present disclosure can include single-layer graphene, multi-layer graphene, or any combination thereof. Other nanomaterials having an extended two-dimensional molecular structure can also constitute the two-dimensional material in the various embodiments of the present disclosure. For example, molybdenum sulfide is a representative chalcogenide having a two-dimensional molecular structure, and other various chalcogenides can constitute the two-dimensional material in the embodiments of the present disclosure. Choice of a suitable two-dimensional material for a particular application can be determined by a number of factors, including the chemical and physical environment into which the graphene or other two-dimensional material is to be terminally deployed.
In an embodiment, the two dimensional material useful in membranes herein is a sheet of graphene-based material. Graphene-based materials include, but are not limited to, single layer graphene, multilayer graphene or interconnected single or multilayer graphene domains and combinations thereof. In an embodiment, graphene-based materials also include materials which have been formed by stacking independent single sheet or multilayer graphene sheets. In embodiments, multilayer graphene includes 2 to 20 layers, 2 to 10 layers or 2 to 5 layers. In embodiments, graphene is the dominant material in a graphene-based material. For example, a graphene-based material comprises at least 30% graphene by weight, or at least 40% graphene, or at least 50% graphene, or at least 60% graphene, or at least 70% graphene, or at least 80% graphene, or at least 90% graphene, or at least 95% graphene. In embodiments, a graphene-based material comprises a range of graphene content selected from 30% to 95%, or from 40% to 80% from 50% to 70%, from 60% to 95% or from 75% to 100%. In embodiments, a graphene-based material comprises a range of up to 35% oxygen by atomic ratio.
As used herein, a “domain” refers to a region of a material where atoms are uniformly ordered into a crystal lattice. A domain is uniform within its boundaries, but different from a neighboring region. For example, a single crystalline material has a single domain of ordered atoms. In an embodiment, at least some of the graphene domains are nanocrystals, having a domain size from 1 to 100 nm or 10-100 nm. In an embodiment, at least some of the graphene domains have a domain size greater than 100 nm to 1 micron, or from 200 nm to 800 nm, or from 300 nm to 500 nm. “Grain boundaries” formed by crystallographic defects at edges of each domain differentiate between neighboring crystal lattices. In some embodiments, a first crystal lattice may be rotated relative to a second crystal lattice, by rotation about an axis perpendicular to the plane of a sheet, such that the two lattices differ in “crystal lattice orientation”.
In an embodiment, the sheet of graphene-based material comprises a sheet of single or multilayer graphene or a combination thereof. In an embodiment, the sheet of graphene-based material is a sheet of single or multilayer graphene or a combination thereof. In another embodiment, the sheet of graphene-based material is a sheet comprising a plurality of interconnected single or multilayer graphene domains. In an embodiment, the interconnected domains are covalently bonded together to form the sheet. When the domains in a sheet differ in crystal lattice orientation, the sheet is polycrystalline.
In embodiments, the thickness of the sheet of graphene-based material is from 0.34 to 10 nm, from 0.34 to 5 nm, or from 0.34 to 3 nm. In an embodiment, a sheet of graphene-based material comprises intrinsic or native defects. Intrinsic or native defects are those resulting from preparation of the graphene-based material in contrast to perforations which are selectively introduced into a sheet of graphene-based material or a sheet of graphene. Such intrinsic or native defects include, but are not limited to, lattice anomalies, pores, tears, cracks or wrinkles. Lattice anomalies can include, but are not limited to, carbon rings with other than 6 members (e.g. 5, 7 or 9 membered rings), vacancies, interstitial defects (including incorporation of non- carbon atoms in the lattice), and grain boundaries.
In an embodiment, a sheet of graphene-based material optionally further comprises non-graphenic carbon-based material located on the surface of the sheet of graphene-based material. In an embodiment, the non-graphenic carbon-based material does not possess long range order and may be classified as amorphous. In embodiments, the non-graphenic carbon-based material further comprises elements other than carbon and/or hydrocarbons. Non-carbon elements which may be incorporated in the non-graphenic carbon include, but are not limited to, hydrogen, oxygen, silicon, nitrogen, copper and iron. In embodiments, the non-graphenic carbon-based material comprises hydrocarbons. In embodiments, carbon is the dominant material in non-graphenic carbon-based material. For example, a non-graphenic carbon-based material comprises at least 30% carbon by weight, or at least 40% carbon, or at least 50% carbon, or at least 60% carbon, or at least 70% carbon, or at least 80% carbon, or at least 90% carbon, or at least 95% carbon. In embodiments, a non-graphenic carbon-based material comprises a range of carbon selected from 30% to 95%, or from 40% to 80%, or from 50% to 70%.
Two-dimensional materials in which pores are intentionally created are referred to herein as “perforated,” such as “perforated graphene-based materials,” “perforated two-dimensional materials,” or “perforated graphene.” Two-dimensional materials are, most generally, those which have atomically thin thickness from single-layer sub-nanometer thickness to a few nanometers and which generally have a high surface area. Two-dimensional materials include metal chalogenides (e.g., transition metal dichalogenides), transition metal oxides, hexagonal boron nitride, graphene, silicene and germanene (see: Xu et al. (2013) “Graphene-like Two-Dimensional Materials) Chemical Reviews 113:3766-3798).
Two-dimensional materials include graphene, a graphene-based material, a transition metal dichalcogenide, molybdenum disulfide, a-boron nitride, silicene, germanene, or a combination thereof. Other nanomaterials having an extended two-dimensional, planar molecular structure can also constitute the two-dimensional material in the various embodiments of the present disclosure. For example, molybdenum disulfide is a representative chalcogenide having a two-dimensional molecular structure, and other various chalcogenides can constitute the two-dimensional material in embodiments of the present disclosure. In another example, two-dimensional boron nitride can constitute the two-dimensional material in an embodiment of the inventive concepts disclosed herein. Choice of a suitable two-dimensional material for a particular application can be determined by a number of factors, including the chemical and physical environment into which the graphene, graphene-based or other two-dimensional material is to be deployed.
The present disclosure is directed, in part, to sheets of graphene-based material or other two-dimensional materials containing a plurality of perforations therein, where the perforations have a selected size and chemistry, as well as pore geometry. In embodiments, the perforated graphene, perforated graphene-based materials and other perforated two-dimensional materials contain a plurality of size-selected perforations ranging from about 3 to 15 angstroms in size. In a further embodiment, the perforation size ranges from 3 to 10 angstroms or from 3 to 6 angstroms in size. The present disclosure is further directed, in part, to perforated graphene, perforated graphene-based materials and other perforated two-dimensional materials containing a plurality of size-selected perforations ranging from about 3 to 15 angstroms in size and having a narrow size distribution, including but not limited to a 1-10% deviation in size or a 1-20% deviation in size. In an embodiment, the characteristic dimension of the perforations is from about 3 to 15 angstroms in size.
The present disclosure is also directed, in part, to perforated graphene, perforated graphene-based materials and other perforated two-dimensional materials containing a plurality of perforations ranging from about 5 to about 1000 angstroms in size. In further embodiments, the perforations range from 10 to 100 angstroms, 10 to 50 angstroms, 10 to 20 angstroms or 5 to 20 angstroms. In a further embodiment, the perforation size ranges from 100 nm up to 1000 nm or from 100 nm to 500 nm. The present disclosure is further directed, in part, to perforated graphene, perforated graphene-based materials and other perforated two-dimensional materials containing a plurality of perforations ranging from about 5 to 1000 angstrom in size and having a narrow size distribution, including but not limited to a 1-10% deviation in size or a 1-20% deviation in size. In an embodiment, the characteristic dimension of the perforations is from 5 to 1000 angstrom.
For circular perforations or apertures, the characteristic dimension is the diameter of the perforation or aperture. In embodiments relevant to non-circular pores, the characteristic dimension can be taken as the largest distance spanning the perforation or aperture, the smallest distance spanning the perforation or aperture, the average of the largest and smallest distance spanning the perforation or aperture, or an equivalent diameter based on the in-plane area of the perforation or aperture. As used herein, perforated graphene-based materials include materials in which non-carbon atoms have been incorporated at the edges of the pores.
The present disclosure particularly describes methods directed to occluding apertures in a sheet of a graphene-based material or other two-dimensional material that are larger than a given threshold size, thereby reducing the plurality of apertures to a desired size and optionally with a specific chemistry. In embodiments, the reduced size of the aperture falls within the perforation and aperture size ranges given above. The threshold size can be chosen at will to meet the needs of a particular application. Perforations or apertures are sized as described herein to provide desired selective permeability of a species (atom, molecule, protein, virus, cell, etc.) for a given application. Selective permeability relates to the propensity of a porous material or a perforated two-dimensional material to allow passage (or transport) of one or more species more readily or faster than other species. Selective permeability allows separation of species which exhibit different passage or transport rates through perforations or apertures. In two-dimensional materials selective permeability correlates at least in part to the dimension or size (e.g., diameter) of perforations or apertures and the relative effective size of the species. Selective permeability of the perforations or apertures in two-dimensional materials such as graphene-based materials can also depend on functionalization of the perforation or aperture (if any) and the specific species that are to be separated. For electrically conductive two dimensional materials, selective permeability can be affected by application of a voltage bias to the membrane. Selective permeability of gases can also depend upon adsorption of a gas species on the filtration material, e.g., graphene. Adsorption at least in part can affect the local concentration of the gas species at the surface of the filtration material. Separation of two or more species in a mixture includes a change in the ratio(s) (weight or molar ratio) of the two or more species in the mixture after passage of the mixture through a perforated two-dimensional material.
The chemistry of the perforated apertures can be the same or different after being occluded according to the embodiments described herein. In various embodiments, occluding the apertures can involve occluding apertures within a particular size range such that no apertures remain within the size range, thereby conferred selectivity to the “healing” of the graphene-based material or other two-dimensional material. The embodiments of the healing processes described herein are applicable to both “through-holes” (i.e., pores in a single two-dimensional sheet) and “intralayer flow” (i.e., passages existing between stacked layers of individual single layer two-dimensional sheets or multiple layer sheets of 2-D material. Passages can include laterally offset pores within multiple two-dimensional sheets. Through-holes can also exist in multiple two-dimensional sheets when the pores are not substantially laterally offset from one another in the various layers
The embodiments described herein allow specific chemistries to be readily applied in a homogenous manner to graphene-based materials and other two-dimensional materials to allow for tunable activity across many applications. While the chemistries described herein can be applied homogenously to an entire surface of the sheet of graphene or other two-dimensional material, they generally provide specific activation of particular perforations or apertures of a given size using a carefully sized moiety that allows for aperture modification to take place. The described techniques can be advantageous in allowing the homogenous application of chemistry to the graphene-based material or other two-dimensional material surface while only occluding perforations or apertures of a certain desired size. The homogenous application of the various chemistries described herein can facilitate scalable production and manufacturing ease. Perforation or aperture modification can confer a specific chemistry to the perforations or apertures (e.g., functional selectivity, hydrophobicity, and the like) and allow for at least partial occlusion of the perforations or apertures to take place in various embodiments. Such selective modification of the apertures can allow selective separations to take place using the graphene-based material, including size-based separations.
For example, perforations or apertures can be selectively modified by various known methods to contain hydrophobic moieties, hydrophilic moieties, ionic moieties, polar moieties, reactive chemical groups, for example, amine-reactive groups (chemical species that react with amines) carboxylate-reactive groups (chemical species that react with carboxylates), amines or carboxylates (among many others), polymers and various biological molecules, including for example, amino acids, peptide, polypeptides, enzymes or other proteins, carbohydrates and various nucleic acids.
Furthermore, the techniques described herein can be configured to at least partially occlude large apertures within the sheet of graphene-based material or other two-dimensional material in preference to smaller apertures, thereby allowing the smaller apertures to remain open and allow flow to be maintained therethrough. This type of selective flow can allow molecular sieving to take place using the graphene-based material or other two-dimensional material, rather than the solution-diffusion model provided by current polymeric solutions. In some aspects, apertures or defects are blocked to provide flow reduction or blockage within a range of 50% or more, 60% or more, 70% or more, 80% or more, 90% or more, 95% or more. In further aspects, however, all the apertures and/or defects in a graphene-based material or other two-dimensional material can be occluded in order to substantially block passage or flow, herein 99% or more through the two-dimensional material or block passage or flow through the two-dimensional material entirely. In an embodiment, a graphene-based material or other two-dimensional material that is occluded in order to substantially or entirely block passage or flow through the material can be used as a starting material for forming a size-selected perforated two-dimensional material. Size-selected perforations can be introduced into the substantially or entirely blocked two-dimensional material employing art known methods for generating perforations of a selected size and, if any, a selected functionalization.
Although the description herein is primarily directed to graphene-based materials, it is to be recognized that other two-dimensional materials or near two-dimensional materials can be treated in a like manner. The at least partially occluded graphene-based materials prepared according to the techniques described herein can be used for occluding fluid flow, particularly liquid or gas flow for separations, including filtration membranes and filtration systems. In addition, they can be used in optical or electronic applications.
In some embodiments, the graphene-based material can be transferred from its growth substrate to a porous substrate in the course of, before or after practicing the embodiments described herein.
By way of example, a sheet of a graphene-based material or sheet of another two-dimensional material can have a plurality of perforations therein, and a direction of fluid flow therethrough can establish an “upstream” side (alternative the top surface) and a “downstream” side (alternatively the bottom surface) of the sheet. The downstream side of the sheet of the graphene-based material or sheet of another two-dimensional material can be next to or in contact with a substrate, such as a porous substrate. In some embodiments, the substrate can provide support to the sheet of the graphene-based material while practicing the various techniques described herein. The perforations in the sheet of a graphene-based material or sheet of another two-dimensional material can be intentionally placed therein, or they can occur natively during its synthesis. According to the embodiments of the present disclosure, the perforations can have a distribution of sizes, which can be known or unknown. By placing an occluding moiety within a flow contacting the graphene-based material or other two-dimensional material, apertures having a desired size profile can become occluded according to the embodiments described herein.
In some embodiments described herein, a fluid containing a sized moiety can be flowed through the sheet of graphene-based material or other two-dimensional material. The sized moiety can lodge in some of the apertures in the sheet and induce occlusion of at least the portion of the apertures in the sheet in which the sized moiety lodges. In other embodiments, a sized moiety can occlude fluid flow on the sheet of graphene-based material or other two-dimensional material from the upstream side of the graphene. Various embodiments of these various flow configurations are described below.
Occluding at least a portion of the apertures in the foregoing manner can result in reducing the size and number of apertures, possibly modifying a flow path and making the graphene-based material or other two-dimensional material suitable for use in an intended application. For example, the graphene-based material or sheet of another two-dimensional material can be processed in the foregoing manner to produce a cutoff pore size in a molecular filter. Depending on the nature of the moiety in the flow path, the moiety can be covalently or non-covalently attached to the graphene-based material, or mechanically connected to the graphene-based material.
In some embodiments, the “downstream” side of the sheet of graphene-based material can be “primed” or functionalized with oxygen via plasma oxidation or the like, such that the graphene-based material can be reactive with a moiety passing through the apertures. In some embodiments, the moiety in the flow path can bind to functional groups introduced to the graphene-based material, such that the moiety binds to the graphene-based material and the apertures become at least partially occluded. Suitable binding motifs can include, but are not limited to, addition chemistry, crosslinking, covalent bonding, condensation reactions, esterification, or polymerization. In various embodiments, the occluding moiety can be sized to reflect a particular cutoff regime, such that it only passes through apertures having a certain threshold size or shape. For example, in various embodiments, the occluding moieties can be a substantially flat molecule or spherical in shape. POSS® silicones (polyhedral oligomeric silsesquioxanes), for example, represent one particular type of occluding moiety that can be made at a very specific size and functionalized to tether to oxygenated functionalization on the apertures. Other examples, of useful occluding moieties include fullerenes, dendrites, dextran, micelles or other lipid aggregates, and micro-gel particles. Some or all of these techniques may be applied to other two-dimensional materials as well.
In various embodiments, the graphene-based material can be perforated and functionalized with oxygen, such as treating the graphene-based material with oxygen or a dilute oxygen plasma, thereby functionalizing the graphene-based material with oxygen moieties. In some embodiments, the graphene based material can be functionalized in this manner while on a copper substrate. Subsequently, the oxygen functionalities can be reacted via a chemistry that converts the oxygenated functionalities into a leaving group (such as a halide group, particularly a fluoro group, or sulfonic acid analogs, such as tosylates, triflates, mesylates, and the like). This chemistry results in sites on the substrate that are vulnerable to nucleophilic attack and can be used for additional chemistry, as detailed above, or allowing the graphene based material to bind to the substrate. In some embodiments, the graphene-based material can functionalized with oxygen so as to provide graphene oxide platelet membranes.
In other embodiments, the downstream side of the graphene-based material or other two-dimensional material can be primed with an occluding substance and a moiety that catalyzes the reaction of the occluding substance with the graphene or other two-dimensional material can pass through the apertures. Thus, in this case, the moiety does not become bonded to the graphene or other two-dimensional material itself.
In the foregoing embodiments, also depicted in
In still further embodiments, carbonaceous or non-carbonaceous materials can be flowed over the graphene based material or other two-dimensional material and become tethered to the open apertures. Suitable materials can include, for example, graphene nanoplatelets (GNPs), fullerenes of various sizes, boron nitride, or carbon nanotubes. In more particular embodiments, tethering of the carbonaceous or non-carbonaceous material can be accomplished by utilizing a light or gentle ion beam, a high temperature annealing step, exposing to light to generate a photo-active reaction. The high temperature annealing step could comprise isocyanate crosslink chemistry. In some embodiments, flow through the two-dimensional material can become completely blocked. In some embodiments, smaller apertures can remain open.
In the depicted embodiments, the carbonaceous or non-carbonaceous materials are flowed laterally across the sheet of graphene-based material or other two-dimensional material, rather than passing through the apertures. In alternative embodiments, the carbonaceous materials or non-carbonaceous materials can be flowed through the sheet of graphene-based material or other two-dimensional material.
In still other embodiments, functionalization or activation of multiple, potentially different layered sheets of graphene-based materials or other two-dimensional material (e.g. complementary chemistries) can be leveraged to allow for flow not only through channels, but also via intralayer flow. Healing or partial occlusion can result from further modification of apertures. That is, layered sheets of two-dimensional material can be differentially functionalized according to the embodiments described herein.
The present disclosure is directed, in part, to composite membranes formed from a porous substrate having a plurality of pores with a sheet of two-dimensional material disposed on the surface of the porous substrate and defining a top surface of the composite membrane. A portion of the pores of the substrate are covered by the two-dimensional material and a portion of the pores of the substrate are not covered by the two-dimensional material due, for example, to defects formed during synthesis of the two-dimensional material, formed during handling of the two-dimensional material, or formed when the two-dimensional material is disposed on the porous substrate. Defects or apertures in the two-dimensional material can result in undesired passage of species through the composite membrane. It is desired for use in filtration applications, that substantially all of the substrate pores are covered by the two-dimensional material so that passage through the membrane is primarily controlled by passage through the two-dimensional material. In a specific embodiment, substantially all pores of the substrate are covered by a two-dimensional material that contains perforations of a desired size range for selective passage through the membrane. In a specific embodiment, perforations in the two-dimensional material have a selected chemistry at the perforation as discussed above. The perforation in the two-dimensional material can have selected size or selected size range and discussed above. In a specific embodiment, the two-dimensional material is a graphene-based material. In a specific embodiment, the two-dimensional material is a graphene-based material which comprises single-layer graphene or multi-layer graphene.
The disclosure provides methods for occluding uncovered substrate pores in the composite membrane as described above. In an embodiment, the method includes introducing one or more occluding moieties at least partially into at least one uncovered pore to occlude the at least one uncovered pore. In specific embodiments, 50% or more of the uncovered substrate pores are occluded. In more specific embodiments, 60% or more, 75% or more, 80% or more, 90% or more, 95% or more or 99% or more of the uncovered substrate pores are occluded. In specific embodiments, occlusion of uncovered pores reduced flow through the composite membrane (compared to the non-occlude membrane) by 50% or more. In specific embodiments, occlusion of uncovered pores reduced flow through the composite membrane (compared to the non-occluded membrane) by 60% or more, 75% or more, 80% or more, 90% or more, 95% or more or 99% or more.
The extent of occlusion of uncovered pores can be assessed by various methods. Detection of uncovered pores can, for example, be assessed using a selected assay fluid, e.g., a detectible gas, such as SF6, to detect the location (or approximate location) of uncovered pores by passage of the assay fluid. Uncovered pores may be detected by use of the passage of detectible chemical species, particles, electrons, UV or visible light through the pores. The presence of uncovered pores can also be detected by various imaging methods. The presence and or location (or approximate location) of pores can be assessed using various imaging methods (including scanning electron microscopy, scanning probe microscopy, scanning tunneling microscopy, atomic force microscopy, transmission electron microscopy, x-ray spectroscopy, etc.); detecting analyte, particles or ions passing through pores (using mass spectrometry, secondary mass spectrometry, Raman spectroscopy, residual gas analysis, detecting Auger electrons, detecting nanoparticles using a microbalance, detecting charged species with a Faraday cup, detecting secondary electrons, detecting movement of analyte through defects, employing an analyte detector, identifying a composition, mass, average radius, charge or size of an analyte; detecting electromagnetic radiation passing through defects; detecting electromagnetic radiation given off by analyte; and detecting electromagnetic radiation or particles back scattered from the membrane.
Uncovered substrate pores include those pores that are only partially covered, but through which non-selective passage can occur.
The porous substrate of the composite membrane can be any porous material compatible with a disposed two-dimensional material and particularly with a graphene-based material. The porous substrate is selected to be compatible with the application for which the composite membrane is intended. For example, compatible with the gases, liquids or other components which are to be in contact with the composite membrane. The porous substrate provides mechanical support for the two-dimensional material and must maintain this support during use. The porous support should substantially retain pores that are covered with two-dimensional material. In specific embodiments, the porous material is made of a polymer, metal, glass or a ceramic
The pores in the substrate can have uniform pore diameter along the length of the pore, or they can have a diameter that varies along this length. Pores or pore openings (entrance or exit) can be shaped, as discussed below, to facilitate retention of occluding moieties in uncovered pores. Pores may be tapered, ridged or provided with one or more ledges to facilitate retention of occluding moieties in uncovered pores. In a specific embodiment, the pore entrance and/or the pore exit is narrowed compared to the rest of the pore to facilitate retention of occluding moieties. In some embodiments, pores in the substrate are preferably of uniform size and uniform density (e.g., uniformly spaced along the substrate). In some embodiments, pores may be independent or may be interconnected with other pores (tortuous). In embodiments, pores sizes (e.g. diameters) can range from 10 nm to 10 microns or more preferably from 50 nm to 500 nm. For methods and composite membranes herein a top surface of the membrane is defined as the surface upon which the two-dimensional material is disposed. One surface contains pore entrance openings and the second surface contains pore exit openings. Introduction of occluding moieties is through pore entry openings so that introduction of such moieties is selectively into pores that are not covered by two-dimension materials. Pore entrance and exits are defined by flow direction through pores.
Occluding moieties most generally include any material that can be selectively introduced into uncovered pores and retained therein to occlude the pore. A step of chemical reaction, application of energy in the form of heat, electromagnetic radiation (e.g., UV, visible or microwave irradiation), or contact with an absorbable material can be applied to deform, swell, polymerize, cross-link or otherwise facilitate retention of occluding materials in a pore. In an embodiment, the occluding materials are one or more particles sized for entrance at least in part into an uncovered pore. Particle size and pore shape may be selected to facilitate retention in the uncovered pores. Particles may be deformable, for example, by application of pressure, heat, microwave radiation or light of a selected wavelength (e.g. UV light), or by ion bombardment. Deformable particles introduced into pores are retained in pores after deformation. Particles may be swellable, where the size of a particle increases on contact with an absorbable material which induces swelling. The absorbable material can, for example, be a fluid including liquids or gases, water or an aqueous solution or a miscible mixture of water and an organic solvent, a polar organic solvent or a non-polar organic solvent. The swellable particle and the absorbable fluid are selected to achieve a desired level of swelling to achieve retention in the pore.
Occluding particles can be made of any suitable material. In specific embodiments, particles selected from metal particles, silica particles, particles of metal oxide, or polymer particles. In specific embodiments, particles are made of melamine, polystyrene or polymethyl methacrylate (PMMA). In a specific embodiment, the particles are made of latex (polystyrene). In specific embodiments, the substrate pore occluding particles are themselves permeable to provide a selective permeability through the occluded pores. In specific embodiments, the substrate pore occluding particles are permeable to fluid flow and provide for separation of components in the fluid. Permeable materials could include hydrogels, polymers, proteins, zeolites, metal-organic framework materials, or thin film solution membranes.
Particle size is generally selected based on the pores sizes present in the substrate so that the particle can enter the pore and be retained in the pore. Particles may be monodisperse if the pore entrance openings are uniform in size. A mixture of particles of different sizes can be employed when pore openings are non-uniform in size. A mixture of particles of different sizes (having a selected particle size distribution or being polydisperse in size) can be used, if pores with different (or unknown sizes) are present in the substrate. In an embodiment, the occluding particle is selected to have particle size that is approximately the same size as a pore entrance opening. The occluding particle may be slightly larger for tapered pores and slightly smaller for non-tapered pores such that the pores have a larger cross-section on the side of the substrate exposed to upstream flow. In an embodiment, particles are sized for at least partial introduction into an uncovered pore, but wherein the particle cannot exit the uncovered pore. Exit from the pore can be inhibited or prevented by providing shaped pores in which the pores are narrowed at some point along its length. Particles useful in the methods herein will in an embodiment range in size from 10 nm to 10 microns.
In an embodiment, employing deformable or swellable particles, the respective particles are deformed or swollen after introduction to an uncovered pore.
In an embodiment occlusion may be facilitated through controlled fouling, where a fluid is flowed to the composite membrane surface, and material from the fluid is bonded to composite membrane pores that are defective. The fouling may be controlled such that it blocks non-selective pores.
In an embodiment occlusion may be facilitated through healing with particles in air or gas. Particles are aerosolized and/or suspended in air and then forced through the membrane, such as by having convective flow of the air through the membrane. The convective flow of the air could be facilitated by applying a pressure differential across the membrane. The particles could be those described herein, with the methods described herein for fixing the particles to the membrane.
In an embodiment, occluding particles carry one or more chemical reactive groups for reaction with compatible reactive groups in the at least one uncovered pore, on the surface of the substrate at the uncovered pore or on other particles to facilitate anchoring of at least one particle in at least one uncovered pore. The particles can carry any one or more of a reactive chemical species, for example, the reactive species may be an amine, a carboxylate acid, an activated ester, a thiol, an aldehyde or a hydroxyl group. Particles useful in the inventive concepts disclosed herein which carry reactive groups can be prepared by known methods or may be obtained from commercial sources. Reactive groups on the particles can react with compatible reactive groups on the surface of the substrate at an uncovered pore, within the pore or at pore openings to facilitate retention in the pore. In an embodiment, particles may react with other particles in the pore to facilitate retention in the pore. One of ordinary skill in the art can employ a variety of chemically reactive groups to facilitate reaction with a pore to facilitate retention and anchoring in the pore. It will be appreciated that chemical reaction between particles, between particles and the pore surface, edges, openings or exits can be activated or induced by introduction of a reactive species, reagent or catalyst into a pore containing at least one occluding particle. It will also be appreciated that a chemical reaction between particles, between particles and the pore surface, edges, openings or exits can be activated or induced, for example, by heating, microwave irradiation, irradiation with light of selective wavelength (e.g., UV radiation) or by application of an ion beam, or by any method known in the art that is compatible with the materials employed.
In an embodiment, the occluding moieties are selected from one or more monomers, oligomers, uncured polymers or uncross-linked polymers. These occluding moieties are introduced selectively into uncovered pores and wherein the monomers, oligomers or polymers are polymerized, cured or cross-linked after they are introduced into the at least one uncovered pore. Polymerization can be effected for example by introduction of a polymerization catalyst, heating, microwave irradiation, or irradiation with light of a selected wavelength or by any method known in the art that is compatible with the materials employed. Curing of an uncured polymer or cross-linking of a polymer can be effected by any art-known method, for example by introduction of a curing or cross-linking reagent or application of heating, microwave irradiation, or irradiation with light of a selected wavelength or by any method known in the art that is compatible with the materials employed.
In an embodiment, the occlusion method further comprising a second step of introducing secondary particles into the at least one uncovered pore having a first particle therein occluding the uncovered pore, where the secondary particles are sized to be smaller than the first particle. In this embodiment, the initial particle and the secondary particles may be deformable or swellable as described above and may be deformed or swollen after introduction of the secondary particles. The initial particle and the secondary particles may carry one or more reactive groups as described above for chemical reaction of particles in the pores to facilitate retention in the pore.
In an embodiment, the composite membrane further comprises a coating layer on the top surface of the porous substrate between that surface and the sheet of two-dimensional material. Chemical reaction of a particle or other occluding moiety with reactive species on this coating at the entrance of the uncovered pore can facilitate anchoring and retention in the pore.
Occluding moieties are introduced to the top surface of the composite membrane where the occluding moieties can enter uncovered substrate pores. Introduction can be by any appropriate method and preferably is by application of a flow of fluid containing a selected concentration of occluding moieties. In a specific embodiment, the fluid is an aqueous solution carrying a selected concentration of occluding moieties. The concentration of occluding moieties in the flow introduced can be readily optimized empirically to optimize the effectiveness or efficiency of occlusion. Effectiveness or efficiency of occlusion can be assessed by measurement of the flow rate through the composite membrane, by accumulation rate of permeate or by an assessment of the selectivity of flow. A decreasing flow rate or a leveling off of permeate accumulation indicates successful occlusion. In an embodiment, the flow of occluding moieties includes a surfactant to decrease or minimize clumping or aggregation of occluding moieties and to facilitate entry of occluding moieties into uncovered pores. The inclusion of an appropriate surfactant is particularly beneficial for the introduction of occluding particles. In a specific embodiment, the surfactant is a non-ionic surfactant, such as (polyethylene glycol sorbitan monooleate). One of ordinary skill in the art can readily select a surfactant appropriate for the methods herein.
In a preferred embodiment, introduction of occluding moieties to the top surface of the composite membrane is by application of a cross-flow to the surface. The velocity of the cross-flow can be varied according to desired results. According to an embodiment, the pressure and flow may be varied as desired. In an embodiment, the shear velocity of the flow may be controlled. In an embodiment, the pressure across the composite membrane may be stopped while shear flowing. In an embodiment, the pressure on both sides of the membrane may be equalized. In an embodiment, the pressure may be controlled in cycles to alternately provide flow forward and then backward. The pressure on one or both sides of the membrane may be pulsed. Further, peristaltic pump rate and dimensions of the channel through the composite membrane may be controlled according to embodiments.
In an embodiment, the pore occlusion method further comprising a step of cleaning the top surface after introduction of occluding moieties into uncovered pores to remove occluding moieties that have not entered uncovered pores. This cleaning step can comprise flow of an appropriate fluid (gas or liquid) to or across the top surface of the membrane. In a specific embodiment, a flow of water or an aqueous solution is applied to or across the top surface of the membrane. In a specific embodiment, the aqueous solution contains a surfactant (as discussed above) to decrease clumping or aggregation of particles on the top surface.
In an embodiment, the introduction and cleaning steps as well any intervening steps to facilitate retention of particles in uncovered pores (e.g., deformation, chemical reaction, swelling or application of energy) are repeated until additional occlusion of pores ends or until a selected level of uncovered pore occlusion is achieved. As discussed above, various methods for accessing the extent or efficiency of pore occlusion can be employed.
In an embodiment, cycles of introduction and cleaning can be repeated until at least 80% of the uncovered pores are occluded. In an embodiment, cycles of introduction and cleaning can be repeated until at least 95% of the uncovered pores are occluded. In an embodiment, cycles of introduction and cleaning can be repeated until at least 99% of the uncovered pores are occluded.
In preferred embodiments, the two-dimensional material is a graphene-based material. In preferred embodiments, the two-dimensional materials is a sheet of graphene containing single layer graphene, few layer graphene (having 2-20 layers) or multilayer graphene.
In an embodiment, the pore occlusion method can be practiced without introducing an occluding moiety into uncovered pores. In this embodiment, a composite membrane as discussed above is provided wherein a sheet of two-dimensional material covers at least a portion of the pores of the substrate; but wherein at least one pore of the substrate is not covered by the two-dimensional material. In this embodiment, the substrate material forming the pores comprises a swellable material. The substrate itself may be made of a swellable material or more preferably the substrate material surrounding the pores is formed of a swellable material. For example, a coating of swellable material can be applied to the inside surfaces of the substrate pores. Selective introduction of an absorbable material into the uncovered pores results in local swelling of the swellable material surrounding the uncovered pore and occlusion of the uncovered pore. In an embodiment, the uncovered pores are selectively contacted with an absorbable fluid.
The disclosure further provides a composite membrane comprising a porous substrate having a plurality of pores and a sheet of two-dimensional material disposed on a surface of the porous substrate and defining a top surface of the membrane, wherein the sheet of two-dimensional material covers at least a portion of the pores of the substrate, wherein at least one pore of the substrate is not covered by the two-dimensional material and wherein at least one uncovered pore of the substrate is occluded with an occluding moiety. In an embodiment, the composite membrane has at least one uncovered pore occluded with one or more particles or occluded with a polymer, cured polymer or cross-linked polymer formed in the at least one uncovered pore.
In embodiments illustrated in
Although the disclosure has been described with reference to the disclosed embodiments, one having ordinary skill in the art will readily appreciate that these are only illustrative of the disclosure. It should be understood that various modifications can be made without departing from the spirit of the disclosure. The disclosure can be modified to incorporate any number of variations, alterations, substitutions or equivalent arrangements not heretofore described, but which are commensurate with the spirit and scope of the disclosure. Additionally, while various embodiments of the disclosure have been described, it is to be understood that aspects of the disclosure may include only some of the described embodiments. Accordingly, the disclosure is not to be seen as limited by the foregoing description.
Every formulation or combination of components described or exemplified can be used to practice the inventive concepts disclosed herein, unless otherwise stated. Specific names of compounds are intended to be exemplary, as it is known that one of ordinary skill in the art can name the same compounds differently. When a compound is described herein such that a particular isomer or enantiomer of the compound is not specified, for example, in a formula or in a chemical name, that description is intended to include each isomers and enantiomer of the compound described individual or in any combination. One of ordinary skill in the art will appreciate that methods, device elements, starting materials and synthetic methods other than those specifically exemplified can be employed in the practice of the inventive concepts disclosed herein without resort to undue experimentation. All art-known functional equivalents, of any such methods, device elements, starting materials and synthetic methods are intended to be included in this inventive concepts disclosed herein. Whenever a range is given in the specification, for example, a temperature range, a time range, or a composition range, all intermediate ranges and subranges, as well as all individual values included in the ranges given are intended to be included in the disclosure. When a Markush group or other grouping is used herein, all individual members of the group and all combinations and subcombinations possible of the group are intended to be individually included in the disclosure.
As used herein, “comprising” is synonymous with “including,” “containing,” or “characterized by,” and is inclusive or open-ended and does not exclude additional, unrecited elements or method steps. As used herein, “consisting of” excludes any element, step, or ingredient not specified in the claim element. As used herein, “consisting essentially of” does not exclude materials or steps that do not materially affect the basic and novel characteristics of the claim. Any recitation herein of the term “comprising”, particularly in a description of components of a composition or in a description of elements of a device, is understood to encompass those compositions and methods consisting essentially of and consisting of the recited components or elements. The inventive concepts disclosed herein illustratively described herein suitably may be practiced in the absence of any element or elements, limitation or limitations which is not specifically disclosed herein.
The terms and expressions which have been employed are used as terms of description and not of limitation, and there is no intention in the use of such terms and expressions of excluding any equivalents of the features shown and described or portions thereof, but it is recognized that various modifications are possible within the scope of the inventive concepts disclosed herein claimed. Thus, it should be understood that although the present inventive concepts disclosed herein has been specifically disclosed by preferred embodiments and optional features, modification and variation of the concepts herein disclosed may be resorted to by those skilled in the art, and that such modifications and variations are considered to be within the scope of the inventive concepts disclosed herein as defined by the appended claims.
In general the terms and phrases used herein have their art-recognized meaning, which can be found by reference to standard texts, journal references and contexts known to those skilled in the art. The preceding definitions are provided to clarify their specific use in the context of the inventive concepts disclosed herein.
All references throughout this application, for example patent documents including issued or granted patents or equivalents; patent application publications; and non-patent literature documents or other source material; are hereby incorporated by reference herein in their entireties, as though individually incorporated by reference, to the extent each reference is at least partially not inconsistent with the disclosure in this application (for example, a reference that is partially inconsistent is incorporated by reference except for the partially inconsistent portion of the reference).
All patents and publications mentioned in the specification are indicative of the levels of skill of those skilled in the art to which the inventive concepts disclosed herein pertains. References cited herein are incorporated by reference herein in their entirety to indicate the state of the art, in some cases as of their filing date, and it is intended that this information can be employed herein, if needed, to exclude (for example, to disclaim) specific embodiments that are in the prior art. For example, when a compound is claimed, it should be understood that compounds known in the prior art, including certain compounds disclosed in the references disclosed herein (particularly in referenced patent documents), are not intended to be included in the claim.
