Polymerized High Internal Phase Emulsion Research Articles

Superhydrophobic/ superoleophilic polystyrene-based porous material with superelasticity for highly efficient and continuous oil/water separation in harsh environments

Three-dimensional separation materials with robust physical/chemical stability have great demand for effective and continuous separation of immiscible oil/water mixtures and water-in-oil emulsions, resulting from chemical leakages and discharge of industrial oily wastewaters. Herein, a superelastic polystyrene-based porous material with superhydrophobicity/superoleophilicity was designed and prepared by high internal phase emulsion polymerization to meet the aforementioned requirements. A flexible and hydrophobic aminopropyl terminated polydimethylsiloxane (NH2-PDMS-NH2) segment was introduced into the rigid styrene-divinylbenzene copolymer through 1, 4-conjugate addition reaction with trimethylolpropane triacrylate. The addition of NH2-PDMS-NH2 simultaneously improved the mechanical and hydrophobic properties of the porous material (the water contact angle from 141.2° to 152.2°). The material exhibited outstanding reversible compressibility (80% strain, even in liquid N2 environments) and superhydrophobic stability, even after being repeatedly compressed 100 times, water contact angle still remained above 150°. Meanwhile, the as-prepared material had outstanding hydrophobic stability in corrosive solutions (strong acidic, alkaline, high-salty, and even strong polar solvent), presence of mechanical interference, strong UV radiations, and high/low temperature environments. More importantly, the material could continuously and efficiently separate immiscible oil/water mixture and water-in-oil emulsions under the above conditions, showing huge potential for the large-scale remediation of complex oily wastewaters.

Water-in-oil emulsion templated polyurethanes with uniform porosity

Porous PU foams have been receiving great attention because of their low density, lightweight, and high surface area. However, preparing PU foams with controlled porosity, pore size, and pore morphology is often difficult with commonly used methods like gas blowing. Here, highly controllable porous PU with small, uniform pore morphology and tunable material properties have been synthesized using water-in-oil polymerized high internal phase emulsion (PolyHIPE) templating and photoinitiated thiol-ene reactions between vinyl-functionalized polyurethane prepolymers and thiol-functionalized crosslinkers. The PolyHIPEs exhibited highly interconnected open-cell structures with pore sizes ranging from 5 to 10 μm. The storage moduli and elastic moduli of PU polyHIPEs derived from flexible HDI-PUs were low compared to stiff IPDI-PU based polyHIPEs. Furthermore, the storage moduli of relatively soft HDI-PU polyHIPEs were affected by the stoichiometric ratio of thiol crosslinker and vinyl-PU whereas no considerable effect on the stiffer IPDI-PU based polyHIPEs. In summary, this work presents an approach to synthesize porous polyurethane polyHIPEs with potential applications in aerospace, automotive, and biomedical industries.

High Internal Phase Emulsion for Constructing Chiral Helical Polymer-Based Circularly Polarized Luminescent Porous Materials.

Polymerized high internal phase emulsions (polyHIPEs) with circularly polarized luminescence (CPL), as an interesting class of porous materials, are of great significance for the development of CPL porous materials but have not been reported so far. Herein, we report the construction of polyHIPE-based CPL porous materials, taking advantage of an adsorption strategy. The pristine polyHIPEs constructed by chiral helical polymers, which acted as a chiral microenvironment, were fabricated by coordination polymerization of chiral acetylene monomers (R/S-SA) using HIPEs as templates. Achiral fluorescent small molecules were dispersed in the pores of the 3D porous organic chiral polymer matrix provided by polyHIPEs through the adsorption strategy, and CPL-active porous materials with blue, cyan, and green emissions were constructed using a fluorescence-selective absorption mechanism that does not rely on chirality transfer at the molecular level. The maximum luminescence dissymmetry factor (glum) value was -2.6 × 10-2. This work establishes a new and simple way for developing CPL porous materials.

Carbon nanotubes in high internal phase emulsion polymer composite for packed-cartridge micro-solid-phase extraction of fluoroquinolones in urine

Aim of this study stands in the evaluation of a carbon nanotubes-based polymerized high internal phase emulsion composite (CNT/polyHIPE) as sorptive phase in biological sample preparation. A micro-solid-phase extraction procedure (µSPE) was developed for trace fluoroquinolone (FQ) antimicrobials, namely Ciprofloxacin, Levofloxacin, Lomefloxacin, Moxifloxacin, Norfloxacin and Sparfloxacin, in human urine samples. PolyHIPEs modified by incorporation of different concentrations of nanotubes (0.2–0.8 wt %) were one-pot synthesized and applied in the packed-cartridge setting. The sorption affinity for the drugs was investigated in tap water and buffered aqueous solutions, demonstrating the key role of the nanotubes embedded in the polymer. The 0.5 wt % CNT composite was selected to develop a straightforward µSPE procedure directly in raw urine (1 mL sample), followed by HPLC-MS/MS. Targets were retained on the sorbent at near neutral pH and, after an aqueous washing (0.1 % v/v formic acid), eluted in a single-step with 4 % v/v ammonia aqueous solution (15 % v/v acetonitrile), thus combining extraction and clean-up. The method allowed accurate quantification of FQs, as evidenced by the recoveries (74–116 %, n = 3) obtained on blank pooled urine samples spiked with 40, 75, 150 µg L−1, accompanied by good inter-day precision (RSD < 14 %, n = 3). To confirm the applicability of the analytical method, some real-life blind samples were processed as a proof of concept.

Fabrication of double imprinted anchor points in cellulose nanocrystals-based hierarchical porous polyHIPEs for selective separation of flavoniods under physiological pH

Previous research had proved that molecular imprinted polymers can be used as separation material for removing Naringin (NRG) from agricultural pomelo wastes effectively. But the adsorption amounts of NRG molecules from traditional MIPs was quite low by using boronic acid as functional monomer because of single affinity interaction. Therefore, we developed the new combination of bifunctional monomers (i.e. low pKa boronate affinity monomer 2,4-difluoro-3-formylphenylboronic acid and dopamine) based on cellulose nanocrystals (CNCs) mixed with polymerized high internal phase emulsion (polyHIPE, PH) through an double layer surface imprinted method. The introduction of polyethylenimine (PEI) can offer abundant anchor units for the growth of more anchor sites to immobilization template molecules. Importantly, largely improved selective adsorption amounts (50.79 μmol g−1), which may be attribute to the fabrication of the uniform growth of double imprinted layers onto the polydopamine (PDA)/boronic acid-based surfaces. In addition, the resulting double recognition molecular imprinted polymers (MIPs) based on hypercrosslinked PH (DR-HCLPH@MIPs) not only exhibited fast adsorption kinetic of NRG molecule, but also possessed excellent selectivity and high adsorption capacities at physiological pH. Meanwhile, the coarse NRG from pomelo waste can be high selectively extracted to 94.74%. Overall, this study provides a versatile approach for fabrication of the sandwich-biscuit-like double imprinting layer porous MIPs for precise identification and ultrafast transport separation of NRG from complex samples.

The multi-sensitive ion-imprinted polymer as a selective absorbent for the separation of ruthenium

In this study, a multi-sensitive ion-imprinted polymer that serves as a highly selective absorption material for ruthenium (Ru(III)) in complicated solutions was designed and prepared with the adoption of Pickering High Internal Phase Emulsions (HIPEs) polymerization technology. Meawhile, acrylamide (AM) and acrylic acid (AA) were used as functional monomers, Ru(III) as template ion, ethylene glycol dimethacrylate (EGDMA) as cross-linking agent and the redox system ammonium persulfate-N,N,N′,N′-tetramethylethylenediamine (AP-TEMED) as initiator for the synthesis of a smart ruthenium ion-imprinted polymer (Ru(III)–SIIP). The chemical structure, morphology and magnetic properties of Ru(III)–SIIP were characterized and subsequently used for the selective adsorption of Ru(III). The results revealed that Ru(III)–SIIP had obvious temperature sensitivity/pH sensitivity/magnetic sensitivity. The maximum adsorption capacity of Ru(III) was 0.191 mmol/g and coupled with a desorption ratio of 82.99%. The screening of the adsorption kinetics of Ru(III)–SIIP indicated that the zero-order and pseudo-first-order kinetic mixed model was more suitable for describing the adsorption process, while the Langmuir model was suitable for describing the isotherm of Ru(III)–SIIP. Furthermore, an adsorption method combined with inductively coupled plasma atomic emission spectrometry (ICP-AES) based on Ru(III)–SIIP was established for Ru(III) and successfully applied in the detection of Ru(III) in mixed solutions. To conclude, Ru(III)–SIIP has broad prospects for the recovery of ruthenium in complex environmental situations.

Facile preparation of Ni@C/hierarchically porous carbon nanocomposites with excellent electrochemical performance from Ni-MOF/porous polymers

High performance supercapacitors are significant for the practical application of the novel renewable energies. Comparisons suggest that hybrid supercapacitor (HSC) is a fairly promising type for application since it combines high power density and high energy density. In this study, hierarchically porous carbons (HPCs) supported Ni@C nanoparticles (Ni@C/HPCs) were obtained by pyrolyzing the precursors of Ni-based MOF/porous polymers (Ni-MOF/polyHIPEs) which were prepared by high internal phase emulsion (HIPE) polymerization followed with solvothermal Ni-MOF growing. The composition and morphology of the Ni@C/HPCs can be controlled by changing the growth time of Ni-MOF. The optimized sample Ni@C/HPC-15 demonstrates a high specific capacity of 215.0 C g−1 at 1 A g−1 and a high rate performance of 82.3% when the current density increases from 1 A g−1 to 10 A g−1. Furthermore, Ni@C/HPC//HPC HSC was assembled and achieved an energy density of 40.9 Wh kg−1 at a power density of 747.2 W kg−1. In particular, the assembled HSC exhibited a remarkable initial capacitance retention of 86.3% after 5000 cycles at 6 A g−1. The reported convenient method may provide inspiration in the preparation and optimization of HPC-based electrode materials with satisfactory performances for energy storage.

Sponge-like polyethyleneimine adsorbents with interconnected open channels enabling ultra-high CO2 adsorption and separation capacity

A novel solid amine adsorbent with interconnect open-cell porous structure was successfully synthesized by crosslinking polyethyleneimine (PEI) with ethylene glycol diglycidyl ether (EGDE) via high internal phase emulsion (HIPE) polymerization. The preparation conditions were optimized. The adsorption performance of the prepared adsorbent for CO2 was evaluated by fixed bed dynamic adsorption experiment. The results indicated that the optimal adsorbent PEI70K-E-HIPE-8 exhibited a record high CO2 adsorption capacity of 14.22 mmol/g, amine efficiency of 83% and ratio of breakthrough capacity to equilibrium capacity of 0.92 (abbreviated as Qb/Qe ratio). Both adsorption capacity and adsorption kinetics are much better than those of PEI70K-E-gel-8 prepared without using HIPE template. The adsorbent also showed good CO2/CH4 separation performance, a CH4 productivity of 54.84 mmol/g could be obtained while using PEI70K-E-HIPE-8 to separated it from a 20 mL CO2/CH4 (20:80, v:v) mixed gas, remarkably higher than that of PEI70K-E-gel-8 (0.28 mmol/g). PEI70K-E-HIPE-8 could keep a stable adsorption and separation performance after at lease 15 adsorption-desorption cycles. The superior CO2 adsorption capacity and adsorption kinetics make it a promising candidate in practical CO2 adsorption and CO2/CH4 separation application.

Highly Porous Polymer Beads Coated with Nanometer-Thick Metal Oxide Films for Photocatalytic Oxidation of Bisphenol A.

Highly porous metal oxide-polymer nanocomposites are attracting considerable interest due to their unique structural and functional features. A porous polymer matrix brings properties such as high porosity and permeability, while the metal oxide phase adds functionality. For the metal oxide phase to perform its function, it must be fully accessible, and this is possible only at the pore surface, but functioning surfaces require controlled engineering, which remains a challenge. Here, highly porous nanocomposite beads based on thin metal oxide nanocoatings and polymerized high internal phase emulsions (polyHIPEs) are demonstrated. By leveraging the unique properties of polyHIPEs, i.e., a three-dimensional (3D) interconnected network of macropores, and high-precision of the atomic-layer-deposition technique (ALD), we were able to homogeneously coat the entire surface of the pores in polyHIPE beads with TiO2-, ZnO-, and Al2O3-based nanocoatings. Parameters such as nanocoating thickness, growth per cycle (GPC), and metal oxide (MO) composition were systematically controlled by varying the number of deposition cycles and dosing time under specific process conditions. The combination of polyHIPE structure and ALD technique proved advantageous, as MO-nanocoatings with thicknesses between 11 ± 3 and 40 ± 9 nm for TiO2 or 31 ± 6 and 74 ± 28 nm for ZnO and Al2O3, respectively, were successfully fabricated. It has been shown that the number of ALD cycles affects both the thickness and crystallinity of the MO nanocoatings. Finally, the potential of ALD-derived TiO2-polyHIPE beads in photocatalytic oxidation of an aqueous bisphenol A (BPA) solution was demonstrated. The beads exhibited about five times higher activity than nanocomposite beads prepared by the conventional (Pickering) method. Such ALD-derived polyHIPE nanocomposites could find wide application in nanotechnology, sensor development, or catalysis.

Modifying pickering polymerized high internal phase emulsion morphology by adjusting particle hydrophilicity

This study investigates the use of submicron polymeric particles with varying crosslinking densities as the sole stabilizer for producing Polymerized High Internal Phase Emulsions (PolyHIPE). We establish a direct correlation between the crosslinking density and the hydrophilicity of the polymer particles. The hydrophilicity of these particles significantly influences the morphology and rheology of HIPEs. These differences manifest as various morphological variations in the resulting PolyHIPE templates. It was discovered that by increasing the crosslinker weight percentage in the particles from 0 % to 100 %, PolyHIPEs with semi-open, open, and closed porous structures can be obtained. Furthermore, non-crosslinked particles were observed to dissolve in the continuous phase, acting as macromolecular surfactants that generate small pores akin to surfactant-stabilized structures in PolyHIPE. These findings offer fresh insights into the relationship between particle localization at the interface, HIPE rheology, and the formation of pore throats in Pickering PolyHIPEs, leading to the creation of either closed or open porous networks. Additionally, interfacial rheological results demonstrate that particles synthesized with varying monomer-to-crosslinker ratios exhibit different interfacial elasticities, which are linked to PolyHIPE morphology.

Versatile, elastomeric and degradable polyHIPEs of poly(glycerol sebacate)-methacrylate and their application in vascular graft tissue-engineering

Polymer scaffolds are an important enabling technology in tissue engineering. A wide range of manufacturing techniques have been developed to produce these scaffolds, including porogen leaching, phase separation, gas foaming, electrospinning and 3D printing. However, all of these techniques have limitations. Delivering suitable scaffold porosity, small feature sizes and macroscopic geometry remain challenging.Here, we present the development of a highly versatile scaffold fabrication method utilising emulsion templating to produce polymerised high internal phase emulsions (polyHIPEs) of the polymer poly(glycerol sebacate) methacrylate (PGS-M). PGS-M is biocompatible, degradable and highly elastic, with tunable mechanical properties. PGS-M was formulated into an emulsion using solvents and surfactants and then photocured into polyHIPE structures. The porosity, degradation behaviour, mechanical properties and biocompatibility of the PGS-M polyHIPEs was investigated.The versatility of the PGS-M polyHIPEs was demonstrated with the production of various complex tubular scaffold shapes, using injection moulding. These shapes were designed for applications in vascular graft tissue engineering and included straight tubes, bends, branches, functioning valves, and a representative aortic arch. The PGS-M polyHIPE scaffolds supported vascular smooth muscle cells (SMCs) in 3D cell culture in a bioreactor.

Covalent organic frameworks based hierarchical porous hybrid monolithic capillary: Synthesis, characterization, and applications in trace metals analysis

The preparation of hierarchical porous monolithic column with high covalent organic frameworks (COF) loading and micropores accessibility is challenging due to the easy aggregability and sedimentation of COFs. Herein, a novel strategy based on high internal phase emulsion (HIPE) polymerization was proposed for preparing COF hybrid capillary monolithic column with hierarchical porosity. COFs with different frameworks including imine COFs (COF-OMe, COF-F and COF-SH), triazine COF (CTF-1) and boron-based COF (COF-5) were selected to investigate the universality of the preparation strategy. The presence of COF in the monolithic capillary was confirmed by scanning electron microscope, X-ray diffraction and fourier transform infrared spectroscopy. Nitrogen adsorption/desorption experiments and thermogravimetric analysis showed that the prepared COF hybrid monolithic capillary exhibited high COF loading (e.g., 28.7% for COF-SH) and accessibility (e.g., 98.5% for COF-SH), mainly due to the thin walls of void-window structures originated from polymerization of HIPE. The successful preparation of water-stable COF-F, COF-OMe, COF-SH and CTF-1 hybrid monolithic columns demonstrated the proposed synthesis strategy is universal to water-stable COF without tedious optimization of dispersion system, effectively avoiding the sedimentation of COF in pre-polymerization solution. Then, the sulfhydryl-modified COF hybrid polymer (poly(COF-SH-HIPE)) monolithic column was evaluated for the extraction of heavy metal ions, and a method based on poly(COF-SH-HIPE) monolithic capillary microextraction on-line coupled with inductively coupled plasma mass spectrometry detection was developed for analysis of trace Cd, Hg and Pb in human fluid samples.

Surfactant-free gelatin-stabilised biodegradable polymerised high internal phase emulsions with macroporous structures.

High internal phase emulsion (HIPE) templating is a well-established method for the generation of polymeric materials with high porosity (>74%) and degree of interconnectivity. The porosity and pore size can be altered by adjusting parameters during emulsification, which affects the properties of the resulting porous structure. However, there remain challenges for the fabrication of polyHIPEs, including typically small pore sizes (∼20-50μm) and the use of surfactants, which can limit their use in biological applications. Here, we present the use of gelatin, a natural polymer, during the formation of polyHIPE structures, through the use of two biodegradable polymers, polycaprolactone-methacrylate (PCL-M) and polyglycerol sebacate-methacrylate (PGS-M). When gelatin is used as the internal phase, it is capable of stabilising emulsions without the need for an additional surfactant. Furthermore, by changing the concentration of gelatin within the internal phase, the pore size of the resulting polyHIPE can be tuned. 5% gelatin solution resulted in the largest mean pore size, increasing from 53μm to 80μm and 28μm to 94µm for PCL-M and PGS-M respectively. In addition, the inclusion of gelatin further increased the mechanical properties of the polyHIPEs and increased the period an emulsion could be stored before polymerisation. Our results demonstrate the potential to use gelatin for the fabrication of surfactant-free polyHIPEs with macroporous structures, with potential applications in tissue engineering, environmental and agricultural industries.

Investigating the Potential of Electroless Nickel Plating for Fabricating Ultra-Porous Metal-Based Lattice Structures Using PolyHIPE Templates.

The use of polymerized high internal phase emulsions (polyHIPEs) as templates for electroless nickel plating is a promising method for producing ultra-porous metallic lattice structures with consistent wall thickness. These structures have desirable properties such as low density, high specific strength, resilience, and absorbency, making them suitable for various applications including battery electrodes, catalyst supports, and acoustic or vibration damping. This study aimed to optimize and investigate the electroless nickel plating process on polyHIPEs. Initially, a surfactant (Hypermer)-stabilized water-in-oil emulsion based on 2-ethylhexyl-acrylate and isobornyl-acrylate was used as a 3D printing resin to create polyHIPE structures. Then, the electroless nickel plating process was optimized using polyHIPE discs. The study also examined the effects of air, argon, and reducing atmospheres during the heating process to remove the polyHIPE template using metallized 3D-printed polyHIPE lattice structures. The findings indicated that different atmospheres led to the formation of distinct compounds. While nickel-coated polyHIPEs were fully oxidized in an air atmosphere, nickel phosphide (Ni3P) structures occurred in argon and reducing atmospheres along Ni metal. Moreover, in argon and reducing atmospheres, the porous structure of the polyHIPEs was retained as the internal structure was completely carbonized. Overall, the study demonstrated that intricate polyHIPE structures can be used as templates to create ultra-porous metal-based lattices for a wide range of applications.

Control of pore interconnectivity in emulsion-templated porous polymers

The applications of porous polymers obtained from polymerized high internal phase emulsions (polyHIPEs) depend on their morphology, especially interconnectivity of pores (openness). For example, an open-cell structure is required for filtration and adsorbent materials, whereas a closed-cell structure is ideal for the applications in energy storage, insulation, and encapsulation. However, the remaining challenge is to control the interconnectivity of polyHIPEs, which is influenced by the complex process of pore throat formation. In this work, we demonstrate that the formation of pore throats can be tuned through varying the attractive interdroplet interactions in the HIPE precursor. The attractive interactions among the droplets are manipulated by employing different surfactants and the refractive index (RI)-matching agent. While the depletion attraction and steric repulsion can be indirectly controlled by changing the surfactant, the van der Waals interaction is controlled by varying the amount of RI-matching agent. The scaled viscoelastic moduli of HIPEs with Laplace pressure are used to further confirm the variation of interdroplet interactions. In addition to the interdroplet interactions, we investigate the potential effect of interfacial rheology on the interconnectivity of polyHIPEs.

In Vivo Bone Regeneration Capacity of Multiscale Porous Polycaprolactone-Based High Internal Phase Emulsion (PolyHIPE) Scaffolds in a Rat Calvarial Defect Model.

Globally, one of the most common tissue transplantation procedures is bone grafting. Lately, we have reported the development of polymerized high internal phase emulsions (PolyHIPEs) made of photocurable polycaprolactone (4PCLMA) and shown their potential to be used as bone tissue engineering scaffolds in vitro. However, it is essential to evaluate the in vivo performance of these scaffolds to investigate their potential in a clinically more relevant manner. Therefore, in this study, we aimed to compare in vivo performances of macroporous (fabricated using stereolithography), microporous (fabricated using emulsion templating), and multiscale porous (fabricated using emulsion templating and perforation) scaffolds made of 4PCLMA. Also, 3D-printed macroporous scaffolds (fabricated using fused deposition modeling) made of thermoplastic polycaprolactone were used as a control. Scaffolds were implanted into a critical-sized calvarial defect, animals were sacrificed 4 or 8 weeks after implantation, and the new bone formation was assessed by micro-computed tomography, dental radiography, and histology. Multiscale porous scaffolds that include both micro- and macropores resulted in higher bone regeneration in the defect area compared to only macroporous or only microporous scaffolds. When one-grade porous scaffolds were compared, microporous scaffolds showed better performance than macroporous scaffolds in terms of mineralized bone volume and tissue regeneration. Micro-CT results revealed that while bone volume/tissue volume (Bv/Tv) values were 8 and 17% at weeks 4 and 8 for macroporous scaffolds, they were significantly higher for microporous scaffolds, with values of 26 and 33%, respectively. Taken together, the results reported in this study showed the potential application of multiscale PolyHIPE scaffolds, in particular, as a promising material for bone regeneration.

Synthesis and Applications of Elastomeric Polymerized High Internal Phase Emulsions (PolyHIPEs).

Polymer foams (PFs) are among the most industrially produced polymeric materials, and they are found in applications including aerospace, packaging, textiles, and biomaterials. PFs are predominantly prepared using gas-blowing techniques, but PFs can also be prepared from templating techniques such as polymerized high internal phase emulsions (polyHIPEs). PolyHIPEs have many experimental design variables which control the physical, mechanical, and chemical properties of the resulting PFs. Both rigid and elastic polyHIPEs can be prepared, but while elastomeric polyHIPEs are less commonly reported than hard polyHIPEs, elastomeric polyHIPEs are instrumental in the realization of new materials in applications including flexible separation membranes, energy storage in soft robotics, and 3D-printed soft tissue engineering scaffolds. Furthermore, there are few limitations to the types of polymers and polymerization methods that have been used to prepare elastic polyHIPEs due to the wide range of polymerization conditions that are compatible with the polyHIPE method. In this review, an overview of the chemistry used to prepare elastic polyHIPEs from early reports to modern polymerization methods is provided, focusing on the applications that flexible polyHIPEs are used in. The review consists of four sections organized around polymer classes used in the preparation of polyHIPEs: (meth)acrylics and (meth)acrylamides, silicones, polyesters and polyurethanes, and naturally occurring polymers. Within each section, the common properties, current challenges, and an outlook is suggested on where elastomeric polyHIPEs can be expected to continue to make broad, positive impacts on materials and technology for the future.

Synthesis of patterned polyHIPE-hydrogel composite materials using thiol-ene chemistry

Elastomeric materials combining multiple properties within a single composite are highly desired in applications including biomaterials interfaces, actuators, and soft robotics. High spatial resolution is required to impart different properties across the composite for the intended application, but many techniques used to prepare these composites rely on multistep and complex methods. There is a need for the development of simple and efficient platforms to design layered composite materials. Here, we report the synthesis of horizontally- and vertically-patterned composites consisting of PDMS-based polymerized high internal phase emulsion (polyHIPE) porous elastomers and PDMS/PEG hydrogels. Composites with defined interfaces that were mechanically robust were prepared, and rheological analysis of the polyHIPE and hydrogel layers showed storage moduli values of ∼ 35 kPa and 45 kPa respectively. The compressive Young’s Modulus and maximum strain of the polyHIPEs were dependent on the thiol to ene ratio in the formulation and obtained values ranging from 6 to 25 kPa and 50–65% respectively. The mechanical properties, total porosity of the polyHIPE, and swelling ratio of the hydrogel were unaffected by the patterning technique compared to non-patterned controls. PolyHIPE-hydrogel composite materials having up to 7-different horizontally pattered layers could be prepared that could expand and contract up hydration and drying.

Acid-Activated Organobentonite-Based Highly Porous Foams via Polymerized High Internal Phase Emulsion: Preparation, Characterization and Machine Learning Prediction

Preparation, characterization, and machine learning prediction of characteristics of acid-treated organobentonite-based highly porous foams via polymerized high internal phase emulsion were reported in this work. The effect of acid-treated organobentonite (AC-BTN) as an inorganic filler on the properties of poly(DVB)HIPE porous foam was experimentally investigated. Incorporating AC-BTN into the continuous phase of the high internal phase emulsion would improve thermal and mechanical properties and also increase the surface area of the resulting materials when compared to the unfilled poly(DVB)HIPE foam. Various amounts of AC-BTN, i.e., 0, 1, 3, 5, 7, and 10 wt.% of AC-BTN, were incorporated into the continuous phase to enhance the properties of poly(DVB)HIPE foam. The surface area and the degradation temperatures (Td) for the series of poly(DVB)HIPE foam filled with AC-BTN increased with increasing filler content from 0 to 10 wt.%. The maximum improvement of mechanical properties was found with the addition of 5 wt.% of AC-BTN into the continuous phase of poly(DVB)HIPE foam. Moreover, the adsorption of CO2 gas by poly(DVB)HIPE foam filled with AC-BTN was found to increase as well. It has been demonstrated in this study that the adsorption of CO2 by poly(DVB)HIPE foam filled with AC-BTN increased by 127% (from 0.00295 to 0.00670 mol/g) compared with neat poly(DVB)HIPE foam. Additionally, the machine learning (ML) method with a linear regression algorithm was employed for the characterization of poly(DVB)HIPE foam and the prediction of properties according to composite composition. Surface area, pore volume, Td, compressive stress, and Young’s modulus were evaluated. The accuracy of prediction using a machine learning application with a linear regression model for properties of poly(DVB)HIPE foam filled with AC-BTN was also reported.

Metal Oxide-Derived MOF-74 Polymer Composites through Pickering Emulsion-Templating: Interfacial Recrystallization, Hierarchical Architectures, and CO2 Capture Performances

Currently, metal-organic framework (MOF)-polymer composites are attracting great interest as a step forward in making MOFs a useful material for industrially relevant applications. However, most of the research is engaged with finding promising MOF/polymer pairs and less with the synthetic methods by which these materials are then combined, albeit hybridization has a significant impact on the properties of the new composite macrostructure. Thus, the focus of this work is on the innovative hybridization of MOFs and polymerized high internal phase emulsions (polyHIPEs), two classes of materials that exhibit porosity at different length scales. The main thrust is the in situ secondary recrystallization, i.e., growth of MOFs from metal oxides previously fixed in polyHIPEs by the Pickering HIPE-templating, and further structure-function study of composites through the CO2 capture behavior. The combination of Pickering HIPE polymerization and secondary recrystallization at the metal oxide-polymer interface proved advantageous, as MOF-74 isostructures based on different metal cations (M2+ = Mg, Co, or Zn) could be successfully shaped in the polyHIPEs' macropores without affecting the properties of the individual components. The successful hybridization resulted in highly porous, co-continuous MOF-74-polyHIPE composite monoliths forming an architectural hierarchy with pronounced macro-microporosity, in which the MOF microporosity is almost completely accessible for gases, i.e., about 87% of the micropores, and the monoliths exhibit excellent mechanical stability. The well-structured porous architecture of the composites showed superior CO2 capture performance compared to the parent MOF-74 powders. Both adsorption and desorption kinetics are significantly faster for composites. Regeneration by temperature swing adsorption recovers about 88% of the total adsorption capacity of the composite, while it is lower for the parent MOF-74 powders (about 75%). Finally, the composites exhibit about 30% improvement in CO2 uptake under working conditions compared to the parent MOF-74 powders, and some of the composites are able to retain 99% of the original adsorption capacity after five adsorption/desorption cycles.