Poor Solvent Research Articles

Cesium lead bromide perovskite nanocrystals synthesized via supersaturated recrystallization at room temperature: comparison of one-step and two-step processes.

Over more than a decade, lead halide perovskites (LHPs) have been popular as a next-generation semiconductor for optoelectronics. Later, all-inorganic CsPbX3 (X = Cl, Br, and I) nanocrystals (NCs) were synthesized via supersaturated recrystallization (SR) at room temperature (RT). However, compared to the hot injection (HI) method, the formation mechanism of NCs via SR-RT has not been well studied. Hence, this study will contribute to elucidating SR-RT based on the LaMer model and Hansen solubility parameter. Herein, we also demonstrate the entropy-driven mixing between two dissimilar polar-nonpolar (DMF-toluene) solvents. Next, we find that, in a poor solvent (toluene ≫ DMF in volume), ∼60 nm sized CsPbBr3 NCs were synthesized in one step, whereas in a marginal solvent (toluene ≈ DMF), ∼3.5 nm sized NCs were synthesized in two steps, indicating the importance of solvent polarity, specifically the 'solubility parameter'. In addition, in the presence of a CuBr2 additive, high-quality cubic NCs (with ∼3.8 nm and ∼21.4 nm edge sizes) were synthesized. Hence, through this study, we present a 'solubility parameter-based nanocrystal-size control model' for SR-RT processes.

Colloidal adsorption in planar polymeric brushes.

The design of nano-functionalised membranes or channels, able to effectively adsorb pollutants in aqueous solutions, is a topic that is gaining a great deal of attention in the materials science community. With this work we explore, through a combination of scaling theories and molecular dynamics simulations, the adsorption of spherical non-deformable colloidal nanoparticles within planar polymeric brushes. Our strategy is twofold: first, we generalise the Alexander-de Gennes theory for planar homopolymeric brushes to the case of diblock copolymer brushes, then we map the adsorbing homopolymeric brushes onto a diblock copolymer system, where the adsorbed colloids and all interacting monomers are considered monomers in bad solvent and we apply the generalised scaling theory to this effective diblock copolymer. This allows the prediction of the average conformation of the grafted substrate, i.e. its average height, as a function of the amount of loaded particles, as well as the introduction of a continuous mapping between a homopolymeric brush, the fraction of loaded particles and the average height of the adsorbing substrate.

Polyelectrolytes: From Seminal Works to the Influence of the Charge Sequence.

We propose a selected tour of the physics of polyelectrolytes (PE) following the line initiated by de Gennes and coworkers in their seminal 1976 paper. The early works which used uniform charge distributions along the PE backbone achieved tremendous progress and set most milestones in the field. Recently, the focus has shifted to the role of the charge sequence. Revisited topics include PE complexation and polyampholytes (PA). We develop the example of a random PE in poor solvent forming pearl-necklace structures. It is shown that the pearls typically adopt very asymmetric mass and charge distributions. Individual sequences do not necessarily reflect the ensemble statistics and a rich variety of behaviors emerges (specially for PA). Pearl necklaces are dynamic structures and switch between various types of pearl-necklace structures, as described for both PE and PA.

Probing conformational properties of conjugated polymers in dilute solutions under variable solvent quality via coarse‐grained modeling

AbstractConjugated polymers (CPs), characterized by rigid conjugation backbones and flexible peripheral side chains, hold significant promise in various organic optoelectronic applications. In this study, we employ coarse‐grained molecular dynamics (CG‐MD) simulations to investigate the intricate interplay of solvent quality, temperature, and chain architecture (e.g., side‐chain length and molecular mass) on the conformational behaviors of CPs in dilute solutions. Our research uncovers distinctive conformational behaviors under varying solvent conditions, highlighting the versatile nature of polymer chains, which can adopt extended configurations in good solvents and transition to aggregated states in poor solvents. Additionally, the mass scaling exponent , a robust structural descriptor, consistently described CPs behavior across diverse architectures and solvent conditions. Furthermore, our study shows that a CP with longer side‐chain exhibits improved solubility, which is further confirmed by experimental observations. Moreover, our analysis of the shape descriptor provided valuable insights into the symmetry and dimensionality of CPs under varying solvent conditions. These findings offer a comprehensive understanding of conformational behaviors of CPs in dilute solution, which are helpful in guiding the conformational design of polymer for specific applications.

Manipulating Nanowires in Interconnecting Layer for Efficient Tandem Organic Photovoltaics†

Comprehensive SummaryOwing to the function of manipulating light absorption distribution, tandem organic solar cells containing multiple sub‐cells exhibit high power conversion efficiencies. However, there is a substantial challenge in precisely controlling the inter‐subcells carrier migration which determines the balance of charge transport across the entire device. The conductivity of “nanowires”‐like conducting channel in interconnecting layer between sub‐cells should be improved which calls for fine engineering on the morphology of polyelectrolyte in interconnecting layer. Here, we develop a simple method to effectively manipulating the domains of conductive components in commercially available polyelectrolyte PEDOT:PSS. The use of poor solvent could effectively modify the configuration of polystyrene sulfonic acid and thus the space for conductive components. Based on our strategy, the insulated shells wrapping conductive domains are thinned and the efficiencies of tandem organic solar cells are improved. We believe our method might provide guidance for the manufacture of tandem organic solar cells.

A Convenient and Universal Strategy toward Solvent‐Tolerant Microporous Structure for High‐Performance Wearable Electronics and Smart Textiles

AbstractMicro/nanostructures can increase effective surface area and enhance the performance of wearable devices, such as the sensitivity of sensors and output of triboelectric nanogenerators. Empowering commercial fibers and fabrics with durable and robust micro/nanostructures has become a major research concern for sustainable wearables. Many technologies are developed to fabricate micron/nanostructures on fibers and textiles, such as breath figure method, electrospinning, and direct imprinting thermal drawing. However, most of these methods have their own limitations toward mass production and real‐life application, including poor solvent resistance, time assuming, requiring expensive equipment, and limited capacity for post‐adjustment of commercial textiles. Herein, a plasma‐enhanced breath figure (PEBF) technique to fabricate solvent‐tolerant microporous structure on existing fabrics with tailored pore size is developed. By combining the wearable nature of fabrics and the surface engineering power of PEBF, the fabricated solvent‐tolerant microporous fabric offers excellent flexibility, washability, breathability, and suitability for large‐scale production, as well as the advantages of cost effectiveness and fast production. Furthermore, wearable triboelectric nanogenerators are fabricated based on solvent‐resistant microporous structured fabrics, revealing the bright future of the PEBF technology in wearable devices and smart textiles.

Simple Donor-π-Acceptor Compounds Exhibiting Aggregation-Induced Emission as Hidden Fingerprints Detecting Agents.

Latent fingerprints are a significant carrier of information for a court expert. To detect this type of forensic trace, what is necessary is a method that is easy to use, compact, and versatile. The research aimed to investigate the physicochemical properties of luminescent substances of donor-π-acceptor systems in terms of their potential use in detecting hidden fingerprints. During the research, a group of fluorene compounds consisting of the (-CH=C(CN)(COOR)) moiety was designed and successfully synthesized. The optical, electrochemical, and aggregation-induced emission properties were studied. The aggregation-induced emission of compounds has been studied in the mixture of THF (as a good solvent) and water (as a poor solvent) with different water fractions ranging from 0% to 99%. Due to the molecular structure, substances showed different affinities to organic traces. As a result, it was noticed that all compounds showed the AIE phenomenon, while during tests on latent fingerprints, it was observed that two substances had particularly forward-looking features in this field.

Crystal growth, HOMO-LUMO engineering and charge-transfer emission of TCNB-based donor-acceptor cocrystals

Using carbazole (CARB), dibenzothiophene (DBZP) and dibenzofuran (DBZF) as electron donors, 1,2,4,5-tetracyanobenzene (TCNB) as electron acceptor, three typical types of luminescent organic cocrystals were synthesized by a simple supramolecular assembly strategy. The cocrystals exhibit interesting optical properties for its charge transfer (CT) interactions. Meanwhile, a series of three-component (CARB)x (DBZP)1-x (TCNB) crystalline microtubes comprising organic CT interactions have been prepared by the self-assembly with poor solvent co-precipitating method. DFT calculations were used to predict the CT interactions and the binding patterns of donor and acceptor, which suggest that the CT interactions can largely influence the energy level and orbital distributions. Moreover, the SXRD analyses verified the cocrystals are constructed by π-π stacking with a face-to-face model. The solid-state cocrystals and microtubes were well characterized by PXRD, UV absorption spectra, emission spectra, fluorescence lifetime and quantum yield analyses. The obvious red-shift in UV–vis absorption spectra and emission spectra with respect to the free monomer indicate the formation of CT interactions. The emission colors of the mixed microtubes can be tailored from green to orange as well as associated photophysical properties with the increasing of dopant concentrations. Therefore, by the combination of experimental and theoretical studies on the cocrystals and microtubes, this work not only reports the new types of crystalline micro-nano materials, but also provides an in-depth understanding of the relationship between structure and fluorescence effect.

Integrating Aggregation Induced Emission and Twisted Intramolecular Charge Transfer via Molecular Engineering

AbstractThe pursuit of sensitive fluorescent chromophores with integrated aggregation‐induced emission (AIE) and twisted intramolecular charge transfer (TICT) properties are attractive due to the tunable emission properties and increased intensity. However, this type of chromophore has yet to be exemplified mechanistically. In this study, a strategy is presented for manipulating the formation of TICT and the AIE effect through molecular engineering. The feasibility of TICT properties is validated by theoretical calculations and ultrafast spectroscopies. By precisely adjusting the hydrophobicity of the donor group, the fluorescence is significantly enhanced through the addition of poor solvent. These findings not only provide mechanistic elucidation for chromophores exhibiting integrated TICT and AIE properties in various environmental conditions but also underscore the critical factors for the systematic design of chromophores with high tunability and strong emissions.

Determination of Hansen solubility parameters of water-soluble proteins using UV–vis spectrophotometry

Determination of solubility parameters by dissolution tests are difficult for some valuable molecules, such as proteins, where the quantities available are small, UV–vis spectroscopy can determine dissolved concentrations of even small amounts of material, but accurate determination of dissolution is difficult in relatively poor solvents, due to difficulty with constructing a reliable calibration curve. In this work we report a new simple procedure to determine the relative dissolution of proteins in various solvents using UV vis spectroscopy for the determination of Hansen solubility parameters (HSP) of proteins. This method allows qualitative determination of the amounts of BSA dissolved in various solvents. The amounts of BSA dissolved in each solvent, can then be used to rank solvents as good or bad for HSP calculation purpose, which gives more reliable ranking than observation alone in dissolution tests. To be able to evaluate the HSP of any solid material, the solubility of the tested material in a range of solvents needs to be determined. Solvents are then scored as good or bad based on observations and from the known properties of those solvents, the HSP of the solute molecule in question can be calculated. Here, bovine serum albumin (BSA) was used as a model protein, but the procedure reported here can be applied to any soluble protein or other macromolecule with a clear UV/vis adsorption peak. This procedure requires the tested material to be highly soluble in water, therefore eliminating the need for the preparation of many standard solutions of BSA in different solvents. Only a set of standard solutions of protein in water is required. UV–vis spectroscopy was used to analyze the remaining solid resuspended in water after centrifugation of solutions of BSA dissolved in other solvents to separate any undissolved protein. The HSP of BSA obtained via this procedure was compared to values previously obtained for BSA using other methods. A very good agreement between the HSP obtained in this work with the that reported by Houen et al. which used amino acid analysis for the estimation of the solubility of BSA in various organic solvents.

Solvent Quality and Aggregation State of Asphaltenes on Interfacial Mechanics and Jamming Behavior at the Oil/Water Interface.

The formation of highly stable water-in-oil emulsions results in complications in both upstream and downstream processing. Emulsion stability in these systems has been connected to the adsorption of surface-active asphaltenes that are assumed to form a rigidified film at the oil/water (o/w) interface. Full characterization of this behavior is needed to allow for engineered solutions for enhanced oil recovery. Interfacial properties, such as surface pressure and interfacial elasticity, are implicated in the stabilizing mechanism for these observed films. Asphaltenes are known to be interfacially active in both good solvents (aromatics) and poor solvents (high ratio of aliphatic to aromatic). However, due to inherent complexities present in asphaltene studies, the details of the mechanical properties of the interface remain poorly understood. Despite the widely accepted perception that asphaltenes form persistent rigid films at fluid-fluid interfaces, the connection between bulk solution properties and interfacial mechanics has not been resolved. Here, the effects of solvent quality on the interfacial properties of asphaltene dispersions are determined by using a well-defined asphaltene/solvent system. Interfacial rigidity is observed only under poor solvent conditions, while the good solvent system remains fluid-like. The interfacial rheology under good and poor solvent conditions is measured simultaneously with surface pressure measurements to track interfacial development. It is shown that surface pressure and dilatational modulus measurements are not indicators of whether an interface demonstrates rigid behavior under large compressions. Finally, conditions required for asphaltene-coated interfaces to exhibit the mechanical behavior associated with a rigidified interface are defined. This work provides a framework for quantifying the impact of the aggregation state of asphaltenes on the stability and mechanics at the o/w interface.

Highly Solvent Resistant Small-Molecule Hole-Transporting Materials for Efficient Perovskite Quantum Dot Light-Emitting Diodes.

Perovskite quantum dot light-emitting diodes (Pe-QLEDs) have been shown as promising candidates for next-generation displays and lightings due to their unique feature of wide color gamut and high color saturation. Hole-transporting materials (HTMs) play crucial roles in the device performance and stability of Pe-QLEDs. However, small-molecule HTMs have been less studied in Pe-QLEDs due to their poor solvent resistance and low hole mobility. In this work, three novel small-molecule HTMs employing benzimidazole as the center core, named X4, X5, and X6, were designed and synthesized for application in Pe-QLEDs. One of the tailored HTM-X6 exhibits excellent solvent resistant ability to the perovskite quantum dot (QD) inks due to its proper solubility and low surface energy. Our result clearly demonstrated that the synergistic effect of poor solubility and low surface energy facilitates the achievement of good solvent resistance to perovskite QD inks. As a result, a promising maximal external quantum efficiency (EQE) of 14.1% is achieved in X6-based CsPbBr3 Pe-QLEDs, which is much higher than that of X4 (9.16%) and X5 (6.60%)-based devices, which is comparable to the PTAA reference (EQE ∼ 15.8%) under the same conditions. To the best of our knowledge, this is the first example that a benzimidazole-based small-molecule HTM demonstrated a good application in Pe-QLEDs. Our work provides new guidance for the rational design of small-molecule HTMs with high solvent resistance for efficient Pe-QLEDs and other photoelectronic devices.

Aggregation-induced electrochemiluminescence-active ruthenium(II) complex for selective detection of dopamine

In this paper, we systematically investigated the aggregation-induced electrochemiluminescence (AIECL) of the ruthenium(II) complex ([Ru(phen)2(phen-O2)](PF6)2, phen-O2: 5,6-diketone-1,10-phenanthroline), which was dissolved in solvents with different water/acetonitrile volume ratios. The fluorescence intensity of the system increased 11.5-fold when the proportion of water (a poor solvent) in the solvent mixture was increased to 90%, and the electrochemiluminescence intensity increased 16-fold when the proportion of water in the solvent was increased to 80%. Transmission electron microscopy and dynamic light scattering confirmed the aggregation of [Ru(phen)2(phen-O2)](PF6)2 molecules into nanoclusters. Aggregation-induced electrochemiluminescence properties were observed to increase with an increase in the proportion of water in H2O/CH3CN. Due to the excellent aggregation-induced luminescence performance of [Ru(phen)2(phen-O2)](PF6)2, the quantitative detection of dopamine was achieved with a good linear range of 100 pM–1uM and a limitation of detection of 33.3 pM. This simple and sensitive method based on the AIECL effect can be widely applied to the detection and analysis of other small biological molecules.

Reduce supply chain financing risks through supply chain integration: dual approaches of alleviating information asymmetry and mitigating supply chain risks

PurposeInformation asymmetry and poor solvency caused by uncertainties in supply chains are the root causes of supply chain financing risks (SCFR). The purpose of this paper is to explore the effect of supply chain integration on reducing SCFR by incorporating the mechanisms of information sharing and controlling supply chain risks (SCR).Design/methodology/approachThis paper proposes hypothesis to discuss the impact of integration on SCFR and the mediating roles of alleviating information asymmetry and mitigating SCR, aiming at discovering factors and mechanisms to reduce SCFR. The research model was validated by applying structural equation modeling on survey data from 321 Chinese small and medium-sized enterprises (SMEs).FindingsIntegration significantly reduces SCFR by dual approaches of information sharing and mitigating SCR, confirming that alleviating information asymmetry to reach information transparency and controlling SCR to reduce uncertainties facilitate less SCFR.Research limitations/implicationsSMEs should enhance integration capability to reduce SCFR as it greatly influences the evaluation of financial service providers on SMEs and the sustainable financing capacity of SMEs. Additionally, any other methods that can improve information sharing and reduce SCR should be attached if possible.Originality/valueThis study represents a pioneering attempt to analyze the impact of integration on reducing SCFR by exploring the specific mechanisms of alleviating information asymmetry and mitigating SCR. Meanwhile, few prior empirical studies have highlighted the importance of SCFR.

Chain folding double-network hydrogels leads to ultra-strong, stretchable and tough sensors

Strong, stretchable and tough sensors are in great demand but challenging. Here, we present a simple and generable strategy toward fabricating high-performance sensors by folding the polymer chains of the ionic double-network (DN) hydrogels via dehydration in poor solvent of ethanol. The combination of chain folding and DN network dramatically improved stress buffering and energy dissipation capacity of hydrogels during the unfolding/stretching process. The as-prepared hydrogels exhibited ultra-high strength (1.06 MPa), stretchability (15,400%) and toughness (88 MJ m−3), representing the most tough hydrogels reported as far as we know. By taking these advantages, the hydrogels were demonstrated as strain sensors with extremely broad work window (0.05–8000%). This chain folding DN concept provides an attractive strategy to improve the whole mechanical properties of hydrogels to new limits and expand the scope of applications.

Nicotinamide-based agglomerates of ibuprofen: formulation, solid state characterization and evaluation of tableting performance with in-silico investigation

BackgroundThe objective of the present investigation was to obtain directly compressible agglomerates of ibuprofen with nicotinamide by a quasi-emulsification solvent diffusion technique. Ibuprofen-nicotinamide agglomerates were prepared by quasi-emulsification solvent diffusion technique using ethanol (good solvent), water (poor solvent), and chloroform (bridging liquid). The prepared agglomerates were characterized by ATR-FTIR, powder X-ray diffraction, differential scanning calorimetry, and scanning electron microscopy and were evaluated for tableting performance and in vitro drug release. To appropriately identify the hydrogen bonding sites, a thorough understanding of the structures of API and coformer is necessary, hence molecular docking approach was implemented to depict the interaction between the proposed coformer and COX-2 protein (PDB Id:4PH9).ResultsThe percent yield of agglomerates was in the range of 85–98 w/w%, and drug content for all batches was in the range of 96–99%. The microphotographs showed irregular circularly shaped agglomerates. ATR-FTIR study showed a strong possibility of hydrogen bonding between ibuprofen and nicotinamide. The crystallinity of ibuprofen was slightly reduced and confirmed by P-XRD and DSC. Crushing strength and friability studies showed good handling qualities of ibuprofen agglomerates. Heckel plot studies showed low mean yield pressure and high tensile strength, indicating excellent compressibility and compactibility of ibuprofen agglomerates. More than 90% drug release was obtained within 60 min in PBS (pH 7.4). The docking studies revealed that nicotinamide individually has –CDOCKER energy 16.8109 where coformer showed 29.0584, which indicates coformer has a better binding affinity to target as compared to nicotinamide individual.ConclusionsIt can be concluded that the agglomerates improved the dissolution, tableting performance, and solid-state properties of ibuprofen and hence can be useful to improve the therapeutic performance of ibuprofen.Graphic

Falling-Leaves Stacking Aggregation of Two-Dimensional Macromolecular Graphene Oxide in Solution.

Understanding the dynamical behaviors of two-dimensional (2D) macromolecules is of fundamental importance for the precise modulation of their assembled structures and material performances. However, considerably less is known about how discrete macromolecular sheets aggregate into extended macroscopic assemblies in solutions. The absence of a quantitative description of the assembly process limits the precise structural control of assemblies. Here, we investigated the aggregation thermodynamic transition and kinetic behavior of 2D macromolecules in the model of single layer graphene oxide (GO). Combining Flory-Huggins theory with experimental observations, we unveiled the critical thermodynamic transition of GO to correlate with the solvent property. We proposed a theoretical falling-leaf model to quantitatively describe the kinetic aggregation process of 2D GO sheets. Experimental analysis validated the theoretical prediction that the thickness of GO aggregates has a power law relation with the poor solvent content. Our work provides a fundamental understanding of phase separation of 2D macromolecules and offers an insight into modulating the aggregated structures of their assembled materials.

Water-Induced Cellulose Nanofibers/Poly(vinyl alcohol) Hydrogels Regulated by Hydrogen Bonding for In Situ Water Shutoff.

Hydrogels have been widely applied to the water shutoff in oilfields due to their excellent three-dimensional network and thermal and physicochemical stability, and it is still a huge challenge to develop new hydrogels with simple preparation, low cost, and high mechanical performance that can meet the requirements of practical applications. Herein, we devised a simple and universal manufacturing method for regulating the hydrogen bonds between poly(vinyl alcohol) (PVA) and cellulose nanofibers (CNF) via the water-diffusion action, thus fabricating a physically tough PVA-CNF hydrogel for the in situ water shutoff. This method allowed the polymer chains to strengthen the molecular interactions between polymers upon replacing with water (a poor solvent) to regulate the cross-linking structure, characterizing by the nano-crystallinity domains and fibrillar segments, which also accounted for the thermal stability, extraordinary elasticity, high stretchability, and toughness of PVA-CNF hydrogel. Further, the obtained PVA-CNF hydrogel exhibited superb plugging performance, that is, the breakthrough pressure gradient could reach 71.56 MPa·m-1, surpassing all currently reported gelling water shutoff agents. This water-induced in situ hydrogelation made it well suited as a water shutoff agent in oilfields and may provide a promising strategy to fabricate mechanically robust smart materials for the water shutoff projects with low cost, simple processing, and high efficiency.

Quantum-Chemical Study of Aggregation of 5-(4'-Dimethylaminobenzylidene)Barbituric Acid

Decreasing fluorescence efficiency in the solid-state is general and is mainly attributed to the intermolecular vibronic interactions, which induce the nonradiative deactivation process. Whereas the isolated dye molecules are virtually non-luminescent in dilute solutions, they become highly emissive upon solution thickening or aggregation in poor solvents or in the solid-state show an increase of luminescence intensity, the phenomenon of the aggregation-induced emission (AIE phenomenon). The development of efficient luminescent materials is a topic of great current interest. Theoretical calculation shows that the dye molecules' aggregation-induced emission characteristics result from intermolecular interactions. Utilizing such features, the molecules can be employed as fluorescent probes for the detection of the ethanol content in aqueous solutions. Quantum-chemical calculations using the method of density functional theory the computations of structure and electronic spectra of aggregated forms of 5-(4’-dimethylaminobenzylidene)barbituric acid and the Gaussian 98 program packages have been performed. The unusual spectral behavior of 5-(4’-dimethylamino-benzylidene)barbituric acid was investigated theoretically by the DFT method and its time-dependent variant TDDFT. Carried out calculations using Zindo, as well as ab initio calculations, confirm the appearance of a new band during aggregation and its shift to the red region when the number of molecules increases.

Improvement of interfacial adhesion between oxide ceramic nanoparticles and epoxy resin by wet-jet milling

Although ceramic/polymer composites are useful for various applications, such as sensors, electronics, automobiles, and aerospace, the aggregation of nanoparticles can lead to the degradation of the mechanical and functional properties of the composites. To mitigate this, the interfacial adhesion between epoxy resin and the oxide ceramic nanoparticles γ-aluminum oxide (Al2O3), silicon dioxide, and magnesium oxide was strengthened by wet-jet milling (WJM) treatment without a chemical modifier. The WJM treatment of the slurry containing nanoparticles and epoxy resin led to the good adsorption of epoxy resin onto the nanoparticle surface, which significantly improved the mechanical properties of the composites. Throughout this process, the amount of epoxy resin adsorbed on the nanoparticle surface and the composite mechanical properties increased with increasing WJM processing pressure, owing to the increased contact between the nanoparticles and epoxy resin droplets and the reduced droplet size. Furthermore, poor solvent was found to be effective for the dispersal of the nanoparticles because the epoxy resin droplets in the slurry were more stable on the nanoparticle surfaces than those in the solvent. When Al2O3 nanoparticles were used as a filler, the amount of epoxy resin adsorbed increased from 3.7 to 70.6 mg g−1, and the composite tensile strength increased from 67.1 to 100.3 MPa in poor solvent and under high WJM processing pressure. This optimized WJM treatment will lead to improvements in the mechanical and functional properties of various composite materials.