Function Of Hydrophobicity Research Articles

High-performance superhydrophobic fly ash based geopolymers with graphene oxide reinforcement for enhanced durability and repellency

While high-performance fly ash geopolymers offer a demonstrably reduced carbon footprint in the construction industry, their inherent affinity for water (hydrophilicity) can facilitate the accumulation of moisture within the material matrix, potentially leading to the initiation and propagation of internal corrosion. The implementation of hydrophobic functionalization strategies on fly ash geopolymers demonstrably enhances their resistance to corrosive degradation. Nevertheless, a crucial challenge persists in the form of mitigating potential declines in mechanical strength. This investigation endeavors to attenuate the deleterious effects exerted by the hydrophobic aluminosilicate hydrate phase on the material's mechanical properties, while concurrently preserving its superhydrophobic character. Our approach involved the incorporation of a novel composite modifier, wherein polymethylhydrosiloxane (PMHS) served as the principal hydrophobic component. Graphene oxide (GO) was strategically introduced to achieve efficient pore filling, owing to its exceptional dispersibility. Furthermore, the presence of GO reinforces the mechanical performance of the composite due to its inherent superior mechanical properties. Additionally, the well-dispersed GO portion forms nano hydrophobic particles by covalently grafting hydrophobic groups, further enhancing the overall hydrophobicity of the composite. This synergistic interplay between PMHS and GO facilitated the successful development of a high-performance fly ash geopolymer composite characterized by exceptional mechanical strength, three-dimensional superhydrophobicity, and enhanced chemical stability. The graphene oxide reinforced high-performance three-dimensional superhydrophobic hybrid hydrogel geopolymer composites maintained high compressive strength while achieving a water contact angle of 153 ° and a water absorption rate of only 1.7 %. Remarkably, the geopolymer retains its high hydrophobicity even after 24 hours in an acid-base solution, with a contact angle exceeding 140° and water absorption rates lower than 4 %.

Hydrophobic Modification of Cellulose Acetate and Its Application in the Field of Water Treatment: A Review.

With the inherent demand for hydrophobic materials in processes such as membrane distillation and unidirectional moisture conduction, the preparation and application development of profiles such as modified cellulose acetate membranes that have both hydrophobic functions and biological properties have become a research hotspot. Compared with the petrochemical polymer materials used in conventional hydrophobic membrane preparation, cellulose acetate, as the most important cellulose derivative, exhibits many advantages, such as a high natural abundance, good film forming, and easy modification and biodegradability, and it is a promising polymer raw material for environmental purification. This paper focuses on the research progress of the hydrophobic cellulose acetate preparation process and its current application in the water-treatment and resource-utilization fields. It provides a detailed introduction and comparison of the technical characteristics, existing problems, and development trends of micro- and nanostructure and chemical functional surface construction in the hydrophobic modification of cellulose acetate. Further review was conducted and elaborated on the applications of hydrophobic cellulose acetate membranes and other profiles in oil-water separation, brine desalination, water-repellent protective materials, and other separation/filtration fields. Based on the analysis of the technological and performance advantages of profile products such as hydrophobic cellulose acetate membranes, it is noted that key issues need to be addressed and urgently resolved for the further development of hydrophobic cellulose acetate membranes. This will provide a reference basis for the expansion and application of high-performance cellulose acetate membrane products in the environmental field.

Nitrogen and Oxygen Co‐Doped Graphene Quantum Dots as a Trace Amphipathic Additive for Dendrite‐Free Zn Anodes

AbstractThe practical implementation of aqueous zinc‐ion batteries (AZIBs) has encountered obstacles stemming from the limited reversibility of the zinc anode, primarily due to dendrite proliferation and water‐induced reactions occurring. In this investigation, a novel bifunctional interphase is proposed by integrating nitrogen and oxygen group graphene quantum dot (N‐O‐GQD) additives into the electrolyte. Experimental results and theoretical calculations demonstrate that the amphipathic N‐O‐GQD additive enhances the stability of the electrode by forming a protection layer on Zn surface. The zincophilic and hydrophobic nitrogen function groups stick to the surface of Zn electrodes to form a hydrophobic layer that shields water molecules from the electrode and promotes the uniform deposition of Zn. The hydrophilic hydroxyl function groups are exposed to the electrolyte to improve the compatibility at the electrode/electrolyte interface. As a result, the amphipathic N‐O‐GQD additive enables a robust cycling performance at high depth of discharge (DOD). Significantly, cells incorporating N‐O‐GQDs demonstrate a remarkable Coulombic efficiency of 99.7% over 900 cycles and sustain dendrite‐free cycling for 564 h (DOD = 51%). Particularly noteworthy is the performance of the modified Zn||ZnVO full cell with robust cycling behavior, enduring 4 000 cycles at 10 A g−1.

Multi-functional finishing of viscose fabrics based on tea polyphenols: Integrated flame retardant, antibacterial, hydrophobic, and UV-resistant functionalities

Tea polyphenols (TP) are endowed with numerous outstanding properties due to their natural structure, and their use in the preparation of multifunctional finishing agents is a novel topic. In this paper, a multifunctional finishing agent, PAT, was prepared by using phytic acid and TP as raw materials and finished on the surface of viscose fabrics to obtain PAT-100. After measurement, the limiting oxygen index of PAT-100 achieved 32.9 %, and the peak heat release rate was reduced by 90 %. Due to the presence of polyphenolic groups, PAT exhibited excellent inhibitory effects on Staphylococcus aureus and Escherichia coli, and the UPF value was improved to 53.2. Furthermore, this system also improved the hydrophobicity of viscose fabrics, and the breaking force retention in the warp and weft directions reached 130 % and 156 %, respectively. This work presents new ideas for TP in the field of multifunctional finishing and increases the added value of viscose fabrics.

Janus Structure Construction of Polyester-Cotton Fabrics for Achieving Excellent Moisture, Moisture-Permeability, and Antibacterial Capability.

Integration of hydrophobic and antibacterial functionalities into polyester-cotton blended (PTCO) textiles has attracted more attention but remains a challenge. Here, a Janus fabric with antibacterial effect, hydrophobicity, and enhanced moisture-permeability is fabricated using a "mist polymerization" approach. The PET fibers in the PTCO fabric are amino-functionalized through ammonolysis reactions of PET molecules with HDA, and mist treatments of poly lauryl methacrylate (PLMA) and poly(DMC-co-MA) (PDM) are applied on the two side surfaces of the PTCO-HDA fabric, respectively. The resulting Janus fabric exhibits an antibacterial rate of 99.9% against both E. coli and S. aureus, along with a hydrophobic property on its single side (PTCO-HDA@PLMA). Additionally, the establishment of a surface-free energy gradient across the fabric confers superior moisture-permeability to the Janus fabric, offering advantages in preserving textile comfort. Moreover, this approach does not significantly compromise the original fabric properties, such as mechanical strength, moisture permeability, and fabric softness. The proposed method offers a straightforward and scalable strategy for textile finishing, demonstrating great potential in expanding the application scope of PTCO fabrics, and it may hold a pivotal role in diverse applications, notably encompassing home textiles, wound dressings, and high-performance sportswear.

Modulating the spirolactone−zwitterion equilibrium of dichlororhodamine via changing its aqueous solubility: A new strategy to construct glutathione fluorogenic probe for bioimaging

The aqueous solubility is one of the key physical properties of a fluorophore. Herein, we synthesized and evaluated a series of 4,5-dichlororhodamine 19 (DCR) derivatives and demonstrated that the spirolactone-zwitterion equilibrium of DCR scaffold is highly dependent on its aqueous solubility: poor water-soluble DCR derivatives predominately adopt as a colorless, non-fluorescent spirolactone in neutral aqueous solution, whereas good water-soluble ones favor a colored, fluorescent zwitterion. To confirm the validity of this strategy, a hydrophobic benzyl thioester functionality was introduced to DCR platform to develop DCR-BTE as a fluorescent probe for glutathione (GSH). The transthioesterification between DCR-BTE and the thiol group of GSH affords a new thioester containing a good water-soluble GSH residue (DCR-GSH), thus shifting the equilibrium toward the fluorescent open form. DCR-BTE was proved to be capable of reporting the variations of GSH levels within the physiological concentration range, and its potential biological utility was shown by monitoring the depletion of GSH in the liver and kidney tissues of mice administrated by an overdose of acetaminophen. The present study provides an appealing strategy to construct fluorogenic probes based on tuning the lactone-zwitterion equilibrium of rhodamine via changing its aqueous solubility.

Hydrophobic, ultraviolet radiation-shielding, and antioxidant functionalities of TEMPO-oxidized cellulose nanofibril film coated with modified lignin nanoparticles

In this study, lignin nanoparticles (LN) and octadecylamine-modified LN (LN-ODA) were utilized as coating materials to enhance the hydrophobic, antioxidant, and ultraviolet radiation-shielding (UV-shielding) properties of a TEMPO-oxidized nanocellulose film (TOCNF). The water contact angle (WCA) of the TOCNF was approximately 53° and remained stable for 1 min, while the modified LN-ODA-coated TOCNF reached over 130° and maintained approximately 85° for an hour. Pure TOCNF exhibited low antioxidant properties (4.7 %), which were significantly enhanced in TOCNF-LN (81.6 %) and modified LN-ODA (10.3 % to 27.5 %). Modified LN-ODA-coated TOCNF exhibited antioxidant properties two to six times higher than those of pure TOCNF. Modified LN-ODA exhibited thermal degradation max (Tmax) at 421 °C, while pure LN showed the main degradation temperature at approximately Tmax 330 °C. The thermal stability of TOCNF-LN-ODA-coated materials remained consistent with that of pure TOCNF, while the crystallinity index of the sample showed a slight decrease due to the amorphous nature of the lignin structure. The tensile strength of TOCNF was approximately 114.1 MPa and decreased to 80.1, 51.3, and 30.3 MPa for LN-ODA coating at 5, 10, and 15 g/m2, respectively.

Integration of Dual Fire Alarm Self-Powered System: Leveraging Intelligent Wearable Flame-Retardant Hydrophobic Cotton Fabric

In the realm of smart textiles, an area garnering significant research attention and demonstrating vast developmental potential, we have conceived and fabricated a multifunctional smart textile with a fire dual-warning function. This innovation integrates thermoelectric performance, triboelectric nanogenerator (TENG), flame retardancy, and hydrophobic functionalities into a cohesive entity. Employing a straightforward impregnation method, we successfully infused cotton fabric (CF) with a novel flame retardant (named AA). Additionally, CF/PPA is modified by incorporating poly(3,4-ethylene dioxythiophene)-poly(styrene sulfonate) (PEDOT:PSS) and polydimethylsiloxane (PDMS) as separate layers, with the former providing thermoelectric properties and the latter enabling TENG functionality in smart textiles. This configuration exhibits excellent voltage output performance, generating a thermoelectric effect of 221 mV under a temperature differential of 76 K and achieving voltage output as high as 138 V at a vertical contact-separation frequency of 5 Hz. The superior dual-warning function, flame-retardant properties, and hydrophobicity of CF/PPA can be integrated into firefighting apparel, thereby establishing fire-alarm systems with remote signal transmission capabilities to enhance personnel safety. Furthermore, CF/PPA holds promising dual warning application prospects in the field of wearable flame-retardant and fire-alarm systems, thus paving new avenues for the utilization of smart textiles in the realm of the Internet of Things (IoT).

Colloidal Probe Technique Optimization for Determination of Young's Modulus of Soft Adhesive Hydrogels.

Atomic force microscopy (AFM) is a valuable tool for determining the Young's modulus of a wide range of materials. However, it faces challenges, particularly when assessing adhesive materials like soft poly(N-isopropylacrylamide) (pNIPAM) hydrogels. This study focuses on enhancing the consistency and reliability of AFM measurements by functionally modifying AFM spherical tip cantilevers to address substrate adhesion issues with these hydrogels. Specifically, hydrophobic functionalization with 1H,1H,2H,2H-perfluorooctyltrichlorosilane (PFOCTS) emerged as the most effective approach, yielding consistent and reliable Young's modulus data across various pNIPAM hydrogel samples. This work highlights the importance of optimizing data acquisition in AFM, rather than relying on postprocessing, to reduce inconsistencies in Young's modulus assessment.

A review on improving the sensitivity and color stability of naturally sourced pH-sensitive indicator films.

Naturally sourced pH-sensitive indicator films are of interest for real-time monitoring of food freshness through color changes because of their safety. Therefore, natural pigments for indicator films are required. However, pigment stability is affected by environmental factors, which can in turn affect the sensitivity and color stability of the pH-sensitive indicator film. First, natural pigments (anthocyanin, betalain, curcumin, alizarin, and shikonin) commonly used in pH-sensitive indicator films are presented. Subsequently, the mechanisms behind the change in pigment color under different pH environments and their applications in monitoring food freshness are also described. Third, influence factors, such as the sources, types, and pH sensitivity of pigments, as well as environmental parameters (light, temperature, humidity, and oxygen) of sensitivity and color stability, are analyzed. Finally, methods for improving the pH-sensitive indicator film are explored, encapsulation of natural pigments, incorporation of a hydrophobic film-forming matrix or function material, and protective layer have been shown to enhance the color stability of indicator films, the addition of copigments or mental ions, blending of different natural pigments, and the utilization of electrospinning have been proved to increase the color sensitivity of indicator films. This review could provide theoretical support for the development of naturally sourced pH-sensitive indicator films with high stability and sensitivity and facilitate the development in the field of monitoring food freshness.

Adsorber Charge Dominates over Hydrophobic or Fluorophilic Functionalization in Influencing Adsorption of PFCA onto Polystyrene Resins

AbstractA systematic series of industrial‐relevant polystyrene‐based anion exchange resins that are functionalized with hydro‐ or fluorocarbon chains are compared regarding their adsorption behavior toward perfluorocarboxylic acids (PFCA) in respect to their charge, chain length, and type of chain. The results clearly show the dominance of electrostatic interactions in the adsorption process as uncharged adsorber materials showed no adsorption at all. In contrast, the charged adsorber materials showed in general a PFCA removal of 80% to 30% over the experiment depending on effluent fraction. Unexpectedly, for perfluorobutanoic acid (PFBA) the highest removal rate is found with consistently >90%. Despite observing significant benefits in the adsorption of PFCA for fluoroalkylated adsorbers in comparison to their non‐fluorinated counterparts, this effect of fluoroalkylation is comparatively small and can not be clearly attributed to fluorophilic interactions between the fluoroalkyl chains. These findings help clarifying that the introduction of fluorocarbon moieties in adsorber materials is not necessary in order to remove fluorocarbon molecules from the environment.

Insight into the hydrophobic functionalization of cellulose microfibrils using the Passerini three-component reaction

The aqueous catalyst-free one-pot Passerini 3-component reaction (P-3CR) was employed for the functionalization of dialdehyde cellulose (DAC) derived from the periodate oxidation of microfibrillated cellulose (MFC) with insights provided by 13C and 15N CP-MAS NMR and FTIR analyses. The kinetics of the P-3CR revealed rapid progress within the initial 2 h, reaching a plateau between 6 and 18 h. The reaction achieved a maximum degree of substitution (DS) with only 1 equivalent of carboxylic acid and isocyanide with respect to the number of aldehydes, therefore demonstrating the atom economy character of the P-3CR performed on MFC. Variable DS values (0.08 to 0.37) were achieved by altering the degree of oxidation of DAC (ranging from 0.48 to 1.1) when reacted with heptanoic acid and tert-butyl isocyanide. Additionally, aliphatic chain lengths of carboxylic acids from C4 to C11 were successfully used for the functionalization of DAC with distinct hydrophobic chains. Furthermore, while cosolvents negatively affected the DS when using heptanoic acid, a significant increase was observed in the case of undecanoic acid due to an improved solubility of the reagent. The aqueous medium P-3CR can thus be considered a versatile tool to tailor the functionalization of MFC and provide it with hydrophobicity.

Preparation and characterization of hydrophobic waterborne polyurethane self‐matting coating

AbstractA green method to synthesize self‐matting waterborne polyurethane acrylic hybrid emulsion with hydrophobic function is introduced in this study. A reactive waterborne polyurethane (RWPU) dispersion containing unsaturated CC double bonds was prepared from epoxidized soybean oil. Subsequently, the RWPU dispersion was copolymerized with fluorinated monomers of different carbon chain lengths to prepare polyurethane acrylic hybrid emulsion (PUF). The results revealed the gloss levels of PUF films to be as low as 12.4 gloss units at 60°. The morphology of PUF films was observed by scanning electron microscope and three‐dimensional surface profilometer, and the relationship between surface roughness and gloss was discussed in detail. In addition, thermal gravimetric analysis was conducted to determine the thermal stability of the PUF films, and the results denoted that these PUF films exhibited excellent thermal stability. Comprehensive performance tests indicated that the RWPU dispersion, which was copolymerized with hexafluorobutyl methacrylate at a weight of 10%, exhibited a low gloss, a high contact angle of 120°, and a high elongation percentage of 423%. Furthermore, the dynamic light scattering results showed small average particle size, revealing the excellent storage stabilities.

Paper-based material with hydrophobic and antimicrobial properties: Advanced packaging materials for food applications.

The environmental challenges posed by plastic pollution have prompted the exploration of eco-friendly alternatives to disposable plastic packaging and utensils. Paper-based materials, derived from renewable resources such as wood pulp, non-wood pulp (bamboo pulp, straw pulp, reed pulp, etc.), and recycled paper fibers, are distinguished by their recyclability and biodegradability, making them promising substitutes in the field of plastic food packaging. Despite their merits, challenges like porosity, hydrophilicity, limited barrier properties, and a lack of functionality have restricted their packaging potential. To address these constraints, researchers have introduced antimicrobial agents, hydrophobic substances, and other functional components to improve both physical and functional properties. This enhancement has resulted in notable improvements in food preservation outcomes in real-world scenarios. This paper offers a comprehensive review of recent progress in hydrophobic antimicrobial paper-based materials. In addition to outlining the characteristics and functions of commonly used antimicrobial substances in food packaging, it consolidates the current research landscape and preparation techniques for hydrophobic paper. Furthermore, the paper explores the practical applications of hydrophobic antimicrobial paper-based materials in agricultural produce, meat, and seafood, as well as ready-to-eat food packaging. Finally, challenges in production, application, and recycling processes are outlined to ensure safety and efficacy, and prospects for the future development of antimicrobial hydrophobic paper-based materials are discussed. Overall, the emergence of hydrophobic antimicrobial paper-based materials stands out as a robust alternative to plastic food packaging, offering a compelling solution with superior food preservation capabilities. In the future, paper-based materials with antimicrobial and hydrophobic functionalities are expected to further enhance food safety as promising packaging materials.

Antimicrobial and hydrophobic cellulose paper prepared by covalently attaching cinnamaldehyde for strawberries preservation

The demand for paper-based packaging materials as an alternative to incumbent disposable petroleum-derived polymers for food packaging applications is ever-growing. However, typical paper-based formats are not suitable for use in unconventional applications due to inherent limitations (e.g., excessive hydrophilicity, lack antimicrobial ability), and accordingly, enabling new capabilities is necessity. Herein, a simple and environmentally friendly strategy was proposed to introduce antimicrobial and hydrophobic functions to cellulose paper through successive chemical grafting of 3-aminopropyltriethoxysilane (APS) and cinnamaldehyde (CA). The results revealed that cellulose paper not only showed long-term antibacterial effect on different bacteria, but also inhibited a wide range of fungi. Encouragingly, the modified paper, which is fluorine-free, displays a high contact angle of 119.7°. Thus, even in the wet state, the modified paper can still maintain good mechanical strength. Meanwhile, the multifunctional composite papers have excellent biocompatibility and biodegradability. Compared with ordinary cellulose paper, multifunctional composite paper can effectively prolong the shelf life of strawberries. Therefore, the multifunctional composite paper represents good application potential as a fruit packaging material.

Synthesis and unambiguous NMR characterization of linear and branched N-alkyl chitosan derivatives

Chitosan, sourced from abundant chitin-rich waste streams, emerges as a promising candidate in the realm of future functional materials and chemicals. While showing numerous advantageous properties, chitosan sometimes falls short of competing with today's non-renewable alternatives. Chemical derivatization, particularly through N-alkylation, proves promising in enhancing hydrophobic functionalities. This study synthesizes fifteen chitosan derivatives (degree of substitution = 2–10 %) using an improved reductive amination method. Next, selective depolymerization through acid hydrolysis reduced the chain rigidity imposed by the polymer backbone. This facilitated unambiguous structural characterization of the synthesized compounds using a combination of common NMR techniques. Two potential side reactions are identified for the first time, emphasizing the need for detailed structural information to unlock the true potential of these derivatives in future applications. HypothesisThe increase in chain mobility induced by the selective depolymerization of aliphatic N-alkyl chitosan derivatives allows for an unambiguous NMR characterization.

Covalent organic frameworks-coated silk membrane for durably efficient oil/water separation

Engineering surface chemistry can effectively improve separation performance of membranes. Herein, we propose a covalent organic framework (COF)-coated strategy to enhance hydrophobicity, corrosion resistance and stability of silk membrane via engineering surface chemistry. 1,3,5-triformylbenzene (TFB) and 1,4-p-phenylenediamine (PDA) are used as monomers dissolved in 1,4-dioxane and ethanol, respectively. Then the two solutions are mixed with pre-treated silk, transferred to an autoclave following heating and the LZU1-COF particles coated silk membrane (Silk@COF) is obtained. LZU1-COF particles are covered on the surface of silk, which enhance the stability, raise the hydrophobic function and rose petal effect of silk membrane. Meanwhile, water can be effectively prevented from penetrating into the pores of Silk@COF, and oil droplets are adsorbed and fall into the collector under the effect of gravity. Not only that, the Silk@COF with lotus effect (water contact angles, WCA = 159.1°) and petal effect exhibits oil/water separation efficiency >98%, especially for dichloromethane (99.65%). This work provides a sustainable and versatile solution for water treatment with excellent eco-friendliness and cost-effectiveness.

In-situ growth of CuS on polyimide film to construct dense and continuous network: Achieving excellent electrothermal and EMI shielding performance

The performance of the electrothermal film is generally determined by conductive filler network. However, it is still challenging to construct a dense network of conductive fillers in the electrothermal film. In this work, we develop a simple and efficient method to construct a dense and continuous network via in-situ growth of CuS nanosheets on the surface of polyimide (PI) film with stable interfacial bonding. The obtained PI@CuS electrothermal film is further packaged by commercially available PTFE and PI tapes to achieve desirable surface hydrophobic self-cleaning function and stability for the use in different environments. By tuning the network density of CuS nanosheets, it imparts excellent electrothermal conversion efficiency and cycling stability to the PI@CuS film, whose surface temperature could rapidly ramp up over 200 °C at 8 V. The film also exhibits excellent photothermal performance, reaching close to 100 °C at 100 mW/cm2. The anti-icing/de-icing experiment shows that the icing time is prolonged significantly at low temperature and the melting time is reduced dramatically. Furthermore, the PI@CuS film also exhibits outstanding electromagnetic interference (EMI) shielding effectiveness of 57.1 dB with a thickness of only 80 μm, and excellent tensile strength of over 90 MPa. The in-situ growth strategy provides a novel route for the fabrication of the electrothermal film with excellent overall performance.

Interfacial Phenomena in Nanostructured Systems with Various Materials.

Interfacial phenomena linked to the behavior of bound water, organic solvents (co-sorbates, dispersion media), hydrogen, methane, acids/bases, and salts bound to various silicas, polymers, and carbon materials were analyzed vs. temperature and concentrations using 1 H NMR spectroscopy, differential scanning calorimetry (DSC) and other methods. The material characteristics were studied using microscopy, infrared spectroscopy (IR), small angle X-ray scattering (SAXS), and nitrogen adsorption. Confined space effects (CSE) result in enhanced freezing point depression (FPD) and stronger diminution of solvent activity and colligative properties of liquid mixtures in narrower pores. Short hydrophobic functionalities (≡Si-CH3 , =Si(CH3 )2 ) at a silica surface and the presence of nanopores result in differentiation of bound water into weakly (WAW, δH =0.2-2.0 ppm) and strongly (SAW, δH =4-6 ppm) associated waters of smaller solvent activity in smaller clusters located in narrower pores and unfrozen below a bulk freezing point. These effects are enhanced in hydrophobic dispersion media. Hydrophobic liquids could displace bound water into narrower pores inaccessible for their molecules larger than water and/or into broader pores to reduce contact area between immiscible liquids. The observed phenomena depend on sorbent/sorbate kinds and play an important role on practical applications of various sorbents.

Poly(vinylpyridine-co-vinylpyridine N-oxide) Excipients Mediate Rapid Dissolution and Sustained Supersaturation of Posaconazole Amorphous Solid Dispersions.

The chemical structure of excipients molecularly mixed in an amorphous solid dispersion (ASD) has a significant impact on properties of the ASD including dissolution behavior, physical stability, and bioavailability. Polymers used in ASDs require a balance between hydrophobic and hydrophilic functionalities to ensure rapid dissolution of the amorphous dispersion as well as sustained supersaturation of the drug in solution. This work demonstrates the use of postpolymerization functionalization of poly(vinylpyridine) excipients to elucidate the impact of polymer properties on the dissolution behavior of amorphous dispersions containing posaconazole. It was found that N-oxidation of pyridine functionalities increased the solubility of poly(vinylpyridine) derivatives in neutral aqueous conditions and allowed for nanoparticle formation which supplied posaconazole into solution at concentrations exceeding those achieved by more conventional excipients such as hydroxypropyl methylcellulose acetate succinate (HPMCAS) or Eudragit E PO. By leveraging these functional modifications of the parent poly(vinylpyridine) excipient to increase polymer hydrophilicity and minimize the effect of polymer on pH, a new polymeric excipient was optimized for rapid dissolution and supersaturation maintenance for a model compound.