Surface Contact Angle Measurements Research Articles

A comparison of antibacterial activity in dark-UV light in perspective of surface and structural properties of spray pyrolysis grown Cu doped Cr2O3 thin films

Thin films of Cr2O3 and Cu doped Cr2O3 thin films were prepared using the spray pyrolysis technique with different Cu/Cr ratios. Precursor solution of 0.2 M was sprayed on a pre-heated (≈ 400 °C) soda lime glass substrate using air as the carrier gas. XRD analysis confirmed polycrystalline nature of the films with rhombohedral structure. Crystallite size and lattice strain have been estimated using Williamson-Hall method. These films were porous and presented a rough morphology and showed a strong signature on the presence of vibrational Cr-O bonding. The solid-liquid surface contact angle measurements revealed a large contact angle which is indicative of reduced surface energy. Vickers hardness measurement reveals that Cr2O3 thin film with 2% Cu/Cr ratio have high hardness value of 903 HV (0.2 kgf). The antibacterial activity of the films was investigated against two gram-positive (Bacillus Subtilus and Bacillus Meurellus) and two gram-negative bacteria (Escherichia Coli and Acetobacter Rhizopherensis). A comparison was established both under dark and UVA light in terms of structural properties of the films. Antibacterial activity was significantly enhanced with the increase in Cu/Cr ratio. Interestingly, the UVA light further facilitated to boost the antibacterial effect against both types of bacteria. A good correlation was found between the structural parameters and the zone of inhibition.

Characterization of Arboblend V2 Nature Textured Surfaces Obtained by Injection Molding

Surface texturing is an engineering technology used in order to improve the surface characteristic of plastic parts obtained by injection molding. Applying this process not only changes the part surface properties, but also its topography. The novel functionalities of plastic products become useful when other materials make contact with the textured surface. Of course, these characteristics may vary depending on the laser positioning, dimensions, and geometry of the texture. The present paper presents the surface characteristics obtained after the laser texturing of the Arboblend V2 Nature biodegradable polymer. Three distinct geometries were studied: hexagonal, square, and triangular, and different behaviors of them were highlighted during surface free energy (SFE) and contact angle (WCA) measurements: a hydrophobic character for square and hexagonal geometry with distilled water as the measure liquid, and a hydrophilic character with diiodomethane as the measure liquid; for triangle geometry, the contact angle measurements were impossible to extract because the drop turns into a flat puddle. Additionally, the friction coefficient varied depending on the geometry texture, with the lowest value being recorded by the sample with hexagonal geometry. The micro-indentation tests highlighted increased surface micro-hardness compared to the basic material. The possibility of use in the practice of textured surfaces is viable; thus, based on the obtained results, there is even the possibility to replace non-biodegradable polymers from different sectors of activity.

Open Questions that Can Bridge Intermolecular Interactions and Macroscopic Wetting/Dewetting Behaviors of Thin Films

AbstractPolymer films and coatings are ubiquitous in nanoscale applications where confined macromolecules experience greater interfacial effects, causing deviations from bulk material properties; however, the fundamental physics dictating their wetting behavior remains poorly understood. This review provides a perspective on thickness‐dependent surface wettability in thin polymer films characterized by critical thickness, where surface energy and contact angle measurements deviate from bulk values. In contrast with dewetting behaviors, which are well‐modeled by van der Waals (vdW) potentials to afford several nanometers of critical thickness, an unexpectedly large critical thickness of ≈100 nm is reported for thin polystyrene films via surface energy and contact angle measurements. This deviation in the critical thickness highlights an opportunity to modify the current theoretical understanding of the vdW potential model. In addition, possible explanations to interpret the long critical length scales are discussed: 1) challenges in sample preparations and contact angle measurements; 2) temperature dependence of surface energy; and 3) the cooperative nature of polymers. This review invites researchers to bridge the knowledge gap between macroscopic behaviors (e.g., wetting/dewetting) and molecular‐level understanding (e.g., vdW potentials) in polymer thin films.

A dendrite suppression coating formulated via electrophoretic deposition using Bi-functional surfactants for Zn-ion batteries

Aqueous Zn-ion batteries (ZIBs) are promising for large-scale energy storage due to their low cost and high safety. However, ZIBs suffer from Zn dendrite growth and side reactions over the charge-discharge processes. Herein, a facile and scalable strategy was developed based on electrophoretic deposition (EPD) of surfactant-stabilized multi-wall carbon nanotubes (MWCNT) to enhance the reversibility of Zn foil. The MWCNT coating provides high surface area and improved electronic conductivity, thus facilitating rapid charge transfer behavior over the Zn 2+ plating/stripping processes. The results indicated that cationic surfactants, cetyltrimethylammonium bromide (CTAB), are feasible to improve the stability of Zn anode as electrolyte additives in parallel to dispersion and charging of MWCNT. Single-crystalline cryptomelane-type α-MnO 2 nanowires were successfully synthesized by oxalate-reduction of potassium permanganate under ambient conditions. The ZIBs, prepared by α-MnO 2 nanowire cathode and MWCNT coated Zn anode, demonstrated surpassing rate capacity and long cycling stability. The interfacial analysis of electrodes, based on surface tension and contact angle measurements, shed some light on the design and development of multi-functional additives for advanced ZIBs. • A dendrite suppression coating was fabricated by electrophoretic deposition. • Surfactants are found to be electrolyte additives paralleled to CNT deposition. • Single-crystalline α-MnO 2 nanowires were synthesized under ambient conditions. • Interfacial properties were analyzed for wettability and tension measurements.

Cotton waste and nanoclay‐based phenolic novolac epoxy composites and evaluation of their properties

AbstractIn this study, two types of biobased epoxy composites were prepared by using only alkali‐treated cotton waste (CtW), or with the nanoclay (NC) in the form of hybrid reinforcement. Phenol novolac‐type epoxy resin (EPN) was used as a matrix. Untreated (CtW) and alkali‐treated (NaOH‐CtW) particles were characterized by scanning electron microscopy (SEM)/energy‐dispersive X‐ray spectroscopy (EDX). The average size for NC was determined as 3838 nm. Composites were prepared at 10–50 wt% NaOH‐CtW and 20 wt% NaOH‐CtW/(1–2–3–4–5) wt% NC ratios. The morphology of the composites was investigated using SEM. The composites' properties were determined by applying thermogravimetric analysis (TGA), and various tests (tensile, hardness, water sorption, and surface contact angle measurement). The tensile strength of pure EPN was 96.6 MPa, while it changed in the range of 74–98 and 81–106 MPa for NaOH‐CtW and hybrid composites, respectively. All hybrid composites exhibited higher Young's modulus values (7.7–8.9 GPa). Thermal values of hybrid composites were found higher and their char percentages varied in the range of 28.9–30.3%. NaOH‐CtW increased the water sorption of the epoxy matrix from 0.59% up to 6% by 50 wt%. In contrast, a decrease in water sorption of NC composites was observed.

Improvement of the durability of cement-based material through surface modification with nano-engineered releasing agents

• Modified releasing agent with NS/NT to make nano-engineered releasing agent. • NS and NT increased the contact angle of releasing agent and help their adhesion on mold. • Reduction of the surface porosity (within 2 mm thick). • Nano-engineered releasing agent can achieve durable concrete surface. Aggressive substances can gain access to the inner structure of cement-based materials through the surface, resulting in deterioration of the structure. This work developed an effective way of improving the quality of cement-based materials surface by applying nanoSiO 2 -/nanoTiO 2 -engineered releasing agents (nSRa/nTRa) on the formwork surface. Continued with our previous work, the positive effects of nSRa/nTRa on cement hydration were used to improve the surface quality of the cement-based samples through its spraying on the mold surface. This work firstly characterized the adhesive properties of these agents on mold surface (contact angle and viscosity measurement), and then their effects on the surface microstructure and the durability of cement-based materials such as 1) sulfate resistance, 2) chloride resistance, and 3) freeze–thaw resistance were determined. Results showed that nanoparticle addition increased the contact angle of releasing agents and helped their adhesion to mold. Applying nSRa/nTRa on cement-based samples benefited the reduction of surface porosity (within 2 mm thick) by 14.2 %, 19.4 %, 8.6 %, and 18.9 % in the nS2Ra-, nS4Ra-, nT4Ra- and nT16Ra-engineered samples. After 120 days of sulfate attack, mortar samples cast in Ra-, nS4Ra-, and nT16Ra-coated molds showed reductions in compressive strength loss of 1.57 %, 0.73 %, and 0.23 %. Noticeable reductions in the chloride migration coefficient of 23.9 % and 26.6 % were found in the nS4Ra-/nT16Ra-modified mortar sample, while their relative dynamic modulus elasticity was 6.72 % and 12 % higher than Ra-sample after 200 freeze–thaw cycles. This work proved that nano-engineered releasing agents can effectively improve the durability of the concrete structure.

Performance Evaluation of an Octadecyltrimethyl Ammonium Chloride-Dimethyl Silicone Oil as a Waterproof Locking Agent in Low-Permeability Reservoirs.

Low porosity and permeability of oil and gas reservoirs make it difficult to develop these resources. To address these problems, we developed and evaluated a novel, environmentally friendly waterproof locking agent, which was prepared using dimethyl silicone oil and octadecyltrimethylammonium chloride and characterized by Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and particle size measurement. The waterproof locking performance of the agent was evaluated in a low-permeability reservoir using surface tension and contact angle measurements, and thermodynamic calculations were performed. The average particle size or median diameter (D50) of a 1% mother liquor was 325 nm at 20 °C and 470.8 nm at 70 °C. The contact angle of clean water on the core surface increased from 10 to 110°. At 70 °C, the surface tension of water was reduced to 24 mN·m–1, indicating good waterproof locking performance. The interaction parameters were calculated in accordance with the Langmuir adsorption theory. The increase in temperature from 20 to 70 °C reduced Γmax from 4.59 × 10–6 to 1.36 × 10–6 mol·m–2 and ΔGθ from −40.93 to −56.54 kJ·mol–1. Thus, the adsorption behavior of the developed locking agent is believed to improve the productivity of oil wells.

Pulse-reverse electrodeposition of a conversion coating based on zinc cation and 3-nitrobenzoic acid on carbon steel to enhance adhesion and protective function of epoxy coating

This work introduces a pulse-reverse electrodeposition method for the application of conversion coating on carbon steel from 0.1 M 3-nitrobenzoic acid and 0.1 M zinc nitrate bath. The impact of current density changes on the surface morphology, composition, and electrochemical characteristics of conversion coatings was explored by surface analysis methods, contact angle, and electrochemical measurements. Results depicted the highest anti-corrosion performance for the sample treated by 0.045 A/cm2. Afterward, an epoxy coating was fabricated over the treated samples. The effect of conversion coating on the epoxy electrochemical behavior and adhesion properties was studied. According to the findings, the adhesion strength and anticorrosion performance of epoxy coating enhanced after the substrate carbon steel being modified by the conversion coating.

Influence of CeO2 and TiO2 Particles on Physicochemical Properties of Composite Nickel Coatings Electrodeposited at Ambient Temperature.

The Ni-TiO2 and Ni-CeO2 composite coatings with varying hydrophilic/hydrophobic characteristics were fabricated by the electrodeposition method from a tartrate electrolyte at ambient temperature. To meet the requirements of tight regulation by the European Chemicals Agency classifying H3BO3 as a substance of very high concern, Rochelle salt was utilized as a buffer solution instead. The novelty of this study was to implement a simple one-step galvanostatic electrodeposition from the low-temperature electrolyte based on a greener buffer compared to traditionally used, aiming to obtain new types of soft-matrix Ni, Ni-CeO2, and Ni-TiO2 coatings onto steel or copper substrates. The surface characteristics of electrodeposited nickel composites were evaluated by SEM, EDS, surface contact angle measurements, and XPS. Physiochemical properties of pure Ni, Ni-CeO2, and Ni-TiO2 composites, namely, wear resistance, microhardness, microroughness, and photocatalytic activity, were studied. Potentiodynamic polarization, EIS, and ICP-MS analyses were employed to study the long-term corrosion behavior of coatings in a 0.5 M NaCl solution. Superior photocatalytic degradation of methylene blue, 96.2% after 6 h of illumination, was achieved in the case of Ni-TiO2 composite, while no substantial change in the photocatalytic behavior of the Ni-CeO2 compared to pure Ni was observed. Both composites demonstrated higher hardness and wear resistance than pure Ni. This study investigates the feasibility of utilizing TiO2 as a photocatalytic hydrophilicity promoter in the fabrication of composite coatings for various applications.

A Novel MATLAB®-Algorithm-Based Video Analysis to Quantitatively Determine Solution Creeping in Intact Pharmaceutical Glass Vials

During the filling process of a biopharmaceutical drug product (DP), a liquid DP film might creep up the inner vial wall which is barely discernible, appears as milky-white haze after lyophilisation and is known as fogging. Creeping and fogging are mainly dependent on the primary packaging material surface and its hydration, vial preparation process as well as DP composition. The occurrence of both can impede visual inspection and might lead to DP rejection. Hence, our studies focused on the early detection of liquid solution and glass vial surface interaction directly after filling. For a fast and highly sensitive evaluation a novel video-based analysis was used. To our knowledge, this is the first time a MATLAB®-algorithm-based video analysis was applied to quantitatively determine creeping time-resolved. Furthermore, creeping in dependence of vial processing sites, surfactant type and concentration, filling temperature, and vial format were investigated. The results were verified using orthogonal conventional methods such as surface tension, wetting behaviour, and contact angle measurements, as well as ToF-SIMS, ICP-MS, and SEM. Additionally, the methods applied were assessed regarding their cross-validation capability. The observations indicate that the vial preparation process can have a pronounced impact on alteration of the glass vial surface and related creeping behaviour of the filled solution.

Carbon and Silane‐based Coatings for Improved Bonding in Hybrid Metal‐Composite Applications

AbstractInterfacial bonding in multi‐material structures is crucial for component performance. The influence of organosilane and Diamond‐Like Carbon coatings were investigated for improved bond strength of additively manufactured AlSi10Mg, CuCr1Zr and Ti6Al4V with carbon fiber reinforced polymer composite. Treated surfaces were evaluated by surface energy, contact angle, film adhesion and thickness measurements, SEM‐EDX analysis and double‐lap‐shear tests. Coating improved the bond strength by around 20 % in case of AlSi10Mg and CuCr1Zr, whereas treatment did not show any significant effect for Ti6Al4V.

Process optimization for extraction of avian eggshell membrane derived collagen for tissue engineering applications

Abstract The avian eggshell membranes’ composition depicts close resemblance with the extracellular matrix of the cells, and therefore being widely employed as potential biomaterials for tissue engineering applications. However, the optimization of process conditions for collagen extraction, the main constituent of eggshell membranes is still challenging. In the present study, extraction of collagen was performed by an enzymatic method optimized through the one-factor-at-a-time (OFAT) technique for three parameters viz. pepsin concentration, treatment time and pH. The process optimization resulted in the maximum yield of 56% collagen with 350 U/mg pepsin concentration at pH 3 treated for 9 days, not reported yet. The collagen extraction was confirmed by OD at 232 nm; and its viscoelasticity behaviour at pH 5. The physico–chemical characterization of extracted collagen with FESEM, ATR-FTIR, surface roughness analysis and contact angle measurement revealed the morphological and topological alteration during the collagen extraction. The process optimization and characterization of eggshell membrane derived collagen can aid in the significant biomaterials development for tissue regeneration.

Controllable hydrophilic titanium surface with micro-protrusion or micro-groove processed by femtosecond laser direct writing

Smart surfaces with switchable wettability have aroused enormous interest, due to their multifunction in chemistry, biology and medicine. In this paper, a controllable hydrophilic titanium surface with either micro-protrusion or micro-groove is processed by femtosecond laser. The relationship between laser processing parameters of defocus value (Df), scanning speed (Vs), power (Po) and the shape/size of structures are systematically studied. Results show that Df and Vs mainly affect the shape of structures, while Vs and Po influence size. The surface structures can change from micro-groove to micro-protrusion, for the first time, by adjusting processing parameters. After laser processing, morphology and chemical composition are analyzed. It is found that the oxygen content in the middle area of micro-protrusion is higher than the recast layer of micro-groove. The formation mechanism can be attributed to the photo-thermal effect and Marangoni convection effect. Furthermore, the surface roughness and contact angle (CA) measurement results show that the surface roughness of micro-groove array is greater than micro-protrusion array, while micro-protrusion array can promote hydrophilicity compared with micro-groove array. Moreover, the micro-protrusion array with high scanning interval (△) can maintain the hydrophilicity better than micro-groove array even after 90 days. The selected area modification of femtosecond laser processing can potentially be applied to improve biological activity in titanium implants.

Validation of adhesion characterization methods for antistick coatings applied in cooking systems

This study aims to validate an effective methodological analysis for the characterization of the adhesion values of antistick coatings employed in cooking systems. The morphology and chemistry of four different industrial products were investigated by roughness measurements, electron microscopy observations and infrared spectroscopy analysis. The adhesion of the coatings was evaluated comparing various techniques, such as the surface contact angle measurements, the pull-off test and the single lap-joint tensile shear method, in synergy with degradation phenomena simulated by P.E.I. abrasion and dishwashing tests. The single lap-joint tensile shear test was able to evaluate evident differences between all the proposed coatings, regardless of their state of deterioration, featuring the best selectivity among the used methods. However, the pull-off test proved to be a viable and more economical alternative for fast evaluation techniques, considering the overall instrument costs. While all the polytetrafluoroethylene-based systems turned out to be totally uninfluenced by the chemical attacks performed during the dishwasher cycles, the sol–gel coating exhibited lower performances of the applied releasing agent, before and after the mechanical degradation tests. Therefore, sol–gel coatings, despite being proposed as valid alternatives to PTFE ones, do not achieve the same quality standards in terms of releasing properties, being in addition much more sensible to degradation and loss in performances.

Birch Wood Surface Characterization after Treatment with Modified Phenol-Formaldehyde Oligomers.

Phenol-formaldehyde (PF) resins with well-established molecular sizes are promising treatment agents for wood bulk protection. However, due to the presence of hydroxyl groups on the periphery, the PF oligomers tend to absorb the water, which can lead to water penetration into the wood. To overcome this drawback different PF pre-polymers have been chemically modified with different long-chain fatty acid chlorides (FAC) via esterification. To obtain the modified PF (M-PF) resins, the PF pre-polymers with average molecular weight (Mw) from 266 to 884 g/mol were esterified with decanoyl, lauroyl, myristoyl, palmitoyl, and stearoyl chloride in pyridine as the reaction medium. Silver birch (Betula pendula) wood specimens (15 × 70 × 150 mm3) were coated with M-PF pre-polymer 5% (w/w) solutions in tetrahydrofuran (THF), and hydrophobic properties of treated birch wood specimens were evaluated using surface contact angle (CA) measurements of water droplets. For all M-PF resin-treated specimens, CA was almost 2–2.5 times higher than for untreated wood (45°) and it remained 80–125° after 60 s. The aging properties of M-PF resin-coated birch wood were analyzed using artificial weathering with ultraviolet (UV) light and combination of both UV and water spray. Results clearly confirm, that the hydrophobic properties of M-PF-treated wood has short-term character and will gradually disappear during long-term application in outdoor conditions.

Surface free energy, wettability and bonding of plywood after fire-retardant treatment with various chemicals

Plywood usage has been increasing recently in the building and furniture industry due to its outstanding surface and resistance properties. Although it has many advantages, the flammability of plywood needs to be improved with fire-retardant chemicals. However, these chemicals which improve panels against burning can be differently influenced many properties of panels. This study aimed to investigate the surface roughness, wettability, and surface free energy of the veneers treated with some fire-retardant chemicals and to determine the changes in the mechanical properties of plywood. The beech, poplar, alder, and pine veneers were used as wood species whilst zinc borate, borax, monoammonium phosphate, and ammonium sulfate were used as fire-retardant chemicals in this study. The surface roughness and contact angle measurements were performed to determine the surface properties of veneers, and then the surface free energy values were calculated. The bonding and bending strength of the plywood panels produced from these veneers were determined according to the relevant standards. As a result of the study, the surface free energy values of veneers with lower contact angles and smoother surfaces were found to be higher. It was also determined that the bonding strength values of plywood panels produced from veneers with high surface energies were also high. Generally, the untreated veneers had higher surface free energy values than the treated veneers. Among the fire-retardant chemicals, zinc borate caused the highest surface free energy values in the beech and alder veneers while borax exhibited the highest values in the poplar and pine veneers.

Adjustable surface activity and wetting ability of anionic hydrocarbon and nonionic short-chain fluorocarbon surfactant mixtures: Effects of Li+ and Mg2+

Achieving wide variation ranges and various adjusting modes of the performances for surfactant mixtures is still a significant challenge which limits the extensive application of surfactant mixtures. Herein, we reported the physicochemical properties and performances of hydrocarbon/fluorocarbon surfactant mixtures constituted with an anionic hydrocarbon surfactant, sodium dodecyl sulfate (SDS), and a tri-block nonionic short-chain fluorocarbon surfactant (F9EG13F9). Meanwhile, the effects of Li+ and Mg2+ on them were investigated. The surface tension and contact angle measurements were adopted to reflect the surface activity and wetting ability of SDS/F9EG13F9 mixtures. The data showed that the surface tensions at the critical micelle concentrations and the contact angles on polytetrafluoroethylene film of these surfactant mixtures are 33.5–21.4 mN/m and 118.0–58.7°, respectively, which indicates that their surface activity and wetting ability possess wide variation ranges. Furthermore, the micellization, adsorption and thermodynamics behaviors of mixed surfactants were also analyzed using a series of theoretical parameters based on the regular solution theory, Clint’s model, Maeda’s model, etc. The results approved that Li+ and Mg2+ immensely reduce the electrostatic repulsion effect of SDS and increase the adsorption of SDS at phase interfaces to enhance mixed monolayer packing, in which the effect of Mg2+ is stronger than that of Li+. Thus, precisely adjustable surface activity and wetting ability can be realized by changing the molar ratio and adding the different cations, which enables SDS/F9EG13F9 mixtures to possess tunable performances to meet various practical application requirements.

Copper Surface Treatment Method with Antibacterial Performance Using "Super-Spread Wetting" Properties.

In this work, a copper coating is developed on a carbon steel substrate by exploiting the superwetting properties of liquid copper. We characterize the surface morphology, chemical composition, roughness, wettability, ability to release a copper ion from surfaces, and antibacterial efficacy (against Escherichia coli and Staphylococcus aureus). The coating shows a dense microstructure and good adhesion, with thicknesses of approximately 20–40 µm. X-ray diffraction (XRD) analysis reveals that the coated surface structure is composed of Cu, Cu2O, and CuO. The surface roughness and contact angle measurements suggest that the copper coating is rougher and more hydrophobic than the substrate. Inductively coupled plasma atomic emission spectroscopy (ICP-AES) measurements reveal a dissolution of copper ions in chloride-containing environments. The antibacterial test shows that the copper coating achieves a 99.99% reduction of E. coli and S. aureus. This study suggests that the characteristics of the copper-coated surface, including the chemical composition, high surface roughness, good wettability, and ability for copper ion release, may result in surfaces with antibacterial properties.

Bidirectional Light-Driven Ion Transport through Porphyrin Metal–Organic Framework-Based van der Waals Heterostructures via pH-Induced Band Alignment Inversion

Bidirectional Light-Driven Ion Transport through Porphyrin Metal–Organic Framework-Based van der Waals Heterostructures via pH-Induced Band Alignment Inversion

Comparison of carboxybetaine with sulfobetaine polyaspartamides: Nonfouling properties, hydrophilicity, cytotoxicity and model nanogelation in an inverse miniemulsion

AbstractZwitterionic polymers are promising non‐fouling materials widely used for surface modification. Here, we report the synthesis of zwitterionic polyaspartamides bearing carboxybetaine and sulfobetaine prepared via combining the ring‐opening reaction of polysuccinimide with 3‐(dimethylamino)‐1‐propylamine and the reaction of the formed tertiary amine side groups with 1,3‐propanesultone and 4‐bromobutyric acid, respectively. Both sulfobetaine and carboxybetaine polyaspartamides have cationic and anionic charged groups on the same repeat unit, but they differ in negatively charged groups. The chemical structures of the synthesized polymers were confirmed by 1H NMR and FT‐IR spectroscopies. The zwitterionic property of polyaspartamides were characterized by zeta potential measurements using wide range of pH. The surface properties mainly anti‐protein adsorption abilities and hydrophilicity were tested by surface plasmon resonance analysis, fluorescence microscopy, and contact angle measurements. Importantly, sulfobetaine polyaspartamides demonstrated better both antifouling performance and ability to form more hydrophilic surfaces than carboxybetaine polyaspartamide. Two zwitterionic carboxybetaine and sulfobetaine nanogels were prepared by horseradish peroxidase‐mediated crosslinking in an inverse miniemulsion. Results from dynamic light scattering and transmission electron microscopy showed the formation of nanosized spherical particles. Additionally, sulfobetaine and carboxybetaine polyaspartamides had remarkable biocompatibilities, indicating their promise as non‐fouling materials for biomedical applications.