Low Surface Free Energy Research Articles

Preparation of dental resin composites with anti-bacterial adhesion against Streptococcus mutans using fluorinated and silicon containing dimethacrylates

ObjectiveThe purpose of this study was to enhance the anti-bacterial adhesion effect against Streptococcus mutans (S. mutans) of fluorinated dimethacrylate (DF MA) based dental resin composites (DRCs) by using silicone dimethacrylate (SMA-MEO). MethodThe SMA-MEO was added into mixture of DFMA and tricyclo (5.2.1.0) decanedimethanol diacrylate (SR833s) (DFMA/SR833s = 50 wt./50 wt.) with mass ratios of 10 wt% and 20 wt% to form resin matrix both with fluorinated and silicon containing dimethacrylates, and then DRCs named DS+ 10 %SMA-MEO and DS+ 20 %SMA-MEO were prepared by mixing the resin matrix with silaned BaAlSiO2 filler particles at a mass ratio of 30 wt./70 wt. Double bond conversion, volumetric shrinkage and shrinkage stress, flexural strength and modulus, water sorption and solubility, contact angle and surface free energy, anti-bacterial adhesion effect against Streptococcus mutans (S. mutans), and cytotoxicity of prepared DRCs were investigated according to standard or referenced methods. Fluorinated dimethacrylate (DFMA) based DRC named DS and 2,2-bis[4-(2-hydroxy-3-methacryloy-loxypropyl)-phenyl]propane (Bis-GMA) based DRC named BT were used as controls. ResultsAdding SMA-MEO into DFMA based DRC could lead to higher double bond conversion (p < 0.05), higher hydrophobicity (p < 0.05), and lower surface free energy (p < 0.05). Only DS+ 10 %SMA-MEO had better anti-bacterial adhesion effect against S. mutans than DS (p < 0.05). The SMA-MEO had no influence on volumetric shrinkage, shrinkage stress, flexural modulus, water sorption and solubility of DRC (p > 0.05), but could reduce flexural strength of dry DRC (p < 0.05). After water immersion, SMA-MEO containing DRCs had comparable flexural strength as DS (p > 0.05). Compared with BT, DS and SMA-MEO containing DRCs had better or comparable physicochemical properties, and lower amount of adherent S. mutans. All of DRCs had comparable cytotoxicity (p > 0.05). SignificanceDRCs with both DFMA and SMA-MEO could have better anti-bacterial adhesion effect against S. mutans than DRC only with DFMA due to increased hydrophobicity and decreased Surface free energy, and the optimal mass fraction of SMA-MEO in DFMA based resin matrix was 10 wt%.

Investigation of Cr2SiC Ceramic MAX Phase Coated Metallic Bipolar Plates in Ex-situ Conditions for Proton Exchange Membrane Fuel Cells

Essential for compact and lightweight proton exchange membrane fuel cell (PEMFC) stacks, metallic bipolar plates (MBPs) suffer from durability and conductivity issues due to surface corrosion and passivation. This study conducts ex-situ characterization of Cr2SiC ceramic MAX phase coatings on stainless steel (SS) 316 L substrates to evaluate their suitability for MBP application. The investigation encompasses coating structure, surface morphology, corrosion resistance, surface wettability, in-plane electrical conductivity, and interfacial contact resistance. X-ray diffraction and X-ray photoelectron spectroscopy confirm the presence of Cr2SiC coatings on SS316L, while energy-dispersive X-ray spectroscopy verifies uniform coverage and elemental weight percentage. Corrosion resistance is evaluated using potentiostatic and potentiodynamic polarization tests, showing excellent resistance with low corrosion current density (Icorr) at both 25 °C (3.29E-03 μA/cm2) and 80 °C (4.32E-02 μA/cm2), meeting US Department of Energy (DOE) technical targets. Potentiodynamic polarization reveals large corrosion potential and small Icorr values at both temperatures, outperforming uncoated samples. Electrochemical impedance spectroscopy post-accelerated corrosion tests show high charge transfer resistance at 25 °C (3.68E+05 Ω cm2) and 80 °C (3.02E+05 Ω cm2), indicating stability in acidic environments. Surface wettability analysis indicates low water affinity with a large contact angle (75°) and low surface free energy (28.92 mJ/m2) for the coated samples as compared to the uncoated samples. Electrical conductivity meets DOE targets with an in-plane conductivity of 4.59E+05 S/m and interfacial contact resistance of 8.04 mΩcm2 after 5-h accelerated corrosion tests at 80 °C. These results suggest that Cr2SiC coated SS316L exhibits excellent corrosion resistance, surface wettability, and electrical characteristics, making them viable for PEMFC applications.

Surface properties and biofilm formation on resins for subtractively and additively manufactured fixed dental prostheses aged in artificial saliva: Effect of material type and surface finishing

Statement of problemAdditive manufacturing (AM) and subtractive manufacturing (SM) have been widely used for fabricating resin-based fixed dental prostheses. However, studies on the effects of material type (AM or SM resin) and surface finishing (polishing or glazing) on the surface properties and biofilm formation are lacking. PurposeThe purpose of this in vitro study was to investigate the effects of material type and surface finishing on the surface roughness, wettability, protein adsorption, and microbial adhesion of the AM and SM resins marketed for fixed restorations under artificial saliva-aged conditions. Material and methodsDisk-shaped specimens (∅10×2 mm) were fabricated using 3 types of resins: AM composite resin with fillers (AMC), AM resin without fillers (AMU), and SM composite resin with fillers (SMC). Each resin group was divided into 2 subgroups based on surface finishing: polished (P) and glazed (G). Therefore, 3 polished surface groups (AMCP, AMUP, and SMCP) and 3 glazed surface groups (AMCG, AMUG, and SMCG) were prepared. Specimens were then categorized according to aging condition in artificial saliva. Surface roughness (Ra and Sa), contact angle, surface free energy (SFE), protein adsorption, and microbial adhesion were measured. The data were analyzed using a nonparametric factorial analysis of variances and post hoc tests with Bonferroni correction (α=.05). ResultsWhen nonaged, significant interactions between material type and surface finishing were detected for Ra, contact angle, SFE, protein adsorption, and microbial adhesion (P≤.008). AMCP showed higher Ra and microbial adhesion than AMUP and SMCP, and higher contact angle and protein adsorption than SMCP (P<.001). AMCG had lower SFE than AMUG (P=.005) and higher bacterial adhesion than SMCG (P<.001). AMC had higher Sa than AMU and SMC (P≤.006). When aged, significant interactions between material type and surface finishing were detected for Ra, Sa, protein adsorption, and microbial adhesion (P≤.026). The contact angle and SFE were significantly affected only by the material type (P≤.001), as AMC exhibited higher wettability than SMC (P≤.004). AMCP had higher Ra and microbial adhesion than AMUP and SMCP (P≤.003). AMCP had higher Sa and protein adsorption than SMCP (P≤.004). AMCG showed lower Ra and higher protein adsorption than AMUG (P≤.001). ConclusionsBoth material type and surface finishing significantly affected surface properties and biofilm formation. AMCP exhibited higher surface roughness, protein adsorption, and microbial adhesion compared with SMCP. Glazing may reduce the differences in surface-biofilm interactions between AMC and SMC.

Innovative CuO-melanin hybrid nanoparticles and polytetrafluoroethylene for enhanced antifouling coatings

Based on current research, a highly effective, completely biocompatible, and eco-friendly antifouling method was developed. Sepia pharaonis was used to synthesize melanin nanoparticles from its ink. To improve the anti-biofouling characteristics, CuO nanoparticles were synthesized from Padina sp., and a CuO-melanin hybrid nanoparticle complex was created under reflux. The XRD spectrum of the hybrid nanoparticles revealed several prominent peaks, indicating the crystalline structure of the nanoparticles. An EDS analysis identified copper, carbon, and oxygen in the hybrid nanoparticles. According to FE-SEM analysis, CuO-melanin hybrid nanoparticles displayed spherical morphology, with sizes ranging from 15 nm to 55 nm. DLS analysis showed that the hydrodynamic diameter of CuO-melanin hybrid nanoparticles was 187.5 nm. The biological test showed that CuO-melanin nanoparticles had the highst effect on marine bacteria (Phaeobacter sp. (6.25 μg/mL), Alteromonas sp. (12.5 μg/mL)), and algae (Isochrysis galbana Parke) (99 %) after 48 h. The CuO-melanin (3 wt%) exhibited the lowest pseudo-barnacle adhesion strength at 0.021 MPa and the lowest surface free energy, measuring 14.22 mN/m. The field immersion study in a marine environment showed that among the panels tested, the one containing 3 wt% CuO-melanin hybrid nanoparticles with polytetrafluoroethylene yielded the most favorable and efficient outcome, since it led to the lowest measured weight of biofouling at 26.44 g. The findings of this study show that CuO-melanin hybrid nanoparticles combined with polytetrafluoroethylene exhibit highly promising characteristics, make them appealing for antifouling applications.

Fabrication of hydrophobic cellulosic paper via physical vapor deposition of alkenyl succinic anhydride.

While plant fibers are abundant and biodegradable natural polymers, their high hydrophilicity often limits their applicability. To broaden the applicability of plant fiber materials across diverse fields, the present study employed cellulosic paper as a substrate and alkenyl succinic anhydride (ASA) as a low surface free energy material to fabricate a series of hydrophobic cellulosic papers (ASAP, ASA-P@Si, ASA-P@Ca, and ASA-P@Ti) through surface coating and physical vapor deposition of ASA. The results demonstrated that, in comparison to uncoated cellulosic paper, the coated variants exhibited significantly improved hydrophobicity. Notably, ASA-P@Si demonstrated superior hydrophobic performance with a contact angle of 140.90° and a sizing degree of 7.2 s, thereby meeting the requirements for specific fine paper grades. In contrast to the traditional ASA internal sizing process, the method in this study necessitates only approximately one-tenth of the conventional ASA internal sizing agent to achieve or even exceed the hydrophobic properties of paper attainable with ASA inter sizing process. Furthermore, the mechanism through which hydrophobic properties are conferred to paper can be elucidated by its surface roughness and low surface free energy, distinguishing it from the traditional ASA internal sizing approach.

Highly Alternating Copolymer of [1.1.1]Propellane and Perfluoro Vinyl Ether: Forming a Hydrophobic and Oleophobic Surface with

Utilizing the unique properties of fluorine substitution is an effective strategy for constructing highly functional materials. Here, we synthesized a novel copolymer composed of [1.1.1]propellane and perfluoro(propyl vinyl ether) (PPVE), rich in alternating sequences. The spin-coated copolymer film was amorphous, and its surface exhibited an extremely low surface free energy (γ). The γ value was lower than that of polytetrafluoroethylene despite containing only 40 mol % PPVE units. This can be attributed to the cancellation of the C-F dipole moments by the entirely random orientation of the fluorine units.

Characterizing the surface compositions of supported bimetallic PtSn clusters: Effects of cluster-support interactions and surface adsorbates

PtSn bimetallic clusters on TiO2(110) and highly oriented pyrolytic graphite (HOPG) surfaces have been characterized by scanning tunneling microscopy, low energy ion scattering (LEIS), X-ray photoelectron spectroscopy, and temperature programmed desorption (TPD); density functional theory (DFT) calculations have also been performed to better understand adsorption of CO and D2 on the PtSn surfaces. On TiO2 at coverages of 2 ML of Pt and 2 ML of Sn, exclusively bimetallic clusters are formed for both orders of deposition because clusters of the first metal completely cover the surface such that all atoms of the second metal are incorporated into the existing clusters. In contrast, on HOPG, the high mobility and weak cluster-support interactions on HOPG result in much larger 2 ML monometallic clusters (∼30 Å high) that do not completely cover the surface, and deposition of the second metal produces larger clusters as well as smaller ones. Despite the difference in cluster morphologies for the different orders of deposition and supports, the LEIS experiments demonstrate that in all cases, the PtSn clusters are rich in Sn at the surface, as expected based on the lower surface free energy for Sn compared to Pt. Furthermore, the +0.2 eV shift in the Sn(3d5/2) binding energy observed on all surfaces in the presence of Pt is consistent with PtSn alloy formation. Deposition of 2 ML of Sn on TiO2 produces two-dimensional clusters with oxidation of Sn and reduction of titania at the cluster-support interface, but addition of Pt to the Sn clusters causes Sn to diffuse away from this interface, leaving Sn in the metallic state. TPD experiments on 2 ML Pt/TiO2 with increasing coverages of Sn show that the number of adsorption sites for D2 sharply decreases to nearly zero at 0.5 ML, while CO adsorption decreases to zero only at much higher Sn coverages of 2 ML. DFT studies for Sn modified Pt surfaces and bulk structures demonstrate that for CO adsorption at low Sn coverages (≤0.25 ML), the strong Pt-CO interactions induce diffusion of Pt to the cluster surface and the formation of a bulk Pt3Sn alloy, whereas D2 adsorption does not lead to interactions with the Pt surface that are strong enough to induce alloy formation. A single Sn adatom prevents D2 adsorption on four neighboring Pt atoms via site-blocking and the donation of electron density to Pt.

Eco-friendly covalently connected silicone hydrogel with negatively charged surface for marine anti-biofouling

In this study, a silicone hydrogel (Gel-TA-Si-x) with amphiphilic and negatively charged surfaces was prepared by combining low surface free energy silicone with highly hydrophilic hydrogel materials using the method of one-step solvent-free bulk polymerization. The hydrogel films exhibited good mechanical properties. This was primarily reflected in the high tensile strength (1 MPa) and elongation at break (358.1 %). Notably, the film exhibited increased hydrophobicity, higher water contact angle and gradual decline in water absorption rate as the mPDMS monomer dosage increased. Despite this, the surface free energy remained low at 22.1 mJ m−2, indicating effective fouling release capability (removal strength against pseudobarnacles was 0.16 MPa). In addition, the surface zeta potential of the hydrogel was as low as −86 mV (at pH = 10). Laboratory antifouling performance tests indicated that the surface negativity of the material enhanced its static antifouling performance and the hydrogel with a negatively charged surface exhibited high bacterial adhesion resistance of 93 % and good resistance to Chlorella adherence and biofilm inhibition. Favorable anti-fouling performance was observed after 180 d of marine field testing. Moreover, the covalent connection of silicone monomers with hydrogel monomers through copolymerization create a stable three-dimension crosslinking network, thereby improving the durability of materials in complex marine environments. This study provides a new idea for developing efficient and environmentally friendly silicone hydrogel antifouling materials.

Coniferous Bark as Filler for Polylactic Acid-Based Biocomposites.

This study explores the possibilities of utilisation of coniferous bark as a filler in wood-polymer composites (WPCs), its impact on properties such as the modulus of rupture (MOR), modulus of elasticity (MOE), thickness swelling (TS) and water absorption (WA) after 2 h and 24 h of immersion in water and the significance of this impact compared to other factors. Six variants of bark-polylactic acid (PLA) WPCs were manufactured, differentiated by their filler content and filler particle size. As a comparison, analogous composites filled with coniferous sawdust were also manufactured. Bark-filled composites were characterised by lower TS and WA after both 2 h and 24 h of immersion, as well as lower water contact angles and surface free energy. The bark filler decreased the composites' MORs and MOEs, while greater differences were noticed for variants filled with small particles. The type of filler was the second most important factor contributing to variance in this study, with the filler content being the most important one.

Molecular dynamics simulation of deposition of high waxy crude oil on different pipeline walls

ABSTRACT Wax deposition occurs in the process of waxy crude oil pipeline transportation, which seriously affects the normal operation of crude oil pipeline. At present, non-metallic pipes have been proved to be effective in delaying the occurrence of wax deposition. Therefore, based on the pipeline walls of 20 G steel, glass fiber reinforced plastic (FRP), and polyethylene (PE), the microscopic mechanism of wax deposition during the pipeline transportation of waxy crude oil was studied by molecular dynamics simulation. The simulation results show that the waxy crude oil clusters undergo diffusion, deposition, reverse diffusion processes, and finally a wax deposition layer is formed on the pipeline surface. On the pipe walls of different materials, the surface free energy affects the interface energy of the solid-liquid contact surface between the waxy crude oil and the pipe wall, which is the main factor for the low surface free energy pipe to have the anti-wax effect. At the same time, according to the analysis of the contact angle on different materials in the simulation results, the difference in pipeline materials can only delay the formation speed of the wax deposition layer and cannot completely prevent the occurrence of wax deposition..

Surface Modification of Feldspathic Ceramic Used for Minimally Invasive Restorations: Effect of Airborne Particle Type on the Surface Properties and Biaxial Flexural Strength.

This study aimed to evaluate the effect of airborne particle abrasion with different particles on the surface free energy, roughness, and biaxial flexural strength of a feldspathic ceramic by comparing it with hydrofluoric acid etching, the standard surface treatment, and polishing. Square-shaped feldspathic ceramic specimens (12 mm × 12 mm × 1.2 mm) were divided into subgroups as airborne particles abraded with alumina (AO3a, AO3b, AO25, AO50a, AO50b, AO90, AO110a, AO110b, AO120a, and AO120b), silica (SO50a, SO50b, SO100, and SO100/200), or nutshell granule (NS100/200), hydrofluoric acid etched, and polished (n = 12). Surface free energy (n = 5), roughness (n = 5), biaxial flexural strength (n = 12), and Weibull moduli (n = 12) were investigated. Data were evaluated with 1-way ANOVA and Tukey HSD tests, and possible correlations were investigated with Pearson's correlation (α = 0.05). SO100/200 mostly had lower surface free energy (p ≤ 0.011), and polishing and etching led to higher surface free energy than AO3a, AO3b, and AO120a (p ≤ 0.031). Polished, SO100, and SO50b specimens mostly had lower roughness and AO125 had the highest roughness (p ≤ 0.029). SO100/200 mostly had lower biaxial flexural strength (p ≤ 0.041), and etched specimens had higher biaxial flexural strength than AO120a, AO120b, and SO50b (p ≤ 0.043). AO3b had the highest (33.56) and AO120b had the lowest (11.8) Weibull modulus. There was a weak positive correlation between the surface free energy and the biaxial flexural strength (r = 0.267, p = 0.011). A larger particle size mostly resulted in higher roughness, which was also affected by the particle shape. Most of the test groups had similar biaxial flexural strength to that of the hydrofluoric acid-etched group. Therefore, for tested feldspathic ceramic, airborne particle abrasion with tested parameters may be a suitable alternative without causing any further damage.

A photocatalyst coupled amphiphobic membrane with enhanced antifouling and self-regenerating properties for oily aerosol filtration

Oily aerosols as the most adhesive particles in the air can cause irreversible fouling of filters. Amphiphobic surface of filters can to some extent reduce membrane fouling, but complex oil fouling will still adhere to the membrane surface, leading to a decrease in membrane separation performance over long-term use. Herein, a silicon carbide (SiC) membrane with amphiphobic properties and catalytic functions was developed to collaboratively combat pollution. Low surface free energy 1H,1H,2H,2H perfluorooctyltrichlorosilane (FOTS) monomer and TiO2 nanoparticles were individually applied to the SiC membrane. PDMS was utilized to protect the monomer from degradation by the catalyst. The membrane exhibits good anti-adhesion and photocatalysis performance for oily aerosols. The membrane exhibits excellent oily aerosol filtration efficiency (98.6 %) with a comparative low filtration resistance of 6.4 kPa, as well as a high capacity for regeneration. Under UV light, the membrane can degrade oily fouling to recover its amphiphobic property. After 5 cycles of filtration, it still maintains good repeatability for oily matter separation and degradation. This study offers a practical approach to designing a membrane that enables long-term and efficient cleaning of oily aerosols.

Synthesis, Characterization, and Structure–Property Investigations of Benzoxazine Resins with Low Surface Free Energy

Synthesis, Characterization, and Structure–Property Investigations of Benzoxazine Resins with Low Surface Free Energy

Hierarchical bio-inspired design and fabrication of all-dimensional superhydrophobic ultra-lightweight high-volume fly ash cement foams using novel ultrasonic-assisted siloxane-encapsulated pickering emulsions

Ultra-lightweight foamed cement (ULFC) exhibits super-high porosity and excellent thermal-insulation capabilities. However, the thermodynamic instability and high water-absorptivity of ULFC with high-volume fly ash have restricted its large-scale application. Superhydrophobic technology can significantly improve the substrates’ hydrophobicity, among which the nanocoating is a popular option but the water-repellent layer may be easily destroyed due to the mechanical damage. Therefore, the intrinsic superhydrophobization becomes a promising alternative to the coating scheme. Here, the internal superhydrophobic ULFC was formulated through introducing the ultrasonic-assisted siloxane-encapsulated Pickering emulsions, in which two Pickering structures containing n-dodecyltrimethoxysilane were stabilized by hydrophobic SiO2 and C–S–H nanoparticles, respectively. Compared with the SiO2 nanoparticles-stabilized dispersion, the droplets of C–S–H nanoparticles-stabilized Pickering emulsion were more stable and controlled-release in cement hydration environment. As such, the incorporation of the latter showed no negative impact on the setting times and static yield stress of the interstitial matrix, optimizing the homogeneity, mechanical strength and heat conductivity of ULFC. The combination of nanoscale foam stabilizer and Pickering emulsions could form the hierarchical waterproof structure with low surface free energy at the gas-solid interfaces, and the multiscale siloxane-grafted intertwined hydration products were responsible for the inner superhydrophobicity of ULFC. Therefore, under the water vapor-saturated environment, the water absorption of superhydrophobic samples showed only a slight increase as a function of time and the ULFC was still hydrophobic with a reduction of apparent water contact angle from 154.6° to 137.8°. From energy consumption analysis, the all-dimensional superhydrophobic ULFC had a potential application in heat-insulation building.

Formation of two-dimensional mixed monolayers of integrated-cellulose nanofibers and starch nanoparticles using cellulose acetate and soluble starch

In this study, mixed monolayers comprising starch and cellulose nanofibers are prepared on the water surface and effectively controlled their surface morphologies. Through the spreading of cellulose acetate on the water surface, we achieve the preparation of integrated films with the spontaneous formation of nanocellulose. It is confirmed that starch, which is insoluble in the spreading solvent, is solubilized through a soluble treatment and spreads into a monolayer on the water surface. Upon mixing the nanocellulose integrated layer and starch particle layer, the morphology changes based on the mixed ratio of these components. In the monolayer film of a 1:1 mixture of cellulose acetate and soluble starch, the morphology predominantly consists of fibers, with particulate aggregates incorporated here and there. Furthermore, when the ratio changes to 1:5, the mixed monolayer transforms into a single particle layer, while the mixed monolayer evolves into a fibrous integrated film at a ratio of 5:1. Meanwhile, from the evaluation of the surface pressure-area isotherms, it is predicted that both components constitute an ideal mesoscopic miscible system. In addition, in the subphase temperature dependence of the cellulose acetate:soluble starch = 1:1 mixed monolayer, fibers are promoted under low-temperature conditions, and substantial domains are formed under high-temperature conditions. Notably, the mixed film remains amorphous at all ratios and exhibits low surface free energy, simultaneously suggesting hydrophobic and oil-repellent properties.

Phosphate Esters: New Coating Materials for a Sustainable Release Paper.

AbstractPaper manufacturers have long used silicone as the coating agent for release liners. However, silicone‐based release paper is very difficult to recycle due to covalent bonds between silicone and fibers. The most suitable solution to overcome this problem is to use alternative coating materials with adequate release properties, provided that they can be easily repulped in typical paper recycling facilities. We proposed a coating agent composed of phosphate esters and dimethylacetamide in order to manufacture a recyclable and efficient release paper. Analyses carried out on coated sheets showed that phosphate esters allowed the formation of a surface with adequate release properties (low peeling force and surface free energy). In addition, the residual adhesion values obtained with phosphate esters confirmed that they are well anchored on the backing paper surface, thus limiting the mass transfer to the adhesive tape.

A Composite Superhydrophobic, Photothermal Coating by Modified Carbon Nanotubes and the Study of Its Anti‐Icing/Deicing Behavior

Linearly structured carbon nanotubes (CNTs) are intertwined to form complex micro‐ and nanoscale structural undulations, and the structural undulations of the coating are further enhanced using large‐size nano‐SiO2. It can be prepared by the composite superhydrophobic coating (S‐C coating) with contact angle of 165.3° and sliding angle of 1°. Small‐size nano‐SiO2 can doped into the 3D‐network structure formed by the CNTs and act as anchor points to fix the structure. This enhances the stability of the coating as well as the abrasion resistance. The coating exhibits good long‐term durability and the ability to face harsh service environments. Due to the presence of the air layer with low heat transfer rate on the coating surface, the S‐C coating demonstrates good anti‐icing properties compared to the uncoated tinplate. By the lower surface free energy and contact area with the ice layer of the coating, the coating also exhibits good deicing performance. The ice adhesion strength of the coating is only 11.5 kPa. The photothermal properties of CNTs and the ability of the micro‐ and nanostructure to reflect light enable the coating to exhibit excellent photothermal properties. This also accelerates the melting and shedding of the ice layer on the coating.

Block copolymers hybrid latex coatings with environment-friendly short-chain perfluoroalkyl: From sequence structure to surface properties

Block copolymers (BCs) of perfluorocarbons (PFCs) show a well-ordered phase separation morphology on the surface that is an ideal structure to fabricate low surface free energy (SFE) environment-friendly short-chained PFCs based coating materials. In this study, a series of block copolymers of 2-(perfluorobutyl) ethyl acrylate hybrid latex coating materials were synthesized via soap-free RAFT emulsion polymerization. The impact of copolymers sequence structure on the surface properties and surface micro-nano structure of hybrid latex films were investigated. The results revealed that the functional chain segments of short-chain perfluorinated were preferentially arranged in the outermost chain segments of the BCs, thereby leading to the stacking of trifluoromethyl (-CF3) groups on the hybrid latex film surfaces and the decrease of SFE. The SFE of BCs latex films were significantly reduced from 21.83 mN/m to 16.03 mN/m compared to that of the random copolymer. Additionally, the SFE of the hybrid latex film can be reduced to 15.32 mN/m under the action of the modified silica crosslinking. Ultimately, the hybrid latex films show excellent superhydrophobic and oleophobic properties on cotton fabrics with water and oil contact angles of 152.5° and 142.4°, respectively, reaching the level of commercial water and oil repellent finishing agents with six fluorocarbon atoms. This study of BCs hybrid latex coatings provides important insights into the mechanism of the sequence structure and surface properties of BCs and offers an environment-friendly superhydrophobic and oleophobic coating material.

Study on laser processing of medical polyether ether ketone surface texture and its improvement on service performance

Polyether ether ketone (PEEK) has excellent chemical stability, x-ray transmittance, and elastic modulus close to human cortical bone, which can effectively reduce the stress shielding effect. Therefore, PEEK can be used as a commonly used medical bone implant material to repair damaged bones. However, due to its low surface free energy, PEEK has a certain degree of biological inertness. Surface modification methods are urgently needed to improve this problem. Laser surface texturing is expected to improve the biological inertia of PEEK materials. In this study, an ultraviolet laser with a wavelength of 355 nm was used to construct textures on the surface of PEEK materials. By biomimetic design on the surface of PEEK materials, textures similar in depth and width to the surface topography of natural bones were processed. We explore the specific improvement of corrugated texture, single line texture, and orthogonal texture on PEEK material performance, aiming at improving the service performance of PEEK material and creating conditions for better service of PEEK material in vivo. Through the evaluation of PEEK surface contact angle, friction and wear properties, and biocompatibility, the research results show that laser surface texture treatment can improve many service properties of PEEK materials.

Robust multifunctional coatings with omniphobic and antistatic properties to repel liquids and solid particles

Multifunctional transparent surfaces, exhibiting omniphobic and antistatic properties to mitigate contamination with both liquids and dust, are reported. The intrinsic electrical conductivity of Laponite (Lap) nanoparticles is combined with the low surface free energy of the perfluoropolyether (PFPE) S10. Lap nanoparticles are functionalized by grafting the PFPE, yielding different S10/Lap ratios. At optimal coating, contact angle values of 114° and 67° are reached for water and hexadecane, respectively, as well as a sheet resistance on the order of 108 Ω/□. Additionally, an excellent ability to repel liquids and reduce the adhesion of dust particles is observed. The mechanical stability of coatings against abrasion is also demonstrated.