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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.

The continuous growth of industrial solid waste production has generated many environmental problems. We evaluated the potential of industrial solid waste as a substitute filler in asphalt mastic, with the aim of increasing the use of sustainable road construction materials. In this study, X-ray fluorescence spectroscopy (XRF) and scanning electron microscopy (SEM) were used to characterize the oxide composition and micromorphology of limestone (LS), red mud (RM), steel slag (SS), and ground granulated blast-furnace slag (GGBFS). Four asphalt mastics containing LS, RM, SS, and GGBFS with a filler-to-binder weight ratio of one were prepared. An evaluation of the rheology and wetting of the solid-waste-filler asphalt mastic was conducted using a frequency sweep, temperature sweep, linear amplitude sweep (LAS), multiple stress creep and recovery (MSCR), and surface free energy (SFE) methods. The results showed that SS increased the complex modulus, elastic component of the asphalt mastic and decreased the nonrecoverable creep compliance at stress levels of 0.1 and 3.2 kPa, which improved the rutting resistance of the asphalt mastic and reduced deformation under high-temperature conditions. The RM and GGBFS increased the fatigue performance of the asphalt mastic under strain loading, enhanced its fatigue life, and maintained good performance under long-term loading. The dispersive component of the SFE parameter of the solid-waste-filler asphalt mastic was larger than the polar component for the largest share of the surface energy composition. The SFE of the asphalt mastic prepared from the industrial solid-waste filler was reduced; however, the difference was insignificant compared to the limestone asphalt mastic. Solid-waste-filler asphalt mastic has performance characteristics, and its actual application can be based on different performance characteristics to select an appropriate solid-waste filler. The results of this study provide new technological solutions for solving the utilization rate of solid waste materials and sustainable road construction in the future.

The article presents the exploration of flax and hemp fibers' surface free energy depending on the chemical composition of the fiber, which is closely related to the plant variety and the method of extracting the fiber. For this purpose, tests of the surface free energy (SFE), evaluation of the percentage content of individual fiber components and FTIR analyses were conducted. The research was carried out with the use of fibrous materials prepared in three different ways: 1. To analyze the effect of subsequent stages of flax fibers refining process on chemical composition and SFE, 2. to explore the dependence of fiber SFE on hemp variety, the water-retting hemp fibers were used, 3. To evaluate the influence of the retting method of hemp fibers BIAŁOBRZESKIE variety on SFE, the fibers extracted with the use of dew and water retting were used as the research material. The study confirmed that the content of individual components in the fiber influenced its sorption capacity and therefore determined its hydrophilic properties. The values of Pearson's linear correlation coefficients determined in the statistical analysis proved that the surface free energy was strongly correlated with the content of individual components in the fibers. Understanding the wettability characteristics of bast fibers will allow modeling the properties of products made of these fibers and designing surface modification processes in order to obtain specific functionality of textile products, depending on their intended utilization.

In order to study the adhesion properties of fast-melting SBS-modified asphalt (SBS-T) at the interface with aggregates, the contact angles of three dosages of SBS-T asphalt with three liquids (distilled water, glycerol, and formamide) were determined by the sessile drop method based on surface free energy theory. The evaluation indexes such as cohesion, asphalt-aggregate adhesion, stripping work and energy ratio of the asphalt were analyzed and the adhesion properties of the asphalt-aggregate system were investigated with the help of micromechanical methods. The results indicate that SBS-T can improve the adhesion properties of the asphalt. Furthermore, as the dosage of the modifier increases, the cohesion work, adhesion work, and energy ratio of the SBS-T asphalt exhibit a similar rise. As the spalling work reduces and the adhesion between asphalt and aggregate improves, it is noteworthy that the SBS-T asphalt-aggregate system exhibits superior adhesion performance compared to the SBS-modified asphalt-aggregate system, despite the same dosage.

This paper presents the experimental results of a study investigating the impact of the machining fluid type, the variable factor, used in slide burnishing on 2D and 3D surface roughness; surface topography; Abbott-Firestone curve shape; microhardness; and SFE (surface free energy). In the experiment, pre-ground, ringed samples of C45 steel were used. The results showed an over eight-fold decrease in the value of the Ra (arithmetical mean deviation) parameter and over a five-fold decrease in the Rt (total height of profile) parameter in relation to their values after grinding. The parameters Rpk (reduced peak height), Rk (core roughness depth), and Rvk (reduced valley depth) were also reduced. The Abbott-Firestone curve after slide burnishing changed its angle of inclination (it was more flattened), and the material ratio Smr increased. The reduction in the Rpk and Rk parameters and increased material ratio will most likely contribute to restoring the functionality of these surfaces (increased resistance to abrasive wear). After slide burnishing, the maximum 25% increase in microhardness was obtained compared to the value after grinding, while the layer thickness was 20 μm. The surface energy of elements subjected to slide burnishing using various machining fluids slightly increased, or its value was close to that of the ground surface. The most favourable properties of the surface layer in terms of mating between two elements were obtained for a part that was slide-burnished with a mixture of oil + polymethyl methacrylate (PMM) + molybdenum disulphide (MoS 2 ).

Erosion and the stripping effect of moisture on asphalt mixtures is one of the main reasons for the shortened service life of asphalt pavements. The common mean of preventing asphalt pavements from being damaged by moisture is adding anti-stripping agents (ASAs) to asphalt mixtures. However, the effect regularity and mechanism of anti-stripping agents on the physicochemical properties of asphalt is not exactly defined. This study compared the physical properties of ASA-modified asphalt (AMAs) to determine the optimal dosage and investigated the rheological and adhesion properties. Based on the roller bottle method and water immersion method, the moisture susceptibility of AMAs with three particle sizes was investigated. The results showed that the modification of asphalt using anti-stripping agents was a physical modification. At the optimum dosage of anti-stripping agents (0.3%), the basic physical properties of AMA1 were the most desirable. ASA2 increased the resistance of asphalt for deformation at high temperature by 46%, and AMA3 had the best low-temperature performance. ASAs enhanced the dispersed and polar components in the asphalt binder, improving the adhesion energy of asphalt. AMA3 had the strongest adhesion to the aggregate, with an increase in adhesion work by 2.8 times and a 45% of increase in ER value. This was attributed to ASA3 containing with a large number of metal cations and polar functional groups. It was shown that ASAs provided the most improvement in the anti-stripping performance of asphalt mixtures with 9.5-13.2 mm particles. The amide ASA, phosphate ASA and aliphatic amine ASA improved the water damage resistance of asphalt by 65%, 45% and 78%, respectively. This study can help engineers realize the effects of different types of ASAs on the physicochemical properties of asphalt and select the most suitable type of ASAs according to the service requirements.

The use of ytterbium laser to obtain colored titanium surfaces is a suitable strategy to improve the aesthetic soft tissue results and reduce implant failures in oral rehabilitation. To investigate the relationship between novel laser-colored surfaces and peri-implant soft tissues, Human Gingival Fibroblasts (HGFs) were cultured onto 12 colored titanium grade 1 light fuchsia, dark fuchsia, light gold, and dark gold disks and their viability (MTT Assay), cytotoxicity (lactate dehydrogenase release), and collagen I secretion were compared to the machined surface used as control. Optical and electronic microscopies showed a HGF growth directly correlated to the roughness and wettability of the colored surfaces. A higher viability percentage on dark fuchsia (125%) light gold (122%), and dark gold (119%) samples with respect to the machined surface (100%) was recorded. All specimens showed a statistically significant reduction of LDH release compared to the machined surface. Additionally, a higher collagen type I secretion, responsible for an improved adhesion process, in light fuchsia (3.95 μg/mL) and dark gold (3.61 μg/mL) compared to the machined surface (3.59 μg) was recorded. The in vitro results confirmed the innovative physical titanium improvements due to laser treatment and represent interesting perspectives of innovation in order to ameliorate aesthetic dental implant performance and to obtain more predictable osteo and perio-osteointegration long term implant prognosis.

Starch-based materials seem to be an excellent alternative for conventional plastics used in various applications. Microfibralted cellulose can be used to improve the surface properties of starch-based materials. This study aims to analyze the surface properties of starch-microfibrillated cellulose materials. The surface properties of films were evaluated by ATR-FTIR, surface roughness, water wettability, and surface free energy. The surface homogeneity between corn starch and microfibrillated cellulose (MFC) fibers was confirmed by scanning electron microscopy (SEM) and atomic force microscopy (AFM). Microscopic analyses of the film surfaces confirm good compatibility of starch and MFC. The addition of MFC increased the surface roughness and polarity of developed starch/MFC materials. The surface roughness parameter has increased from 1.44 ± 0.59 to 2.32 ± 1.13 for pure starch-based materials and starch/MFC material with the highest MFC content. The WCA contact angle has decreased from 70.3 ± 2.4 to 39.1 ± 1.0°, while the surface free energy is 46.2 ± 3.4 to 66.2 ± 1.5 mJ·m -2 , respectively. The findings of this study present that surface structure starch/MFC films exhibit homogeneity, which would be helpful in the application of MFC/starch materials for biodegradable packaging purposes.

The use of modern materials in sports, in terms of chemical composition and surface texture, entails both progress in results and an increasing discrepancy in the technical parameters of the equipment used. This paper aims to demonstrate the differences between balls admitted to a league and world championships in composition, surface texture, and the influence of these parameters on the water polo game. This research compared two new balls produced by top companies producing sports accessories (Kap 7 and Mikasa). To obtain the goal, the measurement of the contact angle, analysis of the material using Fourier-transform infrared spectroscopy, and optical microscopic evaluation were used. The analysis of the surface free energy shows significant differences (Kap 7 32.16 mJ/m 2 , Mikasa 36.48 mJ/m 2 ). In the case of both balls, anisotropies of the structure of the furrows were observed, however, the Mikasa ball is slightly more homogeneous than the Kap 7 ball. The obtained results from the analysis of the contact angle, as well as the composition and real feedback from the players, indicated the need to standardize the material aspect of the regulations so that the sports results are repeatable every time.

The microbiological behavior of dental polymer materials is crucial to secure the clinical success of dental restorations. Here, the manufacturing process and the machining can play a decisive role. This study investigated the bacterial adhesion on dental polymers as a function of manufacturing techniques (additive/subtractive) and different polishing protocols. Specimens were made from polyaryletherketone (PEEK, PEKK, and AKP), resin-based CAD/CAM materials (composite and PMMA), and printed methacrylate (MA)-based materials. Surface roughness (R z ; R a ) was determined using a laser scanning microscope, and SFE/contact angles were measured using the sessile drop method. After salivary pellicle formation, in vitro biofilm formation was initiated by exposing the specimens to suspensions of Streptococcus mutans ( S. mutans ) and Streptococcus sanguinis ( S. sanguinis ). Adherent bacteria were quantified using a fluorometric assay. One-way ANOVA analysis found significant influences ( p < 0.001) for the individual parameters (treatment and material) and their combinations for both types of bacteria. Stronger polishing led to significantly ( p < 0.001) less adhesion of S. sanguinis (Pearson correlation PC = -0.240) and S. mutans (PC = -0.206). A highly significant ( p = 0.010, PC = 0.135) correlation between S. sanguinis adhesion and R z was identified. Post hoc analysis revealed significant higher bacterial adhesion for vertically printed MA specimens compared to horizontally printed specimens. Furthermore, significant higher adhesion of S. sanguinis on pressed PEEK was revealed comparing to the other manufacturing methods (milling, injection molding, and 3D printing). The milled PAEK samples showed similar bacterial adhesion. In general, the resin-based materials, composites, and PAEKs showed different bacterial adhesion. Fabrication methods were shown to play a critical role; the pressed PEEK showed the highest initial accumulations. Horizontal DLP fabrication reduced bacterial adhesion. Roughness < 10 µm or polishing appear to be essential for reducing bacterial adhesion.

Warm Mix Asphalt (WMA) technology can effectively reduce carbon emissions and energy consumption during road project construction. However, it may have a negative impact on the binding properties of asphalt mixtures. In order to effectively evaluate the adhesion performance of asphalt binders and aggregates under the combined influence of WMA and traditional polymer-modified asphalt, this paper provides a comprehensive evaluation at the micro and macro levels. The adhesion between three different modified asphalts (warm mix crumb rubber/ Styrene-Butadiene-Styrene (SBS) composite modified asphalt, warm mix crumb rubber asphalt, and warm mix SBS modified asphalt) and two different aggregates (limestone and granite) under both virgin and short-term aging conditions were analyzed. Regardless of the type of modified asphalt, the results showed that limestone aggregates have better adhesion properties with asphalt binders. In addition, the short-term thermal oxidation aging behavior is conducive to enhancing the asphalt-aggregate adhesion characteristics. Furthermore, WMA additives, crumb rubber, and SBS compound modification can improve the adhesion performance between asphalt and aggregate.

The article presents the effect of anodizing parameters of the EN AW-5251 aluminum alloy on the thickness and roughness of Al 2 O 3 layers as well as their wettability and tribological properties in a sliding combination with the T7W material. The input variables were the current density of 1, 2, 3 A/dm 2 and the electrolyte temperature of 283, 293, 303 K. The tribological tests were performed on the T-17 tester in reciprocating motion, in conditions of technically dry friction. The tests were carried out on a 15 km road with a constant average slip speed of 0.2 m/s and a constant unit pressure of 1 MPa. The measurement of the wettability of the layers was performed using the sitting drop method, determining the contact angles on the basis of which the surface free energy was calculated. The profilographometric measurements were made. The analysis of the test results showed that the anodizing parameters significantly affect the thickness of the Al 2 O 3 layers. The performed correlation analysis also showed a significant relationship between the roughness parameters and the wettability of the surface of the layers, which affects the ability to create and maintain a sliding film, which in turn translates into sliding resistance and wear of the T7W material. The analysis of friction and wear tests showed that the layer with hydrophobic properties produced at a current density of 1 A/dm 2 in an electrolyte at a temperature of 283 K is the most favorable for sliding associations with T7W material.

The utilization of waste rubber tires is of great value for environment protection and resource recovery, which can also improve the properties of matrix asphalt. The adhesion characteristics were evaluated for crumb rubber modified asphalt and limestone aggregate using the surface free energy (SFE) approach. Four types of matrix asphalt and four rubber contents were used to prepare the crumb rubber modified asphalt. The contact angle of matrix and crumb rubber modified asphalt was obtained, and the SFE indicators (dispersion, polar component, and compatibility rate-CR) were calculated. Moreover, the water stability tests were conducted using one matrix and rubber modified asphalt in order to investigate the relationship between SFE and water stability indicators. Results showed that the total SFE, dispersion component, adhesion work, and CR increased with the addition of crumb rubber, while the polar component and spalling work decreased. The types of asphalt had different influences on SFE indicators. The results from analysis of variation (ANOVA) indicated asphalt type and rubber content had significant influence on the adhesion work, spalling work and CR, and the influence of asphalt type was greater than that of rubber content. Additionally, the retained Marshall Stability and tensile strength ratio had better correlation with adhesion work and CR, but less with spalling work. The presented results demonstrated that the type of matrix asphalt played an important role in the adhesion characteristics for the crumb rubber modified asphalt.

New segmented poly(thiourethane-urethane)s (SPTURs) were synthesized by the reaction of 1,1'-methanediylbis (4-isocyanatocyclohexane) ( Desmodur W ® , HMDI) and poly(ε-caprolactone)diol (PCL) and (methanediyldibenzene-4,1-diyl)dimethanethiol as nonconventional polymer chain extender. FTIR spectroscopy was used for the structural analysis of obtained polymers. The molecular weight distribution was examined by GPC chromatography. Based on the measured contact angles, free surface energy parameters were calculated. Thermal properties of polymers were examined by DSC and TGA, while viscoelastic properties were measured by DMTA. The tensile, adhesive and optical properties were also investigated for the obtained polymers. It was shown that SPTURs were transparent or partially transparent solids with high molar masses up to 84,300 Da. These polymers showed a good resistance to hydrolysis during incubation in Optylite ® physiological saline over 8 weeks. Obtained polymers possessed a tensile strength of up to 43.26 MPa, hardness of up to 96.25/59.00 Sh A/D and adhesion to copper of 14.66 MPa. The surface properties of the obtained polymers show that all obtained SPTURs were hydrophilic (CAs for water between 64.07° and 73.12°) with calculated SFE up to 46.69 mN/m.

Surface free energy (SFE) of titanium surfaces plays a significant role in tissue engineering, as it affects the effectiveness and long-term stability of both active coatings and functionalization and the establishment of strong bonds to the newly growing bone. A new contact-mechanics methodology based on high-resolution non-destructive elastic contacting nanoindentation is applied here to study SFE of micro- and nano-structured titanium surfaces, right after their preparation and as a function of exposure to air. The effectiveness of different surface treatments in enhancing SFE is assessed. A time-dependent decay of SFE within a few hours is observed, with kinetics related to the sample preparation. The fast, non-destructive method adopted allowed for SFE measurements in very hydrophilic conditions, establishing a reliable comparison between surfaces with different properties.

Nowadays, a great attention is directed into development of innovative multifunctional composites which may support bone tissue regeneration. This may be achieved by combining collagen and hydroxyapatite showing bioactivity, osteoconductivity and osteoinductivity with such biocompatible polymers as polyvinylpyrrolidone (PVP) and poly(vinyl alcohol) (PVA). Here PVA/PVP-based composites modified with hydroxyapatite (HAp, 10 wt.%) and collagen (30 wt.%) were obtained via UV radiation while two types of collagen were used (fish and bovine) and crosslinking agents differing in the average molecular weight. Next, their chemical structure was characterized using Fourier transform infrared (FT-IR) spectroscopy, roughness of their surfaces was determined using a stylus contact profilometer while their wettability was evaluated by a sessile drop method followed by the measurements of their surface free energy. Subsequently, swelling properties of composites were verified in simulated physiological liquids as well as the behavior of composites in these liquids by pH measurements. It was proved that collagen-modified composites showed higher swelling ability (even 25% more) compared to unmodified ones, surface roughness, biocompatibility towards simulated physiological liquids and hydrophilicity (contact angles lower than 90°). Considering physicochemical properties of developed materials and a possibility of the preparation of their various shapes and sizes, it may be concluded that developed materials showed great application potential for biomedical use, e.g., as materials filling bone defects supporting their treatments and promoting bone tissue regeneration due to the presence of hydroxyapatite with osteoinductive and osteoconductive properties.

Our previous work has shown that for cardiac applications, combining low-temperature plasma oxidation with an amorphous carbon coating (a-C:N:H type) constitutes a prospective solution. In this study, a short-term modification by low-temperature oxygen plasma is proposed as an example and a method for shaping the topography and surface energy of the outer amorphous carbon coating, produced via the Radio-Frequency Chemical Vapour Deposition (RFCVD) method on NiTi alloy oxidized under glow-discharge conditions. This treatment alters the chemical composition of the outer zone of the surface layer. A slight increase is also noted in the surface roughness at the nanoscale. The contact angles were shown to increase by about 20% for water and 30% for diiodomethane, while the surface free energy decreased by ca. 11%. The obtained results indicate that even short-term contact with low-temperature plasma can shape the surface properties of the carbon coating, an outcome which shows potential in terms of its use in medical applications.

It was shown that carbon nonwoven fabrics obtained from polyacrylonitrile fibers (PAN) by thermal conversion may be modified on the surface in order to improve their biological compatibility and cellular response, which is particularly important in the regeneration of bone or cartilage tissue. Surface functionalization of carbon nonwovens containing C-C double bonds was carried out using in situ generated diazonium salts derived from aromatic amines containing both electron-acceptor and electron-donor substituents. It was shown that the modification method characteristic for materials containing aromatic structures may be successfully applied to the functionalization of carbon materials. The effectiveness of the surface modification of carbon nonwoven fabrics was confirmed by the FTIR method using an ATR device. The proposed approach allows the incorporation of various functional groups on the nonwovens' surface, which affects the morphology of fibers as well as their physicochemical properties (wettability). The introduction of a carboxyl group on the surface of nonwoven fabrics, in a reaction with 4-aminobenzoic acid, became a starting point for further modifications necessary for the attachment of RGD-type peptides facilitating cell adhesion to the surface of materials. The surface modification reduced the wettability ( θ ) of the carbon nonwoven by about 50%. The surface free energy (SFE) in the chemically modified and reference nonwovens remained similar, with the surface modification causing an increase in the polar component (ɣ p ). The modification of the fiber surface was heterogeneous in nature; however, it provided an attractive site of cell-materials interaction by contacting them to the fiber surface, which supports the adhesion process.

Starch films can be used as materials for food packaging purposes. The goal of this study is to compare how the starch origin influence the selected starch film properties. The films were made from various starches such as that from maize, potato, oat, rice, and tapioca using 50% w of glycerine as a plasticizer. The obtained starch-based films were made using the well-known casting method from a starch solution in water. The properties of the films that were evaluated were tensile strength, water vapour transition rate, moisture content, wettability, and their surface free energy. Surface free energy (SFE) and its polar and dispersive components were calculated using the Owens-Wendt-Rabel-Kaelbe approach. The values of SFE in the range of 51.64 to 70.81 mJ∙m -2 for the oat starch-based film and the maize starch-based film. The films revealed worse mechanical properties than those of conventional plastics for packaging purposes. The results indicated that the poorest tensile strength was exhibited by the starch-based films made from oat (0.36 MPa) and tapioca (0.78 MPa) and the greatest tensile strength (1.49 MPa) from potato.

Industrial waste from the production of metallic silicon and silicon-iron alloys, which includes silica fumes (microsilica), is subject to numerous applications aiming at its reuse in concrete and polymeric composites. Recycling solves the problem of their storage and adverse environmental impact. Six different formulas of epoxy resins were tested, differing in the type of polymer, the mixing process (sonication or not) and the presence of microsilica. The study showed that microsilica added to the epoxy resin changes its viscosity and free surface energy, and these are the parameters that determine the adhesion of the polymer to the concrete surface. Strength tests and SEM analysis have determined how microsilica molecules can penetrate the structure of polymer macromolecules by filling and forming temporary chemical bonds. Mixing the fillers with the adhesive was achieved by using a sonication process. The analysis of the obtained results showed that, depending on the initial composition of the polymer, the addition of microsilica can change the chemical, physical and mechanical properties of the hardened adhesive to varying degrees. In the case of adhesives used in the construction industry to strengthen and glue structural elements, these changes significantly affect the durability of the adhesive joints.

Poly(hydroxyurethane)s (PHU) are alternatives for conventional polyurethanes due to the use of bis-cyclic dicarbonates and diamines instead of harmful and toxic isocyanates. However, the surface properties of poly(hydroxyurethane)s are not well known. In this work, we focus on the analysis of the surface properties of poly(hydroxyurethane) coatings. Poly(hydroxyurethane)s were obtained by a catalyst-free method from commercially available carbonated diglycidyl ether of bisphenol A (Epidian 6 epoxy resins) and various diamines: ethylenediamine, trimethylenediamine, putrescine, hexamethylenediamine, 2,2,4(2,4,4)-trimethyl-1,6-hexanediamine, m -xylylenediamine, 1,8-diamino-3,6-dioxaoctane, 4,7,10-trioxa-1,13-tridecanediamine, and isophorone diamine, using a non-isocyanate route. The structures of the obtained polymers were confirmed by FT-IR, 1 H NMR and 13 C NMR spectroscopy, and thermogravimetric (TGA) and differential scanning calorimetry (DSC) analyses were performed. The rheological characteristic of the obtained polymers is presented. The static contact angles of water, diidomethane, and formamide, deposited on PHU coatings, were measured. From the measured contact angles, the surface free energy was calculated using two different approaches: Owens-Wendt and van Oss-Chaudhury-Good. Moreover, the wetting envelopes of PHU coatings were plotted, which enables the prediction of the wetting effect of various solvents. The results show that in the investigated coatings, a mainly dispersive interaction occurs.

In line with the current trend of seeking alternative methods for modification of the existing building composites, such as mineral-asphalt mixtures (MAMs), the materials from concrete and ceramics recycling are being used in increasingly wider applications. When added to MAMs as an aggregate, ceramic building material, which has different properties than the raw material (clay), may significantly influence the aggregate properties, including the wettability, porosity, asphalt adhesion, and consequently the mixture durability. The material's microstructure was found using SEM. The wetting properties of mineral-asphalt mixtures were determined by measuring the contact angles (CA) of their surfaces, using water as the measuring liquid. The total surface free energy (SFE) values were determined using the Neumann method. When analyzing the research results, it can be noticed that the chemical composition of the ceramic aggregate has a significant influence on the adhesion of asphalt to its surface due to the chemical affinity. Waste ceramic aggregate, despite its acidic pH value being connected with its elevated silica content, exhibits good adhesive properties.

Scaling commonly occurs at pipe wall during landfill leachate collection and transportation, which may give rise to pipe rupture, thus posing harm to public health and environment. To prevent scaling, this study prepared a low surface energy nanocomposite by incorporating silicone-acrylate polymer and hydrophobically modified nano-SiO 2 into the high-density polyethylene (HDPE) substrate. Through the characterization of contact angle, scanning electron microscopy and thermogravimetry, the results showed that the prepared composite has low wettability and surface free energy, excellent thermal stability and acid-base resistance. In addition, the prepared composite was compared with the commercial HDPE pipe material regarding their performance on anti-scaling by using an immersion test that places their samples into a simulated landfill leachate. It was apparent that the prepared composite shows better scaling resistance. The study further expects to provide insight into pipe materials design and manufacture, thus to improve landfill leachate collection and transportation.

The paper explores the possibility of covering the mortar with the lightweight aggregate by the nanopolymer silane and siloxane as surface hydrophobisation. The investigation involved the mortars with two types of hydrophobic agents diluted with water in a ratio of 1:4 and 1:8. Mortar wetting properties were determined by measuring the absorbability, water vapor diffusion, contact angle (CA) and surface free energy (SFE) of their structure. Surface micro-roughness and 2D topography were evaluated. Scanning electron microscopy (SEM) has shown the microstructure and distribution of pores in mortars. The reduction in absorbency after the first day of testing by 87% was shown. An improvement in frost resistance after 25 cycles by 97% and an 18-fold decrease in weight loss after the sulphate crystallization test were observed. The hydrophobic coating reduces the SFE of mortars and increases the CA. In the case of using silanes, a 9-fold increase CA was observed.

Measurements of forces during machining, especially thin-walled structures typical of the aviation industry, are important in the aspect of instability caused by vibration. One of the last stages of manufacturing by machining is the finishing treatment and deburring of the product's edges. Brushes with ceramic fibres are often employed in deburring, especially for large-sized elements specific to the aviation industry due to the possibility of automatic machining directly on machining centres. This study set out to analyse the effect of variable brushing conditions on axial forces and the selected surface layer properties of AW-7075 aluminium alloy. Experimental studies have examined factors such as surface roughness and topography, axial cutting force in ceramic brush treatment and surface free energy in the aspect of adhesive joints. The tested variable process parameters were the fibre material and the adjustment sleeve spring stiffness. Based on the tests, it was found that the axial force applied by the brush was more strongly connected with the spring stiffness rather than the type of bristle. For most cases, an increase in the value of free surface energy after brushing was observed compared to the initial machining which was milling., Competing Interests: The authors declare no conflict of interest.

The paper reports the results of a study on the Ti6Al4V titanium alloy involving the XPS (X-ray photoelectron spectroscopy) photoelectron spectroscopy method. The position of bands in the viewing spectrum serves as a basis for the qualitative identification of atoms forming the surface layer, while their intensity is used to calculate the aggregate concentration of these atoms in the analyzed layer. High-resolution spectra are used to determine the type of chemical bonds based on characteristic numerical values of the chemical shift. The paper also presents the 3D results of surface roughness measurements obtained from optical profiling, as well as the results of energy state measurements of the Ti6Al4V titanium alloy surface layer after ozone treatment. It was shown that the ozone treatment of the Ti6Al4V titanium alloy removes carbon and increases concentrations of Ti and V ions at higher oxidation states at the expense of metal atoms and lower valence ions. The modification of the surface layer in ozone atmosphere caused a 30% increase in the Ti element concentration in the surface layer compared to the samples prior to ozone treatment. The carbon removal rate from the Ti6Al4V titanium alloy samples amounted to 35%, and a 13% increase was noted in oxides. The tests proved that the value of the surface free energy of the Ti6Al4V titanium alloy increased as a result of ozone treatment. The highest increase in the surface free energy was observed for Variant 4 samples, and amounted to 17% compared to the untreated samples, while the lowest increase was equal to 14%. For the analyzed data, the maximum value of standard deviation was 0.99 [mJ/m 2 ].

Laser surface treatment of the titanium alloy was locally oxidized on the metal surface to improve the joint strength of laser transmission welding of high borosilicate glass with titanium alloy. The results find that the welding strength was increased 5 times. The welding mechanism was investigated by the morphology of the welded parts, the tensile-fracture failure mode, the diffusion of the interface elements, and the surface free energy. The results show that there are many adherents between the titanium alloy and high borosilicate glass after tensile fracture, the welding strength was higher when the laser voltage was 460 V, and the tensile⁻fracture failure mode is mainly ductile fracture. Element-line scanning analysis revealed that elemental diffusion occurred in the two materials, which is an important reason for the high welding strength. Surface free-energy analysis shows that laser surface treatment improves the surface free energy of titanium alloy, promotes the wettability and compatibility, and increases the welding strength of titanium alloy with glass.

To address the difficulty of joining polystyrene (PS) and titanium by laser transmission joining, two methods-laser treatment of the titanium surface and oxygen plasma treatment of the PS surface-are used to compare the laser transmission joint strengths of the different treatment methods. The results of the experiments find that joining with titanium can be achieved only when PS is treated with oxygen plasma. When the laser-treated surface of titanium is jointed to the oxygen plasma-treated PS, the joint strength is the highest, reaching 6.5 MPa. The joining mechanism of oxygen plasma-treated PS and laser oxidation-treated titanium was investigated by joint tensile failure mode, joint micromorphology observation, contact angle and surface free energy experiments, and X-ray photoelectron spectroscopy (XPS). The results show that the failure mode of the joint is an interfacial failure; the size and amount of bubbles play an important role in the joining strength, and the joints with fine and uniform bubbles have the highest joint strength. The two surface treatment methods can improve the surface energy of the joints, improve the compatibility between the two joining surfaces, and enhance the joint strength. Ti⁻C and Ti⁻O chemical bonds are formed at the joints, which are the main reason for the increase in joint strength.

We report the first results of functional properties of nitrogenized silver-permalloy thin films deposited on polyethylene terephthalic ester {PETE (C 10 H₈O₄) n } flexible substrates by magnetron sputtering. These new soft magnetic thin films have magnetization that is comparable to pure Ni 81 Fe 19 permalloy films. Two target compositions (Ni 76 Fe 19 Ag₅ and Ni 72 Fe 18 Ag 10 ) were used to study the effect of compositional variation and sputtering parameters, including nitrogen flow rate on the phase evolution and surface properties. Aggregate flow rate and total pressure of Ar+N₂ mixture was 60 sccm and 0.55 Pa, respectively. The distance between target and the substrate was kept at 100 mm, while using sputtering power from 100-130 W. Average film deposition rate was confirmed at around 2.05 nm/min for argon atmosphere and was reduced to 1.8 nm/min in reactive nitrogen atmosphere. X-ray diffraction, X-ray photoelectron spectroscopy, scanning electron microscopy, vibrating sample magnetometer, and contact angle measurements were used to characterize the functional properties. Nano sized character of films was confirmed by XRD and SEM. It is found that the grain size was reduced by the formation of nitride phase, which in turns enhanced the magnetization and lowers the coercivity. Magnetic field coupling efficiency limit was determined from 1.6-2 GHz frequency limit. The results of comparable magnetic performance, lowest magnetic loss, and highest surface free energy, confirming that 15 sccm nitrogen flow rate at 115 W is optimal for producing Ag-doped permalloy flexible thin films having excellent magnetic field coupling efficiency., Competing Interests: The authors declare no conflict of interest.

The objective of this study was to deposit thin films on PET polymer substrate and examine the functional properties systematically. Their properties have been studied as a function of the N₂-Ar flow rates, deposition time span and Cu doping. Iron nitride film deposited on both sides exhibits ferromagnetic phases, γ'-Fe₄N and ε-Fe₃N co-existed, shows negligible magnetic anisotropy. Other samples show the evolution of N-rich (FeN, Fe₂N) and N-poor (Fe 16 N₂, Fe₃N, Fe₄N) phases under different deposition time conditions. XPS analysis and free energy calculations confirmed that co-sputtered Fe-Cu thin films are more stable than layer deposited counterparts. From VSM results it is evident that the dominant phase, changes steadily from the ferromagnetic α-Fe (N) to the paramagnetic ξ-Fe₂N with the increase of nitrogen flow rates and the ordering of the nitrogen atoms. Binding energy increases steadily from 733 eV to 740 eV with the increasing thickness of thin films from 74 nm to 94 nm. It was observed that surface energy decreases as the contact angle of glycol increases and changes the thin film surface from polar to nonpolar. TEM images indicate that cubic γ'-Fe₄N and ε-Fe₃N nano particles oriented in preferred directions dispersed uniformly in the amorphous iron nitride matrix.