Properties Of Coatings Research Articles

3d Mapping Of Stiffness Evolution Of Hardening Concrete With Saps Using Elastic Wave Tomography

Phenomena occurring during the delicate phase of concrete curing can have a strong influence on the final mechanical properties. Therefore, monitoring the changes during hydration can provide meaningful information on the material properties. Lately, non-destructive techniques have received great attention for monitoring earlyage concrete. This paper aims to assess the ultrasonic velocity and stiffness development of hardening concrete during various curing stages using the Elastic Wave Tomography (EWT) technique. The monitoring of the curing process starts as soon as seven hours after casting and lasts up to seventy hours. A three-dimensional (3D) wave velocity map is created, and conventional concrete is compared to concrete containing SuperAbsorbent Polymers (SAPs), a novel admixture used for shrinkage mitigation by providing internal curing in the cementitious matrix. However, SAPs have been proven to reduce compressive strength when added to concrete, due to the increased porosity they induce. This porosity may also result in the reduction of the wave velocity. However, the internal curing provided by the SAPs can promote the formation of new hydration products in the matrix and thus (partly) compensate for the strength loss making the uniformity of the internal curing another important point of concern. EWT can provide global information on the homogeneity of the influence of the SAPs in the cementitious matrix as opposed to the wave velocity of a single wave path that is usually examined in practice. In addition, the determination of the early-age stiffness evolution can be connected to the final mechanical properties of the material. The dynamic Young’s Modulus is calculated and compared to the static Young’s modulus at 28 days. Predictions towards the static Young’s modulus are also made, showing good agreement.

Advancements in Biofiller-Reinforced PLA Composites for 3D Printing: A Review

Additive manufacturing is key in realizing highly complex and high-performance composite materials. Among all the various kinds of functionality that could be added to a composite component, continuous fiber-reinforced composites have been drawing much attention because of their attractive combination of properties. The comprehensive spectrum of knowledge that ranges from the basics concerned with structure, morphology, synthesis, physical, and chemical properties finally reaches to this analytical study of advanced composites. Most generally, such a composite is structured on a thermoplastic or thermoset polymer matrix that embeds the load-carrying reinforcing fibers; probably best known are carbon, glass, and aramid fibers. These composites, which involve fibers continuously reinforcing, have high strength relative to their weight. They are also anisotropic, meaning they have qualities that vary from one direction to another – something which might be customisable for specific load cases. They warp and shrink less during their life in an outside environment than conventionally made bioplastics due to a fact that short fibers can provide reinforcement to them. This 3-D printing object is manufactured by special additive manufacture technology during the manufacturing process after compounding and extruding the fiber-reinforced composite filament. The final properties of 3D printed parts could be tailorable through changing variables such a fiber type, fiber length, volume fraction, polymer matrix material, orientation of fibers, and printing process parameters. These continuous fiber-reinforced 3D printed composites could achieve tensile strengths up to one GPa, have stiffness values reaching even a rating of countless Gpa, and have ad thicknesses in the range from about 1.4–1.8 g/cm³. This finding could be applied in basically all major industries, from aerospace and the automotive industry to sports gear. Such conclusions from the analysis may be useful in the selection of appropriate materials and techniques while even guiding the development of new applications with respect to such advanced composite materials.

Effect of NaCl replacement by other salt mixtures on myofibrillar proteins: Underlining protein structure, gel formation, and chewing properties.

The protein structure, gel changes, and chewing properties of low-sodium myofibrillar protein (MP) prepared by compound chloride salts (KCl/MgCl2, KCl/CaCl2, and KCl/MgCl2/CaCl2) and different substitution degrees (10%, 25%, and 40%) at same ionic strength (0.6M) were investigated. The results revealed that the low-sodium MP gels containing CaCl2 manifested more liquid loss and less moisture content accompanied by obvious morphological shrinkage, while KCl/MgCl2 contributed to the gel juiciness. At high substitution degree of 40%, KCl/CaCl2 substitution rendered the gel with dense structure and highest strength, but worse water retention capacity. Using other compound chloride salts influenced the chewing efficiency, and CaCl2 substitution made the gel relatively hard to chew. The inhomogeneous structure accompanied by cluster blocks in KCl/CaCl2-substituted MP gel accelerated the overall fracture rate. During heating process, more proteins in CaCl2-substituted MP did not participate in gel formation, intervening the final gel properties. The chloride salt mixtures containing MgCl2, rather than CaCl2, avoided or alleviated the liquid loss and shrinkage of low-sodium MP gel within the substitution degree of 10%-40%, and substitution degree not exceeding 25% was more reasonable for the controlled qualities.

Impact of Carbon Source on Bacterial Cellulose Network Architecture and Prolonged Lidocaine Release

The biosynthesis of bacterial cellulose (BC) is significantly influenced by the type of carbon source available in the growth medium, which in turn dictates the material’s final properties. This study systematically investigates the effects of five carbon sources—raffinose (C18H32O16), sucrose (C12H22O11), glucose (C6H12O6), arabinose (C5H10O5), and glycerol (C3H8O3)—on BC production by Komagataeibacter hansenii. The varying molecular weights and structural characteristics of these carbon sources provide a framework for examining their influence on BC yield, fiber morphology, and network properties. BC production was monitored through daily measurements of optical density and pH levels in the fermentation media from day 1 to day 14, providing valuable insights into bacterial growth kinetics and cellulose synthesis rates. Scanning electron microscopy (SEM) was used to elucidate fibril diameter and pore size distribution. Wide-angle X-ray scattering (WAXS) provided a detailed assessment of crystallinity. Selected BC pellicles were further processed via freeze-drying to produce a foam-like material that maximally preserves the natural three-dimensional structure of BC, facilitating the incorporation and release of lidocaine hydrochloride (5%), a widely used local anesthetic. The lidocaine-loaded BC foams exhibited a sustained and controlled release profile over 14 days in simulated body fluid, highlighting the importance of the role of carbon source selection in shaping the BC network architecture and its impact on drug release profile. These results highlight the versatility and sustainability of BC as a platform for wound healing and drug delivery applications. The tunable properties of BC networks provide opportunities for optimizing therapeutic delivery and improving wound care outcomes, positioning BC as an effective material for enhanced wound management strategies.

Shrouding Gas Plasma Deposition Technique for Developing Low-Friction, Wear-Resistant WS2-Zn Thin Films on Unfilled PEEK: The Relationship Between Process and Coating Properties

In this study, tungsten disulfide–zinc (WS2-Zn) composite films were generated on polyether ether ketone (PEEK) disks by an atmospheric pressure plasma jet (APPJ) equipped with a shrouding attachment. The friction and wear properties of the WS2-Zn coatings were intensively investigated by using a rotational ball-on-disk setup under dry sliding and ambient room conditions. In order to gain more information about the lubrication mechanism, the coating areas as deposited and the worn areas (i.e., in the wear track) were analyzed with a scanning electron microscope (SEM) with regard to their chemical composition in depth by energy-dispersive X-ray spectroscopy (EDS). X-ray photoelectron spectroscopy (XPS) was conducted to obtain precise chemical information from the surface. The results indicated that WS2-Zn coatings significantly improved the tribological properties, exhibiting a coefficient of friction (COF) of <0.2. However, the tribological performance of the coatings is strongly dependent on the plasma process settings (i.e., plasma current, dwell time of the powder particles in the plasma jet), which were tuned to reduce the oxidation by-products of WS2 to a minimum. The COF values achieved of the dry lubricant films were significantly reduced in contrast to the uncoated PEEK by a factor of four.

Mechanical and high-temperature steam oxidation properties of Cr coatings deposited via high-power impulse magnetron sputtering

Applying protective coatings to Zr alloy cladding surfaces is one of the better methods to design fuel tolerant materials. In this study, the surface of a Zr-4 alloy was coated with Cr using high-power impulse magnetron sputtering. Furthermore, the mechanisms by which bias voltages affect the mechanical characteristics, resistance to high-temperature steam oxidation, and coating structure were elucidated. The coating exhibits a strong (200) weave structure with coarse grains at a bias voltage of -100 V. With increasing bias, the energy of deposited particles increases, grains continue to grow, (200) preferential growth orientation disappears, and the coating exhibits a (110) crystal orientation. The growth structure of the coating first shows a tendency to be dense and then loose. For the Cr coating with a (200) crystal orientation, a dense oxide layer is preferentially formed after oxidation, which can effectively block the internal diffusion of O. With increasing oxidation time, coarse Cr grains can effectively block the external diffusion of Zr. Furthermore, the Cr coating exhibiting a (110) crystal orientation was severely oxidized after oxidation, resulting in the formation of cracks at the film base; this accelerated the outward diffusion of Zr.

Exploring the Crystal Structure and Electronic Properties of γ-Al2O3: Machine Learning Drives Future Material Innovations.

For decades, researchers have struggled to determine the precise crystal structure of γ-Al2O3 due to its atomic-level disorder and the challenges associated with obtaining high-purity, high-crystallinity γ-Al2O3 in laboratory settings. This study investigates the crystal structure and electronic properties of γ-Al2O3 coatings under the influence of an external electric field, integrating machine learning with density functional theory (DFT). A potential 160-atom supercell structure was identified from over 600,000 γ-Al2O3 configurations and confirmed through high-resolution transmission electron microscopy and selected area electron diffraction. The findings indicate that γ-Al2O3 deviates from the conventional spinel structure, suggesting that octahedral vacancies can reduce the system's energy. Under an external electric field, the material's band structure and density of states (DOS) undergo significant changes: the bandgap narrows from 3.996 to 0 eV, resulting in metallic behavior, while the projected density of states (PDOS) exhibits peak broadening and splitting of oxygen atom PDOS below the Fermi level. These alterations elucidate the variations in the electrical conductivity of alumina coatings under an electric field. These findings clarify the mechanisms of γ-Al2O3's electronic property modulation and offer insights into its covalent and ionic mixed bonding as a wide-bandgap semiconductor. This discovery is essential for understanding dielectric breakdown in insulating materials.

MPFEM investigation on densification and mechanical structures during ferrous powder compaction

Metal powder compaction is a crucial process in powder metallurgy, significantly affecting the final properties of compacts. However, the quantitative characteristics of multi-scale mechanical structures and the microscopic densification behavior, taking into account the influence of friction conditions, remain unclear. This study utilises a two-dimensional multi-particle finite element method to analyse the ferrous powder compaction. The evolution of powder densification, powder deformation and multi-scale mechanical behaviour under different friction coefficient conditions are analyzed quantitatively and qualitatively. Results reveal that powder densification occurs in distinct stages, with lower friction coefficients promoting greater powder densification, as observed from relative density and coordination number. Additionally, as the axial strain increases, plastic strain gradually rises whilst roundness decreases. Higher friction coefficients are associated with higher equivalent plastic strain but lower powder roundness. The Von Mises stress exhibits different stages of increase with the increment of axial strain. Powders with lower friction coefficients exhibit lower levels of Von Mises stress. As axial strain increases, the number, length, strength and direction coefficient of force chains undergo different evolution processes. Force chains exhibit longer length, fewer numbers, lower strength and lower direction coefficients at lower friction coefficients.

The effect of multi-step cycles on the surface properties of Ni-TiO2 coatings produced by pulse current electrodeposition

ABSTRACT In this study, the Ni-TiO2 coatings were deposited on copper substrates by pulse plating. The effect of multi-step current cycles on the metallurgical properties of produced coatings was investigated. The results showed that the values of applied currents within the periods significantly affect the surface properties of all coatings. Using the negative current cycles, the surface morphologies completely changed from regular and compact to irregular, compared to the deposits that did not have a negative cycle in the coating process. Also, the surface roughness increased by 1.5 times in the best case. Applying the 8-step cycle increased the percentage of TiO2 content inside the Ni-TiO2 layer from 13.13 vol.% to 31.58%. The corrosion and wear analysis results showed that the coating applied by a 4-step cycle with a 90-second off time has the best properties. Therefore, the corrosion and wear properties were not necessarily directly related to the participation percentage of TiO2 particles. Compact morphology with high current efficiency, wide distribution of TiO2 particles (6.31 vol.%) with minimal agglomeration, low coating roughness (Ra = 0.32 µm), high hardness value (436 Vickers), and the participation of (111) plane in the preferred texture improved the corrosion and wear behaviour of the optimal coating.

Impact of molecular architecture and draw ratio on enhancement of targeted mechanical properties of machine direction oriented polyethylene films produced after blown film extrusion

Conventional multi-material multi-layer flexible packaging offers excellent properties. However, it has recycling challenges, necessitating a shift to mono-material multi-layer flexible packaging for example all-polyethylene (PE) packaging which can be tailored through various synthesis and processing methods for different layers. In this work, we study how the key molecular properties (number-average molecular weight ( Mn), weight-average molecular weight ( M w), molecular weight distribution (MWD), comonomer content (short chain branching)) and machine direction orientation (MDO) process draw ratio (MDX) influence the final morphology and mechanical properties of MDO-PE films which are intended as the outer layer of mono-material all-polyethylene multi-layer flexible packaging. Five PE grades and various blends were extruded and blown into films. Selected blown films were machine direction oriented to obtain the final MDO-PE films. Furthermore, one selected PE blown film was processed at different MDO process draw ratios while keeping other process parameters constant. From the molecular properties point of view, the higher molecular weight fractions provide a higher possibility for uniform stretching whereas lower molecular weight fractions provide a higher natural draw ratio and therefore higher modulus and stiffness enhancement. Further, the results show that increasing MDO process draw ratio leads to more fibrillation and increased crystallinity. Consequently, the tensile modulus and stiffness at the higher draw ratios increase as well and are comparable to conventionally used polymers in outer layers of multilayer flexible packaging. Thus, this work demonstrates that MDO-PE films with enhanced modulus can provide sufficient stiffness for the design of outer layer of mono-material multi-layer all-PE packaging which presents higher potential for mechanical recyclability.

Powder Compaction Characteristics and Modeling of Calendering Process for Powder-based Solvent-free Manufacturing of Electrodes for Lithium-ion Batteries

Abstract Powder-based solvent-free manufacturing of electrodes for Li-ion batteries represents an emerging and promising technology in electrode fabrication. This method involves a two-roll powder calendering process, where electrode powder materials are compressed onto a current collector to form electrodes with desired properties. The calendering or compaction of dry powders onto a current collector is a crucial step in solvent-free electrode manufacturing, significantly impacting the microstructures, mechanical properties, and electrochemical performance of the produced electrodes. In this paper, we investigate the compaction characteristics of electrode powders to gain insights into their behavior. A powder-on-current collector calendering model is developed based on Johanson's rolling theory of granular solids. This model enables us to infer the underlying calendering parameters essential for the solvent-free manufacturing of Li-ion batteries. To validate the model, we compare it with experimental calendering results, utilizing measured powder properties and roll design parameters as inputs. This approach offers a comprehensive understanding of the effects of roll geometries, particularly roll diameter, and various equipment design parameters on final electrode properties. Such insights have not been thoroughly explored in the emerging field of solvent-free battery electrode manufacturing, thereby contributing to advancements in this area.

Effects of Ultrasound on Reactive Crystallization and Particle Properties of an Aromatic Amine in Batch and Continuous modes

Ultrasound has shown its benefits in the manufacturing processes of many pharmaceuticals and fine chemicals. This study focused on the reactive crystallization system of an aromatic amine and explored the potential uses of ultrasound in both batch and continuous modes. In batch experiments, we studied the effects of different sonication conditions including power, duration, and starting point on final particle properties. Under ultrasound, the crystal form and crystal morphology remained well maintained. The results of particle size and size distribution suggested that ultrasound reduced the mean sizes by improving the nucleation process and breaking up large particles. Additionally, the presence of ultrasound in continuous experiments was capable of inducing nucleation and the crystal products collected had a suitable distribution. Integrating ultrasound into the beginning of the continuous crystallization process can be an alternative to the seeding technique. The increasing sonication power did not reduce the induction time substantially. This indicated that a rational sonication condition should balance the overall process efficiency and energy consumption. The findings from batch and continuous experiments indicate that ultrasound could intensify industrial crystallization of the aromatic amine. Incorporating energy-efficient ultrasound with the continuous process will potentially lead to increased production efficiency and a well-controlled product quality.

Corrosion Properties of the Composite Coatings Formed on PEO Pretreated AlMg3 Aluminum Alloy by Dip-Coating in Polyvinylidene Fluoride-Polytetrafluoroethylene Suspension.

This paper presents the results of an evaluation of corrosion properties of PEO pretreated AlMg3 aluminum alloy samples with polymer coatings obtained by dip-coating in a suspension of superdispersed polytetrafluoroethylene (SPTFE) in a solution of polyvinylidene fluoride (PVDF) in N-methyl-2-pyrrolidone at different PVDF:SPTFE ratios (1:1, 1:3, 1:5, and 1:10). The electrochemical tests showed that samples with a coating formed at a ratio of PVDF to SPTFE of 1:5 possessed the best corrosion properties. The corrosion current density of these samples was more than five orders of magnitude lower than this parameter for bare aluminum alloy. During the 40-day salt spray test (SST) for samples prepared in a suspension at a PVDF:SPTFE ratio of 1:1-1:5, the formation of any pittings or defects was not detected. The PVDF:SPTFE 1:5 sample demonstrated, as a result of the 40-day SST, an increase in corrosion current density of less than an order of magnitude. The evolution of the protective properties of the studied samples was assessed by a two-year field atmospheric corrosion test on the coast of the Sea of Japan. It was revealed that the samples with the PVDF:SPTFE 1:5 coating had electrochemical parameters that remained consistently high throughout the one year of exposure. After this period, the polymer layer was destroyed, which led to a deterioration in the protective characteristics of the coatings.

Application of Linear Mixed-Effects Model, Principal Component Analysis, and Clustering to Direct Energy Deposition Fabricated Parts Using FEM Simulation Data.

The purpose of this study is to investigate the effects of toolpath patterns, geometry types, and layering effects on the mechanical properties of parts manufactured by direct energy deposition (DED) additive manufacturing using data analysis and machine learning methods. A total of twelve case studies were conducted, involving four distinct geometries, each paired with three different toolpath patterns based on finite element method (FEM) simulations. These simulations focused on residual stresses, strains, and maximum principal stresses at various nodes. A comprehensive analysis was performed using a linear mixed-effects (LME) model, principal component analysis (PCA), and self-organizing map (SOM) clustering. The LME model quantified the contributions of geometry, toolpath, and layer number to mechanical properties, while PCA identified key variables with high variance. SOM clustering was used to classify the data, revealing patterns related to stress and strain distributions across different geometries and toolpaths. In conclusion, LME, PCA, and SOM offer valuable insights into the final mechanical properties of DED-fabricated parts.

Boosting Erosion‐Corrosion Resistance: Collaborative Ni–P Electroless Deposition on Poly‐Amino‐Alcohol@Functionalized GO Matrices

AbstractIn recent years, protective coatings have become crucial in graphene‐based chemical studies. This research investigates the anticorrosive properties of coatings created by co‐depositing carbon compounds. Electroless Ni−P‐PAA@F‐GO coatings were applied to stainless steel by adding various amounts of PAA@F‐GO particles to the Ni−P bath. The coated samples were analyzed using X‐ray diffraction and micro‐hardness tests, revealing a peak hardness of 764 HV at 30 mg/L PAA@F‐GO, compared to 521 HV for standard Ni−P coatings. Corrosion performance was evaluated in a 3 % sodium chloride solution, showing that despite a higher corrosion‐erosion rate. Although the coated samples exhibited a corrosion‐erosion rate 4.7 times higher than untreated samples, the mass loss was notably more pronounced in the untreated samples. The study found that adding PAA@F‐GO particles improved corrosion resistance and durability, with optimal results at a specific particle concentration. The enhanced performance is attributed to the increased roughness, impermeability, and hydrophobicity of the functionalized graphene oxide.

Tuning the Sensitivity of Photonic Sensors Toward Alkanes Through the Textural Properties of Hybrid Xerogel Coatings

AbstractThis work exemplifies how incorporating organosilane modifiers into silica matrices allows for tuning the optical response of reflection photonic sensors through customizing the textural properties of hybrid xerogel sensing films. Xerogels with propyl molar percentages 0, 5, and 10% are used to construct photonic probes (OFS0pTEOS, OFS5pTEOS and OFS10pTEOS, respectively) by dip‐coating upon optimizing film deposition parameters. The time response of these probes toward a battery of volatile organic compounds (VOCs) comprising species with different functionality, size‐shape, and polarity is systematically analyzed through ON/OFF experiments, revealing that a low propyl content makes the poor‐responding OFS0pTEOS film highly sensitive toward non‐aromatic, large molecules with low‐polar or non‐polar character in OFS5pTEOS. This sensor is particularly sensitive toward alkanes, with globular cyclohexane (cyHex) outperforming elongated n‐hexane. Variable‐temperature calibration curves obtained from step‐by‐step experiments and adsorption–desorption cycles corroborate these observations and allow hysteresis to be quantified. The response to cyHex closely follows VOC concentration changes with the most stable signal among analytes, leading to well‐defined curves with low‐to‐negligible hysteresis. The isosteric enthalpies of cyHex adsorption are obtained for both the bulk material and the sensor, demonstrating labile adsorbate‐adsorbent interactions ruling the sensor response and becoming more exothermic for larger VOC concentrations.

Experimental investigation on bond properties of nano-Al2O3 and hydroxypropyl methyl cellulose (HPMC) modified coated steel bar embedded in concrete

In this work, cementitious coatings incorporate nano-Al2O3 (NA) and HPMC were developed applying to the surface of steel bars to enhance bond behavior. A total of 81 pull-out specimens were prepared to evaluated bond properties of different coated steel bars embedded in ordinary performance concrete (OPC), high performance concrete (HPC) and ultra-high-performance concrete (UHPC). The mechanical properties of the cement-based coatings have also been examined. Test results show that flexural and compressive strengths of coating paste exhibited initially increasing and followed by decreasing as NA content increase. Synergistic effect of NA and HPMC results in cement-based coating exhibiting superior mechanical properties. Besides, coating microscopic morphology characterized by scanning electron microscope (SEM) technique revealed that fewer coating defects with NA and HPMC compounding. More importantly, the highest bond strength between coated steel bar and different types concretes was found at 1.0 % NA content in the coatings. Synergistic effect of 1.0 % NA and 0.12 % HPMC improved bond strength of coated steel bar embedded in OPC, HPC and UHPC. It can be obtained from bond-slip curve that, regardless of the HPMC addition to coatings, coated steel bar with 1.0 % NA content shows higher bond stiffness. With both NA and HPMC added, bond stiffness, bond toughness and bond ductility of coated steel bar are superior to those of the coating with NA alone. Moreover, as concrete strength increases, the bond strength, bond stiffness and bond toughness of coated steel bar also increase, respectively.

Atomic-scale insight on nanostructures and electrochemical properties of (NiCrCo)82Ti9Al9 high-entropy alloy coatings by density functional theory calculations

(NiCrCo)82Ti9Al9 high−entropy alloy was attached to act as coating material by combining of laser cladding and laser remelting. In this study, the electrochemical properties of obtained HEA coatings were comparatively investigated using an electrochemical workstation, and the corrosion mechanism was revealed by the density functional theory calculations. The results show that the laser cladded HEA coating is mainly consisted of face-centered and body-centered cubic structures, and the face-centered cubic structure of the laser cladded HEA coating is transferred to the amorphous structure by laser remelting, which provides the stronger anti−corrosion capability compared with the face-centered cubic structure of HEA coating.

Characterization of the Evolution with Temperature of the Structure and Properties of Geopolymer-Cordierite Composites

This work is part of a research project aimed at producing ceramic-like materials, without the need for an initial sintering, for potential applications in catalysis or filtration at temperatures up to 1000 °C. In that context, cordierite-derived materials were prepared from recycled cordierite powder (automotive industry waste) bonded with metakaolin-potassium silicate geopolymer. The principle is that these materials, prepared at temperatures below 100 °C, acquire their final properties during the high-temperature commissioning. The focus is on the influence of the K/Al ratio and cordierite fraction on the stability of the dimensions and porosity during heating at 1000 °C, and on the final Young’s modulus and coefficient of thermal expansion. Conventional and high-temperature XRD evidenced the absence of crystallization of the geopolymer binder and interaction with the cordierite filler during the heating stage when K/Al = 1 or 0.75. By contrast, crystallization of kalsilite and leucite, and diffusion of potassium ions in the structure of cordierite is evidenced for K/Al = 1.5 and 2.3. These differences strongly influence the shrinkage due to sintering and the final properties. It is shown that a K/Al ratio of 0.75 or 1 is favorable to the stability of the porosity, around 25 to 30%. Moreover, a low coefficient of thermal expansion of 4 to 4.5 × 10−6 K−1 and a Young’s modulus of 40 to 45 GPa is obtained.

Renewable Photo-Cross-Linkable Polyester-Based Biomaterials: Synthesis, Characterization, and Cytocompatibility Assessment.

The present work consist of the synthesis of photo-cross-linkable materials, based on unsaturated polyesters (UPs), synthesized from biobased monomers from renewable sources such as itaconic acid and 1,4-butanediol. The UPs were characterized to assess the influence of polycondensation reaction temperature and cross-linking time on their final properties. For this purpose, different UV irradiation exposure periods were tested. Homogeneous, uniform, and transparent films were obtained after 1, 3, and 5 min of UV exposure. These cross-linked films were then characterized. All materials presented high gel content, which was dependent on the reaction's temperature. The thermal behaviors of the UPs were shown to be similar. In vitro hydrolytic degradation tests showed that the materials can undergo degradation in phosphate-buffered saline (PBS) at pH 7.4 and 37 °C, ensuring their biodegradability over time. Finally, to assess the applicability of the polyesters as biomaterials, their cytocompatibility was determined by using human dermal fibroblasts.