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20 pages, 8212 KiB  
Article
Extracted Spent Coffee Grounds as a Performance-Enhancing Additive for Poly(Lactic Acid) Biodegradable Nursery Bags in Agriculture
by Amonrut Waisarikit, Nattawut Suadaung, Benjawan Khantho, Bawan Hadad, Gareth M. Ross, Paul D. Topham, Sukunya Ross and Sararat Mahasaranon
Polymers 2025, 17(5), 561; https://doi.org/10.3390/polym17050561 - 20 Feb 2025
Abstract
This study introduces biodegradable nursery bags using poly(lactic acid) (PLA), a widely used biodegradable polymer, and spent coffee grounds (SCGs), a byproduct of the brewing process in the coffee industry. SCGs were oil-extracted to produce extracted spent coffee grounds (exSCGs), which were characterized [...] Read more.
This study introduces biodegradable nursery bags using poly(lactic acid) (PLA), a widely used biodegradable polymer, and spent coffee grounds (SCGs), a byproduct of the brewing process in the coffee industry. SCGs were oil-extracted to produce extracted spent coffee grounds (exSCGs), which were characterized by their physical properties, chemical functionality, and thermal behavior. The exSCGs were blended with PLA at loadings of 5, 10, and 15 wt%. Analysis showed that exSCGs retained 3–5 wt% residual coffee oil, exhibiting a lower surface area (1.1163 m2/g) compared to SCGs (1.5010 m2/g), along with a higher pore volume (1.148 × 10−3 cm3/g) and pore size (~410 nm). All PLA/exSCG bio-composite films displayed a light brown color, well-dispersed exSCG particles, and excellent UV light barrier properties, with transmittance reduced to 1–2%. The residual coffee oil acted as a plasticizer, reducing the glass transition temperature, melting temperature, and crystallinity with increasing exSCG content. Mechanical testing revealed enhanced flexibility compared to neat PLA. Soil burial tests showed increased biodegradability with higher exSCG content, supported by SEM analysis revealing cracks around exSCG particles. The PLA/exSCG blend containing 10 wt% exSCGs exhibited optimal performance, with a significant increase in melt flow index (from 4.22 to 8.17 g/10 min) and approximately double the melt strength of neat PLA, balancing processability and mechanical properties. This innovation provides a sustainable alternative to plastic nursery bags, addressing waste valorization and promoting eco-friendly material development for agricultural applications. Full article
(This article belongs to the Section Polymer Processing and Engineering)
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Figure 1
<p>Optical images of SCGs (<b>a1</b>) and exSCGs (<b>b1</b>). Surface morphology of SCGs (<b>a2</b>,<b>a3</b>) and exSCGs (<b>b2</b>,<b>b3</b>) via SEM imaging. Particle size distribution of SCGs (<b>c</b>) and exSCGs (<b>d</b>) screened through a 325-mesh sieve, and surface area (<b>e</b>).</p>
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<p>FTIR spectra (<b>a</b>) and TGA thermograms (<b>b</b>) of spent coffee grounds (SCGs), extracted spent coffee grounds (exSCGs), and coffee oil.</p>
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<p>MFI of neat PLA and PLA/exSCGs at various compositions of exSCGs (<b>a</b>). SEM images of PLA/SCGs (<b>b</b>) and PLA/exSCGs (<b>c</b>), highlighting the improvement in interfacial adhesion between PLA and exSCGs when compared to PLA and SCGs.</p>
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<p>Capillary rheology results for neat PLA and PLA/exSCG bio-composites; apparent viscosity versus shear rate (<b>a</b>), Shear stress versus shear rate (<b>b</b>), force versus hau-loff speed showing the melt strength (<b>c</b>) and melt strength with varying concentration of exSCGs (<b>d</b>).</p>
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<p>Color parameter of the film (<b>a</b>) and physical change of the films after soil burial test (<b>b</b>); film appearance by photography (<b>b1</b>), and surface morphology via SEM analysis with surface cracking highlighted by white arrows (<b>b2</b>), of neat PLA and PLA/exSCG bio-composite films before and after soil burial test.</p>
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<p>Transmission (%T) curve (<b>a</b>) and value (<b>b</b>) of the neat PLA and PLA/exSCG bio-composite films.</p>
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<p>Stress–strain curves (<b>a</b>) and tensile mechanical properties (<b>b</b>) of neat PLA and the PLA/exSCG bio-composite films.</p>
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<p>Thermal properties (<b>a</b>) and DSC thermograms of the first (<b>b</b>) and second heating runs (<b>c</b>) of neat PLA and PLA/exSCG bio-composite films.</p>
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<p>SEM images of neat PLA and bio-composite films during natural soil burial tests at 0 and 9 months (<b>a</b>), appearance of the nursery bag showing plant roots emerging from the degraded bag (<b>b-top</b>) and the nursery bags with different thickness and field test times (<b>b-bottom</b>), and tensile mechanical properties (<b>c</b>) of PLA/exSCG10% nursery bags of varying thicknesses after field tests.</p>
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17 pages, 7276 KiB  
Article
No More Purification: A Straightforward and Green Process for the Production of Melamine–Vanillylamine-Based Benzoxazine-Rich Resins for Access to Various Composite Materials
by Lisa Guinebaud, Huihui Qiao, Erwann Guenin, Adama Konate and Frederic Delbecq
J. Compos. Sci. 2025, 9(3), 92; https://doi.org/10.3390/jcs9030092 - 20 Feb 2025
Abstract
A rapid microwave-assisted process minimizing waste was set up to produce bio-based benzoxazine-like monomers produced from vanillylamine and melamine. Without excessive purification, different viscous liquid precursors had a remarkable ability to form four strong and transparent different solid cross-linked thermosets, displaying lower curing [...] Read more.
A rapid microwave-assisted process minimizing waste was set up to produce bio-based benzoxazine-like monomers produced from vanillylamine and melamine. Without excessive purification, different viscous liquid precursors had a remarkable ability to form four strong and transparent different solid cross-linked thermosets, displaying lower curing temperatures under 130 °C. The long and strong adhesive performance of the cured materials was observed using glass slides or aluminum surfaces and they could become a good alternative to adhesive epoxy resin for metal surfaces. At the higher temperatures, these solids could act as efficient flame-retardants proven by thermogravimetric measurements. The best candidates gave a limiting oxidation index value of 41.9. In order to improve the intrinsic surface hydrophobicity of the phenolic resins, slight amounts of silica and iron oxide nanoparticles were dispersed in the polymer matrix, and finally mechanical resistance was pointed out. The most promising of our melamine-based resin was loaded with aluminum pigment to furnish a silver-colored paste ready for being cured to afford a robust solid, which does not undergo contraction or deformation. Full article
(This article belongs to the Special Issue Feature Papers in Journal of Composites Science in 2024)
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<p>Photograph of cured samples. (<b>a</b>) From left to right: <b>MVP2</b>, <b>MVP1</b> and <b>AVP2</b> as transparent solids; (<b>b</b>) molded and cured <b>MVP2</b>; (<b>c</b>) molded and cured <b>MVP1</b> remaining attached on aluminum foil.</p>
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<p>FT-IR spectra of all cured PBZ resins: (<b>a</b>) <b>PBZ-AVP1</b>; (<b>b</b>) <b>PBZ-MVP1</b>; (<b>c</b>) <b>PBZ-AVP2</b>; (<b>d</b>) <b>PBZ-MVP2</b>.</p>
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<p>TGA traces of AVP1, AVP2, MVP1 and MVP2.</p>
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<p>XRD diffractograms from (<b>a</b>) AVP1; (<b>b</b>) MVP1; (<b>c</b>) AVP2; (<b>d</b>) MVP2. (<b>e</b>) Photograph of <b>AVP1</b> cured on glass side; (<b>f</b>) water contact angle tests for PBZ resins on glass slides: from left to the right, <b>MVP1</b>, <b>AVP2</b> and <b>MVP2</b>.</p>
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<p>XRD diffractograms of <b>MVP2</b> loaded with increasing ratios of SiO<sub>2</sub> NPs varying from 10 to 40 wt%.</p>
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<p>FE-SEM pictures of cured <b>MVP2</b> loaded with SiO<sub>2</sub> NPs at different concentrations: (<b>a</b>) 10 wt%; (<b>b</b>) 20 wt%; (<b>c</b>) 30 wt%; (<b>d</b>) 40 wt%. (The scale bars were set up at 40 μm).</p>
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<p>XRD diffractograms of <b>MVP2</b> originally loaded with Fe(OH)O NPs at different ratios.</p>
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<p>FE-SEM photographs of MVP2 loaded with dried iron (III) oxide NPs at different ratios: (<b>a</b>) 10 wt%; (<b>b</b>) 20 wt%; (<b>c</b>) 30 wt%; (<b>d</b>) 40 wt%. (The scale bar was set at 40 μm).</p>
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<p>(<b>a</b>) Picture of a ball made of MVP1 loaded with 40 wt% of aluminum pigment; (<b>b</b>) FE-SEM picture of cured Al-MVP1 (40 wt%) surface; (<b>c</b>) photograph of cured sample of <b>Al-MVP1</b> (40 wt%); (<b>d</b>) FT-IR spectrum of cured <b>Al-MVP1</b> (40 wt%).</p>
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<p>Benzoxazine monomer synthesis and their cationic ring-opening polymerization (ROP) mechanism often catalyzed in acidic conditions to afford PBZ [<a href="#B8-jcs-09-00092" class="html-bibr">8</a>].</p>
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<p>Synthetic pathway for the production of four target benzoxazine monomers from melamine and vanillylamine under microwave irradiation. The materials were isolated as viscous solutions containing the monomers as the main products.</p>
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23 pages, 4007 KiB  
Article
Ageing of Red Wine (cv. Negroamaro) in Mediterranean Areas: Impact of Different Barrels and Apulian Traditional Amphorae on Phenolic Indices, Volatile Composition and Sensory Analysis
by Ilaria Prezioso, Giuseppe Corcione, Chiara Digiorgio, Gabriele Fioschi and Vito Michele Paradiso
Foods 2025, 14(4), 650; https://doi.org/10.3390/foods14040650 - 14 Feb 2025
Abstract
This study investigated the impact of different ageing containers on the volatile composition and quality of Negroamaro wine, a key variety from Apulia, Italy. Seven vessel types were evaluated: traditional Apulian amphorae (ozza), five types of oak barrels (American oak, French oak, European [...] Read more.
This study investigated the impact of different ageing containers on the volatile composition and quality of Negroamaro wine, a key variety from Apulia, Italy. Seven vessel types were evaluated: traditional Apulian amphorae (ozza), five types of oak barrels (American oak, French oak, European oak, a French + European oak and a multi-wood mix) and glass bottles as the control. The impact of the vessels was evaluated after 6 months of ageing through the characterization of phenolic, volatile and sensory profiles. Amphorae allowed a specific evolution of the wine’s primary aromas, such as fruity and floral notes, while enhancing volatile compounds like furaneol, which contributed to caramel and red fruit nuances, and also 3-methyl-2,4-nonanedione, a key compound related to anise, plum and premature ageing, depending on its concentration. This container also demonstrated effectiveness in stabilizing anthocyanin–tannin complexes, supporting color stabilization. Oak barrels allowed different outcomes to be obtained in terms of color stabilization, volatile profile, aroma and astringency. French oak exhibited the highest phenolic and tannin levels, enhancing anthocyanin stabilization and color intensity. European oak followed closely, while American oak excelled in color stabilization, with tannins less reactive to polymers. Mixed wood barrels showed lower phenolic extraction and the best astringency evolution. Full article
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<p>Linear regressions of TT (total tannins) concentration (g L<sup>−1</sup>) and MCPT assay results (mg L<sup>−1</sup>).</p>
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<p>Principal component analysis based on OAVs of volatile compounds found in Negroamaro wines before ageing (T-0) and after ageing in different materials (glass, amphora, mixed, French oak, European oak, American oak, Fre-Eur oak).</p>
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<p>Heatmap with clusterization of the volatile compounds in Negroamaro wine aged in different wooden barrels. Abbreviations for volatile names: 2-m-1-propanol (2-methyl-1-propanol); PEA (phenylethyl alcohol); 3-MND (3-methyl-2,4-nonanedione); 2-AAP (2-aminoacetophenone); ethyl 3-hydroxybutyrate (et-3-OH-but); m-anthranilate (methyl anthranilate); TDN (1,1,5-trimethyl-1,2-dihydronaphthalene).</p>
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<p>Partial least squares discriminant analysis (PLS-DA) of the volatile compounds in Negroamaro wine aged in different wooden barrels. (<b>A</b>) Scores plot with 95% confidence regions. (<b>B</b>) Loading plot of the variables. Abbreviations for volatile names: 2-m-1-propanol (2-methyl-1-propanol); PEA (phenylethyl alcohol); 3-MND (3-methyl-2,4-nonanedione); 2-AAP (2-aminoacetophenone); ethyl 3-hydroxybutyrate (et-3-OH-but); m-anthranilate (methyl anthranilate); TDN (1,1,5-trimethyl-1,2-dihydronaphthalene).</p>
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<p>Partial least squares discriminant analysis (PLS-DA) of the volatile compounds in Negroamaro wine aged in different wooden barrels. (<b>A</b>) Most important variables in the model according to VIP score for component 1. (<b>B</b>) Most important variables in the model according to VIP score for component 2 (the colored boxes on the right indicate the relative concentrations of the corresponding metabolite in each group under study). Abbreviations for volatile names: 2-m-1-propanol (2-methyl-1-propanol); PEA (phenylethyl alcohol); 3-MND (3-methyl-2,4-nonanedione); 2-AAP (2-aminoacetophenone); ethyl 3-hydroxybutyrate (et-3-OH-but); m-anthranilate (methyl anthranilate); TDN (1,1,5-trimethyl-1,2-dihydronaphthalene).</p>
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<p>3-methyl-nonanedione concentration in samples aged in wood, glass and amphorae (<b>A</b>); 3-methyl-nonanedione concentration in samples aged in different types of barrels (<b>B</b>). Different letters mean significant differences at <span class="html-italic">p</span> &lt; 0.05. The red line indicates the concentration of the compound before ageing (T0).</p>
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<p>Furaneol concentrations (mean ± S.D.) in Negroamaro wine aged in different materials (glass, amphora, mixed, French oak, European oak, American oak, Fre–Eur oak). Different letters mean significant differences at <span class="html-italic">p</span> &lt; 0.05. The red line indicates the concentration of the compound before ageing (T0).</p>
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<p>β-damascenone concentrations (mean ± S.D.) in Negroamaro wine aged in different materials (glass, amphora, mixed, French oak, European oak, American oak, Fre-Eur oak). Different letters mean significant differences at <span class="html-italic">p</span> &lt; 0.05. The red line indicates the concentration of the compound before ageing (T0).</p>
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<p>TDN (1,1,5-trimethyl-1,2-dihydronaphthalene) concentrations (mean ± S.D.) in Negroamaro wine aged in different materials (glass, amphora, mixed, French oak, European oak, American oak, Fre-Eur oak). Different letters mean significant differences at <span class="html-italic">p</span> &lt; 0.05. The red line indicates the concentration of the compound before ageing (T0).</p>
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<p>Correspondence analysis of the aroma attributes of the Negroamaro wine before ageing (T-0) and after ageing in different materials (glass, amphora, mixed, French oak, European oak, American oak, Fre-Eur oak). (<b>A</b>) Original scale map; (<b>B</b>) map with the “enlarge the area near origin” function (3×). Red squares correspond to wines and blue bubbles correspond to taste attributes. Size of bubbles represents term frequency.</p>
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<p>Correspondence analysis of the taste attributes of the Negroamaro wine before ageing (T-0) and after ageing in different materials (glass, amphora, mixed, French oak, European oak, American oak, Fre-Eur oak). (<b>A</b>) Original scale map; (<b>B</b>) map with the “enlarge the area near origin” function (3×). Red squares correspond to wines and blue bubbles correspond to odor attributes. Size of bubbles represents term frequency.</p>
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22 pages, 6176 KiB  
Article
The Distribution of Microplastic Pollution and Ecological Risk Assessment of Jingpo Lake—The World’s Second Largest High-Mountain Barrier Lake
by Haitao Wang, Chen Zhao and Tangbin Huo
Biology 2025, 14(2), 201; https://doi.org/10.3390/biology14020201 - 14 Feb 2025
Abstract
To investigate the influence of factors such as tourism, agriculture, and population density on the presence of microplastic (MP) content in aquatic environments and their associated ecological risks, Jingpo Lake, a remote high-mountain lake situated away from urban areas, was selected as the [...] Read more.
To investigate the influence of factors such as tourism, agriculture, and population density on the presence of microplastic (MP) content in aquatic environments and their associated ecological risks, Jingpo Lake, a remote high-mountain lake situated away from urban areas, was selected as the research subject. This study examined the abundance, types, sizes, colors, and polymer compositions of MPs within the water body, fish, and sediments. By considering variables, including fishing practices, agricultural activities, population dynamics, and vegetation cover, an analysis was conducted to unravel the spatial and temporal distribution of MPs concerning human activities, ultimately leading to an assessment of the ecological risks posed by MP pollution. The findings revealed that the average abundance of MPs in the lake’s surface water was recorded as (304.8 ± 170.5) n/m3, while in the sediments, it averaged (162.0 ± 57.45) n/kg. Inside the digestive tracts of fish, the MP abundance was measured at 11.4 ± 5.4 n/ind. The contamination of MPs within the aquatic environment of Jingpo Lake was found to be relatively minimal. Variations in MP loads across time and space were observed, with MPs predominantly falling within the size range of small planktonic organisms (50–1000 μm). Additionally, the prevalent colors of MPs in the water samples were white or transparent, constituting approximately 55.65% of the entire MP composition. Subsequently, they were black, red, and blue. This colors distribution were consistent across MPs extracted from fish and sediment samples. The chemical compositions of the MPs predominantly comprised PE (31.83%) and PS (25.48%), followed by PP (17.56%), PA (11.84%), PET (6.71%), EVA (4.56%), and PC (2.03%). Regarding the seasonal aspect, MP concentrations were highest during summer (46.68%), followed by spring (36.75%) and autumn (16.56%). The spatial distribution of MPs within Jingpo Lake’s water body, fish, and sediments was notably influenced by human activities, as confirmed by Pearson correlation coefficients. A strong association was observed between MP levels and water quality indicators such as ammonium nitrogen (NH4-N), total phosphorus (TP), and chlorophyll-a (Chla), suggesting that human-related pollution contributed significantly to MP contamination. The diversity assessment of MP pollutants exhibited the highest variability in chemical composition (1.23 to 1.79) using the Shannon–Wiener Index. Subsequently, the diversity of colors ranged from 0.59 to 1.54, shape diversity from 0.78 to 1.30, seasonal diversity from 0.83 to 1.10, and size diversity from 0.44 to 1.01. The assessment results of ecological risk highlighted that the risk categories for MPs within the surface water, fish, and sediments of Jingpo Lake were categorized as I for the PHI and PLI and as “Minor” for the PERI. These relatively low-risk values were attributed to the predominantly low toxicity of the distributed MPs within the Jingpo Lake basin. Moreover, the results of the risk assessment were found to be interconnected with the distribution of the local population and agricultural activities around the sampling sections. Usage patterns of coastal land and population density were recognized as influential factors affecting MP loads within the water body, sediments, fish, and other components of the lake ecosystem. Full article
(This article belongs to the Special Issue Global Fisheries Resources, Fisheries, and Carbon-Sink Fisheries)
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<p>Sampling sections in the Jingpo Lake reservoir. S1–S4 locations are close to settlements including densely populated areas, tourist ports, hotels, and related reception infrastructure, while S2, S3, S10, S11, and S12 are closer to farmland, and other sampling sections are areas with less human activity.</p>
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<p>Profile images of typical MPs and occurrence characteristics of MPs in different sampling sections. (<b>A</b>): Fragment(PS); (<b>B</b>): Film(PVC); (<b>C</b>): Fiber(PVC); (<b>D</b>): Microsphere(PS). The outline of microplastic properties is surrounded by yellow lines.</p>
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<p>MP types and temporal–spatial distribution in Jingpo Lake. S1W–S12W: MPs in water; S1S–S12S: MPs in sediments; S1F–S12F: MPs in fish digestive tracts.</p>
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<p>Factors affecting MPs in Jingpo Lake. (<b>a</b>): Correlation between MP content and other environmental physicochemical factors, MPs W−MP content in water, MPs S−MP content in sediments, MPs F−MP content in fish digestive tracts; (<b>b</b>): relationship between MP content and population density; (<b>c</b>): relationship between MP content and land use; (<b>d</b>): relationship between MP content and vegetation type.</p>
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<p>Diversity of MP pollution in Jingpo Lake. S1W–S12W: MPs in water; S1S–S12S: MPs in sediments; S1F–S12F: MPs in fish digestive tracts.</p>
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<p>Risk assessment of MPs in Jingpo Lake. S1W–S12W—MPs in water; S1S–S12S—MPs in sediment; S1F–S12F—MPs in fish digestive tracts.</p>
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19 pages, 3794 KiB  
Article
Generalized Solvent Effect on the Fluorescence Performance of Spiropyran for Advanced Quick Response Code Dynamic Anti-Counterfeiting Sensing
by Junji Xuan, Lingjie Chen and Jintao Tian
Int. J. Mol. Sci. 2025, 26(4), 1531; https://doi.org/10.3390/ijms26041531 - 12 Feb 2025
Abstract
Spiropyran has an attractive and mysterious fluorescence switch and dual-color conversion characteristics, as it exhibits both aggregation-caused quenching (ACQ) in solvents and fluorescence enhancement in polymer matrices. The explanation for this phenomenon has always been of great controversy. Hence, the solvent effect on [...] Read more.
Spiropyran has an attractive and mysterious fluorescence switch and dual-color conversion characteristics, as it exhibits both aggregation-caused quenching (ACQ) in solvents and fluorescence enhancement in polymer matrices. The explanation for this phenomenon has always been of great controversy. Hence, the solvent effect on the emission of spiropyran (SP) was investigated in 16 solvents. By means of molecular orbital theory and the Jablonski diagram, several special parameters (e.g., Hansen solubility parameters and viscosity) were selected for this analysis, with excellent goodness of fit. Subsequently, the main factors that affected the blue shift, red shift, and luminescence efficiency of the emission of the ring-opened form merocyanine (MC) were found to be the hydrogen bonding and polarity, aggregation effect, and viscosity, respectively. A newly modified Jablonski diagram was proposed to clarify the emission behaviors of spiropyran influenced by solvent polarity and isomerization. Meanwhile, the solvent effect could also be extended to a solid polymer matrix (six kinds of polyethylene glycol (PEG) with different molecular weights), which is proposed to be defined as the generalized solvent effect. Accordingly, we have demonstrated that the unique fluorescence properties of spiropyran are dominated by the generalized solvent effect. The security information storage capacity of the simulated quick response (QR) code sensor combined with SP for anti-counterfeiting was significantly improved to six dimensions in taking advantage of the former theoretical analysis. Full article
(This article belongs to the Special Issue Recent Advances in Luminescence: From Mechanisms to Applications)
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Graphical abstract

Graphical abstract
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<p>The spectral properties of <b>SP</b> (7.5 × 10<sup>−5</sup> mol/L) in methanol: (<b>a</b>) absorption spectra (10 min Vis irradiation for <b>SP</b>, and 10 min UV irradiation for <b>MC</b>, the inserts were actual photographs of the experimental samples); (<b>b</b>) emission spectra (ibid); (<b>c</b>) coloration and discoloration processes (the inserts, from left to right, display the actual experimental sample photographs of the coloring process at 0, 2, 4, and 6 min, and the discoloring process at 0.5, 1, 2, 4, 6, 8, 10, and 12 min, respectively); (<b>d</b>) recyclability, the sample was repeatedly treated with 10 min Vis or UV.</p>
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<p>Changes in the emission peak intensity and λ<sub>max</sub> along with the <b>SP</b> concentrations in methanol after 10 min irradiation using a 365 nm UV lamp. The inserted photographs refer to their corresponding Tyndall effect. The original spectral data can be found in <a href="#app1-ijms-26-01531" class="html-app">Figure S3</a>.</p>
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<p>The normalized absorption (<b>a</b>) and fluorescence emission spectra (<b>b</b>) of <b>SP</b> (7.5 × 10<sup>−5</sup> mol/L) and their corresponding photographs in 16 solvents after 10 min UV irradiation. The same number refers to the same solvent. MIN and MAX in (<b>b</b>) refer to the spectra of glycerol and hexane with the minimum and maximum λ<sub>max</sub> values of all solvents, respectively. The original spectral data of (<b>a</b>,<b>b</b>) can be found in <a href="#app1-ijms-26-01531" class="html-app">Figure S4a and S4b</a>, respectively.</p>
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<p>The relationships between λ<sub>max</sub> of the emission band of <b>MC</b> in 16 solvents and different parameters: (<b>a</b>,<b>b</b>) polar force <span class="html-italic">δ</span><sub>P</sub>; (<b>c</b>) hydrogen bonding <span class="html-italic">δ</span><sub>H</sub>; (<b>d</b>) Hansen solubility parameter <span class="html-italic">δ</span><sub>T</sub>; (<b>e</b>,<b>f</b>) a revised parameter <span class="html-italic">δ</span><sub>R</sub> derived from <span class="html-italic">δ</span><sub>T</sub>, the fittings through <span class="html-italic">δ</span><sub>T</sub> were obtained in using statistical method (<b>e</b>) and standard deviation method (<b>f</b>), respectively. The original spectral data used for analyses and fittings can be found in <a href="#app1-ijms-26-01531" class="html-app">Figure S5</a>. Parameters and λ<sub>max</sub> values in different solvents used above and in <a href="#app1-ijms-26-01531" class="html-app">Figure S5 are listed in Table S1</a>.</p>
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<p>The relationships between <span class="html-italic">K</span> of <b>MC</b> in 16 solvents and different parameters: (<b>a</b>) Hansen solubility parameter <span class="html-italic">δ</span><sub>T</sub>; (<b>b</b>) solvent viscosity; (<b>c</b>) square root of the solvent viscosity. <span class="html-italic">A</span>, <span class="html-italic">F</span>, <span class="html-italic">K</span>, <span class="html-italic">δ</span><sub>T</sub>, and viscosity values in different solvents used above are listed in <a href="#app1-ijms-26-01531" class="html-app">Table S2</a>.</p>
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<p>The relationships (<b>a</b>,<b>c</b>) between λ<sub>max</sub> of the emission band of <b>MC</b> (c<sub>SP</sub> = 10<sup>−7</sup> mol/g) in PEG ((<b>a</b>) solidified state, (<b>c</b>) seven d after curing) with different molecular weights (Mn = 2000, 4000, 6000, 8000, 10,000, 20,000) and square root of OHV. (<b>b</b>,<b>d</b>) represent the relationship between λ<sub>max</sub> from (<b>a</b>,<b>c</b>) and all its corresponding fluorescence intensities, respectively. The original spectral data of (<b>a</b>,<b>b</b>) and (<b>c</b>,<b>d</b>) can be found in <a href="#app1-ijms-26-01531" class="html-app">Figures S8 and S9</a>, respectively. OHV values of PEG with different molecular weights used above are listed in <a href="#app1-ijms-26-01531" class="html-app">Table S3</a>.</p>
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<p>Photobleaching of <b>MC</b> (c<sub>SP</sub> = 10<sup>−7</sup> mol/g) in PEG with different molecular weights (Mn = 2000, 4000, 6000, 8000, 10,000, 20,000). The curves were obtained from <a href="#app1-ijms-26-01531" class="html-app">Figure S8a′–f′</a>.</p>
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<p>QR code-sensing application. All QR code sensors are simulated based on the color changes in the 2 × 2 polymer square grid under different stimulations. Without UV irradiation (middle), the non-fluorescent 2 × 2 polymer square grid can produce weak reversible color changes with dark background and light foreground in visible light (middle left, state 1) or dark (middle right, state 2). With UV irradiation (left and right, state 3), the state of the square grid could be reversed with presentation of the dark foreground and light background both in its emission (left) and coloration (right). Meanwhile, the process is also reversible. Three states exist, along with one contrast change and four kinds of color changes.</p>
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<p>Photoisomerization process between the two isomers of <b>SP</b>. The synthesis and characterization of <b>SP</b> are shown in <a href="#app1-ijms-26-01531" class="html-app">Scheme S1, Figures S1 and S2</a>.</p>
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<p>The influence of solvent polarity on the orbital energy of π–π* and n–π* electron transition corresponding to the characteristic molecular structure of <b>SP</b>, <b>MC</b><sub>α</sub>, and <b>MC</b><sub>β</sub>.</p>
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<p>A simplified Jablonski diagram with consideration of the solvent polarity and isomerization of <b>SP</b>. The <b>SP</b><sub>1</sub>*/<b>SP</b><sub>2</sub>* and <b>MC</b><sub>1</sub>*/<b>MC</b><sub>2</sub>* refer to the excited state of the round states <b>SP</b><sub>1</sub>/<b>SP</b><sub>2</sub> and <b>MC</b><sub>1</sub>/<b>MC</b><sub>2</sub> stimulated by UV, respectively. Different solid and dashed arrows denote different processes: (1) absorption (e.g., 365 nm UV); (2) photoisomerization, <b>SP</b>* → <b>MC</b>; (3) vibrational relaxation; (4) fluorescence (radiative transition); (5) external conversion (non-radiative de-excitation); (6) solvent-induced isomerization (non-radiative de-excitation), <b>MC</b>* → <b>SP</b>.</p>
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21 pages, 2477 KiB  
Article
Optical Behavior of Clear Thermoplastic Dental Materials in a Simulated Oral Environment
by Liliana Porojan, Flavia Roxana Bejan, Roxana Diana Vasiliu and Anamaria Matichescu
Polymers 2025, 17(4), 472; https://doi.org/10.3390/polym17040472 - 11 Feb 2025
Abstract
(1) Background: The intra-oral behavior of clear thermoplastic dental materials can be influenced by various intrinsic and extrinsic factors. Aim: The purpose of this in vitro study was to evaluate the optical properties, color changes and whiteness variations of four thermoplastic polymers used [...] Read more.
(1) Background: The intra-oral behavior of clear thermoplastic dental materials can be influenced by various intrinsic and extrinsic factors. Aim: The purpose of this in vitro study was to evaluate the optical properties, color changes and whiteness variations of four thermoplastic polymers used for dental appliances, in a simulated oral environment. (2) Methods: Customized thermoformed specimens of four PETG thermoplastics were selected and investigated in this study: Leone [L], Duran [D], Erkodur [E] and Crystal [C]. The thermoplastic samples were divided into three groups related to pH values (neutral, acidic and basic). A period of 14 days was simulated. Five stages resulted: I. dessicated specimens; II. hydrated in artificial saliva; III. subsequent desiccated; IV. artificial aged; V. further dessicated. Optical CIE L*a*b* coordinates were determined and optical properties, like TP (translucency), OP (opalescence) values, color differences ΔE-NBS, white indexes in dentistry WID and white index differences ΔWID were calculated for all stages of the study, for each group of the materials. Statistical analyses were performed. (3) Results: Optical properties of PETG clear thermoplastic materials, like TP and OP, increase in a simulated oral environment and the changes become significant after artificial aging. Related to pH values, the optical behavior between the materials is significantly different. During artificial aging, the tested materials behave significantly differently in terms of optical properties. (4) Conclusions: After the simulated period of 14 days, TP and OP values increase, with a migration of the color towards red and yellow. Color changes in some cases even reach the level of extremely marked. Whiteness increases, and the differences are mostly perceptible, but partially exceed the limit of acceptability. Full article
(This article belongs to the Section Polymer Applications)
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<p>Translucency (TP) evolution for hydration (<b>a</b>) and desiccation conditions (<b>b</b>), (0) = neutral artificial saliva, (−) = acidic artificial saliva, (+) = basic artificial saliva, L = Leone, D = Duran, C = Crystal, E = Erkodur.</p>
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<p>Opalescence (OP) evolution for hydration (<b>a</b>) and desiccation conditions (<b>b</b>), (0) = neutral, (−) = acidic, (+) = basic, C = Crystal, E = Erkodur, L = Leone, D = Duran.</p>
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<p>Translucency (TP) evolution for hydrothermal aging (<b>a</b>) and desiccation conditions (<b>b</b>), (0) = neutral, (−) = acidic, (+) = basic, C = Crystal, E = Erkodur, D = Duran, L = Leone.</p>
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<p>Opacity (OP) evolution for hydrothermal aging (<b>a</b>) and desiccation conditions (<b>b</b>), (0) = neutral, (−) = acidic, (+) = basic, C = Crystal, E = Erkodur, D = Duran, L = Leone.</p>
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12 pages, 3641 KiB  
Article
Microplastics in Urban Bird Feces: A Methodological Approach and Case Study in Mexico City
by Victoria Amellalli Vazquez-Cruz, Alethia Vázquez-Morillas, Arely Areanely Cruz-Salas, Ana Isabel Hernández-Soriano, Getsemaní Cervantes-Cabrera, Mariana Elizabeth Ballesteros-López and Juan Carlos Alvarez-Zeferino
Microplastics 2025, 4(1), 6; https://doi.org/10.3390/microplastics4010006 - 5 Feb 2025
Abstract
Microplastics (MP) are ubiquitous contaminants in diverse environmental matrices, including biota. Urban birds, such as pigeons (Columba livia), are particularly vulnerable to MP exposure due to their scavenging habits and proximity to human activities. This study developed and applied a methodology [...] Read more.
Microplastics (MP) are ubiquitous contaminants in diverse environmental matrices, including biota. Urban birds, such as pigeons (Columba livia), are particularly vulnerable to MP exposure due to their scavenging habits and proximity to human activities. This study developed and applied a methodology to assess MP presence in pigeon feces, starting with a review of existing methods for extracting MPs from organic matrices. Of all the methodologies investigated, a method was established to be tested, varying the reagent, using pigeon feces collected from the Universidad Autónoma Metropolitana, Azcapotzalco Unit (UAM-A) and 15 virgin microplastics of five different types. Of both reagents, it was found that the method with 50% H2O2 presented better results (degradation of almost all organic matter and recovery efficiency of 93.33%). The selected method was optimized before being applied to feces collected from three sites in Mexico City (n = 10 samples per site). MPs were extracted using a digestion process with 50% hydrogen peroxide, flotation test with CaCl2, staining with red Nile dye and vacuum filtration and analyzed by microscopy and FTIR. Concentrations ranged from 16.4 to 27.8 MP/g dry feces, with fragments (80%) and fibers (20%) being the predominant shapes. The most common colors were black (32%) and white (22%), the polymers identified included polystyrene and polyethylene and the most common size was < 1 mm (54%). These findings suggest that pigeons ingest MP during feeding, likely due to confusion with organic matter, highlighting the risks of urban plastic pollution to avian health. The ingestion of MPs could lead to malnutrition, organ damage, and ecosystem imbalances, underscoring the need for improved waste management in urban areas. This study provides evidence of the pervasive impact of plastic pollution in non-marine environments, demonstrating the potential of urban birds as bio-indicators of local contamination. Full article
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<p>(<b>a</b>) Site 1—truck parking; (<b>b</b>) Site 2—houses; (<b>c</b>) Site 3—train workshop.</p>
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<p>Box-and-whisker diagram of the three sampled sites. Red dots inside the boxes show the average.</p>
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<p>Classification of microplastics: (<b>a</b>) color, (<b>b</b>) shape, (<b>c</b>) polymer and (<b>d</b>) size in millimeters.</p>
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<p>Classification of microplastics: (<b>a</b>) color, (<b>b</b>) shape, (<b>c</b>) polymer and (<b>d</b>) size in millimeters.</p>
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<p>Examples of microplastics (circled in yellow) extracted from pigeon feces.</p>
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25 pages, 5167 KiB  
Article
Optimizing Thermoresponsive and Bioadhesive Systems for Local Application of Erythrosine
by Igor Alves Endrice, Sandy Aline Forastieri Gerarduzzi, Mariana Carla de Oliveira, Marcos Luciano Bruschi and Jéssica Bassi da Silva
Colorants 2025, 4(1), 5; https://doi.org/10.3390/colorants4010005 - 5 Feb 2025
Abstract
Photodynamic therapy (PDT) is a light-activated chemical reaction used for the selective destruction of tissue. For this, various colorants may be applied, such as erythrosine (ERI), a dye already approved by the Food and Drug Administration (FDA) for various purposes. Although promising for [...] Read more.
Photodynamic therapy (PDT) is a light-activated chemical reaction used for the selective destruction of tissue. For this, various colorants may be applied, such as erythrosine (ERI), a dye already approved by the Food and Drug Administration (FDA) for various purposes. Although promising for PDT, ERI has a high hydrophilic profile that impacts its activity. To solve this, the combination of ERI with thermoresponsive and bioadhesive polymers may prove effective. Bio/mucoadhesive and thermoresponsive systems have attracted increasing interest in the development of novel pharmaceutical formulations for topical applications due to their ability to improve adhesion to the mucosa and prolong the residence time at the application site. In this study, systems based on poloxamer 407 (P407) in combination with cellulose derivatives (HPMC and NaCMC) were optimized, aiming at the topical release of ERI for PDT. The results demonstrated that the formulations containing low concentrations of cellulose derivatives exhibited greater adhesiveness and consistency at physiological temperature (37 °C), favoring the maintenance of the system at the application site. Regarding the gelation temperature (Tsol/gel), the formulations displayed values close to body temperature. The formulations with NaCMC showed a slightly higher Tsol/gel compared to HPMC ones, but it was adjustable by the polymer concentration. The addition of ERI influenced the mechanical and adhesive properties of the systems. In formulations containing HPMC, high concentrations of ERI increased bio/mucoadhesiveness, while in systems with NaCMC, the presence of ERI reduced this property. In both cases, the formulations maintained high consistency at 37 °C, contributing to the control of the active release at the application site. Rheological analysis revealed non-Newtonian behavior in all formulations, with greater consistency and elasticity at high temperatures. P407 was mainly responsible for the thermoresponsive transition from sol to gel, conferring desirable characteristics for topical application. Photodynamic activity was relevant in both formulations containing NaCMC and HPMC, which demonstrated greater capacity for degrading uric acid under light exposure. These systems are promising for the controlled release of drugs in photodynamic therapy, providing prolonged retention in the target tissue and maximizing the therapeutic efficacy of ERI. Full article
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<p>Hardness, compressibility, adhesiveness, cohesiveness, and elasticity of polymeric formulations of cellulose derivative (NaCMC or HPMC) at temperatures of 25 and 37 °C.</p>
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<p>Mucoadhesion force and work of the formulations with cellulose derivatives (<span style="color:lime">■</span>HPMC or <span style="color:#3333CC">■</span>NaCMC) in relation to mucin tablets.</p>
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<p>Hardness, compressibility, adhesiveness, cohesiveness, and elasticity of the polymeric formulations with erythrosine (0.1 or 1.0%) at temperatures of 25 and 37 °C.</p>
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<p>Mucoadhesion force and work of the formulations, with or without erythrosine (0.1 or 1.0%), in relation to mucin tablets: (<span style="color:lime">■</span>) binary polymeric system poloxHPMC without ERI; (<span style="color:fuchsia">■</span>) binary polymeric systems poloxHPMC with ERI; (<span style="color:#3333CC">■</span>) binary polymeric system poloxNaCMC without ERI; (<span style="color:purple">■</span>) binary polymeric systems poloxNaCMC with ERI.</p>
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<p>Bioadhesion force and work of the formulations, with or without erythrosine (0.1 or 1.0%), in relation to pig skin tissue: (<span style="color:lime">■</span>) binary polymeric system poloxHPMC without ERI; (<span style="color:fuchsia">■</span>) binary polymeric systems poloxHPMC with ERI; (<span style="color:#3333CC">■</span>) binary polymeric system poloxNaCMC without ERI; (<span style="color:purple">■</span>) binary polymeric systems poloxNaCMC with ERI.</p>
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<p>Flow curves of the formulations, with or without erythrosine, at 25 and 37 °C. The closed symbol represents the outward curve and the open symbol the return curve. Each curve is represented by the average of three analyses performed independently with a coefficient of variation lower than 10%.</p>
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<p>Elastic modulus (●) and viscous modulus (■) as a function of the frequency of the formulations(HPMC or NaCMC), with or without erythrosine, at temperatures of 25 °C and 37 °C. Results are expressed as an average of three analyses performed independently with a coefficient of variation lower than 10%.</p>
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<p>Evaluation of the photodynamic activity of the formulations containing 1% erythrosine (ERI), with or without light exposure.</p>
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<p>Evaluation of the photodynamic activity of the formulations in the absence of erythrosine (ERI), with or without light exposure.</p>
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18 pages, 14835 KiB  
Article
Influence of Food Pigments and Thermal Aging on the Color Stability of Denture Base Resins
by Beatriz Costa, Cristina Bettencourt Neves, João Carlos Roque, Vitor Anes and Virgínia Santos
Appl. Sci. 2025, 15(3), 1503; https://doi.org/10.3390/app15031503 - 1 Feb 2025
Abstract
Color stability of acrylic resins is essential for preserving the aesthetic appearance of denture bases over time. This study explores how food pigments and thermal changes affect the color stability of commonly used denture base resins. Four acrylic resins were tested: three heat-cured [...] Read more.
Color stability of acrylic resins is essential for preserving the aesthetic appearance of denture bases over time. This study explores how food pigments and thermal changes affect the color stability of commonly used denture base resins. Four acrylic resins were tested: three heat-cured acrylic resins with different characteristics (Zhermack® Villacryl H Plus V2, H Plus V4, and H Rapid FN V4) and one self-cured acrylic resin (Zhermack® Villacryl S V4). To simulate the oral environment, the resins underwent 1000 thermal cycles between 5 °C and 55 °C, followed by a 7-day immersion period in beverages such as coffee, red wine, a caramel-colored soft drink (cola), and distilled water (control), forming sixteen group of specimens (n = 5). Color changes (∆E) were measured using the VITA Easyshade V® spectrophotometer, following the CIEDE2000 standard. The findings revealed that thermal aging caused noticeable color changes in all resins (p < 0.001). Red wine led to the most intense discoloration, followed by coffee. The caramel-colored soft drink caused moderate staining, while distilled water had a negligible effect. The type of polymerization did not affect the degree of discoloration, as no significant differences were found between the resins after exposure to beverages (p > 0.05). Overall, this study highlights how both internal and external factors impact the appearance of acrylic resins. Thermal aging can accelerate polymer degradation, while pigments in beverages cause visible staining. Among the tested beverages, red wine proved to be the most aggressive due to its high pigment concentration and low pH. These findings emphasize the need for improved material formulations to enhance the longevity and aesthetic performance of dentures. Full article
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<p>Zhermack<sup>®</sup> acrylic resins. (<b>a</b>) Villacryl H Plus V4, (<b>b</b>) Villacryl H Rapid FN, and (<b>c</b>) Villacryl S.</p>
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<p>Wax mold fabrication: (<b>a</b>,<b>b</b>) pressing the calibrator onto the wax sheet; (<b>c</b>) calibrator and wax mold; (<b>d</b>) wax molds marked on one side.</p>
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<p>(<b>a</b>) Wax patterns on type III gypsum; (<b>b</b>) application of the separating medium on the flask after removal of the wax patterns.</p>
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<p>(<b>a</b>) Acrylic mass in the sealed container; (<b>b</b>) acrylic mass on the flask; (<b>c</b>) flask in the press under 5000 kg pressure; (<b>d</b>) flask in the polymerization unit.</p>
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<p>(<b>a</b>) Specimen after deflask; (<b>b</b>) removal of material using a tungsten carbide bur; (<b>c</b>) manual polishing machine.</p>
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<p>(<b>a</b>) Pumice, polishing paste, and polishing brushes; (<b>b</b>) polishing machine with pumice; (<b>c</b>) brush with polishing paste.</p>
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<p>(<b>a</b>) Box with labeled specimens; (<b>b</b>) black PVC device; (<b>c</b>) VITA Easyshade V<sup>®</sup> display; (<b>d</b>) color measurement of a sample using the VITA Easyshade V<sup>®</sup>.</p>
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<p>(<b>a</b>) Mesh bags with specimens separated and identified by colored rubber bands; (<b>b</b>) thermocycling machine.</p>
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<p>(<b>a</b>) Instant coffee; (<b>b</b>) red wine; (<b>c</b>) carbonated soft drink.</p>
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<p>(<b>a</b>) Dispensing 4 mL of coffee using a graduated syringe; (<b>b</b>) immersion of the specimen in the beverage; (<b>c</b>) specimens wrapped in aluminum foil in an oven at 37 °C; (<b>d</b>) boxes containing specimens immersed in the beverages.</p>
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<p>Experimental protocol design.</p>
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<p>Specimens after 7 days of immersion in the beverages.</p>
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<p>Box plots of ΔE (T1–T0) by Villacryl resin category after thermocycling. (° represents outliers).</p>
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<p>Boxplots of ΔE (T2–T1) according to Villacryl resin and beverage category after immersion in the beverages (°, * represents outliers).</p>
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20 pages, 3010 KiB  
Article
Synthesis of Acrylic–Urethane Hybrid Polymer Dispersions and Investigations on Their Properties as Binders in Leather Finishing
by Selime Keskin, Catalina N. Cheaburu-Yilmaz, Aylin Altinisik Tagac, Raluca Nicoleta Darie-Nita and Onur Yilmaz
Polymers 2025, 17(3), 308; https://doi.org/10.3390/polym17030308 - 24 Jan 2025
Viewed by 250
Abstract
This study investigates the synthesis and application of acrylic–urethane hybrid polymer dispersions as advanced binders for leather finishing. Two polymerization techniques—seeded emulsion and miniemulsion—were used to produce hybrid polymer dispersions by varying the ratios of polyurethane (PU) and acrylic (AC). The synthesized dispersions, [...] Read more.
This study investigates the synthesis and application of acrylic–urethane hybrid polymer dispersions as advanced binders for leather finishing. Two polymerization techniques—seeded emulsion and miniemulsion—were used to produce hybrid polymer dispersions by varying the ratios of polyurethane (PU) and acrylic (AC). The synthesized dispersions, i.e., the hybrid polyurethanes, showed stable, uniform particle sizes, inferring good compatibility and interaction between the PU and AC phases, as confirmed by particle sizes, FTIR, and DSC analyses. The performance of the coating on leather surfaces was assessed by using standard physical tests, including rubbing fastness, flexing endurance, water spot resistance, and grain strength. The results showed that the hybrid polymers outperformed their individual PU and AC counterparts, particularly in terms of abrasion resistance and mechanical integrity. Of the two polymerization techniques, the seeded emulsion hybrids exhibited superior coating properties, providing greater resistance to cracking and abrasion under stress, improved grain strength, and better color retention during rubbing tests. These findings highlight the potential of acrylic–urethane hybrids, particularly those prepared via seeded emulsion polymerization, to address the limitations of traditional binders in high-performance leather applications. Full article
(This article belongs to the Section Polymer Composites and Nanocomposites)
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<p>Particle size distribution curves of the latexes: (<b>a</b>) neat PU and AC latexes, (<b>b</b>) seeded hybrid latexes (S), and (<b>c</b>) hybrid miniemulsions (M).</p>
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<p>FTIR spectra of the PU, prepolymer, and PU monomers.</p>
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<p>FTIR spectra of the PU, AC, and PU–AC hybrid polymers.</p>
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<p>DSC thermograms of PU, AC, and hybrid polymers.</p>
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<p>Images of the finished leather samples after the wet rubbing test.</p>
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<p>Synthesis of waterborne PU.</p>
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<p>Illustration of the PU–AC hybrid synthesis via seeded emulsion polymerization.</p>
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<p>Illustration of the PU–AC hybrid synthesis via miniemulsion polymerization.</p>
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15 pages, 3732 KiB  
Article
Effect of Ultraviolet Aging on Properties of Epoxy Resin and Its Pultruded Fiber-Reinforced Composite
by Shengzong Ci, Baoming Wang, Chengrui Di, Mingyu Wang, Bo Zhu and Kun Qiao
Polymers 2025, 17(3), 294; https://doi.org/10.3390/polym17030294 - 23 Jan 2025
Viewed by 328
Abstract
Polymer matrix composites (PMCs) often undergo aging as a result of ultraviolet (UV) radiation, which significantly impacts their performance and durability. This paper investigated the alterations in the microstructure and macroscopic properties of epoxy resin and its composite used in overhead wires during [...] Read more.
Polymer matrix composites (PMCs) often undergo aging as a result of ultraviolet (UV) radiation, which significantly impacts their performance and durability. This paper investigated the alterations in the microstructure and macroscopic properties of epoxy resin and its composite used in overhead wires during UV aging. Furthermore, the mechanism of UV aging for both resin and composite was revealed. The results showed that UV aging predominantly affected the properties of the surface layer resin. UV aging can induce molecular chain scission, which leads to resin weight change, color deepening, microcrack formation, a decline in mechanical properties, and other performance degradation behaviors under the combined action of many factors. With the increase in aging time, the weight change rate and hardness of the resin increased first and then decreased, while the mechanical properties of the composite decreased rapidly first and gradually tended to be constant. The bending strength and impact strength of the composite decreased by 6.0% and 12.8%, respectively, compared with the initial values. The purpose of this study is to comprehensively understand the UV aging behaviors of epoxy resins and their composites employed in overhead wires, and it also provides essential data for advancing the utilization and durability of epoxy resins and composites across aerospace, marine, and other outdoor applications. Full article
(This article belongs to the Special Issue Mechanical Behaviors and Properties of Polymer Materials, 2nd Edition)
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<p>Overhead transmission lines with different reinforcement cores. (<b>a</b>) Aluminum Conductor Steel Reinforced (ACSR); (<b>b</b>) Aluminum Conductor Composite Core (ACCC).</p>
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<p>Flow chart of resin sample preparation.</p>
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<p>Schematic of pultrusion molding (1. Creel; 2. fiber guide; 3. resin impregnator; 4. mold; 5. tractor; 6. cutter.).</p>
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<p>Weight change rate and density change of epoxy after UV aging. (<b>a</b>): Weight change rate; (<b>b</b>): density.</p>
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<p>Photo of epoxy after UV aging.</p>
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<p>Cross-sectional images of the epoxy after UV aging.</p>
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<p>Hardness change of epoxy before and after UV aging.</p>
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<p>FTIR patterns of epoxy before and after UV aging.</p>
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<p>TG and DTG curve of unaged epoxy resin.</p>
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<p>SEM of the surface of epoxy before and after UV aging. (<b>a</b>) 0 h; (<b>b</b>) 216 h; (<b>c</b>) 360 h; (<b>d</b>) 792 h; (<b>e</b>) 936 h; (<b>f</b>) 1080 h.</p>
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<p>Mechanical property change in CFRP before and after UV aging.</p>
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<p>SEM (500×) of the surface of CFRP before and after UV aging. (<b>a</b>) 0 h; (<b>b</b>) 288 h; (<b>c</b>) 1560 h; (<b>d</b>) 2640 h.</p>
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<p>SEM (5000×) of the surface of CFRP before and after UV aging. (<b>a</b>) 0 h; (<b>b</b>) 240 h; (<b>c</b>) 960 h; (<b>d</b>) 2160 h; (<b>e</b>) 3120 h; (<b>f</b>) 5280 h.</p>
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<p>FTIR spectra of CFRP before and after UV aging.</p>
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18 pages, 2465 KiB  
Article
An In-Vitro Evaluation of Strength, Hardness, and Color Stability of Heat-Polymerized and 3D-Printed Denture Base Polymers After Aging
by Abdulrahman Al-Ameri, Othman Y. Alothman, Omar Alsadon and Durgesh Bangalore
Polymers 2025, 17(3), 288; https://doi.org/10.3390/polym17030288 - 23 Jan 2025
Viewed by 339
Abstract
This study evaluated the strength, hardness, and color stability of 3D-printed denture base resins and compared the outcome with conventional heat-cured denture base resins after aging by thermocycling. A total of 72 specimens from conventional and 3D-printed materials were fabricated in different shapes [...] Read more.
This study evaluated the strength, hardness, and color stability of 3D-printed denture base resins and compared the outcome with conventional heat-cured denture base resins after aging by thermocycling. A total of 72 specimens from conventional and 3D-printed materials were fabricated in different shapes and dimensions based on the mechanical and color tests performed. The specimens were divided into five groups: flexural, tensile, and compressive strengths (n = 20), hardness, and color stability (n = 6). In all these groups, half of the specimens were stored in a distilled water bath at 37 °C for 24 h, and the remaining half of the specimens were subjected to aging by thermocycling. The 3D-printed specimens demonstrated the highest means of tensile strength (32.20 ± 3.8 MPa), compressive strength (106.31 ± 4.07 MPa), and Vickers hardness number (24.51 ± 0.36), and the lowest means of flexural strength (54.29 ± 13.17 MPa) and color difference (ΔE = 2.18 ± 1.09). Conventional heat-cured specimens demonstrated the highest means of flexural strength (59.96 ± 8.39 MPa) and color difference (ΔE = 4.74 ± 2.37) and the lowest means of tensile strength (32.17 ± 9.06 MPa), compressive strength (46.05 ± 4.98 MPa), and Vickers hardness number (10.42 ± 1.05). Aging significantly reduced the flexural strength (−27%), tensile strength (−44%), and hardness (−7%) of 3D-printed resins in contrast to the conventional resin’s compressive strength (−15%) and color stability (p < 0.05). The 3D-printed resin had comparable flexural and tensile strength and significantly superior compressive strength, hardness, and color stability compared with conventional resins. Aging significantly and negatively affected the flexural strength, tensile strength, and hardness of 3D-printed resin. Full article
(This article belongs to the Special Issue 3D Printing and Molding Study in Polymeric Materials)
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<p>Specimen shapes and dimensions used in this study. (<b>a</b>) flexural strength, (<b>b</b>) Tensile strength, (<b>c</b>) compressive strength and (<b>d</b>) hardness and color stability.</p>
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<p>Schematic illustration of strength test set-up. (<b>a</b>) Flexural, (<b>b</b>) Tensile, (<b>c</b>) Compressive.</p>
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<p>Mean flexural strength of conventional and 3D-printed resins at baseline and after thermocycling (Baseline, BL; Thermocycled, AT). Materials with the same lowercase letters are not significantly different.</p>
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<p>Mean elastic modulus of conventional and 3D-printed resins at baseline and after thermocycling (Baseline, BL; Thermocycled, AT). Materials with the same lowercase letters are not significantly different.</p>
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<p>Mean tensile strength of conventional and 3D-printed resins at baseline and after thermocycling (Baseline, BL; Thermocycled, AT). Materials with the same lowercase letters are not significantly different.</p>
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<p>Mean compressive strength of conventional and 3D-printed resins at baseline and after thermocycling (Baseline, BL; Thermocycled, AT). Materials with the same lowercase letters are not significantly different.</p>
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<p>Mean hardness of conventional and 3D-printed resins at baseline and after thermocycling (Baseline, BL; Thermocycled, AT). Materials with the same lowercase letters are not significantly different.</p>
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<p>Mean ΔE of conventional and 3D-printed resins at baseline and after thermocycling (Baseline, BL; Thermocycled, AT). Materials with the same lowercase letters are not significantly different.</p>
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<p>FTIR waveforms of the conventional and 3D-printed resins.</p>
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20 pages, 54914 KiB  
Article
Treatment and Valorization of Waste Wind Turbines: Component Identification and Analysis
by Xiaohan Zhao, Daria Pakuła, Miłosz Frydrych, Roksana Konieczna, Bogna Sztorch, Rafał Kozera, Hongzhi Liu, Hui Zhou and Robert E. Przekop
Materials 2025, 18(2), 468; https://doi.org/10.3390/ma18020468 - 20 Jan 2025
Viewed by 726
Abstract
Recycling end-of-life wind turbines poses a significant challenge due to the increasing number of turbines going out of use. After many years of operation, turbines lose their functional properties, generating a substantial amount of composite waste that requires efficient and environmentally friendly processing [...] Read more.
Recycling end-of-life wind turbines poses a significant challenge due to the increasing number of turbines going out of use. After many years of operation, turbines lose their functional properties, generating a substantial amount of composite waste that requires efficient and environmentally friendly processing methods. Wind turbine blades, in particular, are a problematic component in the recycling process due to their complex material composition. They are primarily made of composites containing glass and carbon fibers embedded in polymer matrices such as epoxies and polyester resins. This study presents an innovative approach to analyzing and valorizing these composite wastes. The research methodology incorporates integrated processing and analysis techniques, including mechanical waste treatment using a novel compression milling process, instead of traditional knife mills, which reduces wear on the milling tools. Based on the differences in the structure and colors of the materials, 15 different kinds of samples named WT1-WT15 were distinguished from crushed wind turbines, enabling a detailed analysis of their physicochemical properties and the identification of the constituent components. Fourier transform infrared spectroscopy (FTIR) identified key functional groups, confirming the presence of thermoplastic polymers (PET, PE, and PP), epoxy and polyester resins, wood, and fillers such as glass fibers. Thermogravimetric analysis (TGA) provided insights into thermal stability, degradation behavior, and the heterogeneity of the samples, indicating a mix of organic and inorganic constituents. Differential scanning calorimetry (DSC) further characterized phase transitions in polymers, revealing variations in thermal properties among samples. The fractionation process was carried out using both wet and dry methods, allowing for a more effective separation of components. Based on the wet separation process, three fractions—GF1, GF2, and GF3—along with other components were obtained. For instance, in the case of the GF1 < 40 µm fraction, thermogravimetric analysis (TGA) revealed that the residual mass is as high as 89.7%, indicating a predominance of glass fibers. This result highlights the effectiveness of the proposed methods in facilitating the efficient recovery of high-value materials. Full article
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<p>Separation method.</p>
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<p>FTIR spectra of: (<b>A</b>) WT1, WT3; (<b>B</b>) WT2, WT5, WT8; (<b>C</b>) WT4, WT6; (<b>D</b>) WT10-12.</p>
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<p>TGA curves of (<b>A1</b>) WT1, WT3; (<b>B1</b>) WT6, WT7; (<b>C1</b>) WT2, WT5, WT8, WT10-12; (<b>D1</b>) WT13-WT15; (<b>E1</b>) WT4 and DTG curves of (<b>A2</b>) WT1, WT3; (<b>B2</b>) WT6, WT7; (<b>C2</b>) WT2, WT5, WT8, WT10-12; (<b>D2</b>) WT13-WT15; (<b>E2</b>) WT4 in nitrogen atmosphere.</p>
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<p>DSC curves of (<b>A</b>) WT1; (<b>B</b>) WT3; (<b>C</b>) WT2, WT6; (<b>D</b>) WT4-5, WT8, WT10; (<b>E</b>) WT11-12; (<b>F</b>) WT13-15.</p>
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<p>Mass sample of different fractions: (<b>a</b>) summed up for GF1-3 and others; (<b>b</b>) based on the size.</p>
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<p>TGA (<b>A1</b>–<b>C1</b>) and DTG (<b>A2</b>–<b>C2</b>) curves of glass fibers in nitrogen atmosphere.</p>
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25 pages, 7109 KiB  
Review
Research Progress on Quantum Dot-Embedded Polymer Films and Plates for LCD Backlight Display
by Bin Xu, Jiankang Zhou, Chengran Zhang, Yunfu Chang and Zhengtao Deng
Polymers 2025, 17(2), 233; https://doi.org/10.3390/polym17020233 - 17 Jan 2025
Viewed by 471
Abstract
Abstract: Quantum dot–polymer composites have the advantages of high luminescent quantum yield (PLQY), narrow emission half-peak full width (FWHM), and tunable emission spectra, and have broad application prospects in display and lighting fields. Research on quantum dots embedded in polymer films and plates [...] Read more.
Abstract: Quantum dot–polymer composites have the advantages of high luminescent quantum yield (PLQY), narrow emission half-peak full width (FWHM), and tunable emission spectra, and have broad application prospects in display and lighting fields. Research on quantum dots embedded in polymer films and plates has made great progress in both synthesis technology and optical properties. However, due to the shortcomings of quantum dots, such as cadmium selenide (CdSe), indium phosphide (InP), lead halide perovskite (LHP), poor water, oxygen, and light stability, and incapacity for large-scale synthesis, their practical application is still restricted. Various polymers, such as methyl methacrylate (PMMA), polyethylene terephthalate (PET), polystyrene (PS), polyvinylidene fluoride (PVDF), polypropylene (PP), etc., are widely used in packaging quantum dot materials because of their high plasticity, simple curing, high chemical stability, and good compatibility with quantum dot materials. This paper focuses on the application and development of quantum dot–polymer materials in the field of backlight displays, summarizes and expounds the synthesis strategies, advantages, and disadvantages of different quantum dot–polymer materials, provides inspiration for the optimization of quantum dot–polymer materials, and promotes their application in the field of wide-color-gamut backlight display. Full article
(This article belongs to the Special Issue Polymers/Their Hybrid Materials for Optoelectronic Applications)
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<p>(<b>a</b>) Photoluminescent liquid crystal display structure schematic diagram. Reprinted with permission from ref. [<a href="#B1-polymers-17-00233" class="html-bibr">1</a>]. Copyright 2020 Springer Nature. (<b>b</b>) Gamut in CIE chromaticity diagram. Reprinted with permission from ref. [<a href="#B4-polymers-17-00233" class="html-bibr">4</a>]. Copyright 2023 Wiley. (<b>c</b>) Current problems and challenges faced by quantum dot materials.</p>
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<p>Group II–VI quantum dots. (<b>a</b>) PL spectra for CdSe/CdS core–shell nanocrystals with different core size and different shell thickness. (<b>b</b>) Photograph of solutions of CdSe/CdS core–shell nanocrystals with different core size and different shell thickness under normal indoor light without UV irradiation. Reprinted with permission from ref. [<a href="#B60-polymers-17-00233" class="html-bibr">60</a>]. Copyright 2005 Wiley. (<b>c</b>) Photographs under ambient room light (<b>top</b>) and UV light (<b>bottom</b>) showing effect of CdCl<sub>2</sub> treatment at increasing CdCl<sub>2</sub> concentrations on QD PL. Reprinted with permission from ref. [<a href="#B68-polymers-17-00233" class="html-bibr">68</a>]. Copyright 2018 American Chemical Society. (<b>d</b>) Cu:Mn-ZnSe-doped QD samples with different amounts of Cu precursors. Reprinted with permission from ref. [<a href="#B64-polymers-17-00233" class="html-bibr">64</a>]. Copyright 2011 Wiley. (<b>e</b>) Solutions of CQWs after different CE reaction times (10 to 60 min) under 365 nm UV light. (<b>f</b>) Normalized absorption and PL spectra of CdZnSe CQWs with respect to the CE reaction time. Reprinted with permission from ref. [<a href="#B66-polymers-17-00233" class="html-bibr">66</a>]. Copyright 2024 Wiley.</p>
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<p>Group III–V quantum dots. (<b>a</b>) The synthesis strategy of InP/Zn(Se,S)/ZnS featuring a core–shell–shell structure and the attainment of multiple emission colors through the adjustment of the composition of the inner shell. (<b>b</b>) Absorbance and emission spectra of InP/ZnSe/ZnS QDs. Reprinted with permission from ref. [<a href="#B80-polymers-17-00233" class="html-bibr">80</a>]. Copyright 2022 American Chemical Society. (<b>c</b>) Absorption spectra of alloyed In<sub>1−x</sub>GaxP cores and the large range of emission colors produced by core−shell In<sub>1−x</sub>GaxP/ZnS samples with varying gallium. (<b>d</b>) In<sub>1−x</sub>GaxP/ZnS emission spectra. Reprinted with permission from ref. [<a href="#B87-polymers-17-00233" class="html-bibr">87</a>]. Copyright 2023 American Chemical Society.</p>
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<p>Perovskite quantum dots (<b>a</b>) FAPbX<sub>3</sub> nanocrystals dispersed in toluene under UV irradiation (λpeak = 365 nm) and PL emission spectra of FAPbX<sub>3</sub> nanocrystals. (<b>b</b>) Corresponding color gamut of FAPbX<sub>3</sub> nanocrystals displayed on the CIE diagram. Reprinted with permission from ref. [<a href="#B93-polymers-17-00233" class="html-bibr">93</a>]. Copyright 2017 American Chemical Society. (<b>c</b>) Scheme of synthesized aqueous-based CsPbBr<sub>3</sub>/CsPb<sub>2</sub>Br<sub>5</sub> PQDs using vacancy inhibitors of PEG, forming a defect-free surface in water (OA refers to oleic acid, and OAm represents oleylamine). Reprinted with permission from ref. [<a href="#B91-polymers-17-00233" class="html-bibr">91</a>]. Copyright 2023 Wiley.</p>
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<p>(<b>a</b>) Schematic diagram of functions by encapsulation illustrated by CsPbX<sub>3</sub> QDs. Reprinted with permission from ref. [<a href="#B20-polymers-17-00233" class="html-bibr">20</a>]. Copyright 2019 Wiley. (<b>b</b>) Radar map of the advantages and disadvantages of three methods of combining QDs with polymers.</p>
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<p>(<b>a</b>) Flowchart of the dual-solvent assisted reprecipitation (DSAR) technique. (<b>b</b>) Photoluminescence spectra (the inset shows photoluminescence quantum yield). (<b>c</b>) Blue light stability test. (<b>d</b>) The 60 °C/90%RH stability test. (<b>e</b>) Color gamut of the fabricated devices using the Cs-DSAR and CsFA-DSAR PQDs. Reprinted with permission from ref. [<a href="#B38-polymers-17-00233" class="html-bibr">38</a>]. Copyright 2023 Elsevier.</p>
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<p>(<b>a</b>) Schematic illustration of the in situ fabrication of MAPbBr<sub>3</sub> NCs-embedded PVDF composite films. (<b>b</b>) Optical images under a UV lamp (365 nm) of color-tunable MAPbX<sub>3</sub>–PVDF composite films with different halogen constitutions on glass substrates. (<b>c</b>) Emission spectrum of the white LED using green emissive MAPbBr<sub>3</sub>–PVDF composite films and red emissive phosphor. (<b>d</b>) The color coordinate (star) and the white triangle (white line) of obtained white LED in CIE 1931 diagram. Reprinted with permission from ref. [<a href="#B32-polymers-17-00233" class="html-bibr">32</a>]. Copyright 2016 Wiley.</p>
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<p>(<b>a</b>) Schematic diagrams of the preparation procedure for yellow PQDF via melt extruding-rolling method. Photographs of the as-prepared PP-encapsulated CsPbX<sub>3</sub>@glass composite particles and the corresponding green and yellow PQDFs. (<b>b</b>) Photograph of yellow monolithic PQDF-based backlit unit and luminescent image of the backlit unit at an operating voltage of 12 V. (<b>c</b>) Schematic structure of an LCD prototype using yellow PQDF as a light converter. (<b>d</b>) Comparison of the display performance of a YAG-based LCD and PQDF-based LCD. (<b>e</b>) Color gamut of PQDF-based LCD (blue solid triangle), NSTC 1953 standard (black dashed triangle), and YAG-based commercial LCD (black solid triangle). Reprinted with permission from ref. [<a href="#B37-polymers-17-00233" class="html-bibr">37</a>]. Copyright 2024 Wiley.</p>
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<p>(<b>a</b>) Schematic structures of the growth of green and red QDs. (<b>b</b>) Light intensity spectra (solid line) and brightness (hatched area) of QD-LED (blue) and phosphor-LED (gray). Inset: color triangles of QD-LED (white) and phosphor-LED (yellow) compared to NTSC1931 (black). (<b>c</b>) Display image of a 46-inch LCD TV panel and a quarter of the white QD-LED backlights (inset). Reprinted with permission from ref. [<a href="#B43-polymers-17-00233" class="html-bibr">43</a>]. Copyright 2010 Wiley. (<b>d</b>) Schematic of syntheses of the ZnS modified green and red QRs. (<b>e</b>) The spectrum of the fabricated QRWLED consists of three emission band peaks at 450, 527, and 624 nm. (<b>f</b>) Schematic of a QRs on-chip backlight with dual-brightness-enhancement film (DBEF) design for displays. Reprinted with permission from ref. [<a href="#B44-polymers-17-00233" class="html-bibr">44</a>]. Copyright 2021 Wiley.</p>
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29 pages, 6394 KiB  
Review
Preparation of Colored Polymer Microspheres
by Lei Wang, Weiting Ma, Shuheng Zhang, Mengke He, Ping Song, Hongying Wang, Xianxiao Song and Botian Li
Molecules 2025, 30(2), 375; https://doi.org/10.3390/molecules30020375 - 17 Jan 2025
Viewed by 356
Abstract
Colored polymer microspheres have attracted significant attention in both academia and industry due to their unique optical properties and extensive application potential. However, achieving a uniform distribution of dyes within these microspheres remains a challenge, particularly when heavy concentrations of dye are used, [...] Read more.
Colored polymer microspheres have attracted significant attention in both academia and industry due to their unique optical properties and extensive application potential. However, achieving a uniform distribution of dyes within these microspheres remains a challenge, particularly when heavy concentrations of dye are used, as this can lead to aggregation or delamination, adversely affecting their application. Additionally, many dyes are prone to degradation or fading when exposed to light, heat, or chemicals, which compromises the long-term color stability of the microspheres. Consequently, the preparation of colored polymer microspheres with high stability continues to be a significant challenge. This review offers a comprehensive overview of the preparation techniques for colored polymer microspheres and their dyeing mechanisms, introducing the fundamental concepts of these microspheres and their applications in various fields, such as biomedicine, optical devices, and electronic display technologies. It further presents a detailed discussion of the different preparation methods, including physical adsorption, chemical bonding, and copolymerization. The advantages, limitations, and potential improvements of each method are explored, along with an analysis of the interactions between dyes and the polymer matrix, and how these interactions influence the properties of the microspheres, including their color uniformity, stability, and durability. Finally, the review discusses future perspectives on the development of colored polymer microspheres, highlighting the advancement of novel materials, innovations in preparation technology, and the exploration of potential new application areas. Full article
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Graphical abstract

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<p>Applications of colored polymer microspheres [<a href="#B2-molecules-30-00375" class="html-bibr">2</a>,<a href="#B3-molecules-30-00375" class="html-bibr">3</a>,<a href="#B4-molecules-30-00375" class="html-bibr">4</a>,<a href="#B5-molecules-30-00375" class="html-bibr">5</a>].</p>
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<p>Chemical structure of (<b>a</b>) methylene blue, (<b>b</b>) Rhodamine B acrylate [<a href="#B52-molecules-30-00375" class="html-bibr">52</a>], (<b>c</b>) ZnAOTPP [<a href="#B55-molecules-30-00375" class="html-bibr">55</a>], (<b>d</b>) Sudan III [<a href="#B56-molecules-30-00375" class="html-bibr">56</a>], (<b>e</b>) RB2 [<a href="#B60-molecules-30-00375" class="html-bibr">60</a>], and (<b>f</b>) pyrene acrylate [<a href="#B61-molecules-30-00375" class="html-bibr">61</a>].</p>
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<p>Synthesis routes of (<b>a</b>) P(AM-BA-AMCO), (<b>b</b>) P(AM-BA-Ac-Flu), and (<b>c</b>) P(AM-BA-RhB); (<b>d</b>) fluorescent images of the three polymer microspheres (A–C: Fluorescent images; A<sub>1</sub>–C<sub>1</sub>: Optical microscope images) [<a href="#B3-molecules-30-00375" class="html-bibr">3</a>].</p>
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<p>(<b>a</b>) Synthesis routes and fluorescence properties of a fluorescent polymer with AIE units [<a href="#B59-molecules-30-00375" class="html-bibr">59</a>]; (<b>b</b>) synthesis routes of a fluorescent polymer with Rhodamine B groups and their fluorescence microscopy (b1: blue light, b2: green light) [<a href="#B53-molecules-30-00375" class="html-bibr">53</a>].</p>
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<p>(<b>a</b>) Chemical structure of PPE; (<b>b</b>) synthesis route of APGMA-PPE-NR fluorescent microspheres; (<b>c</b>) encoding strategy for microspheres that comprises varying the concentrations of PPE and NR in THF solution, as well as their combination [<a href="#B2-molecules-30-00375" class="html-bibr">2</a>].</p>
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<p>Illustration of the preparation of APGMA-CP fluorescent microspheres and the bio-conjugation of BSA-FITC onto the microspheres [<a href="#B66-molecules-30-00375" class="html-bibr">66</a>].</p>
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<p>(<b>a</b>) Synthesis route of polysulfide zinc (II); (<b>b</b>) synthesis route of compound 1 [<a href="#B75-molecules-30-00375" class="html-bibr">75</a>]; (<b>c</b>) illustration of crosslinked shell-coated fluorescent PPV microspheres; (<b>d</b>) chemical structures [<a href="#B76-molecules-30-00375" class="html-bibr">76</a>].</p>
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<p>(<b>a</b>) Preparation of fluorescent nanoparticles via the swelling method [<a href="#B58-molecules-30-00375" class="html-bibr">58</a>]; (<b>b</b>) illustration of quantum dots being embedded into PSDM microspheres [<a href="#B82-molecules-30-00375" class="html-bibr">82</a>]; (<b>c</b>) SB@PS bead preparation process [<a href="#B84-molecules-30-00375" class="html-bibr">84</a>]; (<b>d</b>) preparation process of QD-encoded polymer microspheres, including (I) swelling, (II) temperature increase, and (III) deswelling and rapidly cooling. a1–a2 Dissolution: QDs are mixed with polymer microspheres, which dissolve in chloroform due to hydrophobicity. a2–a3 warming impregnation: warming allows the microspheres to continue to swell and the QDs to penetrate into the microspheres due to the concentration difference. a3–a4 Encapsulation: Remove chloroform and cool quickly to immobilize the molecular chains and encapsulate the QDs [<a href="#B85-molecules-30-00375" class="html-bibr">85</a>].</p>
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<p>(<b>a</b>) Chemical structures of the organic dyes for adsorption; (<b>b</b>) equilibrium adsorption capacity of PDA microspheres for different dyes [<a href="#B91-molecules-30-00375" class="html-bibr">91</a>]; (<b>c</b>) synthesis of polymer microspheres; (<b>d</b>) UV–Vis absorption spectra of dyed microspheres with different amounts of VBC; (<b>e</b>) variation in the dye content incorporated into dyed microspheres [<a href="#B92-molecules-30-00375" class="html-bibr">92</a>].</p>
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<p>(<b>a</b>) Synthesis route of RB2, (<b>b</b>) absorption spectra of RB1 and RB2, and (<b>c</b>) emission spectra [<a href="#B60-molecules-30-00375" class="html-bibr">60</a>].</p>
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<p>(<b>a</b>) Synthesis route of rosin-derived CCRM via the suspension polymerization strategy; (<b>b</b>) adsorption capacity of CCRM for different dyes [<a href="#B96-molecules-30-00375" class="html-bibr">96</a>]; (<b>c</b>) synthesis route of CMPSF; (<b>d</b>) synthesis route of porous hollow microspheres; (<b>e</b>) synthesis route of porous hollow carboxylated polysulfone microspheres; (<b>f</b>) purification performance; and (<b>g</b>) UV–Vis spectra of PH-PSF and PH-CPSF microspheres [<a href="#B97-molecules-30-00375" class="html-bibr">97</a>].</p>
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<p>Bright-field (<b>a</b>–<b>d</b>) and fluorescence (green channel) (<b>e</b>–<b>h</b>) microscope images of PS microspheres loaded with chlorophyll a at different dye loading levels: (<b>a</b>,<b>e</b>) 1 wt%, (<b>b</b>,<b>f</b>) 2.5 wt%, (<b>c</b>,<b>g</b>) 4 wt%, and (<b>d</b>,<b>h</b>) 10 wt% [<a href="#B99-molecules-30-00375" class="html-bibr">99</a>].</p>
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<p>(<b>a</b>) Effect of pH on MB adsorption using PAM/SA [<a href="#B96-molecules-30-00375" class="html-bibr">96</a>]; (<b>b</b>) effect of temperature on MB adsorption using PAM/SA [<a href="#B103-molecules-30-00375" class="html-bibr">103</a>]; (<b>c</b>) change in relative concentration of RhB in solution 1 under different irradiation times [<a href="#B108-molecules-30-00375" class="html-bibr">108</a>].</p>
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