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    <title>Advances in Science and Technology</title>
    <link>https://www.scientific.net/AST</link>
    <description>Latest Results for Advances in Science and Technology</description>
    <language>en-us</language>
    <image>
      <title>Advances in Science and Technology</title>
      <link>https://www.scientific.net</link>
      <url>https://www.scientific.net/Image/JournalCover/14</url>
    </image>
    <item>
      <title>Preface</title>
      <link>https://www.scientific.net/AST.179.-1</link>
      <description>Publication date: 19 June 2026
&lt;br /&gt;Source: Advances in Science and Technology Vol. 179
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      <pubDate>Fri, 19 Jun 2026 00:00:00 +0200</pubDate>
      <feedDate>Fri, 3 Jul 2026 01:19:40 +0200</feedDate>
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      <title>Study on the Setting Characteristics, Mechanical Properties, and Volumetric Stability of Alkali-Activated Metakaolin-Based Composite Materials</title>
      <link>https://www.scientific.net/AST.179.3</link>
      <guid>10.4028/p-d6GvAX</guid>
      <description>Publication date: 19 June 2026
&lt;br /&gt;Source: Advances in Science and Technology Vol. 179
&lt;br /&gt;Author(s): An Cheng, Pin Chien Cheng, Qi Zhen Huang, Yuan Ho Cheng, Kai En Lan, Hui Mi Hsu
&lt;br /&gt;Traditional Portland cement production generates substantial CO₂ emissions, hindering sustainable low-carbon building materials. This study develops a cement-free alkali-activated geopolymer using metakaolin as the primary binder, blended with 0%, 10%, and 20% ground granulated blast-furnace slag (GGBFS) by weight, activated by sodium hydroxide and sodium silicate. It examines physical properties, including setting time, compressive strength, and volumetric stability, under varying GGBFS levels, with chemical analysis via FTIR and DTG. Increasing GGBFS accelerates polymerization, reducing initial setting time from 4 hours (0% GGBFS) to 2 hours (20% GGBFS), with final setting time similar. Compressive strengths (MPa) under ambient curing at 1, 7, and 28 days for M100S0, M90S10, and M80S20 are 8.34/13.34/26.28 at 1 day, 31.77/45.90/45.68 at 7 days, and 34.8/45.4/42.1 at 28 days. Early-age strength improves with higher GGBFS due to additional calcium facilitating C-S-H gel formation, while strengths stabilize beyond 28 days. Volumetric stability shows no significant shrinkage or expansion within three days across mixtures, with maximum strain below 0.12%, indicating excellent stability. FTIR shows enhanced Si-O-Al bond intensity (~1050 cm⁻¹) in GGBFS samples, reflecting greater Al incorporation into silicate tetrahedra and denser amorphous structure. The O-H stretching peak (~3400 cm⁻¹) narrows slightly, signifying reduced water and improved polymerization. DTG corroborates enhanced polymerization efficiency with GGBFS. These results highlight superior mechanical properties and stability of GGBFS-blended metakaolin geopolymers, positioning them as promising for subgrade soil stabilization, improving early bearing capacity and long-term durability for sustainable construction.
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      <pubDate>Fri, 19 Jun 2026 00:00:00 +0200</pubDate>
      <feedDate>Fri, 3 Jul 2026 01:19:40 +0200</feedDate>
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      <title>A Damage Mechanics–Based Analysis of CNT-Modified Self-Sensing Cementitious Composites</title>
      <link>https://www.scientific.net/AST.179.9</link>
      <guid>10.4028/p-fKuhH5</guid>
      <description>Publication date: 19 June 2026
&lt;br /&gt;Source: Advances in Science and Technology Vol. 179
&lt;br /&gt;Author(s): Seungyeol Oh, Hyeona Kwon, Seongwon Hong
&lt;br /&gt;Smart construction systems require materials capable of autonomously detecting structural damage with high precision and reliability. This study develops self-sensing cementitious composites and evaluates their feasibility using a damage-mechanics-based framework. Mechanical loading tests were performed while monitoring electrical resistance, and the correlation between fractional change in resistance and damage variable was quantitatively assessed. The conductive network generated by dispersed functional fibers enabled deformation-induced electrical variation, providing real-time sensing capability. Unlike prior studies focusing solely on electrical response, this work integrates continuum damage mechanics to establish a predictive electro-mechanical relationship. Results demonstrate a strong correlation between electrical response and internal damage evolution, validating the feasibility of applying these self-sensing composites to smart structural systems for health monitoring and early-stage damage detection.
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      <pubDate>Fri, 19 Jun 2026 00:00:00 +0200</pubDate>
      <feedDate>Fri, 3 Jul 2026 01:19:40 +0200</feedDate>
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      <title>Feasibility of AMPS Hydrogel for Surface Cleaning in Art Conservation</title>
      <link>https://www.scientific.net/AST.179.15</link>
      <guid>10.4028/p-nYx3JM</guid>
      <description>Publication date: 19 June 2026
&lt;br /&gt;Source: Advances in Science and Technology Vol. 179
&lt;br /&gt;Author(s): Passanun Chuangjaroen, Sutinee Girdthep
&lt;br /&gt;This study investigated the feasibility of using hydrogels based on 2-acrylamido-2-methylpropane sulfonic acid sodium salt (AMPS-Na⁺) as rigid solvent gels for cleaning art surfaces. Hydrogels were synthesized from AMPS-Na⁺ (10–50 %w/v) using ethylene glycol dimethacrylate (EGDM, 0.05–0.25 mol%) as a crosslinker and 2,2′-azobis (2-methylpropionamidine) dihydrochloride (CPAD, 0.05–0.25 mol%) as an initiator under UV irradiation. The gel formation, swelling capacity, and water retention were evaluated to determine the optimal composition. Results showed that 50% AMPS combined with 0.25 mol% EGDM and 0.25 mol% CPAD produced a stable, transparent hydrogel with excellent swelling ability (6,793%) and structural uniformity. FTIR spectra confirmed successful copolymerization of AMPS, EGDM, and CPAD, maintaining functional groups such as –SO₃⁻ and C=O without chemical degradation. DSC thermograms revealed improved thermal stability and homogeneity at higher CPAD concentrations. The optimized hydrogel exhibited high water uptake, controlled evaporation, and reusability, suggesting strong potential as a safe and effective cleaning.
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      <pubDate>Fri, 19 Jun 2026 00:00:00 +0200</pubDate>
      <feedDate>Fri, 3 Jul 2026 01:19:40 +0200</feedDate>
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      <title>Polyvinyl Alcohol/ Cinnamon Essential Oils-Loaded Porous Rice Starch Composite Film for Active Food Packaging with Slow Release</title>
      <link>https://www.scientific.net/AST.179.23</link>
      <guid>10.4028/p-a1JVjJ</guid>
      <description>Publication date: 19 June 2026
&lt;br /&gt;Source: Advances in Science and Technology Vol. 179
&lt;br /&gt;Author(s): Elok Pawening Maharani, Priyanto Triwitono, Yudi Pranoto, Djagal Wiseso Marseno
&lt;br /&gt;Porous starch (PS) was used as a carrier agent for cinnamon essential oil (CEO) for the development of an active food packaging film. This study aimed to investigate polyvinyl alcohol (PVA), PVA incorporated with CEO (PVA-CEO), and a composite PVA film enriched with PS loaded with CEO (PVA-PSCEO). The results showed that the PVA-PSCEO film exhibited a tensile strength (TS) of 24.48 ± 0.70 MPa, an elongation at break (EAB) of 365.94 ± 6.76%, and a water vapor permeability (WVP) of 4.3523×10⁻⁸± 3.1008×10⁻⁸ gH2O.m/m²·h·Pa. The PVA-PSCEO significantly increased thickness and UV-protection ability compared with PVA and PVA-CEO. The CEO release profile of the PVA-PSCEO film also demonstrated a slow-release behavior. Films containing either CEO or PS-CEO both exhibited antioxidant activity and antimicrobial properties. SEM analysis revealed that the loading of CEO into PS improved the dispersion of CEO within the film. FTIR spectra indicated the presence of interactions among PVA, PS, and CEO. Therefore, this slow-release active film shows strong potential for food packaging applications.
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      <pubDate>Fri, 19 Jun 2026 00:00:00 +0200</pubDate>
      <feedDate>Fri, 3 Jul 2026 01:19:40 +0200</feedDate>
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      <title>Encapsulation of Cold-Pressed Avocado Oil Using Beta-Cyclodextrin: Study of Physical and Chemical Properties</title>
      <link>https://www.scientific.net/AST.179.31</link>
      <guid>10.4028/p-BuWb3D</guid>
      <description>Publication date: 19 June 2026
&lt;br /&gt;Source: Advances in Science and Technology Vol. 179
&lt;br /&gt;Author(s): Viwat Simmasood, Rittichai Assawarachan, Thitiphan Chimsook
&lt;br /&gt;This study aimed to develop β-cyclodextrin (β-CD) microcapsules containing cold-pressed avocado oil (AO) using an optimized co-precipitation method. The AO was extracted by cold pressing, yielding 31.12%. Prior to microencapsulation, the antioxidant activity and total phenolic content of AO were analyzed, showing an antioxidant activity of 85.25 ± 1.22% and a total phenolic content of 95.34 ± 1.10 mg GAE/L of oil. The effect of varying ethanol concentrations (30%, 40%, 60%, 80%, and 100% v/v) on encapsulation efficiency was systematically investigated. Using β-cyclodextrin as the encapsulating agent and 80% ethanol produced the highest encapsulation performance, with a microcapsule recovery yield of 89.45 ± 0.71% and an encapsulation efficiency of 75.25 ± 0.54% for AO. Characterization of the AO-β-cyclodextrin inclusion complex by scanning electron microscopy (SEM), Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), and thermal analysis revealed notable changes in spectra and thermal profiles, confirming the formation of the inclusion complex. The antioxidant activity and total phenolic content of the microcapsules prepared with 80% ethanol and an AO-to-β-cyclodextrin ratio of 1:0.5 w/w were evaluated after 1.5 months of storage. The results demonstrated the antioxidant activity and total phenolic content of 87.01±0.54% and 98.29±0.19 mg GAE/L of oil, respectively. The results indicated that the microcapsules effectively stabilized AO. These findings suggest that the AO-β-cyclodextrin inclusion complex is a promising bioactive system for the development of functional foods and cosmetic formulations.
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      <pubDate>Fri, 19 Jun 2026 00:00:00 +0200</pubDate>
      <feedDate>Fri, 3 Jul 2026 01:19:40 +0200</feedDate>
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      <title>Asymmetric Titanium Dioxide-Polylactic Acid Membranes for Microfiltration and Photocatalytic Dye Removal</title>
      <link>https://www.scientific.net/AST.179.41</link>
      <guid>10.4028/p-P0aBn5</guid>
      <description>Publication date: 19 June 2026
&lt;br /&gt;Source: Advances in Science and Technology Vol. 179
&lt;br /&gt;Author(s): Khor Yee Chow, Amira Mohd Nasib, Enche Ab Rahim Siti Kartini, Mohamad Syahmie Mohamad Rasidi, Mohammad Firdaus Abu Hashim, Peng Yong Hoo
&lt;br /&gt;This research aims to fabricate and analyze asymmetric polylactic acid (PLA) membranes and evaluate their performance in the removal of methyl orange (MO) dye through a microfiltration process. The asymmetric PLA membranes were synthesized via the non-solvent induced phase separation (NIPS) method. A polymer solution containing 14 wt.% PLA dissolved in 86 wt.% N,N-dimethylacetamide (DMAc) was prepared with varying amounts of TiO₂ (0, 0.5, and 1.0 wt.%). The cast membranes were immersed in a coagulant bath consisting of methanol and distilled water in an 80:20 ratio. Several characterization methods were employed: membrane porosity was measured using the gravimetric method and hydrophilicity was assessed by water contact angle. Membrane performance was evaluated in terms of water flux and permeability under a transmembrane pressure of 1 bar, as well as the removal efficiency of methyl orange dye. In addition, the photocatalytic activity of the membranes was investigated to determine its effect on dye removal. The results showed that membrane porosity decreased with increasing TiO₂ content (from 53.7% to 45.1%), while water contact angle also decreased (from 72.7° to 56.1°), indicating improved hydrophilicity. The incorporation of TiO₂ enhanced water flux (11,526.8–14,628.4 L/m²h), permeability (5763.4–7314.2 L/m²h·bar), and methyl orange removal efficiency (65–69.8%). Furthermore, photocatalytic reactions further improved dye removal efficiency with increasing TiO₂ content (up to 84.3%).
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      <pubDate>Fri, 19 Jun 2026 00:00:00 +0200</pubDate>
      <feedDate>Fri, 3 Jul 2026 01:19:40 +0200</feedDate>
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      <title>Production and Application of Microalgae Residue-Based Biochar for Soil Amendment</title>
      <link>https://www.scientific.net/AST.179.47</link>
      <guid>10.4028/p-STk8bu</guid>
      <description>Publication date: 19 June 2026
&lt;br /&gt;Source: Advances in Science and Technology Vol. 179
&lt;br /&gt;Author(s): Farah Aina Abdullah, Umi Fazara Md Ali, Nor Ashikin Ahmad, Mohd Irfan Hatim Mohamed Dzahir, Nur Hidayah Azmi
&lt;br /&gt;This study investigates the production and application of biochar derived from Nannochloropsis gaditana residue for sustainable soil amendment. Pyrolysis conditions were optimized by varying temperature and residence time: 300°C for 30 minutes (Sample A), 500°C for 60 minutes (Sample B), and 700°C for 90 minutes (Sample C). Biochar characterization included SEM (morphology), FTIR (functional groups), pH analysis, and ICP-MS (trace elements). Sample B, produced at 500°C for 60 minutes, showed the most favorable properties; high porosity, balanced functional groups, and optimal alkalinity (pH 9.41). Sample C was highly porous and alkaline (pH 9.83) but lacked reactive groups, while Sample A retained labile nutrients with moderate porosity and pH (7.64). These results demonstrate the potential of microalgae-based biochar to improve nutrient-poor, acidic soils and support environmentally friendly alternatives to chemical fertilizers in Malaysia.
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      <pubDate>Fri, 19 Jun 2026 00:00:00 +0200</pubDate>
      <feedDate>Fri, 3 Jul 2026 01:19:40 +0200</feedDate>
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      <title>The Application of Magnesium Nitrate Hexahydrate/Carrot Nanocellulose/ Graphene-Based Phase Change Aerogel in Solar Thermal Energy Storage</title>
      <link>https://www.scientific.net/AST.179.55</link>
      <guid>10.4028/p-2eZOWn</guid>
      <description>Publication date: 19 June 2026
&lt;br /&gt;Source: Advances in Science and Technology Vol. 179
&lt;br /&gt;Author(s): Yeng Fong Shih, Wen Ying Lin, Tzu Min Wu, Teng Hsiang Hsu
&lt;br /&gt;In this study, flexible aerogels were fabricated using carrot cellulose nanofibers (CCNF) combined with graphene oxide (GO) or reduced graphene oxide (RGO). GO was thermally treated to produce RGO in order to enhance the material's thermal conductivity, while retaining some functional groups that react with CCNF to form the aerogel. The 3D porous structure of these aerogels effectively supports phase change materials (PCMs). Magnesium nitrate hexahydrate (MNH) was then adsorbed onto the aerogels as the PCM to form the phase change aerogels. These phase change aerogels can adsorb up to 96.0% of MNH, and their phase change enthalpy reaches 100.9 J/g. The thermal conductivity of the aerogels is 0.4021 W/m·K, and the photothermal conversion storage efficiency reaches 0.591. Therefore, this composite phase change material, with its outstanding photothermal conversion and storage properties, shows promising potential for use as a solar thermal energy storage material.
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      <pubDate>Fri, 19 Jun 2026 00:00:00 +0200</pubDate>
      <feedDate>Fri, 3 Jul 2026 01:19:40 +0200</feedDate>
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      <title>Material and Geometric Design of Helical and Finned Tube Heat Exchangers for Ice Thermal Energy Storage in Infrastructure Cooling</title>
      <link>https://www.scientific.net/AST.179.63</link>
      <guid>10.4028/p-89BuDR</guid>
      <description>Publication date: 19 June 2026
&lt;br /&gt;Source: Advances in Science and Technology Vol. 179
&lt;br /&gt;Author(s): Suppawut Laohachote, Jetsadaporn Priyadumkol
&lt;br /&gt;Ice thermal energy storage offers an effective solution for sustainable infrastructure cooling by producing ice during off-peak hours and utilizing the stored cooling during peak demand. The performance of such systems is strongly influenced by the geometry and material selection of the embedded heat exchangers, which determine heat transfer, durability, and fabrication feasibility. This study presents a novel direct comparison of helical and finned tube coils under identical operating conditions, rarely addressed in prior ITES research. Both configurations, fabricated from copper tubing, were tested in a 200-liter insulated tank using water as the secondary refrigerant. Performance was evaluated through ice formation rate, cooling capacity delivery, and overall efficiency. The helical coil consistently outperformed the finned tube coil, producing more uniform ice distribution, a greater ice mass of 58.4 kilograms compared with 49.83 kilograms, and an extended cooling duration of 5 hours and 30 minutes compared with 4 hours and 15 minutes. The originality of this work lies in isolating coil geometry effects on ITES performance, offering reproducible evidence for design optimization. Limitations include the use of a single refrigerant and a laboratory-scale system, which may affect scalability to real applications. Nevertheless, the findings provide practical guidance for selecting coil designs that improve efficiency and reliability in infrastructure cooling systems.
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      <pubDate>Fri, 19 Jun 2026 00:00:00 +0200</pubDate>
      <feedDate>Fri, 3 Jul 2026 01:19:40 +0200</feedDate>
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      <title>Thermal Mechanical Performance Mapping of Insulation Material under Extreme Desert Conditions: A Modeling-Based Comparative Study</title>
      <link>https://www.scientific.net/AST.179.69</link>
      <guid>10.4028/p-7Esi1G</guid>
      <description>Publication date: 19 June 2026
&lt;br /&gt;Source: Advances in Science and Technology Vol. 179
&lt;br /&gt;Author(s): Abeer Abdullah Al Anazi
&lt;br /&gt;Lightweight modular buildings deployed in desert environments operate under severe climatic stress, facing extreme daytime temperatures, large diurnal swings and intense solar radiation. These conditions drive continuous heat ingress into the interior and impose thermal fatigue on the building envelope. While insulation materials are typically selected based on steady-state thermal conductivity values, these metrics do not capture transient heat penetration, thermal lag or the mechanical response induced by cyclic temperature loads. This work presents a thermal–mechanical performance-mapping framework that evaluates insulation materials under realistic desert boundary conditions. A multilayer cabin wall is modeled using measured Kuwait summer temperature cycles and solar-equivalent heat flux. Transient one-dimensional heat-transfer analysis is combined with thermo-elastic stress estimation to evaluate polyurethane foam, polyisocyanurate, expanded polystyrene and mineral wool. Dynamic indicators—including interior temperature moderation, thermal lag and normalized daily heat gain—are used to compare performance. The findings reveal substantial discrepancies between laboratory-rated and climate-specific behavior and highlight the need for integrated evaluation when selecting insulation for buildings in extreme climates.
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      <pubDate>Fri, 19 Jun 2026 00:00:00 +0200</pubDate>
      <feedDate>Fri, 3 Jul 2026 01:19:40 +0200</feedDate>
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      <title>Investigation of Membrane Thickness Effects on PEM Fuel Cell Performance Using OpenFOAM</title>
      <link>https://www.scientific.net/AST.179.77</link>
      <guid>10.4028/p-sMLY89</guid>
      <description>Publication date: 19 June 2026
&lt;br /&gt;Source: Advances in Science and Technology Vol. 179
&lt;br /&gt;Author(s): Chayanid Seanglumlert, Arom Boekfah, Machimontorn Promtong, Yodsadej Kanokmedhakul, Wonsiri Punurai, Chakrit Suvanjumrat
&lt;br /&gt;This study investigates the effect of membrane thickness on proton exchange membrane fuel cell (PEMFC) performance through high-fidelity computational fluid dynamics (CFD) simulations using the open-source platform OpenFOAM. Seven membranes with thicknesses of 20, 25, 30, 40, 50, 127, and 183 μm were evaluated to generate polarization and power density characteristics. Results reveal that membrane thickness exerts a substantial influence on PEMFC efficiency, with thinner membranes reducing ohmic resistance and enhancing proton conductivity, albeit with trade-offs related to water management and gas crossover. The findings underscore the necessity of optimizing membrane thickness to achieve an optimal balance between efficiency, durability, and operational stability, offering valuable insights for the design and development of next-generation PEMFC systems.
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      <pubDate>Fri, 19 Jun 2026 00:00:00 +0200</pubDate>
      <feedDate>Fri, 3 Jul 2026 01:19:40 +0200</feedDate>
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      <title>Effects of Electrolyte Salt on the 15°C Performance of a SiOx–C Negative Electrode for Lithium-Ion Batteries</title>
      <link>https://www.scientific.net/AST.179.85</link>
      <guid>10.4028/p-8Lfsqh</guid>
      <description>Publication date: 19 June 2026
&lt;br /&gt;Source: Advances in Science and Technology Vol. 179
&lt;br /&gt;Author(s): Yeongung Cho, Soon Ki Jeong
&lt;br /&gt;Silicon oxide–carbon (SiOx–C) negative electrodes exhibit diminished performance at reduced temperature. This study isolates the role of electrolyte salt in EC/DMC half‑cells by holding the electrode formulation, separator, potential window, and current density constant and comparing 25°C and 15°C. Galvanostatic profiles and electrochemical impedance spectroscopy were used to quantify polarization, capacity, and interfacial resistance. On lowering to 15°C, all salts showed increased polarization; the severity followed LiCF3SO3 ≳ LiClO4 &amp;gt; LiPF6 ≫ LiBF4. Nyquist spectra exhibited the same ordering in the growth of the mid‑frequency arc. At 25°C, the durable capacity ranking was LiBF4 &amp;gt; LiPF6 &amp;gt; LiClO4 &amp;gt; LiCF3SO3. Under the fixed protocol, capacities at 15°C collapsed toward low values for all salts, indicating a kinetic penalty sufficient to trigger premature voltage cutoffs. LiBF4 minimized the increase in interfacial resistance but did not preserve capacity at 15°C. The data show salt-dependent low-temperature kinetics in SiOx–C and indicate that operation near 15°C requires lower current density, adjusted potential windows, or deliberate control of interphase and solvation chemistry.
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      <pubDate>Fri, 19 Jun 2026 00:00:00 +0200</pubDate>
      <feedDate>Fri, 3 Jul 2026 01:19:40 +0200</feedDate>
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