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COMPOSITES PART A-APPLIED SCIENCE AND MANUFACTURING · 2025 · IF 8.9

Organic-Inorganic hybrid polymeric flame retardant coating for fire safety rigid polyurethane foam

Hongliang Ding,Chuanshen Wang,Jue Wang,Lini Wu,Na Sun,Hongfei He,Lu Liu,Wei Wang,Keqing Zhou,Wei Zhang,Bin Yu

Rigid polyurethane foams (RPUFs) are widely used for their excellent performance but are limited by their flammability. Flame-retardant coatings are an effective solution to address this issue without compromising their mechanical properties. Herein, flame-retardant copolymer poly(HBA-co-VBS) is synthesized via radical copolymerization of hydroxybutyl acrylate (HBA) and sodium 4-vinylbenzenesulfinate (VBS). A series of transition metal oxide-loaded halloysite nanotubes (Mo-HNTs, Co-HNTs) and hexagonal boron nitride (Mo-BN, Co-BN) are synthesized via impregnation method to prepare organic–inorganic hybrid flame-retardant coatings. The coated RPUFs reach V-0 rating in the UL-94 test with higher LOI over 31 %. Co-HNTs sample exhibits the best flame-retardant performance with the lowest PHRR (142.5 kW m −2 ) and lowest THR (49.9 MJ m −2 ). Inorganic nanoparticles reduce toxic gas emissions, especially CO emission, due to the catalysis effect of Mo and Co. This research provides a novel approach to design high-performance flame-retardant coatings.

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SEPARATION AND PURIFICATION TECHNOLOGY · 2024 · IF 8.1

Development of efficient CO2 adsorbents: Synthesis and performance evaluation of dopamine-modified halloysite nanotubes loaded with ZIF-8

Shuqian Meng,Xiaoqian Ju,Jingwen Wang,Baolu Cui,Yuxi Liu,Haosheng Ma,Dechao Wang,Zhiyuan Yang

Carbon capture, utilization, and storage (CCUS) is a crucial technology for achieving carbon reduction targets. The key to CCUS technology lies in developing and designing efficient and low-cost CO 2 capture materials. Metal-organic frameworks (MOFs) have emerged as promising CO 2 adsorbents in the field of carbon capture. However, high agglomeration of nanoparticles and high cost have severely hindered the application of MOF-based solid adsorbents. This study employs an in-situ growth method to prepare a novel “corncob-shaped” PHNT@ZIF-8 composite material. During the reaction process, surface modification of halloysite nanotubes (HNT) enhances the interaction between HNT and ZIF-8. The resulting PHNT@ZIF-8 exhibits an enhanced CO 2 adsorption capacity of 1.48 mmol/g. Notably, the functionalized PHNT@ZIF-8 as CO 2 adsorbents demonstrated significant adsorption properties: a high specific surface area of 409.74 m 2 /g, good selectivity in simulated flue gas composition of 15%/85% (CO 2 /N 2 ) (39.1), excellent thermal stability, and superior regenerability. Moreover, PHNT@ZIF-8 adsorbs CO 2 primarily through van der Waals forces, which involve low energy and are easily reversible. After eight adsorption–desorption cycles, CO 2 capacity retention rate remains as high as 93% (1.37 mmol/g). This work enriches the repertoire of solid CO 2 composite adsorbents, providing a novel pathway for enhancing CO 2 adsorption performance.

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ANALYST · 2024 · IF 3.6

Curcumin/kaolin composite for advanced latent fingerprint imaging with fluorescence quantification

Jiujiang Wang,Dawu Li,Jianghua Zhang,Zijian Gao,Jinke Han

Latent fingerprints (LFPs) are invisible impressions that need to be developed before being used for criminal investigation; however, existing fingerprint visualization techniques face challenges, such as complex preparation and poor contrast. To advance practical fingerprint detection, green-emissive micron-sized curcumin/kaolin composites were synthesized via a facile and cost-effective one-step physical cross-linking method, which exhibited unprecedented performance in developing diversified marks, including LFPs, knuckle prints, palm prints, and footprints, with clear three-level details on various substrates. Notably, the powders successfully developed LFPs that were aged for 30 days and even up to 100 days, meeting the stringent requirements for comprehensive forensic application. Afterward, a novel method, termed Fingerprint Fluorescence Intensity Ratio (FFIR), was developed to quantify the contrast between fingerprint signals and background noise and to compare the efficacy of full-color developing agents. Compared with the existing grayscale conversion strategy, the proposed FFIR method achieved tunable multi-color fingerprint image enhancement for the first time, which helped to eliminate background fluorescence interference and improved visual perception. The feasibility of FFIR and its sensitivity in tracking image capture parameters were demonstrated by the established mathematical model. Hence, the newly synthesized modified composites and the mathematical model-validated method demonstrate profound practical significance in comprehensive fingerprint imaging.

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ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH · 2024 ·Vol. 31 ·期 20 ·29232-29245 · IF 0

Effects of tire–road wear particles on the adsorption of tetracycline by aquatic sediments

Fan Xiulei,Cao Binwen,Wang Shenpeng,Li Huixian,Zhu Mingxian,Sha Haidi,Yang Yangyang

Tire–road wear particles (TRWPs) are formed by friction between the tire and the road. TRWPs are ubiquitous across the globe, especially in sediments. However, the possible effects of TRWPs on tetracycline (TC) in aquatic sediments are unknown. To investigate the potential role of TRWPs as carriers of co-pollutants, this study investigated the pore surface properties and TC adsorption behavior of TRWP-contaminated sediments and explored the TC behavior in water sediments, as well as the role of aging processes and TRWPs abundance. The results showed that the surface morphology of TRWP-contaminated sediments changed and the adsorption capacity of sediments to TC increased. The TC adsorption capacity of sediments contaminated by 2% TRWPs increased from 3.15 to 3.48 mg/g. Moreover, the surface physical and chemical properties of TRWPs after UV aging changed, which further increased the TC adsorption capacity. The TC adsorption capacity of the sediments contaminated by aged TRWPs increased from 3.48 to 3.65 mg/g. Changing the proportion of aged TRWPs, we found that the adsorption capacity of sediments contaminated by different proportions of TRWPs for TC was 2% > 1% > 0.5% > 4% > blank sediment. These results may contribute to predicting the potential environmental risks of TRWPs in aquatic sediments.

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WATER ENVIRONMENT RESEARCH · 2024 ·Vol. 96 ·期 6 ·e11058 · IF 2.5

Catalytic ozonation of reverse osmosis membrane concentrates by catalytic ozonation: Properties and mechanisms

Wenquan Sun,Yueqian Cheng,Zhiqiang Xiao,Jun Zhou,Kinjal J. Shah,Yongjun Sun

Ni-Mn@KL ozone catalyst was prepared for the efficient treatment of reverse osmosis membrane concentrates. The working conditions and reaction mechanism of the ozone-catalyzed oxidation by Ni-Mn@KL were systematically studied. Then, a comprehensive CRITIC weighting–coupling coordination evaluation model was established. Ni-Mn@KL was characterized by scanning electron microscopy, BET, X-ray diffraction, X-ray photoelectron spectroscopy, energy-dispersive spectrometry, and X-ray fluorescence spectrometry and found to have large specific surface area and homogeneous surface dispersion of striped particles. Under the optimum working conditions with an initial pH of 7.9 (raw water), a reaction height-to-diameter ratio of 10:1, an ozone-aeration intensity of 0.3 L/min, and a catalyst filling rate of 10%, the maximum COD removal rate was 60.5%. Free-radical quenching experiments showed that OH oxidation played a dominant role in the Ni-Mn@KL-catalyzed ozone-oxidation system, and the reaction system conformed to the second-order reaction kinetics law. Ni-Mn@KL catalysts were further confirmed to have good catalytic performance and mechanical performance after repeated utilization. Practitioner Points Ni-Mn@KL catalyst can achieve effective treatment of RO film concentrated liquid. High COD removal rate of RO membrane concentrated liquid was obtained at low cost. Ni-Mn@KL catalyst promotes ozone decomposition to produce ·OH and O 2 − · oxidized organic matter. The Ni-Mn@KL catalyst can maintain good stability after repeated use. A CRITIC weight–coupling coordination model was established to evaluate the catalytic ozonation.

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JOURNAL OF THERMAL ANALYSIS AND CALORIMETRY · 2024 · IF 3

Catalytic role of various clay minerals during the thermal reaction process with oxidized and pyrolyzed oils

Luo Chen,Liu Huiqing,Zhou Song,Li Jingpeng,Li Xiang,Huang Yaowei

This study evaluated this thermal reaction behavior of oxidized and pyrolyzed oils containing diverse clay minerals by means of differential scanning calorimetry (DSC) technology. The catalytic role of various clay minerals for thermal reaction processes involving oxidized oil and pyrolyzed oil during in situ combustion (ISC) was investigated in conjunction with kinetic calculation methods as well. The results demonstrated that all four clay minerals could shorten its temperature region of oxidized oil low-temperature oxidation (LTO) stage, with the peak temperature during the LTO stage of oxidized oil containing montmorillonite being dramatically reduced. The catalytic role of montmorillonite and illite on oxidized oil is more powerful in the high-temperature oxidation (HTO) stage with higher peak heat flow. The Lewis acid sites within clay minerals affect free radical reactions within the crude oil pyrolysis process, and in situ reforming performance of 400°C pyrolyzed oils containing clay minerals is less effective, along with low heat release in the LTO stage. Clay minerals can considerably minimize the activation energy during thermal reaction of oxidized oil, contributing to the coke generation and conversion in the fuel deposition (FD) stage and boosting the success rate of the ISC procedure. The catalytic role of clay minerals in the oxidation and pyrolysis reactions of crude oil contributes to the prediction of fuel deposition and the expansion of the combustion front during ISC under diverse types of rock conditions.

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Journal of Central South University · 2024 ·Vol. 31 ·期 10 ·3382-3393 · IF 3.7

Corrosion behavior of B10 copper-nickel alloy beneath a deposit caused by sulfate-reducing bacteria with carbon source starvation in marine environments

Jin Zheng-yu,Wang Zhi,Fan Yu-xing,Liu Hai-xian,Liu Ruo-ling,Zhang Yi,Yin Yan-sheng,Liu Hong-fang,Fan Shao-jia,Liu Hong-wei

Copper-nickel alloys can suffer severe localized corrosion in marine environments containing sulfate-reducing bacteria (SRB), but the effect of SRB on the under-deposit corrosion of copper-nickel alloys is unknown. In this work, the corrosion behavior of B10 copper-nickel alloy beneath a deposit caused by SRB with carbon source starvation in artificial seawater was studied based on electrochemical measurements and surface analysis. Results demonstrate that SRB with an organic carbon starvation can survive in artificial water but most SRB cells have died. The survived SRB cells can attach to the bare and deposit-covered B10 copper-nickel alloy, leading to the corrosion acceleration. Due to the limitation of organic carbon source, the pitting corrosion of B10 copper-nickel alloy caused by SRB is not serious. However, serious pitting corrosion of the deposit-covered B10 copper-nickel alloy can be found both in abiotic and biotic conditions, and the pitting corrosion and uniform corrosion are further accelerated by SRB. There is a galvanic effect between the bare and deposit-covered specimens in the presence of SRB in the early stage but the galvanic effect after 5 d of testing can be neglected due to the low OCP difference values.

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APPLIED THERMAL ENGINEERING · 2024 · IF 6.1

A DFT-based kinetic equation for Co3O4 decomposition reaction in high-temperature thermochemical energy storage

Lei Liu,Kexin Li,Hanzi Liu,Zhiqiang Sun

Thermal energy storage supports stable grid integration of variable renewable energy sources by reducing power curtailment and generation costs. Thermochemical energy storage (TCES) offers high energy density and long-duration, long-distance storage advantages, making it a focus in large-scale applications such as concentrated solar power plants. Metal oxide systems like Co 3 O 4 /CoO are widely used due to their operational flexibility, yet limited understanding of their decomposition kinetics hinders optimization of TCES materials and reactor design. In this study, we developed a rate equation based on density functional theory and transition state theory to identify the reaction mechanisms and rate constants at the gas–solid interface, prior to predict Co 3 O 4 decomposition kinetics. A microkinetic model was then constructed to couple surface reactions with oxygen ion diffusion across the bulk, which was integrated into a reactor model accounting for mass transfer steps. The model’s accuracy was validated against the data from the micro-fluidized bed thermogravimetric analyzer experiments. For particles smaller than 150 μm, the formation step of adsorbed O 2 (energy barrier of 0.8 eV) controls the reaction rate, while gas diffusion dominates the reaction rate for particles larger than 500 μm. To conclude, the optimal conditions for maximizing charge–discharge kinetics in TCES applications were identified as: 850–900 °C, 0–10 vol% O 2 , and 150–500 μm. This model provides theoretical guidance for optimizing TCES materials and reactor design, reducing experimental costs while maintaining accuracy.

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Desalination and Water Treatment · 2024 · IF 1

Adsorption of Cr(VI) from aqueous solutions using inorganic clays modified magnetic chitosan adsorbent: Kinetic and thermodynamic study

Jinfeng Yuan,Weidong Lu

Inorganic clays modified magnetic chitosan adsorbent (ICMMCA) was successfully prepared and systematically characterized in chemical structure and morphology. Effect of variables including initial pH and concentration of Cr(VI) in the solution, adsorption time, adsorption temperature and coexisting ions on the performance of ICMMCA in Cr(VI) removal from water were evaluated. Furthermore, the kinetic and thermodynamic studies were conducted to elucidate the adsorption mechanisms and thermodynamic characteristics of the adsorption process. The results demonstrated that the maximum Cr(VI) adsorption capacity of 94.67 mg/g could be achieved when the adsorbent loading was 1 g/L, the initial concentration of Cr(VI) was 100 mg/L, the adsorption time was 60 min and solution pH was at 5. The adsorption data could be well fitted by the Freundlich isotherm model. The thermodynamic parameters indicated that the adsorption process was spontaneous and endothermic in nature. The adsorption process could be described by the pseudo-second-order kinetic model.

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RARE METALS · 2025 · IF 11

Adsorption of rare earth elements and aluminum on the surface of kaolinite: insights from sequential chemical extractions, XAFS, and DFT

Pan Jia-Xin,Zhao Long-Sheng,Li Zheng,Feng Zong-Yu,Liu De-Peng,Chen Jun,Huang Xiao-Wei

To achieve selective leaching of ion adsorption rare earth, it is necessary to thoroughly reveal the differences in the adsorption mechanisms of aluminum and rare earth elements. In this study, we investigated the adsorption processes of Dy and Al on the surface of K–homoionic kaolinite using batch experiments and sequential chemical extractions. The results revealed that the adsorption of Dy and Al, as well as the desorption of K, followed the Langmuir model. The maximum ion-exchangeable capacity of Dy was higher (9.39 mmol·kg −1 ) than that of Al (6.30 mmol·kg −1 ). The ion exchange stoichiometry ratios of Dy–K and Al–K derived from the Langmuir model were 2.0 and 2.6. The analysis of X-ray absorption fine structure (XAFS) and density functional theory (DFT) revealed that Dy and Al were adsorbed onto kaolinite as outer-sphere hydrated complexes via hydrogen bonds. Dy was adsorbed as [Dy(H 2 O) 10 ] 3+ , and Al was adsorbed as [Al(OH) 2 (H 2 O) 4 ] + . In particular, the adsorption of Al resulted in protonation of the hydroxyl groups on the surface of the kaolinite. Based on the above insights, the higher ion exchange stoichiometry ratios are attributed to closer adsorption distances (6.04 Å for Dy and 3.69 Å for Al) and lower adsorption energies (− 223.72 kJ·mol −1 for Dy and − 268.33 kJ·mol −1 for Al). The maximum ion-exchangeable capacity is related to the change of the surface electrical properties of kaolinite. The zeta potential was increased to − 7.3 mV as the protonation resulted from aluminum adsorption, while Dy adsorption had a minor effect, maintaining a value of − 17.5 mV. Graphical abstract

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ANTI-CORROSION METHODS AND MATERIALS · 2024 ·Vol. 71 ·期 5 ·514-528 · IF 2.3

Anti-corrosive superhydrophobic coatings for reinforcement protection: recycling of concrete garbage

Xiaohu Wen,Xiangkang Cao,Xiao-ze Ma,Zefan Zhang,Zehua Dong

PurposeThe purpose of this paper was to prepare a ternary hierarchical rough particle to accelerate the anti-corrosive design for coastal concrete infrastructures.Design/methodology/approachA kind of micro-nano hydrophobic ternary microparticles was fabricated from SiO2/halloysite nanotubes (HNTs) and recycled concrete powders (RCPs), which was then mixed with sodium silicate and silane to form an inorganic slurry. The slurry was further sprayed on the concrete surface to construct a superhydrophobic coating (SHC). Transmission electron microscopy and energy-dispersive X-ray spectroscopy mappings demonstrate that the nano-sized SiO2has been grafted on the sub-micron HNTs and then further adhered to the surface of micro-sized RCP, forming a kind of superhydrophobic particles (SiO2/HNTs@RCP) featured of abundant micro-nano hierarchical structures.FindingsThe SHC surface presents excellent superhydrophobicity with the water contact angle >156°. Electrochemical tests indicate that the corrosion rate of mild steel rebar in coated concrete reduces three-order magnitudes relative to the uncoated one in 3.5% NaCl solution. Water uptake and chloride ion (Cl-) diffusion tests show that the SHC exhibits high H2O and Cl-ions barrier properties thanks to the pore-sealing and water-repellence properties of SiO2/HNTs@RCP particles. Furthermore, the SHC possesses considerable mechanical durability and outstanding self-cleaning ability.Originality/valueSHC inhibits water uptake, Cl-diffusion and rebar corrosion of concrete, which will promote the sustainable application of concrete waste in anti-corrosive concrete projects.

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SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY · 2024 · IF 4.3

A novel turbidity compensation method for fluorescence spectroscopy and application in the detection of two algae species

Ruizhuo Li,Jing Dong,Guojun Wu,Limin Gao,Min Yang

Turbidity interference in measurements can reduce the accuracy of fluorescence detection. Conventional turbidity compensation methods directly establish the relationship between turbidity value and fluorescence but cannot accurately characterize the complex interference of turbidity on fluorescence detection. This paper introduces a novel turbidity compensation technique that separates the interference caused by turbidity particles into scattering intensifying and scattering-absorption attenuating components and corrects them separately. First, the scattering spectrum overlapping with fluorescence is estimated and subtracted from the actual sample spectrum to mitigate the fluorescence intensification caused by scattering. Then, attenuation coefficients at different turbidity intervals are calculated to compensate for fluorescence attenuation. Finally, the two components are combined to obtain the final corrected result. Based on the proposed method, the fluorescence spectra data of Platymonas helgolandica var. tsingtaoensis and Synechococcus elongatus undeod is evaluated. The core problem for comper different turbidity interferences were analyzed. Intensifying and attenuating coefficients based on turbidity values and scattering spectra were determined, ensuring adaptability to known and unknown turbidity conditions. The study results show that the fluorescence variation at different concentrations and turbidity levels are influenced by sample concentration and turbidity, exhibiting nonlinear behavior. The compensation model developed was applied to experimental data, achieving a mean relative error of less than 4% and a satisfactory root-mean-square error, significantly enhancing prediction accuracy. This method offers a straightforward and rapid application to detect a wide range of fluorescent substances.

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