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Time-resolved fluorescence measurements of dissolved organic matter (DOM) as a function of environmental parameters in estuarine waters

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Environmental science and Pollution Research 2025年第4期32卷 1952-1970页

作者： de Bruyn, Warren J. Manickam, Dhivya Harrison, Aaron W. Clark, Catherine D. Chemistry and Biochemistry Program Schmid College of Science Chapman University One University Drive OrangeCA92866 United States Department of Chemistry Austin College 900 N. Grand Ave. ShermanTX75090 United States Department of Chemistry College of Science and Engineering Western Washington University 516 High Street BellinghamWA98229 United States

Fluorescent lifetimes of dissolved organic matter (DOM) and associated physicochemical parameters were measured over 14 months in an estuary in Southern California, USA. Measurements were made on 77 samples from sites near the inlet, mid-estuary, and outlet to maximize the range of physicochemical variables. Time-resolved fluorescence data were well fit to a triexponential model with an intermediate lifetime component (τ1: 1 to 5 ns), a long lifetime component (τ2: 2 to 15 ns), and a short lifetime component (τ3: © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2025.

关键词： Fluorescence quenching

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Nano-enhanced potassium biostimulants: augmenting wheat yield, antioxidant activity, and micronutrient bioavailability in arid agricultural systems

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Nanotechnology for Environmental engineering 2025年第2期10卷 1-14页

作者： Shahryari, Ali Esmaeilzadeh Bahabadi, Sedigheh Beyzaei, Hamid Mohammadi, Yasaman Nusrat, Easmin Sharifan, Hamidreza Department of Biology Faculty of Basic Sciences University of Zabol Zabol Iran Department of Chemistry Faculty of Basic Sciences University of Zabol Zabol Iran Environmental Science and Engineering Program University of Texas at El Paso El PasoTX United States Department of Chemistry and Biochemistry University of Texas at El Paso El PasoTX United States

The development of agricultural biostimulants (BS) has marked a significant advancement in bolstering crop resilience against environmental stressors. This study investigates synthesizing and applying six novel nano-based potassium (K)-enriched biostimulants that enhance micronutrient availability, nitrogen uptake, and subsequent plant growth during seed germination and developmental phases. Using Nuclear Magnetic Resonance (NMR) and Fourier-transform infrared Spectroscopy (FTIR), the synthesized biostimulants were characterized before their application in soil-supporting wheat (Triticum aestivum L.) cultivation. The biostimulants’ effects at three concentrations (0.1, 0.2, and 0.5 mmol) and were evaluated on physiological and biomolecular parameters. To assess nutrient availability, soil mineral content was analyzed via X-ray Photoelectron Spectroscopy (XPS). An increase in biostimulant concentration led to a marked rise in seed germination rates, correlating with elevated bioavailability of nitrates, ammonia, sulfur, potassium, and other key micronutrients. At a threshold concentration of 0.2 mmol, a notable improvement in the bioavailability of nutrients and a significant increase in the total phenol and flavonoid content was observed. The phenolic content was measured using the Folin-Ciocalteu method and expressed as Gallic Acid Equivalents (GAE), while flavonoids were quantified based on quercetin equivalents. These phytochemicals were correlated with enhanced antioxidant activities, measured using the Ferric Reducing Antioxidant Power (FRAP) assay. The results indicated an 80% increase in antioxidant capacity, particularly for biostimulant BS6 at the 0.2 mmol concentration. Furthermore, biostimulants demonstrated a positive effect on the elongation of radicles and plumules, contributing to improved plant vigor. Overall, the study highlights the potential of synthesized K-based biostimulants to significantly enhance crop productivity, nutrient uptake, and antio

关键词： Fourier transform infrared spectroscopy

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MXene:From synthesis to environment remediation

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Chinese Journal of Chemical engineering 2023年第9期61卷 260-280页

作者： Ali Nikkhah Hasan Nikkhah Hadis langari Alireza Nouri Abdul Wahab Mohammad Ang Wei Lun Ng law Yong Rosiah Rohani Ebrahim Mahmoudi Department of Chemical and Process Engineering Faculty of Engineering and Built EnvironmentUniversiti Kebangsaan MalaysiaBangi 43600Malaysia Department of Mechanical and Aerospace Engineering University at BuffaloBuffaloUSA Department of Chemical and Biomolecular Engineering University of ConnecticutStorrsUSA Department of Chemistry and Medicinal Chemistry University at BuffaloBuffaloUSA Chemical and Water Desalination Engineering Program College of EngineeringUniversity of SharjahSharjah 27272United Arab Emirates Lee Kong Chian Faculty of Engineering and Science Universiti Tunku Abdul RahmanJalan Sungai LongBandar Sungai LongKajangSelangorMalaysia

A new burgeoning family of two-dimensional(2D)transition metal carbides/nitrides,better known as MXenes,have received extensive attention because of their distinct properties,such as metallic conductivity,good hydrophilicity,large surface area,good mechanical stability,and *** 40 different MXenes have been synthesized,and dozens more structures and properties have been theoretically ***,the recent progress in MXenes development is not well covered in chronological order based on different *** review article focuses on emerging synthesis methods,the properties of MXenes,and mainly the applications of MXenes and MXene-based material family in environmental remediation,a comprehensive review of gaseous and aqueous pollutants treatment.

关键词： MXene 2D materials Wastewater treatment CO_(2)capture Adsorption Photodegradation

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Methacrylic acid/Tween 80 engineered amorphous calcium phosphate as an effective bioactive reinforcing nanofillers in dental adhesive

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Dental Materials Journal 2025年第2期44卷 190-200页

作者： Maimansomsuk, Siripatsorn Teangrom, Paremai Teanchai, Chayada Sinthuvanich, Chomdao Ruengket, Pakorn Attarataya, Jakrada Akkarachaneeyakorn, Khrongkhwan Department of Chemistry Faculty of Science Kasetsart University Bangkok10900 Thailand Center of Excellence for Innovation in Chemistry Faculty of Science Kasetsart University Bangkok10900 Thailand Research Center Faculty of Dentistry Mahidol University Bangkok10400 Thailand Department of Biochemistry Faculty of Science Kasetsart University Bangkok Thailand Faculty of Science Kasetsart University Bangkok Thailand Genetic Engineering and Bioinformatics Program Graduate School Kasetsart University Bangkok Thailand Nakhon Ratchasima30000 Thailand

Bioactive fillers in dental adhesives are designed to release beneficial ions, such as calcium and phosphate, to help in remineralization process, and preventing secondary caries. Their incorporation also aims to improve the longevity of dental restorations. Herein, CaP nanoparticles were synthesized through a water-in-oil emulsion method using Tween80 as a surfactant and methacrylic acid (MAA). MAA officiated as a co-surfactant and reduced the size of CaP nanoparticle, including improved compatibility with the components of dental adhesive. The incorporation of 2% T80/CaP/MAA nanofillers into dental adhesive demonstrated increased efficiency, as evidenced by a higher degree of conversion (%DC) and greater micro-tensile bond strength (μTBS). More importantly, T80/CaP/ MAA nanofillers were able to induce remineralization process in the dental structure, which was confirmed by EDX mapping and IR imaging. Finally, a cytotoxicity assessment of the dental adhesive containing T80/CaP/MAA showed no significant adverse effects on human fibroblast cells. © 2025, Japanese Society for Dental Materials and Devices. All rights reserved.

关键词： Stem cells

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Machine intelligence-accelerated discovery of all-natural plastic substitutes

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Nature Nanotechnology 2024年第6期19卷 782-791页

作者： Chen, Tianle Pang, Zhenqian He, Shuaiming Li, Yang Shrestha, Snehi Little, Joshua M. Yang, Haochen Chung, Tsai-Chun Sun, Jiayue Whitley, Hayden Christopher Lee, I-Chi Woehl, Taylor J. Li, Teng Hu, Liangbing Chen, Po-Yen Department of Chemical and Biomolecular Engineering University of Maryland College ParkMD United States Department of Mechanical Engineering University of Maryland College ParkMD United States Department of Chemistry and Biochemistry University of Maryland College ParkMD United States Department of Biomedical Engineering and Environmental Sciences National Tsing Hua University Hsinchu Taiwan Department of Materials Science and Engineering University of Maryland College ParkMD United States Maryland Robotics Center College ParkMD United States

One possible solution against the accumulation of petrochemical plastics in natural environments is to develop biodegradable plastic substitutes using natural components. However, discovering all-natural alternatives that meet specific properties, such as optical transparency, fire retardancy and mechanical resilience, which have made petrochemical plastics successful, remains challenging. Current approaches still rely on iterative optimization experiments. Here we show an integrated workflow that combines robotics and machine learning to accelerate the discovery of all-natural plastic substitutes with programmable optical, thermal and mechanical properties. First, an automated pipetting robot is commanded to prepare 286 nanocomposite films with various properties to train a support-vector machine classifier. Next, through 14 active learning loops with data augmentation, 135 all-natural nanocomposites are fabricated stagewise, establishing an artificial neural network prediction model. We demonstrate that the prediction model can conduct a two-way design task: (1) predicting the physicochemical properties of an all-natural nanocomposite from its composition and (2) automating the inverse design of biodegradable plastic substitutes that fulfils various user-specific requirements. By harnessing the model’s prediction capabilities, we prepare several all-natural substitutes, that could replace non-biodegradable counterparts as exhibiting analogous properties. Our methodology integrates robot-assisted experiments, machine intelligence and simulation tools to accelerate the discovery and design of eco-friendly plastic substitutes starting from building blocks taken from the generally-recognized-as-safe database. © The Author(s) 2024.

关键词： Neural networks

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Characterizing catalyst function and transformations in the plasma reduction of CO₂ on atomic layer deposition-synthesized catalysts

RSC Applied Interfaces

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RSC Applied Interfaces 2024年第3期1卷 552-563页

作者： Conlin, Samuel K. Mehrabi, Hamed Parette, David N. Nichols, Eva M. Coridan, Robert H. Department of Chemistry and Biochemistry University of Arkansas Fayetteville 72701 AR United States Materials Science and Engineering Program University of Arkansas Fayetteville 72701 AR United States Department of Chemistry University of British Columbia Vancouver V6T 1Z1 BC Canada

The enhancement of CO2 reduction in atmospheric-pressure, non-thermal plasma has been shown using a variety of catalyst systems with ranging composition, particle sizes, and morphologies. Improvements in CO2 conversio...

The enhancement of CO₂ reduction in atmospheric-pressure, non-thermal plasma has been shown using a variety of catalyst systems with ranging composition, particle sizes, and morphologies. Improvements in CO₂ conversion can be attained by choice of catalyst material. However, inhomogeneity in the material distribution arising from the synthesis affects the catalytically active surface area and dielectric environment that modulates the plasma properties near the catalyst. Atomic layer deposition (ALD) can be used to control the composition of ultra-thin layers on support materials. We used ALD to synthesize metal oxide catalyst coatings on high surface area supports. We found that TiO₂ achieved significantly higher yields of CO₂ conversion (to CO and O₂) at low reactor power compared to ZnO or Al₂O₃, materials commonly used as a support for other catalysts. We also observed an unexpected increase in the catalytic activity on ZnO with increasing power. The results here suggest that ALD can unambiguously isolate the catalytic effects of materials in plasma reactors. © 2024 RSC.

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Pt_(1)/Ni_(6)Co_(1)layered double hydroxides/N-doped graphene for electrochemical non-enzymatic glucose sensing by synergistic enhancement of single atoms and doping

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Nano Research 2023年第1期16卷 318-324页

作者： Baojun Long Peiyu Cao Yuanmeng Zhao Qianqian Fu Yan Mo Yueming Zhai Juejing Liu Xingyi Lyu Tao Li Xiaofeng Guo Changsheng Shan Minghua Zeng Ministry-of-Education Key Laboratory for the Synthesis and Application of Organic Functional Molecules College of Chemistry and Chemical EngineeringHubei UniversityWuhan 430062China Key Laboratory for the Chemistry and Molecular Engineering of Medicinal Resources School of Chemistry and Pharmaceutical SciencesGuangxi Normal UniversityGuilin 541004China The Institute for Advanced Studies(IAS) Wuhan UniversityWuhan 430072China Material Science and Engineering Program Washington State UniversityPullmanWA 99164USA Department of Chemistry and Alexandra Navrotsky Institute for Experimental Thermodynamics Washington State UniversityPullmanWA 99164USA X-ray Science Division Argonne National LaboratoryArgonneIL 60439USA Department of Chemistry and Biochemistry Northern Illinois UniversityDeKalbIL 60115USA

The development of novel single-atom catalysts is important for highly efficient electrochemical catalysis and *** this work,a novel Pt single atoms(SAs)supported on Ni_(6)Co_(1)layered double hydroxides/nitrogen-doped graphene(Pt_(1)/Ni_(6)Co_(1)LDHs/NG)was constructed for electrochemical enzyme-free catalysis and sensing towards *** loading of Pt single atoms increases with doping of Co atoms that generate more anchoring sites for Pt *** resulting Pt_(1)/Ni_(6)Co_(1)LDHs/NG exhibits low oxidative potential of 0.440 V with high sensitivity of 273.78μA·mM^(−1)·cm^(−2)toward glucose,which are 85 mV lower and 15 times higher than those of Ni(OH)_(2),***_(1)/Ni_(6)Co_(1)LDHs/NG also shows excellent selectivity and great stability during 5-week *** and experimental results show that the boosted performance of Pt_(1)/Ni_(6)Co_(1)LDHs/NG originates from its stronger binding energy with glucose and the synergistic effect of Pt SAs,Co doping,and *** work provides a general strategy of designing highly active SACs for extending their application in electrochemical sensing.

关键词： single-atom catalysts electrochemical sensor layered double hydroxides nitrogen-doped graphene synergistic effect

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NGenE 2022: Electrochemistry for Decarbonization

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ACS ENERGY LETTERS 2023年第1期8卷 740-747页

作者： Cabana, Jordi Alaan, Thomas Crabtree, George W. Huang, Po-Wei Jain, Akash Murphy, Megan N'Diaye, Jeanne Ojha, Kasinath Agbeworvi, George Bergstrom, Helen Gersib, Simon Harb, Hassan Stejer, Adrien Quiles-Galarza, Genesis Rodriguez, Oliver Caruso, Isabella Goncalves, Josue M. Chen, Grace Y. Fernandez, Carlos A. Pan, Hanqing Ritter, Kabian Yang, Yingjie Zhang, Haozhe Garcia-Alvarez, Ana Cristina Ilic, Stefan Kumar, Khagesh Silcox, Rachel Yao, Yu Song, Hakhyeon Stoyanov, Stoyan Saraf, Mohit Chen, Celine H. Subasinghe, S. M. Supundrika Gomes, Reginaldo Lang, Shuangyan Murphy, Eamonn Thind, Arashdeep Singh Zheng, Yu Department of Chemistry University of Illinois at Chicago Chicago Illinois 60607 United States Department of Physics University of Illinois at Chicago Chicago Illinois 60607 United States Joint Center for Energy Storage Research Argonne National Laboratory Lemont Illinois 60439 United States School of Chemical & Biomolecular Engineering Georgia Institute of Technology Atlanta Georgia 30332 United States Materials Science Division Argonne National Laboratory Lemont Illinois 60439 United States Department of Chemistry Beckman Institute for Advanced Science University of Illinois at Urbana−Champaign Urbana−Champaign Urbana Illinois 61801 United States Department of Chemistry and Biochemistry University of Oregon Eugene Oregon 97403-1253 United States Department of Chemistry Texas A&M University College Station Texas 77843-3255 United States Department of Chemical and Biomolecular Engineering University of California Berkeley California 94720 United States Department of Chemical and Biomolecular Engineering University of California Irvine California 92697 United States Department of Chemical and Biomolecular Engineering University of Pennsylvania Philadelphia Pennsylvania 19104 United States Department of Materials Science and Engineering Massachusetts Institute of Technology Cambridge Massachusetts 02139 United States Department of Mechanical and Industrial Engineering University of Illinois at Chicago Chicago Illinois 60607 United States Division of Chemistry and Chemical Engineering California Institute of Technology Pasadena California 91125 United States George W. Woodruff School of Mechanical Engineering Georgia Institute of Technology Atlanta Georgia 30332 United States Department of Chemistry University of Nevada Reno Nevada 89557 United States Department of Chemistry University of California Davis Davis California 95616 United States Pritzker School of Molecular Engineering The University of Chicago Chicago Illinois 60637 United State

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A Coordinated-Anion-Enriched Electrolyte for Lean-Electrolyte Li-S Batteries (vol 9, pg 3869, 2024)

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ACS ENERGY LETTERS 2024年第9期9卷 4524-4525页

作者： Qin, Kaiqiang Li, Shi Yen, Dean Zhang, Weiran Yang, Zhenzhen Kamphaus, Ethan Phillip Kim, Eric Youngsam Huang, Jinghao Shea, John J. Hu, Enyuan Cheng, Lei Wang, Chunsheng Luo, Chao Department of Chemistry and Biochemistry George Mason University Fairfax Virginia 22030 United States Materials Science Division Argonne National Laboratory Lemont Illinois 60439 United States Chemistry Division Brookhaven National Laboratory Upton New York 11973 United States Department of Chemical and Biomolecular Engineering University of Maryland College Park Maryland 20742 United States Chemical Sciences and Engineering Division Argonne National Laboratory Lemont Illinois 60439 United States Department of Chemical Environmental and Materials Engineering University of Miami Coral Gables Florida 33146 United States Chemical Sciences Division Oak Ridge National Laboratory Oak Ridge Tennessee 37831 United States Quantum Science & Engineering Center George Mason University Fairfax Virginia 22030 United States

The solid electrolyte interphase (SEI) on Li and cathode electrolyte interphase (CEI) at sulfurized polyacrylonitrile (SPAN) formed in the commonly used liquid electrolytes cannot accommodate the large volume change of both Li anode and SPAN cathode, resulting in severe electrolyte and Li consumption and fast capacity decay under high mass loading and lean electrolyte conditions. Herein, a LiF-rich SEI and a LiF–LixNyOzcoenriched CEI are simultaneously formed by adding ionic liquid (Py13TFSI) in the localized high-concentration electrolyte (LHCE), which forms a coordinated-anion-enriched solvation structure. The LiF-rich interphase results in less stress/strain during large volume changes of Li and SPAN, therefore achieving obviously improved stability even at a high areal capacity. Consequently, Li (50 μm)||SPAN (6 mg cm–2) pouch cells under the lean electrolyte conditions (E/S ratio of 5 mL gSPAN–1) deliver a stable cycle life of 120 cycles with 79.2% capacity retention, demonstrating great promise for high-energy-density lithium–sulfur batteries.

关键词： Cathodes

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21-Component compositionally complex ceramics: Discovery of ultrahigh-entropy weberite and fergusonite phases and a pyrochlore–weberite transition

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Journal of Advanced Ceramics 2022年第4期11卷 641-655页

作者： Mingde QIN Heidy VEGA Dawei ZHANG Sarath ADAPA Andrew J.WRIGHT Renkun CHEN Jian LUO Department of Nano Engineering University of California San DiegoLa Jolla 92093USA Department of Chemistry and Biochemistry University of California San DiegoLa Jolla 92093USA Program of Materials Science and Engineering University of California San DiegoLa Jolla 92093USA Department of Mechanical and Aerospace Engineering University of California San DiegoLa Jolla 92093USA

Two new high-entropy ceramics(HECs)in the weberite and fergusonite structures,along with the unexpected formation of ordered pyrochlore phases with ultrahigh-entropy compositions and an abrupt pyrochlore–weberite transition,are discovered in a 21-component oxide *** the Gibbs phase rule allows 21 equilibrium phases,9 out of the 13 compositions examined possess single HEC phases(with ultrahigh ideal configurational entropies:~2.7kB per cation or higher on one sublattice in most cases).Notably,(15RE_(1/15))(Nb_(1/2)Ta_(1/2))O_(4) possess a single monoclinic fergusonite(C2/c)phase,and(15RE_(1/15))_(3)(Nb_(1/2)Ta_(1/2))_(1)O_(7) form a single orthorhombic(C222_(1))weberite phase,where 15RE_(1/15) represents Sc_(1/15)Y_(1/15)La_(1/15)Pr_(1/15)Nd_(1/15)Sm_(1/15)Eu_(1/15)Gd_(1/15)Tb_(1/15)Dy_(1/15)Ho_(1/15)Er_(1/15)Tm_(1/15) Yb_(1/15)Lu_(1/15).Moreover,a series of eight(15RE_(1/15))_(2+x)(Ti_(1/4)Zr_(1/4)Ce_(1/4)Hf_(1/4))_(2−2x)(Nb_(1/2)Ta_(1/2))_(x)O_(7) specimens all exhibit single phases,where a pyrochlore–weberite transition occurs within 0.75

关键词： compositionally complex ceramics high-entropy ceramics(HECs) weberite pyrochlore fergusonite ultrahigh-entropy ceramics many-component ceramics

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