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Effect of calcination temperature on hydrotalcite for organic dye waste elimination from aqueous solution via adsorption

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AIP Conference Proceedings 2023年第1期2540卷

作者： Lina Mahardiani Risma Arinda Finly Khoirunnisa Arabbani 1Chemistry Education Study Program Faculty of Teacher Training and Education Sebelas Maret University Surakarta Indonesia 2Material Science and Engineering Program National Taipei University of Technology Taipei Taiwan

Hydrotalcite as one of the advanced materials is applied in wide range of aspects like adsorption. This research aims to study the capability of the hydrotalcite like compound Mg-Al-CO3 material to remove the organic dye, namely, congo red and methylene blue in water through adsorption. Prior to the adsorption process, hydrotalcite like compound Mg-Al-CO3 was calcined within temperature ranges of 300-750°C. The adsorption process was carried out by batch method with variations in calcination temperature of the hydrotalcite material and variations in contacting time. The performance effectiveness of hydrotalcite was evaluated through the adsorption percentages based on the absorbance measurement data using the UV-Vis instrument. The results showed excellent hydrotalcite's capability of removing both organic dyes. Hydrotalcite calcined at 600°C was able to remove 94% of the organic dyes within 30 minutes.

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Attributional life cycle assessment of recycling and disposal strategies for construction and demolition waste

Cleaner Environmental Systems

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Cleaner Environmental Systems 2025年 18卷

作者： Kanwal, Qudsia Xu, Guochang Gari, Ziad Alhusainan, Ream S. Al-Ghamdi, Sami G. Environmental Science and Engineering Program Biological and Environmental Science and Engineering Division King Abdullah University of Science and Technology Thuwal23955-6900 Saudi Arabia KAUST Climate and Livability Initiative King Abdullah University of Science and Technology Thuwal23955-6900 Saudi Arabia Material Cycles Division National Institute for Environmental Studies Onogawa 16-2 Tsukuba305-8506 Japan

The management of Construction and Demolition Waste (CDW) poses significant environmental challenges in Saudi Arabia, exacerbated by rapid urbanization and the Giga Projects under Vision 2030. This study presents a Life Cycle Assessment (LCA) of CDW management practices across seventeen municipalities, providing the first region-specific evaluation of environmental impacts using comprehensive data. By integrating primary and secondary data from local sources, Ecoinvent 3.91, and GaBi Sphera, the study evaluates key CDW disposal methods: sanitary landfilling, incineration, and recycling. The findings reveal that advanced recycling infrastructure (e.g., compactor trucks, recycling facilities) significantly reduces non-renewable energy use, Global Warming Potential (GWP), and downstream emissions, particularly in high CDW-generating regions like Riyadh and Jeddah. Notably, recycling achieves a GWP reduction of up to 75 million kg CO2-eq annually for key materials like mixed soil and concrete. Furthermore, the study contributes to global CDW management literature by presenting a replicable LCA framework that can be applied to other rapidly urbanizing economies facing similar waste management challenges. This framework offers valuable insights for policymakers, urban planners, and researchers seeking to develop sustainable CDW management strategies aligned with circular economy principles and international sustainability goals. © 2025 The Authors

关键词： Project management

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Profile of bovine teeth potency as hydroxyapatite scaffold

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AIP Conference Proceedings 2023年第1期2536卷

作者： Endanus Harijanto Anita Yuliati Prihartini Widiyanti Dental Material Department Faculty of Dentistry Universitas Airlangga Surabaya Indonesia Biomedical Engineering Study Program Department of Physics Faculty of Science and Technology Universitas Airlangga Surabaya Indonesia

Background: Bone destructions in the oral cavity are due to trauma, chronic infection, congenital malformations, or resection surgery, most often by using an autologous bone graft technique. The problem using this technique are limited donors and suppliers, high cost, host potential imune response becauce accepts foreign bone tissue also potential transmission diseases. Another solution in tissue engineering techniques is using the scaffold. Hidroxyapatite is one of the osteoconductive potentialy ceramic materials in scaffold fabrication. Objective: To prove that bovine teeth hydroxyapatite have characteristic as scaffold for bone tissue regeneration. Methods: HA was obtained by calcining bovine teeth at 1000°C for 3 hours, Fourier Transform Infra Red Spectroscopy (FTIR) test , Energy Dispersive X-Ray (EDX) test and X-Ray Diffraction (XRD) test. Results: Bovine teeth hydroxyapatite to showed of hydroxyl, phosphate and carbonate functional groups (FTIR test). Average Ca/P=1.97. Conclusion: Hydroxyapatite from bovine teeth has potency as scaffold through the chemistry and physical characteristics.

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Correction: materials laboratories of the future for alloys, amorphous, and composite materials (MRS Bulletin, (2025), 50, 2, (190-207), 10.1557/s43577-024-00846-y)

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MRS Bulletin 2025年 1-2页

作者： Banerjee, Sarbajit Meng, Y. Shirley Minor, Andrew M. Zhang, Minghao Zaluzec, Nestor J. Chan, Maria K.Y. Seidler, Gerald McComb, David W. Agar, Joshua Mukherjee, Partha P. Melot, Brent Chapman, Karena Guiton, Beth S. Klie, Robert F. McCue, Ian D. Voyles, Paul M. Robertson, Ian Li, Ling Chi, Miaofang Destino, Joel F. Devaraj, Arun Marquis, Emmanuelle A. Segre, Carlo U. Liu, Huinan H. Yang, Judith C. Momeni, Kasra Misra, Amit Abdolrahim, Niaz Medvedeva, Julia E. Cai, Wenjun Sehirlioglu, Alp Dizbay-Onat, Melike Mehta, Apurva Graham-Brady, Lori Maruyama, Benji Rajan, Krishna Warner, Jamie H. Taheri, Mitra L. Kalinin, Sergei V. Reeja-Jayan, B. Schwarz, Udo D. Simon, Sindee L. Brown, Craig M. Department of Chemistry and Department of Materials Science & Engineering Texas A & M University College Station United States Pritzker School of Molecular Engineering The University of Chicago Chicago United States Department of Materials Science & Engineering University of California Berkeley Berkeley United States National Center for Electron Microscopy Molecular Foundry Lawrence Berkeley National Laboratory Berkeley United States Center for Nanoscale Materials Argonne National Laboratory Lemont United States Department of Physics University of Washington Seattle United States Department of Materials Science & Engineering The Ohio State University Columbus United States Department of Mechanical Engineering and Mechanics Drexel University Philadelphia United States School of Mechanical Engineering Purdue University West Lafayette United States Department of Chemistry University of Southern California Los Angeles United States Department of Chemistry Stony Brook University The State University of New York Stony Brook United States Department of Chemistry University of Kentucky Lexington United States Department of Physics University of Illinois at Chicago Chicago United States Department of Materials Science & Engineering Northwestern University Evanston Bangladesh Department of Materials Science & Engineering University of Wisconsin–Madison Madison United States Department of Materials Science and Engineering University of Pennsylvania Philadelphia United States Department of Mechanical Engineering and Materials Science Duke University Durham United States Department of Chemistry Creighton University Omaha United States Physical and Computational Sciences Directorate Pacific Northwest National Laboratory Richland United States Department of Materials Science & Engineering University of Michigan–Ann Arbor Ann Arbor United States Department of Physics Illinois Institute of Technology Chicago United States Department of Bioengineering and the Mater

This article was updated to correct Minghao Zhang’s affiliation from "Pritzker School of Molecular Engineering, The University of Chicago, Chicago, USA" to "Pritzker School of Molecular Engineering, The University of Chicago, Chicago, USA;Argonne National Laboratory, Lemont, USA." Argonne National Laboratory was left off the original publication. © The Author(s) 2025.

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Crystal structure-controlled synthesis of NiMoO4/NiO hierarchical microspheres for high-performance supercapacitors and photocatalysts

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Journal of Energy Storage 2024年 97卷

作者： Lee, Kuen-Chan Huang, Jen-Hsien Wu, Yen-Ju Wang, Kuan-Syun Cho, Er-Chieh Hsu, Shih-Chieh Liu, Ting-Yu Department of Science Education National Taipei University of Education No. 134 Sec. 2 Heping E. Road Da-an District Taipei City106 Taiwan Ph.D. Program in Medical Neuroscience College of Medical Science and Technology Taipei Medical University 250 Wuxing Street Taipei City110 Taiwan Department of Green Material Technology Green Technology Research Institute CPC Corporation No.2 Zuonan Rd. Nanzi District Kaohsiung City81126 Taiwan 1-2-1 Sengen Tsukuba Ibaraki305-0047 Japan Department of Materials Engineering Ming Chi University of Technology New Taipei City243303 Taiwan School of Pharmacy College of Pharmacy Taipei Medical University 250 Wuxing Street Taipei City110 Taiwan Department of Chemical and Materials Engineering Tamkang University No. 151 Yingzhuan Road Tamsui District New Taipei City25137 Taiwan Department of Chemical Engineering and Materials Science Yuan Ze University Taoyuan City32003 Taiwan College of Engineering & Center for Sustainability and Energy Technologies Chang Gung University Taoyuan33302 Taiwan

Global environmental challenges and energy crises have driven researchers to develop multifunctional and highly efficient nanomaterials. This study presents dual-functional NiMoO4 (NMO)/NiO hierarchical microspheres that can serve as supercapacitors and photocatalysts prepared using a microwave-assisted hydrothermal method. The α- and β-phase contents of NMO can be regulated by controlling the post-annealing temperature and pH value of the precursor solution. The as-prepared NMO/NiO nanocomposites exhibited dual Faradaic redox reactions attributed to NMO and NiO, leading to remarkable supercapacitor performance. In addition, the constructed heterojunction between NMO and NiO also improved charge separation, leading to excellent photocatalytic capability. Based on the results, NMO with a higher β-phase content showed better supercapacitive and photocatalytic performance owing to its higher conductivity. The optimal NMO/NiO composite displayed a specific capacitance of 943 F g−1 at 1 A/g and excellent cycling stability, with 83.1 % retention at 5 A/g after 4000 cycles. Additionally, it demonstrated an outstanding photocatalytic capability for the degradation of methylene blue (MB), achieving a rate constant of (0.0113 min−1). © 2024 Elsevier Ltd

关键词： Supercapacitor

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Effective strategies to reduce triethylene glycol consumption in natural gas processing plants

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Case Studies in Chemical and Environmental Engineering 2022年 5卷

作者： Trueba, Luis Gaston, Tyler Brackin, James Miller, Joseph You, Byoung-Hee Department of Engineering Technology Texas State University San Marcos 78666 TX United States Material Science Engineering and Commercialization Program Texas State University San Marcos 78666 TX United States Ingram School of Engineering Texas State University San Marcos 78666 TX United States

Triethylene glycol (TEG) is the desiccant most frequently used in natural gas processing plants to decrease natural gas water vapor content to levels at or below those required by salable gas standards (less than 7 lb per MMSCF (112 mg/Sm³) in the U.S.). Several parameters have a significant influence on the successful operation of TEG dehydration systems. Identifying and controlling these parameters can reduce major TEG losses and temporary shutdowns of gas plants. This can be accomplished by creating standard operating procedures so that TEG is only utilized when the water vapor content of the natural gas is greater than above salable levels. In doing so, TEG needs to be stored at ideal temperatures in a manner that shields it from oxygen. Isolating the dehydration system and automating TEG dispersion based on the gas water vapor content limits TEG loss to vapor, corrosion of gas handling equipment, and operational excursions. The solutions discussed are automatic variation of TEG circulation rates, use of an inert gas in TEG storage tanks, a simplified TEG usage monitoring system, and improving the function of the flash gas separator. The results of the study show a significant reduction in operating costs for a typical gas plant if all solutions are fully implemented. © 2022 The Authors

关键词： Natural gas dehydration TEG consumption Triethylene glycol (TEG)

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Effect of pyrolysis temperature on characteristics of tunable magnetic biochar synthesized from watermelon rind and its tetracycline adsorption performance

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Journal of the Taiwan Institute of Chemical Engineers 2024年 160卷

作者： Thairattananon, Phisit Le, Giang T.T. Matsumura, Yukihiko Wu, Kevin C.W. Charinpanitkul, Tawatchai Department of Chemical Engineering Faculty of Engineering Center of Excellence in Particle and Material Processing Technology Chulalongkorn University Bangkok10330 Thailand Institute of Fundamental and Applied Sciences Duy Tan University Ho Chi Minh700000 Viet Nam Faculty of Environmental and Chemical Engineering Duy Tan University Da Nang550000 Viet Nam Mechanical Engineering Program Graduate School of Advanced Science and Engineering Kagamiyama Hiroshima Higashi-Hiroshima739-8527 Japan Department of Chemical Engineering National Taiwan University Taipei10617 Taiwan Department of Chemical Engineering and Materials Science Yuan Ze University Chung-Li Taoyuan Taiwan Research Network of NANOTEC-KU on Nanocatalyst and Nanomaterials for Sustainable Energy and Environment Bangkok10900 Thailand

Background: Tetracycline is an emerging contaminant in water reservoirs, causing undesirable influences on human society. The promising usage of magnetic biochar (MBC) derived from watermelon rind has been explored in the adsorption of various contaminants owing to its high specific surface area and separability;however, the temperature-dependent changes of MBC and its sorption ability toward antibiotics have not been widely examined. Method: Tunable MBCs could be synthesized via simple pyrolysis of watermelon rind impregnated with FeCl3 at different temperatures (700–900 °C). The as-synthesized MBCs were characterized using scanning electron microscopy (SEM), an elemental analyzer, N2 adsorption/desorption, Fourier-transform infrared spectroscopy (FTIR), Raman spectroscopy, X-ray diffractometry (XRD), and vibrating sample magnetometry (VSM). Then Tetracycline, an emerging contaminant in water reservoirs, was employed as the target contaminant, while adsorption kinetics, isotherm, the effect of pH, and reusability were investigated. Significant findings: The tunability of as-synthesized MBCs could be observed by their distinct changes in structural characteristics when varying pyrolysis temperature. MBC synthesized at 900 °C (MBC900) possessed a high-specific surface area (401 m2.g−1) and saturation magnetization (55.29 emu.g−1), resulting in a greater amount of sorption sites. Tetracycline adsorption by MBCs followed a pseudo-second-order kinetic model and fitted well with the Freundlich model. MBC900 is an excellent adsorbent with a maximum adsorption capacity of 77.6 mg.g−1 and could be used for at least five cycles with an insignificant decrease in the adsorption capacity. © 2024 Taiwan Institute of Chemical Engineers

关键词： Adsorption

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Frustrated metastable-to-equilibrium grain boundary structural transition in NbMoTaW due to segregation and chemical complexity

arXiv

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arXiv 2023年

作者： Geiger, Ian Apelian, Diran Pan, Xiaoqing Cao, Penghui Luo, Jian Rupert, Timothy J. Material and Manufacturing Technology University of California IrvineCA92697 United States Department of Materials Science and Engineering University of California IrvineCA92697 United States Department of Physics and Astronomy University of California IrvineCA92697 United States Department of Mechanical and Aerospace Engineering University of California IrvineCA92697 United States Department of NanoEngineering University of California San Diego La Jolla CA92093 United States Program in Materials Science and Engineering University of California San Diego La Jolla CA92093 United States

Grain boundary structural transitions can lead to significant changes in the properties and performance of materials. In multi-principal element alloys, understanding these transitions becomes complex due to phenomena such as local chemical ordering and multi-component segregation. Using atomistic simulations, we explore a metastable-to-equilibrium grain boundary structural transition in NbMoTaW. The transition, characterized by structural disordering and reduced free volume, shows high sensitivity to its local chemical environment. Most notably, the transition temperature range of the alloy is more than twice that of a pure metal. Differences in composition between coexisting metastable and equilibrium structures highlight the change in local site availability due to structural relaxation. Further examination of grain boundaries with fixed chemical states at varying temperatures reveals that the amount of segregation significantly influences the onset temperature yet has minimal effect on the transition width. These insights underscore the profound effect of chemical complexity and ordering on grain boundary transitions in complex concentrated alloys, marking a meaningful advancement in our understanding of grain boundary behavior at the atomic level. Copyright © 2023, The Authors. All rights reserved.

关键词： Grain boundaries

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Ultrathin-shell epitaxial Ag@Au core-shell nanowires for high-performance and chemically-stable electronic, optical, and mechanical devices

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Nano Research 2021年第11期14卷 4294-4303页

作者： Yangzhi Zhu Sanggon Kim Xuezhi Ma Peter Byrley Ning Yu Qiushi Liu Xiaoming Sun Da Xu Sangshan Peng Martin C.Hartel Shiming Zhang Vadim Jucaud Mehmet R.Dokmeci Ali Khademhosseini Ruoxue Yan Department of Chemical and Environmental Engineering Bourns College of EngineeringUniversity of California-RiversideRiversideCA92521USA Terasaki Institute for Biomedical Innovation Los AngelesCA90064USA Department of Electrical and Computer Engineering University of California-RiversideRiversideCA92521USA State Key Laboratory of Chemical Resource Engineering Beijing University of Chemical TechnologyBeijing100029China State Key Laboratory of Chemo/Biosensing and Chemometrics College of Chemistry and Chemical EngineeringHunan UniversityChangsha410082China Department of Bioengineering University of California-Los AngelesLos AngelesCA90095USA Department of Electrical and Electronic Engineering The University of Hong KongHong KongChina Material Science and Engineering Program University of California-RiversideRiversideCA92521USA

Silver nanowires (AgNWs) hold great promise for applications in wearable electronics, flexible solar cells, chemical and biological sensors, photonic/plasmonic circuits, and scanning probe microscopy (SPM) due to their unique plasmonic, mechanical, and electronic properties. However, the lifetime, reliability, and operating conditions of AgNW-based devices are significantly restricted by their poor chemical stability, limiting their commercial potentials. Therefore, it is crucial to create a reliable oxidation barrier on AgNWs that provides long-term chemical stability to various optical, electrical, and mechanical devices while maintaining their high performance. Here we report a room-temperature solution-phase approach to grow an ultra-thin, epitaxial gold coating on AgNWs to effectively shield the Ag surface from environmental oxidation. The Ag@Au core-shell nanowires (Ag@Au NWs) remain stable in air for over six months, under elevated temperature and humidity (80 °C and 100% humidity) for twelve weeks, in physiological buffer solutions for three weeks, and can survive overnight treatment of an oxidative solution (2% H2O2). The Ag@Au core-shell NWs demonstrated comparable performance as pristine AgNWs in various electronic, optical, and mechanical devices, such as transparent mesh electrodes, surface-enhanced Raman spectroscopy (SERS) substrates, plasmonic waveguides, plasmonic nanofocusing probes, and high-aspect-ratio, high-resolution atomic force microscopy (AFM) probes. These Au@Ag core-shell NWs offer a universal solution towards chemically-stable AgNW-based devices without compromising material property or device performance.

关键词： epitaxial growth core-shell nanowire plasmonic waveguides atomic force microscopy(AFM)probe transparent electrode wearable electronics

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Facile Li-Ion Transport via LLTO Scaffold with Crosslinked Polyethylene Glycol Composite Electrolyte for Solid-State Batteries

SSRN

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SSRN 2025年

作者： Lee, Jungkuk Counihan, Michael J. Barai, Pallab Burns, Meghan E. Singh, Vibhu V. Jamnuch, Sasawat Pascal, Tod A. Shrinivasan, Venkat Tepavcevic, Sanja Zhang, Yuepeng Applied Materials Division Argonne National Laboratory LemontIL60439 United States Materials Science Division Argonne National Laboratory LemontIL60439 United States Department of Chemistry University of Illinois Chicago ChicagoIL60607 United States ATLAS Materials Physics Lab Aiiso Yufeng Li Family Department of Chemical and Nano Engineering University of California San Diego La Jolla CA92093 United States Microscopy and Microanalysis Research Group Materials Measurement Science Division National Institute of Standards and Technology GaithersburgMD20899 United States Material Science and Engineering Program University of California San Diego La Jolla CA92093 United States Chemical Sciences and Engineering Division Argonne National Laboratory LemontIL60439 United States

Composite polymer electrolytes (CPEs) hold significant promise for solid-state batteries due to their ability to combine the benefits of inorganic fillers and polymer matrices. However, agglomeration of inorganic fillers can disrupt the formation of a percolation pathway, hindering lithium-ion transport. Here, we developed a stable, porous, and interconnected 3-dimentional LLTO (Li0.33La0.557TiO3) nanofiber scaffold and fabricate CPEs using in-situ crosslinked polyethylene glycol (xPEG). The resulting self-standing LLTOxPEG-65 achieved an ionic conductivity of 5.0 × 10−4 S/cm at 30 °C and a critical current density of 0.5 mA/cm2. A significantly lower activation energy (~0.2 eV) was observed in LLTOxPEG-65 compared to pristine xPEG (0.44 eV), indicating a transition of lithium-ion transport pathways from xPEG to the LLTO scaffold. However, increasing the xPEG content led to a decrease in ionic conductivity and a rise in activation energy, approaching that of pristine xPEG. DFT calculations revealed that Li+ transport in the [010] and [001] planes of LLTO predominantly takes place within the bulk rather than along the surface, while a concerted diffusion mechanism was observed in the [100] plane. Additionally, mesoscale-level computational analysis indicated that the high LLTO scaffold fraction (90 wt %) can ensure transport through the bulk of the fibers even with larger interfacial charge transfer resistance, around 1 Ω·cm2 between LLTO and xPEG. Presence of the highly percolated LLTO scaffold helps to promote efficient Li+ transport through the bulk of LLTO. © 2025, The Authors. All rights reserved.

关键词： Activation energy

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