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Crystallization study of boscalid monohydrate using γ-valerolactone-water as a green solvent system: Mechanisms and powder properties optimization

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chemical engineering Research and Design 2025年 218卷 597-618页

作者： Shang, Zeren Hu, Weiguo Wang, Guangle Hou, Baohong Guo, Shengzheng Wang, Jingkang Gong, Junbo State Key Laboratory of Chemical Engineering School of Chemical Engineering and Technology Tianjin University Tianjin300072 China North China Pharmaceutical Co. Ltd Shijiazhuang050015 China School of Chemistry and Chemical Engineering Qinghai Minzu University Xining810007 China

The thrust to enhance the greenness of boscalid monohydrate crystallization process, improve its powder properties and explore related mechanisms has been augmenting in academia and industry. Therefore, the anti-solvent crystallization of monohydrate using γ-valerolactone as the good solvent and water as the poor solvent is developed for the first time. And the formation of boscalid-water molecular aggregates similar to the supramolecular structure of monohydrate facilitates the nucleation of monohydrate in the anti-solvent crystallization. Boscalid-water-γ-valerolactone phase diagrams and thermodynamic analysis show monohydrate is more stable than form II when the activity of water exceeds a certain value. Based on the monitoring results, it is evident that the nucleation of monohydrate and the dissolution of form II respectively act as the rate-controlling step in the initial stage and later stage of the solution-mediated transformation from form II to monohydrate. The main effects diagrams show the different effects of mass fraction of water and three other factors on the induction time and transformation time of this solution-mediated transformation. Furthermore, the solid-state phase transformation of monohydrate involving the dehydration kinetics and mechanism has been investigated. Finally, the HPMC coated monohydrate spherical particle with improved powder properties is induced by HPMC in the γ-valerolactone-water system. © 2025 Institution of chemical Engineers

关键词： Setting

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Investigation and optimization of high-valent Ta-doped SrFeO_(3-δ)as air electrode for intermediate-temperature solid oxide fuel cells

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International Journal of Minerals,Metallurgy and Materials 2024年第9期31卷 2102-2109页

作者： Shanshan Jiang Hao Qiu Shaohua Xu Xiaomin Xu Jingjing Jiang Beibei Xiao Paulo Sérgio Barros Juliao) Chao Su Daifen Chen Wei Zhou School of Energy and Power Jiangsu University of Science and TechnologyZhenjiang 212100China WA School of Mines:Minerals Energy and Chemical EngineeringCurtin UniversityPerth WA6102Australia Institute of Analysis and Testing Beijing Academy of Science and TechnologyBeijing 100089China State Key Laboratory of Materials-Oriented Chemical Engineering College of Chemical EngineeringNanjing Tech UniversityNanjing 211816China

To explore highly active and thermomechanical stable air electrodes for intermediate-temperature solid oxide fuel cells(ITSOFCs),10mol%Ta5+doped in the B site of strontium ferrite perovskite oxide(SrTa_(0.1)Fe_(0.9)O_(3-δ),STF)is investigated and *** effects of Ta^(5+)doping on structure,transition metal reduction,oxygen nonstoichiometry,thermal expansion,and electrical performance are evaluated *** 10mol%Ta^(5+)doping,the thermal expansion coefficient(TEC)decreased from 34.1×10^(-6)(SrFeO_(3-δ))to 14.6×10^(-6) K^(-1)(STF),which is near the TEC of electrolyte(13.3×10^(-6) K^(-1) for Sm_(0.2)Ce_(0.8)O_(1.9),SDC),indicates excellent thermomechanical *** 550-750℃,STF shows superior oxygen vacancy concentrations(0.262 to 0.331),which is critical in the oxygen-reduction reaction(ORR).Oxygen temperature-programmed desorption(O_(2)-TPD)indicated the thermal reduction onset temperature of iron ion is around 420℃,which matched well with the inflection points on the thermos-gravimetric analysis and electrical conductivity *** 600℃,the STF electrode shows area-specific resistance(ASR)of 0.152Ω·cm^(2) and peak power density(PPD)of 749 mW·cm^(-2).ORR activity of STF was further improved by introducing 30wt%Sm_(0.2)Ce_(0.8)O_(1.9)(SDC)powder,STF+SDC composite cathode achieving outstanding ASR value of 0.115Ω·cm2 at 600℃,even comparable with benchmark cobalt-containing cathode,Ba_(0.5)Sr_(0.5)Co_(0.8)Fe_(0.2)O_(3-δ)(BSCF).Distribution of relaxation time(DRT)analysis revealed that the oxygen surface exchange and bulk diffusion were improved by forming a composite *** 650℃,STF+SDC composite cathode achieving an outstanding PPD of 1117 mW·cm^(-2).The excellent results suggest that STF and STF+SDC are promising air electrodes for IT-SOFCs.

关键词： strontium ferrite-based perovskite Ta doping composite cathode intermediate-temperature solid oxide fuel cells

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Real-time fluorescent detection of food spoilage with doped quantum dots-anchored hydrogel sensor

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Nano Research 2024年第12期17卷 10467-10475页

作者： Chenying Li Jianzhong Li Lei Ji Yibin Zhu Jiajia Liu Jiatao Zhang School of Materials Science and Engineering Beijing Key Laboratory of Construction-Tailorable Advanced Functional Materials and Green ApplicationsBeijing Institute of TechnologyBeijing 100081China School of Chemistry and Chemical Engineering MIIT Key Laboratory of Medical Molecule Science and Pharmaceutical EngineeringMOE Key Laboratory of Cluster ScienceBeijing Institute of TechnologyBeijing 100081China

Spermine assumes a pivotal role in assessing food safety due to its potential to induce a spectrum of diseases upon excessive ***,contemporary spermine detection methodologies,exemplified by high-performance liquid chromatography(HPLC),demand costly instrumentation and the expertise of skilled *** address this challenge,the study introduces a portable fluorescence sensing *** fluorescent probes were realized through the utilization of CdS quantum dots deeply doped with Ag^(+)(CdS:Ag QDs)and nitrogen-doped carbon quantum dots(N-CQDs).Hydrogen bonds formed between CdS:Ag QDs and spermine result in the formation of the assembly and the decreasing of the fluorescence *** an effort to broaden the applicative scope and streamline deployment processes,fluorescent sensing hydrogels were meticulously engineered,capitalizing on the swelling properties inherent in polyvinyl alcohol(PVA)*** systematic delineation of the correlation between 1-R/B and spermine concentration facilitates the quantitative determination of spermine *** incorporation of this composite construct serves to alleviate environmental influences on the probes,thereby augmenting their *** portable fluorescent sensing platform proves pivotal in expeditiously measuring spermine concentration within the fluorescent sensing hydrogel,enabling a quantitative assessment of pork *** utilization of this platform for food freshness evaluation imparts the benefits of convenience,cost-effectiveness,and intuitive operation.

关键词： Ag^(+)doped CdS quantum dots nitrogen-doped carbon quantum dots ratiometric fluorescent sensing hydrogel portable platform spermine detection

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Decarboxylative cyanation and thiocyanation via catalytic electron donor-acceptor complex with copper catalysis

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Science China Chemistry 2024年第9期67卷 3019-3028页

作者： Hongping Zhao Xiaoxiang Xi Tianbao Wu Zimin Chen Minyan Wang Weiming Yuan Key Laboratory of Material Chemistry for Energy Conversion and Storage Ministry of EducationHubei Key Laboratory of Bioinorganic Chemistry and Materia MedicaSchool of Chemistry and Chemical EngineeringHuazhong University of Science and Technology(HUST)Wuhan 430074China State Key Laboratory of Coordination Chemistry School of Chemistry and Chemical EngineeringNanjing UniversityNanjing 210093China Shenzhen Huazhong University of Science and Technology Research Institute Shenzhen 518000China

A new catalytic decarboxylative cyanation and thiocyanation via a synergistic Na I/Cu catalysis is *** photoexcited electron donor-acceptor complex by assembly of Na I,R3P,and N-acyloxy-phthalimide ester(NHPI ester)triggers the generation of alkyl radical species,which then engages in Cu-catalyzed radical coupling *** to success of this dual catalytic transformation is the reliable charge transfer between I·and Cu(I).This dual catalytic platform can eliminate the use of expensive iridium-based photocatalyst or synthetically elaborate organic dyes.A series of primary,secondary,and tertiary alkyl nitriles and thiocyanates are easily ***,an asymmetric decarboxylative cyanation by applying a chiral Cu catalyst is also developed to afford chiral nitriles in high *** mechanistic details and the origin of the high enantioselectivity are further investigated by the mechanistic experiments and the density functional theory calculations.

关键词： electron donor-acceptor catalysis copper catalysis cyanation thiocyanation asymmetric synthesis

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Research progress on the substrate for metal-organic framework(MOF) membrane growth for separation

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Chinese Journal of chemical engineering 2023年第4期56卷 299-313页

作者： Wufeng Wu Xilu Hong Jiang Fan Yanying Wei Haihui Wang School of Chemistry&Chemical Engineering South China University of TechnologyGuangzhou 510640China Beijing Key Laboratory for Membrane Materials and Engineering Department of Chemical EngineeringTsinghua UniversityBeijing 100084China

During the last decade, metal-organic frameworks(MOFs) have been applied in various fields due to their unique chemical and functional advantages. One of the widespread research hotspots is MOF-based membranes for separations, specifically continuous defect-free MOF membranes, which are usually grown on porous substrates. The substrate not only serves as the MOF layer support but also has a great influence on the membrane fabrication process and the final separation performance of the resultant membrane. In this review, we mainly introduce the progress focused on the substrates for MOF membranes fabrication. The substrate modifications and seeding methods aimed at synthesizing highquality MOF membranes are also summarized systematically.

关键词： Membrane separation MOF membrane Metal-organic frameworks Support Synthesis

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Insight into the role of ethylene glycol on thermodynamics and nucleation kinetics of dimethyl terephthalate in mixed solvent system

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Particuology 2024年第2期85卷 1-12页

作者： Yujin Zhang Chunyan Shi Jing Tang Li Liu Dongxia Yan Qing Zhou Xingmei Lu Songyan Jia College of Chemical Engineering Shenyang University of Chemical TechnologyShenyang110142China Bejing Key Laboratoryoflonic Liquids Clean Process CAS Key LaboratoryofGreen Process and EngineeringState Key Laboratoryof Multiphase Complex SystemsInstitute of Process EngineeringChinese Academy of SciencesBeijing100190China School of Chemistry and Chemical Engineering Qingdao UniversityQingdao266071China Henan Institute of Advanced Technology Zhengzhou UniversityZhengzhou450001China School of Chemical Engineering University of Chinese Academy of SciencesBeijing100049China

Dissolution and nucleation are two essential processes for industrial *** paper in-vestigates the effect of ethylene glycol addition on the crystallization behavior of dimethyl terephthalate(DMT)in *** DMT solubility in mixed solvent system(methanol-ethylene glycol)was deter-mined by isothermal satiation approach,and the solubility was associated using seven *** model fitting results were consistent with the experimental *** on the results,the metastable zone width(MSZW)of DMT was detected by the polythermal approach;the modified Sangwal's theory was used to investigate the nucleation behavior,which can provide a new way of thought for better analysis of the crystallization *** results demonstrated that MSZW was associated with various elements,such as cooling rate,saturation temperature and mass fraction of ethylene *** addition of ethylene glycol slowed down the nucleation rate as shown by the broadening of *** derive the solid-liquid interface energy,the nucleation driving force,the critical nucleation size and the critical Gibbs free energy according to the classical nucleation *** is demonstrated that the nucleation driving force and the solid-liquid interface energy are dependent and jointly influence the MSZW.

关键词： Dissolution Nucleation Solubility Apparent thermodynamic parameters Metastable zone width Solid-liquid interface energy

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Tailor-made high elasticity and low-hysteresis hydrogels based on asymmetric H-bonding crosslinking for wearable applications

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Science China Chemistry 2025年第3期68卷 1117-1125页

作者： Xiaofang Shi Nan Shi Miaomiao Dang Chengyu Ji Yingjie Li Peiyi Wu Zhiguo Hu Collaborative Innovation Centre of Henan Province for Green Manufacturing of Fine Chemicals Henan Engineering Laboratory of Chemical Pharmaceutical and Biomedical MaterialsSchool of Chemistry and Chemical EngineeringHenan Normal UniversityXinxiang 453007China State Key Laboratory for Modification of Chemical Fibers and Polymer Materials College of ChemistryChemical Engineering and Biotechnology&Center for Advanced Low-dimension MaterialsDonghua UniversityShanghai 201620China

The conventional method of fabricating hydrogels constantly confronts the conflict between elasticity and toughness,limiting their repetitive *** the desired elasticity through a simple and low-cost approach is a significant challenge for hydrogels,particularly through rational molecular ***,low-hysteresis and high-toughness hydrogels are developed from the design of a new feature monomer,N-acryloylethylsemicarbazide(NACE).Based on a concept of“asymmetric Hbonding design”,the unique double and triple H-bonding of NACE can result in a novel asymmetric crosslinking polymer with alternating strong and weak H-bonding *** NACE is copolymerized with acrylamide(AM)to regulate the mechanical properties of hydrogel via H-bonding *** P(NACE-AM)ionic hydrogels are obtained simply and rapidly via one-step photopolymerization without a chemical cross-linking *** P(NACE-AM)hydrogels combine superb mechanical elasticity and toughness,and excellent ionic conductivity,showing great potential as durable ionic conductive devices for wearable utilization.

关键词： new feature monomer asymmetric H-bonding low-hysteresis hydrogel wearable sensor

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Preparation and properties of high-energy-density aluminum/boroncontaining gelled fuels

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Chinese Journal of chemical engineering 2024年第1期65卷 230-242页

作者： Yi Chen Kang Xue Yang Liu Lun Pan Xiangwen Zhang Ji-Jun Zou Key Laboratory for Green Chemical Technology of the Ministry of Education School of Chemical Engineering and TechnologyTianjin UniversityTianjin 300072China Collaborative Innovative Center of Chemical Science and Engineering(Tianjin) Tianjin 300072China Haihe Laboratory of Sustainable Chemical Transformations Tianjin 300192China Zhejiang Institute of Tianjin University Ningbo 315201China

Energetic nanofluid fuel has caught the attention of the field of aerospace liquid propellant for its high energy density(HED), but it suffers from the inevitable solid-liquid phase separation problem. To resolve this problem, herein we synthesized the high-Al-/B-containing(up to 30%(mass)) HED gelled fuels, with low-molecular-mass organic gellant Z, which show high net heat of combustion(NHOC), density, storage stability, and thixotropic properties. The characterizations indicate that the application of energetic particles to the gelled fuels obviously destroys their fibrous network structures but can provide the new particle-gellant gelation microstructures, resulting in the comparable stability between 1.0%(mass) Z/JP-10 + 30%(mass) Al or B and pure JP-10 gelled fuel. Moreover, the gelled fuels with high-content Al or B exhibit high shear-thinning property, recovery capability, and mechanical strength, which are favorable for their storage and utilization. Importantly, the prepared 1.0%(mass) Z/JP-10 + 30%(mass) B(or 1.0%(mass) Z/JP-10 + 30%(mass) Al) shows the density and NHOC 1.27 times(1.30) and 1.43 times(1.21)higher than pure JP-10, respectively. This work provides a facile and valid approach to the manufacturing of HED gelled fuels with high content of energetic particles for gel propellants.

关键词： Gelled fuels Energetic aluminum/boron Low-molecular-mass organic gellant Fuel property

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Regulation of interlayer channels of graphene oxide nanosheets in ultra-thin Pebax mixed-matrix membranes for CO_(2) capture

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Chinese Journal of chemical engineering 2024年第3期67卷 257-267页

作者： Feifan Yang Yuanhang Jin Jiangying Liu Haipeng Zhu Rong Xu Fenjuan Xiangli Gongping Liu Wanqin Jin State Key Laboratory of Materials-Oriented Chemical Engineering College of Chemical EngineeringNanjing Tech UniversityNanjing 211816China Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology School of Petrochemical EngineeringChangzhou UniversityChangzhou 213164China Shandong Production and Research Long Membrane Technology Development Co. Ltd.Yantai Economic Development ZoneYantai 265505China

For the application of carbon capture by membrane process,it is crucial to develop a highly permeable CO_(2)-selective *** this work,we reported an ultra-thin polyether-block-amide(Pebax)mixedmatrix membranes(MMMs)incorporated by graphene oxide(GO),in which the interlayer channels were regulated to optimize the CO_(2)/N_(2) separation *** membrane preparation conditions were systematically investigated on the influence of the membrane structure and separation performance,including the lateral size of GO nanosheets,GO loading,thermal reduction temperature,and *** results demonstrated that the precisely regulated interlayer channel of GO nanosheets can rapidly provide CO_(2)-selective transport channels due to the synergetic effects of size sieving and preferential *** GO/Pebax ultra-thin MMMs exhibited CO_(2)/N_(2) selectivity of 72 and CO_(2) permeance of 400 GPU(1 GPU=106 cm^(3)(STP)·cm^(2)·s^(-1)·cmHg^(-1)),providing a promising candidate for CO_(2) capture.

关键词： Mixed-matrix membrane Ultra-thin membrane Pebax Graphene oxide CO_(2) capture

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Interfacial charge effects of supported-metal-cluster heterostructures on azo hydrogenation catalyzation

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Nano Research 2024年第5期17卷 3853-3862页

作者： Zhenhua Gu Jingli Zhang Zijun Zhang Qingxue Mu Liangchong Yu Taolei Sun Lei Shen Guanbin Gao State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China Hubei Key Laboratory of Nanomedicine for Neurodegenerative Diseases School of ChemistryChemical Engineering and Life ScienceWuhan University of TechnologyWuhan 430070China

The impact of interfacial charge on catalytic performance of supported-metal-cluster(SMC)heterostructures remains unclear,hindering efforts to develop high-performance SMC *** we systematically investigated interfacial charge effects of SMCs using a model system of graphene-supported gold-nanoclusters(AuNCs/rGO)for azo *** types of SMCs with different interfacial charges were synthesized by anchoring electropositive 2-aminoethanethiol(CSH),amphoteric cysteine(Cys),and electronegative 3-mercaptopropionic-acid(MPA)onto AuNCs/rGO,*** three SMCs exhibited high and selective catalytic activity to azo-hydrogenation in four representative azo *** catalytic activity of Cys@AuNCs/rGO was lower than that of CSH@AuNCs/rGO but higher than that of MPA@AuNCs/***,the cyclic stability of Cys@AuNCs/rGO was inferior to that of both CSH@AuNCs/rGO and MPA@AuNCs/*** mechanistic studies revealed that amino ligands modified CSH@AuNCs and Cys@AuNCs agglomerated into large-size gold nanoparticles on rGO surface during catalytic reaction under NaBH_(4) action,leading to reduced efficiency and cyclic ***,non-amino ligand modified MPA@AuNCs only partially detached from rGO surface without agglomeration,resulting in better cyclic *** of amino groups in ligands such as modifying-NH_(3)^(+)group in Cys into imine to form N-isobutyryl-L-cysteine(NIBC)substantially improved the cyclic stability while maintaining the high activity in the NIBC@AuNCs/rGO catalyst *** work provides an approach for developing a highly-active and stable SMC heterostructure catalyst via manipulating interfacial charges in SMC.

关键词： interfacial charge effect supported-metal-cluster catalyst azo hydrogenation graphene supported gold nanoclusters

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