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Mitochondria-targeted NIR molecular probe for detecting viscosity of gland damage and SO2 in actual samples 线粒体靶向近红外分子探针,用于检测腺体损伤的粘度和实际样品中的二氧化硫
IF 5.9 3区 工程技术 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-09-29 DOI: 10.1016/j.jiec.2024.09.046
Peng Lei , Ruifang Wang , Chuan Dong , Shaomin Shuang , Minglu Li
Glandular damage can be caused by various factors, including disease, trauma, or other abnormalities within the organism. The viscosity of the gland is one of the important indicators to measure the degree of damage. Sulfur dioxide (SO2) is widely used as an important food additive due to its preservative and bleaching properties, but its overuse has serious negative impacts on the environment, so it is urgent to develop a simple detection method. Herein, we designed and synthesized a mitochondria-targeted near-infrared (NIR) fluorescence probe (BDC) for the detection of viscosity and SO2. BDC consisted of a donor-π-acceptor (D-π-A) structure and extended double bonds bridging rotor, which enabled sensitive response to viscosity and intense fluorescence emission. The TICT (twisted intramolecular charge transfer) of BDC was inhibited with an increase in viscosity, accompanied by a significant enhancement of red fluorescence signal with emission wavelength beyond 800 nm. Notably, BDC was able to noninvasively and sensitively monitor the viscosity changes in the glands of non-obese diabetic (NOD) mice model. BDC was utilized for monitoring SO2 in food and environmental samples through Michael addition reactions, providing a straightforward tool for SO2 detection in food safety and environmental monitoring.
腺体损伤可由多种因素造成,包括疾病、创伤或机体内的其他异常情况。腺体的粘度是衡量损伤程度的重要指标之一。二氧化硫(SO2)因其防腐和漂白特性被广泛用作重要的食品添加剂,但其过度使用会对环境造成严重的负面影响,因此开发一种简便的检测方法迫在眉睫。在此,我们设计并合成了一种线粒体靶向近红外(NIR)荧光探针(BDC),用于检测粘度和二氧化硫。BDC 由供体-π-受体(D-π-A)结构和延伸双键桥接转子组成,能对粘度做出灵敏反应并发出强烈的荧光。随着粘度的增加,BDC 的 TICT(扭曲分子内电荷转移)受到抑制,同时红色荧光信号显著增强,发射波长超过 800 纳米。值得注意的是,BDC 能够无创、灵敏地监测非肥胖糖尿病(NOD)小鼠模型腺体的粘度变化。通过迈克尔加成反应,BDC 被用于监测食品和环境样品中的二氧化硫,为食品安全和环境监测中的二氧化硫检测提供了一种直接的工具。
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引用次数: 0
Advanced Z-scheme H-g-C3N4/Bi2S3 nanocomposites: Boosting photocatalytic degradation of antibiotics under visible light exposure 先进的 Z 型 H-g-C3N4/Bi2S3 纳米复合材料:在可见光照射下促进抗生素的光催化降解
IF 5.9 3区 工程技术 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-09-26 DOI: 10.1016/j.jiec.2024.09.045
Govinda Raj Muniyandi , Jeyapaul Ubagaram , Abinaya Srinivasan , Daisy Rani James , Nalandhiran Pugazhenthiran , Chandramohan Govindasamy , John Alphin Joseph , Aruljothy John Bosco , Shanmugam Mahalingam , Junghwan Kim
Abnormal concentrations of antibiotics found in aquatic environments have raised serious environmental concerns. For the efficient degradation of antibiotics, it is necessary to develop photocatalysts that react to visible light. In this work, calcination and hydrothermal methods were used to synthesize bare H-g-C3N4 and Bi2S3, respectively. Various analytic methods, such as XRD, XPS, FT-IR, HR-SEM, and HR-TEM, were utilized to verify the accomplished synthesis of the materials produced. The results of ultraviolet–visible diffuse reflectance spectroscopy (UV–DRS) showed that the synthesized nanocomposites exhibited a lower band gap than the bare materials and thus greater visible-light absorption. The degradation efficacy of the bare materials and hydrothermally synthesized nanocomposites over ciprofloxacin were investigated. A high degradation efficiency of 92 % was demonstrated for ciprofloxacin using the H-g-C3N4/Bi2S3 (5 %) nanocomposite. This remarkable efficiency underscores the potential of this nanocomposite in removing antibiotic pollutants from wastewater. In addition, the electron transfer dynamics amid the two materials (H-g-C3N4 and Bi2S3) within the heterojunction was elucidated. The findings provide valuable insights into the mechanisms underlying the enhanced photocatalytic activity of nanocomposites, paving the way for further optimization and development of advanced photocatalytic systems for environmental remediation.
水生环境中发现的抗生素浓度异常已引起严重的环境问题。为了有效降解抗生素,有必要开发能对可见光产生反应的光催化剂。本研究采用煅烧法和水热法分别合成了裸露的 H-g-C3N4 和 Bi2S3。利用 XRD、XPS、傅立叶变换红外光谱、HR-SEM 和 HR-TEM 等多种分析方法验证了材料的合成过程。紫外-可见光漫反射光谱(UV-DRS)的结果表明,合成的纳米复合材料的带隙低于裸材料,因此可见光吸收能力更强。研究了裸材料和水热合成纳米复合材料对环丙沙星的降解效果。使用 H-g-C3N4/Bi2S3 (5%)纳米复合材料对环丙沙星的降解效率高达 92%。这一出色的降解效率凸显了这种纳米复合材料在去除废水中抗生素污染物方面的潜力。此外,还阐明了异质结内两种材料(H-g-C3N4 和 Bi2S3)之间的电子传递动力学。这些发现为了解纳米复合材料增强光催化活性的机制提供了宝贵的见解,为进一步优化和开发先进的光催化系统用于环境修复铺平了道路。
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引用次数: 0
Eco-friendly corrosion inhibition of steel using phenolic compounds from Cynara syriaca 利用西洋菜中的酚类化合物对钢铁进行环保型缓蚀处理
IF 5.9 3区 工程技术 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-08-27 DOI: 10.1016/j.jiec.2024.08.038
Meriem Kemel
This study evaluates the corrosion inhibition performance of the n-butanol (n-BuOH) fraction derived from Cynara syriaca on mild steel in acidic environments. The n-BuOH fraction achieved up to 94 % inhibition at 500 ppm, as assessed through gravimetric analysis, potentiodynamic polarization (PDP), and electrochemical impedance spectroscopy (EIS). Key phenolic compounds, including kaempferol, naringenin, myricetin, chlorogenic acid, and quercetin, were identified by UPLC-MS/MS. These compounds form stable flavonoid-metal complexes, as confirmed by UV–Vis spectroscopy. FT-IR and SEM-EDS analyses revealed the formation of protective coatings and interactions with the steel surface. Polarization curves indicate that the n-BuOH fraction acts as a mixed-type inhibitor, predominantly affecting the anodic reaction. The inhibition efficiency decreased from 94.14 % to 73.43 % with increasing temperatures. Thermodynamic analysis showed an increase in activation energy (Ea = 58.20 kJ/mol) and a positive ΔH value of 56.17 kJ/mol, which can be attributed to the increased thickness of the double layer, enhancing the activation energy of the corrosion process. A Gibbs free energy (ΔG0ads) value of −25.48 kJ/mol confirms that the adsorption process is spontaneous and involves both physisorption and chemisorption. pKa analysis identified specific adsorption sites. This research underscores the potential of the n-BuOH fraction as a novel, eco-friendly corrosion inhibitor, offering valuable insights for sustainable corrosion control strategies.
本研究评估了从西洋菜(Cynara syriaca)中提取的正丁醇(n-BuOH)馏分在酸性环境中对低碳钢的缓蚀性能。通过重量分析、电位极化(PDP)和电化学阻抗光谱(EIS)评估,正丁醇馏分在 500 ppm 时的缓蚀效果高达 94%。通过 UPLC-MS/MS,确定了主要的酚类化合物,包括山奈酚、柚皮苷、杨梅素、绿原酸和槲皮素。紫外可见光谱法证实,这些化合物形成了稳定的类黄酮-金属复合物。傅立叶变换红外光谱(FT-IR)和扫描电子显微镜(SEM-EDS)分析表明了保护层的形成以及与钢表面的相互作用。极化曲线表明,正丁醇部分是一种混合型抑制剂,主要影响阳极反应。随着温度的升高,抑制效率从 94.14% 降至 73.43%。热力学分析表明,活化能(Ea = 58.20 kJ/mol)增加,ΔH 值为 56.17 kJ/mol,这可能是由于双层厚度增加,提高了腐蚀过程的活化能。吉布斯自由能(ΔG0ads)值为 -25.48 kJ/mol,这证实了吸附过程是自发的,同时涉及物理吸附和化学吸附。这项研究强调了正丁醇馏分作为一种新型环保缓蚀剂的潜力,为可持续腐蚀控制策略提供了宝贵的见解。
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引用次数: 0
Synthesis, characterization, theoretical, and experimental evaluation of novel imidazolone − based compounds as eco-friendly corrosion inhibitors for mild steel 作为低碳钢环保型缓蚀剂的新型咪唑啉酮化合物的合成、表征、理论和实验评估
IF 5.9 3区 工程技术 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-08-26 DOI: 10.1016/j.jiec.2024.08.042
W. Ettahiri , A. El Moutaouakil Ala Allah , J. Lazrak , E.H. Safir , K.K. Yadav , B. Hammouti , A.J. Obaidullah , Z. Rais , Y. Ramli , M. Taleb
This study investigates the corrosion inhibition properties of two newly synthesized namely (E)-2-(2-benzylidenehydrazineyl)-5,5-diphenyl-3,5-dihydro-4H-imidazol-4-one denoted Ph-DDI and (E)-2-(2-(4-methylbenzylidene)hydrazineyl)-5,5-diphenyl-3,5-dihydro-4H-imidazol-4-one denoted CH3Ph-DDI, on mild steel (MS) in a 1 M HCl solution. These compounds demonstrated high inhibition efficiencies of 98.3 % and 98.7 %, respectively. Structural characterization was performed using FT-IR, 1H NMR, 13C NMR, and HRMS-ESI. Theoretical evaluations indicated high reactivity and potent inhibition capacity. Electrochemical tests confirmed a concentration-dependent inhibition effectiveness up to 328 K. Adsorption studies suggested that the compounds displace water molecules to form an adsorbed protective layer. Microscopy analysis provided insights into the corrosion inhibition mechanisms, confirming the formation of protective layers and iron/inhibitor complexes. Further molecular structure analysis using Monte Carlo (MC) simulations and density functional theory (DFT) calculations elucidated the structural features contributing to the compounds’ effective corrosion inhibition properties.
本研究探讨了两种新合成物,即(E)-2-(2-亚苄基肼基)-5,5-二苯基-3,5-二氢咪唑-4-酮和(E)-2-(2-(4-甲基亚苄基)肼基)-5,5-二苯基-3,5-二氢咪唑-4-酮在 1 M HCl 溶液中对低碳钢 (MS) 的缓蚀性能。这些化合物的抑制率分别高达 98.3% 和 98.7%。利用 FT-IR、H NMR、C NMR 和 HRMS-ESI 进行了结构表征。理论评估表明,该化合物具有很高的反应活性和很强的抑制能力。吸附研究表明,这些化合物取代了水分子,形成了吸附保护层。显微镜分析深入揭示了腐蚀抑制机制,证实了保护层和铁/抑制剂复合物的形成。利用蒙特卡罗(MC)模拟和密度泛函理论(DFT)计算进行的进一步分子结构分析阐明了化合物有效缓蚀特性的结构特征。
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引用次数: 0
A novel S-scheme photocatalyst Fe2O3/Bi2O3/g-C3N4 with enhanced visible-light photocatalytic performance for antibiotic degradation and CO2 reduction: RSM-based optimization 一种新型 S 型光催化剂 Fe2O3/Bi2O3/g-C3N4 具有增强的可见光光催化性能,可用于抗生素降解和二氧化碳还原:基于 RSM 的优化
IF 5.9 3区 工程技术 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-08-10 DOI: 10.1016/j.jiec.2024.08.002
Abdelfattah Amari , Hakim S. Sultan Aljibori , Zaina Algarni , Noureddine Elboughdiri , M.A. Diab , Kwang-Hyun Baek , Ibrahim Mahariq
The degradation of pollutants and reduction of CO2 to hydrocarbon fuels using photocatalysis is a potential approach to reducing CO2 emissions and decreasing environmental contamination. This study introduces an innovative S-scheme photocatalyst (Fe2O3/Bi2O3/g-C3N4) synthesized through simple methods for the first time. The structural, morphological, and optical properties of the synthesized photocatalysts were comprehensively characterized using XRD, XPS, FTIR, SEM, TEM, HR-TEM, BET, UV–vis DRS, PL, ESR, and mott-Schottky analyses, respectively. The visible light photodegradation of tetracycline (TC) antibiotic and CO2 conversion were carried out in order to evaluate the photocatalytic performance of these synthesized materials. Using the RSM-CCD approach, the influence of key variables on TC degradation were optimized. The results indicated that the optimized photocatalyst (45-FeBiC) exhibited higher photocatalytic performance (99.87 %) compared to other samples via photogenerated •O2, and •OH. Additionally, four cycle studies verified that the 45-FeBiC nanocomposite had adequate photostability. After 6 h of visible light illumination, the 45-FeBiC catalyst generated 33.84 μmol/g of CO and maintained 96.2 % of its initial photocatalytic activity after 30 h of reaction. The enhanced photocatalytic efficiency of the 45-FeBiC nanocomposite is attributed to the photosensitization effect of 3 wt%-Fe2O3/Bi2O3 on g-C3N4 within the S-scheme photocatalytic framework.
利用光催化技术降解污染物并将一氧化碳还原为碳氢化合物燃料,是减少一氧化碳排放和降低环境污染的一种潜在方法。本研究首次介绍了一种通过简单方法合成的创新型 S 型光催化剂(FeO/BiO/g-CN)。分别采用 XRD、XPS、FTIR、SEM、TEM、HR-TEM、BET、UV-vis DRS、PL、ESR 和 mott-Schottky 分析方法对合成光催化剂的结构、形貌和光学性质进行了综合表征。为了评估这些合成材料的光催化性能,对其进行了四环素(TC)抗生素的可见光光降解和 CO 转化实验。利用 RSM-CCD 方法优化了关键变量对 TC 降解的影响。结果表明,与其他样品相比,优化后的光催化剂(45-FeBiC)通过光生成 -O 和 -OH 表现出更高的光催化性能(99.87%)。此外,四次循环研究验证了 45-FeBiC 纳米复合材料具有足够的光稳定性。在可见光照射 6 小时后,45-FeBiC 催化剂生成了 33.84 μmol/g CO,并在反应 30 小时后保持了 96.2% 的初始光催化活性。45-FeBiC 纳米复合材料光催化效率的提高归功于 S 型光催化框架中 3 wt%-FeO/BiO 对 g-CN 的光敏效应。
{"title":"A novel S-scheme photocatalyst Fe2O3/Bi2O3/g-C3N4 with enhanced visible-light photocatalytic performance for antibiotic degradation and CO2 reduction: RSM-based optimization","authors":"Abdelfattah Amari ,&nbsp;Hakim S. Sultan Aljibori ,&nbsp;Zaina Algarni ,&nbsp;Noureddine Elboughdiri ,&nbsp;M.A. Diab ,&nbsp;Kwang-Hyun Baek ,&nbsp;Ibrahim Mahariq","doi":"10.1016/j.jiec.2024.08.002","DOIUrl":"10.1016/j.jiec.2024.08.002","url":null,"abstract":"<div><div>The degradation of pollutants and reduction of CO<sub>2</sub> to hydrocarbon fuels using photocatalysis is a potential approach to reducing CO<sub>2</sub> emissions and decreasing environmental contamination. This study introduces an innovative S-scheme photocatalyst (Fe<sub>2</sub>O<sub>3</sub>/Bi<sub>2</sub>O<sub>3</sub>/g-C<sub>3</sub>N<sub>4</sub>) synthesized through simple methods for the first time. The structural, morphological, and optical properties of the synthesized photocatalysts were comprehensively characterized using XRD, XPS, FTIR, SEM, TEM, HR-TEM, BET, UV–vis DRS, PL, ESR, and mott-Schottky analyses, respectively. The visible light photodegradation of tetracycline (TC) antibiotic and CO<sub>2</sub> conversion were carried out in order to evaluate the photocatalytic performance of these synthesized materials. Using the RSM-CCD approach, the influence of key variables on TC degradation were optimized. The results indicated that the optimized photocatalyst (45-FeBiC) exhibited higher photocatalytic performance (99.87 %) compared to other samples via photogenerated •O<sub>2</sub><sup>−</sup>, and •OH. Additionally, four cycle studies verified that the 45-FeBiC nanocomposite had adequate photostability. After 6 h of visible light illumination, the 45-FeBiC catalyst generated 33.84 μmol/g of CO and maintained 96.2 % of its initial photocatalytic activity after 30 h of reaction. The enhanced photocatalytic efficiency of the 45-FeBiC nanocomposite is attributed to the photosensitization effect of 3 wt%-Fe<sub>2</sub>O<sub>3</sub>/Bi<sub>2</sub>O<sub>3</sub> on g-C<sub>3</sub>N<sub>4</sub> within the S-scheme photocatalytic framework.</div></div>","PeriodicalId":363,"journal":{"name":"Journal of Industrial and Engineering Chemistry","volume":"140 ","pages":"Pages 599-616"},"PeriodicalIF":5.9,"publicationDate":"2024-08-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142211298","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Corrigendum to “Zn-doped aerogel for Ni2+ adsorption (Zn-A-Ni) and reuse of Zn-A-Ni to create Zn, Ni-co-doped carbon aerogel for applications in adsorption and energy storage” [J. Ind. Eng. Chem. (2024) 7534] 用于吸附 Ni2+ 的掺锌气凝胶(Zn-A-Ni)以及重复利用 Zn-A-Ni 制备用于吸附和储能的掺锌、掺镍碳气凝胶》[J. Ind. Eng. Chem. (2024) 7534] 更正
IF 5.9 3区 工程技术 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-08-08 DOI: 10.1016/j.jiec.2024.07.048
Nguyen Huu Hieu , Phan Minh Tu , Nguyen Hoang Kim Duyen , Cao Vu Lam , Dang Ngoc Chau Vy , Ta Dang Khoa , Nguyen Truong Son , Vo Nguyen Dai Viet , Pham Trong Liem Chau
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引用次数: 0
Optimal growth conditions and heavy metal removal of Coelastrella sp. CORE-3 isolated from wastewater 利用从废水中分离出来的 CORE-3 螺旋藻优化生长条件并去除重金属
IF 5.9 3区 工程技术 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-07-17 DOI: 10.1016/j.jiec.2024.07.034
J.S. Park , D.W. Kim , J.B. Kwon , S.H. Park , K.Y. Chung
This study was investigated to optimize growth conditions of native microalgae (Coelastrella sp. CORE-3) from wastewater, evaluate the removal of Cu2+, Zn2+, Cd2+ and Ni2+ and compare both isolated microalgae and Ankistrodesmus bibraianus, and describe their sorption mechanisms on the cell surface. The effects of the pH, light: dark cycle and temperature on the growth of the isolated Coelastrella sp. CORE-3 was optimized. The optimal L:D cycle, temperature, and pH conditions were 14:10 hr, 25℃, pH 7. The growth of isolated microalgae, Coelastrella sp. CORE-3. was compared with A. bibraianus. The removal efficiency of heavy metals by Coelastrella sp. CORE-3 and A. bibraianus were found as follows, respectively: (live cell) Zn2+ > Cd2+ > Cu2+ > Ni2+, (dead cell) Cu2+ > Cd2+ > Zn2+ > Ni2+. SEM analysis indicated that more cell surface deformation occurred in A. bibraianus compared to Coelastrella sp. after exposure to heavy metals. This result suggests that Coelastrella sp. CORE-3 has more resistant to heavy metal toxicity. In addition, based on the FT-IR analysis, the live cells of Coelastrella sp. CORE-3 and A. bibraianus showed the interactions of heavy metals with the functional groups: alcohol, alkane, amide, amine on their cell surfaces.
本研究旨在优化废水中本地微藻(Coelastrella sp. CORE-3)的生长条件,评估其对 Cu2+、Zn2+、Cd2+ 和 Ni2+ 的去除效果,并对分离微藻和 Ankistrodesmus bibraianus 进行比较,描述其在细胞表面的吸附机制。优化了 pH 值、光-暗周期和温度对离体鞘藻 CORE-3 生长的影响。最佳光暗周期、温度和 pH 条件为 14:10 hr、25℃、pH 7。CORE-3 和 A. bibraianus 对重金属的去除率分别为:(活细胞)Zn2+ > Cd2+ > Cu2+ > Ni2+,(死细胞)Cu2+ > Cd2+ > Zn2+ > Ni2+。扫描电镜分析表明,暴露于重金属后,A. bibraianus 的细胞表面变形比 Coelastrella sp.这一结果表明,Coelastrella sp. CORE-3 对重金属毒性的抵抗力更强。此外,根据傅立叶变换红外光谱分析,CORE-3 和 A. bibraianus 的活细胞显示出重金属与细胞表面的功能基团(醇、烷、酰胺、胺)的相互作用。
{"title":"Optimal growth conditions and heavy metal removal of Coelastrella sp. CORE-3 isolated from wastewater","authors":"J.S. Park ,&nbsp;D.W. Kim ,&nbsp;J.B. Kwon ,&nbsp;S.H. Park ,&nbsp;K.Y. Chung","doi":"10.1016/j.jiec.2024.07.034","DOIUrl":"10.1016/j.jiec.2024.07.034","url":null,"abstract":"<div><div>This study was investigated to optimize growth conditions of native microalgae (<em>Coelastrella</em> sp. CORE-3) from wastewater, evaluate the removal of Cu<sup>2+</sup>, Zn<sup>2+</sup>, Cd<sup>2+</sup> and Ni<sup>2+</sup> and compare both isolated microalgae and <em>Ankistrodesmus bibraianus</em>, and describe their sorption mechanisms on the cell surface. The effects of the pH, light: dark cycle and temperature on the growth of the isolated <em>Coelastrella</em> sp. CORE-3 was optimized. The optimal L:D cycle, temperature, and pH conditions were 14:10 hr, 25℃, pH 7. The growth of isolated microalgae, <em>Coelastrella</em> sp. CORE-3. was compared with <em>A. bibraianus.</em> The removal efficiency of heavy metals by <em>Coelastrella</em> sp. CORE-3 and <em>A. bibraianus</em> were found as follows, respectively: (live cell) Zn<sup>2+</sup> &gt; Cd<sup>2+</sup> &gt; Cu<sup>2+</sup> &gt; Ni<sup>2+</sup>, (dead cell) Cu<sup>2+</sup> &gt; Cd<sup>2+</sup> &gt; Zn<sup>2+</sup> &gt; Ni<sup>2+</sup>. SEM analysis indicated that more cell surface deformation occurred in <em>A. bibraianus</em> compared to <em>Coelastrella</em> sp. after exposure to heavy metals. This result suggests that <em>Coelastrella</em> sp. CORE-3 has more resistant to heavy metal toxicity. In addition, based on the FT-IR analysis, the live cells of <em>Coelastrella</em> sp. CORE-3 and <em>A. bibraianus</em> showed the interactions of heavy metals with the functional groups: alcohol, alkane, amide, amine on their cell surfaces.</div></div>","PeriodicalId":363,"journal":{"name":"Journal of Industrial and Engineering Chemistry","volume":"140 ","pages":"Pages 589-598"},"PeriodicalIF":5.9,"publicationDate":"2024-07-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141844650","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Synergistic effect of spinning drawing and preoxidation stretching on the orientation structure of mesophase pitch carbon fibers 纺丝拉伸和预氧化拉伸对介相沥青碳纤维取向结构的协同效应
IF 5.9 3区 工程技术 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-06-25 DOI: 10.1016/j.jiec.2024.06.031

Mesophase pitch carbon fiber has shown remarkable prospects in specialty carbon material. The mechanical properties of mesophase pitch carbon fiber (CF) cannot be precisely controlled because of the difficulty of forming process regulation. The early forming of carbon fiber (precursor fiber (PF) and pre-oxidation fiber (OF)) is difficult to regulate, such as carbon microcrystal and carbon layer texture, while cause the irreversible growth of carbonization process. Herein, a synergy strategy of spinning drawing and preoxidation stretching is developed to optimize orientation structure, eliminate morphology defects and improve mechanical properties. A synergistic effect of superior spinning drawing and suitable preoxidation stretching is beneficial to adjust the more order rearrangement of carbon microcrystals. The tensile strength of carbon fibers with spinning drawing and preoxidation stretching is increased by 1.7 times, and their defects are reduced by 40%. The results show that the excellent mechanical property of carbon fiber is contributed by the extrusion stress caused by high oxidation crosslinked surface layer under tension, and the micro-flow and rearrangement of carbon microcrystals induced by extrusion stress. A mechanical strengthening mechanism of carbon fiber is proposed, which provides guidance for high-performance mesophase pitch carbon fiber.

介相沥青碳纤维在特种碳材料领域有着广阔的发展前景。介相沥青碳纤维(CF)的力学性能无法精确控制,原因在于成型工艺难以调控。碳纤维的早期成型(原纤维(PF)和预氧化纤维(OF))难以调控,如碳微晶和碳层质地,同时造成碳化过程的不可逆生长。在此,我们开发了一种纺丝拉伸和预氧化拉伸的协同策略,以优化取向结构、消除形态缺陷并改善力学性能。优异的纺丝拉伸和适当的预氧化拉伸的协同效应有利于调整碳微晶的有序重排。通过纺丝拉拔和预氧化拉伸,碳纤维的拉伸强度提高了 1.7 倍,缺陷减少了 40%。研究结果表明,碳纤维优异的力学性能得益于高氧化交联表层在张力作用下产生的挤压应力,以及挤压应力引起的碳微晶的微流动和重排。提出了碳纤维的力学强化机理,为高性能介相沥青碳纤维的制备提供了指导。
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引用次数: 0
PMMA microspheres-embedded Ti3C2Tx MXene heterophotocatalysts synergistically working for multiple dye degradation PMMA 微球嵌入 Ti3C2Tx MXene 异种光催化剂协同作用于多种染料降解
IF 5.9 3区 工程技术 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-06-22 DOI: 10.1016/j.jiec.2024.06.006
We developed a novel MXene/polymer hybrid material for enhanced photodegradation of multiple organic dyes. Specifically, uniform-sized PMMA microspheres and multilayer Ti3C2Tx MXene were integrated through a facile solution process to form PMMA/Ti3C2Tx composites. The hybridization of the two components significantly increased the specific surface area and pore volume. An optimized composite showed high photocatalytic activity, demonstrating 93 and 98 % degradation efficiencies for orange G (OG) and rhodamine B (RhB) in 60 min of light illumination. Furthermore, the composite revealed good recyclability without a significant performance drop even after four cycles. Moreover, the composite retained its high photocatalytic activity at various conditions, including elevated temperatures, a wide range of pH levels, and in tap water. These results manifest that the PMMA/Ti3C2Tx hetero-photocatalyst is well suited for use in wastewater treatment and environmental cleanup.
我们开发了一种新型 MXene/聚合物混合材料,用于增强多种有机染料的光降解。具体来说,通过一种简便的溶液工艺,将均匀尺寸的 PMMA 微球和多层 TiCT MXene 融合在一起,形成 PMMA/TiCT 复合材料。两种成分的杂化大大增加了比表面积和孔隙率。优化后的复合材料具有很高的光催化活性,在 60 分钟的光照下,橙 G(OG)和罗丹明 B(RhB)的降解效率分别达到 93% 和 98%。此外,该复合材料还具有良好的可回收性,即使经过四个周期后性能也不会明显下降。此外,该复合材料在各种条件下都保持了很高的光催化活性,包括在高温、各种 pH 值和自来水中。这些结果表明,PMMA/TiCT 异种光催化剂非常适合用于废水处理和环境净化。
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引用次数: 0
A review on the application of perovskite catalysts for sulfate radical-based advanced oxidation processes 过氧化物催化剂在基于硫酸根的高级氧化过程中的应用综述
IF 5.9 3区 工程技术 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-06-14 DOI: 10.1016/j.jiec.2024.06.007
In today’s increasingly serious problem of emerging contaminants (ECs), sulfate radical-based advanced oxidation processes (SR-AOPs) have become one of the options for deep wastewater purification and water remediation. The heterogeneous activation of persulfate without external energy is of great significance. However, how to choose a suitable persulfate activation method to meet the practical requirements is an urgent problem to be solved. Perovskite-based catalysts have been widely used in SR-AOPs because of their advantages such as low cost, high catalytic activity, variety and tunable structures. In this paper, the history, structure and preparation method of perovskite are introduced. Next is the design of perovskite catalyst, include the selection of elements, modification methods and preparation of perovskite-based composites. The synergistic effect of generating oxygen vacancies (OVs) through cation substitution and utilizing bimetallic oxides is a common method in the field of perovskite-mediated SR-AOPs. Finally, the shortcomings and future development direction of this field are discussed. This work helps researchers and practitioners to better select and design perovskite catalysts and perovskite-based composites.
在新兴污染物(ECs)问题日益严重的今天,基于硫酸根的高级氧化工艺(SR-AOPs)已成为废水深度净化和水修复的选择之一。无外部能量的过硫酸盐异质活化具有重要意义。然而,如何选择合适的过硫酸盐活化方法以满足实际要求是一个亟待解决的问题。过硫酸盐基催化剂具有成本低、催化活性高、种类多、结构可调等优点,已被广泛应用于 SR-AOPs 中。本文首先介绍了过氧化物的历史、结构和制备方法。接下来介绍了透辉石催化剂的设计,包括元素的选择、改性方法和基于透辉石的复合材料的制备。通过阳离子置换产生氧空位(OVs)和利用双金属氧化物的协同效应是包晶石介导的 SR-AOPs 领域的常用方法。最后,讨论了该领域的不足之处和未来发展方向。这项工作有助于研究人员和从业人员更好地选择和设计包晶催化剂和基于包晶的复合材料。
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Journal of Industrial and Engineering Chemistry
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