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Engineered hybrid iron-cobalt metal oxide nanoparticles for effective adsorption of malachite green dye 用于有效吸附孔雀石绿染料的工程混合铁钴金属氧化物纳米粒子
IF 2.8 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pub Date : 2024-08-28 DOI: 10.1002/jctb.7737
Nasira Hussain, Shanza Shafaat, Ambreen Sarfraz, Muhammad Usman, Muhammad Saqib Khan, Asad Muhammad Khan, Rafaqat Ali Khan, Bilal Ahmad Zafar Amin, Muhammad Bilal, Ahson Jabbar Shaikh

BACKGROUND

Hybrid iron and cobalt metal oxide nanoparticles are well known; however, are not optimized in terms of size and stability. We engineered these hybrid nanoparticles using the co-precipitation method and characterized them by various techniques, which are then used for the effective adsorption and removal of malachite green (MG) dye.

RESULTS

The ideal conditions for synthesis are determined to be 50:50 ratio of Fe2O3 and CoO, pH of 11, temperature range of 40 °C–60 °C, and reactant addition time of 20 min. These hybrid nanoadsorbents effectively eliminated MG dye from aqueous solutions. Factors such as initial MG dye concentration, pH of the medium, contact time, temperature, and nanoadsorbent dose were optimized for the MG removal to achieve a maximum removal efficiency of 96.9%. Non-linear fitting of data indicates that both Langmuir and Freundlich models provided the best fit, suggesting the presence of both monolayer and multilayer adsorption of MG on hybrid nanoparticles. The kinetics of MG dye removal are better controlled by the intraparticle diffusion (IPD) phenomenon. The adsorption of MG onto the hybrid nanoparticles was confirmed to be endothermic, with negative ΔG and positive ΔH values. The optimized synthetic conditions also positively impacted the hybrid nanoparticles which enhanced the adsorption and exhibited ferromagnetic behavior as compared to the superparamagnetic behavior reported in the literature, making them significantly important for dye removal applications.

CONCLUSION

These findings demonstrate the potential of optimized hybrid nanoparticles as effective nanoadsorbents for dye removal applications, with implications for further applications in photocatalysis and sensing. © 2024 Society of Chemical Industry (SCI).

背景众所周知,铁和钴金属氧化物杂化纳米粒子在尺寸和稳定性方面尚未达到最佳状态。我们采用共沉淀法设计了这种混合纳米粒子,并通过各种技术对其进行了表征,然后将其用于有效吸附和去除孔雀石绿(MG)染料。结果理想的合成条件是 Fe2O3 和 CoO 的比例为 50:50,pH 值为 11,温度范围为 40 ℃-60 ℃,反应物添加时间为 20 分钟。这些混合纳米吸附剂能有效去除水溶液中的 MG 染料。在去除 MG 的过程中,对 MG 染料的初始浓度、介质的 pH 值、接触时间、温度和纳米吸附剂的剂量等因素进行了优化,以达到 96.9% 的最高去除率。数据的非线性拟合表明,Langmuir 模型和 Freundlich 模型都提供了最佳拟合,表明混合纳米粒子上存在单层和多层 MG 吸附。颗粒内扩散(IPD)现象更好地控制了 MG 染料的去除动力学。混合纳米粒子对 MG 的吸附被证实是内热的,ΔG 值为负,ΔH 值为正。优化的合成条件也对杂化纳米粒子产生了积极影响,增强了吸附能力,与文献报道的超顺磁性相比,杂化纳米粒子表现出铁磁性,这使其在染料去除应用中具有重要意义。© 2024 化学工业学会(SCI)。
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引用次数: 0
Rapid precipitation of vanadium from solution using melamine as precipitant with high efficiency 以三聚氰胺为沉淀剂从溶液中高效快速沉淀钒
IF 2.8 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pub Date : 2024-08-28 DOI: 10.1002/jctb.7738
Bo Wang, Qiaowen Yang, Ting Li, Sifan Cui, Pengqiang Feng, Xuan Hou

BACKGROUND

Selective catalytic reduction (SCR) can effectively remove NOx from flue gas in a coal-fired power plant. As the core of SCR technology, the catalyst has a limited lifespan. The process of reducing acid leaching and roasting water leaching can efficiently extract vanadium and tungsten from spent SCR catalyst. For vanadium recovery in solution, the traditional vanadium precipitation process by NH4Cl has the disadvantages of consuming high precipitant dosage and producing large amounts of waste water.

RESULTS

This study focused on the vanadium precipitation process using a solution containing vanadium obtained from adopting some steps to handle the spent SCR catalyst. First, melamine was screened out as the vanadium precipitant. Then, the vanadium precipitation conditions were optimized as follows: solution pH value of 1.0, n(C3H6N6)/n(V) = 0.8, 110 °C and 30 min. Under the best precipitation conditions, the vanadium precipitation efficiency of melamine can reach 99.32%. Finally, the mechanisms of vanadium precipitation by NH4Cl and melamine were discussed, respectively.

CONCLUSION

The results showed that the vanadium precipitation process by NH4Cl followed the chemical reactions between NH4+ and vanadium ions, while the vanadium precipitation process by melamine followed the redox and complexation reactions which essentially belonged to the types of chemical adsorption. The vanadium precipitation product was roasted at 550 °C for 2 h to obtain the vanadium product. The main component of the vanadium product was V2O5, with a purity of 93.27 wt%. The total recovery efficiency of vanadium from spent SCR catalyst was 78.24%. © 2024 Society of Chemical Industry (SCI).

背景选择性催化还原(SCR)可有效去除燃煤发电厂烟气中的氮氧化物。作为 SCR 技术的核心,催化剂的使用寿命有限。还原酸浸出和焙烧水浸出工艺可从废 SCR 催化剂中有效提取钒和钨。对于溶液中的钒回收,传统的 NH4Cl 钒沉淀工艺存在沉淀剂用量大、产生大量废水的缺点。首先,筛选出三聚氰胺作为钒沉淀剂。然后,对钒沉淀条件进行了如下优化:溶液 pH 值为 1.0,n(C3H6N6)/n(V) = 0.8,温度为 110 °C,时间为 30 分钟。在最佳沉淀条件下,三聚氰胺的钒沉淀效率可达 99.32%。结果表明,NH4Cl沉钒过程遵循NH4+与钒离子之间的化学反应,而三聚氰胺沉钒过程遵循氧化还原和络合反应,本质上属于化学吸附类型。钒沉淀产物在 550 ℃ 下焙烧 2 小时后得到钒产物。钒产品的主要成分是 V2O5,纯度为 93.27%。从废 SCR 催化剂中回收钒的总效率为 78.24%。© 2024 化学工业学会(SCI)。
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引用次数: 0
Zinc-based metal–organic frameworks for encapsulation and sustained release of ciprofloxacin for excellent antibacterial activities 用于包封和持续释放环丙沙星的锌基金属有机框架,具有卓越的抗菌活性
IF 2.8 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pub Date : 2024-08-23 DOI: 10.1002/jctb.7736
Abdul Rauf, Mohsin Javed, Muhammad Jahangir, Mehdi Hassan, Anam Tariq, Wajahat Ali, Ali Bahadur, Shahid Iqbal, Sajid Mahmood, Khalid M Alotaibi, Matar Alshalwi

BACKGROUND

In terms of crystalline nanoporous materials, metal–organic frameworks (MOFs) are relatively new. They are self-assembling structures made of organic ligands that serve as linkers between metal centers and metal ions that function as coordination centers. Due to MOFs' high porosity, absence of nonaccessible bulk volume, vast surface areas and variety of pore sizes and topologies, drug delivery via them is becoming more and more common.

RESULTS

Zn-MOF and Zn-MOF@drug were produced using a solvothermal approach in this study and characterized using a variety of methods, including Fourier transform infrared spectroscopy, powder X-ray diffraction and scanning electron microscopy. Utilizing the zone of inhibition and minimum inhibitory concentration approaches, Zn-MOF and Zn-MOF@drug were evaluated for their antibacterial capability against Escherichia coli and Bacillus subtilis, two types of bacteria.

CONCLUSION

The antibacterial potential of Zn-MOF@drug was greater than that of the metal salt, commercially available ZnO, Zn-MOF and ligand alone. The mechanism of antibacterial activity of Zn-MOF@drug was also discussed. © 2024 Society of Chemical Industry (SCI).

背景 在结晶纳米多孔材料方面,金属有机框架(MOFs)相对较新。它们是由有机配体自组装而成的结构,有机配体是金属中心与作为配位中心的金属离子之间的连接体。由于 MOFs 具有高孔隙率、无不可获取的体积、巨大的表面积以及各种孔隙大小和拓扑结构,通过它们进行药物输送正变得越来越普遍。研究结果本研究采用溶热法制备了 Zn-MOF 和 Zn-MOF@药物,并使用傅立叶变换红外光谱、粉末 X 射线衍射和扫描电子显微镜等多种方法对其进行了表征。结论 Zn-MOF@drug 的抗菌潜力大于金属盐、市售 ZnO、Zn-MOF 和单独的配体。此外,还讨论了 Zn-MOF@drug 的抗菌机制。© 2024 化学工业学会(SCI)。
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引用次数: 0
Adsorption of vanadium using a new anionic Schiff Base adsorbent and its application to vanadium separation from boiler ash 新型阴离子席夫碱吸附剂对钒的吸附及其在锅炉灰中钒分离中的应用
IF 2.8 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pub Date : 2024-08-22 DOI: 10.1002/jctb.7733
Mohamed Abdalla

Background

This study reports the preparation of 2-hydroxy-3-(4-(((2-((2-(((E)-4-(2-hydroxy-3-(trimethylammonio)propoxy)-3-methoxybenzylidene)amino)ethyl)amino)ethyl)imino)methyl)-2-methoxyphenoxy)-N,N,N-trimethylpropan-1-aminium (HYM/QA). The adsorbent was employed to extract and concentrate vanadium from its solutions and boiler ash samples.

Results

The impact of initial dosage, pH, reaction time and temperature on the sorption behavior of V(V) was examined. Under optimal conditions (pH 5, 0.08 g dose, 45 min at room temperature), a sorption capacity of 392.25 mg g−1 was achieved. The uptake of V(V) on HYM/QA was effectively reversed using 1 mol L−1 NaOH, regenerating the material. After six cycles of sorption and elution, the sorption capability remained at 91.4% of its initial value. The efficiency and selectivity of HYM/QA toward V5+ ions were assessed using the separation factor parameter, revealing limited interference from heavy metals such as Mn2+, Cr3+, Pb2+, Si4+, Al3+, NO32−, HCO3 and Zn2+. The uptake process of HYM/QA for V(V) conformed to the Langmuir and Dubinin–Radushkevich isotherm models and the pseudo-second-order kinetic model. HYM/QA was characterized by infrared, Brunauer–Emmett–Teller surface area, 1H NMR, 13C NMR and gas chromatography–mass spectrometry analyses, confirming successful preparation. Thermodynamic assessments suggested that the sorption process is endothermic, spontaneous and becoming more favorable with rising temperature.

Conclusion

The optimized conditions were used to adsorb vanadium from boiler ash samples, and the obtained vanadium pentaoxide was analyzed and confirmed using various tools, demonstrating the material's effectiveness for vanadium extraction. © 2024 Society of Chemical Industry (SCI).

背景本研究报道了2-羟基-3-(4-(((2-((2-(((E)-4-(2-羟基-3-(三甲基氨基)丙氧基)-3-甲氧基亚苄基)氨基)乙基)氨基)乙基)亚氨基)甲基)-2-甲氧基苯氧基)-N,N,N-三甲基丙-1-铵(HYM/QA)的制备。结果考察了初始用量、pH 值、反应时间和温度对钒吸附行为的影响。在最佳条件下(pH 值 5,0.08 克剂量,室温下 45 分钟),吸附容量达到 392.25 毫克 g-1。使用 1 mol L-1 NaOH 可以有效地逆转 HYM/QA 对 V(V) 的吸收,使材料再生。经过六次吸附和洗脱循环后,吸附能力保持在初始值的 91.4%。使用分离因数参数评估了 HYM/QA 对 V5+ 离子的效率和选择性,结果显示重金属(如 Mn2+、Cr3+、Pb2+、Si4+、Al3+、NO32-、HCO3- 和 Zn2+)的干扰有限。HYM/QA 对 V(V)的吸收过程符合 Langmuir 和 Dubinin-Radushkevich 等温线模型以及假二阶动力学模型。对 HYM/QA 进行了红外、Brunauer-Emmett-Teller 表面积、1H NMR、13C NMR 和气相色谱-质谱分析,确认制备成功。热力学评估表明,吸附过程是内热的、自发的,并且随着温度的升高变得更加有利。结论利用优化的条件从锅炉灰烬样品中吸附钒,并利用各种工具对所获得的五氧化二钒进行分析和确认,证明了该材料提取钒的有效性。© 2024 化学工业学会(SCI)。
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引用次数: 0
Ibuprofen removal by modified natural zeolite: characterization, modeling, and adsorption mechanisms 用改性天然沸石去除布洛芬:表征、建模和吸附机理
IF 2.8 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pub Date : 2024-08-22 DOI: 10.1002/jctb.7729
Anna Carla Ribeiro, Wardleison Martins Moreira, Bruna Bruguer Ferri, Débora dos Federici Santos, Mara Heloisa Neves Olsen Scaliante, Elizabeth de da Costa Neves Fernandes Almeida Duarte, Rosângela Bergamasco

BACKGROUND

Developing robust technologies to remove emerging pollutants from water is urgent since conventional treatments are not technically prepared to remove them. This paper investigated the ibuprofen (IBU) adsorption capacity onto natural zeolite (NZ) and hydrothermally modified zeolite in an acidic medium followed by impregnation with the cationic surfactant cetyltrimethylammonium bromide (CTAB) (MZHT-CTAB). The materials characterization included scanning electron microscopy (SEM), X-ray diffraction (XRD), atomic absorption spectroscopy (AAS), Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA/DTG), N2 adsorption/desorption isotherm (BET), Zeta Potential (ZP), and Point of Zero Charge (pHPZC). The adsorptive capacity studies were carried out by varying the pH solution, a kinetic study at three concentrations (25, 50, and 100 mg L−1), and the contaminant concentration influence (5–100 mg L−1).

RESULTS

The results showed that the MZHT-CTAB obtained both the highest removal efficiency (~ 37%) and the highest adsorption capacity (~ 14 mg g−1) at pH 5.0. The Pseudo Second-Order (PSO) model, which showed the best fit to the experimental data, is significant as it indicates the reliability of our results. The maximum adsorption capacity for the concentration of 100 mg L−1 was 11.93 mg g−1. According to Giles's classification, the isotherm was classified as S-3 type, indicating the competition between the adsorbate and water molecules for the active sites on the adsorbent surface.

CONCLUSION

The adsorption studies demonstrate that the novel adsorbent (MZHT-CTAB) is highly effective in removing IBU, presenting a significant removal capacity and feasibility. This promising result contributes to the ongoing search for alternative materials for water treatment. © 2024 Society of Chemical Industry (SCI).

背景由于传统的处理方法在技术上无法去除水中的新污染物,因此迫切需要开发强有力的技术来去除这些污染物。本文研究了布洛芬(IBU)在酸性介质中天然沸石(NZ)和水热改性沸石上的吸附能力,然后用阳离子表面活性剂十六烷基三甲基溴化铵(CTAB)(MZHT-CTAB)进行浸渍。材料表征包括扫描电子显微镜 (SEM)、X 射线衍射 (XRD)、原子吸收光谱 (AAS)、傅立叶变换红外光谱 (FTIR)、热重分析 (TGA/DTG)、N2 吸附/解吸等温线 (BET)、Zeta 电位 (ZP) 和零电荷点 (pHPZC)。结果表明,在 pH 值为 5.0 时,MZHT-CTAB 获得了最高的去除效率(约 37%)和最高的吸附容量(约 14 mg g-1)。伪二阶(PSO)模型与实验数据的拟合效果最好,这表明我们的结果是可靠的。浓度为 100 mg L-1 时的最大吸附容量为 11.93 mg g-1。根据 Giles 的分类,等温线被归类为 S-3 型,表明吸附剂表面的活性位点存在吸附剂和水分子之间的竞争。这一令人鼓舞的结果为目前寻找水处理替代材料做出了贡献。© 2024 化学工业学会(SCI)。
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引用次数: 0
Ferrate(VI) green oxidant: electrochemical generation, self-decomposition, and application for reactive red 195 azo dye treatment 六价铬铁绿色氧化剂:电化学生成、自分解及在活性红 195 偶氮染料处理中的应用
IF 2.8 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pub Date : 2024-08-22 DOI: 10.1002/jctb.7734
Thi Van Anh Nguyen, Thi Thanh Thuy Mai, Thi Binh Phan, Huu Quang Tran, Minh Quy Bui

BACKGROUND

Ferrate(VI), an environmentally friendly oxidant, has recently emerged as one of the most promising chemicals for water and wastewater treatment due to its versatile application as an oxidant, coagulant, and disinfectant. In this paper, the factors affecting the electrosynthesis process of ferrate using ductile iron anode were studied. Besides, the obtained ferrate was used to remove reactive red 195 (RR195).

RESULTS

The optimal ferrate electrochemical synthesis conditions were determined, including 14 mol L−1 NaOH electrolyte solution, a current density of 40 mA cm−2, and electrolysis time of approximately 5–6 h. Furthermore, the kinetics of the ferrate's self-decomposition reaction was also studied at different temperatures. The decomposition process of ferrate in a 14 mol L−1 NaOH environment followed second-order kinetics, with reaction rate constants of 4.70 × 10−9, 7.31 × 10−8, 1.95 × 10−7, and 4.70 × 10−7 (L mol−1 s−1) at temperatures of 4, 10, 20, and 30 °C, respectively. RR195 treatment efficiency by ferrate reached 96.3% in a short time of 3 min at pH 3 with a ferrate/RR195 molar ratio of 30/1.

CONCLUSION

This study identified the optimal conditions for the electrochemical synthesis of ferrate using a ductile iron anode. Ferrate was stable at a low temperature of 4 °C, so unused ferrate needs to be stored at low temperatures to avoid decomposition of ferrate. The ferrate green oxidant demonstrated high efficiency in the treatment of RR195 in a short time. © 2024 Society of Chemical Industry (SCI).

背景资料 硫酸铁(VI)是一种环境友好型氧化剂,由于其可用作氧化剂、混凝剂和消毒剂等多种用途,最近已成为水和废水处理领域最有前途的化学品之一。本文研究了影响使用球墨铸铁阳极电合成铁酸盐过程的因素。结果确定了最佳的铁酸盐电化学合成条件,包括 14 mol L-1 NaOH 电解质溶液、40 mA cm-2 的电流密度和约 5-6 h 的电解时间。在 14 mol L-1 NaOH 环境中,铁酸盐的分解过程遵循二阶动力学,在温度为 4、10、20 和 30 °C 时,反应速率常数分别为 4.70 × 10-9、7.31 × 10-8、1.95 × 10-7 和 4.70 × 10-7 (L mol-1 s-1)。在 pH 值为 3、铁/RR195 摩尔比为 30/1 的条件下,铁酸对 RR195 的处理效率在 3 分钟的短时间内达到 96.3%。铁酸酯在 4 ℃ 的低温下稳定,因此未使用的铁酸酯需要在低温下储存,以避免铁酸酯分解。铁酸绿色氧化剂可在短时间内高效处理 RR195。© 2024 化学工业协会(SCI)。
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引用次数: 0
Textile waste pretreatment for anaerobic digestion: a review and technology feasibility study 用于厌氧消化的纺织废物预处理:综述和技术可行性研究
IF 2.8 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pub Date : 2024-08-21 DOI: 10.1002/jctb.7728
Naveenrajah Tharmarajah, Kaveh Shahbaz, Saeid Baroutian

The increasing volume of textile waste in landfills and incineration poses severe environmental challenges. Waste valorisation of textile waste via anaerobic digestion (AD) is preferable, as it offers economic and environmental benefits, but it is hindered by textile complexity, necessitating effective pretreatment technologies to improve biogas production. This study aims to evaluate various pretreatment technologies for biogas production from textile fibres via AD. A weighted-scoring analysis (WSA) assessed pretreatment methods based on technical, economic, environmental and operational criteria. Hydrothermal pretreatment emerged as the most technically effective method, scoring 140 owing to its substantial methane enhancement. Economically, shredding was the most viable option, scoring 125, as a consequence of low capital and O&M cost. Environmentally, hydrothermal and deep eutectic solvent (DES) pretreatments were top performers with 100 points owing to low environmental impact and positive heat reactions. In a case study conducted in the Auckland region, the potential environmental impact (PEI) obtained from hydrothermal and DES were 169 and 92 per year, respectively, resulting in minimal environmental impact. Operationally, ultrasonic and biological pretreatments scored highest owing to their ease of operation, and minimal health and safety requirements. Overall, hydrothermal pretreatment achieved the highest WSA score of 340, reflecting its balanced performance across all criteria. Hydrothermal pretreatment is the most promising technology for enhancing biogas production from textile waste. Its technical efficiency, economic feasibility and environmental benefits regarding the WSA score make it suitable for upscaling and providing a viable solution for managing textile waste in the AD plant. © 2024 The Author(s). Journal of Chemical Technology and Biotechnology published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry (SCI).

垃圾填埋和焚烧产生的纺织废物数量不断增加,给环境带来了严峻的挑战。通过厌氧消化(AD)对纺织废弃物进行废物价值化是可取的,因为它具有经济和环境效益,但它受到纺织品复杂性的阻碍,需要有效的预处理技术来提高沼气产量。本研究旨在评估通过 AD 从纺织纤维中生产沼气的各种预处理技术。加权评分分析法(WSA)根据技术、经济、环境和操作标准对预处理方法进行了评估。热水解预处理是技术上最有效的方法,得分 140 分,因为它能大量增加甲烷。在经济上,粉碎是最可行的选择,得分为 125 分,因为资本和运营及维护成本较低。在环境方面,水热法和深共晶溶剂(DES)预处理法因对环境影响小和热反应积极而表现最佳,得分为 100 分。在奥克兰地区进行的一项案例研究中,水热法和 DES 每年对环境的潜在影响(PEI)分别为 169 分和 92 分,对环境的影响极小。在操作方面,超声波预处理和生物预处理得分最高,因为它们易于操作,对健康和安全的要求最低。总体而言,热液预处理的 WSA 得分最高,为 340 分,反映了其在所有标准中的均衡表现。热液预处理是最有希望提高纺织废料沼气产量的技术。它的技术效率、经济可行性和 WSA 分数方面的环境效益使其适合升级,并为厌氧消化(AD)工厂管理纺织废物提供了可行的解决方案。作者:© 2024。化学技术和生物技术期刊》由约翰威利和桑斯有限公司代表化学工业学会(SCI)出版。
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引用次数: 0
Exploring enhanced syngas production via the catalytic performance of metal-doped X-Ni/CeO2 (X = Zr, La, Sr) in the dry reforming of methane 探索掺杂金属的 X-Ni/CeO2(X = Zr、La、Sr)在甲烷干转化过程中的催化性能,以提高合成气产量
IF 2.8 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pub Date : 2024-08-20 DOI: 10.1002/jctb.7732
Wan Nabilah Manan, Wan Nor Roslam Wan Isahak, Zahira Yaakob, Salma Samidin, Khairul Naim Ahmad, Mohd Nor Latif, Ali Faris Aldoghachi, Yun Hin Taufiq-Yap

Background

The quest to manufacture large amounts of syngas to bridge fossil fuels and the renewable energy ecosystem stimulates the creation of efficient and stable heterogeneous catalysts. The NiCeO2 catalysts, synthesized via ultrasonic-assisted citric acid complexation, are highly efficient for the dry reforming of methane (DRM) reaction. Different promoter metals (Zr, La and Sr) were tested for catalytic performance and syngas production. A range of analyses, including X-ray diffraction (XRD), N2 physisorption, H2 temperature-programmed reduction, CO2 temperature-programmed desorption, field emission scanning electron microscopy (FESEM), transmission electron microscopy and X-ray photoelectron spectroscopy, were employed to characterize the physicochemical properties of the catalysts.

Results

XRD results indicated the formation of NiO, CeO2, solid solution ceria–zirconia, perovskite LaNiO3 and SrNiO3 crystalline phases. FESEM results showed the promoted catalysts (Zr, La, Sr) produce large pores to facilitate reactant diffusion, with zirconia specifically creating a spiderweb morphology. At 800 °C, the CH4 and CO2 conversions follow the sequence of NiCeO2 catalyst (CH4 = 54%, CO2 = 45%) < Sr/NiCeO2 (CH4 = 60%, CO2 = 67%) < La/NiCeO2 (CH4 = 85%, CO2 = 84%) < Zr/NiCeO2 (CH4 = 95%, CO2 = 87%). The integration of promoters in DRM catalysts has notably improved carbon formation resistance, as evidenced by the following ranking: Zr/NiCeO2 (5.1 wt%) < commercial catalyst (6.0 wt%) < La/NiCeO2 (7.85 wt%) < Sr/NiCeO2 (10.9 wt%) < NiCeO2 (11.3 wt%).

Conclusion

This study demonstrates that incorporating promoters, particularly Zr, in NiCeO2 significantly enhances resistance to carbon formation. It offers valuable insights into selecting metal catalyst promoters for excellent catalytic performance in DRM. © 2024 Society of Chemical Industry (SCI).

背景 为生产大量合成气,在化石燃料和可再生能源生态系统之间架起一座桥梁,对高效、稳定的异相催化剂的需求不断增长。通过超声波辅助柠檬酸络合合成的 NiCeO2 催化剂在甲烷干转化(DRM)反应中具有很高的效率。对不同的促进金属(Zr、La 和 Sr)的催化性能和合成气产量进行了测试。采用了一系列分析方法,包括 X 射线衍射 (XRD)、N2 物理吸附、H2 温度编程还原、CO2 温度编程解吸、场发射扫描电子显微镜 (FESEM)、透射电子显微镜和 X 射线光电子能谱,来表征催化剂的物理化学特性。 结果 XRD 结果表明形成了 NiO、CeO2、固溶体铈氧化锆、包晶 LaNiO3 和 SrNiO3 结晶相。FESEM 结果表明,促进催化剂(Zr、La、Sr)产生了大孔,以促进反应物的扩散,特别是氧化锆形成了蛛网状形态。800 °C 时,CH4 和 CO2 的转化率依次为 NiCeO2 催化剂(CH4 = 54%,CO2 = 45%);Sr/NiCeO2(CH4 = 60%,CO2 = 67%);La/NiCeO2(CH4 = 85%,CO2 = 84%);Zr/NiCeO2(CH4 = 95%,CO2 = 87%)。在 DRM 催化剂中加入促进剂可显著提高抗碳形成能力,具体排名如下:Zr/NiCeO2(5.1 wt%);商用催化剂(6.0 wt%);La/NiCeO2(7.85 wt%);Sr/NiCeO2(10.9 wt%);NiCeO2(11.3 wt%)。 结论 本研究表明,在 NiCeO2 中加入促进剂(尤其是 Zr)可显著提高抗碳形成的能力。它为在 DRM 中选择金属催化剂促进剂以获得优异的催化性能提供了宝贵的见解。© 2024 化学工业协会 (SCI)。
{"title":"Exploring enhanced syngas production via the catalytic performance of metal-doped X-Ni/CeO2 (X = Zr, La, Sr) in the dry reforming of methane","authors":"Wan Nabilah Manan,&nbsp;Wan Nor Roslam Wan Isahak,&nbsp;Zahira Yaakob,&nbsp;Salma Samidin,&nbsp;Khairul Naim Ahmad,&nbsp;Mohd Nor Latif,&nbsp;Ali Faris Aldoghachi,&nbsp;Yun Hin Taufiq-Yap","doi":"10.1002/jctb.7732","DOIUrl":"https://doi.org/10.1002/jctb.7732","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Background</h3>\u0000 \u0000 <p>The quest to manufacture large amounts of syngas to bridge fossil fuels and the renewable energy ecosystem stimulates the creation of efficient and stable heterogeneous catalysts. The NiCeO<sub>2</sub> catalysts, synthesized via ultrasonic-assisted citric acid complexation, are highly efficient for the dry reforming of methane (DRM) reaction. Different promoter metals (Zr, La and Sr) were tested for catalytic performance and syngas production. A range of analyses, including X-ray diffraction (XRD), N<sub>2</sub> physisorption, H<sub>2</sub> temperature-programmed reduction, CO<sub>2</sub> temperature-programmed desorption, field emission scanning electron microscopy (FESEM), transmission electron microscopy and X-ray photoelectron spectroscopy, were employed to characterize the physicochemical properties of the catalysts.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>XRD results indicated the formation of NiO, CeO<sub>2</sub>, solid solution ceria–zirconia, perovskite LaNiO<sub>3</sub> and SrNiO<sub>3</sub> crystalline phases. FESEM results showed the promoted catalysts (Zr, La, Sr) produce large pores to facilitate reactant diffusion, with zirconia specifically creating a spiderweb morphology. At 800 °C, the CH<sub>4</sub> and CO<sub>2</sub> conversions follow the sequence of NiCeO<sub>2</sub> catalyst (CH<sub>4</sub> = 54%, CO<sub>2</sub> = 45%) &lt; Sr/NiCeO<sub>2</sub> (CH<sub>4</sub> = 60%, CO<sub>2</sub> = 67%) &lt; La/NiCeO<sub>2</sub> (CH<sub>4</sub> = 85%, CO<sub>2</sub> = 84%) &lt; Zr/NiCeO<sub>2</sub> (CH<sub>4</sub> = 95%, CO<sub>2</sub> = 87%). The integration of promoters in DRM catalysts has notably improved carbon formation resistance, as evidenced by the following ranking: Zr/NiCeO<sub>2</sub> (5.1 wt%) &lt; commercial catalyst (6.0 wt%) &lt; La/NiCeO<sub>2</sub> (7.85 wt%) &lt; Sr/NiCeO<sub>2</sub> (10.9 wt%) &lt; NiCeO<sub>2</sub> (11.3 wt%).</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusion</h3>\u0000 \u0000 <p>This study demonstrates that incorporating promoters, particularly Zr, in NiCeO<sub>2</sub> significantly enhances resistance to carbon formation. It offers valuable insights into selecting metal catalyst promoters for excellent catalytic performance in DRM. © 2024 Society of Chemical Industry (SCI).</p>\u0000 </section>\u0000 </div>","PeriodicalId":15335,"journal":{"name":"Journal of chemical technology and biotechnology","volume":"99 11","pages":"2420-2433"},"PeriodicalIF":2.8,"publicationDate":"2024-08-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142430199","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Construction of magnetic bimetallic oxide-decorated attapulgite-based adsorbents for arsenic ion adsorption 构建用于砷离子吸附的磁性双金属氧化物装饰阿塔蓬石基吸附剂
IF 2.8 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pub Date : 2024-08-09 DOI: 10.1002/jctb.7727
Bo Yu, Xiaoning Li, Jiao Ma, Han Yan, Ke Lian, Pengfei Shen

BACKGROUND

Arsenic contamination can exert severe detrimental effects on the ecological environment and human health. It can cause acute or chronic poisoning, resulting in cell distortion or cancer when humans come into contact with or consume arsenic-containing water. Adsorption technology is one of the effective methods for arsenic removal. In this study, using attapulgite (ATP) as a support for bimetallic iron–manganese oxides, a series of adsorbents (Fe-Mn/ATP) with different manganese-to-iron molar ratios were prepared via the coprecipitation method. Scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy mapping, X-ray diffraction and zeta potential measurements were used to analyze the structure and properties of Fe-Mn/ATP. In addition, the adsorption performance of the material for arsenic ions was investigated by static adsorption and dynamic adsorption experiments.

RESULTS

A novel Fe-Mn/ATP adsorbent was prepared using ATP as the raw material and manganese-to-iron molar ratio was 1:3 by coprecipitation at 60 °C for 1 h. The adsorption efficiency of arsenic ions was optimal at an Fe-Mn/ATP dosage of 2 g L−1, pH 4 and a contact time of 10 min, reaching a maximum adsorption capacity of 38.27 mg g−1 at room temperature. The adsorption process followed the pseudo-second-order kinetic model and the Langmuir isotherm adsorption model, indicating that arsenic ion adsorption by Fe-Mn/ATP was mainly monolayer chemical adsorption. Furthermore, Fe-Mn/ATP showed a removal rate for arsenic ions of over 80% after four cycles of regeneration, revealing a great potential for practical application.

CONCLUSION

This study offers a promising Fe-Mn/ATP adsorbent for removal of arsenic ions from wastewater. © 2024 Society of Chemical Industry (SCI).

砷污染会对生态环境和人类健康造成严重危害。当人类接触或饮用含砷的水时,会引起急性或慢性中毒,导致细胞畸变或癌症。吸附技术是去除砷的有效方法之一。本研究以阿塔波来石(ATP)作为双金属铁锰氧化物的载体,通过共沉淀法制备了一系列不同锰铁摩尔比的吸附剂(Fe-Mn/ATP)。利用扫描电子显微镜结合能量色散 X 射线光谱图、X 射线衍射和 zeta 电位测量分析了 Fe-Mn/ATP 的结构和性质。以 ATP 为原料,锰-铁摩尔比为 1:3,在 60 ℃ 共沉淀 1 小时,制备了新型铁-锰/ATP 吸附剂。在铁锰/ATP 的用量为 2 g L-1、pH 值为 4、接触时间为 10 分钟时,砷离子的吸附效率最佳,室温下的最大吸附容量为 38.27 mg g-1。吸附过程遵循伪二阶动力学模型和 Langmuir 等温线吸附模型,表明 Fe-Mn/ATP 对砷离子的吸附主要是单层化学吸附。此外,Fe-Mn/ATP 经过四次再生后对砷离子的去除率超过 80%,显示出巨大的实际应用潜力。© 2024 化学工业学会(SCI)。
{"title":"Construction of magnetic bimetallic oxide-decorated attapulgite-based adsorbents for arsenic ion adsorption","authors":"Bo Yu,&nbsp;Xiaoning Li,&nbsp;Jiao Ma,&nbsp;Han Yan,&nbsp;Ke Lian,&nbsp;Pengfei Shen","doi":"10.1002/jctb.7727","DOIUrl":"10.1002/jctb.7727","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> BACKGROUND</h3>\u0000 \u0000 <p>Arsenic contamination can exert severe detrimental effects on the ecological environment and human health. It can cause acute or chronic poisoning, resulting in cell distortion or cancer when humans come into contact with or consume arsenic-containing water. Adsorption technology is one of the effective methods for arsenic removal. In this study, using attapulgite (ATP) as a support for bimetallic iron–manganese oxides, a series of adsorbents (Fe-Mn/ATP) with different manganese-to-iron molar ratios were prepared via the coprecipitation method. Scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy mapping, X-ray diffraction and zeta potential measurements were used to analyze the structure and properties of Fe-Mn/ATP. In addition, the adsorption performance of the material for arsenic ions was investigated by static adsorption and dynamic adsorption experiments.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> RESULTS</h3>\u0000 \u0000 <p>A novel Fe-Mn/ATP adsorbent was prepared using ATP as the raw material and manganese-to-iron molar ratio was 1:3 by coprecipitation at 60 °C for 1 h. The adsorption efficiency of arsenic ions was optimal at an Fe-Mn/ATP dosage of 2 g L<sup>−1</sup>, pH 4 and a contact time of 10 min, reaching a maximum adsorption capacity of 38.27 mg g<sup>−1</sup> at room temperature. The adsorption process followed the pseudo-second-order kinetic model and the Langmuir isotherm adsorption model, indicating that arsenic ion adsorption by Fe-Mn/ATP was mainly monolayer chemical adsorption. Furthermore, Fe-Mn/ATP showed a removal rate for arsenic ions of over 80% after four cycles of regeneration, revealing a great potential for practical application.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> CONCLUSION</h3>\u0000 \u0000 <p>This study offers a promising Fe-Mn/ATP adsorbent for removal of arsenic ions from wastewater. © 2024 Society of Chemical Industry (SCI).</p>\u0000 </section>\u0000 </div>","PeriodicalId":15335,"journal":{"name":"Journal of chemical technology and biotechnology","volume":"99 11","pages":"2395-2406"},"PeriodicalIF":2.8,"publicationDate":"2024-08-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141925017","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Production of magnetic photocatalysts from TiO2, Fe(NO3)3 and sucrose and their application for the degradation of model organic contaminants 利用二氧化钛、Fe(NO3)3 和蔗糖生产磁性光催化剂并将其用于降解模型有机污染物
IF 2.8 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pub Date : 2024-08-08 DOI: 10.1002/jctb.7725
Leydiane de Oliveira Pereira, Iara do Rosario Guimarães, Luana Pereira Zampiere, Isabela Sales Marques, Stéfany Gonçalves de Moura, Aline Aparecida Caetano, Fabiano Magalhães

BACKGROUND

Photocatalysis is an efficient method for the removal of organic contaminants in wastewater. In this study, different magnetic photocatalysts for the degradation of organic compounds were prepared.

RESULTS

Ti/C/Fe photocatalysts were prepared by supporting TiO2 (20, 40 and 60% w/w) on a carbon/iron oxide (C/Fe) magnetic carrier. Characterization via Raman spectroscopy, X-ray diffractometry, thermal analysis, X-ray fluorescence, scanning electron microscopy and energy-dispersive X-ray spectroscopy/elemental mapping and magnetic property analysis by vibrating-sample magnetometry confirmed the presence of TiO2, Fe3O4, Fe3C and char in the photocatalysts as well as their magnetic properties. The results of specific surface area analysis showed that the C/Fe support had a surface area of 183 m2 g−1 and that this area decreased with an increasing amount of supported TiO2, reaching up to 129 m2 g−1. Diffuse reflectance spectroscopy characterization revealed that the bandgap values obtained for the photocatalysts (Ti/C/Fe) were lower than 3.2 eV. The prepared photocatalysts showed high efficiency in degrading the contaminants Remazol Black (RB5) (99%), paracetamol (77%) and phenol (90%). Recovery and reuse experiments using RB5 showed that after the fourth reaction, the photocatalytic efficiency was reduced by 50%, and the recovery reached up to 70%. Sedimentation kinetics showed that while only 6% of the TiO2 was deposited, up to 89% of the photocatalysts were deposited.

CONCLUSIONS

These results indicate that the photocatalysts showed excellent photocatalytic efficiency for different contaminants and can be easily and quickly separated from the reaction medium by magnetic separation. © 2024 Society of Chemical Industry (SCI).

光催化是去除废水中有机污染物的一种有效方法。通过在碳/氧化铁(C/Fe)磁性载体上支撑 TiO2(20%、40% 和 60% w/w),制备了 Ti/C/Fe 光催化剂。通过拉曼光谱、X 射线衍射仪、热分析、X 射线荧光、扫描电子显微镜和能量色散 X 射线光谱/元素图谱进行表征,并通过振动样品磁力计进行磁性分析,证实了光催化剂中 TiO2、Fe3O4、Fe3C 和炭的存在及其磁性。比表面积分析结果表明,C/Fe 支持物的比表面积为 183 m2 g-1,随着支持物 TiO2 含量的增加,比表面积减小,最高为 129 m2 g-1。漫反射光谱表征显示,光催化剂(Ti/C/Fe)的带隙值低于 3.2 eV。所制备的光催化剂在降解污染物雷马唑黑(RB5)(99%)、扑热息痛(77%)和苯酚(90%)方面表现出很高的效率。使用 RB5 进行的回收和再利用实验表明,经过第四次反应后,光催化效率降低了 50%,回收率最高达到 70%。沉积动力学表明,虽然只有 6% 的 TiO2 被沉积,但高达 89% 的光催化剂被沉积。这些结果表明,光催化剂对不同污染物具有出色的光催化效率,并且可以通过磁分离法方便快捷地从反应介质中分离出来。© 2024 化学工业学会(SCI)。
{"title":"Production of magnetic photocatalysts from TiO2, Fe(NO3)3 and sucrose and their application for the degradation of model organic contaminants","authors":"Leydiane de Oliveira Pereira,&nbsp;Iara do Rosario Guimarães,&nbsp;Luana Pereira Zampiere,&nbsp;Isabela Sales Marques,&nbsp;Stéfany Gonçalves de Moura,&nbsp;Aline Aparecida Caetano,&nbsp;Fabiano Magalhães","doi":"10.1002/jctb.7725","DOIUrl":"10.1002/jctb.7725","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> BACKGROUND</h3>\u0000 \u0000 <p>Photocatalysis is an efficient method for the removal of organic contaminants in wastewater. In this study, different magnetic photocatalysts for the degradation of organic compounds were prepared.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> RESULTS</h3>\u0000 \u0000 <p>Ti/C/Fe photocatalysts were prepared by supporting TiO<sub>2</sub> (20, 40 and 60% w/w) on a carbon/iron oxide (C/Fe) magnetic carrier. Characterization via Raman spectroscopy, X-ray diffractometry, thermal analysis, X-ray fluorescence, scanning electron microscopy and energy-dispersive X-ray spectroscopy/elemental mapping and magnetic property analysis by vibrating-sample magnetometry confirmed the presence of TiO<sub>2</sub>, Fe<sub>3</sub>O<sub>4</sub>, Fe<sub>3</sub>C and char in the photocatalysts as well as their magnetic properties. The results of specific surface area analysis showed that the C/Fe support had a surface area of 183 m<sup>2</sup> g<sup>−1</sup> and that this area decreased with an increasing amount of supported TiO<sub>2</sub>, reaching up to 129 m<sup>2</sup> g<sup>−1</sup>. Diffuse reflectance spectroscopy characterization revealed that the bandgap values obtained for the photocatalysts (Ti/C/Fe) were lower than 3.2 eV. The prepared photocatalysts showed high efficiency in degrading the contaminants Remazol Black (RB5) (99%), paracetamol (77%) and phenol (90%). Recovery and reuse experiments using RB5 showed that after the fourth reaction, the photocatalytic efficiency was reduced by 50%, and the recovery reached up to 70%. Sedimentation kinetics showed that while only 6% of the TiO<sub>2</sub> was deposited, up to 89% of the photocatalysts were deposited.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> CONCLUSIONS</h3>\u0000 \u0000 <p>These results indicate that the photocatalysts showed excellent photocatalytic efficiency for different contaminants and can be easily and quickly separated from the reaction medium by magnetic separation. © 2024 Society of Chemical Industry (SCI).</p>\u0000 </section>\u0000 </div>","PeriodicalId":15335,"journal":{"name":"Journal of chemical technology and biotechnology","volume":"99 11","pages":"2366-2380"},"PeriodicalIF":2.8,"publicationDate":"2024-08-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141929240","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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Journal of chemical technology and biotechnology
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