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CELLULOSE · 2020 ·Vol. 27 ·期 6 ·3287-3300 · IF 4.21

Recyclable ZIF-9@CA-Fe3O4/RGO/cellulose composite membrane as efficient catalysts for activating peroxymonosulfate to degrade methylene blue

Zhang Su-Feng,Li Hao,Hou Chen,Liu Li-Na,Wang Yang,Zhao Meng-Ke,Liang Chen

Abstract The treatment of dyes in wastewater is important to solve environmental problems. Advanced oxidation processes has been proved to be an effective treatment. In this work, a novel nanocomposite catalyst of ZIF-9@Fe 3 O 4 (cobalt-containing zeolitic imidazolate framework-9 coated Fe 3 O 4 nanocomposite) modified reduced graphite oxide (RGO) was prepared for the first time and coded as ZIF-9@CA-Fe 3 O 4 /RGO. Then, ZIF-9@CA-Fe 3 O 4 /RGO was immobilized on a cellulose membrane to obtain a composite membrane, which was used as a composite catalyst for activating peroxymonosulfate to degrade methylene blue (MB). The results demonstrated that the composite membrane could efficiently degrade approximately 96% of MB in 9 min without adjusting the initial pH and maintain good catalytic activity even after seven cycles. Furthermore, the composite membrane can be easily separated from the solution at the end of the reaction. This work indicates that the composite membrane has a broad application prospect in industrial applications. Graphic abstract

CAS / MDL: 51-17-2
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APPLIED SURFACE SCIENCE · 2021 · IF 6.707

Enhanced adsorption of Eu(III) from wastewater using Solidago canadensis-derived biochar functionalized by Ca/Al-LDH and hydroxyapatite

Lijia Dong,Shengbo Li,Yefei Jin,Baowei Hu,Guodong Sheng

In this paper, CaAl hydrotalcite or hydroxyapatite decorated invasive plant ( Solidago canadensis )-derived biochar were synthesized by co-precipitation and high temperature pyrolysis method. The three composites and bare biochar were characterized by Scanning electron microscopy (SEM), X-ray spectroscopy (EDX), the Fourier transform infrared spectroscopy (FT-IR), X-ray diffractometer (XRD), and X-ray photoelectron spectroscopy (XPS) techniques, and employed to remove Eu(III) from wastewater under a series of environmental conditions. The results indicated that the Eu(III) adsorption on BC@LDH@HAP was higher than that on BC, BC@LDH, and BC@HAP, and belonged to multi-layer adsorption, which was different from the monolayer adsorption of biochar. The adsorption could be fitted best by Langmuir model and the maximum adsorption capacity of Eu(III) on BC@LDH@HAP was up to 714 mg/g at pH ~ 6. The characterization results suggested that this excellent adsorption of BC@LDH@HAP arose from the abundant P-, C-, O-containing functional groups rather than larger specific surface area. The spectra of XPS, FT-IR, and XRD uncovered that the adsorption mechanisms of Eu(III) on BC@LDH@HAP involved surface complexation, ion exchange, and precipitation. Moreover, the absorbed Eu(III) was formed into two precipitate induced by P-containing groups and carbonate groups. This research confirmed BC@LDH@HAP is a promising material for the removal of Eu(III) in wastewater.

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ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH · 2019 ·Vol. 26 ·期 11 ·11170-11178 · IF 2.914

Effect of cation type in mixed Ca-Na systems on transport of sulfonamide antibiotics in saturated limestone porous media

Sun Kaixuan,Sun Yuanyuan,Gao Bin,Xu Hongxia,Wu Jichun

Retention and transport of sulfonamides (SAs) in subsurface can strongly affect groundwater quality. In this work, a range of laboratory batch sorption and column transport experiments were conducted to determine the effect of cation type in mixed Ca-Na systems on the retention and transport of two typical SAs, sulfadimethoxine (SDM) and sulfacetamide (SCA), in saturated limestone porous media. Column experimental data showed divalent cation Ca 2+ played a more important role than monovalent cation Na + in decreasing the transport of only SDM in co-cation systems in the saturated limestone media. Further, in the single-cation (i.e., including either Ca 2+ or Na + ) system, increasing ionic strength (IS) of either NaCl or CaCl 2 had little effect on SCA transport; however, increasing of IS of CaCl 2 promoted the retention of SDM in the saturated limestone porous media. This is mainly due to the cation bridging effect of Ca 2+ on SDM and limestone. Overall, SDM showed much higher retention in the limestone columns than SCA, which can be attributed to the two SAs’ different physicochemical properties. Moreover, limestone showed stronger ability to retain the two SAs than quartz sand. Findings in this study suggest that cation type and the concentration of certain electrolyte (e.g., CaCl 2 ) as well as medium type play an important role in controlling the environmental fate and transport of antibiotics.

CAS / MDL: 144-80-9 1037-50-9
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Materials · 2018 ·Vol. 12 ·期 1 ·83 · IF 2.467

Efficient Catalytic Production of Biodiesel with Acid-Base Bifunctional Rod-Like Ca-B Oxides by the Sol-Gel Approach

Anping Wang,Hu Li,Heng Zhang,Hu Pan,Song Yang

The search for acid-base bifunctional catalysts has become a hot topic in the preparation of biofuels from renewable resources. In the present work, a series of novel acid-base bifunctional metal-boron catalysts were successfully prepared by a sol-gel method and characterized by XRD, IR, SEM, TEM, TGA, BET, and TPD. Among those bifunctional solid materials, the Ca-B(700) catalyst had the highest density of both acid and base sites and showed excellent catalytic performance in the production of biodiesel from nonedible oils with high acid value. Under the optimal reaction conditions of 20/1 methanol/oil mole ratio and 4 wt % catalyst dosage at 105 °C for 2 h, a high biodiesel yield of 96.0% could be obtained fromJatrophacurcas oil in one-pot. In addition, Ca-B(700) was also applicable to producing biodiesel fromFirmiana platanifolia L.f.oil in a relatively low acid value, with an almost quantitative yield (98.5%) at 65 °C after 2 h. The Ca-B(700) catalyst had good stability and reusability, which is a promising acid-base bifunctional catalytic material for the preparation of biodiesel.Keywords:sol-gel synthesis;acid-base bifunctional materials;high/low acid value oils;transesterification;biofuels

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Inorganic Chemistry Frontiers · 2018 ·Vol. 5 ·期 10 ·2657-2665 · IF 5.106

Macroscopic and microscopic investigation of uranium elimination by Ca–Mg–Al-layered double hydroxide supported nanoscale zero valent iron

Hongwei Pang,Yihan Wu,Shuyi Huang,Congcong Ding,Shun Li,Xiangxue Wang,Shujun Yu,Zhongshan Chen,Gang Song,Xiangke Wang

In the past few decades, uranium (235, 238U(VI)) has turned into a forefront environmental issue due to its extensive use in the nuclear industry and its toxicity and radioactivity. Herein, nanoscale zero valent iron (nZVI), which was supported on Ca–Mg–Al-layered double hydroxide (Ca–Mg–Al-LDH/nZVI), was fabricated via an in situ growth route and employed for U(VI) decontamination from aqueous solutions. Spectroscopy and microscopy (SEM, TEM, FTIR, XRD, BET, and XPS) technologies were applied for the investigation of the properties of Ca–Mg–Al-LDH/nZVI and the U(VI) elimination mechanism. Ca–Mg–Al-LDH/nZVI had a remarkable BET surface (426.8 m2 g−1), abundant functional groups (i.e., Fe–O, Al–O, –OH, etc.), high efficiency (4 h to achieve equilibrium) and large adsorption capacities (Qmax = 216.1 mg g−1) for U(VI) removal. The decontamination process of U(VI) was observed to be pH-dependent and ionic strength-independent, suggesting that the adsorption was predominated by inner-sphere surface coordination. XPS spectroscopy analyses indicated that the reduction and adsorption of nZVI and the adsorption of Ca–Mg–Al-LDH dominated U(VI) elimination on Ca–Mg–Al-LDH/nZVI. The environmentally friendly synthesis method, excellent physicochemical properties and remarkable removal performance suggested that Ca–Mg–Al-LDH/nZVI was applicable as a potential adsorbent for U(VI) decontamination from wastewater in environmental pollution remediation.

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FOOD HYDROCOLLOIDS · 2014 · IF 4.28

Microencapsulation of Lactobacillus acidophilus CGMCC1.2686 via emulsification/internal gelation of alginate using Ca-EDTA and CaCO3 as calcium sources

Sha Cai,Meng Zhao,Yapeng Fang,Katsuyoshi Nishinari,Glyn O. Phillips,Fatang Jiang

Emulsification/internal gelation is an effective encapsulation method to protect probiotics from adverse environment. In this paper, microcapsules of Lactobacillus acidophilus CGMCC1.2686 were prepared by emulsification and gelation of alginate solutions with slow release of Ca 2+ ions from calcium carbonate (CaCO 3 ) and calcium disodium ethylenediaminetetraacetate (Ca-EDTA). Physical characterization of the two types of microcapsules showed that alginate-Ca-EDTA microcapsule was more uniform in size than alginate-CaCO 3 , with a span factor of 0.96 and 1.20, respectively. Mechanical measurements demonstrated that alginate-CaCO 3 microcapsule was more robust and elastic, which was supported by its denser structure as observed by electron scanning microscopy. Bacteria encapsulation yields in the two microcapsules were similar, 37.9% for alginate-CaCO 3 and 36.9% for alginate-Ca-EDTA. However, alginate-CaCO 3 microcapsule exhibited much higher cell survivals in both simulated gastric juice and bile salts solution (22.2% and 2.6*10 −2 %, respectively) than alginate-Ca-EDTA (7.1% and 0%, respectively), indicating a more effective protection of L. acidophilus CGMCC1.2686. The protection efficiency was discussed in relation to the mechanical properties of the microcapsules and the calcium sources used.

CAS / MDL: 62-33-9
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Chemical Engineering and Processing-Process Intensification · 2024 · IF 3.8

Enhanced ORR kinetics and stability through synergy of Pt-Ni clustering and porous N-doped C/Ca aerogel support

Muhammad Umair Mushtaq,Zhu Lin,Danni Li,Khurram Shahzad Ayub,Zain Abbas,Waqas Qamar Zaman,Ji Yang

The oxygen reduction reaction (ORR) is fundamental in numerous electrochemical energy conversion technologies, necessitating efficient catalysts to enhance reaction kinetics and reduce precious metal usage. This study focuses strategic clustering of Pt-Ni on Calcium Oxide/activated carbon (C/Ca) aerogels. Electrochemical analyses confirmed that incorporating Ni into Pt matrices significantly enhanced ORR activities with Pt 25 Ni 75 -C/Ca composition emerged as optimum. A positive shift in half-wave potential (905 mV vs. RHE) and impressive mass activity (72.50 Ag −1 at 85 V) highlight the potential of this composite as a highly effective and stable ORR catalyst. Pt-C/Ca demonstrated performance fluctuation, while Pt 25 Ni 75 -C/Ca showed remarkable stability after 40,000 cycles. Furthermore, C/Ca aerogels exhibited a significantly increased BET surface area, and the presence of Pt-Ni/pyridinic-N species on its surface C/Ca aerogel provided supplementary active sites that facilitated the adsorption and reduction of O 2 during ORR.

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Journal of Cleaner Production · 2017 · IF 5.715

Study of reaction mechanism between guaiacol and Ca(OH)2 in water: Development of a novel phenol extraction method

De-Bin Li,Yun-Quan Liu,Yue-Yuan Ye,Shui-Rong Li,Duo Wang

Experiments were conducted to elucidate the mechanism of reaction between guaiacol and Ca(OH) 2 in water based on in situ FT-IR, 1 H NMR, ICP-AES and TGA analyses. Three phases were revealed for this reaction when guaiacol was dropped into the solution of Ca(OH) 2 , and the final molar ratio of guaiacol to Ca 2+ reaches 4. It was found that an acid–base reaction occurs in the first reaction phase. However, the second reaction phase includes not only the acid-base reaction, but also the accompanied coordination reaction between oxygen atom of hydroxyl group in guaiacol and Ca 2+ . The third reaction phase is also the coordination reaction, particularly, the one between the hydrogen atom in guaiacol and Ca 2+ . Based on the mechanism study, a novel circulating precipitation agent was developed and tested for the extraction of phenolic compounds from the simulated wastewater. The result showed that 96.63% guaiacol could be extracted from the simulated wastewater with the novel extraction technology at the optimum reaction conditions.

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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2024 · IF 7.7

Improved interfacial compatibility between unsaturated polyester resin and rice straw fibers after non-washing treatment with Ca(OH)2

Liwen Shen,Feiyang Zhao,Huijuan Liu,Jicheng Li,Yang Lu,Jun Liu,Nianzhao Gao,Shuangfei Xiang,Shujun Zhao,Guocheng Zhu,Parpiev Khabibulla,Juramirza Kayumov,Feiya Fu,Xiangdong Liu

The agricultural industry produces a substantial volume of rice straw (RS) annually, highlighting the importance of recycling RS for sustainable materials. However, the poor interfacial compatibility between RS and polymers often leads to drawbacks in their composites, such as water-swelling and limited tensile strength. Here, we propose a novel approach using Ca(OH) 2 that offers several distinct advantages: enhancement of interfacial compatibility, elimination of the need for water washing, and formation of calcified hybrid particles on fiber surfaces by capturing CO 2 from the atmosphere. The non-washing calcified rice straw (NCRS) fibers were used to fabricate composites with unsaturated polyester resin (UPR), resulting in NCRS/UPR composites exhibiting significant enhancements in water resistance and mechanical properties compared to RS/UPR composites. The NCRS/UPR composites achieved a water absorption rate below 25 %, thickness swelling rate below 10 %, and tensile strength of 19.9 MPa. This work comprehensively explored the mechanism underlying these achievements through experimental studies. Findings suggest that CaCO 3 particles involving with released lignin act as an interfacial bridge between RS fiber surface and UPR, resulting in significantly improved properties. This approach demonstrates promising prospects as a simple and eco-friendly methodology for manufacturing RS-based composite materials.

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JOURNAL OF HAZARDOUS MATERIALS · 2017 · IF 6.065

Enhanced adsorption of U(VI) and 241Am(III) from wastewater using Ca/Al layered double hydroxide@carbon nanotube composites

Haijun Chen,Zhe Chen,Guixia Zhao,Zhibin Zhang,Chao Xu,Yunhai Liu,Jing Chen,Li Zhuang,Tasawar Haya,Xiangke Wang

Ca/Al layered double hydroxide decorated carbon nanotube (Ca/Al-LDH@CNTs) composites were fabricated by co-precipitation method and hydrothermal aged treatment. The prepared Ca/Al-LDH@CNTs was characterized by SEM, TEM, EDS, XRD, FT-IR, UV–vis and XPS techniques, and applied to remove U(VI) from aqueous solutions under various environmental conditions (i.e., pH, ionic strength, temperature and contact time). The results indicated that the adsorption of U(VI) on Ca/Al-LDH@CNTs was four times higher than that of U(VI) on bare CNTs. The kinetic investigations reflected the chemisorption of U(VI) on Ca/Al-LDH@CNTs through oxygen-containing functional groups. The adsorption isotherms demonstrated that the adsorption of U(VI) was well fitted by Langmuir model and the maximum adsorption capacity of U(VI) on Ca/Al-LDH@CNTs was calculated to be 382.9 mg g −1 at 289.15 K. The thermodynamic parameters calculated from temperature-dependent isotherms suggested that U(VI) adsorption on Ca/Al-LDH@CNTs were endothermic and spontaneous process. Furthermore, Ca/Al-LDH@CNTs could remove ∼91% of 241 Am(III) at pH = 8.0, which confirmed Ca/Al-LDH@CNTs as a promising material for multiply low level radionuclides’ pollution remediation.

CAS / MDL: 308068-56-6
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY · 2024 · IF 8.1

Efficient and sustainable H2 production from aqueous-phase reforming of methanol over Cu@CA-Val catalyst at low temperatures

Jiajin Li,Minglei Lu,Yuxin Ge,Weiwei Lu,Zidi Liu,Hongde Xu,Yu Zhang,Zhihui Li,Zhuoyu Zheng,Pengxiang Gao,Qian Zhang,Tiejun Wang

Aqueous-phase reforming of methanol (APRM) is an important method for H 2 production, widely used in energy fields like polymer electrolyte membrane fuel cells (PEMFCs). However, traditional noble metal catalysts , being expensive and vulnerable to CO poisoning, restrict their practical application. Therefore, developing robust non-noble metal catalysts for efficient and sustainable H 2 production with low CO levels in APRM at low temperatures is highly significant. In this study, a novel approach was employed to synthesize carbon-encapsulated Cu catalyst via controlled pyrolysis , leading to Cu@CA-Val catalyst with excellent low-temperature catalytic activity. The optimal Cu@CA-Val-300 catalyst exhibited a high hydrogen production rate of 0.2–27.0 μmolH 2 /g cat /s over a wide temperature of 135–180 °C (base-free), surpassing the most Cu-based and Pt-based catalysts. The Cu@CA-Val-300 catalyst exhibited exceptional hydrothermal stability during continuous operation in a fixed reactor for 200 h. Efficient H 2 production was attributed to good wettability , enabling the diffusion of CH 3 OH and H 2 O molecules into Cu + /Cu 0 sites for activation, with CO being suppressed and transformed through the formate formation.

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SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY · 2025 · IF 4.6

A novel fluorescence and colorimetric dual sensing system for rapid and sensitive detection of histidine based on TSPP-CA

Dajie Zou,Chenyan Lu,Yanyan Jia,Huan Wang,Jiuli Wang

Histidine (His) plays an important role in human health and life activities. It will harm human health when His intake is insufficient or excessive. Its residue also will pollute the natural environment. Therefore, establishing a reliable and sensitive method for detecting histidine is particularly important. However, most of the existing detection methods of His rely on the single change of single signal, which are susceptible to interference from testing environmental factors and prone to generating false positive results. In contrast, the fluorescence and colorimetric dual-signal sensing system can not only effectively improve the reliability of detection, but also significantly reduce the risk of false positives. Therefore, the dual-signal sensing system has gradually become the research hotspot. Based on this, 5,10,15,20-tetra-(4-sulfophenyl) porphyrin (TSPP) was selected as the fluorescence and colorimetry dual-signal probe for the rapid detection of His in this study. Since TSPP could interact with many substances due to the specificity of molecular structure, it is the best choice to build an “ON-OFF-ON” sensing system in order to improve the specificity of the sensing system. Therefore, citric acid (CA) as an intermediate based on TSPP probe was successfully developed fluorescence and colorimetric dual-sensing system for the quantitative detection of histidine in real samples. The signal of the dual sensing system was “turned on” when the red TSPP solution obtained the fluorescence emission wavelength of 642 nm at the 514 nm optimal excitation wavelength and the UV–Vis absorption at 413 nm, respectively. The fluorescence intensity and absorbance of TSPP gradually decreased with the introduction of CA. At this time, the signal of the dual-sensing system became “turned off”, and the color of the solution changed from light pink to light green. The quenched fluorescence intensity and absorbance, however, was restored upon the introduction of histidine into the system. Simultaneously, the color of the solution changed from light green to light pink, and the dual-sensing system became “turned on”. Therefore, a novel fluorescence and colorimetric dual-signal sensing system based on TSPP was proposed for histidine detection. The results indicated that the linear ranges of the fluorescence sensing system were 8.34 × 10 −6  M − 1.51 × 10 −4  M and 1.85 × 10 −4  M − 1.4 × 10 −3  M with detection limits of 0.282 μM and 10.91 μM (LOD, S/N = 3), respectively. The linear range of the colorimetric sensing system was 2.04 × 10 −4  M–4.35 × 10 −4  M with a detection limit of 11.97 μM (LOD, S/N = 3). Meanwhile, the dual-sensing system provided a promising platform for practical samples sensing applications.

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