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SEPARATION AND PURIFICATION TECHNOLOGY · 2022 · IF 9.136

Salt sacrificial template strategy and in-situ growth of lamellar La(OH)3 on a novel PVDF foam for the simultaneous removal of phosphates and oil pollution without VOCs emission

Yunyun Wang,Li Chen,Yinhua Jiang,Xinyan Yang,Jiangdong Dai,Xiaohui Dai,Mingdong Dong,Yongsheng Yan

Applying polyvinylidene fluoride (PVDF) monolith for phosphates removal can improve the operability of the adsorption process compared with some other powder nanomaterials. However, as the commonly used synthesis strategy, non-solvent induced phase separation (NIPS) was deemed not environmentally friendly enough since the dissolution of PVDF often involved volatile organic compounds (VOCs). This article designed a salt sacrificial template method to fabricate a 3D porous PVDF monolith, and then in-situ growth of lamellar La(OH) 3 on the PVDF foam was realized to enhance the adsorption affinity to phosphates pollution. No VOCs were used or released during the whole synthesis process. The adsorption for phosphates was as high as 56.2 mg g −1 , and easy reusability of the novel PVDF monolith was realized. In addition, this PVDF-La(OH) 3 foam exhibited good adsorption properties in both oil and water environments, which implied it could not only adsorb phosphates in actual water samples but also separate oil contaminants from water. All these implied that this PVDF-La(OH) 3 foam could be a potential candidate for large-scale industrial adsorption and separation of phosphates. This PVDF-La(OH) 3 foam could be a potential candidate for large-scale industrial adsorption and separation of phosphates.

研究领域: 环境科学 · 材料科学
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MICROPOROUS AND MESOPOROUS MATERIALS · 2023 · IF 5.2

High-silica FAU zeolite through controllable framework modulation for VOCs adsorption under high humidity

Qiang Yu,Wenna Zhang,Junjie Li,Wen Liu,Yanan Wang,Weifeng Chu,Xinbao Zhang,Longya Xu,Xiangxue Zhu,Xiujie Li

Although FAU zeolites have been widely used as absorbents for volatile organic compounds (VOCs) removal, preparation of high-silica FAU zeolite to expand its application under high humidity is still a big challenge. Here, two high-silica FAU zeolites were successfully prepared through the controllable framework modulation strategy. By carefully matching the degrees of dealumination and Si-insertion, the zeolite (FAU-H) with an ultra-high SiO 2 /Al 2 O 3 ratio of 957 was obtained. FAU-H exhibited similar high adsorption capacities of VOCs (e.g. m-xylene and toluene) under dry and humid conditions, more importantly, its adsorption capacity of m-xylene was 25% higher than the industrial high-silica FAU zeolite (HSZ-390HUA) from Tosoh Corporation. When the dealumination degree was mismatched with that of Si-insertion, imperfect FAU-M (SiO 2 /Al 2 O 3  = 108) with the existence of some defect sites was obtained that becomes a good candidate for the adsorption removal of small VOCs molecules (e.g. isopropanol). The moderate interaction between VOCs and zeolite framework is proved a key factor for small molecules adsorption on basis of the DFT calculations. Moreover, the fitted kinetic models, desorption tests, and adsorption−desorption cycling tests proved the good regenerability of FAU-H and FAU-M. Therefore, the proposed high-silica FAU zeolites are promising adsorbents for VOCs removal.

CAS / MDL: 108-38-3 10026-04-7
研究领域: 材料科学 · 环境工程 · 化学工程
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CHEMICAL ENGINEERING JOURNAL · 2017 · IF 6.216

Preparation of highly-hydrophobic novel N-coordinated UiO-66(Zr) with dopamine via fast mechano-chemical method for (CHO-/Cl-)-VOCs competitive adsorption in humid environment

Peng Hu,Xiaopeng Liang,Muhammad Yaseen,Xiaodan Sun,Zhangfa Tong,Zhongxing Zhao,Zhenxia Zhao

A novel mechano-chemical strategy using dopamine to modify UiO-66(Zr) by N-coordination was proposed to enhance its competitive adsorption for acetaldehyde, chlorobenzene/H 2 O, both thermodynamically and kinetically. The newly synthesized material was characterized by SEM, EDX, XPS, PXRD, FT-IR, TGA/DTG and BET techniques. Results showed that N was successfully grafted into UiO-66(Zr) frameworks through coordination interaction with Zr-O clusters resulting in M-UiO-66(Zr-N 3.0 ). The obtained M-UiO-66(Zr-N 3.0 ) exhibited a significant increase in adsorption of chlorobenzene (4.94   mmol/g) and acetaldehyde (9.42   mmol/g) compared to parent UiO-66(Zr) and UiO-66(Zr)-NH 2 . The H 2 O adsorption uptake of M-UiO-66(Zr-N 3.0 ) decreased by 20% that of UiO-66(Zr) and 47% of UiO-66(Zr)-NH 2 indicating higher hydrophobicity of the modified material. Kinetic performance indicated that diffusivity of chlorobenzene on M-UiO-66(Zr-N 3.0 ) was about 7.8 and 40   times higher than that of the parent UiO-66(Zr) and UiO-66(Zr)-NH 2 respectively and 15.4   times higher than that of H 2 O on itself. Based on the results, the current N-modification strategy can be deemed as an efficient way to improve MOFs competitive adsorption towards VOCs under humid conditions and it might play active role in industries involving adsorbent applications.

研究领域: 材料科学 · 环境科学
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2024 · IF 4.9

In-situ growth of MIL-101(Fe) onto PET base for high-efficiency adsorption of low concentrations benzene series VOCs and easy recycling

Shu-Huan Chen,Huma Javeria,Xu-Hui Sun,Zhen-Xia Du

With the proliferation of vehicles in households, people are spending more and more time in their cars, so it is important to ensure the air quality and safety of the car. In this research, environmentally friendly, green PET@PDA@MIL-101(Fe) (PPM) was prepared by in-situ solvothermal growth and acid etching methods, which was categorized by SEM, FTIR, XRD, XPS, and BET. PPM was used to adsorb benzene, toluene, and m-xylene at low concentrations. The maximum amount of adsorption of PET@PDA@MIL-101(Fe) (PPM) for benzene, toluene, and m-xylene was 68.72 mg/g, 91.63 mg/g, and 78.47 mg/g respectively. The adsorption process of PPM is well fitted by the pseudo-first-order kinetic model and Langmuir isothermal adsorption model. Furthermore, PPM exhibited excellent toluene removal performance in simulated vehicles and excellent cycling capability in adsorption-desorption experiments. As a result, PPM can be used to treat and manage toluene volatile organic compounds (VOCs) at low concentrations.

CAS / MDL: 71-43-2 77-86-1
研究领域: 环境科学 · 材料科学 · 化学工程
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ANALYST · 2024 · IF 3.6

Qualitative and quantitative rapid detection of VOCs differentially released by VAP-associated bacteria using PTR-MS and FGC-PTR-MS

Wei Xu,Xue Zou,Yueting Ding,Qi Zhang,Yulan Song,Jin Zhang,Min Yang,Zhou Liu,Qiang Zhou,Dianlong Ge,Qiangling Zhang,Wencheng Song,Chaoqun Huang,Chengyin Shen,Yannan Chu

Ventilator-associated pneumonia (VAP) is a prevalent disease caused by microbial infection, resulting in significant morbidity and mortality within the intensive care unit (ICU). The rapid and accurate identification of pathogenic bacteria causing VAP can assist clinicians in formulating timely treatment plans. In this study, we attempted to differentiate bacterial species in VAP by utilizing the volatile organic compounds (VOCs) released by pathogens. We cultured 6 common bacteria in VAP in vitro, including Acinetobacter baumannii, Enterobacter cloacae, Escherichia coli, Pseudomonas aeruginosa, Stenotrophomonas maltophilia, and Staphylococcus aureus, which covered most cases of VAP infection in clinic. After the VOCs released by bacteria were collected in sampling bags, they were quantitatively detected by a proton transfer reaction-mass spectrometry (PTR-MS), and the characteristic ions were qualitatively analyzed through a fast gas chromatography-proton transfer reaction-mass spectrometry (FGC-PTR-MS). After conducting principal component analysis (PCA) and analysis of similarities (ANOSIM), we discovered that the VOCs released by 6 bacteria exhibited differentiation following 3 h of quantitative cultivation in vitro. Additionally, we further investigated the variations in the types and concentrations of bacterial VOCs. The results showed that by utilizing the differences in types of VOCs, 6 bacteria could be classified into 5 sets, except for A. baumannii and E. cloacae which were indistinguishable. Furthermore, we observed significant variations in the concentration ratio of acetaldehyde and methyl mercaptan released by A. baumannii and E. cloacae. In conclusion, the VOCs released by bacteria could effectively differentiate the 6 pathogens commonly associated with VAP, which was expected to assist doctors in formulating treatment plans in time and improve the survival rate of patients.

研究领域: 医学 · 微生物学 · 分析化学
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CHEMICAL ENGINEERING JOURNAL · 2024 · IF 13.3

Three birds with one stone: Constructing Janus multilayer carbon fabric to boost solar-driven interfacial evaporation, electrical power generation and inhibit VOCs volatilization

Keyu Ding,Yaqin Yang,Yanan Mao,Dongdong Tong,Shizhou Lu,Bo Song

Solar-driven interfacial evaporation technology has great potential to address both the freshwater and energy crises in a low-cost, environmentally friendly, and sustainable method. How to achieve highly efficient freshwater and energy harvesting simultaneously is still challenging. Here, a Janus-structured multilayer carbon fabric (JMCF) solar evaporator is proposed to effectively overcome the bottleneck in the cogeneration of fresh water and electricity. The Janus structure of the multilayer fabric effectively controls water supply upwards, improves light absorption and photothermal conversion, increases evaporation surface area, facilitates water vapor escape and inhibits VOCs volatilization. Accordingly, the optimized JMCF solar evaporator can achieve a high evaporation rate of 3.12 kg m -2 h −1 and an output voltage of 0.577 V in 3.5 wt% seawater under 1 sun irradiation. In addition, the JMCF evaporation system also demonstrates good working stability, self-cleaning capacity, environmental adaptability, and economic feasibility. This work provides new ideas and inspiration for the design of high efficiency solar-driven interfacial evaporation system to address the freshwater scarcity, energy crisis, global change problem, etc.

研究领域: 材料科学 · 环境科学 · 能源工程
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SEPARATION AND PURIFICATION TECHNOLOGY · 2024 · IF 8.1

The design of core–shell ZSM-5@NiAl-LDH composites for efficient adsorption of VOCs under high humidity

Wei Zhao,Yinan Xu,Yuehui Qiao,Rui Sun,Jie Qian,Yixue Wang,Quan Liu,Zhekun Shi,Fandong Meng,Xiaoli Zhan,Qinghua Zhang

Zeolites have been widely utilized in the adsorption of volatile organic compounds (VOCs) due to their high specific surface area and robust stability. However, the adsorption capacity of zeolites for VOCs is considerably reduced under humid conditions due to the competitive adsorption between water and VOCs, thereby limiting their industrial applicability. Herein, we report a core–shell ZSM-5@NiAl-LDH (Z-L) composites designed specifically for efficient adsorption of VOCs under high humidity conditions. The core–shell architecture is achieved by introducing active sites onto the ZSM-5 framework pretreated with high-alkalinity agents, followed by the growth of NiAl-LDH on its surface, creating a regular, vertically staggered structure. Compared with ZSM-5 zeolite, Z-L composites show a larger specific surface area, wider pore size, and larger mesopore volume, allowing a high adsorption capacity of the VOCs. Contact angle and static adsorption tests of water molecules reveal that the LDH shell effectively increases the hydrophobicity of Z-L composites. The dynamic adsorption behavior for m-xylene demonstrates that Z-L composites exhibit significantly enhanced adsorption capacity, 3.79 times that of ZSM-5 zeolite. Furthermore, Z-L composites exhibit a higher selectivity for m-xylene at 60 % relative humidity, achieving a Q wet /Q dry ratio of 86.7 %, outperforming most porous adsorption materials. Kinetic model analysis reveals that the augmentation of mesopores in Z-L composites enhances the effective diffusion space for synthesized samples, resulting in exceptional adsorption performance. This novel synthetic material is anticipated to be a promising candidate for VOCs pollution control in high-humidity environments.

CAS / MDL: 108-38-3 13478-00-7
研究领域: 材料科学 · 环境工程 · 化学工程
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Nanoscale · 2017 ·Vol. 9 ·期 17 ·5433-5444 · IF 7.367

Multifunctional hybrid porous filters with hierarchical structures for simultaneous removal of indoor VOCs, dusts and microorganisms

Yang Zhao,Ze-Xian Low,Shasha Feng,Zhaoxiang Zhong,Yong Wang,Zhong Yao

Air purification often requires multiple layers of filters with different functions to remove various air pollutants, which lead to high pressure drop, high air flow path and frequent filter replacement. In this work, a novel multifunctional Ag@MWCNTs/Al2O3 hybrid filter with a depth-type hierarchical structure for simultaneous removal of fine particles, microorganisms and VOCs was designed and fabricated. The novel hybrid air filter showed leading air purification performances to date, achieving 82.24% degradation of formaldehyde at room temperature, 99.99% formaldehyde degradation at 55 °C and complete retention of indoor airborne microorganisms. The complete particle retention rate (100% retention) based on the most penetrating particle size (MPPS, aerodynamic diameter ≦300 nm) of Ag@MWCNTs/Al2O3 was achieved at an only 35.60% pressure drop compared with the pristine Al2O3 filter, leading to the highest quality factor (Qf) ever reported. Furthermore, the Ag@MWCNTs/Al2O3 hybrid filter showed excellent water repellency (water contact angle of 139.6 ± 2.9°), prolonging the service life of the filters and improving the air purification efficiency. The novel Ag@MWCNTs/Al2O3 hybrid filter exhibits remarkable air purification performance in both laboratory synthetic conditions as well as in the “real world” and shows great promise as an effective single replacement for multiple layers of air purifying filters.

CAS / MDL: 102-54-5
研究领域: 环境科学 · 材料科学 · 化学工程 · 气溶胶科学
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APPLIED CATALYSIS A-GENERAL · 2020 · IF 5.006

Preparation of nickel-foam-supported Pd/NiO monolithic catalyst and construction of novel electric heating reactor for catalytic combustion of VOCs

Xiao Chen,Jianyu Li,Yue Wang,Ying Zhou,Qiulian Zhu,Hanfeng Lu

Metal-based monolithic catalysts have excellent electrical and thermal conductivity, impact resistance, ductility, and mechanical properties. Thus, they have a broader application prospect than ceramic-based monolithic catalysts. In this work, high-dispersion Pd nanoparticle dispersion liquid was synthesized by using the solvothermal method. Moreover, nickel-foam-supported Pd/NiO (Pd/NiO/Ni foam) monolithic catalyst with good catalytic combustion performance was prepared successfully by simply spraying the dispersion liquid on the surface of Ni foam, which was oxidized at high temperature to grow NiO film. A novel electric heating catalytic combustion reactor with fast response and safety was constructed by nesting Pd/NiO/Ni foam with an insulated heating rod. Notably, even at the high space velocity of 50,000 h −1 , the constructed reactor can completely degrade 2500 ppm of toluene at 230 ℃ and exhibits good catalytic activity for hydrocarbons and oxygen-containing and heteroatom-containing organic compounds.

CAS / MDL: 112-90-3 112-80-1
研究领域: 催化 · 环境工程 · 化学工程
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SURFACE & COATINGS TECHNOLOGY · 2019 · IF 3.192

A semi-packed micro GC column for separation of the NAFLD exhaled breath VOCs

Baoqing Han,Guishan Wu,Hao Huang,Tinghan Liu,Jiuhong Wang,Jianhai Sun,Hairong Wang

The separation and detection of human breath play a significant role in early and non-invasive disease diagnosis. Various volatile organic compound (VOC) gases are considered as the biomarkers of a nonalcoholic fatty liver disease (NAFLD) patient. In this paper, a micro gas chromatography (GC) column used for VOCs separation of the NAFLD breath sample was presented, from its design, fabrication and separation performance testing. The serpentine column made using microelectromechanical system (MEMS) technology was chosen for its relatively small band broadening. The micro pillar configuration was simulated and optimized. The 3 m and 1 m long column with a cross-section of 200 μm × 240 μm was fabricated by deep-reactive-ion-etching (DRIE) method and sealed with anodic bonding. The stationary phase was coated to the inner wall of the column by static coating. The column was installed into the conventional gas chromatography to test separation performance of the GC. The nonpolar alkane mixture containing the NAFLD biomarker gas pentane was separated and the experimental factors such as the temperature and the carrier gas flow rate were studied. The results indicated that the micro GC column can effectively separate alkanes from C 5 -C 12 within 5 min. This could help the micro detector of micro GC system to quickly identify the contents or concentrations of characteristic alkanes. The micro GC column can meet the requirements of the micro GC system for the breath analysis of the NAFLD or other metabolic liver diseases. The micro column assembled with micro gas detector and preconcentrator can be hopefully developed into a portable breath analysis device.

研究领域: 分析化学 · 医学诊断 · 生物医学工程 · 微流控
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2022 · IF 24.319

Defect-band bridge photothermally activates Type III heterojunction for CO2 reduction and typical VOCs oxidation

Jingwei Li,Jianrui Feng,Xiaomin Guo,Hongli Fang,Jiayi Chen,Churong Ma,Ruchun Li,Yuya Wang,Zebao Rui

This work reports a novel strategy to activate type III heterojunction through introducing defect sites at the interfaces and making use of the defect band as the bridge for storage, secondary excitation, and interband transfer of the photothermal induced charges for constructing two-component Type B heterojunction photothermocatalyst. Type III heterojunction WO 3−x /GdCrO 3 is activated by defect-band state W 5/4+ at WO 3−x interface under photothermal conditions, achieving efficient charge separation, high redox potential, and full visible light absorption. The as-bridged (or Type B) heterojunction WO 3−x -R/GdCrO 3 as non-noble metal catalyst demonstrates excellent photothermocatalytic performance in toluene degradation with a reaction rate five times higher than that of WO 3−x /GdCrO 3 with less interfacial defect sites as well as in CO 2 reduction with high CO and CH 4 yielding rates of 49.6 μmol g −1 h −1 and 18.5 μmol g −1 h −1 in gas-solid reaction system without sacrifice agent, evidently better than those reported in the literature.

研究领域: 材料科学 · 催化 · 环境科学 · 化学
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SEPARATION AND PURIFICATION TECHNOLOGY · 2025 · IF 9

Electron beam irradiation defective UiO-66 supported noble metal catalysts for binary VOCs removal: Insight into the synergistic degradation mechanism of mutual promotion

Yaofei Zhang,Jiani Chen,Tegexi Buren,Zhuo Li,Xiaojin Zhang,Shuting Ma,Jiafeng Wei,Fukun Bi,Xiaodong Zhang

Electron beam (EB) irradiation has emerged as an effective post-synthetic strategy to modify the structural properties of metal-organic frameworks (MOFs), offering enhanced defect engineering and improved active site dispersion. In this study, UiO-66-100, pretreated under the optimal EB irradiation dose of 100 kGy with abundant structural defects, was selected as the support to synthesize supported noble metal catalysts M-UiO-66-100 (M = Pt, Pd, Ru, Ag, Au). The catalytic performance of M-UiO-66-100 was evaluated by toluene and 2-propanol degradation. Among them, Pt-UiO-66-100 exhibited superior performance for toluene oxidation (T 90  = 187 °C), while Pd-UiO-66-100 showed excellent activity for 2-propanol degradation (T 90  = 229 °C). Both catalysts exhibited distinct physicochemical properties and adsorption behaviors in single-component Volatile organic compound (VOC) systems. Interestingly, further studies revealed that both Pt- and Pd-based catalysts displayed significantly enhanced catalytic activity for toluene and 2-propanol mixture oxidation, highlighting a mutual promotion effect. VOC- temperature-programmed desorption/oxidation (TPD/TPO) and thermal desorption-gas chromatography–mass spectrometry (TD-GC–MS) results elucidated the mutual promotion effect that compared with single VOC systems, Pd-UiO-66-100 and Pt-UiO-66-100 produce fewer intermediates during mixed VOC degradation, which reduced the accumulation of intermediates on the catalysts surface, released the surface active sites, and accelerated their mineralization. This work provides a rational design approach for EB-modified MOF-supported catalysts and deepens the insights into the synergistic oxidation mechanism in mixed-VOC systems.

研究领域: 材料化学 · 环境催化 · 纳米催化 · 多孔材料 · 大气污染控制
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