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DALTON TRANSACTIONS · 2018 ·Vol. 47 ·期 18 ·6394-6403 · IF 4.099

H5PV2Mo10O40 encapsulated in MIL-101(Cr): facile synthesis and characterization of rationally designed composite materials for efficient decontamination of sulfur mustard

Yanqin Li,Qi Gao,Lijuan Zhang,Yunshan Zhou,Yuxu Zhong,Ying Ying,Mingcai Zhang,Chunqian Huang,Yong'an Wang

Currently extensive effort is compulsively expended to decontaminate efficiently banned chemical war agents. In this work, H5PV2Mo10O40 molecules have been encapsulated in mesoporous MIL-101(Cr), which features two types of mesoporous cages (internal diameters of 29 Å and 34 Å) and microporous windows (diameters of 12 Å and 16 Å), leading to the formation of a new composite H5PV2Mo10O40@MIL-101(Cr) through a simple impregnation method. The composite was characterized thoroughly by elemental analysis, FT-IR spectroscopy, powder X-ray diffraction, scanning electron microscopy, energy dispersive X-ray spectroscopy, TG/DTA, and textural analysis thereby confirming the encapsulation of the H5PV2Mo10O40 into MIL-101(Cr). The decontamination efficiency of sulfur mustard (4 μL HD in 40 μL of petroleum ether) by 20 mg of the composite is found to be 97.39% in 120 min under ambient conditions. GC-MS analysis on the decontaminated products using 2-chloroethyl ethyl sulfide (CEES), which has been widely used as a simulant of sulfur mustard, showed that MIL-101(Cr) just decontaminates CEES by adsorption, while CEES can be decontaminated under ambient conditions by a synergetic combination of adsorption of MIL-101(Cr) and subsequent chemical oxidation degradation to nontoxic 2-chloroethyl ethyl sulfoxide (CEESO) due to the presence of highly dispersed H5PV2Mo10O40 within the composites.

研究领域: 材料科学 · 化学工程 · 环境科学
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DALTON TRANSACTIONS · 2020 ·Vol. 49 ·期 24 ·8122-8135 · IF 4.174

A dual-function all-inorganic intercluster salt comprising the polycation ε-[Al13O4(OH)24(H2O)12]7+ and polyanion α-[PMo10V2O40]5− for detoxifying sulfur mustard and soman

Jialin Yu,Qi Gao,Lijuan Zhang,Yunshan Zhou,Yuxu Zhong,Jianbo Yin,Yuanyuan Zhou,Fangsheng Tao,Yong'an Wang

ε-[Al13O4(OH)24(H2O)12]7+, which shares similarity with the phosphotriesterase active site ZnII–OH–ZnII, was specially chosen to interact with the cluster α-PMo10V2O405− to form a new three-dimensional intercluster, which crystallized in the monoclinic space group P21/m with Z = 2, for the decontamination of chemical warfare agents. The experimental results showed that 50 mg of the compound decontaminated 96.4% (within 120 min) and 99.5% (within 40 min) of sulfur mustard (HD) (4 μL) and soman (GD) (4 μL), respectively, in ambient conditions. The decontamination processes followed first-order reaction kinetics with a rate constant and half-life of 0.01234 min−1 and 56.15 min for HD and 0.1198 min−1 and 5.78 min for GD, respectively. It was concluded that the α-PMo10V2O405− moiety was responsible for the catalytic oxidation of HD into non-toxic sulfoxide, while the ε-[Al13O4(OH)24(H2O)12]7+ moiety was responsible for the catalytic hydrolysis of HD and GD into nontoxic hydrolysates. Besides, the compound showed notable efficacy for the decontamination of HD on guinea pig skin and of GD on Kunming mouse skin, indicating high potential for use in human skin protection and treatment.

CAS / MDL: 92-87-5 10140-63-3
研究领域: 化学 · 生物学 · 医学
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Journal of Water Process Engineering · 2023 · IF 7

Plasma jet decontamination of sulfur mustard and its analogues in water by oxidation effect

Ruixue Wang,Zhongwen Li,Xiaosen Li,Peiwen Guo,Haibo Wang,Xuan Guo,Jinyi Zhong

Atmospheric pressure plasma jet (APPJ), as an emerging clean and efficient technology, has been found a great potential for chemical warfare agents (CWAs) decontamination. In this study, we first proposed APPJ for the degradation of sulfur mustard (HD) and its surrogate 2-chloroethyl ethyl sulfide (2-CEES) in water. Under optimal conditions, the degradation efficiency of 2-CEES and HD reached 100 % after 5 min or 6 min plasma treatment. The degradation products of 2-CEES and HD were mainly non-toxic alcohols or low toxic sulfones, which can be degraded and converted into some small molecules (HCl, SO 2 , or CO 2 ) under further plasma treatment. We then identified two dominant short-lived reactive species (·OH and 1 O 2 ) and long-lived reactive molecule (H 2 O 2 ) and distinguished the effect of these three active particles during the degradation process of 2-CEES in water. This work provides detailed evidence of a novel decontamination strategy for HD and 2-CEES.

研究领域: 环境科学 · 化学工程 · 等离子体技术
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ACS Applied Materials & Interfaces · 2022 · IF 10.383

Ultrafast Degradation and High Adsorption Capability of a Sulfur Mustard Simulant under Ambient Conditions Using Granular UiO-66-NH2 Metal–Organic Gels

Chuan Zhou,Bo Yuan,Shouxin Zhang,Guang Yang,Lin Lu,Heguo Li,Cheng-an Tao

Zirconium-based metal–organic frameworks (Zr-MOFs) have been considered as prospective materials for the degradation of nerve chemical warfare agents (CWAs) but show poor catalytic performance toward blister agents. Moreover, the powder issues and the poor adsorption capability also remain as the major challenges for the application of Zr-MOFs in practical CWA detoxification. Herein, a series of defected granular UiO-66-NH2 metal–organic gels are synthesized via adjusting the amount of added concentrated hydrochloric acid for the decontamination of 2-chloroethyl ethyl sulfide (2-CEES), a sulfur mustard simulant. The half-life of 2-CEES decontaminated by defected granular UiO-66-NH2 metal–organic gels can be shortened to 7.6 min, which is the highest reported value for MOFs under ambient conditions. The mechanism of decontamination is that the amino group on the linkers in UiO-66-NH2 MOGs undergoes a substitution reaction with 2-CEES to yield 2-(2-(ethylthio)ethylamino)terephthalic acid, which is less toxic and fixed in the frameworks. The recycling test corroborates that the granular UiO-66-NH2 xerogels possess good stability and reusability. Static adsorption and desorption tests show that UiO-66-NH2 xerogels possess a high 2-CEES vapor adsorption capacity of 802 mg/g after exposure for 1 d and only 28 wt % desorption capacity after air exposure for 7 d. The dual function of ultrafast degradation and high adsorption capability provide a firm foundation for using UiO-66-NH2 xerogels as a future protection media.

CAS / MDL: 64-17-5 68-12-2
研究领域: 化学战剂 · 材料科学 · 环境化学 · 催化
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