CHEMICAL ENGINEERING JOURNAL
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2016
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IF 5.31
Hong Zhang,Xiaoyu Yang,Zhaohui Liu,Yanzhao Yang
An arisen and environment-friendly method of cloud point extraction (CPE) which involved Octylphenoxypolyethoxyethanol (TX-114) as surfactant and 2-Mercaptobenzothiazole-functionalized ionic liquid as extractant was carried out to separate Ru(III) from aqueous phase to bottom surfactant phase for the first time. A host of variable ( e.g. , the extractant concentration, hydrochloric acid concentration, nitric acid concentration, TX-114 mass fraction, TX-114 volume and sodium chloride concentration) were evaluated and optimized to investigate the extraction behavior. At optimized experimental conditions, the extraction percentage of Ru(III) was found to be 82%, together with the enrichment factor of 40. A special complexation extraction mechanism of Ru(III) in CPE process was studied systemically and confirmed via job method, UV–vis spectrum and FT-IR spectrum in detail. Taking together, the rational-designed functional ionic liquid as a novel extractant exhibited superior extractability for Ru(III) in CPE system.
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BIOMETALS
·
2017
·Vol. 30
·期 3
·441-447
·
IF 2.183
Wang Qingming,Sun Huifang,Sha Weilin,Chen Juan,Gu Liuyue,Wang Dong,Tang Xinhui
A novel S2O3 2− luminescent sensor (Cu2+-p-CPIP) was developed and the presence of S2O3 2− caused an obvious fluorescence enhancement at 420 nm upon excitation at 330 nm, which could be distinguished with the naked eye under a UV lamp. Remarkably, the compound exhibited excellent selective and sensitive response to S2O3 2− over other common anions with a micromolar limit of detection (0.442 μM) in DMSO/H2O (v/v, 1:1) buffer. The absorbance intensity and the color of Cu2+-p -CPIP solution changed gradually with the increase of S2O3 2− concentration. The proposed method was applied to the determination of S2O3 2− in milk samples and the recoveries were 97.5–105%. The preparation of Cu2+-p -CPIP exhibited the quick, simple and facile advantages. The results showed that Cu2+-p -CPIP can be a good candidate for simple, rapid and sensitive colorimetric detection of S2O3 2− in aqueous solution.
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ACS Sustainable Chemistry & Engineering
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2016
·
IF 5.267
Yanbing Wang,Kai Yu,Da Lei,Wei Si,Yajun Feng,Lan-Lan Lou,Shuangxi Liu
An environmentally benign and homogeneous base-free route for 5-hydroxymethyl-2-furfural (HMF) aerobic oxidation to 2,5-furandicarboxylic acid (FDCA) in water was reported using Mg–Al–CO3 hydrotalcite-supported Pd nanoparticles (xPd/HT-n) as catalyst. The influences of the Mg/Al molar ratio of hydrotalcite and Pd loading amount on the catalytic performance of these catalysts were originally systematically investigated. These catalysts exhibited excellent catalytic activity and FDCA selectivity in the HMF oxidation, especially for 2%Pd/HT-5 and 2%Pd/HT-6; >99.9% FDCA yields were achieved for 8 h under ambient pressure and homogeneous base-free conditions. The remarkably improved catalytic performance could be attributed to the suitable basicity of the Mg–Al–CO3 hydrotalcite and the abundant OH– groups on the surface of hydrotalcite. The plausible reaction mechanism was proposed based on the results of a series of controlled experiments. Furthermore, these catalysts were quite stable and could be reused at least five times without obvious loss in reaction activity.
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RESEARCH ON CHEMICAL INTERMEDIATES
·
2015
·Vol. 42
·期 3
·2035-2045
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IF 1.221
Yu Zhi-Yu,Fang Qiu-Sheng,Zhou Jia,Song Zhi-Bin
A simple, efficient, and eco-friendly aerobic procedure for synthesis of 2-substituted benzothiazoles catalyzed by facile prepared [N 2222 ][Pro] in a biomass medium (ethyl lactate) has been developed. The reactions afford the target 2-arylbenzothiazoles in good to excellent yields (>80 %) under air condition and was observed without use of chromatography. In addition, this proline-based ionic liquid catalyst can be easily recycled six times without loss of catalytic activity in gram scale synthesis.
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BIOSENSORS & BIOELECTRONICS
·
2014
·
IF 6.451
Jia-Cheng Wang,Yong-Sheng Wang,Jin-Hua Xue,Bin Zhou,Qiu-Mei Qian,Yong-Song Wang,Ji-Cheng Yin,Hui Zhao,Hui Liu,Shan-Du Liu
We developed a highly sensitive label-free assay of 8-hydroxy-2′-deoxyguanosine (8-OHdG) using 8-OHdG-aptamer (Apt) as the recognition element. The Apt was adsorbed onto the surface of gold nanoparticles (AuNPs), which prevents them from aggregating under high-salt conditions. Upon addition of 8-OHdG, the conformation of the Apt changes to form a G-quadruplex structure, which leads to the aggregation of the AuNPs along with the increase of the resonance light scattering intensity. The mechanism of 8-OHdG that induces Apt to form G-quadruplexes structure was studied by circular dichroism . The response signals linearly correlated with the concentration of 8-OHdG ranging from 90.8 pM to 14.1 nM with a detection limit of 27.3 pM, which is much lower than that obtained by other methods. This method does not need any label steps and sophisticated equipment. The application for detection of 8-OHdG in real samples further demonstrated its reliability. This strategy would be helpful for developing a universal analytical method by simply replacing corresponding aptamers for various target molecules.
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EUROPEAN JOURNAL OF INORGANIC CHEMISTRY
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2015
·Vol. 2015
·期 28
·4708-4714
·
IF 2.942
Xiao-Qing Huang,Hao Yang,Shun-Ping Zhao,Jian-Lan Liu,Xiao-Ming Ren
Graphical An anhydrous proton conductor is achieved by inserting 2-picolinic acid into the layer space of kaolinite, and the proton transport in this intercalated hybrid material is mainly through the vehicle mechanism owing to the absence of a dense H-bond network. Kaolinite intercalated with 2-picolinic acid was prepared and characterized by scanning electron microscopy, powder X-ray diffraction, infrared spectroscopy, and thermogravimetric analysis. The proton conductivity ( σ ) of the material is 1.85 × 10 –10 S cm –1 at 353 K and gradually increases to 1.7 × 10 –7 S cm –1 at 393 K under N 2 (anhydrous environment) with an activation energy of E a = 1.93 eV, whereas σ = 1.56 × 10 –7 S cm –1 under 80 % relative humidity at 353 K with E a = 0.91 eV. The crystal structure optimized with the Cambridge Sequential Total Energy Package discloses the absence of a dense H-bond network in the layer space of kaolinite, which explains the low proton conductivity and high proton transfer activation energy of the intercalated proton conductor.
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ACS Applied Materials & Interfaces
·
2014
·
IF 5.9
Zhi Chen,Zanyong Zhuang,Qing Cao,Xiaohong Pan,Xiong Guan,Zhang Lin
The mechanism of the interaction between nano-Mg(OH)2 adsorbent and uranyl in water was studied. At trace levels, the uranyl is adsorbed as a monolayer on nano-Mg(OH)2, and occupied a small proportion of the adsorption sites. As the uranyl concentration crosses over a threshold, continuous increase of adsorption capacity takes place. It indicates that, by taking the pre-adsorbed uranyl as the nucleation centers, the additional uranyl crystallizes and forms U-rich nanocrystals well-scattered on the surface of nano-Mg(OH)2. A strategy of inducing fast crystal growth of nano-Mg(OH)2 to micrometer-sized Na2Mg(CO3)2 enables the desorption and enrichment of uranyl. The recycling and reuse of nano-Mg(OH)2 can be achieved simultaneously. The finding in this work provides fundamental understanding of the efficient usage of nano-Mg(OH)2 in practical applications.
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Catalysis Science & Technology
·
2013
·Vol. 4
·期 3
·773-779
·
IF 3.753
Qinzhuo Zhou,Bo-Geng Li,Suyun Jie,Na Zheng
A series of phosphine-containing cobalt complexes [CoCl2(PRPh2)2, R = Ph (1), Cy (2), nPr (3), Et (4), Me (5), H (6)] has been used for the highly active and stereospecific polymerization of 1,3-butadiene upon activation with ethylaluminum sesquichloride (EASC). The high catalytic activities and polybutadienes with high cis-1,4 selectivity were obtained in the solution polymerization in toluene. The conversion of butadiene and the microstructure and molecular weight of the resulting polymers were affected by reaction parameters and the R group on the phosphine ligand. The dispersion medium was also a sensitive factor for the current catalytic systems, influencing the catalytic activity and properties of products. In comparison with the solution polymerization in toluene, the heterogeneous polymerization in isooctane yielded slightly lower catalytic activity, cis-1,4 content and molecular weight under similar reaction conditions.
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JOURNAL OF APPLIED POLYMER SCIENCE
·
2014
·Vol. 131
·期 17
·
IF 1.64
Hongming Yuan,Zaochuan Ge,Shaojun Chen,Shiguo Chen,Haipeng Yang,Haitao Zhuo
This article demonstrates a comparative investigation about the effect of diisocyanate on pyridine containing shape memory polyurethanes (Py-SMPUs), which are synthesized with N , N -bis(2-hydroxylethyl)isonicotinamide (BINA) and four different diisocyanates: 1,6-hexanediisocyante (HDI), isophorone diisocyanate (IPDI), methylene diphenyl diisocyanate (MDI), and tolylene diisocyanate (TDI). Results show that all BINA–SMPU systems have amorphous reversible phase. Comparatively, the MDI–BINA and TDI–BINA systems show higher T g ; and the HDI–BINA and IPDI–BINA systems show better thermal stability. In addition, the HDI–BINA and the IPDI–BINA systems exhibit good thermal-induced shape memory effect and good moisture-sensitive shape memory effect due to their better moisture absorption properties. Particularly, the HDI–BINA system has better response speed and better shape recovery. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131 , 40721.
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JOURNAL OF HAZARDOUS MATERIALS
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2014
·
IF 4.331
Zhixing He,Chengzhen Niu,Zhenmei Lu
The bacterial strain DP-2, identified as Rhodococcus ruber , is able to effectively degrade di-n-butyl phthalate (DBP) and phenol. Degradation kinetics of DBP and phenol at different initial concentrations revealed DBP and phenol degradation to fit modified first-order models. The half-life of DBP degradation ranged from 15.81 to 27.75 h and phenol degradation from 14.52 to 45.52 h under the initial concentrations of 600–1200 mg/L. When strain DP-2 was cultured with a mixture of DBP (800 mg/L) and phenol (700 mg/L), DBP degradation rate was found to be only slightly influenced; however, phthalic acid (PA) accumulated, and phenol degradation was clearly inhibited during synchronous degradation. Transcriptional levels of degradation genes, phenol hydroxylase ( pheu ) and phthalate 3,4-dioxygenase ( pht ), decreased significantly more during synchronous degradation than during individual degradation. Quantitative estimation of individual or synchronous degradation kinetics is essential to manage mixed hazardous compounds through biodegradation in industrial waste disposal.
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Chemistry-An Asian Journal
·
2013
·Vol. 8
·期 7
·1504-1513
·
IF 4.572
Si-Hai Wu,Yu-Wu Zhong,Jiannian Yao
Graphical NN-CNN breaking news : 2,3-Di(2-pyridyl)-5-phenylpyrazine, which is able to bind two metals through a NN-CNN-type coordination mode, has been designed and synthesized. A RuPt heterobimetallic complex with this bridging ligand shows near-infrared emission at 750 nm, with a quantum yield of 0.41 % and an excited-state lifetime of 170 ns. en This link goes to a English section zh This link goes to a English section A new bridging ligand, 2,3-di(2-pyridyl)-5-phenylpyrazine (dpppzH), has been synthesized. This ligand was designed so that it could bind two metals through a NN-CNN-type coordination mode. The reaction of dpppzH with cis -[(bpy) 2 RuCl 2 ] (bpy=2,2′-bipyridine) affords monoruthenium complex [(bpy) 2 Ru(dpppzH)] 2+ ( 12+ ) in 64 % yield, in which dpppzH behaves as a NN bidentate ligand. The asymmetric biruthenium complex [(bpy) 2 Ru(dpppz)Ru(Mebip)] 3+ ( 23+ ) was prepared from complex 12+ and [(Mebip)RuCl 3 ] (Mebip=bis( N -methylbenzimidazolyl)pyridine), in which one hydrogen atom on the phenyl ring of dpppzH is lost and the bridging ligand binds to the second ruthenium atom in a CNN tridentate fashion. In addition, the RuPt heterobimetallic complex [(bpy) 2 Ru(dpppz)Pt(CCPh)] 2+ ( 42+ ) has been prepared from complex 12+ , in which the bridging ligand binds to the platinum atom through a CNN binding mode. The electronic properties of these complexes have been probed by using electrochemical and spectroscopic techniques and studied by theoretical calculations. Complex 12+ is emissive at room temperature, with an emission λ max =695 nm. No emission was detected for complex 23+ at room temperature in MeCN, whereas complex 42+ displayed an emission at about 750 nm. The emission properties of these complexes are compared to those of previously reported Ru and RuPt bimetallic complexes with a related ligand, 2,3-di(2-pyridyl)-5,6-diphenylpyrazine. en This link goes to a English section zh This link goes to a English section 1
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APPLIED CATALYSIS A-GENERAL
·
2014
·
IF 3.674
Xiuquan Jia,Jiping Ma,Min Wang,Zhongtian Du,Fang Lu,Feng Wang,Jie Xu
The promoted effect of Cu(NO 3 ) 2 on aerobic oxidation of 5-hydroxymethylfurfural (HMF) to 2,5-diformylfuran (DFF) catalyzed by VOSO 4 in acetonitrile was intensively investigated. It was revealed that Cu(NO 3 ) 2 facilitated the activation of VOSO 4 to generate active V 5+ species via the generation of NO x gas. The high DFF selectivity is ascribed to Cu 2+ cation which can effectively prohibit oxidative C C bond cleavage reaction of HMF and prevent radical reaction of DFF to humins. In addition, the polarity of solvent plays a great role on high selectivity of DFF.
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