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排序方式: 共有1164条查询结果,搜索用时 156 毫秒
1.
In this work, tin dioxide (SnO2) Nanoparticles (NPs) were synthesized through green synthesis, using Citrus × paradisi extract as a stabilizing (capping). The extract concentrations used were 1, 2 and 4% in relation to the aqueous solution. The resulting SnO2 NPs were used for the degradation of Methyl Orange (MO), Methylene Blue (MB) and Rhodamine B (RhB), under both solar and UV radiation. The NPs were characterized via Attenuated Total Reflectance Infrared Spectroscopy (ATR-IR), X-Ray Diffraction (XRD), Scanning Electron Microscopy (SEM) and Transmission Electron Microscopy (TEM-SAED), the Brunauer-Emmett-Teller (BET) theory, Ultraviolet to Visible spectroscopy (UV–Vis), and Photoluminescence spectroscopy (PL); while the photocatalytic degradation was evaluated using UV-VIS. The results showed that the Citrus × paradisi extract is a good medium for the formation of SnO2 NPs. These NPs presented quasi-spherical morphology, particle sizes of 4–8 nm, with a rutile phase crystalline structure, and with banned gap of 2.69 at 3.28 eV. The NPs had excellent photocatalytic properties under solar radiation, degrading 100% of the OM in 180 min. Furthermore, under UV radiation, 100% degradation of the three dyes was achieved in a short time; 20 min for MO, and 60 min for MB and RhB. Therefore, green synthesis is a feasible medium for the formation of SnO2 NPs with good photocatalytic properties.  相似文献   
2.
Epoxidized methyl esters (EMO) with their high oxirane ring reactivity, acts as a raw material in the synthesis of various industrial chemicals including polymers, stabilizers, plasticizers, glycols, polyols, carbonyl compounds, biolubricants etc. EMO has been generally quantified by the gas chromatography (GC) and high-performance liquid chromatography (HPLC) techniques. Taking into the account of the limitations of these techniques, two qHNMR-based equations have been proposed for the quantification of EMO in the mixture of EMO and methylesters (MO). The validity of the proposed method was determined using standard mixtures of MO and EMO having different molar concentrations. The developed equations have been applied on the samples of EMO prepared from oleic acid in two-step process viz., esterification followed by epoxidation. The qHNMR-based EMO quantification showed acceptable agreement with the results obtained from HPLC analysis.  相似文献   
3.
In the present study we made an effort to deploy eco-friendly synthesized reduced graphene oxide/Lanthanum Alluminate nanocomposites (RGO-LaAlO3) and Lanthanum Alluminate (LaAlO3) as adsorbents to remove dye from the synthetic media. XRD, SEM, BET surface area and EDX have been used to characterize the above-mentioned adsorbents. The impacts of different factors like adsorbent dosage, the concentration of adsorbate and PH on adsorption were studied. The best fit linear and nonlinear equations for the adsorption isotherms and kinetic models had been examined. The sum of the normalized errors and the coefficient of determination were used to determine the best fit model. The experimental data were more aptly fitted for nonlinear forms of isotherms and kinetic equations. Pseudo-second-order and Freundlich isotherm model fits the equilibrium data satisfactorily. Methyl orange (MO) has been used as model dye pollutant and maximum adsorption capacity was found to be 469.7 and 702.2 mg g?1 for LaAlO3 and RGO-LaAlO3, respectively.  相似文献   
4.
The technology for transesterification reactions between methyl esters and alcohols is well established by using classical homogeneous alkaline catalysts, which provide high conversion of methyl esters to specialty or nonindigenous esters. However, in certain products where the purity of the esters is of concern, the removal of homogeneous catalysts after the completion of the reaction is a challenge in terms of production cost and water footprint. Therefore, a study to investigate the potential of heterogeneous catalysts was conducted on reactions between methyl palmitate and triethanolamine. The degree of basicity and active surface area of calcium oxide (CaO), zinc oxide (ZnO), and magnesium oxide (MgO) were first characterized by using temperature-programmed desorption (TPD-CO2) and Brunauere–Emmett–Teller (BET), respectively. Among the metal oxides investigated, the CaO catalyst showed the best catalytic activity toward the transesterification process as it gave the highest conversion of methyl palmitate and yielded fatty esteramine compositions similar to the conventional homogeneous catalyst. The optimum transesterification condition by using the CaO catalyst utilized a lower vacuum system of approximately 200 mbar, which could minimize a considerable amount of energy consumption. Furthermore, low CaO dosage of 0.1% was able to give a conversion of 94.5% methyl ester and formed esteramine at 170 °C for 2 h. Therefore, the production of esterquats from esteramine may become more economically feasible through the methyl ester route by using the CaO catalyst, which can be recycled three times.  相似文献   
5.
目的 评定采用高效液相色谱-电感耦合等离子体质谱(High performance liquid chromatography combined with inductively coupled plasma-mass spectrometry, HPLC-ICP-MS)法检测鱼肉中甲基汞、乙基汞含量的不确定度。方法 分析整个检测过程中存在的不确定度因素,建立数学模型,分别从称样量、稀释体积、标准溶液、标准曲线拟合以及方法回收率等几个方面进行分析,对测量结果的不确定度进行评定。结果 影响测量结果的不确定度主要来源于样品前处理和标准曲线拟合。鱼肉样品中结果表示分别为:甲基汞含量(0.48±0.046) mg/kg;乙基汞含量为(0.34±0.051) mg/kg, k=2。结论 该方法准确度高,适用于鱼肉中甲基汞、乙基汞的检测,为提高数据准确性提供有效指导。  相似文献   
6.
The transesterification of dimethyl carbonate with phenol to methyl phenyl carbonate (MPC) was investigated on novel catalysts such as titanium diisopropoxide bis(ethyl acetoacetate) and titanium dibutoxide bis(ethyl acetoacetate) in a closed batch reactor at 185–206 °C under high pressure. The produced methanol could be removed efficiently by reactive distillation in order to overcome the equilibrium. The prepared catalysts have higher resistance to water than titanium alkoxides. Phenol conversion as high as 86.4 % with an MPC selectivity of 99.4 % was achieved under optimal reaction conditions within 9 h. Most of the catalytic activity was retained after repeated use for ten times.  相似文献   
7.
Monoclinic scheelite-type BiVO4 is currently considered as one of the most promising non-titania photocatalysts, wheras tetragonal zircon-type BiVO4 is still poorly understood. Herein, a new and simple synthetic approach was applied and nanostructured single-phase zircon-type BiVO4 was successfully prepared by a controllable ethylene-glycol colloidal route. In addition, nanostructured monoclinic scheelite-type BiVO4 powders were also fabricated through annealing of the as-prepared samples. A comparative study of the two BiVO4 polymorphs was conducted and it turned out that the novel synthetic approach had a significant impact on porosity and photocatalytic performance of zircon-structured BiVO4. All the prepared materials, as-prepared and annealed, were mesoporous, while measured values of specific surface area of some zircon-structured samples (~34?m2/g) were ~7 times higher than those reported thus far for this phase. Interestingly, for the first time, zircon-type BiVO4, previously considered to be a poor photocatalyst, exhibited a better overall performance in degradation of methyl orange compared to monoclinic scheelite-type BiVO4. Hence, it could be expected that the here-presented synthesis and observations will both arouse interest in scarcely studied tetragonal zircon-type BiVO4 and facilitate as well as speed up further research of its properties.  相似文献   
8.
In this article, morphology, structure and size controllable chitosan microspheres with high mechanical strength were synthesized by microfluidic technology combining chemical crosslinking and used as an adsorbent for methyl orange. The synthesized adsorbents were characterized using scanning electron microscopy(SEM),Fourier transform infrared spectroscopy(FTIR), and an Energy Dispersive Spectrometer(EDS). The effect of pH revealed that the adsorption process depended on pH and the pH variation of methyl orange solution after adsorption indicated that adsorption capacity was affected through the associated role of chitosan nature and pH variation. Experimental results suggested that the as-prepared chitosan microspheres were controlled within a narrow size distribution(coefficients of variation is 1.81%), whose adsorption capacity reached to 207 mg·g~(-1) and mechanical strength was suitable to resist forces. In addition, the adsorption isotherm was well fitted with the Langmuir model, and the adsorption kinetic was best described by the pseudo-second-order kinetic model.The high performance microfluidic-synthesized chitosan microspheres have promising potentials in the applications of removing dyes from wastewater.  相似文献   
9.
Wearable energy storage devices that can be used in the garment industry are strongly required to power E-textiles. In this article, polypyrrole (PPy) nanorods were deposited on cotton fabrics via in situ polymerization of pyrrole in the presence of the fibrillar complex of FeCl3 and methyl orange as a reactive self-degraded template. The obtained fabrics could be directly used as supercapacitor electrodes, with a maximum specific capacitance of 325 F g−1 and an energy density of 24.7 Wh kg−1 at a current density of 0.6 mA cm−2. The capacitance remained higher than 200 F g−1 after 500 cycles.  相似文献   
10.
《Advanced Powder Technology》2019,30(10):2363-2368
The heterostructure of Cu7.2S4 nanosheets/trisoctahedron Cu2O were successfully constructed on the {3 3 2} high-index facets of Cu2O. The results show that oxygen defects amount of the Cu7.2S4/Cu2O samples are closely related to the thickness of Cu7.2S4 nanosheets. Compared with the unmodified cuprous oxide and the Cu7.2S4/Cu2O modified with thick Cu7.2S4 nanosheets, the Cu7.2S4/Cu2O grafted with 10 nm thickness of Cu7.2S4 show higher oxygen defects content and photocatalytic performance for MO decoloration. UV–VIS DRS and PL detection show that the Cu7.2S4 nanosheets grafting on Cu2O with high-index facets accelerates the charge carrier separation, which results in an elevated degradation properties for MO.  相似文献   
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