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1.
Elemental mercury capture on heat-treated activated carbon (TAC) was studied using a laboratory-scale fixed bed reactor. The capability of TAC to perform Hg0 capture under both N2 and baseline gas atmospheres was studied and the effects of common acid gas constituents were evaluated individually to avoid complications resulting from the coexistence of multiple components. The results suggest that surface functional groups (SFGs) on activated carbon (AC) are vital to Hg0 capture in the absence of acid gases. Meanwhile, the presence of acid gas components coupled with defective graphitic lattices on TAC plays an important role in effective Hg0 capture. The presence of HCl, NO2, and NO individually in basic gases markedly enhances Hg0 capture on TAC due to the heterogeneous oxidation of Hg0 on acidic sites created on the carbon surface and catalysis by the defective graphitic lattices on TAC. Similarly, the presence of SO2 improves Hg0 capture by about 20%. This improvement likely results from the deposition of sulfur groups on the AC surface and oxidation of the elemental mercury by SO2 due to catalysis on the carbon surface. Furthermore, O2 exhibits a synergistic effect on Hg0 oxidation and capture when acid gases are present in the flue gases.  相似文献   

2.
The chemisorption properties of N18O adsorption on TiO2(110) surface were investigated by experimental and theoretical methods. The results of temperature programmed desorption (TPD) indicated that the temperatures of the three desorption peaks of the main N2 molecules were at (low) temperature of 230 K, 450 K and (high) temperature of 980 K. This meant that N18O decomposed and recombined during the process of N2 desorption after N18O was exposed. Analysis of the stable combination and orbital theory calculation of the surface reaction of NO adsorption on the TiO2(110) cluster model showed that there was clear preference for the Ti-NO orientation.  相似文献   

3.
Systematic studies of the transport properties of La0.67Ca0.33Mn1?xFe x O3 (x=0–0.3) systems showed that with increasing Fe-doping contentx the resistance increases and the insulator-metal transition temperature moves to lower temperature. For small doping content, the transport property satisfies metal transport behavior below the transition temperature, and above the transition temperature it satisfies the small polaron model. This behavior can be explained by Fe3+ doping, which easily forms Fe3+?O2??Mn4+ channel, suppressing the double exchange Mn3+?O2??Mn4+ channel and enhancing the spin scattering of Mn ions induced by antiferromagnetic clusters of Fe ions.  相似文献   

4.
Surface morphologies of Zr52.5 Al10 Ni10 Cu15 Be12.5 bulk metallic glass after being rolled at both a temperature around T9 and near （ Tx - 50） K were investigated with a scanning electron microscopy. Macroscopic and microscopic observation results show that squamae, cracks, steps and wedges exist on the surface when the samples were rolled at temperatures around Ty. However, a smooth and fiat surface appears when the samples were rolled at temperatures near （ Tx - 50） K. These results indicate that the mode of deformation in the supercooled liquid region is a partially homogeneous flow at a temperature around T9, and a fully homogeneous one at temperatures near （ Tx - 50） K. According to the results, it is more feasible to roll the amorphous alloys at temperatures near （ Tx - 50） K to obtain parts with smooth and fiat surface.  相似文献   

5.
A Gram-negative, aerobic, non-motile, rod-shaped bacterial strain, designated 25-1T, was isolated from the air inside giant panda enclosures at the Chengdu Research Base of Giant Panda Breeding, China. Strain 25-1T grew optimally at pH 7.0–8.0, at 28–30 °C and in the presence of NaCl concentrations from 0.0% to 0.5 %. 16S rRNA gene sequence analysis indicated that strain 25-1T belongs to the genus Chryseobacterium within the family Flavobacteriaceae and is related most closely to C. carnis G81T (96.4% similarity), C. lathyri RBA2-6T (95.8% similarity), and C. zeae JM1085T (95.8% similarity). Its genomic DNA G+C molar composition was 36.2%. The major cellular fatty acids were iso-C15:0 (44.0%), iso-C17:0 3OH (19.8%) and C16:1 ω7c/16:1 ω6c (12.7%). The only isoprenoid quinone was menaquinone 6 (MK-6). The major polar lipids were phosphatidylethanolamine, two unidentified amino lipids and two unidentified lipids. The DNA-DNA relatedness between strain 25-1T and C. lathyri RBA2-6T was 38%. Phenotypic, genotypic, and phylogenetic characteristics indicated that strain 25-1T is a novel member of the genus Chryseobacterium, for which the name C. chengduensis sp. nov. is proposed. The type strain is 25-1T (CCTCC AB2015133T=DSM 100396T).  相似文献   

6.
1Introduction Oxide dilutedmagneticsemiconductors(O DMS)havedrawnmuchattentioninthelastdecadebecause thesematerialsappeartohavegreatpotentialforuse inspin dependentelectronicdevices[1].Recently,iron cobalt dopedtitaniumdioxideswithroomtemperature ferromagnetismhavebeenreported[2].Specially,the resultsofmagneticpropertiesofFexTi1-xO2(x=0.065and0.250)indicatethatferromagnetismwitha Femagneticmomentislargerthantheonereported forCo[3].ThefabricationmethodsofFe Co doped TiO2includepulsedlaser…  相似文献   

7.

Objectives

To investigate the effects of different nitrate sources on the uptake, transport, and distribution of molybdenum (Mo) between two oilseed rape (Brassica napus L.) cultivars, L0917 and ZS11.

Methods

A hydroponic culture experiment was conducted with four nitrate/ammonium (NO3 ?:NH4 +) ratios (14:1, 9:6, 7.5:7.5, and 1:14) at a constant nitrogen concentration of 15 mmol/L. We examined Mo concentrations in roots, shoots, xylem and phloem sap, and subcellular fractions of leaves to contrast Mo uptake, transport, and subcellular distribution between ZS11 and L0917.

Results

Both the cultivars showed maximum biomass and Mo accumulation at the 7.5:7.5 ratio of NO3 ?:NH4 + while those were decreased by the 14:1 and 1:14 treatments. However, the percentages of root Mo (14.8% and 15.0% for L0917 and ZS11, respectively) were low under the 7.5:7.5 treatment, suggesting that the equal NO3 ?:NH4 + ratio promoted Mo transportation from root to shoot. The xylem sap Mo concentration and phloem sap Mo accumulation of L0917 were lower than those of ZS11 under the 1:14 treatment, which suggests that higher NO3 ?:NH4 + ratio was more beneficial for L0917. On the contrary, a lower NO3 ?:NH4 + ratio was more beneficial for ZS11 to transport and remobilize Mo. Furthermore, the Mo concentrations of both the cultivars’ leaf organelles were increased but the Mo accumulations of the cell wall and soluble fraction were reduced significantly under the 14:1 treatment, meaning that more Mo was accumulated in organelles under the highest NO3 ?:NH4 + ratio.

Conclusions

This investigation demonstrated that the capacities of Mo absorption, transportation and subcellular distribution play an important role in genotype-dependent differences in Mo accumulation under low or high NO3 ?:NH4 + ratio conditions.
  相似文献   

8.
A Pr-doped TiO2-NTs/SnO2-Sb electrode was prepared by a simple method, cyclic voltammetry(CV). The methyl orange(MO)aqueous solution was selected as a simulated wastewater. The ordered microstructural TiO2-NTs substrate was synthesized by an electrochemical method to obtain large specific surface area and high space utilization. The phase structure, electrode surface morphology and electrochemical properties of electrodes were characterized by XRD, SEM and electrochemical technology, respectively. The results showed that praseodymium oxide was successfully doped into the SnO2-Sb film by CV method. Due to the doped Pr, the oxygen evolution potential increased from 2.25 V to 2.40 V. The degradation of MO was investigated by UV-vis. The C t /C 0 (φ) was studied as a function to obtain the optimal parameters, such as the amount of doped Pr, current density and initial dye concentration. In addition, the degradation process followed pseudo-first-order reaction kinetics and the rate constant was 0.099 3 min-1. The result indicated that the introduction of Pr reduced the formation of oxygen vacancies or enhanced the formation of adsorbed hydroxyl radical groups on the surface, thus leading to better activity and stability.  相似文献   

9.
文章基于密度泛函理论,研究了本征及Nb,Fe单原子掺杂单层MoSe2的电子结构及光学性质。计算发现,本征单层MoSe2和Nb-MoSe2为直接带隙半导体,Fe-MoSe2为间接带隙结构;Fe-MoSe2较本征单层MoSe2导电性大大提高,实现了由半导体向半金属的过渡。由态密度分析得出了本征及Nb,Fe单原子掺杂单层MoSe2能量状态主要由Mo 4d,Se 4p轨道电子所贡献的结论,并对各原子掺杂体系轨道电子的能量贡献和掺杂类型做了探讨。此外,还详细分析了费米能级附近的自旋态密度、杂质带、磁性之间的联系。光学性质方面,比较了本征单层MoSe2与各掺杂体系的复介电常数和光吸收系数,在红外光区Fe-MoSe2的吸收系数高于本征单层MoSe2。本征单层MoSe2的光吸收系数为9.69×104 cm-1,是区域最大吸收峰。上述研究表明,通过对单层MoSe2的Nb,Fe掺杂可使电子输运特性得到了增强,为高活性自旋电子和光电子器件设计和研究开辟了新的前景。  相似文献   

10.
Nanostructures enhance phonon scattering and improve the figure of merit of thermoelectric materials. Nanosized CoSb3 skutterudite was synthesized by solvothermal methods using CoCl2 and SbCl3 as the precursors. A “two-step” model was suggested for the formation of CoSb3 based on the X-ray diffraction analysis. The first step is the formation of cobalt diantimonide in the earlier stage during the synthesis process. Diantimonide was then combined with antimony atoms to form the skutterudite structured triantimonide, CoSb3, in the later stage of the synthesis process as the second step. The synthesized CoSb3 powders consist of irregular particles with sizes of about 20 nm and sheets of about 80 nm. Project supported by the National Natural Science Foundation of China (No. 50171064) and the Hi-Tech Research and Development Program (863) of China (No. 2002AA302406)  相似文献   

11.
In this study, supported nonmetal （boron） doping TiO2 coating photocatalysts were prepared by chemical vapor deposition （CVD） to enhance the activity under visible light irradiation and avoid the recovering of TiO2. Boron atoms were successfully doped into the lattice of TiO2 through CVD, as evidenced from XPS analysis. B-doped TiO2 coating catalysts showed drastic and strong absorption in the visible light range with a red shift in the band gap transition. This novel B-TiO2 coating photocatalyst showed higher photocatalytic activity in methyl orange degradation under visible light irradiation than that of the pure TiO2 photocatalyst.  相似文献   

12.
Using SnxTi1-xO2 as carriers, CuO/Sn0.9Ti0.1O2 and CuO/Sn0.7Ti0.3O2 catalysts with different loading amounts of copper oxide (CuO) were prepared by an impregnation method. The catalytic properties of CuO/Sn0.9Ti0.1O2 and CuO/Sn0.7Ti0.3O2 were examined using a microreactor-gas chromatography (GC) NO CO reaction system and the methods of BET (Brun- auer-Emmett-Teller), TG-DTA (themogravimetric and differential thermal analysis), X-ray diffraction (XRD) and H2-temperature programmed reduction (TPR). The results showed that NO conversions of Sn0.9Ti0.1O2 and Sn0.7Ti0.3O2 were 47.2% and 43.6% respectively, which increased to 95.3% and 90.9% at 6 wt% CuO loading. However, further increase in CuO loading caused a decrease in the catalytic activity. The nitrogen adsorption-desorption isotherm and pore-size distribution curve of Sn0.9Ti0.1O2 and Sn0.7Ti0.3O2 represented type IV of the BDDT (Brunauer, Deming, Deming and Teller) system and a typical mesoporous sample. There were two CuO diffraction peaks (2θ 35.5° and 38.7°), and the diffraction peak areas increased with increasing CuO loading. TPR analysis also detected three peaks (α, β and γ) from the CuO-loaded catalysts, suggesting that the α peak was the reduction of the highly dispersed copper oxide, the β peak was the reduction of the isolated copper oxide, and the γ peak was the reduction of crystal phase copper oxide. In addition, a fourth peak (δ) of the catalysts meant that the SnxTi1-xO2 mixed oxides could be reductive.  相似文献   

13.
Well-cubic perovskite lanthanum aluminate (LaAlO3) film on (110) silicon substrate was fabricated by sol-gel method with corresponding inorganic salts. Lanthanum acetate and aluminum acetate glacial acetic acid solutions were prepared via ligand exchange starting from lanthanum nitrate hexahydrate and aluminum nitrate hexahydrate after being refluxed. (CH3CO)2O removed nitrates and the crystallized H2O completely, acetylacetone (AcAc) was partially bidentated with metallic ion of the metallic acetates and formed La(OAc)3−x (AcAc) x which were hydrolyzed into La(AcAc)3−x(OH) x by adding 10 ml 0.4% methyl cellulose (MCL) solution. The La(AcAc)3−x (OH) x , polymerizing and combining with MCL, formed the LaAlO3 sol precursor with heteropolymeric structure and formed film easily. The epitaxial LaAlO3 film on Si(110) substrate was crystallized after being annealed in thermal annealing furnace for 650–750 °C/30 min. The morphologies and microstructures were characterized. The refractive index of the LAO film was 1.942 to 2.007; the dielectric constant and the dissipation factors were estimated to be 23–26 and 2.1×10−4−2.4×10−4 respectively. Project (No. 2002CB613305) supported by the National Basic Research Program (973) of China  相似文献   

14.
Based on the laboratory experiments with the saltwater and freshwater replacing each other in the level sand column, taking the kaolin, illite, smectite, bivalent hydrargyrum ion (Hg2+) and phenol (C6H5OH) as examples, this paper studies the applications of water sensitivity in situ remediation in saltwater-freshwater transition zone. In the water sensitivity process, the release and migration of clay minerals can make the hydraulic conductivity (HC) decrease and pollutants remove. A new type of low penetrable or impenetrable purdah can be built by adding clay minerals into the sand media to replace the underground concrete impenetrable wall to prevent seawater intrusion, and a number of the heavy metals and organic pollutants in the sand media can be removed by in situ remediation. The results show that the content of kaolin and illite influences the water sensitivity process slightly, and HC of the sand columns descends from 0.011 cm/s to 0.001 4 cm/s and 0.001 2 cm/s respectively even if the content reaches 12% (weight ratio, sic passim). However, for smectite, HC descends sharply to about 1×10−8 cm/s when its content reaches 4%, and no water can flow through the sand columns beyond 5%. The particle release and migration processes can remove the Hg2+ and C6H5OH out of the sand columns efficiently, the removing rate of Hg2+ is 31.68% when the freshwater and saltwater are filtered through the sand columns polluted by Hg2+, while it is 67.55% when the water sensitivity occurs. With the same method, the removing rates of C6H5OH under the fluid flow and water sensitivity are 55.71% and 43.43% respectively. Supported by National Natural Science Foundation of China (No. 40572142). HAN Zhiyong, born in 1976, male, Dr, associate Prof.  相似文献   

15.
A new concept of low-cost direct air capture technology integrated with a fertilization system is proposed, as an alternative to the application of air derived CO2. A moisture swing sorbent can elevate the CO2 concentration from 400 parts per million (ppm) to several thousand ppm, and this can be used to cultivate plants. Desorption isotherms were determined and are described well by a Langmuir model. The adsorption rate constant and the desorption rate constant were gained at 25 °C, 35 °C, and 45 °C under 1000 ppm concentration of CO2. In accelerated cultivation experiments, the effects of CO2 concentration, light intensity, and spectrum on the CO2 uptake rate of the plants were investigated. A multi-bed desorption system which is capable of providing a continuous and stable CO2 supply for a greenhouse is demonstrated based on the desorption characteristic and CO2 uptake feature of plants. An energy and cost assessment for the integrated system was performed and the results indicated that minimum energy requirements and cost estimate of CO2 are 35.67 kJ/mol and 34.68 USD/t, respectively. This makes direct air capture a competitive and sustainable carbon source for agriculture.  相似文献   

16.
TiO2 nanoparticles(NPs)were prepared via the hydrothermal route of TiO2 xerogel in nitric acid, hydrochloric acid and acetic acid. The physico-chemical properties of the powders were characterized by X-ray diffraction(XRD)and N2 adsorption desorption techniques. The effects of the different acids on the structure(crystal phase)and texture(primary particle size and porosity)of the TiO2 powders were explored. Results indicated that acetic acid facilitated the formation and stability of pure anatase phase. On the other hand, nitric acid and hydrochloric acid led to the transformation from anatase to rutile. The catalyst synthesized via the hydrothermal route of TiO2 xerogel in the low concentration hydrochloric acid solution(Ti-HCl-0.15)had the highest photocatalytic activity than the catalysts obtained in the other two acid solutions. The effects of the different acids were discussed in terms of acid strength, chelating effect and the thermal stability of the adsorbed acidic anions.  相似文献   

17.
With the increasing occurrence of haze during the summer, the physicochemical characteristics and toxicity differences in PM2.5 in different seasons are of great concern. Hangzhou is located in an area that has a subtropical monsoon climate where the humidity is very high during both the summer and winter. However, there are limited studies on the seasonal differences in PM2.5 in these weather conditions. In this test, PM2.5 samples were collected in the winter and summer, the morphology and chemical composition of PM2.5 were analyzed, the toxicity of PM2.5 to human bronchial cells BEAS-2B was compared, and the correlation between PM2.5 toxicity and the chemical composition was discussed. The results showed that during both the winter and summer, the main compounds in the PM2.5 samples were water-soluble ions, particularly SO42?, NO3?, and NH4+, followed by organic components, while heavy metals were present at lower levels. The higher the mass concentration of PM2.5, the greater its impact on cell viability and ROS levels. However, when the mass concentration of PM2.5 was similar, the water extraction from the summer samples showed a greater impact on BEAS-2B than that from the winter samples. The cytotoxicity of PM2.5 was closely associated with heavy metals and organic pollutants but less related to water-soluble ions.  相似文献   

18.
Magnetic properties of nanocrystalline Fe60 Cr40 powders prepared by mechanical alloying in vacuum and air were investigated by utilizing the measurements of magnetization, X-ray diffraction, and ^67Fe M（oe）ssbauer spectrum. The results show that the Fe60 Cr40 powders keep the bcc structure during milling in air and vacuum. The saturation magnetization of the Fe60 Cr40 powders milled in vacuum and air decreases with the increase of the milling time up to 45 h. The decrease of saturation magnetization of the Fe60Cr40 powders milled in vacuum is due to the formation of Fe-Cr solid solution, while in air it is due to the formation of paramagnetic disorder structure and solid solution.  相似文献   

19.
This paper describes the preparation and properties of TiNx-SiO2 double-layered antireflective(AR) coatings that were applied with print process. The coating material was analyzed and TiNx was used instead of TiO2 as high refractive material. The influence of solution concentration on AR property was studied. The testing result shows that the coatings using print process are featured with excellent mechanical property and the AR property is comparable to American Southwall AR product. It is expected that the study would promote the industrialization progress in AR coatings.  相似文献   

20.
In this study, liquid-phase aerobic oxidation of toluene catalyzed by Mn–Mo oxide was conducted in a 1.0 L batch reactor. The macroscopic kinetics of toluene consumption and benzaldehyde generation at 413–443 K were obtained from a combination of experimental observation and hypothetical models. The results clearly showed that both the oxidation rate of toluene and generation rate of the aromatic product were proportional to the concentration of the substrate, the partial pressure of oxygen and the surface area of the catalyst. The energy barrier of toluene oxidation to benzyl alcohol was the highest(≈ 81 kJ mol~(-1)), while that of benzyl alcohol oxidation to benzaldehyde was the lowest(≈ 57 kJ mol~(-1)). Moreover, the activation energy of further oxidation of benzaldehyde in an acetic acid solvent was only slightly lower(≈ 1.9 kJ mol~(-1)) than that of toluene oxidation. Significantly, the transformation of benzyl alcohol indeed contributed to the generation of benzaldehyde and this step conformed to a first-order parallel-consecutive model. Increased reaction temperature and residence time favored the transformation of benzyl alcohol to benzaldehyde. In addition, doping with molybdenum at Mn/Mo = 3/1 enhanced the catalytic performance of the heterogeneous catalyst and was attributed to the presence of a synergetic effect between different metal cations. Regarding the microscopic kinetics, the LH-OS-ND mechanism(Langmuir–Hinshelwood adsorption of reagents on the same type of active sites and non-dissociative adsorption of oxygen) was verified as responsible for the heterogeneous oxidation of toluene. Oxygen and benzaldehyde were weakly adsorbed(Δ H_(ads,Oxy) ≈~(-1)5 kJ mol~(-1), Δ H _(ads)0,Bald) ≈-30 kJ mol~(-1)), but showed strong mobility(Δ S_(ads,Oxy) ≈-22 J mol~(-1) K~(-1)), Δ S_(ads,Bald) ≈-39 J mol~(-1) K~(-1)). The fundamental intrinsic rates were deduced based on the LH-OS-ND mechanism and showed great consistency with the macroscopic results.  相似文献   

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