黔桂喀斯特区域河流水体离子对底栖硅藻群落的影响

为了建立喀斯特地区河流底栖硅藻对水环境变化的响应模型,定量研究了中国西南喀斯特地区黔桂珠江水系典型岩溶水体中的离子、电导率与底栖硅藻群落分布的关系.研究发现,电导率的范围为20～2070μS.cm-1,并且Ca2+与(HCO3-+CO32-)是岩溶水体的主要优势离子.对离子、电导率与硅藻群落结构进行主成分分析(PCA)、对应分析(CA)、加权平均分析(WA)和相关性分析,结果表明,水体离子(HCO3-+CO32-、SO42-、NO3-、Cl-、Ca2+、Na+、Mg2+、K+)与电导率环境变量都能用于解释底栖硅藻的群落分布特征;而Ca2+、(HCO3-+CO32-)和Na+浓度是影响物种组成的显著因素.通过研究确定了以上8种水体离子和电导率的相应指示种值(最适值Optima),以及这些离子环境下的硅藻分布特征.该结果为中国西南喀斯特地区硅藻种群生态学、个体生态学以及水质评价的研究提供了理论依据.

广东车八岭国家级自然保护区空气负离子水平及其主要影响因子

空气负离子(Negative air ion,NAI)是综合反映空气质量的重要指标,对人类的生活环境具有重大意义。该研究选定广东车八岭国家级自然保护区内10个典型观测点,在5月份(夏季)和10月份(秋季)进行NAI观测。结果表明:保护区内NAI浓度较高,均高于700个·cm^(-3);各观测点的NAI浓度基本呈现水体>森林>草坪>楼内的规律;秋季10个观测点的NAI浓度从高到低依次为博物馆旁河中央、漂流起点、小瀑布口、小瀑布支柱、针阔混交林、针叶林、博物馆前草坪、单竹坑、吊桥、办公楼内;观测点漂流起点、小瀑布口、小瀑布支柱、博物馆旁河中央的NAI水平与单竹坑、吊桥、博物馆前草坪、办公楼内、针阔混交林、针叶林均有显著差异。夏季各观测点的NAI浓度从高到低依次为小瀑布口、博物馆旁河中央、小瀑布支柱、漂流起点、针阔混交林、针叶林、单竹坑、博物馆前草坪、吊桥、办公楼内,其中观测点漂流起点、小瀑布口、小瀑布支柱、博物馆旁河中央显著高于其它地点,观测点针阔混交林、针叶林显著高于单竹坑、吊桥、博物馆前草坪、办公楼内,观测点办公楼内显著低于其他点。区内NAI浓度受到季节、水体、植被类型等因子的影响。

Structure and corrosion resistance of modified micro-arc oxidation coating on AZ31B magnesium alloy

A hydrophobic surface was fabricated on a micro-arc oxidation (MAO) treated AZ31 Mg alloys via surface modification with myristic acid. The effects of modification time on the wettability of the coatings were investigated using the contact angle measuring device. The surface morphologies and structure of the coatings were evaluated using SEM, XRD and FT-IR. The corrosion resistance was investigated by potentiodynamic polarization curves and long-term immersion test. The results showed that the water contact angle (CA) increases gradually with modification time from 0 to 5 h, the highest CA reaches 138° after being modified for 5 h, and the number and size of the micro pores are decreased. The modification method hardly alters crystalline structure of the MAO coating, but improves the corrosion resistance based on the much positive potential and low current density. Moreover, the corrosion resistance and hydrophobicity can be enhanced with increasing the alkyl chain. The wetting and spreading for the alkylcarboxylate with low surface energy become easier on the micro-porous surface, and alkylcarboxylate monolayer will be formed through bidentate bonding, which changes the surface micropores to a sealing or semi-sealing structure and makes the MAO coating dense and hydrophobic. All the results demonstrate that the modification process improves the corrosion protection ability of the MAO coating on AZ31B Mg alloy.

Solvatochromic Parameters and Preferential Solvation Behavior for Binary Mixtures of 1,3-Dialkylimidazolium Ionic Liquids with Water

Binary mixtures of 1,3-dialkylimidazolium based ionic liquids （ILs） and water were selected as solvent systems to investigate the solute-solvent and solvent-solvent interactions on the preferential solvation of solvatochromic indicators at 25 ℃. Empirical solvatochromic pa- rameters, dipolarity/polarizability （π^＊）, hydrogen-bond donor acidity （α）, hydrogen-bond acceptor basicity （β）, and Reichardt＇s polarity parameters （ET^N） were measured from the ultraviolet-visible spectral shifts of 4-nitroaniline, 4-nitroanisole, and Reichardt＇s dye. The solvent properties of the IL-water mixtures were found to be influenced by IL type and IL mole fraction （XIL）. All these studied systems showed the non-ideal behavior. The max- imum deviation to ideality for the solvatochromic parameters can be obtained in the XIL range from 0.i to 0.3. For most of the binary mixtures, the π^＊ values showed the synergistic effects instead of the ETN, α and β values. The observed synergy extent was dependent on the studied systems, such as the dye indicator and IL type. A preferential solvation model was utilized to gather information on the molecular interactions in the mixtures. The dye indicator was preferentially solvated on the following trend： IL〉IL-water complex〉water.

Mechanism of Reverse Snapback on I-V Characteristics of Power SITHs with Buried Gate Structure

The reverse snapback phenomena （RSP） on I-V characteristics of static induction thyristors （SITH） are physically researched. The I-V curves of the power SITH exhibit reverse snapback phenomena, and even turn to the conducting-state,when the anode voltage in the forward blocking-state is increased to a critical value. The RSP I-V characteristics of the power SITH are analyzed in terms of operating mechanism, double carrier injection effect, space charge effect, electron-hole plasma in the channel, and the variation in carrier lifetime. The reverse snapback mechanism is theoretically pro- posed and the mathematical expressions to calculate the voltage and current values at the snapback point are presented. The computing results are compared with the experiment values.

Ternary System of Fe-based Ionic Liquid,Ethanol and Water for Wet Flue Gas Desulfurization

Fe-based ionic liquid （Fe-IL） was synthesized by mixing FeCl3·6H2O and 1-butyl-3-methylimidazolium chloride [Bmim]C1 in this paper. The phase diagram of a ternary Fe-IL, ethanol and water system was investigated to construct a ternary desulfurization solution for wet flue gas desulfurization. The effects of flow rate and concentration of SO2, reaction temperature, pH and Fe-IL fraction in aqueous desulfurization solution on the desulfiariza- tion efficiency were investigated. The results shows that the best composition of ternary desulfurization solution of Fe-IL, ethanol and water is 1 ： 1.5 ： 3 by volume ratio, and pH should be controlled at 2.0. Under such conditions, a desulfurization rate greater than 90% could be obtained. The product of sulfuric acid had inhibition effect on the wet desulfurization process. With applying this new ternary desulfurization solution, not only the catalyst Fe-IL can be recycled and reused, but also the product sulfuric acid can be separated directly from the ternary desulfurization system.

基于CDs@MIL-101-NH_(2)复合材料的水体铅离子荧光检测方法及效果分析

为探究CDs@MIL-101-NH_(2)对铅离子的荧光法检测性能及荧光淬灭机理,采用水热法制备了碳点(N,S,I-CDs)修饰MIL-101-NH_(2)(Fe)的复合材料,使用TEM、XRD、FT-IR、XPS对复合材料进行了表征。结果表明:采用水热法成功构建了CDs@MIL-101-NH_(2)复合材料,碳点的引入未对MIL-101-NH_(2)结构造成很大影响,且氨基修饰于MOF框架上;CDs@MIL-101-NH_(2)复合材料在激发波长为340 nm、发射波长为436 nm、材料的质量浓度为10 mg·L^(−1)、pH为7的条件下具有最佳荧光强度;CDs@MIL-101-NH_(2)荧光探针可对水体铅离子做出荧光响应,有较好的选择性,在1.22~500μmol·L^(−1)内具有良好的拟合度(R2=0.9988),检出限为1.22μmol·L^(−1);荧光探针与铅离子结合后发生荧光淬灭现象,可能是由于复合材料上的氨基与铅离子发生相互作用引起的,且荧光碳点修饰提高了MIL-101-NH_(2)检测水体铅离子的性能;在实际水样的铅离子检测中,样品回收率为97.24%~106.16%,相对标准偏差RSD<4%,说明这一新型的CDs@MIL-101-NH_(2)复合材料可用于荧光法检测水体中的铅离子。本研究结果可为灵敏高效的荧光探针的设计与制备提供一种新思路,亦可为便捷的原位检测铅离子荧光方法的进一步开发和应用提供参考。

An Efficient and Stable Ionic Liquid System for Synthesis of Ethylene Glycol via Hydrolysis of Ethylene Carbonate

An ionic liquid system of [Bmim]X/[Bmim]OH(X Cl,BF4,and PF6,) was developed for the hydroly-sis of ethylene carbonate to ethylene glycol. The important parameters,such as the variety of ionic liquids,molar ratio of [Bmim]X to [Bmim]OH,amount of ionic liquid,molar ratio of water to ethylene carbonate,reaction tem-perature,pressure and reaction time,were investigated systematically. Excellent yield(>93%) and high selectivity(99.5%) of ethylene glycol were achieved. Under the optimum reaction conditions,the ionic liquid system could be reused at least five times and the selectivity of ethylene glycol remained higher than 99.5%.

Plasmonic Field Enhancement for Vibration Spectroscopy at Metal/Water Interfaces

Electrochemical （EC） reactions play vital roles in many disciplines, and its molecular-level understanding is highly desired, in particular under reactions. The vibration spectroscopy is a powerful in situ technique for chemical analysis, yet its application to EC reactions is hindered by the strong attenuation of infrared （IR） light in both electrodes and electrolytes. Here we demonstrate that by incorporating appropriate sub-wavelength plasmonic structures at the metal electrode, the IR field at the EC interface can be greatly enhanced via the excitation of surface plasmon. This scheme facilitates in situ vibrational spectroscopic studies, especially using the surface-specific sum-frequency generation technique.

Effect of Mono- and Di-ethanolammonium Formate Ionic Liquids on the Volatility of Water, Ethanol, and Methanol

Vapor pressures were measured for six binary systems containing water, ethanol, or methanol with one of the two ionic liquids(ILs) at different component concentrations and temperatures using a quasi-static ebulliometer,with the ILs mono-ethanolammonium formate([HMEA][HCOO]) and di-ethanolammonium formate([HDEA][HCOO]).The vapor pressures of the IL-containing binary systems are well correlated using the NRTL model with an overall average absolute relative deviation(AARD) of 0.0062. The effect of ILs on the vapor pressure depression of solvents at 0.050 mole fraction of IL is that [HDEA][HCOO]>[HMEA][HCOO], and the vapor pressure lowering degree follows the order of water>methanol>ethanol. Further, the activity coefficients of three solvents(viz. water,ethanol, and methanol) for the binary systems {solvent(1) + IL(2)} predicted based on the fitted NRTL parameters at T 333.15 K indicate that the two ILs generate a negative deviation from Raoult's law for water and methanol and a positive deviation for ethanol to a varying degree, change the relative volatility of a solvent. [HMEA][HCOO]may be a promising entrainer to efficiently separate ethanol aqueous solutions by special rectification.

Interfacial engineering of heterogeneous molecular electrocatalysts using ionic liquids towards efficient hydrogen peroxide production

Efficient and selective oxygen reduction reaction(ORR)electrocatalysts are critical to realizing decentralized H_(2)O_(2)production and utilization.Here we demonstrate a facile interfacial engineering strategy using a hydrophobic ionic liquid(IL,i.e.,[BMIM][NTF2])to boost the performance of a nitrogen coordinated single atom cobalt catalyst(i.e.),cobalt phthalocyanine(CoPc)supported on carbon nanotubes(CNTs).We find a strong correlation between the ORR performance of CoPc/CNT and the thickness of its IL coatings.Detailed characterization revealed that a higher O_(2)solubility(2.12×10^(−3)mol/L)in the IL compared to aqueous electrolytes provides a local O2 enriched surface layer near active catalytic sites,enhancing the ORR thermodynamics.Further,the hydrophobic IL can efficiently repel the as‐synthesized H_(2)O_(2)molecules from the catalyst surface,preventing their fast decomposition to H_(2)O,resulting in improved H_(2)O_(2)selectivity.Compared to CoPc/CNT without IL coatings,the catalyst with an optimal~8 nm IL coating can deliver a nearly 4 times higher mass specific kinetic current density and 12.5%higher H2O2 selectivity up to 92%.In a two‐electrode electrolyzer test,the optimal catalyst exhibits an enhanced productivity of 3.71 molH2O2 gcat^(–1)h^(–1),and robust stability.This IL‐based interfacial engineering strategy may also be extended to many other electrochemical reactions by carefully tailoring the thickness and hydrophobicity of IL coatings.

Upland rice and lowland rice exhibited different P/P expression under water deficit and ABA treatment

Aquaporins play a significant role in plant water relations. To further understand the aquaporin function in plants under water stress, the expression of a subgroup of aquaporins, plasma membrane intrinsic proteins （PIPs）, was studied at both the protein and mRNA level in upland rice （Oryza sativa L. cv. Zhonghan 3） and lowland rice （Oryza sativa L. cv. Xiushui 63） when they were water stressed by treatment with 20% polyethylene glycol （PEG）. Plants responded differently to 20% PEG treatment. Leaf water content of upland rice leaves was reduced rapidly. PIP protein level increased markedly in roots of both types, but only in leaves of upland rice after 10 h of PEG treatment. At the mRNA level, OsPIP1,2, OsPIP1,3, OsPIP2;1 and OsPIP2;5 in roots as well as OsPIP1,2 and OsPIP1;3 in leaves were significantly up-regulated in upland rice, whereas the corresponding genes remained unchanged or down-regulated in lowland rice. Meanwhile, we observed a significant increase in the endogenous abscisic acid （ABA） level in upland rice but not in lowland rice under water deficit. Treatment with 60 μM ABA enhanced the expression of OsPIP1;2, OsPIP2;5 and OsPIP2;6 in roots and OsPIP1;2, OsPIP2;4 and OsPIP2;6 in leaves of upland rice. The responsiveness of PIP genes to water stress and ABA were different, implying that the regulation of PIP genes involves both ABA-dependent and ABA-independent signaling oathways during water deficit.

Rational design of stratified material with spatially separated catalytic sites as an efficient overall water-splitting photocatalyst

The development of metal sulfide catalysts with remarkable activity toward efficient overall photocatalytic water splitting remains challenging owing to the dominant charge recombination and deficient catalytic active sites.Moreover,in the process of water oxidation catalysis,the inhibition of severe photocorrosion is an immense task,requiring effective photogenic hole-transfer kinetics.Herein,stratified Co-MnO_(2)@CdS/CoS hollow cubes with spatially separated catalytic sites were rationally designed and fabricated as highly efficient controllable catalysts for photocatalytic overall water splitting.The unique self-templated method,including a continuous anion/cation-exchange reaction,integrates a Co-doped oxidation co-catalyst(Co-MnO_(2))and a reduction co-catalyst(CoS)on the nanocubes with uniform interface contact and ultrathin two-dimensional(2D)nanometer sheets.We demonstrate that the stratified Co-MnO_(2)@CdS/CoS hollow cubes can provide an abundance of active sites for surface redox reactions and contribute to the separation and migration of the photoionization charge carriers.In particular,CoS nanoparticles dispersed on the walls of CdS hollow cubes were identified as reduction co-catalysts accelerating hydrogen generation,while Co-MnO_(2) nanosheets attached to the inner walls of the CdS hollow cube were oxidation co-catalysts,promoting oxygen evolution dynamics.Benefiting from the desirable structural and compositional advantages,optimized stratification of Co-MnO_(2)@CdS/CoS nanocubes provided a catalytic system devoid of precious metals,which exhibited a remarkable overall photocatalytic water-splitting rate(735.4(H_(2))and 361.1(O_(2))μmol h^(−1) g^(−1)),being among the highest values reported thus far for CdS-based catalysts.Moreover,an apparent quantum efficiency(AQE)of 1.32%was achieved for hydrogen evolution at 420 nm.This study emphasizes the importance of rational design on the structure and composition of photocatalysts for overall water splitting.

Influence of Nonionic Surfactant Addition on Drag Reduction of Water Based Nanofluid in a Small Diameter Pipe

The goal of this research was to determine the impact of nonionic surfactants on drag reduction effect in water and metal oxide nanofluid. Two nonionic surfactants （Rokacet 07 and Rokanol KT） and copper（II） oxide wa- ter-based nanofluid were examined. Friction factors in a 4 mm diameter pipe for the Reynolds number between 8000 and 50000 were determined. Results showed that addition of nonionic surfactants caused the decrease of fric- tion factor in water and nanofluid. The drag reduction effect was similar in both cases. Presence of nanoparticles in the system has no great influence on drag reduction effect.

Probing Molecular Interactions in 1-Butyl-3-methylimidazolium Chloride-Water and 2,6-Dimethoxyphenol Mixtures Using Attenuated Total Reflection Infrared Spectroscopy

Molecular interactions of the ternary mixtures of 1-butyl-3-methylimidazolium chloride （[C4C1im]Cl）-water-2,6-dimethoxyphenol （2,6-DMP, a phenolic monomer lignin model compound） were investigated in comparison with the [C4C1im]Cl-water binary systems through attenuated total reflection infrared spectroscopy. Results indicated that the microstructures of water and [C4C1im]Cl changed with varying mole fraction of [C4C1im]Cl （xIL） from 0.01 to 1.0. This change was mainly attributed to the interactions of [C4C1im]Cl-water and the self-aggregation of [C4C1im]Cl through hydrogen bonding. The band shifts of C-H on imidazolium ring and the functional groups in 2,6-DMP indicated that the occurrence of intermolecular interactions by different mechanisms （i.e., hydrogen bonding or π-π stacking） resulted in 2,6-DMP dissolution. In the case of xIL=0.12, the slightly hydrogen-bonded water was fully destroyed and [C4C1im]Cl existed in the form of hydrated ion pairs. Interestingly, the maximum 2,6-DMP solubility （238.5 g/100 g） was achieved in this case. The interactions and microstructures of [C4C1im]Cl-water mixtures influenced the dissolution behavior of 2,6-DMP.

Composite Cathode based on Mn-doped Perovskite Niobate-Titanate for Efficient Steam Electrolysis

Redox-active Mn is introduced into the B site of redox-stable perovskite niobate-titanate to improve the electrocatalytic activity of composite cathode in an oxide-ion-conducting solid oxide electrolyzer. The XRD and XPS results reveal the successful partial replacement of Ti/Nb by Mn in the B site of niobate-titanate. The ionic conductivities of the Mndoped niobate-titanate are significantly improved by approximately 1 order of magnitude in reducing atmosphere and 0.5 order of magnitude in oxidizing atmosphere compared with bare niobate-titanate at 800 ℃. The current efficiency for Mn-doped niobate-titanate cathode is accordingly enhanced by ,-25% and 30% in contrast to the bare cathode with and without reducing gas flowing over the cathode under the applied voltage of 2.0 V at 800 ℃ in an oxide-ion-conducting solid oxide electrolyzer, respectively.

Adsorption of Heavy Metal Ions by Adsorbent from Waste Mycelium Chitin

The adsorption properties of chitin adsorbent from mycelium of fermentation industries for the removal of heavy metal ions were studied. The result shows that the chitin adsorbent has high adsorption capacity for many heavy metal ions and Ni2+ in citric acid. The influence of pH was significant:When pH is higher than 4.0, the high adsorption capacity is obtained,otherwise H+ ion inhibits the adsorption of heavy metal ions. The comparison of the chitin adsorbent with some other commercial adsorbents was made, in which that the adsorption behaviorchitin adsorbent is close to that of commercial cation exchange adsorbents, and its cost is much lower than those commercial adsorbents.

Atmospheric-pressure Air Plasma Treatment of Polyester Fabrics for Inkjet Printing with Pigment Inks

Without any preprocessing,polyester fabric has lower ability to hold on water and inks due to the smooth morphology of polyester fibers. Therefore, patterns directly printed with pigment inks have poor color yields and bleed easily. Pretreatments of polyester fabric were carried out with atmospheric air plasma under different experimental conditions. After plasma treatment the samples were printed with magenta pigment ink. Scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS) analyses indicated that the enhanced color performance was mainly contributed by not only the etching effect but also oxygen-containing polar groups induced onto fiber surfaces through plasma treatment. Thereby the surface modification of polyester fabrics using atmospheric-pressure air plasma offers a potential way to fabric pretreatment for pigment inkjet printing with the advantages of environmental friendly and energy saving over traditional pretreatment methods.

Effects of Different Organic Residues on Rice Yield and Soil Quality

Calcaric regosols are a valuable land resource, distributed widely across western China. Soil quality has deteriorated considerably in recent years owing to the blind pursuit of economic benefits. A 2-year field experiment was carried out to evaluate the effects of using spent mushroom compost, leguminous plant (Vicia sepium L.) compost, and a combination of the two (at a 1:1 and 2:1 ratio), on rice yield and soil quality in a suburb of China. Vicia sepium L. composted with spent mushroom compost at a 1:1 ratio produced the highest grain and stover yield, grain and stover phosphorus concentration, and phosphorus uptake of rice; they were 56.5%, 93.2%, 89.3%, 198.6% and 22.2% greater than control soil, respectively. The 2:1 ratio (Vicia sepium L.: spent mushroom compost) produced the highest grain N concentration, stover N concentration, and N uptake; they were 31.6%, 31.4%, and 40.7% higher than control, respectively. Soil physical, chemical, and environmental properties were improved with the application of Vicia sepium L. composted with spent mushroom compost at a 2:1 ratio. In particular, soil water-stable aggregates, organic carbon, particulate organic carbon, total nitrogen, available potassium, and cation exchange capacity increased, whereas bulk density, pH, and phytoavailable heavy metals decreased. This organic treatment is beneficial to improve soil quality indicators, and contribute to soil restoration.

Parameterizations of different hydrometeor spectral relative dispersion in the convective clouds

Spectral relative dispersion of different hydrometeors is vital to accurately describe sedimentation.Here,the Weather Research and Forecasting model with spectral bin microphysics is used to simulate convective clouds in Shouxian of Anhui province in China to study the spectral relative dispersion of different hydrometeors.Firstly,regardless of clean or polluted conditions,the relative dispersion of ice crystal spectra and its volume-mean diameter are negatively correlated,while the relative dispersion of other hydrometeor spectra is positively related to their respective volume-mean diameter.The correlations for cloud droplets and raindrops are affected by the process of collision-coalescence;the correlations for ice crystals,graupel particles,and snow particles could be affected by the deposition,riming,and aggregation processes,respectively.Secondly,relative dispersion parameterizations are developed based on a comprehensive consideration of the relationships between the relative dispersion and volume-mean diameter under both polluted and clean conditions.Finally,the relative dispersion parameterizations are applied to terminal velocity parameterizations.The results show that for cloud droplets,ice crystals,graupel particles,and snow particles,assuming the shape parameter in the Gamma distribution is equal to 0 underestimates the shape parameter and overestimates the relative dispersion;and for raindrops,assuming the shape parameter is equal to 0 is close to the relative dispersion parameterizations.The most appropriate constant shape parameters are recommended for different hydrometeors.The relative dispersion parameterizations developed here shed new light for further optimizing the terminal velocity parameterizations in models.