KNO_3在γ-Al_2O_3上分解及表面碱位形成的研究

用浸渍法制备KNO3／Al2O3样品。热重-差热（TG-DTA）结果显示KNO3分解经两个过程，分别对应873K和973K的吸热峰。拉曼光谱显示973K抽空的样品KNO3已完全分解成K2O。微量吸附量热结果表明973K抽空的样品碱性比纯MgO的还强。这种强碱性应为KNO3完全分解成K2O物种所致，而γ-Al2O3载体的存在可增强KNO3的分解。

固体碱催化剂研究进展

综述了固体碱催化剂的研究情况 ,包括固体碱催化剂类型及各种固体碱催化剂碱位的产生及作用机理 。

钴(Ⅱ)席夫碱配合物氧载体性能研究

对三种钻（Ⅱ）席夫碱配合物氧载体进行戴氧性能研究，实验证明它们的载氧性能与批配住碱的性质有关．

KF/Al_2O_3在Michael加成反应中的应用及其机理

综述了KF/Al2O3固体碱催化剂应用于Michael加成反应中,对反应产率和立体构型的影响。论述了该催化剂的表面活性碱位及其在Michael加成反应中的催化机理的研究现状,提出目前普遍认同的几种催化机理,并就此提出自己的观点。

表面、界面的作用与粘接机理(二)

介绍了材料粘接过程界面区的酸碱作用与化学反应对粘接性能的贡献,其内容包括氢键力的作用,酸碱配位作用的考查,酸碱作用对粘接性能的影响和界面化学结合的形成途径及其对粘接性能的影响。

Abnormal Secondary Growth and Histochemical Localization of Alkaloids in Root System of Aconitum flavum Hand.-Mazz.

[Objective] The purpose of this study was to clarify the structure,growth pattern and histochemical localization of alkaloids in root system of Aconitum flavum Hand.-Mazz.[Method] Paraffin sectioning and histochemistry were employed for performing the analysis in this study.[Result] The root system of Aconitum flavum Hand.-Mazz.consists of taproot,lateral root and adventitious root.The primary structure of root system is normal,but secondary structure shows abnormal.The cambium and the extra cambium of taproot form a ＂U＂-shaped secondary vascular bundle and tertiary bundle in abnormal secondary structure.The sieve tube group is made of little sieve tube group which is differentiated from primary phloem and cambium.Meanwhile,the secondary xylem in tuberous root also appears to be a ＂U＂ shape.Parenchyma cells of secondary phloem occupy most of the tuberous root.The sieve tube group of tuberous root is mainly differentiated from parenchyma cell of secondary phloem.[Conclusion] The difference in abnormal secondary structure of taproot and tuberous root are attributed to their varied cambium compose and activity pattern.Alkaloids are mainly accumulated in parenchyma cell of the inside cortex and between bundle in taproot,while parenchyma of secondary phloem and pith in tuberous root.

Effect of solanine on the membrane potential of mitochondria in HepG_2 cells and [Ca^(2+)]i in the cells

AIM： To observe the effect of solanine on the membrane potential of mitochondria in HepG2 cells and [Ca^2＋]i in the cells, and to uncover the mechanism by which solanine induces apoptosis.METHODS： HepG2 cells were double stained with AO/EB, and morphological changes of the cells were observed using laser confocal scanning microscopy （LCSM）. HepG2 cells were stained with TMRE, and change in the membrane potential of mitochondria in the cells were observed using LCSM. HepG2 cells were double stained with Fluo-3/AM, and change of [Ca^2＋]i in the cells were observed using LCSM. HepG2 cells were double stained with TMRE and Fluo-3/AM, and both the change in membrane potential of mitochondria and that of [Ca^2＋]i in the cells were observed using LCSM.RESULTS： Cells in treated groups showed typical signs of apoptosis. Staining with TMRE showed that solanine could lower membrane potential; staining with Fluo-3/AM showed that solanine could increase the concentration of Ca^2＋ in tumor cells; and those of double staining with TMRE and Fluo-3/AM showed that solanine could increase the concentration of Ca^2＋ in the cells at the same time as it lowered the membrane potential of mitochondria.CONCLUSION： Solanine opens up the PT channels in the membrane by lowering the membrane potential, leading to Ca^2＋ being transported down its concentration gradient, which in turn leads to the rise of the concentration of Ca^2＋ in the cell, turning on the mechanism for apoptosis.

Removal of SO_2 and NO_x by Pulsed Corona Combined with in situ Ca(OH)2 Absorption

Removal of SO2 and NOx by pulsed corona combined with in situ alkali absorption was experimentally investigated.In the reactor,a plate-wire-plate combination is devised for generating pulsed corona and then alkaline absorbent slurries were introduced into the reactor by a continuous band conveying system to capture the gaseous reaction products.It was found that both SO2 and NO could be removed by corona combined with in situ alkali absorption.The removal of SO2 increased to 75%with the corona discharge,compared with 60%removal only with Ca(OH)2 absorption.About 40%removal of NO was reached by pulsed corona combined with in situ Ca(OH)2 absorption.It was found that SO2 and NO in the gas stream are oxidized to SO3 and NO2 by pulsed corona respectively,and then absorbed by the alkali in the reactor.The removals of SO2 as well as NO were higher with Ca(OH)2 as the absorbent,compared with using CaCO3 or ZnO.

Iron-incorporated nitrogen-doped carbon materials as oxygen reduction electrocatalysts for zinc-air batteries

The application of electrocatalysts for the oxygen reduction reaction(ORR) is vital in a variety of energy conversion technologies. Exploring low-cost ORR catalysts with high activity and long-term stability is highly desirable, although it still remains challenging. Herein, we report a facile and reliable route to convert ZIF-8 modified by Fe-phenanthroline into Fe-incorporated and N-doped carbon dodecahedron nanoarchitecture(Fe-NCDNA), in which carbon nanosheets are formed in situ as the building blocks with uniform Fe-N-C species decoration. Systematic electrochemical studies demonstrate that the as-synthesized Fe-NCDNA electrocatalyst possesses highly attractive catalytic features toward the ORR in terms of activity and durability in both alkaline and neutral media. The Zn-air battery with the optimal Fe-NCDNA catalyst as the cathode performs impressively, delivering a power density of 184 m W cm^–2 and a specific capacity of 801 m Ah g^–1;thus, it exhibits great competitive advantages over those of the Zn-air devices employing a Pt-based cathode electrocatalyst.

Inhibition effect of a synthesized N,N′-bis(2-hydroxybenzaldehyde)-1,3-propandiimine on corrosion of mild steel in HCl

The corrosion inhibition of mild steel in 1 mol/L HC1 by N, N＇-bis （2-hydroxybenzaldehyde）- 1, 3-propandiimine （2-HBP） has been investigated by using potentiodynamic polarization, electrochemical impedance spectroscopy （EIS） and chronoamperometry measurements. The experimental results suggest that this compound is an excellent corrosion inhibitor for mild steel and the inhibition efficiency increases with the increase in inhibitor concentration. Polarization curves reveal that this organic compound is a mixed type inhibitor. The effect of temperature on the corrosion behavior of mild steel with the addition of the Schiff base was studied in the temperature range from 25 ℃ to 65℃. The experimentally obtained adsorption isotherms follow the Langmuir equation. Activation and thermodynamic adsorption parameters such as Ea, △H, △S,Kads and AG,ds were calculated by the corrosion currents at different temperatures and using the adsorption isotherm. The morphology of mild steel surface in the absence and presence of 2-HBP was examined by atomic force microscope （AFM） images.

Self-assembled three-dimensional carbon networks with accessorial Lewis base sites and variational electron characteristics as efficient oxygen reduction reaction catalysts for alkaline metal-air batteries

Heteroatom-doped carbon has been demonstrated to be one of the most promising non-noble metal catalysts with high catalytic activity and stability through the modification of the electronic and geometric structures.In this study,we develop a novel solvent method to prepare interconnected N,S co-doped three-dimensional（3D）carbon networks with tunable nanopores derived from an asso-ciated complex based on melamine and sodium dodecylbenzene sulfonate（SDBS）.After the intro-duction of silica templates and calcination,the catalyst exhibits 3D networks with interconnected 50-nm pores and partial graphitization.With the increase of the number of Lewis base sites caused by the N doping and change of the carbon charge and spin densities caused by the S doping,the designed N,S co-doped catalyst exhibits a similar electrochemical activity to that of the commercial 20-wt%Pt/C as an oxygen reduction reaction catalyst.In addition,in an aluminum-air battery,the proposed catalyst even outperforms the commercial 5-wt%Pt/C catalyst.Both interconnected porous structures and synergistic effects of N and S contribute to the superior catalytic perfor-mance.This study paves the way for the synthesis of various other N-doped and co-doped carbon materials as efficient catalysts in electrochemical energy applications.

The genetic relationship between Habo alkaline intrusion and its surrounding deposits, Yunnan Province, China: geological and S–Pb isotopic evidences

The Habo alkaline intrusion, which is located in the south of the Sanjiang area, Yunnan Province, China, is a typical Cenozoic alkaline intrusion. There are a series of small to medium-sized Au and Pb-（Zn） deposits around this intrusion. Those deposits are spatially associated with the Habo alkaline intrusion. （1） The δ^34S values of sulfides from Au deposits range from -1.91‰ to 2.69 ‰, which are similar to those of Pb-（Zn） deposits （-3.82 ‰ to -0.05 ‰） and both indicate a much greater contribution from magma. （2） The Habo alkaline intrusion has relatively homogeneous Pb isotopic compositions with ^206pb/^204pb ranging from 18.608 to 18.761, ^207pb/^204pb from 15.572 to 15.722 and ^20spb/^204pb from 38.599 to 39.110. These Pb isotope ratios are similar to those of Au deposits, whose ^206pb/^204pb range from 18.564 to 18.734, ^20Tpb/^20apb from 15.582 to 15.738 and ^208pb/^204pb from 38.592 to 39.319. Pb ratios in both the intrusion and Au deposits suggest that Pb mainly derived from the depth, probably represents a mixture of mantle and crust. Pb-（Zn） deposits, however, show a decentralized trait, and most of them are similar to that of the alkaline intrusion with ^206pb/^204pb ranging from 18.523 to 18.648, ^207pb/^204pb from 15.599 to 15.802, and ^20spb/^204pb from 38.659 to 39.206. （3） In the plumbotectonic diagram ^20Tpb/^204pb versus ^206pb/^204pb, almost all of Au and Pb-（Zn） deposits have the same projection area with the Habo alkaline intrusion, which indicates that those deposits almost share the same source with the alkaline intrusion. （4） Isotopic age of the Habo alkaline intrusion is 36-33 Ma, which is similar to that of Beiya, whose ore- related alkaline porphyries age is 38-31 Ma and molybdenite Re-Os age is 36.9 Ma. Therefore, along with S-Pb isotope traits, we suggest that the Habo Au and Pb-（Zn） deposits should be typically Ailaoshan-Red RiverCenozoicalkaline-related deposits and ore-forming ages of these deposits should be later than that of the Habo alkaline intrusion.

Effect of Schiff base as corrosion inhibitor on AZ31 magnesium alloy in hydrochloric acid solution

Schiff base derived from the condensation reaction of analar grade 1-amino-2-naphthol 4-sulphonic acid with cinnamaldehyde was prepared under microwave condition.The Schiff base was analysed by infrared spectroscopy.This Schiff base as a corrosion inhibitor of AZ31 magnesium alloy in 0.05 mol/L HCl solution was studied.The inhibition effect of the Schifif base compound（4Z）-4-（3-phenyl allylidene amino）-3-hydroxy naphthalene-1-sulfonic acid（AC） on AZ31 magnesium alloy corrosion was studied using mass loss,potentiodynamic polarization technique,electrochemical impedance spectroscopy methods.The potentiodynamic polarization curve shows that Schiff base AC inhibits both anodic and cathodic reactions at all concentration,which indicates it is a mixed type inhibitor.EIS results indicate that as the additive concentration is increased,the polarization resistance increases whereas double-layer capacitance decreases.The adsorption of AC on the AZ31 magnesium alloy surface in 0.05 mol/L HCl obeys the Langmuir adsorption isotherm.

Synthesis of thiadiazole-based Schiff base metal complexes and their inhibition rate to superoxide anion free radical

A new series of Schiff base ligands were synthesized by the condensation of 2-amino-5-mercaptan-l,3,4-thiadiazole and salicylaldehyde or 2,4-dihydroxybenzaldehyde and their derivatives with choroacetic acid, and further reaction with corresponding metal acetate to form metal complexes. The compositions and structures of the ligands and their complexes were characterized by elemental analysis, molar conductivities, electronic absorption spectra and infra-red spectra. Their inhibition rates to free radical, such as O2, were also tested. The results show that all of the obtained complexes display significant activities, among which the copper（Ⅱ） complexes have the best inhibitive effects.

Histochemical localization and characterization of AKP,ACP,NSE,and POD from cultured Apostichopus japonicus

We investigated the distribution of four enzymes involved in the immune response of Apostichopus japonicus. We collected samples of the tentacles, papillate podium, integument, respiratory tree, and digestive tract and stained them for acid phosphatase （ACP）, alkaline phosphatase （AKP）, non-specific esterase （NSE） and peroxidase （POD） activity. The distribution and content of ACE AKP, NSE, and POD differed among the tissues. The coelomic epithelium of the tentacle, papillate podium, and integument and the mucous layer of respiratory tree were positive for ACP activity. The coelomic epithelium and cuticular layer of the tentacle, papillate podium, and integument and the mucous layer and tunica externa of the respiratory tree and digestive tract stained positive or weakly positive for AKP activity. Almost all the epithelial tissues stained positive, strongly positive, or very strongly positive for NSE activity. The cuticular layer of the tentacle and integument and the mucous layer, tunica submucosa, and tunica externa of the respiratory tree and digestive tract stained positive for POD activity. We hypothesize that these enzymes play a role in the immune response in A. japonicus.

In Situ Synchrotron X-ray Diffraction Studies of Single-walled Carbon Nanotubes for Electric Double-layer Capacitors

In situ synchrotron X-ray diffraction experiments of SWCNT （single-walled carbon nanotube） electrode in alkali halide aqueous electrolyte at several applied potentials were performed, and the change in the diffraction pattern of SWCNTs was observed. It was found that the position of the 100 diffraction peak does not change with applied potential while the peak intensity decreases with anion adsorption. It was concluded that the space inside the tube would be the important ion adsorption site for the well-gown SWCNT bundles.

铈基固溶体上CO_2和甲醇直接合成碳酸二甲酯

以柠檬酸为络合剂,制备掺杂不同金属的铈基固溶体。XRD表征表明成功合成了铈基固溶体。甲醇和二氧化碳直接合成碳酸二甲酯活性测试结果表明,掺杂镧的固溶体具有较好的活性,加入锌的固溶体活性最差。对掺杂不同金属的铈基固溶体的NH_3-TPD和CO_2-TPD表征表明,中强酸碱位和强酸碱位是催化剂的活性中心。具有较多中强酸碱位和强酸碱位的铈镧固溶体表现出最好的活性。

The electrochemical stability of ionic liquids and deep eutectic solvents

Room temperature ionic liquids （ILs） composed of cations and anions, as well as deep eutectic solvents （DESs） composed of hydrogen bond donors （HBDs） and hydrogen bond acceptors （HBAs）, are regarded as green solvents due to their low volatility. They have been used widely for electrochemically driven reactions because they exhibit high conductivity and excellent elec- trochemical stability. However, no systematic investigations on the electrochemical potential windows （EPWs）, which could be used to characterize the electrochemical stability, have been reported. In this regard, the EPWs of 33 ILs and 23 DESs have been studied utilizing cyclic voltammetry （CV） method and the effects of structural factors （cations and anions of ILs, and HBDs and HBAs of DESs） and external factors （electrode, water content） on the EPWs have been comprehensively investi- gated. The electrochemical stability of selected 1Ls comprising five traditional cations, namely imidazolium, pyridinium, pyr- rolidinium, piperidinium and ammonium and 13 kinds of versatile anions was studied. The results show that for ILs, both cati- on and anion play an important role on the reductive and oxidative potential limit. For a same IL at different working electrode, for example, glassy carbon （GC）, gold （Au） and platinum （Pt） electrode, the largest potential window is almost observed on the GC working electrode. The investigations on the EPWs of choline chloride （ChCl）, choline bromide （ChBr）, choline iodide （ChI）, and methyl urea based DESs show that the DES composed of ChCl and methyl urea has the largest potential window. This work may aid the selection of ILs or DESs for use as a direct electrolyte or a solvent in electrochemical applications.

Synthesis of ultrathin Co2AlO4 nanosheets with oxygen vacancies for enhanced electrocatalytic oxygen evolution

In this work, we reported the synthesis of twodimensional spinel structure of ultrathin Co2AlO4 nanosheets via dealloying and subsequent annealing processes. Oxygen vacancy defects were further introduced into Co2AlO4 nanosheets by a mild solvothermal reduction method, resulting in large electrochemical surface area and high active site densities, making the related Co atoms get electrons, and producing more empty orbitals. The positive charge of Co and Al atoms adjacent to the O vacancies in VO-rich Co2AlO4 reduced significantly, that is, more electrons are concentrated on the Co and Al atoms. Those electrons closed to the Fermi level have a promoting effect during the H2O activation. As a result, the obtained ultrathin Co2AlO4 nanosheets with oxygen vacancies show a low overpotential of 280 m V at the current density of 10 mA cm^-2 and a small Tafel slope of70.98 m V dec^-1. Moreover, it also displays a remarkable stability in alkaline solution, which is superior to most of the reported Co3O4 electrocatalysts. The present work paves a new way to achieve efficient new energetic materials for sustainable community.

Highly efficient oxygen evolution and stable water splitting by coupling NiFe LDH with metal phosphides

It is a great challenge to develop highly active oxygen evolution reaction(OER)electrocatalysts with superior durability.In this study,a NiFe layered double hydroxidedecorated phosphide(NiFe LDH@CoP/NiP_(3))was constructed to display satisfactory OER activity and good stability for water splitting in alkaline media.At an overpotential of 300 mV,NiFe LDH@CoP/NiP_(3) achieved a current density of 82 mA cm^(-2) for the OER,which was 9.1 and 2.3 times that of CoP/NiP_(3) and NiFe LDH,respectively.Moreover,the reconstruction behavior,during which oxyhydroxides formed,was studied by a combination of X-ray photoelectron spectroscopy,Raman spectroscopy,and scanning electron microscopy.A synergistic effect between NiFe LDH and CoP/NiP_(3) was also observed for the hydrogen evolution reaction.Furthermore,when NiFe LDH@CoP/NiP_(3) acted as both the cathode and anode for overall water splitting,a high current density of 100 mA cm^(-2) was maintained for more than 275 h.In addition,under Xe light irradiation,a solar-to-hydrogen efficiency of 9.89% was achieved for solar-driven water splitting.This work presents the coupling of different active compositions,and can provide a reference for designing bifunctional electrocatalysts.