类风湿性关节炎患者氧化还原物水平的测定

目的通过检测类风湿性关节炎(RA)患者体内氧化还原物水平,探讨氧化还原物水平与类风湿性关节炎发生、发展的关系。方法选择83例RA患者,采用高效液相色谱电化学法检测其血浆总抗坏血酸(TAA)、脱氢抗坏血酸/总抗坏血酸(DHAA/TAA)、维生素E、晚期蛋白质氧化产物(AOPP)、血浆丙二醛(MDA)等氧化还原指标;对RA患者血浆AOPP、MDA及高敏C-反应蛋白(hs-CRP)做相关分析,并以30名健康人作为对照进行统计分析。结果RA患者血浆MDA、AOPP及DHAA/TAA水平显著高于正常人(P<0.05),AOPP增高则极为显著(P<0.01);维生素E与正常人无显著差异(P>0.05)。RA患者MDA与hs-CRP明显相关(P<0.01),AOPP与hs-CRP则无相关性(P>0.05)。结论RA患者体内氧化还原水平明显升高,是RA病程发展的重要机制;AOPP、MDA两项指标可反映RA患者体内的高氧化水平。

Environmental Stresses and Redox Status of Ascorbate

To investigate the effects of environmental stresses on ascorbic acid content and its redox status, the effects of freezing and drought on ascorbate and dehydro-ascorbate content and activities of four enzymes involved in the ascorbate-glutathione cycle in some conifers were studied. The results showed that both freezing and drought induced the decrease in ascorbate content and the increase in dehydro-ascorbate content. The activities of ascorbate peroxidase (APX) and monodehydro-ascorbate reductase (MDAR) were decreased by freezing stress. At the beginning of exposure to air, water loss from detached needles induced the increase in the activities of APX and MDAR. Further water loss turned to decrease the APX and MDAR activities. The activities of dehydro-ascorbate reductase (DHAR) and glutathione reductase (GR) were not sensitive to changes in temperature and water content of the needles. It is concluded that moderate temperature or water stresses may induce the acclimation and increase in the ability of the H2O2 scavenging system, while strong stresses decrease the ability and induce injury of plant tissues. Correlation between ascorbate content and activities of related enzymes and cold tolerance of conifers were also reported.

Catalytic reduction of SO_2 by CO over CeO_2-TiO_2 mixed oxides

The structure and catalytic desulfurization characteristics of CeO2-TiO2 mixed oxides were investigated by means ofX-ray diffraction （XRD）, X-ray photoelectron spectroscopy （XPS） and catalytic activity tests. According to the results, a CeO2-TiO2solid solution is formed when the mole ratio of cerium to titanium n（Ce）：n（Ti） is 5：5 or greater, and the most suitable n（Ce）：n（Ti） isdetermined as 7：3, over which the conversion rate of SO2 and the yield of sulfur at 500℃ reach 93% and 99%, respectively.According to the activity testing curve, Ce0.7Ti0.3O2 （n（Ce）：n（Ti）=7：3） without any pretreatment can be gradually activated by reagentgas after about 10 min, and reaches a steady activation status 60 min later. The XPS results of Ce0.7Ti0.3O2 after different time ofSO2＋CO reaction show that CeO2 is the active component that offers the redox couple Ce4＋/Ce3＋ and the labile oxygen vacancies, andTiO2 only functions as a catalyst structure stabilizer during the catalytic reaction process. After 48 h of catalytic reaction at 500℃,Ce0.7Ti0.3O2 still maintains a stable structure without being vulcanized, demonstrating its good anti-sulfur poisoning performance.

Comparative Studies on Degradation of Methyl Orange by Nanostructured Zinc and Zinc Oxide Films

Nanostructured zinc and zinc oxide films were prepared by magnetron sputtering processes and succeeded air annealing treatments. Comparison of reductive degradation rate of methyl orange （MO） by zinc films and photocatalytic degradation rate of MO by zinc oxide films was carried out. Both reductive degradation and photocatalytic degradation process of MO by zinc and zinc oxide films can be described by first order kinetic model. It was found that although MO liquid was most quickly decolorized by metallic zinc films, the mineraliza- tion of MO was not thorough. Observation of extra ultraviolet absorption peaks indicated the formation of aromatic intermediates. On the other hand, although the photocatalytic degradation rate of MO liquid by ZnO films was only as about 1/4 large as the reductive degradation rate by zinc films, no signs of aromatic intermediates were found. Moreover, it was found that partially oxidized zinc oxide film showed higher photocatalytic efficiency than the totally oxidized ZnO films. Synergy effect between zinc and zinc oxide phase in the partially oxidized films was considered to be responsible for the higher photocatalytic efficiency.

Carbon monoxide oxidation on copper manganese oxides prepared by selective etching with ammonia

A series of copper manganese oxides were prepared using a selective etching technique with various amounts of ammonia added during the co-precipitation process. The effect of the ammonia etching on the structure and catalytic properties of the copper manganese oxides was investigated using elemental analysis, nitrogen physisorption, X-ray powder diffraction, scanning and transmission electron microscopy, X-ray photoelectron spectroscopy, H2 temperature-programmed reduc- tion, and Oz temperature-programmed desorption combined with catalytic oxidation of CO. It was found that ammonia can selectively remove copper species from the copper manganese oxides, which correspondingly generates more defects in these oxides. An oxygen spillover from the man- ganese to the copper species was observed by H2 temperature-programmed desorption, indicating that ammonia etching enhanced the mobility of lattice oxygen species in these oxides. The Oz tem- perature-programmed desorption measurements further revealed that ammonia etching improved the ability of these oxides to release lattice oxygen. The improvement in redox properties of the copper manganese oxides following ammonia etching was associated with enhanced catalytic performance for CO oxidation.

4-Desoxypicropodophyllin and 4’-Demethyl-4-desoxypicropodophyllin Obtained from System (CH_3)_3SiCl/NaI/MeCN

文献报道鬼臼脂素在 (CH3)3SiCl/Nal/MeCN 反应体系中得到氧化产物4-去氧-C环芳构化鬼臼脂素。而本文作者采用a-不饱和苦鬼臼脂素在同样的反应体系中却得到了部分还原产物C环氧化鬼臼脂素。根据鬼臼脂素和苦鬼臼脂素的结构差异,作者对发生这一现象的原因进行了报道和分析。

Synthesis of a chabazite-supported copper catalyst with full mesopores for selective catalytic reduction of nitrogen oxides at low temperature

A series of meso‐microporous copper‐supporting chabazite molecular sieve（CuSAPO‐34） catalysts with excellent performance in low‐temperature ammonia selective catalytic reduction（NH3‐SCR）have been synthesized via a one‐pot hydrothermal crystallization method. The physicochemical properties of the catalysts were characterized by scanning electron microscopy, transmission electron microscopy, N2 adsorption‐desorption measurements, X‐ray diffraction, 27 Al magic angle spinning nuclear magnetic resonance, diffuse reflectance ultraviolet‐visible spectroscopy, inductively coupled plasma‐atomic emission spectroscopy, X‐ray photoelectron spectroscopy, temperature‐programmed reduction measurements, and electron paramagnetic resonance analysis. The formation of micro‐mesopores in the Cu‐SAPO‐34 catalysts decreases diffusion resistance and greatly improves the accessibility of reactants to catalytic active sites. The main active sites for NH3‐SCR reaction are the isolated Cu^2＋ species displaced into the ellipsoidal cavity of the Cu‐SAPO‐34 catalysts.

Promotional effects of Zr on K^+-poisoning resistance of CeTiO_x catalyst for selective catalytic reductionof NO_x with NH_3

CeTiOx and CeZrTiOx catalysts were prepared by a coprecipitation method and used for selective catalytic reduction of NOx by NH3 （NH3‐SCR）. Various amounts of KNO3 were impregnated on the catalyst surface to investigate the effects of Zr addition on the K＋‐poisoning resistance of the CeTiOx catalyst. The NH3‐SCR performance of the catalysts showed that the NOx removal activity of the Zr‐modified catalyst after poisoning was better than that of the CeTiOx catalyst. Brunau‐er‐Emmett‐Teller data indicated that the Zr‐containing catalyst had a larger specific surface area and pore volume both before and after K＋poisoning. X‐ray diffraction, Raman spectroscopy, and transmission electron microscopy showed that Zr doping inhibited anatase TiO2 crystal grain growth, i.e., the molten salt flux effect caused by the loaded KNO3 was inhibited. The Ce 3d X‐ray photoelectron spectra showed that the Ce3＋/Ce4＋ratio of CeZrTiOx decreased more slowly than that of CeTiOx with increasing K＋loading, indicating that Zr addition preserved more crystal defects and oxygen vacancies; this improved the catalytic performance. The acidity was a key factor in the NH3‐SCR performance; the temperature‐programmed desorption of NH3 results showed that Zr doping inhibited the decrease in the surface acidity. The results suggest that Zr improved the K＋‐poisoning resistance of the CeTiOx catalyst.

Gold stabilized on various oxide supports catalyzing formaldehyde oxidation at room temperature

Gold stabilized on reducible oxide （CeO2 and FeOx） and irreducible oxide （γ‐Al2O3, SiO2, and HZSM‐5） were prepared by deposition precipitation method and tested for catalytic oxidation of formaldehyde （HCHO） at room temperature under high GHSV of 600000 ml/（g＆#183;s）. Au/γ‐Al2O3 cata‐lyst showed distinctive catalytic performance, presenting the highest initial HCHO conversion and stability. Correlating the reaction rate with Au particle size, there is a linear relationship, suggesting that the smaller Au particle size with higher dispersion possesses high reactivity for HCHO oxida‐tion. All the catalysts deactivated at high GHSV （600000 ml/（g＆#183;s））, but in a quite different rate. Re‐ducible oxide （CeO2 and FeOx） could stabilize gold through O linkage and therefore exhibits a better stability for HCHO oxidation reaction. However, the aggregation of gold particles occurred over Au/SiO2 and Au/HZSM‐5 catalysts, which result in the fast deactivation. Therefore, our results sug‐gest that the reducibility of the supports for Au catalysis has no direct influence on the activity, but affects the catalytic stability.

Octahedral Cu_2O-modified TiO_2 nanotube arrays for efficient photocatalytic reduction of CO_2

A photocatalyst composed of TiO 2 nanotube arrays（TNTs） and octahedral Cu2 O nanoparticles was fabricated,and its performance in the photocatalytic reduction of CO2 under visible and simulated solar irradiation was studied. The average nanotube diameter and length was 100 nm and 5 μm,respectively. The different amount of octahedral Cu2 O modified TNTs were obtained by varying electrochemical deposition time. TNTs modified with an optimized amount of Cu2 O nanoparticles exhibited high efficiency in the photocatalysis,and the predominant hydrocarbon product was methane. The methane yield increased with increasing Cu2 O content of the catalyst up to a certain deposition time,and decreased with further increase in Cu2 O deposition time. Insufficient deposition time（5 min） resulted in a small amount of Cu2 O nanoparticles on the TNTs,leading to the disadvantage of harvesting light. However,excess deposition time（45 min） gave rise to entire TNT surface being most covered with Cu2 O nanoparticles with large sizes,inconvenient for the transport of photo-generated carriers. The highest methane yield under simulated solar and visible light irradiation was observed for the catalysts prepared at a Cu2 O deposition time of 15 and 30 min respectively. The morphology,crystallization,photoresponse and electrochemical properties of the catalyst were characterized to understand the mechanism of its high photocatalytic activity. The TNT structure provided abundant active sites for the adsorption of reactants,and promoted the transport of photogenerated carriers that improved charge separation. Modifying the TNTs with octahedral Cu2 O nanoparticles promoted light absorption,and prevented the hydrocarbon product from oxidation. These factors provided the Cu2O-modified TNT photocatalyst with high efficiency in the reduction of CO2,without requiring co-catalysts or sacrificial agents.

Phosphorus in Interstitial Water Induced by Redox Potential in Sediment of Dianchi Lake,China

The sediment redox potential was raised in the laboratory to estimate reduction of internal available phosphorus loads,such as soluble reactive phosphorus(SRP)and total phosphorus(TP),as well as the main elements of sediment extracts in Dianchi Lake.Several strongly reducing substances in sediments,which mainly originated from anaerobic decomposition of primary producer residues,were responsible for the lower redox potential.In a range of -400 to 200 mV raising the redox potential of sediments decreased TP and SRP in interstitial water.Redox potentials exceeding 320 mV caused increases in TP,whereas SRP maintained a relatively constant minimum level.The concentrations of Al,Fe, Ca^(2+),Mg^(2+),K^+,Na^+ and S in interstitial water were also related to the redox potential of sediments,suggesting that the mechanism for redox potential to regulate the concentration of phosphorus in interstitial water was complex.

Promotional effects of Er incorporation in CeO_2(ZrO_2)/TiO_2 for selective catalytic reduction of NO by NH_3

A series CeO2（ZrO2）/TiO2 catalysts were modified with Er using a sol-gel method.The catalytic activity of the obtained catalysts in the selective catalytic reduction（SCR） of NO with NH3 was investigated to determine the appropriate Er dosage.The catalysts were characterized using X-ray diffraction,N2 adsorption,NH3 temperature-programmed desorption,H2 temperature-programmed reduction,photoluminescence spectroscopy,electron paramagnetic resonance spectroscopy,and X-ray photoelectron spectroscopy.The results showed that the optimum Er/Ce molar ratio was 0.10;this catalyst had excellent resistance to catalyst poisoning caused by vapor and sulfur and gave more than 90% NO conversion at 220–395 ℃ and a gas hourly space velocity of 71 400 h^-1.Er incorporation increased the Ti^3＋ concentrations,oxygen storage capacities,and oxygen vacancy concentrations of the catalysts,resulting in excellent catalytic performance.Er incorporation also decreased the acid strength and inhibited growth of TiO2 and CeO2 crystal particles,which increased the catalytic activity.The results show that high oxygen vacancy concentrations and oxygen storage capacities,large amounts of Ti^3＋,and low acid strengths give excellent SCR activity.

A review on TiO_2-based Z-scheme photocatalysts

TiO2‐based Z‐scheme photocatalysts have attracted considerable attention because of the low recombination rate of their photogenerated electron–hole pairs and their high photocatalytic efficiency.In this review,the reaction mechanism of Z‐scheme photocatalysts,recent research progress in the application of TiO2‐based Z‐scheme photocatalysts,and improved methods for photocatalytic performance enhancement are explored.Their applications,including water splitting,CO2reduction,decomposition of volatile organic compounds,and degradation of organic pollutants,are also described.The main factors affecting the photocatalytic performance of TiO2‐based Z‐scheme photocatalysts,such as pH,conductive medium,cocatalyst,architecture,and mass ratio,are discussed.Concluding remarks are presented,and some suggestions for the future development of TiO2‐based Z‐scheme photocatalysts are highlighted.

Preparation of low-oxygen-containing Ti-48Al-2Cr-2Nb alloy powder by direct reduction of oxides

A high-purity Ti-48Al-2Nb-2Cr alloy powder with an oxygen content as low as 0.0572 wt.%and a particle size of<150μm was produced from a mixture of TiO_(2),Al_(2)O_(3),Nb_(2)O_(5),and Cr_(2)O_(3)powders through reduction with magnesium and deoxidation with calcium.The phase and composition of the products were analyzed.The final product mainly includedγ-TiAl and minorα_(2)-Ti_(3)Al phases,and Ti,Al,Cr,and Nb were homogenously distributed in the powder with a mole ratio of 49.73:43.51:2.05:1.98.The reduction and deoxidation mechanisms were investigated by thermodynamic modeling using the HSC Chemistry software and Pandat software based on the Ti alloy database.

Land Management Effects on Biogeochemical Functioning of Salt-Affected Paddy Soils

Most lowlands in Northeast Thailand(Isaan region)are cultivated with rice and large areas are affected by salinity, which drastically limits rice production.A field experiment was conducted during the 2003 rainy season to explore the interactions between salinity and land management in two fields representative of two farming practices:an intensively managed plot with organic inputs and efficient water management,and one without organic matter addition.Field measurements,including pH,Eh,electrical conductivity(EC),and soil solution chemistry,were performed at three depths, with a particular focus on Fe dynamics,inside and outside saline patches. High reducing conditions appeared after flooding particularly in plots receiving organic matter and reduction processes leading to oxide reduction and to the release of Fe and,to a lesser extend,Mn to the soil solution.Oxide reduction led to the consumption of H^+ and the more the Fe reduction was,the higher the pH was,up to 6.5.Formation of hydroxy-green rust were likely to be at the origin of the pH stabilization.In the absence of organic amendments,high salinity prevented the establishment of the reduction processes and pH value remained around 4.Even under high reduction conditions,the Fe concentrations in the soil solution were below commonly observed toxic values and the amended plot had better rice production yield.

Effects of surface physicochemical properties on NH_3-SCR activity of MnO_2 catalysts with different crystal structures

α‐,β‐,δ‐,andγ‐MnO2nanocrystals are successfully prepared.We then evaluated the NH3selective catalytic reduction(SCR)performance of the MnO2catalysts with different phases.The NOx conversion efficiency decreased in the order:γ‐MnO2>α‐MnO2>δ‐MnO2>β‐MnO2.The NOx conversion with the use ofγ‐MnO2andα‐MnO2catalysts reached90%in the temperature range of140–200°C,while that based onβ‐MnO2reached only40%at200°C.Theγ‐MnO2andα‐MnO2nanowire crystal morphologies enabled good dispersion of the catalysts and resulted in a relatively high specific surface area.We found thatγ‐MnO2andα‐MnO2possessed stronger reducing abilities and more and stronger acidic sites than the other catalysts.In addition,more chemisorbed oxygen existed on the surface of theγ‐MnO2andα‐MnO2catalysts.Theγ‐MnO2andα‐MnO2catalysts showed excellent performance in the low‐temperature SCR of NO to N2with NH3.

Kinetic Model and Simulation of Promoted Selective Non-catalytic Reduction by Sodium Carbonate

Abstract The detailed kinetic model of selective non-catalytic reduction （SNCR） of nitric oxide, including so-dium species reactions, was deyeloped on the basis of recent studies on thermal DeNOx mechanism, NOxOUTmechanism and promotion mechanism of Na2CO3. The model was validated by comparison with several experi-mental findings, thus providing an effective tool for the primary and promoted SNCR process simulation. Experimental and simulated results show part-per-million level of sodium carbonate enhances NO removal efficiency andextend the effective SNCR temperature range in comparison with use of a nitrogen agent alone. The kinetic modeling, sensitivity and rate-of-production analysis suggest that the performance improvement can be explained as ho-mogeneous sodium species reactions producing more reactive OH radicals. The net result of sodium species reac-tions is conversion of H2O and inactive HO2 radicals into reactive OH radicals, i.e. H2O＋HO2=3OH, which enhances the SNCR performance of nitrogen agents by mainly increasing the production rate of NH2 radicals. More-over, N2O and CO are eliminated diversely via the reactions Na＋N20=NaO＋N2, NaO＋CO=Na＋CO2 andNaO2＋CO =NaO＋CO2, in.the pro.moted SNCR process, especially in the NOxOUT process.

A review of the interactions between ceria and H2 and the applications to selective hydrogenation of alkynes

Cerium oxide(ceria) has found a wide variety of applications in catalysis including as a catalyst, a modifier, or a support, largely thanks to its robust redox properties and versatile acid-base function. While it is often utilized for oxidation reactions, ceria has recently attracted intense research interest for its unusual ability to selectively hydrogenate alkynes to alkenes. The intriguing hydrogenation ability of ceria has sparked renewed research efforts to understand how pure ceria works as a hydrogenation catalyst. In this review, recent advances in both experimental and computational studies of ceria are summarized, focusing on the interaction of ceria with H2 and in hydrogenation reactions. Significant insights from various studies including in situ spectroscopy/microscopy and theoretic modeling of ceria in hydrogen-involved reactions are discussed, which shed light on the origin of the hydrogenation ability of ceria and the reaction mechanisms involved in ceria-catalyzed alkyne hydrogenation. Ways to further improve both the mechanistic understanding and catalytic performance of ceria-based materials for hydrogenation reactions are proposed at the end in the summary and outlook section.

Characterization of Gleyization of Paddy Soils in the Middle Reaches of the Yangtze River

The gleyisation of representative paddy soils in the middle reaches of the Yangtze caver was characterized,taking oxidation-reduction potential(Eh),the amount of active reducing substances and the forms of iron and manganese as the parameters.The Eh value was linearly related with the logarithm of the amount of active reducing substances, which was contributed by ferrous iron by 83% on an avers.The degree of gleyization of dament horizons was graded as ungleyed,slightly gleyed,mildly gleyed and gleyed.The Eh of the four grades was>500,300-500,100-300 and<100 mV,respectively, and the corresponding amoks of active reducing substances was<1,1-7,7-30 and>30 mmol.kg(-1),respectively.The amount of ferrous iron of the four grades was<0.5,0.5-5,5-25 and > 25 mmol kg-1,respectively.The extent of gleyisation of a soil was classified as upper-gleyed, middle-gleyed and lower-gleyed, depending on whether the depth of the gley horbon was less than 30 cm,30-60 cm or more than 60 cm.

Efficient photoelectrocatalytic CO_2 reduction by cobalt complexes at silicon electrode

Two homogeneous photoelectrocatalytic systems composed of simple polypyridyl Co complexes[Co(tpy)2](PF6)2and[Co(bpy)3](PF6)2as electrocatalysts and a Si wafer as the photoelectrode were used for combined photoelectrochemical reduction of CO2to CO.A high photocurrent density of1.4mA/cm2was observed for the system with the[Co(tpy)2](PF6)2catalyst and a photovoltage of400mV was generated.Faradaic efficiencies of CO were optimized to83%and94%for the[Co(tpy)2](PF6)2and[Co(bpy)3](PF6)2complexes,respectively,in acetonitrile solution with10%methanol(volume fraction,same below)as a protic additive.Addition of2%water volume fraction induced a large amount of non‐specific H2evolution by the Si photoelectrode.