农田生态系统温室气体排放研究进展

自1985年起,中国科学院大气物理研究所利用自行设计制造的自动观测仪器系统,历时十六年先后对我国四大类主要水稻产区的甲烷排放规律及其与土壤、气象条件和农业管理措施的关系进行了系统野外观测实验,并对稻田甲烷产生、转化和输送机理进行了理论研究,探讨了控制稻田甲烷排放的实用措施,建立了估算和预测稻田甲烷排放的数值模型.在甲烷排放的时空变化规律和转化率研究方面有一系列新的发现,在稻田甲烷产生率、排放率及其与环境条件的关系方面取得一系列新的成果,以充分证据改变了国际上关于全球和中国稻田甲烷排放总量的估算.在对稻田甲     

Studies of Nitrous Oxide Emission from Farmlands in North China

Measurements of nitrous oxide emission from agricultural lands were conducted. The results show that nitrous oxide fluxes on several soils are at the range of 2-60 μg . N / m2 h. Factors influencing the production rates of nitrous oxide from the soils, such as soil temperature, soil moisture and fertilization, are discussed. The calculated amount of nitrous oxide emission from China farmlands is 9.8 × 107 Kg . N per year, which accounts for about 10% of the total source strength in China areas.     

Laboratory study of the rates and products of the phototransformations of naphthalene adsorbed on samples of titanium dioxide,ferric oxide,muscovite, and fly ash

The photodegradation of naphthalene (NPH), chosen as a model of polynuclear aromatic pollutants, has been studied in the presence of a layer of four water-insoluble inorganic solids which can be found in the troposphere (TiO₂, Fe₂O₃, muscovite, and a fly ash sample). Direct photolysis of NPH is negligible at >340 nm. Dark adsorption of NPH on TiO₂ (mainly anatase, nonporous, 50 m² g^–1) at 293 K corresponds to a surface coverage ofca. 50% at equilibrium. Under these conditions (saturated surface), the stationary-state photocatalytic degradation reaches 0.4 molecule nm^–2 h^–1 (>340 nm, radiant fluxca. 22 mW cm^–2). Dioxygen is required and its partial pressure in air is such that the degradation is zero order in O₂. Water vapor markedly increases the rate. The other particulates have also an effect, less important than that of TiO₂, however quite noticeable with respect to surface area unit for the fly ash sample which contains 3.2% Fe₂O₃. Apart from 1,4-naphthoquinone, which is the main intermediate product in all cases, 2-naphthol, phthalide, phthaldialdehyde, phthalic acid, acetophenone, benzaldehyde, benzoic acid are also formed on dry TiO₂. Depending on their volatility, these compounds are transferred to the gas phase or remain principally adsorbed on the solid particles where they are further transformed. For instance, phthalic acid (or anhydride) and benzoic acid are generated from 1,4-naphthoquinone. Degradation mechanisms are briefly discussed.     

Kinetics of redox cycling of iron coupled with fulvic acid

The kinetics of conversion of iron(III) (hydr)oxides to ferrous iron mediated by fulvic acid have been investigated in order to improve the understanding of the redox cycling of iron at the oxic-anoxic boundary in natural waters. Under the conditions similar to natural waters, fulvic acid is able to reduce the iron(III) (hydr)oxide. The kinetics of the reaction depend on the reactivity of iron(III) (hydr)oxides and the reducing power of the fulvic acid. The rate of reaction is 60 nm/h obtained under following conditions: total concentration of Fe(III) 1.0 × 10^–4 M, pH 7.5, fulvic acid 5 mg/L. The rate is considered as a net result of reduction and oxidation in the > Fe^III-OH/Fe(II) wheel coupled with fulvic acid. In a real natural water system, reductants other than fulvic acid may be of importance. The results obtained in the laboratory, however, provide evidence that the Fe(OH)₃(s)/Fe(II) redox couple is able to act as an electron-transfer mediator for the oxidation of natural organic substances, such as fulvic acid by molecular oxygen either in the absence of microorganisms or as a supplement to microbial activity.     

Synthesis of todorokite by refluxing process and its primary characteristics

Todorokite is one of the common manganese ox-ides in manganese ore deposits, weathering product of manganese-bearing rocks, soils and sediments. It is also an important component in the abundant marine manganese nodules. Since todorokite was firstly found in Japanese Todoroki mine in 1934, its properties and origination have appeared to be very interesting to many researchers[1—3]. It has a stable structure similar to porous molecular sieves, constructed of triple MnO6 octahedral chains. Th…     

Preparation of Nano‐Lepidocrocite and an Investigation of Its Ability to Remove a Metal Complex Dye

Lepidocrocite (γ‐FeOOH) nanoparticles were synthesized from iron(II) sulfate solution and characterized using X‐ray diffraction (XRD), transmission electron microscopy (TEM), Fourier transform‐IR (FT‐IR), nitrogen adsorption, and point of zero charge pH (pH_PZC) analyses. TEM, XRD, and FT‐IR analyses proved the synthesis of nano‐lepidocrocite. Surface area and pH_PZC of the synthesized lepidocrocite were 68.1 m² g^?1 and 4.8, respectively. Utilization of the synthesized lepidocrocite in the adsorption of Lanacron brown S‐GL (LBS‐GL) from aqueous solutions was investigated, and the effect of lepidocrocite dosage, pH, temperature, and contact time on this process were optimized and modeled using response surface methodology approach. The lepidocrocite dosage of 0.015 g, pH 3.5, temperature of 38°C, and contact time of 100 min were determined as optimum adsorption conditions. Isotherm and kinetics of the adsorption process were analyzed at the optimum conditions. The equilibrium data were fitted well to the Langmuir isotherm model. The maximum monolayer adsorption capacity was 528.21 mg g^?1. The adsorption process was described by the pseudo‐second‐order kinetic model. Furthermore, the effect of pH on the desorption of LBS‐GL was investigated. High LBS‐GL desorption efficiency was achieved at a high pH value.     

Nitric oxide profiles measured in situ during the Globus '85 campaign

Nitric oxide profiles obtained from three flights of chemiluminescent instruments during the Globus '85 campaign held in France in the autumn of 1985 are reported. When the profile obtained in the early morning of 20 September is compared with the flight made the previous afternoon, an average morning to midday NO ratio of 0.7 for the region between 26 and 33 km is obtained. This value is in good agreement with theoretical studies involving the photolysis of N₂O₅ and the establishment of the NO₂–NO equilibrium.     

第一原理计算过渡金属掺杂尖晶石型LiMn2O4的电子结构

尽管对过渡金属掺杂锰酸锂后放电平台的升高现象有众多实验研究,但对其机理的研究却鲜见报道.采用第一原理的密度泛函理论,计算了过渡金属M(M=Ti、Cr、Fe、Co、Ni、Cu、Zn)掺杂尖晶石型LiMn2O4的电子结构,并以此分析放电平台的升高机理.电子态密度分析发现由于M-3d能带的诱导作用,出现了新的O-2p能带,而锂脱出时获得的电子,主要是由费米能级附近O-2p能带提供的.当过渡金属M由Ti变化到Zn时,M-3d能带逐渐向低能量的方向移动,新的O-2p能带出现的位置也随之下移,当Li脱出时,需要更多的能量才能从低能量的O-2p能带上获得电子,因而体系能够获得较高的嵌入电压.     

山西余吾井田山西组沉积环境演化及聚煤规律

通过对研究区163个钻孔岩心、测井资料以及煤矿开采揭露资料进行解释和对比,同时结合岩石组合、沉积构造、剖面结构、测井相组合以及华北晚古生代早二叠世陆表海盆地地质背景,分析了山西组的岩性组合、展布特征及演化历史。研究认为,山西组底部为陆表海环境,含菱铁质泥岩是有力证据;区内主采3号煤层形成于华北大海退之后废弃的三角洲前缘之上,煤层厚度的变化主要受沉积环境的控制和后期局部冲刷的影响,与基底环境关系不大;井田山西组沉积环境演化及厚煤层展布特征表明华北晚古生代早二叠世为一个稳定的克拉通盆地。     

游离氧化铁形态转化对红粘土工程性质的影响

本文通过模拟环境中的有机质使游离氧化铁形态转化对典型红粘土工程性质的影响试验,系统地测试了游离氧化铁的形态分布与物性指标的关系。试验结果表明,在渍水条件下,游离氧化铁的形态转化对红粘土性质的影响不显著,但在渗水条件下,由于游离氧化铁的流失使得胶结作用减弱,它对红粘土工程性质的影响逐渐明显,其潜在的危害仍然是不容忽视的。