共查询到20条相似文献，搜索用时 718 毫秒
1.
Geometry and vibrational frequencies of the ground state of Si2O2 molecule are studied using density function theory (DFT) at the level of cc-pvtz and 6-311++G**. It is found that the optimizing value by B3lyp/cc-pvtz is closer to the experimental data. The excited properties under different external electric fields are also investigated by the time-dependent-DFT method. Transitions from the ground state of Si2O2 molecule to the first singlet state under different external electric fields can take place more easily. The corresponding absorption spectral line is about 360 nm in wavelength and the excitation energy is about 3.4 eV. 相似文献
2.
3.
This paper evaluates the simultaneous measurement of dissolved gases (CO2 and O2/Ar ratios) by membrane inlet mass spectrometry (MIMS) along the 180° meridian in the Southern Ocean. The calibration of pCO2 measurements by MIMS is reported for the first time using two independent methods of temperature correction. Multiple calibrations and method comparison exercises conducted in the Southern Ocean between New Zealand and the Ross Sea showed that the MIMS method provides pCO2 measurements that are consistent with those obtained by standard techniques (i.e. headspace equilibrator equipped with a Li–Cor NDIR analyser). The overall MIMS accuracy compared to Li–Cor measurements was 0.8 μatm. The O2/Ar ratio measurements were calibrated with air-equilibrated seawater standards stored at constant temperature (0 ± 1 °C). The reproducibility of the O2/Ar standards was better than 0.07% during the 9 days of transect between New Zealand and the Ross Sea.The high frequency, real-time measurements of dissolved gases with MIMS revealed significant small-scale heterogeneity in the distribution of pCO2 and biologically-induced O2 supersaturation (ΔO2/Ar). North of 65°S several prominent thermal fronts influenced CO2 concentrations, with biological factors also contributing to local variability. In contrast, the spatial variation of pCO2 in the Ross Sea gyre was almost entirely attributed to the biological utilization of CO2, with only small temperature effects. This high productivity region showed a strong inverse relationship between pCO2 and biologically-induced O2 disequilibria (r2 = 0.93). The daily sea air CO2 flux ranged from − 0.2 mmol/m2 in the Northern Sub-Antarctic Front to − 6.4 mmol/m2 on the Ross Sea shelves where the maximum CO2 influx reached values up to − 13.9 mmol/m2. This suggests that the Southern Ocean water (south of 58°S) acts as a seasonal sink for atmospheric CO2 at the time of our field study. 相似文献
4.
The TiO2--Mn--TiO2 multilayers are successfully grown on glass and silicon substrates by alternately using radio frequency reactive magnetron sputtering and direct current magnetron sputtering. The structures and the magnetic behaviours of these films are characterised with x-ray diffraction, transmission electron microscope (TEM), vibrating sample magnetometer, and superconducting quantum interference device (SQUID). It is shown that the multi-film consists of a mixture of anatase and rutile TiO2 with an embedded Mn nano-film. It is found that there are two turning points from ferromagnetic phase to antiferromagnetic phase. One is at 42 K attributed to interface coupling between ferromagnetic Mn3O4 and antiferromagnetic Mn2O3, and the other is at 97 K owing to the interface coupling between ferromagnetic Mn and antiferromagnetic MnO. The samples are shown to have ferromagnetic behaviours at room temperature from hysteresis in the M--H loops, and their ferromagnetism is found to vary with the thickness of Mn nano-film. Moreover, the Mn nano-film has a critical thickness of about 18.5 nm, which makes the coercivity of the multi-film reach a maximum of about 3.965times 10 - 2 T. 相似文献
5.
采用化学沉淀法成功制备了Cu2+/SnO2复合纳米光催化剂,采用XRD、SEM等测试手段对复合纳米光催化剂的粒径、形态等进行表征。在紫外光条件下,分别改变催化剂掺杂比、催化剂煅烧温度、催化剂投加量、柴油初始含量和光照时间等单因素,探究不同条件对Cu2+/SnO2复合纳米光催化剂降解海洋柴油污染物的影响。结果表明,自制复合纳米光催化剂可以有效降解海水中的柴油污染物,在紫外光作用下,于400℃下煅烧Cu/Sn掺杂比为0. 03的Cu2+/SnO2复合纳米光催化剂、投加量为0. 2 g/dm3、柴油初始含量为0. 15 g/dm3、H2O2溶液含量为0. 2 g/dm3、溶液的p H为7、光照时间3 h时效果最好,海水中柴油的去除率最高,达到86. 98%。Cu2+/SnO2复合纳米光催化剂用聚丙烯纳米球负载后可以实际应用于海洋中,便于回收。 相似文献
6.
生物固氮作用是一个重要的海洋新氮来源，在海洋生物地球化学循环中扮演着不可替代的角色。基于稳定同位素（15N2）示踪吸收法，是目前直接测定海洋生物固氮速率最有效的手段。其中，高效、洁净地将15N2引入海水培养体系，并准确定量培养体系底物的同位素示踪水平，是同位素示踪吸收法准确获取固氮速率的关键。本研究针对15N2同位素示踪剂引入这一关键环节进行了探讨，确认改进气泡法是将15N2引入海水培养体系的首选操作。在对培养体系造成的较小扰动的情况下，可将培养体系氮气底物的15N原子丰度提升至10%以上，相对于另一种导入同位素示踪剂的手段——预溶解海水法，改进气泡法将培养瓶中氮气底物的15N原子丰度提升了近200%。此外，改进气泡法还具有最小化痕量金属沾污、操作简便等优点。将改进气泡法结合与稳定同位素比值质谱测定结合，是准确测定水体生物固氮速率的推荐方法。 相似文献
7.
8.
CO2升高和阳光紫外辐射对坛紫菜生长和光合特性的耦合效应 总被引：1，自引：0，他引：1
大气CO2持续升高,导致溶入海水中的CO2增多,海水表层的H+浓度增加,从而引起海洋酸化。为了探讨近岸定生大型海藻对这种环境变化的响应,本文选择经济海藻坛紫菜为实验材料,研究海洋酸化与紫外辐射对藻体生长以及光合特性的影响。实验分两个CO2处理,分别为正常空气水平(390 ppmv)和高CO2水平(800 ppmv); 三种辐射处理,分别为全波长辐射(PAB)、滤除紫外线B(PA)和仅接受可见光处理(PAR)。研究结果表明,CO2培养下的坛紫菜,在仅有可见光(P)或者同时有紫外线A(PA)存在的情况下,显著促进藻体的生长;但在全波长辐射处理下(PAB),这种作用不明显。高CO2降低了藻体在P和PA处理下的光合作用速率,但对PAB处理作用不显著。高CO2处理下的藻体,UV-B显著降低了全波长辐射下藻体紫外吸收物质的含量,但在正常CO2水平下,紫外辐射的作用不显著。这表明高CO2导致的生长优势被紫外辐射的负面效应所抵消,在全球变化的过程中,紫外辐射的进一步加强在海洋酸化的背景下甚至有可能降低坛紫菜的产量。 相似文献
9.
10.
《Journal of Sea Research》2004,51(1):3-10
Hydrogen peroxide (H2O2) was measured in marine surface waters of the eastern Atlantic Ocean between 25°N and 25°S. H2O2 concentrations decreased from 80 nM in the north to 20 nM in the south, in agreement with earlier observations. A diel cycle of H2O2 production as a function of sunlight in surface waters was followed twice whilst the ship steamed southward. Around 23°N a distinct diel cycle could be measured which correlated well with irradiance conditions.The wavelength dependency of H2O2 formation was studied near the equator. For 16 hours, water samples were incubated with wavelength bands of the solar spectrum, i.e. visible (VIS: 400–700 nm), VIS and ultraviolet A radiation (UVAR: 320–400 nm) and VIS, UVAR and ultraviolet B radiation (UVBR: 280–320 nm). A significant relationship was found between wavelength band and the production of H2O2. In addition, a clear positive relationship between intensity and production was found. UVAR was 6.5 times more efficient than VIS in producing 1 nM of H2O2, whereas UVBR was 228 times more efficient than VIS. When these data were weighted with respect to the energy of the solar spectrum at zenith hour, 28% of the H2O2 was formed by VIS, 23% was formed by UVAR and 48% was formed by UVBR. Considering the strong attenuation of UVBR in marine waters as compared with UVAR and VIS radiation, the role of UVAR deeper in the water column is recognised. Furthermore results of this research emphasise the importance of VIS radiation in the formation of H2O2. 相似文献
11.
Photorefractive properties of Hf:Fe:LiNbO3 crystals with various [Li]/[Nb] ratios have been investigated at 488 nm wavelength based on the two-wave coupling experiment. High diffraction efficiency and large recording sensitivity are observed and explained. The decrease in Li vacancies is suggested to be the main contributor to the increase in the photoconductivity and subsequently to the induction of the improvement of recording sensitivity. The saturation diffraction efficiency is measured up to 80.2%, and simultaneously the recording sensitivity of 0.91 cm/J is achieved to in the Hf:Fe:LiNbO3 crystal grown from the melt with the [Li]/[Nb] ratio of 1.20, which is significantly enhanced as compared with those of the Hf:Fe:LiNbO3 crystal with the [Li]/[Nb] ratio of 0.94 in melt under the same experimental conditions. Experimental results definitely show that increasing the [Li]/[Nb] ratio in crystal is an effective method for Hf:Fe:LiNbO3 crystal to improve its photorefractive properties. 相似文献
12.
In this work, the influence of a small-molecule material, tris(8-hydroxyquinoline) aluminum (Alq3), on bulk heterojunction (BHJ) polymer solar cells (PSCs) is investigated in devices based on the blend of poly(2-methoxy-5-(2-ethylhexyloxy)-1,4-phenylenevinylene) (MEH-PPV) and [6,6]-phenyl-C61-butyric acid methyl ester (PCBM). By doping Alq3 into MEH-PPV:PCBM solution, the number of MEH-PPV excitons can be effectively increased due to the energy transfer from Alq3 to MEH-PPV, which probably induces the increase of photocurrent generated by excitons dissociation. However, the low carrier mobility of Alq3 is detrimental to the efficient charge transport, thereby blocking the charge collection by the respective electrodes. The balance between photon absorption and charge transport in the active layer plays a key role in the performance of PSCs. For the case of 5 wt.% Alq3 doping, the device performance is deteriorated rather than improved as compared with that of the undoped device. On the other hand, we adopt Alq3 as a buffer layer instead of commonly used LiF. All the photovoltaic parameters are improved, yielding an 80% increase in power conversion efficiency (PCE) at the optimum thickness (1 nm) as compared with that of the device without any buffer layer. Even for the 5 wt.% Alq3 doped device, the PCE has a slight enhancement compared with that of the standard device after modification with 1 nm (or 2 nm) thermally evaporated Alq3. The performance deterioration of Alq3-doped devices can be explained by the low solubility of Alq3, which probably deteriorates the bicontinuous D-A network morphology; while the performance improvement of the devices with Alq_3 as a buffer layer is attributed to the increased light harvesting, as well as blocking the hole leakage from MEH-PPV to the aluminum (Al) electrode due to the lower highest occupied molecular orbital (HOMO) level of Alq3 compared with that of MEH-PPV. 相似文献
13.
本实验以新月菱形藻为受试生物,研究了低浓度不同粒径TiO2颗粒(21nm、60nm和400nm)对海洋微藻生长、抗氧化酶活性(超氧化物歧化酶SOD、过氧化氢酶CAT和过氧化物酶POD)、脂质过氧化产物(MDA)含量的影响,并测定了相应的活性氧自由基(ROS)的含量,初步探讨了TiO2颗粒对海洋微藻的作用机制。结果表明,1mg/L TiO2颗粒对新月菱形藻生长的抑制作用随着粒径的减小而逐渐增强,第48h、72h、96h呈现出显著的纳米效应。TiO2颗粒可以诱导藻细胞内ROS的含量增加,对藻细胞产生氧化胁迫,新月菱形藻的抗氧化酶活性发生应激响应,以清除过量的ROS,但剩余的ROS对藻细胞产生氧化损伤,导致MDA含量升高,并且纳米级TiO2颗粒对新月菱形藻的氧化损伤大于微米级颗粒。在不同粒径TiO2颗粒的胁迫下,藻细胞SOD和CAT活性的响应也存在差异。本研究将为开展人工纳米材料对海洋生态系统影响的潜在风险评估提供科学依据。 相似文献
14.
The generalised gradient approximation based on density functional theory is used to study the structural and electronic properties of the endohedral fullerene dimer (N2@C60)2. Four N atoms sit at the cage centres in the form of two N_2 molecules. The density of states and Mulliken charge analysis explore that the energy levels from -6 to -10 eV are mainly influenced by the N2 molecules. 相似文献
15.
The mechanisms regulating N2O production in an estuarine sediment (Tama Estuary, Japan) were studied by comparing the change in N2O production with those in nitrification and denitrification using an experimental continuous-flow sediment–water system with15N tracer (15N-NO−3 addition). From Feburary to May, both nitrification and denitrification in the sediment increased (246 to 716 μmol N m−2 h−1and 214 to 1260 μmol N m−2 h−1, respectively), while benthic N2O evolution decreased slightly (1560 to 1250 nmol N m−2 h−1). Apparent diffusion coefficients of inorganic nitrogen compounds and O2at the sediment–water interface, calculated from the respective concentration gradients and benthic fluxes, were close to the molecular diffusion coefficients (0·68–2·0 times) in February. However, they increased to 8·8–52 times in May except for that of NO−2, suggesting that the enhanced NO−3 and O2supply from the overlying water by benthic irrigation likely stimulated nitrification and denitrification. Since the progress of anoxic condition by the rise of temperature from February to May (9 to 16 °C) presumably accelerated N2O production through nitrification, the observed decrease in sedimentary N2O production seems to be attributed to the decrease in N2O production/occurrence of its consumption by denitrification. In addition to the activities of both nitrification and denitrification, the change in N2O metabolism during denitrification by the balance between total demand of the electron acceptor and supply of NO−3+NO−2 can be an important factor regulating N2O production in nearshore sediments. 相似文献
16.
An improved model is presented for the calculation of the solubility of carbon dioxide in aqueous solutions containing Na+, K+, Ca2+, Mg2+, Cl−, and SO42− in a wide temperature–pressure–ionic strength range (from 273 to 533 K, from 0 to 2000 bar, and from 0 to 4.5 molality of salts) with experimental accuracy. The improvements over the previous model [Duan, Z. and Sun, R., 2003. An improved model calculating CO2 solubility in pure water and aqueous NaCl solutions from 273 to 533K and from 0 to 2000 bar. Chemical Geology, 193: 257–271] include: (1) By developing a non-iterative equation to replace the original equation of state in the calculation of CO2 fugacity coefficients, the new model is at least twenty times computationally faster and can be easily adapted to numerical reaction-flow simulator for such applications as CO2 sequestration and (2) By fitting to the new solubility data, the new model improved the accuracy below 288 K from 6% to about 3% of uncertainty but still retains the high accuracy of the original model above 288 K. We comprehensively evaluate all experimental CO2 solubility data. Compared with these data, this model not only reproduces all the reliable data used for the parameterization but also predicts the data that were not used in the parameterization. In order to facilitate the application to CO2 sequestration, we also predicted CO2 solubility in seawater at two-phase coexistence (vapor–liquid or liquid–liquid) and at three-phase coexistence (CO2 hydrate–liquid water–vapor CO2 [or liquid CO2]). The improved model is programmed and can be downloaded from the website http://www.geochem-model.org/programs.htm. 相似文献
17.
浒苔对NH+4-N与NO-3-N吸收的相互作用 总被引：1，自引：0，他引：1
在国内首次研究了大型海洋绿潮藻浒苔(Ulva prolifera)对NH4+-N与NO 3--N两种氮源的选择吸收作用。结果表明:当两种氮源等浓度比例存在时,随着NH4+-N与NO3--N浓度升高,藻体对NH4+-N的吸收速率逐渐升高,而对NO3--N吸收受到抑制;当NO3--N和NH 4+-N高浓度比存在时,藻体对NH4-N的吸收速率随着NO3--N/NH4+-N比例的升高和NH4-N浓度的下降而降低;当NO3--N和NH4+-N低浓度比存在时,藻体对NH+4-N保持较高的吸收速率,而对NO3--N的吸收效率随着NO3--N浓度的降低而降低;浒苔具有同时利用水体中较高浓度的NH+4-N和NO3--N的能力,只有当NH4+-N或NO3--N浓度较低时,才以吸收相对应的氮源为主。这说明浒苔能够快速、大量地吸收水体中氮源,为爆发性增殖贮备物质条件。同时,即便两种氮源同时存在,浒苔对NH+4-N的吸收速率也远高于对NO3--N的吸收速率,因此,控制NH4+-N的大量输入仍是预防浒苔绿潮爆发的关键。 相似文献
18.
The exploitation of different plant materials for the biosynthesis of nanoparticles is considered a green technology because it does not involve any harmful chemicals. In this study, iron oxide nanoparticles (Fe3O4-NPs) were synthesized using a completely green biosynthetic method by reduction of ferric chloride solution using brown seaweed water extracts. The two seaweeds Padina pavonica (Linnaeus) Thivy and Sargassum acinarium (Linnaeus) Setchell 1933 were used in this study. The algae extract was used as a reductant of FeCl3 resulting in the phytosynthesis of Fe3O4-NPs. The phytogenic Fe3O4-NPs were characterized by surface plasmon band observed close to 402 nm and 415 nm; the obtained Fe3O4-NPs are in the particle sizes ranged from 10 to 19.5 nm and 21.6 to 27.4 nm for P. pavonica and S. acinarium, respectively. The strong signals of iron were reported in their corresponding EDX spectra. FTIR analyses revealed that sulphated polysaccharides are the main biomolecules in the algae extracts that do dual function of reducing the FeCl3 and stabilizing the phytogenic Fe3O4-NPs. The biosynthesized Fe3O4-NPs were entrapped in calcium alginates beads and used in Pb adsorption experiments. The biosynthesized Fe3O4-NPs alginate beads via P. pavonica (Linnaeus) Thivy had high capacity for bioremoval of Pb (91%) while that of S. acinarium (Linnaeus) Setchell 1933 had a capacity of (78%) after 75 min. The values of the process parameters for the maximum Pb removal efficiency by Fe3O4-NPs alginate beads synthesized via P. pavonica (Linnaeus) Thivy were also estimated. 相似文献
19.
过氧化氢(H2O2)等活性氧(ROS)物质因具有绿色高效的特点,在废水处理、杀菌消毒等领域受到研究者广泛关注。利用电催化生成H2O2是一种实时提供活性氧物质的有用方法。然而,目前报道的大多数高性能催化材料都是粉体形式,不便于在实际场景中的应用。因此,制备可直接应用的电极材料显得尤为重要。本研究利用喷涂-热解的制备方法,制备了高活性氧催化活性的氧化炭黑(O−CB)/多孔碳毡电极,通过聚四氟乙烯(PTFE)的修饰优化电极表面的氧气传质,成功制备氧掺杂碳气体扩散电极。研究结果表明,O−CB/PTFE-5 wt%电极具有最高的催化性能,其合成H2O2的速率达27.19 mg·L-1(mg catalyst)-1·cm-1·h-1。海洋典型污损微生物假单胞菌(Pseudomonas sp.)的抗菌实验表明,该电极电催化作用60 min产生的活性氧对Pseudomonas sp.的杀菌率可达到97.69%,作用120 min的杀菌率可达到99.99%。 相似文献
20.
微藻固碳是一种新型节能减排技术，具有长期可持续发展的潜力。本文对两株富油微藻（球等鞭金藻和微拟球藻）进行了富碳培养下生长特性及中性脂积累特性的研究。两株富油微藻的最佳培养条件为10%CO2浓度和f培养基。本研究对两株富油微藻的最大生物量产率、总脂含量、最大油脂产率、微藻的C含量和CO2固定率进行了测定。球等鞭金藻的各参数指标分别为：142.42±4.58g/（m2·d），39.95%±0.77%，84.47±1.56g/（m2·d），45.98%±1.75%和33.74±1.65g/（m2·d）。微拟球藻的各参数指标分别为：149.92±1.80g/（m2·d），37.91%±0.58%，89.90±1.98g/（m2·d），46.88%±2.01%和34.08±1.32g/（m2·d）。实验结果显示，两株海洋微藻均属于高固碳优良藻株，适合应用于微藻烟气减排技术开发，具备用于海洋生物质能耦合CO2减排开发的潜力。 相似文献