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1.
Variation of reactivity of particulate and sedimentary organic matter along the Zhujiang River Estuary 总被引：3，自引：0，他引：3
To investigate organic matter source and reactivity in the Zhujiang River (Pearl River)Estuary and its adjacent areas, particulate organic carbon (POC), particulate hydrolysable amino acids (PHAA), and Chl a during two cruises in July 1999 and July 2000 were measured. The highest POC and PHAA concentration was observed in the waters with maximum Chl a. The spectra distribution,relative content (dry weight in milligram per gram), PHAA-C% POC and other indicators such as the ratios of amino acids vs. amino sugars (AA/AS) and glucosamine vs. galactosamine (Glum/Gal) suggested that particulate amino acids in the water column and sediments in the Zhujiang River Estuary were mainly derived from biogenic processes rather than transported from terrestrial erosion. In inner estuary where high turbidity was often observable, organic matter was mainly contributed by re-suspension of bottom sediments with revealed zooplankton, microbial reworked characteristics, which suggest that these organic matters were relatively “old“. In the estuarine brackish region, organic matter in water column is mainly contributed by relatively fresh, easily degradable phytoplankton derived organic matter.During physical - biological processes within the eastuary, organic matter derived from phytoplankton was subjected to alteration by zooplankton grazing and bacterial reworking. 相似文献
2.
近年来武汉市臭氧污染日益严峻,成为影响空气质量达标的瓶颈,弄清臭氧及其前体物非线性关系是臭氧防控的关键和基础.本研究基于武汉中心城区2018年4—9月臭氧及其前体物在线观测数据,分析出武汉市臭氧浓度受前体物和气象条件等因素的共同影响,呈较为明显的季节变化和日变化特征.观测期间武汉市大气挥发性有机物（VOCs）平均体积分数为32.5×10-9,烷烃是武汉市VOCs的主要组分,其次是含氧VOCs （OVOCs）和卤代烃.利用基于观测的模型定量分析臭氧与前体物之间的关系,发现削减VOCs会引起臭氧生成潜势的显著下降,而削减氮氧化物则会使臭氧生成潜势升高,说明武汉市臭氧生成处于VOCs控制区.在人为源VOCs中,间/对二甲苯和邻二甲苯的相对增量反应活性（RIR）最高,是影响臭氧生成的关键组分. 相似文献
3.
矿物表面活性及其量度 总被引：6，自引：1，他引：6
矿物及其材料的表面活性及其表面反应性的具体表征，它是由矿物表面功能基所控制。由于矿物表面金属原子的电负性不同，以及它所处的配位环境不同，常表现出不同的极性、荷电性和Lewis酸碱性，它与溶质和溶剂分子之间反应（成键）能力也不同。在热力学上表现为反应自由能变化也不同。因此，量度矿物表面活性就是量度其表面极性、荷电性和Lewis酸碱性，它既可用化学方法，也可用热力学的方法。前者是通过反应作用量来量度，后者通过反应作用能来量度。然而现代矿物谱学的方法更能给出矿物及其材料表面反应活性的本质和详细信息。 相似文献
4.
A statistically relevant correlation between the reaction rate coefficient, k
OH, for the OH radical reaction with 161 organic compounds in the gas phase at 300 K, and the corresponding vertical ionisation energies E
i,v, reveals two classes of compounds: aromatics where –log(k
OH/cm3s-1)3/2E
i,v(eV)–2 and aliphatics where –log(k
OH/cm3s-1)4/5E
i,v(eV)+3. The prediction of the rate coefficient, k
OH, for the reaction of OH with organic molecules from the above equations has a probability of about 90%. Assuming a global diurnal mean of the OH radical concentration of 5×105 cm3, the upper limit of the tropospheric half-life of organic compounds and their persistence can be estimated. 相似文献
5.
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 > FeIII-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. 相似文献
6.
以富营养化的胶州湾一个柱状沉积物为例，用细化的铁形态分析及量化的铁氧化物还原活性相结合的方法研究了沉积物中铁的成岩作用过程。结果表明，这两种方法相结合的结果能更详细示踪铁的转化并能从多视角提供铁成岩作用的细微差别。这一方法有望应用于其它研究中更好地揭示复杂的铁和硫的生物地球化学循环。铁微生物还原在上部沉积物铁的还原中起重要作用，但12 cm深度以下铁被硫化物的化学还原为主要过程。最具生物活性的无定形铁氧化物是铁微生物还原的主要参与者，然后依次为弱晶态铁氧化物和磁铁矿，晶态铁氧化物几乎不参与铁的成岩循环。沉积物上部铁微生物还原的重要作用主要是活性铁含量高而活性有机质含量低共同作用的结果，且后者也是沉积物中硫酸盐还原速率以及硫化物积累的最终制约因素。对比研究表明，通过还原性溶解动力学方法表征的微生物可还原的铁氧化物主要由无定形和弱晶态铁氧化物组成，其总体活性常数相当于老化的水铁矿，且随深度增加而减低。 相似文献
7.
M. Frank M.M. Rutgers van der LoeffPeter W. Kubik Augusto Mangini 《Earth and Planetary Science Letters》2002,201(1):171-186
We present the first transect of dissolved 10Be depth profiles across the Antarctic Circumpolar Current (ACC) in the Atlantic sector. North of the Polar Front the 10Be concentrations increase continuously from very low values at the surface to values of up to 1600 atoms/g at depth. Deep water 10Be concentrations of particular water masses are consistent with earlier results obtained further north. South of the Polar Front and in the Weddell Sea the distribution of 10Be is also characterised by low surface concentrations but below 1000 m depth the concentrations are relatively constant and significantly higher (up to 2000 atoms/g) than further north, probably as a result of mixing and advection of water masses of Pacific origin. Overall the deep water 10Be distribution is obviously not significantly affected by scavenging processes or ice melt and comparison with the density distribution suggests that 10Be can be viewed as a quasi-conservative tracer. This provides a tool for an improved understanding of the behaviour of other more particle reactive trace metals in the Southern Ocean such as 230Th: in deep waters north of the ACC/Weddell Gyre boundary (AWB) 10Be/230Th has a relatively constant value (1.7±0.3×109 atoms/dpm) over a wide density range whereas south of the AWB the ratio is significantly lower (1.1±0.2×109 atoms/dpm). This normalisation to 10Be corroborates that 230Th is enriched by 50% due to accumulation south of the AWB as a consequence of minimal particulate fluxes. The quasi-conservative behaviour deduced from our results also implies that 10Be can only be used as a tracer for Southern Ocean particle fluxes in the past if ocean circulation patterns and water mass residence times did not change significantly. 相似文献
8.
P.V. Sivapullaiah J.P. Prashanth A. Sridharan B.V. Narayana 《Geotechnical and Geological Engineering》1998,16(3):239-250
The use of fly ash in geotechnical engineering depends greatly on its pozzolanic reactivity. Though many factors influence the reactivity of fly ash it is well recognized that reactive silica and lime content play a major role. A new, accurate and reliable method for the determination of reactive silica content of fly ash has been established. The reactive silica content, obtained as acid soluble silica in about 2 to 3 N hydrochloric acid, is found to correlate well with unconfined compressive strength of fly ashes. The reactive silica content of fly ash is also important in the stabilization of soils using fly ash. © Rapid Science Ltd. 1998 相似文献
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10.
纳米硫化亚铁（Nano-FeS）粒径小、比表面积大、反应活性高，但易团聚、易氧化的特点使其在地下水修复中的应用受到限制，通过改性可提高Nano-FeS的分散性和稳定性。本文选用羧甲基纤维素钠（CMC）及羟基铝柱撑膨润土（Alb）两种改性剂，制备了稳定型改性的CMC-FeS和负载型的Alb-FeS。分别从分散性、抗沉降性、抗氧化性、反应性和迁移性考察了两种改性Nano-FeS的性能。结果表明：Alb-FeS与CMC-FeS的分散性均较Nano-FeS得到明显改善；3 d后Nano-FeS完全沉降氧化，CMC-FeS沉降3 cm且开始氧化，而Alb-FeS沉降16 cm却未氧化；在相同的实验条件下，Alb-FeS、Nano-FeS、CMC-FeS对Cr （Ⅵ）的去除能力从强到弱，去除率分别是85.16%、84.90%、82.78%。在粗砂、中砂与细砂介质中，3种FeS的迁移能力从强到弱依次为CMC-FeS、Alb-FeS、Nano-FeS；在3种介质中CMC-FeS的最大迁移距离分别是Nano-FeS的6.1倍、6.4倍和3.4倍，而Alb-FeS与Nano-FeS相比迁移性没有明显提高。综合考虑分散性、抗沉降性、稳定性、反应活性及迁移能力，实际应用中宜优先选择CMC-FeS作为Cr （VI）污染地下水的原位修复材料。 相似文献