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温度、浓度对流体中氟钛络合物水解的影响:对深部地质过程中钛元素活动的制约 总被引：6，自引：3，他引：3
Ti是自然界中丰度最高的高场强元素(HFSE),其主要赋存矿物——金红石的溶解度决定了俯冲带HFSE的活动与循环。而富氟流体被认为是影响Ti等HFSE能否活化、迁移的重要因素。本文对不同浓度的氟钛络合物(K2Ti F6)在100MPa压力和200~500℃温度下的稳定性进行了研究,结果显示其在热液条件下发生显著水解,水解程度与温度和初始浓度密切相关,即温度越高、初始浓度越低,则水解程度越剧烈。对实验数据进行拟合,首次获得了K2Ti F6的表观水解常数与温度的关系式:-ln K=(8972±788)/T-(4.16428±1.40362),其中获得的热力学参数为:ΔrHΘ=74.59±6.55k J/mol,ΔrSΘ=34.62±11.67J/(mol·K)。同时,运用上述获得的关系式将温度推广到俯冲带条件,计算了金红石溶解度和流体中Ti的最大迁移量之间的关系。结果显示,当金红石的溶解度大于1000μg/m L时,富F流体能有效迁移的Ti大于1μg/m L;随着金红石溶解度的增加,Ti的有效迁移百分比也逐渐增大,但俯冲流体中Ti的最大迁移量可能不超过6700μg/m L,比之前的预计要低得多。本文的研究证实了富F流体能最大程度活化并迁移Ti等HFSE。其中,对于岩浆-热液体系而言,F主要通过在岩浆中预富集,然后再大量分配进入晚期流体中而形成富F流体;对于俯冲带而言,多硅白云母的脱水或热解是形成富F流体/超临界流体的有效途径。 相似文献
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沉淀-陈化-返溶作用和压力对热液中氟钛络合物高温水解的影响及地质意义 总被引：3，自引：3，他引：0
钛是自然界中最不活泼的金属元素之一,然而越来越多的证据显示钛可以在特定条件下能进入热液流体中发生迁移,其中氟可能在其中扮演着重要的角色。本文研究了300℃和50~400MPa压力条件下氟钛络合物(K2Ti F6)的稳定性以及沉淀-陈化-返溶作用和压力对氟钛络合物水解行为的影响。研究结果显示,氟钛络合物水解的过程中,由于Ti O2沉淀物的陈化作用,在稳定的温度和压力条件下,沉淀物的返溶很难发生;但在缓慢降温和机械性振荡过程中,沉淀物的返溶会明显发生。而且,在温度不变的情况下,压力的改变对K2Ti F6水解并没有显著的影响,显示氟钛络合物不管在高压还是低压环境下均遵循近似的水解规律。本文认为主要的原因在于压力的增高会促进水解反应沉淀物的陈化,进而抑制沉淀物的返溶,但并不破坏水解反应的平衡。最后,本文提出金属络合物的形成-水解-沉淀/返溶-陈化过程是水-岩作用或热液成矿过程中高场强元素活化、迁移和成矿的主要机制。 相似文献
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The observation that a fraction of organic matter produced in marine systems evades the concerted efforts of microbial communities and is buried in sediments suggests that there are ‘speed bumps’ in carbon degradation pathways that impede microbially driven remineralization processes. The initial step in degradation of macromolecules, extracellular enzymatic hydrolysis, is often stated to be ‘the’ rate-limiting step in carbon remineralization. Experimental investigations described here, however, demonstrate that at least in certain cases, microbes produce extracellular enzymes on time scales of hours to tens of hours in response to substrate addition, and hydrolysis is extremely rapid. If enzymatic hydrolysis can be rapid, what factors slow or stop organic matter degradation? A lack of the correct inducer to initiate enzyme production, and/or a lack of the correct organism to produce the required enzyme, may result in a complete lack of hydrolysis in certain environments—a barricade, rather than a speed bump. Preliminary evidence supporting this hypothesis includes a comparison of polysaccharide hydrolysis in seawater and sediments, which demonstrates that the spectrum of enzymes active in seawater and sediments are fundamentally different. Furthermore, a survey of enzyme activities in surface waters from a range of locations suggests that pelagic microbial communities also differ widely in their abilities to express specific extracellular enzymes. Trans-membrane transport through porins is yet another potential location of structure-related selectivity.Our efforts to identify speed bumps and barricades are hampered by our inability to structurally characterize in sufficient detail the macromolecular structures present in marine systems. Furthermore, assessments of organic matter ‘quality’ from a chemical perspective do not necessarily accurately reflect the availability of organic carbon to microbial communities. For these communities, in fact, ‘quality’ may be a variable, which depends on the enzymatic and uptake capabilities of community members. To begin to assess substrate structure and quality from a microbial perspective, we will have to combine specific knowledge of macromolecular structures with detailed investigations of the enzymatic and transport capabilities of heterotrophic marine microbes. 相似文献
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以华北陆块南部豫西偃师县龙门镇地区全取芯铝土矿钻孔ZK4704为主要研究对象,通过岩芯观察和垂向上连续取样,运用扫描电镜、能谱分析、X射线衍射分析、差热分析、红外光谱分析等手段对本溪组含铝岩系的矿物学特征及其垂向变化规律进行了分析。研究表明,偃龙地区本溪组含铝岩系的矿物均为自生矿物,除后期重结晶作用的影响外,主要以隐晶质或微晶存在,矿物成分在垂向上具有明显的变化规律:下部和上部泥岩以粘土矿物为主,但下部泥岩以伊利石为主,上部泥岩以高岭石为主。中部铝矿物含量较高,粘土矿物含量较少。在上述分析基础上,以化学风化作用的基本原理和产生的条件为联结本溪组含铝岩系矿物学特征和原岩的纽带,分析了铝土矿的原岩。认为,可以迅速水解的火山灰是最有可能的含铝岩系的原岩,而由弱碱性的海相环境逐渐转变为弱酸性沼泽环境的海退序列可以很好地解释水解过程中化学环境的变化,含铝岩系基底强烈的古岩溶作用,可以为硬水铝石的产生提供良好的泄水条件。偃龙地区本溪组铝土矿的火山灰物源可由华北陆块北缘和我国西部地区同时期强烈活动的火山作用提供。 相似文献
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两类榴辉岩的石榴石变形特征差异——来自TEM研究的证据 总被引：9，自引：4，他引：9
大陆碰撞造山带中超高压榴辉岩从变形程度上通常可以分为面理化榴辉岩和块状榴辉岩两类。本文利用透射电子显微镜对中国大陆科学钻探主孔岩心中面理化榴辉岩和块状榴辉岩的石榴石变形特征进行了比较研究。结果表明:(1)面理化榴辉岩中石榴石的位错密度比块状榴辉岩中石榴石的位错密度高大约3个数量级,位错密度达1.2×1010/cm2。并且有水分子团与高密度位错共存,表明主导石榴石发生强烈塑性变形的机制为水弱化的位错滑移。(2)块状榴辉岩中石榴石的位错密度低,没有观察到水分子团,虽然在局部发现有位错网,但总体上仍呈刚性。(3)两类榴辉岩的石榴石中占主导地位的位错滑移系都是1/2<111>{110},其次为<100>{010}。本文对变形石榴石晶体中水的赋存状态、水弱化机制及变形石榴石形态优选方位与晶格优选方位不协调问题进行了讨论:(1)水在石榴石晶体中有三种可能赋存状态:第一种是吸附于位错管道中的极化水分子;第二种是通过晶体表面以及位错管道扩散进入晶格的间隙水分子;第三种是以4OH-替代SiO44-形式的结构水。(2)石榴石水弱化机制有两种可能:一种是水弱化促进的位错滑移机制,在面理化榴辉岩石榴石的塑性变形中起主导作用;另一种是水弱化促进的扩散和颗粒边界滑移机制,在面理化榴辉岩石榴石的塑性变形中只起次要作用。(3)变形石榴石不产生明显的LPO是由其晶体结构本身特征所决定的,并不能排除其主导变形机制仍然是位错滑移的可能性。 相似文献
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The activities and substrate specificities of extracellular enzymes in natural systems are not well understood, despite their critical role in microbial remineralization of organic carbon. These enzymes initiate organic carbon degradation by selectively hydrolyzing high molecular weight substrates to lower molecular weight products which can be transported into cells. A set of single- and dual-labeled fluorescent polysaccharides was synthesized and characterized to explore a variety of approaches for measuring enzymatic hydrolysis of biopolymers via photophysical techniques, focusing particularly on rapid and robust optical techniques which are amenable to field measurements in remote locales. A shotgun-labeling approach yielded dual-labeled probes that exhibited substantial donor fluorophore quenching. The photophysical response of these probes to hydrolysis via purified enzymes was investigated in the lab, and fluorescence polarization proved to be a rapid and reliable technique for monitoring probe hydrolysis. Initial field results were also obtained from hydrolysis experiments in sediment porewaters. Because polarization measurements are rapid and simple, this approach could be used to follow the extracellular enzymatic hydrolysis of a wide range of biopolymers which fuel microbial metabolism. 相似文献
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虾蛄肉酶法制备抗氧化肽的工艺优化和活性研究 总被引：1，自引：1，他引：0
以虾蛄(Oratosquillaoratoria)肉为研究的对象,用胰蛋白酶水解得到抗氧化肽,以1,1-二苯基-2-三硝基苯肼(DPPH)自由基清除率为指标,采用L16(45)正交试验和三因素三水平的响应面分析法,对酶解工艺进行分析优化。结果表明最佳的酶解工艺条件为:温度51.1°C,pH7.07,加酶量1500U/g,料液比1︰3.09,酶解时间2h,DPPH自由基清除率47.3466%,理论值与预测值相差很小,说明该方法可行。在此条件下测得羟基自由基的清除率为88.9%,超氧阴离子清除率为29.13%,还原力A700为0.243,表明虾蛄肉酶解多肽有较强的抗氧化性,可以进一步分离纯化从中提取抗氧化肽。 相似文献
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During spring the atmospheric concentration of Peroxyacetyl Nitrate, PAN, in the UK varies over three orders of magnitude due to long range transport and local photochemical production. An experiment at Great Dun Fell was used to determine which of these sources of PAN controlled spring time concentrations and to quantify the contribution of PAN to oxidised nitrogen in cloud water. The gas phase mixing ratio of a wide range of trace gas pollutants, including PAN, along with cloud water chemical composition and aerosol/cloud droplet distributions were measured. A chemical model was developed to determine the contribution of PAN hydrolysis to cloud water nitrification and to quantify the sink strengths of PAN. Chemical reaction following thermal decomposition was found to be the dominant sink mechanism in the model but transport was the most important factor controlling PAN concentration. During cloud episodes PAN concentrations varied from 100 ppt to over 1 ppb but the calculated inorganic oxidised nitrogen loading in the cloud due to PAN dissolution and hydrolysis was an insignificant fraction of the observed total oxidised nitrogen loading of the cloud. Extrapolation of the model to persistent cloud in marine conditions showed that PAN has a negligible effect on cloud nitrification. It was concluded that PAN concentrations were heavily influenced by regional concentrations and that the hydrolysis of PAN in cloud water was an insignificant source of oxidised nitrogen in cloud water. 相似文献