褐藻酸苄酯的合成与表征     

甘纯玑  蔡乐琤 《海洋科学》1990,14(2):45-47

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Trends in the solubility of iron,aluminium, manganese and phosphorus in aerosol collected over the Atlantic Ocean     

A.R. Baker  T.D. Jickells  M. Witt  K.L. Linge 《Marine Chemistry》2006

The solubility of iron, aluminium, manganese and phosphorus has been determined in aerosol samples collected between 49°N and 52°S during three cruises conducted in the Atlantic Ocean as part of the European Union funded IRONAGES programme. Solubilities (defined at pH 4.7) determined for Fe and Al in samples of Saharan dust were significantly lower (medians 1.7% and 3.0%, respectively) than the solubilities of these metals in aerosols from other source regions (whole dataset medians 5.2% and 9.0%, respectively). Mn solubility also varied with aerosol source, but the median solubility of Mn in Saharan dust was very similar to the median for the dataset as a whole (55% and 56%, respectively). The observed solubility of aerosol P was ∼ 32%, with P solubility in Saharan aerosol perhaps as low as 10%. Laboratory studies have indicated that aerosol Fe solubility is enhanced by acid processing. No relationship could be found between Fe solubility and the concentrations of acid species (non-seasalt SO₄²⁻, NO₃⁻) nor the net acidity of the aerosol, so we are unable to confirm that this process is significant in the atmosphere. In terms of the supply of soluble Fe to oceanic ecosystems on a global scale, the observed higher solubility for Fe in non-Saharan aerosols is probably not significant because the Sahara is easily the dominant source of Fe to the Atlantic. On a smaller scale however, higher solubility for aerosol Fe may alter our understanding of Fe cycling in regions such as the remote Southern Ocean.  相似文献   

超临界流体中MoO3与WO3溶解度实验探讨   总被引：1，自引：1，他引：1  

龚庆杰  於崇文岑况 王玉荣 《岩石学报》2005,21(1):240-244

超临界地质流体以其独特的性质对金属成矿元素具有超强的萃取、层析和搬运能力,在热液矿床成矿机制研究中对揭示成矿物质的源、流和汇起着特殊和重要作用。本文利用分析纯H2MoO4在高温下脱水制备了MoO3(白色斜方晶系),在冷封式高压釜中实验测定了417℃超临界条件下,MoO3在纯水中的溶解度分别为7.3(29MPa)、14.2(45MPa)、21.6(55MPa)、27.7(78MPa)、32.5(100MPa)、和34.2(150MPa)mmol/l,热液中钼的存在形式为H2MoO4。依据前人的实验方案,补充测定了WO3在4.0%NaCl水溶液中于450%条件下的溶解度,其值分别为27.51(50MPa)和30.52(100MPa)mmol/l。结合前人研究结果发现,MoO3、WO3的溶解度在临界区域内具有超临界现象,在超临界条件下其溶解度与石英的超临界溶解度行为基本相似,表现为溶解度随体系温度和压力的升高而增大,这对揭示岩浆热液型和石英脉型钨、钼矿床的形成机制具有重要指导作用。  相似文献   

KCl-KNO3-CH3OH/H2O和KNO3-NH4NO3-CH3OH/H2O三元体系在25℃时的溶解度          下载免费PDF全文

刘亦凡  谢爱华  钟杰  董殿权 《盐湖研究》2003,11(1):66-69

测定了 2 5℃时KCl KNO3 CH3 OH H2 O和KNO3 NH4NO3 CH3 OH H2 O三元体系的溶解度 ,并与 2 5℃时相应体系在水中的溶解度进行了比较。  相似文献   

The effect of water on accessory phase solubility in subaluminous and peralkaline granitic melts   总被引：4，自引：0，他引：4  

Robert L. Linnen   《Lithos》2005,80(1-4):267-280

The solubilities of columbite, tantalite, wolframite, rutile, zircon and hafnon were determined as a function of the water contents in peralkaline and subaluminous granite melts. All experiments were conducted at 1035 °C and 2 kbar and the water contents of the melts ranged from nominally dry to approximately 6 wt.% H₂O. Accessory phase solubilities are not affected by the water content of the peralkaline melt. By contrast, solubilities are affected by the water content of the subaluminous melt, where the solubilities of all the accessory phases examined increase with the water content of the melt, up to 2 wt.% H₂O. At higher water contents, solubilities are nearly constant. It can be concluded that water is not an important control of accessory phase solubility, although the water content will affect diffusivities of components in the melt, thus whether or not accessory phases will be present as restite material. The solubility behaviour in the subaluminous and peralkaline melts supports previous spectroscopic studies, which have observed differences in the coordination of high field strength elements in dry vs. wet subaluminous granitic glasses, but not for peralkaline granitic glasses. Lastly, the fact that wolframite solubility increases with increasing water content in the subaluminous melt suggests that tungsten dissolved as a hexavalent species.  相似文献   

柴达木低品位固体钾矿溶解转化率与品位关系   总被引：1，自引：1，他引：0       下载免费PDF全文

王兴富  王石军  王罗海  田红斌  刘万平  刘斌山 《盐湖研究》2020,28(3):61-65

我国是缺钾大国,探明的可溶性钾盐十分有限,柴达木盆地是我国盐湖钾盐的聚集地,含水层骨架中含有数亿吨低品位固体钾矿,开发出这些低品位固体钾盐对增加国内钾肥供给,保障粮食安全具有重大意义。青海盐湖工业股份有限公司历经十年开发出低品位固体钾盐的浸泡式溶解转化方法,试验表明,固体钾盐的溶解转化率随固体钾品位的增加而增加,累计溶解转化率为56%～98%。该技术在柴达木多个盐湖得到推广应用,察尔汗盐湖保有固体钾盐达2.96×10~8 t,平均品位KCl为1.24%,根据试验数据回归分析溶解转化率77%,可溶解转化出钾盐(KCl)约2.28×10~8 t,柴达木盆地盐湖保有3.43×10~8 t固体钾盐,平均品位KCl为1.25%,溶解转化率78%,可溶解转化出钾盐(KCl)2.68×10~8 t,大幅度增加了钾盐储备量。  相似文献   

Phosphate mineral accumulation in lake sediment to form a secondary phosphate source: A case study in lake sediment around Eppawala Phosphate Deposit (EPD) in Sri Lanka   总被引：1，自引：0，他引：1  

Nimila Dushyantha  Nalin Ratnayake  Hemalal Panagoda  Chulantha Jayawardena  Amila Sandaruwan Ratnayake 《国际泥沙研究》2021,36(4):532-541

Global phosphorus scarcity will result in significant consequences for future food security with the depletion of current phosphate reserves.Therefore,exploration of new phosphorus sources is essential to address future phosphorus scarcity.The current study investigated the geochemical potential of lake sediment around the Eppawala Phosphate Deposit(EPD)in Sri Lanka to be used as a low-grade phosphorus source for agricultural purposes.Jaya-Ganga is a man-made water canal that drains through the EPD feeding three lakes,namely,upstream Ihalahalmilla Lake and Koon Lake,and downstream Kiralogama Lake with respect to the EPD.Three cores(cores A,B,and C)were collected from the above three lakes and major oxides and minerals distributions along the cores were analyzed.Notable high enrichment of phosphorus pentoxide(P2O5)content and high P2O5 solubility values were measured in the top 60 cm sediment layer in Core B and throughout the Core C compared to the Core A.This high enrichment of P2O5 content in the same sediment columns were confirmed by the comparison with the Upper Continental Crust(UCC)values and literature survey.According to the X-ray Diffraction(XRD)results,phosphate minerals,such as fluorapatite,crandallite,and millisite were abundantly found in the same sediment columns.Therefore,these phosphate minerals can be considered as pathfinding minerals for soluble phosphates in sediment cores.Thus,sediment with high P2O5 content and high solubility in downstream Kiralogama Lake showed the potential for application of these sediments as a direct phosphate source in agricultural purposes.Furthermore,the current study has introduced a new area of interest,i.e.,soil and sediments around major phosphate deposits,for the exploration of new phosphate sources to meet future phosphorus demand.  相似文献   

三元体系Li~+,Mg~(2+)∥SO_4~(2-)—H_2O 25℃相关系及溶液物化性质的研究          下载免费PDF全文

李冰  房春晖  王庆忠  李军  宋彭生 《盐湖研究》1993,(3)

研究了三元体系Li~+,Mg~(2+)∥SO_4~(2-)—H_2O在25℃时的相关系和平衡液相的密度、粘度、折光率、电导等物化性质,该体系为简单共饱型,两段溶解度曲线对应于体系的两种原始组份Li_2SO_4·H_2O和MgSO_4·7H_2O的结晶区,无复盐和固溶体形成,亦无脱水作用发生,应用电解质溶液Pitzer模型检测该体系25C的溶解度,并用经验或半经验公式对平衡液相的密度和折光率进行了理论计算,计算值与实验值非常接近。  相似文献   

An analytical solution to multi-component NAPL dissolution equations     

Scott K. Hansen  Bernard H. Kueper 《Advances in water resources》2007

This note presents a novel method for determining the changing composition of a multi-component NAPL body dissolving into moving groundwater, and the consequent changes in the aqueous phase solute concentrations in the surrounding pore water. A canonical system of coupled non-linear governing equations is derived which is suitable for representation of both pooled and residual configurations, and this is solved. Whereas previous authors have handled such problems numerically, it is shown that these governing equations succumb to analytical solution. By a suitable substitution, the equations become decoupled, and the problem collapses to a single first-order equation. The final result is expressed implicitly, with time as a function of the number of moles of the least soluble component, m₁. The number of moles of each other component is expressed explicitly in terms of m₁. It is shown that the time-m₁ relationship has a well behaved inverse. An example is given in which the analytic solution is verified against traditional finite difference analysis, and its computational efficiency is shown.  相似文献   

Behaviour of H₂O₂, NH₃, and black carbon in mixed-phase clouds during CIME     

Paolo Laj  Andrea I. Flossmann  Wolfram Wobrock  Sandro Fuzzi  Giordano Orsi  Loretta Ricci  Stephan Mertes  Alfons Schwarzenbck  Jost Heintzenberg  Harry Ten Brink 《Atmospheric Research》2001,58(4):256

We investigated the partitioning of trace substances during the phase transition from supercooled to mixed-phase cloud induced by artificial seeding. Simultaneous determination of the concentrations of H₂O₂, NH₃ and black carbon (BC) in both condensed and interstitial phases with high time resolution showed that the three species undergo different behaviour in the presence of a mixture of ice crystals and supercooled droplets. Both H₂O₂ and NH₃ are efficiently scavenged by growing ice crystals, whereas BC stayed predominantly in the interstitial phase. In addition, the scavenging of H₂O₂ is driven by co-condensation with water vapour onto ice crystals while NH₃ uptake into the ice phase is more efficient than co-condensation alone. The high solubility of NH₄⁺ in the ice could explain this result. Finally, it appears that the H₂O₂–SO₂ reaction is very slow in the ice phase with respect to the liquid phase. Our results are directly applicable for clouds undergoing limited riming.  相似文献