利用盐湖常见元素的助烧结作用绿色制备氧化镁及磷酸镁水泥

低活性氧化镁是制备磷酸镁水泥(MPC)的关键原材料。现行低活性氧化镁的生产方式导致了制备MPC具有能耗高和成本高的缺点,不利于其推广应用。利用盐湖中常见元素如B,Na、K和Cl的助烧结作用,在≤1 200℃煅烧盐湖提锂镁渣、外掺B的轻烧镁粉和水氯镁石的热解产物制备低活性氧化镁。介绍了低活性氧化镁的粒径、比表面积、孔隙率、化学组成、矿物组成和形貌等物理特征,以及低活性氧化镁制备MPC的凝结时间、水化产物、微观结构、抗压强度、体积稳定性等凝结硬化性能,并分析了烧结温度对低活性氧化镁的理化性能及MPC的凝结硬化性能的影响。相比现有技术,利用盐湖共存元素的助烧结作用可将氧化镁的烧结温度由1 500～1 800℃降低到1 200℃以下,有利于实现低活性氧化镁及MPC的低能耗、低成本绿色制备,促进MPC的推广应用。     

东海北部营养盐分布的季节变化及成因探讨

基于美国国家海洋大气管理局(NOAA)2007年发布的全球海域营养盐数据库资料和美国国家地球物理数据中心(NGDC)2006年发布的全球地貌数据库资料,在MATLAB计算机平台上,利用研发的数值分析与成图技术,对东海北部海域营养盐分布的季节变化特征进行分析。结果表明:(1)东海北部海域NO3--N、PO43--P分布总特征为由沿岸向离岸递减,由表层向底层递增;西北高,东南低,呈扇形向东南扩展;SiO3--Si有两个浓度高值区,一个为研究区域的西北角,另一个在东北角;(2)在0~50 m的表层营养盐平均浓度均是冬季最高;50~200 m的中层NO3--N、SiO3--Si夏季最高;200 m以下的底层四季变化微弱,其中400~500m层PO43--P、SiO3--Si浓度值秋季最高。NO3--N变异系数表层最大,PO3--P中层最大、SiO3--Si底层最大,其中NO3--N相应各层变异系数大于PO43--P、SiO3--Si;(3)研究区域四季均存在高营养盐水团。高PO43--P、SiO3--Si水团中心分别位于125.5°E、30.5°N和128.5°E、30.5°N;高NO3--N水团中心,随冬-春-夏-秋、从南往东北再向西、最后向东南,在125°~128°E、29°~31°N范围内移动。     

Dissolved nutrient balance and net ecosystem metabolism in a Mediterranean-climate coastal lagoon: San Diego Bay

The temporal and spatial variability of dissolved inorganic phosphate (DIP), nitrogen (DIN), carbon (DIC) and dissolved organic carbon (DOC) were studied in order to determine the net ecosystem metabolism (NEM) of San Diego Bay (SDB), a Mediterranean-climate lagoon. A series of four sampling campaigns were carried out during the rainy (January 2000) and the dry (August 2000 and May and September 2001) seasons. During the dry season, temperature, salinity and DIP, DIC and DOC concentrations increased from oceanic values in the outer bay to higher values at the innermost end of the bay. DIP, DIC and DOC concentrations showed a clear offset from conservative mixing implying production of these dissolved materials inside the bay. During the rainy season, DIP and DOC increased to the head, whereas salinity decreased toward the mouth due to land runoff and river discharges. The distributions of DIP and DOC also showed a deviation from conservative mixing in this season, implying a net addition of these dissolved materials during estuarine mixing within the bay. Mass balance calculations showed that SDB consistently exported DIP (2.8–9.8 × 10³ mol P d⁻¹), DIC (263–352 × 10³ mol C d⁻¹) and DOC (198–1233 × 10³ mol C d⁻¹), whereas DIN (5.5–18.2 × 10³ mol N d⁻¹) was exported in all samplings except in May 2001 when it was imported (8.6 × 10³ mol N d⁻¹). The DIP, DIC and DOC export rates along with the strong relationship between DIP, DIC or DOC and salinity suggest that intense tidal mixing plays an important role in controlling their distributions and that SDB is a source of nutrients and DOC to the Southern California Bight. Furthermore, NEM ranged from −8.1 ± 1.8 mmol C m⁻² d⁻¹ in September to −13.5 ± 5.8 mmol C m⁻² d⁻¹ in January, highlighting the heterotrophic character of SDB. In order to explain the net heterotrophy of this system, we postulate that phytoplankton-derived particulate organic matter, stimulated by upwelling processes in the adjacent coastal waters, is transported into the bay, retained and then remineralized within the system. Our results were compared with those reported for the heterotrophic hypersaline coastal lagoons located in the semi-arid coast of California–Baja California, and with those autotrophic hypersaline systems found in the semi-arid areas of Australia. We point out that the balance between autotrophy and heterotrophy in inverse estuaries is dependent on net external inputs of either inorganic nutrients or organic matter as it has been indicated for positive estuaries.     

滇东昆阳磷矿成矿物质来源及其沉积环境

昆阳磷矿位于滇池西南部,为探讨该磷矿的成矿物质来源及其沉积环境,从岩相学和元素地球化学两方面对磷矿石展开了研究.研究结果显示,磷块岩矿石的主要矿物成分为胶磷矿,矿体w(P2 O5)平均含量为26.16％,磷块岩P2 O5含量由地表向地下沿倾向逐渐降低,酸不溶物含量逐渐增加,在垂直剖面上,矿区中部P2 O5含量相对上部和...     

长江口理化因子影响初级生产力的探索Ⅲ.长江河口区水域磷酸盐供给的主要水系组成

长江口水域的水系组成和特征的综合研究结果表明,长江、台湾暖流、气旋型涡旋和32°N附近的上升流从东、南、西、北四个方向向长江口水域提供了丰富的磷酸盐,并且均以不同的时间、方式和强度提供磷酸盐。长江口的浅海区南侧有上升流出现,这可由物理海洋、海洋化学和海洋生物调查数据予以证实。这样,展示了整个长江河口区水域磷酸盐的输送过程,为研究长江河口区磷酸盐的分布成因和浮游植物的生长过程提供了科学基础。     

坡缕石粘土的磷吸附机制及其铁负载效果研究

比较了3种天然坡缕石粘土对不同程度磷污染水体的吸附净化能力,通过等温吸附实验和吸附动力学实验探讨了坡缕石粘土的磷吸附机制,并研究了不同形态铁负载对坡缕石粘土吸附净化磷污染水体性能和机制的影响.结果发现,3种天然坡缕石粘土对不同程度磷污染水体均有一定的吸附净化能力,其中含白云石较多的坡缕石粘土的磷吸附能力最强,吸附等温曲线呈S型,且Freundlich方程(R2=0.977 6)比Langmuir方程(R2=0.924 9)拟合效果更好;准一级方程、冥函数方程、抛物线扩散方程、准二级方程均能较好地模拟坡缕石粘土对磷的吸附动力学过程,说明坡缕石粘土对磷的吸附可能属于不均匀介质的多分子层吸附.此外,不同形态铁负载均能显著增强坡缕石粘土对不同程度磷污染水体的吸附净化能力,吸附等温曲线呈L型,Langmnir方程(Fe2 :R2=0.96,Fe3 :R2=0.967 7)比Freundlich方程(Fe2 :R2=0.965 7,Fe3 :R2=0.936 1)能略好地拟合铁负载坡缕石粘土的磷吸附等温结果,说明铁负载坡缕石粘土的磷吸附过程可能是均匀介质的单分子吸附.适量白云石有助于提高坡缕石粘土的磷吸附净化性能,铁负载可能通过改变坡缕石的表面电荷和吸附活性位点来改变其磷吸附机制,从而提高其磷吸附性能.     

Removal of Lead,Copper, Zinc and Cadmium from Water Using Phosphate Rock

Removal of Pb^2＋, Cu^2＋, Zn^2＋ and Cd^2＋ from aqueous solutions by sorption on a natural phosphate rock （FAP） was investigated. The effects of the contact time and initial metal concentration were examined in the batch method. The percentage sorption of heavy metals from solution ranges generally between 50% and 99%. The amount of sorbed metal ions follows the order Cu〉Pb〉Cd〉Zn. Heavy metal immobilization was attributed to both surface complexation of metal ions on the surface of FAP grains and partial dissolution and precipitation of a heavy metal-containing phosphate. The very low desorption ratio of heavy metals further supports the effectiveness of FAP as an alternative and low-cost material to remove toxic Pb^2＋, Cu^2＋, Zn^2＋ and Cd^2＋ from polluted waters.     

离子色谱法同时测定地质样品中氟氯磷硫

本文研究了离子色谱同时测定地质样品中F~-、Cl~-、PO_4~(3-)、SO_4~(2-)的前处理过程,选择了色谱测定最佳条件。在Na_2CO_3全熔的样品溶液中,加入(NH_4)_2CO_3使Si、Al随大多数金属离子同时沉淀;再用预处理柱除去熔剂引入的大量Na~+及CO_3~(2-)消除其干扰;并在流出液中补加相应试剂与淋洗液相匹配,实现了多种地质样品中F~-、Cl~-、PO_4~(3-)和SO_4~(2-)的测定。方法检出限(3s,μg/ml)分别为F~-0.05、Cl~-0.1、PO_4~(3-)0.3、SO_4~(2-)0.5。测定范围为F~-0.05—3μg/ml,Cl~-0.1—6μg/ml,PO_4~(3-)0.3 —30μg/ml,SO_4~(2-)0.5—30μg/ml。     

Study of inorganic ligand-chromium(III)-surface ternary complexes by ESR spectroscopy

Cr(III) sorbed at the solid/water interface of latex and hectorite was studied by ESR spectroscopy in the presence of different inorganic ligands. The ESR spectra of the surface obtained in the presence of selenite, phosphate and fluoride can be explained in terms of ternary surface complex formation. This is contrasted by the behaviour of sulfate and selenate ions which were found to have no effect on the ligand field of Cr(III), either in the adsorbed state or in solution.     

Oxyanion Concentrations in Eastern Sierra Nevada Rivers – 2. Arsenic and Phosphate

Water samples were collected from the Truckee River-Pyramid Lake system, the Walker River-Walker Lake system, and the Carson River, all located in eastern California and western Nevada, U.S.A., at three different times (i.e., summer 1991, spring 1992, and autumn 1992) over a two year period. The concentrations of As, Na, Cl, PO4, and pH were measured in these river samples and the associated terminal lakes. Arsenic values ranged from below 13 nmol/kg near Truckee, California to 160 nmol/kg at Nixon, Nevada in the Truckee River, from 40 nmol/kg in the headwaters of both West and East Walker Rivers to 270 nmol/kg below Weber Reservoir on the main branch of the Walker River, and from <27 nmol/kg to 234 nmol/kg for the lower Carson River system. Arsenic concentrations in Steamboat Creek (0.91 mol/kg–1.80 mol/kg) in the Truckee River catchment are above the U.S. EPA drinking water maximum contaminant level of 0.67 mol/kg, as are the As concentrations in both Pyramid Lake (1.33 mol/kg–1.57 mol/kg ) and Walker Lake (13.7 mol/kg–18.7 mol/kg). Sources of As for all three rivers include weathering of As-rich rocks and/or regolith and input of high-As geothermal spring waters, both processes primarily, although not exclusively, adding As to the headwater regions of these rivers. Steamboat Hot Springs (29 mol/kg As 54.5 mol/kg), for example, is identified as a source of As to the Truckee River via Steamboat Creek. The high As concentrations in Pyramid and Walker Lakes are likely due to (1) desorption of arsenate from aquatic particulate matter in these high pH waters (9.0 pH 9.5), (2) limited biologic uptake of arsenate, and (3) evaporative concentration of the lake waters. Evaluation of molar PO4}/As ratios of river waters and geothermal spring waters (e.g., Steamboat Hot Springs), indicates that phosphate is substantially enriched in Steamboat Creek as well as the mid to lower reaches of the Walker and Carson Rivers. These regions of each river are dominated by agricultural interests and, additionally, in the case of Steamboat Creek, residential areas and golf courses. Our data strongly imply that phosphate-rich agricultural return flow has likely added P to these streams and, consequently, increased their respective P:As ratios.