高纯球形-准球形亚微米晶质SiO2材料的制备与表征

以天然粉石英为基本原料,通过氢氟酸与盐酸混合酸溶蚀技术和机械强力搅拌处理,制备了高纯球形-准球形亚微米晶质SiO2材料。XRD,SEM表征结果表明,制备的高纯球形亚微米晶质SiO2材料为纯结晶SiO2相,粒子呈球形-准球形,球化-准球化率达80%～90%,粒径一般为300 nm～800 nm;其化学组成为:w(SiO2)99.90%,w(Al2O3)192×10-6,w(Fe2O3)33×10-6,w(Mg)1×10-6,w(Ca)2×10-6,w(Cl-)20×10-6。     

重金属离子在胡敏酸-高岭石复合体上的吸附

本文研究了胡敏酸存在下高岭石对重金属离子的吸附行为。实验结果表明:①胡敏酸和Cu2 溶液按先后顺序或同时加入高岭石中反应,在Cu2 平衡浓度<10mg/L时,3种加入顺序对Cu2 的吸附量基本相同,当Cu2 平衡浓度>10mg/L时,(K Cu) HA和(K Cu HA)两种加入顺序对Cu2 的吸附量比(K HA) Cu的略大。②在pH=5时,胡敏酸-高岭石复合体对Cu2 的吸附量明显大于纯高岭石。这是由于胡敏酸含有大量的羧基和酚羟基等活性基团,吸附在高岭石上的胡敏酸增加了其表面吸附位,在复合体表面形成了S—HA—Cu三元配合物,且Cu2 的吸附量与复合体中胡敏酸的含量在一定范围内成正相关;③溶液pH值在4～7之间变化可调控复合体对Cu2 的吸附机制。④在Cu2 和Cd2 共存时,随着金属离子初始浓度的增大,Cu2 的吸附量呈直线上升,而Cd2 的吸附量增加缓慢,表明复合体对Cu2 的吸附能力比对Cd2 强。     

磺化层柱状有机膦酸锆的合成及催化反应研究

在氢氟酸溶液中,混合亚磷酸、4,4’-联苯二膦酸和锆离子反应生成4,4’-联苯二膦酸锆／亚磷酸锆（简称MCZP）,改变有机酸和亚磷酸的比例,可以合成具有相同组分但结构不同的一系列化合物。通过磺化反应,在苯环上接上磺酸基团后,它具有类似强酸性阳离子交换树脂特性．该文首次对这类化合物催化酯化、醚化等典型的酸催化有机反应进行了研究,结果表明其催化转化率高、催化剂可重复使用和再生,是一种很有发展前途的新型固体酸催化剂．     

酸法地浸采铀的地下水生态环境问题

本文综述了利用酸法地浸采铀对采铀区及其周围地下水生态环境的影响方式、影响程度以及针对这些影响所采用的各种治理手段和效果。并就我国刚刚起步不久的酸法地浸采铀中地下水生态环境的保护和恢复,提出了一些建议。     

亚南极冰川雪冰内MSA的季节变化(英)

Methanesulphonate was investigated as a potential contributor to the sulphur budget based on the analysis on Antarctic snow/ice from Coffins Ice Cap, King George Island (62°10' S, 58°50,W). The anion was found to be present at a mean concentration of 0. 17 μeq. L-1 with a maximum of 0.73 μeq. L-1. A distinct seasonal variation exists in the top 10 m of the core, equivalent to more than two years of deposition. Dating resulted from δ18O profile suggests that the principal peaks of methanesulphonate are associated with snow deposited in autumn and secondary peaks in spring. The seasonal patterns of methanesulphonate in the subantarctic snow displays a phase difference from that observed in marine air from low and middle latitudes.     

山西孙家庄中酸性杂岩体及其邻近地区的找矿远景评价

通过“面型”岩石测量和多子样剖面岩石测量,对山西孙家庄中酸性杂岩体作出找矿远景评价,并对其邻近地段进行矿化追踪。确定该岩体的主要指示元素和伴生元素,圈出以Cu为主的斑岩矿化多元素组合异常,在Cu异常浓集中心发现斑岩矿化。孙家庄岩体周围地区,存在斑岩型矿化—接触交代矿化—热液多金属矿化的环带状分布模式。     

有机酸对高岭石形成影响的模拟试验研究

利用富里酸、胡敏酸和盐酸与天然矿物－长石、蒙脱石和云母在常温常压下进行反应,探讨矿物溶解及高岭石形成机理。实验表明富里酸对这些矿物具有较大的溶解能力,其原因是由于形成了具有较大溶解度和活动性的有机硅和有机铝复合体。在中性－碱性条件下有利于有机硅复合体的形成,酸性条件下有利于有机铝复合体的形成。在富里酸作用下,蒙脱石和云母分别在４个月和８个月有少量转化成高岭石,说明层状硅酸盐矿物比架状硅酸盐矿物更易     

Measurements of Reaction Coefficients of NO2 and HONO on Aerosol Particles

The reaction coefficients of nitrogen dioxide and nitrous acid with monodisperse sodium chloride and ammonium sulphate aerosols have been measured in a flow reactor at atmospheric pressure. These experiments were performed at relative humidities above and below the deliquescence points of both aerosols (r.h. 50 and 85%) at 279 K. The results for NO₂ afford a reaction coefficient in the range (2.8–10) × 10^-4 and for HONO, (2.8–4.6) × 10^-3. For both species, there appears to be an enhancement of the reaction coefficient on sodium chloride aerosol at 50% r.h. The results are compared with reaction coefficients determined by other experimental methods. A good agreement is found for both gases between this method and the coated denuder method previously developed in our research laboratories (Msibi et al., 1993) and with the majority of other published data for NO₂. In the case of HONO, our estimate of reaction coefficient is smaller than, or at the lower limits of the ranges reported by other published studies.     

Fast Oxidation Reaction of Nitrite by Dissolved Oxygen in the Freezing Process in the Tropospheric Aqueous Phase

Nitrite oxidation in the tropospheric aqueous phase by freezing was evaluated by freezing a field sample. Nitrite oxidation by dissolved oxygen in the freezing process is much faster than by other oxidation processes, such as reactions with ozone, hydrogen peroxide or dissolved oxygen in an aqueous solution at pHs 3 to –6. At pH 4.5 and 25°C, the lifetime of nitrite in the aqueous phase is ca. 1 hr in oxidation by ozone (6×10^-10 mol dm^-3), ca. 10 hr in oxidation by H₂O₂ (2×10^-4 mol dm^-3), and 7.5 hr (Fischer and Warneck, 1996) in photodissociation at midday in summer. Under the same conditions at a temperature below 0°C, the lifetime of nitrite in the freezing process is estimated as ca. 2 sec when the droplets are frozen within a second. The reaction by freezing is affected by the presence of salts, such as NaCl or KCl, or orgnaic compounds, such as methanol or acetone. The results of freezing a field rain or fog sample showed that nitrite oxidation proceeds below pH 6, and the conversion ratio of nitrate from nitrite increases with decreasing pH. The oxidation of nitrite by freezing was also observed in freezing fog particles generated by an ultrasonic humidifier. The ratios of the concentrations of ions in the winter sample to those in the summer sample (or those in the fog sample) were almost the same values. However, the concentration of nitrite in the winter sample was lower than that estimated by the ratios of other ions. From the present study, it seems that the freezing process plays an important role in the nitrite sink process in the tropospheric aqueous phase.     

Aminostratigraphy and sea-level history of the Pleistocene Bridgewater Formation,Mount Gambier region,southern Australia

A geochronological framework based on amino acid racemisation (AAR) and constrained by previously reported optically stimulated luminescence (OSL) ages is presented for the evolution and paleosea-level record of the Pleistocene Bridgewater Formation of the Mount Gambier region, of southern Australia. Within the study area, the Bridgewater Formation is represented by late early Pleistocene [Marine Isotope Stage (MIS) 23 at 933 ka] to Holocene barrier shoreline successions deposited during sea-level highstands. Regional monotonic uplift (0.13 mm yr^–1) and pervasive calcrete development during the Pleistocene have preserved the sequence of calcarenite (mixed quartz-skeletal carbonate sand) shoreline complexes from denudation. AAR analyses confirm that the barriers generally increase in age landwards and correlate with sea-level highstands associated with interglacials as defined by the marine oxygen isotope record. AAR analyses on the benthic foraminifer Elphidium crispum have proved more reliable than the whole-rock method in extending the age range of AAR dating of these relict shoreline successions. Paleosea-levels from the coastal plain are as follows: MIS 7, –9 ± 2 m; MIS 9, 4 ± 1 m; and a minimum sea-level of 2 ± 2 m is derived for MIS 11. Paleosea-level could not be determined for MIS 15, 19 or 23 as diagnostic sea-level indicators were not identified within these sedimentary successions. Dismal Range, dated at 933 ± 145 ka (MIS 23), represents a correlative feature to the East Naracoorte Range but is some 25 km seaward of the Kanawinka Fault compared with the same barrier at Naracoorte. Mingbool Range (788 ± 18 ka) is of similar age to the West Naracoorte Range (MIS 19) and formed as an arcuate shoreline complex that became attached to the higher relief of the area represented by the Mount Burr Volcanic Province. The higher topographical relief resulted from crustal doming of the Oligo-Miocene Gambier Limestone caused by the intrusion of magma associated with the volcanic province. The AAR age of 788 ± 118 ka for Mingbool Range indicates that the Mount Burr volcanics predate the deposition of this shoreline complex.