二水硫酸钙结晶动力学研究

主要研究了过饱和溶液中CaSO4 ·2H2 O晶体成核及生长现象 ,同时对垢的形成机理进行了探讨。实验表明 ,成核延迟时间随溶液过饱和度增大而减小 ;CaSO4 ·2H2 O晶体生长属于表面反应控制 ,且与粒径相关 ,当温度为 3 0℃ ,粒径为2 8～ 67μm ,Ca2 + 浓度为 0 .0 3 5mol/L时 ,晶体生长速度在 0 .5× 10 - 8～ 5 .8× 10 - 8m/s之间     

湖北省宜昌硅钙质磷块岩选矿工艺研究

湖北省宜昌硅钙质沉积磷块岩,是难选的中低品位沉积磷块岩,主要磷酸盐矿物为泥晶磷灰石,主要脉石矿物为白云石、石英、玉髓.从获得高品位精矿、高回收率选矿工艺指标的角度,对含泥量较高的中低品位硅钙质沉积磷块岩,进行选矿工艺研究。确定分级-反浮选（常温）最佳选矿工艺路线为：选矿技术指标为磨矿细度-0．074mm（-200目）,含量占67．7％,原矿品位P2O5 25．89％,精矿产率58．61％、品位P2O5 35．22％,回收率80．00％.通过工艺流程试验研究的论述,旨在向年轻的选矿工作者传达一种工作思路,同时对于选别同类型磷矿的矿山企业也有一定的参考价值、     

菹草(Potamogeton crispus)叶面CaCO3-P沉淀物产生的关键影响因子分析

沉水植物光合作用形成的微环境有利于水体中钙和磷形成CaCO₃-P共沉淀,但在不同水环境因子下水体中钙和磷形成CaCO₃-P共沉淀的能力不同。本研究以菹草(Potamogeton crispus)为研究对象,研究不同钙浓度(0、20、35、50、65 mg/L)、碱度(0、100、200、300、400 mg/L CaCO₃)、磷浓度(0、0.1、0.2、0.3、0.4 mg/L)和温度(11、14、17、20℃)对菹草削减水体磷的能力及对CaCO₃-P共沉淀产生的差异,并通过分析无植物对照组培养液的饱和指数变化趋势,揭示植物介导下CaCO₃-P的发生规律,为湖泊生态修复中沉水植物的选择提供理论依据。结果表明:①在菹草培养组中,总磷(TP)和溶解性磷酸盐(SRP)浓度显著下降,并且不同处理组之间存在显著差异。随着钙浓度的增加,各处理组的TP和SRP浓度均呈减小趋势,而添加钙浓度导致减幅进一步提高。相比之下,在无菹草对照组中,TP和SRP浓度没有显著变化。这表明菹草的引入促进了水中磷的去除效率。②各处理组CaCO₃-P共沉淀量随碱度的增加而增加,碱度为400 mg/L CaCO₃时,产生最大CaCO₃-P共沉淀量,说明菹草在碱性水环境中更有利于产生CaCO₃-P共沉淀。共沉淀在中等磷水平(0.2 mg/L)产生量最高,每株菹草每天平均产生23.12 mg共沉淀量。实验验证了自然水体磷浓度对菹草叶面CaCO₃-P共沉淀量的产生差异较小,共沉淀在中等温度水平(17℃)含量最高,每株菹草每天平均产生16.61 mg共沉淀量,说明菹草在适宜温度下产生共沉淀的差异不大。以上结果表明,碱度相较于磷浓度及温度对菹草的CaCO₃-P共沉淀量影响更大。③在水环境因子相同的情况下,无菹草对照组碳酸钙饱和指数(方解石和霰石饱和指数)均大于0,说明有结晶趋势,但在实验期间并未产生沉淀,而添加菹草的处理组产生了不等量的CaCO₃-P共沉淀,表明沉水植物也可通过共沉淀的方式削减水体磷负荷,为湖泊富营养化的治理提供理论支撑。     

三元体系CaCl2-SrCl2-H2O相平衡在高钙锶比卤水体系中分离提取氯化锶的应用

采用等温溶解平衡法测定了三元体系CaCl₂-SrCl₂-H₂O温度在353.15 K时共饱和点的溶解度。基于实验结果和文献已有报道的该体系多温下的相平衡数据,模拟了南翼山油田卤水中氯化钙和氯化锶在温度323.15 K下的分离实验。模拟钙锶分离实验结果表明,物质的量比为25.41∶1的CaCl₂和SrCl₂的混合溶液在323.15 K下蒸发结晶提纯后的固相中钙锶物质的量比降低为1.73∶1,SrCl₂的回收率为52.47%,将所得一次固相产品在323.15 K下溶解并再次蒸发后,钙和锶的物质的量比从1.73∶1降至1.1∶1,SrCl₂的回收率为78.67%,SrCl₂的总回收率为41.28%。     

乌贼墨黑色素对铅中毒小鼠的排铅作用及其对体内钙、锌和铜含量的影响

本文研究了乌贼墨黑色素对铅中毒小鼠的排铅作用及对小鼠体内钙、锌和铜含量的影响。采用48只小鼠为实验对象,按体质量随机分为阴性对照组,醋酸铅模型对照组,乌贼墨黑色素低(50mg/kg)、中(100mg/kg)、高(200mg/kg)剂量组以及阳性对照组(1.5g/60 kg),除阴性对照组外其余各组均每天腹腔注射醋酸铅溶液(7mg/kg)10天。第11天起各剂量组用乌贼墨黑色素灌胃,阴性对照组及醋酸铅模型对照组灌胃去离子水,阳性对照组灌胃二巯基丁二酸(DMSA),连续进行28d。采用原子吸收分光光度法测定小鼠的血液、肝、肾及脑组织中的铅、钙、锌和铜的含量。研究发现乌贼墨黑色素高剂量组(200mg/kg)显著降低了血铅含量,下降28.15%;乌贼墨黑色素中剂量组(100mg/kg)显著降低了肝铅含量,下降15.89%。同时,乌贼墨黑色素高剂量组对铅中毒小鼠肝铜、肾锌以及脑锌的含量高于醋酸铅模型对照组(P0.05),而与阴性对照组相比无统计学差异(P0.05)。以上结果表明高剂量、中剂量乌贼墨黑色素对血铅与肝铅有一定的排铅作用,同时高剂量的乌贼墨黑色素对小鼠肝脏中的铜、肾脏中的锌以及脑中的锌有保护作用。     

Phosphorus in Bottom Sediments of Pomeranian Bay (Southern Baltic—Poland)

The paper presents the results of determination of inorganic and organic forms of phosphorus in bottom sediments of Pomeranian Bay. The sediments were collected in March and July of 1996. The following characteristics of the sediments were determined: organic matter content, forms of inorganic phosphorus: loosely adsorbed phosphorus and phosphorus bound to aluminium, calcium and iron, as well as total inorganic phosphorus. Pomeranian Bay is a shallow basin, with depth averaging between 12 and 15 m and sandy sediments prevailing. Smaller silt fractions occur only in the vicinity of the wina River estuary and in deeper northern regions of the Bay. Calcium-bound phosphorus is the dominant form of inorganic phosphorus in the Pomeranian Bay. Iron-bound phosphorus is the second most prevailing form, and aluminium-bound phosphorus the third. Loosely bound phosphorus was present in the lowest amounts. Total inorganic phosphorus in the Bay consisted of the four forms listed above, except in estuarine regions where an additional form of phosphorus occurred, most probably occluded phosphorus. High organic phosphorus concentrations were found at the wina River estuary and in the northern part of the Bay (Saßnitz Deep) corresponding to the higher organic matter content of these sediments. Sediments of Pomeranian Bay contained less phosphorus than those from the Gulf of Gda sk or Puck Bay and other parts of the Baltic Sea, suggesting that the amount of phosphorus in the sediments was determined by a number of inter-related factors, such as sediment type, amount of organic matter, the chemical composition of the sediment and oxygen content of near-bottom water.     

羽毛复合氨基酸钙配合物降解有机磷农药的研究

有机磷农药在我国农作物生产中已被广泛应用,但常因使用不当造成作物产品中残留超标。采用硫酸水解羽毛制取复合氨基酸,并与碳酸钙反应制得复合氨基酸钙配合物,该配合物可以通过水解有机磷农药中的磷酸酯键降低作物中的农药残留。将配合物分别喷施已施有机磷农药的茶叶、黄瓜和西红柿,5d后采摘茶叶鲜叶,按绿茶加工工艺进行处理,测定其毒死蜱含量,毒死蜱的残留量减少了75.80%;喷施配合物次日采摘黄瓜和西红柿样品,并测定其毒死蜱与乐果的残留量,黄瓜中毒死蜱残留量为空白对照的70.75%,乐果完全降解;西红柿中毒死蜱残留量为空白对照的71.33%,乐果的残留量为67.79%。     

末次间冰期以来渭河上游气候演化的黄土记录研究

对渭河上游樊家台剖面末次间冰期以来黄土地层的粒度与CaCO3进行综合分析表明,末次间冰期时,受夏季风影响较大,粒度较细,CaCO3有较强的淋溶与淀积,气候呈现较为暖湿的特点;末次冰期时,受冬季风影响较强,粒度较粗,CaCO3淋溶淀积微弱,气候较为干冷。间冰期早期（相当于深海氧同位5e阶段）由于夏季风较强,粉尘堆积较少,古土壤向下发育,并与下部土壤融合,导致粒度较5a、5c阶段粗;2阶段的早期,由于粉尘源区出现了高湖面,环境湿度大,造成此时段早期黄土粒度较晚期细;表现出区域气候的特点。     

Analysis of Ca+ K plage area for short period variation

We have analysed the observations of Solar Ca⁺K daily plage area for the period 1951-1977 to find evidence for the existence of short period (around 12–13 days) variation in the data. We divided the data in three groups—two corresponding to 10–20‡N and 10–20‡S latitude belts, and one corresponding to the total plage area—and used the power spectrum and autocorrelation techniques for the analysis. Both the techniques clearly show the 27-day periodicity due to solar rotation modulation in all the sets. A 12–13 day periodicity is seen in only 3, out of a total of 57 data sets when autocorrelation technique is used. A generally weak peak around 12–13 days is, however, seen in the power spectrum of all the data sets. The relative power in the 12–13 day peak is found to be significantly higher in those three data sets where the autocorrelation also shows this periodicity. On these two epochs the sunspot area distribution showed the existence of two distinct active longitudes separated by about 140–170 degrees. This seems to be the cause for the existence of a periodicity around 12–13 days in the autocorrelation and enhancement in the relative power of the 12–13 days peak in the power spectrum of these two epochs     

Characterization of lake water and ground water movement in the littoral zone of Williams Lake,a closed‐basin lake in north central Minnesota

Williams Lake, Minnesota is a closed‐basin lake that is a flow‐through system with respect to ground water. Ground‐water input represents half of the annual water input and most of the chemical input to the lake. Chemical budgets indicate that the lake is a sink for calcium, yet surficial sediments contain little calcium carbonate. Sediment pore‐water samplers (peepers) were used to characterize solute fluxes at the lake‐water–ground‐water interface in the littoral zone and resolve the apparent disparity between the chemical budget and sediment data. Pore‐water depth profiles of the stable isotopes δ¹⁸O and δ²H were non‐linear where ground water seeped into the lake, with a sharp transition from lake‐water values to ground‐water values in the top 10 cm of sediment. These data indicate that advective inflow to the lake is the primary mechanism for solute flux from ground water. Linear interstitial velocities determined from δ²H profiles (316 to 528 cm/yr) were consistent with velocities determined independently from water budget data and sediment porosity (366 cm/yr). Stable isotope profiles were generally linear where water flowed out of the lake into ground water. However, calcium profiles were not linear in the same area and varied in response to input of calcium carbonate from the littoral zone and subsequent dissolution. The comparison of pore‐water calcium profiles to pore‐water stable isotope profiles indicate calcium is not conservative. Based on the previous understanding that 40–50 % of the calcium in Williams Lake is retained, the pore‐water profiles indicate aquatic plants in the littoral zone are recycling the retained portion of calcium. The difference between the pore‐water depth profiles of calcium and δ¹⁸O and δ²H demonstrate the importance of using stable isotopes to evaluate flow direction and source through the lake‐water–ground‐water interface and evaluate mechanisms controlling the chemical balance of lakes. Published in 2003 by John Wiley & Sons, Ltd.