秦岭山地丹江流域土地利用变化的土壤侵蚀效应评价

论文采用ArcGIS 10.0及InVEST土壤保持模型,分析2000—2010年秦岭山地丹江流域土地利用类型变化特征,模拟流域不同时期不同土地利用类型土壤侵蚀及土壤保持量的变化规律,并着重探讨土地利用类型方式转变对流域土壤侵蚀的影响。结果表明：1）2000—2010年间,流域裸地大比例减少90.18%（831.06 hm²）,主要转移至水域,耕地大面积减少5 197.24 hm²（4.11%）,主要流向灌丛和城镇;坡耕地还林还草初见成效,湿地的保护与恢复成效显著。2）2000—2010年间,流域土壤侵蚀状况较为严重,整体处于中度侵蚀至强度侵蚀级别,但10 a间侵蚀状况有减缓趋势;在该研究时段内,耕地大面积转为灌丛是该流域由土地利用类型变化引起的土壤侵蚀减缓的主要原因;另外,耕地转为林地以及裸地面积的减少也起到了减轻土壤侵蚀的作用;以自然生态系统为主的林地、灌丛及草地转为耕地时,土壤侵蚀强度则会明显增加。3）生态系统土壤保持功能受多方因素共同影响;2000、2010年研究区实际土壤保持量分别为5.35×10⁸、5.47×10⁸ t;占全区面积一半以上的林地和灌丛单位面积土壤保持量较为稳定,全区土壤保持功能有所提高。保证一定面积的林地、在人工干预下合理安排坡耕地还林还草区域的空间分布是秦岭山地丹江流域减少土壤侵蚀的必要措施,同时应注重对可利用耕地的保护。     

Inhibition of pyrite oxidation by surface coating: a long-term field study

Pyrite and other iron sulfides are readily oxidized by dissolved oxygen in aqueous phase, producing acidity and Fe²⁺, which causes significant environmental problems. Applications of surface coating agents (Na₂SiO₃ and KH₂PO₄) were conducted at Boeun (Chungbuk, South Korea) outcrop site, and their efficiencies to inhibit the oxidation of sulfide minerals were monitored for a long-term period (449 days). The rock sample showed positive Net Acid Production Potential (NAPP = 20.23) and low Net Acid Generation pH (NAGpH = 2.42) values, suggesting that the rock sample was categorized in the potential acid-forming group. For the monitored time period (449 days), field study results showed that the application of Na₂SiO₃ effectively inhibited the pyrite oxidation as compared to KH₂PO₄. Na₂SiO₃ as a surface coating agent maintained pH 5–6 and reduced oxidation of pyrite surface up to 99.95 and 97.70 % indicated by Fe²⁺ and SO₄ ^2? release, respectively. The scanning electron microscope and energy-dispersive X-ray spectrometer analysis indicated that the morphology of rock surface was completely changed attributable to formation of iron silicate coating. The experimental results suggested that the treatment with Na₂SiO₃ was highly effective and it might be applicable on field for inhibition of iron sulfide oxidation.     

新生鼠PFOS低剂量慢暴露对成年后神经行为的影响

为观察新生鼠全氟辛烷磺酸(PFOS)低剂量慢暴露对其成年后神经行为和海马组织影响,选取出生后5-7 d雄性SD幼鼠80只,按体重随机分为4组,分别为对照组(Con)、低剂量组(P5)、中剂量组(P10)、高剂量组(P20),每组各20只。从PND7开始染毒,共染毒12周,动态记录体重,并进行水迷宫、旷场实验、滚轮实验观察神经行为变化,同时取材进行HE染色,观察海马形态学改变。结果显示与Con组比较,P20组染毒8 d后出现体重增长减缓(P0.05),4周时P10和P20组死亡率明显升高;并且P10、P20组在4周,P5组在8周时,水迷宫实验逃逸潜伏期延长,目标象限停留时间缩短;P10、P20组大鼠在4周,P5组在8周时,旷场实验中央格停留时间延长,站立次数减少,行走总距离缩短;滚轮试验中,对照组和P5组肢体运动协调能力无显著性差异。P5组在染毒12周时出现海马神经元排列紊乱,胞核固缩及胞体胀大,CA1区细胞和齿状回闩区神经前体细胞数量明显少于Con组(P0.01)。上述结果表明,大鼠幼年PFOS低剂量慢暴露可损害其成年后空间学习记忆及自主探究能力,这种损害可能与海马神经元发生不足有关     

Improved blending strategy for membrane modification by virtue of surface segregation using surface-tailored amphiphilic nanoparticles

Membrane modification is one of the most feasible and effective solutions to membrane fouling problem which tenaciously hampers the further augmentation of membrane separation technology. Blending modification with nanoparticles (NPs), owing to the convenience of being incorporated in established membrane production lines, possesses an advantageous viability in practical applications. However, the existing blending strategy suffers from a low utilization efficiency due to NP encasement by membrane matrix. The current study proposed an improved blending modification approach with amphiphilic NPs (aNPs), which were prepared through silanization using 3-(Trimethoxysilyl)propyl methacrylate (TMSPMA) as coupling agents and ZnO or SiO₂ as pristine NPs (pNPs), respectively. The Fourier transform infrared and X-ray photoelectron spectroscopy analyses revealed the presence of appropriate organic components in both the ZnO and SiO₂ aNPs, which verified the success of the silanization process. As compared with the pristine and conventional pNP-blended membranes, both the ZnO aNP-blended and SiO₂ aNP-blended membranes with proper silanization (100% and 200%w/w) achieved a significantly increased blending efficiency with more NPs scattering on the internal and external membrane surfaces under scanning electron microscope observation. This improvement contributed to the increase of membrane hydrophilicity. Nevertheless, an extra dosage of the TMSPMA led to an encasement of NPs, thereby adversely affecting the properties of the resultant membranes. On the basis of all the tests, 100% (w/w) was selected as the optimum TMSPMA dosage for blending modification for both the ZnO and SiO₂ types.

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金盆水库汛期高浊水径流的潜入及热分层水体水质响应

以西安金盆水库为研究对象,在汛期通过对河流区至库区的水温、浊度、DO和营养盐等水质指标进行连续监测,探究降雨径流的潜入规律及热分层水体水质动态响应特性.结果表明:在外界气温变化条件下,水库出现季节性热分层现象.汛期径流的汇入导致下温跃层消亡,热分层稳定性减弱;汛期径流水体携带大量颗粒态营养盐物质和泥沙以异重流形式潜入,其流态从过渡区的底层潜流向主库区间层流转变,潜入初期间层流厚度达20m.降雨早期异重流的潜入导致中下层水体的TN、TP、TOC显著增加,水体平均TN、TP、TOC、浊度最高分别超出平时0.2,2,0.6,16倍,水质呈现短时高污染负荷.底层潜流水体水温较高,大量沉降于沉积物中的颗粒态污染物分解速率加快,內源污染负荷进一步提高,底层水体中TN、TP、TOC浓度高达1.88,0.05,4.6mg/L;汛期可通过分层取水方案和排放高浊水来保障供水安全.     

基于霍尔三维结构绿色建筑标准体系构建研究

为了建立科学的标准体系并能保证标准之间的协调性,通过分析标准体系层次性和复杂性的特点,引入霍尔三维结构理论,从目标、专业、时间3个维度构建覆盖绿色建筑全生命周期的标准体系。     

超高效液相色谱-串联质谱法测定污水中14种有机磷酸酯阻燃剂

建立了超高效液相色谱-串联质谱(UPLC-MS/MS)联用法同时测定污水中14种有机磷酸酯阻燃剂(OPEs)的分析方法.样品采集后,经GF/C膜过滤,HLB固相萃取小柱净化后进样分析.以BEH C18色谱柱为分离柱,乙腈和水混合液为流动相(0.2 mL min-1)梯度洗脱,15 min内可完成14种OPEs的分离.在电喷雾正离子模式下,采用多反应监测模式(MRM)进行质谱测定.在加标浓度为1.0μg·L-1时,14种OPEs在污水处理厂进水和出水中的回收率分别为52.1%—119%、43.6%—114%,相对标准偏差(RSD)分别为1.2%—16.2%、0.4%—9.2%,方法的检出限(LOD)在0.3—6.0 ng·L-1间.方法精密度好,准确度高,可满足同时对污水样品中的14种OPEs进行定性及定量分析的要求.     

陡河水库鱼体汞的生物积累初探

为了解陡河燃煤电厂大气汞释放对毗邻的陡河水库水生生态系统中鱼体汞含量、生物积累和放大等的影响,本研究采集陡河水库野生鱼、虾和螺蛳,分别测定了鱼样等生物样品中的总汞和甲基汞,并对部分代表性样品测定稳定碳氮同位素比值。鱼汞分布特征和δ13C‰和δ15N‰同位素比值分布特征显示:鱼体(鲜样)中总汞和甲基汞平均含量分别为56.4±26.7和15.5±8.4 ng·g-1,总汞含量最高的是杂食性的白条鱼为133 ng·g-1。不同食性的鱼体δ13C和δ15N稳定同位素值变化范围分别为-28.1‰~-24.4‰和12.0‰~16.1‰,Log10[Hg]与δ15N的线性相关斜率值为负值。以上结果表明:陡河水库鱼体汞总体偏低,没有发现高生物积累和生物放大,其主要原因在于陡河水库水环境中汞含量较低,且陡河水库靠近市区,过度捕捞使可以捕获的鱼样种类和数量偏少,且鱼龄较低。     

硅藻土地区桥梁灌注桩成孔测试研究∗

硅藻土作为一种特殊的黏性土,在分布上具有一定的区域性,目前针对该类型土的工程特性以及硅藻土地区灌注桩成孔方法的研究都较少。以杭绍台高铁项目为工程依托,为了研究硅藻土层中灌注桩的成孔方法,开展了灌注桩成孔方法现场试验;分别采用冲击锤锤击成孔、旋挖干钻成孔和旋挖泥浆护壁成孔三种方法进行施工,对三种方法的成孔质量进行分析对比。研究结果表明:在硅藻土地区施工灌注桩,旋挖干钻成孔工艺施工速度较快,效率高,桩长、桩径、桩位偏差和垂直度均能满足设计要求,成孔后孔壁稳定性好,成孔质量更为可靠;冲击锤法成孔,成孔速度较慢,且存在桩孔扩径现象;旋挖泥浆护壁法成孔后平稳性较差,波动性较大,且存在局部塌孔现象,成孔效果较差。因此建议硅藻土地段优先考虑采用旋挖干钻法施工桥梁灌注桩。     

Low-temperature CO oxidation over Au-doped 13X-type zeolite catalysts: preparation and catalytic activity

Au-supported 13X-type zeolite (Au/13X) was synthesized using a common deposition–precipitation (DP) method with a solution of sodium carbonate as a precipitate agent. Further testing was conducted to test for catalytic oxidation of CO. A study was conducted on the effects of different preparation conditions (i.e., chloroauric acid concentration, solution temperature, pH of solution, and calcinations temperature) on Au/13X for CO oxidation. In respect to the catalytic activity, the relationship between different the preparation conditions and gold particles in 13X zeolite was analyzed using X-ray diffraction, TEM and XPS. The activity of Au/13X catalysts in CO oxidation was dependent on the chloroauric acid concentration. From XRD results, a higher chloroauric acid concentration induced larger gold nanoparticles, which resulted in lower catalytic activity. Results revealed that higher temperatures induced higher Au loading, homogeneous deposit, and smaller gold clusters on the support of 13X, resulting in higher CO activity. Furthermore, a pH of 5 or 6 generated greater amounts of Au loading and smaller Au particles on 13X than at a pH of 8 or 9. This may be a result of an effective exchange between Au(OH)2Cl2- and Au(OH)₃Cl^- on specific surface sites of zeolite under the pH’s 5 and 6. The sample calcined at 300°C showed the highest activity, which may be due to the sample’s calcined at 200°C inability to decompose completely to metallic gold while the sample calcined at 400°C had larger particles of gold deposited on the support. It can be concluded from this study that Au/13X prepared from a gold solution with an initial chloroauric acid solution concentration of 1.5 × 10^-3 mol·L^-1 gold solution pH of 6, solution temperature of around 90°C, and a calcination temperature of 300°C provides optimum catalytic activity for CO oxidation.