论湘中城市群经济的融合耦动与可持续发展

本文以湘中（长株潭）城市群作为研究对象,概述了湘中城市群经济融合的总体特征,对其城市群空间生长演化过程中存在的问题和应采取的对策,经济如何实现可持续发展进行了探讨。     

Growth responses of the newly-discovered Cd-hyperaccumulator Rorippa globosa and its accumulation characteristics of Cd and As under joint stress of Cd and As

Rorippa globosa has been identified as a newly-found Cd-hyperaccumulating species. In the present study, growth responses of Rorippa globosa and its accumulation characteristics of Cd and As were examined under joint stress of Cd and As. The results showed that Cd and As had an antagonistic effect on enhancing the growth of Rorippa globosa plants and Cd uptake and accumulation under the low concentration Cd and As treatments. When the concentration of Cd in the soil was 10 mg/kg and the concentration of As was 50 mg/kg, the highest growing height of the plant was up to 35.9 cm and the dry weight of the shoots was up to 2.2 g/pot, respectively. Meanwhile, the accumulation of Cd in the leaves under the joint stress was higher than that at the same level under single Cd pollution. However, there were synergic adverse effects on plant growth and Cd uptake under the combined pollution from a high concentration of Cd and As. Meanwhile, the accumulation of As in the roots was greater than that in the shoots, the translocation factor (TF) was ?0.3 and the bioaccumulation factor (BF) was ?0.6, thus showing that Rorippa globosa had an excluding effect on As uptake. These results confirmed that Rorippa globosa had a strong tolerant ability to the joint stress of Cd and As, and the potential for phytoremediation of soils contaminated by Cd and As.     

Biogenic volatile organic compound analyses by PTR-TOF-MS: Calibration, humidity effect and reduced electric field dependency

Green leaf volatiles(GLVs) emitted by plants after stress or damage induction are a major part of biogenic volatile organic compounds(BVOCs). Proton transfer reaction time-of-flight mass spectrometry(PTR-TOF-MS) is a high-resolution and sensitive technique for in situ GLV analyses, while its performance is dramatically influenced by humidity, electric field,etc. In this study the influence of gas humidity and the effect of reduced field(E/N) were examined in addition to measuring calibration curves for the GLVs. Calibration curves measured for seven of the GLVs in dry air were linear, with sensitivities ranging from 5 to10 ncps/ppbv(normalized counts per second/parts per billion by volume). The sensitivities for most GLV analyses were found to increase by between 20% and 35% when the humidity of the sample gas was raised from 0% to 70% relative humidity(RH) at 21°C, with the exception of(E)-2-hexenol. Product ion branching ratios were also affected by humidity,with the relative abundance of the protonated molecular ions and higher mass fragment ions increasing with humidity. The effect of reduced field(E/N) on the fragmentation of GLVs was examined in the drift tube of the PTR-TOF-MS. The structurally similar GLVs are acutely susceptible to fragmentation following ionization and the fragmentation patterns are highly dependent on E/N. Overall the measured fragmentation patterns contain sufficient information to permit at least partial separation and identification of the isomeric GLVs by looking at differences in their fragmentation patterns at high and low E/N.     

Activated carbon coated palygorskite as adsorbent by activation and its adsorption for methylene blue

An activation process for developing the surface and porous structure of palygorskite/carbon(PG/C) nanocomposite using ZnC l2 as activating agent was investigated. The obtained activated PG/C was characterized by X-ray diffraction(XRD), Fourier transform infrared spectroscopy(FTIR), field-emission scanning electron microscopy(SEM), and Brunauer–Emmett–Teller analysis(BET) techniques. The effects of activation conditions were examined,including activation temperature and impregnation ratio. With increased temperature and impregnation ratio, the collapse of the palygorskite crystal structure was found to accelerate and the carbon coated on the surface underwent further carbonization. XRD and SEM data confirmed that the palygorskite structure was destroyed and the carbon structure was developed during activation. The presence of the characteristic absorption peaks of C_C and C–H vibrations in the FTIR spectra suggested the occurrence of aromatization. The BET surface area improved by more than 11-fold(1201 m2/g for activated PG/C vs. 106 m2/g for PG/C) after activation, and the material appeared to be mainly microporous. The maximum adsorption capacity of methylene blue onto the activated PG/C reached 351 mg/g. The activated PG/C demonstrated better compressive strength than activated carbon without palygorskite clay.     

Do vehicular emissions dominate the source of C6–C8 aromatics in the megacity Shanghai of eastern China?

The characteristic ratios of volatile organic compounds(VOCs) to i-pentane, the indicator of vehicular emissions, were employed to apportion the vehicular and non-vehicular contributions to reactive species in urban Shanghai. Two kinds of tunnel experiments, one tunnel with more than 90% light duty gasoline vehicles and the other with more than 60% light duty diesel vehicles, were carried out to study the characteristic ratios of vehicle-related emissions from December 2009 to January 2010. Based on the experiments, the characteristic ratios of C6–C8aromatics to i-pentane of vehicular emissions were 0.53 ± 0.08(benzene), 0.70 ± 0.12(toluene),0.41 ± 0.09(m,p-xylenes), 0.16 ± 0.04(o-xylene), 0.023 ± 0.011(styrene), and 0.15 ± 0.02(ethylbenzene), respectively. The source apportionment results showed that around 23.3% of C6–C8 aromatics in urban Shanghai were from vehicular emissions, which meant that the non-vehicular emissions had more importance. These findings suggested that emission control of non-vehicular sources, i.e. industrial emissions, should also receive attention in addition to the control of vehicle-related emissions in Shanghai. The chemical removal of VOCs during the transport from emissions to the receptor site had a large impact on the apportionment results. Generally, the overestimation of vehicular contributions would occur when the VOC reaction rate constant with OH radicals(k OH) was larger than that of the vehicular indicator, while for species with smaller k OH than the vehicular indicator, the vehicular contribution would be underestimated by the method of characteristic ratios.     

HF对Cu-SSZ-13/堇青石的原位合成及脱除NO_x的影响

以Cu-TEPA为模板剂原位水热合成一系列具有优良deNOx特性的Cu-SSZ-13/堇青石整体式催化剂.为进一步改善其氨的选择性催化还原氮氧化物的活性,在制备过程中添加HF对原位制备Cu-SSZ-13/堇青石整体式催化剂进行改性.利用XRD、SEM、XPS、BET、ICP-AES等对样品进行了表征.结果表明,当nHF/nAl在0.015—0.0375时,晶化72 h的Cu-SSZ-13/堇青石表现出了优异的脱硝性能和抗老化性能,其最大转化率为99.8%,NOx转化率保持在90%以上的最宽活性温度窗口为280—640℃,而无HF的新鲜样品的NOx转化率保持在90%以上的活性温度窗口为300—580℃;720℃老化50 h处理后,nHF/nAl=0.015—0.0375样品的NOx转化率保持在90%以上的最宽活性温度窗口为360—520℃,未添加HF的老化样品相应的活性温度窗口为400—500℃.无论新鲜还是老化,nHF/nAl=0.015—0.0375样品在低温段200—300℃和高温段500—700℃的NOx转化率基本都大于未添加HF的样品.结合表征结果,在催化剂原位水热合成过程中HF的加入既提高了样品的相对结晶度和负载量,又增大了样品的比表面积和比孔容,且提高了Cu-SSZ-13/堇青石骨架结构的稳定性,进而在一定程度上改善了Cu-SSZ-13/堇青石的高温脱硝活性和水热稳定性.     

不同基质组合对氮磷吸附能力的研究

就地利用菜地改建小型湿地系统可能是实现农村生活污水消纳和资源化利用的一种有效途径,其中菜园土与吸附基质的组合直接关系水体污染物中氮磷的净化效果. 选取沸石、谷壳、活性炭、陶粒和菜园土作为试验基质,使用BET比表面积孔径分析仪、扫描电子显微镜和Ｘ射线衍射仪(EDX)对其进行表征,通过等温吸附试验分别筛选出对氮磷吸附效果较好的沸石和陶粒,设置菜园土∶陶粒∶沸石质量占比基质组合:F1(10∶0∶0)、F2(6∶2∶2)、F3(8∶1∶1)、F4(8∶2∶0)、F5(8∶0∶2)、F6(6∶1∶3)和F7(6∶3∶1). 在低、中、高3种氮磷浓度下,通过吸附动力学试验筛选出去除效果最好的基质组合. 结果表明:①5种单一基质中,活性炭、陶粒的比表面积(35.72、33.23 m2/g)和微孔体积(2.20×10?1、8.25×10?2 cm2/g)均较大;沸石和陶粒表面呈粗糙多孔结构. ②Freundlich和Langmuir等温吸附模型均能较好地拟合5种单一基质对氮磷的吸附,各基质对氮的饱和吸附量表现为沸石(2.00 mg/g)>陶粒(1.47 mg/g)>菜园土(1.17 mg/g)>活性炭(0.99 mg/g)>谷壳(0.21 mg/g),对磷的饱和吸附量表现为陶粒(1.28 mg/g)>活性炭(1.25 mg/g)>沸石(1.16 mg/g)>谷壳(0.80 mg/g)>菜园土(0.50 mg/g). ③7种基质组合对氮磷吸附具有相似的动力学特征,Elovich模型、双常数速率模型和一级反应动力学模型均能较好地模拟基质组合对不同污染负荷条件下氮磷的吸附规律. ④7种基质组合对氮磷的吸附速率均呈现先快后慢的趋势,最终于12~48 h趋于稳定. 研究显示,F2、F4和F7基质组合对氮磷的去除效果均较好,但考虑菜地改造的简易性和可操作性,F4为最佳基质组合,其在3种不同氮磷浓度下对氮、磷的吸附量分别为0.36~0.68和0.10~0.39 mg/g.      

火焰原子吸收光度法测定水中铝的方法改进

研究了在盐酸介质中，壬基酚聚氧乙烯-7醚（NP-7）活化下，火焰原子吸收光度法测定环境水体中铝的方法改进。在25mL容量瓶中，加入5．0mL体积分数为50％的盐酸、2．0mL质量浓度为0．01g／mL NP-7和4．0mL质量浓度为75．0μg/mL的铝标准溶液，在原子吸收分光光度计的最佳测定条件下测定吸光度。根据吸光度与铝质量浓度绘制了工作曲线，线性范围3．0～24．0μg/mL，检出限1．32μg/mL。该法用于环境水体中铝含量的测定，加标回收率为94．4％～101．4％，最大相对标准偏差5．8％，方法对比最大相对误差4．1％。