情感诉求对交通安全广告效果的影响

为检验交通公益广告中情感诉求变化对广告效果的影响,采用试验法操作广告情感诉求类型,使用眼动技术和Go/no-go联想测验(GNAT),通过比较不同效价和唤醒度的情感诉求广告对受众的注意力和内隐态度的影响,评估交通安全广告情感诉求类型的说服效果。研究发现:被试对低唤醒广告文字区的眼动注视时间和注视点个数显著长于/多于对高唤醒广告文字区的注视时间和注视点个数;被试观看高唤醒消极的广告后,正确驾驶行为的积极态度显著下降,而低唤醒消极/高唤醒积极/低唤醒积极的公益广告对于被试的内隐态度的改变没有显著差异。结果表明,高唤醒度积极广告能够提升受众的注意力,而高唤醒度消极广告则会损害受众对正确驾驶行为的内隐态度。     

1968～2018年洞庭湖江湖连通河道松滋口冲淤变化特征

探究江湖连通河道演变态势是评估重大人类活动事件对江湖关系变化影响的重要环节。以洞庭湖—荆江三口中松滋口河道为研究对象，通过建立其河道长期的水位—流量关系曲线分析其河道的冲淤变化特征，对其河道冲淤变化驱动因素进行分析，并采用实测河道断面资料验证其结果的可靠性。结果表明：水位—流量关系曲线法分析河道地形冲淤演变特征与实测横断面地形资料分析结果一致，松滋口河道同流量下水位下降对应于该时期河道冲刷，同流量下水位上升对应于河道淤积。不同时期松滋口东西分支河道冲淤变化主要驱动因素不同。1968～1981年间，下荆江裁弯引起的河势变化是西支新江口河道冲刷与东支沙道观河道淤积的主要诱因。1981～2003年间，其东西两支河道淤积主要是由于葛洲坝运行后引起的上荆江河道冲刷导致的。2003～2018年间，其河道冲刷主要是由于三峡大坝运行引起的河道水沙比例的大幅改变导致的。     

生态足迹影响因子的定量分析

人口的膨胀和人类工业化进程的加剧，使得人类向自然界获取越来越多的资源，同时向环境源源不断的输入废弃物，已经严重超过了自然生态系统的供给能力和环境容量，生态环境日益恶化，水土流失、草场退化、植被消亡、生物多样性锐减、全球变暖等情况已经严重到难以遏制的地步，危及到人类自身的生存。在和平与发展成为世界两大主题的今天，人们越来越关注可持续发展的问题。在现有资料的基础上，利用主成分分析方法，定量地讨论了中国各省（区市）1999年生态足迹大小与其影响因子间的关系。结果表明，生态足迹的大小是各省（区市）的大中型企业个数、全社会固定生产投资等众多因子共同作用的结果，其中总人口和GDP是生态足迹大小的主要影响因子，其因子载荷量分别达到了0.940和0.913。值得一提的是非农业人口与生态足迹的相关系数超过了农业人口，这说明由于消费模式和生活水平等的差异，非农业人口对生态足迹的影响大于农业人口对生态足迹的影响。在此基础上建立了生态足迹影响因子的多元线性回归模型，以期为生态足迹在进行区域可持续发展评价的方法上提供新的思路。     

湖泊水质模型研究进展

湖泊是最重要的淡水资源之一，对社会和经济的发展起着不可估量的作用。保护和改善湖泊水环境问题已成为当前世界关注的一个焦点。湖泊水质模型是一种利用数学语言来描述湖泊污染过程中的物理、化学、生物化学及生物生态各方面之内在规律和相互联系的手段。作为湖泊水环境污染治理、规划决策分析中的一个重要工具，它可以为湖泊的综合整治和科学管理提供科学的依据，在环境保护领域中发挥着举足轻重的作用。分别介绍了湖泊水质模型国内外研究动态、类型、常用软件（WASP、EFDC、CE QUAL W2、CE QUAL R1、CE QUAL ICM、MIKE、SMS等）和应用实例，并综观湖泊水质模型的研究历史和应用前景，系统分析了湖泊水质模型研究的发展趋势。     

电解锰渣基方沸石的制备及其对Pb2+的吸附性能

以电解锰渣为原料,经过"弱酸除杂-碱融活化-室温陈化-晶化"水热合成反应体系,在分别外加铝源和硅源的条件下制备方沸石ANA-A及ANA-S,运用XRF、XRD、SEM-EDS和BET等表征手段对2种方沸石的化学组成、晶相结构、微观形貌和比表面积进行分析。结果表明:在煅烧温度750℃、合成温度180℃、水热反应时间8 h的条件下,外加铝源和硅源均可合成方沸石。进一步研究2种沸石对水溶液中Pb2+的静态吸附性能,其所合成的电解锰渣基ANA-A及ANA-S方沸石均可以很好地用Langmuir等温模型拟合,属于单分子层吸附,饱和吸附量分别为161.29,185.19 mg/g,对初始浓度为100 mg/L的Pb2+去除率分别为93.69%和95.47%,且均符合Lagergren准二级动力学模型,属于化学吸附;两者中ANA-S的吸附效果更好。     

Hygroscopicity measurement of sodium carbonate, β-alanine and internally mixed β-alanine/Na2CO3 particles by ATR-FTIR

Water-uptakes of pure sodium carbonate(Na_2CO_3),pure β-alanine and internally mixedβ-alanine/Na_2CO_3 aerosol particles with different mole ratios are first monitored using attenuated total reflectance Fourier transform infrared spectroscopy(ATR-FTIR) technique.For pure Na_2CO_3 aerosol particles,combining the absorptions at 877 and 1422 cm-1 with abrupt water loss shows the efflorescence relative humidity(ERH) of 62.9%–51.9%.Upon humidifying,solid Na_2CO_3 firstly absorbs water to from Na_2CO_3·H2 O crystal at 72.0% RH and then deliquesces at 84.5% RH(DRH).As for pure β-alanine particles,the crystallization takes place in the range of 42.4%–33.2% RH and becomes droplets at ～ 88.2% RH.When β-alanine is mixed with Na_2CO_3 at various mole ratios,it shows no efflorescence of Na_2CO_3 whenβ-alanine to Na_2CO_3 mole ratio(OIR) is 2:1.For 1:1 and 1:2 β-alanine/Na_2CO_3 aerosols,the ERHs of Na_2CO_3 are 51.8%–42.3% and 57.1%–42.3%,respectively.While β-alanine crystal appears from 62.7% RH for 2:1 and 59.4% RH for both 1:1 and 1:2 particles and lasts to driest state.On hydration,the DRH is 44.7%–75.2% for Na_2CO_3 with the OIR of 1:1 and 44.7%–69.0%for 1:2 mixture,and those of β-alanine are 74.8% for 2:1 mixture and 68.9% for two others.After the first dehumidification–humidification,all the water contents decrease despite of constituent fraction.And at ～ 92% RH,the remaining water contents are 92%,89% and 82%at ～ 92% RH,corresponding to OIR of 2:1,1:1 and 1:2 mixed system,respectively.     

Synergistic effects of Cu species and acidity of Cu-ZSM-5 on catalytic performance for selective catalytic oxidation of n-butylamine

In this work, a series of Cu-ZSM-5 catalysts with different SiO₂/Al₂O₃ ratios (25, 50, 100 and 200) were synthesized and investigated in n-butylamine catalytic degradation. The n-butylamine can be completely catalytic degradation at 350°C over all Cu-ZSM-5 catalysts. Moreover, Cu-ZSM-5 (25) exhibited the highest selectivity to N₂, exceeding 90% at 350°C. These samples were investigated in detail by several characterizations to illuminate the dependence of the catalytic performance on redox properties, Cu species, and acidity. The characterization results proved that the redox properties and chemisorption oxygen primarily affect n-butylamine conversion. N₂ selectivity was impacted by the Brønsted acidity and the isolated Cu²⁺ species. Meanwhile, the surface acid sites over Cu-ZSM-5 catalysts could influence the formation of Cu species. Furthermore, in situ diffuse reflectance infrared Fourier transform spectra was adopted to explore the reaction mechanism. The Cu-ZSM-5 catalysts are the most prospective catalysts for nitrogen-containing volatile organic compounds removal, and the results in this study could provide new insights into catalysts design for VOC catalytic oxidation.     

Photodegradation of Hexafluoropropylene Oxide Trimer Acid under UV Irradiation

As a novel alternative to traditional perfluoroalkyl substances (PFASs), including perfluorooctanoic acid (PFOA) and perfluorooctane sulfonate (PFOS), hexafluoroproplyene oxide trimer acid (HFPO-TA) has been detected worldwide in surface water. Moreover, recent researches have demonstrated that HFPO-TA has stronger bioaccumulation potential and higher hepatotoxicity than PFOA. To treat these contaminants e.g. PFOA and PFOS, some photochemical techniques by adding exogenous substances had been reported. However, there is still no report for the behavior of HFPO-TA itself under direct UV irradiation. The current study investigated the photo-transformation of HFPO-TA under UV irradiation in aqueous solution. After 72 hr photoreaction, 75% degradation ratio and 25% defluorination ratio were achieved under ambient condition. Reducing active species, i.e., hydrated electrons and active hydrogen atoms, generated from water splitting played dominant roles in degradation of HFPO-TA, which was confirmed by different effects of reaction atmospheres and quenching experiments. A possible degradation pathway was proposed based on the products identification and theoretical calculations. In general, HFPO-TA would be transformed into shorter-chain PFASs, including hexafluoropropylene oxide dimer acid (HFPO-DA), perfluoropropionic acid (PFA) and trifluoroacetate (TFA). This research provides basic information for HFPO-TA photodegradation process and is essential to develop novel remediation techniques for HFPO-TA and other alternatives with similar structures.     

基于SVR的长江经济带水环境承载力评价

基于DPSIRM模型构建区域水环境承载力评价指标体系,并基于SVR模型构建了区域水环境承载力评价模型,利用交叉验证法对SVR模型参数进行优化选择,进一步提高模型预测精度.运用该模型研究了长江经济带2009~2018年的水环境承载力演变趋势及空间差异,结果表明：长江经济带水环境承载力等级整体呈现升高趋势,其中上游城市群承载等级由II级（超载）提升到了IV级（弱可承载）;中游城市群承载等级由II级（超载）提升到了IV级（弱可承载）;下游长三角区域承载等级由I级（重超载）提升到了IV级（弱可承载）.将评价结果与熵权-TOPSIS法的评价结果相比较,相同率达到91.7%,说明SVR模型评价区域水环境承载力可行,评价结果可靠.以下游区域为例,分别对其6个子系统的承载力进行剖析,并运用单因素轮换OAT法对各子系统内的评价指标进行敏感性分析,便于决策者识别指标敏感性.     

洪泽湖不同入湖河流沉积物磷形态特征及生物有效性

为揭示洪泽湖入湖河流沉积物磷形态空间差异性及影响因素,分析了洪泽湖自西北向西南7条入湖河流65个表层沉积物中不同磷（P）形态,并探讨了磷形态空间赋存特征的影响因素及环境意义.研究表明：沉积物总磷（TP）含量为488.90mg/kg~960.22mg/kg,无机磷（Pi）为主要形态,相对含量为65.81%~76.16%.西部入湖流域沉积物有机磷（Po）以非活性有机磷（NLOP）为主,汴河最高,相对含量约占Po的50.41%,生物有效态无机磷（BAP）相对含量最高,占Pi的66.84%,污染程度最高;西南和西北入湖流域Po则以中活性有机磷（MLOP）为主,Pi以钙结合态无机磷（HCl-Pi）为主.西北入湖流域由于受当地地质背景的影响,HCl-Pi所占Pi相对含量最高（43.02%）,从而减缓了磷的移动能力,污染程度最低.随着沉积物污染程度的增加,生物有效态Po含量增加,但所占Po相对含量降低;HCl-Pi含量增加,所占Pi相对含量降低,这一现象和我国其它典型地区沉积物磷形态空间分布类似.西部和西南入湖流域主要受水土流失、有机面源污染及藻类生长的影响,有机质环境较高,水交换能力弱,可被有机质降解的Po组分高于可被矿化的Po组分,大部分难降解Po组分易沉积,导致西部和西南入湖流域较高的BAP和NLOP含量,富营养化程度较高.沉积物OM是各形态磷之间相互转化的关键因素,和沉积物内源磷地球生物化学循环密切相关.洪泽湖入湖流域沉积物磷形态空间差异性主要由农业面源污染物的输入而导致内源磷负荷加剧.洪泽湖西部和西南入湖流域应重点控制农田水土流失及养殖业面源污染,建设滨岸修复带,遵循少量多次增施有机肥原则,减少农用地水土流失.健全农村养殖业废水废渣处理;划定科学养殖区;提倡铜围网箱,增加水体交换率.而对于洪泽湖西北入湖流域则应重点防止过度城镇化带来的水土流失及对生态功能保护区过高的污染负荷.