Estimation of Similarity in the Qualitative Composition of Humic Substance in Marine Sediments By Means of an Uv-Spectroscopic Library

In this paper a method for the study of the qualitative similarity of extractable humic substance (EHS) in marine sediments based on the realisation of UV spectral library of EHS is described. the spectral library was built including the digitised spectra of humic substance extracted from several marine sediments (46 samples) and two samples of standard materials (lignin sulphonate and humic substance) in a Statistica data file. the data matrix was elaborated by means of different multivariate statistic techniques such as Cluster Analysis (CA), Principal Components Analysis (PCA) and the univariate technique Spectral Correlation Analysis (SCA). This approach allows us to show the contribution of different organic compounds (aromatic, lipid and acid) to the composition of EHS and moreover it evidences also the structural characteristics of EHS in terms of similarities in the qualitative composition of samples such as presence of terrestrial and/or vegetal contributions. the UV library is an objective tool to study the qualitative composition of EHS and it represents a complementary approach to the most common methods based on the application of spectroscopic (IR, ¹³CNMR), potentiometric and chromatographic techniques.     

Characterization of fulvic acids during olive mill waste composting (Elemental,Thermal and fluorescence analyses)

Elemental analysis, fluorescence spectroscopy and differential scanning calorimetry (DSC) were applied to the study of fulvic acids isolated from different stages during olive mill waste composting. The fulvic extracted acids are characterized by a high nitrogen content and O/C ratio values that may result from the high degree of humification and the synthesis of more condensed humic complexes. This was confirmed by fluorescence spectroscopy in the synchronous-scan mode by the decrease of shoulder intensities at intermediate wavelengths indicating the increase of polycondensation and conjugation of unsaturated structures and the greater uniformity of fluorophores. Fluorescence spectra in the emission, excitation and synchronous modes became simpler with compost maturation. This was confirmed by DSC results which proved the high degree of polycondensation of aromatic nuclei of fulvic acid molecules during olive mill waste composting.     

Application and mechanism of polysaccharide extracted from Enteromorpha to remove nano-ZnO and humic acid in coagulation process

Green source Ep was extracted from marine alga waste. The molecule model structure of Ep was studied and constructed. PAC-Ep coagulation system improves the efficiency of removal efficiency. Synergistic effects between NPs and HA make a big difference to enhance efficiency. Mechanism is charge neutralization, hydrogen bonding and adsorbing-complexing Enteromorpha polysaccharide (Ep) extracted from alga a novel green coagulant aid for nanoparticles (NPs) and heavy metal ions removal and the structure of EP was intensively studied in this study. The integration of Ep with polyaluminum chloride (PAC-Ep) coagulants exhibited higher coagulation performance than that of the polyaluminum chloride (PAC) because of the negatively charged NPs suspension and humic aid (HA) solution. Significant high removal efficiencies of dissolved organic matter (94.1%), turbidity (99.3%) and Zn ions (69.3%) were achieved by the PAC-Ep coagulants. The dual-coagulation properties of PAC-Ep for different pollutants was based on multiple mechanisms, including (i) Al³⁺ charge neutralization; (ii) hydroxy aluminum hydroxyl bridging formed polynuclearhydroxy complexes bridge and sweep colloidal particles; (iii) adsorption and bridging of Ep chain for the NPs and heavy metal ions. Results indicated that the destabilization of colloid was induced by the coexisting HA and higher removal was achieved as ions adsorption was enhance in the presence of HA complexation. On the basis of that, the extraction of polysaccharide is a promising candidate for its high coagulation performance in water treatment.     

石化企业VOCs无组织排放源强的反演模拟

针对石化行业面源无组织排放VOCs难以准确定量的问题,建立了基于开路式傅里叶变换红外光谱技术(OP-FTIR)的面源污染源源强反演模型,并进行了现场模拟试验。试验结果表明,风向、风速、大气稳定度、监测距离、数据处理周期等都是影响反演模型准确性的重要灵敏度参数。以反演源强Q_P与实际排放量Q的比值(Q_P/Q)为量化指标,对各影响因素进行优化处理,确定了构建反演模型适用的边界条件。当各灵敏度参数稳定于适用边界条件之内时,Q_P/Q为0.85~0.90。     

Characterization of humic acids extracted from the sediments of the various rivers and lakes in China

The humic acids (HAs) isolated from the sediments of the various rivers,lakes,and reservoirs in China were studied using elemental analyzer,fourier transform infrared (FT-IR),and CP/MAS 13C nuclear magnetic resonance (NMR) spectroscopy.The results showed that the HAs were characterized by some common chemical and physicochemical properties,but they also pose some differences in the C-containing functional groups.The C/N,C/H,O/C,and O/H ratios differ widely for the various HAs,showing that the elemental comp...     

不同面源强度影响下城市河流溶解性有机质光谱特征变化

采用紫外-可见吸收光谱（UV-vis）和三维荧光光谱结合平行因子法（EEMs-PARAFAC）研究两条面源输入强度不同的城市河流春夏两季水体中溶解性有机质（DOM）含量和组成变化.结果表明,两条河流夏季水体DOM腐殖化程度和相对分子质量均显著高于春季（P<0.01）. PARAFAC模型共解析出C1（UVC类富里酸）、 C2（类色氨酸）、 C3（类胡敏酸）和C4（UVA类富里酸）这4个化学组分,C1[（31±6）%]和C2[（31±4）%]为水体DOM中主要荧光组分.高面源输入水平的河流春季各组分荧光强度均低于夏季,而低面源输入水平的河流与之相反.随机森林回归模型表明,C3%对河流水质变化敏感度最高（R²=0.75,P<0.001）,具有很好的指示作用;水面覆盖率（Cover）对C4%有显著预测重要性（P<0.001）, C4%易受光化学氧化作用影响.主成分分析（PCA）和Adonis检验表明,氮和磷为水体自生源过程的重要推动力,面源输入强度和季节变化对城市河流水体状况有显著影响（R²=0.775,P<0.001）.城...     

城市污水处理过程中溶解性有机物及荧光物质的变化规律

以锦州市W污水处理厂为研究对象,利用三维荧光光谱分析技术和荧光区域积分(FRI)方法考察了城市污水处理过程中溶解性有机物及荧光物质的去除状况.利用XAD树脂将DOM分为5个部分:疏水性有机酸(HPO-A)、疏水性中性有机物(HPO-N)、过渡亲水性有机酸(TPIA)、过渡亲水性中性有机物(TPI-N)和亲水性有机物(HPI).结果表明,HPO-A和HPI是该污水处理厂进水中的主要DOM组分,并且DOM中的荧光物质主要为类芳香族蛋白质荧光物质和类富里酸荧光物质.在该污水处理厂内,生物降解作用是TPI-A和HPI的主要去除机制,HPO-N和TPI-N主要是由深度处理工艺(絮凝-沉淀-过滤)去除的,生物处理工艺和深度处理工艺对HPO-A的去除能力接近,而生物处理工艺和深度处理工艺对TPI-N的去除效果均较差.生物处理工艺对HPO-A、TPI-A和HPI中的荧光物质有较强的去除能力,而对HPO-N和TPI-N中荧光物质的去除效果较差.深度处理工艺能够有效去除HPO-A和HPO-N中的荧光物质,而对TPI-A、TPI-N和HPI中的荧光物质无明显去除作用.     

航空压力环境对锂离子电池热解气体爆炸极限影响*

针对航空锂离子电池热失控释放气体安全性研究不足的问题,采用气体拉曼光谱技术、气相色谱仪(Gas Chromatography,GC)和质谱(Mass Spectroscopy,MS)耦合来探究压力和荷电状态(State of Charge,SOC)对锂离子电池早期故障气体类型、气体动态演变及气体潜在危险性等特征的影响规律,同时综合考虑压力、电压和电池温度等多种因素分析锂离子电池热失控危害。研究结果表明:电池SOC越高且环境压力越低,电池越早触发热失控,爆炸极限越宽,其中30 kPa下100%SOC电池热解气体爆炸极限为8.01%~53.35%;SOC和环境压力越高,电池热失控越危险,释放的气体体积越多;CO,CO2,PF3,C2H4及电解液（C3H6O2、C3H6O3、C4H8O2）等气体可作为航空锂离子电池早期故障诊断特征。研究结果对保障锂离子电池在航空领域的安全运输及应用具有重要意义。     

环糊精对腐植酸-芘、蒽相互作用影响初探

利用吸收光谱、荧光猝灭法、圆二色谱法及芘荧光探针法,探讨了环糊精(CDs)对腐植酸(HA)与以芘为代表的多环芳烃(PAHs)相互作用的影响.β-CD与HA的吸收光谱和荧光光谱测定结果表明:β-CD能够包络HA的芳环部分;荧光猝灭法和圆二色谱法测定结果表明:HA能够与被β-CD空腔包络的芘分子发生相互作用,CDs和HA之间存在与芘相互作用的竞争;用荧光猝灭法测定了四种不同CDs存在下HA和芘的结合常数,并用芘为荧光探针进行测定,结果表明:CDs浓度较低时,HA对芘的作用占优势;反之,CDs占优势.与其它三种CDs不同,γ-CD存在下HA与芘的结合常数随其浓度的升高一直增大.     

Mapping of temperature and line-of-sight errors in constituent retrievals for MIPAS/ENVISAT measurements

An optimized code for the near real-time retrieval of line of sight, temperature and volume-mixing ratio profiles of five key species (O₃, H₂O, HNO₃, CH₄ and N₂O) from infrared limb spectra recorded by the Michelson Interferometer for Passive Atmospheric Sounding (MIPAS) experiment on board the ENVISAT-1 satellite was developed as part of an ESA-supported study. In this code line of sight and temperature are retrieved simultaneously among themselves, but sequentially with respect to the volume-mixing ratio of the five key species. The sequential retrieval leaves unaccounted the mapping of line of sight and temperature errors in the retrieved volume-mixing ratio of the constituents. This paper illustrates an algorithm that provides the a-posteriori evaluation of temperature and line-of-sight-induced error on the retrieved volume-mixing ratio of the MIPAS key species. It is shown that in most cases temperature and line-of-sight-induced error provides a significant contribution to the total volume-mixing ratio error. The variability of this error as a function of latitude, season and atmospheric model is also analyzed.