基于SVM模型的妫水河叶绿素a浓度的遥感反演

以北京市妫水河为研究区,基于2011年9月25日和2012年9月30日的两期叶绿素a浓度实测数据和准同步的环境一号卫星(HJ-1A)多光谱数据,分别构建一元线性和多元支持向量机模型(SVMM),通过决定系数R²和平均相对误差对模型的精度进行检验,用模型进行水体叶绿素a浓度的反演,并分析其时空分布特征。研究表明:在样本数较少的情况下,SVM具有很强的非线性映射能力,能够取得较好的预测结果,更适用于反演叶绿素a浓度。时间分布上,研究区叶绿素a浓度呈增加趋势,均值上升了6.86 μg/L;空间分布上,深水区叶绿素a浓度值低于浅水区,上游高于下游。国产HJ-1A CCD2多光谱数据以其4 d的时间分辨率,在水质动态变化监测方面具有优势。     

Gasoline composition determined by H NMR spectroscopy

A fast and simple ¹H NMR spectroscopic method was developed for the concentration measurement of aromatic, olefinic and aliphatic fractions in gasoline samples. Simultaneously, individual components such as benzene, methyl tert-butyl ether and several dienes could be determined. The method relies on only a few, well-established assumptions about the molecular compositions and is therefore applicable to a broad range of gasolines. It is well suited for laboratories with high sample throughput since measurement time is short and all concentrations are determined within one NMR experiment. The method was applied to commercial gasolines and samples used in European round robin tests. Comparisons of NMR and round robin test results showed excellent agreement.     

二聚炔醇酸性介质缓蚀剂的合成与应用

对二聚炔醇化合物ＤＭＨ的合成、分子结构及缓蚀作用机理进行了论述。因ＤＭＨ化合物具有独特的分子结构，形成了稳定的络合体系及基团的屏蔽效应，增加了缓蚀被膜厚度及缓蚀体系的化学稳定性，实验证实ＤＭＨ是酸性介质中的高效缓蚀剂。     

乙烯二聚制高纯丁烯－1技术经济评价

本文对生产高纯度丁烯－１的Ａｌｐｈａｂｎｔｏｌ工艺进行了技术经济评价，认为该工艺条件简单、反应条件温和，而且投资少，所以很适合事在发展中国家应用。     

Synthesis, characterization, and catalytic properties of polysiloxanes with pendant 4-(3-pyridinyl)butyl and 4-(1-oxypyridin-3-yl)butyl groups

New silane monomers with the pendant 4-(3-pyridine)butyl group have been synthesized by hydrosilation of 3-(3-butenyl)pyridine with Me _n Si(OEt)_3-n H (n=0, 1) using a platinum catalyst. Only -addition products were observed. The products were characterized by elemental analysis, infrared,¹H- and¹³C-NMR spectroscopy, and gas chromatography-mass spectrometry. Hydrolysis-polycondensation of the difunctional monomer with a basic catalyst, Me₄NOH, gave a mixture of cyclic oligomers, principally cyclic tetramer, and linear homopolymer. Under similar reaction conditions, the trifunctional monomer gave crosslinked material which was soluble in common organic solvents. The linear homopolymer and crosslinked polymer were trimethylsilyl end-blocked with hexamethyldisilazane. The cyclic and end-blocked polymers were characterized by elemental analysis and spectroscopic methods. Molecular weights of the polymers were obtained by end-group analysis using¹H-NMR spectral data, size exclusion chromatography, and direct insertion-probe mass spectrometry. The cyclic, linear, and crosslinked materials were N-oxidized withm-chloroperoxybenzoic acid and characterized by spectroscopic methods. The polymeric N-oxide derivatives were shown to be effective transacylation catalysts in the synthesis of mixed carboxylic acid anhydrides in immiscible solvents (H₂O/CH₂Cl₂) under phase-transfer conditions. The implications of the results on the mechanism of catalysis are discussed.     

Crystallization and phase transformation kinetics of poly(1-butene)/MWCNT nanocomposites

Poly(1-butene)/MWCNT nanocomposites were prepared by simple melt processing technique. Crystallization, crystal-to-crystal phase transformation and spherulitic morphology were studied using differential scanning calorimetry (DSC), wide angle X-ray diffraction (WAXD) and optical microscopy (OM). The non-isothermal crystallization exhibited higher values of Z_t derived from Avrami theory and lower values of F(T) obtained from Avrami-Ozawa analysis, while the isothermal crystallization revealed a significant increase in crystallization temperatures and lower crystallization half times compared to pristine PB. The observed changes in the crystallization kinetics were ascribed to the enhanced nucleation of PB in the presence of MWCNT. The nucleating activity calculated from the non-isothermal crystallization data revealed that the MWCNTs provide an active surface for the nucleation of PB. The optical micrographs exhibited significantly smaller crystallites with disordered morphology for the nanocomposites compared to the well defined spherulitic morphology for pristine PB. The rate of phase transformation from kinetically favored tetragonal to thermodynamically stable hexagonal form was noticeably enhanced as evidenced by the reduction in the half time for phase transformation from 58 h to 25 h for PB reinforced with 7% MWCNT.     

含给电子Z-N催化剂催化乙烯/1-丁烯共聚的研究

研究了两种含有给电子体分别为对硝基苯胺、乙二醇二甲醚的Ziegler-Natta催化剂催化乙烯与1-丁烯高压的共聚反应性能,主要考察了反应条件对聚合活性、聚合物物理性质的影响,同时采用红外光谱法测定了聚合物的支化度.研究表明,给电子体为乙二醇二甲醚的催化剂催化活性高于对硝基苯胺.反应条件如反应压力、温度、铝钛比对聚合活性、丁烯的插入率以及聚合物性质都有明显影响.高的反应压力有利于1-丁烯插入和聚合物堆密度的提高;反应温度在50℃时的聚合活性最大,聚合物的支化度较高,聚合物熔点较低;铝钛比为500时聚合活性高于低铝钛比的聚合活性.     

再生丁基橡胶与非极性不饱和橡胶共混物的性能研究

对再生丁基橡胶(RIIR)与非极性不饱和橡胶共混物的性能进行了研究。结果表明,RIIR易以填料的形式加入到非极性不饱和橡胶中使用,当RIIR以填料的形式加入到NR、BR及SBR中时,不仅使它们的耐热氧老化性及耐屈挠龟裂性得到明显改善,而且使NR及BR的撕裂强度及扯断伸长率提高;RIIR作为生胶与BR及NR共混,可改善BR的耐热氧老化性,提高NR的撕裂强度;SBR与RIIR共混,均使拉伸强度及撕裂强度降低;非极性不饱和二烯类橡胶与RIIR共混后,均使耐磨性降低。