近红外分析网络共享平台中复杂工作流实现算法

近红外分析共享平台中的采集工作流是一个以数据为中心的工作流。对系统中复杂采集工作流的跳转执行过程进行了详细分析,针对自由工作流跳转造成的数据和状态不一致性的问题,提出了一个任务执行优先关系算法,计算采集工作流中各个活动任务执行次序关系值,并构造一个执行次序关系树,记录各任务活动的状态信息;在流程回退、撤销、跳转时保证了数据和状态的一致性,较好地实现了跨任务活动的跳转。应用结果表明,此算法能够正确高效地实现复杂流程的跳转。     

过量TiO2助烧剂对Ba0.998La0.002TiO3陶瓷晶粒生长的影响

采用电性能测定和微观结构分析等方法研究了过量TiO2助烧剂对Ba0.998La0.002TiO3陶瓷晶粒生长的影响.结果表明:对于Ba0.998La0.002TiO3陶瓷在有液相参与烧结的晶粒溶解-淀析过程中,晶粒生长的必要条件是不仅要有液相的形成,而且BaTiO3晶粒必须在液相中有一定的溶解度.由于BaTiO3晶粒在Ba6Ti17O40和Ba2TiSi2O8液相中有足够的溶解度,促进了晶粒的生长,同时旌主掺杂离子进入晶格而释放氧,形成半导性的陶瓷,而BaTiO3晶粒不能溶解于Ba2Ti2SiP2O13液相中,抑制了晶粒的生长.     

分子筛对轻汽油醚化反应的催化性能影响

在固定床反应器中研究了不同分子筛催化剂对催化裂化轻汽油和甲醇醚化反应的催化性能。结果表明，Hβ沸石的催化活性远远高于HZSM-5、HY沸石分子筛催化剂，与D005型树脂催化剂的催化活性相当。B和Mo改性对Hβ沸石的催化活性提高较小，水蒸汽处理使Hβ沸石的催化活性有提高。粒径比小于0．023即可消除扩散影响。填加30％的氧化铝粘结剂对Hβ沸石的催化活性没有影响。在最佳的反应条件下，叔碳烯烃转化率可达57．68％。     

Studies on the semirigid chain polyamide—poly(1,4-phenyleneterephthalamide)

In this article, the polycondensation of terephthaloyl chloride and p-phenylenediamine was systematically studied, including the liquid–crystalline state of the solution and the spinning of poly(1,4-phenyleneterephthalamide) (PPTA). High-molecular-weight PPTA with ε_inh = 5–7 was prepared and the main factors influencing the solution polycondensation of 1,4-phenylenediamine with terephthaloyl chloride were studied in detail. Experimental results showed that the water content of the reaction system, reactant concentration, and volume ratio of mix solvents have a great influence on the inherent viscosity of the poly(1,4-phenyleneterephthalamide) obtained. The highest ε_inh was obtained at 0.3M/liter reactant concentration in a mixed solvent ratio HMPA/DMAC of 4/1 (by volume), at 0.35M/liter reactant concentration in a mixed solvent of HMPA/NMP = 7/3, and at 0.5M/liter of reactant concentration in a mixed solvent of HMPA/THF = 9/1. The water content must be controlled to less than 100 ppm in the polymerization system. In the early stage of the polycondensation process, the ε_inh of the polymer obtained increased rapidly with time. The system gelled within 2 or 3 min, while the monomer conversion reached about 100%. However, the reaction of polycondensation continued after gelation and the ε_inh of the polymer increased appreciably. We have studied the viscosity behavior at 20–155°C for the anisotropic solution of PPTA in 100% sulfuric acid (ε_inh of PPTA 2.5–4.9). Experimental results showed that, at low concentrations the viscosity of isotropic solution increases with the increase of polymer concentration to reach a maxium near the critical polymer concentration, beyond which the solution changes to an anisotropic liquid–crystalline solution. The appropriate spinning region was obtained as shown in the phase diagram determined by viscosity, degree of depolarization anisotropy, and region of thermal depolymerization. Fibers of PPTA with high modulus and high tenacity were obtained by dry-jet wet spinning. The fibers obtained have a tenacity of ～22 g/denier, a modulus of ～600 g/denier, and elongation at break ～3.5%.     

基于个性诊断的路段缺失速度值估计

针对基于GPS的浮动车技术因无法做到对路网的时空间全覆盖导致部分路段实时交通状态缺失问题,提出基于热门路段个性化诊断(personality diagnosis base on popular road,PDPR)模型对各路段上的缺失速度值进行估计。使用K均值算法对所有原始数据作离散化处理,根据数据覆盖率对路段进行分类;以高覆盖率路段的速度数据为辅助,使用个性诊断算法(personality diagnosis,PD)对低覆盖率路段进行缺失速度估计,把估计值映射到连续型空间。实验结果表明,PDPR模型估计误差比PPCA(probabilistic principal component analysis)算法低32.84%,比滑动平均法低5.70%。     

氯溴异氰尿酸的高效液相色谱分析方法

介绍了使用反相高效液相色谱法对氯溴异氰尿酸烟剂进行定量分析。HPLC法使用C18柱,以V(甲醇)﹕V(水)﹕V(冰乙酸)=15﹕85﹕0.1为流动相,紫外检测波长215nm。方法的变异系数为0.44%,回收率在98%～102%之间。     

金刚石合成机制的研究

孤立原子不存在轨道混合问题。碳原子在形成金刚石时，原子间互相影响，使电子运动状态发生变化，形成sp^3的杂化轨道，C-C形成共价键。文章分析了金刚石合成的机理，论述和比较了片状触媒和粉状触媒合成金刚石的过程和差异，提出了“单间生长机制”的观点，认为在粉状触媒工艺中金刚石生长的环境条件优越，合成出的金刚石晶体均匀对称，品质良好。     

双环戊二烯改性不饱和聚酯树脂研究进展

较详细地介绍了双环戊二烯改性不饱和聚酯树脂的机理、合成路线(初始法、半酯化法、酸酐法、后期法、封端法和水解法)及国内外双环戊二烯改性不饱和聚酯树脂在气干性、低苯乙烯挥发、低收缩性与力学性能方面的研究进展,提出了今后的研究方向。     

PVG输送带覆盖胶性能的研究

用粉末丁腈P83来改性PVC研制PVG输送带覆盖胶,研究了P83对覆盖胶的拉伸强度、撕裂强度、表面电阻、热空气加速老化性能和阻燃性能的影响。实验结果表明,P83与PVC共混的性能较好,可达到性能互补的效果。综合考察,P83用量在30份时,PVG输送带覆盖胶的综合性能较佳。     

开放水热法制备莫来石复相纳米晶体的影响因素

以天然高岭土为原料,经精细化处理煅烧制备莫来石.用常压、开放水热技术制备出莫来石复相纳米晶体材料.实验表明:常压、开放水热条件下制备莫来石复相纳米晶粉体的水热反应中,采用质量比为m(Na2O)/m(SiO2)=2.8,m(H2O)/m(Na2O)=35～30,0～80℃控温升温1 h,在80℃保温2 h,可制备出尺寸为80～100 nm莫来石复相纳米晶体.所制备的莫来石纳米晶体的水热溶液相变驱动力△μ为(3.609～4.672)×10-20 J/mol;水热体系溶解度控制在3.891×10-6 mol/L;熔解热△E为18.846 kJ/mol;晶体生长速率常数选择0.85～0.92,有利于快速成核和晶体生长,并且可以很好地控制晶体尺寸和分散度.