自燃煤矸石轻集料混凝土结构耐久性综述

为了探讨自燃煤矸石轻集料混凝土结构耐久性能．通过对自燃煤矸石轻集料、自燃煤矸石轻集料混凝土的耐久性科研成果分析、工程应用情况、有关耐久性调查及长期自然环境下自燃煤矸石混凝土碳化试验研究后说明，只要制定合理标准。严格执行、精心设计、合理选材、加强管理、自燃煤矸石混凝土是可以满足结构耐久性要求。     

Detecting Fixed Patterns in Chordal Graphs in Polynomial Time

The Contractibility problem takes as input two graphs G and H, and the task is to decide whether H can be obtained from G by a sequence of edge contractions. The Induced Minor and Induced Topological Minor problems are similar, but the first allows both edge contractions and vertex deletions, whereas the latter allows only vertex deletions and vertex dissolutions. All three problems are NP-complete, even for certain fixed graphs H. We show that these problems can be solved in polynomial time for every fixed H when the input graph G is chordal. Our results can be considered tight, since these problems are known to be W[1]-hard on chordal graphs when parameterized by the size of H. To solve Contractibility and Induced Minor, we define and use a generalization of the classic Disjoint Paths problem, where we require the vertices of each of the k paths to be chosen from a specified set. We prove that this variant is NP-complete even when k=2, but that it is polynomial-time solvable on chordal graphs for every fixed k. Our algorithm for Induced Topological Minor is based on another generalization of Disjoint Paths called Induced Disjoint Paths, where the vertices from different paths may no longer be adjacent. We show that this problem, which is known to be NP-complete when k=2, can be solved in polynomial time on chordal graphs even when k is part of the input. Our results fit into the general framework of graph containment problems, where the aim is to decide whether a graph can be modified into another graph by a sequence of specified graph operations. Allowing combinations of the four well-known operations edge deletion, edge contraction, vertex deletion, and vertex dissolution results in the following ten containment relations: (induced) minor, (induced) topological minor, (induced) subgraph, (induced) spanning subgraph, dissolution, and contraction. Our results, combined with existing results, settle the complexity of each of the ten corresponding containment problems on chordal graphs.     

Use of laser scanning confocal microscopy for characterizing changes in film thickness and local surface morphology of UV-exposed polymer coatings

Laser scanning confocal microscopy (LSCM) has been used to characterize the changes in film thickness and local surface morphology of polymer coatings during the UV degradation process. With the noninvasive feature of LSCM, one can obtain thickness information directly and nondestructively at various exposure times without destroying the specimens or deriving the thickness values from IR measurement by assuming uniform film ablation. Two acrylic polymer coatings were chosen for the study, and the physical and chemical changes of the two systems at various exposure times were measured and analyzed. Those measurable physical changes caused by UV exposure include film ablation, formation of pits and other surface defects, and increases in surface roughness. It was found in both coatings that changes in measured film thickness by LSCM were not correlated linearly to the predicted thickness loss using the changes in the CH band obtained by the Fourier Transform Infrared (FTIR) spectroscopy measurements in the later degradation stages. This result suggested it was not a uniform film ablation process during the UV degradation. At later stages, where surface deformation became severe, surface roughness and profile information using LSCM were also proven to be useful for analyzing the surface degradation process Presented at the 81st Annual Meeting of the Federation of Societies for Coatings Technology, November 13–14, 2004 in Philadelphia, PA.     

甲基丙烯酸甲酯（MMA）生产中水解和酯化反应特性的研究

用间歇式搅拌反应器，对丙酮氰醇（ＨＣＮ）法甲基丙烯酸甲酯生产中水解和酯化反应的特性进行了研究。研究表明：（１）甲基丙烯酰胺硫酸盐的水解反应有较高的平衡转化率，其动力学方程为ｋ１＝６．５２×１０＾６ｅｘｐ（－６９．８／ＲＴ）；（２）甲基丙烯酸与甲醇间酯化反应的平衡转化率较低，故生产中必须加以提高。测得的液相和汽－液相酯化反应的活化能分别为４９．４ｋＪ／ｍｏｌ和５４．４ｋＪ／ｍｏｌ。     

B_2O_3和CaF_2对C_3S-C_(2.75)B_(1.25)A_3-C_2S-C_3A水泥熟料矿物体系力学性能影响

研究了B2O3和CaF2对C3S-C2.75B1.25A3S珚-C2S-C3A熟料矿物体系的组成、结构与力学性能的影响。研究结果表明:在该熟料体系中C3S,C2.75B1.25A3S珔,C2S和C3A的适宜含量分别为50%,10%,25%和15%,B2O3和CaF2的适宜掺量为2%和1.5%。在最佳组成和制备工艺条件下,合成的阿利特-硫铝酸钡钙水泥的1d,3d和28d抗压强度分别达到18MPa,48MPa和95MPa以上,展现了良好的早期力学性能。同时,掺加CaF2能有效降低熟料中游离氧化钙的含量,促进阿利特在低温条件下形成。利用SEM-EDS,XRD等测试手段对熟料的组成、结构及性能进行了分析。     

Free energy barrier for compact chains escaping from a small sphere

In this paper, the process of compact polymer chains escaping from a small sphere to a large one in the view of thermodynamics is investigated in detail based on the pruned-enriched-Rosenbluth method (PERM), which is quite efficient for the three-dimensional polymers on the simple-cubic lattice. In our simulation, three representative states of a polymer chain during the escaping process are studied, and some statistical properties of the chain size and the chain shape, such as mean-square radius of gyration per bond 〈S²〉/N and the shape factor 〈δ^∗〉 are investigated. Our aim is to illuminate how the size and shape of the compact chains change during the escaping process. The changes of 〈S²〉/N and 〈δ^∗〉 are not monotone and it is due to the fact that the chain should stretch itself in the escaping process. In the meantime, some thermodynamic properties are also calculated here. The hole is designed to be small enough to allow only one monomer at a time and it thus reduces the number of allowed chain conformations and breaks contacts between monomers at the beginning of the process. Additionally, we discuss the free energy barrier per bond H₂ − H₁ = ΔH of a compact chain, and here H₂ is the maximum free energy per bond during the process and H₁ is the minimum one when the compact chain is within the small sphere. Averaging free energy barrier over chain length N is convenient for the comparison with different chain lengths. ΔH as a function of chain length N and radius r₁ of the small sphere is also studied and our result shows that ΔH for longer chains is lower means that it is relatively easier for each bond in longer chains to surmount the free energy barrier to escape. Some discussions about the self-avoiding walk (SAW) and swollen chains are also made for the comparison, and our results also show that the restriction of the small sphere on the SAW and the swollen chains is more effective because of their relatively looser intrinsic structure.     

Dehydration of aldoximes on rare earth exchanged (La<Superscript>3+</Superscript>, Ce<Superscript>3+</Superscript>, RE<Superscript>3+</Superscript>, Sm<Superscript>3+</Superscript>) Na–Y zeolites: A facile route for the synthesis of nitriles

Rare earth exchanged Na–Y zeolites, H-mordenite, K-10 montmorillonite clay and amorphous silica-alumina were effectively employed for the continuous synthesis of nitriles. Dehydration of benzaldoxime and 4-methoxybenzaldoxime were carried out on these catalysts at 473 K. Benzonitrile (dehydration product) was obtained in near quantitative yield with benzaldoxime whereas; 4-methoxybenzaldoxime produces both Beckmann rearrangement (4-methoxyphenylformamide) as well as dehydration products (4-methoxy benzonitrile) in quantitative yields. The production of benzonitrile was near quantitative under heterogeneous reaction conditions. The optimal protocol allows nitriles to be synthesized in good yields through the dehydration of aldoximes. Time on stream (TOS) studies show decline in the activity of the catalysts due to neutralization of acid sites by the basic reactant and product molecules and water formed during the dehydration of aldoximes.     

电解氧化法制取葡萄糖酸钠

研究了在无隔膜槽中电解氧化葡萄糖制取葡萄糖酸钠的方法，得出了最佳工艺条件，为电解法制取葡萄糖酸钠的工业化提供了依据。     

PC／PA1010共混物的热行为

利用热失重、微分热失重和显示扫描量热法研究了聚碳酸酯／尼龙１０１０共混物的热行为和解降解过程。结果表明：共混物在６００℃以下分两步降解，降解温度随尼龙１０１０用量增加有下降趋势；共混物的熔点随尼龙１０１０用量增加而升高。     

Effect of the Chiral Center Position of an Optically Active Terminal Group on the Induction of Optical Activity in Polysilanes

Summary Polysilanes with an optically active alkoxy group, i.e., (S)-(+)-2-butoxy, (R)-(-)-2-butoxy, (S)-(-)-2-methyl-1-butoxy, and (S)-(+)-3,7-dimethyl-1-octoxy, at the terminal positions, the chiral carbon centers of which were located at the α, β, and γ positions relative to the oxygen, respectively, were prepared, and the effect of the position of chiral center of the terminal optically active group on the induction of optical activity in polysilanes was investigated. The circular dichroism (CD) spectra of these polymers showed positive Cotton signals around 340 nm at temperatures below -20 °C, but the intensities were small, indicating that the optically active groups at the terminal positions have some ability, albeit small, to induce optical activity to the polysilanes. Further, the optically active (S)-(+)-2-butoxy and (R)-(-)-2-butoxy groups did not control the helical sense direction of the polymers, despite the different chiral stimuli from the 2-butoxy groups introduced to the terminal positions. To control the helical structure of polysilanes by the use of optically active terminal groups, appropriate optically active groups are required.