仙霞路框架中桥基坑工程施工监测分析

在仙霞路框架中桥基坑施工过程中,根据基坑开挖方法及支护结构形式,合理设置监测点.通过对支护结构深层土体水平位移、支撑轴力及地下水位的动态监测,及时掌握基坑支护结构的稳定状态,判断土体的变形趋势,分析基坑开挖施工与土体变形之间的关系,并据此控制基坑开挖及降水速率,指导施工,确保了基坑在开挖施工过程中的安全.     

Soluble Dietary Fiber from Canna edulis Ker By-Product and its Enzymatic and Antioxidant Activities

Soluble dietary fiber (SDF) was prepared from Canna edulis Ker by-product by physical-enzymatic method and its structure was characterized using GC, FT-IR, ¹H-NMR, and solid ¹³C-NMR spectroscopy. The results exhibit that SDF is mainly composed of polysaccharides with minor phenolic compounds. Moreover, influences of SDF on protease hydrolysis of β-lactoglobulin (β-lg) and lipase hydrolysis of tributyrin (TBG) were determined. The results indicate that SDF promotes N release of β-lg by pepsin, despite it inhibiting the enzymatic activity of pepsin. Inversely, tryptic hydrolysis of β-lg is inhibited by the addition of SDF, which has no obvious effect on tryptic activity. SDF also inhibits lipase hydrolysis of TBG and the inhibition rate increases with increasing SDF concentration. Furthermore, antioxidant activities of SDF were evaluated by six different modes, and the relationship between concentration and activity was discussed. The results indicated different activities determined by different methods, suggesting that antioxidant mechanisms of SDF are complicated.     

Highly soluble perylene dyes: Synthesis, photophysical and electrochemical characterizations

Highly soluble perylene diimide derivatives with symmetrical and unsymmetrical secondary, tertiary alkyl side chains were synthesized and their photophysical properties, redox potentials and thermal stabilities were measured and compared with previously reported 1-pentylhexyl substituted swallow-tailed perylene diimide. Diasteroisomers of the novel, unsymmetrical swallow-tailed substituted perylene diimide compound could not be detected using low temperature NMR spectroscopy. The novel dyes were soluble in a range of organic solvents indicating potential for photo-electronic applications and photocatalytic reactions. Two dyes were not only soluble in organic solvents but also showed solubility in aqueous media as the hydrochloride salt, thus offering potential use in biological applications.     

Hydrogen transfer during co-liquefaction of Elbistan lignite and biomass: liquid product characterization approach

In this study, Elbistan lignite (EL) and manure were liquefied under catalytic conditions in an inert atmosphere. Red mud, tetralin, and distilled water were used as a catalyst and solvent, respectively. The liquefaction studies were carried out under catalytic conditions in the catalyst concentration of 9%, solvent/solid ratio of 3/1, reaction time of 60 min, waste/lignite ratio of 1/3, and at temperature of 400°C. Stirring speed and initial nitrogen pressure were kept constant at 400 rpm and 20 bar, respectively. At the end of liquefaction process, the soluble liquefaction products were separated by successive solvent extraction to preasphaltene, asphaltene, and oils. Oil products characterized by H-NMR to be able to differ hydrogen transfer from manure to EL surface. To obtain the hydrogen transfer way, liquefaction experiments conducted under inert atmosphere which does not related to hydrogen reaction, other above experimental conditions were kept same but only solvent type changed. The reason of using distilled water instead of tetraline is tetraline known as hydrogen donor but not water. Because water behaves supercritical conditions during the liquefaction stage. EL liquefied alone while using tetraline however EL liquefied with manure with using distilled water as a solvent. The obtained oil products form both experiments characterized by H-NMR. The radical groups diffraction and range values are not changed significantly shows that manure behaved as an hydrogen donor. So, EL with manure is the one great option to reduce cost of hydrogen source for direct coal liquefaction plant.     

Growing Innovative Calcium Carbonate Morphologies by Utilizing the Colloidal Gas Aphron System as a Surfactant-Based Template Method

Many studies have been conducted to study the various polymorphs and morphologies of calcium carbonate crystals in nature and living organisms. In this experimental work, a novel method has been employed to crystallize calcium carbonate by using colloidal gas aphron dispersion. The polymorph and morphology of prepared particles were investigated using scanning electron microscopy (SEM), X-ray diffraction (XRD), and Fourier transform infrared spectrometry techniques. SEM and XRD analyses demonstrated that the morphology of synthesized CaCO₃ can be changed from spherical (vaterite phase) to novel rod and plate-like shapes (mixture of vaterite and calcite phases) with changes in the surfactant concentration. The quantitative examination results of different calcium carbonate polymorph orientations showed that the precursor concentrations had no significant effect on the orientation of calcite phase, but rather they affected the orientation development of vaterite phase at a higher surfactant concentration.     

线性支架回采工艺在榆家梁煤矿的使用与推广

根据神东煤炭分公司历年房采工作面的回采现状,以及神府矿区煤层赋存及顶底板岩性等情况,结合榆家梁煤矿42220房采工作面使用线性支架回采的尝试及效果,简单阐述新回采工艺在安全、效率、效益方面相对于以往回采工艺所具备的优势。     

4-硝基苯乙烯基吡啶类氢键液晶的合成及表征

该文用4-硝基苯甲醛和4-甲基吡啶合成了质子受体4-硝基苯乙烯基吡啶,用无水乙醇重结晶得黄色固体,其熔点126.8～128.9℃,产率27%。用4-羟基苯甲酸和1-溴代正烷合成了质子供体4-烷氧基苯甲酸,用体积分数为95%的乙醇重结晶,所得4种中间体产率都在20%左右。最后,以上述两个中间体为原料,制备了系列4-硝基苯乙烯基吡啶类氢键型液晶。IR和1H NMR证实了各中间体结构。POM、IR、DSC检测了各复合物。POM拍摄的向列相、近晶相液晶织构表明,3种该氢键复合物均呈现明显的液晶态,且n=3时为向列相,n=5、8时为近晶相;IR图谱3500～2500cm-1处峰的变化及羰基向高波数位移,证明了羧基和吡啶间的分子间氢键代替了羧基间的分子间氢键。各复合物的液晶区间范围比各相应单体增大了1倍,表明羧酸吡啶间氢键起到了稳定液晶态的作用。     

Synthesis and characterization of a thermotropic liquid crystalline hyperbranched polyester

BACKGROUND: Hyperbranched polymers have received increasing attention in the fields of medicine, homogeneous catalysis and materials science. Hydroxyl‐functional aliphatic polyesters are one of the most widely investigated families of hyperbranched polymers. The research reported here is based on the preparation of a novel hyperbranched polyester and the modification of its terminal hydroxyl groups by biphenyl mesogenic units. RESULTS: 2,2,6,6‐Tetramethylolcyclohexanol as a core and 8‐[4′‐propoxy(1,1‐biphenyl)yloxy]octanoic acid as a mesogenic unit were synthesized. A hyperbranched polyester (HPE) was synthesized in one step and subsequently substituted by reaction of its terminal hydroxyl groups with the biphenyl mesogenic units to yield a novel liquid crystalline hyperbranched polyester (HPE‐LC). The chemical structures of all compounds were confirmed using Fourier transform infrared, ¹H NMR and ¹³C NMR spectroscopy. The thermal behavior and the mesogenic properties of the biphenyl mesogenic unit and HPE‐LC were investigated using differential scanning calorimetry, polarized optical microscopy and wide‐angle X‐ray diffraction. The results demonstrated that the degree of branching of the HPE is ca 0.63. Both HPE‐LC and the biphenyl mesogenic unit exhibit mesomorphic properties, but HPE‐LC has a lower isotropic transition temperature and a wider transition temperature range than the biphenyl mesogenic unit. CONCLUSION: A novel liquid crystalline hyperbranched polyester was successfully synthesized, which exhibits mesomorphic properties. This polymer has good solubility in highly polar solvents and good thermal stability. Copyright © 2009 Society of Chemical Industry