海底管道测温探头的研制

温度对于金属在不同环境下的腐蚀都有着直接或者间接的影响,对于海底管道而言,不仅管道内的流体性质影响腐蚀,流体的温度更是一个不容忽视的因素。本文采用TMP35作为温度敏感元件,研制开发了海底管道测温探头。利用该测温探头采集的数据,绘制了温度与电位关系变化曲线,并依据温度与电位关系变化曲线:E=9.0159 T-87.139或者T=0.1109 E+9.665,编译了测温应用软件。目前该管道测温探头已在海底管道腐蚀检测中得到了应用。     

A Comparative Study on the Biosorption of Cd2+ onto Paecilomyces lilacinus XLA and Mucoromycote sp. XLC

The filamentous fungi XLA and XLC isolated from Cd-contaminated soil were identified morphologically and phylogenetically as Paecilomyces lilacinus and Mucoromycote sp., respectively. The minimum inhibitory concentrations (MICs) of Cd²⁺, Co²⁺, Cu²⁺, Zn²⁺, Cr³⁺ and Cr⁶⁺ in minimum mineral (MM) medium agar plates were 29,786, 2945, 9425, 5080, 1785 and 204 mg·L⁻¹ for XLA and 11,240, 884, 9100, 2540, 3060 and 51 mg·L⁻¹ for XLC, respectively. Favorable biosorption conditions for adsorption of Cd²⁺ by the tested fungi were investigated. Efficient performances of the biosorbents were described using Langmuir isotherm model, and the predicted maximum biosorption capacities for Cd²⁺ were 77.61 mg·g⁻¹ of XLA and 79.67 mg·g⁻¹of XLC. Experiments on desorption potential of biosorbents validated their efficacy at a large scale. Results showed that XLA obtained a desorption rate of 84.7% by 2% EDTA and XLC gained a desorption rate of 78.9% by 0.1 M HCl. Analysis by Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy/energy dispersive X-ray spectroscopy (SEM/EDS) and X-ray photoelectron spectroscopy (XPS) suggested that groups of C–N, COO– for XLA and C–N, CH₂ and phosphate for XLC were the dominant binding sites for Cd²⁺ biosorption. Our results indicated that the fungus XLA, rather than XLC, could potentially be used as an inexpensive, eco-friendly and effective bioremediation agent for the removal of Cd²⁺ from wastewater.     

基于ANSYS某自动化机械手大跨距支撑横梁的结构分析

针对超高运行的自动化机械手可靠性及安全性问题,对其超大跨距第七轴机械手支撑横梁的设计进行验证分析。主要基于ANSYS仿真对某型汽车拆解线的大跨距横梁进行有限元结构静力分析,研究其变形及应力应变情况,并确定机械手行走稳定性影响。分析结果可以对横梁的设计提供参考,对大型自动化工程具有通用性和参考意义。     

Characterizations,relationship, and potential sources of outdoor and indoor particulate matter bound polycyclic aromatic hydrocarbons (PAHs) in a community of Tianjin,Northern China

Polycyclic aromatic hydrocarbons (PAHs) are among the most toxic air pollutants in China. However, because there are unsubstantial data on indoor and outdoor particulate PAHs, efforts in assessing inhalation exposure and cancer risk to PAHs are limited in China. This study measured 12 individual PAHs in indoor and outdoor environments at 36 homes during the non‐heating period and heating period in 2009. Indoor PAH concentrations were comparable with outdoor environments in the non‐heating period, but were lower in the heating period. The average indoor/outdoor ratios in both sampling periods were lower than 1, while the ratios in the non‐heating period were higher than those in the heating period. Correlation analysis and coefficient of divergence also verified the difference between indoor and outdoor PAHs, which could be caused by high ventilation in the non‐heating period. To support this conclusion, linear and robust regressions were used to estimate the infiltration factor to compare outdoor PAHs to indoor PAHs. The calculated infiltration factors obtained by the two models were similar in the non‐heating period but varied greatly in the heating period, which may have been caused by the influence of ventilation. Potential sources were distinguished using a diagnostic ratio and a mixture of coal combustion and traffic emission, which are major sources of PAHs.     

Kinetic study of the competitive hydrogenation of glycolaldehyde and glucose on Ru/C with or without AMT

The competitive hydrogenation of glycolaldehyde and glucose over 1% Ru/C catalyst was studied in a batch reactor at 373–403 K and 6 MPa hydrogen pressure, with or without the presence of ammonium metatungstate (AMT). It was found that the presence of AMT retarded significantly the hydrogenation of both aldoses, and this suppressing effect was more pronounced on the glucose hydrogenation. The hydrogenation of glycolaldehyde occurred always preferentially to the glucose hydrogenation, with or without the presence of AMT. The kinetic data in the absence of AMT were well modeled based on Langmuir–Hinshelwood–Hougen–Watson kinetics assuming the surface reaction being rate‐determining and noncompetitive adsorption of dissociatively chemisorbed hydrogen and aldose. However, in the presence of AMT, the complexing between AMT and aldose and the strong adsorption of AMT on Ru surface must be considered in the development of new kinetic model. The as‐modified model described the data satisfactorily. © 2014 American Institute of Chemical Engineers AIChE J, 61: 224–238, 2015     

Fluidized‐bed CVD of unstacked double‐layer templated graphene and its application in supercapacitors

Graphene is inclined to stack with each other that greatly hinders the full utilization of its intrinsic extraordinary properties. Introducing protuberant spacers is a straightforward strategy to avoid the stacking of graphene nanosheets, resulting in a novel unstacked double‐layer templated graphene (DTG) structure. Herein, a family of layered double hydroxides were used for the bulk chemical vapor deposition (CVD) of DTG in a fluidized‐bed reactor. A high specific surface area of 1554.2 m² g^?1 and a large pore volume of 1.70 cm³ g^?1 were achieved. When used as the electrode material for supercapacitors, the DTG afforded a specific capacitance of 65.5 F g^?1 at a sweep rate of 5.0 mV s^?1 and a capacitance retention of 77% when the sweep rate was increased to 500 mV s^?1. Therefore, the DTG obtained via fluidized bed CVD is a promising electrode material for supercapacitor applications. © 2014 American Institute of Chemical Engineers AIChE J, 61: 747–755, 2015     

Ethylene polymerization with homogeneous and heterogeneous catalysts based on bis(4‐fluorophenyl)methyl‐substituted bis(imino)pyridyliron complexes

A series of bis(4‐fluorophenyl)methyl‐substituted bis(imino)pyridyliron chloride complexes were immobilized on oxide supports. The kinetics of ethylene polymerization by both homogeneous and heterogeneous systems was followed, the catalysts mostly demonstrating high activities. The effect of the ligands nature and reaction conditions on the catalytic activities and molecular weights of the resultant polyethylenes was examined. In contrast to homogeneous systems, the supported iron complexes were found to exhibit high and stable activity upon activation with triisobutyl aluminium, producing high‐molecular‐weight polyethylene with good morphology. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42674.     

Influence of fiber surface treatment on mechanical performance of Xanthoceras sorbifolia bunge husk fibers/PP composites

The PP Composites containing Xanthoceras sorbifolia Bunge husks fibers with different surface treatments were prepared. The mechanical properties such as tensile properties and impact properties of the composites were investigated. It is revealed that the composites with fibers treated by alkali and the following treatments of silane coupling agents KH570, titanate coupling agent JN‐9A, acetic anhydride, MAPP, or bleach, all performed higher in tensile properties than that with untreated fibers, while lower in impact properties. Meanwhile, all treated fibers performed better thermal stability than untreated fibers. The fibers treated by alkali followed by KH570 treatment were added into PP with different contents. It is found that as the fiber content increases, the elastic modulus and impact strength of the composites increase sharply at first followed by a decrease, while the tensile strength decrease initially and increase with a peak at 10%, then decrease continuously. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41217.     

Development of a superporous hydroxyethyl cellulose‐based hydrogel by anionic surfactant micelle templating with fast swelling and superabsorbent properties

The self‐assembling anionic surfactant, sodium n‐dodecyl sulfonate (SDS) micelles were used as pore‐forming templating for fabricating novel superporous hydroxyethyl cellulose‐grafting‐poly(sodium acrylate)/attapulgite (HEC‐g‐PNaA/APT) hydrogels. The network characteristics, morphologies of the hydrogels and removing of SDS micelles from the final product by washing with ethanol/water (v/v, 7 : 3) procedure were determined by Fourier transform infrared spectroscopy and scanning electron microscopy, as well as by determination of swelling ratio, swelling rate, and stimuli response to salts and pHs. The results showed that the added‐SDS concentration significantly affected the morphologies and pore structure of the hydrogel, and 2 mM SDS facilitates to form a homogeneous and well‐defined pore structure in the gel network to extremely improve the swelling ratio and swelling rate. The 2 mM SDS‐added superporous HEC‐based hydrogel not only had highest equilibrium swelling ratio (Q_eq, 1118, 102 g g^?1 in distilled water and 0.9 wt % NaCl solution), rapid swelling rate (k_is, 5.2840 g g s^?1), also showed multistimulus responses to salts and pHs, which may allow its applications in several areas such as adsorption, separation and biomedical materials. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42027.