材料表面性质对微生物附着行为的影响

利用荧光显微镜计数法,研究了微生物在4种不同材料表面的初始附着行为,对微生物附着进行了定量描述,初步获得以下结果:(1)不同材料表面,细菌的附着量呈现如下差异:316L不锈钢＞PVC＞玻璃,在有机硅材料(道康宁T2)表面的附着变动性很大;(2)同种材料表面,不同细菌的附着量也不同,表现为:Shewanella oneidensis MR-1菌株和Pseudomonas aeruginosa PAO1菌株均大于Escherichia coli JM 109菌株.并由此对其附着差异和影响因素进行了讨论.     

Buckling and postbuckling of composite ship panels stiffened with preform frames

The U.S. shipbuilding industry recently has started incorporating composite materials in the construction of both military and commercial ships due to the advantages of composite construction. These advantages include the reduction in total life costs, corrosion resistance, high strength- and stiffness-to-weight ratios, and improved stealth for military applications. One disadvantage is the higher costs of composites compared to steel and other conventional materials. Therefore, new higher quality materials with lower costs and new fabrication methods need to be developed before composite materials will be fully accepted for the construction of large ships. A new composite preform framing technology shows promise in the reduction of fabrication costs for large ship construction. There already has been significant cost savings using this framing technology in the construction of small recreational boats and large yachts. This framing technology involves casting a dry glass fiber-reinforced plastic (GRP) fabric into shape in a closed mold with a foam core. One unresolved issue using this framing technology is the orientation of the fiber for the frames. This paper summarizes experimental results of the testing of composite panels stiffened with preform frames under in-plane uniaxial compressive loads. Biaxial (0,90), quadaxial (0,90,+45,−45), and triaxial (+45,−45,0) laminates were used in the frames.     

Development of an online analyzer of atmospheric H2O2 and several organic hydroperoxides for field campaigns

An online automated instrument was developed for atmospheric measurements of hydroperoxides with separation and quantification of H₂O₂ and several organic hydroperoxides. Samples were trapped in aqueous solutions in a scrubbing glass coil. Analyses were performed on an HPLC column followed by para-hydroxyphenylacetic acid (POPHA) acetic acid and peroxidase derivatization and fluorescence detection. Analytical and sampling tests were performed on different parameters to obtain optimum signal-to-noise ratios, high resolution and collection efficiencies higher than 95% for H₂O₂ and organic hydroperoxides. The obtained performances show large improvements compared to previous studies. The sampling and analytical devices can be coupled providing an online analyzer. The device was used during two field campaigns in the Marseilles area in June 2001 (offline analyzer) and in July 2002 (online analyzer) at rural sites at low and high altitudes, respectively, during the ESCOMPTE and BOND campaigns. During the ESCOMPTE campaign, H₂O₂ was detected occasionally, and no organic hydroperoxides was observed. During the BOND campaign, substantial amounts of H₂O₂ and 1−HEHP+MHP were often detected, and two other organic hydroperoxides were occasionally detected. These observations are discussed.     

Differentiation and magma mixing on Kilauea's east rift zone: a further look at the eruptions of 1955 and 1960. Part II. The 1960 lavas

 New and detailed petrographic observations, mineral compositional data, and whole-rock vs glass compositional trends document magma mixing in lavas erupted from Kilauea's lower east rift zone in 1960. Evidence includes the occurrence of heterogeneous phenocryst assemblages, including resorbed and reversely zoned minerals in the lavas inferred to be hybrids. Calculations suggest that this mixing, which is shown to have taken place within magma reservoirs recharged at the end of the 1955 eruption, involved introduction of four different magmas. These magmas originated beneath Kilauea's summit and moved into the rift reservoirs beginning 10 days after the eruption began. We used microprobe analyses of glass to calculate temperatures of liquids erupted in 1955 and 1960. We then used the calculated proportions of stored and recharge components to estimate the temperature of the recharge components, and found those temperatures to be consistent with the temperature of the same magmas as they appeared at Kilauea's summit. Our studies reinforce conclusions reached in previous studies of Kilauea's magmatic plumbing. We infer that magma enters shallow storage beneath Kilauea's summit and also moves laterally into the fluid core of the East rift zone. During this process, if magmas of distinctive chemistry are present, they retain their chemical identity and the amount of cooling is comparable for magma transported either upward or laterally to eruption sites. Intrusions within a few kilometers of the surface cool and crystallize to produce fractionated magma. Magma mixing occurs both within bodies of previously fractionated magma and when new magma intersects a preexisting reservoir. Magma is otherwise prevented from mixing, either by wall-rock septa or by differing thermal and density characteristics of the successive magma batches. Received: July 10, 1995 / Accepted: October 10, 1995     

关于曹妃甸某排水管道CIPP壁厚设计的歧义

本文根据曹妃甸某排水管道的招标文件,概要介绍了曹妃甸厂区待修复排水管道的运行状况和修复实践,并分别就不同CIPP工法（软管翻转法、软管拉入加热固化法、软管拉入紫外线固化法）遵照ASTMF1216—05规定,计算出内衬层厚度,并与招标文件对比,指出其不足。希望引起排水业界对CIPP工艺适用范围的关注,在应用中加强技术评价工作,以进一步促进管道非开挖修复事业在我国的健康发展。     

A pre-edge analysis of Mn K-edge XANES spectra to help determine the speciation of manganese in minerals and glasses

High-resolution manganese K-edge X-ray absorption near edge structure spectra were collected on a set of 40 Mn-bearing minerals. The pre-edge feature information (position, area) was investigated to extract as much as possible quantitative valence and symmetry information for manganese in various “test” and “unknown” minerals and glasses. The samples present a range of manganese symmetry environments (tetrahedral, square planar, octahedral, and cubic) and valences (II to VII). The extraction of the pre-edge information is based on a previous multiple scattering and multiplet calculations for model compounds. Using the method described in this study, a robust estimation of the manganese valence could be obtained from the pre-edge region at 5% accuracy level. This method applied to 20 “test” compounds (such as hausmannite and rancieite) and to 15 “unknown” compounds (such as axinite and birnessite) provides a quantitative estimate of the average valence of manganese in complex minerals and silicate glasses. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Microfocus X-ray computed tomography analysis of corroded glass objects

Microfocus X-ray computed tomography (µCT) is a useful tool for non-destructive analysis of corroded archaeological glass objects and for monitoring restoration and conservation processes for these materials. This was demonstrated by µCT analysis of artificially corroded laboratory-produced glasses and corroded archaeological glasses retrieved from soil environments. Corrosion layers with a thickness of 20 µm or more can be detected as areas with lower X-ray attenuation values than the non-corroded glass. Features that are revealed by µCT analyses include the degree and patterns of corrosion and the presence of various internal structures in the corrosion layers. The study of restored corroded glasses demonstrates that mechanical and laser cleaning can be monitored efficiently. The study of consolidation practices, using test objects, requires the use of additives to increase X-ray attenuation values of the organic compounds that are used.     

Petrology and sulfur and chlorine emissions of the 1963 eruption of Gunung Agung,Bali, Indonesia

 The 1963 eruption of Gunung Agung produced 0.95 km³ dense rock equivalent (DRE) of olivine±hornblende-bearing, weakly phyric, basaltic andesite tephra and lava. Evidence for magma mixing in the eruptive products includes whole-rock compatible and incompatible trace element trends, reverse and complex compositional zoning of mineral phases, disequilibrium mineral assemblages, sieve-textured plagioclase phenocrysts, and augite rims on reversely zoned orthopyroxene. Basalt magma mixed with pre-existing andesite magma shortly before eruption to yield basaltic andesite with a temperature of 1040–1100  °C at an assumed pressure of 2 kb, f O₂>NNO, and an average melt volatile content (H₂O±CO₂) of 4.3 wt.%. Magma-mixing end members may have provided some of the S and Cl emitted in the eruption. Glass inclusions in phenocrysts contain an average of 650 ppm S and 3130 ppm Cl as compared with 70 ppm and 2220 ppm, respectively, in the matrix glass. Maximum S and Cl contents of glass inclusions approach 1800 and 5000 ppm, respectively. Application of the petrologic method to products of the 1963 eruption for estimating volatile release yields of 2.5×10¹²g (Mt) of SO₂ and 3.4 Mt of Cl released from the 0.65 km³ of juvenile tephra which contributed to stratospheric injection of H₂SO₄ aerosols on 17 March and 16 May, when eruption column heights exceeded 20 km above sea level. An independent estimate of SO₂ release from atmospheric aerosol loading (11–12 Mt) suggests that approximately 7 Mt of SO₂ was injected into the stratosphere. The difference between the two estimates can be most readily accounted for by the partitioning of S, as well as some Cl, from the magma into a water-rich vapor phase which was released upon eruption. For other recent high-S-release eruptions of more evolved and oxidized magmas (El Chichón, Pinatubo), the petrologic method gives values two orders of magnitude less than independent estimates of SO₂ emissions. Results from this study of the Agung 1963 magma and its volatile emissions, and from related studies on eruptions of more mafic magmas, suggest that SO₂ emissions from eruptions of higher-S-solubility magma may be more reliably estimated by the petrologic method than may those from more-evolved magma eruptions. Received: 29 June 1994 / Accepted: 25 April 1996     

Composition dependence of elasticity in aluminosilicate glasses

The elastic properties of two types of aluminosilicate (basaltic and rhyolitic) glasses have been studied using both Brillouin and Raman spectroscopy at ambient conditions. It has been found that the elastic moduli of the basaltic glasses decrease with increasing SiO₂ concentration. The shear moduli displayed the least dependence on SiO₂ content. The bulk moduli of the basaltic glasses strongly depend on the sum of the Q ³ and Q ⁴ anionic units. Among the modifiers, iron cations showed the strongest effect on the elastic properties of the rhyolitic glasses. For the elastic moduli of rhyolitic glasses, the major effect of alkaline earth cations is on shear modulus; however, both iron and alkali cations showed stronger effects on bulk modulus and similar relative contribution between bulk and shear moduli (based on the equivalent M⁺ cation). The dependences of elastic moduli on bulk NBO/T observed in both types of glasses suggest that the elastic modulus of an aluminosilicate glass depends on the concentration of effective modifying cations rather than the apparent concentration of all non-network-forming cations. An analysis of data also indicated that the ideal molar mixing model is failed in prediction of the elastic properties of the present multicomponent glasses by using the known parameters.     

High‐Precision Sr‐Nd‐Hf‐Pb Isotopic Composition of Chinese Geological Standard Glass Reference Materials CGSG‐1, CGSG‐2, CGSG‐4 and CGSG‐5 by MC‐ICP‐MS and TIMS

To assess the homogeneity of and provide the first Sr‐Nd‐Hf‐Pb isotopic reference values for the Chinese Geological Standard Glasses CGSG‐1, CGSG‐2, CGSG‐4 and CGSG‐5, we measured these isotopes in several measurement sessions over the course of nearly 3 years. The results were obtained by high‐precision MC‐ICP‐MS and TIMS. Our investigation indicates that these CGSG glass reference materials are homogenous with regard to Sr‐Nd‐Hf‐Pb isotopic distribution and are therefore suitable geochemical materials for Sr‐Nd‐Hf‐Pb isotope measurements. Clear differences in Sr‐Nd‐Hf‐Pb isotopic composition were observed between the glasses and the original powdered rock reference materials (CGSG‐2 and GSR‐7, and especially CGSG‐5 and GSR‐2) because of flux addition during preparation of the glasses. The new Sr‐Nd‐Hf‐Pb isotope data provided here might be useful to the geochemical community for in situ and bulk analysis.