Dissolution of Ti wires in sulphuric acid and hydrochloric acid solutions

Ti wire electrodes were immersed in acidic solutions containing H₂SO₄ and HCl of various concentrations at 353 K to evaluate corrosion rate by measurement of electric resistance change (resistometry). Addition of hydrochloric acid to sulphuric acid solution promoted depassivation of Ti. After depassivation, the immersion potential dropped to the hydrogen evolution potential and a hydride layer was formed on the surface. The hydride layer dissolved continuously in the acidic solution. SEM observation showed that Ti wires dissolved almost uniformly in the early stage and that the dissolution then trace became irregular due to nonuniform growth of the hydride layer. Dissolution rate of a Ti wire was estimated almost accurately by resistometry.     

钙矾石膨胀机理的SEM研究

本文利用扫描电镜观察了在具有不同矿物组成的系统中生成的钙矾石的形成与膨胀机理。发现能够产生膨胀的钙矾石是由局部化学反应所生成；它们在未水化的铝酸盐矿物表面原地结晶，呈放射状生长。通过溶解，沉淀生成的钙矾石不能凝结，没有膨胀性。     

Preparation of flat-polished specimens for SEM-backscattered electron imaging and X-ray microanalysis—importance of epoxy impregnation

Representative and quantitative microstructural information of cement-based materials can be obtained in the backscattered electron and X-ray modes of the scanning electron microscope (SEM). One prerequisite, of several, is to use flat specimens. Microstructures that are minimally affected by the grinding and polishing necessary to produce the flat surface can be obtained. It is essential to fill the pores of the specimen with epoxy resin prior to grinding and polishing. After hardening, the epoxy stabilizes the microstructure and enables it to withstand the stresses of grinding and polishing without alteration. In the present paper, we describe a preparation technique that we consider to have produced excellent polished specimens. The importance of epoxy impregnation is demonstrated.     

Antimicrobial finishing of regular and modified polyethylene terephthalate fabrics

An effective two-stage method has been developed for imparting antimicrobial properties to regular polyethylene terephthalate (R-PET), polyethylene glycol modified polyethylene terephthalate (PEG-M-PET), R-PET/Cotton blend (R-PET/C) and PEG-M-PET/Cotton blend (PEG-M-PET/C) fabrics. The method consists of partial hydrolysis of the fabrics to create carboxylic groups in PET macromolecules followed by subsequent reaction with dimethylalkylbenzyl ammonium chloride (DMABAC) under alkaline conditions. The reaction conditions such as pH, reaction temperature and time, carboxylic content, and DMABAC concentration were studied. Characterization of the finished fabrics was carried out through scanning electron microscopy (SEM) and Fourier transform infrared spectra (FTIR). All the modified PET fabrics showed excellent antibacterial activity towards Gram-positive (Bacillus mycoides), Gram-negative (Escherichia coli), and nonfilamentous fungus (Candida albicans). The achieved antimicrobial functions on the PET fabrics are durable in repeated laundering processes. Even after laundering 10 times the fabrics could still provide more than 85% of its antimicrobial activity against B. mycoides, E. coli, and C. albicans. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Morphological aspects of rubber fracture and wear

Morphology of carbon black (CB)‐filled rubber was studied with AFM and SEM and the classification of filler agglomerates, based on their internal structure and filler–matrix interactions, has been proposed. It varies according to the activity of CB and the kind of rubber. It has been shown that fracture of rubber starts either inside filler agglomerates (de‐cohesion) or in a filler–matrix interphase (de‐adhesion) initiating wear of the material. Microscopic observations correlate well with TGA and EPR data of wear debris collected during friction of rubber. The increase of thermal stability of CB and the appearance of additional spin signals, respectively, for elongated samples or debris, are proposed to be associated with de‐cohesion or de‐adhesion of the agglomerates. New approach to the fracture of rubber called “fatal agglomerate concept” is presented. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Compatibility between Polyamide 6 and Polycarbonate

Polyamide （PA6） and polycarbonate （PC） were prepared by a Brabender mixer （ PLV- 151） at 240℃ with 30 rpm for duration of 8 and 6 minutes respectively. The epoxy resin （E） addition can lead to substantial microstructural changes in the PA6/PC blends. Scanning electron microscope （SEM） was used to observe the mixtures characterized by the domains of clearly segregated homophases and voids between the two polymers. PA6/PC of polyamide 6 and polycarbonate with epoxy resin addition under the composition ratio of 20/80, 20/80/1, 40/60/1 and 40/60, were tested to verify the key role of epoxy in promoting the compatibility of PA6 with PC during blending.     

An application of rapid freezing,freeze substitution–fixation for scanning electron microscopy

A combined technique of the rapid freezing, freeze substitution–fixation method and the osmium–DMSO-osmium method was devised. By this combined method we clearly observed the architecture of intracellular components in three dimensions. Morphological characteristics were generally similar to those of tissue prepared by the osmium–DMSO-osmium method but different in some respects. Mucigen droplets in intestinal goblet cells, for example, appeared as separated spheres, while in specimens prepared by chemical fixation they were observed as a mass of fused droplets. In the Golgi complex, all cisternae were extremely flat, although they usually dilated on the cis side after chemical fixation. Particles on the mitochondrial tubules of liver cells were well distinguished. They were mushroom shaped, as are those observed by negative staining. The combined method, that is, the rapid freezing, osmium–DMSO-osmium method, is thought to be effective for studying the true structure of intracellular components by scanning electron microscopy.     

导线物证的扫描电镜及能谱鉴定方法

对导线物证同一性的鉴定，可先用X射线能谱仪快速确定物证为同一物的必要条件，再用扫描电镜对物证的特征条纹或金相组织进行最后判定。该方法简便，可靠。     

特种钢用结晶器铜管破裂原因分析

通过对某特钢厂破裂的结晶器铜管进行金相实验、扫描电镜和能谱分析,并结合结晶器的生产、使用及失效过程情况,综合受力分析,认为铜管破裂原因主要是环境介质硫渗入形成硫化物,在拉应力作用下,裂纹沿脆性质点扩展导致的破坏。     

Experimental investigation and thermodynamic modeling of the Mg–Sn–Sr ternary system

The isothermal sections of the Mg–Sn–Sr ternary system in the Mg-rich region at 415 and 350 °C have been determined using the scanning electron microscopy (SEM) equipped with energy dispersive X-Ray spectrometry (EDS). The existence of the MgSnSr ternary compound was confirmed in these two isothermal sections. Two new compounds, named Mg₅Sn₃Sr and Mg₂₅Sn₂₄Sr_14, were found in the present work based on the SEM/EDS results. Thermodynamic optimization of the Sn–Sr binary and Mg–Sn–Sr ternary systems were carried out using the CALPHAD (CALculation of PHAse Diagrams) technique. The Modified quasi-chemical model (MQM) was used for the liquid solution which exhibits a high degree of short-range ordering behavior. The solid phases were described with the Compound energy formalism (CEF). Finally, a self-consistent thermodynamic databases for the Mg–Sn–Sr ternary system has been constructed in the present work, which can be an efficient and convenient guidance to investigate and develop the Mg-based alloys.