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101.
Gun Wirtanen Timo Alanko Tiina Mattila-Sandholm 《Colloids and surfaces. B, Biointerfaces》1996,5(6):319-326
Biofilm growth of Bacillus subtilis, Pseudomonas fragi, Pediococcus inopinatus and Listeria monocytogenes was studied on stainless steel surfaces at room and low temperatures to evaluate the results of traditional hygiene measures. The results were compared with those of image analysis of stainless steel surfaces in an epifluorescence microscope. Statistical analyses were carried out to determine the variations between the conventional cultivation swab method, the glycocalyx amount obtained using swabbing, and the values of the areas of the biofilm, slime and cells. As a general rule, old biofilms showed total counts at approximately the same levels as the young biofilm. The results showed that temperature affected the results for all strains except B. subtilis. The strains of Pe. inopinatus and Ps. fragi showed increased attachment at 6°C and L. monocytogenes at 25°C. The biofilm slime was more easily detached than the cells. The results indicated that the traditional swab method is not reliable for the measurement of biofilm formation on surfaces. 相似文献
102.
A.?AsanEmail author M.?Kabasakaloglu M.?L.?Aksu 《Russian Journal of Electrochemistry》2005,41(2):154-158
In this study, the coverage conditions of mild steel with polypyrrole (PPy) were investigated. It was observed that the surface was passive up to 0.6 V, to the oxidation potential of pyrrole in oxalic acid solution. The PPy coverage was obtained with 0.1 M oxalic acid + 0.2 M pyrrole. A passivity mechanism supported with current potential curves was proposed. The PPy deposition was also investigated according to pyrrole and oxalic acid concentrations by successive voltammetric scans.This article was submitted by the authors in English.From Elektrokhimiya, Vol. 41, No. 2, 2005, pp. 175–180.Original English Text Copyright © 2005 by Asan, Kabasakaloglu, Aksu.This revised version was published online in April 2005 with corrections to the article note and article title and cover date. 相似文献
103.
The inhibition performance of five azomethine derivatives such as: 1-(4-Methyloxy phenylimino)-1-(phenylhydrazono)-propan-2-one (SB1), 1-(4-Methylphenylimino)-1-(phenylhydrazono) propan-2-one (SB2), 1-(phenylimino)-1(phenylhydrazono)-propan-2-one (SB3), 1-(4-Bromo phenylimino)-1(phenylhydrazono)-propan-2-one (SB4) and 1-(4-Chlorophenylimino)-1(phenylhydrazono) -propan-2-on (SB5) as corrosion inhibitors for mild steel in sulfuric acid 0.5 ?M were investigated using different methods. All experimental results demonstrate that these compounds are eficients inhibitors. The inhibition efficiencies () increase with inhibitors concentration. At 7.5 10?5 ?M, the was 97.27%, 96.31%, 94.23%, 93.19 and 91.64% for SB1, SB2, SB3, SB4 and SB5, respectively. The potentiodynamic polarization results indicated that all the studied inhibitors act as mixed type. The adsorption process on mild steel surface obeyed Langmuir isotherm. The associated activation parameters and thermodynamic have been calculated and discussed. The adsorbed film formed on the metal surface was characterized by SEM and EDX. 相似文献
104.
表面电沉积Ni—La2O3复合镀层的Fe26Cr1Mo不锈钢的氧化行为研究 总被引:3,自引:0,他引:3
Fe26Cr1Mo不锈钢在900℃氧化时,生成的氧化层在冷却过程中大量剥落,经表面共电沉积NiLa2O3复合镀层后,抗热循环能力明显提高。 相似文献
105.
M. Menning C. Schelle A. Duran J.J. Damborena M. Guglielmi G. Brusatin 《Journal of Sol-Gel Science and Technology》1998,13(1-3):717-722
Glass-like sol-gel coatings have been investigated as corrosion protective coatings on stainless steel. Magnesium- and borosilicate coatings with thickness of about 100–700 nm and methyl-modified SiO2 coatings with a thickness of about 2 m were deposited on stainless steel plates by dip-coating. The coatings were densified between 400°C and 500°C in different atmospheres (N2, air) for 1 h. The corrosion protection against gaseous attack was investigated by accelerated corrosion tests, at 800°C in air for 1 h. A corrosion protection factor was calculated from the relation Fe/Fe2O3, determined by XRD on the surface of coated and uncoated samples. Methyl-modified SiO2 coatings showed a protection factor, which was 2 orders of magnitude higher than for the other coatings. Electrochemical investigations were performed on samples submerged in a NaCl solution for 200 h. The corrosion propagation, polarization resistance and impedance vector were measured. For accelerated corrosion tests, polarization intensity curves were determined for high potentials of up to 1 V. Again excellent results were obtained for the methyl-modified SiO2 coatings, which remained passive for 200 h. Results of the salt spray corrosion test, however, showed no corrosion protection by the sol-gel coatings. After 2000 h in the salt spray chamber the steel was corroded and the coatings peeled off. It is concluded that for the further development of these coatings an improved interfacial passivation will be required. 相似文献
106.
以tiron作为柱前衍生试剂,用含3mmol·L-1pH 3.8的HOAc-NaOAc,40mmol·L-1TBA-Br和2mmol·L-1tiron的甲醇-水溶液(53+47)作流动相,在C18柱上,于15min内实现了WO42-、MoO42-的分离测定。钨和钼的检出限分别为5.98和3.20ng·ml-1。方法快速,选择性好,用于钢及合金中高含量钨和钼的测定,结果与标准值相符。 相似文献
107.
108.
Tarek M. Madkour Rasha A. Azzam 《Journal of polymer science. Part A, Polymer chemistry》2002,40(14):2526-2536
Polyurethane elastomers of a controlled molecular architecture were synthesized using a two‐step polymerization technique. The building blocks of the elastomeric materials included urea–urethane prepolymers end‐capped with diisocyanate groups and had an exact number of urea groups at both ends. Two‐dimensional bifurcated hydrogen‐bonding networks incorporating the urea groups were, with differential scanning calorimetric and dynamic mechanical thermal analyzer techniques, responsible for the increase in the glass‐transition temperature (Tg) of the hard block and sharp interface morphology between the pure “hard” domains and pure “soft” domains. The higher extent of the phase separation between the two phases contributed to higher elastic moduli for the hard blocks and higher tensile strength for the elastomeric samples. Higher elongation values were attributed to the liberation of the elastomeric chain ends that otherwise would have been constrained in the interface region. The higher Tg values of the hard blocks corresponded to an increase in the hardness values and a decrease in the tear‐strength values. The increase in the amount of urea groups within the hard segments, as a result of the increased amount of water and blowing catalyst, resulted in elastomeric foams with higher open‐cell content. This resulted in lower resilience values as measured using the pendulum rebound test and was attributed to the ability of the open cells to absorb and dissipate energy. © 2002 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 40: 2526–2536, 2002 相似文献
109.
《Surface and interface analysis : SIA》2003,35(6):525-535
We investigated the association of uranium with clean and corroded surfaces of 1010 carbon steel. Studying steel contaminated by uranium species will have an important effect on the development of methods used to clean radioactively contaminated metal waste. X‐ray photoelectron spectroscopy, synchrotron infrared microspectroscopy and laboratory‐based Fourier transform infrared analysis of steel surfaces exposed to uranyl nitrate showed the presence of crystallized hydrated uranyl oxides, uranyl hydroxides, iron oxyhydroxides and iron oxides. In general, heavily corroded areas physically shield the uranium species, which tended to associate spatially with hydroxyl groups and lepidocrocite. Lightly corroded areas contained uranium species with stronger axial U–O bonding. Infrared spectroscopy, Rutherford backscattering spectroscopy and energy‐dispersive spectroscopy mapping analysis revealed that the uranium species are well distributed within the upper micron of the thick corrosion layer and associated more with areas of high hydroxide content. Parameters such as the concentration of uranyl nitrate solution used to expose the carbon steel coupons, the method of contamination (dipped or sprayed with dilute uranyl nitrate solution) and the degree of corrosion (accelerated corrosion before and/or after contamination) played significant roles in the distribution and nature of the uranyl hydroxide/iron oxyhydroxide corrosion products found on the surface of all coupons. These factors must be considered in the development and optimization of decontamination processes for metal waste. Copyright © 2003 John Wiley & Sons, Ltd. 相似文献
110.
The reversed-phase high-performance liquid Chromatographic (RP-HPLC) behaviour of the binary chelates of V(V) and V(IV) with 4-(2-pyridylazo) resorcinol (PAR) and ternary chelates of vanadium with PAR and auxiliary ligands: hydrogen peroxide, hydroxylamine, tartrate and citrate were studied using a C18 column. The complex double-peak chromatograms of V(IV)/V(V)-PAR systems were studied and the origin of each peak was proved. Vanadium in ternary systems with PAR and hydrogen peroxide was found exclusively in V(V)-H2O2-PAR complex (single peak on the chromatogram) despite its initial oxidation state. The double role of hydroxylamine (complex agent and reductor) in vanadium systems with PAR was confirmed: in the V(V) system three species were identified (V(V)-PAR, V(V)-NH2OH-PAR and V(IV)-PAR), but in the V(IV) system only two: V(IV)-PAR and V(V)-NH2OH-PAR. Citrate and tartrate giving single peak were found as auxiliary ligands in ternary V(V) systems of analytical importance. Due to its masking potential towards iron (III) ions, citrate was chosen as the most suitable third component of a ternary vanadium system with PAR, to form the basis of an RP-HPLC method for direct determination of V in steel. 相似文献