Laccase Immobilized on Mesoporous Silica Materials and Its Corrosion Inhibition Performance in Circulating Cooling Water System

Mesoporous SiO_2 microspheres were synthesized using the sol-gel method and were characterized by TEM, FT-IR and BET techniques. The diameter of the microspheres is about 100—150 nm, and the average mesopore diameter is 2.55 nm, while the specific surface area is 1 088.9 m2/g. Mesoporous SiO_2 microspheres adsorb glutaraldehyde and immobilize laccase by means of the aldehyde group in glutaral which can react with the amidogen of laccase. The immobilization conditions were optimized at a glutaraldehyde concentration of 0.75%, a crosslinking time of 8 h, a laccase concentration of 0.04 L/L and an immobilization time of 10 h. When diesel leakage concentration was 80 mg/L, the highest corrosion inhibition efficiency of immobilized laccase reached 49.23%, which was slightly lower than the corrosion inhibition efficiency of free laccase(59%). The diesel degradation ratio could reach up to 45%. It has been proved that the immobilized laccase could degrade diesel to inhibit corrosion.

Mechanical and electrochemical characteristics in sea water of 5052-O aluminum alloy for ship

The optimum corrosion protection potentials were examined for 5052-O Al alloy,which is mainly used in ships.Various electrochemical experiments were carried out and the surface morphologies of specimens were observed by scanning electron microscopy（SEM） in order to determine the optimum corrosion protection potential to overcome pitting,corrosion,stress corrosion cracking（SCC）,and hydrogen embrittlement in sea water.An optimum protection potential range of-1.3 V to-0.7 V was determined under the application of an impressed current cathodic protection（ICCP） system.The low current densities were shown in the range of-1.3 V to-0.7 V in the electrochemical experiments and good specimen surface morphologies were observed after potentiostatic experiment.

Shear Strength of Reinforced Concrete Beams Under Sea Water

The marine structures such as harbour,pier and inshore concrete terrace are exposed in adverse circumstances in a long period of time .Owing to the attack of external corrosive medium,their safety,durability and reliability decline.Especially the reinforced concrete(RC) structures in the wave splash area are more likely to be subjected to destruction and the loss is vast. Now the safety ,durability and reliability of structure have become increasingly an important subject to be studied.By way of the soaking and drying cycle test on the different mix proportions oblique section of 10 pieces of RC beams suffered artificial sea water(ASW) corrosion under 0,35,70,105,140 times of dry-wet cycles,the compared results of exerting pressure test of these beams under simply supporting were investigated. The law about the changes of the mechanical performance for RC beams with different mix proportions under different time periods for suffering corrosion of dry-wet cycles is as follows: the resistivity to ASW corrosion of the concrete specimens with various water cement ratio(various initial strength)is different;the characters of oblique section failure for RC beams attacked by sea water are about the same as those for ordinary RC beam; along with the extension of the time for sea water attack, the bearing capacity for oblique section of RC beams varies wave upon wave.The specimens attacked by sea water for about 35 times of corrosion cycle achieve minimum bearing capacity.

典型溶蚀丘陵系统岩溶发育特征及其水资源开发条件分析——以湖南省新化县桑梓镇为例

我国典型溶蚀丘陵型岩溶发育区主要分布于湘中的新化县 -涟源县一带。受中国大陆梯级地形、复杂地质背景、气候水文等内外环境因子的联合作用 ,发育了一系列独具特色的不同类型的岩溶地貌及形态组合。宏观岩溶地貌主要有四种类型 :丛丘谷地、丘岭谷地、峰丛洼地谷地和峰丘谷地。不同单元岩溶发育特征差异明显。溶蚀速度在10 .2 6～ 30 .0 4 m3 / km2 · a,总体上侵蚀作用大于溶蚀作用 ,以流水溶蚀-侵蚀形态为主导特征。开发利用岩溶水应从地貌差异和岩溶水系统多层多块结构特点出发 ,因地制宜 ,蓄、引、提、堵等多种开发方式相结合。

溶蚀丘陵型岩溶流域概念性水文模型及其应用

为弥补传统概念性水文模型在岩溶水文模拟上的缺陷,基于三水源新安江模型,采用多个线性水库表达岩溶地下系统的异质性,同时引入流域虚拟面积系数修正岩溶流域的非闭合性。将改进的概念性水文模型应用于湘中南典型溶蚀丘陵型岩溶流域,并在此基础上探讨岩溶流域非闭合性的动态变化。研究结果表明:①改进模型的日径流模拟精度提高11.21%,水量平衡误差及低水误差分别降低23.29%、27.64%;②岩溶地下汇流系统的多向性导致流域非闭合状态具有双重性;③地下汇流面积与时段降雨量呈正相关,然而受地下饱和程度的制约,地下汇流面积的变化率随时段降雨量的增大而减小;④由于岩溶地貌的蓄水滞水作用,地下流域受外侧补给的过程存在滞后性。模型的改进与拓展研究可为岩溶水文模拟提供新思路。

Hydroxyl carboxylate based non-phosphorus corrosion inhibition process for reclaimed water pipeline and downstream recirculating cooling water system

A combined process was developed to inhibit the corrosion both in the pipeline of reclaimed water supplies（PRWS） and in downstream recirculating cooling water systems（RCWS）using the reclaimed water as makeup. Hydroxyl carboxylate-based corrosion inhibitors（e.g.,gluconate, citrate, tartrate） and zinc sulfate heptahydrate, which provided Zn^2＋ as a synergistic corrosion inhibition additive, were added prior to the PRWS when the phosphate（which could be utilized as a corrosion inhibitor） content in the reclaimed water was below 1.7 mg/L, and no additional corrosion inhibitors were required for the downstream RCWS.Satisfactory corrosion inhibition was achieved even if the RCWS was operated under the condition of high numbers of concentration cycles. The corrosion inhibition requirement was also met by the appropriate combination of PO4^3- and Zn^2＋ when the phosphate content in the reclaimed water was more than 1.7 mg/L. The process integrated not only water reclamation and reuse, and the operation of a highly concentrated RCWS, but also the comprehensive utilization of phosphate in reclaimed water and the application of non-phosphorus corrosion inhibitors. The proposed process reduced the operating cost of the PRWS and the RCWS, and lowered the environmental hazard caused by the excessive discharge of phosphate. Furthermore, larger amounts of water resources could be conserved as a result.

Water vapor corrosion behaviors of high-entropy pyrosilicates

In this study,the water vapor corrosion resistance of two types of high-entropy pyrosilicates((Yb_(0.2)Y_(0.2)Lu_(0.2)Ho_(0.2)Er_(0.2))_(2)Si_(2)O_(7)((5RE1/5)_(2)Si_(2)O_(7))and(Yb_(0.2)5Lu_(0.2)5Ho_(0.2)5Er_(0.2)5)_(2)Si_(2)O_(7)((4RE_(1/4))_(2)Si_(2)O_(7)))and two single-component pyrosilicates(Yb_(2)Si_(2)O_(7) and Lu_(2)Si_(2)O_(7))were evaluated at 1350℃ for 50e100 h,and the initial corrosion behaviors of these pyrosilicates were studied.The results showed that the final corrosion products of the four types of pyrosilicates were all X2-type monosilicates,exhibiting similar corrosion phenomena.However,(4RE_(1/4))_(2)Si_(2)O_(7) generated many nanoscale monosilicate grains during corrosion.The corrosion resistance of Lu_(2)Si_(2)O_(7) was clearly better than those of the others,and(4RE_(1/4))_(2)Si_(2)O_(7) exhibited the worst corrosion resistance.The corrosion mechanism of the pyrosilicate blocks was analyzed from the perspectives of grain size,bulk hydrophobicity,and binding energy.This study potentially provides a theoretical basis for the preparation of high-entropy pyrosilicates with different atomic ratios according to the different properties of the various rare earth elements.

Crack Initiation Mechanism of Z3CN20.09M Duplex Stainless Steel during Corrosion Fatigue in Water and Air at 290 °C

The crack initiation mechanism of a Z3CN20.09M duplex stainless steel （DSS） during corrosion fatigue （CF） in water and air at 290 ℃ was investigated by using a CF cracking machine and a scanning electron microscopy （SEM）. The cracks were initiated successively at the persistent stip bands （PSBs）, phase boundaries （PBs） and pitting corrosion points （PCPs） of the specimens when they were tested in water at 290 ℃, while in airat 290 ℃ the cracks were only initiated at the PSBs and PBs. And the cracks were found mainly to initiate at the PSBs and PBs when the specimens were tested in water and air at 290 ℃, respectively. The results also reveal that the cracks were likely to be initiated at the first 20% of fatigue life of the specimens tested in water at 290 ℃. However, the cracks were not found until 50% of fatigue life when tested in air at 290 ℃. Moreover, the crack numbers of the specimens tested in water at 290 ℃ were much more than those tested in air at 290 ℃.

Corrosion Behavior of Ni–20Cr–18W–1Mo Superalloy in Supercritical Water

The corrosion behavior of Ni–20Cr–18 W–1Mo superalloy in supercritical water 500 °C/25 MPa for 200 h is investigated using gravimetry, SEM/EDS, XPS, and TEM. The oxide films show a layered structure with Ni rich in the outer layer, and Cr rich in the inner layer, consisting of an outer Ni（OH）2and NiO layer, including some Cr（OH）3, and an inner Cr2O3, Ni Cr2O4, and WO3 layer. Mo elements are not oxidized. The oxide films grow via a mixed mechanism,namely metal dissolution/oxide precipitation mechanism and solid-state growth mechanism. The effects of secondary and primary carbides on the weight-gain trend and oxide formation are discussed.

Analysis of Oxides Formed on the Surface of the Alloy 690 in Hydrogenated Supercritical Water

The oxides formed on the surface of the alloy 690 in hydrogenated supercritical water at 400℃ for 1000 h were investigated using scanning electron microscopy,transmission electron microscopy,scanning transmission electron microscopy and energy-dispersive X-ray spectroscopy.The oxides on me surface of the alloy 690 exhibited multi-layer structure：an outer layer consisted of granular crystallites（NiO and NiFe_2O_4） and a compact inner layer（spinel and Cr_2O_3）.Chemical analysis indicated that the outer layer was enriched in nickel but depleted in chromium,whereas the inner layer was enriched in chromium and iron but depleted in nickel.The inner layer was also characterized as layered structure by Fe-rich spinel on top of continuous Cr_2O_3 layer.Besides,Cr_2O_3 nodules were readily observed at the oxides/alloy interface.

Characteristics of Oxidation and Oxygen Penetration of Alloy 690 in 600°C Aerated Supercritical Water

The oxide films formed on Alloy 690 exposed to 600 ℃ supercritical water were characterized using mass measurement, X-ray diffraction. Raman spectroscopy, scanning electron microscopy equipped with energy dispersive X-ray spectroscopy and X-ray photoelectron spectroscopy. It was found that the mass gain of the alloy in supercritical water decreased with increasing exposure time. The oxide films have a double-layer structure, with an inner layer rich in Cr and outer layer rich in Ni and Fe after short time and long time exposure. The penetration of the oxide along the grain boundaries was observed, and the penetration depth increased with increasing exposure time. The grain boundaries and voids are the short-path of oxygen diffusion into the metal.