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31.
针对镀液温度变化的非线性和滞后性,设计了采用专家规则的镀液温度实时控制系统。该系统在实时监测的基础上,构建了综合评判镀液温度偏差和镀液温度偏差变化率的专家规则,实现了镀液温度的自适应快速调节。仿真分析结果表明,该系统克服了非线性和滞后性的不良影响,能够实现镀液温度的实时控制。 相似文献
32.
With increasing consumption of natural gas (NG), small NG reservoirs, such as coalbed methane and oil field associated gas, have recently drawn significant attention. Owing to their special characteristics (e.g., scattered distribution and small output), small-scale NG liquefiers are highly required. Similarly, the mixed refrigerant cycle (MRC) is suitable for small-scale liquefaction systems due to its moderate complexity and power consumption. In consideration of the above, this paper reviews the development of mobile miniature NG liquefiers in Technical Institute of Physics and Chemistry (TIPC), China. To effectively liquefy the scattered NG and overcome the drawbacks of existing technologies, three main improvements, i.e., low-pressure MRC process driven by oil-lubricated screw compressor, compact cold box with the new designed heat exchangers, and standardized equipment manufacturing and integrated process technology have been made. The development pattern of “rapid cluster application and flexible liquefaction center” has been eventually proposed. The small-scale NG liquefier developed by TIPC has reached a minimum liquefaction power consumption of about 0.35 kW·h/Nm3. It is suitable to exploit small remote gas reserves which can also be used in boil-off gas reliquefaction and distributed peak-shaving of pipe networks. 相似文献
33.
负载型金属催化剂在水处理中起着重要的作用,浸渍法是制备负载型催化剂的重要方法。为了克服传统浸渍方法的缺点,本文通过使用甘氨酸/盐酸作为缓冲溶液,严格控制pH,获得高分散的活性组分并以此方法制备了铁基类芬顿催化剂。对苯酚催化降解的实验表明,使用缓冲溶液法制备的催化剂比未使用的样品可以更高效地去除苯酚,1h内对苯酚的降解可达89.3%。此外,通过调节浸渍温度、浸渍时间和缓冲溶液的pH等参数来精确控制活性组分的量和催化活性。更重要的是,此催化剂制备方法可以用于其他负载型金属催化剂的制备,比如过硫酸盐催化剂,并取得了良好的催化效果。 相似文献
34.
《International Journal of Hydrogen Energy》2020,45(20):11749-11760
To make SOFC high efficiency energy generation devices, thin ceramic films are proposed as their main components. The rate of the oxygen reduction reaction is relevant for the overall performance of the SOFC, hence a lot of attention is given to the cathodes and their interfaces. The airbrushed solution combustion (ASC) method was used to fabricate an LSM thin film on a dense YSZ substrate. A single phase LSM perovskite was obtained with very thin and interconnected porosity, and a small average grain size (55 nm). The nanostructured LSM thin film electrode showed a low total activation energy (1.27 eV) at high temperatures, but a high area specific resistance at 850°C (55 Ω.cm2). The activation energy for the dissociative adsorption and diffusion of oxygen was significantly low (1.27 eV), while the charge transfer and oxygen ion migration activation energy at the LSM/YSZ interface (1.28 eV) was closer to those usually reported. 相似文献
35.
《International Journal of Hydrogen Energy》2020,45(20):11593-11604
Biogas is a renewable biofuel that contains a lot of CH4 and CO2. Biogas can be used to produce heat and electric power while reducing CH4, one of greenhouse gas emissions. As a result, it has been getting increasing academic attention. There are some application ways of biogas; biogas can produce hydrogen to feed a fuel cell by reforming process. Urea is also a hydrogen carrier and could produce hydrogen by steam reforming. This study then employes steam reforming of biogas and compares hydrogen-rich syngas production and carbon dioxide with various methane concentrations using steam and aqueous urea solution (AUS) by Thermodynamic analysis. The results show that the utilization of AUS as a replacement for steam enriches the production of H2 and CO and has a slight CO2 rise compared with pure biogas steam reforming at a temperature higher than 800 °C. However, CO2 formation is less than the initial CO2 in biogas. At the reaction temperature of 700 °C, carbon formation does not occur in the reforming process for steam/biogas ratios higher than 2. These conditions led to the highest H2, CO production, and reforming efficiency (about 125%). The results can be used as operation data for systems that combine biogas reforming and applied to solid oxide fuel cell (SOFC), which usually operates between 700 °C to 900 °C to generate electric power in the future. 相似文献
36.
37.
《Contact lens & anterior eye》2020,43(4):338-344
PurposeTo compare the sensitivity of two genotypes of P. aeruginosa to various disinfectant solutions and analyze the attached bacteria on worn cosmetic contact lenses (cosCLs).MethodsIn this prospective study, healthy volunteers wore etafilcon (brown), nelfilcon (gray), or hilafilcon (black) cosCLs and microbial adhesion analysis was performed. A rub-off test determined pigment dislodgement. Disinfectant sensitivity to Optifree Replenish (Alcon), Optifree Pure Moist (Alcon), Renu Fresh (Bausch & Lomb), and AoSept Plus (Ciba Vision) was tested at various disinfection times and compared between various genotypes and Type III secretion (T3S) system mutants.ResultsOf the 1152 cosCLs collected, 364 were culture positive (32%). The highest rate of culture-positive lens was hilafilcon (chi square, P = 0.0001). Hilafilcon also had a significantly greater number of isolates than etafilcon (P < 0.0001). Hilafilcon was the only lens to fail the rub-off test. Cytotoxic strains were significant more resistant to Renu Fresh than were invasive strains, even at 100% of recommended disinfection time (P = 0.0005). Of the tested disinfectants, Renu Fresh was significantly less effective in killing both genotypes of P. aeruginosa compared to AoSept Plus at all time points (25%, 50%, 75%, and 100% recommended disinfection time, P = 0.0001, 0.0001, 0.0005, and 0.0005, respectively). When the T3S system was dysfunctional, mutant strains were all susceptible to disinfectants (P = 0.0001 for both invasive and cytotoxic strains).ConclusionPseudomonas species is commonly found on cosCLs of asymptomatic individuals. Wearers of cosCLs that dislodge pigments may be predisposed to microbial contamination. Cytotoxic strains are more resistant to disinfectant solutions, especially to Renu Fresh. P. aeruginosa disinfectant resistance requires a functional T3S system. 相似文献
38.
39.
《Ceramics International》2020,46(11):18623-18631
Low haze and anti-reflective glass has high potential applications in automobile and optoelectronic fields. Etching is a novel and effective method to fabricate gradient refractive index anti-reflective layer on glass surface. However, the gradient layer on glass surface prepared by the etching method usually characterizes rough porous structure, and the structural defect results in high haze and low abrasion resistance to restrict its applications. In this paper, a hydrothermal etching method has been explored to prepare anti-reflective glass. It has demonstrated to be a new and facile method successfully to tailor the porous nanostructure of gradient refractive index layer and largely decrease the haze of the glass, by adding complex compound in the etching solution. Compared with the etching solution containing NaOH, adding the complex compound of C6H5Na3O7 in the etching solution has the advantage to overcome the defects. The grain diameter of the graded porous anti-reflective film decreases from ~63 nm to ~18 nm, the etched film thickness increases from 0.44 μm to 1.55 μm, the haze decreases drastically from 23.76% to 1.00%, the reflectivity decreases from 5.88% to 1.08% and the abrasion resistance greatly increases. However, when changing the complex compound from C6H5Na3O7 to Na2HPO4, the haze is 23.44% and has no effect on decreasing haze. Structural characterizations show that the grain size in the porous gradient layer can be easily tailored by changing the ion radius of complex anion in the etching solution, and the optical properties can be controlled. The paper provides new insights into the nanostructures and the preparation approach of anti-reflective glass. 相似文献
40.
在1400℃下,将平均尺寸φ15 mm?10 mm的石灰块投入CaO?SiO2?FeO及CaO?SiO2?FeO?P2O5两组渣系中,研究了静态条件下石灰在两组渣系中的溶解行为。结果表明,两组渣系在反应界面周围形成四个区域,即基体渣层、C2S渗透层、铁酸钙渗透层和石灰层。渗透层为石灰中的Ca2+与液渣中的Fe2+相互渗透所形成的一个多相共存区域,存在致密固相层影响石灰的溶解。渗透层中的铁酸钙层逐渐被C2S层取代,C2S层厚度不断增加最终溶解于液相渣中。5~60 s两组渣系石灰溶解速度相近,60~80 s含磷渣系石灰溶解速度显著加快。当渣中加入P2O5时,磷会固溶于C2S中形成C2S?C3P固溶体层,该层的形成会排挤FeO进入渣中,提高渣的渗透能力,加速石灰溶解。 相似文献