印尼褐煤无黏结剂型煤自燃与燃烧特性研究

在内辊式高压型煤机上将一种印度尼西亚褐煤压制成高强度的无黏结剂型煤,对其比表面积、孔容积和表面官能团进行分析,测定了型煤的相对着火温度和绝热氧化升温速率,研究了其热解和燃烧行为特性.结果表明,印尼褐煤在干燥和高压成型过程中,发生了孔的收缩和崩塌,特别是微孔收缩程度要更大一些;干燥和成型过程中有羟基、羰基和羧基含氧官能团的分解;经过提质处理后,褐煤的自燃着火倾向降低,热解和燃烧反应性降低.     

Mixing processes in the cavity transfer mixer: A thorough study

In many industrial applications, the quality of mixing between different materials is fundamental to guarantee the desired properties of products. However, properly modeling and understanding polymer mixing presents noticeable difficulties, because of the variety and complexity of the phenomena involved. This is also the case with the Cavity Transfer Mixer (CTM), an add‐on to be mounted downstream of existing extruders, to improve distributive mixing. The present work proposes a fully three‐dimensional model of the CTM: a finite element solver provides the transient velocity field, which is used in the mapping method implementation to compute the concentration field evolution and quantify mixing. Several simulations are run assessing the impact on mixing of geometrical and functioning parameters. In general, the number of cavities per row should be limited and the cavity size rather big to guarantee good mixing quality. © 2017 American Institute of Chemical Engineers AIChE J, 64: 1034–1048, 2018     

Synthesis of sulfides via reaction of aryl/alkyl halides with S8 as a sulfur-transfer reagent catalyzed by Fe3O4-magnetic-nanoparticles-supported L-Histidine-Ni(II)

One-pot synthesis of symmetrical diaryl/alkyl sulfides in high yields from the reaction between aryl/alkyl halides and S₈ can be carried out in a short period, using Fe₃O₄@SiO₂@His@Ni(II) as a reusable catalyst. The present approach offers the advantages of a clean reaction, simple methodology and high efficiency, and avoids the use of a toxic catalyst.     

Investigation of the effect of magnetic field on mass transfer parameters of CO2 absorption using Fe3O4‐water nanofluid

In this study, the enhancement of physical absorption of carbon dioxide by Fe₃O₄‐water nanofluid under the influence of AC and DC magnetic fields was investigated. Furthermore, a gas‐liquid mass transfer model for single bubble systems was applied to predict mass transfer parameters. The coated Fe₃O₄ nanoparticles were prepared using co‐percipitation method. The results from characterization indicated that the nanoparticles surfaces were covered with hydroxyl groups and nanoparticles diameter were 10–13 nm. The findings showed that the mass transfer rate and solubility of carbon dioxide in magnetic nanofluid increased with an increase in the magnetic field strength. Results indicated that the enhancement of carbon dioxide solubility and average molar flux gas into liquid phase, particularly in the case of AC magnetic field. Moreover, results demonstrated that mass diffusivity of CO₂ in nanofluid and renewal surface factor increased when the intensity of the field increased and consequently diffusion layer thickness decreased. © 2016 American Institute of Chemical Engineers AIChE J, 63: 2176–2186, 2017     

Absorption Enhancement in Ultrathin Structures Based on Crystalline-Si/Ag Parabola Nanocones Periodic Arrays with Broadband Antireflection Property

In this study, we examine the optical properties and unique features of a novel design of a parabola nanocone consisting of a homogenous shell-like cover layer of crystalline silicon (c-Si) and an Ag core which provides an enhanced absorption efficiency and significant photocurrent conversion during exposure to an incident light. Determining the geometrical sizes of the c-Si/Ag parabola nanocone, we designed an antireflection nanostructure based on certain arrays of investigated cone arrays on a GaAs substrate. We proved that the examined nanostructure shows a low percentage of reflectance of 6.24 % and a significant short current density of ~37.2 mA/m ² as well as broadband antireflection facility. This understanding paves the way for novel methods toward the use of a simple and two layer nanoparticle in designing efficient and high performance antireflection layers of photovoltaics and solar cells that are able to function over a wide range of spectrum.     

Investigating the effect of nano-silica on efficiency of the foam in enhanced oil recovery

Due to the vast production of crude oil and consequent pressure drops through the reservoirs, secondary and tertiary oil recovery processes are highly necessary to recover the trapped oil. Among the different tertiary oil recovery processes, foam injection is one of the most newly proposed methods. In this regard, in the current investigation, foam solution is prepared using formation brine, C₁₉TAB surfactant and air concomitant with nano-silica (SiO₂) as foam stabilizer and mobility controller. The measurements revealed that using the surfactant-nano SiO₂ foam solution not only leads to formation of stable foam, but also can reduce the interfacial tension mostly considered as an effective parameter for higher oil recovery. Finally, the results demonstrate that there is a good chance of reducing the mobility ratio from 1.12 for formation brine and reservoir oil to 0.845 for foam solution prepared by nanoparticles.     

Synthesis of polybutadiene nanoparticles by emulsion polymerization: The effect of electrolyte and initiator type on particle size and reaction kinetics

Emulsion polymerization of the butadiene (Bu) was performed in the presence of disproportionate potassium rosinate (DPR) as anionic emulsifier, potassium hydroxide (KOH), and potassium carbonate (K₂CO₃) as electrolytes, and three different initiators including potassium persulfate (KPS), 2,2^′-azobisisobutyronitrile (AIBN) or 4,4′-azobis(4-cyanovaleric acid) (ACVA, also known as VAZO) at 70 °C. Latexes were prepared with a solid content of about 30 wt%. The particle size and its distribution were measured by dynamic light scattering (DLS) analysis, while the polymerization conversion was determined gravimetrically at different time intervals. Results on the emulsion polymerization of Bu in the presence of KOH and K₂CO₃ co-electrolytes showed that adding KOH to the reaction media decreases the polymerization rate. Positive effect of co-electrolytes on the control over polybutadiene latex (PBL) particles size and its distribution was also confirmed, where K₂CO₃ played roles as electrolyte and pH buffer and KOH served double roles as electrolyte and alkaline supplier of the reaction media. Complete solubility of the AIBN in Bu resulted in higher rate of polymerization in the presence of AIBN in comparison to other initiators, i.e., VAZO or KPS. The results showed that initiator type plays a significant role on the formation of PBL nanoparticles and kinetics of the polymerization. The kinetic studies revealed that emulsion polymerization of Bu follows case 1 (i.e., \(\bar{n}\) ?0.5, where \(\bar{n}\) indicates average number of the propagating chains per particle) of the Smith-Ewart kinetics.     

The Ablation and Oxidation Behaviors of SiC Coatings on Graphite Prepared by Slurry Sintering and Pack Cementation

SiC coatings were generated on graphite using slurry sintering (SS) and pack cementation (PC). The samples’ ablation features were assessed by an oxyacetylene torch. The rates of mass ablation of the PC–SiC and SS–SiC coatings were approximated 2.17?×?10^?3 and 9.52?×?10^?3 g s^?1, respectively, decreased by 84.1 and 29.6% compared to the uncoated samples. It was mainly attributed to the formation of a SiO₂ layer on the surface. The continuous SiO₂ molten film formed via the PC–SiC oxidation generates a sealing mechanism which can be an obstacle against the oxygen diffusion and hinder more ablation. This is while discontinuous SiO₂ film formed from the thin SS–SiC cannot protect the graphite effectively. The non-isothermal oxidation test shows that without the SiC coating, the sample weight is lost largely from 25 to 1500 °C, and its weight loss was 2.2% after the TGA. However, after coating, the samples possessed excellent oxidation protection and weight losses of SS–SiC and PC–SiC coatings are down to 1.3 and 0.6%, respectively. The more oxidation of the graphite substrate occurred due to the formation of macrocracks in the coating during the TGA and also the formation of holes on SiO₂ glass layer owing to release of CO or CO₂.     

The synergistic effect of seawater's parameters on the corrosion rate of the austenitic stainless steel 304

In this article the corrosion rate of the austenitic stainless steel type 304, under the synergistic effect of environmental factors has been assessed via potentiodynamic polarization scan. Salinity, velocity, pH and temperature are the factors which induce effects on the corrosion rate of the considered metal. Quantitative analysis is applied using the full two-level factorial experimental design method, which results in the contribution value of each parameter in changing the quantity of average corrosion rate in both individual and synergistic cases. Besides this quantitative analysis, qualitative analysis has been used to predict the variation direction. These two analyses show the important role of the synergistic action, which changes the variation direction of corrosion rate and the contribution percentage of each parameter in varying the value of corrosion rate. Applying both these analyses can show the magnitude and quality of each parameter’s effect, which is remarkably valuable in marine applications.