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近年来,国际政治经济形势发生了深刻变革,中国的石油行业面临着严峻的多维挑战。在高成本开采压力之下,采取油气技术+互联网的方式,借助机器视觉技术建设智能油田有望成为当前油田降本增效的有效途径。通过调研机器视觉技术在油田应用现状及进展,对融合过程中存在的问题进行了分析挖掘,前瞻性地探讨了机器视觉与油田深度融合的建设目标、建设模式和建设方向。 相似文献
3.
为了提高RH无铬真空槽的使用寿命及保证使用过程的稳定性,通过对影响RH真空槽使用寿命的因素进行机理分析,有针对性地开展了技术攻关。采取改进浸渍管与环流管砌砖工艺、增加挡墙工艺、优化下部槽钢结构、RH真空槽焊接漏点检测和化冷钢技术等措施,使某公司RH真空槽浸渍管寿命从100炉提升到135炉左右,实现了1套下部槽与2套浸渍管与环流管配套使用,提高生产的稳定性,取得了良好的经济效益和社会效益。 相似文献
4.
概述了水泥行业碳排放的主要来源,分析了目前水泥工业碳减排的主要渠道,指出错峰生产和产能减量置换政策已成为压减水泥过剩产能的两大政策抓手。 相似文献
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Rui-Qi Zhang Ang Ma Xiang Liang Li-Min Zhao Hui Zhao Zhong-Yong Yuan 《Frontiers of Chemical Science and Engineering》2021,15(6):1550
The low cost and highly efficient construction of electrocatalysts has attracted significant attention owing to the use of clean and sustainable energy technologies. In this work, cobalt nanoparticle decorated N-doped carbons (Co@NC) are synthesized by the pyrolysis of a cobalt covalent organic framework under an inert atmosphere. The Co@NC demonstrates improved electrocatalytic capabilities compared to N-doped carbon without the addition of Co nanoparticles, indicating the important role of cobalt. The well-dispersed active sites (Co–Nx) and the synergistic effect between the carbon matrix and Co nanoparticles greatly enhance the electrocatalytic activity for the oxygen reduction reaction. In addition, the Co content has a significant effect on the catalytic activity. The resulting Co@NC-0.86 exhibits a superb electrocatalytic activity for the oxygen reduction reaction in an alkaline electrolyte in terms of the onset potential (0.90 V), half-wave potential (0.80 V) and the limiting current density (4.84 mA·cm–2), and a high selectivity, as well as a strong methanol tolerance and superior durability, these results are comparable to those of the Pt/C catalyst. Furthermore, the superior bifunctional activity of Co@NC-0.86 was also confirmed in a home-built Zn-air battery, signifying the possibility for application in electrode materials and in current energy conversion and storage devices. 相似文献
7.
在软锰矿湿法浸出过程中,采用传统搅拌桨反应器,容易出现流体“打旋”现象,导致传质效果差,进而降低反应效率。因而,本研究将刚柔组合桨应用于软锰矿的还原浸出过程,强化浸出过程的传质行为,提高锰矿浸出率。结果表明,在黄铁矿与软锰矿质量比为0.20,硫酸浓度为1.5 mol/L,液固比为10,温度为363 K下,软锰矿中锰的浸出率达到90.12%,与传统桨叶相比,锰浸出率提高5.5%。同时,研究发现浸出过程遵循核收缩模型且受表面化学反应控制,黄铁矿与软锰矿质量比、初始硫酸浓度、液固比的反应级数分别为1.2679、0.4182、1.1959,反应动力学方程为1- (1-X)1/3=0.96×103( )1.2679 [H2SO4]0.4182(L/S)1.1959exp(-41.75 ×103/RT)t,浸出反应的表观活化能为41.75 kJ/mol。刚柔组合桨体系下的软锰矿浸出反应表观活化能相比传统搅拌体系下的软锰矿浸出反应表观活化能的文献报道值降低4.515~20.54 kJ/mol。 相似文献
8.
张常兴 《石油化工腐蚀与防护》2021,(1)
某炼油厂12 Mt/a常减压蒸馏装置减压塔洗涤段填料局部产生严重结焦。从原料性质、操作参数、异常工况、设备问题和加工负荷等方面分析,结焦原因为:全厂停电、紧急停工导致洗涤油突然中断和填料层局部过热;洗涤油个别喷头堵塞,导致局部填料润湿不均匀;劣质原油及重污油掺炼比例提高和减压塔加工负荷的增大加剧了洗涤段结焦。提出了控制劣质原油及重污油掺炼比例、优化操作参数、设备和工艺技术改造等措施。 相似文献
9.
《Ceramics International》2021,47(21):29908-29918
The cellulose derived carbon/graphene/ZnO aerogel composite was prepared as an electrode in order to investigate the electrochemical properties. Carbon aerogel was synthesized using paper as an available cellulose source, and the composite was obtained through a new and simple preparation method including the immersion of monolithic carbon aerogel in graphene oxide/Zn2+ suspension and subsequent chemical reduction and freeze drying. The morphology, functional groups and crystalline structure of the samples were studied with Scanning Electron Microscopy (SEM), Fourier Transform Infrared Spectroscopy (FTIR) and X-ray Diffraction Spectroscopy (XRD), respectively. Electrochemical performance of the prepared binder free electrodes was examined using Cyclic Voltammetry (CV), Galvanostatic Charge-Discharge (GCD) and Electrochemical Impedance Spectroscopy (EIS). The data revealed that flexible carbon/graphene/ZnO composite resulted in a low density (0.035 g cm−3) electrode with the capacitance of 900 mF cm−2 at a high current density of 10 mA cm−2, lower IR drop and high cyclic stability (capacitance retention of 96%) after 1000 cycles, at 10 mA cm−2. These features were due to the presence of 3D porous conductive network, highly reduced graphene oxide, and the formation of ZnO nanoparticles on graphene sheets. Moreover, polyaniline (PANI) was introduced to carbon/graphene/ZnO composite electrode using electro-oxidation method at different reaction time and aniline concentration in order to achieve remarkably improved capacitance of 2500 mF cm−2 (at 10 mA cm−2) and low charge transfer resistance. Also, after the supercapacitor device assembly, the capacitance was retained. Based on the results, the synthesized composite is a promising material for new generation of lightweight freestanding electrodes with the high electrochemical performance. 相似文献
10.
In this work, one step process of synthesis of silver nanoparticles (Agnp) embedded in insitu formed calcium alginate (CA) beads is stated. CA, formed from the reaction between sodium alginate and calcium hydroxide, acts as reducing and stabilizing agent as well as support for nanoparticles. The reaction mechanism for the formation and stabilization of Agnp is proposed where the vicinal dihydroxy groups of alginate are assumed to act as the reducing agent for Ag+ to Ag°. Transmission electron microscopy (TEM), x‐ray diffraction (XRD), UV‐vis spectroscopy, field emission scanning electron microscopy (FESEM), and atomic absorption spectroscopy (AAS) were used to characterize the Agnp. The formation of spherical nanoparticles with average size range of 4‐5 nm was confirmed by TEM. Catalytic activity of this nano silver‐calcium alginate (Agnp‐CA) composite was evaluated in the reduction of p‐nitrophenol. Concentrations of sodium alginate, calcium hydroxide, and AgNO3 are found to be the parameters that critically affect the synthesis of Agnp. The efficacy of the catalyst is expressed on the basis of suitable reaction parameters. Both pseudo‐homogeneous and heterogeneous kinetic models are proposed for the reaction to find the best model and the Eley‐Riedel model is found to fit well with the experimental data. The novelty of this work is that the tandem process of CA bead formation, Agnp formation, and Agnp entrapment in CA have been transformed into a single‐step process. Moreover, elaborations of each step of the ionic mechanisms of Agnp formation and p‐NP reduction with Agnp and the establishment of a heterogeneous kinetic model for the reaction are reported for the first time here. 相似文献