综述:多工况切换下同步磁阻电机动态响应增强型主动电流预测方法

《Processes》:A Dynamic-Response-Enhanced Active Current Prediction Method for Synchronous Reluctance Motors Under Multi-Operating-Condition Switching

【字体: 大 中 小 】 时间:2026年07月01日 来源:Processes 3.4

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  降黏剂是水基钻井液(WBDF)中用于对抗深井与超深井钻探中普遍存在的高温高盐环境所诱发流变性劣化的关键添加剂。本文系统综述了该领域的研究进展,将降黏剂划分为三大体系:改性天然材料、工业废弃物利用以及合成聚合物。改性天然材料降黏剂源自木质素、腐殖酸等可再生资源,

  
降黏剂是水基钻井液(WBDF)中用于对抗深井与超深井钻探中普遍存在的高温高盐环境所诱发流变性劣化的关键添加剂。本文系统综述了该领域的研究进展,将降黏剂划分为三大体系:改性天然材料、工业废弃物利用以及合成聚合物。改性天然材料降黏剂源自木质素、腐殖酸等可再生资源,经化学改性后具备环境友好特性;工业废弃物制备的降黏剂在实现资源循环利用的同时兼具经济效益;合成聚合物降黏剂通过引入磺酸基、羧酸基等功能单体并进行合理分子设计,可实现220 °C以上的耐温性能以及优异的耐盐耐钙能力,是当前领域内的主流研究方向。本文深入分析了各类降黏剂的作用机理,总结了其性能特征、合成方法及应用现状,并指出了在构效关系阐释、极端工况适应性以及技术转化效率方面存在的挑战。最后,本文讨论了未来的发展趋势,重点关注精准分子设计、超深井极限性能需求、环境可持续途径以及标准化评价体系建立。本综述旨在为深层油气资源的高效开发提供理论见解与实践指导。
A Dynamic-Response-Enhanced Active Current Prediction Method for Synchronous Reluctance Motors Under Multi-Operating-Condition Switching
Abstract
Viscosity reducers are essential additives for water-based drilling fluids (WBDFs), serving to counteract the rheological degradation induced by the high-temperature and high-salinity conditions commonly encountered in deep and ultra-deep well drilling. This paper systematically reviews the research progress in this field, categorizing viscosity reducers into three major systems: modified natural materials, industrial waste utilization, and synthetic polymers. Modified natural material viscosity reducers, derived from renewable materials such as lignin and humic acid via chemical modification, are environmentally friendly products. The preparation of viscosity reducers from industrial wastes realizes both resource recycling and economic benefits. Synthetic polymer viscosity reducers, incorporated with functional monomers such as sulfonic and carboxylic groups, achieve high performance with temperature resistance exceeding 220 °C as well as excellent salt and calcium tolerance via rational molecular design, and represent the current mainstream research direction in the field. This paper provides an in-depth analysis of the action mechanisms of various viscosity reducers, summarizes the performance characteristics, synthesis methods and application status, and identifies challenges in structure–property relationship elucidation, extreme working condition adaptability, and technology transfer efficiency. Finally, future development trends are discussed, with emphasis on precision molecular design, ultimate performance requirements for ultra-deep wells, environmentally sustainable approaches, and the establishment of standardized evaluation protocols. This review aims to provide both theoretical insights and practical guidance to support the efficient development of deep oil and gas resources.
1. Introduction
As global energy demand continues to grow and conventional oil and gas resources become increasingly depleted, oil and gas exploration and development are progressively expanding into deep, ultra-deep, and complex geological formations. Deep and ultra-deep well drilling has become an inevitable trend in the petroleum industry, which brings unprecedented technical challenges. As the “blood” of drilling engineering, drilling fluid directly affects the safety, efficiency, and cost of drilling operations. During deep well drilling, the downhole temperature increases significantly with well depth, often exceeding 150 °C and potentially reaching above 240 °C [1]. Simultaneously, salt-gypsum layers and high-salinity formations are more and more frequently encountered than ever before. High-temperature and high-salinity environments pose serious threats to the rheological properties of water-based drilling fluids. High temperature intensifies clay particle hydration expansion and polymer degradation, while high-concentration electrolytes compress the electrical double layer of clay particle surfaces, weakening the electrostatic repulsion between particles [2]. These effects collectively cause sharp increases in drilling fluid viscosity and gel strength, which in turn, result in troublesome problems under the downhole environment.
To effectively control drilling fluid rheological properties under harsh conditions, viscosity reducers are widely used as key additives. Their core function is to disrupt or inhibit the formation of spatial network structures among clay particles, thereby reducing viscosity and gel strength of drilling fluids and restoring or maintaining good fluidity. Traditional viscosity reducers, such as ferrochrome lignosulfonate (FCLS), exhibit good temperature and salt resistance; however, the chromium ions (especially highly toxic hexavalent chromium) generated during their production and application pose serious environmental and health hazards and have been restricted or banned by environmental regulations in many countries [2,3]. Under the global consensus of green, low-carbon, and sustainable development, the development of efficient, environmentally friendly viscosity reducers capable of adapting to extreme conditions (high temperature, high salinity, and high density) has become an urgent research topic in drilling fluid chemistry.
In recent years, researchers worldwide have conducted extensive work on water-based drilling fluid viscosity reducers and formed diverse technical approaches and product systems. Historically, inorganic and organic phosphates represent one of the earliest classes of viscosity reducers. These include sodium-based organic phosphates such as ethylenediamine tetramethylene phosphonic acid (EDTMPS), which, however, exhibits poor salt tolerance, as well as inorganic phosphates like sodium phosphate, sodium tripolyphosphate, and sodium hexametaphosphate [4,5]. However, the broader family of phosphate-based viscosity reducers generally suffers from low temperature resistance, typically not exceeding 80 °C for most conventional types. Due to this inherent limitation, they are not suitable for the high-temperature conditions encountered in deep and ultra-deep wells, which are the primary focus of this review. Therefore, these early phosphate-based additives are not covered in the review.
According to the material sources and synthesis strategies, the viscosity reducers that are the focus of this review can be divided into three main categories: modified natural materials, industrial waste utilization, and synthetic polymers, as shown in Figure 1. Among these, modified natural materials will be introduced first, followed by industrial waste-derived products, with synthetic polymers receiving the most detailed attention as the current mainstream research direction. These studies have not only promoted the development of high-performance viscosity reducer products but also deepened understanding of the microscopic viscosity reduction mechanism. This paper aims to comprehensively and systematically review the research progress on the development and application of water-based drilling fluid viscosity reducers. By elaborating on the molecular design principles, synthesis methods, performance characteristics, and mechanisms of various viscosity reducers, this review summarizes the current technological achievements and existing deficiencies and discusses future development trends and key research directions, so as to provide valuable references for subsequent innovative research and engineering applications in this field.
Figure 1.Main categories of water-based drilling fluid viscosity reducers: modified natural materials, industrial waste utilization, and synthetic polymers.
2. Structure and Properties of Bentonite High-Temperature Thickening Mechanism
Water-based drilling fluids are multiphase dispersion systems composed of water, clay (primarily bentonite), and various additives. The main component of bentonite is montmorillonite, whose structural characteristics determine the basic properties of drilling fluids. Therefore, understanding its structure and fundamental properties is essential for comprehending the high-temperature resistance and viscosity reduction mechanisms of viscosity reducers.
Montmorillonite is a layered silicate mineral belonging to the 2:1 layer-type clay mineral. Its crystal structure consists of one aluminum-oxygen octahedral sheet sandwiched between two silicon-oxygen tetrahedral sheets [6]. Adjacent crystal layers in montmorillonite allow exchangeable cations, water molecules, and other polar molecules to easily enter between layers, causing changes in the physicochemical properties of montmorillonite [7]. Due to isomorphous substitution in layered crystal particles, montmorillonite layers adsorb cations and polar water molecules, giving clay surfaces a permanent negative charge. Clay particle edges may carry positive or negative charges due to broken bonds or adsorption. Lowering the medium pH increases positive charges on particle edges, while raising the pH converts edge charges to negative. Clay particles form large, thick sheet structures through different associations, which are significantly influenced by electrolytes and pH [8,9,10].
The anisotropic charge distribution of montmorillonite—permanently negative basal surfaces and pH-dependent positively charged edges—directly governs the particle–particle interactions (edge-to-face, edge-to-edge, and face-to-face associations) that determine the rheological behavior of drilling fluids [11,12]. Specifically, the edge-to-face “card-house” network, which
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