Production chemistry is an important field in the petroleum industry to study the physicochemical changes in the production system and associated impact on production fluid flow from reservoir to topsides facilities. Mineral scale deposition and metal corrosion are among the top three water-related production chemistry threats in the petroleum industry, particularly for offshore deepwater and shale operations. Mineral scale deposition is mainly driven by local supersaturation due to operational condition change and/or mixing of incompatible waters. Corrosion, in contrast, is an electrochemical oxidation–reduction process with local cathodic and anodic reactions taking place on metal surfaces. Both mineral scaling and metal corrosion can lead to severe operational risk and financial loss. The most common engineering solution for oilfield scale and corrosion control is to deploy chemical inhibitors, including scale inhibitors and corrosion inhibitors. In the past few decades, various chemical inhibitors have been prepared and applied for scaling and corrosion control. Phosphorus-based polymers are an important class of chemical inhibitors commonly adopted in oilfield operations. Due to the versatile molecular structures of these chemicals, phosphorus-based polymeric inhibitors have the advantage of a higher calcium tolerance, a higher thermal stability, and a wider pH tolerance range compared with other types of inhibitors. However, there are limited review articles to cover these polymeric chemicals for oilfield scale and corrosion control. To address this gap, this review article systematically reviews the synthesis, laboratory testing, and field applications of various phosphorus-based polymeric inhibitors in the oil and gas industry. Future research directions in terms of optimizing inhibitor design are also discussed. The objective is to keep the readers abreast of the latest development in the synthesis and application of these materials and to bridge chemistry knowledge with oilfield scale and corrosion control practice.

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Hydrophobic hydrogels with high strength and great stretchability hold immense potential in various fields, such as soft robots, 3D printing, and flexible sensors. However, the formation of large hydrophobic domains in a hydrophobic hydrogel can lead to a heterogeneous structure in the bulk hydrogel. This phenomenon will result in the hydrophobic hydrogel becoming opaque, having a large energy hysteresis during stretching, poor strain-sensitivity, and slow self-recovery. In this study, we successfully developed a series of transparent hydrophobic hydrogels that exhibit excellent mechanical properties (low hysteresis and high toughness of ∼1.8−2.5 MJ m −3 ) with a desirable strain-sensitivity. The key factor in achieving this was the ability to tune large, inhomogeneous hydrophobic structures into small, well-ordered domains at the scale of 16.50−52.08 nm by introducing a small number of electrostatic groups into the hydrophobic networks. The hydrophobic hydrogels were able to form strong dual physical interactions, including electrostatic interactions and hydrophobic associations, making them ideal materials for fabricating wearable sensors with both in air and underwater applications. This facile and effective approach provides a novel method to prepare hydrophobic hydrogels with good mechanical performance, low hysteresis, and good strain-sensitivity, opening up new potential for their applications in various fields.

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