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Natural environment hosts a considerable amount of accessible energy, comprising mechanical, thermal, and chemical potentials. Environment-induced nanogenerators are nanomaterial-based electronic chips that capture environmental energy and convert it into electricity in an environmentally friendly way. Polymers, characterized by their superior flexibility, lightweight, and ease of processing, are considered viable materials. In this paper, a thorough review and comparison of various polymer-based nanogenerators were provided, focusing on their power generation principles, key materials, power density and stability, and performance modulation methods. The latest developed nanogenerators mainly include triboelectric nanogenerators (TriboENG), piezoelectric nanogenerators (PENG), thermoelectric nanogenerators (ThermoENG), osmotic power nanogenerator (OPNG), and moist-electric generators (MENG). Potential practical applications of polymer-based nanogenerator were also summarized. The review found that polymer nanogenerators can harness a variety of energy sources, with the basic power generation mechanism centered on displacement/conduction currents induced by dipole/ion polarization, due to the non-uniform distribution of physical fields within the polymers. The performance enhancement should mainly start from strengthening the ion mobility and positive/negative ion separation in polymer materials. The development of ionic hydrogel and hydrogel matrix composites is promising for future nanogenerators and can also enable multi-energy collaborative power generation. In addition, enhancing the uneven distribution of temperature, concentration, and pressure induced by surrounding environment within polymer materials can also effectively improve output performance. Finally, the challenges faced by polymer-based nanogenerators and directions for future development were prospected. [ABSTRACT FROM AUTHOR]

Anti-gel fouling is a key problem faced by membrane desalination, especially for applications in organic acid-rich seawater. In this paper, a chemical crosslinking-based method was used to reconstruct and characterize the gel pollutants produced under the actual operating conditions of seawater desalination. In addition to the calcium alginate/calcium humate three-dimensional network skeleton, salt ions (K+, Na+, Mg2+, Cl−) in solution were also considered to ensure that the reconstructed gel was similar to pollutant gels on membranes under practical operating conditions. Characterizations showed that the reconstructed gel has high thermal insulation and stability, thus adjusting the temperature has no removal effect. Two detergents (sodium citrate and sodium hydroxide) were investigated, and their gel-removal mechanism was elucidated by molecular dynamics simulation. Numerical analysis showed that the electrostatic attraction interaction had a significant role in the gel cleaning process. Owing to the attraction of the lower electrostatic potential region in the cleaning agent, the ion exchange between Na+ in the cleaning agent and Ca2+ in the gel led to the breaking of the Ca2+-induced intermolecular bridge in the complex. As the adhesion of fouling gels decreased, the gel water solubility was increased, resulting in a decrease in weight and strength of the gel. Therefore, the integrity of the gel fouling layer was weakened and can be effectively removed. This study provides a theoretical basis for the removal of gel-like membrane fouling during actual seawater desalination. [ABSTRACT FROM AUTHOR]