Search

Black-odor water is a serious environmental issue in many developing counties. Iron sulfides and chromophoric dissolved organic matter are considered possible blackening substances. However, the specific type of blackening iron sulfides and the contributions of blackening substances are unclear. This study performed a laboratory simulation experiment to identify the blackening iron sulfides and quantify the contribution of blackening substances. The environmental conditions for forming blackening substances and their blackening process were also determined. We demonstrated that the black iron sulfide was mackinawite. Humic acid is another substance that absorbs light. The equivalent contributions of mackinawite and humic acid were 18.94 m -1 /mg Fe 2+ and 1.11 m -1 /mg DOC, respectively. A pH of more than 6 is a precondition for producing mackinawite. The production of black substances is the foundation of the blackening process, but the suspension of black substances is essential in causing water blackening. Fulvic acid stabilizes the suspension by changing the surface charge of blackening substances. Moreover, blackening substances can also be suspended with microbial flocs. Determining blackening substances and their role during the blackening process would allow for developing precise and targeted control technologies, improving urban water over the long term., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have influenced the work reported in this paper., (Copyright © 2022 Elsevier B.V. All rights reserved.)

Film-forming techniques and the control of heat release in micro-energetic chips or devices create challenges and bottlenecks for the utilization of energy. In this study, promising nano-Al/MoO 3 metastable intermolecular composite (MIC) chips with an uniform distribution of particles were firstly designed via a convenient and high-efficiency electrophoretic deposition (EPD) technique at room temperature and under ambient pressure conditions. The mixture of isopropanol, polyethyleneimine, and benzoic acid proved to be an optimized dispersing agent for EPD. The kinetics of EPD for oxidants (Al) and reductants (MoO 3 ) were systematically investigated, which contributed to adjusting the equivalence ratio of targeted energetic chips after changing the EPD dynamic behaviors of Al and MoO 3 in suspension. In addition, the obtained nano-Al/MoO 3 MIC energetic chips showed excellent heat-release performance with a high heat release of ca. 3340 J/g, and were successfully ignited with a dazzling flame recorded by a high-speed camera. Moreover, the fabrication method here is fully compatible with a micro-electromechanical system (MEMS), which suggests promising potential in designing and developing other MIC energetic chips or devices for micro-ignition/propulsion applications.

This paper presents the results of a comparative study of methods to prevent the loss of barium during the formation of thin-film proton-conducting electrolyte BaCe 0.89 Gd 0.1 Cu 0.01 O 3-δ (BCGCuO) on La 2 NiO 4+δ -based (LNO) cathode substrates by electrophoretic deposition (EPD). Three different methods of the BCGCuO film coating were considered: the formation of the BCGCuO electrolyte film without (1) and with a protective BaCeO 3 (BCO) film (2) on the LNO electrode substrate and the formation of the BCGCuO electrolyte film on a modified La 1.7 Ba 0.3 NiO 4+δ (LBNO) cathode substrate (3). After the cyclic EPD in six stages, the resulting BCGCuO film (6 μm) (1) on the LNO substrate was completely dense, but the scanning electron microscope (SEM) analysis revealed the absence of barium in the film caused by its intensive diffusion into the substrate and evaporation during the sintering. The BCO layer prevented the barium loss in the BCGCuO film (2); however, the protective film possessed a porous island structure, which resulted in the deterioration of the film's conductivity. The use of the modified LBNO cathode also effectively prevented the loss of barium in the BCGCuO film (3). A BCGCuO film whose conductivity behavior most closely resembled that of the compacts was obtained by using this method which has strong potential for practical applications in solid oxide fuel cell (SOFC) technology.