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[Display omitted] • Highly stable perovskite nanocrystals in water were obtained by modifing wool keratin (WK) and crosslinking agent (PAPI). • CPB/WK-PAPI nanocrystals show excellent photoluminescence retention over time even after 512 days (>40 %). • Portable, low cost, and visualize test strips for amines were successfully made from these nanocrystals. Perovskite nanocrystals (PNCs) have emerged as promising candidates for fluorescent probes owing to their outstanding photoelectric properties. However, the conventional CsPbBr 3 (CPB) NCs are extremely unstable in water, which has seriously limited their sensing applications in water environment. Herein, we present a powerful ligand engineering strategy for fabricating highly water-stable CPB NCs by using a biopolymer of wool keratin (WK) as the passivator and the polyaryl polymethylene isocyanate (PAPI) as the cross-linking agent. In particular, WK with multi-functional groups can serve as a polydentate ligand to firmly passivate CPB NCs by the ligand exchange process in hot toluene; and then the addition of PAPI can further encapsulate CPB NCs by the crosslinking reaction between PAPI and WK. Consequently, the as-prepared CPB/WK-PAPI NCs can maintain ∼ 80 % of their relative photoluminescence (PL) intensity after 60 days in water, and they still maintain ∼ 40 % of their relative PL intensity even after 512 days in the same environment, which is one of the best water stabilities compared previously reported polymer passivation methods. As a proof-of their application, the portable CPB/WK-PAPI NCs-based test strips are further developed as a fluorescent nanoprobe for real-time and visual monitoring amines and food freshness. Among various amine analytes, the as-prepared test strips exhibit higher sensitivity towards conjugated amines, achieving a remarkable detection limit of 18.3 nM for pyrrole. Our research not only introduces an innovative strategy involving natural biopolymers to enhance the water stability of PNCs, but also highlights the promising potential of PNCs for visually and portably detecting amines and assessing food freshness. [ABSTRACT FROM AUTHOR]

The dissolution of silica and transparent exopolymer particles (TEP) can deposit on the membrane surface and cause serious membrane fouling in reverse osmosis (RO) technology. Coagulation, as a common pretreatment process for RO, can effectively intercept pollutants and alleviate membrane fouling. In this study, FeCl 3 and AlCl 3 coagulants and polyacrylamide (PAM) flocculants were used to explore the optimal coagulation conditions to reduce the concentration of silica and TEP in the RO process. The results showed that the two coagulants had the best removal effect on pollutants when the pH was 7 and the dosage was 50 mg/L. Considering the proportion of reversible fouling after coagulation, the removal rate of pollutants, and the residual amount of coagulation metal ions, the best PAM dosage was 5 mg/L for FeCl 3 and 1 mg/L for AlCl 3. After coagulation pretreatment, the Zeta potential decreased, and the particle size distribution increased, making pollutants tend to aggregate, thus effectively removing foulants. The removal mechanisms of pollutants by coagulation pretreatment were determined to be adsorption, electric neutralization and co-precipitation. This study determined the best removal conditions of silica and TEP by coagulation and explored the removal mechanism. • The removal mechanism of silica and transparent extracellular polymeric particles by coagulation was explored. • The optimal conditions for coagulation to mitigate membrane fouling caused by silica and transparent extracellular polymeric particles was determined. • FeCl 3 demonstrates a more effective membrane fouling mitigation compared to AlCl 3. [ABSTRACT FROM AUTHOR]

Dissolved silica and transparent exopolymer particles (TEP) are the primary foulants in reverse osmosis (RO) desalinated brackish water and wastewater. In this study, we investigated the fouling properties of varying silica concentrations with TEP on the membrane surface and discovered a synergistic fouling effect between the silanol group (Si–OH) and the TEP carboxyl group (-COOH). The membrane fouling experiments showed that silica fouling approached saturation at 6 mM, with little variation in membrane flux as the silica concentration increased. Furthermore, the –OH functional group of the monosilicate molecule can chemically react with the -COO- functional group on the membrane surface to create hydrogen bonds, allowing monosilicate deposition directly on the membrane. Silica-silica interactions reacted with aggregates at high silica concentrations and joined with TEP to create a more substantial, more complex cross-linked network, resulting in severe membrane fouling. At pH 9, silica fouling was most severe due to the dramatic increase in the solubility of monosilicic acid dissolution in solution and the decreased polymerization rate. This work reveals the essential process of membrane fouling induced by silica and TEP, significantly increasing knowledge on silica-TEP fouling. The contamination of reverse osmosis membranes by silica and transparent exopolymer particles (TEP) was investigated using a laboratory-scale reverse osmosis plant. The mechanism of interaction was also mapped through multiple characterisations to explain the complexation mechanism of the two contaminants causing membrane fouling. [Display omitted] • At 6 mM, silica saturated the reverse osmosis membrane fouling. • The TEP was easily transformed from colloid to particles when silica levels increased. • The silane alcohol group (Si–OH) and the carboxyl group (-COOH) of TEP have a synergistic impact. • The solubility of silica solution was greatest at pH 9, and membrane fouling was the most severe. [ABSTRACT FROM AUTHOR]

This paper examines the causal impact of LEED (Leadership in Energy & Environmental Design) certification on energy consumption among federally owned buildings that were retrofitted over the period 1990–2019. Using a difference-in-differences propensity score matching approach, the paper has two findings. First, despite energy savings being an explicit federal goal, LEED-certified retrofits of federal buildings did not have statistically significant energy savings on average. Second, LEED buildings with higher energy scores had greater energy efficiency post-certification, and the improvements were economically meaningful. The absence of energy savings on average appears to be driven by three factors — trade-offs across energy and other areas in acquiring points for certification, possible changes in energy use after the official performance period for LEED certification ended, and improvements in the energy efficiency of all federal buildings. [ABSTRACT FROM AUTHOR]