Water quality management and load reduction are subject to inherent uncertainties in watershed systems and competing decision objectives. Therefore, optimal decision-making modeling in watershed load reduction is suffering due to the following challenges: (a) it is difficult to obtain absolutely ``optimal'' solutions, and (b) decision schemes may be vulnerable to failure. The probability that solutions are feasible under uncertainties is defined as reliability. A reliability-oriented multi-objective (ROMO) decision-making approach was proposed in this study for optimal decision making with stochastic parameters and multiple decision reliability objectives. Lake Dianchi, one of the three most eutrophic lakes in China, was examined as a case study for optimal watershed nutrient load reduction to restore lake water quality. This study aimed to maximize reliability levels from considerations of cost and load reductions. The Pareto solutions of the ROMO optimization model were generated with the multiobjective evolutionary algorithm, demonstrating schemes representing different biases towards reliability. The Pareto fronts of six maximum allowable emission (MAE) scenarios were obtained, which indicated that decisions may be unreliable under unpractical load reduction requirements. A decision scheme identification process was conducted using the back propagation neural network (BPNN) method to provide a shortcut for identifying schemes at specific reliability levels for decision makers. The model results indicated that the ROMO approach can offer decision makers great insights into reliability tradeoffs and can thus help them to avoid ineffective decisions. (C) 2015 Elsevier B.V. All rights reserved.
Fe3O4@SiO2 magnetic nanoparticles modified by grafting poly(1-vinylimidazole) oligomer (FSPV) was fabricated as a novel adsorbent to remove Hg(II) from water. Fourier transform infra-red spectroscopy confirmed the successful grafting of oligomer, and thermogravimetric analysis showed FSPV had a high grafting yield with organic content of 22.8%. Transmission electron microscopy image displayed that FSPV particles were polymer-coated spheres with size of 10–20 nm. With saturation magnetization of 44.7 emu/g, FSPV particles could be easily separated from water with a simple magnetic process in 5 min. The Hg(II) adsorption capacity of FSPV was found to be 346 mg/g at pH 7 and 25 °C in 10 mM NaCl. Moreover, the removal of Hg(II) by FSPV was not obviously affected by solution pH (from 4 to 10) or humic acid (up to 8 mg/L as TOC). The presence of seven common ions including Na+, K+, Ca2+, Mg2+, Cl−, NO3−, and SO42− (up to 100 mM ionic strength) slightly increased the adsorption of Hg(II) by FSPV. X-ray photoelectron spectroscopy analysis revealed that the N atom of the imidazole ring was responsible for the bonding with Hg(II), whereas the bonding of Hg with N did not result in cleavage of Hg–Cl bond in HgCl2 and HgClOH. The regeneration of Hg(II)-loaded FSPV could be achieved with 0.5 M HCl rapidly in 10 min, and the removal of Hg(II) maintained above 94% in five consecutive adsorption–desorption cycles. Therefore, FSPV could serve as a promising adsorbent for Hg(II) removal from water.
Ye et al. have determined a maximum nitrous acid (HONO) yield of 3% for the reaction HO2 center dot H2O + NO2, which is much lower than the yield used in our work. This finding, however, does not affect our main result that HONO in the investigated Po Valley region is mainly from a gas-phase source that consumes nitrogen oxides.
[6,6]-Phenyl-C61-butyric acid-4'-hydroxyl-azobenzene ester (PCBAb) was synthesized and used as the acceptor in the fabrication of reversible UV-VIS response bi-state polymer solar cells (PSCs) based on the photoinduced cis-trans isomerization of PCBAb. The device can be switched between ``active'' and ``sleep'' by the irradiation of UV and visible light, respectively. The active device has a PCE of 2.0%. With UV irradiation, the device goes to ``sleep'' with a lowered PCE (0.4%), and simultaneously decreased J(sc), V-oc and FF, while after visible light treatment, the device is made ``active'' again. The mechanism of the bi-state process involves the different electron mobilities of the isomers. (C) 2015 Elsevier B.V. All rights reserved.