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A new Cost-Effective Inertial Dimension Method pertaining to Following Motion and also Causing Kinesthetic Comments inside Lower-Limb Prosthesis Customers.
Nanometer-size zero-valent iron (NZVI) is an efficient reducing agent, but its surface is easily passivated with an oxide layer, leading to reaction inefficiency. In our study, oxalate (OA) was introduced into this heterogeneous system of NZVI, which could form ferrioxalate complexes with the NZVI surface-bound Fe3+ and dissolved Fe3+ in the solution. Photolysis of ferrioxalate complexes can facilitate the generation of Fe2+ from Fe3+ and CO2•- radical, both species have strong reduction capacity. Hence, a "photo-oxalate-Fe(0)" system through sunlight induction was established, which not only prohibited the formation of a surface passivation layer, but also displayed a synergetic mechanism of ferrioxalate photolysis to enhance reduction, exhibiting remarkably higher degradation activity (several times faster) toward the model pollutant Cr(VI) than the mechanism with NZVI alone. Factor tests suggested that both NZVI dosage and OA content markedly affected the reduction rate. Low pH was beneficial to the reduction efficiency. Moreover, recyclability experiment showed that the reduction rate decreased from 0.21706 to 0.03977 min-1 after three cycles of reuse due to the NZVI losing reaction activity generally, but the system still maintained considerable reduction capacity. Finally, a mechanism was revealed whereby NZVI would transform to Fe oxides after the exhaustion of its reductive power, and the photolysis of ferrioxalate to promote the cycling of iron species played the predominant role in providing extra reduction ability. These features confirm that introduction of OA into Cr(VI) reduction by NZVI through sunlight induction is advantageous and promising. V.In this study, sodium tripolyphosphate (STPP) was used to promote the removal of organic pollutants in a zero-valent copper (ZVC)/O2 system under neutral conditions for the first time. 20 mg/L p-nitrophenol (PNP) can be completely decomposed within 120 min in the ZVC/O2/STPP system. The PNP degradation process followed pseudo-first-order kinetics and the degradation rate of PNP gradually increased upon the decreasing ZVC particle size. The optimal pH of the reaction system was 5.0. Our mechanism investigation showed that Cu+ generated by ZVC corrosion was the main reducing agent for the activation of O2 to produce ROS. ·OH was identified as the only ROS formed during the degradation of PNP and its production pathway was the double-electron activation of O2 (O2→H2O2→·OH). In this process, STPP did not only promote the release of Cu+ through its complexation, but also promoted the production of ·OH by reducing the redox potential of Cu2+/Cu+. In addition, we could initiate and terminate the reaction by controlling the pH. At pH 8.1, the reaction was terminated. STPP was recycled to continuously promote the corrosion of ZVC and O2 activation as long as the pH was less then 8.1. This study provided a new and efficient way for O2 activation and organic contaminants removal. V.The leaching concentrations of different metals in stainless steel pickling residue (SSPR) were determined and the toxic metals were treated using Na2S∙xH2O, FeSO4∙6H2O, and phosphoric acid. A modified European Community Bureau of Reference (BCR) sequential extraction was used to identify the speciation of the concerned metals. Results showed that SSPR contains a large amount of Ca (58.41%), Fe (29.44%), Cr (3.83%), Ni (2.94%), Mn (2.82%) and some of Al, Cu, Mg, Zn. Among them, Cr and Ni were the most toxic metals in SSPR, thus the raw SSPR falls into hazardous waste category due to the leaching amount of Cr. In addition, the leached Cr was identified as Cr6+ (MgCrO4) in the waste. BCR test revealed that risk assessment code (RAC) of Cr and Ni were 33.29% and 61.7%, indicating they posed "high" and "very high" risk to the environment, respectively. After fixing by Na2S∙xH2O and FeSO4∙6H2O, the leaching concentrations of Cr and Ni were less than 1.5 and 0.5 mg/L, respectively. After fixing by Na2S∙xH2O and FeSO4∙6H2O the treated SSPR can be safely reused as roadbed materials, concrete and cement aggregates. This study provides a useful implication in treatment and beneficial reuse of heavy metal-containing hazardous wastes. V.Coal-based olefin (CTO) industry as a complement of traditional petrochemical industry plays vital role in China's national economic development. However, high CO2 emission in CTO industry is one of the fatal problems to hinder its development. In this work, the carbon emission and mitigation potentials by different reduction pathways are evaluated. The economic cost is analyzed and compared as well. According to the industry development plan, the carbon emissions from China's CTO industry will attain 189.43 million ton CO2 (MtCO2) and 314.11 MtCO2 in 2020 and 2030, respectively. With the advanced technology level, the maximal carbon mitigation potential could be attained to 15.3% and 21.9% in 2020 and 2030. If the other optional mitigation ways are combined together, the carbon emission could further reduce to some extent. In general, the order of mitigation potential is followed as feedstock alteration by natural gas > CO2 hydrogenation with renewable electricity applied > CCS technology. selleck screening library The mitigation cost analysis indicates that on the basis of 2015 situation, the economic penalty for feedstock alteration is the lowest, ranged between 186 and 451 CNY/tCO2, and the cost from CCS technology is ranged between 404 and 562 CNY/tCO2, which is acceptable if the CO2 enhanced oil recovery and carbon tax are considered. However, for the CO2 hydrogenation technology, the cost is extremely high and there is almost no application possibility at present. V.Dissolved oxygen (DO) concentration is regarded as one of the crucial factors to influence partial nitrification process. However, achieving and keeping stable partial nitrification under different DO concentrations were widely reported. The mechanism of DO concentration influencing partial nitrification is still unclear. Therefore, in this study two same sequencing batch reactors (SBRs) cultivated same seeding sludge were built up with real-time control strategy. Different DO concentrations were controlled in SBRs to explore the effect of DO concentration on the long-term stability of partial nitrification process at room temperature. It was discovered that ammonium oxidation rate (AOR) was inhibited when DO concentration decreased from 2.5 to 0.5 mg/L. The abundance of Nitrospira increased from 1011.5 to 1013.7 copies/g DNA, and its relative percentage increased from 0.056% to 3.2% during 190 operational cycles, causing partial nitrification gradually turning into complete nitrification process. However, when DO was 2.
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