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Focused on the key areas of energy, buildings, industry, and transportation, with 2020 as the base year and 2035 as the target year, we respectively designed the baseline scenario, policy scenario, and enhanced scenario, calculated the emission reduction potential of air pollutants and CO2 of Beijing, and constructed an assessment method of co-control effect gradation index to evaluate the co-control effect of air pollutants and CO2 in the policy scenario and enhanced scenario. The results showed that in the policy scenario and enhanced scenario, the reduction rates of air pollutants emissions will reach 11%-75% and 12%-94%, respectively, and reduction rates of CO2 emissions will reach 41% and 52%, respectively, compared with those from the baseline scenario. Optimizing vehicle structure had the largest contribution to the emission reduction of NOx, VOCs, and CO2, and the emission reduction rates will reach 74%, 80%, and 31% in the policy scenario and 68%, 74%, and 22% in the enhanced scenario, respectively. Replacing coal-fired with clean energy in rural areas had the largest contribution to the emission reduction of SO2; the emission reduction rates will reach 47% and 35% in the policy scenario and enhanced scenario, respectively. Improving the green level of new buildings had the largest contribution to the emission reduction of PM10; the emission reduction rates will reach 79% and 74% in the policy scenario and enhanced scenario, respectively. Optimizing travel structure and promoting green development of digital infrastructure had the best co-control effect. The co-control effect of replacing coal-fired with clean energy in rural areas, optimizing vehicle structure, and promoting green upgrading of the manufacturing industry will be improved to a better status in the enhanced scenario. More attention should be paid to improving the proportion of green trips, implementing the promotion of new energy vehicles, and the green transportation of goods to reduce emissions in the field of transportation. At the same time, with the continuous improvement in electrification level in the end energy consumption structure, the proportion of green electricity should be increased by expanding local renewable energy power production and increasing external green electricity transmission capacity, to enhance the co-control effect of pollution and carbon reduction.
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Bottom ash, a power plant waste, was used to remove the organic pollutants in coking wastewater and papermaking wastewater. Particular attention was paid on the effect of bottom ash particle size and dosage on the removal of chemical oxygen demand (COD). UV-vis spectra, fluorescence excitation-emission matrix (FEEM) spectra, Fourier transform infrared (FTIR) spectra, and scanning electron microscopic (SEM) photographs were investigated to characterize the wastewaters and bottom ash. The results show that the COD removal efficiencies increase with decreasing particle sizes of bottom ash, and the COD removal efficiency for coking wastewater is much higher than that for papermaking wastewater due to its high percentage of particle organic carbon (POC). Different trends of COD removal efficiency with bottom ash dosage are also observed for coking and papermaking wastewaters because of their various POC concentrations. Significant variations are observed in the FEEM spectra of wastewaters after treatment by bottom ash. New excitation-emission peaks are found in FEEM spectra, and the fluorescence intensities of the peaks decrease. A new transmittance band in the region of 1400-1420 cm(-1) is observed in FTIR spectra of bottom ash after adsorption. The SEM photographs reveal that the surface of bottom ash particles varies evidently after adsorption.
Assuntos
Coque , Resíduos Industriais , Papel , Centrais Elétricas , Eliminação de Resíduos Líquidos/métodos , Poluentes da Água/química , Adsorção , Carbono/análise , Cor , Microscopia Eletrônica de Varredura , Tamanho da Partícula , Espectroscopia de Infravermelho com Transformada de FourierRESUMO
The effect of immobilized microorganism technique on the micro-polluted river water was studied by four kinds of gaia-biological aerated filter (G-BAF), which were formed by special microorganism (BP35) and four different carriers, including haydite, FPUFS, aquamats flexible carrier and artificial aquatic mat. The removal rates of NH4(+) -N, chlorophyll and turbidity were 83.0%-89.0%, 77.5%-89.0% and 84.4%-95.2%, respectively, and they were all higher than the removal rates of COD, UV254 and TP. The FPUFS contained reactive groups, such as hydroxyl, epoxy and acylamide groups, which made FPUFS load a great amount of enzymes and microorganisms. Therefore, the removal rates of pollutants for FPUFS-G-BAF were higher than those for the other three kinds of G-BAF. Hydraulic retention time (HRT) had little effect on the removal rate of NH4(+) -N, while affected the removal rate of COD significantly. When the concentration of dissolved oxygen (DO) increased from < 2 mg/L to > 4 mg/L, for the four kinds of G-BAF, the removal rates of COD and NH4(+) -N increased 11.9%-18.0% and 12.7%-16.1%, respectively. The result of GC-MS showed that the technique of G-BAF could effectively degrade the macro-molecule refractory organics into small-molecule substance.
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Bactérias/metabolismo , Reatores Biológicos/microbiologia , Rios , Poluentes Químicos da Água/metabolismo , Bactérias/citologia , Bactérias/crescimento & desenvolvimento , Biodegradação Ambiental , Células Imobilizadas , Filtração/métodos , Compostos Orgânicos/metabolismoRESUMO
In this study, nanoscale Fe(0) was immobilized in and on poly(vinyl alcohol) (PVA) microspheres by the inverse suspension crosslinked method. Two different sizes of Fe(0)/PVA microspheres were synthesized in the presence and absence of dispersant. The chelating action between Fe(2+) and PVA was identified by Fourier transform infrared and X-ray photoelectron spectroscopy. The morphology and distribution of the obtained Fe(0)/PVA microspheres were characterized by environmental scanning electron microscope, energy-dispersive X-ray spectrometry, and X-ray diffraction. Nanoscale Fe(0) particles were mostly dispersed over the surface of the microspheres. They were distributed more homogeneously on the surfaces of Fe(0)/PVA microspheres with diameter of 600-700 microm than those with diameter of 10-12 microm. The nitrobenzene (NB) reduction reactions followed pseudo-first-order kinetics. The normalized surface rate constants (k(SA)) values were determined to be 0.162 L h(-1)m(-2) for L-Fe(0)/PVA microspheres, 0.098 L h(-1)m(-2) for S-Fe(0)/PVA microspheres, and 0.023 L h(-1)m(-2) for nanoscale Fe(0) particles. Furthermore, with the analysis of the products by GC/MS, possible reductive pathways of NB by Fe(0)/PVA microspheres were suggested. The recovery rates of iron in microspheres were determined to be 81.17% for large Fe(0)/PVA and 60.31% for small Fe(0)/PVA.