Ferroelectric polarization effect on the photocatalytic activity of Bi0.9Ca0.1FeO3/CdS S-scheme nanocomposites

BiFeO₃ (BFO), as a kind of narrow band-gap semiconductor material, has gradually emerged advantages in the application of photocatalysis. In this paper, Ca doped BFO nanoparticles Bi_0.9Ca_0.1FeO₃ (BCFO) were prepared by sol-gel method. And BCFO and CdS nanocomposites with two morphologies were obtained by controlling the time of loading CdS under a low temperature liquid phase process. It is found that the band gap becomes narrower after doping Ca into BFO, which is conducive to the absorption of visible light. Among all the samples, the composite of CdS nanowires and BCFO nanoparticles obtained by reaction time of 10 min has the best photocatalytic performance. The degradation rate of Methyl Orange solution was 94% after 90 min under visible light irradiation, which was much higher than that of pure BCFO and CdS. Furthermore, significant enhancement in the degradation rate (100% degradation in 60 min) can be achieved in poled samples after electric polarization process. The highest degradation rate is due to the promoted separation of photogenerated carriers induced by the internal polarization field and the formation of S-scheme heterostructure between BCFO and CdS. Such BCFO-CdS nanocomposites may bring new insights into designing highly efficient photocatalyst.     

Porous FeOx/BiVO4-δS0.08：Highly efficient photocatalysts for the degradation of Methylene Blue under visible-light illumination

Porous S-doped bismuth vanadate with an olive-like morphology and its supported iron oxide （y wt.% FeOx/BiVO4-δS0.08, y = 0.06, 0.76, and 1.40） photocatalysts were fabricated using the dodecylamine-assisted alcohol-hydrothermal and incipient wetness impregnation methods, respectively. It is shown that the y wt.% FeOx/BiVO4-δS0.08 photocatalysts contained a monoclinic scheetlite BiVO4 phase with a porous olive-like morphology, a surface area of 8.8-9.2 m^2/g, and a bandgap energy of 2.38-2.42 eV. There was co-presence of surface Bi^5＋, Bi^3＋, V^5＋, V^3＋, Fe^3＋, and Fe^2＋ species in y wt.% FeOx/BiVO4-δS0.08. The 1.40 wt.% FeOx/BiVO4-δS0.08 sample performed the best for Methylene Blue degradation under visible-light illumination. The photocatalytic mechanism was also discussed. We believe that the sulfur and FeOx co-doping, higher oxygen adspecies concentration, and lower baudgap energy were responsible for the excellent visible-light-driven catalytic activity of 1.40 wt.% FeOx/BiVO4-δS0.08.     

活性炭催化过硫酸钠降解金橙G动力学

采用颗粒活性炭(granular active carbon,GAC)催化过硫酸钠(sodium persulfate,PDS)产生具有强氧化性的硫酸根自由基,以偶氮染料金橙G(orange G,OG)为目标污染物,研究了其降解过程及动力学.结果表明,GAC/PDS体系能通过氧化作用有效地去除金橙G,其中氧化降解速率主要与PDS投量、GAC投加量、溶液的初始浓度及反应温度有关,升高温度和GAC投量可以显著地加快OG的降解.且在初始浓度为0.050～0.125 mmol·L-1、pH值为5.0、n(PDS)/n(OG)为10/1～160/1、GAC投量为0.1～1.6 g·L-1、温度为298～338 K的实验范围内,反应的氧化降解符合一级动力学模型且与实验值吻合良好.另外还对GAC重复使用之后的催化效果进行了初步考察.     

Efficient visible light photo-Fenton-like degradation of organic pollutants using in situ surface-modified BiFeO3 as a catalyst

The visible light photo-Fenton-like catalytic performance of BiFeO₃ nanoparticles was investigated using Methyl Violet (MV), Rhodamine B (RhB) and phenol as probes. Under optimum conditions, the pseudo first-order rate constant (k) was determined to be 2.21×10^-2, 5.56×10^-2 and 2.01×10^-2 min^-1 for the degradation of MV (30 μmol/L), RhB (10 μmol/L) and phenol (3 mmol/L), respectively, in the BiFeO₃-H₂O₂-visible light (Vis) system. The introduction of visible light irradiation increased the k values of MV, RhB and phenol degradation 3.47, 1.95 and 2.07 times in comparison with those in dark. Generally, the k values in the BiFeO₃-H₂O₂-Vis system were accelerated by increasing BiFeO₃ load and H₂O₂ concentration, but decreased with increasing initial pollutant concentration. To further enhance the degradation of pollutants at high concentrations, BiFeO₃ was modified with the addition of surface modifiers. The addition of ethylenediamineteraacetic acid (EDTA, 0.4 mmol/L) increased the k value of MV degradation (60 μmol/L) from 1.01×10^-2 min^-1 in the BiFeO₃-H₂O₂-Vis system to 1.30 min^-1 in the EDTA-BiFeO₃-H₂O₂-Vis system by a factor of 128. This suggests that in situ surface modification can enable BiFeO₃ nano-particles to be a promising visible light photo-Fenton-like catalyst for the degradation of organic pollutants.     

Assembly of SPS/MgSi assisted by dopamine with excellent removal performance for ciprofloxacin

In this work, magnesium silicate-based sulfonated polystyrene sphere composites (SPS/MgSi) were synthesized by one-step (SMD1) and two-step (SMD2) methods. For SMD1, MgSi particles were densely assembled on the surface of SPS, assisted by complexation between Fe³⁺ and hydroxyl phenol. For SMD2, SPS/SiO₂ was firstly obtained by the same method as SMD1, and then SPS/SiO₂ was transformed directly to SPS/MgSi under hydrothermal conditions. Therefore, MgSi obtained by the two-step method had an interwoven structure. Compared to SPS, MgSi and SMD1, SMD2 presented a larger specific surface area and more negative surface charges. Therefore, SMD2 showed superior adsorption performance toward CIP with concentrations of 5, 10 and 50 mg/L, and for 50 mg/L, the equilibrium adsorption capacity could reach 329.7 mg/g. The adsorption process is fast and can be described by the pseudo-second-order kinetic model. The relationship between pH value and Zeta potential demonstrated that electrostatic interaction dominated the adsorption process. In addition, competitive adsorption showed that the effect of Na⁺ was negligible but the effect of Ca²⁺ was dependent on its concentration. Humid acid (HA) could slightly promote the absorption of CIP by SMD2. After five rounds of adsorption-desorption, the equilibrium adsorption capacity of SMD2 still remained at 288.6 mg/L for 50 mg/L CIP. Notably, SMD2 presented likewise superior adsorption capacity for CIP with concentrations of 10 and 50 mg/L in Minjiang source water. All the results indicated that this synthesis method is universal and that SMD2 has potential as an adsorbent for CIP removal from aquatic environments.     

Mediterranean shrublands carbon sequestration: environmental and economic benefits

To date, only a few attempts have been done to estimate the contribution of Mediterranean ecosystems to the global carbon cycle. Within this context, shrub species, composition and structure of the Mediterranean shrublands developing along the Latium coast (Italy) were analyzed in order to evaluate their contribution to carbon (C) sequestration, also taking into consideration the economic benefits at a national level. The considered shrublands had a shrub density of 1,200?±?500 shrubs ha^?1. Shrubs were classified into small (S), medium (M) and large (L), according to their volume (V) and leaf area index (LAI). The total yearly carbon dioxide (CO₂) sequestration per species (SC_y) was calculated multiplying the total photosynthetic leaf surface area (spt) of each species by the mean yearly photosynthetic rate and the total yearly photosynthetic activity time (in hours). Q. ilex and A. unedo had the highest SC_y (46.2?±?15.8 kg CO₂ year^?1, mean value), followed by P. latifolia (17.5?±?6.2 kg CO₂ year^?1), E. arborea, E. multiflora, C. incanus, P. lentiscus, R. officinalis, and S. aspera (6.8?±?4.2 kg CO₂ year^?1, mean value). The total yearly CO₂ sequestration per shrub (SC_shy) was 149?±?5 kg CO₂ year^?1 in L, decreasing 30 % in M and 80 % in S shrubs. Taking into account the frequency of S, M and L and their SC_shy, the total CO₂ sequestration of the Mediterranean maquis was quantified in 80 Mg CO₂ ha^?1?year^?1, corresponding to 22 Mg C ha^?1?year^?1. From a monetary viewpoint, this quantity could be valued to more than 500 US$ ha^?1?year^?1. Extending this benefit to the Mediterranean shrublands throughout the whole country, we obtained a nationwide estimated annual benefit in the order of $500 million.     

Preparation of MnO2 decorated Co3Fe1Ox powder/monolithic catalyst with improved catalytic activity for toluene oxidation

In this paper, KMnO₄ was used to pre-treat Co₃Fe-layered double hydroxides (LDH) precursor to prepare MnO₂ decorated Co₃Fe₁O_x catalyst. The toluene oxidation performance of the catalyst was investigated systematically. The optimized 0.1MnCF-LDO catalyst exhibited the best catalytic performance, and the temperatures of 50% and 90% toluene conversion (T₅₀ and T₉₀) were 218 and 243°C, respectively. The apparent activation energy (E_a) was 31.6 kJ/mol. The characterization results showed that the pre-redox reaction by KMnO₄ could increase the specific surface area, Co³⁺ species amount and oxygen defect concentration of the catalyst, which are the main reason of the improved toluene catalytic activity. Besides, this method was also applied to enhance toluene oxidation of iron mesh based monolithic catalyst. The 0.1MnCF-LDO/Iron mesh (IM) catalyst showed a 90% toluene conversion at around 316°C which was much lower than that of without MnO₂ addition (359°C). In addition, the water resistant of all the catalysts was studied as well, all the samples showed relatively good water resistance. The toluene conversion still remained to be over >80% even in the presence of 10 vol.% water vapor.     

Advanced treatment of biologically pretreated coal gasification wastewater by a novel heterogeneous Fenton oxidation process

Sewage sludge from a biological wastewater treatment plant was converted into sewage sludge based activated carbon(SBAC) with Zn Cl2 as activation agent, which was used as a support for ferric oxides to form a catalyst(Fe Ox/SBAC) by a simple impregnation method.The new material was then used to improve the performance of Fenton oxidation of real biologically pretreated coal gasification wastewater(CGW). The results indicated that the prepared Fe Ox/SBAC significantly enhanced the pollutant removal performance in the Fenton process, so that the treated wastewater was more biodegradable and less toxic. The best performance was obtained over a wide p H range from 2 to 7, temperature 30°C, 15 mg/L of H2O2 and 1 g/L of catalyst, and the treated effluent concentrations of COD, total phenols,BOD5 and TOC all met the discharge limits in China. Meanwhile, on the basis of significant inhibition by a radical scavenger in the heterogeneous Fenton process as well as the evolution of FT-IR spectra of pollutant-saturated Fe Ox/BAC with and without H2O2, it was deduced that the catalytic activity was responsible for generating hydroxyl radicals, and a possible reaction pathway and interface mechanism were proposed. Moreover, Fe Ox/SBAC showed superior stability over five successive oxidation runs. Thus, heterogeneous Fenton oxidation of biologically pretreated CGW by Fe Ox/SBAC, with the advantages of being economical, efficient and sustainable, holds promise for engineering application.     

CO2 emissions from tropical drained peat in Sumatra,Indonesia

With the increasing use of tropical peatland for agricultural development, documentation of the rate of carbon dioxide (CO₂) emissions is becoming important for national greenhouse gas inventories. The objective of this study was to evaluate soil-surface CO₂ fluxes from drained peat under different land-use systems in Riau and Jambi Provinces, Sumatra, Indonesia. Increase of CO₂ concentration was tracked in measurement chambers using an Infrared Gas Analyzer (IRGA, LI-COR 820 model). The results showed that CO₂ flux under oil palm (Elaeis guineensis) plantations ranged from 34?±?16 and 45?±?25 Mg CO₂ ha^–1 year^–1 in two locations in Jambi province to 66?±?25 Mg CO₂ ha^–1 year^–1 for a site in Riau. For adjacent plots within 3.2 km in the Kampar Peninsula, Riau, CO₂ fluxes from an oil palm plantation, an Acacia plantation, a secondary forest and a rubber plantation were 66?±?25, 59?±?19, 61?±?25, 52?±?17 Mg ha^–1 year^–1, respectively, while on bare land sites it was between 56?±?30 and 67?±?24 Mg CO₂ ha^–1 year^–1, indicating no significant differences among the different land-use systems in the same landscape. Unexplained site variation seems to dominate over land use in influencing CO₂ flux. CO₂ fluxes varied with time of day (p?<?0.001) with the noon flux as the highest, suggesting an overestimate of the mean flux values with the absence of night-time measurements. In general, CO₂ flux increased with the depth of water table, suggesting the importance of keeping the peat as wet as possible.     

Potassium ferrate pretreatment promotes short chain fatty acids yield and antibiotics reduction in acidogenic fermentation of sewage sludge

During the acidogenic fermentation converting waste activated sludge (WAS) into short-chain fatty acids (SCFA), hydrolysis of complex organic polymers is a limiting step and the transformation of harmful substances (such as antibiotics) during acidogenic fermentation is unknown. In this study, potassium ferrate (K₂FeO₄) oxidation was used as a pretreatment strategy for WAS acidogenic fermentation to increase the hydrolysis of sludge and destruct the harmful antibiotics. Pretreatment with K₂FeO₄ can effectively increase the SCFA production during acidogenic fermentation and change the distribution of SCFA components. With the dosage of 0.2 g/g TS, the maximum SCFA yield was 4823 mg COD/L, which is 28.3 times that of the control group; acetic acid accounts for more than 90% of the total SCFA. The higher dosage (0.5 g/g TS) can further increase the proportion of acetic acid, but inhibit the overall performance of SCFA production. Apart from the promotion of hydrolysis and acidogenesis, K₂FeO₄ pretreatment can also simultaneously oxidizes and degrades part of the antibiotics in the sludge. When the dosage is 0.5 g/g TS, the degradation efficacy of antibiotics is the most significant, and the contents of ofloxacin, azithromycin, and tetracycline in the sludge are reduced by 69%, 42%, and 50%, respectively. In addition, K₂FeO₄ pretreatment can also promote the release of antibiotics from sludge flocs, which is conducive to the simultaneous degradation of antibiotics in the subsequent biological treatment process.     

微波预处理面包酵母对锶的吸附研究

采用微波预处理的面包酵母作为生物吸附剂吸附处理Sr2＋,研究了其吸附特性、生物吸附动力学、吸附平衡过程和吸附机理.实验结果表明,微波预处理能有效提高酵母的吸附效能.酵母对Sr2＋吸附10min即可达到平衡,吸附过程可以很好地用准二级动力学方程来描述（R2=0.9999）,平衡吸附量qe为4.69mg·g^-1,二级吸附...     

Government environmental control measures on CO2 emission during the 2014 Youth Olympic Games in Nanjing: Perspectives from a top-down approach

Strict air pollution control measures were conducted during the Youth Olympic Games（YOG） period at Nanjing city and surrounding areas in August 2014.This event provides a unique chance to evaluate the effect of government control measures on regional atmospheric pollution and greenhouse gas emissions.Many previous studies have observed significant reductions of atmospheric pollution species and improvement in air quality,while no study has quantified its synergism on anthropogenic CO₂...     

Survival of Norovirus Surrogate on Various Food-Contact Surfaces

Norovirus (NoV) is an environmental threat to humans, which spreads easily from one infected person to another, causing foodborne and waterborne diseases. Therefore, precautions against NoV infection are important in the preparation of food. The aim of this study was to investigate the survival of murine norovirus (MNV), as a NoV surrogate, on six different food-contact surfaces: ceramic, wood, rubber, glass, stainless steel, and plastic. We inoculated 10⁵ PFU of MNV onto the six different surface coupons that were then kept at room temperature for 28 days. On the food-contact surfaces, the greatest reduction in MNV was 2.28 log₁₀ PFU/coupon, observed on stainless steel, while the lowest MNV reduction was 1.29 log₁₀ PFU/coupon, observed on wood. The rank order of MNV reduction, from highest to lowest, was stainless steel, plastic, rubber, glass, ceramic, and wood. The values of d _R (time required to reduce the virus by 90 %) on survival plots of MNV determined by a modified Weibull model were 277.60 h (R ² = 0.99) on ceramic, 492.59 h (R ² = 0.98) on wood, 173.56 h on rubber (R ² = 0.98), 97.18 h (R ² = 0.94) on glass, 91.76 h (R ² = 0.97) on stainless steel, and 137.74 h (R ² = 0.97) on plastic. The infectivity of MNV on all food-contact surfaces remained after 28 days. These results show that MNV persists in an infective state on various food-contact surfaces for long periods. This study may provide valuable information for the control of NoV on various food-contact surfaces, in order to prevent foodborne disease.     

Relationships between chemical elements of PM2.5 and O3 in Shanghai atmosphere based on the 1-year monitoring observation

Mass level of fine particles (PM_2.5) in main cities in China has decreased significantly in recent years due to implementation of Chinese Clean Air Action Plan since 2013, however, O₃ pollution is getting worse than before, especially in megacities such as in Shanghai. In this work, O₃ and PM_2.5 were continuously monitored from May 27, 2018 to March 31, 2019. Our data showed that the annual average concentration of PM_2.5 and O₃ (O₃-8 hr, maximum 8-hour moving average of ozone days) was 39.35 ± 35.74 and 86.49 ± 41.65 µg/m³, respectively. The concentrations of PM_2.5 showed clear seasonal trends, with higher concentrations in winter (83.36 ± 18.66 µg/m³) and lower concentrations in summer (19.85 ± 7.23 µg/m³), however, the seasonal trends of O₃ were different with 103.75 ± 41.77 µg/m³ in summer and 58.59 ± 21.40 µg/m³ in winter. Air mass backward trajectory, analyzing results of potential source contribution function model and concentration weighted trajectory model implied that pollutants from northwestern China contributed significantly to the mass concentration of Shanghai PM_2.5, while pollutants from areas of eastern coastal provinces and South China Sea contributed significantly to the mass level of ozone in Shanghai atmosphere. Mass concentration of twenty-one elements in the PM_2.5 were investigated, and their relationships with O₃ were analyzed. Mass level of ozone had good correlation with that of Ba (r = 0.64, p < 0.05) and V (r = 0.30, p > 0.05), suggesting vehicle emission pollutants contribute to the increasing concentration of ozone in Shanghai atmosphere.     

Efficacy of Cinnamaldehyde Against Enteric Viruses and Its Activity After Incorporation Into Biodegradable Multilayer Systems of Interest in Food Packaging

Cinnamaldehyde (CNMA), an organic compound that gives cinnamon its flavor and odor, was investigated for its virucidal activity on norovirus surrogates, murine norovirus (MNV) and feline calicivirus (FCV), and hepatitis A virus (HAV). Initially, different concentrations of CNMA (0.1, 0.5 and 1 %) were individually mixed with each virus at titers of ca. 6–7 log₁₀ TCID₅₀/ml and incubated 2 h at 4 and 37 °C. CNMA was effective in reducing the titers of norovirus surrogates in a dose-dependent manner after 2 h at 37 °C, while HAV titers were reduced by 1 log₁₀ after treatment with 1 % of CNMA. When incubation time was extended, HAV titers were reduced by 3.4 and 2.7 log₁₀ after overnight incubation at 37 °C with 1 and 0.5 % of CNMA, respectively. Moreover, this paper analyzed, for the first time, the antiviral activity of adding an active electrospun interlayer based on zein and CNMA to a polyhydroxybutyrate packaging material (PHB) in a multilayer form. Biodegradable multilayer systems prepared with 2.60 mg/cm² (~9.7 %) of CNMA completely inactivated FCV according to ISO 22196:2011, while MNV titers were reduced by 2.75 log₁₀. When the developed multilayer films were evaluated after one month of preparation or at 25 °C, the antiviral activity was reduced as compared to freshly prepared multilayer films evaluated at 37 °C. The results show the excellent potential of this system for food contact applications as well as for active packaging technologies in order to maintain or extend food quality and safety.     

Root- and peat-based CO2 emissions from oil palm plantations

Measured carbon dioxide (CO₂) flux from peat soils using the closed chamber technique combines root-related (autotrophic + heterotrophic where rhizosphere organisms are involved) and peat-based (heterotrophic) respiration. The latter contributes to peat loss while the former is linked to recent CO₂ removal through photosynthesis. The objective of this study was to separate root- from peat-based respiration. The study was conducted on peatland under 6 and 15 year old oil palm (Elaeis guineensis Jacq.) plantations in Jambi Province, Indonesia in 2011 to 2012. CO₂ emissions were measured in the field from 25 cm diameter and 25 cm tall closed chambers using an infrared gas analyser. Root sampling and CO₂ emissions measurements were at distances of 1.0, 1.5, 2.0, 2.5, 3.0, 3.5, 4.0, and 4.5 m from the centre of the base of the palm tree. The emission rate for the six and 15 year old oil palm plantations at ≥3.0 m from the centre of the tree were 38.2?±?9.5 and 34.1?±?15.9 Mg CO₂ ha^?1 yr^?1, respectively. At distances <2.5 m, total respiration linearly decreased with distances from the trees. Heterotrophic respirations were 86 % of the 44.7?±?11.2 and 71 % of 47.8?±?21.3 Mg CO₂ ha^?1 yr^?1 of weighted surface flux, respectively for the 6 and 15 year old plantations. We propose that CO₂ flux measurements in oil palm plantations made at a distance of ≥3 m from the tree centre be used to represent the heterotrophic respiration that is relevant for the environmental impact assessment.     

垃圾渗滤液浓缩液高铁酸钾联合PAC处理技术研究

以碟管式反渗透(DTRO)处理垃圾渗滤液产生的浓缩液为研究对象,采用高铁酸钾联合聚合氯化铝(PAC)处理浓缩液.结果表明,在单独采用高铁酸钾的条件下,DTRO浓缩液COD、UV_(254)和色度去除率随着高铁酸钾投加量的增加而升高.高铁酸钾投加量为10 g·L~(-1),pH为5时,COD、UV_(254)和色度去除效果最佳,反应在40 min内基本完成,COD、UV_(254)、色度去除率分别为38.5%、35.7%和68.5%.通过响应曲面法分析高铁酸钾联合PAC处理DTRO浓缩液效果可得,高铁酸钾投加量在10.0～13.0 g·L~(-1)之间,pH调节至3.0～4.0,PAC投加量为13.0～15.0 g·L~(-1)时,DTRO浓缩液COD去除率可达74%.     

Enhanced dewaterability of waste activated sludge by UV assisted ZVI-PDS oxidation

Ultraviolet（UV） assisted zero-valent iron（ZVI）-activated sodium persulfate（PDS） oxidation（UV-ZVI-PDS） was used to treat waste activated sludge（WAS） in this study.The dewaterability performance and mechanism of WAS dewatering were analyzed.The results showed that UV-ZVI-PDS can obtain better sludge dewatering performance in a wide pH range（2.0-8.0）.When the molar ratio of ZVI/PDS was 0.6,UV was 254 nm,PDS dosage was 200 mg/g TS（total solid）,pH was 6.54,reaction time was 20 min,the CST（capillary s...     

Carbon storage and sequestration potential of selected tree species in India

A dynamic growth model (CO2FIX) was used for estimating the carbon sequestration potential of sal (Shorea Robusta Gaertn. f.), Eucalyptus (Eucalyptus Tereticornis Sm.), poplar (Populus Deltoides Marsh), and teak (Tectona Grandis Linn. f.) forests in India. The results indicate that long-term total carbon storage ranges from 101 to 156 Mg C?ha^?1, with the largest carbon stock in the living biomass of long rotation sal forests (82 Mg C?ha^?1). The net annual carbon sequestration rates were achieved for fast growing short rotation poplar (8 Mg C?ha^?1?yr^?1) and Eucalyptus (6 Mg C?ha^?1?yr^?1) plantations followed by moderate growing teak forests (2 Mg C?ha^?1?yr^?1) and slow growing long rotation sal forests (1 Mg C?ha^?1?yr^?1). Due to fast growth rate and adaptability to a range of environments, short rotation plantations, in addition to carbon storage rapidly produce biomass for energy and contribute to reduced greenhouse gas emissions. We also used the model to evaluate the effect of changing rotation length and thinning regime on carbon stocks of forest ecosystem (trees?+?soil) and wood products, respectively for sal and teak forests. The carbon stock in soil and products was less sensitive than carbon stock of trees to the change in rotation length. Extending rotation length from the recommended 120 to 150 years increased the average carbon stock of forest ecosystem (trees?+?soil) by 12%. The net primary productivity was highest (3.7 Mg ha^?1?yr^?1) when a 60-year rotation length was applied but decreased with increasing rotation length (e.g., 1.7 Mg ha^?1?yr^?1) at 150 years. Goal of maximum carbon storage and production of more valuable saw logs can be achieved from longer rotation lengths. ‘No thinning’ has the largest biomass, but from an economical perspective, there will be no wood available from thinning operations to replace fossil fuel for bioenergy and to the pulp industry and such patches have high risks of forest fires, insects etc. Extended rotation lengths and reduced thinning intensity could enhance the long-term capacity of forest ecosystems to sequester carbon. While accounting for effects of climate change, a combination of bioenergy and carbon sequestration will be best to mitigation of CO₂ emission in the long term.     

赤泥活化过一硫酸盐降解环丙沙星:性能和机制

为提高赤泥的综合利用及抗生素有机废水的深度处理,以赤泥（red mud,RM）为催化剂、环丙沙星（ciprofloxacin,CIP）为目标污染物,系统研究了RM活化过一硫酸盐（peroxymonosulfate,PMS）降解CIP的效果和机制.结果表明,含有Fe、Al和Ca等金属氧化物,具有较大比表面积（10.96 m²·g^-1）和复杂孔道结构的RM能够有效增强PMS对CIP的降解速率和效果.自由基捕获剂甲醇、叔丁醇和苯酚的抑制实验结果进一步说明,体系产生的SO₄^-·和HO·在RM表面与CIP发生氧化反应.温度、PMS浓度和RM投加量影响CIP的降解.温度升高反应速度加快,反应活化能为5.74 kJ·mol^-1; PMS浓度增加,体系产生更多SO₄^-·和HO·,CIP的降解率升高; RM存在最佳投加量1.0 g·L^-1.HPLC/MS/MS共检测到8种降解产物,CIP分子中的哌嗪环易受活性物质进攻,CIP主要通过2种途径进行降解.本研究表明RM是一种极具潜力的廉价催化剂,可用于活化过一硫酸盐处理含抗生素的污染废水.