Microplastic pollution and enrichment of distinct microbiota in sediment of mangrove in Zhujiang River estuary,China

The microbial communities colonized on microplastics(MPs)have attracted widespread attention.However,few studies focused on the MPs impacts on mangrove ecosystems,particularly on bacterial communities.We investigated the MPs pollution in mangrove of Zhujiang(Pearl)River estuary(ZRE).To study the potential risk posed by MPs to the mangrove ecosystems,the differences in bacterial communities,functions,and complexity between MPs and sediment samples were reported for the first time.Microplastics(2991±1586 items/kg dry weight(dw))in sediment were mainly fibers and polyethylene,mostly transparent,and in size less than 0.5 mm.Bacterial communities and functions significantly differed from MPs in mangrove sediment.Compared with sediment,MPs significantly enriched members of Proteobacteria,Bacteroidetes,and Actinobacteria,as well as the bacteria associated with plastic-degrading and human diseases on their surface,suggesting that microbial communities on MPs may promote MPs degradation and the spread of diseases,posing potential risk to mangrove ecosystems and human health.Although bacteria on MPs exhibited a lower diversity,the co-occurrence network analysis indicated that network of bacteria colonized on MPs was bigger and more complex than those of mangrove sediment,illustrating that MPs can act as a distinct habitat in this special ecosystem.This study provides a new perspective for increasing our understanding of microplastic pollution in mangrove ecosystems.

中国农村家庭能源消费结构:基于Meta方法的研究

农村家庭能源转型事关农村居民的生活水平与生活质量,是能源消费革命的重要组成部分。此前文献研究中对我国能源消费结构存在不同的判断,一种观点认为目前仍以生物质能源为主,另一种观点认为农村家庭能源消费已经过渡到以煤炭为主。为了判断现有的农村能源消费结构,本文基于已有的可得文献,采用Meta分析方法提取了35篇文献中的73组效应值进行定量分析。结果表明:已有文献在研究对象、样本特征、模型方法、解释变量等维度上存在显著的异质性,由此导致了文献之间结论不一致。本文在控制住这些因素后发现,我国农村家庭能源消费结构已经发生根本性转变,家庭收入是驱动能源消费转型的主要因素。伴随着收入的持续增长,劣质能源(生物质能)显著减少,电力等高品质商品能源显著增加,而煤炭、沼气等低品质能源消费量逐步趋于稳定。不同的稳健性检验也支持这一结论。

空气过滤用微纳米纤维多层梯度复合材料的制备与性能

将薄微米纤维网作为静电纺丝的基材,静电纺聚丙烯腈(PAN)纳米纤维网形成微纳单层复合纤网,再将多个不同过滤精度的单层复合纤网按照一定顺序叠加,经热风粘合工艺加固制备具有逐层变化结构的微纳米纤维多层梯度复合空气过滤材料,分别研究了以纺丝时间为梯度、微米纤维网面密度为梯度的多层梯度复合滤料的孔径及过滤性能。研究结果表明:以纺丝时间为梯度的多层梯度复合滤料的平均孔径、最大分布的孔径均减小;对≥0.3μm颗粒的过滤效率提高了13%,而过滤阻力略微增大,但均在26-30 Pa之间。以微米纤网面密度为梯度的多层梯度复合滤料的平均孔径、最大分布的孔径相近;在过滤阻力保持稳定的情况下,对≥0.3μm颗粒的过滤效率提高幅度较小。因此,不同类型的梯度结构可在阻力略微增大或保持不变的情况下,提高复合材料的整体过滤性能,为制备高效低阻、可实际应用的复合滤料提供思路。

纳米纤维复合空气过滤材料的研究进展

纳米纤维是制备空气过滤材料的重要纤维元素,引入纳米纤维可极大地提高滤料的过滤性能。针对纳米纤维复合滤料的研究现状,介绍了制备纳米纤维常用的聚合物、基材的原料和分类,着重阐述了纳米纤维和微米级基布的复合方式和加固方式,指出了这种方式制备的叠层复合过滤材料的优缺点;综述了纳米纤维与微米纤维混合过滤材料的3种制备方法及其优缺点,为开发新型高效低阻的复合空气过滤材料提供了研究思路。

Methanation of carbon dioxide on Ni/ZrO_2-Al_2O_3 catalysts:Effects of ZrO_2 promoter and preparation method of novel ZrO_2-Al_2O_3 carrier

The novel nickel-based catalysts with a nickel content of 12 wt% were prepared with the zirconia-alumina composite as the supports. The new carriers, ZrO2 improved alumina, were synthesized by three methods, i.e., impregnation-precipitation, co-precipitation, and impregnation method. The catalytic properties of these catalysts were investigated in the methanation of carbon dioxide, and the samples were characterized by X-ray diffraction （XRD）, X-ray photoelectron spectroscope （XPS）, temperature-programmed reduction （TPR） and temperature-programmed desorption （TPD） techniques. The new catalysts showed higher catalytic activity and better stability than Ni/γ-Al2O3. Furthermore, as a support for new nickel catalyst, the ZrO2-Al2O3 composite prepared by the impregnation-precipitation method was more efficient than the other supports in the methanation of carbon dioxide. The highly dispersed zirconium oxide on the surface of γ-Al2O3 inhibited the formation of nickel aluminate-like phase, which was responsible for the better dispersion of Ni species and easier reduction of NiO species, leading to the enhanced catalytic performance of corresponding catalyst.

中国农村居民煤炭消费及影响因素研究

农村居民煤炭消费牵涉到农村居民生活方式与能源转型、北方供暖清洁化改革、大气污染治理等重大改革实践,如何准确理解和研判现有的农村居民煤炭消费现状,并进而识别出科学、有效的减煤措施,已成为改善农村居民能源结构、治理农村地区煤炭消费、改善北方地区大气质量的重要手段之一。然而,现有对农村居民煤炭消费的统计数据可能存在一定低估,基础性数据的匮乏与不足严重阻碍了科学研究和公共决策。为了准确了解我国农村居民煤炭消费的现状、特征与空间分布,本文采用第三次中国家庭能源消费调查数据对农村居民的煤炭消费进行了核算,并针对户均煤炭消费量和地区农村居民煤炭消费总量进行了比较,在此基础上还考察了气候差异、资源禀赋、收入水平等因素对农村居民煤炭需求的影响。研究结果表明,2014年中国农村居民生活用煤炭消费总量为6 585.7万tce,平均每户煤炭消费量为347.2 kgce,其中供暖用煤占比96.9%,烹饪用煤占比3.1%。各省的户均煤炭消费和煤炭消费总量呈现显著的空间差异,其中:东北、西部地区农村居民户均煤炭消费量显著高于其他地区,北京及周边的河北、山东、山西、内蒙、辽宁和天津7个省、市的农村居民共消费了全国55%的农村生活用煤,其中北京周边的河北、山东和山西三省农村居民消费了全国46.6%的农村煤炭消费。地区煤炭资源禀赋、农村居民住房面积与供暖用煤需求显著正相关,而冬季户外温度、居民收入水平同煤炭需求之间关系不显著。未来政府应通过改善农村居民民生需求、推动农村能源转型、提高农村能源统计水平等途径来有效治理农村散煤消费。

Theoretical insight into the enhanced CH_4 desorption via H_2O adsorption on different rank coal surfaces

The density functional theory was used to investigate the adsorption of CH4and H2O on different rank coal surfaces. The coal rank is the dominant factor in affecting the adsorption capacity of coal. In order to better understand gas and water interaction with coal of different maturity, we developed fourteen coal models to represent the different rank coal. The interactions of CH4and H2O with coal surfaces were studied and characterized by their adsorption energies, Mulliken charges and electrostatic potential surfaces. The results revealed that the interaction between coal and CH4was weak physical adsorption, and that the interaction between coal and H2O consisted of physical and chemical adsorption. Adsorption energy of coal–H2O system was larger than that of coal–CH4on all rank coals, suggesting that the adsorption priority in the coal models is H2O > CH4. Consequently, the injection of H2O into the different rank coal could effectively enhance the coal bed methane (CBM) recovery. © 2016 Science Press

Electro-Optically Switchable Optical True Delay Lines of Meter-Scale Lengths Fabricated on Lithium Niobate on Insulator Using Photolithography Assisted Chemo-Mechanical Etching

Optical true delay lines(OTDLs)of low propagation losses,small footprints and high tuning speeds and efficiencies are of critical importance for various photonic applications.Here,we report fabrication of electro-optically switchable OTDLs on lithium niobate on insulator using photolithography assisted chemo-mechanical etching.Our device consists of several low-loss optical waveguides of different lengths which are consecutively connected by electro-optical switches to generate different amounts of time delay.The fabricated OTLDs show an ultra-low propagation loss of^0.03dB/cm for waveguide lengths well above 100 cm.

Catalytic performances of Ni/mesoporous SiO_2 catalysts for dry reforming of methane to hydrogen

Several mesoporous silicas with different morphologies were controllably prepared by sol-gel method with adjustable ratio of dual template, and they were further impregnated with aqueous solution of nickel nitrate, followed by calcination in air. The synthesized silica supports and supported nickel samples were characterized using N2-adsorption/desorption, X-ray diffraction (XRD), H2temperature-programmed reduction (H2-TPR), Scanning electron microscope (SEM), Transmission electron microscope (TEM) and thermo-gravimetric analysis (TGA-DTG) techniques. The Ni nanoparticles supported on shell-like silica are highly dispersed and yielded much narrower nickel particle-size than those on other mesoporous silica. The methane reforming with dioxide carbon reaction results showed that Ni nanoparticles supported on shell-like silica carrier exhibited the better catalytic performance and catalytic stability than those of nickel catalyst supported on other silica carrier. The thermo-gravimetric analysis on used nickel catalysts uncovered that catalyst deactivation depends on the type and nature of the coke deposited. The heterogeneous nature of the deposited coke was observed on nickel nanoparticles supported on spherical and peanut-like silica. Much narrower and lower TGA derivative peak was founded on Ni catalyst supported on the shell-like silica. © 2016 Science Press

Improvement of catalytic stability for CO_2 reforming of methane by copper promoted Ni-based catalyst derived from layered-double hydroxides

Copper-promoted nickel-based metal nanoparticles (NPs) with high dispersion and good thermal stability were derived from layered-double hydroxides (LDHs) precursors that were facilely developed by a co-precipitation strategy. The copper-promoted Ni-based metal NPs catalysts were investigated for methane reforming with carbon dioxide to hydrogen and syngas. A series of characterization techniques including XRD, N2adsorption and desorption, H2-TPR, XPS, CO2-TPD, TEM, TGA and in situ CH4-TPSR were utilized to determine the structure-function relationship for the obtained catalysts. The copper addition accelerated the catalyst reducibility as well as the methane activation, and made the Ni species form smaller NPs during both preparation and reaction by restricting the aggregation. However, with higher copper loading, the derived catalysts were less active during methane reforming with CO2to syngas. It was confirmed that the catalyst with 1 wt% Cu additive gave the higher catalytic activity and remained stable during long time reaction with excellent resistance to coking and to sintering. Furthermore, the mean size of metal NPs changed minimally from 6.6 to 7.9 nm even after 80 h of time on stream at temperature as high as 700 °C for this optimized catalyst. Therefore, this high dispersed anti-coking copper-promoted nickel catalyst derived from LDHs precursor could be prospective catalyst candidate for the efficient heterogeneous catalysis of sustainable CO2conversion. © 2016 Science Press

Catalytic properties of Cu-Co catalysts supported on HNO_3-pretreated CNTs for higher-alcohol synthesis

HNO 3 -pretreated CNTs were employed as supports, and a special ultrasound-assisted impregnation method was designed to prepare supported Cu-Co catalysts for higher-alcohol synthesis from syngas. The catalysts used in this work were characterized by N 2 adsorption-desorption, TEM, XRD, H 2 -TPR, CO-TPD techniques. It was found that the pre-treatment procedure of CNTs remarkably promoted the catalytic properties of the Cu-Co/CNTs catalysts. For the Cu-Co catalyst supported on CNTs pre-treated by 68 wt% HNO 3 , some active components were introduced into the CNTs channels, their dispersions and the amount of strongly adsorbed CO-species were improved. The CO conversion and alcohol yield on the HNO 3 -pretreated Cu-Co/CNTs catalyst were increased by ～21% and ～69%, respectively, compared with those on the normal Cu-Co/CNTs catalyst.

Ordered mesoporous Sn-SBA-15 as support for Pt catalyst with enhanced performance in propane dehydrogenation

A series of Sn‐incorporated SBA‐15materials with high specific surface areas and highly orderedmesoporous structures were synthesized by a facile one‐pot method and used as catalyst supports.A reference sample was also prepared using a conventional impregnation method.The catalystswere characterized using various methods,and their activities in propane dehydrogenation wereinvestigated.The incorporation of Sn into the SBA‐15matrix led to strong interactions between Snspecies and the support,and these helped to maintain the oxidation states of Sn species during thereaction.Substitution with Sn changed the interfacial properties of the Pt species and improved thefunction and effect of the Sn promoter.The catalytic activities and stabilities of the Pt catalysts supportedon Sn‐incorporated SBA‐15were better than those of the impregnated sample.However,thecatalytic performance deteriorated when an excessive amount of Sn was introduced and the interactionsamong Pt,Sn species,and the support became weaker.The Pt/0.5Sn‐SBA‐15catalyst gavethe best propene selectivity,i.e.,98.5%,with a corresponding propane conversion of about43.8%.

基于城乡视角的居民能源消费影响因素研究

2002-2016年,伴随着2.91亿农村人口的城镇化,中国居民能源消费量增长了190%。在这一背景下,准确识别城乡居民能源消费模式差异及影响因素显得至关重要。本文基于城乡视角,重新界定居民能源消费,涵盖了建筑用能和交通用能两部分;同时在模型中创新性地引入了财富效应和强度效应,结合结构效应、城镇化效应和人口效应进行定量研究。利用对数平均迪氏分解法,基于我国2002-2012年城镇、农村居民数据,本文考察了不同驱动因素对城镇和农村能源消费的异质性影响。结果表明,建筑能耗强度和住房面积的增长是驱动居民能源消费增长的主要因素,机动车数量的增加也对城镇居民能源消费有明显的正向作用。由于较高的增长率,农村建筑能耗强度和人均住房面积增加对能耗增量的贡献已经逐渐超过城市。此外,分解结果表明,城镇化对居民能源消费的正向效应在逐年递减。这为"城镇化导致居民能源消费增加"提供了间接反证。

Remarkable carbon dioxide catalytic capture (CDCC) leading to solid-form carbon material via a new CVD integrated process (CVD-IP): An alternative route for CO_2 sequestration

Through our newly-developed ＂chemical vapor deposition integrated process （ISVD-IP）＇＂ using carbon OlOXlae （t..u2） as me raw matenal and only carbon source introduced, CO2 could be catalytically activated and converted to a new solid-form product, i.e., carbon nanotubes （CO2-derived） at a quite high yield （the single-pass carbon yield in the solid-form carbon-product produced from CO2 catalytic capture and conversion was more than 30% at a single-pass carbon-base）. For comparison, when only pure carbon dioxide was introduced using the conventional CVD method without integrated process, no solid-form carbon-material product could be formed. In the addition of saturated steam at room temperature in the feed for CVD, there were much more end-opening carbon nano-tubes produced, at a slightly higher carbon yield. These inspiring works opened a remarkable and alternative new approach for carbon dioxide catalytic capture to solid-form product, comparing with that of CO2 sequestration （CCS） or CO2 mineralization （solidification）, etc. As a result, there was much less body volume and almost no greenhouse effect for this solid-form carbon-material than those of primitive carbon dioxide.

Catalytic combustion of methane over nano ZrO_2-supported copper-based catalysts

The nano ZrO2-supported copper-based catalysts for methane combustion were investigated by means of N2 adsorption, TEM, XRD, H2-TPR techniques and the test of methane oxidation. Two kinds of ZrO2 were used as support, one （ZrO2-1） was obtained from the commercial ZrO2 and the other （ZrO2-2） was issued from the thermal decomposition of zirconium nitrate. It was found that the CuO/ZrO2-2 catalyst was more active than CuO/ZrO2-1. N2 adsorption, H2-TPR and XRD measurements showed that larger surface area, better reduction property, presence of tetragonal ZrO2 and higher dispersion of active component for CuO/ZrO2-2 than that of CuO/ZrO2-1. These factors could be the dominating reasons for its higher activity for methane combustion.

Exploring a broadened operating pH range for norfloxacin removal via simulated solar-light-mediated Bi_2WO_6 process

Semiconductor photocatalysis can be operated over a narrow pH range for wastewater treatment. In this study, a simulated solar-light-mediated bismuth tungstate (SSL/Bi2WO6) process is found to be effective for norfloxacin degradation over a narrow pH range. To broaden the operating pH range of the SSL/Bi2WO6 process, an NH4+ buffer system and an Fe3+ salt were introduced under extremely basic and acidic pH conditions, respectively. The NH4+ buffer system continuously supplied hydroxyl ions to generate ·OH radicals and prevented acidification of the solution, resulting in improved norfloxacin removal and mineralization removal under alkaline conditions. In contrast, the Fe3+ salt offered an additional homogeneous photo-sensitization pathway. The former treatment assisted in norfloxacin decay and the latter increased the collision frequency between the photo-generated hole and hydroxyl ions. Moreover, the effect of parameters such as pH and Fe3+ dosage was optimized.

Degradation of methotrexate by UV/peroxymonosulfate:Kinetics,effect of operational parameters and mechanism

Methotrexate(MTX)is one of the most consumed anti-cancer drugs in the pharmaceutical market around the world.The widespread occurrence of MTX in aquatic environment through hospital effluent has attracted increasing concern due to its potential to induce water pollution.In the present study,the degradation of MTX in aqueous medium was investigated by UV-activated peroxymonosulfate(PMS).A significant improvement in degradation rate by increasing UV intensity and PMS concentration while the decrease in degradation efficiency with the increase of solution p H and initial concentration of MTX was observed.The proposed UV/PMS process could achieve more than 90%MTX degradation in 30 min with a good mineralization degree(65%).A pseudofirst order kinetic model was employed and successfully predicted the degradation of MTX.The effect of other operational parameters such as the initial concentration of the targeted compound,dosage of oxidant(PMS),solution p H and UV intensity on the degradation rate were investigated.At the last,the main transform intermediates were identified using LC–MS and possible degradation pathways were proposed.The results show that UV/PMS can be used as an efficient technology to treat pharmaceuticals such as methotrexate containing water and wastewater.

Effects of Ce/Zr ratio on the structure and performances of Co-Ce_(1-x)Zr_xO_2 catalysts for carbon dioxide reforming of methane

The Co-incorporated Ce1-xZrxO2 catalysts were prepared by co-precipitation for carbon dioxide reforming of methane.The ratio of Ce to Zr was varied to optimize the performances of co-precipitated Co-Ce-Zr-Ox catalysts.The prepared catalysts were characterized by various physico-chemical characterization techniques including TPR,X-ray diffraction,N2 adsorption at low temperature,XPS and CO2-TPSR.The co-precipitated Co-Ce0.8Zr0.2O2 sample containing 16% CoO exhibited a higher catalytic activity among the five catalysts,and the activity was maintained without significant loss during the reaction for 60 h.Under the conditions of 750 ℃,0.1 MPa,36000 ml/（h gcat）,and CO2/CH4 molar ratio of 1：1,the CO2 conversion over this catalyst was 75% while the CH4 conversion was 67%.The cubic Ce0.8Zr0.2O2 facilitated a higher dispersion and a higher reducibility of the cobalt component,and the apparent activation energy for Co-Ce0.8Zr0.2O2 sample was 49.1 kJ/mol in the CO2/CH4 reforming reaction.As a result,the Co-Ce0.8Zr0.2O2 sample exhibited a higher activity and stability for the reforming of CH4 with CO2.

Ultrathin nanosheets of cobalt-nickel hydroxides hetero-structure via electrodeposition and precursor adjustment with excellent performance for supercapacitor

A homogeneous better-dispersed ultrathin nanosheets（ca. 5 nm） of cobalt-nickel layered double hydroxides（LDH） supported on nickel foam scaffold was synthesized using controllable electrodeposition approach for high efficiency electrode materials of new supercapacitor. The morphology and electrochemical performances of the samples can be controlled by adjusting the precursor ratio, i.e., Ni（OAc）2/Co（NO3）2 molar ratio in the electrodeposition approach. With the increase of this molar ratio, the electrochemical performances give a volcano trend. When the optimized molar ratio is 0.64/0.36, the hybrid delivered a high specific capacitance of 1587.5 F g-1 at a current density of 0.5 A g-1, with good rate capability（1155 F g-1 was retained even at 10 A g-1） and a robust recycle stability（remaining 91.5% after 1000 cycles at 5 A g-1）. The good performance could be attributed to the enlarged interlayer spacing, ultrathin nanosheets and synergistic effects between Co（OH）2 and Ni（OH）2. Furthermore, an asymmetric supercapacitor with a high energy density of 34.5 Wh kg-1 at 425 W kg-1 and excellent cycling stability of 85.4% after 5000 charge-discharge cycles at 2 A g-1 was fabricated. We believe that this fantabulous new electrode material would have encouraging applications in electrochemical energy storage and a wide readership.

Microwave-Assisted Synthesis of NiCo_2O_4 Double-Shelled Hollow Spheres for High-Performance Sodium Ion Batteries

The ternary transitional metal oxide NiCo_2O_4 is a promising anode material for sodium ion batteries due to its high theoretical capacity and superior electrical conductivity. However, its sodium storage capability is severely limited by the sluggish sodiation/desodiation reaction kinetics. Herein, NiCo_2O_4 double-shelled hollow spheres were synthesized via a microwave-assisted, fast solvothermal synthetic procedure in a mixture of isopropanol and glycerol, followed by annealing. Isopropanol played a vital role in the precipitation of nickel and cobalt,and the shrinkage of the glycerol quasi-emulsion under heat treatment was responsible for the formation of the double-shelled nanostructure. The as-synthesized productwas tested as an anode material in a sodium ion battery,was found to exhibit a high reversible specific capacity of 511 m Ahg^(-1) at 100 m Ag^(-1), and deliver high capacity retention after 100 cycles.