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国家自然科学基金(41071210)

作品数:7 被引量:284H指数:5
相关作者:陈宝梁陈再明方远徐义亮周丹丹更多>>
相关机构:浙江大学台州市环境科学设计研究院更多>>
发文基金:国家自然科学基金浙江省自然科学基金国家高技术研究发展计划更多>>
相关领域:环境科学与工程理学轻工技术与工程更多>>

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Metal composition of layered double hydroxides(LDHs) regulating ClO_4^- adsorption to calcined LDHs via the memory effect and hydrogen bonding被引量:5
2014年
A series of calcined carbonate layered double hydroxides(CLDHs) with various metal compositions and different M2+/M3+ ratios were prepared as adsorbents for perchlorate. Adsorption isotherms fit Langmuir model well, and the adsorption amount followed the order of MgAl-CLDHs > MgFe-CLDHs >>> ZnAl-CLDHs. The isotherms of MgAl-CLDHs and MgFe-CLDHs displayed a two-step shape at low and high concentration ranges and increased with an increase in the M2+/M3+ ratio from 2 to 4. The two-step isotherm was not observed for ZnAl-CLDHs, and the adsorption was minimally affected by the M2+/M3+ ratio. The LDHs, CLDHs and the reconstructed samples were characterized by X-ray diffraction, SEM, FT-IR and Raman spectra to delineate the analysis of perchlorate adsorption mechanisms. The perchlorate adsorption of MgAl-CLDHs and MgFe-CLDHs was dominated by the structural memory effect and the hydrogen bonds between the free hydroxyl groups on the reconstructed-LDHs and the oxygen atoms of the perchlorates. For ZnAl-CLDHs, the perchlorate adsorption was controlled by the structural memory effect only, as the hydroxyl groups on the hydroxide layers preferred to form strong hydrogen bonds with carbonate over perchlorate, which locked the intercalated perchlorate into a more confined nano-interlayer. Several distinct binding mechanisms of perchlorate by CLDHs with unique M2+ ions were proposed.
Yajie LinQile FangBaoliang Chen
关键词:LANGMUIR模型层状双氢氧化物
变色栓菌和黄孢原毛平革菌共培养产漆酶增强BaP的氧化
<正>多环芳烃(PAHs)是环境中普遍存在的一类典型有机污染物。由于PAHs排放量大、来源广泛且具有半挥发性、低溶解性、难生物降解性,常常在土壤中长期存在、大量积累。PAHs污染土壤修复技术主要有化学修复、植物修复、微生...
钱林波陈宝梁
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水稻秸秆生物碳对重金属Pb^2+的吸附作用及影响因素被引量:136
2012年
以农业废弃物水稻秸秆为原料,采用限氧裂解法制备了不同温度(350、500和700℃)下的秸秆生物碳(RC350、RC500和RC700),研究了生物碳对Pb2+的吸附性能、作用机制及影响因素,为准确预测生物碳还田固碳对土壤中重金属迁移行为的影响提供理论参考.结果表明,生物碳对Pb2+的吸附行为符合准一级动力学方程,Pb2+在RC350、RC500、RC700上的吸附速率分别为0.167h-1、0.154h-1、0.388h-1;其等温吸附曲线符合Langmuir方程,最大吸附量分别为65.3、85.7和76.3mg·g-1,是原秸秆生物质RC100的5~6倍、活性炭AC的2~3倍.生物碳单位面积上的有效吸附点位比AC高约10倍.经酸化去除表面矿物成分后,RC350和RC700对Pb2+的吸附能力急剧下降,其最大吸附量、吸附亲和力与AC相近;红外光谱分析表明,去灰分后生物碳上有机碳官能团并无明显减少,而无机矿物(如SiO2)含量显著降低.生物碳中的有机碳组分和无机矿物组分对其吸附Pb2+均有重要贡献,其中无机矿物组分的吸附量及亲和力均大于有机碳组分.
陈再明方远徐义亮陈宝梁
关键词:生物碳秸秆
Enhanced oxidation of benzo[a]pyrene by crude enzyme extracts produced during interspecific fungal interaction of Trametes versicolor and Phanerochaete chrysosporium被引量:4
2012年
The effects of interspecific fungal interactions between Trametes versicolor and Phanerochaete chrysosporium on laccase activity and enzymatic oxidation of polycyclic aromatic hydrocarbons(PAHs) were investigated.A deadlock between the two mycelia rather than replacement of one fungus by another was observed on an agar medium.The laccase activity in crude enzyme extracts from interaction zones reached a maximum after a 5-day incubation,which was significantly higher than that from regions of T.versicolor or P.chrysosporium alone.The enhanced induction of laccase activity lasted longer in half nutrition than in normal nutrition.A higher potential to oxidize benzo[a]pyrene by a crude enzyme preparation extracted from the interaction zones was demonstrated.After a 48 hr incubation period,the oxidation of benzo[a]pyrene by crude enzyme extracts from interaction zones reached 26.2%,while only 9.5% of benzo[a]pyrene was oxidized by crude extracts from T.versicolor.The oxidation was promoted by the co-oxidant 2,2'-azinobis-3ethylbenzthiazoline-6-sulphonate diammonium salt(ABTS).These findings indicate that the application of co-culturing of white-rot fungi in bioremediation is a potential ameliorating technique for the restoration of PAH-contaminated soil.
Linbo Qian
关键词:苯并[A]芘酶促氧化
Biosorption and biodegradation of polycyclic aromatic hydrocarbons by Phanerochaete chrysosporium in aqueous solution被引量:8
2013年
Biosorption and biodegradation of phenanthrene and pyrene by live and heat-killed Phanerochaete chrysosporium are investigated to elucidate the bio-dissipation mechanisms of polycyclic aromatic hydrocarbons(PAHs) in aqueous solution and its regulating factors.The effects of nutrient conditions(carbon source and nitrogen source concentrations),the co-existing Cu 2+,and repeated-batch feed of PAHs on the biosorption and biodegradation are systematically studied.The removal of PAHs by dead bodies of P.chrysosporium is attributed to biosorption only,and the respective partition coefficients of phenanthrene and pyrene are 4040 and 17500 L/kg.Both biosorption and biodegradation contribute to the dissipation of PAHs by live P.chrysosporium in water.After a 3-d incubation,the removal percentage via biosorption are 19.71% and 52.21% for phenanthrene and pyrene,respectively.With the increase of the incubation time(3 40 d),biodegradation gradually increases from 20.40% to 60.62% for phenanthrene,and from 15.55% to 49.21% for pyrene.Correspondingly,the stored-PAHs in the fungal bodies decrease.Under the carbon-rich and nitrogen-limit nutrient conditions,the removal efficiency and biodegradation of phenanthrene and pyrene are significantly promoted,i.e.99.55% and 92.77% for phenanthrene,and 99.47% and 83.97% for pyrene after a 60-d incubation.This phenomenon is ascribed to enhanced-biosorption due to the increase of fungal biomass under carbon-rich condition,and to stimulated-biodegradation under nitrogen-limit condition.For the repeated-batch feed of phenanthrene,the pollutant is continuously removed by live P.chrysosporium,and the contribution of biodegradation is enhanced with the repeated cycles.After 3 cycles,the biodegradation percentage is up to 90% with each cycle of a 6-d incubation.
DING JieCHEN BaoLiangZHU LiZhong
关键词:营养条件多环芳香烃
黄孢原毛平革菌菌球对多环芳烃的生物吸附和生物降解作用被引量:10
2012年
以黄孢原毛平革菌(Phanerochaete chrysosporium,Pc)为代表,研究了死体和活体Pc菌球对水中菲、芘等多环芳烃(PAHs)的生物吸附和生物降解作用及其相对贡献,探讨了碳源、氮源浓度和共存Cu2+的影响,考察了连续多次输入下菲的生物吸附和生物降解作用,试图为准确掌握微生物作用下PAHs的迁移转化行为及其调控作用提供理论指导.结果表明,死体Pc菌球对水中菲、芘的去除机制为生物吸附,分配系数分别为4040和17500L/kg.活体Pc菌球的去除机制包括生物吸附和生物降解,3d时生物吸附对水中菲、芘的去除率分别为19.71%和52.21%;随着作用时间延长(3~40d),生物降解对菲、芘的去除作用逐渐增大(20.40%~60.62%和15.55%~49.21%),且菌体中PAHs残留量不断下降.富碳限氮营养条件下,活体Pc菌球对PAHs的去除作用和降解效果最优,在60d时分别为99.55%和92.77%(菲),99.47%和83.97%(芘),主要源于富碳增加Pc菌体生物量而增强生物吸附、限氮则触发Pc对PAHs的生物降解作用.活体Pc菌球在富碳限氮强化条件下可连续多次去除和降解新输入的PAHs,其中单次生物降解率随循环次数(6d/次)增加而增大,循环3次后菲的生物降解率高达90%.
丁洁陈宝梁朱利中
关键词:生物吸附生物降解黄孢原毛平革菌多环芳烃生物修复
有机污染物与生物炭的相互作用:吸附模型、机理和热力学
<正>生物炭是农林废弃物和畜禽粪质等材料在缺氧或无氧条件下低温(<700℃)裂解产生的富炭固体,主要被用作土壤改良剂以提升土壤肥力和增强土壤固碳。进入土壤后,生物炭会与土壤组分、微生物或植物根之间发生溶解-沉淀、吸附-脱...
陈宝梁陈再明陈文远周丹丹方远
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氧化石墨烯表面氧化碎片的原位观测及分布位点研究
氧化石墨烯结构的研究对于其实际应用具有重要意义。已有文献表明[1],在氧化石墨烯制备过程中产生的氧化碎片会吸附在氧化石墨烯片层表面,会降低其催化、吸附、电导等性能。但是目前并未有直接证据证实氧化石墨烯表面氧化碎片的存在。...
陈笑笑陈宝梁
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水稻秸秆生物碳的结构特征及其对有机污染物的吸附性能被引量:124
2013年
以水稻秸秆为原料,采用限氧裂解法制备了不同温度(100~700℃)的秸秆生物碳,用TG-DTG热重分析、CHNO元素分析、FTIR、BET-N2比表面及孔径分布等手段表征生物碳的组成与结构,研究生物碳吸附水中硝基苯、对硝基甲苯、萘、菲等有机污染物的性能及影响因素,探讨其作用机制及构-效关系,试图为高效利用废弃农业秸秆资源、制备廉价的有机物吸附材料提供理论依据.结果表明,水稻秸秆生物碳含有丰富的有机碳组分和无机矿物组分,随着裂解温度升高,生物碳中有机组分的含碳量逐渐升高、极性减弱、芳香性增强,而无机矿物组分的相对含量则不断增加;当裂解温度从300℃升至400℃时,比表面积突然增大(0.16→110m·2g-1)、微孔结构被打开,主要由于水稻秸秆中纤维素组分大量分解所致.水稻秸秆生物碳吸附有机污染物的主要介质为有机组分,等温吸附曲线符合Freundlich方程,回归参数N、logKf与生物碳的芳香性指数(H/C原子比)呈良好的线性关系;定量描述了分配作用和表面吸附作用的相对贡献.随碳化温度升高,等温吸附曲线由线性变为非线性,吸附机制从分配作用→分配作用+表面吸附作用→表面吸附作用;分配作用部分与有机污染物的logKow呈正相关,而表面吸附则与污染物的疏水性、分子尺寸及其与生物碳的极性匹配性有关.
陈再明陈宝梁周丹丹
关键词:生物碳水稻秸秆有机污染物
不同裂解温度制备的松木屑生物炭对萘的吸附动力学行为
<正>有机化合物在土壤、底泥等天然颗粒上的吸附、脱附过程往往表现出快、慢两个阶段。快吸附阶段一般在几天内完成,而慢吸附阶段可以持续几个星期甚至几年。慢吸附行为是有机化合物在环境中长期迁移转化和生物有效性的限速步骤。生物炭...
陈再明陈宝梁
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