长株潭城市群核心区土地利用生态风险评价

随着长株潭城市群的快速发展,人类活动导致的土地利用结构及方式改变对生态环境构成了巨大压力。运用G IS和景观生态学方法的土地利用生态风险评价,以长株潭城市群核心区为研究区域,选择湘江岸线为典型样带,建立了基于源与汇景观功能的土地利用生态风险评价指标体系,并构建了评价模型,对生态风险进行了空间分析和综合评价。结果表明,长沙市建成区的土地利用生态风险指数整体最高,株洲和湘潭居次。其中,从城市群建成区向外,风险指数逐渐降低,长沙、株洲、湘潭三市交界处生态风险指数也较低。根据研究区域生态风险状况、变化和分布特征,提出了相应的风险调控策略和管理方法,为实现区域土地利用与生态、社会、经济的可持续发展提供决策依据。     

Effects of reductive inorganics and NOM on the formation of chlorite in the chlorine dioxide disinfection of drinking water

Chlorine dioxide (ClO₂) disinfection usually does not produce halogenated disinfection by-products, but the formation of the inorganic by-product chlorite (ClO₂^–) is a serious consideration. In this study, the ClO₂^– formation rule in the ClO₂ disinfection of drinking water was investigated in the presence of three representative reductive inorganics and four natural organic matters (NOMs), respectively. Fe²⁺ and S^2– mainly reduced ClO₂ to ClO₂^– at low concentrations. When ClO₂ was consumed, the ClO₂^– would be further reduced by Fe²⁺ and S^2–, leading to the decrease of ClO₂^–. The reaction efficiency of Mn²⁺ with ClO₂ was lower than that of Fe²⁺ and S^2–. It might be the case that MnO₂ generated by the reaction between Mn²⁺ and ClO₂ had adsorption and catalytic oxidation on Mn²⁺. However, Mn²⁺ would not reduce ClO₂^–. Among the four NOMs, humic acid and fulvic acid reacted with ClO₂ actively, followed by bovine serum albumin, while sodium alginate had almost no reaction with ClO₂. The maximum ClO₂^– yields of reductive inorganics (70%) was higher than that of NOM (around 60%). The lower the concentration of reductive substances, the more ClO₂^– could be produced by per unit concentration of reductive substances. The results of the actual water samples showed that both reductive inorganics and NOM played an important role in the formation of ClO₂^– in disinfection.     

石油降解菌XD-1产表面活性剂的性能

从含油废水中筛选分离到1株原油降解菌XD-1,鉴定为假单胞菌（Pseuomonas sp.）.初步实验表明菌XD-1具有较强的产表面活性剂乳化原油的作用,对该菌的产表面活性剂性能进行了研究.实验证明,菌XD-1所产表面活性剂为脂肽类物质,菌在生长对数期产表面活性剂,表面活性剂的产生为生长相关型;充足的碳源是产表面活性剂的必需条件,菌利用原油为碳源时能持续大量地产表面活性剂;原油和尿素为产表面活性剂的最适碳源和氮源,菌XD-1产表面活性剂的最佳营养培养基组成为葡萄糖10 g,尿素4 g,磷酸二氢钾1 g,微量元素液4 mL,水1 L,pH 8.0.     

How does anti-corruption affect enterprise green innovation in China’s energy-intensive industries?

Environmental Geochemistry and Health - Rampant corruption exists in China’s energy-intensive industries. However, we know little about the nexus of corruption and enterprise green innovation...     

Biocompatible self-healing hydrogels based on boronic acid-functionalized polymer and laponite nanocomposite for water pollutant removal

Environmental Chemistry Letters - Global water pollution by organic dyes and metals may be solved by adsorption. In particular, hydrogel adsorbents display unique...     

Product identification and toxicity change during oxidation of methotrexate by ferrate and permanganate in water

• Oxidation of methotrexate by high-valent metal-oxo species was first explored. • Fe(VI) presented a higher reactivity to MTX than Mn(VII) at pH 8.0. • Ketonization and cleavage of peptide bond were two initial reaction pathways. • Products of MTX were not genotoxic, neurotoxic, or endocrine-disrupting chemicals. • The less biodegradable products exhibited developmental and acute/chronic toxicity. Accompanying an annual increase in cancer incidence, the global use of anticancer drugs has remarkably increased with their worldwide environmental prevalence and ecological risks. In this study, the oxidation of methotrexate (MTX), a typical anticancer drug with ubiquitous occurrence and multi-endpoint toxicity, by ferrate(VI) (Fe(VI)) and permanganate (Mn(VII))) was investigated in water. Fe(VI) exhibited a higher reactivity with MTX (93.34 M⁻¹ s⁻¹) than Mn(VII) (3.01 M⁻¹ s⁻¹) at pH 8.0. The introduction of Cu(II) and Fe(III) at 1.0 mM improved the removal efficiency of 5.0 μM MTX by 100.0 μM Fe(VI) from 80% to 95% and 100% after 4 min, respectively. Seven oxidized products (OPs) were identified during oxidative treatments, while OP-191 and OP-205 were characterized as specific products for Fe(VI) oxidation. Initial ketonization of the L-glutamic acid moiety and cleavage of the peptide bond of MTX were proposed. Additionally, a multi-endpoint toxicity evaluation indicated no genotoxicity, neurotoxicity, or endocrine-disrupting effects of MTX and its OPs. Particularly, serious developmental toxicity in zebrafish larvae was observed in the treated MTX solutions. Based on the acute and chronic aquatic toxicity prediction, OP-190, OP-192, OP-206, and OP-208 were deemed toxic or very toxic compared to harmful MTX. Furthermore, the reduced biodegradability index from 0.15 (MTX) to −0.5 to −0.2 (OP-192, OP-206, and OP-468) indicated the formation of lower biodegradable OPs. Overall, this study suggests that Fe(VI) and Mn(VII) oxidation are promising treatments for remediating anticancer drug-contaminated water. However, the environmental risks associated with these treatments should be considered in the evaluation of water safety.     

Fabrication of novel bio-adsorbent and its application for the removal of Cu(II) from aqueous solution

Environmental Science and Pollution Research - As eco-friendly adsorption material, hydroxyapatite (Ca5(PO4)3OH, HA) has been extensively applied to the removal of heavy metal ions. However,...     

Can anti-corruption improve the quality of environmental information disclosure?

Environmental Science and Pollution Research - This study takes the anti-corruption campaign of the 18th CPC National Congress in China as an exogenous impact build a double difference (DID) model,...     

Testing the efficacy of camera-trap sampling designs for monitoring giant pandas in a heterogeneous landscape

Environmental Science and Pollution Research - The use of camera traps is prevalent in the ecological study of giant pandas (Ailuropoda melanoleuca). The reliability of camera-trap surveying...     

等离子体改性对活性炭纤维表面化学结构的影响

采用放电等离子体对活性炭纤维表面进行改性,通过改变活性炭纤维的化学官能团来强化活性炭纤维对SO2和NOx的吸附和催化作用。利用XPS、FTIR等方法对改性活性炭纤维的化学性质进行表征,研究了活性炭纤维表面官能团在等离子体改性过程中的转化规律和机理。实验结果表明:放电改性过程可以有效地向活性炭纤维表面引入有利于脱硫脱氮的含氧、含氮官能团;当电压为8kV,放电时间为5min时,放电改性活性炭纤维的效果最佳。