BPA暴露对本体和子代胰岛β细胞转录组差异对比分析

双酚A(BPA)作为一种典型的环境内分泌干扰物,与二型糖尿病和肥胖症等代谢类疾病密切相关.在这项研究中,旨在探讨BPA直接暴露以及围产期暴露对本体和子代胰岛β细胞影响的差异,从而实现对不同易感人群的精准预防与治疗.通过对GEO数据库中GSE126297和GSE82175两个数据集进行分析,共筛选出108个共有的差异基因...     

城市污泥中温厌氧消化过程中厌氧耐药菌的分布与去除研究

城市污泥中含有大量的耐药菌,具有向环境传播耐药菌与抗性基因的潜在危险,但目前缺乏对城市污泥厌氧消化过程中耐药菌的研究.为此对某城市污水处理厂卵形消化池污泥进行了为期1 a的调查研究,考察了中温厌氧消化过程中四环素类与β-内酰胺类抗生素厌氧耐药菌的污染特征与去除效果,并分析了耐药菌的季节性变化规律.结果表明,厌氧进泥中四环素类耐药菌浓度与耐药率均低于β-内酰胺类.中温厌氧消化过程可以去除1.48~1.64 log单位的耐药菌(P<0.05),但经过厌氧消化后氨苄西林与头孢噻吩耐药率有显著增长(分别增加了12.0%与14.3%,P<0.05).厌氧进泥中耐药菌分布有明显的季节特征,除金霉素耐药菌外,其它耐药菌的浓度均为寒冷季显著高于温暖季(P<0.05).     

Evaluation of soil washing process with carboxymethyl-β-cyclodextrin and carboxymethyl chitosan for recovery of PAHs/heavy metals/fluorine from metallurgic plant site

Polycyclic aromatic hydrocarbons(PAHs)/heavy metals/fluorine(F) mixed-contaminated sites caused by abandoned metallurgic plants are receiving wide attention. To address the associated environmental problems,this study was initiated to investigate the feasibility of using carboxymethyl-β-cyclodextrin(CMCD) and carboxymethyl chitosan(CMC) solution to enhance ex situ soil washing for extracting mixed contaminants. Further,Tenax extraction method was combined with a first-three-compartment model to evaluate the environmental risk of residual PAHs in washed soil. In addition,the redistribution of heavy metals/F after decontamination was also estimated using a sequential extraction procedure. Three successive washing cycles using50 g/L CMCD and 5 g/L CMC solution were effective to remove 94.3% of total PAHs,93.2% of Pb,85.8% of Cd,93.4% of Cr,83.2% of Ni and 97.3% of F simultaneously. After the 3rd washing,the residual PAHs mainly existed as very slowly desorbing fractions,which were in the form of well-aged,well-sequestered compounds; while the remaining Pb,Cd,Cr,Ni and F mainly existed as Fe–Mn oxide and residual fractions,which were always present in stable mineral forms or bound to non-labile soil fractions. Therefore,this combined cleanup strategy proved to be effective and environmentally friendly.     

β-环糊精衍生物对甲基对硫磷的增溶洗脱和光降解

研究了3种新型β-环糊精衍生物(谷氨酸-β-环糊精、乙二胺-β-环糊精、羧甲基-β-环糊精)对甲基对硫磷的增溶作用、土壤中甲基对硫磷的洗脱作用以及对甲基对硫磷的光降解作用.研究表明,这三种β-环糊精衍生物都能显著地增加甲基对硫磷在水中的溶解度,并且相对增溶倍数与β-环糊精衍生物的浓度成正相关;120g/L的上述3种β-环糊精衍生物溶液中,甲基对硫磷的溶解度比在纯水中分别提高了117.82倍、80.99倍、47.28倍;β-环糊精衍生物能有效洗脱去除土壤中的甲基对硫磷,其中120g/L的谷氨酸-β-环糊精溶液的累积去除率最高,达103.9%,洗脱液浓度是影响洗脱去除率的主要因素;β-环糊精衍生物能促进甲基对硫磷的光降解,在3g/L的谷氨酸-β-环糊精、乙二胺-β-环糊精、羧甲基-β-环糊精溶液中甲基对硫磷光解速率分别为80.26%、91.53%、76.39%。     

生物炭和碳纳米管固定化漆酶去除水体雌二醇

漆酶是一类具有高效的催化氧化能力的含铜多酚的氧化酶,而固定化漆酶技术在有机废水处理领域受到了越来越多的关注。通过比较吸附法和包埋法利用木炭(WB)、竹炭(BB)和碳纳米管(CNT)固定游离漆酶去除水体雌二醇(E2)。在25 °C 、pH=5条件下,固定化漆酶经120 h 贮存仍保留80%的活性。经过5次循环研究,固载的漆酶仍保留了27%~58%的剩余活性。结合扫描电子显微镜和傅里叶变换红外光谱,证实了漆酶成功地负载在碳基材料上。仅在 8 h内,50 mg·L⁻¹ E2通过吸附法制备的WB、BB、CNT固定化漆酶去除了42.92%、47.66%、43.92%,而包埋法制备的WB、BB、CNT固定化漆酶分别去除84.08%、87.20%、87.86%。结果表明,包埋法固定化漆酶对E2的去除效率更优,这是由于包埋固载在生物炭和CNT的漆酶更为稳定。此外,K⁺和Mn²⁺离子可能通过干扰漆酶的电子传递过程影响漆酶的活性,从而抑制E2的去除。本研究旨在为固定化漆酶在有机废水处理的实际应用提供指导。     

β-环糊精接枝羧甲基壳聚糖吸附剂的制备及其性能

采用γ-氨丙基三乙氧基硅烷化学修饰活化后的硅胶,以戊二醛为交联剂,接上羧甲基壳聚糖,继而接枝上β-环糊精作为功能单体,制备了一种用于分离富集水样中Cu(Ⅱ)的固相萃取新材料。利用红外光谱(FT-IR)、比表面分析(BET)、X射线衍射光谱(XRD)以及热重分析(TG)等方法对吸附剂进行结构表征。采用火焰原子吸收(FAAS)作为检测手段,考察了溶液pH、振荡时间、吸附剂用量、样品流速、洗脱液浓度和体积等对吸附剂吸附Cu(Ⅱ)的影响。吸附剂饱和吸附容量为9.37 mg/g,最大富集倍数高达350。吸附过程能用准二级动力学模型和Langmuir等温吸附方程进行很好的拟合。应用于环境水样中Cu(Ⅱ)的分离富集与测定,回收率在96.8%~105.2%之间,效果较好。     

磁性Fe3O4/石墨烯纳米复合材料催化降解水中17β-雌二醇

利用化学沉淀法制备磁性四氧化三铁 /石墨烯(Fe3O4 /GE)纳米复合材料,并将其与H2O2构成非均相Fenton体系用于催化降解水中微量的17β-雌二醇(E2),研究了初始pH值,初始H2O2浓度,催化剂用量对E2降解的影响。结果表明,Fe3O4/GE纳米复合材料在无需外加光源的条件下能够有效催化降解E2。在pH 7.0,E2初始浓度为1 mg/L,初始H2O2浓度为15 mmol/L,Fe3O4 /GE投加量为15 mg/L的条件下,反应8 h后可去除92.9%的E2。Fe3O4/GE具有便捷的磁分离特性和稳定的催化活性,经过7次循环使用后对E2的降解效率仍保持在91.5%左右。     

Assessing the biodegradation potential of polymers in screening- and long-term test systems

This paper presents a test scheme for assessing the biodegradation potential of polymers, starting with aquatic screening systems (aerobic and anaerobic) and continuing to long-term systems. At the end of the scheme the material has to prove its behavior under the relevant disposal conditions. Aerobic screening was performed mainly under aquatic conditions, but also in soil, using BOD-respirometry. Carbon balances were performed to obtain a better evaluation of the biodegradation potential. Under anaerobic conditions, biodegradation in an aquatic medium was followed by measuring CH₄ and CO₂ production. Polymers not fully degraded in the screening systems were tested in aquarium systems for at least 1 year. Biodegradation was followed by monitoring the DOC released in the water, mass loss, and microbial growth on the samples and in the water as well as via FTIR spectroscopy and SEM pictures. Results are presented for the polymers PHB, PHBV, PCL, Mater-Bi AI05H and ZF03U, and Bioceta. By combining the data from the screening with the aquarium system, a good picture of the degradation behavior of the polymers is obtained.Paper presented at the Bio/Environmentally Degradable Polymer Society—Third National Meeting, June 6–8, 1994, Boston, Massachusetts.     

Crystallization behavior of predominantly syndiotactic poly(β-hydroxybutyrate)

Predominantly syndiotactic poly(-hydroxybutyrate), syn-PHB, of variable syndioregularity (syndyad fractions 0.59, 0.62, 0.64, and 0.71) and molecular weight was prepared by the dibutyltin dimethoxide catalyzed ring opening of racemic-butyrolactone (BL). The crystallization behavior of the syn-PHB polymers was investigated by DSC and X-ray diffraction analyses. DSC of films after melting and annealing showed at least one, and often two distinct melting transitions occuring over a broad (often 40°C) temperature range. These results indicate that syn-PHB chain segments of variable syndioregularity form crystalline regions with very different thermodynamic stabilities. Maximum degrees of crystallinity for melt annealed 0.64- and 0.71-syn-PHB was observed at an annealing temperature (T _c ) of 30°C. AtT _c values at 45°C and higher, crystallization of relatively lower syndioregular chain segments was apparently excluded to variable degrees dependent onT _c and sample syndiotactic dyad content. After crystallization of syn-PHB samples at elevated temperatures, ambient temperature annealing resulted in an observed lower temperature melting transition at 50°C. This result showed little to no dependence on syn-PHB syndio-regularity andT _c . Both solution precipitated 0.62-syn-PHB and 0.71-syn-PHB have WAXS patterns with poorly resolved crystalline reflections superimposed on amorphous haloes indicating low levels of crystallinity (17% and 25%, respectively) and poorly formed crystals. Isothermal crystallization monitored by DSC showed that the syn- and natural origin PHB showed fastest crystallization rates at temperatures between 50°C and 70°C and 60°C and 90°C, respectively. From the dependence of the higher melting transition onT _c it was determined that the equilibrium melting temperatures for 0.62-syn-PHB (M _n =83,700 g/mol) and a 0.64-syn-PHB (M _n =11,900 g/mol) were 157 and 154°C, respectively. An Avrami analysis of syn-PHB yielded results similar to that found for natural origin PHB indicating that crystal growth occurs by a two-dimensional mechanism.Guest Editor: Dr. Graham Swift, Rohm & Haas.     

Biodegradability and compostability of polymers—test methods and criteria for evaluation

The treatment of solid waste in controlled composting facilities is an important possibility for reducing garbage. Natural and synthetic polymeric materials can be used for many purposes, for example, as packaging materials, where compostability is required. A prerequisite for official regulations and the decision as to which materials may be composted is investigations on their biodegradability and the quality of the compost produced. Several standardization groups at the ISO, CEN, and DIN are developing definitions, test methods, and classification systems for differentiating compostable from noncompostable materials. The concept which will be standardized and used in Germany is described in detail. It includes characterization of the test material, determination of the biodegradability using laboratory tests such as simple aquatic batch tests and a controlled aerobic composting test, investigation of the disintegration of the test material in industrial or bench-scale composting facilities, and finally, chemical and ecotoxicological analysis of the compost produced.