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52.
张文杰 《中国环境管理干部学院学报》1999,(4)
本文通过对居室环境概念的阐述,剖析了人与居室环境功能的关系,并指出了居室环境对人行为的规范作用及营造良好居室环境的重要性。 相似文献
53.
该文就常熟市农业资源的实际出发,从改造中低产田、开发长江滩地、复耕零星废弃地、利用庭园空间、立体利用水面、开发杂草资源、加工植物蛋白饲料及发展棉田套作等8个方面的途径,评价了农业开发潜力,说明在经济发达地区的农业开发是大有可为的。文章提出了相应的实施对策。 相似文献
54.
55.
呼伦湖是我国北方生态安全屏障的重要组成部分,为探究呼伦湖水体中有机物的组成及来源,利用三维荧光光谱(EEMs)结合平行因子(PARAFAC)分析技术进行溶解性有机物(DOM)荧光特征及来源研究。结果表明:呼伦湖DOM中含有3种荧光组分,分别为类色氨酸(C1)、类腐殖酸(C2)和类富里酸(C3);平水期、丰水期和枯水期的C2和C3荧光强度占比约70%,表明呼伦湖水体DOM以腐殖质类物质为主,其中不同水期生态补水工程入湖口的C2和C3荧光强度均高于其他区域;平水期、丰水期和枯水期的荧光指数、生物指数和腐殖化指数平均值分别为1.50~1.54、0.85~1.00和4.12~4.68,表明呼伦湖DOM由陆源和自生源混合组成,具有明显的自生源特征;水质监测数据表明,2021年呼伦湖平水期、丰水期和枯水期水质均为GB 3838—2002《地表水环境质量标准》劣Ⅴ类,其中平水期和丰水期的BOD5平均值高于枯水期,而平水期总有机碳平均浓度高于丰水期和枯水期;不同水期C2和C3的荧光强度均呈显著正相关,表明DOM中组分C2和C3的产生及来源具有一致性。
相似文献56.
采集朔州市市区采暖季和非采暖季季PM10样品,测定其中元素碳(EC)和有机碳(OC)含量,并对碳组分的浓度水平、时空分布特征和主要来源进行了研究,结果表明:朔州市市区PM10中OC、EC平均浓度分别为(25.95±9.36)μg/m3和(26.58±10.36)μg/m3,总碳气溶胶(TAC)在PM10中的平均百分含量为30.1%;采暖季OC和EC浓度大于非采暖季,且OC、EC质量浓度大小在5个采样点位均呈现出点位5(工业开发区) > 点位2(居民区) > 点位1(商业、居民混合区) > 点位3(商业、文教混合区) > 点位4(相对清洁区)的变化规律,其中,点位5的OC、EC质量浓度最大,分别为(29.66±8.72)μg/m3和(31.40±10.42)μg/m3;PM10中OC/EC在采暖季和非采暖季比值均低于2,一次污染严重;OC和EC相关性较好,相关系数(R2)分别为0.85(采暖季)和0.69(非采暖季),说明PM10中的碳气溶胶主要来源于一次排放源,加强对燃煤烟尘、机动车尾气和生物质的燃烧等空气污染来源的控制对于改善朔州市环境空气质量有重要作用。 相似文献
57.
Hongyu Liu Hu Zhang Shan Chen Dongbo Liu Hongmei Xia 《Journal of Polymers and the Environment》2006,14(4):419-426
An extracellular poly (β-hydroxybutyrate) (PHB) depolymerase was purified from a Penicillium sp. DS9701-09a by centrifugation, ultrafiltration, precipitation and gel filtration chromatography. The specific activity of the purified enzyme was 37.9-folds higher than that of the culture supernatant and the recovery yield was 11.8%. The PHB deploymerase molecular mass was 44.8 kDa from analysis of both Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and Matrix-assisted laser desorption-time-of-flight (MALDI-TOF) mass spectrometer. The isoelectric point of 6.7 for the enzyme was determined by a two-dimensional electrophoresis. The optimum enzyme activity was observed at a temperature of 50 °C and pH 5.0. The apparent K
m of the enzyme was found to be 1.35 mg/mL. The PHB depolymerase consisted of 16 kinds of normal amino acids. The secondary structure of the enzyme was determined by CD spectrum. α-helix and β-turn were found to be 66% and 34% for the enzyme without ammonium sulphite. Chemical inhibition on the PHB depolymerase activity was examined and EDTA was found to have a significantly inhibitory effect. 相似文献
58.
Jiang W Zhang S Shan XQ Feng M Zhu YG McLaren RG 《Environmental pollution (Barking, Essex : 1987)》2005,138(2):285-289
An attempt has been made to elucidate the effects of soil properties on arsenate adsorption by modeling the relationships between adsorption capacity and the properties of 16 Chinese soils. The model produced was validated against three Australian and three American soils. The results showed that nearly 93.8% of the variability in arsenate adsorption on the low-energy surface could be described by citrate-dithionite extractable Fe (Fe(CD)), clay content, organic matter content (OM) and dissolved organic carbon (DOC); nearly 87.6% of the variability in arsenate adsorption on the high-energy surface could be described by Fe(CD), DOC and total arsenic in soils. Fe(CD) exhibited the most important positive influence on arsenate adsorption. Oxalate extractable Al (Al(OX)), citrate-dithionite extractable Al (Al(CD)), extractable P and soil pH appeared relatively unimportant for adsorption of arsenate by soils. 相似文献
59.
Analysis of chemical compositions contributable to chemical oxygen demand (COD) of oilfield produced water 总被引:1,自引:0,他引:1
This work was to give a comprehensive estimation for the chemical compositions contributable to COD of the produced water treatment system. For this purpose, the wastewater samples were collected from an onshore wastewater treatment plant. The chemical compositions of the wastewater were investigated, and the COD contributed by each component was estimated. The results showed that the COD levels of O&G and SS presented decreasing trends during the whole process and achieved total removal percentages of 95.1% and 62.3%, respectively. The final COD of organic acids and low-molecular-weight carbonyl compounds were respectively lowered to nearly 64% and 35% of their initial levels, and no regular trends were found for the COD of these chemicals during the whole treatment process. The COD of inorganic components presented minor variations at all sampling spots. The majority of COD was originated from O&G in raw wastewater. The COD contributed by O&G decreased greatly with continuous treatment and finally was lower than 17% of measured COD. At each sampling spot, the ratios of COD contributed by SS did not exceed 7.6% of measured COD. Other measured chemicals, including organic acids, carbonyl compounds, volatile phenols, reductive anions, metals and TDP were not the main sources of COD during the whole treatment process, and the ratio of COD was below 9% at each sampling spot. Most of the soluble components contributable to residual COD were still unknown after biological treatment, and the COD contributed by these components was greater than 57% of measured COD. 相似文献
60.
Pei ZG Shan XQ Wen B Zhang S Yan L Khan SU 《Environmental pollution (Barking, Essex : 1987)》2006,139(3):541-549
The effect of copper on adsorption of p-nitrophenol on two typical Chinese soils was investigated using a batch-equilibration method. Adsorption experiments were carried out when both copper and p-nitrophenol were adsorbed simultaneously, and when copper was previously adsorbed on soils. It was observed that adsorption of p-nitrophenol decreased with increasing copper concentrations thereby indicating a competition between copper and p-nitrophenol for occupying the adsorption sites on soils. Moisture increased the hydrated sphere and the acidity of water surrounding the cation, which further reduced the adsorption of p-nitrophenol. Fourier transform infrared spectroscopy study provided the direct evidence for the coordination of p-nitrophenol sorbed by soils with metal cation in n-hexane system. It was observed that the perturbations included a red shift of the nu(asym) (NO) band, a concomitant blue-shift of the nu(sym) (NO) band and a blue-shift of C-N band when compared with the infrared spectra obtained from water solution. 相似文献