城市污水处理厂污泥及剩余麻黄废渣堆肥化研究

对城市污水污泥与麻黄废渣进行堆肥无害化处理，考察了温度、水分、pH及各有机成分的变化趋势，探讨了堆肥腐熟度的指标。     

水中总α、总β、~(238)U放射性水平及其与残渣含量的关系

本文报道了新疆地区37个不同水源水中总α、总β、~(238)U放射性比活度和残渣含量的调查结果.结果表明,水中总α、总β、~(238)U放射性比活度和残渣含量的算术均值和标准偏差分别为0.84±0.74,0.48±0.37, 0.24±0.16(Bg/L)和1.27±0.72(g/L).水中总α放射性主要是天然铀系核素贡献.水中总α、总β和~(238)U放射性水平与残渣含量呈直线正相关,且可用通式y=a+bx描述.     

土壤微生物群落对玉米根茬和茎叶残体碳的利用特征

以沈阳农业大学连续29a棕壤长期定位施肥试验为基础,以¹³C标记的玉米植株为试验试材,采用田间原位培养方法和磷脂脂肪酸-稳定同位素示踪联用（PLFA-SIP）技术,研究土壤不同粒级团聚体中微生物群落对残体碳的同化状况,及土壤有机碳的固定这一关键生物地球化学过程.结果表明：植物残体添加显著增加了全土及各粒级团聚体中各微生物群落PLFAs含量,其中以真菌PLFAs含量增幅最高,细菌中以革兰氏阴性菌含量增幅最高;但不同残体类型并未对全土中各群落PLFAs含量产生显著影响.茎叶碳与根茬碳的矿化率无显著差异;根茬碳对总PLFAs碳库的贡献是茎叶碳的3.9倍,说明根茬碳更有利于通过微生物合成的方式贡献于土壤有机碳库.残体碳占不同微生物群落PLFAs碳库的比例以真菌最高,表明真菌对植物残体碳具有最强的同化能力;而残体碳对PLFAs的贡献在革兰氏阳性菌和革兰氏阴性菌之间却差异不大.残体碳含量、PLFAs含量和残体碳占微生物PLFAs碳库的比例均在较小粒级的团聚体中（0.25~1mm和<0.25mm）更高,而细菌/真菌比在较大粒级团聚体（>2mm和1~2mm）中更高,说明较小粒级团聚体已经成为微生物对残体进行同化固定的主要位点.植物残体在土壤中的腐解过程与残体类型、土壤团聚体组成和微生物群落密切相关.     

高浓度废水处理技术在柴油碱渣处理中的应用

炼厂柴油碱渣废水中含有成分复杂的酚及硫化物,因而其浓度较高。大港石化公司运用高浓度废水处理技术进行生物前期处理,其装置试运及柴油碱渣标定应用表明该技术先进。在生物处理过程中,工艺系统运行安全可靠,各项技术指标都达到或超过设计目标。其中,CODCr由处理前的34744mg/L降低到370mg/L,氨氮控制在50mg/L以下。高浓度废水处理技术流程简单,对周边环境无污染。     

湿法磷酸生产中磷石膏废渣制硫酸钾铵的中间试验研究

在湿法磷酸生产中要排出大量的磷石膏废渣 ,不仅要占用大量土地堆放而且污染环境。作者介绍了以磷石膏废渣作原料 ,生产硫酸钾铵的 3 0 0 0t a中间试验装置 ,包括磷石膏与碳酸铵复分解反应制备硫铵及硫铵与氯化钾复分解反应制取硫酸钾铵     

氧化铬渣培烧过程中有机废气的治理

对氧化铬焦油渣焙烧处理中含尘、酸、苯及苯系物烟气的治理，提出一级喷淋水膜除尘并回收低浓度醋酸，二级涅式捕集苯系有机物净化技术。运行结果表明，该工艺醋酸回收率达95％，苯、甲苯、二甲苯去除率分别达到97．9％、99．7％、99．9％，达到了国家规定的排放标准。     

林地变为玉米地后土壤轻质部分有机碳的13C/12C比值的变化

为了观察森林生态系统转变为农业生态系统后土壤有机碳的变化，选择贵州喀斯特森林区为研究对象，采集了林地和邻近的玉米地土壤剖面样品，并按土壤密度把土壤样品分级成轻质部分和重质部分。林地和玉米地土壤均为石灰土。玉米地土壤风化相对较强，淋溶严重而贫瘠，并且所返还的植物残留物数量很少。实验结果表明，林地土壤轻质部分的(13C值明显低于重质部分，而玉米地土壤轻质部分的(13C值明显高于重质部分，说明植物残留物首先进入到轻质部分。然而，由于当地的耕作习惯，输入到玉米地土壤轻质部分的玉米残留物的数量很少，只有48%，这是初级生产力低下的主要原因。     

多效唑在番茄和土壤中的残留与降解动态研究

研究了多效唑（paclobutrazol）在番茄（Lycopersicon eseulentum）和土壤中的残留分析方法及残留动态。建立番茄和土壤样品中多效唑残留的固相萃取-高效液相色谱（SPE-HPLC）检测方法,样品用乙腈提取,再用φ（甲醇-二氯甲烷）=5∶95混合溶剂经LC-NH2固相萃取柱净化,以φ（乙腈-水）=55∶45作流动相,Shiseido C18色谱柱（4.6 mm×250 mm,5μm）于222 nm波长检测,外标法定量。在0.1~5.0 mg·L-1范围内,多效唑峰面积与其质量浓度之间呈良好线性关系,相关系数为0.9995。采用田间试验方法,在番茄幼苗期施用不同多效唑质量分数50、100、200、600 mg·kg-1,研究在不同处理时间1、6 h,1、2、3、7、14、21、30、45、60 d,多效唑在番茄以及土壤中的残留动态变化。添加质量分数水平为0.05、0.1、0.5 mg·kg-1时,多效唑在果实、植株和土壤中的添加回收率分别为92.45%~103.70%、94.52%~98.85%和94.30%~102.10%,变异系数分别为3.69%~5.00%、1.58%~4.53%和1.28%~3.35%。结果表明：多效唑在番茄植株和土壤中的降解规律均符合一级动力学方程C=Coe-kt。当施用质量分数为600 mg·kg-1时,其在番茄植株中的残留半衰期为1.66 d,在土壤中的半衰期为2.78 d;在植株中的降解速率大于在土壤中的降解速率。按照推荐使用的施用浓度,采收时多效唑在番茄和土壤中无残留,证明推荐施用浓度是合理的。     

Effect of long-term application of corn stalks and inorganic fertilizers on fluorescence characteristics of water extractable organic matter in a meadow black soil of northeast China

ABSTRACT

Returning crop residues into fields, either alone or in combination with inorganic fertilizer, is considered as a practical way to enhance soil fertility. However, information concerning the effects of crop residues and inorganic fertilizer application on water extractable organic matter (WEOM) in soil is scarce. The aim of this study was to examine the 10-year effect of corn residue (CR) return with or without the application of nitrogen, phosphorus, and potassium (NPK) fertilizer on the quantity and quality of WEOM in a black soil of northeast China by means of ultraviolet absorbance, fluorescence excitation--emission matrix, and derived spectroscopic indices. The application of NPK fertilizers and CR, alone or together, increased the content of total soil organic carbon (SOC), water extractable organic carbon (WEOC), and ratio of WEOC/SOC, with the sequence being NPK + CR > CR > NPK > CK. Compared with control treatment, the individual application of NPK fertilizer decreased the aromaticity of WEOM. In contrast, elevated proportion of tryptophan-like fluorophore and microbially derived fulvic acid-like components with low molecular weight was detected in the WEOM. The amendment with CR alone resulted in increase in aromaticity of WEOM and proportion of plant-derived humic acid-like component with large molecular weight, accompanied by reduced proportion of tyrosine-like compounds. For the soil with CR restoration, the application of NPK fertilizer increased aromaticity of WEOM, and large molecular weight fulvic acid-like and humic acid-like compounds were found. However, the proportions of tyrosine-like and tryptophan-like compounds were diminished. The quantitative and qualitative analysis of WEOM using fluorescence spectroscopy describes responses to be observed in long-term different fertilization strategies.     

Characteristics and risk assessment of organochlorine pesticide residues in surface sediments collected at the Qingshitan Reservoir

ABSTRACT

An ultrasonic extraction – gas chromatography – electron capture detector analytical method was used to measure the concentration and types of organochlorine (OC) pesticides in sediment to obtain a better understanding of the characteristics and hidden ecological risks associated with OC pesticide exposure in surface sediment of the Qingshitan Reservoir. Fifteen types of OC pesticides were detected in the sediment, and the sum concentration of these chemicals was in the 149.32–490.19 ng/g range (mean value: 319.39 ng/g). The concentrations of detected OC pesticides occurred in the following order: hexachlorohexanes (HCHs) (mean value: 200.17 ng/g) > DDTs (mean value: 36.92 ng/g) > heptachlors (mean value: 32.74 ng/g) > methoxychlor (mean value: 24.13 ng/g). There was a 100% detection rate for HCH isomers, and their concentrations occurred in the following order: β-HCH > δ-HCH > γ-HCH > α-HCH. β-HCH was the main component of HCHs. Ratios between α-HCH/γ-HCH and β-/(α+γ)-HCH were used to investigate the sources of pollution. Most of the surveyed areas were polluted by lindane, which originated from past pesticide residue usage, and no new inputs of HCHs were found. DDT was the major component of the DDTs, and accounted for 52%–87% of the DDTs. The ratios of (DDE+DDD)/DDT at all sample collection points were less than 1, indicating that degradation rate of DDTs in sediment was low and there was a new input of DDTs in these surveyed areas. The ratio of DDD/DDE was less than 1 at most of the sample collection points, indicating that the degradation of DDT in the sediments primarily took place under aerobic conditions. Comparison of OC pesticide residual levels in the underwater sediment collected at the Qingshitan Reservoir to other states and countries showed the pollution level of these chemicals of the Qingshitan Reservoir was relatively high. The ecological risk was assessed based on guideline values of effects range-low (ERL) and effects range-medium (ERM). The results showed that DDD, DDE, DDTs and endrin residues in the sediment posed a moderate ecological risk, but DDT and γ-HCH showed high ecological risk. These OC pesticides might adversely affect biological systems, and need to be addressed.