氯碱企业生产过程中的重大危害分析及对策

分析了氯碱企业生产过程中的重大危害为中毒和火灾爆炸,提出了相应的对策.     

巢湖周围池塘氮、磷和有机质研究

巢湖周围池塘众多,根据池塘位置和地表径流补给差异,池塘可以分为村庄内池塘、毗邻村庄池塘和农田区域池塘(远离村庄的池塘).本研究采集了巢湖周围136口池塘上覆水和沉积物样品,调查巢湖周围池塘中氮、磷以及有机质污染现状.结果表明,池塘上覆水中总氮、氨氮、硝态氮、亚硝态氮、总磷、溶解态磷和COD平均含量分别为2.53、0.65、0.18、0.02、0.97、0.38和51.58mg·L-1;池塘沉积物中总氮、氨氮、硝态氮、亚硝态氮、总磷、无机磷、有机磷和烧失量平均含量分别为1575.36、35.73、13.30、2.88、933.19、490.14、414.75mg·kg-1和5.44%;90%以上的池塘总氮、总磷含量达到或超过富营养化水平.位于村庄内的池塘上覆水和沉积物中总氮和氨氮的含量显著高于位于农田区域的池塘.上覆水和沉积物中无机氮表现为:氨氮硝态氮亚硝态氮.池塘上覆水和沉积物中有机质与总氮、总磷之间存在显著的正相关性.池塘中氮、磷和有机物质主要为陆源性输入,池塘位置和径流补给方式明显影响其中的氮、磷和有机质含量.通过截留径流中的氮、磷和有机质,池塘能够有效减少进入巢湖的营养盐含量.     

不同氮、磷肥用量下双季稻田的CH4和N2O排放

以红壤双季稻田为研究对象,采用静态暗箱-气相色谱法对2009年水稻生长期内不施肥（CK）,平衡施肥（BF）、减氮磷一（DNP1）、减氮磷二（DNP2）和增氮磷（INP）等5个处理的CH4和N2O排放通量以及环境因素进行观测.结果表明,早稻生长期间BF、DNP1、DNP2和INP的CH4平均排放通量为4.57、5.42、...     

东莞市蔬菜基地土壤中喹诺酮类抗生素的污染特征研究

抗生素作为新兴环境污染物在区域农业土壤污染特征研究中鲜见报道.本文利用固相萃取-高效液相色谱-串联质谱分析方法,调查了东莞市18个区镇24个代表性蔬菜基地土壤中喹诺酮类抗生素(QNs)的含量与分布特征.结果表明,4种喹诺酮类化合物的检出率均在90%以上,以环丙沙星(平均含量24.93μg·kg-1)和恩诺沙星(平均含量...     

Mn对超富集植物短毛蓼和水蓼生长、Mn吸收及氮素代谢的影响

采用水培的方法,研究了不同浓度Mn(0.0003、0.5、1、2、4、8 mmol · L^-1)对Mn超富集植物短毛蓼(Polygonum pubescens Blume)和水蓼(Polygonum hydropiper L.)叶片铵态氮、硝态氮、游离脯氨酸、可溶性蛋白质含量及氮素代谢关键酶:硝酸还原酶(NR)、谷氨酰胺合成酶(GS)、谷氨酸合酶(GOGAT)和谷氨酸脱氢酶(GDH)活性的影响.结果表明,随着Mn处理浓度的增加,短毛蓼和水蓼的根、茎、叶中Mn含量显著增加(p<0.05),在相同Mn处理浓度下短毛蓼中Mn含量均大于同部位水蓼中Mn含量.在Mn处理浓度小于1 mmol · L^-1时,Mn对短毛蓼的株高、株重影响不显著,但对水蓼的影响显著(p<0.05),表明短毛蓼比水蓼更耐Mn污染.Mn处理显著降低了短毛蓼硝态氮含量(p<0.05),提高了可溶性蛋白质含量,浓度为8 mmol · L^-1的Mn处理显著提高了水蓼硝态氮、铵态氮、可溶性蛋白质含量及短毛蓼、水蓼游离脯氨酸含量(p<0.05).Mn引起了短毛蓼和水蓼氮素代谢关键酶活性的变化,显著降低了水蓼叶片NR、短毛蓼叶片GS活性(p<0.05);在Mn处理浓度为1 mmol · L^-1时,短毛蓼叶片NR活性最高,为对照的1.91倍,而2、4、8 mmol · L^-1 Mn处理显著降低了短毛蓼和水蓼GOGAT活性(p<0.05).另外,Mn处理显著提高了短毛蓼和水蓼叶片GDH活性(p<0.05),在Mn处理浓度为8 mmol · L^-1时,短毛蓼、水蓼叶片GDH活性分别为对照的16.29倍和1.29倍.     

江西省陆地生态系统氮平衡的时空分布规律研究

利用系统物质平衡模型,对1995-2005年江西省陆地生态系统的N收支平衡进行了核算,并分析了不同来源N收支量的时间序列特征以及N盈余强度的空间分布特征,探讨了自然灾害和政策实施对N平衡的影响.结果表明:江西省陆地生态系统的N输入量变化范围是(155.5-184.2)×107kg·a-1,平均值为168.5 ×107 ...     

青岛大气气溶胶中氨基化合物的分布特征

氨基化合物是大气气溶胶和雨水中常被检出的一类有机氮化合物,由于其可作为生物生长直接的氮源,因此可能对海洋生态系统产生直接作用.利用2008年1～12月在青岛采集的66个总悬浮颗粒物样品,采用邻苯二甲醛/N-乙酰-L-半胱氨酸柱前衍生高效液相色谱法,分析了其中溶解态(DAC)和颗粒态氨基化合物(PAC)的浓度.气溶胶中DAC浓度为2.4～40.9nmol·m-3,在春季最高,夏季次之,秋季、冬季最低.PAC浓度为0.7～76.1nmol·m-3,呈现春季冬季秋季夏季的变化趋势.不同季节氨基化合物的组成不同.依据气团的后向轨迹,气溶胶样品可分为受北方陆源、南方陆源和海洋源影响,DAC和PAC在受南方陆源影响的气溶胶中浓度最高,北方陆源次之,海洋源气溶胶中最低.不同来源的气溶胶中氨基化合物的组成不同,蛋白质类氨基化合物对总氨基化合物的贡献在海洋源气溶胶中最高,在南方源气溶胶中最低.     

污水地下渗滤系统强化脱氮试验研究

构建了3套以5%炉渣+95%草甸棕壤为基质的地下渗滤系统室内模拟试验装置,在水力负荷为0.1m3/(m2·d)条件下进行了生活污水处理试验.结果表明,当分流位置位于系统内110cm处,分流比为1:1时,可提高地下渗滤对总氮的去除效率,总氮的去除率由59.37%提高至68.41%,且对COD和总磷的去除效果没有影响.     

Nitrogen cycle of a typical Suaeda salsa marsh ecosystem in the Yellow River estuary

The nitrogen (N) biological cycle of the Suaeda salsa marsh ecosystem in the Yellow River estuary was studied during 2008 to 2009. Results showed that soil N had significant seasonal fluctuations and vertical distribution. The N/P ratio (15.73±1.77) of S. salsa was less than 16, indicating that plant growth was limited by both N and P. The N absorption coefficient of S. salsa was very low (0.007), while the N utilization and cycle coefficients were high (0.824 and 0.331, respectively). The N turnover among compartments of S. salsa marsh showed that N uptake from aboveground parts and roots were 2.539 and 0.622 g/m2, respectively. The N translocation from aboveground parts to roots and from roots to soil were 2.042 and 0.076 g/m2, respectively. The N translocation from aboveground living bodies to litter was 0.497 g/m2, the annual N return from litter to soil was far less than 0.368 g/m2, and the net N mineralization in topsoil during the growing season was 0.033 g/m2. N was an important limiting factor in S. salsa marsh, and the ecosystem was classified as unstable and vulnerable. S. salsa was seemingly well adapted to the low-nutrient status and vulnerable habitat, and the nutrient enrichment due to N import from the Yellow River estuary would be a potential threat to the S. salsa marsh. Excessive nutrient loading might favor invasive species and induce severe long-term degradation of the ecosystem if human intervention measures were not taken. The N quantitative relationships determined in our study might provide a scientific basis for the establishment of effective measures.     

Modeling assessment for ammonium nitrogen recovery from wastewater by chemical precipitation

Chemical precipitation to form magnesium ammonium phosphate (MAP) is an effective technology for recovering ammonium nitrogen (NH4 +-N). In the present research, we investigated the thermodynamic modeling of the PHREEQC program for NH4 +-N recovery to evaluate the effect of reaction factors on MAP precipitation. The case study of NH4 +-N recovery from coking wastewater was conducted to provide a comparison. Response surface methodology (RSM) was applied to assist in understanding the relative significance of reaction factors and the interactive effects of solution conditions. Thermodynamic modeling indicated that the saturation index (SI) of MAP followed a polynomial function of pH. The SI of MAP increased logarithmically with the Mg2+/NH4 + molar ratio (Mg/N) and the initial NH4 +-N concentration (CN), respectively, while it decreased with an increase in Ca2+/NH4 + and CO3 2??/NH4 + molar ratios (Ca/N and CO3 2??/N), respectively. The trends for NH4 +-N removal at different pH and Mg/N levels were similar to the thermodynamic modeling predictions. The RSM analysis indicated that the factors including pH, Mg/N, CN, Ca/N, (Mg/N) (CO3 2??/N), (pH)2, (Mg/N)2, and (CN)2 were significant. Response surface plots were useful for understanding the interaction effects on NH4 +-N recovery.