"全糟厌氧+UASB+好氧"工艺在酒糟废水治理中的应用

将污染治理和综合利用作为一个整体考虑,利用“厌氧＋UASB＋好氧”工艺处理酒糟废水,各项指标均取得了较好的处理效果：同时通过回收沼气获得了一定的经济效益。找到了一条技术先进、运行可靠、经济可行的治理工艺路线。     

盐城凹陷凝析油地球化学特征

运用碳同位素、气相色谱、色谱 质谱、流体包裹体技术 ,研究了盐城凹陷凝析油地球化学特征 ,并与永安凹陷永 7井凝析油、下扬子海相原油进行了对比。该凝析油碳同位素为 -2 8 8‰～ 3 0 5‰ ,全油色谱中含有一定的长链正构烷烃 ,Pr/Ph为 1 5 6,三环萜烷含量高 ,伽玛蜡烷含量低 ,重排甾烷含量高 ,C2 9甾烷 >>C2 7甾烷 >C2 8甾烷。石蜡指数、庚烷值表明原油为高成熟凝析油 ,甲基菲指数MPI表明原油为未熟—低熟原油 ,C2 9甾烷 2 0S/ (2 0S+2 0R)值表明原油为成熟原油。这种成熟度的差异可能与不同成熟度原油的混合作用有关。油气主要充注时间为 6～ 1 5Ma。凝析油的主体可能源于泰州组烃源岩 ,凝析油的形成与蒸发分馏作用密不可分     

敞开式微气泡富氧曝气活性污泥新工艺

活性污泥法在降解污水中所含有机物时,如增加污水中的溶解氧量,可大幅度提高污泥中微生物的活力,显著改善污水处理效率.但过去由于氧气成本高,纯氧曝气法一直处于试验阶段,未能很好地推广应用.变压吸附现场制氧可提供廉价氧气源,结合微气泡富氧曝气技术,同时实现了充氧和混合工艺,氧的利用率大幅提高,显著降低了纯氧曝气处理污水的综合投资和运行成本,是一种高效、低能耗的污水处理新工艺,具有很好的应用前景.     

物化-厌氧-好氧-溶气吸附工艺在毛条废水治理中的应用

介绍了应用物化 厌氧 好氧 溶气吸附工艺治理毛条废水（ＣＯＤＣｒ浓度１３８０００～１５６００ｍｇ／Ｌ）的工程实例。一年多的运行情况表明ＣＯＤＣｒ去除率达９９３％。     

粤东花岗岩类地球化学特征及成因探讨

粤东花岗岩类的SiO_2、K_2O及ALK值偏高,Al_2O_3、Fe_2_O_3、FeO及MgO偏低,ANKC值、Na/K比及CaO、Na_2O含量介于华南改造型花岗岩和同熔型花岗岩之间;负铕异常明显,轻稀土显著富集,中稀土(Tb—Tm)略有亏损;铅同位素高于地幔铅和下地壳铅同位素组成,略低于华南中生代上地壳铅同位素组成;锶、氧同位素具正相关关系,不相容元素比与其他元素间无相关关系。其岩浆起源于上、下地壳间的过渡带,该过渡带由上地壳物质及侵入其中的幔源物质组成,岩浆上升定位过程中,未发生过明显的分异结晶一同化作用。     

南方天然水体DOM的化学分级、变化特征及三卤甲烷生成势(THMFP)特性研究

采用XAD树脂吸附法,在春季内(3～5月)连续对南方深圳水库中的水体溶解性有机物(DOM)进行化学分级表征.结果表明,天然水体DOM的总量和单个化学分级组分含量在一个季节会发生一定的波动,但总的分布特征在季节内未发生根本变化,即憎水酸(HoA)和亲水部分(HiM)浓度始终较高,而憎水碱(HoB)、憎水中性物(HoN)、弱憎水酸(WHoA)浓度则相对较低.同时,选取代表性时间点对DOM各化学分级组分进行了消毒副产物三卤甲烷生成势(THMFP)的研究,发现三卤甲烷(THMs)的主要前驱物为憎水和弱憎水有机部分,对THMFP的贡献共占约80%.进一步研究发现,憎水中性物、憎水酸、弱憎水酸的THMs生成能力较强,总体上与紫外吸收能力基本一致;但弱憎水酸表现略有不同,其SUVA(100×UV254/DOC)值并不十分突出,但三卤甲烷生成能力却明显较高,说明DOM的紫外吸收特性不能完全作为THMFP特性的替代指标.亲水物质(HiM)的SUVA值也不高,但其THMs生成能力接近憎水酸部分,值得水处理工艺研究重点关注.     

Effect of dissolved oxygen on methane production from bottom sediment in a eutrophic stratified lake

Clarifying the role of sulfate and dissolved oxygen (DO) in methane production may allow for precise and accurate modeling of methane emissions in eutrophic lakes. We conducted field observations of sulfate, methane, and DO concentrations in Lake Abashiri, a typical brackish and eutrophic lake in a cold region, to develop a DO-based method for quantitively estimating methane production in a eutrophic lake and analyzed the results. We found that sulfate concentrations decreased rapidly from 900.0 mg/L in water overlying the sediments to nearly 0.0 mg/L in the bottom sediment. Methane production was almost uniform across sediment depths of 0.05 to 0.25 m, ranging from 1400 to 1800 µmol/m²/day. Also, methane production was found to be a function of DO concentrations in water overlying the bottom and could be modeled by a logistic function: constant production at 1,400 µmol/m²/day for DO concentrations of 0.0 to 3.0 mg/L, rapidly decreasing to 0 µmol/m²/day for DO concentrations of 3.0 to 6.0 mg/L. This methane model was verified using a simple one-dimensional numerical model that showed good agreement with field observations. Our results thus suggest that the proposed methane model reduces uncertainty in estimating methane production in a eutrophic lake.     

Direct hydride derivatization of methyl- and ethylmercury chlorides in aqueous solution with KBH4

ＩｎｔｒｏｄｕｃｔｉｏｎＲａｐｉｄａｎｄｓｅｎｓｉｔｉｖｅａｎａｌｙｔｉｃａｌｍｅｔｈｏｄｓｆｏｒｔｈｅｄｅｔｅｒｍｉｎａｔｉｏｎｏｆｍｅｒｃｕｒｙａｎｄｒｅｌａｔｅｄｃｏｍｐｏｕｎｄｓｉｎｅｎｖｉｒｏｎｍｅｎｔａｌｓａｍｐｌｅｓａｒｅｉｍｐｅｒａｔｉｖｅｌｙｄｅｍａｎｄｅｄｓｉｎｃｅｖａｒｉｏｕｓｃｈｅｍｉｃａｌｆｏｒｍｓｏｆｍｅｒｃｕｒｙｉｎｔｈｅｎａｔｕｒａｌｅｎｖｉｒｏｎｍｅｎｔｃａｎｂｅｈａｖｅｄｉｆｆｅｒｅｎｔｌｙ ,ｔｈｅｒｅｂｙａｆｆｅｃｔｉｎｇｉｔｓｂｉｏｇｅｏｃｈｅｍｉｃａｌｂ…     

基于超高效液相色谱串联质谱法的番茄果实和土壤中氟吡菌胺残留测定

建立了番茄果实和土壤中氟吡菌胺残留的超高效液相色谱-串联质谱(UPLC-MS/MS)检测方法。用乙腈水溶液提取样品中的氟毗菌胺,以C_(18)柱为分析柱、乙腈-甲酸水溶液为流动相,采用超高效液相色谱-串联质谱多反应监测、电喷雾正离子源、外标法定量。氟吡菌胺在0.05~1.00 mg/L范围内与峰面积呈良好的线性关系,线性方程为y=6964.10x-143.28,决定系数为0.996 8。向对照番茄果实、对照土壤中分别添加氟吡菌胺标样,使其添加量分别为0.10 mg/kg、0.40 mg/kg和2.00 mg/kg,平均回收率分别为92.43%~103.32%和92.75%~104.46%,相对标准偏差分别为3.8%~4.9%和3.4%~4.4%。番茄果实和土壤中氟吡菌胺的定量限分别为1.0μg/kg和1.7μg/kg,检出限分别为0.3μg/kg和0.5μg/kg。     

An integrated chemical mass balance and source emission inventory model for the source apportionment of PM2.5 in typical coastal areas

The source apportionment of PM_2.5 is essential for pollution prevention. In view of the weaknesses of individual models, we proposed an integrated chemical mass balance-source emission inventory (CMB-SEI) model to acquire more accurate results. First, the SEI of secondary component precursors (SO₂, NO_x, NH₃, and VOCs) was compiled to acquire the emission ratios of these sources for the precursors. Then, a regular CMB simulation was executed to obtain the contributions of primary particle sources and secondary components (SO₄^2?, NO₃^-, NH₄⁺, and SOC). Afterwards, the contributions of secondary components were apportioned into primary sources according to the source emission ratios. The final source apportionment results combined the contributions of primary sources by CMB and SEI. This integrated approach was carried out via a case study of three coastal cities (Zhoushan, Taizhou, and Wenzhou; abbreviated WZ, TZ, and ZS) in Zhejiang Province, China. The regular CMB simulation results showed that PM_2.5 pollution was mainly affected by secondary components and mobile sources. The SEI results indicated that electricity, industrial production and mobile sources were the largest contributors to the emission of PM_2.5 gaseous precursors. The simulation results of the CMB-SEI model showed that PM_2.5 pollution in the coastal areas of Zhejiang Province presented complex pollution characteristics dominated by mobile sources, electricity production sources and industrial production sources. Compared to the results of the CMB and SEI models alone, the CMB-SEI model completely apportioned PM_2.5 to primary sources and simultaneously made the results more accurate and reliable in accordance with local industrial characteristics.