放射性核素在海水、底质及海洋生物间的转移--Ⅰ.核素进入海水后的初始状态

作者在建立的人工小生境中,研究了具有生态学意义的~(137)Cs、~(134)Cs、~(65)Zn、~(60)Co、~(59)Fe、~(54)Mn等核素在海水、底质及海洋生物间的转移规律.本文是该项研究的第一部分,研究悬浮物、底质对核素的富集和吸附,考察了核素进入海水后的初始状态.     

热带假丝酵母314号固定化细胞分解苯酚的研究

1.比较了三种生长培养基对热带假丝酵母314号细胞分解苯酚活力的影响。在以苯酚为碳源的培养基中生长的细胞酶活力较高,125mg湿细胞一小时可分解苯酚5425.8μg。用3.0%的琼脂固定化后,固定化细胞酶的相对活力为44.4%。诱导能显著地提高固定化细胞的酶活力,最适的诱导时间为12—18个小时。 2.比较了固定化细胞和自然细胞的某些性质。两种细胞反应的最适温度均为37℃;反应的pH范围均在3.5—11之间;固定化细胞热稳定性稍差;Cu~(2 )和Zn~(2 )对自然细胞的活性有一定抑制作用;CN-明显抑制两种细胞酶活力。 3.固定化细胞装柱后连续处理浓度约为150ppm的苯酚溶液,20天内的出水酚浓度平均为0.29ppm,在此条件下固定化细胞的半衰期为11天。 4.连续处理苯酚过程中,固定化细胞所丧失的酶活力可以通过再培养得到恢复。     

蓟运河汞污染化学地理特征

通过对蓟运河汞污染化学地理研究,查清了河水沉积物中汞和甲基汞的含量范围,水平和垂直变化,以及空间分布;研究了汞存在的形态;揭示了汞在河流中的富集区;作出了河流汞污染状况的分区,初步提出了治理河道汞污染的途径。     

Stability analysis of alkaline nitrobenzene-containing wastewater by a catalyzed Fe-Cu treatment process

Iron and copper bimetallic system (catalyzed Fe-Cu process) is a promising technology for alkaline nitrobenzene-containing wastewater treatment. However, little is currently known about the changes of treatment efficiency with time going. This research investigated the long-term performance of the catalyzed Fe-Cu process to reduce nitrobenzene (NB) in alkaline wastewater. In addition, the changes of the metal surfaces morphologies and matters before and after the reaction were analyzed by scanning electron microscopy (SEM) in conjunction with energy-dispersion spectroscopy (EDS) and X-ray diffraction spectroscopy (XRD). The results showed that the surface properties of copper almost remained unchanged after weeks of operation, which spelled its strong chemical stability and resistance to poisoning. Moreover, the results indicated that there were two reasons for the treatment efficiency decreasing with time. One was the gradual iron element consumption due to corrosion. The other was iron reactivity weakened due to the precipitates accumulation on the surfaces that were mainly Fe₃O₄ and FeCO. __________ Translated from Environmental Pollution & Control, 2006, 28(10): 783–785 [译自: 环境污染与防治]     

An assessment of how distance and diesel oxidation catalyst will impact thermal decomposition behaviors of particles

Decomposition mass loss and pyrolysis products analyses of particles sampled at various locations along the tailpipe of a Euro-IV diesel engine were performed using a thermogravimetry in conjunction with Fourier transformation infrared spectrometry-mass spectrum. Diesel particles were collected at the same location with and without diesel oxidation catalyst (DOC) mounted on the test engine separately. The three poles in thermal gravity-differential thermal gravity images suggested that the decomposition process of diesel particles could be divided into three stages which correspond to the decompositions of lower boiling substances, higher boiling substances and soot respectively. It is noticed that no matter whether DOC was mounted or not, the further the particles were sampled away from the engine block, the lower the peak temperatures and the heavier the mass losses within the first two stages, which indicated that the soluble organic fraction in the particle samples increased and therefore lowering the activation energy of thermal decomposition. Hydroxyl, ammonia, C_xH_y fragments, benzene, toluene, and phenol were found to be the primary products of particle decomposition, which didn't change with the location of particle sample point. The employment of DOC increased the activation energy for particle oxidation and resulted in a higher peak temperature and lower mass loss within the first-stage. Moreover, the CO stretching bands of aldehyde and ketone at 1771 cm^?1 was only detected without a DOC, while the NO₂ peak at 1634 cm^?1 was solely noticed with the presence of DOC. Compared to the first-stage pyrolysis products, more polycyclic aromatic hydrocarbons and less C_xH_y fragments were seen in the second-stage.     

化工铬渣冷固结球团还原解毒实验研究

采用铬渣冷固结球团方法来处理铬渣，研究了不同原料配比的铬渣冷固结球团的成球性能和强度，并用煤气进行了球团的还原实验。结果表明：铬渣的成球性能较好，在自然养护20d后，球团的抗压强度可达30kg／球以上。在900℃用煤气还原铬渣冷固结球团后，铬渣中的Cr^6含量在5mg／L以下：在1200℃还原后，有的铬渣中未检出Cr^6铬渣完全解毒，还原后的铬渣冷固结球团可进行综合利用。     

O3/UV降解喹啉过程中不同氧化剂的相对重要性

研究O3 /UV降解自配喹啉水溶液时水体中存在的不同氧化剂对喹啉降解的相对重要性的结果表明 ,O3 和·OH是喹啉降解过程的主要氧化剂 .通过靛蓝二磺酸钠法和·OH探针化合物 (对氯苯甲酸 )法分别测定了水体中的O3 浓度和·OH浓度 ,定量地计算了O3 和·OH在降解喹啉时的相对重要性 ,得到喹啉与·OH的二级反应速率常数为 6 65× 1 0 9mol·(L·s) - 1.在本试验条件下 ,由·OH引起的喹啉去除率占总去除率的 88% ,而由O3 引起的喹啉去除率占总去除率的 1 2 % .提高水体中·OH的浓度有利于提高喹啉的总降解速率 .     

水泥土桩复合地基桩土应力参数研究

本文首先通过理论分析，认为桩土应力比、桩土荷载分担比等是反映水泥土桩复合地基工作性状的重要参数。然后通过现场试验，研究桩土应力比、桩土荷载分担比随荷载变化的规律。结果认为：随着荷载增加，桩土应力比逐渐减小，当比值达到某一特征值后，不再发生明显变化；桩土应力比、桩土荷载分担比不为常数，其变化是桩土变形协调的结果。最后得出有一定参考价值的结论。     

无排泥条件下HRT对膜生物反应器硝化性能的影响及其生物群落结构分析

以无机氨氮废水(NH+4 N,500mg·L-1)为处理对象,在不排泥条件下逐渐缩短膜生物反应器的水力停留时间(HRT,30h～5h),连续运行260d.在反应器内的氨氮容积负荷和污泥负荷分别为1 2kg·(d·L)-1和2 13kg·kg-1·d-1时,氨氮去除率达98 2%以上.当HRT减少至7h时开始出现NH+4 N和NO-2 N的积累.尽管反应器内MLSS随着运行时间的延长在逐步上升,氨氧化菌(AOB)和亚硝酸氧化菌(NOB)的数量分别从HRT10h和15h起开始下降.16SrDNA聚合酶链式反应结合变性梯度凝胶电泳(PCR DGGE)的分析发现反应器内生物多样性随着运行时间的延长而增加,测序结果表明进行氨氧化作用的主要是亚硝化单胞菌属(Nitrosomonassp.),进行亚硝酸氧化的主要是硝化螺菌属(Nitrospirasp.).尽管反应器只进行无机氨氮配水,仍存在大量的异养菌,估计其生长是以胞外分泌产物和细胞裂解产物为基质.     

北极沉积物中硫酸盐还原菌与生物地球化学要素的相关分析

对北极楚科奇海、白令海测区34个沉积物样品的硫酸盐还原菌(SRB)含量与CaCO3、Si、S、P、Cd、Fe、Ti、Pb、Hg等地球化学要素作了相关分析．同时分析了SRB与其所在沉积物粒度与底层水温间的关系．结果表明：SRB与Si、砂及底层水温为正相关；SRB与CaCO3、Fe、Ti、P、Pb、Hg、粉砂、粘土为负相关；而SRB与Cd、S的相关性因海区不同而不同．既有负相关．也有正相关．分析了这些相关状况及其原因．