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91.
The catalyst of Fe-Mo/ZSM-5 has been found to be more active than Fe-ZSM-5 and Mo/ZSM-5 separately for selective catalytic reduction (SCR) of nitric oxide (NO) with NH3. The kinetics of the SCR reaction in the presence of O2 was studied in this work. The results show that the observed reaction orders were 0.74-0.99, 0.01-0.13, and 0 for NO, O2 and NH3, respectively, at 350-450℃. And the apparent activation energy of the SCR was 65 kJ/mol on the Fe-Mo/ZSM-5 catalyst. The SCR mechanism was also deduced. Adsorbed NO species can react directly with adsorbed ammonia species on the active sites to form N2 and H2O. Gaseous O2 might serve as a reoxidizing agent for the active sites that have undergone reduction in the SCR process. It is also important to note that a certain amount of NO was decomposed directly over the Fe-Mo/ZSM-5 catalyst in the absence of NH3. 相似文献
92.
Bioaccumulation of heavy metals in fishes from Taihu Lake, China 总被引:9,自引:0,他引:9
The Cr,Zn,Cu,Cd,Pb contents were determined in Cyprinus carpio Linnaeus,Carassius auratus Linnaeus,Hypophthalmichthys molitrix and Aristichthys nobilis,which were caught from Meiliang Bay,Taihu Lake,a large,shallow and eutrophic lake of China.The results showed that:(1)the Cr,Cu,Pb,Cd contents in the edible parts of the four fish species were much lower than Chinese Food Health Criterion(1994),but the Zn contents were higher than the Criterion;(2)Cd contents were the highest in the liver of fish,Pb contents were almost the same in all organs of fish,Cr contents mainly enriched in the skin and gonads,Zn contents were the highest in the gonad(♀),and Cu contents were the highest in the liver;(3)the total metal accumulation was the greatest in the liver and the lowest in the muscle.The total metal accumulation was the highest in C.auratus L.This investigation indicated that fish products in Taihu Lake were still safe for human consumption,but the amount consumed should be controlled under the Chinese Food Health Criterion to avoid excessive intake of Zn. 相似文献
93.
94.
95.
崇西湿地冬季潮滩鱼类种类组成及多样性分析 总被引:8,自引:0,他引:8
根据2006年冬季在崇西湿地进行的光滩和草滩插网渔获调查,首次对冬季长江口潮滩鱼类种类组成、多样性及相关环境因子作了分析。结果表明:冬季崇西湿地潮滩鱼类主要由淡水小型鱼类组成,共23种,隶属7科,20属。光滩和草滩插网的最大优势种皆为油,两种网具的渔获种类组成具一定的相似性。在一个潮周期内,3种多样性指数D、H′ 和J值波动范围较大,小汛潮时多样性指数比其它潮汛低。白天和晚上潮水的鱼类种类数无显著变化(P>0.5),但在个体数和生物量上白天较晚上潮水高(P<0.5)。水温、潮汐大小对潮滩鱼类丰度影响较大,而与盐度相关较小。此外,天气状况也是影响潮滩鱼类的一个重要因子。总之,潮滩鱼类的种类组成和多样性受到各种环境因子的综合影响。 相似文献
96.
三峡库区悬移质泥沙对磷污染物的吸附解吸特性 总被引:3,自引:0,他引:3
就三峡库区悬移质泥沙对磷污染物的吸附解吸特性从野外同步监测和室内试验研究两个方面展开研究。选取长江干流、嘉陵江和乌江共7个监测断面于2002年和2003进行野外同步监测,测试结果表明:水中的悬移质泥沙对水中各种覆存形态的磷污染物浓度具有显著影响,单位重量泥沙对磷的吸附量与水体总泥沙含量、泥沙粒径有密切关系。采集寸滩断面泥沙对磷酸盐吸附解吸特性进行室内试验研究,并根据Langmuir吸附动力学方程对吸附解吸过程进行了拟合,发现吸附速率常数k随着泥沙粒径的增加而呈递增变化,而磷酸盐初始浓度对k值的影响并不明显,同时,磷酸盐解吸量随着泥沙浓度的增加和粒径的增加呈递减变化,k值随着泥沙粒径的增加而呈递增变化,泥沙浓度对k值的影响不明显。 相似文献
97.
Competition of three bloom-forming marine phytoplankton (diatom Skeletonema costatum, and dinoflagellates Prorocentrum
minimum and Alexandrium tamarense) was studied through a series of multispecies cultures with di erent nitrate (NaNO3) and
phosphate (NaH2PO4) levels and excess silicate to interpret red tide algae succession. S. costatum outgrew the other two dinoflagellates
in nitrate and phosphate replete cultures with 10 mol/L Na2SiO3. Under nitrate limited (8.82 mol/L NaNO3) conditions, the growth
of S. costatum was also dominant when phosphate concentrations were from 3.6 to 108 mol/L. Cell density of the two dinoflagellates
only increased slightly, to less than 400 and 600 cells/mL, respectively. Cell density of S. costatum decreased with time before day
12, and then increased to 4000 cells/mL (1.5 mg/L dry biomass) at NaNO3 concentrations between 88.2 and 882 mol/L with limited
phosphate (0.36 mol/L NaH2PO4) levels. In addition, P. minimum grew well with a maximal cell density of 1690–2100 cells/mL
(0.5–0.6 mg/L dry biomass). Although S. costatum initially grew fast, its cell density decreased quickly with time later in the growth
phase and the two dinoflagellates were dominant under the nitrate-limited and high nitrate conditions with limited phosphate. These
results indicated that the diatom was a poor competitor compared to the two dinoflagellates under limited phosphate; however, it grew
well under limited nitrate when growth of the dinoflagellates was near detection limits. 相似文献
98.
Removal of phosphate by Fe-coordinated amino-functionalized 3D mesoporous
silicates hybrid materials
Phosphate removal from aqueous waste streams is an important approach to control the eutrophication downstream bodies of water.
A Fe(III) coordinated amino-functionalized silicate adsorbent for phosphate adsorption was synthesized by a post-grafting and metal
cation incorporation process. The surface structure of the adsorbent was characterized by X-ray di raction, N2 adsoropion/desoprotion
technique, and Fourier transform infrared spectroscopy. The experimental results showed that the adsorption equilibrium data were well
fitted to the Langmuir equation. The maximum adsorption capacity of the modified silicate material was 51.8 mg/g. The kinetic data
from the adsorption of phosphate were fitted to pseudo second-order model. The phosphate adsorption was highly pH dependent and
the relatively high removal of phosphate fell within the pH range 3.0–6.0. The coexistence of other anions in solutions has an adverse
e ect on phosphate adsorption; a decrease in adsorption capacity followed the order of exogenous anions: F?? > SO2?? 4 > NO??3 > Cl??. In
addition, the adsorbed phosphate could be desorbed by NaOH solutions. This silicate adsorbent with a large adsorption capacity and
relatively high selectivity could be utilized for the removal of phosphate from aqueous waste streams or in aquatic environment. 相似文献
99.
Tao Zhang Qiucheng Li Lili Ding Hongqiang Ren Ke Xu Yonggang Wu Dong Sheng 《环境科学学报(英文版)》2011,23(6):881-890
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. 相似文献
100.
Removal of phosphate from wastewater using alkaline residue 总被引:2,自引:0,他引:2
Yubo Yan Xiaodong Liu Xiuyun Sun Fangbian M Lianjun Wang Jiansheng Li Jinyou Shen 《环境科学学报(英文版)》2014,26(5):970-980
Alkaline residue(AR) was found to be an efficient adsorbent for phosphate removal from wastewater. The kinetic and equilibrium of phosphate removal were investigated to evaluate the performance of modified alkaline residue. After treatment by NaOH(AR-NaOH), removal performance was significantly improved, while removal performance was almost completely lost after treatment by HCl(AR-HCl). The kinetics of the removal process by all adsorbents was well characterized by the pseudo second-order model. The Langmuir model exhibited the best correlation for AR-HCl, while AR was effectively described by Freundlich model. Both models were well fitted to AR-NaOH. The maximum adsorption capacities calculated from Langmuir equation were in following manner: AR-NaOH AR AR-HCl. Phosphate removal by alkaline residue was pH dependent process. Mechanisms for phosphate removal mainly involved adsorption and precipitation, varied with equilibrium pH of solution. For AR-HCl, the acid equilibrium pH( 6.0) was unfavorable for the formation of Ca-P precipitate, with adsorption as the key mechanism for phosphate removal. In contrast, for AR and ARNaOH, precipitation was the dominant mechanism for phosphate removal, due to the incrase on pH( 8.0) after phosphate removal. The results of both XRD and SEM analysis confirmed CaHPO4·2H2O formation after phosphate removal by AR and AR-NaOH. 相似文献