氮肥水平对不同土壤CH4排放的影响

鉴于氮肥施用对农田CH₄排放的影响还有很大不确定性,室外盆栽试验于2002年在南京农业大学实施.选取3个供试土壤,各土壤设置对照和低、中、高3个不同氮肥水平,施入尿素量分别为0 g/盆钵(对照) ,0.64g/盆钵,(低氮水平) ,1.28g/盆钵(中氮水平) ,1.93g/盆钵(高氮水平) .结果表明在水稻生长季,不同氮肥(尿素)施用量对稻田土壤CH₄排放影响表现为不同土壤之间,及不同氮肥水平之间CH₄排放均存在显著差异.无氮肥施入的情况下,3种土壤的CH₄季节性累积排放量存在显著差异,分别为6.7g/m²,12.6g/m² 和8.3g/m².施加氮肥后,3种土壤的CH4排放量随氮肥施入量的增加,均表现为降低趋势,不同土壤CH₄排放量存在差异,土壤背景氮含量最高的F(江苏溧水)土壤的CH4排放都比相应氮肥水平下的G(江苏涟水)和H(江苏农科院)土壤的CH₄排放低1倍左右.更进一步发现从低氮到中氮水平,3种土壤CH₄排放量随氮肥用量的增加降低幅度最大,而此时各土壤的NH₄-N含量随氮肥用量增加明显提高,推断造成CH₄排放降低的主要可能原因是各土壤的氨态氮含量的增加所致.从中氮到高氮水平3种土壤的CH₄排放量的变化不尽相同,G和H土壤的CH₄排放量随氮肥用量的增加而降低,而F土壤在中氮和高氮水平下的CH4排放量没有明显变化,值分别为30g/m².     

有机肥施用对田面水氮磷流失风险的影响

为探明化肥配施有机肥对田面水氮、磷流失及水稻系统养分吸收的影响,采用田间小区试验,设置常规施肥处理（FN）、常规施肥减氮磷量20%处理（F0）、减氮磷20%+有机肥处理（F1~F4处理有机肥施用量分别为1 500、3 000、4 500和6 000 kg/hm2）共6个处理,探索化肥减量20%配施有机肥的最优组合.结果表明:不同施肥处理下,田面水中ρ（TN）、ρ（NH₄+-N）均于施肥后第1天达到峰值,随后迅速下降,于第7天后逐渐趋于稳定,ρ（TN）和ρ（NH₄+-N）分别维持在各自峰值的5.1%~10.9%与4.8%~9.6%,田面水中ρ（TP）的变化趋势与ρ（TN）相似;F0与F1处理均能有效降低田面水中ρ（TN）和ρ（TP）.与FN处理相比,F1处理下ρ（TN）、ρ（NH₄+-N）与ρ（TP）平均值分别降低了6.5%、9.1%和3.1%,该处理能够有效地降低氮、磷养分流失风险,且增施有机肥可使水稻增产0.2%~19.8%,地上部分氮、磷累积量随有机肥施用量的增加而显著增加（P < 0.05）.综合水稻产量、养分吸收和田面水养分动态等指标发现,F1处理不仅能提高区域双季稻产量,还能有效控制田面水氮、磷养分浓度,降低氮、磷地表径流产生的农田面源污染风险,是针对南方双季稻田的一项"控源节流"优化施肥模式.      

水肥用量对玉米季土壤CO2排放的综合影响

为揭示水肥用量对农田生态系统土壤CO_2排放的综合影响,试验设高水W1(90 mm)、中水W0.85(76.5 mm)、低水W0.7(63 mm)这3个灌水水平,300、255、210和0 kg·hm~(-2)这4个施氮水平和90、76.5、63和0 kg·hm~(-2)这4个施磷水平,采用静态暗箱-气相色谱法对夏玉米地土壤CO_2排放进行原位观测,分析土壤CO_2排放对水肥调控的动态响应.结果表明,玉米季农田土壤CO_2排放呈双峰曲线,主峰值出现在拔节期至抽雄期,次峰出现在抽雄至灌浆期,其他阶段排放通量较低.W1在高肥F1(N 300 kg·hm~(-2),P2O590 kg·hm~(-2))和低肥F0.7(N 210 kg·hm~(-2),P2O563 kg·hm~(-2))水平下全生育期土壤CO_2平均排放通量均显著高于W0.7(P0.05);中肥F0.85(N 255 kg·hm~(-2),P2O576.5 kg·hm~(-2))和F0.7水平下,W0.85与W0.7差异不显著(P0.05).W1水平下,F1比F0.7显著增大14.82%(P0.05);W0.85水平下,F0.85比F0.7显著增大8.03%(P0.05);而W0.7水平下各施肥水平间无显著性差异.单施氮(N 210 kg·hm~(-2))或磷(P2O563 kg·hm~(-2))、氮磷配施(N 210 kg·hm~(-2)、P2O563kg·hm~(-2))较不施肥处理分别显著增加23.70%、19.00%和12.30%,且氮磷交互作用极显著(P0.01).方差分析表明,供应水平相差15%时,水肥交互作用对全生育期土壤CO_2平均排放通量影响不显著(P0.05),而对土壤CO_2累计排放量影响显著(P0.05);供应水平相差30%时水肥交互作用对全生育期土壤CO_2平均排放通量和累计排放量均影响显著(P0.05).可见,灌水量、施氮量、施磷量单因素均显著促进土壤CO_2排放,而氮磷配施起抑制作用.土壤CO_2排放与水、肥供应水平均有密切关系,水肥交互显著促进了土壤CO_2排放,通过水肥联合调控可有效调节土壤CO_2排放.     

胶州湾潮间带和沿岸区的耐铬菌

本文首次报道了胶州湾潮间带和沿岸区的耐铬菌数量分布。讨论了耐铬菌的若干生态意义。发现沉积物表层的耐铬菌数量大,但水中的耐铬菌出现频率高于沉淀物的。找到了CT/AA与样品含铬量间的正相关。指出CT/AA可作为环境铬污染的一个重要指数。试验了耐铬菌耐Cr~(3+)、Cr~(6+)、Hg~(2+)和降解原油的能力。认为耐铬菌对环境污染有适应、忍耐、抵抗乃至降解的能力。耐铬菌在环境污染物(首先是铬污染)的迁移、转化活动中起重要作用。它们是水生微生物区系的一个重要组成部分。耐铬菌的耐铬能力为它能参于铬污染的消除活动赋于强大活力。     

生物炭配施缓控释肥对稻田田面水氮素动态变化及径流流失的影响

在太湖流域,通过田间试验研究了控释肥(CRF)、生物炭配施控释肥(BC+CRF)、生物炭配施稳定性肥(BC+SF)、生物炭配施控释肥和稳定性肥(BC+CRF+SF)4种施肥处理对稻田田面水p H、氮素动态变化、氮素径流流失的影响.结果表明,田面水平均p H介于5.64~8.15,生物炭配施控释肥和稳定性肥田面水p H降低3.16%~4.48%.田面水平均全氮(TN)质量浓度介于19.05~25.23 mg·L~(-1),生物炭配施控释肥和稳定性肥田面水TN质量浓度显著降低4.75%~6.58%.田面水无机氮素以铵态氮(NH_4~+-N)为主,NH_4~+-N和硝态氮(NO_3~--N)平均质量浓度分别介于0.01~17.26 mg·L~(-1)和0.24~3.11mg·L~(-1).与单施控释肥相比,各处理田面水NH_4~+-N和NO_3~--N质量浓度分别显著降低35.89%~48.78%和20.54%~37.01%.生物炭配施稳定性肥显著降低了田面水NH_4~+-N和NO_3~--N质量浓度,有效减少无机氮素径流流失风险.TN、NH_4~+-N、NO_3~--N径流流失量分别介于16.24~18.09、1.76~2.22、0.76~1.38 kg·hm~(-2).与单施控释肥相比,各处理TN、NH_4~+-N、NO_3~--N径流流失均有不同程度削减.生物炭配施控释肥和稳定性肥显著削减了氮素径流流失,有效降低区域稻田氮素面源污染风险.     

Effect of fertilization and irrigation schedule on water and fertilizer solute transport for wheat crop in a sub-humid sub-tropical region

In order to increase the water and fertilizer use efficiency and decrease the losses of water and fertilizer solutes (N and P), it is necessary to assess the influence of level of fertilization and irrigation schedule on movement and balance of water and fertilizers in the root zone. With this goal, the reported study was undertaken to determine the effect of fertilization and irrigation schedule on water movement and fertilizer solute transport in wheat crop field in a sub-tropical sub-humid region. Field experiments were conducted on wheat crop of cultivar Sonalika (Triticum aestivum L.) during the years 2002–2003, 2003–2004 and 2004–2005. Each experiment consisted of four fertilizer treatments and three irrigation treatments during the wheat growth period. During the experiment, the irrigation treatments were: I₁ = 10% maximum allowable depletion (MAD) of available soil water (ASW); I₂ = 40% MAD of ASW; I₃ = 60% MAD of ASW. The fertilizer treatments during the experiment were: F₁ = control treatment with N:P₂O₅:K₂O as 0:0:0 kg ha⁻¹; F₂ = fertilizer application of N:P₂O₅:K₂O as 80:40:40 kg ha⁻¹; F₃ = fertilizer application of N:P₂O₅:K₂O as 120:60:60 kg ha⁻¹ and F₄ = fertilizer application of N:P₂O₅:K₂O as 160:80:80 kg ha⁻¹. The results of the investigation revealed that low volume high frequency irrigation results in higher deep percolation losses than the low frequency high volume irrigation with different levels of fertilization for wheat crop in coarse lateritic soil, whereas different levels of fertilization did not significantly affect soil water balance of the wheat crop root zone during all the irrigation schedules. Level of fertilization and irrigation schedule had significant effect on nitrogen leaching loss whereas irrigation schedules had no significant effect on nitrogen uptake under different levels of fertilization. On the other hand, the leaching loss of phosphorus was not significantly influenced by the irrigation schedule and level of fertilization of wheat crop. This indicated that PO₄–P leaching loss was very low in the soil solution as compared to nitrogen due to fixation of phosphorus in soils. From the observed data of nitrogen and phosphorus use efficiency, it was revealed that irrigation schedule with 40% maximum allowable depletion of available soil water with F₂ fertilizer treatment (N:P₂O₅:K₂O as 80:40:40 kg ha⁻¹) was the threshold limit for wheat crop with respect to nitrogen and phosphorus use, crop yield and environmental pollution.     

Towards a better hydraulic cleaning strategy for ultrafiltration membrane fouling by humic acid: Effect of backwash water composition

As a routine measurement to alleviate membrane fouling, hydraulic cleaning is of great significance for the steady operation of ultrafiltration (UF) systems in water treatment processes. In this work, a comparative study was performed to investigate the effects of the composition of backwash water on the hydraulic cleaning performance of UF membranes fouled by humic acid (HA). Various types of backwash water, including UF permeate, Milli-Q water, NaCl solution, CaCl₂ solution and HA solution, were compared in terms of hydraulically irreversible fouling index, total surface tension and residual HA. The results indicated that Milli-Q water backwash was superior to UF permeate backwash in cleaning HA-fouled membranes, and the backwash water containing Na⁺ or HA outperformed Milli-Q water in alleviating HA fouling. On the contrary, the presence of Ca^2 + in backwash water significantly decreased the backwash efficiency. Moreover, Ca^2 + played an important role in foulant removal, and the residual HA content closely related to the residual Ca^2 + content. Mechanism analysis suggested that the backwash process may involve fouling layer swelling, ion exchange, electric double layer release and competitive complexation. Ion exchange and competitive complexation played significant roles in the efficient hydraulic cleaning associated with Na⁺ and HA, respectively.     

Reducing phosphorus in dairy diets improves farm nutrient balances and decreases the risk of nonpoint pollution of surface and ground waters

Reducing phosphorus (P) in dairy diets may result in different types of manure with different chemical composition. Application of these manures to soils may affect the soil P solubility and lead to different environmental consequences. A laboratory incubation study determined the impact of 40 dairy manures on P dynamics in two soil types, Mattapex silt loam (Aquic Hapludult) and Kalmia sandy loam (Typic Hapludult). The manures were fecal samples of lactating cows, collected from commercial dairy farms located in Northeastern and Mid-Atlantic United States, with a wide range of dietary P concentrations (from 2.9 to 5.8 g P kg⁻¹ feed dry matter, DM). Dried and ground fecal samples were mixed with surface horizon (0–15 cm) of soils at 150 kg P ha⁻¹ and the mixtures were incubated at 25 °C for 21 days. At the end of incubation, water soluble P (WS-P) and Mehlich-3 P (M3-P) in the soil–manure mixtures were substantially higher than the control (soil alone) but were lower than the soils receiving fertilizer KH₂PO₄ at 150 kg P ha⁻¹. Similarly, the relative extractability of P in soils amended with low- and high-P manures was always lower (<93%) than KH₂PO₄ suggesting that fertilizer P is more effective at increasing soil solution P in the short-term. Concentrations of WS-P or M3-P in soil–manure mixtures did not differ regardless of the source of manure (i.e. different farms and different diets). This suggests that when the same amount of P is added to soils through manure applications, the solubility or bioavailability of P in soils will be the same. However, P concentrations in feces correlate significantly with that in diets (r = 0.82^**); and when the manures were grouped into high-P diets (averaging 5.1 g P kg⁻¹) versus low-P diets (3.6 g P kg⁻¹), manure P was 40% greater in the high-P group (10.6 g kg⁻¹ DM) than the low-P group (7.6 g kg⁻¹ DM). Thus, lowering excess P in diets would reduce P excretion in manures, P accumulation in soils, improve P balance on farms, require less area for land disposal, and decrease potential for P loss to waters.     

施氮和水分管理对光合碳在土壤-水稻系统间分配的量化研究

施肥和水分管理是影响水稻生长的两个关键因素,探讨水肥耦合条件下光合碳在"水稻-土壤"系统输入与分配动态,对深入解析稻田土壤碳循环具有重要意义.本研究通过盆栽试验,选用籼性常规水稻品种(中早39),采用13C-CO_2连续标记技术,量化研究施氮和水分管理对光合碳在"水稻-土壤"系统中分配的影响.结果表明:施氮增加了水稻地上部干物质重和碳、氮含量,却显著降低了水稻根冠比;干湿交替使施氮条件下的水稻地上部全碳、全氮含量较持续淹水处理分别提高了22%和33%,根系中全碳、全氮含量分别提高了36%、44%,这表明施氮有利于水稻地上部生长,而干湿交替显著促进了水稻根系的生长.施氮显著增加水稻地上部13C含量,与不施氮处理相比增加了32%~83%;施氮使光合碳在水稻地上部的回收率增加6%~32%,在根系的回收率减少18%~59%.水分管理对13C分配的影响表现为:连续标记22 d后,在施氮条件下,干湿交替使水稻地上部、根系13C量均有一定量的增加;不施氮条件下,干湿交替与持续淹水处理相比,地上部13C量减少10.3mg·pot-1,回收率降低了11%~12%;根系13C量增加1.9 mg·pot-1,回收率提高了24%~57%.施氮和干湿交替都显著增加了13C在根际土壤中的累积与回收率.因此,施氮增加了光合碳在土壤-水稻系统中的累积,但降低了光合碳在根系中的分配,干湿交替比持续淹水更利于光合碳向土壤中的传输与累积,水肥耦合管理显著调控了光合碳的传输与分配.该研究进一步量化了水肥管理条件下水稻光合碳的分配及其在土壤有机碳库中的传输特征,为稻田水肥管理、水稻土有机质积累持续机制提供了理论依据和数据支撑.     

松花江水中天然有机物的提取分离与特性表征

将反渗透与XAD大孔树脂吸附技术相结合,对松花江水中天然有机物(NOM)进行了浓缩和分离,并采用紫外光谱、红外光谱、液相凝胶色谱、官能团滴定1、HNMR核磁共振等分析手段,对松花江水中NOM及其各分离组分和一种商用腐殖酸CHA的特性进行了比较和表征.结果表明,利用反渗透进行NOM浓缩对水中有机物具有很高的回收率;松花江水中NOM组成为:富里酸>腐殖酸>亲水部分;各组分芳香性为:腐殖酸>憎水部分>富里酸>亲水部分,E₄/E₆与芳香性之间缺乏必然的联系;腐殖酸和商用腐殖酸具有较高的不饱和性,NOM和亲水部分次之,憎水部分和富里酸中饱和烃含量较多;紫外吸收较弱的有机成分对NOM分子量的贡献较大;NOM及其分离组分的总酸度为9.84～12.15meq/g,羧酸含量为CHA>亲水>憎水>NOM>富里酸>腐殖酸;NOM及其各分离组分的溶解性有机物构成以脂肪烃为主.     

Preliminary investigation of phosphorus adsorption onto two types of iron oxide-organic matter complexes

Iron oxide(FeO)coated by natural organic matter(NOM)is ubiquitous.The associations of minerals with organic matter(OM)significantly changes their surface properties and reactivity,and thus affect the environmental fate of pollutants,including nutrients(e.g.,phosphorus(P)).In this study,ferrihydrite/goethite-humic acid(FH/GE–HA)complexes were prepared and their adsorption characteristics on P at various p H and ionic strength were investigated.The results indicated that the Fe O–OM complexes showed a decreased P adsorption capacity in comparison with bare Fe O.The maximum adsorption capacity(Q_(max))decreased in the order of FH(22.17 mg/g)FH-HA(5.43 mg/g)GE(4.67 mg/g)GE-HA(3.27 mg/g).After coating with HA,the amorphous FH–HA complex still showed higher P adsorption than the crystalline GE–HA complex.The decreased P adsorption observed might be attributed to changes of the Fe O surface charges caused by OM association.The dependence of P adsorption on the specific surface area of adsorbents suggests that the Fe O component in the complexes is still the main contributor for the adsorption surfaces.The P adsorptions on Fe O–HA complexes decreased with increasing initial p H or decreasing initial ionic strength.A strong dependence of P adsorption on ionic strength and p H may demonstrate that outer-sphere complexes between the OM component on the surface and P possibly coexist with inner-sphere surface complexes between the Fe O component and P.Therefore,previous over-emphasis on the contributions of original minerals to P immobilization possibly over-estimates the P loading capacity of soils,especially in humic-rich areas.     

Response surface method for modeling the removal of carbon dioxide from a simulated gas using water absorption enhanced with a liquid-film-forming device

This paper presents the results from using a physical absorption process to absorb gaseous CO_2mixed with N_2using water by producing tiny bubbles via a liquid-film-forming device(LFFD)that improves the solubility of CO_2in water.The influence of various parameters—pressure,initial CO_2concentration,gas-to-liquid ratios,and temperature—on the CO_2removal efficiency and its absorption rate in water were investigated and estimated thoroughly by statistical polynomial models obtained by the utilization of the response surface method(RSM)with a central composite design(CCD).Based on the analysis,a high efficiency of CO_2capture can be reached in conditions such as low pressure,high CO_2concentration at the inlet,low gas/liquid ratio,and low temperature.For instance,the highest removal efficiency in the RSM–CCD experimental matrix of nearly 80%occurred for run number 20,which was conducted at 0.30 MPa,CO_2concentration of 35%,gas/liquid ratio of 0.71,and temperature of 15°C.Furthermore,the coefficients of determination,R~2,were 0.996 for the removal rate and 0.982 for the absorption rate,implying that the predicted values computed by the constructed models correlate strongly and fit well with the experimental values.The results obtained provide essential information for implementing this method properly and effectively and contribute a promising approach to the problem of CO_2capture in air pollution treatment.     

九龙江河流-库区系统沉积物磷特征及其生态学意义

采用沉积物磷形态的标准测试方法 (SMT)分析了九龙江北溪河流-库区系统16个站位的沉积物磷含量和形态组成,探讨了该系统沉积物磷的空间分布、形态特征及其生态学意义.结果表明,沉积物总磷(TP)的含量为387～2 092 mg.kg-1,平均1 032 mg.kg-1.以无机磷(IP)为主要赋存形态,IP占TP的48%～98%,而IP中以铁铝结合态磷(Fe/Al-P)为主,占IP的43%～99%.TP和Fe/Al-P含量呈现上游高、下游低的空间分布规律,与表层水DTP含量和陆源污染负荷的分布一致.北溪沉积物TP含量的高低主要受Fe/Al-P控制.沉积物富磷、高Fe/Al-P比例(释放潜力大)以及"上游高下游低"的空间分布特征,加上九龙江上游水体较低的氮磷比值属于藻类生长磷弱限制,极可能是九龙江水华首先在上游暴发并向下游库区蔓延的主要原因.九龙江沉积物磷的这些特征在水华过程中具有重要的调控作用和生态学意义.     

负载磁性废茶生物炭活化过一硫酸盐高效降解水中腐殖酸和富里酸

城市污水厂二级处理出水中含有大量的溶解性有机物（Dissolved organic matters,DOM）会对生物和受纳水体构成潜在的危害,因此有必要对二级处理出水进行深度处理.本研究以农业废弃物茶叶渣为原料,通过对废弃茶叶改性和负磁制备一种磁性废茶生物炭（Fe-tea biochar,Fe-TB）,用于活化过一硫酸盐（Peroxymonosulfate,PMS）氧化降解水中的腐殖酸（Humic acid,HA）和富里酸（Fulvic acid,FA）.考察Fe-TB铁负载量、PMS浓度、Fe-TB投加量、初始pH、HA和FA的初始浓度对Fe-TB/PMS体系氧化降解HA和FA的影响.结果表明,在铁碳比为2/1（W/W）、PMS=0.2 g·L^-1,2Fe-TB投加量分别为0.6 g·L^-1（HA体系）和0.4 g·L^-1（FA体系）、初始pH=7条件下,50 min时对初始浓度为20 mg·L^-1的HA和FA的去除率分别达到95.3%和77.4%;经过4次重复循环使用,HA和FA的去除率均在59.0%以上,表明其良好的稳定性和重复使用性.淬灭实验及电子顺磁共振（EPR）分析结果证明2Fe-TB/PMS体系以单线态氧（¹O₂）为主要氧化活性物种降解HA和FA.实际二级处理出水中的DOM降解结果表明,2Fe-TB /PMS体系可以有效降解实际水体中的DOM,具有良好的应用前景.     

Investigation of potential interferences on the measurement of dissolved reactive phosphate using zirconium oxide-based DGT technique

A diffusive gradients in thin films (DGT) technique based on hydrous zirconium oxide (Zr-oxide) has been recently developed for the measurement of dissolved reactive phosphate (DRP). In this study, the detailed performance of the DGT technique is reported. Spiking experiments revealed that several orthophosphate monoester compounds contributed to the Zr-oxide DGT measurements of DRP. However, such a phenomenon is unlikely to occur during field conditions due to the low concentration of organic P in typical natural waters. The presence of Cl- (up to 106 g/L), SO42- (up to 16 g/L), HCO3- (up to 817 g/L), and AsO2- and AsO 3 4 (both up to 1 mg As/L) in solutions had negligible effects on the measurement of DRP. The threshold concentrations of Cl-, SO42- and HCO3- have been increased from previous reports for the measurements of DRP using other adsorbent-based DGT techniques. The capacity for DGT measurements of DRP decreased with increasing solution pH (4.2-9.2). The lowest capacity (95 μg P/m2 at pH 9.2) was still greater than that of other DGT techniques that are usually used for the measurement of DRP (2-12 μg P/cm2 ). The Zr-oxide binding gel could be stored for up to 2 years without any aging effect. This period of validity was considerably longer than the ferrihydrite binding gel that is commonly used in present DGT devices (6 months). The field application revealed that the concentrations of DRP measured in three fresh water samples using the Zr-oxide DGT technique were in agreement with those of the traditional colorimetric method.     

应用大型原状土柱渗漏计测定冬小麦-夏玉米轮作期硝态氮淋失

从 1998— 2 0 0 0年 ,利用土壤溶液提取器和大型原状土柱渗漏装置 (面积 0 18m2 ,2m深 )田间观测了北京地区冬小麦 夏玉米轮作期间的NO-3 N淋失 .设置对照和常量氮肥水平两个处理 .土柱渗出液的NO-3 N平均浓度 ,对照处理为 35 0mg L ,常量施氮土柱为 5 5 6mg L ;NO-3 N淋失通量 ,对照处理为 1 3g (m2 ·a) ,常量施氮土柱为 2 0g (m2 ·a) ;氮肥表观淋失百分数分别为 10 %、0 86 %和 0 5 4%,受年降雨变化的影响非常明显 .常量氮肥施用条件下 0— 2 0 0cm土壤提取液和土柱底部渗出液的NO-3 N浓度 ,都超过饮用水卫生标准 10mg L ,因此 ,常量施氮水平引起的硝态氮对浅层地下水的污染不容忽视 .     

羟胺强化亚铁活化过硫酸盐降解对乙酰氨基酚的研究

采用羟胺(HA)强化Fe~(2+)/过硫酸盐(PS)体系降解对乙酰氨基酚(ACT),考察了Fe~(2+)、PS、HA投加浓度以及反应初始pH值对ACT降解效果的影响.结果表明,在反应时间为30 min,亚铁浓度为0.05 mmol·L~(-1), PS浓度为0.8 mmol·L~(-1)和初始pH为3.0的条件下,0.5 mmol·L~(-1) HA可将ACT的去除率从13%提高到90%.适量增加Fe~(2+)或HA浓度可以提高ACT的降解率,但是过高的Fe~(2+)和HA浓度会抑制ACT的降解.ACT的降解率随着PS浓度升高而提升,当PS浓度达到1.2 mmol·L~(-1)时,30 min内ACT几乎可以完全降解.ACT的降解效果随着pH的升高而降低.EPR实验表明Fe~(2+)/PS/HA体系中主要的自由基是SO■和HO~·.Na_2SO_3、NaNO_2和Na_2S_2O_3等常见的还原剂均能够强化Fe~(2+)/PS体系对ACT的降解效果,但是其对Fe~(2+)/PS体系的强化效果均比HA低.     

东莞石马河流域水化学特征时空差异及来源辨析

石马河流域对东江饮用水源地城镇供水具有重要战略意义.为研究石马河水化学特征,分别于2012年2月、6月和11月采集石马河河水水样共39个,分析测定了水体主离子(K+、Na+、Ca2+、Mg2+、Cl-、SO2-4和HCO-3)及营养盐(PO3-4、NO-3和NH+4)浓度,探讨了水化学组成的时空差异、控制因素并对其来源进行了初步辨析.结果表明,水化学组成的时空差异显著,不同时期的河水TDS及营养盐平均浓度排序为11月2月6月;河水阴离子以HCO-3为主,2月和11月时,河水阳离子以Na++K+为主,为HCO-3-Na+水,6月时则以Ca2+为主,为HCO-3-Ca2+水;营养盐浓度在空间上的差异主要受人类活动导致N、P废水排放影响,3个时期的石马河出水口处(R7)N∶P为18.4,有利于浮游植物的生长,河道出现了富营养化的现象;Gibbs图显示,2月和11月的河水主离子受蒸发岩溶解的影响较为显著,而蒸发岩和碳酸盐岩风化共同控制6月的水化学组分;海盐沉降对石马河河水物质的贡献率较小;部分Na+、Mg2+、Cl-和SO2-4来自化肥的施用和工业废水的排放;NH+4-N、PO3-4-P和NO-3-N主要分别来源于家禽养殖废水和生活废水.     

三峡库区汉丰湖水体氮磷及化学计量比季节变化特征

在分析2017年3月至2018年2月汉丰湖水体氮磷营养盐质量浓度季节性变化的基础上,利用氮磷化学计量摩尔比评估水体氮磷养分限制状态.结果表明：湖体TN、DN和NO₃^--N平均质量浓度分别为1.60、1.25和0.91 mg·L^-1,三者季节变化过程相似,均呈现出冬季最高、夏季最低的特点.NO₃^--N对水体TN贡献较大,NH₄⁺-N和NO₂^--N质量浓度维持在较低水平且变化平稳.TP、DP和PO₄^3--P平均质量浓度分别为0.13、0.09和0.06 mg·L^-1,TP和DP质量浓度变化相似,呈春夏季升高,秋冬季先降低再升高的趋势,而PO₄^3--P质量浓度则波动降低.TN/TP范围在11.07~56.02之间,均值为29.23,TN/TP呈季节性波动变化,最高值出现在冬季,最低值出现在夏季.汉丰湖水体多数时间适宜藻类生长繁殖,少数时间处于N限制状态,极少数时间处于P限制状态.降雨径流、肥料使用、污水排放和水生生物活动等因素皆会影响TN/TP的季节变化,同时根据汉丰湖水质特征提出保护建议.