改变垫水层沸点的薄层扬沸实验研究

扬沸是油池火灾的一种特殊现象,燃料和垫水层交界面的过热温度和沸腾状态是决定扬沸是否发生以及发生时间的最主要因素,过热温度由沸点决定。在垫水层中添加氯化钠能够改变垫水层的沸点,从而改变交界面的过热温度。在垫水层添加氯化钠使其成为饱和氯化钠水溶液,对此条件下的油池火燃烧进行实验探究,以验证前人关于扬沸临界条件的研究结果,并为扬沸防治提供思路。垫水层改变为饱和氯化钠溶液后,柴油实验组均没有发生扬沸,且观察到火焰温度和热辐射强度的下降。表明此方法可以有效抑制扬沸的发生。     

Biosorption of cesium（Ⅰ） from aqueous solution by a novel exopolymers secreted from Pseudomonas fluorescens C-2： Equilibrium and kinetic studies

The biosorption characteristics of Cs(I) ions from aqueous solution using exopolymers (PFC02) produced from Pseudomonas fluorescens C-2 were investigated as a function of pH, biosorbent dosage, contact time and initial concentration. pH played a major role in the adsorption process, and the optimum pH for the removal of Cs(I) was 8.0. Langmuir, Freundlich and Dubinin-Radushkevich (D-R) models were applied to describe the biosorption isotherm of the Cs(I) ions by PFC02. The Lagergren first-order, pseudo second-order kinetic and intraparticle diffusion models were used to test the kinetic data. Langmuir model and D-R model fitted the equilibrium data better than the Freundlich isotherm. The monolayer adsorption capacities of PFC02 as obtained from Langmuir isotherm at 25°C was found to be 32.63 mg/g. From the D-R isotherm model, the mean free energy was calculated as 26.73 kJ/mol, indicating that the biosorption of cesium was chemisorption. The biosorption process was rapid, and the kinetic rates were best fitted to the pseudo second-order model, which indicated the biosorption process operated through chemisorption mechanism. FT-IR analysis of PFC02 showed the possible functional groups responsible for cesium adsorption were hydroxyl, carboxyl, carbonyl and sulphonate groups. SEM analysis showed the porous structure of the material while EDX analysis confirmed the adsorption of Cs(I) on PFC02. Cesium adsorbed onto the PFC02 could be desorbed efficiently using 1 mol/L HNO3, and the enrichment factor was 50.0. Furthermore, PFC02 could be reused five times with only about 8.25% regeneration loss. The developed method was successfully utilized for the removal of Cs(I) ions from aqueous solution.     

Material conversion from paper sludge ash in NaOH solution to synthesize adsorbent for removal of Pb^2＋, NH^4＋ and PO4^3- from aqueous solution

Material conversion from paper sludge ash (PSA) in NaOH solution was attempted to synthesize the adsorbent for removal of inorganic pollutants, such as Pb2+, NH4 + and PO4 3?? from aqueous solution. PSA of 0.5 g was added into 10 mL of 3 mol/L NaOH solution, and then heated at 80, 120, and 160°C for 6–48 hr to obtain the product. PSA mainly composed of two crystalline phases, gehlenite (Ca2Al2SiO7) and anorthite (CaAl2Si2O8), and amorphous phase. Hydroxysodalite (Na6Al6Si6O24 8H2O) was formed at 80°C, and anorthite dissolved, whereas gehlenite remained una ected. Katoite (Ca3Al2SiO4(OH)8) was formed over 120°C, and hydroxycancrinite (Na8(OH)2Al6Si6O24 2H2O) was formed at 160°C, due to the dissolution of both gehlenite and anorthite. Specific surface areas of the products were almost same and were higher than that of raw ash. Cation exchange capacities (CECs) of the products were also higher than that of raw ash, and CEC obtained at lower temperature was higher. Removal abilities of products for Pb2+, NH4 +, and PO4 3?? were higher than that of raw ash.With increasing reaction temperature, the removal e ciencies of Pb2+ and NH4 + decreased due to the decrease of CEC of the product, while removal e ciency for PO4 3?? was almost same. The concentrations of Si and Al in the solution and the crystalline phases in the solid during the reaction explain the formation of the product phases at each temperature.     

Experimental studies on ozonation of ethylenethiourea

The experimental study on ozonation of ethylenethiourea(ETU) is conducted.The reaction of gas-phase ETU with 0.63 × 10-6 mol/L ozone is carried out in a 200-L reaction chamber.The secondary organic aerosol(SOA) resulted from the ozonation of gas-phase ETU is observed with a scanning mobility particle size(SMPS).The rapid exponential growth of SOA reveals that the atmospheric lifetime of ETU vapor towards ozone reaction is less than four days.The ozonation of dry ETU particles,ETU-contained water droplets an...     

A kinetic model of Ti（IV）-catalyzed H2O2/O3 process in aqueous solution

A kinetic model for the Ti(IV)-catalyzed H₂O₂/O₃ process was established, and the experimental results demonstrated that the model could well describe this ozone-based oxidative system mathematically and chemically.     

Benzene removal by nano magnetic particles under continuous condition from aqueous solutions

Benzene removal evaluated using Fe304 nano continuous condition. A 44 initial benzene concentration, from aqueous solutions was magnetic particles （NM） in factorial design including NM dose, contact time and pH was investigated in 16 experiments （Taguchi OA design）. The results indicated that all factors were significant and the optimum condition was： pH 8, NM dose of 2000 mg.L-1, benzene concentrations of 100 mg.L-1 and contact time of 14min. The maximum benzene uptake and distribution ratio in the optimum situation were 49.4mg.g-1 and 38.4L.g-1, respectively. The nano particles were shown to capture 98.7% of the benzene in optimum batch condition and 94.5% in continuous condition. The isotherm data proved that the Bmnauer-Emmett-Teller model fit more closely and produced an isotherm constant （b） less than one, indicating favorable adsorption. Regeneration studies verified that the benzene adsorbed by the NM could be easily desorbed by temperature, and thereby, NM can be employed repeatedly in water and wastewater management.     

Oxidative treatment of aqueous monochlorobenzene with thermally-activated persulfate

The oxidation of aqueous monochlorobenzene （MCB） solutions using thermally- activated persulfate has been investigated. The influence of reaction temperature on the kinetics of MCB oxidation was examined, and the Arrenhius Equation rate constants at 20℃, 30℃, 40℃, 50℃, and 60℃ for MCB oxidation performance were calculated as 0, 0.001, 0.002, 0.015, 0.057 min-1, which indicates that elevated temperature accelerated the rate. The most efficient molar ratio ofpersulfate/MCB for MCB oxidation was determined to be 200 to 1 and an increase in the rate constants suggests that the oxidation process proceeded more rapidly with increasing persulfate/MCB molar ratios. In addition, the reactivity of persulfate in contaminated water is partly influenced by the presence of background ions such as CI-, HCO3, SO2 , and NO3. Importantly, a scavenging effect in rate constant was observed for both C1 and CO2- but not for other ions. The effective thermally activated persulfate oxidation of MCB in groundwater from a real contaminated site was achieved using both elevated reaction temperature and increased persulfate/MCB molar ratio.     

根系分泌物对五氯酚的增溶作用和影响机制

采用室内模拟培养方法研究了植物根系分泌物对五氯酚(PCP)溶解性的影响及其反应机制,结果表明,根系分泌物属于表面活性物质,提高了PCP溶解性,增加了PCP的表观溶解度,而且其对PCP增溶作用与根系分泌物浓度呈线性正相关,向日葵根系分泌物中大分子组分含量比紫花苜蓿的高,其对PCP的增溶效果比紫花苜蓿的大,根系分泌物降低了PCP的正辛醇/水溶液分配系数,且各体系中IgKow分配系数的大小顺序与增溶作用大小顺序正好相反,产生上述结果是因为根系分泌物中的大分子组分能够形成疏水微区,促进PCP的分配作用,提高PcP的溶解性,而且根系分泌物中大分子组分愈多,其对PCP增溶作用愈强.     

氯离子浓度对硝酸基复合肥水溶液热安全性影响研究

为了研究复合肥洗涤液中氯离子浓度对硝酸基复合肥水溶液热稳定性影响,利用自行研制的临界爆炸测试装置对硝酸基复合肥水溶液的热安全性进行测试。结果表明,不同浓度氯离子对硝酸基复合肥水溶液临界爆炸温度影响较大,复合肥水溶液的分解温度随着氯离子浓度的增大呈先降低后升高的趋势。研究结果对硝酸基复合肥的安全生产具有指导意义。     

含盐水中苯并[a]芘在模拟太阳光下的降解

主要研究了在模拟太阳光照射下,含盐水溶液中苯并[a]芘(BaP)的光降解,讨论了氯离子浓度、pH值、苯并[a]芘浓度、腐殖酸、助溶剂、电子供体、固体颗粒物等对苯并[a]芘光降解的影响.这些影响因素从不同的路径促进或抑制苯并[a]芘的光降解,得出了光照条件下BaP可能的转化路径.同时通过进行GC-MS检测确定了苯并[a]芘光降解后有6-氯代苯并[a]芘和苯并[a]芘二酮物质生成.