A study on oxidative degradation of polyacrylamide in wastewater with UV/FENTON/C4H4O62−

The degradation of polyacrylamide (PAM) in simulate wastewater was studied in UV/Fenton/C₄H₄O₆^2? system. The factors such as molecular ratio of H₂O₂/Fe²⁺/C₄H₄O₆^2?, pH, and the dosage of Fenton reagent that could affect the PAM degradation in the UV/Fenton/C₄H₄O₆^2? system were investigated. The experimental results showed that adding C₄H₄O₆^2? to UV/Fenton system could form photosensitive ferrous complexes, which led to higher degradation efficiency of PAM. The degradation rate of PAM could be up to 95.2% under the following conditions: the concentration of H₂O₂, Fe²⁺, and C₄H₄O₆^2? were 22.5, 2.25, and 2.25 mmol/L, respectively (i.e., molecular ratio of H₂O₂/Fe²⁺/C₄H₄O₆^2? was 10:1:1), the pH value was 3.0.     

Petrophysical analysis to investigate the effects of carbon dioxide storage in a subsurface saline aquifer at Ketzin, Germany (CO2SINK)

To test the injection behaviour of CO₂ into brine-saturated rock and to evaluate the dependence of geophysical properties on CO₂ injection, flow and exposure experiments with brine and CO₂ were performed on sandstone samples of the Stuttgart Formation representing potential reservoir rocks for CO₂ storage. The sandstone samples studied are generally fine-grained with porosities between 17 and 32% and permeabilities between 1 and 100 mD.Additional batch experiments were performed to predict the long-term behaviour of geological CO₂ storage. Reservoir rock samples were exposed over a period of several months to CO₂-saturated reservoir fluid in high-pressure vessels under in situ temperature and pressure conditions. Petrophysical parameters, porosity and the pore radius distribution were investigated before and after the experiments by NMR (Nuclear Magnetic Resonance) relaxation and mercury injection. Most of the NMR measurements of the tested samples showed a slight increase of porosity and a higher proportion of large pores.     

Photocatalytic remediation of γ-hexachlorocyclohexane contaminated soils using TiO2 and montmorillonite composite photocatalyst

TiO2 and montmorillonite composite photocatalysts were prepared and applied in degrading γ-hexachlorocyclohexane(γ-HCH)in soils.After being spiked with γ-HCH,soil samples loaded with the composite photocatalysts were exposed to UV-light irradiation.The results indicated that the photocatalytic activities of the composite photocatalysts varied with the content of TiO2 in the order of 10%＜70%＜50%＜30%.Moreover,the photocatalytic activity of the composite photocatalysts with TiO2 content 30% was higher than that of the pure P25 with the same mass of TiO2.The strong adsorption capacity of the composite photocatalysts and quantum size effect may contribute to its increased photocatalytic activities.In addition,effect of dosage of composite photocatalysts and soil pH on γ-HCH photodegradation was investigated. Pentachlorocyclohexene,trichlorocyclohexene,and dichlorobenzene were detected as photodegradation intermediates,which were gradually degraded with tlle phOtOdegradation evolution.     

高原生境不同水力停留时间下A2/O工艺活性污泥微生物代谢机制研究

在高原生境下构建不同水力停留时间(HRT)运行工况的A²/O系统,结合水质分析及对好氧池活性污泥的16S rRNA基因测序,对微生物优势菌属功能和代谢途径进行研究。结果表明:高原生境下HRT为26.25 h时A²/O工艺处理效果总体最好,微生物优势菌属代谢功能以有机物降解、反硝化脱氮和聚磷菌除磷为主,代谢途径以碳氮磷代谢为主;在高原生境下,应对外界环境变化的细菌双组分调节功能(ko02020)丰度较大,该代谢途径在适应环境变化中有显著作用,是高原生境下的优势代谢途径;微生物细胞中rpoE基因丰度偏大,为微生物适应高原环境提供了保障。HRT为26.25 h时微生物功能基因总丰度最大,可见26.25 h是高原生境下A²/O工艺最佳HRT运行工况。     

上海地区二氧化硫浓度和风速的统计关系

应用上海市1986年6月至1987年5月间5个自动监测站的全年每日逐时SO_2浓度平均值和同步的风速平均值资料,按季进行比较、归纳,得到风速—SO_2浓度的诊断判据,并利用1984年全年的相应资料进行验证,准确率达85％;得到了各季浓度—风速的回归方程,和浓度—风速、温差的二元回归方程、复相关系数。     

外源水杨酸对梨叶片感染轮纹病菌后抗氧化酶活性及Ca2+浓度的影响

为了解水杨酸(Salicylic acid,SA)缓解轮纹病菌伤害植物的机理,用0.3 mmol L-1的SA预先处理梨叶片,3 d后接种轮纹病菌(Physalospora Piricola Nose),接种4 d后开始测定各种指标,随后每隔3 d测定1次,共5次.结果表明,经0.3 mmol L-1 SA处理后,梨叶片的超氧化物歧化酶(SOD)、过氧化物酶(POD)、过氧化氢酶(CAT)、抗坏血酸过氧化物酶(APX)、愈创木酚过氧化物酶(GPX)和谷胱甘肽还原酶(GR)的活性分别比对照组(CK1)提高了30.65%、25.36%、28.55%、21.11%、35.67%和26.45%.电镜观察表明,感染轮纹病菌的梨叶片,Ca2+较多分布在细胞膜内侧、细胞质及一些细胞器(叶绿体)上.经SA处理后感染轮纹病菌的梨病叶,Ca2+较多分布在细胞壁外侧及细胞间隙中,与正常梨叶片Ca2+的分布情况相似.表明较低浓度的SA可缓解轮纹病菌对梨叶片的伤害作用.     

H_2O_2致大鼠RTE细胞系氧化应激作用及GSH保护作用的体外研究

许多具有氧化作用的空气污染物,均能使细胞产生氧化损伤,使胸腺基质淋巴生成素(thymic stromal lymphopoietin,TSLP)含量上升。而TSLP是一种启动过敏性炎症的重要因子,会导致哮喘等疾病发生率的上升。在本研究中用过氧化氢(H_2O_2)模拟具有氧化作用的空气污染物进行染毒,研究细胞氧化应激水平的变化,并讨论还原型谷胱甘肽(GSH)对细胞受氧化损伤的保护作用。将大鼠支气管上皮细胞(RTE)分组培养,每组设置6个平行实验,分别用低、中、高剂量H_2O_2染毒3 h;高剂量设置1个重复,作为保护组,在染毒前用GSH保护2 h。结果显示,高剂量组H_2O_2(3.2 mmol·L~(~(-1)))染毒的细胞,其细胞活力下降(P0.01),丙二醛(MDA)水平上升(P0.01),TSLP水平上升(P0.05),与之相比,用GSH保护后的同剂量染毒组,上述指标得到全面缓解(P0.01)。这表明高浓度的H_2O_2会损伤细胞活力,并使MDA及TSLP水平上升,而GSH对TSLP及MDA的升高有极显著的抑制作用,即对细胞有一定的保护作用。     

利用废旧锌锰电池制备光催化剂净化甲苯

针对废旧锌锰电池回收利用难,以及光催化剂 TiO2活性低的问题,以废旧锌锰电池和商业二氧化钛为原料,通过球磨法制备了新型复合光催化剂.在紫外光灯照射下,进行了废旧锌锰电池复合改性TiO2对甲苯的光催化氧化实验,并重点探究空速、光照强度、相对湿度和氧气体积分数等关键实验条件对甲苯净化效率的影响.结果表明,改性后的催化剂对...     

普光天然气净化厂投料试车H2S泄漏安全管理

普光气田天然气净化厂是中国石化集团公司"川气东送工程"的关键组成部分,在投料试车期间,富含高浓度H2S的原料气决定了净化过程中的泄漏中毒高风险,尤其在投料试车过程中,实时监测现场H2S气体浓度是试车安全管理的关键。介绍了天然气净化厂净化工艺,分析了试车安全风险;利用安全监测系统、GasFindIR红外成像仪、有毒挥发气体分析仪等先进仪器设备建立了实时安全管理监测方法,实时监测现场H2S气体浓度。结果表明,该方法在天然气净化厂投料试车阶段发现H2S气体泄漏及时,泄漏点定位准确,泄漏量检测精确,保证了普光气田天然气净化厂投料试车作业安全的顺利进行,为高含H2S气田投料试车作业的安全管理提供了参考。     

Experimental and theoretical research on the inhibition performance of ethanol gasoline/air explosion by C6F12O

The safety issue of ethanol gasoline and the methods to control or weaken its explosion have attracted attention. To clarify the effect of C₆F₁₂O (perfluoro(2-methyl-3-pentanone)) on the explosion of ethanol gasoline-air mixtures and intrinsic mechanism, the explosion overpressure and flame propagation behavior under different equivalence ratios (φ = 0.6–0.8) and C₆F₁₂O concentrations (χ_inh = 0–4.0%) were experimentally obtained. The detailed inhibitor reaction process was also obtained by CHEMKIN based on a new assembly kinetic mechanism. The results show that the effects of C₆F₁₂O on the explosion characteristics of ethanol gasoline varied with χ_inh and φ. For rich flames, C₆F₁₂O is more effective than and heptafluoropropane (C₃HF₇) and nitrogen (N₂) in suppressing explosions; for lean and equivalence ratio flames, the addition of C₆F₁₂O may result in more severe explosions. The decrease in chemical reactivity is mainly because the mole fractions of OH and H radicals and the proportion of paths H radicals involved decrease after adding C₆F₁₂O, and R1500: CF₃COF + H = CF₃CO + HF, R965: CF₂:O + H = CF:O + HF, R863: CF₃ + H = CF₂ + HF are main suppressing reactions.