RGO/TiO2光催化降解2,4-二氯苯氧乙酸研究

通过Hummers法及紫外光/热还原工艺制得还原氧化石墨烯(RGO),采用溶胶-凝胶-煅烧法,以RGO和钛酸酊脂为前驱体制备出RGO/TiO2光催化复合材料,并利用XRD、FT-IR等对其进行了表征.对RGO/TiO2光催化降解性能的研究发现,复合光催化剂RGO/TiO2对2,4-二氯苯氧乙酸(2,4-D)的光催化降解活性显著优于纯TiO2,并且发现负载量和pH值对光催化降解性能有较大的影响:RGO/TiO2投加量为1.2g·L~(-1)、RGO负载量2%、pH为3、初始浓度为50 mg·L~(-1)反应12 h,2,4-D去除率达到98.75%;2,4-D降解率随着RGO/TiO2投加量的增大先增大后减小;RGO/TiO2对2,4-D的降解为脱氯还原和催化氧化过程,产生氯酚、苯酚等中间产物.     

优化热脱附技术对十溴联苯醚污染土壤的适用性及修复效果

为了探索绿色、高效、环保的修复PBDEs污染土壤的技术,在热脱附技术基础上将木炭同时作为尾气吸附剂和燃烧热源,处理不同十溴联苯醚污染水平的PBDEs(多溴联苯醚)污染土壤,通过14种不同溴代PBDEs同系物分析十溴联苯醚的降解产物组分并计算其去除率. 结果表明:在热脱附技术处理后,十溴联苯醚初始污染水平分别为500、800和1 000 μg/kg,污染土壤中PBDEs的去除率分别为63%、81%、94%. 14种不同溴代PBDEs同系物在热脱附反应后的残留产物中均有检出,其中热脱附处理后的土壤中以三溴和四溴PBDEs产物占优势,而尾气中则以四溴和五溴PBDEs产物为主. 根据热脱附试验前后土壤中PBDEs的结构组成对比及分析可知,降解和脱溴反应在整个热脱附反应过程中发挥了重要作用. 另外,XAD树脂吸附柱中虽有少量的氯代和溴代二英类物质(PCDD/Fs和PBDD/Fs)被检出,但其毒性当量浓度均小于0.1 ng/m3,符合欧盟、日本及我国所规定的二英物质排放标准. 研究显示,在利用优化的热脱附技术修复十溴联苯醚污染土壤过程中,PBDEs的去除率与污染土壤中其污染水平相关,并且热脱附过程以降解及逐级脱溴反应为主.      

LRM 模块载荷分解方法研究

目的根据综合模块化航空电子设备的特点,研究LRM模块的载荷分解方法。方法通过仿真和试验方法,对LRM模块所承受的温度和振动载荷进行分解,并详细论述两种方法的具体实现过程。结果将模块载荷分解方法成功运用于某工程系统中,验证了方法的有效性。结论 LRM模块的载荷分解方法能够指导其他类似综合模块化航空电子设备的载荷分解,推动LRM模块合理的独立环境试验及交付。     

光催化氧化技术降解水中双酚A的研究进展

目前环境雌激素双酚A(bisphenol A,BPA)所带来的危害已成为学术研究的热点问题。光催化氧化技术作为新兴的高级氧化技术,可快速降解水中双酚A。介绍了几种主要的光催化氧化技术降解双酚A的机理,并综述了国内外利用新型光催化剂在降解双酚A领域所取得的研究进展,为光催化氧化技术在双酚A降解领域的研究提供参考。     

等离子体分解SO2实验

介绍了在低温常压条件下,应用等离子体分解有害气体ＳＯ２的实验结果,通过实验总结出ＳＯ２浓度,气体流量以及烟气温度ＳＯ２分解率的影响规律,比较了脉冲叠加正、负直流电压产生的等离子体分解ＳＯ２的能耗和分解量。实验结果表明,该项技术耗能低,ＳＯ２分解率高。每消耗１ｋＷ·ｈ电能可分解１．６１－１．９７ｋｇＳＯ２气体,分解率达８０％以上。     

基于双向门控循环单元的地表水氨氮预测

为提高水环境中NH4+-N的预测精度,提出了一种互补完全集合经验模式分解(CCEEMDAN)和双向门控循环单元(BiGRU)神经网络的混合预测模型(CCB).首先,通过CCEEMDAN将NH4+-N数据分解成一系列较为简单的模态成份;然后利用BiGRU神经网络对各成份进行预测,将所有分解成份的预测结果相加即可获得最终预...     

Organic residue decomposition: The minicontainer-system a multifunctional tool in decomposition studies

The Minicontainer-test, first described by Eisenbeis (1993), was designed to study the kinetics of organic residue decomposition at a microsite level. It is derived from the litterbag technique and consists of polyethylene minicontainers (volume about 1.5 cm³) filled with a test substrate (litter, straw, cellulose, etc.). The minicontainers (MCs) are closed at either end with plastic gauze discs of variable mesh size (e.g. 20 μm, 250 μm, 500 μm or 2 mm). A definite number of such units are inserted into PVC-bars, which can be implanted into the soil horizontally or vertically, or be exposed on the soil surface horizontally. The bars are very stable and can be exposed in different environments for months to years. If required, the bars can be removed temporarily and stored, e.g. during soil cultivation. Should fresh litter be used, two phases of decomposition can be distinguished: a fast initial phase, which can be mainly related to the effect of leaching, and a second slow phase depending mainly on the activity of soil organisms and litter quality. Several questions can be addressed to investigations using MCs, e.g. 1) parts of the soil fauna which are involved in decomposition (nematodes, microarthropods, and smaller specimens of the macrofauna, e.g. enchytraeidae, diplopods and dipteran larvae) can be extracted from the litter substrate using a miniscale high gradient extractor, 2) the organic mass loss of litter can be determined, 3) microbial biomass (C_mic, N_mic) can be assessed by fumigation extraction and 4) microbial activity (respiration) in the test substrate can also be assessed by use of standardised methods. Compared to litterbag studies, the larger number of small replicate units improves the statistical evaluation. Until today the Minicontainer-test has been applied in forestry and agriculture, e.g. studying the effects of liming, soil restoration and the application of insecticides, e.g. Diflubenzuron (Dimilin) and Btk (Bacillus thuringiensis var.kurstaki).     

混合堆肥过程中挥发性固体含量的层次效应及动态变化

城市污泥与猪粪混合堆肥表明:升温期和高温期堆体上部有机物降解的差异较大,降温期堆体下部各层有机物降解的差异较大,且堆体内挥发性固体(VS)含量已形成明显的层次效应,腐熟期堆体中部有机物降解的差异较大,堆体内VS含量的层次效应仍很明显;不同堆肥期堆体内VS含量的差异由大到小分别为:降温期≥腐熟期>高温期>升温期,不同部位有机物降解程度由大到小为:上部>中部>下部;VS含量随时间的变化满足一级反应动力学方程,城市污泥和猪粪混合堆肥过程中VS的降解速率约为0.3kg·d^-1,VS含量降低了8.2%.     

三氧化钨光催化法脱色处理化纤厂废水

以WO3粉体作为催化剂对化纤厂废水采用光催化氧化法进行脱色处理,讨论了光催化氧化法的反应机理,以及化纤厂废水的pH值、光催化剂的投入量、光照时间各因素对废水色度去除率的影响。实验结果表明：WO3粉体的投入量为1．000g／L,pH值为3．00时,利用300W高压汞灯光照7h后,废水试样的吸光度由0.596降低至0．020,色度去除率达到96．6％。     

Photocatalytic remediation of γ-HCH contaminated soil induced by α-Fe2O3 and TiO2

Heterogeneous photocatalytic degradation of γ-HCH on soil surfaces was carried out to evaluate the photocatalytic effectiveness of α-Fe2O3 and TiO2 toward degrading γ-HCH on soil surfaces. After being spiked with γ-HCH, soil samples were loaded with α-Fe2O3 or TiO2 and exposed to UV-light irradiation. Different catalyst loads(0%, 2%, 5%, 7%, and 10% (wt). α-Fe2O3; 0%, 0.5%, 1%, 2% wt. TiO2) were tested for up to 7 d irradiation. The effects of soil thickness, acidity, and humic substances were also investigated. The obtained results indicated that the γ-HCH photodegradation follows the pseudo-first-order kinetics. The addition of α-Fe2O3 or TiO2 accelerates the photodegradation of γ-HCH, while the photodegradation rate decreases when the content of α-Fe2O3 exceeds 7%(wt.). The degradation rate increases with the soil pH value. Humic substances inhibit the photocatalytic degradation of γ-HCH. Pentachlorocyclohexene, tetrachlorocyclohexene, and trichlorobenzene are detected as photodegradation intermediates, which are gradually degraded with the photodegradation evolution.