低温环境汽油机颗粒捕集器再生间隔里程评估方法

对汽油机颗粒捕集器（gasoline particulate filter,GPF）碳载量估算的温度修正方法,以及低温环境下的GPF再生间隔里程进行研究。利用发动机台架试验测量了GPF颗粒物再生反应速率,通过对数作图法拟合反应速率得到再生反应活化能,氧和颗粒物的反应活化能为81.6~91.4 kJ/mol,二氧化碳和颗粒物的反应活化能为159.2~218.9 kJ/mol。基于反应活化能计算了不同环境温度下颗粒物再生反应速率的修正系数;测量试验车低温冷启动阶段颗粒物累积速度,计算颗粒物排放的温度修正系数。以轻型车排放国六标准I型试验为基础,利用颗粒物再生反应速率和排放的温度修正系数对低温环境下GPF主动再生间隔里程进行了仿真。与寒区道路试验中获得的实际GPF颗粒物累积数据对比,仿真结果能较为准确地预测GPF在寒区不同工况下的颗粒物累积速度。试验和仿真结果均显示车辆低速行驶时GPF内颗粒物累积速度更易受低温环境影响。

     

腐殖酸定向修饰Ce-Co铁基生物焦汞吸附机理

使用腐殖酸对铁基改性生物焦进行定向修饰,并借助固定床吸附装置考察改性后生物焦汞吸附性能,探究了不同腐殖酸负载量下的铁基改性生物焦的汞吸附能力.采用BET、XPS、FTIR表征手段,考察了定向修饰后生物焦的孔隙结构、表面元素价态及表面功能基团的组成,通过SEM扫描电镜探究生物焦微观形貌,并利用EDS能谱分析生物焦表面活性金属成分分布.结果表明,使用腐殖酸对铁基改性生物焦定向修饰后的生物焦汞脱除性能大幅提高,使用5%质量分数包裹后的生物焦汞脱除性能最高,3h单位累积汞吸附量为18025ng/g,相较于未被修饰的铁基改性生物焦汞吸附性能提高65%;负载腐殖酸后的生物焦以介孔为主,表面活性金属种类丰富,有利于单质汞的氧化;样品表面羧基、醇羟基等含氧官能团数量增加,定向修饰后生物焦表面出现大量氨基等利于重金属吸附的含氮官能团;定向修饰后的生物焦表面出现团聚现象,包裹量过高会将生物焦表面活性位点完全包裹,阻碍了氧化还原反应的进行,不利于汞的进一步氧化;汞在生物焦表面的吸附过程同时存在化学吸附与物理吸附.     

Propane oxidation and steam reforming over Pd/LaFe(0.8) Co(0.2) O3 catalyst: effects of the reactant composition and steam

The effects of reactant composition and steam on propane combustion over Pd/LaFe0.8Co0.2O3 catalyst were investigated.Propane conversion and the oxidation state of palladium were strongly affected by the redox ration of reactants.Higher propane conversion could be obtained under rich conditions and explained as a complex balance between oxidation and steam reforming.Water produced in the oxidation could promote the propane conversion by steam reforming.However,the presence of excess steam would bring about inhibition.     

Adsorption behavior of condensed phosphate on aluminum hydroxide

Sodium pyrophosphate （pyro-P, Na4P2OT）, sodium tripolyphosphate （tripoly-P, Na3P3O10）, and sodium hexametaphosphate （meta-P, （NaPO3）6） were selected as the model compounds of condensed phosphate to investigate the adsorption behavior of condensed phosphate on aluminum hydroxide. The adsorption was found to be endothermic and divisible into two stages： （1） fast adsorption within 1 h; and （2） slow adsorption between 1 and 24 h. The modified Freundlich model simulated the fast adsorption stage well; the slow adsorption stage was described well by the first-order kinetics. The activation energies of pyro-P, tripoly-P, and meta-P adsorption on aluminum hydroxide were determined to be 20.2, 22.8 and 10.9 kJ/mol P adsorbed, respectively, in the fast adsorption stage and to be 66.3, 53.5 and 72.5 kJ/mol P adsorbed, respectively, in the slow adsorption stage. The adsorption increased the negative charge of the aluminum hydroxide surface. Transmission electron microscopy and energy dispersive X-ray analysis analyses provided evidence that the adsorption was not uniform on the surface and that the small crystals contributed more to the fast adsorption than the normal sites did. The results from X-ray fluorescence spectrometry and X-ray photoelectron spectroscopy tests also revealed the uneven adsorption of condensed phosphate as a function of the penetration depth. More condensed phosphates were adsorbed on the outer surface of aluminum hydroxide than in its inner parts.     

污泥过热蒸汽干燥单因素试验

为了研究污泥常压过热蒸汽干燥过程中各干燥因素对干燥性能指标的影响规律,研制了一套污泥常压过热蒸汽干燥试验装置。利用研制的过热蒸汽干燥试验装置进行了不同温度、污泥质量和蒸汽流量的干燥试验。试验结果表明:蒸汽温度在180~260℃,污泥质量在6~30 g,蒸汽流量在18~40 m~3/h时,随着过热蒸汽温度升高、蒸汽流量增大,相对单位能耗值均是先减小后增大,平均干燥强度一直增大;随着污泥质量增大,相对单位能耗是先减小后增大,平均干燥强度一直减小。     

土壤中稀土元素的含量和分布

利用仪器中子活化分析方法(INAA)对我国一些典型地区的364个表层土壤样品中La、Ce、Nd、Sm、Eu、Tb、Yb和Lu等八个稀土元素进行了测定.文中报告了各地区及所研究的全部土壤中稀土元素的平均含量和分布特征.     

用煤矸石合成4A沸石分子筛处理氨氮废水

以煤矸石为原料,采用碱熔一水热法合成4A沸石分子筛。由于煤矸石中铝、硅主要以高岭土形式存在,其活化过程是合成4A沸石分子筛关键环节。为提高4A沸石分子筛钙离子的交换能力,增加对模拟废水氨氮的去除率,实验考察了碳酸钠与煤矸石质量比、活化温度、活化时间、晶化温度和晶化时间对4A沸石分子筛钙离子交换能力的影响,同时也考察了模拟废水的pH、4A沸石分子筛加入量及吸附时间对氨氮去除率的影响。结果表明,最佳工艺条件为,碳酸钠与煤矸石质量比为0．9、活化温度为800％、活化时间1．5h、晶化温度90％和晶化时间3h。合成4A沸石分子筛的钙离子交换能力为310mg／g,在pH为6的100mL模拟氨氮废水中加入6g4A沸石分子筛吸附40min后,废水中氨氮的去除率达到86％。通过最佳工艺条件合成4A沸石分子筛,在处理氨氮废水方面具有一定的应用前景。     

A novel graphene oxide-carbon nanotubes anchored α-FeOOH hybrid activated persulfate system for enhanced degradation of Orange II

Persulfate activation has been applied as one of the efficient advanced oxidation processes(AOPs) to remediate polluted environments. In this study, a novel α-FeOOH anchored by graphene oxide(GO)-carbon nanotubes(CNTs) aerogel(α-FeOOH@GCA) nanocomposite activated persulfate system(α-FeOOH@GCA + K_2S_2O_8) was applied for decolorization of Orange Ⅱ(OⅡ). The decolorization of OⅡ was remarkably enhanced to a level of ～ 99% in this system compared with that of pristine α-FeOOH(～ 44%) or GO-CNTs(～18%). The enhanced catalytic activity of α-FeOOH@GCA was due to the formation of a heterojunction byα-FeOOH and GO-CNTs as confirmed by the presence of Fe–O–C chemical bonds. The degradation intermediates of OⅡ were comprehensively identified. The proposed degradation pathway of OⅡ begins with the destruction of the conjugated structures of OⅡ by the dominant reactive oxygen species, surface-bound SO_4~(·-). The decolorization efficiency of OⅡ by the α-FeOOH@GCA activated persulfate system decreased from the first to third cycle of recycling. Ultraviolet(UV) irradiation or introduction of a small amount of Fe~(2+) could restore the activation of this system. The results show that the α-FeOOH@GCA persulfate activation system promises to be a highly efficient environmental remediation method for organic pollutants.     

热活化过硫酸盐联合混凝处理微乳浊液的机理

在冶金冷轧微乳浊液中,醚链较长、αH较多的非离子型表面活性剂的存在导致体系稳定性极高而难于降解,利用热活化过硫酸盐(PS)进行破乳预处理,并联合混凝作用,以实现高效的油水分离.本文研究了PS浓度、体系温度、pH值对上述反应的影响,根据电子顺磁共振等分析技术确定了作用自由基类型及其贡献率,利用气相色谱-质谱联用法分析了反...     

Fe (II)活化过硫酸盐处理喹啉工艺参数优化及生物毒性

以喹啉为处理目标物,采用Fe²⁺活化K₂S₂O₈（PS）的高级氧化体系在不同环境因素下降解喹啉.结果表明：与单一PS体系和Fe²⁺体系相比,Fe²⁺/PS体系可以有效降解喹啉.在初始喹啉浓度为250mg/L,喹啉/PS物质的量比为1：10,PS/Fe²⁺物质的量比为3,初始pH3,反应温度为45℃,反应时间为80min的条件下,喹啉降解率可达100%.提高PS和Fe²⁺浓度均能有效提高喹啉降解率,但超过一定限值后对喹啉去除效果不明显.Fe²⁺/PS去除喹啉的过程符合一级反应动力学.溶液初始pH值越高,喹啉去除率越低;反应温度越高,喹啉去除率越高.自由基淬灭实验证实,Fe²⁺活化PS体系中有SO₄^-·和OH·的存在,其中由SO₄^-·产生的OH·对喹啉的降解占主导地位.通过GC/MS检测到2种中间产物8-羟基喹啉和2（1H）-喹啉酮,据此推测基于硫酸根自由基强化喹啉降解的可能路径.大肠杆菌急性毒性实验结果证实,虽然Fe²⁺/PS体系去除喹啉过程中产生了毒性更强的中间产物,但酸性条件和较高的反应温度有利于体系脱毒.