Preparation and performance of novel APP/NaY–Fe suppressant for coal dust explosion

Coal dust explosion occurs easily in the coal chemical industry. To ensure safety in industrial production, NaY zeolite was used as carrier modified with Fe ions and combined with ammonium polyphosphate (APP) to prepare a novel composite suppressant for coal dust explosion. The explosion suppression performance of novel APP/NaY–Fe suppressant was investigated by flame propagation inhibition experiments. The results show that Fe ion modification can effectively improve the explosion suppression performance. By increasing content, the explosion suppression performance of the explosion suppressant increases. The maximum explosion pressure P_max of coal dust drops to 0.13 MPa when 50 wt% explosion suppressants were added, and the coal dust explosion cannot continue to expand. Complete suppression of explosion could be achieved by adding 66 wt% explosion suppressants. Combined with XRD, SEM and TG results, the explosion suppression mechanism was proposed. The novel explosion suppressant has high thermal stability, good dispersity and its explosion suppression components distribute uniformly. It shows good explosion suppression performance by the synergistic effect among explosion-suppression components.     

几种表面防护体系耐盐雾性能研究

目的通过对比试验室加速腐蚀试验结果,获得耐盐雾腐蚀性能最佳的表面防护体系。方法选用2024铝合金的几种不同表面防护体系,进行盐雾腐蚀试验。通过宏观腐蚀形貌和涂层失光率变化来分析判定表面防护体系耐腐蚀性能,获得抗腐蚀性能优异的表面防护体系。结果综合内外部防护体系宏观腐蚀形貌和失光率情况来看,阿洛丁氧化和所配套的三套涂层系统的盐雾适应性较差。结论内部防护体系推荐采用铬酸阳极化+10P4-X底漆防护体系;外部防护体系推荐采用铬酸阳极化+10P20-X底漆+ECL面漆防护体系。     

除镉最佳混凝剂的筛选及应用条件研究

通过采用聚合氯化铝铁（PAFC）、氯化铁（FeCl3）及聚合硫酸铁（PFS）对含镉废水的处理研究表明,三种混凝剂对含镉水体均有良好的处理效果,同等条件下,三种混凝剂对含镉水体去除率分别为98.22%、92.19%和93.63%。研究了PAFC对含镉水体的混凝沉淀效果,实验结果表明：碱性条件有利于镉离子的沉淀,当pH为9～11时,去除率可达98.00%左右;对于初始浓度为4.000 0 mg.L-1的含镉废水,经处理后,水体浓度可降至0.184 0 mg.L-1,对于初始浓度为0.400 0 mg.L-1的含镉废水,经处理后水体浓度降至0.007 2 mg.L-1;废水中投加一定量的石灰乳对PAFC除镉起一定的作用,投加量达30.00 mg.L-1时,其去除率达99.91%;通过对PAFC除镉动力学拟合,符合一级线性动力学方程。     

3-氨丙基三乙氧基硅烷改性蒙脱石的表征及其对Sr(Ⅱ)的吸附研究

3-氨丙基三乙氧基硅烷(APTES)作为偶联剂在粘土功能化方面具有特殊的研究意义.因此,本文采用X射线衍射(XRD)、扫描电镜(SEM)及红外光谱(FTIR)等方法对不同离子交换容量(1.0CEC、1.5CEC、2.0CEC、2.5CEC、3.0CEC、4.0CEC)的APTES改性蒙脱石(APTES-Mt)的结构及表面进行表征与分析,同时对Sr(Ⅱ)的吸附性能进行了研究.结果表明,改性蒙脱石对Sr(Ⅱ)的吸附平衡时间为24h,吸附量随溶液pH(1.0～10.0)的增大而增强,且改性蒙脱石的吸附量是原始蒙脱石吸附量的3倍.改性蒙脱石对Sr(Ⅱ)的吸附作用较强,吸附后的Sr(Ⅱ)不易从材料中解吸出来.XRD、SEM和FTIR等分析结果显示,APTES已经成功插入层间,改性蒙脱石对Sr(Ⅱ)的吸附机理主要为配位吸附.     

泥炭预处理吸附垃圾渗滤液中的COD

通过对泥炭改性去除水中COD进行了试验研究。探讨了磷酸、硫酸、盐酸、硝酸和氢氧化钠对COD去除效果的影响和吸附机理。结果表明,在酸、碱改性过程中,用5%的硫酸改性的泥炭去除COD的效果最佳,改性泥炭用量为每10 g/100 mL,吸附时间为60 min,pH为10的试验条件下,COD的去除率为68.5%以上,磷酸较硫酸次之,去除率为55%左右,而盐酸和硝酸较差分别为45%和38%,氢氧化钠为40%左右。并对其吸附机理进行了研究,其吸附等温线符合Freundlich型。通过扫描电镜观察泥炭表面的结构,硫酸改性后的泥炭表面结构比较粗糙,比表面积最大,与实验结果相吻合。用原子吸收法对泥炭处理前后的水样进行比较,表明泥炭对重金属也有很好的去除率。本研究为泥炭利用提供了可借鉴的思路。     

地下空间在节能减排中的应用及展望

在能源短缺和环境污染的双重压力下,我国出台多项措施加大节能减排力度。总结概括了地下空间的几种类型,认为盐岩洞穴、废弃矿洞、废弃油井、枯竭油气层等地下空间经过技术改造,可以埋存CO2、固体垃圾、废弃核原料,储存油气,地热利用等,能创造可观的社会价值和环境保护效益,可作为节能减排的一种有效措施。以山东地区为例,调研分析了山东多处地下空间利用现状,给出了地下空间的三种发展方向。     

SnAgCu焊料中Sn元素在模拟土壤溶液中的浸出行为

研究了Sn-3.5Ag-0.75Cu无铅焊料及其与Cu基板的钎焊接头在模拟土壤的NaCl,NaCl-Na2SO4和NaCl-Na2SO4-Na2CO3溶液中Sn元素的浸出行为.结果表明:焊料在NaCl-Na2SO4-Na2CO3溶液中Sn的浸出相对严重;而接头在NaCl溶液中Sn的浸出量最多.在Sn浸出量多的焊料和接头表面形成厚而疏松的腐蚀产物,XRD分析表明其产物主要由SnO,SnO2和Sn4(OH)6Cl2组成.动电位极化测试分析表明接头中Cu基板与焊料合金之间的电偶腐蚀是焊料合金与接头在同种溶液中Sn元素浸出差异的主要原因.     

上海中心城区土地利用变化对区域降雨径流的影响研究

土地利用变化导致的城市下垫面改变对降雨径流关系有着重要影响。选择高度城市化的上海中心城区,利用初损和径流量修正方法并经实测数据验证后的SCS-CN修正模型,在城市集水区尺度上,初步探讨模拟了1947—2006年中心城区在0.5～10 a一遇设计暴雨重现期条件下持续1 h的降雨事件和丰、平、枯降雨年份下的径流系数,并分析了土地利用方式、前期土壤湿润程度(AMC)和降雨因素对中心城区60 a降雨径流关系的影响。结果表明:①60 a间,AMCⅠ和0.5～10 a一遇设计暴雨重现期条件下的径流系数相对增长17.21%～6.14%,枯、平和丰水年的年径流系数相对增长分别为20.49%、11.83%和10.02%;②土地利用类型、土壤入渗能力和AMC类型,与降雨强度共同构成影响降雨径流关系的两方面重要因素。随着降雨强度的增大,在AMCⅠ→Ⅲ过程中,土地利用改变对降雨径流关系的影响趋小,降雨类型起决定作用;而降雨强度越小,土壤AMC越干燥,土地利用改变对降雨径流关系影响越强;③不同降雨强度和降水年条件下的径流系数均随CN值的增大而增加,其径流系数与CN值之间分别可用线性(R20.999)和指数(R20.987)关系表示。     

Improved source assessment of Si, Al and related mineral components to PM10 based on a daily sampling procedure

Samples obtained from an industrialized valley in the East Alpine region were collected daily for a half year and analyzed using X-ray fluorescence to examine the elements Si,Al,Fe,Ca,Mg,Na,K,Zn,P,S and Cl.Some factors affecting the changes of these elements were considered,including time,elemental correlations,weekday,weekend and seasonal changes.Diagnostic analysis provided an insight into a decoupling behavior that occursin siliceous and carbonates minerals.A decrease in Si and Al and an increase in carbonates,Na,K,Zn and P were observed during the cold season.However,a consistently high correlation of Si and Al was observed in all seasons.It was established that such high levels originated from street surface abrasion.The increase in variability and absolute levels of carbonates during the cold season was demonstrated by adding carbonates to the street surface as gritting material to increase the grip on snowy surfaces.A marked increase in Na and Cl was observed in winter which may have been caused by thaw salt that is widely used in winter in Austria.This was associated with a significant increase in K,Zn,and P in the cold season that was the result of domestic space heating with wood.PM10 levels in December were 12 μg/m3 and were higher than levels detected in July.It was established that such high levels originated from mineral oxides,wood smoke,and inorganic ionic material(s).     

Removal of humic acid from aqueous solution by cetylpyridinium bromide modified zeolite

Natural zeolite was modified by loading cetylpyridinium bromide (CPB) to create more e cient sites for humic acid (HA) adsorption. The natural and CPB modified zeolites were characterized with X-ray di raction, field emission scanning electron microscopy, Fourier transform infrared spectroscopy and elemental analysis. The e ects of various experimental parameters such as contact time, initial HA concentration, solution pH and coexistent Ca2+, upon HA adsorption onto CPB modified zeolites were evaluated. The results showed that natural zeolite had negligible a nity for HA in aqueous solutions, but CPB modified zeolites exhibited high adsorption e ciency for HA. A higher CPB loading on natural zeolites exhibited a larger HA adsorption capacity. Acidic pH and coexistent Ca2+ were proved to be favorable for HA adsorption onto CPB modified zeolite. The kinetic process was well described by pseudo second-order model. The experimental isotherm data fitted well to Langmuir and Sips models. The maximum monolayer adsorption capacity of CPB modified zeolite with surfactant bilayer coverage was found to be 92.0 mg/g.