载铁改性沸石粉体抑制甲烷/空气扩散火焰试验研究

为发展洁净高效新型粉体灭火介质,以沸石粉体为基体,采用盐酸活化和氯化铁溶液浸泡方法制备载铁改性沸石粉体灭火剂。采用X-射线衍射仪(XRD)、扫描电镜(SEM)和X-射线荧光光谱仪(XRF)等仪器对该粉体灭火剂的结构和形貌进行表征。通过小尺度的杯式燃烧器试验研究载铁沸石粉体对甲烷/空气扩散火焰的灭火效果,并和未改性沸石粉体进行对比。试验结果表明,载铁改性沸石粉体灭火剂的灭火效能明显高于未改性沸石粉体。改性沸石灭火效能提高,主要是由于所负载的铁离子在火焰中转化为活性铁原子,参与清除火焰自由基的催化反应。     

Simultaneous removal of ammonia and N-nitrosamine precursors from high ammonia water by zeolite and powdered activated carbon

When adding sufficient chlorine to achieve breakpoint chlorination to source water containing high concentration of ammonia during drinking water treatment, high concentrations of disinfection by-products(DBPs) may form. If N-nitrosamine precursors are present, highly toxic N-nitrosamines, primarily N-nitrosodimethylamine(NDMA), may also form. Removing their precursors before disinfection should be a more effective way to minimize these DBPs formation. In this study, zeolites and activated carbon were examined for ammonia and N-nitrosamine precursor removal when incorporated into drinking water treatment processes.The test results indicate that Mordenite zeolite can remove ammonia and five of seven N-nitrosamine precursors efficiently by single step adsorption test. The practical applicability was evaluated by simulation of typical drinking water treatment processes using six-gang stirring system. The Mordenite zeolite was applied at the steps of lime softening, alum coagulation, and alum coagulation with powdered activated carbon(PAC) sorption. While the lime softening process resulted in poor zeolite performance, alum coagulation did not impact ammonia and N-nitrosamine precursor removal. During alum coagulation, more than67% ammonia and 70%–100% N-nitrosamine precursors were removed by Mordenite zeolite(except 3-(dimethylaminomethyl)indole(DMAI) and 4-dimethylaminoantipyrine(DMAP)). PAC effectively removed DMAI and DMAP when added during alum coagulation. A combination of the zeolite and PAC selected efficiently removed ammonia and all tested seven N-nitrosamine precursors(dimethylamine(DMA), ethylmethylamine(EMA), diethylamine(DEA), dipropylamine(DPA), trimethylamine(TMA), DMAP, and DMAI) during the alum coagulation process.     

粉煤灰提铝中间产物合成4A分子筛对氨氮的吸附行为研究

采用粉煤灰提铝中间产物合成4A分子筛,利用XRD、SEM、热重分析、化学成分分析、阳离子交换容量对4A分子筛进行表征.考察吸附时间、pH、分子筛投加量、氨氮初始浓度、共存阳离子对其吸附性能的影响,研究其对模拟废水中氨氮的吸附效果,并结合准二级动力学方程、吸附等温线研究吸附性能和机理.结果表明,初始浓度为50 mg·L~(-1)、4A分子筛投加量为5 g·L~(-1)、pH值为6~9、吸附时间为80 min时氨氮去除率可达71.34%;随着氨氮初始浓度升高,其去除率降低,吸附容量增加;共存阳离子Na~+、K~+、Ca~(2+)对NH_4~+有强烈的竞争吸附,Mg~(2+)无明显竞争作用.吸附过程符合准二级动力学方程和Freundlich模型.Langmuir吸附等温线显示最大吸附容量为20 mg·g~(-1).     

在沸石对高放废液水泥固化体中Cs~+浸出率的影响

文章主要研究模拟高放废液加入沸石预处理经碱矿渣水泥固化后Cs+的浸出性能。实验结果表明,处理含Cs+高放废液固化体中加入沸石,能使Cs+浸出率降低";两步法"掺入沸石固化体抗Cs+浸出性能更有所提高;pH值升高Cs+的吸附比增大。     

水热条件对粉煤灰沸石离子交换性能的影响

沸石的离子交换性能是决定其应用价值的一个重要指标。为衡量粉煤灰沸石的应用性能,本研究主要考察了反应温度、反应时间以及添加剂等水热反应条件对合成粉煤灰沸石产品离子交换性能(CEC,Cation Exchange Capacity)的影响。结果表明,产品的CEC值随着反应温度和反应时间增加而增大,至120℃、6h达到最大。添加剂十六烷基三甲基溴化铵和95%乙醇有效促进了NaP1沸石的结晶过程,均可使产品CEC值提高10%以上。合成NaP1型粉煤灰沸石的最佳水热反应条件为:反应温度120℃,反应时间6h,液固比(mL/g)为8,氢氧化钠浓度为2mol/L,95%乙醇作为添加剂。所得粉煤灰沸石产品CEC值达到最大值198.31cmol/kg。     

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.     

An experimental study on the influence of zeolite on changes of pH and alkalinity in anaerobic treatment of compost leachate

With the increase of urbanization, municipal solid waste has also increased. Therefore, the need for solid waste management is also increasing compared with earlier decades. Composting is a good option for the recycling of solid waste; however, it produces leachate, which requires proper treatment systems to prevent environmental degradation. Due to high chemical oxygen demand (COD) concentrations in compost leachate, anaerobic treatment is the best option for handling the effluent, and an anaerobic baffled reactor (ABR) is one such anaerobic reactor that can be used for its treatment. Because of high ammonia and heavy metal concentrations, as well as the possibility of sludge washout in ABRs, it is important to use proper media, such as zeolite, which can reduce inhibition effects and sludge washout from the reactor. Anaerobic treatment, especially during the methanogenesis phase, is sensitive, and pH and alkalinity are parameters that influence the treatment. Therefore, adjusting these parameters within a normal range is very important to the proper functioning of anaerobic systems. In this study, a pilot‐scale ABR was used, and the last 4 of the 8 ABR compartments were filled with zeolite. The bioreactor was operated at hydraulic retention times (HRT) of 3, 4, and 5 days, with zeolite filling ratios of 10%, 20%, and 30%, and influent COD concentrations of 10,000, 20,000, and 30,000 milligrams per liter (mg/L). In this study, pH value was 6.43 ± 0.1, 6.96 ± 0.3, and 6.96 ± 0.25 at filling ratios of 10%, 20%, and 30%, respectively. According to the results, in all filling ratios, no significant changes were observed in the pH value when the organic loading rate increased and its amount was within a constant range. Influent alkalinity was equal to 2015 ± 510, 2884 ± 505, and 4154 ± 233 milligrams of calcium carbonate per liter (mg CaCO₃/L) at influent COD concentrations of 10,000, 20,000, and 30,000 mg/L, respectively, and in effluent, they were 2536 ± 336, 3379 ± 639, and 4377 ± 325 mg CaCO₃/L, respectively. The amount of alkalinity in the effluent increased compared with the alkalinity in the influent. The results show that the amount of alkalinity in the influent and effluent was similar, and the alkalinity enhancement was lower when the filling ratio was increased from 10% to 20%, and 20% to 30%. Comparisons of the results from zeolite with and without biofilm showed that, in cases of zeolite with biofilm, the amounts of silica and oxygen decreased and the amount of carbon increased, and it showed the formation of biofilm on the surface of zeolite. In addition, the absence of sodium in the zeolite with the biofilm indicated that sodium was exchanged with ammonium ions. According to the results, zeolite can be used in anaerobic reactors as a medium, and it also reduces fluctuations in pH and alkalinity at different organic loading rates, providing a normal range for anaerobic treatment.     

Two-step fast microwave-assisted pyrolysis of biomass for bio-oil production using microwave absorbent and HZSM-5 catalyst

A novel technology of two-step fast microwave-assisted pyrolysis(f MAP) of corn stover for bio-oil production was investigated in the presence of microwave absorbent(Si C) and HZSM-5catalyst. Effects of f MAP temperature and catalyst-to-biomass ratio on bio-oil yield and chemical components were examined. The results showed that this technology, employing microwave, microwave absorbent and HZSM-5 catalyst, was effective and promising for biomass fast pyrolysis. The f MAP temperature of 500°C was considered the optimum condition for maximum yield and best quality of bio-oil. Besides, the bio-oil yield decreased linearly and the chemical components in bio-oil were improved sequentially with the increase of catalyst-to-biomass ratio from 1:100 to 1:20. The elemental compositions of bio-char were also determined. Additionally, compared to one-step f MAP process, two-step f MAP could promote the bio-oil quality with a smaller catalyst-to-biomass ratio.     

稻壳沸石的合成及其对磷酸盐的吸附/脱附动力学

以稻壳为原料采用煅烧-水热合成法制备了合成沸石,运用XRD和SEM表征了合成沸石的特性,通过静态实验,研究了合成沸石对磷酸盐的吸附和脱附机理。结果表明:12 h后产物发现了Na P沸石的特征峰和亚晶结构,延长水热合成晶化的时间有利于沸石晶核的形成。沸石对磷酸盐的吸附机理符合伪二级模型,实测值与伪二级吸附动力学模型的拟合值相差在1.1%以内。颗粒内扩散速率是由膜扩散和内扩散共同控制,颗粒内扩散速率常数kp随初始浓度的增加而减小。升温有利于磷酸盐的脱附,MNa OH/P>8.0时(MNa OH/P为Na OH物质的量与吸附的磷酸盐物质的量之比),磷酸盐的脱附率可达82.9%。伪二级脱附动力学模型的拟合结果优于伪一级,拟合值与实测值相差在1.7%以内。     

改性Y沸石催化降解聚苯乙烯的研究

用热重分析方法研究了HY沸石与改性Y沸石(UHY)作为催化降解聚苯乙烯的催化剂对聚苯乙烯催化降解的作用及影响,对聚苯乙烯的催化降解与热降解反应产物进行了比较。结果表明,催化剂的存在能显著地降低聚苯乙烯的降解温度,催化剂的酸量和孔结构对聚苯乙烯的降解温度、活化能、积炭的生成量及裂解产物有很大的影响。