生物滤料滤池处理姚江微污染水源水

通过中试试验,考察了不同滤料介质的生物滤池对于姚江微污染水源水的处理效果。结果表明,双层生物滤料滤池能够有效地去除有机物、氨氮等污染物质,可以延长滤池反冲洗周期,并能在短时间内恢复到正常处理能力,适合于传统滤池的改造。采用颗粒活性炭-石英砂滤料滤池的综合处理效果优于同类型的颗粒活性炭-沸石滤料滤池,通过加入少量臭氧(0.8～1.0mg/L)可以提高生物滤池的去除效果。     

Kinetics of and catalyst decay accompanying the gas phase rearrangement of cyclohexanone-oxime over a hy ultrastable zeolite

The kinetics of the rearrangement of cyclohexanone-oxime has been studied in a fixed bed, glass tubular reactor at atmospheric pressure and temperatures of 240, 270, 300 and 335°C, using ultrastable HY zeolite catalyst. Several kinetic models, including the Langmuir-Hinshelwood type, have been derived and the best statistical fit has been obtained with a pseudo-first order kinetic equation. The rate constants and activation energies for the formation of the products caprolactam, cyclohexanone and 5-cyanopent-l-ene have been calculated. Based on the evolution of the selectivity with temperature, and the I.R. spectra of the poisoned catalyst, different decay models have been deduced and discussed.     

MCM-22沸石催化剂的苯与长链烯烃烷基化性能

用NH3-TPD法研究了4种不同硅铝摩尔比的MCM-22沸石的酸性质,在常压间歇式反应器中考察了它们在苯与长链烯烃烷基化反应中的催化性能,并与HY和HZSM-5沸石催化剂进行了比较。实验结果发现MCM-22的催化活性与其强酸量有一致的关系,与其硅铝摩尔比无对应关系;MCM-22的活性比HY低,但对2-P的选择性远远高于HY,这说明了MCM-22对2-P具有形状选择作用。     

Selective O-methylation of phenol with dimethyl carbonate over X-zeolites

The O-methylation of phenol with dimethyl carbonate proceeds selectively in the vapor phase over alkali ion exchanged X-zeolites. Thus, a 76% yield of anisole was obtained with a 93% selectivity over NaX at 553 K. The participation of basic sites in the O-methylation is suggested.     

NO adsorption on Cu-ZSM-5: assignment of IR band at 2133 cm−1

The adsorption of nitrogen oxides on Cu-ZSM-5 was studied by infrared spectroscopy to elucidate the species associated with the band at 2133 cm^–1. The band was found for both NO and NO₂ adsorption. Labeling experiments with¹⁵NO revealed that the associated surface species contained nitrogen and, most likely, an N-O bond. Co-adsorption experiments of NO and oxygen produced adsorbed nitronium, NO ₂ ⁺ , as the principal, associated species. Adsorption of nitrogen oxides on dispersed CuO and the HZSM-5 support demonstrated that the 2133 cm^–1 band was not necessarily associated with copper ions. A relatively strong correlation between the bands at 2133 and 3615 cm^–1 indicates that the primary adsorption sites of NO ₂ ⁺ are the strongly protic, bridging Si(OH)Al framework hydroxyls. Once these were filled, other, weaker acid sites began to adsorb NO ₂ ^O .     

Effect of zeolite in surface discharge plasma on the decomposition of toluene

Toluene was decomposed in a surface discharge plasma reactor packed with various zeolites. The positioning effect of the zeolite bed was also investigated Reactor-B, in which the zeolite bed was located upstream, performed much better than Reactor-A, in which the zeolite bed was located downstream. Furthermore, the decomposition efficiency in Reactor-B increased with the capacity for toluene adsorption on zeolite, while that in Reactor-A did not. The toluene adsorbed in micropores was not decomposed effectively by direct electron impact, but was decomposed by active oxygen species generated in the plasma zone on the zeolite surface. A good correlation was also observed between toluene decomposition and ozone consumption in the downward-type reactor.     

HZSM-5分子筛催化合成1，3-苯并二嗯茂烷类化合物

研究了HZSM-5分子筛催化邻苯二酚与环己酮、丁酮、丙酮、丙醛、丁醛、异丁醛、戊醛、异戊醛、正己醛、正辛醛、苯甲醛、二苯甲酮等10余种醛（酮）的缩合反应。考察了反应时间、酚与醛（酮）的配比、HZSM-5分子筛用量等因素对邻苯二酚与醛（酮）反应的影响。结果表明，当n（邻苯二酚）：n（醛（酮）]=1：1．4，催化剂用量为3．5g／mol邻苯二酚，反应5h，选择性一般在99．2％以上，转化率也一般在30％以上，表明，HZSM-5分子筛对邻苯二酚与醛（酮）的反应有较好的催化性能。     

Quick Activation of Optimized Zeolites with Microwave Heating and Utilization of Zeolites for Reusable Desiccant

Effectiveness of microwave heating in an activation treatment of zeolites was studied and utilization of zeolites for reusable desiccant was examined. X zeolite was chosen as a target material for its large adsorption capacity. Na-X zeolite easily caused a thermal runaway by microwave radiation of 500 W but Ca contained X zeolite merely reached ca. 573 K under the same conditions. Mixtures of Na-X and Ca-X with suitably mixed ratios did not cause the thermal runaway and their heating temperatures were controlled (>573 K) at will. Under the most suitable conditions, the mixture reached a dehydration degree of 92%. A degradation degree of adsorptive capacity of the mixture for water was examined after three treatments. The average degradation degree was 1.5% per treatment. The heating method is promising as a quick and easy technique to activate zeolite. By applying the method, the zeolites with suitable mixing ratios are usable as a reusable desiccant for home use.     

Molecular simulation of hydrogen adsorption in organic zeolite

The adsorption of molecular hydrogen on model zeolites has been simulated employing Grand Canonical Monte Carlo (GCMC) procedure. The effects of cation type, available volume, surface area, temperature, pressure and pre-adsorbed organics such as benzene on the hydrogen uptake are analyzed. The hydrogen adsorption can be affected mainly by the available volume and surface area per g-zeolite at the same temperature and pressure. Increase of temperature results in the decrease of sorption intensity and capacity. The adsorption capacity correlates well with the pressure with high linearity at room temperature. Adsorption is lowered by the pre-adsorbed benzene molecule. The orientation and the number of benzene molecule in zeolite affect the adsorption capacity. The organic zeolite with larger available volume shows larger adsorption capacity.     

Measurement of zeolite,silicate, and phosphate in laundry detergent products by inductively coupled plasma atomic emission spectrometry

This paper reports the development of a method for simultaneously measuring zeolite, silicate, and phosphate in laundry detergent products by inductively coupled plasma atomic emission spectrometry. A sample is decomposed under alkaline oxidative conditions to decompose zeolite, silicate, phosphate, and organic substances. Then hydrochloric acid is added to the decomposed solution to dissolve aluminum hydroxide precipitate before analysis. This sample preparation procedure was investigated by using a total organic carbon analyzer and was confirmed to be applicable to simultaneous measurements of zeolite, silicate, and phosphate. Relative standard deviation for the analysis is less than 2.1%, recovery is more than 99.0%, and the calibration curve gives a correlation coefficient ofR=1.000. The detection limit of this method for aluminum and silicon is 0.1%, and for phosphorus, 0.2% by weight in the product. This method is applicable to various laundry detergent products that contain zeolite, silicate, or phosphate and is five times faster than the three wet chemical methods.