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应用错流式动态膜-生物反应器(CDMBR)对己内酰胺废水进行了180 d的实验,实验过程中测定反应器的膜出水和上清液的水质,并对污泥进行了耗氧呼吸速率测定.结果表明,上清液COD一直保持在100mg/L以下,而膜出水的则保持在50 mg/L以下,膜对上清液的COD去除率达50%,而对氮的去除没有贡献.可溶性细胞产物(SMP)在反应器内容易积累,停留足够的时间后能被生物降解.通过投加抑制剂测定耗氧呼吸速率,发现异养菌、硝化细菌和亚硝化细菌的活性由于F/M的降低和SMP积累受到一定的抑制,但不影响系统的处理效率.跨膜压力、膜面流速越大,通量衰减得也就越快. 相似文献
144.
Information about temporal changes in soil organic carbon (C) pools may be obtained indirectly from changes in input-output budgets of organically combined nutrients such as sulphur (S). Sulphur budgets were therefore evaluated for Northern Ireland (NI) for the period 1940-1990, inclusive. These budgets indicated that the land or soil had acted first as a sink but then as a source for S, and that reserves of soil S built up between 1940 and 1965 were totally depleted by the mid-1980s. Pooled data from six long-term soil-monitoring sites on undisturbed grassland suggested that negative S budgets from the late-1970s onwards had been due to the net mineralization of soil organic matter and thus were indicative of net losses of organic C from surface soil horizons. There was some evidence that the decline in rainfall and fertiliser S inputs from the mid-1960s may have precipitated the breakdown of soil organic matter. 相似文献
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采用上流式分段污泥床(upflow staged sludge bed)反应器对聚酯废水进行了预处理试验研究.反应器内厌氧污泥经过近70 d的培养驯化后,用于处理聚酯废水.当进水COD值为800~2000 mg/L,HRT约为16~20 h时,其COD去除率基本能稳定在50%~55%之间;聚酯废水经预处理后,其BOD5/COD值由原来的0.3左右提高到约为0.6,取得了较好的预处理效果.但系统的总产气量由培养期的约13 L/d降至0.8 L/d左右,其中甲烷气体的含量也由50%下降至约6%. 相似文献
147.
α-MnO_2 nanotubes and their supported Au-Pd alloy nanocatalysts were prepared using hydrothermal and polyvinyl alcohol-protected reduction methods, respectively. Their catalytic activity for the oxidation of toluene/m-xylene, acetone/ethyl acetate, acetone/m-xylene and ethyl acetate/m-xylene mixtures was evaluated. It was found that the interaction between Au-Pd alloy nanoparticles and α-MnO_2 nanotubes significantly improved the reactivity of lattice oxygen, and the 0.91 wt.% Au0.48 Pd/α-MnO_2 nanotube catalyst outperformed the α-MnO_2 nanotube catalyst in the oxidation of toluene, m-xylene, ethyl acetate and acetone. Over the0.91 wt.% Au0.48 Pd/α-MnO_2 nanotube catalyst,(i) toluene oxidation was greatly inhibited in the toluene/m-xylene mixture, while m-xylene oxidation was not influenced;(ii) acetone and ethyl acetate oxidation suffered a minor impact in the acetone/ethyl acetate mixture; and(iii) m-xylene oxidation was enhanced whereas the oxidation of the oxygenated VOCs(volatile organic compounds) was suppressed in the acetone/m-xylene or ethyl acetate/m-xylene mixtures. The competitive adsorption of these typical VOCs on the catalyst surface induced an inhibitive effect on their oxidation, and increasing the temperature favored the oxidation of the VOCs. The mixed VOCs could be completely oxidized into CO_2 and H_2 O below 320°C at a space velocity of 40,000 m L/(g·hr). The 0.91 wt.% Au0.48 Pd/α-MnO_2 nanotube catalyst exhibited high catalytic stability as well as good tolerance to water vapor and CO_2 in the oxidation of the VOC mixtures. Thus, the α-MnO_2 nanotube-supported noble metal alloy catalysts hold promise for the efficient elimination of VOC mixtures. 相似文献
148.
目的:了解北京地区加油站职业病危害现状。方法:按照国家相关标准规范对北京市137家加油站的工作场所进行了汽油、苯、甲苯、二甲苯和噪声的检测。结果:加油站职业病危害因素浓/强度均符合国家职业接触限值要求,确定汽油为主要职业病危害因素。结论:北京市加油站职业危害较小,但长期接触低浓度的汽油,加之劳动强度大、作业时间长等特点会损害人体的免疫功能。 相似文献
149.
Shubo Deng Danmeng Shuai Qiang Yu Jun Huang Gang Yu 《Frontiers of Environmental Science & Engineering in China》2009,3(2):171-177
Perfluorooctane sulfonate (PFOS), as a potential persistent organic pollutant, has been widely detected in water environments,
and has become a great concern in recent years. PFOS is very stable and difficult to decompose using conventional techniques.
Sorption may be an attractive method to remove it from water. In this study, the molecularly imprinted polymer (MIP) adsorbents
were prepared through the polymerization of 4-vinylpyridine under different preparation conditions in order to remove perfluorooctane
sulfonate (PFOS) from water. The MIP adsorbents using perfluorooctanoic acid (PFOA) as the template had good imprinting effects
and could selectively remove PFOS from aqueous solution. The sorption behaviors including sorption kinetics, isotherms, and
effect of pH, salt, and competitive anions were investigated. Experimental results showed that the sorption of PFOS on the
MIP adsorbents was very fast, pH-dependent, and highly selective. The achieved fast sorption equilibrium within 1 h was attributed
to the surface sorption on the fine adsorbents. The sorption isotherms showed that the sorption selectivity of PFOS on the
MIP adsorbents decreased at high PFOS concentrations, which may be due to the double-layer sorption and the formation of PFOS
micelles on the sorbent surface. The sorption of PFOS on the MIP adsorbents was mainly dominated by the electrostatic interaction
between the protonated vinylpyridine on the adsorbent surface and the anionic PFOS. The prepared MIP adsorbents can potentially
be applied in water and wastewater treatment for selective removal of PFOS. 相似文献
150.