气浮-生化处理-砂滤工艺处理高浓度食品生产废水

食品生产废水属于高浓度有机废水,具有排水量大、污染物浓度、水质水量变化大的特点,如不处理就直接排放,将会对水环境造成严重的污染.本工程中废水原水水质参数为:CODCr＜5000mg/L,BOD5＜3000mg/L,SS＜500mg/L,pH5.0～7.5,水温20～30℃.针对该废水水质特点,采用气浮-生化-砂滤工艺处理食品生产废水.运行结果表明,该处理工艺具有处理效率高、操作管理简便、抗冲击负荷、污泥量小、出水水质稳定、运行成本低等优点,处理后出水CODCr85mg/L,BOD524.3mg/L,SS56.2mg/L,pH6～8,达到<污水综合排放标准>(GB8978-1996)中的一级标准.     

Will Simplified Modalities and Procedures Make More Small-Scale Forestry Projects Viable Under the Clean Development Mechanism?

Simplified modalities and procedures (M&P) are expected to increase the viability of small-scale project activities under the Clean Development Mechanism (CDM). A small-scale afforestation or reforestation (AR) project is defined as a project removing less than 8 kilotons of carbon dioxide equivalent (CO₂e) per year. Depending on the project type and the method for measuring scale, 8 kilotons of CO₂e per year correspond to highly diverse areas, possibly ranging from 200 to 6000 ha. Using a model to calculate the minimum project scale above which the CDM is a positive financial incentive for eligible AR project activities, the paper analyzes whether a reduction of transaction costs under simplified M&P will be a sufficient incentive to motivate small-scale participation in the CDM. Model results show that, even under optimistic assumptions on carbon market conditions and transaction costs, small-scale project activities will not benefit from simplified M&P. Results also show that project activities removing more than 8 kilotons of CO₂e per year and registered as small-scale would be the ones that could benefit the most from simplified M&P. It is concluded that the participation of small-scale project activities to the CDM requires more than simplified M&P, the price of expiring Certified Emission Reductions being one of the most critical parameters.     

现代卷烟行业清洁生产审核

现代卷烟行业工艺技术成熟、自动化水平高,形成了产污较少、能耗高的行业特点。在对某卷烟厂进行的清洁生产审核中,针对行业特点,结合企业自身情况,提出并实施无、低费方案11项,中、高费方案6项。改善了车间环境,每年可节水约6万t,节电约20万kW·h,节约蒸汽约400t,减少废水排放约8万m3,节约资金514余万元,取得了良好的效益。     

颗粒活性炭对UASB处理垃圾渗滤液促进作用的研究

通过对比研究,考查了用UASB处理垃圾渗滤液时,投加颗粒活性炭对加速UASB反应器中污泥颗粒化进程、缩短启动时间、提高处理效果的影响。结果显示:启动时间缩短了近1/3,最大有机负荷提高近40%且出现了更大颗粒污泥,但COD去除效率没有明显提高。     

中国广告人才现状研究

广告人作为广告业的主体,是广告公司竞争发展的首要因素,也是广告业发展的决定因素。本文从中国广告业迅猛发展的情势入手,分析了中国广告业求贤若渴的势态,以及我国广告从业人员的现状和广告公司需要什么样的广告人等几个要素。     

Comparison of Black Carbon,Total Organic Carbon,and PAH Concentrations in Surface Sediments from Two Main Rivers in Henan Province,China

Black carbon (BC) in surface sediments from Henan section of Yellow River and Huaihe River, China, was determined. Average content of BC in Huaihe River was 0.33%, higher than that in Yellow River (n?=?23) with mean value of 0.15%. Distribution patterns of BC in Yellow River and Huaihe River were similar, namely that tributaries had higher BC content than main stream. In addition, BC content in the mainstream of Yellow River and Huaihe River decreased with altitude. The BC content presented a significant positive correlation with clay (r?=?0.672; p?<?0.01) content in Yellow River, while neither did in Huaihe River. The ratio of BC/TOC ranged from 1.8–57.4% (median 29.6%), evidencing pyrogenic fossil fuel source of BC in Yellow River. Relatively low values of BC/TOC in Huaihe River (5.3%–28.8%, median 7.5%,) reflected that the origin of BC is from burning of biomass. In addition, Pearson rank correlation analysis showed that BC was in strong correlation with lighter PAH in Yellow River, while BC was in significant correlation with heavier PAH in Huaihe River. The ratio of BC/TOC indicated that BC in Yellow River mainly came from fossil fuel combustion, while BC in Huaihe River was primarily from biomass burning.     

非均相催化湿式氧化法活性炭再生

使用浸渍法制备的CuO Al2 O3催化剂对吸附苯酚饱和的活性炭进行非均相催化湿式氧化再生研究 ,考察了反应温度、反应时间、催化剂投加量、反应氧分压、投炭量、蒸馏水量对非均相催化湿式氧化再生活性炭的影响结果 ,同时在该实验中得到非均相CuO Al2 O3催化湿式氧化再生活性炭的最佳条件。对催化剂进行了X衍射分析 ,并通过对催化剂的稳定性进行实验 ,得出该催化剂在进行催化湿式氧化再生活性炭的过程中具有较好的稳定性     

电极材料对电解法处理循环式准好氧垃圾填埋场渗滤液效果的影响研究

分别用3种不同材料电极（不锈钢、Ti／Pt和Ti／RuO2-IrO2）作阳极、石墨电极作阴极在同一条件下分别对循环式准好氧填埋垃圾场渗滤液进行电解处理对比研究。研究结果表明，随着电解时间的变化，渗滤液中的COD、BOD5、BOD5／COD、重金属离子浓度、色度和pH值均会发生改变。当电解时间为10—20min时，用上述3种电极作阳极电解均会出现渗滤液COD、BOD5、BOD5／COD增大的现象；当电解时间为30—40min时，用Ti／RuO2-IrO2或Ti／Pt电极作阳极电解均可使渗滤液的色度降为0；当电解时间为120min时，分别用3种电极作阳极电解都可使渗滤液中的COD、BOD5和重金属得到有效的去除，其中用Ti／RuO2-IrO2电极作阳极电解对COD、BOD5的去除效果最好：用Ti／Pt电极作阳极电解对Pb^2＋的去除效果最好。     

Kinetics of benzene adsorption onto activated carbon

An activated carbon bed adsorption process is influenced by the adsorbents' characteristics, volatile organic compound (VOC) characteristics, and process conditions. In the literatures, the adsorption processes of the adsorbents and VOCs were usually considered to be in equilibrium. In this study, the VOC adsorption processes by activated carbon were considered to be a kinetic process, i.e. they are not in equilibrium. Then, isothermal adsorption curves and a small column experiment were simulated.     

Development of a continuously stirred flow cell for investigating sorption mass transfer

This paper introduces a new reversible-flow design for a continuously stirred reactor used to study sorption mass transfer in soil and solvent systems. The stirred reactor has potential advantages over conventional packed column or batch reactors because it isolates intraparticle sorption rate limitations from advective-dispersive transport, yet allows changes to flux through the reactor for analysis of sorption kinetics under dynamic conditions. Previously, stirred reactors have often failed due to clogging of sediment on the effluent frit. The reverse-flow backwashing design allows longer life and higher confidence in maintaining mixed conditions than previous designs. Mass transfer 'rate coefficients estimated from stirred and column experiments are compared; both techniques produced results consistent with a published correlation. The data also show that fitted sorption mass transfer coefficients can be strongly dependent on the choice of equilibrium partition coefficient (i.e. batch or first-moment derived values), and that the conventional two-site sorption kinetics model fails to accurately predict sorption mass transfer in the presence of changing solvent velocity through the reactor.