西部地区经济发展与水环境质量的相关分析

认识经济发展与水环境污染的关系,以求西部地区经济与环境的协调发展。文章运用环境库兹涅茨理论和自回归分析模型,对1995～2004年我国西部地区人均GDP与废水排放量的分析,可知西部地区的人均GDP增加1%,则污水排放量增加0.582%,经济发展伴随着水环境质量的持续恶化,说明西部地区目前处于环境库兹涅茨曲线的左半部分。因此有必要加强对水环境的规制和治理,改善经济发展和水环境质量之间的这种两难关系。还表明自回归模型对于西部地区水环境质量的预测也是有效的。     

灰色理论模型预测城市垃圾量

利用灰色理论模型 ,采用非线性微分方程拟合 ,可较好地预测城市垃圾的产生量。运用最小二乘法 ,通过MATALAB程序求出了模型中的参数 ,假设检验结果表明 ,该模型有较高的预测精度。根据上述模型 ,预测娄底市未来30a的总垃圾预测量为 80 4 90万t     

应用线性和非线性法求解有机物生物降解动力学参数

根据苯甲酸类化合物在水体中不同时间的生化需氧量，用线性和非线性合法对化合物生物降解随时间变化的动力学过程进行曲线拟合，得到各化合物2个数值不同的安全生化需氧量、生物降解速率常数和生物降解滞后期。根据各化合物2种不同的生物降解动力学模型所得到的生化需氧量拟合值与实测值的误差相比较，发现用非线性法拟合得到的有机物生物降解动力学模型，更符合化合物真实生物降解规律，因此用非线性法拟合化合物的生物降解动态变化，比用线性方法更精确。     

人工神经元网络对水处理系统建模适应性的研究

针对水处理系统的特点和研究中的难点，引入人工神经元网络的理论和思想，提出了水处理系统的神经网络分析方法．通过建立基于ＢＰ人工神经元网络的臭氧生物活性炭系统的模型，具体地考察了人工神经元网络对水处理系统建模的适应性，使水处理系统的研究迈向智能化和控制化．     

Determination and discussion hydraulic retention time in membrane bioreactor system

Based on the microorganism kinetic model, the formula for computing hydraulic retention time in a membrane bioreactor system (MBR) is derived. With considering HRT as an evaluation index a combinational approach was used to discuss factors which have an effect on MBR. As a result, the influencing factors were listed in order from strength to weakness as: maximum specific removal rate K, saturation constant Ks, maintenance coefficient m, maximum specific growth rate ,ua and observed yield coefficient Yobs. Moreover, the formula was simplified, whose parameters were experimentally determined in petrochemical wastewater treatment. The simplified formula is θ= 1.1( 1/β -1)(Kｓ S)/KXo , for oetroehemical wastewater treatment K and Ko eaualed 0.185 and 154.2, resoectively.     

RS、GIS在内陆湖泊水质研究中的应用

:遥感 (RS)、地理信息系统 (GIS)技术的综合应用在许多研究领域广泛推广并日渐成熟 ,表现出广阔的发展前景。将 RS、GIS相结合 ,综合应用于内陆湖泊水质的监测和分析 ,充分体现了其快速、经济、高效的强大优势。本文首先回顾了一般监测方法的特点及局限性 ,主要讨论了 RS、GIS的特点及在内陆湖泊监测和分析中的优势所在。最后提出了此领域的发展方向展望     

Cu／A1-Ce-PILC在丙烯选择性催化还原NO反应中的失活研究

采用聚合羟基复合阳离子合成交联黏土A1-Ce-PILC，经SO4^2-改性后，以浸渍法制备了铜基交联黏土催化剂Cu／A1-Ce-PILC，并将其应用于C3H6选择性催化还原NO的反应，350℃时NO转化率达到最大值56％，700℃时下降至22％．为探究催化剂高温失活的原因，采用XPS、TPR、TGA、Py-IR和DSC对反应前后催化剂的物化性能进行了表征．结果表明，经过H2预处理活化后活性组分Cu物种以Cu^＋形式存在，而高温反应后Cu物种除以Cu^＋和Cu^2＋ 2种形式存在外，还出现了少量CuO物种；高温反应过程中A1-Ce-PILC上结构羟基和SO4^2-流失导致催化剂表面酸性减弱；此外，还存在表面积炭覆盖了部分活性中心并堵塞了催化剂孔道的现象．这三者的共同影响促进了C3H6深度氧化，抑制了NO还原，从而导致催化剂的失活．     

Carbon isotope ratios in logged and unlogged boreal forests: Examination of the potential for determining wildlife habitat use

Due to assimilation of recycled CO₂ from litter decomposition and photosynthetic changes in carbon fractionation at low light levels, the foliage at the base of a forest is often more depleted in¹³C compared to that exposed to the atmosphere in either the canopy or in open clearings. This is referred to as the canopy effect. African research has indicated that these habitat differences in foliar ¹³C can be substantial enough to affect the carbon isotope ratios of resident fauna. Previous work documenting a 30-year chronology on moose teeth from Isle Royale National Park indicated a progressive depletion in¹³C and suggested that this could be due to forest regrowth following extensive burning. The present study examined the assumption implicit in this hypothesis that foliar ¹³C varies between open and closed boreal forest sites. I found a marginal canopy effect of 2 ¹³C difference between upper canopy and ground flora for a forest in northwestern Ontario and an average difference of 1.2 in under- and mid-story vegetation between closed forests and open clear-cuts. Because of these small differences, the utility of carbon isotope analysis in quantifying temporally integrated exploitation of deforested habitats will be low for northern boreal locations. In denser forests, such as those in the tropics or western North American where the canopy effect can be expected to be much greater, ¹³C analysis may still offer some promise for determining selection by wildlife of disturbed habitats.     

Synthesis and biodegradation of poly(γ-butyrolactone-co-l-lactide)

Biodegradable polyesters were synthesized by ring-opening copolymerization of -butyrolactone (BL) and its derivatives withl-lactide (LLA). Although tetraphenyl tin was the main catalyst used, other organometallic catalysts were used as well.¹H and¹³C NMR spectra showed that poly(BL-co-LLA)s were statistical and that their number-average molecular weights were as high as 7×10⁴. The maximum BL content obtained from copolymerization BL/LLA was around 17%. TheT _m andT _g values of the copolymers showed a gradual depression with an increase in BL content. NoT _m was obtained for the copolymers containing more than 13 mol% BL. The biodegradability of the copolyesters was evaluated by enzymatic hydrolysis and nonenzymatic hydrolysis tests. The enzymatic hydrolysis was carried out at 37°C for 24 h using lipases fromRhizopus arrhizus andR. delemar. Hydrolyses by both lipases showed that an increase in BL content of the copolymer resulted in enhanced biodegradability. Nonenzymatic accelerated hydrolysis of copolymers at 70°C was found to increase proportionally to their exposure time. The hydrolysis rate of these copolymers was considerably faster than that of PLLA. The higher hydrolyzability was recorded for the BL-rich copolymers. The copolymerization of -methyl--butyrolactone (MBL) or -ethyl--butyrolactone (EBL) with LLA resulted in relatively LA-rich copolymers.     

Enzymatic degradation of poly([R,S] β-hydroxybutyrate)

The synthetic analogue of a bacterially produced polyester, poly(-hydroxybutyrate) (PHB) was synthesized from racemic -butyrolactone using anin situ trimethyl aluminum-water catalyst. The polymer was fractionated into samples differing in molecular weight and isotactic diad content. The latter was closely related to degree of crystallinity. The biodegradation of these fractions were examined by monitoring mass loss over time in the presence of anAlcaligenes faecalis T1 extracellular bacterial poly(-hydroxybutyrate) depolymerase. The fraction with high isotactic diad tacticity content showed little or no degradation over a 50 hour incubation period, whereas the fraction of intermediate isotactic diad content degraded in a continuous steady fashion at a rate that was less than that for bacterial PHB. The low isotactic diad fraction underwent a rapid initial degradation, followed by no further mass loss. The presence of stereoblocks in the polymer structure of the various fractions was an influence on the degree of susceptibility towards degradation and is related to sample crystallinity.