东北地区农业现代化与新型城镇化协调发展研究

新型城镇化与农业现代化作为"三化"、"四化"乃至"五化"战略的重要核心内容,研究新型城镇化与农业现代化的协调发展对于开创中国未来城乡经济社会发展一体化的新格局至关重要。以东北三省34个地级城市为研究对象,构建农业现代化与新型城镇化的评价指标体系,结合熵值赋权、变异系数赋权的综合确权法测算城市农业现代化与新型城镇化的发展水平,基于耦合协调度模型探讨二者的耦合度与协调发展度,并划分其阶段类型,研究表明:(1)东北三省新型城镇化的发展水平排序:辽宁省吉林省黑龙江省,农业现代化的发展优势排序:黑龙江省辽宁省吉林省;辽宁与吉林省的新型城镇化发展速度超前于农业现代化,仅黑龙江省的新型城镇化发展滞后于农业现代化;(2)东北三省新型城镇化的高值区分布在以哈尔滨为核心的黑龙江省西南、以长春为核心的吉林省中部、以沈阳和大连为核心的辽宁省中部及南端,农业现代化的高值区分布在哈—大—齐—绥沿线的松嫩平原;沈阳、大连、哈尔滨、长春新型城镇化水平居于东北三省前列,哈尔滨、沈阳、齐齐哈尔、绥化农业现代化水平位于首位;(3)辽宁省新型城镇化与农业现代化的耦合协调发展度均强于黑龙江省,吉林省略低;耦合度高值区位于黑龙江省东北部的三江平原、辽宁省的沿海经济带,协调发展度高值区位于黑龙江省西南部的松嫩平原及以长春、沈阳、大连为核心的小范围圈层区域;仅哈尔滨与沈阳市处于勉强协调阶段,多数城市处于高强度、中高强度拮抗耦合与轻度、中度失调阶段。     

老垃圾填埋场渗滤液回灌工艺参数研究

根据理论分析,通过回灌能够实现对老垃圾填埋场所产生渗滤液的场内处理,改善渗滤液水质,同时能加速老填埋场的稳定化进程.以深圳市10座老垃圾填埋场为研究对象,提出渗滤液回灌工艺及其参数.回灌方式以水平渗沟为主,设置聚乙烯罐调节水量.渗滤液回灌加速了填埋气体产生速率,降低了有效应力,可能引起垃圾体边坡失稳.较大的渗滤液回灌量(1.6%)导致较低的垃圾边坡安全系数(1.96).确定满足加速垃圾稳定化和填埋场稳定性的最佳回灌量是填埋场渗滤液回灌大规模应用需要解决的重要问题.     

Influence of start-up on PCDD/F emission of incinerators

This study aims to evaluate the influence of start-up on polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans (PCDD/Fs) concentration in the stack flue gas of incinerators and its contributing PCDD/F emission. The PCDD/F emission of the first sample among three consecutive stack flue gas samples of five intermittent incinerators, which sampled at a stable combustion condition after start-up, is 2-3 times higher than the mean of the others. For verifying the PCDD/F characteristics of incinerators during start-up, one continuous MSWI was investigated for two years. The elevated PCDD/F emissions of the MSWI during start-up could reach 96.9 ng I-TEQN m(-3) and still maintained a high PCDD/F emission (40 times higher than the Taiwan emission limit) even 18 h after the injection of activated carbon, indicating the memory effect. Taking the MSWI for example, which consists of four incinerators, the estimated annual PCDD/F emission from normal operational conditions was 0.112 g I-TEQ. However, one start-up procedure can generate approximately 60% of the PCDD/F emissions for one whole year of normal operations. And the PCDD/F emission, which is the result of the start-ups of four incinerators, was at least two times larger than that of a whole year's normal operations, without consideration for the PCDD/F emission contributed by the long lasting memory effect.     

Remediation of soil contaminated with pyrene using ground nanoscale zero-valent iron

The sites contaminated with recalcitrant polycyclic aromatic hydrocarbons (PAHs) are serious environmental problems ubiquitously. Some PAHs have proven to be carcinogenic and hazardous. Therefore, the innovative PAH in situ remediation technologies have to be developed instantaneously. Recently, the nanoscale zero-valent iron (ZVI) particles have been successfully applied for dechlorination of organic pollutants in water, yet little research has investigated for the soil remediation so far. The objective in this work was to take advantage of nanoscale ZVI particles to remove PAHs in soil. The experimental factors such as reaction time, particle diameter and iron dosage and surface area were considered and optimized. From the results, both microscale and nanoscale ZVI were capable to remove the target compound. The higher removal efficiencies of nanoscale ZVI particles were obtained because the specific surface areas were about several dozens larger than that of commercially microscale ZVI particles. The optimal parameters were observed as 0.2 g iron/2 mL water in 60 min and 150 rpm by nanoscale ZVI. Additionally, the results proved that nanoscale ZVI particles are a promising technology for soil remediation and are encouraged in the near future environmental applications. Additionally, the empirical equation developed for pyrene removal efficiency provided the good explanation of reaction behavior. Ultimately, the calculated values by this equation were in a good agreement with the experimental data.     

Improving the activity of Mn/TiO2 catalysts through control of the pH and valence state of Mn during their preparation

In this study, the authors investigated the influence of the valence state of Mn on the efficacy of selective catalytic reduction using a Mn-based catalyst. The nitrogen oxides (NOx) conversion rate of the catalyst was found to be dependent on the type of TiO2 support employed and on the temperature, as the catalyst showed an excellent conversion of > 80% at a space velocity of 60,000 hr(-1) when the temperature was above 200 degrees C. Brunauer-Emmett-Teller, X-ray diffraction, and X-ray photoelectron spectroscopy analyses confirmed that catalyst displaying the highest activity contained the Mn4+ species and that its valence state was highly dependent on the pH during the catalyst preparation.