GdFeO3上CO氧化的Redox机理动力学

ＧｄＦｅＯ３用柠檬酸络合制备。用ＸＲＤ测定ＧｄＦｅＯ３为钙钛矿结构。用ＣＯ还原脉冲及用Ｏ２再氧化脉冲证实在ＧｄＦｅＯ３上ＣＯ氧化为Ｒｅｄｏｘ机理。用外循环流动无梯度反应顺研究了ＣＯ氧化稳态动力学。用正交设计法估计动力学方程中的参数。还原催化剂再氧化为控制步骤。     

土地资源承载力若干问题浅析

本文就当前土地资源承载力研究中所遇到的若干问题,从土地资源承载力定义的理解、土地生产力的计算、单产预测、土地资源评价和土地利用结构调整等5个方面进行了探讨。 如何定义和理解土地资源人口承载力是进行这项研究的关键。以研究土地资源人口承载力为目的的土地资源评价是进行土地生产力计算和土地利用结构调整必不可少的基础。根据统计资料预测的作物单产,不能反映出土地生产力,而使用农业生态地带法计算作物单产目前也存在着一些问题。     

Influence of no-tillage on the distribution and lability of phosphorus in Finnish clay soils

No-tillage (NT) is a method adopted to reduce erosion and particulate phosphorus (P) load from arable land to watercourses. However, it has been found to increase the loss of dissolved P with surface runoff, but the reasons for that have rarely been examined in detail. The objective of the present study was to determine the chemical factors explaining this response by investigating the impact of NT on the type and distribution of P reserves as well as on organic carbon (C) in the 0–35 cm topsoil layer of clay soil profiles (Vertic Cambisols). Soil samples were taken from two experimental fields (Jokioinen and Aurajoki) at 0–5, 5–20 and 20–35 cm depths in conventionally tilled (CT) and non-tilled (for 4–5 years) plots. The plots had been cultivated and fertilized according to the common field practices in Finland (15–18 kg P and 100–128 kg N ha⁻¹ year⁻¹).Inorganic and organic P reserves characterized by a modified Chang and Jackson fractionation procedure were not significantly affected by the cultivation methods. However, in the uppermost soil layer (0–5 cm) in NT of the Jokioinen field, the labile P determined by water extraction (P_w) increased significantly, whereas the increase in P extracted with acid ammonium acetate (P_AAC) remained statistically insignificant. The increase in labile P coincided with a significant increase in organic carbon (C), which supports the theory that competition between organic anions and phosphate for the same sorption sites on oxide surfaces will enhance the lability of soil P. In the Aurajoki field with distinct soil cracking, P_w and P_AAC were not affected by NT in the uppermost soil layer, but they increased in the deepest soil layer (20–35 cm) concomitantly with an increase in Al-bound P and organic C. However, the increases were not statistically significant. In both fields, soil acidification due to the repeated application of N fertilizers at a shallow soil depth as well as the accumulation of organic C lowered pH of the uppermost soil layer in NT compared to the deeper soil layers. The results indicated that even short-term NT can increase the labile P in clay soil. However, further studies are needed to assess the long-term changes in lability of surface soil P and, consequently, the possible need for readjustment of the fertilization level in NT.     

沈阳市中水回用对策研究及前景分析

为了解决全市水资源严重短缺问题，缓解污水排放对生态环境造成的破坏，沈阳市在今后5～10a内将建成中水回用系统，使城市中水回用率达到50％。结合沈阳市中水回用现状，分析了目前全市中水供应能力及市场需求，进行了2010年相应指标的预测，同时探讨了沈阳市中水回用存在的问题和解决方法。     

高压脉冲电凝聚技术处理活性染料废水试验研究

难生物降解有机废水是废水处理的难点。阐述了高压脉冲电凝聚技术处理高浓度、难生物降解有机废水的最新机理。采用高压脉冲电凝聚技术处理活性染料（活性红）生产废水．研究了影响高压脉冲电凝聚技术处理活性染料废水效果的操作条件及影响因素．结果表明，在最佳处理工艺条件下。CODCr浓度12628mg／L的生产废水经处理后CODCr去除率为65％左右。再经后续混凝沉淀，最终出水CODCr可降低到1000mg／L以下。     

Comparison of UV-based advanced oxidation processes for the removal of different fractions of NOM from drinking water

This study examined the effectiveness for degradation of hydrophobic (HPO), transphilic (TPI) and hydrophilic (HPI) fractions of natural organic matter (NOM) during UV/H₂O₂, UV/TiO₂ and UV/K₂S₂O₈ (UV/PS) advanced oxidation processes (AOPs). The changing characteristics of NOM were evaluated by dissolved organic carbon (DOC), the specific UV absorbance (SUVA), trihalomethanes formation potential (THMFP), organic halogen adsorbable on activated carbon formation potential (AOXFP) and parallel factor analysis of excitation–emission matrices (PARAFAC-EEMs). In the three UV-based AOPs, HPI fraction with low molecular weight and aromaticity was more likely to degradate than HPO and TPI, and the removal efficiency of SUVA for HPO was much higher than TPI and HPI fraction. In terms of the specific THMFP of HPO, TPI and HPI, a reduction was achieved in the UV/H₂O₂ process, and the higest removal rate even reached to 83%. UV/TiO₂ and UV/PS processes can only decrease the specific THMFP of HPI. The specific AOXFP of HPO, TPI and HPI fractions were all able to be degraded by the three UV-based AOPs, and HPO content is more susceptible to decompose than TPI and HPI content. UV/H₂O₂ was found to be the most effective treatment for the removal of THMFP and AOXFP under given conditions. C1 (microbial or marine derived humic-like substances), C2 (terrestrially derived humic-like substances) and C3 (tryptophan-like proteins) fluorescent components of HPO fraction were fairly labile across the UV-based AOPs treatment. C3 of each fraction of NOM was the most resistant to degrade upon the UV-based AOPs. Results from this study may provide the prediction about the consequence of UV-based AOPs for the degradation of different fractions of NOM with varied characteristics.     

Catalytic oxidation effect of MnSO4 on As(III) by air in alkaline solution

The catalytic oxidation effect of MnSO₄ on As(III) by air in an alkaline solution was investigated. According to the X-ray diffraction (XRD), scanning electron microscope-energy dispersive spectrometer (SEM-EDS) and X-ray photoelectron spectroscopy (XPS) analysis results of the product, it was shown that the introduction of MnSO₄ in the form of solution would generate Na_0.55Mn₂O₄·1.5H₂O with strong catalytic oxidation ability in the aerobic alkaline solution, whereas the catalytic effect of the other product MnOOH is not satisfactory. Under the optimal reaction conditions of temperature 90°C, As/Mn molar ratio 12.74:1, air flow rate 1.0 L/min, and stirring speed 300 r/min, As(III) can be completely oxidized after 2 hr reaction. The excellent catalytic oxidation ability of MnSO₄ on As(III) was mainly attributed to the indirect oxidation of As(III) by the product Na_0.55Mn₂O₄·1.5H₂O. This study shows a convenient and efficient process for the oxidation of As(III) in alkali solutions, which has potential application value for the pre-oxidation of arsenic-containing solution or the detoxification of As(III).     

皮革和毛皮加工废水处理技术

采用混凝沉淀-酸化水解-悬挂链曝气-生物接触氧化组合工艺处理皮革和毛皮加工生产废水。实验结果表明;进水COD为2400mg/L,处理后出水COD≤100mg/L,去除率≥95.8%。各项水质指标均稳定地达到了GB8978-96污水综合排放一级标准。     

Promotional effect of cobalt doping on catalytic performance of cryptomelane-type manganese oxide in toluene oxidation

The cryptomelane-type manganese oxide (OMS-2)-supported Co (xCo/OMS-2; x = 5, 10, and 15 wt.%) catalysts were prepared via a pre-incorporation route. The as-prepared materials were used as catalysts for catalytic oxidation of toluene (2000 ppmV). Physical and chemical properties of the catalysts were measured using the X-ray diffraction (XRD), Fourier transform infrared spectroscopic (FT-IR), scanning electron microscopic (SEM), X-ray photoelectron spectroscopy (XPS), and hydrogen temperature-programmed reduction (H₂-TPR) techniques. Among all of the catalysts, 10Co/OMS-2 performed the best, with the T_90%, specific reaction rate at 245°C, and turnover frequency at 245°C (TOF_Co) being 245°C, 1.23 × 10⁻³ mol_toluene/(g_cat·sec), and 11.58 × 10⁻³ sec⁻¹ for toluene oxidation at a space velocity of 60,000 mL/(g·hr), respectively. The excellent catalytic performance of 10Co/OMS-2 were due to more oxygen vacancies, enhanced redox ability and oxygen mobility, and strong synergistic effect between Co species and OMS-2 support. Moreover, in the presence of poisoning gases CO₂, SO₂ or NH₃, the activity of 10Co/OMS-2 decreased for the carbonate, sulfate and ammonia species covered the active sites and oxygen vacancies, respectively. After the activation treatment, the catalytic activity was partly recovered. The good low-temperature reducibility of 10Co/OMS-2 could also facilitate the redox process accompanied by the consecutive electron transfer between the adsorbed O₂ and the cobalt or manganese ions. In the oxidation process of toluene, the benzoic and aldehydic intermediates were first generated, which were further oxidized to the benzoate intermediate that were eventually converted into H₂O and CO₂.     

接触氧化-电解工艺处理印染废水

主要介绍了采用生物接触氧化 电解工艺处理印染废水的设计及运行情况。处理系统运行结果表明 :当进水CODCr、BOD5和色度分别为 764 5mg L、2 63 7mg L和 42 0倍时 ,系统出水CODCr、BOD5和色度分别为 160 5mg L、48 9mg L和 12倍 ,去除率分别为 79%、81 5 %和 97 1%。该工艺运行稳定 ,操作控制方便