废醋酸锌催化剂回收醋酸锌工艺研究

对从废醋酸锌催化剂中浸取醋酸锌进行了实验研究,考察了废催化剂颗粒大小,浸取剂种类和用量、温度和浸取时间等因素对醋酸锌浸取率的影响。     

The influence of degree of substitution on blend miscibility and biodegradation of cellulose acetate blends

In this account, we report our findings on blends of cellulose acetate having a degree of substitution (DS) of 2.49 (CA2.5) with a cellulose acetate having a DS of 2.06 (CA2.0). This blend system was examined over the composition range of 0–100% CA2.0 employing both solvent casting of films (no plasticizer) and thermal processing (melt-compressed films and injection molding) using poly(ethylene glycol) as a common plasticizer. All thermally processed blends were optically clear and showed no loss in optical quality after storage for several months. Thermal analysis and measurement of physical properties indicate that blends in the middle composition range are partially miscible, while those at the ends of the composition range are miscible. We suggest that the miscibility of these cellulose acetate blends is influenced primarily by the monomer composition of the copolymers. Bench-scale simulated municipal composting confirmed the biodestructability of these blends and indicated that incorporation of a plasticizer accelerated the composting rates of the blends.In vitro aerobic biodegradation testing involving radiochemical labeling conclusively demonstrated that both the lower DS CA2.0 and the plasticizer significantly enhanced the biodegradation of the more highly substituted CA2.5.While this work was in progress, Robert Gardner was struck with cancer and died on June 6, 1995. This paper is dedicated to his memory and to his contributions as a friend and colleague.     

Ag~+改性复合钛铌酸钾盐对二甲基硫醚和乙硫醇吸附与光催化氧化研究

采用高温固相法合成具有不同Nb/Ti摩尔比的复合钛铌酸钾盐,通过Ag+离子交换对其进行改性。在静态下评价了Ag+改性复合钛铌酸钾盐对二甲基硫醚(DMS)和乙硫醇(EM)的吸附与紫外光催化氧化作用,使用红外光谱技术对催化剂表面滞留物种进行表征。结果表明,Ag+改性复合钛铌酸钾盐对DMS的吸附作用力比EM弱。随着Nb/Ti摩尔比增加,Ag+改性复合钛铌酸钾盐对EM的吸附作用力增强。在紫外光辐射下,Ag+改性的复合钛铌酸钾盐将DMS氧化为亚砜、砜和硫酸盐,而EM则被氧化为磺酸和单齿硫酸盐。     

系列混合碳源在EBPR系统颗粒化进程中的影响研究

在SBR反应器中接种富含聚磷菌的活性污泥,以一系列不同比例的丙酸与乙酸混合为碳源条件,进行了EBPR系统颗粒化培养,考察了混合碳源中丙酸所占质量分数(以COD质量浓度计)的提高对EBPR系统颗粒化进程中颗粒粒径生长、污泥沉降性能、系统除磷效率等宏观特性的影响规律.结果表明,EBPR系统污泥颗粒生长速率随碳源中丙酸所占质量分数的增加而提高;碳源中丙酸所占质量分数较高的反应器污泥SVI值相对较高.经90 d培养,碳源中丙酸所占质量分数分别为0%、25%、50%、75%及100%的系统中成熟颗粒体积平均粒径分别为550.64、599.41、642.38、680.99和745.08μm,污泥SVI值分别稳定在30、40、50、60及75 mL.g-1左右.在相同的磷处理负荷下,各试验系统除磷性能产生了显著性差异.0%、25%、50%、75%及100%丙酸碳源系统平均净除磷能力(以MLSS计)分别为0.78、2.29、2.96、3.23及3.77 mg.g-1,平均除磷效率分别为31.5%、56.5%、77.4%、85.9%及97.0%.     

Residual dynamics of thiacloprid in medical herbs marjoram, thyme, and camomile and in soil

Thiacloprid is a new insecticide of the chloronicotinyl family. To assess its risk after application, residual characteristics of thiacloprid in marjoram, thyme, and camomile and in soil were studied under field conditions. The active ingredient was extracted from the plant material using a mixture of acetone-water. After filtration, the extract was concentrated to the aqueous phase, diluted with water, and portioned against ethyl acetate on a matrix solid phase dispersion column. Thiacloprid was extracted from soil using a mixture of methanol-water, filtered, and re.extracted （clean up） with dichloromethane. The residues were quantified using HPLC-MS-MS. The methods were validated by recovery experiments. Thiacloprid residues in marjoram, thyme, and camomile and in soil persisted beyond 10, 14, 14, and 21 d but no residues were detected after 14, 21, 21, and 28 d, respectively. The data obtained in this study indicated that the biexponential model is more suitable than the first-order function to describe the decline of thiacloprid in fresh marjoram, fresh thyme, and dried camomile flowers with half-life （t1/2） of 1.1, 0.7, and 1.2 d, respectively. However, both the first-order function and biexponential model were found to be applicable for dissipation of thiacloprid in soil with almost the same t1/2 values of 3.5 and 3.6 d. The results indicated that thiacloprid dissipates rapidly and does not accumulate in the tested herbs and in soil.     

我国14个站点降水中甲酸和乙酸浓度及对酸性的贡献

为了较全面地掌握我国大气降水中有机酸含量及其对降水酸性的贡献,于2007年全年在我国14个区域代表性较好的站点采集了降水样品,利用离子交换色谱法分析了样品中的甲酸和乙酸2种重要有机酸的浓度,对所得各站数据进行了统计分析,计算了2种酸的湿沉降通量和对降水酸性的相对贡献.观测到的14个站点甲酸和乙酸平均浓度范围分别为0.96～3.43μmol/L和0～5.13μmol/L,接近国外偏远地区观测结果,也接近我国过去短期观测结果的低端值.比较显示,偏远地区有机酸含量低于城市附近地区.估算的甲酸和乙酸湿沉降通量范围分别为0.38～4.18mmol/(m2.a)和0.06～5.87mmol/(m2.a),南方站点有机酸湿沉降通量大于北方.有机酸对降水酸性的贡献范围是0.02%～51.6%,总平均贡献为2.95%,这一结果表明,虽然我国酸雨主要是硫、氮排放造成的,但有机酸在部分地区及部分时段甚至有很显著的致酸作用,应该成为酸雨观测研究内容之一.     

β-环糊精/醋酸纤维素纳米纤维的制备及对染料废水的处理

制备了不同β-环糊精(β-CD)含量的醋酸纤维素(CA)纳米纤维膜,并对纤维膜的结构形貌、尺寸分布、孔隙率、比表面积以及纤维膜的力学性能进行表征分析。随后研究了不同β-CD含量、初始浓度、吸附时间下,纳米纤维膜对甲基红染料的截留性能和吸附性能。结果表明:过量(≥30%)的β-环糊精会使纳米纤维产生珠节,纤维的形貌和力学性能变差;吸附试验表明,β-CD的加入提高了CA纳米纤维膜对染料的吸附,MR吸附率可达93.48%,最大平衡吸附量可达181.74 mg/g,比纯CA纳米纤维膜提高了将近40%;此外,染料的截留实验表明,纳米纤维膜对染料的截留效果较差,最大截留率为50.35%。     

电子供体对地下水中高氯酸盐生物去除的影响研究

通过静态实验,考察了电子供体类型及用量对厌氧条件下微生物去除地下水中高氯酸盐的影响.结果表明,电子供体醋酸盐和H₂的加入,可以明显提高ClO₄^-的去除率,驯化后的微生物去除ClO₄^-的速率比未加入电子供体时提高约1.4~3倍.Monod动态模型能很好地拟合两种电子供体环境下ClO₄^-的微生物去除过程,分别以醋酸盐和H₂作为电子供体时,基质半饱和常数K_s为12.6 mg·L^-1和2.2 mg·L^-1,最大比基质消耗速率V_m为0.45 d^-1和0.08 d^-1.动力学参数表明,本实验条件下,异养型混合菌去除ClO₄^-的效果明显优于自养型混合菌;在少数受高浓度ClO₄^-污染的地下水环境中,为了提高ClO₄^-的去除速率只有通过增加菌体浓度或提高微生物酶的活性来实现.随着电子供体醋酸盐用量增加,ClO₄^-的(比)消耗速率逐渐增大.当初始CH₃COO^-与ClO₄^-的比例为3.80 mg(COD)/mg(ClO₄^-)时,比消耗速率v最大(0.27 d^-1).     

气相色谱法测定大气中乙酸乙酯和甲基丙烯酸甲酯

建立了用气相色谱法测定大气中乙酸乙酯和甲基丙烯酸甲酯的方法。大气中乙酸乙酯和甲基丙烯酸甲酯活性炭吸附,二硫化碳解吸,DB-200毛细管柱分离,直接进样分析,氢火焰离子化检测器检测,时间定性,峰面积定量。本方法前处理简便,分离度好,分析灵敏度高,满足环境分析要求。     

Effects of metal and acidic sites on the reaction by-products of butyl acetate oxidation over palladium-based catalysts

Catalytic oxidation is widely used in pollution control technology to remove volatile organic compounds. In this study, Pd/ZSM-5 catalysts with different Pd contents and acidic sites were prepared via the impregnation method. All the catalysts were characterized by means of N2 adsorption- desorption, X-ray fluorescence （XRF）, HE temperature programmed reduction （H2-TPR）, and NH3 temperature programmed desorption （NH3-TPD）. Their catalytic performance was investigated in the oxidation of butyl acetate experiments. The by-products of the reaction were collected in thermal desorption tubes and identified by gas chromatography/mass spectrometry. It was found that the increase of Pd content slightly changed the catalytic activity of butyl acetate oxidation according to the yield of CO2 achieved at 90%, but decreased the cracking by-products, whereas the enhancement of strong acidity over Pd-based catalysts enriched the by-product species. The butyl acetate oxidation process involves a series of reaction steps including protolysis, dehydrogenation, dehydration, cracking, and isomerization. Generally, butyl acetate was cracked to acetic acid and 2- methylpropene and the latter was an intermediate of the other by-products, and the oxidation routes of typical by-products were proposed. Trace amounts of 3-methylpentane, hexane, 2-methylpentane, pentane, and 2-methylbutane originated from iso4merization and protolysis reactions.