硫酸生产尾气的回收

我国中、小型硫酸生产中 ,仍有一些厂家采用一转一吸工艺流程 ,二氧化硫的转化率约为 90 %～95%。含 SO2 的炉气虽经转化吸收 ,排放尾气中 SO2的含量仍在 0 .4 %～ 0 .5% (质量分数 )。一家年产 4 .5万 t的硫酸厂 ,排放尾气中的 SO2 可达 540 0 t,既浪费资源 ,又污染环境。尾气的回收势在必行。目前 ,SO2 回收方法中应用较多的为氨酸法 ,但由于此法选用的设备结构及操作条件不尽合理 ,使尾气很难达到国家排放标准。我们采用氨酸法对某硫酸厂尾气的回收工艺条件及设备进行合理选择 ,不仅使尾气达到国家排放标准 ,同时生产出合格的液体 SO…     

用MnSO4作催化剂测定废水中的COD

介绍了用MnSO4代替Ag2SO4作催化剂定废水中COD的方法。该方法可降低分析成本,且使回流时间缩短为30min,方法的变异系数、回收率分别为0．65％和96．8％－100．8％。     

赖氨酸废水的处理和氨回收

对赖氨酸浓废水调 p H沉淀处理后的澄清水进行预处理 :先加入石灰乳 ,搅拌、沉淀 ,SO42 -从 2 0 0 0 0 m g/ L 左右降至 130 0 mg/ L 左右 ,去除率为 94%左右 ,然后进行空气吹脱 ,NH3- N从 5 0 0 0 mg/ L左右降至 80 m g/ L左右 ,去除率 >98%。吹脱出水经厌氧生化处理后 ,再进行空气吹脱 ,NH3- N从 70 0 mg/ L 左右降至 85 mg/ L 左右 ,去除率 >86 %。再吹脱出水与稀废水混合后进行好氧生化和 A/ O、O系统处理 ,出水的 COD<10 0 m g/ L,BOD5<2 0 mg/ L,SS<70 mg/ L,NH3- N<2 5 m g/ L。对浓废水与石灰乳混合后搅拌过程中及两次空气吹脱过程中挥发的 NH3进行回收 ,将其与 H2 SO4反应 ,生成的 (NH4) 2 SO4回用于生产     

可再生湿法烟气脱硫过程有机胺吸收液中硫酸根的测定

为了快速准确测定可再生湿法烟气脱硫过程有机胺吸收液中的p(SO2-4),建立了以茜素红为指示剂,用BaCl2直接滴定测定有机胺吸收液中p(SO2-4)的方法.实验结果表明:当试样pH为4.0 ～4.5时,方法的相对误差为0.28％-0.62％,加标回收率均在97％以上;SO2-3的存在会使p(SO2-4)的测定结果偏大...     

SO42-/TiO2-WO3光催化氧化邻硝基苯酚

研究了用H2SO4溶液浸渍处理TiO2-WO3，制备SO4^2-／TiO2-WO3催化剂的方法；考察了该催化剂对邻硝基苯酚的光催化氧化性能。TiO2-WO3的最佳处理工艺条件：H2SO4浓度为0．2mol/L，WO3加入量为3％，于550℃焙烧3h。实验结果表明，反应30min后SO4^2-／TiO2-WO3催化剂可使邻硝基苯酚降解97％；邻硝基苯酚的光催化氧化降解过程遵循一级动力学规律。     

环境友好固体超强酸SO2-4/Fe2O3 催化合成阿斯匹林的研究

制备固体超强酸SO2-4/Fe2O3,并测定其红外光谱,首次将其作为催化剂应用于合成阿斯匹林.考察了反应时间、反应温度、催化剂用量、酸醇摩尔比等对水杨酸酰化反应的影响.研究结果表明,最佳条件下收率可达88.8%.SO2-4/Fe2O3对合成阿斯匹林的反应具有良好的催化作用,是能代替浓硫酸作为水杨酸乙酰化的对环境友好的优良催化剂.     

磁性铁矿石对CO还原SO2的催化活性

采用磁性强弱不同的铁矿石以及制备的Fe3O4作为催化剂,催化CO还原SO2。实验结果表明:在3种催化剂中弱磁性铁矿石对CO还原SO2的催化活性最好;当反应温度为700℃时,在弱磁性铁矿石催化作用下的SO2转化率达84.3%。该方法既可以有效去除炼油厂催化裂化再生装置排放的SO2,同时又利用了低品位的磁性铁矿石,实现了SO2的治理和资源的综合利用。     

液膜分离法处理石灰法草浆纸厂废水

用乳状液膜法处理石灰法草浆纸厂废水,选择膜体系为T152-煤油-TOA-H2SO4.研究了膜体系的组成和工艺条件对COD去除率的影响.在试验条件下经一级处理COD去除率可达44%.采用低电压破乳,破乳后油相可重复使用.该方法具有处理成本低、无二次污染的优点.     

硫酸生产中废钒催化剂回收工艺研究

采用H2SO4浸取、NH4HSO3还原、NH4NO3氧化、KOH精制的方法回收废钒催化剂中的V2O5。实验结果表明,还原反应的最佳条件为：n（NH4HSO3）／n（V2O5）=1．10,还原反应温度90℃,还原反应时间2．0h。氧化反应的最佳条件为：n（KOH）／n（VO^＋）=1．10,氧化反应温度60℃,液固比8,氧化反应时间60min。该方法V2O5回收率达90．3％以上,V2O5纯度达82％以上。     

湿法烟气脱硫石膏制备硫酸铵

采用湿法烟气脱硫石膏为原料,与( NH4)2CO3反应,制备(NH4)2SO4.通过X射线衍射仪表征可知:脱硫石膏的主要成分为CaSO4,反应后CaSO4中的Ca2+大部分以CaCO3形式存在于固体沉淀物中,CaCO3粉末平均粒径为80 nm;而原先CaSO4中的不溶性SO2-4则与NH+4结合生成(NH4)2SO4,...     

紫外光谱结合正交试验设计同时测定水中苯系物

利用正交试验设计,以光谱预处理、特征筛选及多元校正方法为考察因素,每个因素的4种不同方法为水平,确定了水中3种苯系物（苯酚、苯胺及苯甲酸）紫外光谱数据的最佳分析方法,从而建立了其定量校正模型。对于苯酚、苯胺及苯甲酸,其光谱预处理、特征筛选及多元校正分别采用一阶导数+无信息变量消除法（UVE）+偏最小二乘回归（PLSR）,Savitzky-Golay平滑+变量结合种群分析法（VCPA）+PLSR,Savitzky-Golay平滑+移动窗口偏最小二乘法（MWPLS）+PLSR。在独立测试集上3组分的预测误差均方根（RMSEP）分别为0.809 4、0.796 3和0.945 4。水样加标回收实验的回收率为97.79%~103.84%,相对标准偏差（RSD）小于3%。该方法可作为一种同时测定水中苯系物的简便有效方法。     

固相微萃取—气相色谱法测定水中痕量硝基苯类化合物

建立了固相微萃取种类与气相色谱联用测定地下水中12种硝基苯类化合物的分析方法,对萃取头种类、萃取时间、萃取温度、进样口衬管种类等分析条件进行了优化。实验结果表明,该方法的检出限为0.001~0.050 μg/L,线性范围0.005~500 μg/L（相关系数大于0.997）,加标回收率为72.1%~122.0%,相对标准偏差为3.65%~12.60%。应用该方法对地下水及地表水样品进行分析,结果表明该方法具有环保、灵敏、快速、简便等特点,适用于水中痕量硝基苯、硝基甲苯类化合物和硝基氯苯类化合物的测定。     

Precision determination for the dynamic respirometric index (DRI) method used for biological stability evaluation on municipal solid waste and derived products

Dynamic respiration index (DRI) is an effective respirometric method to measure the biological stability of municipal solid waste (MSW). It allows testing MSW biological stability under standardized conditions and is now used as a routine analytical method. However, the method needs to be studied for precision parameters to ensure the quality of results generated.This work reports on a DRI validation study, detecting repeatability (r) and reproducibility limits (R). To perform the study, 4-6 Italian laboratories took part in an interlaboratory test for the validation of the DRI method on four different municipal solid wastes from different mechanical-biological treatment full-scale plants. Precision values (r and R) of DRI, expressed as relative standard deviation, were in the range of 3.6% and 15.5%, and were acceptable when compared with previous data obtained in another respirometric test. On the other hand, no regressions were found between r and R, and DRI, and as a consequence prediction of precision values was not possible a priori for different DRI levels, unless the same typology of waste was considered.     

Effects of equipment loadings on geosynthetic-lined slope behaviour.

When combined in the lining and covering of waste-containment facilities, soil and geosynthetic components protect the environment by acting as a hydraulic barrier. Equipment loading may significantly increase the tensile stress induced in geosynthetic components, leading to a potential stability problem. Large equipment loadings may also result in a localized circular slip surface during construction operations. New analytical method based on discrete element modelling is proposed for estimating the distribution of tensile force developed in the individual geosynthetic components of the lining system and for evaluating the safety factor of slope failure due to equipment loading. The analytical results of an example are presented to demonstrate the applicability of the analytical method for the lining system of a waste landfill. The analyses of the example show that equipment loading provide a substantial increase in the tensile forces of the geosynthetic components of a lining system and that the possibility of shallow failure due to equipment loading increases as the slope becomes steeper. This method is a useful tool for analysing the lining system of waste landfills with complex lining components.     

Monitoring of odor compounds produced by solid waste treatment plants with diffusive samplers

Nuisance caused by odors is one of the most important problems for waste management plants. To control an odor nuisance, it must first be quantified. The analytical difficulties in odor measurements are related to the high number of volatile components (belonging to several chemical classes), above all when the concentration is lower than the detection limit of the technique used for the measurement. In this work, 2-butanone, alpha-pinene, tetrachloroethylene, dimethyldisulfide, beta-pinene, limonene, phenol and benzoic acid are determined, because they are representative of some important classes of compounds with higher odor impact. The compounds are sampled with thermal desorbable radial diffusive samplers Radiello containing Tenax cartridges. The analytical repeatability and the complete thermal desorption of the cartridges were verified for each odor compound; the relative standard deviations for repeated samples and the recovery percentage were, respectively, less than 7% and about 97% for all compounds. The measurements of the linearity of sampling showed no systematic difference according to the collection period. The comparison between the odor threshold and the limit of detection demonstrated that this method is reliable for the recognition and quantification of odor compounds, allowing Public Administration to impose legal limits and the control agencies to verify them.     

Calculation of carbon balances for evaluation of the biodegradability of polymers

Establishing carbon balances has been proven to be an applicable and powerful tool in testing biodegradability of polymers. In controlled degradation tests at a 4-L scale with the model polymer poly(-hydroxybutyrate) (PHB), it was shown that the degree of degradation could not be determined with satisfactory accuracy from CO₂ release alone. Instead, the course of degradation was characterized by means of establishing carbon balances for the degradation of PHB withAcidovorax facilis and a mixed culture derived from compost. Different analytical methods for determining the different carbon fractions were adapted to the particular test conditions and compared. Quantitative determination of biomass and residual polymer were the main problems in establishing carbon balances. Amounts of biomass derived from protein measurements depend strongly on assumptions of the protein content of the biomass. Selective oxidation of biomass with hypochlorite was used as alternative, but here problems arose from insoluble metabolic products. Determination of soluble components with the method of chemical oxygen demand (COD) also includes empirical assumptions but seems acceptable if the dissolved carbon fraction is in the range of some 10% total carbon. Results confirm both analytical assays and theoretical approaches, in ending up at values very close to 100%, within an acceptable standard deviation range under test conditions comparable to standard test practice.Paper presented at the Bio/Environmentally Degradable Polymer Society—Third National Meeting, June 6–8, 1994, Boston, Massachusetts.     

Optimization for solidification of low-level-radioactive resin using Taguchi analysis

Solidification of low-level-radioactive (LLW) resin was optimized using Taguchi analytical methodology. The ingredients in LLW mortar which caused the solidification of cement were evaluated through consecutive measurements of the effects of various concentrations of ingredients. Samples selected according to Taguchi's method were separated into 18 different categories and measured at the 7th, 21st, and 28th day after fabrication on developing effects. Evaluations of the various samples focused on whether the compressive and bending strength fulfilled the special criteria of the Taiwan Power Company (TPC). Similar results indicated that both furnace slag and fly ash were the dominant material resulting from the solidification of LLW mortar. The superior combination was obtained as furnace slag 24 wt.%, fly ash 24 wt.%, and cement 8 wt.% to mix 24 wt.% of resin with 20 wt.% of water, to fulfill the contemporary requirements of TPC.     

The evaluation of an analytical protocol for the determination of substances in waste for hazard classification

The classification of waste as hazardous could soon be assessed in Europe using largely the hazard properties of its constituents, according to the the Classification, Labelling and Packaging (CLP) regulation. Comprehensive knowledge of the component constituents of a given waste will therefore be necessary. An analytical protocol for determining waste composition is proposed, which includes using inductively coupled plasma (ICP) screening methods to identify major elements and gas chromatography/mass spectrometry (GC–MS) screening techniques to measure organic compounds. The method includes a gross or indicator measure of ‘pools’ of higher molecular weight organic substances that are taken to be less bioactive and less hazardous, and of unresolved ‘mass’ during the chromatography of volatile and semi-volatile compounds. The concentration of some elements and specific compounds that are linked to specific hazard properties and are subject to specific regulation (examples include: heavy metals, chromium(VI), cyanides, organo-halogens, and PCBs) are determined by classical quantitative analysis. To check the consistency of the analysis, the sum of the concentrations (including unresolved ‘pools’) should give a mass balance between 90% and 110%. Thirty-two laboratory samples comprising different industrial wastes (liquids and solids) were tested by two routine service laboratories, to give circa 7000 parameter results. Despite discrepancies in some parameters, a satisfactory sum of estimated or measured concentrations (analytical balance) of 90% was reached for 20 samples (63% of the overall total) during this first test exercise, with identified reasons for most of the unsatisfactory results. Regular use of this protocol (which is now included in the French legislation) has enabled service laboratories to reach a 90% mass balance for nearly all the solid samples tested, and most of liquid samples (difficulties were caused in some samples from polymers in solution and vegetable oil). The protocol is submitted to French and European normalization bodies (AFNOR and CEN) and further improvements are awaited.     

模糊综合评价在焦化废水处理技术中的应用

采集某焦化厂废水处理系统的数据,选取当前常用的3种焦化废水处理技术和该焦化厂现用废水处理技术建立了较为完整的模糊综合评价数学模型,选择技术综合评价的评价因素集,利用判断矩阵分析法确定各评价因素的权重,建立了各定量因素指标的隶属函数,确定了各定性因素指标的模糊评语集,最后以模糊矩阵的合成运算完成模糊综合评价.4种焦化废水处理技术的综合性能优劣次序为:该焦化厂现用废水处理技术>普通活性污泥法>湿式催化氧化法>多相光催化氧化法.