The determination and matching analysis of pinch point temperature difference in evaporator and condenser of organic rankine cycle for mixed working fluid

Exergo-economic analysis of the pinch point temperature difference (PPTD) in both evaporator and condenser of sub-critical organic Rankine cycle system (ORCs) are performed based on the first and second laws of thermodynamics. Taking mixture R13I1/R601a as a working fluid and the annual total cost per net output power Z as exergo-economic performance evaluation criterion, the effects of PPTD in evaporator ΔT_e, and the PPTD ratio of condenser to evaporator y, on the exergo-economic performance of ORCs are analyzed. Moreover, how some other parameters influence the optimal PPTD in evaporator ΔT_e,opt and the optimal PPTD ratio of condenser to evaporator y_opt are also discussed. It has been found that the exergo-economic performance of ORCs is remarkably influenced by ΔT_e and y, and there exists ΔT_e,opt and y_opt. In addition, ΔT_e,opt and y_opt are affected by heat transfer coefficient ratio of condenser to evaporator ß, the temperature of working fluid at dew point in condenser T_1a, and composition of R13I1/R601a: larger ß and T_1a lead to lower ΔT_e,opt and y_opt; by contraries, larger mass fraction of R13I1 makes ΔT_e,opt and y_opt increase, and y_opt increases linearly. The effects of the temperature of working fluid at bubble point in evaporator T_3a, mass flow rate of exhaust flue gas m_g, and inlet temperature of exhaust flue gas T_gi on ΔT_e,opt and y_opt are very slight. For comparison, three additional working fluids, namely R601a, R245fa, and 0.32R245fa/0.68R601a, are also taken into account.     

Clam shell catalyst for continuous production of biodiesel

Continuous flow transesterification of waste frying oil (WFO) with methanol for the biodiesel production was tested in a laboratory scale jacketed reactive distillation (RD) unit packed with clam shell based CaO as solid catalyst. The physiochemical properties of the clam shell catalysts were characterized by X-ray Diffraction (XRD), Brunauer–Emmett–Teller (BET), Scanning Electron Microscopy (SEM), and Energy Dispersive Atomic X-ray Spectrometry (EDAX). The effects of the reactant flow rate, methanol-to-oil ratio, and catalyst bed height were studied to obtain the maximum methyl ester conversion. Reboiler temperature of 65°C was maintained throughout the process for product purification and the system reached the steady state at 7 hr. The experimental results revealed that the jacketed RD system packed with clam shell based CaO showed high catalytic activity for continuous production of biodiesel and a maximum methyl ester conversion of 94.41% was obtained at a reactant flow rate of 0.2 mL/min, methanol/oil ratio of 6:1, and catalyst bed height of 180 mm.     

煤炭资源耗减价值及其“利益共享、风险共担”补偿机制研究

煤炭行业清费建税,资源税从价计征引起了社会各界对资源税费制度改革的热议,而资源耗减价值是资源税费制度改革的重要依据之一。将资源回采率纳入使用者成本模型,科学计量了我国2000-2011年间煤炭资源的耗减价值。分析表明:2000-2011年间,4%折现率下煤炭资源耗减价值增加了22倍之多,而资源税费却仅仅增长了7倍,煤炭资源耗减价值与资源税费实际征收额之间存在有巨大缺口得不到补偿;国家资源所有者权益的实现度与煤炭经济形势呈逆向分布,煤炭工业利润率的上升并没有带来国家资源所有者权益的增加,导致这种错位的原因与我国不合理的资源税收机制有很大关系;资源税税率的理论区间为1.11%-8.85%,与国家规定的2%-10%高度重合,从而说明国家决策的合理性。为使资源所有者权益的实现度与煤炭工业经济形势相"挂钩",以资源税收入等于资源耗减价值为切入点,对资源所有者权益的实现度进行数理分析,求得了资源税税率与当期资源价格的关系,发现固定税率的资源税难以适应市场波动,于是提出"资源税+利润税"的组合税收工具,确定了利润税的起征点,计算得出了资源税和利润税的税率组合。该组合税制在一定程度上能够平抑经济周期对煤炭工业造成的影响,同时又维护国家资源所有者权益,从而实现国家与煤炭工业"利益共享、风险共担"。     

A method to estimate the impact of clear-cutting on nutrient concentrations in boreal headwater streams

Large-scale forestry operations, like clear-cutting, may impair surface water quality if not done with environmental considerations in mind. Catchment and country level estimates of nutrient loads from forestry are generally based on specific export values, i.e., changes in annual exports due to the implemented forestry operations expressed in kg ha⁻¹. We introduce here a specific concentration approach as a method to estimate the impact of clear-cutting on nutrient concentrations and export in headwater streams. This new method is potentially a more dynamic and flexible tool to estimate nutrient loads caused by forestry, because variation in annual runoff can be taken into account in load assessments. We combined water quality data from eight boreal headwater catchment pairs located in Finland and Sweden, where the effect of clear-cutting on stream water quality has been studied experimentally. Statistically significant specific concentration values could be produced for total nitrogen, nitrate, ammonium, and phosphate. The significant increases in the concentrations of these nutrients occurred between 2 and 6 years after clear-cutting. Significant specific concentration values could not be produced for total phosphorus and total organic carbon with the whole dataset, although in some single studies significant increases in their concentrations after clear-cutting were observed. The presented method enables taking into account variation in runoff, temporal dynamics of effects, and the proportional size of the treated area in load calculations. The number of existing studies considering large site-specific variation in responses to clear-cutting is small, and therefore further empirical studies are needed to improve predictive capabilities of the specific concentration values.     

快腐剂对畜禽粪便堆肥过程中腐熟度的影响

以牛粪、菌糠和鸡粪等为材料按照两种比例调配为混合基质,在添加或不添加快腐剂的条件下在发酵桶中进行为期38 d的堆肥发酵实验,通过对发酵产物的温度、p H值、总有机碳、C/N、硝铵态氮含量和种子发芽指数等指标变化的研究,揭示了快腐剂对发酵过程的影响。结果表明,虽然快腐剂对有机物料的温度、C/N比无显著的影响,但可以促进铵态氮向硝态氮的转化,在16 d时使发酵产物NH+4-N/NO-3-N比值降为0.15,达到腐熟标准(0.16);提升种子发芽指数,在腐解29 d时使种子发芽指数达到82.76%,达到完全腐熟指标(0.8),比不添加快腐剂的处理提前了4 d左右。快腐剂的作用效果受腐解物料配比的影响。     

Fe~(3+)和Cu~(2+)对饮用水氯消毒副产物三卤甲烷形成的影响

为了研究水中存在Br-的情况下,Fe3+和Cu2+对三卤甲烷(THMs)的生成及CHCl3、CHBr Cl2、CHBr2Cl、CHBr34种消毒副产物相对分布的影响,以腐殖酸模拟氯消毒过程中的前体物进行实验。结果表明,在p H为6、7和9 3种条件下,Fe3+抑制了THMs的生成,p H=6时只有CHCl3生成量随着Fe3+浓度的增加逐渐减少,其余3种消毒副产物均在增加,p H=7时4种消毒副产物浓度均减小并在Fe3+浓度为2 mg/L时生成量最低,p H=9时的生成趋势与p H=6时类似。Cu2+能促进THMs的生成,在p H为6、7和9时,当加入0.5 mg/L Cu2+时,THMs总量分别增加了16.7%、22.6%和2.5%,随着p H增加,THMs总量增加。在3种p H环境中,Cu2+对THMs生成的影响大于Fe3+,在偏酸性环境中,Fe3+影响THMs生成,产生的致癌风险高,当金属离子浓度为2.5 mg/L时,致癌风险相差最高为15%,在中性和偏碱性环境中,Cu2+影响THMs生成,产生的致癌风险高。     

一种新型铋基光催化剂的合成及其可见光催化性能

采用水热法合成铋基光催化剂Bi4VO8Br,通过X-射线粉末衍射、扫描电镜等手段对其进行表征.选择甲基橙为目标降解物来评价不同条件下合成的Bi4VO8Br在可见光下的光催化活性,发现pH 3、反应时间15 h、反应温度160℃为材料水热合成的最佳条件.考察了Bi4VO8Br在可见光及紫外光下对几种农药和增塑剂的光催化降解性能,显示了Bi4VO8Br对不易光解的含苯环有机物的可见光高活性.五氯酚的光催化过程影响因素优化结果表明,可见光和紫外光分别照射120 min和20 min,其降解率分别达到97％和99％,Bi4VO8Br表面上活性基团的捕获即空穴的氧化作用是主要反应原理.     

用生物滴滤床处理H2S和挥发性有机物混合废气

用生物滴滤床（BTF）处理某化工厂污水站的H2S和挥发性有机物（VOCs）混合废气,当废气中H2S质量浓度为120～400mg／m^3、VOCs质量浓度为115～340mg／m^时,运行稳定后H2S和VOCs的去除率为95％和85％。考察了影响BTF运行的循环水水质情况,试验结果表明：加入Na2CO3可使循环水pH控制在3～6;循环水中含盐量、Cl^-质量浓度和SO4^2-质量浓度分别为2200～3300,600～800,1200～1400mg／L,均未达到抑制微生物的水平。     

超声强化高级氧化技术降解水中有机污染物的研究进展

介绍了用于降解水中有机污染物的超声强化技术,分析了超声与臭氧氧化、Fenton试剂氧化和光催化氧化等高级氧化技术联用的机理,综述了这些联用技术在降解有机污染物方面的研究进展,并展望了超声强化高级氧化技术的发展前景。     

长江口区域水体半挥发性有机污染物健康风险评价

近年来长江口区域水体的有机物污染日渐严重.主要应用美国环境保护局(USEPA)的健康风险评价方法,并对其进行了一定的修改和补充,对长江口区域水体半挥发性有机污染物的健康风险进行了初步评价.结果表明:长江口区域水体半挥发性有机污染物的非致癌风险指数均小于1,其中单环芳香族类的非致癌风险值均在10-3数量级,卤代烃类的风险值在10-4数量级,均偏高于其他类物质;各类物质的致癌风险指数均在10-4数量级以下,其中六氯苯、双(2-氯乙基)醚和咔唑的风险指数相对较高,在10-5数量级.根据USEPA的建议值,初步认为目前长江口区域水体中单一半挥发性有机污染物不会对人体产生明显的健康危害.由于缺少相关的研究资料,因此各种有机污染物的联合健康效应评价尚无法进行.