餐厨垃圾发酵废液组分表征

餐厨垃圾发酵废液是在利用餐厨垃圾发酵产乙醇的过程中蒸馏后产生的废液。为研究分析餐厨垃圾发酵废液的组成成分,利用国家标准方法对其常规水质指标、无机离子进行了检测,并利用三维荧光光谱技术和固相萃取—GC/MS技术对其有机物组分进行了分析。结果表明:餐厨垃圾发酵废液为SS=1 000 mg/L,COD=60 000 mg/L的高悬浮物、高浓度有机废液,TN和TP含量分别为700 mg/L和180 mg/L,废液可生化性好;其金属阳离子和无机阴离子以Na+、Cl-为主,浓度分别为1 200 mg/L和2 200 mg/L;有机物组分以芳香族蛋白质类物质为主,约占有机物总量的80%;在可挥发性有机组分中,餐厨垃圾发酵废液中以酸类和醇类物质为主,易于生物降解,且有可回收利用价值。     

餐厨垃圾高温厌氧消化

在中试规模下,研究餐厨垃圾高温厌氧消化试验,通过监测餐厨垃圾厌氧消化过程中产气量、气体组成等产气情况和消化液中pH值、SCOD、NH4+-N、VFAs等化学指标含量变化,确定餐厨垃圾厌氧消化的最大有机负荷,并分析餐厨垃圾高温厌氧消化技术的可行性,结果表明,在工程上餐厨垃圾单独进行高温厌氧消化产甲烷具有技术可行性,但难以保证系统长时间安全稳定运行;餐厨垃圾厌氧消化正常运行时最大有机负荷可达2.551 kg VS/(m3.d);当系统有机负荷为2.551 kg VS/(m3.d)时,每天每千克VS最高可产生甲烷量0.622 m3;氨氮对餐厨垃圾厌氧消化产甲烷影响明显;餐厨垃圾中固有Na+含量对厌氧消化产甲烷影响不明显。     

我国餐厨垃圾厌氧处理技术现状分析及建议

随着我国餐厨垃圾排放量的持续增加,已造成严重的环境污染防控压力。为促进我国餐厨垃圾的资源化利用和无害化处理处置,在文献调研的基础上,梳理了我国大中型餐厨沼气工程的发展现状,分析了导致沼气产率低、沼气回用量大等餐厨沼气亟待解决的低经济效益难题的根本原因,并结合实际情况提出餐厨垃圾厌氧消化技术相关的建议,以期为我国提高餐厨垃圾的资源化、无害化处理能力和水平提供参考。     

脂肪酶强化餐厨垃圾厌氧产甲烷及其影响因素研究

油脂降解缓慢是影响餐厨垃圾厌氧发酵的重要原因。应用脂肪酶强化餐厨垃圾厌氧产甲烷,探究了脂肪酶投加量、温度和pH对产甲烷的影响。结果表明,脂肪酶能够促进餐厨垃圾厌氧发酵的水解和酸化,为产甲烷菌提供物质基质,还能提高脱氢酶的活性。脂肪酶最佳投加量为0.4g/L,最适温度为35℃,最适pH为7.0。     

酸化餐厨垃圾厌氧消化产氢研究

分析了餐厨垃圾酸化过程中的pH、挥发性脂肪酸(VFA)产量及含水量等参数的变化,考察了酸化餐厨垃圾厌氧消化过程中的产氢情况,并探讨了调节初始pH对酸化餐厨垃圾产氢的影响.结果表明,餐厨垃圾的酸化是一个前期极为快速的过程,经过1d的酸化,新鲜餐厨垃圾的pH就从6.0左右下降到4.5左右,而后pH缓慢下降,经过5～6 d的酸化,pH下降到4.0以下;餐厨垃圾酸化过程中,产生的VFA主要是异戊酸,其浓度变化与VFA的浓度变化趋势较为一致;酸化时间为1、3、4、5、6d的餐厨垃圾体系产生的氢气的最高体积分数呈递减趋势,产氢量也呈现出相同的变化趋势;初始pH对酸化餐厨垃圾体系的产氢影响是很大的,调节到相同初始pH的不同体系,产氢的结果可以相近.因此,pH是酸化餐厨垃圾厌氧消化产氢过程中必须控制的关键因素之一.     

烷基多苷对餐厨垃圾干式厌氧发酵的影响

近年来,餐厨垃圾厌氧发酵生产挥发性脂肪酸(VFA)得到广泛的研究,水解反应是餐厨垃圾厌氧发酵的限速步骤。利用生物表面活性剂——烷基多苷(APG)强化餐厨垃圾厌氧发酵生产VFA,考察了APG投加量对餐厨垃圾干式厌氧发酵的影响,分析了APG对餐厨垃圾厌氧发酵的强化机制。结果表明,APG的最佳投加量为0.5g/L,在此投加量下VFA的最大累积量为18.5g/L,VFA的转化率为38%;APG能够强化餐厨垃圾的水解反应,使溶解性蛋白质和溶解性多糖含量明显增加,为后续产酸细菌提供了更多的发酵基质。APG自身分解对VFA有一定贡献,但贡献量远远小于餐厨垃圾的产生量。     

竹叶与餐厨垃圾厌氧共消化工艺

将黄金竹和毛竹的竹叶分别与餐厨垃圾厌氧共消化,通过分析消化过程中的产气量、pH、COD、NH4+-N和VFAs变化,探讨添加不同竹叶对餐厨垃圾厌氧消化效果的影响.实验结果表明,添加毛竹叶显著增强了餐厨垃圾的厌氧消化能力.毛竹叶+餐厨垃圾组的总产气量是餐厨垃圾对照组单独厌氧消化总产气量的3.28倍,甲烷总产量为10.1 L,COD去除率高达83.0％.而添加黄金竹叶对餐厨垃圾厌氧消化的影响则不明显,可能因为黄金竹叶在消化过程中释放了大量挥发性脂肪酸(VFAs),造成体系酸中毒.     

茅草添加与温度变化对餐厨垃圾厌氧水解产酸的影响简

比较了茅草添加在温度变化条件下对餐厨垃圾厌氧水解过程小分子有机酸产量的影响，提出一种新型餐厨垃圾的资源化方式。研究结果显示，餐厨垃圾在55℃条件下厌氧水解主要产物为乳酸，达到25.7 g/L，其干物质转化率可以达到32.1% （g TS），而餐厨+茅草处理在同样条件下的乳酸产量为20.1 g/L，干物质转化率为25.1%。温度下降为37℃后继续进行的的厌氧水解，得到的主要产物是乙酸、丙酸和丁酸，餐厨处理和餐厨+茅草处理这两者的峰值分别为6.5、2.8、8.0和6.1 g/L、2.7 g/L和5.9 g/L。结果显示茅草添加可以在一定程度上调节水解产物的比例，而温度变化可以调控小分子有机酸的产量。本研究结果表明，厌氧水解是一种有潜力的小分子有机酸生产与餐厨垃圾资源化处理途径。     

餐厨垃圾厌氧发酵特性的研究

为了实现餐厨垃圾低成本现场能源化处理，利用单相法，采用正交试验法，研究了接种率、温度和含水率对餐厨垃圾厌氧发酵过程中运行特性的影响。结果表明，接种率、含水率、发酵温度以及它们之间的交互作用对餐厨垃圾产气效果影响显著，其中以接种率与温度的交互作用影响最为显著，其次是含水率。采用单相法进行55℃高温厌氧发酵，保证65%左右的接种率和90%以上的含水率，完全可以实现餐厨垃圾现场处理。     

含油量对餐厨垃圾厌氧发酵的影响

在35℃条件下，研究了不同含油量（0％、1％、2％、3％、4％、5％）餐厨垃圾中温厌氧消化过程中日产气量、甲烷含量、总固体（TS）、挥发性固体（VS）、干物质产气率等的变化，为后续餐厨垃圾连续发酵的预处理提供参考。结果表明：5％含油量餐厨厌氧发酵周期最长，累计产气量最大，为5800mL。在消化过程中，沼气中甲烷含量先上升后下降，最高可达76％；于物质产气率随含油量增大而增大，依次为497．4、506．1、543．8、554．4、590．7和600．1mL／gTS；5％含油餐厨垃圾的TS和VS去除率最大，分别为34．4％和42．9％。     

次氯酸钠发生器的研制

介绍了电解法生产次氯酸钠的原理 ,并在原有生产工艺的基础上进行了重新设计和对设备的重新选择、改造 ,得出了各个工艺参数的最佳值 ,生产出高品质的次氯酸钠     

An application of the theory of kinematics of mixing to the study of tropospheric dispersion

The most common technique used for numerical simulations of tracer mixing is that of the numerical solution of the advection–diffusion equation with the unresolved fluxes parameterized using the similarity theory. Despite correct predictions of the overall directions of transport, models based on a numerical solution of the advection–diffusion equation lack sufficient accuracy to correctly reproduce the coupling of mixing with small scale processes which are sensitive to the microstructure of the tracer distribution. The objective of this paper is to revisit the basic formalism employed in numerical models used to investigate atmospheric tracers. The main mathematical method proposed here is the theory of kinematics of mixing which could be applied effectively for simulations of atmospheric transport processes. At the beginning of the paper, we introduce simple mathematical transformations in order to demonstrate how complex topological structures are created by mixing processes. These idealistic flow systems are essential to explain transport properties of much more complex three-dimensional geophysical flows. An example of the application of the kinematics of mixing to the analysis of tracer transport on a planetary scale is presented in the following sections. The complex filamentary structures simulated in the numerical experiment are evaluated using some commonly applied statistical measures in order to compare the results with the data published in the literature. The results of the experiment are also analysed with the help of simple conceptual models of fluid filaments. The microstructure of the tracer distribution introduced in the paper is essential to increase our understanding of atmospheric transport and to develop more realistic parameterizations of small-scale mixing. The presented results could also be used to improve calculations of the coupling between microphysical processes and tracer mixing.     

Estimation of uncertainty of sampling for analysis of pesticide residues

Abstract

A computer model was used to take random samples from primary sample populations obtained from field trials to simulate the uncertainty of sampling for residue analysis of plant commodities and soil. The results indicate about 40%, 30% and 20% relative uncertainty when random samples of size 5, 10 and 25 are taken respectively, from a single lot. Therefore the sample size should be the same for establishing and enforcing legal limits.     

Evaluation of the presence of drugs of abuse in tap waters

A total of seventy samples of drinking water were tested for non-controlled and illicit drugs. Of these, 43 were from Spanish cities, 15 from seven other European countries, three from Japan and nine from seven different Latin American countries. The most frequently detected compounds were caffeine, nicotine, cotinine, cocaine and its metabolite benzoylecgonine, methadone and its metabolite EDDP. The mean concentrations of non-controlled drugs were: for caffeine 50 and 19 ng L⁻¹, in Spanish and worldwide drinking water respectively and for nicotine 13 and 19 ng L⁻¹. Illicit drugs were sparsely present and usually at ultratrace level (<1 ng L⁻¹). For example, cocaine has mean values of 0.4 (Spain) and 0.3 ng L⁻¹ (worldwide), whereas for benzoylecgonine, these mean values were 0.4 and 1.8 ng L⁻¹, respectively. Higher concentrations of benzoylecgonine were found in Latin American samples (up to 15 ng L⁻¹). No opiates were identified in any sample but the presence of methadone and EDDP was frequently detected. Total mean values for EDDP were 0.4 ng L⁻¹ (Spain) and 0.3 ng L⁻¹ (worldwide). Very few samples tested positive for amphetamines, in line with the reactivity of chlorine with these compounds. No cannabinoids, LSD, ketamine, fentanyl and PCP were detected.     

Mechanisms of biodegradation of dibenzoate plasticizers

Biodegradation mechanisms were elucidated for three dibenzoate plasticizers: diethylene glycol dibenzoate (D(EG)DB), dipropylene glycol dibenzoate (D(PG)DB), both of which are commercially available, and 1,6-hexanediol dibenzoate, a potential green plasticizer. Degradation studies were done using Rhodococcus rhodochrous in the presence of pure alkanes as a co-substrate. As expected, the first degradation step for all of these systems was the hydrolysis of one ester bond with the release of benzoic acid and a monoester. Subsequent biodegradation of the monobenzoates of diethylene glycol (D(EG)MB) and dipropylene glycol (D(PG)MB) was very slow, leading to significant accumulation of these monoesters. In contrast, 1,6-hexanediol monobenzoate was quickly degraded and characterization of the metabolites indicated that the biodegradation proceeded by way of the oxidation of the alcohol group to generate 6-(benzoyloxy) hexanoic acid followed by β-oxidation steps. This pathway was blocked for D(EG)MB and D(PG)MB by the presence of an ether function.The use of a pure hydrocarbon as a co-substrate resulted in the formation of another class of metabolites; namely the esters of the alcohols formed by the oxidation of the alkanes and the benzoic acid released by hydrolysis of the original diesters. These metabolites were biodegraded without the accumulation of any intermediates.     

混凝试验搅拌器的研制

影响混凝效果的因素众多,混凝沉淀烧杯试验是进行水的混合、絮凝、沉淀工艺研究、设计和生产指导的最有效方法之一,阐述了智能型混凝试验搅拌器的设计原理和技术性能.     

不同泥源对厌氧氨氧化反应器启动的影响

采用2套上流式生物膜反应器,分别接种少量厌氧氨氧化污泥和大量硝化污泥,考察其对厌氧氨氧化反应器启动的影响。污泥接种入反应器后,测得接种厌氧氨氧化污泥的反应器(R1)内MLSS为0.22 g/L,另一个反应器(R2)MLSS为2.7 g/L。与直接接种厌氧氨氧化污泥相比,R1经过72 d的运行才显现出厌氧氨氧化特性。经过114 d的培养,前者氮去除速率由0.23 kg/(m3.d)提升到5.29 kg/(m3.d),总氮去除率大于89%;R2的氮去除速率由0.01 kg/(m3.d)提升到1.1 kg/(m3.d),总氮去除率大于84.6%。说明普通污泥启动需要一个较长的筛选过程,直接接种少量的厌氧氨氧化污泥比接种普通的污泥能够更快启动厌氧氨氧化反应器。     

生物质快速热裂解主要参数对生物油产率的影响

以松木木屑为原料,在自制的小型流化床上,开展了生物质热裂解温度、生物质粒径和进料速率对生物油产率的影响实验研究.结果表明,在热裂解温度分别为450、475、500、525和550℃条件下,当热裂解温度为500℃时,生物油产率最高,平均产率达到53.33%（质量百分比）.反应温度越高,炭产量越低,不可冷凝气体产量越高,气体发热值越高;粒径＜1 mm的生物质其粒径对生物油产率影响不大;生物质进料速率增加时,生物油产率增加.本研究为生物能的利用提供了新的途径.     

生物质快速热裂解主要参数对生物油产率的影响

以松木木屑为原料,在自制的小型流化床上,开展了生物质热裂解温度、生物质粒径和进料速率对生物油产率的影响实验研究.结果表明,在热裂解温度分别为450、475、500、525和550℃条件下,当热裂解温度为500℃时,生物油产率最高,平均产率达到53.33%(质量百分比).反应温度越高,炭产量越低,不可冷凝气体产量越高,气体发热值越高;粒径＜1 mm的生物质其粒径对生物油产率影响不大;生物质进料速率增加时,生物油产率增加.本研究为生物能的利用提供了新的途径.     

Visualisation of the complexity of EUSES

The interdependencies of parameters applied in the models of EUSES are visualised in a directed connectivity graph. The parameters (inputs, defaults, state variables, outputs) are represented by boxes (nodes) and their relations by lines (edges). The visualisation, on the one hand, clarifies the complexity of the models in EUSES and, on the other hand, creates an overview and transparency. The parameters’ relations to each other can be recognised faster, and the models can be better understood. The complexity was quantified by the number (variety), kind (substance parameter, physico-chemical parameter, concentration, other parameters), and depth (dimension) of the parameter and the number of relations (connectivity). The variety of EUSES (without the modelsSimple Treat andSimple Box whose interior structure is not documented and without the effect and risk characterisation) amounts to 466, the connectivity to 961, and the maximal dimension is 21.