油菜秸秆直接液化为液体油工艺探讨

为了实现油菜秸秆的综合利用,将其在高温高压下催化液化制备液体油。结果表明:(1)油菜秸秆中的纤维素、半纤维素、木质素质量分数分别为25.45%、11.57%、28.73%,木质素最高,其次是纤维素。(2)油菜秸秆和残渣元素分析可知,液化反应前后油菜秸秆各元素含量无明显变化,热值(HHV)分别为10.58、10.47MJ/kg。(3)硫酸盐催化作用优于氯化物催化剂,硫酸铁和硫酸亚铁在中性反应溶剂条件下催化效果较佳,特别是在酮类反应溶剂中。在实验条件为固液比1.0∶19.3(油菜秸秆与混合溶剂的质量比)、反应时间4h、催化剂用量1%(质量分数)、丙酮作反应溶剂、硫酸铁作催化剂时,转化率可达47.106%。(4)预先将油菜秸秆浸泡在1%(质量分数)KOH溶液中12h,对生物质中纤维素、半纤维素和木质素有溶胀作用,能提高转化率。(5)通过热重(TG)/差热(DTG)曲线分析,残渣的燃烧反应性更好,活化能略低于油菜秸秆。     

NaOH预处理对玉米秸秆固态厌氧消化的影响

实验主要研究了NaOH预处理对玉米秸秆厌氧消化产气量和产气效率的影响。采用质量分数分别为1.0%、2.5%、5.0%和7.5%NaOH溶液对玉米秸秆进行24 h浸泡和未浸泡等预处理,测定其厌氧消化过程中各指标的变化。结果表明,经质量分数为5.0%NaOH浸泡24 h后,玉米秸秆木质素降解率最大,为38.67%;厌氧发酵累积产气量为226.75L/kg VS,与未经碱处理实验组相比提高了38.5%。该结果提示,5.0%NaOH溶液浸泡24 h后可使玉米秸秆厌氧消化的产气量和产气效率显著提高。     

NaOH预处理对杂交狼尾草厌氧发酵产沼气的影响

研究了Na OH预处理对杂交狼尾草厌氧消化制沼气的影响。采用质量分数分别为0%、2%、4%、6%和8%的Na OH溶液对杂交狼尾草进行碱预处理,在中温(35℃)、TS质量分数6%、接种率20%及初始p H为7.0条件下,进行厌氧发酵实验。对比了处理前后原料木质纤维素含量,探讨了不同浓度预处理对发酵过程沼气产量、甲烷浓度、p H以及产气速率的影响。结果表明,Na OH预处理有助于提高杂交狼尾草厌氧发酵的产气量和产气速率,其中4%Na OH预处理为较优条件。经4%Na OH溶液常温浸润24 h后,杂交狼尾草木质素降解率最大,比未处理实验组提高了31.2%;厌氧发酵总产气量比未处理实验组提高了31.6%。     

石灰预处理和干发酵对稻草热解特性影响

深入研究生物质热解有助于热解机理的理解,利用热重分析来探讨石灰预处理和干发酵对稻草热解特性的影响。结果表明:预处理使木质素和半纤维素含量增加,而干发酵使VS、半纤维素和纤维素含量降低;预处理和干发酵改变稻草热解特性,但未改变稻草的热反应机理;热解一级动力学方程很好模拟稻草热解的主失重阶段,稻草热解活化能数值为42.3～47.8 kJ/mol,属于正常范围;预处理降低反应活化能,而干发酵增加反应活化能。这为秸秆及其干发酵残渣的气化提供了重要的设计依据。     

氧化氨解预处理对稻草秸秆还田肥效的影响

采用氧化氨解方法预处理稻草秸秆,加速难降解物质的分解,同时提高产物氮含量,增加其腐殖化程度,从而实现稻草秸秆快速还田增肥。结果表明,经单因素实验和正交实验优化,氧化氨解预处理稻草秸秆的最佳条件为氨水(质量分数25%~28%)用量15.0mL、双氧水(质量分数30%)用量25.0 mL、反应时间150 min、初始固液比1g∶1 mL,产物全氮质量分数达到3.06%,黄腐酸质量分数达到0.32%。反应机理主要是双氧水和氨水与木质素及半纤维素发生反应,最主要的是氮元素嫁接到木质素中成为氨化木质素,在土壤微生物作用下缓慢释放有机氮。     

NaOH预处理对秸秆与蓝藻混合厌氧发酵产沼气的影响

以稻秸和蓝藻为原料,在实验室自制小型发酵装置内进行混合物料厌氧发酵实验,研究不同质量分数NaOH预处理对秸秆与蓝藻混合厌氧发酵产沼气的影响。结果表明,经过NaOH预处理后,稻秸组分被破坏,产气量较对照组有明显增加,发酵时间缩短。扫描电镜观察显示,经碱性预处理过的稻草秸秆孔隙度增大,机械组织暴露,酶解的有效比表面积增大,酶解速率加快。NaOH质量分数为6%的处理组产气效果最好,总产气量比对照组高出248%,且甲烷平均含量达到58.89%,预处理效果最为理想。     

腐秆剂对水稻秸秆腐解性能的影响

以水稻秸秆为代表性秸秆,研究了腐秆剂对秸秆腐解性能的影响。对秸秆中施用腐秆剂后各项基本指标(腐解率,C/N)进行测定,探索了不同时间、腐秆剂用量、p H、温度、含水量和尿素用量对秸秆腐解的影响。对腐解前后的秸秆进行了红外光谱(IR)分析。结果表明,秸秆在腐解25 d后速率趋于平缓;腐解的适宜p H为7.0、温度为30℃、含水量为80%、尿素用量和腐秆剂用量均为秸秆质量的1%,此条件下腐解25 d,腐解率可达40.73%。对比腐解前后秸秆的红外谱图发现,腐解后的秸秆中纤维素、木质素和半纤维素等碳水化合物发生分解,使羟基和亚甲基基团减少,同时也表明酚类化合物被氧化成醌类物质;秸秆中的蛋白质和氨基酸分解后生成酰胺类化合物、硝酸盐和铵盐。     

水稻与棉花秸秆不同预处理厌氧发酵产沼气

以猪粪为接种物,以棉花秸秆和水稻秸秆为发酵原料,分别对秸秆进行稀碱法预处理和稀碱法与超声波联合预处理,在发酵温度为(37±1)℃的条件下进行厌氧发酵产沼气的研究。结果表明,以联合预处理的秸秆为发酵原料,厌氧发酵的各项指标均比以稀碱预处理秸秆发酵的效果好,其中累积产气量和沼气中甲烷含量分别提高35.23%和2.4%,发酵后TS、VS含量相对减少2.6%～10.94%,发酵液代谢产物中的有机酸丙酮酸、乙酸和柠檬酸含量相对减少23.9%～25.9%、20.24%～24.53%和41.08%～45.91%。     

玉米芯水热预处理条件优化及木质素的结构表征

利用基于3因素3水平的Box-Behnken设计响应曲面实验,研究了添加干冰为辅助介质的水热预处理条件:预处理温度,预处理时间以及辅助介质添加量这3个因素以及这3个因素中两两交互作用对木质素含量的影响,并对水热预处理条件进行了优化。并采用13C固体核磁波谱(NMR)和红外(FT-IR)光谱分析了木质素的结构变化。根据方差分析,辅助介质添加量对木质素含量的影响最为显著,其次是预处理时间,预处理温度的影响最弱。以木质素含量最小为目标,根据二元回归方程预测出最佳的预处理条件为:温度180℃,时间90 min,0.47 g辅助介质添加量,在最优条件下,木质素含量预计为21.2%,脱除率达到31.6%。固体13C NMR和FTIR分析表明,在水热预处理过程中,木质素的致密结构遭到了破坏,木质素高聚体进行了解聚,产生了单体和低聚体。并且确定玉米芯中的木质素主要是紫丁香基型木质素和愈创木基型木质素。     

不同接种量的微生物秸秆腐熟剂对蔬菜副产物堆肥效果的影响

为了明确不同接种量的微生物秸秆腐熟剂对蔬菜副产物堆肥效果的影响,以玉米秸秆为调理剂,在调节初始物料含水率为63％和C/N为28的条件下,设置了B1(堆肥混合物+1％秸秆腐熟剂)、B2(堆肥混合物+3％秸秆腐熟剂)、B3(堆肥混合物+5％秸秆腐熟剂)和CK(堆肥混合物+3％灭菌惰性载体)4个处理,测定不同堆肥处理对温度、含水率、碳氮比(C/N)、半纤维素、纤维素、木质素、总养分含量、发芽指数等指标的影响.结果表明,蔬菜副产物堆肥接种微生物秸秆腐熟剂均能够使堆肥周期缩短,有效降低堆肥含水率,提高有机质的降解幅度,并且使堆肥中半纤维素、纤维素、木质素降解率分别提高1.03％、1.16％和1.47％;氮磷钾养分含量也比不接种处理平均提高0.48％.4个处理的总体堆肥效果表现为:B2＞B1 ＞B3＞CK.     

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.     

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。     

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.     

造纸废水混凝处理中SFT助凝替代性研究

中小造纸厂废水处理常用PAC作混凝剂 ,PAM作助凝剂。由于PAM成本很高 ,影响了处理设备的投运率。用超细滑石粉 (SFT)替代PAM助凝 ,与混凝剂PAC配合 ,其混凝处理效果基本相当 ,但是处理成本降低 0 .10元 /m3 。由于SFT属环境无害材料 ,不会给排泥带来二次污染     

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.     

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.