底物浓度对玉米秸秆乙醇发酵及残渣甲烷发酵的影响

为研究底物浓度对玉米秸秆乙醇发酵过程中乙醇产率和乙醇发酵剩余残渣厌氧发酵产气特性的影响,在中温(37±0.2)℃条件下,利用实验室自制小型厌氧发酵装置,在底物浓度为2%、3%、4%和5%下开展周期为50 d的序批式厌氧发酵实验,探索不同底物浓度下玉米秸秆发酵乙醇产率和乙醇发酵剩余残渣厌氧发酵产气特性。结果表明:底物浓度对玉米秸秆乙醇发酵影响显著,当底物浓度为3%时,玉米秸秆厌氧发酵乙醇产量最大,达到39.04 g;底物浓度过低或过高均不适合后期厌氧发酵产甲烷的进行,当底物浓度为3%时,玉米秸秆乙醇发酵残渣表面纤维结构被破坏最明显,残渣厌氧发酵产甲烷实验最早在3 d出现产气峰值,挥发性固体单位甲烷产量为26.82 mL·g~(-1),并且累积产气量最高,挥发性固体单位累积甲烷产量达到270.01 mL·g~(-1),玉米秸秆乙醇发酵残渣还有较高的产气潜能;通过质量平衡分析得到,底物浓度为3%时,玉米秸秆生物转化过程中TS和VS去除率最高,分别为59.12%和79.07%。该研究可为玉米秸秆乙醇发酵工程提供参考。     

汽爆秸秆高温固态发酵沼气的研究

沼气液态深层发酵及秸秆的物理、化学和生物预处理方式存在效率低、污染重等问题。为了解决这些问题,对蒸汽爆破预处理方式以及固态发酵在玉米秸秆沼气化中的应用进行了研究。秸秆经过蒸汽爆破预处理后,在50℃的高温条件下进行固态发酵沼气,甲烷产量达到138.2 mL/g TS。通过单因素实验优化,确定最佳发酵条件为：固液比1∶7,初始pH值7.5,接种量35%,NH₄HCO₃添加量0.04 g/g干汽爆秸秆,纤维素酶用量30 IU/g干汽爆秸秆,发酵温度50℃。在上述实验条件下,汽爆秸秆的甲烷产量提高至153.0 mL/g TS,是未汽爆秸秆的2.9倍。发酵后秸秆纤维素和半纤维素的降解率分别为59.86%和67.22%。因此,蒸汽爆破预处理有助于提高秸秆的产气量和降解率。高温固态发酵不仅可以缩短发酵延迟期,提高产气效率,而且发酵结束后不会产生大量废液,对环境友好。     

牛粪和玉米秸秆厌氧消化产甲烷潜力及动力学

为了评价牛粪和玉米秸秆的产甲烷潜力,研究其厌氧消化过程动力学方程,采用自制序批式厌氧发酵实验装置对某养殖场牛粪和秸秆的最大甲烷生产潜力及其发酵过程进行研究。通过实验研究,测得接种物、牛粪和玉米秸秆的累计甲烷产量分别为64.87、244.0和466.54 m L CH4/g VS。根据实测的产气量变化曲线,按照modified Gompertz equation模型进行方程拟合,牛粪组和玉米秸秆组拟合方程的相关性系数分别为0.983和0.991,表明运用modified Gompertz equation模型预测牛粪和玉米秸秆的产甲烷潜力方法可行。通过对产甲烷过程的动力学研究得到:接种物、牛粪和玉米秸秆的最大产甲烷潜力分别为66.07、213.93和458.57 m L CH4/g VS,与实测值的误差率分别为1.8%、12.3%和1.7%;牛粪和玉米秸秆的最大甲烷日产气率(Rm)和延滞期时间(λ)分别是13.14 m L CH4/(g VS·d)、30.76 m L CH4/(g VS·d)和0.35 d、0.71 d。综上,玉米秸秆厌氧消化的停滞期长,但总产气量和最大甲烷日产期率都比牛粪高。     

猪粪与玉米秸秆混合中温发酵产气效果

以猪粪及碱液预处理后的玉米秸秆为原料,在恒温35℃和料液总固体质量分数为5%的条件下,以实验室内培养的不产气厌氧活性污泥为接种物,研究猪粪与玉米秸秆不同配比(干物质比分别为1∶3、1∶2、1∶1、2∶1、3∶1和0∶1(单一猪粪))混合发酵对产气效果的影响。研究结果表明,在35℃条件下,猪粪与玉米秸秆以2∶1配比的累积产气量最大,为15 157 mL;其次是1∶1样品,累积产气量为15 088 mL。但甲烷产量最高为1∶1样品,56 d共产甲烷9 137 mL,甲烷气占总产气量的60.6%。通过对发酵过程中pH及COD的测定,证明经碱液预处理后的玉米秸秆能与猪粪混合稳定发酵,发酵前后厌氧消化液中COD的降解率可达50%以上。进一步研究分析得出,将玉米秸秆和猪粪按一定比例混合发酵不仅可以缩短发酵周期、提高产气速率,而且可以大幅提升原料的产气潜力。     

非混合接种对猪粪厌氧干发酵产气特性的影响

为达到缓解猪粪厌氧干发酵时有机酸的积累并能够同时提高产气性能的目的,采用小试批式实验,在中温(37℃)、总固体(TS)为20％的条件下研究了猪粪接种物全混合发酵、猪粪非混合接种发酵、猪粪玉米秸秆与接种物全混合发酵及猪粪玉米秸秆混合原料非混合接种发酵这4种方式对发酵体系的有机酸积累及产甲烷特性的影响.结果表明,猪粪接种物...     

单室双阳极微生物电解池利用氢发酵废水产氢

为提高微生物电解池(MEC)利用氢发酵废水产氢速率,以丁酸为底物在微生物燃料电池(MFC)中驯化富集阳极产电微生物,采用单室双阳极MEC处理玉米秸秆的氢发酵废水,通过对关键过程参数的优化,实现氢发酵废水高效产氢。结果表明,当外加电压为0.8 V时,产氢速率和玉米秸秆氢发酵废水中COD的去除率分别达到(5.31±0.13)m~3·(m~3·d)~(-1)和(58±2)%。其中,乙酸、丁酸、丙酸、乙醇的去除率分别达到(95±2)%、(76.2±0.8)%、(93±3)%、(98±1)%。与单室单阳极MEC相比,单室双阳极MEC利用玉米秸秆氢发酵废水进行深度产氢的速率提高了1.22倍。此外,MEC生物阳极驯化方式对MEC利用玉米秸秆氢发酵废水产氢具有重要影响。与利用乙酸为底物驯化富集的生物阳极相比,以丁酸为底物驯化富集的生物阳极去除COD的能力和MEC产氢速率都有提高。     

利用三七渣固态发酵灵芝菌的研究

以川芝6号为发酵菌种,对三七渣固态发酵灵芝菌的培养基制备条件进行了研究和优化。结果表明,优化的培养基制备条件为采用过60目筛的三七渣,酵母粉添加量5%(质量分数,下同),磷酸二氢钾添加量0.025%,培养基含水量70%,不调节初始pH。在此条件下进行灵芝发酵,发酵培养物中灵芝菌丝体的质量分数最高可达31.27%。     

纤维素酶添加时间对碱性双氧水预处理玉米秸秆高温厌氧消化的影响

研究了纤维素酶添加时间对玉米秸秆高温厌氧消化的影响。玉米秸秆首先进行碱性双氧水预处理,结果表明,预处理最佳条件为Na OH投加量4 g/L,H_2O_2投加量17 g/L,固液比1∶40,预处理时间4 h。预处理后的玉米秸秆在50℃下进行序批式高温厌氧消化,分别在发酵前期(第1天)、发酵中期(第10天)和发酵后期(第20天)向系统中添加15 m L(20 FPU/g)纤维素酶液。结果表明,添加纤维素酶能有效促进厌氧发酵过程中的生物质水解,对随后产酸产甲烷过程的直接影响较小。和对照组相比,发酵前期、中期和后期添加纤维素酶时系统的累积产气量分别提高18.66%、10.39%和1.93%,VS转化率分别提高13.51%、8.00%和2.90%。前期、中期和后期添加纤维素酶均能提高厌氧消化产气,但厌氧消化前期添加纤维素酶效果更为明显。     

温度和初始pH对农业固体废物暗发酵产氢的影响

以猪粪、鸡粪、玉米秸秆、餐厨垃圾和厨余垃圾等5种农业固体废物为底物,采用修正的Gompertz模型,研究了典型农业固体废物暗发酵产氢动力学和代谢产物变化规律,探讨了不同温度和初始pH条件下的主要产氢代谢途径。结果表明:温度和初始pH对农业固体废物暗发酵产氢具有显著影响;高温组累积产气量和氢气百分含量显著高于中温组。在55℃高温且pH为6.0的条件下,餐厨垃圾暗发酵产氢效果最佳,累积产气量和氢气百分含量最大,为1 100 mL和73.58%,最大产氢速率和产氢潜力分别为37.11 mL·h~(-1)和660.30 mL;厨余垃圾暗发酵产氢效果次之,鸡粪产氢潜力最差。在暗发酵产氢末期,以鸡粪为底物的代谢产物的氨氮浓度最高,过高的氨氮浓度可能抑制了产氢过程。VFA分析表明:不同底物和条件下丁酸浓度均最高,且含有少量乙醇、乙酸、丙酸等;暗发酵产氢代谢途径是以丁酸型发酵为主的混合型发酵。通过温度、初始pH等非生物性控制因素的优化调控,显著提高了农业固体废物暗发酵产氢潜力和底物利用效率,为生物制氢的技术研发与工程应用提供参考。     

调理剂和通风方式对污泥生物干化效果的影响

采用了自主设计的污泥生物干化实验室模拟系统,研究了调理剂、物料配比和通风方式等实验条件对脱水污泥生物干化的影响效果。研究结果表明,与锯末相比,秸秆有利于反应物料温度的上升,含水率下降程度更大;利用秸秆调节污泥初始含水率在60%和65%的实验条件下时,物料的平均含水率分别下降了7%和6%,当初始含水率65%时,生物堆体的温度和含水率没有明显的变化;与连续通风相比较,间歇通风的实验条件有利于生物堆体的温度的升高和干化效果;在该实验中,最佳的生物干化条件是以秸秆为调理剂,初始含水率调至65%以下,以间歇方式进行通风。     

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.     

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     

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.     

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。     

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.     

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     

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.     

产油微藻培养与回收的关键技术研究进展

寻找廉价而高效的替代原料是实现生物柴油产业化的关键所在.微藻以含油量高、生长周期短、环境适应能力强、生物产量高等优点,有望成为一种极具潜力的生物柴油生产原料.然而,目前尚存在微藻培养低效成本高和微藻回收效率低两大难题.综述了微藻培养与回收过程中的关键技术,并对存在的两大难题及其改进技术进行了详细的探讨.最后,总结并展望了微藻培养、回收技术未来的发展趋势.     

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.