162 resultados para SBR
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Cross-link density, microstructure and mechanical properties of styrene butadiene rubber (SBR) composites filled with different particle sized kaolinites are investigated. With the increase of kaolinite particle size, the cross-link density of the filled SBR composites, the dispersibility and orientation degree of kaolinite particles gradually decrease. Some big cracks in filled rubber composites are distributed along the fringe of kaolinite aggregates, and the absorbance of all the absorption bands of kaolinites gradually increase with the increase of kaolinite particle size. All mechanical property indexes of kaolinite filled SBR composites decrease due to the decrease of cross-linking and reduction of interface interaction between filler and rubber matrix.
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Ultrasonic degradation of commercially important polymers, styrene-butadiene (SBR) rubber, acrylonitrile-butadiene (NBR) rubber, styrene-acrylonitrile (SAN), polybutadiene rubber and polystyrene were investigated. The molecular weight distributions were measured using gel permeation chromatography (GPC). A model based on continuous distribution kinetics approach was used to study the time evolution of molecular weight distribution for these polymers during degradation. The effect of solvent properties and ultrasound intensity on the degradation of SBR rubber was investigated using different pure solvents and mixed solvents of varying volatility and different ultrasonic intensities. (C) 2011 Elsevier B.V. All rights reserved.
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The paper focuses on the use of oxygen and steam as the gasification agents in the thermochemical conversion of biomass to produce hydrogen rich syngas, using a downdraft reactor configuration. Performance of the reactor is evaluated for different equivalence ratios (ER), steam to biomass ratios (SBR) and moisture content in the fuel. The results are compared and evaluated with chemical equilibrium analysis and reaction kinetics along with the results available in the literature. Parametric study suggests that, with increase in SBR, hydrogen fraction in the syngas increases but necessitates an increase in the ER to maintain reactor temperature toward stable operating conditions. SBR is varied from 0.75 to 2.7 and ER from 0.18 to 0.3. The peak hydrogen yield is found to be 104g/kg of biomass at SBR of 2.7. Further, significant enhancement in H-2 yield and H-2 to CO ratio is observed at higher SBR (SBR=1.5-2.7) compared with lower range SBR (SBR=0.75-1.5). Experiments were conducted using wet wood chips to induce moisture into the reacting system and compare the performance with dry wood with steam. The results clearly indicate the both hydrogen generation and the gasification efficiency ((g)) are better in the latter case. With the increase in SBR, gasification efficiency ((g)) and lower heating value (LHV) tend to reduce. Gasification efficiency of 85.8% is reported with LHV of 8.9MJNm(-3) at SBR of 0.75 compared with 69.5% efficiency at SBR of 2.5 and lower LHV of 7.4 at MJNm(-3) at SBR of 2.7. These are argued on the basis of the energy required for steam generation and the extent of steam consumption during the reaction, which translates subsequently in the LHV of syngas. From the analysis of the results, it is evident that reaction kinetics plays a crucial role in the conversion process. The study also presents the importance of reaction kinetics, which controls the overall performance related to efficiency, H-2 yield, H-2 to CO fraction and LHV of syngas, and their dependence on the process parameters SBR and ER. Copyright (c) 2013 John Wiley & Sons, Ltd.
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Gasification is an energy transformation process in which solid fuel undergoes thermochemical conversion to produce gaseous fuel, and the two most important criteria involved in such process to evaluate the performance, economics and sustainability of the technology are: the total available energy (exergy) and the energy conserved (energy efficiency). Current study focuses on the energy and exergy analysis of the oxy-steam gasification and comparing with air gasification to optimize the H-2 yield, efficiency and syngas energy density. Casuarina wood is used as a fuel, and mixture of oxygen and steam in different proportion and amount is used as a gasifying media. The results are analysed with respect to varying equivalence ratio and steam to biomass ratio (SBR). Elemental mass balance technique is employed to ensure the validity of results. First and second law thermodynamic analysis is used towards time evaluation of energy and exergy analysis. Different component of energy input and output has been studied carefully to understand the influence of varying SBR on the availability of energy and irreversibility in the system to minimize the losses with change in input parameters for optimum performance. The energy and exergy losses (irreversibility) for oxy-steam gasification system are compared with the results of air gasification, and losses are found to be lower in oxy-steam thermal conversion; which has been argued and reasoned due to the presence of N-2 in the air-gasification. The maximum exergy efficiency of 85% with energy efficiency of 82% is achieved at SBR of 0.75 on the molar basis. It has been observed that increase in SBR results in lower exergy and energy efficiency, and it is argued to be due to the high energy input in steam generation and subsequent losses in the form of physical exergy of steam in the product gas, which alone accounts for over 18% in exergy input and 8.5% in exergy of product gas at SBR of 2.7. Carbon boundary point (CBP), is identified at the SBR of 1.5, and water gas shift (WGS) reaction plays a crucial role in H-2 enrichment after carbon boundary point (CBP) is reached. Effects of SBR and CBP on the H-2/CO ratio is analysed and discussed from the perspective of energy as well as the reaction chemistry. Energy density of syngas and energy efficiency is favoured at lower SBR but higher SBR favours H-2 rich gas at the expense of efficiency. Copyright (C) 2014, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
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We have developed a real-time imaging method for two-color wide-field fluorescence microscopy using a combined approach that integrates multi-spectral imaging and Bayesian image reconstruction technique. To enable simultaneous observation of two dyes (primary and secondary), we exploit their spectral properties that allow parallel recording in both the channels. The key advantage of this technique is the use of a single wavelength of light to excite both the primary dye and the secondary dye. The primary and secondary dyes respectively give rise to fluorescence and bleed-through signal, which after normalization were merged to obtain two-color 3D images. To realize real-time imaging, we employed maximum likelihood (ML) and maximum a posteriori (MAP) techniques on a high-performance computing platform (GPU). The results show two-fold improvement in contrast while the signal-to-background ratio (SBR) is improved by a factor of 4. We report a speed boost of 52 and 350 for 2D and 3D images respectively. Using this system, we have studied the real-time protein aggregation in yeast cells and HeLa cells that exhibits dot-like protein distribution. The proposed technique has the ability to temporally resolve rapidly occurring biological events.
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A partir da publicação, em 1994, de um relatório que afirmava que a presença de óleos aromáticos pesados, com altos teores de compostos policíclicos, em formulações de borrachas estaria relacionada ao desenvolvimento de doenças como o câncer, associado ao fato da crescente conscientização ambiental na fabricação de produtos elastoméricos, foi iniciado um estudo sobre a substituição do óleo aromático de origem do petróleo por óleos vegetais de menor risco. Nessa Dissertação de Mestrado foi proposta a substituição do óleo aromático derivado do petróleo por óleos vegetais como o de tungue, palma e linhaça, em composições de borracha natural (NR) contendo diferentes teores do copolímero de butadieno-estireno (0, 10 e 50 phr) e diferentes tipos de carga (negro de fumo N330 e negro de fumo N375). As composições obtidas foram avaliadas quanto a propriedades reométricas, mecânicas e fractográficas. Foi observado que não houve variação significativa na viscosidade Mooney, na resistência à tração, no alongamento na ruptura e na dureza Shore das composições de NR SBR1502 quando o óleo aromático foi substituído pelos óleos vegetais, quando diferentes negros de fumo foram utilizados como carga reforçante e quando foram utilizados teores crescentes de SBR1502. Por outro lado, a resistência ao rasgamento das composições de NR SBR1502 apresentaram melhores resultados quando o negro de fumo N375 foi utilizado. A adição de teores crescentes de SR 1502 levou à diminuição dos valores de rasgo. A natureza do óleo utilizado influenciou esse resultado e melhores valores foram obtidos com o óleo de tungue. Os resultados obtidos foram corroborados pela morfologia do material, avaliadas por microscopia eletrônica de varredura
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A hipotensão pós-exercício (HPE) é um fenômeno de relevância clínica, mas dúvidas persistem no tocante ao efeito do modo e da forma de execução (contínua vs. acumulada) do exercício aeróbio para sua manifestação, bem como o papel do controle autonômico cardíaco como mecanismo fisiológico associado à HPE. Assim, a presente tese objetivou: a) investigar a HPE induzida por sessões aeróbias de exercício isocalórico contínuo e acumulado; b) comparar as respostas de pressão arterial sistólica (PAS) e diastólica (PAD) após teste cardiopulmonar de exercício máximo (TCPE) em três modalidades; c) verificar a influência do modo de exercício e do controle autonômico cardíaco em repouso sobre a reativação vagal após TCPE. No primeiro estudo, 10 homens saudáveis (idade: 27,6 3,5 anos) realizaram TCPEs de corrida e ciclismo para medida do consumo de oxigênio de pico (VO2pico) e sessões contínuas (400 kcal) e acumuladas (2 x 200 kcal) de corrida e ciclismo à 75%VO2reserva. A PAS e PAD reduziram similarmente após exercício contínuo e acumulado (4,6 2,3 vs. 5,2 2,3 mmHg, 2,6 2,5 vs. 3,6 2,5 mmHg, respectivamente, P > 0,05). Porém, a corrida provocou maior declínio na PAS do que o ciclismo (P < 0.05). A atividade simpática (componente de baixa frequência, LF) e parassimpática (componente de alta frequência, HF) aumentou (P < 0,001) e diminuiu (P < 0,001) em relação à sessão controle, elevando o balanço simpato-vagal (razão LF:HF) (P < 0,001) que foi inversamente correlacionado ao ΔPAS e ΔPAD (r = -0,41 a -0,70; P < 0.05). No segundo e terceiro estudos, 20 homens saudáveis (idade: 21.2 3.0 anos) realizaram três TCPEs (ciclismo, caminhada e corrida). No segundo estudo, investigou-se a resposta aguda da PA, débito cardíaco (Q), resistência vascular periférica (RVP), sensibilidade do barorreflexo arterial (SBR), variabilidade da frequência cardíaca (VFC) e dispêndio energético durante 60 min após os TCPEs e sessão controle. Comparado ao controle, somente a corrida modalidade envolvendo maior dispêndio energético total (P < 0,001) - foi capaz de reduzir a PAS no pós-exercício (P < 0,001). Mudanças na RVP, SBR, LF, e razão LF:HF foram negativamente correlacionadas às variações na PAS (-0,69 a -0,91; P < 0,001) e PAD (-0,58 a -0,93; P ≤ 0,002). No terceiro estudo, examinou-se a reativação parassimpática após cada TCPE pela raiz quadrada da média do quadrado das diferenças entre intervalos R-R normais adjacentes em janelas de 30 s (rMSSD30s). Apesar da menor FCpico, VO2pico e dispêndio energético no ciclismo vs. caminhada e corrida (P < 0,001), a reativação parassimpática foi significativamente mais rápida após o ciclismo (P < 0,05). Outrossim, o Δ rMSSD30-180s foi positivamente correlacionado ao HF (rs = 0,90 a 0,93; P < 0,001) e negativamente correlacionado ao LF e a razão LF:HF medidos no repouso (rs = -0,73 a -0,79 e -0,86 a -0,90, respectivamente; P < 0,001). Em conclusão, a forma de execução do exercício aeróbio não interfere na magnitude da HPE, mas a HPE é dependente do modo ou o volume total de exercício. Os resultados também indicam que o padrão de recuperação do controle autonômico cardíaco pela análise espectral da VFC pode ter um papel importante na indução da HPE.
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A corrosão causada por H2S biogênico frequentemente resulta em danos extensos na indústria do petróleo. O presente trabalho avaliou parâmetros de crescimento microbiano e aplicou metodologias de determinação de sulfetos por técnicas espectrofotométrica na região da luz visível e radiorespirométrica para avaliação da atividade metabólica, correlacionando com a população de bactérias redutoras de sulfato, determinada através da técnica do Número Mais Provável (NMP). Amostras de água de formação e consórcio de BRS foram avaliadas através do arraste de sulfetos estáveis produzidos biogenicamente e quantificados por espectrofotometria. O cálculo das velocidades instantâneas e específicas de produção de sulfetos permitiu avaliar de que maneira alguns parâmetros de crescimento microbiano podem afetar o metabolismo das BRS. A detecção de concentrações traço de sulfetos biogênicos pode ser realizada através de ensaios radiorespirométricos. Para isto, diluições em série de água do mar sintética com três amostras distintas foram avaliadas. Os testes realizados indicam que o acréscimo do tempo de incubação de cultura microbiana anaeróbia mista contribuiu para o aumento das capacidades de redução de sulfato, assim como o aumento das fontes de carbono. Ambas as técnicas provaram ser um rápido teste para a detecção de sulfetos biogênicos, particularmente aqueles associados aos produtos de corrosão, sendo uma ferramenta muito útil para monitoração e controle de tanques de armazenamento de água e óleo, plataformas continentais de petróleo e diversos tipos de reservatórios. O presente trabalho prevê a continuidade dos experimentos, através de avaliação de um maior universo de amostras da indústria do petróleo e medições menos espaçadas da técnica espectrofotométrica, além da avaliação radiorespirométrica em modo contínuo, evitando os efeitos inibitórios do H2S
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To demonstrate the utility of distributional surveys for assessing relative abundance and trends in counts for a discrete area of coastline, aerial survey data from Sarasota County, Florida, USA, were analyzed for the years 1987 to 2006. The study area was divided into 3 regions: the Sarasota Bay Region (SBR; N = 353 surveys), Lemon Bay (N = 368), and the Myakka River (N = 209). Manatee counts varied significantly across seasons (p < 0.0001) for all 3 regions. Manatees within Sarasota County utilized open bays primarily in the warmer months. Such usage may have been influenced by resource availability. Conversely, usage of the Myakka River peaked in winter months when manatees seek warm-water refugia such as Warm Mineral Spring. Marginal means for yearly counts within Lemon Bay and the SBR increased significantly, beginning midway through the survey period (1996) until the early 2000s. In contrast, mean yearly counts within the Myakka River decreased over this time period. After record lows in 2003 for Lemon Bay and the Myakka River, and a considerable decline in 2004 for the SBR, mean yearly counts for all 3 regions showed an increasing trend over the remaining 2 yr of the study. Greater protection of manatee habitat and availability of forage coincided with the increase in numbers of manatees using Sarasota County waters during the 1990s, and the subsequent decline in numbers may be indicative of the increase in mortality in recent years due to watercraft collisions and severe red tide events.
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本文研究了低密度聚乙烯/乙烯、乙酸乙烯(LDPE/EVA),低密度聚乙烯/1,2—聚丁二烯(LDPE/1,2-PDB),乙丙橡胶/丁苯橡胶(EPR/SBR),以及聚偏氟乙烯/聚丙烯酸乙酯(PVF_2/PEA),聚氧化乙烯/聚乙酸乙烯酯(PEO/PVAc)五个共混体系的辐射关联反应情况。其中采用了机械共混、溶液共混两种方法制备了第一个共混体系,而后四个共混体系均只采用了溶液共混一种制备方法。首先,采用了电子显微镜以及DSC等方法,研究了以上五个共混体系组分间的相溶性。结果表明前三个共混体系属于多相聚合物共混体系。电子显微镜观察表明LDPE/1.2-PBD以及EPR/SBR两共混体系存在着明显的相分离现象,当LDPE含量为50%左右,EPR含量为30~50%时两共混体系均有相倒转发生。对于LDPE/1.2-PBD共混体系,共混样品的熔点虽然随加入1.2-PBD的量的增加而下降,但下降很小,不符合由热力学导出的表示相溶半晶聚合物共混体系熔点随组成变化的关系式:1/(φ1) (1/(Tm) - 1/(Tm)) = - (R V_(2u))/V_(1u) H_(2u))[(1/(u_2) - 1/(u_1)) + X_(12 φ_1]。而PVF_2/PEA、PEO/PVAc二共混体系相溶性明显提高。二共混体系结晶聚合物的溶点均随加入另一组分而急剧下降,由上式求得PVF_2/PEA、PEO/PVAc二共混体系的lory-Huggins相互作用参数X_(12)分别为:-0.28和-0.35。正是由于组分间有强烈的相互作用,至使以上二共混体系相溶性提高。LDPE/1.2-PDB和PVF_2/PEA二共混体系,在被r—射线照射击后,性能的变化情况很不一样。对于PVF_2/PEA共混体系在被r—射线照射后,我们首次发现共混样品用DSC测得的熔融峰由未照射时的一个分裂成照射后的两个。由此近似求得PVF_2/PEA共混体系中含有含PEA为19%及6%的两种结晶相。而LDPE/ 1。2-PBD共混体系组分间相溶性差,共混样熔融峰没有分裂现象,只是熔点随辐照剂量稍有下降。以上五个共混体系发生辐射交联后,其溶胶分数S与辐照剂量R的关系仍可用下式R(S + S~(1/2)) = 1/(q_oU_1) + (α_o)/(q_o)R~β表示。但发现,有些含有双链及分子链较柔顺的橡胶态单一聚合物(丁苯橡胶、PEA、1.2-PBD)的β值有极低的值(<0.5)。我们把此现象归因于以上这些聚合物发生辐射交联反应时有强化交联效应。对于共混样的β值—β_b值,与共混组分、组分间相溶性、及共混比例有并,实验结果表明以上关系可由下式近似表示。β_b = [(β_1 + (K'β_2 - β_1)φ_2]/[1 + (K' - 1)φ_2]式中,β_b为共混样的β值;β_1,β_2分别为组分1及2的β值;φ_2分别为组分1及2的体积分数;而K’值为一特征参数,它与共混体系性质有关。实验结果表明,共混体系组分间相溶性愈好,X_(12)值愈负,则K’值偏离1愈远。K’值表示了组分间参加反应时的协同效应。
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本论文主要包括以下三方面的工作:1. 傅立叶变换红外光谱法对含有特殊相互作用的高聚物共混体系的相容性及其他性质进行了研究。实验表明,在EVA/CPE(PVC)体系中,当两组分分子间处于互容的情况时,属于EVA的羰基伸缩振动频率向低频移动且谱峰加宽。利用这一光谱上的特征,可以表征出共混体系的相容性。得出,该体系的相容性与EVA中VA含量以及CPE中氯含量成正比。由升温实验还得出了EVA(VA:40%)/CPE(Cl:64%)共混体系的相图。运用同样的手段,考察了PcL/SAN体系的相容性。通过计算机分峰,得出PcL的羰基伸缩振动的结晶谱带和非晶变带。发现,随着SAN加入量的增多,上述PcL的非晶谱带ν_(c=o)向低频移动。说明该体系中PcL的非晶部分与SAN在室温下是相容的。FT-IR还用来研究了该体系中PcL的等温结晶过程。利用红外中的差谱技术,考察了PVF_2/PMMA共混体系的相容性。实验得出,当PMMA含量较高时,体系处于相容状态;而当PMMA含量较低时,由于体系中PVF_2 的结晶度较大,妨碍了PVF_2与PMMA分子的相互“混溶“,则为不相容状态。初步考察了涂膜法制备不同晶型PVF_2/PMMA样品的条件。2. 首次运用FT-IR法,对不含有特殊相互作用的高聚物共混体系(LLDPE/NR,LLDPE/SBR)的相容性进行了研究。发现,在这两个体系中皆发生相类似的光谱现象,即LLDPE的加入,使得分别属于NR和SBR的=CH-面外摇摆振动峰,强度增大,峰宽变窄。通过一系列实验证明,上述变化与PE中的非晶含量有关,得出LLDPE的非晶部分与NR或SBR分子间存在着一定程度的相互渗透。其他实验手段测得的结果支持了上述解释。3. 详细研究了LLDPE在LLDPE/SBR共混体系中的结晶动力学和熔融热力学过程。发现SBR的加入,对LLDPE的平衡熔点Tm°影响不大,晶体表面能略有增大。根据这实验现象,提出了该体系中LLDPE的晶体结构模型。实验表明,SBR的加入,还对共混体系中LLDPE的结晶度,微晶尺寸,球晶结构,片层结构等产生较大的影响。
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电感耦合等离子体发射光谱(ICP-AES)已有20多年的历史,经过20年来的发展,ICP-AES已成为世界各地分析化学实验室制备的分析手段之一。目前ICP-AES已经应用于生物样品、地质样品,合金等各种样品的分析中。虽然ICP-AES已成为溶液分析最理想、最有效的方法之一,但由于样品组成的复杂性,也使分析化学工作者面临着许多困难。如在钢铁及合金分析中,样品主成份的分析需准确度要好于1%,精密度≤0.3%,采用ICP-AES法的非内标法通常是达不到要求的。对于一些较纯的水溶液样品,一般可以采用简单的水样标准化,而含有复杂的、可变的基体成份就不适合于基体匹配。为了使冶金样品主成份分析的精度小于0.3%,准确度好于1%,我们将ICP摄谱法广泛应用的内标法应用到光电直读光谱仪中。内标法的作用达到了这一目的。使用内标法,就是要使内标元素能起到在等离子体激发过程中变动的补偿作用同时,还能起到在样品引入过程中,对样品喷雾量和提升率变动的补偿作用以提高分析方法精度和准确度。在初步的试验中,我们考察了28种元素谱线强度随等离子体操作参数变化的情况。(a)谱线强度与正向功率的关系;(b)谱线强度与观察高度的关系;(c)谱线强度与载气流速的关系。这样各元素在等离子体中的行为就因所给定的条件不同而异。根据上述28种元素在等离子体中的行为进行分类,为选择合适的内标元素奠定了基础。我们还对等离子体的正向功率、载气流量、观察高度、酸度等实验条件做了研究。发现,当各操作参数等主要条件改变时,谱线强度往往改变较大,但选择的内标元素谱线亦有类似的变化。因此,在采用内标法后,可以使这种变动得到一定的补偿,从而提高了分析结果的精度。本工作选用的折衷工作条件为:正向功率:1.30KW;载气流量:0.75 l/min; 观察高度:17 mm; 酸度:10% HNO_3(v/v)。研究了单一酸对分析元素谱线强度的影响。结果表明,单一酸的酸度在20%(v/v)以内,对分析元素与内标元素的谱线净强度的比值无影响。在折衷工作条件下,我们用合成水溶液体系研究了共存元素引起的物理干扰对分析元素谱线强度的影响。实验结果表明,随着试液中共存元素(Cu)浓度的增加,粘度明显增加,并导致提升量的急剧降低,谱线强度相应下降。但是当气溶胶导入量发生变化的时候,同时也引起内标元素和分析元素的原子或离子在等离子体中浓度分布的发迹内标元素与分析元素严格一致,可以较正共存元素引起的物理干扰。当共存元素达到一定的浓度时,由于内标元素与分析元素不严格一致,内标法失去作用。我们又考察了内标元素的浓度对分析元素的影响,内标元素的加入量从5~500μg/ml变化。当内标元素的浓度为200μg/ml时,对Mo, Ni, Pb, Ti及Mg略有影响,对其它元素无影响。我们选定内标元素的浓度为10 PPm。在折衷工作条件下,我们绘制了含有Y作内标的一套工作曲线及相应的不含Y的工作曲线,并分析了BMn40-1.5锰白铜样品。结果表明,当含量大于0.3%时,测定精度均低于0.3%,并得出以下结论:(1)各种元素在等离子体中的行为依测定条件而异,因此内标元素的选择最好是从在等离子体中行为相似的一组内选择。(2)在光电直流光谱仪中动用内标法可以提高样品中主成份元素的精度和准确度。(3)内标法在SBR较高的情况下可以起到较好的效果,但当SBR较小时,内标法就会失去作用。样品分解是样品分析的关键步骤。在现有的分解方法中,常用的有干灰化法和湿灰化法等。然而这些方法各有其缺点。因此,我们试图寻找一种快速的湿法消解技术,微波炉快速样品溶解似乎很具有吸引力。我们利用国产微波炉和全聚器氟乙烯密封溶器结合,系统地考查了微波炉溶解茶叶及茶树叶,利用ICP-AES测定的可行性,并与湿式消解法,加压密封法等进行了比较,获得满意结果。首先,我们选择了微波炉消化处理的最佳条件,确定了最佳溶解方案,已证明HNO_3-HF(5:1)混合酸溶解样品是令人满意的。又研究了微波炉加热对分析无素挥发性的影响。结果表明,微波炉加热与不经微波炉加热样品的浓度没有明显差异。按上述确定的工作条件,我们分析茶叶及茶树叶样品,并与不同的处理方法进行了比较。采用干灰化法处理茶叶(茶树叶)至少需8小时,而且还极易损失和沾污,但干灰化法用的酸量较少,空白较低,对Cr等的测定有利。湿法消解由于使用HClO_4-HF混酸,B大部分损失或完全挥发挥失。然而采用微波炉完全溶解样品只需19分钟即可,而且由于未使用HClO_4,样品溶液最后只需蒸至近干,有效地防止了易挥发元素的损失及某些不溶性高氯酸盐的生成。微波炉混合酸消酸系统是一种合适的溶解各种各样样品的技术,它为分解各种各样样品以进行多元素测定提供了一种快速、准确、经济的方法。该方法对于通常在敞口溶器中分解易于损失的挥发性元素特别有用,而且还特别适用于样品个数多,量少的生物样品等的微量元素的分析测定。
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本工作对几个不同类型的聚合物/聚合物共混体系-PS/SBR,EVA/CPE,PVF_2/PEMA和PMAA/PEO-的相容性和共混物中分子基团的相互作用进行了探讨和研究。主要结果有:(1)对不同PS分子量的PS/SBR聚合物共混体系进行了形态观察和Tg测量,结果表明共混物的相容性随PS组分的分子量、组成和温度变化。(2)用固体NMR测量进一步证实了EVA/CPE是分子之间均匀混合的相容共混体系。T_1值在测试温度范围内都符合自旋强相互作用偶合的加和式。(3)对PVF_2/PEMA共混体系进行了固体NMR研究,测量得到~1H的T_1和T_2随温度的变化曲线,用PC/MAS技术得到共混体系的高分辨~(13)C MNR谱,并从各个化学位移峰强对交叉极化接触时间的变化曲线拟合得到不同基团的~1H T_(1p)和T_(CH)。(4)用二维NMR技术通过质子自旋交换相互作用,考察了聚电解质与水溶性聚合物的共混物PMAA/PEO中各个化学基团之间的空间接近程度。
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根据石油废水的代表性目标污染物,从石油废水和污泥中分离、筛选到一大批有价值的微生物降解菌株,对降解菌株的降解特性、降解机理进行了研究。利用合成石油废水和洛阳石化石油废水分别进行了复合SBR工艺和脉冲SBR工艺实验室小试研究。同时对不同来源的石油废水分别进行了不同工艺的批式试验。通过试验研究得到以下结论:1.分离到一株以环已烷为唯一碳和能源的降解菌株LHGl、LHCl菌株能够利用环烷烃、环烷酮、链烃、芳烃和酚类。环已酮对LHGl菌株羟化酶具有特异诱导能力。GC/MS分析表明,LHGl菌株降解环已烷和环戊酮的代谢产物与已知途径代诱导产物不同。经质粒检测,在LHGl菌株中没有发现质粒。2.复合SBR工艺与脉冲SBR工艺对石油废水污染物的去除均具有很好的效果,两工艺均可获得较高的总氮去除效率。3.GC/MS分析表明,复合SBR工艺处理石油废水后,绝大部分污染物得到完全降解,出水中仅检出微生物部分代谢产物和微量难降解污染物。4.投加优势菌种后,能够提高SBR工艺对石油废水污染物的去除效率,能够正常处理含盐量达2.0%的石油废水。5.投加碳源能够显著提高SBR工艺对低浓度石油废水的污染物去除效率,增强微生物的活性,改善微生物的絮凝性能。
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OLAND两阶段生物脱氮系统是一项正在开发且极具应用前景的处理高氨氮、低COD废水的新技术。在实验室水平,对OLAND系统限氧亚硝化阶段MBR反应器和厌氧氨氧化阶段SBR反应器的启动和运行进行了系统研究。MBR反应器控制参数在DO0.1-0.3mg/L,pH7.8±0.1,温度30±0.5℃,SRT无穷大的条件下,可实现在较高的容积负荷By=IO00mgN/L,水力停留时间HRT:ld下稳定的亚硝酸型硝化,使NH4+-N和NO2-N的出水比例达到理想的比值(1:1.20±0.20),保证厌氧氨氧化阶段SBR反应器的理想进水;SBR反应器在完全厌氧、pH7.8-8.2,温度30±0.5℃,SRT无穷大的条件下,无需外加任何有机碳源,在较高总氮负荷550mgN/L下,可实现NH4+-N和NO2--N同时稳定的去除,二者的消耗比例为1:(1.21±0.05),总氮去除率高达92%。采用巢式PCR、DGGE、 FISH等分子技术对MBR反应器硝化菌群随溶解氧的动态变化规律和SBR反应器厌氧氨氧化菌群结构、组成进行了研究,并探讨了硝化菌群与氮素组成变化之间的内在联系。结果表明:在限氧亚硝化阶段硝化菌群中氨氧化菌受溶解氧浓度的影响较大,其种群结构从反应器启动初期到稳定后期发生了非常明显的变化。亚硝酸氧化菌NOB的种群组成受溶氧影响并不明显,从启动初期到稳定后期其种群结构无明显变化。硝化菌群中氨氧化菌 AOB与亚硝酸氧化菌NOB的数量比例关系随溶解氧的降低而不断升高,从最初的3.6:1升高到稳定后期的5.5:1。MBR反应器优势硝化菌群主要由A、B、C三类氨氧化菌和硝化杆菌D、硝化螺菌F组成,其中优势菌C为维持MBR反应器稳定出水比例的主要功能菌。硝化菌群组成和结构的变化,带来了不同N素之间组成和比例的规律性变化。厌氧氨氧化阶段基本由厌氧氨氧化菌AnAOB和ANAMMOX两类菌组成,二者空间结构紧密,在反应器中的活菌数量比例分别为55%和42%。厌氧氨氧化菌AnAOB种群多样性相对比较丰富,主要由条带I和H所代表的两种优势菌组成;ANAMMOX菌种群多样性变化较小,其种群主要由优势菌K和J组成。对MBR和SBR反应器中的优势菌进行了克隆、测序和系统发育学分析,结果表明:限氧亚硝化阶段MBR反应器启动初期的优势菌A属于Nitrosomonadaceae科,是否是一个新属,还有待于进一步鉴定。运行中期优势菌B与Nitroso)nonaseurooaea亲缘关系最近,同源性高达99.1%,暂命名为Nilrosomonas sp.BI。稳定后期优势菌C与Nitrosomonas eutroPha亲缘关系最近,同源性为96.3%,暂命名为Nifrosomonas sp.cl。硝化杆菌属优势菌D与Nitrobacter alkalicus、Nitrobacter hambllrgensts和Nitlobac招rwinograsky 亲缘关系较近,同源性分别为95.5-97%、96.5~97%和95.8~96.8%。SBR反应器中AnAOB优势菌I与MBR反应器优势菌B亲缘关系最近,同源性高达98.7%,与Nitlosomonas euroPaea同源性为98.3%。根据序列比较和生理特性分析,优势菌I与优势菌B应为Nitrosomonas属两个不同的种,暂将优势菌I命名为Nitrosomonas sp.II。优势菌H与MBR反应器优势菌C亲缘关系最近,同源性达97.9%,与Nitrosomonas eutropha同源性为96.3%。结合其生理特性分析,二者应为Nitrosomonas属两个不同的种,暂将优势菌H命名为Nitrosomollas sp.Hl。ANAMMox优势菌K与未培养的 Planctomycete和已鉴定的另一种ANAMMoX菌尤uenenia sf况ttgartiensis亲缘关系较近,同源性分别为99.8%和96.6%。优势菌J与Gen bank收录的所有菌的相似性均低于76%,说明该菌是OLAND系统厌氧氨氧化阶段比较独特的菌,是迄今为止在厌氧反应过程中未发现的一个新菌。