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A kinetic model for partial oxidation of ethane to acetic acid on promoted VPO catalyst 促进型VPO催化剂上乙烷部分氧化制乙酸的动力学模型
Pub Date : 2000-12-01 DOI: 10.1002/1097-4660(200012)75:12<1160::AID-JCTB330>3.0.CO;2-#
A. Fakeeha, Y. Fahmy, M. Soliman, Saeed M. Alwahabi
The partial oxidation of ethane to acetic acid on promoted VPO with Mo, using an Mo/V ratio of 0.2, has been investigated experimentally and theoretically. The reaction was carried out in a differential reactor at 1360 kPa, in the temperature range 548–623 K, with space times of 1.2–3.6 s and oxygen concentrations of 5–20%. The rate of oxidation of ethane was found to be approximately first order in ethane and zero order in oxygen at 548 K. At 623 K, the order of reaction with respect to ethane decreased to about 0.5, while that for oxygen increased to about 0.27. A kinetic model has been developed, which assumes that adsorbed oxygen reacts with ethane to form ethene, acetic acid, CO and CO2. Ethene is further oxidized to acetic acid, CO and CO2 through a redox mechanism. The model exhibits good agreement with the experimental data. © 2000 Society of Chemical Industry
在Mo/V比为0.2的条件下,对乙烷在促进的VPO上部分氧化生成乙酸进行了实验和理论研究。反应在差速反应器中进行,温度为1360 kPa,温度范围为548 ~ 623 K,反应时间为1.2 ~ 3.6 s,氧浓度为5 ~ 20%。在548 K时,乙烷的氧化速率近似为一级,氧的氧化速率为零级。在623 K时,乙烷的反应阶数下降到0.5左右,而氧的反应阶数上升到0.27左右。建立了吸附氧与乙烷反应生成乙烯、乙酸、CO和CO2的动力学模型。乙烯通过氧化还原机制进一步氧化为乙酸、CO和CO2。模型与实验数据吻合较好。©2000化学工业协会
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引用次数: 7
Fast detection of high molecular weight substances in wastewater based on an enzymatic hydrolysis combined with the Arxula BOD sensor system 基于酶解结合Arxula BOD传感器系统的废水中高分子量物质的快速检测
Pub Date : 2000-11-01 DOI: 10.1002/1097-4660(200011)75:11<1080::AID-JCTB311>3.0.CO;2-#
K. Tag, Alex W. K. Kwong, M. Lehmann, Chiyui Chan, R. Renneberg, K. Riedel, G. Kunze
A microbial amperometric sensor based on the yeast Arxula adeninivorans LS3 was tested for its suitability to measure the biochemical oxygen demand incurred by the use of high molecular weight substances, such as starch, cellulose and milk powder. As with other sensors, the untreated samples varied strongly from the corresponding BOD 5 . Digestion of macromolecules with α-amylase, cellulase and protease for 30min at 37°C resulted in sensor BOD values which correlated better with BOD 5 values when corrected for the enzyme blank signal.
以酵母菌Arxula adeninivorans LS3为原料,设计了一种微生物安培传感器,用于测定淀粉、纤维素和奶粉等高分子量物质的生化需氧量。与其他传感器一样,未经处理的样品与相应的BOD 5差异很大。α-淀粉酶、纤维素酶和蛋白酶在37℃条件下酶切30min得到的传感器BOD值与BOD 5值的相关性较好,校正了酶空白信号。
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引用次数: 13
Secretion of heterologous and native proteins, growth and morphology in batch cultures of Aspergillus niger B1‐D at varying agitation rates 不同搅拌速率下黑曲霉B1 - D分批培养中外源和原生蛋白的分泌、生长和形态
Pub Date : 1999-08-01 DOI: 10.1002/(SICI)1097-4660(199908)74:8<821::AID-JCTB114>3.0.CO;2-#
A. Wongwicharn, L. Harvey, B. McNeil
The influence of bioreactor operational conditions on the micromorphology of batch cultures of Aspergillus niger B1-D, containing a hen egg white lysozome (HEWL) marker protein, was examined using computerised image analysis. Significant differences in micromorphology were observed with increased stirrer speed, with shorter organisms with shorter hyphal elements occurring as agitation speed increased, even though mean tip numbers were similar. This may explain the observed increase in the total extracellular protein, since the ratio of synthetic (tip) to non-synthetic zones became increasingly favourable. HEWL concentrations fell above 500rpm, probably due to the effects of DOT (dissolved oxygen tension) on the glucoamylase HEWL fusion. HEWL was susceptible to proteolytic degradation, by native proteases, during the autolytic phase. Such insights may indicate why a gene from one mould expressed in a close relative can give production levels equivalent to levels of native enzymes, while secretion of a gene from a 'distant' source, eg a higher eukaryotic gene, occurs at much lower levels.
采用计算机图像分析技术,研究了生物反应器操作条件对含有蛋清溶酶体(HEWL)标记蛋白的黑曲霉B1-D批培养菌微观形态的影响。随着搅拌速度的增加,观察到微形态的显著差异,随着搅拌速度的增加,即使平均尖端数相似,也会出现更短的菌丝元素。这也许可以解释观察到的细胞外蛋白总量的增加,因为合成区(尖端)与非合成区的比例变得越来越有利。HEWL浓度下降到500rpm以上,可能是由于DOT(溶解氧张力)对葡萄糖淀粉酶HEWL融合的影响。在自溶阶段,HEWL易受天然蛋白酶的蛋白水解降解。这些见解可能表明,为什么在近亲中表达的来自一个霉菌的基因可以产生相当于天然酶水平的产量,而来自“遥远”来源的基因(例如高级真核基因)的分泌水平要低得多。
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引用次数: 20
Combined biological and chemical oxidation of ferrous sulfate using immobilised Thiobacillus ferrooxidans 固定化氧化亚铁硫杆菌生物化学联合氧化硫酸亚铁的研究
Pub Date : 1999-06-01 DOI: 10.1002/(SICI)1097-4660(199906)74:6<562::AID-JCTB75>3.0.CO;2-#
M. Nemati, C. Webb
Thiobacillus ferrooxidans immobilised in biomass support particles with activated carbon coating were used in a packed-bed bioreactor to study the combined effects of chemical and biological catalysis on the oxidation of ferrous iron. The effect of ferrous iron concentration (in the range 5–30 kg m−3) and of its volumetric loading on the kinetics of reaction were investigated. With low concentrations of ferrous iron, 5–10 kg m−3, the combined catalysis did not offer a significant advantage to oxidation of ferrous iron and the kinetics of reaction were slightly faster than those achieved with just the biological catalyst. With ferrous iron at a concentration of 20 kg m−3, the combination of chemical and biological catalysis resulted in a remarkable enhancement of the reaction rate. The maximum oxidation rate of ferrous iron in the presence of combined catalysts, 21.9 kg m−3 h−1, was twice as high as that achieved with just the biological catalyst. © 1999 Society of Chemical Industry
在填料床生物反应器中,采用活性炭包覆固定化在生物质载体颗粒中的氧化亚铁硫杆菌,研究了化学催化和生物催化对亚铁氧化的联合作用。研究了亚铁浓度(5-30 kg m−3)及其体积负荷对反应动力学的影响。在低浓度的亚铁(5-10 kg m−3)条件下,组合催化剂对亚铁的氧化没有明显的优势,反应动力学比单独使用生物催化剂的反应略快。当铁的浓度为20 kg m−3时,化学和生物联合催化可显著提高反应速率。复合催化剂作用下亚铁的最大氧化速率为21.9 kg m−3 h−1,是单纯生物催化剂作用下氧化速率的两倍。©1999化学工业学会
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引用次数: 19
Removal of toxic metals from aqueous mixtures. Part 1: Biosorption 从含水混合物中去除有毒金属。第一部分:生物吸附
Pub Date : 1999-05-01 DOI: 10.1002/(SICI)1097-4660(199905)74:5<429::AID-JCTB62>3.0.CO;2-#
A. Zouboulis, E. Rousou, K. A. Matis, I. Hancock
The biosorption of toxic metals from an aqueous mixture containing zinc, copper and nickel, in the presence of calcium and sodium ions (usual co-existing cations in related systems) has been investigated. Industrial biomass samples of different origin have been examined batchwise as effective sorbents, including bacteria (Streptomyces rimosus), fungi (Penicillium chrysogenum) and yeasts (Saccharomyces carlsbergensis and Saccharomyces cerevisiae). The effect of solution pH was evaluated in the range of 3–11.5. Selectivity was observed, particularly for the removal of copper. The observed removal of metals by the application of biosorption was also compared in laboratory experiments with other more conventional separation techniques (filtration, centrifugation and flotation). © 1999 Society of Chemical Industry
研究了在钙和钠离子(相关体系中通常共存的阳离子)存在下,从含锌、铜和镍的水溶液中吸附有毒金属的情况。不同来源的工业生物质样品作为有效吸附剂进行了批量检测,包括细菌(链霉菌)、真菌(青霉菌)和酵母(卡尔斯伯根酿酒酵母和酿酒酵母)。在3-11.5范围内评价溶液pH的影响。观察到选择性,特别是对铜的去除。在实验室实验中,还将生物吸附法对金属的去除效果与其他更传统的分离技术(过滤、离心和浮选)进行了比较。©1999化学工业学会
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引用次数: 87
Simulation and optimisation of integrated bioprocesses: a case study 综合生物过程的模拟和优化:一个案例研究
Pub Date : 1999-03-01 DOI: 10.1002/(SICI)1097-4660(199903)74:3<289::AID-JCTB26>3.0.CO;2-#
Yuhong Zhou, N. Titchener-Hooker
Biotech companies need to reduce time to market and to raise the efficiency of processing in order to lower costs. This paper presents results of the application of computer-based simulations for the rapid formulation of integrated bioprocesses designs and demonstrates the use of simulations to explore the nature and impact of the interactions that exist in a typical bioprocess. An approach for the optimisation of such integrated bioprocesses is presented. Data from a continuous fermentation, with models for cell harvesting, cell disruption and cell debris removal, verified by comparison with pilot-scale data, have been integrated and used to demonstrate the consequences of different process designs and operating decisions on the resulting process performance.
生物技术公司需要缩短上市时间,提高加工效率,以降低成本。本文介绍了基于计算机的模拟在快速制定综合生物过程设计中的应用结果,并演示了如何使用模拟来探索典型生物过程中存在的相互作用的性质和影响。提出了一种优化这种综合生物过程的方法。通过与中试规模数据的比较验证,来自连续发酵的数据,以及细胞收获、细胞破坏和细胞碎片去除的模型,已被整合并用于演示不同工艺设计和操作决策对最终工艺性能的影响。
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引用次数: 13
Simultaneous oxidative conversion and CO2 or steam reforming of methane to syngas over CoO–NiO–MgO catalyst 甲烷在co - nio - mgo催化剂上的同步氧化转化和CO2或蒸汽重整制合成气
Pub Date : 1998-12-01 DOI: 10.1002/(SICI)1097-4660(199812)73:4<345::AID-JCTB961>3.0.CO;2-#
V. Choudhary, A. S. Mamman
CO2 reforming, oxidative conversion and simultaneous oxidative conversion and CO2 or steam reforming of methane to syngas (CO and H2) over NiO–CoO–MgO (Co: Ni: Mg=0·5: 0·5:1·0) solid solution at 700–850°C and high space velocity (5·1×105 cm3 g−1 h−1 for oxidative conversion and 4·5×104 cm3 g−1 h−1 for oxy-steam or oxy-CO2 reforming) for different CH4/O2 (1·8–8·0) and CH4/CO2 or H2O (1·5–8·4) ratios have been thoroughly investigated. Because of the replacement of 50 mol% of the NiO by CoO in NiO–MgO (Ni/Mg=1·0), the performance of the catalyst in the methane to syngas conversion process is improved; the carbon formation on the catalyst is drastically reduced. The CoO–NiO–MgO catalyst shows high methane conversion activity (methane conversion >80%) and high selectivity for both CO and H2 in the oxy-CO2 reforming and oxy-steam reforming processes at ⩾800°C. The oxy-steam or CO2 reforming process involves the coupling of the exothermic oxidative conversion and endothermic CO2 or steam reforming reactions, making these processes highly energy efficient and also safe to operate. These processes can be made thermoneutral or mildly exothermic or mildly endothermic by manipulating the process conditions (viz. temperature and/or CH4/O2 ratio in the feed). © 1998 Society of Chemistry Industry
研究了不同CH4/O2(1·8-8·0)和CH4/CO2或H2O(1·5 - 8·4)比下,在700-850℃、高空速(氧化转化为5·1×105 cm3 g - 1 h - 1,氧-蒸汽或氧-CO2转化为4·5×104 cm3 g - 1 h - 1)条件下,在nio - cooo - mgo (CO: Ni: Mg=0·5:0·5·1·0)固溶体上,甲烷转化为合成气(CO和H2)的CO2重整、氧化转化和同时氧化转化和CO2或蒸汽重整为CO2或蒸汽重整为CO2和H2。在NiO - mgo (Ni/Mg=1·0)中,CoO取代了50 mol%的NiO,提高了催化剂在甲烷制合成气过程中的性能;催化剂上的碳生成量大大减少。CO - nio - mgo催化剂在小于或等于800°C的氧- co2重整和氧-蒸汽重整过程中显示出高甲烷转化活性(甲烷转化bbb80 %)和CO和H2的高选择性。氧蒸汽或CO2重整过程涉及到放热氧化转化和吸热CO2或蒸汽重整反应的耦合,使这些过程非常节能且操作安全。这些过程可以通过控制工艺条件(即进料中的温度和/或CH4/O2比)来实现热中性或轻度放热或轻度吸热。©1998化学工业学会
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引用次数: 52
Enzyme flow microcalorimetry—a useful tool for screening of immobilized penicillin G acylase 酶流动微量热法——一种筛选固定化青霉素G酰化酶的有效工具
Pub Date : 1998-09-01 DOI: 10.1002/(SICI)1097-4660(199809)73:1<31::AID-JCTB930>3.0.CO;2-#
A. Vikartovská-Welwardová, E. Michálková, P. Gemeiner
Screening of a representative series of immobilized penicillin G acylase biocatalysts (enzyme, cells) using enzyme Now microcalorimetry is described. Immobilized penicillin G acylase biocatalysts were either prepared in the labor- atory by various techniques or obtained from four commercial manufacturers. An industrial strain of Escherichia coli was entrapped in (poly)acrylamide gel or hardened calcium pectate gel. Semi-puri-ed enzyme was immobilized in various waysEeither by covalent binding to oxirane-acrylic beads or chlorotriazine bead cellulose or by entrapment in (poly)acrylamide gel. The validity of the enzyme Now microcalorimetry results was corroborated by a pH-stat method, showing enzyme Now microcalorimetry to be a suitable method for rapid screening of immobilized biocatalysts regardless of the immobilization technique, carrier type or the biocatalyst source. 1998 Society of Chemical Industry ( J. Chem. T echnol. Biotechnol. 73 ,3 1 E36 (1998)
用酶Now微量热法筛选具有代表性的固定化青霉素G酰化酶生物催化剂(酶、细胞)。固定化青霉素G酰化酶生物催化剂可以通过各种技术在实验室中制备,也可以从四个商业制造商那里获得。用(聚丙烯酰胺)凝胶或硬化果胶钙凝胶包埋大肠杆菌工业菌株。半纯化的酶以不同的方式固定,要么是共价结合到氧丙烷-丙烯酸珠或氯三嗪珠纤维素或包埋在(聚)丙烯酰胺凝胶。通过pH-stat法验证了Now酶微热法结果的有效性,表明Now酶微热法是一种适合快速筛选固定化生物催化剂的方法,无论固定化技术、载体类型或生物催化剂来源如何。化学工业学会[j]。T echnol。生物技术。73,31 E36 (1998)
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引用次数: 2
Stabilisation of β-glucosidase entrapped in alginate and polyacrylamide gels towards thermal and proteolytic deactivation 海藻酸盐和聚丙烯酰胺凝胶包裹的β-葡萄糖苷酶在热和蛋白水解失活方面的稳定性
Pub Date : 1998-09-01 DOI: 10.1002/(SICI)1097-4660(199809)73:1<7::AID-JCTB921>3.0.CO;2-#
N. Ortega, M. D. Busto, M. Perez-Mateos
β-D-Glucosidase was immobilised by entrapment in two different matrices (calcium alginate and polyacrylamide gels), in order to compare how the immobilisation could stabilise the enzyme towards thermal and proteolytic deactivation. While the enzyme trapped in polyacrylamide gel showed an optimum temperature for activity at 10°C lower than that of the free enzyme, the optimal temperature after immobilisation in alginate beads was not altered (60°C). The immobilisation of enzyme in alginate beads caused a larger increase in the thermal stability than the entrapment in polyacrylamide gels. The stabilisation factors obtained as 55, 60 and 65°C for β-glucosidase immobilised in alginate and polyacrylamide gels were 2·03, 3·06, 2·19 and 2·04, 0·35, 1·01, respectively. In contrast, the β-glucosidase immobilised in polyacrylamide gels was more resist-ant in proteolysis than that trapped in alginate beads. © 1998 Society of Chemical Industry
通过将β- d -葡萄糖苷酶固定在两种不同的基质(海藻酸钙和聚丙烯酰胺凝胶)中,以比较固定如何使酶在热和蛋白水解失活时稳定下来。在聚丙烯酰胺凝胶中捕获的酶显示出比游离酶低10°C的最佳活性温度,而在海藻酸盐珠中固定后的最佳温度(60°C)没有改变。将酶固定在海藻酸酯微球中比在聚丙烯酰胺凝胶中更能提高酶的热稳定性。在55、60和65℃条件下,海藻酸盐和聚丙烯酰胺凝胶固定β-葡萄糖苷酶的稳定因子分别为2.03、3.06、2.19和2.04、0.35、1.01。相比之下,固定在聚丙烯酰胺凝胶中的β-葡萄糖苷酶在蛋白质水解方面比捕获在海藻酸珠中的β-葡萄糖苷酶更具抗性。©1998化学工业协会
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引用次数: 23
A novel synthesis of high‐area alumina via H2O2‐precipitated boehmite from sodium aluminate solutions 用H2O2沉淀薄水铝石从铝酸钠溶液中合成高面积氧化铝的新方法
Pub Date : 1998-08-01 DOI: 10.1002/(SICI)1097-4660(199808)72:4<320::AID-JCTB911>3.0.CO;2-#
E. A. El-Katatny, S. Halawy, M. A. Mohamed, M. Zaki
A novel procedure was devised, whereby crystalline boehmite, γ-AlO(OH), was efficiently precipitated from sodium aluminate solutions, NaAlO 2 (aq), following controlled addition of H 2 O 2 aqueous solution. The effects of the aluminate solution variables (viz. concentration, volume, caustic ratio, pH and temperature), as well as the H 2 O 2 /Al 2 O 3 molar ratio, on the amount and composition of the yield, were examined. Accordingly, optimal conditions for 98% recovery of the aluminium content of the parent aluminate solution were realized. The remaining NaOH can be recycled and used to extract further amounts of aluminium from bauxite (Bayer process). Thermal stability of the resulting boehmite was explored by thermogravimetry and differential thermal analysis. Accordingly, various calcination products of the boehmite were obtained at some selected temperatures in the range 400-1100°C and characterized by chemical analysis, X-ray powder diffractometry, and surface charge and specific area measurements. The results obtained indicated the synthesis of relatively high surface area transitional aluminas of industrial and catalytic merits.
设计了一种新工艺,在控制h2o2水溶液的加入下,从naal2 (aq)铝酸钠溶液中有效地析出结晶薄水铝石γ-AlO(OH)。考察了铝酸盐溶液的浓度、体积、烧碱比、pH和温度以及h2o / al2o3的摩尔比对收率和组成的影响。据此,实现了母铝酸盐溶液铝含量回收率98%的最佳工艺条件。剩余的氢氧化钠可以回收利用,用于从铝土矿中提取更多的铝(拜耳法)。用热重法和差热分析法考察了所得薄铝石的热稳定性。在400 ~ 1100℃范围内,通过化学分析、x射线粉末衍射、表面电荷和比面积测量等方法,获得了不同温度下的薄铝石煅烧产物。研究结果表明,该方法具有合成高比表面积过渡氧化铝的工业和催化价值。
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引用次数: 26
期刊
Journal of Chemical Technology & Biotechnology
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