非粮原料燃料乙醇发酵关键技术的研究

生物质燃料乙醇是一种高度清洁的交通液体燃料，是减少温室气体排放，缓解大气污染的最佳技术选择。以非粮原料生产燃料乙醇可以在进行能源生产的同时保证粮食安全，有利于产业的可持续发展。在众多的非粮原料中，甘薯是我国开发潜力最大的生物质能源作物之一。我国占世界甘薯种植总面积和产量的90％。同时，甘薯的单位面积燃料乙醇产量远大于玉米和小麦。其成本是目前酒精中最低廉的，因此利用甘薯生产乙醇是发展生物质燃料乙醇的首要选择。目前采用薯类全原料主要采用分批发酵生产乙醇，其技术水平低，发酵强度低，一般在0.7－2.5g/（L•h），乙醇浓度低，甘薯发酵乙醇为6－8％(v/v)，能耗高，环境负荷大，污染严重。针对上述问题，本文从菌株选育、原料预处理、中试放大、残糖成分分析等方面进行研究。 为了研究乙醇发酵生产规模扩大过程中，大型发酵罐底部高压条件下，CO2对酵母乙醇发酵的影响，我们通过CO2 加压的方法进行模拟试验，研究结果表明，发酵时间随压强的升高而逐渐延长，高压CO2 对乙醇发酵效率影响不大，在0.3 MPa 以下时，发酵效率均可达到90%以上。高压CO2 对发酵的抑制作用是高压和CO2 这两个因素联合作用的结果。高压CO2 条件下，酵母胞外酶和胞内重要酶类的酶活均表现出特征性。0.2 MPa 下，酶活性的变化趋势和0.1 MPa 条件下的较为一致。而0.3 MPa 下的酶活变化趋势与0.4 MPa 下的酶活更为接近。通过全基因表达分析发现在CO2 压力为0.3 MPa 下，乙醇发酵途径中多个基因表达量下调，同时海藻糖合成酶和热激蛋白基因表达量上调。 筛选耐高温的乙醇酵母菌株能够解决糖化温度和发酵温度不协调的矛盾，实现真正意义上的边糖化边发酵。高温发酵还能够降低发酵时的冷却成本，实现乙醇的周年生产。本研究筛选出一株高温发酵菌株Y-H1，进而我们对该菌株的胞外酶和胞内乙醇代谢重要酶类的酶活性进行了分析。结果表明Y-H1 能够在40 ℃条件下正常进行乙醇发酵，发酵33h，最终乙醇浓度达到10.7%（w/w），发酵效率达到90%以上。同时发酵液最终pH 在3.5 左右，显示菌株具有一定的耐酸性能力。同时观察到40 ℃下，菌株的胞外酶和胞内乙醇代谢重要酶类的酶活性发生了变化，乙醇发酵途径中关键酶基因表达下调，而海藻糖合成酶与热激蛋白基因表达量上调，这些结果为进一步研究酵母菌耐热调控机理提供了依据。 糖蜜是一种大规模工业生产乙醇的理想原料，本研究利用选育高浓度乙醇发酵菌株结合配套的发酵稳定剂，研究了糖蜜高浓度乙醇发酵情况。结果表明采用冷酸沉淀预处理糖蜜溶液，采用分批补料的发酵方式，乙醇浓度最高达到了10.26% (w/w)，发酵时间为42 h。同时观察到在糖蜜发酵中，乙醛含量与乙醇浓度存在一定的相关性。 快速乙醇发酵对于缩短乙醇生产周期、降低乙醇生产成本、减少原料腐烂损失具有重要意义。本研究诱变和筛选得到了一株快速乙醇发酵菌株10232B。在优化后的发酵条件下，采用10L 发酵罐进行分批乙醇发酵，经过18h,乙醇的最终浓度达到88.5g/L,发酵效率93.6%，平均乙醇生产速度达到4.92 g/L/h。此菌株在保持较高乙醇生产浓度的同时，拥有快速生产乙醇的能力，适合作为快速乙醇发酵生产菌种。 由于鲜甘薯具有粘度大的特点，传统液化糖化处理很难在短时间内充分糖化原料；高粘度的醪液也难以进行管道输送，容易堵塞管路；同时，也会降低后续的乙醇发酵效率。 本文采用了快速粘度分析法对鲜甘薯糊化粘度特性进行了分析，进而对预处理条件进行了研究，在最佳预处理条件下，糖化2h 后，醪液葡萄糖值最高可达99.3，粘度4.5×104 mPa.s，而采用传统糖化工艺，醪液DE 值仅为85.8，粘度大于1.0×105 mPa.s。 此预处理方法也可用于快速糖化不加水的醪液。后续的乙醇发酵试验表明，通过此预处理方法获得的糖化醪液对乙醇发酵无负面影响。 在前期已实现了实验室水平的鲜甘薯燃料乙醇快速乙醇发酵基础上，进一步将发酵规模扩大到500L，在中试水平上对甘薯乙醇发酵进行了研究。结果表明在500L 中试规模，采用边糖化边发酵（SSF）工艺，在料液比为3∶1，发酵醪液最高粘度为6×104mPa.s 条件下，发酵37h，乙醇浓度达到了12.7%（v/v），发酵效率91%，发酵强度为2.7 g/（L•h）。与目前国内的薯类乙醇发酵生产技术水平具有明显的优越性。 为研究甘薯、木薯乙醇发酵中残糖的组成，采用了高效液相色谱—蒸发光散射检测法，对乙醇发酵残糖进行了分析。结果表明，甘薯、木薯乙醇发酵残糖均为寡聚糖，主要由葡萄糖、木糖、半乳糖、阿拉伯糖和甘露糖构成。随着发酵时间延长，寡聚糖中的葡萄糖、半乳糖、甘露糖可被缓慢的水解释放。提高糖化酶量仅在一定程度上降低残糖，过量的糖化酶反而会导致残糖增加。同时发现3, 5-二硝基水杨酸法不能准确测定甘薯、木薯乙醇发酵中的残总糖含量。进一步筛选了两株残糖降解菌株，对甘薯乙醇发酵残糖的降解利用率均达到了40%以上，而且还能显著降低发酵醪液粘度。经形态学和rRNA ITS 序列分析，确定这两株菌分别属于为木霉属和曲霉属黑曲霉组。 通过对以甘薯原料为代表的非粮原料发酵技术研究开发，以期形成乙醇转化率高，能耗低，生产效率高、季节适应性好，原料适应性广，经济性强，符合清洁生产机制的燃料乙醇高效转化技术，为具有我国特色的燃料乙醇发展模式提供技术支持。 Sweet potato is one of the major feedstock for the fuel ethanol production in China. The planting area and the yield in China take 90% of the world. Sweet potato is an efficient kind of energy crops. The energy outcome per area is higher than corn or wheat. And the manufacture cost of ethanol is the lowest, compared with corn and wheat. So sweet potato is the favorable crop for the bioethanol production in China. However, the low-level fermentation technology restricts the development of ethanol production by sweet potato, including slow ethanol production rate, low ethanol concentration and high energy cost. To solve these problems, we conducted research on the strain breeding, pretreatment, pilot fermentation test and residual saccharides analysis. To study the impact of hyperbaric condition at bottom of the large fermentor on yeast fermentation, high pressure carbon dioxide (CO2) was adopted to simulate the situation. The results showed that the fermentation was prolonged with the increasing pressure. The pressure of CO2 had little impact on the ethanol yield which could reach 90% under the pressure below 0.3 MPa. The inhibition was combined by the high pressure and CO2. Under the high CO2 pressure, the extracellular and important intracellular enzyme activities were different from those under normal state. The changes under 0.1 MPa and 0.2 MPa were similar. The changes under 0.3 MPa were closer to those under 0.4 MPa. The application of thermotolerance yeast could solve the problem of the inconsistent temperature between fermentation and saccharificaton and fulfill the real simultaneous saccharification and fermentation. And it could reduce the cooling cost. A thermotolerance strain Y-H1 was isolated in our research. It gave high ethanol concentration of 10.7%（w/w）at 40 ℃ for 33 h. The ethanol yield efficiency was over 90%. At 40 ℃, the extracellular and important intracellular enzyme activities of Y-H1 showed the difference with normal state, which may indicate its physiological changes at the high temperature. Molasses is another feedstock for industrial ethanol production. By our ethanol-tolerance strain and the regulation reagents, the fermentation with high ethanol concentration was investigated. In fed-batch mode combined with cold acid deposition, the highest ethanol concentration was 10.26% (w/w) for 42h. The aldehyde concentration in fermentation was found to be related to ethanol concentration. The development of a rapid ethanol fermentation strain of Zymomonas mobilis is essential for reducing the cost of ethanol production and for the timely utilization of fresh material that is easily decayed in the Chinese bioethanol industry. A mutant Z. mobilis strain, 10232B, was generated by UV mutagenesis. Under these optimized conditions, fermentation of the mutant Z. mobilis 10232B strain was completed in just 18 h with a high ethanol production rate, at an average of 4.92 gL-1h-1 per batch. The final maximum ethanol concentration was 88.5 gL-1, with an ethanol yield efficiency of 93.6%. This result illustrated the potential use of the mutant Z. mobilis 10232B strain in rapid ethanol fermentation in order to help reduce the cost of industrial ethanol production. As fresh sweet potato syrup shows high viscosity, it is hard to be fully converted to glucose by enzymes in the traditional saccharification process. The high-viscosity syrup is difficult to be transmitted in pipes, which may be easily blocked. Meanwhile it could also reduce the later ethanol fermentation efficiency. To solve these problems, effects of the pretreatment conditions were investigated. The highest dextrose equivalent value of 99.3 and the lowest viscosity of 4.5×104 mPa.s were obtained by the most favorable pretreatment conditions, while those of 85.8 and over 1.0×105 mPa.s was produced by traditional treatment conditions. The pretreatment could also be applied on the material syrup without adding water. The later experiments showed that the pretreated syrup had no negative effect on the ethanol fermentation and exhibited lower viscosity. The fuel ethanol rapid production from fresh sweet potato was enlarged in the 500L pilot scale after its fulfillment on the laboratory level. The optimal ratio of material to water was 3 to 1 in 500L fermentor. With low-temperature-cooking (85 ℃) using SSF, the Saccharomyces cerevisiae was able to produce ethanol 97.44 g/kg for 37h, which reached 92% of theoretical yield. The average ethanol production rate was 4.06 g/kg/h. And the maximum viscosity of syrup reached 6×104mPa.s. The results showed its superiority over current industrial ethanol fermentation. The compositions of the residual saccharides in the ethanol fermentation by sweet potato and cassava were analyzed by high performance liquid chromatography coupled with evaporative light-scattering detector. The results showed that all the residual saccharides were oligosaccharides, mainly composed of glucose, xylose, galactose, arabinose and mannose. The glucose, galactose and mannose could be slowly hydrolyzed from oligosaccharides in syrup during a long period. To increase the glucoamylase dosage could lower the residual saccharides to a certain extent. However, excess glucoamylase dosage led to more residual saccharides. And the method of 3, 5-dinitrosalicylic acid could not accurately quantify the residual total saccharides content. Two residual saccharides degrading strains were isolated, which could utilize 40% of total residual saccharide and lower the syrup viscosity. With the analysis of morphology and internal transcribed spacer sequence, they were finally identified as species of Trichoderma and Aspergillus niger.

注氦尖晶石的红外光谱研究

利用傅立叶变换红外光谱仪对注He尖晶石样品随退火温变化而引起光吸收性能的变化进行了研究。发现尖晶石样品在626.4cm-1附近的吸收峰随注入剂量的增加向小波数方向移动,而在随后退火过程该吸收峰随退火温度的增加而向大波数方向回复。该吸收峰的回复行为依赖于注入剂量和退火温度。认为在626.4cm-1附近吸收峰随注入剂量和退火温度的这种变化与尖晶石中He的俘获以及释放有关。

~(12)C~(6+)重离子辐照大葱的细胞学和RAPD分析

用309、0和180Gy12C6+重离子辐照处理大葱干种子,研究其对大葱根尖的细胞学效应,并采用随机扩增多态性DNA(RAPD)技术初步分析了其变异类型。不同剂量12C6+的重离子照射能有效诱导大葱根尖细胞微核和染色体畸变。随着辐照剂量的增加,幼苗根尖细胞微核形成几率明显增大,微核率、多微核率和染色体总畸变率呈线性上升。但除去微核以外的染色体畸变率则呈U型变化。RAPD结果表明,大葱不同处理之间的DNA存在明显差异,所用35种引物中有28种出现了特异性条带,既有新增条带,又有缺失条带,还有迁移率的差异。30、90和180Gy剂量辐照引起的RAPD变异率分别为29.91%、41.05%和22.14%。结果发现高微核率和染色体变异过大会导致高致死效应,使得染色体总畸变率高的处理组在当代生长苗的DNA变异率变小。

基于ARM920T的HIRFL-CSR前端总线控制器FBC-01

本文论述用于兰州重离子加速器冷却存储环(HIRFL-CSR)控制系统的前端总线系统控制器FBC-01的硬件设计。该控制器是基于0.8mmBGA封装的AT91RM9200(ARM9)处理器,运行嵌入式LINUX操作系统。控制器可以连接标准的VGA显示器、键盘、鼠标,具有通用的10M/100M以太网接口、USB接口、RS-232接口、485接口、CANBUS接口。可以带SD卡、CF卡存储器。该控制器采用现场可编程的FPGA器件设计背板接口,并采用具有64mA高驱动能力的总线驱动器,不仅符合VME规范的电气要求,而且具有灵活的接口信号定义可编程能力,是HIRFL-CSR控制系统的关键部件。

~(143)Dy和~(141)Dy的β缓发质子衰变与自旋指认

分析了143Dy和141Dy的β缓发质子衰变的数据,对比计算了这两种核的核位能面。从中看到了143Dy的衰变包括有1/2+基态和11/2-同核异能态的两种衰变成分,并且确定了它们的半衰期分别为(6.0±1.5)s和(3.0±0.5)s。同时也测定了141Dy的半衰期为(0.9±0.2)s,并指认了它的自旋宇称为9/2-。

热核物质中基态关联修正下的单核子势和核子有效质量

以有限温度Brueckner-Hartree-Fock(BHF)方法为基础,利用质量算子的空穴线展开,计算了不同温度和密度下的核物质中单核子势和核子有效质量,特别是研究和讨论了基态关联效应和三体核力贡献对热核物质中单核子势的影响.研究表明,基态关联和三体核力对单核子势的密度和温度依赖性均有重要影响.基态关联导致的重排修正具有排斥性,大大减弱了低动量区域单核子势的吸引性,而且基态关联效应对单核子势的贡献随密度增大而增强,随温度升高而减弱.三体核力对基态关联的影响是导致单核子势中重排项贡献减小.在高密度区域包含基态关联效应和三体核力贡献的单核子势的排斥性在整个动量范围内随温度升高而增强.

质子滴线附近的β缓发质子衰变

简要回顾了我们小组在 1996~2004 年中发表的有关质子滴线附近β缓发质子衰变的实验结果, 即运用氦喷嘴快速带传输系统 +“p-γ”符合方法, 在稀土区质子滴线附近首次观测了 9种新核素的β缓发质子衰变, 在 A= 90 核区的 N = Z线附近获得了 5 种核素的β缓发质子衰变的新数据. 同时着重补充了一些重要的实验技术细节. 汇总了这 14 种核素的半衰期、自旋、宇称、形变以及生成反应截面的实验结果, 并与流行的核模型理论预言进行了系统的对比讨论. 从中看出:(ⅰ) Mo, Rh 以及“等待点”核 Ru 和 Pd 半衰期的实验值比近期 M?ller 等 85 92 89 93人的宏观-微观理论预言值长 5~10 倍, 因而明显地影响天体 rp-过程的核素丰度;(ⅱ) 实验指认的质子滴线核 Ho 和 Pm 的自旋和宇称, 与流行理论预言不符, 142 128但用 Woods-Saxon-Strutinsky 方法计算得到的位能面可以解释自旋和宇称的实验值; (ⅲ) 实验估计的 9 种稀土核的生成截面比通用的 Alice和 HIVAP 程序的计算值要小 1～2 个数量级.

奇奇核~(90)Nb的高自旋态研究

用能量为80MeV的19F束通过反应76Ge(19F,5n)90Nb布居了90Nb的高自旋态.通过在束γ测量分析90Nb退激γ射线的符合级联关系,发现了19条新的属于90Nb的γ跃迁,建立了90Nb的高自旋态能级纲图.通过经验壳模型计算指定了部分能级的组态,并结合实验DCO比值和与相邻N=49核素的系统比较,确认了新能级的自旋和宇称.

γ射线对A172胶质瘤细胞的生物学效应

以不同剂量照射后的细胞存活率、微核率和微核细胞率作为生物学终点,研究了γ射线对A172细胞的生物学效应.结果表明:细胞存活率与剂量之间满足回归方程lgY=-0.06427X+1.83354,其回归系数r=-0.9886,P<0.01.剂量为1Gy时微核率和微核细胞率达到最大值,此时的微核率为(66.75±3.564)%,微核细胞率为(53.9±0.7849)%,微核率和微核细胞率均随着剂量的增大先增大后减小,并分别维持在42%和37%左右.

重离子束治癌相关生物学效应及机理研究

重离子束治癌是当今放射治疗中最科学、最先进、最有效的方法，是有代表性的高技术。目前仅有美、日、德实现了该技术，并已取得常规疗法难以实现的疗效。我国近年来开展了“重离子束治癌技术的基础研究”，其中，放射生物学及机理研究是重要内容。本论文从细胞、DNA分子、以及动物个体的三个不同层次上分别研究了重离子束治癌相关的生物学问题。在细胞研究方面。采用HeLa、B 16两种细胞分别研究了X一射线和重离子在水介质中入射的深度与相应细胞的存活率(1一失活率)，结果表明：X一射线对细胞的损伤随深度而逐渐衰减(或细胞存活随深度逐渐增加)，而重离子对细胞的损伤则为Bragg曲线(或细胞存活为倒Bragg曲线)。研究了25MeV／u ~(40)Ar~(14+)辐照人肝癌细胞SMMC一7721的微核及存活的动态变化，结果表明： 单次照射与分次照射的微核率随时间的变化规律在96h内没有明显区别，受照(单次、分次) 肝癌细胞的存活数随时间表现出衰减趋势，微核率与细胞存活数关系的动态变化为负相关性。研究了6MV X-射线和125．5keV／μm的重离子辐照B 1 6、V79细胞的2Gy存活率(SF2)，结果表明：B16和V79细胞的存活率(P<0．01)依赖于不同的辐射性质(X-射线、~(12)C离子)，其X-射线与~(12)C离子辐射这两种细胞的存活率之比分别为5．4和1．43，即~(12)C离子辐射增强了X-射线抗性细胞系的敏感性，从而显示了重离子治疗癌症的优势。研究了125．5keV／um的碳离子辐照小鼠黑色素瘤B16、人的宫颈癌HeLa、中国仓鼠肺V79、人的肝癌SMMC-7721四种细胞的相对生物学效率(RBE)，得．到了RBE依赖于细胞种类的关系、RBE随细胞存活水平的升高而增加的关系、以及当LET≥125．5keV／μm时，RBE随着LET的增大而变小的关系。在DNA分子研究方面。研究了125．5keV／μm~(12)C~(6+)辐照小鼠黑色素瘤B 16、中国仓鼠肺V79、人的宫颈癌HeLa、人的肝癌SMMC一7721细胞的灵敏度(由D50表示)、DNA双链断裂(DSB)和DNA双链断裂片段分布，结果表明：细胞敏感性与DNA双链断裂之间没有一致的关系，提出了细胞辐射敏感性的一种可能的分子机理，即DNA序列敏感性位点协同DNA双链断裂互补性机理。由此解释了四种细胞系的不同敏感性问题。在动物个体研究方面。研究了57．28MeV／u氧离子50Gy一次性局部照射对B16黑色素瘤小鼠肿瘤生长的抑制作用，并观测了受照小鼠的死亡情况，结果表明：照射B16黑色素瘤后第10天观察，肿瘤生长延迟为6天、肿瘤抑制率为66％，耐受剂量小于50Gy。研究了50MeV／u ~(12)C~(6+)离子辐照对小鼠移植性肿瘤S180的抑制作用、控制率、治愈率和病理组织学变化，结果表明：各剂量组对S180肉瘤的抑制作用均大于90％，高剂量组抑瘤作用明显强于低、中剂量组(P

FEBIAD-II离子源少参数质量公式和核质量计算

第一篇FEBIAD－II离子源根据物理实验的要求本文设计和加工了一套有别于中空阴极源的FEBIAD－II离子源系统，在文中对离子源结构和特点进行了分析。测试了离子源引出离子束的发散情况，得到了此离子源的工作温度，引出离子流与高压、引出板电压、网栅电流的关系曲线，进而给出本源的工作参数。第二篇少参数质量公式和核质量计算本文介绍一个少参数的原子核质量公式，并计算了28≤Z≤81的1440个原子核质量和S_(2n)，与实验比较，核质量和S_(2n)的方均根偏差分别为1.01和0.57MeV。计算的双中子分离能曲线很好地重现了N＝50、82的主壳效应，Z＝40时N＝56的亚壳效应，以及N≥60和90时的原子核发生大形变的特性

Study on bioactivity of extracts from marine sponges in Chinese Sea

The bioactivity screening of fractions from two inter-tidal sponges collected from the north of China Yellow Sea and one sponge collected from the South Chinese Sea was reported in this study. In sponge Hymeniacidon perleve there were 9 fractions out of 15 from CHCl3 extract with anti Staphylococcus aureus activity, 9 fractions out of 19 from BuOH extract with anti Escherichia coli activity, and three fractions from CHCl3 extract which had moderate to strong activity in inhibiting Bacillus subtilis, Candida albicans, and Aspergilus niger. The fractions of Reniochalina sp. showed bioactivity against bacteria and fungi. The fractions of Acanthella acuta Schmidt showed bioactivity against S. aureus and fungi. One compound from H. perleve obtained by the bioactively directing isolation was tested for bioactivity against the human hepatoma cell line Qgy7701 (IC50 10.1 mug/ml), Burkitt's lymphoma cell line Raji (IC50 9.76 mug/ml) and chronic myelogenous leukemia K562 (IC50 1.90 mug/ml). (C) 2003 Elsevier B.V. All rights reserved.

Analysis of sulfur-containing compounds in crude oils by comprehensive two-dimensional gas chromatography with sulfur chemiluminescence detection

This paper reports an analytical method for separating, identifying, and quantifying sulfur-containing compounds in crude oil fraction (IBP-360degreesC) samples based on comprehensive two-dimensional gas chromatography coupled with a sulfur chemiluminescence detector. Various sulfur-containing compounds and their groups were analyzed with one direct injection. 3620 peaks were detected including 1722 thiols/thioethers/ disulfides/1-ring thiophenes, 953 benzothiophenes, 704 dibenzothiophenes, and 241 benzonaphthothiophenes. The target sulfur compounds and their groups were identified based on the group separation feature and structured retention of comprehensive two-dimensional gas chromatography as well as standard substances. The quantitative analysis of major sulfur-containing compounds and total sulfur was based on the linear response of the sulfur chemiluminescence detector using the internal standard method. The sulfur contents of target sulfur compounds and their groups in 4 crude oil fractions were also determined. The recoveries for standard sulfur-containing compounds were in the range of 90-102%. The quantitative result of total sulfur in the Oman crude oil fraction sample was compared with those from ASTM D 4294 standard method (total S by X-ray fluorescence spectrometry), the relative deviation (RD%) was 4.2% and the precision of the method satisfactory.