<Emphasis Type="Italic">Penicillium</Emphasis> sp. ZD-Z1 chitosanase immobilized on DEAE cellulose by cross-linking reaction

Chitosanase obtained fromPenicillium sp.ZD-Z1 was immobilized on DEAE cellulose with glutaraldehyde by cross-linking reaction. The optimal conditions of immobilization were as follows: 0.1 g DEAE cellulose was treated with 5 ml 5% glutaraldehyde solution; then 2.3 mg chitosanase was immobilized on the carrier. The optimal temperature and pH was 60 °C and 4.0, and the K _m value was 18.87 g/L. Under optimal conditions, the activity of immobilized enzyme is 1.5 U/g, and the recovery of enzyme activity is 81.3%. After immobilization, the optimal temperature and K _m value increased (from 50 °C to 60 °C, from 2.49 g/L to 18.87 g/L), whereas the optimal pH was reduced (from 5.0 to 4.0). The enzyme activity loss was less than 20% after 10 times batch reaction; the immobilized enzyme showed good operation stability.     

Hydrothermal synthesis of LA-MN-Hexaaluminates for the catalytic combustion of methane

Hydrothermal synthesis by using urea hydrolysis at 1.0-3.0 MPa and 120-130 ‡C was employed to prepare Mn-substituted hexaaluminate catalysts for methane combustion. The results from DTA-MS demonstrated that CO_3- and Off anions co-exist in the hydrothermal reaction. XRD reveals that the components of carbonates and hydroxides in the hydrothermal reaction are more favorable than those in the (NH₄)₂CO₃ co-precipitation for the formation of the Mn-substituted hexaaluminate phase. After calcination at 1,200 ‡C for 2 h, LaMnAl₁₁O₁₉ is the major phase of the catalyst prepared by the hydrothermal synthesis method while LaAlO₃ is the major one of the catalysts prepared by NH₄OH and (NH₄)₂CO₃ co-precipitation. The catalyst prepared by hydrothermal synthesis has higher activity than that prepared by NH₄OH and (NH₄)₂CO₃ co-precipitation. The major reason is that more Mn²⁺ ions have incorporated into the hexaaluminate lattice. The effect of drying methods on the formation of hexaaluminate phase was also discussed.     

Catalytic degradation of waste polyolefinic polymers using spent FCC catalyst with various experimental variables

Liquid-phase catalytic degradation of waste polyolefinic polymers (HDPE, LDPE, PP) over spent fluid catalytic cracking (FCC) catalyst was carried out at atmospheric pressure with a stirred semi-batch operation. The effect of experimental variables, such as catalyst amount, reaction temperature, plastic types and weight ratio of mixed plastic on the yield and accumulative amount distribution of liquid product for catalytic degradation was investigated. The initial rate of catalytic degradation of waste HDPE was linearly increased with catalyst amount (4-12 wt%), while that was exponentially increased with reaction temperature (350-430 ‡C). Spent FCC catalyst in the liquid-phase catalytic degradation of polymer was not deactivated fast. The product distribution from catalytic degradation using spent FCC catalyst strongly depended on the plastic type. The catalytic degradation of mixed plastic (HDPE: LDPE: PP: PS=3: 2: 3: 1) showed lower degradation temperature by about 20 ‡C than that of pure HDPE.     

Synthesis and Polymerization of Cationic bis(cyclopentadienyliron)arene Complexes Containing Arylazo Dyes

The synthesis of the title complexes was achieved via the reaction of -p-dichlorobenzene- -cyclopentadienyliron cations with 4,4′-bis(4-hydroxyphenyl)valeric acid to produce the diiron complexes which were then reacted with a number of arylazo dyes to give cationic bis(cyclopentadienyliron)arene complexes containing the arylazo dyes. These iron-containing monomers were subsequently polymerized via nucleophilic aromatic substitution using 1,8-octanedithiol, 4,4′-thiobisbenzenethiol, or bisphenol A to produce the desired coloured cationic organoiron polymers. The weight – average molecular weights were estimated to range from 11,800 to 31,600. UV–vis studies conducted in dimethylformamide (DMF) showed that the metallated polymers exhibited of 412–491 nm. Addition of HCl to the polymer solution caused a bathochromic shift into the range of 515–530 nm. Thermogravimetric analysis (TGA) revealed that the iron moieties were cleaved between 205 and 248 °C while the polyether/thioether backbone degraded between 380 and 613 °C. Differential scanning calorimetry (DSC) showed that the polymers exhibited glass transition temperatures (Tg) ranging from 106 to 184°C.This paper is dedicated to Professor Richard J. Puddephatt in recognition of his outstanding contribution to the field of metal-containing polymers.     

(<Emphasis Type="Italic">Z,Z</Emphasis>)-6,9-Heneicosadien-11-One: Major Sex Pheromone Component Of Painted Apple Moth, <Emphasis Type="Italic">Teia anartoides</Emphasis>

(Z, Z)-6,9-Heneicosadien-11-one (Z6Z9-11-one-21Hy) was identified as the major sex pheromone component of the painted apple moth (PAM), Teia anartoides (Lepidoptera: Lymantriidae), on the basis of (1) comparative gas chromatographic-electroantennographic detection (GC-EAD) analyses, GC-mass spectrometry (MS), high-performance liquid chromatography (HPLC)-MS, and HPLC-UV/visible spectroscopy of pheromone gland extracts and authentic standards; (2) GC-EAD analyses of effluvia of calling females; and (3) wind tunnel and field trapping experiments with a synthetic standard. In field experiments in Australia, synthetic Z6Z9-11-one-21Hy as a single component attracted male moths. Wind tunnel experiments suggested that a 4-component blend consisting of Z6Z9-11-one-21Hy, (6Z,9R,10S)-cis-9,10-epoxy-heneicosene (Z6-9R10S-epo-21Hy), (E, E)-7,9-heneicosadien-6,11-dione (E7E9-6,11-dione-21Hy), and 6-hydroxy-(E, E)-7,9-heneicosadien-11-one (E7E9-6-ol-11-one-21Hy) (all present in pheromone gland extracts) might induce more males to orient toward, approach, and contact the source than did Z6Z9-11-one-21Hy as a single component. Additional experiments are needed to determine conclusively whether or not Z6-9R10S-epo-21Hy, E7E9-6,11-dione-21Hy, and E7E9-6-ol-11-one-21Hy might be minor sex pheromone components of PAM. Moreover, attractiveness of synthetic pheromone and virgin PAM females needs to be compared to determine whether synthetic pheromone could replace PAM females as trap baits in the program to monitor eradication of exotic PAM in New Zealand.     

Experiences from using heat integration software to determine retrofit opportunities within a refinery process

Heat integration techniques can be used to optimize the energy requirement for both new and retrofit plant designs. Software tools for identifying retrofit options are becoming available. This paper reports our experiences from using heat exchanger network (HEN) optimization software for a retrofit case study of an oil refinery process. The HEN optimization software was used to automate the search for the most beneficial retrofit designs following the twostage process proposed by Asante and Zhu. The software provided three potential retrofit designs. Results from this analysis were used as the basis of a rigorous mass and energy balance simulation of the plant. The simulation corroborated the energy savings, but there were some important differences. The simulation required 20% more heat exchange area. Furthermore, the retrofit design involving one topology change was shown to be less economic than an alternative design. These differences are discussed and a revised methodology is proposed.     

Associations between apolipoprotein E genotype and circulating F<Subscript>2</Subscript>-isoprostane levels in humans

Apolipoprotein E (apoE), an important determinant of plasma lipoprotein metabolism, has three common alleles (ε2, ε3, and ε4). Population studies have shown that the risk of diseases characterized by oxidative damage, such as coronary heart disease and Alzheimer’s disease, is significantly higher in ɛ4 carriers. We evaluated the association between apoE genotypes and plasma F₂-isoprostane levels, an index of lipid peroxidation, in humans. Two hundred seventy-four healthy subjects (104 males, 170 females; 46.9±13.0 yr; 200 whites, 74 blacks; 81 nonsmokers, 64 passive smokers, and 129 active smokers) recruited for a randomized clinical antioxidant intervention trial were included in this analysis. ApoE genotype was determined by PCR and restriction enzyme digestion. Free plasma F₂-isoprostane was measured by GC-MS. Genotype groups were compared using multiple regression analysis with adjustment for sex, age, race, smoking status, body mass index, plasma ascorbic acid, and β-carotene. Subjects with ε3/ε4 and ε4/ε4 genotype (ε4-carriers) and with ε2/ε3 and ε3/ε3 (non-ε4-carriers) were pooled for analysis. In subjects with high cholesterol levels (total cholesterol above 200 mg/dl), plasma F₂-isoprostane levels were 29% higher in ε4 carriers than in non-ε4-carriers (P=0.0056). High-cholesterol subjects that are ε4 carriers have significantly higher levels of lipid peroxidation as assessed by circulating F₂-isoprostane levels.     

气候变化背景下流域生态需水预估−以好溪流域为例

为探究未来气候变化对流域生态需水量的影响,保障河流生态需水量,针对好溪流域进行生态需水量计算 及预测。基于好溪流域气象数据及下垫面条件建立流域生态需水模型,并根据 GF1-WFV 遥感影像数据订正后的 地表反射率和作物种植结构提升模型模拟精度。选择 CanESM2气候模式下的 RCP2.6、RCP4.5 和 RCP8.5 这 3 种 排放情景,建立气候变化背景下流域生态需水预测方法,计算现状年并预测未来年份的生态需水量及生态需水保 障程度。结果表明,基于光学遥感影像进行数据订正后,模型模拟精度有所提升,率定期的模型精度 R2从 0.80 提 升为 0.85,验证期的 R2从 0.75 提升至 0.78。应用提升精度后的模型进行生态需水预测,在 RCP2.6、RCP4.5 和 RCP8.5 情景下,2025—2100 年的年均生态需水分别增加了 0.27 亿、0.21 亿和 0.29 亿 m3,其中 RCP8.5 情景下生态 需水保障程度最高,RCP4.5 情景下生态需水保障程度最低。     

基于云模型的山东省干旱时空分布特征

基于山东省 29 个气象站 1951—2017 年的实测气象数据,主要采用降水量距平百分率作为气象干旱等级评 价指标,通过云模型分析山东省干旱时空分布的均匀性和稳定性特征,并采用 ArcGIS 的反距离权重法分析不同 时间尺度下的干旱频次空间分布特征。结果表明：山东省降水量距平百分率呈逐年波动式下降趋势,但下降趋势 不明显,干旱发生具有明显的季节性,呈现出季节性连旱现象;从时间尺度来看,年尺度上干旱分布的模糊性和随 机性较小,干旱的确定性更容易度量,干旱分布不均匀性的稳定程度较低;对季节间云数字特征的对比显示,多年 来冬、秋季干旱分布的模糊性和随机性较大,冬季干旱分布的确定性最难以度量;在稳定性方面秋季最稳定,春季 次之,夏季最不稳定;在空间尺度上,鲁西北地区发生干旱、严重干旱和特大干旱的频次最高;发生轻度干旱的频 次最高区位于胶东半岛,鲁南地区次之;发生中度干旱的频次最高区位于鲁中地区,鲁南地区次之;由超熵值大小 判定干旱分布不均匀性的稳定程度,表现为鲁西北地区最稳定,鲁中地区次之,胶东半岛最不稳定;从干旱分布的 均匀性分析得出鲁西南地区干旱分布最不均匀,鲁西北地区干旱分布最均衡;山东省干旱频次在空间上的分布表 现为春旱和冬旱呈从西北向东南递减的趋势,秋旱比较严重。云模型针对半湿润地区的干旱分布具有较好的应 用前景。     

冲积河流推移质输沙最优河道形态影响因素理论分析

为从理论上确定水沙动力、阻力和边界条件对冲积河流推移质输沙最优河道形态和最小比降的影响,基于 水力半径分割方法将河床整体糙率划分为河岸糙率和河底糙率;采用河道形态自动调整变分方法,以等腰梯形为 河道过水断面,推导推移质输沙率与河道形态的关系,分析河岸与河底相对糙率、河岸坡角、流量、输沙率、中值 粒径和河底糙率对最优河道形态和最小比降的影响。结果表明：最优河道形态和最小比降随河岸与河底相对糙 率的增大而减小,随河岸坡角的增大而增大。流量或者河底糙率的增加将使最小比降减小,同时造成最优河道形 态趋向窄深。输沙率或者中值粒径的增加将使最小比降增大,但两者对最优河道形态演变的影响不同,输沙率增 大将使最优河道形态向宽浅发展,而中值粒径增加将使最优河道形态向窄深发展。