生物质转化的共性问题研究——生物质科学与工程学的建立与发展

生物质资源的高值转化是研究热点。由于现有的生物质利用技术存在的技术单一,缺乏系统性理论指导等问题,导致原料利用率低,经济效益差,难以实现工业化生产,迫切需要建立新的理论体系。通过深入分析生物质转化过程中的共性问题,在综合多学科知识的基础上,提出了生物质科学与工程学这一理念,从生物质原料工程学,生物质转化过程工程学和生物质产品工程学三方面对生物质利用技术进行了全面、系统的研究,为生物质类可再生资源的高值化利用提供了新的研究思路。     

超细纤维素胶体和丙烯酰胺的接枝共聚

本文用纤维素材料经酸分解制备具有平衡聚合度（LODP）的微晶纤维素，再分散成超细纤维素胶体（准均相纤维素体系）。用扫描电镜（SEM）观察处理前后的纤维素颗粒尺寸，并比较它们和丙烯酰胺接枝共聚的反应速率、聚合转化率、接枝率、接技效率、聚丙烯酰胺支链的分子量及其分布的情况。     

Isolation,identification, and function of the Dufour gland secretion ofXylocopa virginica texana (Hymenoptera: Anthophoridae)

The Dufour's gland secretion ofXylocopa virginica texana possesses short-term repellency for conspecifics when applied to passion flowers. This secretion contains a number of straight-chain hydrocarbons. The two major components are the methyl esters of palmitic and myristic acid. A mixture of the two esters and two of the available hydrocarbons were as effective as the Dufour's gland extract in eliciting a response in females to the passion flower,Passiflora incarnata, to which the extract was applied.Approved as TA13387 by the Director, Texas Agricultural Experiment Station and conducted in cooperation with the USDA. Supported in part by NSF-DEB-76-03963.     

STEAM OXIDATION OF CARBON FORMED BY THERMAL DEGRADATION OF PMMA IN ALUMINA

In the processing of multilayer ceramic multichip modules (MCM's), a ceramic substrate, such as alumina, along with a polymer, such as poly(methyl methacrylate) (PMMA), solvents, plasticizers, flocculants, is thermally degraded before sintering. The thermal degradation of PMMA from the green body of oxide ceramics leaves behind some amount of residual carbon in the ceramic. Carbon concentration above 100 ppm has a deleterious effect on the physical properties such as fkxural strength, density, breakdown voltage and dcnsification behavior of the ceramic. This paper discusses the kinetics of oxidation of carbon formed by the thermal degradation of poly(methyt methacrylate) in alumina. Pellets of 5 urn and I urn size alumina were made at 6000 psig in a single step change. Kinetic runs were made in the temperature range of 673 to 993 K with steam as the oxidant at a flow rate of 9.96E-03 g/cm² sec. The organics (polymethyl methacrylate, methyl ethyl ketone, methanol) concentration was varied from 5 to 20 by weight%. The oxidation products were analyzed using a Varian 3700 gas chromatograph coupled with CDS 111 integrator, and by volumetric analysis. Carbon analysis was carried out at the IBM Fishkill center using a Leco analyzer. Kinetic rates and activation energies are evaluated.     

Antioxidant efficacy of amino acids in methyl linoleate at different relative humidities

Antioxidant efficacy of the amino acids methionine, tryptophan, aspartic acid, serine, alanine and arginine in methyl linoleate were compared to a methyl linoleate control at 2,50 or 79% relative humidity (RH) at 37°C. Antioxidant efficacy varied with RH and the individual amino acids. Arginine had the highest antioxidant efficacy at all RH values compared to the control. The efficacy of alanine was equal to that of arginine at RHs of 50 and 79% but was lower at 2% RH. The presence of aliphatic, alkaline amino, hydroxyl or thiol groups in the side chain of the amino acids increased the antioxidant efficacy at high RHs.     

2-羟基-3-氰甲基-5-甲基苯乙酮的合成

探索黄酮醋酸类化合物中间体的合成方法。通过酰基化、Fries重排、氯甲基化和氰化合成2 -羟基 - 3-氰甲基 - 5 -甲基苯乙酮 ,获得了满意的收率 ( 88.5 % )。采用新方法合成了鲜见文献报道的新化合物 2 -羟基 - 3-氰甲基 - 5 -甲基苯乙酮。该方法具有反应时间短、操作简便、收率好等优点。     

接种固氮菌对纤维素分解过程的影响

从纤维素分解菌与联合固氮菌的接种配比,研究了混合培养对滤纸分解的影响。试验共设6个处理样,总接种量均为10%(V/V):处理Ⅰ,2%固氮菌+8%纤维素分解菌;处理Ⅱ,4%固氮菌+6%纤维素分解菌;处理Ⅲ,6%固氮菌+4%纤维素分解菌;处理Ⅳ,10%纤维素分解菌;处理Ⅴ,10%固氮菌;CK(空白对照)。结果显示:与处理Ⅳ相比,处理Ⅰ、Ⅱ的CMC酶活力及处理Ⅰ、Ⅱ、Ⅲ的滤纸分解率有明显提高。接种固氮菌的各处理样中,培养液中氮素含量与CK相比均有显著提高(P<0.05),且培养过程中pH值比较平稳,而未接种固氮菌处理培养液的氮素则低于CK,pH急剧降低。所有处理样中,接种2%固氮菌效果最佳,培养192h,其CMC酶活力与滤纸分解率比处理Ⅳ分别提高43.4%、240%;与处理Ⅴ相比,固氮菌数有显著增加(P<0.05),培养液中氮含量提高28.0%。     

Electrochemical insertion of sodium into hard carbons

The electrochemical insertion of sodium ions into different types of hard carbons was achieved in electrolytes composed of ethylene carbonate as the solvent and NaClO₄ as the salt. For all the materials studied the sodium uptake increases when the carbon highest heat treatment temperature (HTT) decreases. PAN-based carbon fibres appear to be suitable structures to allow significant sodium insertion. Thus, T650 ex-PAN fibres lead to a reversible capacity close to 209 mAh g⁻¹. In that case, sodium insertion occurs in two main ways: one is the adsorption on the single graphene layers and the other is the concomitant insertion into the porosity that occurs below 0.1 V versus Na⁺/Na. This second mechanism, which is indicated by a low-voltage plateau on the electrochemical curves, allows significant insertion. The compared electrochemical study of two saccharose-coke samples corresponding to different regions of Dahn's classification underlines the importance of the carbon precursor and of the manufacture process. The reversible capacity is equal to 184 mAh g⁻¹ for the sample heat treated at 800 °C which presents a high hydrogen content whereas it is close to 145 mAh g⁻¹ for the one characterized by a HTT of about 1500 °C and a low hydrogen content. The best electrochemical performances are obtained for pyrolyzed cellulose carbons. Indeed, the reversible capacity is about 279 mAh g⁻¹. Outgassing these carbons at 950 °C results in such a decrease of the reversible capacity down to 145 mAh g⁻¹. That can be related either to the thermal elimination of heteroelements or to modifications of the pore size distribution. Consequently, the most suitable hard carbon material for anodic applications in rechargeable sodium-ion batteries should both present a high residual hydrogen content and a significant microporosity.     

Effects of octadecanoid metabolites and inhibitors on induced nicotine accumulation inNicotiana sylvestris

We examined the effects of inhibitors of the octadecanoid pathway (n-propyl gallate, acetosalicylic acid, salicylhydroxamic acid, methyl salicylate, and antipyrine) on wound- and jasmonate-induced nicotine accumulation and compared the nicotine-inducing ability of exogeneous additions of linolenic acid (18:3) and its methyl ester, linoleic acid (18:2), abscisic acid, traumatic acid, and methyl dihydrojasmonate to the nicotine-inducing ability of exogenous additions of methyl jasmonate (MJ). The first four of these inhibitors significantly reduced wound-induced nicotine accumulation when applied in a lanolin paste to wounded tissues immediately after wounding at concentrations of 89–90µg/plant. When methyl salicylate and propyl gallate were mixed individually with MJ, neither inhibited MJ-induced nicotine synthesis, which suggests that the inhibitors block jasmonate synthesis or release from stored pools and not its effects. Linolenic acid or its methyl ester applied to undamaged plants or damaged plants (to either damaged or undamaged leaves) or to the roots of hydroponically growing plants did not induce nicotine accumulation or increase nicotine accumulation above levels found in damaged plants. Similarly, traumatic acid, linoleic acid, and abscisic acid did not induce nicotine accumulations. Methyl dihydrojasmonate, which is biosynthetically derived from linoleic acid, had 12–56% of the nicotine-inducing acitivity of MJ when added to the roots of hydroponically grown plants. The signal transduction pathway mediating wound-induced nicotine production therefore shares many features of the pathway eliciting wound-induced proteinase inhibitor production but differs in not being regulated at the lipase step in jasmonic acid production and not being responsive to abscisic acid.     

Aldol condensation in gaseous phase by zeolite catalysts

Vapour-phase reactions of, in situ, prepared formaldehyde with methyl propionate were studied using X, Y and ZSM-5 zeolite catalysts. Base properties of these zeolites were enhanced by KOH or NaN₃ treatment. The niobium and molybdenum ZSM-5 zeolite supported oxides were also tested for their catalytic activity. The results are discussed in terms of an ability of zeolite catalysts to synthesize methyl methacrylate.