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.     

凝固条件对纤维素/丝素蛋白纤维相形态及性能的影响

蛋白质纤维具有光滑柔顺、透气吸湿等优点,然而天然蛋白纤维产量有限。再生蛋白纤维的制备通常采用与其它成纤高分子接枝或共混的方法,有利于提高再生蛋白纤维的断裂强度。选用同为天然高分子的纤维素为基体,以共溶剂溶解纤维素与蛋白质,进而纺丝成形制得力学性能满足要求的纤维素/丝素蛋白共混纤维。为了探究凝固剂组成对纤维素/丝素蛋白共混纤维相形态及性能的影响,选用水、乙醇、乙醇/1-丁基-3-甲基咪唑氯盐([BMIM]Cl)等作为凝固剂。研究发现:乙醇作为凝固剂时,纤维素与丝素蛋白能很好地同时凝固;而当在乙醇凝固浴中加入适量的[BMIM]Cl径向均匀分散。通过对凝固剂组成的调控能有效提升纤维的力学强度。     

氧化纤维素的制备研究

介绍了氧化纤维素 (DAC)的制备过程 ,用正交法探讨了以NaIO4 作氧化纤维素时反应温度、溶液pH值、氧化剂浓度、反应时间以及交互作用对DAC醛基含量的影响 ,找到了影响醛基含量的主要因素为反应温度、反应温度与NaIO4 的交互作用、反应温度与溶液 pH值的交互作用。初步确定了制备氧化纤维素的反应工艺 ,使醛基含量较高时的最佳反应条件为 :反应温度 3 5℃ ,反应时间 3h ,NaIO4 质量分数 6.78% ,pH值为 2时 ,醛基含量达 68.2 0 %。     

2,4-D/CMC接枝物纳米粒子的制备与缓释性能研究

以羧甲基纤维素钠（CMC）为基材，甲基丙烯酸甲酯（MMA）和二甲基二烯丙基氯化铵（DMDAAC）为改性单体，通过乳液聚合制备了CMC-g-P(MMA-DMDAAC)共聚物，采用自组装方法负载2,4-二氯苯氧乙酸（2,4-D）得到2,4-D/CMC-g-P(MMA-DMDAAC)纳米药物缓释体系。利用傅里叶红外光谱（FTIR）、差示扫描量热法（DSC）、热重分析（TGA）、扫描电镜（SEM）、粒度分析仪对其结构和形貌进行表征，并探究其载药性能和缓释性能。结果表明，2,4-D/CMC-g-P(MMA-DMDAAC)载药粒子呈笼状结构，粒度分布为160～425 nm；其载药率随着CMC∶MMA∶DMDAAC的摩尔比增大而提高，最高可达40.8%；其药物累计释放率随CMC∶MMA∶DMDAAC的摩尔比增大而降低，其释放行为符合Weibull模型，遵循Fick扩散机理。     

纤维素衍生物液晶相转变和织态结构

本文综述了纤维素衍生物液晶态相转变和织态结构。描述了纤维素衍生物从各向同性态向液晶态的转变过程和液晶态的织构特征。讨论了溶液浓度和温度对液晶相织构的影响。探讨了各种因素,如溶剂、取代基含量、外加力场和外加磁场等对液晶相的形成及织态结构的影响。     

Infrared study of salt free and salt treated cellulose pyrolysis under nitrogen atmosphere

The pyrolysis under nitrogen of salt free and salt treated cellulose was studied by infrared spectroscopy. The results confirm the unzipping mechanism suggested by DTA and TGA studies, and show this mechanism to apply to the untreated and salt treated samples. The results also show the unzipping to stop at the stage of char formation. The onset of this stage was found to occur after the volatilization of only 45–50% of the initial sample of the borax treated cellulose, compared with 65–70% of the KCl treated cellulose and 80–85% of the untreated cellulose.     

HEC influence on cement hydration measured by conductometry

Cellulose ethers are of universal use in factory-made mortars, though their influences on mortar properties at a molecular scale are poorly understood. Recent studies dealt with the influence of hydroxyethylmethyl cellulose (HEMC) and hydroxypropylmethyl cellulose (HPMC) molecular parameters on cement hydration. It was concluded that the degree of substitution is the most relevant factor on cement hydration kinetics, contrary to the molecular weight. Nevertheless, the major role played by the substitution degree has not been verified for other types of cellulose ethers such as hydroxyethyl cellulose (HEC), which generally possesses a higher hydration retarding capacity compared to HPMC and HEMC. In this frame, a study of the impact of HEC molecular parameters on cement hydration was performed. A negligible influence of the molecular weight was observed. Moreover, the results emphasize that the hydroxyethyl group content mainly determines the delay of cement hydration.     

纤维素醚的特点、制备及在工业中的应用

综述了纤维素醚的种类、制备方法、性能和特点,以及纤维素醚在石油、建筑、造纸、纺织、医药、食品、光电材料及日化工业中的应用,介绍了一些具有发展前景的纤维素醚类衍生物的新品种并展望其应用前景。     

纤维素/NMMO·H_2O溶液体系流变性能的研究

利用 Brookfield DV-Ⅱ型粘度计对纤维素/NMMO·H2O 溶液体系的流变性能进行了研究,讨论了温度、纤维素浓度、浆粕聚合度及添加剂等对溶液粘度的影响。结果表明,纤维素/NMMO·H2O 溶液的流动活化能较低,因此其表观粘度随温度的变化不大;纤维素浓度和浆粕聚合度的增加都可使溶液粘度增大,但纤维素浓度对溶液粘度的影响更显著;抗氧化剂没食子酸丙酯(GPE)的加入减缓了加热时溶液粘度的下降,降低了纤维素的氧化降解;二甲亚砜(DMSO)的加入可有效地控制溶液粘度,改善溶液的加工性能。