碱处理棉纤维结构及其在LiCi/DMAc中的溶解特性

采用NaOH溶液对棉纤维进行处理.通过X射线衍射研究了不同碱处理条件下棉纤维的晶面结构变化,表征了棉纤维的结晶度和晶粒尺寸.考察了碱处理棉纤维在LiCl/DMAc中的溶解性和溶解稳定性.结果表明碱处理后,棉纤维的晶面结构明显变化,棉纤维衍射峰发生明显的变化,结晶度和晶粒尺寸也有变化,且随碱的质量分数的变化非常明显,而处...     

酵母多基因表达载体在纤维素生物转化中应用

构建含酿酒酵母组成型强启动子PGK、G418抗性基因及rDNA片段的整合型载体pScIKP,利用rDNA多个同源重组位点,将外源基因以多拷贝整合到酵母染色体上,无需诱导即可持续表达;利用载体位于表达盒两端同尾酶,可插入多个基因表达盒,实现多基因稳定共表达.为检验共表达情况,反转录从绿色木霉中获得纤维素酶基因eg3和cbh2, 克隆并转化获得重组酵母菌株S.cerevisiae-ec. 该重组酵母能降解羧甲基纤维素形成水解圈;用羧甲基纤维素还原糖法和滤纸酶活力法测定酶活力,其最适温度和最适pH值与所表达单酶相似,表明共表达未影响两种酶的生物学特性;且双酶具有协同作用,能更有效降解非结晶纤维素.pScIKP载体能成功用于多个外源基因共表达和产物协同作用的研究,为构建能直接降解纤维素的酿酒酵母菌株,实现纤维素可再生能源的生物利用奠定了基础.     

Study on volume ratio and plasticizer screening of free coating membranes composed of ethyl cellulose and chitosan

The aim of this study was to optimize the formula of free blended coating membrane of ethyl cellulose (EC) and chitosan (CS), including their suitable ratio range and the best plasticizer used. The dry films were produced by a casting/solvent evaporation method, with different volume ratio of EC and CS solution plasticized by various plasticizers, respectively. The wet films were prepared by immersing dry films in pH 6.8 phosphate buffer saline (PBS) for 24 h. The promising ratio range of EC/CS was below 20/5 or 20/6 with various plasticizer, which was determined by comparing the viscosity of the blended solutions and the morphology of the blended films. The efficiency of plasticization was evaluated by measuring glass transition temperature (T_g). All the testing plasticizers have good compatibility with EC or CS and dibutyl phthalate (DBP) have the strongest efficiency inducing the lowest T_g (39.9°C) of the film. Mechanical properties were evaluated by the ratio of tensile strength (T) to elastic modulus (E). In the wet state, the films with DBP had the highest T/E value (1.2). The results of leaching of plasticizers also verified that DBP was the most stable plasticizer in the films. The release rates of tetramethylpyrazine phosphate (TMPP) through the pellets coated with the blended films of EC/CS (20 : 6 v/v) plasticized by various plasticizers showed that the more water‐soluble the plasticizer was, the more quickly TMPP dissolved from the coated pellets, which further indicated that the water‐insoluble plasticizers (such as DBP) could be more applicable to keep the sustained or controlled release property of the blended films in wet state. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 1932–1939, 2006     

Study of the influence of reaction conditions on the degree of substitution,intrinsic viscosity,and yield of oxidized cellulose acetate by factorial experimental design

A half‐fraction, two‐level, four‐factor factorial experimental design was used to study the effects of the acetic anhydride concentration, reaction temperature, reaction time, and sulfuric acid concentration on the degree of substitution, intrinsic viscosity, and yield of oxidized cellulose acetate (OCA). Oxidized cellulose containing 20% (w/w) carboxylic acid was used as the starting material. The data were fitted by multiple regression analysis with SAS software. The correlation coefficients obtained from plots of the predicted and observed values for the degree of substitution, intrinsic viscosity, and yield were 0.985, 0.993, and 0.991, respectively. Residual normal plots of the regression models showed a linear relationship. Lenth and main‐factor‐effect plots revealed an increase in the degree of substitution of OCA with an increasing concentration of acetic anhydride. The latter had no effect on the intrinsic viscosity and yield of OCA. An increase in the reaction temperature led to an increase in the degree of substitution and a decrease in the intrinsic viscosity and yield of OCA. The influence of the reaction time on the degree of substitution and intrinsic viscosity followed a trend similar to that observed with the reaction temperature, but the yield of OCA was unaffected. Increasing the concentration of sulfuric acid reduced the degree of substitution, intrinsic viscosity, and yield of OCA. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 96: 696–705, 2005     

聚合度对纤维素表面性能的影响

根据Washburn浸渍理论和van Oss-Good-Chaudhury组合理论及应用柱状灯芯技术测试了具有不同聚合度(DP)的纤维素的表面性能,同时与已报道的纤维素的表面能进行了比较。结果表明:纤维素的表面能随分子量的增加而增大,但主要是其Lifshitz-van der Waals力在起主导作用。研究还发现纤维素的表面能γS与聚合度DP之间的关系大致可以描述为:γS=37.56+0.02 DP,而纤维素的极性率P与聚合度DP之间的关系则是一种非线性关系,如:P=11.88-0.02 DP+9.10 DP2。     

海藻酸钠与纳米晶纤维素共混膜制备与性能研究

借助冷冻干燥技术制备了海藻酸钠与纳米晶纤维素共混膜以达到增强目的;探讨了不同含量的纳米晶纤维素与海藻酸钠共混膜的微观形貌、力学性能、吸水性能及孔隙率的变化;综合评价确定最佳的纳米晶纤维素含量在0.75%至1.00%之间。     

硅藻土/纤维素复合助滤剂在微污染原水处理中的应用

以硅藻土和纤维素为原料,通过溶胶-凝胶法制备出了新型硅藻土/纤维素复合助滤剂,探究了各种制备条件对助滤剂的影响,并在高岭土悬浊液中对硅藻土、纤维素和硅藻土/纤维素的助滤性能进行了比较,同时研究了硅藻土/纤维素助滤剂对实际微污染水过滤的影响。研究结果表明:复合助滤剂的最佳制备条件为纤硅比0.67,氨水浓度5.0×10^-4mol/L,蒸馏水/纤维素40 mL/g,EtOH/硅藻土20 mL/g,60℃恒温水浴;硅藻土/纤维素复合助滤剂的助滤性能要明显优于硅藻土和纤维素助滤剂;在微污染原水直接过滤过程中,投加硅藻土/纤维素助滤剂可提高各微污染物的去除率,结合微滤膜深度处理工艺,最终出水水质满足《生活饮用水卫生标准》(GB 5749-2006)的要求。     

改性细菌纤维素硫酸酯对Pb(Ⅱ)吸附性能的影响

以廉价且资源丰富的细菌纤维素为原料,研究制备了改性细菌纤维素硫酸酯吸附材料,并对其进行表征分析。以典型重金属污染物Pb(Ⅱ)为去除目标,考察了不同反应时间、溶液p H和反应温度等对改性细菌纤维素吸附Pb(Ⅱ)的影响。结果表明:经改性后细菌纤维素的吸附性能有所增加;其对Pb(Ⅱ)的平衡吸附量随p H的增大而增加,随温度的增加而减小;吸附过程符合拟二级反应方程和Langmuir吸附等温方程。     

Mechanical properties of silica aerogels prepared from a mixture of TEOS and organo-alkoxysilanes of type R1SiX3

Silica aerogels were prepared from a mixture of tetraethylorthosilicate and organo- alkoxysilanes. The effects of organo-alkoxysilanes on the mechanical properties of the silica aerogels were studied. The flexibility of silica aerogels was significantly improved by incorporation of organo-alkoxysilanes. When MTES and TEOS were combined as precursors of silica areogels, with the increased amount of MTES, the apparent elastic modulus and apparent compressive strength monotonously rose. At the same organo- alkoxysilanes to TEOS ratio, the size of alkyl groups of the organo-alkoxysilanes had little effect on the mechanical properties. In series of MTES and TEOS, the lowest elastic modulus of silica skeleton and the highest compressive strength of silica skeleton were observed at MTES to TEOS ratio of around 50：50. At a certain organo-alkoxysilanes to TEOS ratio, the elastic modulus of silica skeleton increased and the compressive strength of silica skeleton decreased with the size increase of the alkvl grouns.     

Preparation and properties of PMMA modified silica aerogels from diatomite

Diatomite was used as raw material to prepare sodium silicate with a modulus of 3.1 by alkalidissolution method and the resulted sodium silicate solution was employed as a precursor. Methyl methacrylate monomers were introduced in wet gels through solution-immersion, and upon heating at 70 ℃, the mesoporous surfaces throughout the skeletal framework were coated with the polymer layer. PMMA modified silica aerogels were successfully synthesized via ambient pressure drying. The properties were investigated by FTIR, NMR, TGA, nitrogen adsorption-desorption, FESEM and nano-indentation, etc. Results indicate that with the increasing of PMMA incorporated into silica aerogels, the bulk density and the BET surface area increase, the porosity decreases. Through the observation of FESEM, it is found that the interconnecting pores and the big pores add, the pore size distribution expands from 5-17 to 28-150 nm. By comparison, the PMMA modified silica aerogels achieve a 52-fold increase in hardness and a 10-fold increase in modulus.