Fabrication and characterization of electrospun porous cellulose acetate nanofibrous mats incorporated with capric acid as form-stable phase change materials for storing/retrieving thermal energy

Electrospun cellulose acetate (CA) nanofibrous mats incorporated with capric acid was studied to fabricate form-stable phase change materials (PCMs) for storing/retrieving thermal energy. Electrospun CA nanofibrous mats with different porous structures and specific surface areas were firstly prepared through regulating the volume ratio of mixture solvent of acetone/dichloromethane (DCM). Effects of different volume ratio of mixture solvent and mat thickness on the morphological structure, specific surface area, and absorption capacity of CA nanofibrous mats were systematically investigated. The results indicated that CA nanofibrous mats were highly porous on the surface; hence, they were capable of absorbing a large amount of capric acid. The maximum absorption capacity of CA mats via electrospinning with volume ratio of acetone/DCM being 5/5 was ~95.8 wt%, due to its higher specific surface area of ~17.1 m²/g. The specific surface area and capric acid absorption capacity of CA nanofibrous mats increased with the increases of mat thickness. As the thickness of nanofibrous mats increased from 10 to 85 μm, the corresponding specific surface area and capric acid absorption capacity of mats increased respectively from 7.2 to 29.0 m²/g and 92.1 to 98.5%. Morphological structures, as well as the properties of thermal energy storage and thermal insulation of the fabricated form-stable PCMs, were studied by scanning electron microscopy, differential scanning calorimetry, and measurement of freezing times, respectively. The results indicated that the resulting form-stable PCMs could well maintain their phase transition characteristics and demonstrated great thermal energy storage capability and temperature regulation ability.     

水体沉积物中有效砷的测试新方法研究

一种氧化铁/醋酸纤维素复合膜(FeO/CAM)被用于太湖沉积物中砷的生物有效性评估.结果发现,在水介质中,FeO/CAM对沉积物中砷的富集量随土水比增加而呈乘幂函数减少,在土水质量比为0.025(即1:40)之后趋于某一平台值;在土水比为0.025并得到充分振荡的条件下,沉积物中释放的有效砷被FeO/CAM富集至膜中,并随时间增加而增加,至24 h后逐渐趋于平衡,这一过程恰当地模拟了生物对砷的吸收.因此,FeO/CAM可以用于有效砷的体外测试.利用FeO/CAM对12个总砷含量为6.4～34.6 mg·kg-1的太湖沉积物样品中的有效砷进行了测定.结果发现,FeO/CAM提取的有效砷含量与磷酸盐缓冲液提取的有效砷含量之间显著相关.太湖沉积物中的有效砷含量与总砷、总磷、有机质和吸附磷含量以及磷吸附饱和度显著相关,说明沉积物理化属性对有效砷含量有重要影响.FeO/CAM克服了化学试剂提取过程中引起的非有效态砷释放的根本缺陷,因此,FeO/CAM方法在沉积物有效砷含量的测定时比化学试剂提取法可能更准确.     

白腐菌降解纤维素和木质素的研究进展

纤维素和木质素是潜在的可再生资源，近年来，利用微生物对它们进行降解已成为研究的热点。虽然纤维素较木质素易降解，但其被木质素包裹，故降解的关键问题就是木质素的降解。本文从木质纤维素的生物可降解性出发，重点讨论白腐菌降解木质素酶系及其作用机理。     

改性枸杞枝作为反硝化脱氮碳源的研究

为提高枸杞枝作为反硝化碳源的效能,采用甲醇（体积占比分别为0、20%、50%、100%）-水-NaOH （0.01 g·mL^-1）体系（分别简称为0组、20%组、50%组、100%组）对枸杞枝进行改性处理,研究原枸杞枝的静态释碳、改性前后枸杞枝的静态反硝化特性、表面形态和脱氮动力学.结果表明,原枸杞枝释碳过程同时符合二级动力学方程和Ritger-Peppas方程;第I阶段（1~3 d）为碳源快速释放期,第II阶段（4~21 d）为碳源稳定释放期;改性后枸杞枝纤维素和半纤维素含量占比增加了8.7%~35.2%;不同甲醇-水-NaOH体系改性枸杞枝平均反硝化速率依次为20%组>50%组>0组>100%组>对照组,20%甲醇-水-NaOH组反硝化速率最高（0.76 mg·g^-1·d^-1）,表明20%甲醇-水-NaOH （0.01 g·mL^-1）是枸杞枝改性的最佳条件;改性后的枸杞枝表面结构粗糙、不规则且有大量的孔洞产生,适合脱氮微生物附着生长,其反硝化脱氮过程符合Monod动力学方程（R²=0.96）.     

Adsorption of heavy metal ions from aqueous solution by carboxylated cellulose nanocrystals

A novel nanoadsorbent for the removal of heavy metal ions is reported.Cotton was first hydrolyzed to obtain cellulose nanocrystals(CNCs).CNCs were then chemically modified with succinic anhydride to obtain SCNCs.The sodic nanoadsorbent(NaSCNCs) was further prepared by treatment of SCNCs with saturated NaHCO 3 aqueous solution.Batch experiments were carried out with SCNCs and NaSCNCs for the removal of Pb 2+ and Cd 2+.The effects of contact time,pH,initial adsorption concentration,coexisting ions and the regeneration performance were investigated.Kinetic studies showed that the adsorption equilibrium time of Pb 2+ and Cd 2+ was reached within 150 min on SCNCs and 5 min on NaSCNCs.The adsorption capacities of Pb 2+ and Cd 2+ on SCNCs and NaSCNCs increased with increasing pH.The adsorption isotherm was well fitted by the Langmuir model.The maximum adsorption capacities of SCNCs and NaSCNCs for Pb 2+ and Cd 2+ were 367.6 mg/g,259.7 mg/g and 465.1 mg/g,344.8 mg/g,respectively.SCNCs and NaSCNCs showed high selectivity and interference resistance from coexisting ions for the adsorption of Pb 2+.NaSCNCs could be efficiently regenerated with a mild saturated NaCl solution with no loss of capacity after two recycles.The adsorption mechanisms of SCNCs and NaSCNCs were discussed.     

pH影响下小麦根吸附极性有机物的行为研究

文章以标准纤维素为对照吸附剂,以菲为对照吸附质,采用批量平衡振荡法进行吸附实验,研究不同pH条件下,小麦根吸附极性污染物(2,4-二氯苯酚和硝基苯)的行为差异。结果表明:污染物吸附以疏水性分配为主,吸附系数(K_d)值随化合物疏水性的增强而增强;非解离型极性污染物(硝基苯)的吸附与疏水性污染物(菲)类似,吸附等温线呈线性,相关系数(R²)均大于0.98,同时pH对吸附的影响无显著性差异(P>0.05);解离型极性污染物(2,4-二氯苯酚)的吸附随pH增加而降低,仅在pH 5.0时呈现吸附线性,在pH 7.0和8.0时均呈非线性,等温线逐渐向浓度轴弯曲,这源于疏水作用以及解离的2,4-二氯苯酚与吸附剂之间静电作用的共同影响。根的吸附能力大于纤维素,这与根中含有类脂物质有关。     

二乙烯三胺改性花生壳纤维素对水中刚果红的吸附

采用环氧氯丙烷和二乙烯三胺对花生壳中纤维素进行改性,制备了二乙烯三胺花生壳纤维素（DMPSC）,运用红外光谱（FTIR）进行表征,并探究了DMPSC对刚果红的吸附性能和机理。结果表明,DMPSC的吸附率明显高于其他吸附剂。在原始pH,吸附剂用量为1 g·L-1,吸附时间为180 min,温度为8、30和50℃时,100 mg·L-1的刚果红溶液吸附量分别达到83.24、99.04和99.78 mg·g-1。吸附过程符合Langmuir等温线模型,在8℃时饱和吸附量（qm）为111.86 mg·g-1。准二级动力学方程能更好地描述吸附动力学过程,表观活化能Ea为56.88 kJ·mol-1,升高温度有利于DMPSC对刚果红的吸附,该过程属于化学吸附。     

改性纤维素吸附剂的合成及其对铜离子的吸附

建立了一种简单方便的纤维素改性的固相合成方法。采用普遍廉价的滤纸作为原料,用固相合成法将预处理后的滤纸纤维经琥珀酸酐进行酯化改性,制备成新型的纤维素吸附剂,通过质量增比、扫描电镜、傅里叶红外光谱仪和X射线衍射仪对制备的吸附剂进行了分析表征,并且探究了离子初始浓度、溶液pH和吸附时间对改性纤维素吸附铜离子的影响。结果表明,在室温下初始离子浓度为1 000 mg/L,离子溶液体积为50 mL,加入0.1 g纤维改性剂,pH 为 4.0~5.0,吸附平衡时间为50 min时,滤纸纤维改性后最大吸附铜离子质量可达470 mg/g,铜离子去除率达到94%。     

半-IPN羧甲基纤维素/聚(丙烯酰胺-共-甲基丙烯酸钠)水凝胶制备及其吸附性能

羧甲基纤维素(CMC)水溶液中,通过自由基共聚制备半-互穿网络(IPN)羧甲基纤维素(CMC)/聚(丙烯酰胺-共-甲基丙烯酸钠)(poly(AAm-co-NMR))水凝胶。研究CMC含量对半-IPN水凝胶溶胀率及对甲基紫的吸附性能影响。IPN-0.25、IPN-0.50和IPN-1.00对甲基紫的平衡吸附容量分别为111.0、182.3和237.6 mg/g。分别采用拟一级、拟二级和粒内扩散模型拟合实验数据,结果表明,拟二级动力学模型最符合该体系,其相关系数R2最高,说明水凝胶对甲基紫的吸附主要为化学吸附。     

纤维素-铝-硅复合物的制备及对重金属离子的吸附

以微晶纤维素为基质 ,制备了带有 NH2 基团的纤维素 -铝 -硅复合物 ,测定了该复合物对水溶液中 Hg2 + 、Cu2 + 的吸附性能。讨论了溶液温度、p H值、金属离子浓度及时间对吸附性能的影响 ,结果表明它对Hg2 +和 Cu2 +具有较高的吸附容量和较快的吸附速度。