Alkylated ureas: mineralization and evaluation as N sources

An incubation experiment was conducted for 11 weeks to study the mineralization of ten alkylated ureas and urea in soil. Six of the alkylated ureas viz. methylurea(MU), 1,3-dimethylurea(1,3DMU), 1,1-dimethylurea(1,1DMU), ethylurea(EU), 1,3-diethylurea(1,3DEU) and butylurea(BU) and urea mineralized during the experiment. Urea mineralized immediately, while alkylated ureas mineralized after an incubation period ranging from less than a week to four weeks (delay period of mineralization). The delay period increased in the following sequence MU < 1,3DMU < EU < BU < 1,1DMU < 1,3DEU, but after the delay period was over the compounds mineralized almost as rapidly as urea. The delay period varied according to the number of carbon atoms in the alkyl group and their position with respect to each other on the molecule. It appeared to be specific for each compound and was apparently not influenced by the presence of urea or other alkylated ureas. This character can be used to develop mixture of various alkylated ureas to obtain N mineralization at the desired time. Rapid evolution of CO₂ and N₂O was observed during the mineralization of urea as well as alkylated ureas. Increase in soil pH was also observed during this period. The simultaneous ocurrence of these events suggested the formation of urea as an intermediate during the mieralization of alkylated ureas. None of the alkylated ureas showed adverse affect on emergence of wheat seedlings and except DEU and BU at high concentration no other alkylated urea showed any adverse effect on initial growth of wheat seedlings.     

UV-固化光纤色标油墨

报导了一类新型的化学功能材料———ＵＶ固化光纤色标油墨。该材料由可ＵＶ固化的有机硅环氧安息香酸丙烯酸酯（ＳＥＢＡ）和脂环族环氧丙烯酸酯（ＡＣＥＡ）两种光敏预聚物为基料，以自行合成的光敏染料———分散红氨基甲酸酯丙烯酸酯（ＲＵＡ）、分散蓝氨基甲酸酯丙烯酸酯（ＢＵＡ）和吖啶黄氨基甲酸酯丙烯酸酯（ＹＵＡ）为着色剂，加入必要的添加剂配制而成的ＵＶ固化光纤色标油墨。该色标油墨已在光纤生产中得到应用。     

一种新型有机非线性光学材料的光折效应及其产生机理

本文介绍了一种新近研制的光折聚合物。实验表明，除去吸收和反射，入射光束经聚合物后的第一布拉格衍射效率高达８６％，材料也显示出双光束耦合的净增益高于２４０ｃｍ＾－１。这些结果表明，这种新型研制的光折聚合物材料是替代无机光折晶体的实用材料。     

NH4SCN从ROH-CTMAB-C12H26载金有机相中反萃金

研究了硫氰酸铵（NH4SCN）从混合醇（ROH）－十六烷基三甲基溴化铵（CTMAB）－正十二烷（C12H26）载金有机相中反萃金，考察了平衡时间，PH值，反萃剂浓度，温度等因素对反萃率的影响及有机相的循环使用，绘制了反萃等温曲线，结果表明，NH4SCN对金具有较高反萃率，可顺利实现金的反萃。     

饮用水中天然有机物的分析与表征方法

天然有机物(NOM)是一类分布广泛、成分复杂的有机混合物,可严重影响饮用水的处理效率,并可能对出水水质产生严重的不利影响。因此,为了改进和优化饮用水的处理过程,在研究和实际应用阶段对NOM进行表征和定量以了解其结构特性和反应性具有重要意义。文中先对NOM的富集方法进行了介绍,接着梳理了不同分离方法的依据及作用,最后总结了各类表征方法的原理及应用,以期有助于对NOM和饮用水处理的深入研究。     

Room-Temperature Solid-State Lithium Metal Batteries Using Metal Organic Framework Composited Comb-Like Methoxy Poly(ethylene glycol) Acrylate Solid Polymer Electrolytes

Solid polymer electrolyte with good thermal stability and flexibility is an excellent candidate for solid-state lithium metal batteries, while its low ionic conductivity caused by high crystallinity limits its application at ambient temperature. Here a metal organic framework (zeolitic imidazolate framework-8, ZIF-8) composited comb-like methoxy poly(ethylene glycol) acrylate polymer electrolyte (MCPE) with high ionic conductivity (9.96 × 10⁻⁵ S cm⁻¹ at 30 °C) is prepared by an in situ UV polymerization method. The as-prepared MCPE exhibits improved mechanical property due to the introduction of porous ZIF-8 nanofillers, which is beneficial to suppress the growth of lithium dendrites. Consequently, the LiFePO₄||MCPE||Li cells show a high capacity of 116 mAh g⁻¹ at 30 °C and 0.5 C, and maintain 89.4% of initial capacity after 150 cycles with the average Coulombic efficiency of 99.9%. These results demonstrate that the MCPE shows great potential in solid-state lithium metal batteries near room temperature.     

纳米粉及添加剂对压电陶瓷材料性能的影响

采用高能球磨法研磨出PZT-5纳米粉料，添加外购的纳米有机添加剂，按照传统的固相工艺法制备出了压电陶瓷材料，研究分析纳米粉料和纳米有机添加剂对压电陶瓷性能的影响。通过测试分析可以看出，纳米压电粉料与纳米有机添加剂的综合作用，降低了材料的烧结温度、相对介电常数εr,Qm值和以d31，提高了压电应变常数d333，从而压电电压常数g33、gh、dh成倍提高，这些对制作宽带、高灵敏度的换能器是很有好处的。     

铸件内析出性气孔形成及演化的直接观察与分析

采用透明模型合金实时观察了铸件析出性气孔的形成发展,结果发现,纯物质凝固时,析出性气孔的产生发生于凝固型壳形成之后,随着凝固自型壁向中心凝固,呈现自周边向中心的气条生长。对于合金凝固,析出性气孔在凝固基本完成之后伴随着热裂及缩松的发生开始产生,呈现一定的偏聚现象。浇注前熔体过热度的提高将使析出性气孔更加密集,铸型和环境温度的降低有利于降低气孔的数量及分布范围,采用真空除气,可有效地抑制析出性气孔的产生和热裂缩松缺陷的形成。     

Polynitroalcohols obtained through nitro aldol reaction between nitro oligomers and C1‐C2‐aldehydes

Polynitroalcohols (PNA) were obtained by A_N‐reaction of nitro oligomers from ground waste rubbers (NO‐GWR) with C₁‐C₂‐aldehydes in presence of organic bases triethanolamine, triethylamine and cyclopropylamine. The A_N‐reaction was studied at temperatures from 30 to 50°C, time 4 h, and NO‐GWR : aldehyde = 1 : 0.5/2.0 mass ratios in the solution. PNA were characterized by elemental analyses, such as ¹H NMR spectra, IR spectroscopy—baseline method with internal standard and thermal analyses. The quantitative functional composition of PNA (%NO₂, %C?O, and %OH groups) was proved to be similar to the composition of PNA obtained from model butadiene–styrene nitro oligomer (BSNO). It was concluded that NO‐GWR could replace NO based on elastomers in nitro aldol reaction with formaldehyde and acetaldehyde. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 3241–3250, 2006     

气相色谱法测定有机化合物的蒸发热

本文用气相色谱测定了多种烷烃、芳烃、醇类和酯类的蒸发热。结果表明,测定数据与文献数据基本一致,误差一般在±5%以内。是一种简单、快捷的测定方法。