氮掺杂纳米TiO_2改性涂料及其抗菌性能

将自制的氮掺杂锐钛矿型纳米二氧化钛光催化剂作为功能性组分,加入耐光催化氧化的硅丙乳胶涂料中,制备出一种新型光催化功能性建筑涂料,实现了可见光光催化效应。使用紫外-可见光吸收光谱研究该功能性涂料对紫外线的吸收能力;采用菌落计数法研究该涂料在可见光照射下对金黄色葡萄球菌的杀灭性能。同时分析了纳米粉体种类、引入量及方式对涂料紫外线的吸收性能和抗菌性能的影响。     

2,6-二乙酰基吡啶合成方法的改进

优化了2，6—二乙酰基吡啶的合成工艺。以2，6—吡啶二羧酸为原料，经过醇化及克莱森酯缩合反应，合成了2，6—二乙酰基吡啶，2，6—吡啶二羧酸二乙醇和2，6—二乙酰基吡啶的分离收率分别为94．1％和88．9％，2，6—二乙酰基毗啶的质量分数大于99％。     

从假性紫罗兰酮合成β-紫罗兰酮中主要副产物(I)的分离鉴定

假性紫罗兰酮在浓硫酸及 - 2 0°C低温条件下反应 ,主要生成 β-紫罗兰酮 ,少量的 α-及 γ-紫罗兰酮 ,同时生成副产物 ( I)及 ( II)。用 IR、1H NMR及 MS光谱分析方法 ,对副产物 ( I)进行了结构鉴定 ,结构为 3,4,4a,5 ,8,8a-六氢 - 2 ,5 ,5 ,8a-四甲基 - 2 H - 1 -苯并吡喃     

B_2O_3和CaF_2对C_3S-C_(2.75)B_(1.25)A_3-C_2S-C_3A水泥熟料矿物体系力学性能影响

研究了B2O3和CaF2对C3S-C2.75B1.25A3S珚-C2S-C3A熟料矿物体系的组成、结构与力学性能的影响。研究结果表明:在该熟料体系中C3S,C2.75B1.25A3S珔,C2S和C3A的适宜含量分别为50%,10%,25%和15%,B2O3和CaF2的适宜掺量为2%和1.5%。在最佳组成和制备工艺条件下,合成的阿利特-硫铝酸钡钙水泥的1d,3d和28d抗压强度分别达到18MPa,48MPa和95MPa以上,展现了良好的早期力学性能。同时,掺加CaF2能有效降低熟料中游离氧化钙的含量,促进阿利特在低温条件下形成。利用SEM-EDS,XRD等测试手段对熟料的组成、结构及性能进行了分析。     

SBR反应器中反硝化条件下去除苯酚工艺

基于异养反硝化原理,在序批式间歇反应器(SBR)中对反硝化同时降解苯酚的菌种进行了149 d的驯化,驯化通过逐步提高进水中苯酚和NO3--N的浓度进行.驯化结束后,进水苯酚质量浓度达到360 mg/L,葡萄糖质量浓度达到100 mg/L,NO3--N质量浓度达到240 mg/L,水力停留时间6 h,苯酚和NO3--N去除率均大于98%.反应器运行结果表明:进水苯酚质量浓度低于720 mg/L时,SBR反应器运行稳定;高浓度NO2--N(＞60 mg/L)可以严重影响微生物对苯酚以及NO3--N的去除能力,同时反应器中20.5%～23.5%的COD可被用于微生物的细胞合成.     

Isobutane/2-butene alkylation on MCM-22 catalyst. Influence of zeolite structure and acidity on activity and selectivity

The catalytic behavior of the novel MCM-22 zeolite for the continuous alkylation of isobutane with 2-butene has been investigated at a temperature of 50°C, 2.5 MPa total pressure, and a variety of olefin space velocities. At high olefin conversions the MCM-22 zeolite showed a very high initial cracking activity attributable to strong Brønsted acid sites, as well as to the existence of strong diffusional restrictions of the TMP's (formed inside the zeolite) to exit through the channels. At short times on stream (TOS), TMP's account for ca. 40% of the C₈ fraction. The olefin conversion and the cracking activity rapidly decline with TOS, while the alkylate product became richer in dimethylhexenes, indicating a predominance of 2-butene dimerization and a loss of hydrogen transfer activity as the catalyst aged. Moreover, MCM-22 gives less TMP's than large-pore zeolites (USY, beta, mordenite), but more than the mediumpore ZSM-5 at similar 2-butene conversion. The latter catalyst was much more selective for olefin dimerization than for isobutane alkylation, presumably because formation of the bulkier TMP's was strongly impeded in its smaller pores.     

生物膜载体吸附剂对Zn2+的吸附

本文对生物膜吸附Zn^2＋的行为进行了准一级动力学方程和Elovich模型方程的拟合，对实验测定的吸附等温线用Langmuir与Freundlich吸附模型进行拟合；考察了pH值及温度对生物膜吸附Zn^2＋的影响。结果表明，Zn^2＋在生物膜载体吸附剂上的吸附动力学过程与Elovich方程有较好的拟合度，R^2=0．99994。单一等温吸附过程与Langmuir方程具有较好的拟合度，R^2=0．99785；pH=6～8，室温25℃对Zn^2＋分有较高的去除率。     

Mg(OH)2及其与红磷复配阻燃聚丙烯复合材料的性能研究

研究了Mg(OH)2和Mg(OH)2/红磷复配体系阻燃聚丙烯材料的性能,选用热塑性弹性体POE对阻燃聚丙烯复合材料进行了增韧改性,结果表明:Mg(OH)2与红磷复配可以减少Mg(OH)2用量,降低对材料力学性能的损耗;POE较好地改善了材料的冲击性能,其添加量为15份时,材料的冲击强度可由8.14kJ/m2增大至12.83kJ/m2。最后利用锥形量热仪验证了Mg(OH)2/红磷复配体系的协同阻燃效应。     

Syntheses of TiO2 photocatalysts by the molten salts method: Application to the photocatalytic degradation of Prosulfuron

Titania photocatalysts were synthesised by the molten salts method by reaction of a titanium precursor with three different alkali metal nitrates (LiNO₃, NaNO₃, KNO₃). The titania powders obtained have been characterised using TEM, XRD, BET and UV-Vis absorption spectroscopy. Their photoactivities were evaluated by degrading a commercial sulfonylurea herbicide, Prosulfuron^®. It has been found that the rate constants increased in the following order: Li2 prepared in KNO₃, with a rate constant 1.4 times smaller than that of P25. The effect of calcination was also studied, especially for the sample prepared in NaNO₃ (TiO₂[Na]). An improvement in photocatalytic activity was observed when TiO₂[Na] was calcined in the region of 700–800 °C. Even though the photocatalytic activities obtained did not exceed or even equal to that of Degussa P25, nevertheless, this study constitutes the first attempt to synthesise titania photocatalysts by the molten salts method.     

用D_2EHPA-煤油溶剂萃取分离L-异亮氨酸

本文研究了从发酵液中用D2EHPA－煤油溶剂萃取分离L－异亮氨酸工艺．考察了萃取时pH值、萃取剂浓度和异亮氨酸浓度对于异亮氨酸和缬氨酸的萃取分配比的影响．在计算机上进行回归，得到以下分配模型：当1≤pH≤3．5时lgDIle＝0．09906pH2＋0．8625pH＋2．2696lgCHR－0．09188lg2CIle＋0．1766lgCIle－1．366lgDrmVal＝－0．0293pH2＋0．550pH＋1．2659lgCHR－0．2420lg2CIle＋0．4549lgCIle－1．696用此模型，应用分馏萃取理论，进行逐级计算，求取了萃取工艺的主要参数，并在φ20mm的多级离心萃取器上对上述结果进行了验证．结果表明：当CHR浓度为1．5mol／L，相比V：L：L’＝2：1：2，N’＝3，N＝6时，异亮氨酸的收率达到90％以上，纯度＞99％．实验取得了较为满意的结果．