溴代双酚A型不饱和聚酯树脂的阻燃机理

利用TGA、DSC、热解-电导率仪,研究了文题内容。实验结果说明了溴的引入,使树脂具有良好的阻燃性,当溴含量大于7.63%(wt)时,树脂即能自熄。溴使树脂热解过程成碳倾向增加,分解生成的溴化氢是有效的自由基捕获剂。三氧化二锑和溴同时引入,对阻燃具有协同效应。     

壳聚糖的γ射线辐射降解研究

动力学;无规降解;断链机理;壳聚糖的γ射线辐射降解研究     

TiO2光催化降解4-氯苯酚过程中的电分析监测

采用循环伏安法和紫外光谱法对有机物的光催化降解进行机理研究和在线监测.以标准光催化剂DegussaP25在紫外光照射下催化降解4-氯苯酚,发现在降解过程中至少有两对氧化还原中间产物对苯二酚-苯醌和羟基氢醌-羟基苯醌.由4-氯苯酚及中间产物的电极响应,可以观测到它们在光催化降解过程中的含量变化,从而对整个过程实现在线监测,并由此全面了解光催化反应机理.从不同反应时间后测得的紫外光谱可以看到,苯环特征峰逐渐消失.这表明4-氯苯酚的苯环逐渐被打开,直至被彻底降解.     

聚氧化乙烯/苯乙烯-马来酸钠共聚物共混体系性能研究

用热分析（DSC、TG）和FTIR对聚氧化乙烯（PEO）/苯乙烯-马来酸钠（St-alt-MANa,简称SMANa)共聚物共混体系的相容性、分子间作用、热失重等性质进行了研究。结果表明,共混物可以任意比互溶,它们之间的相互作用是PEO的醚键“-O-”和共聚物盐中的“-COOH”之间形成了氢键。TG分析结果表明,随温度的升高,首先形成了酸酐,这可由FTIR光谱确定。热降解产如CO2作为酸酐和共聚物中羧基的降解产物。与不饱和结构相关的谱带（1774cm^-1、1449cm^-1)在350℃和450℃的红外光谱中可观察到,这可能是主要的碳-碳链断裂的结果。共混体系的Tg随SMANa含量的增加而增加,而体系结果温度Tc、熔融温度Tm却略有下降,这说明两组分间具有良好的溶混性。     

Dynamic and Isothermal Thermogravimetric Degradation of Poly(vinyl Chloride)/Chlorinated Poly(ethylene) Blends

The thermal degradation of poly(vinyl chloride)/chlorinated poly(ethylene) (PVC/CPE) blends of different compositions was investigated by means of dynamic and isothermal thermogravimetric analysis in flowing atmosphere of nitrogen. Kinetic parameters (the apparent activation energy E, and pre-exponential factor Z) were calculated after Flynn-Wall-Ozawa method for the first stage of dynamic degradation of PVC/CPE blends, and after Flynn method for the isothermal degradation. In both cases, there is the compensation dependence between the values E and logZ. The values of compensation ratios as well as the characteristics of TG and DTG curves, confirm the stabilizing effect of CPE on PVC dehydrochlorination. This revised version was published online in July 2006 with corrections to the Cover Date.     

Production of oxychemicals from precipitated hardwood lignin

Lignin is a major byproduct in the biomass-to-ethanol process. The lignin produced from acid treatment of biomass has characteristics suitable for further conversion to organic chemicals. It is free of contaminants and has a relatively low molecular weight. In this study, catalytic oxidative conversion of the acid-soluble lignin precipitated from acid hydrolysates of hardwood was investigated. The process is based on aqueous alkaline oxidation of lignin with dissolved O₂ in the presence of Fe³⁺ and Cu²⁺ catalysts at moderate reaction temperatures (160–180°C). Aromatic aldehydes, ketones, and organic acids are found to be the primary products identifiable on extraction with ether. The combined weight yield of the total ether extractable products is about 20–25% of the initial lignin. The yield of the aldehydes (vanillin + syringaldehyde) is in the vicinity of 15% with an additional 3 to 4% of aromatic ketones. The yields of aldehydes plus ketones observed in this work far exceeded those obtainable from the conventional alkaline air oxidation of spent sulfite liquors. This article also provides comprehensive batch reaction data on conversion and product distribution.     

掺杂TiO2纳米粉的合成、表征及催化性能研究

 考察了制备方法对掺杂Fe2O3,ZrO2或SnO2的TiO2纳米粉的XRD谱及催化性能的影响．结果表明,用共沉淀法制备的Fe2O3·TiO2对其XRD谱强度的影响较大,而负载法制备Fe2O3／TiO2对其XRD谱的强度无影响;两种方法制备的掺杂ZrO2或SnO2的TiO2样品对XRD谱均无影响．TEM结果表明,TiO2纳米粉的晶粒均匀,粒径为14～18nm．苯酚水溶液的光催化氧化分解反应结果表明,与TiO2样品相比,负载型Fe2O3／TiO2的催化活性明显较高,但ZrO2／TiO2,SnO2／TiO2和共沉淀型Fe2O3·TiO2的催化活性变化不大．可以认为,对掺杂Fe2O3的TiO2催化剂,负载法是较好的制备方法．     

TiO_2制备方法对光催化分解十二烷基苯磺酸钠的影响

本文以TiCl4 为前体 ,采用沉淀法、气相沉积法和溶胶 凝胶法分别制备了TiO2 光催化剂 ,比较了它们在十二烷基苯磺酸钠 (SDBS)光解反应中的催化活性。结果表明 ,以日光灯作光源时 ,气相沉积法获得的催化剂效果最好 ;以 5 0 0W紫外线高压汞灯作光源时 ,沉淀法获得的催化剂活性最高 ,10 0ml初始化学需氧量 (COD)为381mg/L的SDBS溶液 ,在 0 .1g催化剂作用下 ,室温光照 8h ,COD去除率可达 98 8%。在沉淀法制备的催化剂上 ,SDBS溶液的催化光解为一级反应     

壳聚糖及其衍生物与金属配位的研究进展

本文综述了壳聚糖、壳聚糖衍生物及其降解产物与金属配位的性能,形成某些配位化合物的条件、组成、结构及其表征,阐述了它们的应用。     

Photocatalytic degradation of trichloroethylene over BiOCl under UV irradiation

In this study, BiOCl samples were synthesized under different pH values and characterized by XRD, SEM, UV‐vis DRS, BET, photoelectrochemical measurement and PL. The photocatalytic performances of the as‐prepared samples were evaluated through the decomposition of trichloroethylene (TCE) under UV irradiation. The influences of several parameters such as solution pH and common inorganic anions on TCE removal were investigated. Results indicated that BiOCl‐0.6 exhibited better photocatalytic performance than BiOCl‐6.0 because of its higher migration ability of photo‐induced carrier. The photocatalytic degradation of TCE over BiOCl‐0.6 followed pseudo first‐order kinetics and appeared to be more efficient in acidic solution than in alkaline. TCE was almost completely dechlorinated in 120 minutes. The inhibiting effect of naturally occurring anions was in the order of HCO₃^‐ >SO₄^2‐ >NO₃^‐, while Cl^‐ exhibited a dual effect. Moreover, BiOCl‐0.6 exhibited superior reusability after three cycles of repetition tests.