沉淀酵母菌对Pb(Ⅱ)的吸附机理研究

应用红外光谱(FTIR)和X射线光电子能谱(XPS)等研究了沉淀酵母菌对Pb(Ⅱ)的吸附机理.从扫描电镜图片可以看出,吸附Pb(Ⅱ)后沉淀酵母菌细胞发生变形,细胞之间相互粘连;能量分析谱证实Pb(Ⅱ)与细胞表面的K进行了交换吸附;比较吸附Pb(Ⅱ)前后沉淀酵母菌的红外光谱可以发现,糖醛酸COOH基团C-O伸缩振动蓝移了13.59cm-1,C=O伸缩振动红移了5.42 cm-1,N-H伸缩振动峰红移了4 cm-1,C-O伸缩振动蓝移了2.86 cm-1,说明了COOH、C=O、C-O、N-H为沉淀酵母菌吸附Pb(Ⅱ)的主要活性基团.X射线光电子能谱进一步证实了吸附后Pb(Ⅱ)主要同N、O、P等元素形成配合物.沉淀酵母菌对Pb(Ⅱ)的吸附是离子交换和表面络合共同作用的结果.     

2-氢七氟丙烷熄灭聚甲基丙烯酸甲酯燃烧火焰的实验研究

采用二视窗小型燃烧室和数码摄像技术分别研究了2-氢七氟丙烷和二氧化碳对聚甲基丙烯酸甲酯(RMMA)燃烧火焰的熄灭过程;探讨了2-氢七氟丙烷对PMMA的点火延迟时间、火焰形貌和燃烧速率的影响;同时,运用傅立叶变换红外光谱(FTIR)对PMMA熄火表面的化学成份进行了分析.结果发现:极低浓度的2-氢七氟丙烷不仅不能灭火反而还能够促进PMMA的点火和燃烧,但在灭火剂浓度相对较高的情况下,2-氢七氟丙烷抑制样品点火和燃烧的能力要远高于二氧化碳.与二氧化碳灭火剂相比,2-氢七氟丙烷具有灭火浓度低、灭火效率高和灭火速度快等明显优点.此外,FTIR的分析结果显示PMMA熄火表面的化学成份没有明显变化,这表明2-氢七氟丙烷对RMMA燃烧火焰的熄灭作用可能主要是发生在气相中.     

Biodegradation of Poly(ε-caprolactone) (PCL) Film by <Emphasis Type="Italic">Alcaligenes faecalis</Emphasis>

The biodegradation behavior of PCL film with high molecular weight (80,000 Da) in presence of bacterium Alcaligenes faecalis and the analysis of degraded polymer film have been carried out. Thin Films of PCL were prepared by means of solution casting method and the bacterial degradation behavior was carried in basal medium, in presence of bacteria with time variation after UV treatment. It was observed that after UV treatment the degradation of polymer film was increased and the degradation rate followed a three steps degradation mechanism. The degraded polymer film was analyzed by means of Differential Scanning Calorimeter (DSC), Thermo Gravimetric Analyzer (TGA) and Fourier Transform Infrared Spectroscope (FTIR). DSC results revealed that at the initial stages of the degradation up to 15–20 days, the bacterium preferentially degrades the amorphous parts of the polymer film over the crystalline zone. Thermo gravimetric analysis highlighted the low temperature stability of degraded films with extent of degradation. FTIR results showed the chain scission mechanism of the polymer chains and also supported the preferential degradation of amorphous phase over crystalline phase in the initial stages of the degradation.     

The effect of the activation of carboxyl group and hydrogen migration on reaction pathway during the pyrolysis of triglycerides

ABSTRACT

This study investigated the activation of carboxyl group and hydrogen migration on the pyrolysis products of triglycerides. It was found that the activation of carboxylic group determined the efficiency of the decarboxylation reactions. The activation of carboxyl group influenced the pyrolysis products. The glycerol mono-stearate and glycerol mono-oleate were used as the model compounds to analyze the cracking of the ester bond. It was found that the first intermediate formed was RCOO·, but not RCO·. Large amount of ketone was found in the pyrolysis of stearate, while not in that of oleate. In comparison, alcohol was found in pyrolysis products of oleate, while not in stearate. The results indicated that during the pyrolysis process, the carbon-carbon double bond influenced both the cracking of the C-C bond and the transformation of the oxygen-containing functionalities. The activation of carboxyl group and hydrogen migration played essential roles in the determination of the formation of the pyrolysis products. In addition, the mechanism for the evolution of the acid, ester, ketone, aldehyde, alcohol, and other heavy compounds during the pyrolysis was also proposed.     

板栗内皮对水溶液中镉的吸附研究

采用生物吸附法去除水体重金属污染具有重要的现实意义.本文以板栗内皮为吸附剂,研究了溶液pH值、反应时间、吸附剂投加量对水溶液中镉的吸附量与去除率的影响;通过模型拟合、离子交换实验、电镜扫描（SEM）和红外光谱（FTIR）分析,对吸附机理进行了探讨.结果表明：板栗内皮是一种理想的镉吸附剂,适应pH值范围宽（3～6）,达到...     

Copper(II) ions’ removal from aqueous solution using green horse-chestnut shell as a low-cost adsorbent

The adsorption of copper(II) ions from aqueous solutions by the green horse-chestnut shell was studied in a batch adsorption system. It was determined how the parameters of the adsorption process, such as time, pH, copper(II) ions concentration and sorbent dose, influence the effectiveness of copper(II) ions’ removal. The adsorption process was fast and equilibrium was established about 10?min, and near 95–97% of Cu(II) ions were removed from aqueous solution. Maximum copper(II) ions’ adsorption occurred at around pH 5. The adsorption kinetics are also described, using pseudo-first-order model and pseudo-second-order model of type 1 and 2. A comparison of the kinetics models on the overall adsorption rate showed that the adsorption system was best described by the pseudo-second-order model of type 1 (r²?=?0.999) for all initial concentrations. Another key part of this study was the use of the Freundlich model to determine the adsorption isotherm and the experimental data were in strong correspondence with this model.     

TG/FTIR analysis on co-pyrolysis behavior of PE,PVC and PS

The pyrolysis and co-pyrolysis behaviors of polyethylene (PE), polystyrene (PS) and polyvinyl chloride (PVC) under N₂ atmosphere were analyzed by Thermal gravimetric/Fourier transform infrared (TG/FTIR). The volatile products were analyzed to investigate the interaction of the plastic blends during the thermal decomposition process. The TGA results showed that the thermal stability increased followed by PVC, PS and PE. The pyrolysis process of PE was enhanced when mixed with PS. However, PS was postponed when mixed with PVC. As for PE and PVC, mutual block was happened when mixed together. The FTIR results showed that the free radical of the decomposition could combine into a stable compound. When PE mixed with PVC or PS, large amount of unsaturated hydrocarbon groups existed in products while the content of alkynes was decreased. The methyl (CH₃) and methylene (CH₂) bonds were disappeared while PVC mixed with PE.     

Molecular changes of aquatic humic substances formed from four aquatic macrophytes decomposed under different oxygen conditions

Aquatic macrophytes’ decomposition is a source of recalcitrant carbon in the long term contributing to humic substances (HS) formation. Understanding the influence of plant detritus quality and oxygen availability over molecular changes of these compounds provides ecological information related to their cycling. This study described the molecular variation of dissolved HS from Eichhornia azurea, Egeria najas, Oxycaryum cubense and Salvinia molesta decomposition under aerobic and anaerobic conditions. The aquatic HS formed from the four aquatic macrophytes showed similar features (e.g. molecular weight and aromaticity). This fact indicates little influence of the detritus quality or availability of oxygen on the fulvic acids (FA) and humic acid characteristics. Under aerobic condition a decrease in the polysaccharides content in FA occurred. HS from E. najas were related to less-recalcitrant features, while HS from S. molesta were related to recalcitrant.     

Methidathion Complexes with Homoionic and Surfactant-Modified Montmorillonites

Abstract

The formation of the insecticide methidathion (S-[(5-methoxy-2-oxo-1,3,4-thiadiazol-3(2H)-yl)methyl] O,O-dimethyl phosphorodithioate) complexes with inorganic cation-saturated (Mg²⁺, Ca²⁺, Cu²⁺, and Ni²⁺) montmorillonites was investigated. The nature and structure of the complexes was determined by X-ray diffraction and infrared spectroscopy. The arrangement of the pesticide molecule in the interlayer space was also considered from ab initio calculations using simpler related molecules. The insecticide methidathion penetrated the interlayer spaces of the homoionic clay samples. The ligand–cation interactions in these complexes depend on the nature and characteristics of the saturating cations. Mechanisms involving water bridges and direct coordination with the exchange cation were proposed for the adsorption of methidathion by inorganic cation-saturated montmorillonites. The effect of the inorganic cations on the sorption of the cationic surfactant tetradecyltrimethylammonium bromide (TDTMA) by montmorillonite was also studied and the subsequent sorption of methidathion in TDTMA⁺-Montmorillonite determined. Van der Waals bonds constitute the methidathion adsorption mechanism by montmorillonite saturated with TDTMA⁺. The arrangements of methidathion and of the cationic surfactant molecules in the montmorillonite interlayer space were demostrated.     

铊在黄铁矿中的相态分布及碳酸盐在其释放过程中的作用

采用分级提取-电感耦合等离子体质谱法,对黄铁矿中铊的相态分布进行了考察.结果表明,黄铁矿中的铊主要以存在于硅酸盐相中和以酸可交换的形式存在于矿物结构中的铊为主,这部分铊分别占到58.3%和25.1%;以可氧化态形式结合在黄铁矿(FeS2)中的铊次之,占11.2%;以易还原态形式存在于铁氧化物相中的铊最少,为5.4%.自然条件下铊的释放主要是酸可交换态铊和可氧化态铊的释放迁移过程.漫反射红外光谱表征发现,黄铁矿在表面氧化过程中其表面羟基增多,表明存在表面溶解及表面酸化现象.进一步的释放机理探讨认为,铊在黄铁矿表面存在一种"溶解-吸附沉淀"平衡,这一平衡由碳酸盐中和作用和黄铁矿表面氧化共同控制,并决定了铊的释放迁移.