聚乳酸—聚乙二醇嵌段共聚物及其交联聚氨酯弹性体的性能研究

通过改变聚乙二醇（ＰＥＧ）的用量，将丙交酯（ＬＡ）与聚乙二醇共聚制成嵌段预聚体，用二苯基甲烷二异氰酸酯（ＭＤＩ）扩链后再用三羟甲基丙烷（ＴＭＰ）交联，制得系列聚氨酯型弹性体。通过对其性能研究表明，随着ＰＥＧ含量的增加，共聚物的特性粘度降低，玻璃化转变温度（Ｔｇ）降低，拉伸强度先升后降；聚氨酯弹性体的玻璃化转变温度降低，拉伸强度降低，而降解速度却加快。

Syntheses,structures,and properties of three coordination polymers based on 5⁃ethylpyridine⁃2,3⁃dicarboxylic acid and N⁃containing ligands

Three coordination polymers[Mn(epda)(2,2'⁃bipy)(H_(2)O)](1),[Mn(epda)(phen)](2),and[Co_(2)(epda)2(bpe)2(H_(2)O)_(4)]·5H_(2)O(3)(H2epda=5⁃ethyl⁃pyridine⁃2,3⁃dicarboxylic acid,2,2'⁃bipy=2,2'⁃bipyridine,phen=phenanthroline,bpe=1,2⁃bis(4⁃pyridyl)ethylene)were synthesized by solvothermal reactions and characterized by single⁃crystal X⁃ray diffraction,thermogravimetric analyses,IR spectroscopy and elemental analysis.1 displays a 1D chain struc⁃ture,and these chains are joined by O-H…O hydrogen bonding andπ⁃πstacking interactions to generate a 2D layer structure.2 displays a 2D layer structure,and adjacent layers are generated 3D architecture throughπ⁃πstacking interactions.3 displays a 1D chain structure,and adjacent chains are generated double layer structure through O-H…O hydrogen bonding.The fluorescent properties of 1 and 3 indicate that they can potentially be used as a luminescent sensor.1 was highly selective and sensitive towards o⁃nitrophenol through different detection mechanisms,however,3 was highly selective and sensitive towards 2,4,6⁃trinitrophenol.In addition,the magnetic behavior of 2 has also been investigated.CCDC:2172533,1,2355773,2,2355774,3.

改性纳米SiO_2填充PLA/PBAT复合体系结晶与流变性能研究

通过熔融共混挤出法制备聚乳酸(PLA)/聚己二酸-对苯二甲酸-丁二酯(PBAT)/改性纳米二氧化硅(SiO_2)复合材料,利用差示扫描量热仪(DSC)、X射线衍射仪(XRD)、旋转流变仪等仪器,对其结晶性能、流变特性等进行了研究。研究表明:随着改性纳米SiO_2填充量的增加,复合体系的熔融结晶温度(Tc)和熔融温度(Tm)逐渐降低,结晶度由26.81%增加到32.89%。对添加改性纳米SiO_2前后复合材料的流变性能进行了研究,并将线性流变学测试的结果与非线性流变学的结果进行了对比,考察Cox-merz关系式是否适用。

改性纳米SiO_2填充PLA/PBAT复合体系的结晶动力学研究

利用Avrami方程,研究PLA及PLA/PBAT/SiO_2复合材料的等温结晶动力学,研究结果表明:PLA及其共混物的Avrami指数n值分别为2.06~2.29和1.91~3.05;样品的结晶常数K(T)、半结晶时间t_(1/2)和结晶速率τ_(1/2)均随结晶温度的升高先增大后减小;在相同的结晶温度条件下,PLA/PBAT/SiO_2样品的K(T)和t_(1/2)均高于纯PLA的。采用改进的Avrami方程,分析PLA及PLA/PBAT/SiO_2复合材料样品的非等温结晶过程。研究结果表明:PLA及其共混物的Avrami指数n_1数值范围为1.31~4.88,表明晶体生长模式均为二维生长和三维生长并存;所有样品的n_1均随着升温速率的增大而增大,且n_1均小于n2,Z_(c1)和Z_(c2)也随升温速率的增大而增大。基于Mo方程分析结果与基于改进的Avrami方程分析结果一致,进一步证实了纳米SiO_2的引入提高了PLA的结晶速率;且PLA/PBAT/SiO_2样品的结晶活化能ΔE均大于纯PLA的,说明PBAT及SiO_2的引入阻碍了PLA主链的链段向晶体生长表面的迁移过程。

PBAT全生物降解地膜在土壤试验中的降解行为研究

研究了以聚己二酸/对苯二甲酸丁二酯(PBAT)为主要原料的全生物降解地膜在实地埋土降解实验过程中的降解行为。采用红外光谱、X射线光电子能谱、凝胶渗透色谱、热失重分析、扫描电子显微镜对PBAT薄膜在降解过程中化学结构、表面元素、热稳定性、表面微观形貌以及分子量的变化进行分析。结果表明,随埋土时间的延长,PBAT地膜红外光谱中C—O吸收峰的峰强减弱,分子链中酯键发生断裂;表面O/C原子个数比由0.27升高至0.77,结合能下降,热稳定性降低,聚集态发生改变;在埋土实验过程中,PBAT发生了分子级别的降解过程,以PBAT为主要原料的全生物降解膜在埋土实验中可完全降解。

TiO_2/SiO_2催化酯交换法合成PES的工艺

采用凝胶–溶胶法合成TiO_2/SiO2催化剂(TSP–44),用于催化丁二酸二甲酯(DMS)和乙二醇(EG)酯交换法合成高分子量聚丁二酸乙二酯(PES)。采用FTIR和1H-NMR确定聚合物结构,系统考察了催化剂浓度、聚合反应温度和时间对聚合反应的影响。经常压酯交换后获得的预聚体在230℃条件下缩聚4.0h后,合成PES的特性黏数[η]可达到0.693dL/g,重均分子量(Mw)和数均分子量(Mn)分别可以达到91 546和52 015,分子量分布系数(PDI)为1.76。热稳定性测试结果显示,酯交换法合成PES失重1%的温度和最大热解速率的温度(Tmax)分别为310℃和398℃。

IN-SITU POLYMERIZED SYNTHESIS AND PROPERTIES OF NANO-ZnO/PEG/PET COMPOSITE

Nano-ZnO particle （nZnOp） reinforced polyethylene glycol （PEG）/polyethylene terephthalate （PET） （nZnOp/PEG/PET） copolymeric composites with different mass fractions and molecular weights of PEG are synthesized via in-situ polymerization. The dispersion of nZnOp in copolymer matrixes and the effects of PEG and nZnOp particles on the crystallization behavior of the composites are studied by TEM, differential scanning calorimetry（DSC）, XRD and Fourier thansform infrared spectroscopy （FTIR ）. The results reveal that nZnOp particles are dispersed in the matrixes with nano-scale, and the addition of PEG induces more homogeneous dispersion of nZnOp. Simultaneously, these nanoparticles become nucleating centers during the crystallization of the matrixes. PEG segments can improve the flexibility of the PET molecular chain, resulting in the drop of the cold crystallization temperature and the rise of the crystallization rate of the composites. Furthermore, PEG （4 000） with the mass fraction of 10% can promote the crystallization rate of the composites. The mechanical properties show that the nano-particles strengthen and toughen the PET matrix, whereas PEG weakens these improve- ments.

Intestinal preparation prior to capsule endoscopy administration

In order to have an adequate view of the whole small intestine during capsule endoscopy, the preparation recommended consists of a clear liquid diet and an overnight fast. However, visualization of the small bowel during video capsule endoscopy can be impaired by intestinal contents. To improve mucosal visualization, some authors have evaluated different regimens of preparation. There is no consensus about the necessity of intestinal preparation for capsule endoscopy and it should be interesting to develop adequate guidelines to improve its efficacy and tolerability. Moreover, the effect of preparation type (purgative) on intestinal transit time is not clear. Since a bowel preparation cannot defini-tively improve its visibility (and theoretically the yield of the test), it is not routinely recommended.

Fabrication of a Knitted Biodegradable Stents for Tracheal Regeneration

Endoluminal stents for reinforcement and regeneration of human trachea have been developed by weft-knitting method on a small-diameter circular knitting machine. The constituent materials of the stent are Polyglactin, Polypropylene and Chitosan with Polyglactin and Polypropylene plate-stitched fabric acting as backbone while chitosan as matrix, respectively. The fabrication procedures including knitting and coating are described in this paper. Mechanical and animal tests have been carried out to evaluate the mechanical properties of the stents.

Preparation of Iminodiacetic Acid-Polyethylene Glycol for Immobilized Metal Ion Affinity Partitioning

The synthesis route was investigated and optimized for the preparation of iminodiacetic acid-polyethylene glycol (IDA-PEG) for immobilized metal ion affinity partitioning in aqueous two-phase systems. IDA-PEG was synthesized from PEG in two steps by the reaction of iminodiacetic acid with a monosubstituted derivative of epichlorohydrin-activated PEG. The Cu2+ content combined with IDA-PEG was determined by atomic absorption spectrometry as 0.5 mol·mol^-1 (PEG). Furthermore, the affinity partitioning behavior of lactate dehydrogenase in polyethylene glycol/hydroxypropyl starch aqueous two-phase systems was studied to clarify the affinity effect of the Cu(Ⅱ)-IDA-PEG.

Simultaneous Synthesis of Dimethyl Carbonate and Poly（ethylene terephthalate） Using Alkali Metals as Catalysts

Dimethyl carbonate （DMC） and poly（ethylene terephthalate） was simultaneously synthesized by the transesterification of ethylene carbonate （EC） with dimethyl terephthalate （DMT） in this paper. This reaction is an excellent green chemical process without poisonous substance. Various alkali metals were used as the catalysts. The results showed alkali metals had catalytic activity in a certain extent. The effect of reaction condition was also studied. When the reaction was carded out under the following conditions： the reaction temperature 250℃, molar ratio of EC to DMT 3 ： 1, reaction time 3h, and catalyst amount 0.004 （molar ratio to DMT）, the yield of DMC was 68.9%.

Preparation and Properties of Poly(Ethylene Terephthalate)/Boehmite Nanocomposite

Colloidal boehmite particles have been included into a polyethylene terephthalate matrix by in situ polymerization. Boehmite nanoparticles were produced by the controlled hydrolysis of aluminium isopropylate. The nanoparticles were characterized using Transmitted Electronic Microscopy (TEM) and X-ray Diffraction (XRD), which revealed the particles of magnitude about 10 nm. The particles have been used without any surface modification. Characterization of the nanocomposite has been carried out using TEM and differential scanning calorimetry (DSC). TEM images indicate that the particles have been homogeneously dispersed in the polymer. DSC results show that the presence of boehmite affects the process of crystallization of polyethylene terephthalate.

Electrochemical study on adsorption behavior of surfactants at β-2CaO·SiO2/NaAlO2 interface

β-2CaO＇SiO2 was obtained with analytical grade reagents. Polyethylene glycol （PEG）, sodium polyacrylate （PAAS） and their mixture were used to inhibit the decomposition of β-2CaO·SiO2 in sodium aluminate solution. The potential of solid-liquid interface and the adsorption mechanism were studied by the methods of Zeta potential measurement and XPS. The results indicate that PEG and PAAS have synergistic effect on the inhibition of secondary reaction. The inhibitory effect is the best when the volume ratio of PAAS to PEG is 1：1 and the total concentration is 12.5 mg/L. PAAS adsorbs on the surface of β-2CaO-SiO2 by the formation of --COOCa coordinate bond, and the negative charge enters into Stem layer, which results in the decrease of particle potential and the obvious change of binding energy of Ca 2p, Si 2p and O Is. PEG only physically adsorbs on the surface ofβ-2CaO·SiO2, and had little effect on particle potential and binding energy of Ca 2p, Si 2p and O Is.

Research on characterization of thermotropic polyurethane membrane of PDAG/BDO/MDI

Adopting Poly（ethylene glycol） adipate Dilpoly- （ethylene glycol）] adipate polydiglycol adipate glycol （PDAG）, 1,4-butanediol （BDO）, hydroxy silicone oil, methylene diphenyl diisocyanate （MDI） as the raw material, a new polyurethane elastic body can be made through prepolymerization. After measurement of the moisture permeability, adsorption quantity and mechanical properties of the membrane made with the elastic body, we also proofed its formula by infrared spectroscopy. The result showed that the moisture permeability of the membrane, with a certain intelligent thermotropic quality, will increase by 3 to 4 times when the temperature is between 25℃-45℃.

A Structure-properties Study of MDI-based Hydrophilic Polyether-polyester Polyurethane

A series of segmented polyether-polyester polyurethane with amorphous hydrophilic soft segment domains were prepared from 4,4'- diphenylmethane diisocyanate (MDI), polybutylene adipate (Glycol) 2000 (PBA2000), and polyethylene glycol 1000 (PEG1000), with 1,4-butanediol (BDO) as the chain extender. Furthermore, several representative properties of the polyurethanes, such as moisture permeability, water resistance, hydrophilic property, and phase inversion temperature, were investigated. The studies show that the structure and concentration of soft segment have a remarkable effect on the main application properties of polyurethane. On the contrary, the functional properties of the polyurethane are almost not affected by its hard segment.

Comparing reduced-dose sodium phosphate tablets to 2L of polyethylene glycol: A randomized study

To compare the tolerability and quality of bowel cleansing between 2 L polyethylene glycol (PEG) and reduced-dose sodium phosphate (NaP) tablets as a preparation for colonoscopy. METHODSTwo hundred patients were randomly assigned to the PEG or NaP groups at the same ratio. The NaP group patients took 30 tablets with 2 L of clear liquid, while the PEG group patients took 2L of PEG. Tolerability was assessed by a questionnaire about taste, volume, and the overall impression. The bowel cleansing quality was evaluated by colonoscopists. RESULTSAlthough NaP showed better tolerability in terms of taste, volume and overall impression (P < 0.01, P < 0.01 and P = 0.02, respectively), the overall cleansing quality was better in the PEG group (P < 0.01). A subgroup analysis, stratified by sex and age, indicated that NaP was associated with better tolerability and equivalent bowel cleansing quality in females of < 50 years of age. CONCLUSIONDespite the better tolerability, the use of 30 NaP tablets with 2 L of clear liquid should be limited due to its lower cleansing quality; however, in certain cases the regimen may deserve consideration, particularly in cases involving young women.

Biodegradation of DTP and PET Fiber by Microbe

The degradation of diethylene glycol terephthalate (DTP) and polyethylene terephthalate (PET) fiber by microbe was studied.The degree of DTP degradation was determined by High Performance Liquid Chromatography (HPLC) to be more than 90%.The products after degradation of DTP and PET fiber were various.The degradation of DTP can be described by the first-order reaction model.The degradation of PET fiber was found to be little,but surface erosion of PET fiber could be clearly seen from the SEM photographs indicating there occurred some traces of biodegradation on the PET fiber surface.

Synthesis of Novel Electron Donors and Their Application to Propylene Polymerization

A series of electron donors,including 1,1-cyclopentanecarboxylic acid diethyl ester (CPCADEE),1,1cyclopentanedimethanol acetic diester (CPDMAD),1,1-biethoxymethyl pentane (BEMP),2,2-diethyl diethylmalonate (DEDEM)and 2,2-diethyl-1,3-propanediol acetic diester (DEPDADE),were synthesized by diethyl malonate (DEM).The purities and structures of the above products were characterized by gas chromatography (GC) and gas chromatography-mass spectrometer (GC-MS),respectively.Furthermore,the possible optimal three-dimensional structures of these donors were simulated by means of Gaussian 03 and Chem 3D.Then these electron donors were coordinated with tetrachloro titanium (TiCl 4) and chloride magnesium (MgCl 2)to obtain the catalysts for the polymerization of propylene.The catalytic activities and properties of polypropylene are greatly improved by adding external donor(ED) when CPCADEE or DEPDADE is used as internal donor(ID).However,when BEMP was used as ID,the highest catalytic activity is obtained without adding ED,which can reduce production costs and simplify catalytic synthesis.The experiments indicate that BEMP has the shortest distance of oxygen atoms and the highest electronegativity.

Properties of Surface Cyclic Oligomers Present on Polyester Fiber

The effects of different treatments, such as dry heat,wet heat, solvent vapor and ultrasonic, on propertiesof the cyclic oligomers on the surface of polyester fiberare studied. The components of surface oligomers areanalyzed through Thin-Layer Chromatograph. Theresult shows that: all of the treatment, especially solvent vapor treatment,call significantly increase the content of surface cyclic oligomers.The content of cyclic triIner is increased more considerably than other oligomers. Moreover,the morphology and thedistribution of surface cyclic oligomers are also different from different treatments:Dry heat and wet heat cause larger polygonal solids distributed evenly on the surface of fiber;solvent vapor nlakes fiber surface exhibit irregular rodlike crystal shapes randomly;ultrasonic treatment induces some obscureand smaller deposi^on the surface of fiber.