聚苯乙烯型双季铵树脂的制备及性能研究

三乙烯二胺和四甲基乙二胺与氯甲基聚苯乙烯反应,得到同时含有季铵和叔胺的强-弱碱型树脂,再用碘甲烷季铵化叔胺,制备聚苯乙烯双季铵树脂;另一种方法是将二甲基苄胺型叔胺树脂用4-溴丁基三甲基溴化铵季铵化引入4碳链双季铵基团。反应结果表明,两类强弱碱基树脂的季铵化反应结果并不理想,二甲基苄胺型叔胺树脂季铵化反应的转化率最高为36%。考察了这些新型双季铵树脂的热稳定性及对水溶液中有机酸(如苯磺酸和对-硝基苯乙酸)的吸附、脱附性能。     

四乙烯五胺功能化酚醛树脂作为Knoevenagel缩合反应的高活性酸碱双功能催化剂（英文）

通过市售酚醛树脂(PR)和四乙烯五胺经由氨化反应制备四乙烯五胺官能化酚醛树脂(TEPA-PR),并应用于催化Knoevenagel缩合反应.通过傅里叶转移红外光谱(FTIR)、X射线衍射光谱(XRD)和元素分析(EA)表征TEPA-PR结构.TEPA-PR可高效催化芳香醛的Knoevenagel缩合反应,具有产率高,底物适用性广的优势.此外,该反应可在不同极性溶剂中进行.该新型树脂催化剂表现出良好的可循环使用性,使用5次后其催化活性没有显着降低.     

氧化叔胺树脂的合成及其对苯酚的吸附性能研究

将D301树脂的叔胺基氧化，合成了大孔交联氧化叔胺树脂．比较D301树脂与氧化叔胺树脂对正己烷溶液中和水溶液苯酚的吸附性能，发现氧化叔胺树脂对苯酚的吸附量比D301树脂的有明显的增加．为弄清吸附量增加的原因，根据氧化叔胺树脂对正己烷溶液中苯酚的吸附等温线，利用热力学函数关系计算了等量吸附焓、吸附Gibbs自由能和吸附熵，发现叔胺树脂氧化后，与苯酚的相互作用和吸附的自发倾向增强，但吸附过程仍为氢键吸附．     

大孔吸附树脂的合成及其对黄芩甙的吸附性能

用吸附树脂纯化分离中药黄芩中的黄苓甙是天然药物研究新技术。但吸附树脂交联聚苯乙烯疏水性强,水相与树脂之间的界面能较大,通过氯甲基化引入极性基团可以改善树脂的吸附性能。本文通过对氯甲基化后的交联聚苯乙烯(氯球)进行后交联以改善树脂孔结构,并通过胺化反应增加树脂的极性和亲水性,研究所合成一系列大孔吸附树脂的碱基含量对黄苓甙的静态吸附性能的影响。     

一种有机膦树脂的合成及在锂镁分离中的应用

本文以线性酚醛树脂为母体,其经溴甲基化、三乙氧基磷亲核取代及Arbuzov重排反应,合成一种有机膦树脂。该树脂经红外,电镜扫描,热重等方法进行了表征。另外,通过Gauss软件对产物结构单元类似物的单体进行频率计算,得到其理论计算红外图谱,与产物红外图谱进行比对,表明对酚醛树脂高分子骨架上官能团改造是成功的,合成了一种有机膦树脂。用该树脂对锂镁分离进行了简单的分离实验,结果表明该有机膦树脂对锂镁吸附的分离系数(β)为2.3。     

氦原子碰撞诱导解离表征原子团簇上小分子的吸附

研究原子团簇上小分子的吸附和反应对认识一些复杂化学过程的微观机理非常重要,为了表征小分子如何吸附在原子团簇上,我们研制了一套氦原子碰撞诱导解离串级飞行时间质谱装置.该装置配有激光溅射团簇源,团簇在快速流动管里与一氧化碳、水等小分子发生反应,产物团簇通过第一级飞行时间质谱选质后与一束氦气(He)发生碰撞,使用第二级飞行时间质谱检测碰撞碎片的分布.结果表明:一些过渡金属氧化物团簇上小分子的弱吸附、强吸附以及氧化性吸附能够通过该实验装置进行表征.     

酚醛树脂包覆氧化天然石墨作为锂离子电池负极材料

天然石墨经过浓硫酸氧化处理,酚醛树脂包覆并高温碳化后形成具有核壳结构的碳包覆氧化天然石墨复合材料.采用扫描电子显微镜(SEM),透射电子显微镜(TEM),X射线衍射(XRD),激光显微拉曼光谱(Raman)等检测技术对氧化处理以及酚醛树脂热解碳包覆前后天然石墨材料的结构与形貌进行分析与表征.结果表明,氧化处理与适量的酚醛树脂热解碳包覆有效修复了天然石墨表面的一些缺陷结构,使其表面更为光滑.电化学测试结果显示,经过氧化处理与酚醛树脂热解碳包覆后天然石墨材料电化学性能得到明显提高.酚醛树脂包覆量为9%时,复合材料表现出最好的电化学性能,其首次放电比容量为434.0mAh·g-1,40次循环后,放电比容量保持在361.6mAh·g-1,而未经处理的天然石墨放电比容量仅为332.3mAh·g-1.该改性方法有效提高了天然石墨材料的比容量,对其进一步应用具有重要意义.     

复分解-配位反应与三硫化二铋的溶解性

通过实验和理论计算论证了三硫化二铋在无氧化性强酸中的溶解性.结果表明,三硫化二铋不能溶于稀硫酸中.三硫化二铋能溶于氢卤酸(除HF外)、稀硫酸与碱金属卤化物的混合液中,应是其溶解过程发生了复分解-配位两步反应的缘故.明确指出并修正了教科书中有失精当之处.     

复分解–配位反应与三硫化二铋的溶解性

通过实验和理论计算论证了三硫化二铋在无氧化性强酸中的溶解性.结果表明,三硫化二铋不能溶于稀硫酸中.三硫化二铋能溶于氢卤酸(除HF外)、稀硫酸与碱金属卤化物的混合液中,应是其溶解过程发生了复分解-配位两步反应的缘故.明确指出并修正了教科书中有失精当之处.     

疏水缔合型丙烯酰胺类聚合物Ⅰ.疏水单体N-苯基甲酰胺-丙烯酰胺的合成与表征

通过异氰酸苯酯和丙烯酰胺(AM)的取代反应,制备了疏水缔合型单体N-苯基甲酰胺-丙烯酰胺(HMAM)。用红外光谱、核磁共振氢谱、质谱、元素分析和差示扫描量热仪对HMAM进行表征。结果表明,HMAM单体含有疏水和亲水基团,可用于制备新型水溶性疏水缔合型聚合物,该聚合物不溶于水和丙酮等强极性溶剂,但能溶于二甲亚砜和N,N-二甲基甲酰胺等中等极性的溶剂中。     

Preparation and properties of a thermo-sensitive latex film

Polymer particles with hydrophobic core and hydrophilic shell were prepared via a three-step method. First, poly(butyl methacrylate-co-methyl methacrylate) (p-(BMA-MMA)) latex was prepared through emulsion polymerization. Then, a shell of poly(glycidyl methacrylate) (p-GMA) was introduced around the p-(BMA-MMA) particles by using a redox initiation system under kinetically controlled conditions. Finally, part of the epoxy groups existing in the shell were converted into quaternary ammonium salts, resulting in an ionic hydrophilic shell. The core-shell particles could be redispersed in water to form a stable emulsion. The contact angle of the core-shell latex film with water was around 16° at 25 °C, which became larger than 90° after the film was heated at 150 °C for a short period of time. This showed that the latex film was completely switched from hydrophilicity to hydrophobicity by the action of heat. Additionally, the latex film before heat treatment could be easily washed away from the substrate with neutral water, but it could no longer be removed after the heat treatment. When an IR dye with the maximum absorption at 830 nm was incorporated into the film, it became sensitive to LD laser emitting at 830 nm and gave negative image after exposed by LD laser and developed with neutral water. This showed that the latex film might find uses in chemical-free thermal laser imaging applications.     

Spectroscopic characterization of intramolecular charge transfer of sodium 4-(N,N-dimethylamino)naphthalene-1-sulfonate

In this paper, a new dual fluorescent N,N-dimethylaminonaphthalene derivative, sodium 4-(N,N-dimethylamino)naphthalene-1-sulfonate (SDMDNS), was reported. It was found that SDMDNS emits dual fluorescence only in highly polar solvent water but not in organic solvents such as methanol, dioxane and acetonitrile. Only a single broad band emission at ca. 420 nm was observed in the short wavelength region in organic solvents. The dual fluorescence of SDMDNS in water was found at 423 and 520 nm, respectively. Introduction of organic solvent as ethanol into aqueous solution of SDMDNS leads to blue shift of the long-wavelength emission, and this was evidently supported by introduction of cyclodextrin or surfactant in the aqueous solution. It indicates that a highly polar solvent was required to bring out dual fluorescence; furthermore, the short wavelength fluorescence is emitted from locally excited (LE) state and the long wavelength fluorescence is emitted from charge transfer (CT) state. The pH dependence of the dual fluorescence of SDMDNS demonstrates that the neutral form of the molecular has a higher ratio of CT band intensity to LE band. Temperature effect on the excited state of SDMDNS was also examined and gave stabilization enthalpy (-DeltaH ) of the CT reaction 8.7 kJ mol(-1).     

Photoinduced intramolecular charge transfer of sodium 4-(N,N-dimethylamino) benzenesulfonate

A new dual fluorescent N,N-dimethylaniline derivative, sodium 4-(N,N-dimethylamino)-benzenesulfonate (SDMAS), is reported. In SDMAS, the electron acceptor is linked to the phenyl ring via a sulfur atom at the para-position of the electron donor. It was found that SDMAS emits dual fluorescence only in highly polar solvent water but not in organic solvents such as formamide, methanol and acetonitrile. In organic solvents only a single-band emission at ca.360 nm was observed in the short wavelength region. The dual fluorescence of SDMAS in water was found at 365 and 475 nm, respectively. Introduction of organic solvent such as ethanol, acetonitrile, and 1,4-dioxane into aqueous solution of SDMAS leads to blue-shift and quenching of the long-wavelength emission. Measurements of steady-state and picosecond time-resolved fluorescence indicate that the long wavelength fluorescence is emitted from a charge transfer (CT) state that is populated from the locally excited (LE) state, with the latter giving off the     

Ion-exchange resins in non-aqueous solvents-III Solvent-uptake properties of ion-exchange resins and related adsorbents

Solvent-uptake properties for several synthetic resins and common adsorbents were determined by the centrifugation method. Data are reported for eighteen different solvents, which include water and the common polar and non-polar organic solvents. The cation-exchange resins are of two varieties: the microreticular or gel type and the macroreticular or porous type. The latter resin being rigid and porous takes up all types of solvents, whereas the former resin, which relies on swelling of the resin matrix, does not take up the nonpolar solvents. Data for the H(+) form and Na(+) form macroreticular resin are compared. Unsulphonated polystyrene-divinylbenzene polymers which possess similar micro- and macroreticular properties to the cation-exchange resins were also studied in the same solvents. The swelling properties of these non-polar resins are compared with each other and with the polar cation resins. Other adsorbents, which are frequently used as supports in chromatography were also examined in the same solvents. Several of these have large average pore diameters and surface areas like the macroreticular resin.     

Adsorption of a polymeric siloxane surfactant on carbon black particles dispersed in mixtures of water with polar organic solvents

The adsorption of a rake-type polymeric siloxane surfactant (polydimethylsiloxane-graft-polyether copolymer) on carbon black (CB) particles dispersed in mixtures of water with polar organic solvents (ethanol, formamide, or glycerol) has been investigated. The adsorption obeys the Langmuir isotherm at low surfactant concentrations (below the critical micelle concentration, CMC). At these conditions, the average surface area occupied by one siloxane surfactant follows the sequence water+glycerol mixture >plain water >water+ethanol mixture. At higher surfactant concentrations in the solution in contact with the particles, a sharp increase in the adsorbed amount is observed. The adsorbed layer thickness has been determined by dynamic light scattering. Below the CMC the adsorbed layer thickness is less than 10 nm. Above the CMC, the adsorbed layer thickness increases to 20-30 nm, a length scale comparable to the diameter of the siloxane surfactant micelles in aqueous solution. This fact, together with SANS data that we have obtained in the absence of added polar organic solvent, indicates that the structure of the adsorbed layer is similar to that of micelles. The findings presented here are relevant to waterborne coatings and ink formulations, where polymeric surfactants are used in conjunction with polar organic solvents.     

应用漫反射红外光谱技术优化2-聚苯乙烯磺酰胺基乙醇树脂的合成

本文采用漫反射红外光谱法优化一种新的固相合成载体2－江西 乙烯磺酰胺基乙醇树脂的合成。聚苯乙烯磺酰氯树脂在有或没有溶剂和／或催化剂存在下与乙醇铵反应得到2－聚苯乙烯磺酰胺基乙醇树脂。漫反射红外光谱跟踪整个反应过程。结果表明，漫反射红外光谱技术是优化制备新的功能基化聚合物条件的有力工具。2－聚苯乙烯磺酰胺基乙醇树脂的优化制备条件是：聚苯乙烯磺酰氯，乙醇胺在60℃反应30min。     

Correlation between physical properties and conformational rigidity of some aromatic polyimides having pendant phenolic groups

Soluble polyimides based on an aromatic diamine containing pendant phenolic group and four different dianhydrides have been synthesized by two-step polycondensation reaction in solution. The polyimides were easily soluble in polar organic solvents and even in less polar solvents and showed high thermal stability, with initial decomposition temperature being above 420 °C. Monte Carlo method was used to calculate conformational rigidity parameters of these polyimides. Some physical properties such as solubility, glass transition temperature and initial decomposition temperature were investigated and compared with those of related polyimides which did not contain any pendant groups based on the same dianhydrides and a diamine without pendant phenolic group. All data were discussed in relation to the rigidity of the chain.

     

Multilayer films from phenolic resin-sodium dodecyl sulfate complex and polycations

Novel multilayer ultrathin films of PR-SDS-PC were fabricated by employing the complex of phenolic resin (PR) and sodium dodecyl sulfate (SDS) as a "complex polyanion" and various polycations (PCs). The resulting films were etched quickly when being immersed in polar organic solvents due to the weak hydrophobic interaction between PR and SDS. By employing the photosensitive diazo resin (DR) as PC, the stability of the PR-SDS-DR film increases significantly after UV irradiation, because a covalent crosslinking structure forms in the film.     

Synthesis of Multidentate Spuaraines

To search for more better sensitizer of organic solar cell,a series of multidentate squarines(Sq1~6)were synthesized,the structures wcre determined by elemental analysis,IR, UV-vis,1H NMR and MS spectroscopies. The squaraines have good solubility in polar solvents such as EtOH, CH3CoCH3, CHCl3 etc. as well as strong absorption band over 600~700 nm spectral range.