Phosphonic acid-functionalized hollow silica spheres by nitroxide mediated polymerization

A new strategy to prepare phosphonic acid-functionalized hollow silica spheres is proposed via nitroxide mediated polymerization of diisopropyl p-vinylbenzyl phosphonate on the surface of hollow silica spheres (HSSs) and hydrolysis thereafter. The thickness of the organic layer of PVBPA can be controlled by the quantity of the monomers. The structure and morphology of poly(vinylbenzyl phosphonic acid) (PVBPA) grafted HSSs (HPSSs) are confirmed by FTIR and TEM. The addition of HPSS in PVBPA membranes can improve the water retentivity of the composite membranes. The composite membranes with HPSSs exhibit higher water uptake and proton conductivity than the pure PVBPA membranes.     

Hollow spherical nanocapsules of poly(pyrrole) as a promising support for Pt/Ru nanoparticles based catalyst

Poly(pyrrole) hollow spherical nanocapsules (HSNCs-PPy) were prepared and used as an efficient support matrix to PtRu nanoparticles. γ-Radiation was utilized to load PtRu nanoparticles into Ppy-HSNC matrix. The advantageous characteristics of HSNCs-Ppy/PtRu catalyst as a support matrix for loading PtRu catalysts are presented.     

混合丁烯催化齐聚及齐聚产物利用技术开发

剩余丁烯催化齐聚是企业消除瓶颈、挖潜增效的途径。齐聚产物可用于生产高辛烷值汽油组分、异壬醇、对叔辛基酚等石化产品 ,效益显著。本文介绍该技术及其前景 ,并说明了有关的工艺过程及产物的主要用途。     

稀土草酸盐直接制备氟化物的试验研究

稀土草酸盐中直接加氢氟酸置换生成氟化稀土,选择加入１２０％理论量的氢氟酸有较高的转化率和回收率。置换后草酸溶液循环使用,降低了成本。     

Investigation of self-assembled monolayer treatment on SiO2 gate insulator of poly(3-hexylthiophene) thin-film transistors

We have investigated self-assembled monolayer (SAM) treatment on SiO₂ gate insulator of poly(3-hexylthiophene) (P3HT) thin-film transistor (TFT), and demonstrated a correlation between mobility and surface free energy of the insulator. The device with lower surface free energy shows higher mobility. The docosyltrichlorosilane (DCTS)-treated device exhibits the best performance among the various SAM-treated devices examined. Field-effect mobility, on/off ratio and threshold voltage of the DCTS-treated P3HT TFT were 0.015 cm²/Vs, >10⁵ and −14 V, respectively.     

Silicon oxynitride gas barrier coatings on poly(ether sulfone) by plasma-enhanced chemical vapor deposition

Thin silicon oxynitride (SiO_xN_y) has been deposited for a gas barrier layer on the surface of poly(ether sulfone) film using plasma-enhanced chemical vapor deposition (PECVD) of a mixture of hexamethyldisiloxane (HMDSO) and ammonia. The chemical structure of the deposited layer varied from organic to inorganic structures depending on RF plasma input power applied to the reaction system. A silicon-based undercoat layer, which has an organic/inorganic hybrid structure, was used as an interfacial buffer layer between the organic PES and inorganic SiO_xN_y layer. With the help of the undercoat layer, the dense inorganic SiO_xN_y layer gave a superior oxygen barrier property of 0.2 cm³/m² day at a critical coating thickness of ca. 20 nm. In a highly stressed SiO_xN_y film, the effect of the undercoat layer was remarkable in preventing crack formation during bending tests.     

Selective removal of Cr(VI) ions from aqueous solutions including Cr(VI), Cu(II) and Cd(II) ions by 4-vinly pyridine/2-hydroxyethylmethacrylate monomer mixture grafted poly(ethylene terephthalate) fiber

In this study, a new reactively fibrous adsorbent was prepared by grafting 4-vinly pyridine (4-VP) and 2-hydroxyethylmethacrylate (HEMA) monomer mixture onto poly(ethylene terephthalate) (PET) fibers for removal of Cr(VI), Cu(II) and Cd(II) metal ions from aqueous solution by using batch adsorption method. The influence of various parameters such as graft yield (GY), pH, adsorption time, initial ion concentration and adsorption temperature was investigated. The selectivity of the reactive fiber was also examined. The results show that the adsorbed amount of metal ions followed as given in the order Cr(VI) > Cd(II) > Cu(II). At pH 3, Cr(VI) was removed by 99% while the initial concentration of ions was at 5 mg L⁻¹ and by 94% at 400 mg L⁻¹. It was found that the grafted fiber is more selective for Cr(VI) ions in the mixed solution of Cr(VI)–Cu(II), Cr(VI)–Cd(II) and Cr(VI)–Cu(II)–Cd(II) at pH 3 and it was observed that the grafted fibers are stable and regenerable by acid and base without losing their activity.     

Low Risk Synthesis of Energetic Poly(3‐Azidomethyl‐3‐Methyl Oxetane) from Tosylated Precursors

Azidated oxetanic polymers such as poly(3‐azidomethyl‐3‐methyl oxetane), are under investigation as “energetic” binder to be used as an alternative to polybutadiene in solid rocket propellants. The classic synthetic route for the production of the polymer is through an azidated monomer where the N₃⁻ functionality has been previously introduced by nucleophilic displacement of a suitable, usually a halogen, leaving group. However, this could involve critical steps with manipulation of a highly unstable liquid monomer. Here it is shown that the azidation can be performed as the final step of the preparation by substitution of the tosyl group in a preformed polymer. The procedure assures good yield and purity of the product and satisfactory rate of reaction, being the energetic functionality always kept in a safe form, which shows low shock and friction sensitivity. Poly(3‐azidomethyl‐3‐methyl oxetane) was prepared by azidation of poly(3‐tosyloxymethyl‐3‐methyl oxetane) in dimethylsulfoxide, testing several operating conditions. Moreover, hypothesizing a second order kinetics, the rate constant and the activation energy for the azidation step have been estimated.     

Aspects of the kinetics and solubility of silica and calcium oxalate composites in sugar solutions

Fouling of industrial surfaces by silica and calcium oxalate can be detrimental to a number of process streams. Solution chemistry plays a large roll in the rate and type of scale formed on industrial surfaces. This study is on the kinetics and thermodynamics of SiO₂ and calcium oxalate composite formation in solutions containing Mg²⁺ ions, trans-aconitic acid and sucrose, to mimic factory sugar cane juices. The induction time (t_i) of silicic acid polymerization is found to be dependent on the sucrose concentration and SiO₂ supersaturation ratio (SS). Generalized kinetic and solubility models are developed for SiO₂ and calcium oxalate in binary systems using response surface methodology. The role of sucrose, Mg, trans-aconitic acid, a mixture of Mg and trans-aconitic acid, SiO₂ SS ratio and Ca in the formation of composites is explained using the solution properties of these species including their ability to form complexes.     

Synthesis of Hydroxypropyl Methacrylate/Polysaccharide Graft Copolymers as Matrices for Controlled Release Tablets

ABSTRACT

Hydrophilic matrices are an interesting option when developing drug delivery systems. With this aim, hydroxypropyl methacrylate was grafted onto hydroxypropyl starch and hydroxypropyl cellulose substrates by following the Ce(IV) redox initiation method. Different amounts of ethyleneglycol dimethacrylate, 7 and 34 mol%, as the crosslinking monomer, were also added. The drying of grafted products was carried out by lyophilization, obtaining white powders. Reaction yields (percent grafting, grafting efficiency, etc.) and some physical characteristics of the powders (particle size, moisture uptake, density, morphology, etc.) were determined. These parameters indicate how useful these products may be as potential matrices for direct compressed tablets. In this light, the powder flowability and the binding properties of each copolymer were determined. The graft copolymers can be considered of great interest as direct compression excipients. Due to their different chemical structure and composition, they showed differences in viscoelastic properties that revealed an interesting range of possibilities for use in drug delivery formulations. Tablets formulated with conventional excipients were also tested. Dissolution tests of various tablets were carried out. In 12 hr, 60–80% of the model drugs was released.