pH-Sensitive Dye-Polyether Derivatives as Dispersants for Its Parent Dye. Part 1: Synthesis and Hydrolysis Behavior

A series of dye-polyether derivatives, supposedly to be used as dispersants for parent dye, were synthesized by grafting poly(oxyalkylene)-amines based on differing both molecular weights and degrees of hydrophilicity/hydrophobicity, onto C.I. disperse red 60 via a stable urea linkage. The structures of the dye-polyether derivatives were characterized by FTIR, ¹H NMR, and SEC. The influence of pH on the hydrolysis behaviors of the dye-polyether derivatives were studied in buffered aqueous solutions within the pH range of 4 to 10. The hydrolysis of dye-polyether derivatives was pH dependent and relatively faster in mild alkaline buffer solution than in acidic one. The influence of poly(oxyalkylene)-amine structure on the hydrolysis behavior was also investigated; it was found that the hydrolysis rate is affected little by the molecular weight and increases with the increasing hydrophilicity of the poly(oxyalkylene)-amine.     

Nanocomposites: Industrial opportunity or challenge?

Polymer nanocomposites based on organically modified layered silicates are an area of substantial scientific interest and of emerging industrial practice. Despite the proven benefits of nanocomposites such as mechanical properties, barrier properties and contribution to fire retardancy, polymer nanocomposites are used today only in niche applications. The reasons for the limited growth of nanocomposites are explained through the availability of alternative solutions, processing and dispersion challenges and inferior oxidative and photooxidative stability. Recent developments show the improved dispersion of unmodified nanoclays in polyolefins with the help of selected copolymer structures. The (photo)oxidative instability of nanocomposites is compensated with adjusted stabilizer systems.     

Choice of dispersants for the nano-apatite filler of polylactide-matrix composite biomaterial

The aim of this study is to compare de-aggregative ability of common organic dispersants for the acicular nano-apatite crystallite with main composition of calcium hydroxyapatite (HA) as a filler of composite containing polylactide (PLA) matrix. Firstly, the acicular nano-apatite powders with an average length of 70–120 nm were synthesized based on traditional chemical co-precipitation and freeze-drying techniques. Common organic dispersants including tetrahydrofuran, acetone, chloroform, N,N-dimethyl formamide (DMF) and ethanol were then employed to disperse synthetic freeze-dried ultra-fine nano-powders. The observations and weight of sediments showed that nano-apatite suspension dispersed by DMF and ethanol presented homogeneous and stable colloid after vigorly stirred for 24 h and then kept still for same time, respectively. Results of particle measurements and viscosity measurement illuminated that a large number of the nano-apatite particles with an average dimension of 297.86 nm and viscosity of 0.8872 cP in DMF suspension could be dispersed up to 91.28 nm by the DMF dispersant and the DMF dispersant could minimize agglomeration between the apatite ultra-fine nano-powders. DMF is a more effective and appropriate dispersant to disperse the apatite nano-fillers than chloroform, tetrahydrofuran, acetone and ethanol, when the nano-apatite/PLA composite biomaterials were prepared.     

Preparation of stable colloidal suspensions of superdisintegrants via wet stirred media milling

Superdisintegrants are cross-linked polymers that can be used as dispersants for fast release of drug nanoparticles from nanocomposite microparticles during in vitro and in vivo dissolution.Currently available superdisintegrant particles have average sizes of approximately 5-130 μm,which are too big for drug nanocomposite applications.Hence,production of stable superdisintegrant suspensions with less than5 μm particles is desirable.Here,we explore the preparation of colloidal suspensions of anionic and nonionic superdisintegrants using a wet stirred media mill and assess their physical stability.Sodium starch glycolate(SSG) and crospovidone(CP) were selected as representative anionic and nonionic superdisintegrants,and hydroxy propyl cellulose(HPC) and sodium dodecyl sulfate(SDS) were used as a steric stabilizer and a wetting agent/stabilizer,respectively.Particle sizing,scanning electron microscopy,and zeta potential measurements were used to characterize the suspensions.Colloidal superdisintegrant suspensions were prepared reproducibly.The extensive particle breakage was attributed to the swelling-induced softening in water.SSG suspensions were stable even in the absence of stabilizers,whereas CP suspensions required HPC-SDS for minimizing particle aggregation.These findings were explained by the higher absolute(negative) zeta potential of the suspensions of the anionic superdisintegrant(SSG) as compared with those of the nonionic superdisintegrant(CP).