Stabilizing effect of the cyclodextrins additive to spray-dried particles of curcumin/polyvinylpyrrolidone on the supersaturated state of curcumin

Although curcumin is considered to have various therapeutic effects, its use as a functional food or supplement is restricted owing to its low water solubility and bioavailability. To increase the solubility of curcumin in water, the use of polyvinylpyrrolidone (PVP) and vinylpyrrolidone-vinyl acetate copolymers with a pyrrolidone skeleton was noted to be promising. In particular, the bi-component formulations of curcumin/PVP prepared through spray drying exhibited an amorphous state in powder X-ray diffraction observations and temporally increased the apparent solubility of curcumin to over 5000 times that of untreated curcumin; nevertheless, after 24 h, the solubility decreased owing to the unstable supersaturated state of curcumin. The addition of α-cyclodextrin (α-CyD) in the bi-component curcumin/PVP formulation helped maintain the supersaturated state of curcumin, whereas the addition of β- and γ-CyD led to the collapse of the supersaturated state. The addition of α-CyD can likely help inhibit the nucleation and crystal growth of curcumin, through the interaction among the solubilized units of curcumin/PVP and α-CyD.     

Evaluation of maleic acid-based copolymers containing polyoxyethylene ether as inhibitors for CaCO3 scale

Polymer scale inhibitors have been widely used to reduce the loss caused by mineral scaling in circulating cooling water systems. In this article, four maleic acid-based copolymers [hydrolyzed polymaleic anhydride (HPMA)-AEO] containing different fatty alcohol polyoxyethylene ether (such as AEO-9, AEO-10, AEO-15, and AEO-20) are prepared by the way of free-radical copolymerization and characterized using Fourier transform infrared (FTIR), ¹H NMR, and gel permeation chromatographic (GPC) techniques. The effects of HPMA-AEO on CaCO₃ scale are studied in several aspects (such as dose, Ca²⁺ concentration, temperature, inhibition time, pH, the ratio of EO:carboxyl, and the relative supersaturation of CaCO₃ solution) by static experiments. The CaCO₃ scaling process with dosing of HPMA-AEO-9 is investigated under dynamic tests. CaCO₃ deposits and precipitate in the presence of HPMA-AEO-9 are analyzed using scanning electronic microscope (SEM) and X-ray diffraction (XRD). The results show that the performance of HPMA-AEO against CaCO₃ scale highly depends upon the ratio of EO:carboxyl; the introduction of AEO group can significantly improve the performance of HPMA-AEO to tolerate high alkalinity, high hardness, and high temperature; the presence of HPMA-AEO-9 can obviously affect the CaCO₃ scaling process on the tube wall through interfering with nucleation process and crystal growth process and significantly alter the surface morphology and crystal form of CaCO₃ deposits. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47470     

Anthocyanin-rich fruit vinegar from Grewia and Cantaloupe fruit blends

Grewia is a tropical berry rich in anthocyanins and antioxidants but highly perishable in nature. In this study, desirable composite blend of overripe Grewia (Phalsa) berries and cantaloupe was sought for conversion to acetic acid. Composition of raw macerate, and the alcoholic and acetic ferments was analysed for sugars, alcohol and acetic acid. The primary alcohol yield varied significantly (5.75–99.44%) with blend composition. Vinegar from select blend attained 4.98% acidity with 138.57 mg mL⁻¹ of phenols and high anthocyanins retention (74.77%). Gompertz model was used to fit the growth curves of S. cerevisiae and A. aceti (R²> 0.92) during fermentation. Presence of ethyl acetate, iso-pentyl alcohols explained pleasant sweet fruity aroma of resulting vinegar. Thus, high quality functional red fruit vinegar can be obtained to prevent spoilage and utilise the functional potential of this delicate and nutritious berry.     

Study of the composition and structure of ion-conducting membranes based on polyvinyl alcohol by 1H NMR spectroscopy

One of the alternative types of proton-conducting membranes for a hydrogen-air solid polymer fuel cell is the type of hybrid membranes based on polyvinyl alcohol (PVA) crosslinked with aldehyde, modified by sulfonic acid. Earlier, for the first time, we obtained new ion – conducting membranes based on furfural-crosslinked PVA modified aminosulfonic acid (ASA) and tetraethoxysilane (TEOS), as well as membranes not crosslinked with furfural (FUR) or unmodified ASA and TEOS, by a liquid-phase synthesis method, in an organic medium-dimethyl sulfoxide. The values of their ionic conductivity and the degree of swelling in water are presented. In this work, the composition and structure of the obtained ion-conducting membranes are studied using liquid-phase nuclear magnetic resonance (NMR) spectroscopy on ¹H nuclei. In the ¹H NMR spectrum of an ion – conducting membrane not cross-linked with the «PVA/ASA», the signal of free OH groups of PVA is observed to disappear, but at the same time a characteristic triplet at 7.1 ppm. is preserved, having a constant of ～51 Hz and components of the same intensity (1:1:1), which corresponds to protons of ¹⁴NH₄⁺ hydrolyzed ASA. The disappearance of the expanded signal at 9.6 m. d. of protons of the free sulfo group of ASA and a narrow singlet signal at 5.8 m. d. of free protons of the NH₂ group of ASA indicates the interaction of ASA with OH groups of PVA. In the ¹H NMR spectrum of an ion – conducting membrane crosslinked with FUR – «PVA/ASA/FUR», signals of protons of the furan ring of FUR and a signal of its aldehyde group are observed, which is shifted to a strong field, which is determined by the formation of a chemical bond between FUR and the polymer chain of PVA. In the ¹H NMR spectra of all membranes modified by ASA, the appearance of a second weaker-field ¹⁴NH₄⁺ triplet is observed, and in the spectra of a number of ion – conducting hybrid membranes modified by TEOS – «PVA/ASA/FUR/TEOS», signals of the third type of ¹⁴NH₄⁺ triplets shifted in a strong field relative to the other two ¹⁴NH₄⁺ triplets were detected. The appearance of additional ¹⁴NH₄⁺ triplets indicates the formation of several bound forms of the ammonium ion.     

Effect of functionalized silicon carbide nano-particles as additive in cross-linked PVA based composites for vibration damping application

In this research study, a comprehensive effort has been made to functionalize silicon carbide particles using the acidic oxidation with nitric acid to obtain homogeneous stabilized distribution of activated SiC particles within a polymer matrix, and develop functionalized silicon carbide (f-SiC) particle reinforced polyvinyl alcohol (PVA) based cross-linked composite. After fabrication of functionalized silicon carbide (f-SiC) particle reinforced polyvinyl alcohol based cross-linked composite with varying f-SiC weight percentages of PVA (0%, 1%, 2%, 3%, and 4%) were placed to various investigations. Processed samples are initially examined based by the physical tests (water absorption tests), followed by mechanical test (tensile test) and then micro-structural tests (scanning electron microscopy). Lastly, thermal tests were also concluded which involved the dynamic mechanical, differential thermal and thermo gravimetric analysis. The cross-linked polyvinyl alcohol-based composite with 2 weight % of f-SiC content is observed to be the superlative of all the compositions under this research study that was confirmed by the mechanical and micro-structural tests. This composite material shows high storage modulus with visco-elastic behavior, therefore, the material can be utilized to diminish the transmission of noise, as a shock absorber and vibration isolator.     

二硫代焦磷酸酯微胶囊阻燃PVA纤维的制备及性能

采用原位聚合的方法制备了以新戊二醇二硫代焦磷酸酯(DDPS)为核、三聚氰胺甲醛树脂(MF)为壳的阻燃微胶囊(MDDPS),分别将DDPS和MDDPS无卤阻燃剂与聚乙烯醇(PVA)共混纺丝,制备了无卤阻燃PVA纤维;表征了MDDPS的结构及形貌,研究了纯PVA纤维、DDPS/PVA纤维、MDDPS/PVA纤维的力学性能、阻燃性能、热稳定性、燃烧前后的形貌。结果表明:微胶囊MDDPS的平均粒径增大至7.82μm,仍能满足共混纺丝要求;DDPS及MDDPS的加入,PVA纤维力学性能下降;MDDPS/PVA纤维阻燃性能较好,极限氧指数达31.3%,燃烧时膨胀较为明显,且600℃时残炭率达到19.1%,炭层较为致密,有气泡产生,释放不燃性气体阻止了燃烧。     

Polymer brush coatings for combating marine biofouling

A variety of functional polymer brushes and coatings have been developed for combating marine biofouling and biocorrosion with much less environmental impact than traditional biocides. This review summarizes recent developments in marine antifouling polymer brushes and coatings that are tethered to material surfaces and do not actively release biocides. Polymer brush coatings have been designed to inhibit molecular fouling, microfouling and macrofouling through incorporation or inclusion of multiple functionalities. Hydrophilic polymers, such as poly(ethylene glycol), hydrogels, zwitterionic polymers and polysaccharides, resist attachment of marine organisms effectively due to extensive hydration. Fouling release polymer coatings, based on fluoropolymers and poly(dimethylsiloxane) elastomers, minimize adhesion between marine organisms and material surfaces, leading to easy removal of biofoulants. Polycationic coatings are effective in reducing marine biofouling partly because of their good bactericidal properties. Recent advances in controlled radical polymerization and click chemistry have also allowed better molecular design and engineering of multifunctional brush coatings for improved antifouling efficacies.     

用异丙醇精制胆固醇

选用异丙醇分别重结晶熔点140℃和147℃的胆固醇,优化了所用异丙醇的最佳质量分数为75%,重结晶时胆固醇溶解完全,单步收率达到92.0%,所得产品指标分别达到147℃胆固醇和液晶用胆固醇的质量要求,并将异丙醇和其他常用胆固醇精制方法作了比较。     

A straightforward preparation and characterization of novel poly(vinyl alcohol)/organoclay/silver tricomponent nanocomposite films

In the present investigation, novel poly(vinyl alcohol)/organoclay/silver (PVA/OMMT/Ag) tricomponent nanocomposite (NC) films with different compositions were prepared by solution intercalation method under ultrasonic irradiation process. The NC films were obtained by mixing a colloidal solution consisting of Ag nanoparticles (NPs) (3, 5, 7 and 9 wt%) with a water solution of PVA and OMMT (10 wt%) via solution casting method. The scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction, Fourier transform infrared spectroscopy, and thermogravimetric analysis (TGA) were utilized to characterize the morphology and properties of the PVA/OMMT/Ag NC films. TGA confirmed that the heat stability of the nanocomposite was improved. The enhancement in the thermal properties of the hybrid materials was due to strong hydrogen bonding between OH groups of PVA, free acid functionalized groups of OMMT, and the Ag NPs. SEM and TEM results also showed that the OMMT and Ag NPs were dispersed homogeneously in the PVA matrix on nanoscale.