Gamma Ray Radiation Effect on Bi2WO6 Photocatalyst

The development of Bi2WO6-based materials has become one of research hotspots due to the increasing demands on high-efficient photocatalyst responding to visible light.In this work,the effect of high energy radiation(γ-ray)on the structure and the photocatalytic activity of Bi2WO6 nanocrystals was first studied.No morphological change of Bi2WO6 nanocrystals was observed by SEM underγ-ray radiation.However,the XRD spectra of the irradiated Bi2WO6 nanocrystals showed the characteristic 2θof(113)plane shifts slightly from 28.37o to 28.45o with the increase of the absorbed dose,confirming the change in the crystal structure of Bi2WO6.The XPS results proved the crystal structure change was originated from the generation of oxygen vacancy defects under high-dose radiation.The photocatalytic activity of Bi2WO6 on the decomposition of methylene blue(MB)in water under visible light increases gradually with the increase of absorbed dose.Moreover,the improved photocatalytic performance of the irradiated Bi2WO6 nanocrystals remained after three cycles of photocatalysis,indicating a good stability of the created oxygen vacancy defects.This work gives a new simple way to improve photocatalytic performance of Bi2WO6 through creating oxygen vacancy defects in the crystal structure by-ray radiation.

Polyaniline Nanotubes Prepared by One-Step Synergistic Polymerization of Aniline and Acrylic Acid

The electrochemical property of electrode materials greatly depends on their morphologies. This report introduces a novel and facile synthesis method for polyaniline (PANI) nanotubes from one-step synergistic polymerization of aniline and acrylic acid in an aqueous solution induced by the addition of ammonium persulfate (APS). The molar ratio of aniline to AA (X{ani/AA}) is found to have great in fluence on the morphology of the produced PANI. Hollow PANI nanotubes with an average inner diameter of 80 nm and outer diameter of 180 nm can be mainly produced when X{ani/AA} is not higher than 1. The electrochemical properties of the prepared PANI nanotubes have been investigated using a three-electrode system. The specific capacitance of PANI nanotubes can reach 436 F/g at a current density of 0.5 A/g in 1 mol/L H2SO4 solution. Furthermore, the specific capacitance of the PANI nanotube maintains 89.2% after 500 charging/discharging cycles at a current density of 0.5 A/g, indicating a good cycling stability.

THERMALLY STIMULATED SHAPE MEMORY BEHAVIOR OF(ETHYLENE OXIDE-BUTYLENE TEREPHTHALATE)SEGMENTED COPOLYMER

The thermally stimulated shape memory behavior of ethylene oxide-butylene terephthalate (EOBT) segmented copolymers with different soft segment molecular weight and hard segment content was investigated. The deformation recovery ratio R-f of the EOBT samples increases with the soft segment molecular weight and the hard segment weight content, while the average overall deformation recovery speed V-r increases with the hard segment content. The temperature of maximum deformation recovery speed (T-M) is determined by the melting temperature of the soft segment crystals and the stability of the crystallized hard segment domains.

COMPOSITIONAL HETEROGENEITY OF ETHYLENE OXIDE-BUTYLENE TEREPHTHALATE SEGMENTED COPOLYMER

A series of ethylene oxide-butylene terephthalate (EOBT) segmented copolymers with different soft segment length and hard segment content were synthesized. The compositional heterogeneity was studied by solvent extraction. The results show that the compositional heterogeneity increases when soft segment length and hard segment content increase. The compositional heterogeneity is also reflected in the crystallization behavior and morphology of soft and hard segment in EOBT segmented copolymer. The more compositional heterogeneous the EOBT segmented copolymer is, the more different the morphology and the crystallization behavior between separated fractions. Compared with ethylene oxide-ethylene terephthalate (EOET) segmented copolymer, compositional heterogeneity in EOBT segmented copolymer is weaker. But the compositional heterogeneity in EOBT segmented copolymer with long soft segment and high hard segment content is still obvious.

In-situ Enhanced Toughening of Poly（ethylene terephthalate）/elastomer Blends via Gamma-Ray Radiation at Presence of Trimethylolpropane Triacrylate

Gamma-ray radiation has always been a convenient and effective way to modify the inter- facial properties in polymer blends. In this work, a small amount of trimethylolpropane triacrylate （TMPTA） was incorporated into poly（ethylene terephthalate） （PET）/random terpolymer elastomer （ST2000） blends by melt-blending. The existence of TMPTA would induce the crosslinking of PET and ST2000 molecular chains at high temperatures of blend- ing, resulting in the improvement in the impact strength but the loss in the tensile strength. When the PET/ST2000 blends were irradiated by gamma-ray radiation, the integrated me- chanical properties could be enhanced significantly at a high absorbed dose. The irradiated sample at a dose of 100 kGy even couldn＇t be broken under the impact test load, and at the same time, has nearly no loss of tensile strength. Based on the analysis of the impact- fractured surface morphologies of the blends, it can be concluded that gamma-ray radiation at high absorbed dose can further in situ enhance the interfacial adhesion by promoting the crosslinking reactions of TMPTA and polymer chains. As a result, the toughness and strength of PET/ST2000 blend could be dramatically improved. This work provides a facial and practical way to the fabrication of polymer blends with high toughness and strength.

Synthesis and Optical Properties of ZnO Nanoparticles in Submicron PS Hollow Reactors

ZnO nanoparticles were first encapsulated in submicron PS hollow microspheres through two-step swelling process of core-shell structured PMMA/PS （PMMA： polymethyl methao- rylate） microspheres in acid-alkali solution, and the ZnO precursors, i.e. the ethanol solu- tions of （CHaCOO）2Zn and LiOH. The transmission electron microscope, X-ray diffraction, and thermogravimetric analysis results show that the feeding order of ethanol solutions of （CH3COO）2Zn and LiOH in the second swelling step has great influence on the loading efficiency and the size of ZnO nanoparticles, but little on their crystal form. The photolumi- nescence and UV-Vis absorption behavior of ZnO/PS microspheres show that the PS shell can effectively avoid the fluorescence quenching effect.

Magnetic Nano-Amorphous-Iron-Oxide-Based Drug Delivery System with Dual Therapeutic Mechanisms

Smart nanoparticles that respond to pathophysiological parameters,such as p H,GSH,and H2O2,have been developed with the huge and urgent demand for the high-efficient drug delivery systems(DDS)for cancer therapy.Herein,cubic poly(ethylene glycol)(PEG)-modified mesoporous amorphous iron oxide(AFe)nanoparticles(AFe-PEG)have been successfully prepared as p H-stimulated drug carriers,which can combine doxorubicin(DOX)with a high loading capacity of 948 mg/g,forming a novel multifunctional AFe-PEG/DOX nanoparticulate DDS.In an acidic microenvironment,the AFe-PEG/DOX nanoparticles will not only release DOX efficiently,but also release Fe ions to catalyze the transformation of H2O2 to·OH,acting as fenton reagents.In vitro experimental results proved that the AFe-PEG/DOX nanoparticles can achieve combination of chemotherapeutic(CTT)and chemodynamic therapeutic(CDT)effects on Hela tumor cells.Furthermore,the intrinsic magnetism of AFePEG/DOX makes its cellular internalization efficiency be improved under an external magnetic field.Therefore,this work develops a new and promising magnetically targeted delivery and dual CTT/CDT therapeutic nano-medicine platform based on amorphous iron oxide.

Preparation and Structure-Property Regulation Mechanism of Reversible Thermochromic Polydiacetylene

The thermochromic mechanism and the structure-property regulation principle of reversible thermochromic polydiacetylene(PDA)materials have always been a challenging issue.In this work,a series of diacetylene monomers(m-PCDA)containing phenyl and amide or carboxyl groups were synthesized from 10,12-pentacosadiynoic acid(PCDA)through the esterification or amidation reactions.The effects of the number and the distribution of the functional groups in m-PCDA molecules on their solid-state polymerization capability,and the thermochromic mechanism of their corresponding polymers(m-PDA)were investigated and discussed in detail.The results show that the m-PCDA monomers containing both benzene ring and groups that can form hydrogen bonding interactions have strong intermolecular interaction,and are easy to carry out the solid phase polymerization under 254-nm UV irradiation to obtain the corresponding new thermochromic m-PDA materials.The thermochromic behavior of m-PDA depends on its melting process.The initial color-change temperature(blue to red)is determined by the onset melting tem perature,and the temperature range in which reversible color recovery can be achieved by repeat heating-cooling treatment is determined by its melting range.According to the proposed thermochromic mechanism of PDA,various new PDA materials with precise thermochromic temperatu res and reversible thermochromic temperature ra nges can be designed and synthesized through the appropriate introduction of benzene ring and groups that can form hydrogen bonding interactions into the molecular structure of linear diacetylene monomer.This work provides a perspective to the precise molecular structure design and the property regulation of the reversible thermochromic PDA materials.

具有近红外光控释功能的邻苯二酚改性壳聚糖基可注射生物黏合剂的制备及性能

在制备邻苯二酚基团改性壳聚糖(CS-pC)的基础上,将CS-pC乙酸水溶液与β-甘油磷酸钠(β-GP)水溶液混合形成可注射溶胶,该溶胶加热至体温附近(37°C)时发生溶胶-凝胶转化,得到无细胞毒性且有优良抗菌和黏附性能的水凝胶(CS-pC/β-GP).该水凝胶黏附在猪皮上的临界剥离强度可达4.9 kPa,是纯壳聚糖(CS)基水凝胶临界剥离强度(0.6 kPa)的8倍.进一步在CS-pC/β-GP溶胶形成过程中加入水溶性药物盐酸多西环素(DH)和近红外光热剂金纳米棒(AuNR),即可以形成具有近红外光控释功能的CSpC/β-GP/DH/AuNR水凝胶,其负载的DH在808 nm近红外激光照射下的释放速率是无光照下的6倍.本工作为开发高效可注射型多功能邻苯二酚改性壳聚糖基生物黏合剂提供了新思路.

Fabrication of macroporous polystyrene/graphene oxide composite monolith and its adsorption property for tetracycline

Macroporous polystyrene microsphere/graphene oxide（PS/GO） composite monolith was first prepared using Pickering emulsion droplets as the soft template. The Pickering emulsion was stabilized by PS/GO composite particles in-situ formed in an acidic water phase. With the evaporation of water and the oil phase（octane）, the Pickering emulsion droplets agglomerated and combined with each other, forming a three-dimensional macroporous PS/GO composite matrix with excellent mechanical strength. The size of the macrospores ranged from 4 mm to 20 mm. The macroporous PS/GO composite monolith exhibited high adsorption capacity for tetracycline（TC） in an aqueous solution at p H 4–6. The maximum adsorption capacity reached 197.9 mg g 1at p H 6. The adsorption behaviour of TC fitted well with the Langmuir model and pseudo-second-order kinetic model. This work offers a simple and efficient approach to fabricate macroporous GO-based monolith with high strength and adsorption ability for organic pollutants.

Synthesis and morphology control of raspberry-like poly(ethylene terephthalate)/polyacrylonitrile microspheres

The fabrication of raspberry-like poly（ethylene terephthalate）/polyacrylonitrile（PET/PAN） microspheres by g-ray radiation-induced polymerization of acrylonitrile on micron-sized PET microspheres were first reported in this work. A PET emulsion was firstly prepared by dispersing a PET solution with 1,1,2,2-tetrachloroethane/phenol mixture as the solvent into an aqueous solution of sodium dodecyl sulfate.Then, PET microspheres were formed by precipitating the PET emulsion droplets from ethanol. The influence of the PET solvent and the weight ratio of ethanol to PET emulsion on the morphology of the PET microspheres had been investigated. After the surface of the prepared PET microspheres was grafted with poly（acrylic acid）, the grafting polymerization of AN also had been successfully initiated by g-ray radiation to form PAN microspheres with a size of about 100 nm on the PET microspheres. This work provides a new method to fabricate micron-sized PET microspheres, and further expands the functionalization of PET and its application fields.

One-step synthesis of self-healable hydrogels by the spontaneous phase separation of linear multi-block copolymers during the emulsion copolymerization

Self-healable polyacrylamide-based hydrogels were prepared at room temperature via a one-step emulsion copolymerization of acrylamide（AM）,dodecyl 2-methacryIate（DM）,and 5-acetylaminopentyl acrylate（AAPA） using sodium dodecyl sulfonate（SDS） as the emulsifier and ammonium persulfate（APS）as the initiator.The produced linear multi-block copolymer chains are composed of randomly-linked hydrophilic polyacrylamide segments（PAM） and hydrophobic segments constituted by DM and AAPA units（P（DM-co-AAPA））.The P（DM-co-AAPA） segments will self-aggregate into hydrophobic microdomains during the polymerization process driven by the hydrophobic interactions,and finally separate from water phase,acting as the crosslinks and leading to the formation of strong hydrogels with a storage modulus as high as 400 Pa.These hydrophobic microdomains will be dissolved in water when the temperature increases to 70℃,resulting in a temperature-responsive reversible sol-gel transition of the prepared hydrogels.Furthermore,the prepared hydrogels have excellent self-healing ability.The broken hydrogels can be automatically healed into a body with a same strength within 2-min＇s contact.This work provides a new simple way to prepare reversible physical crosslinked hydrogel with high strength and self-healing efficiency.