RESUMO
Vitrimers, possessing associative covalent adaptable networks, are cross-linked polymers exhibiting malleable (glass-like) feature and recyclable and reprocessable (thermoplastics-like) properties. The dynamic behaviors of vitrimer are dependent on both chain/molecular mobility (glass transition temperature, Tg) and dynamic bond-exchanging reaction rate (topology freezing transition temperature, Tv). This work aims on probing the effect of high Tg on the stress relaxation and physical recyclability of vitrimers, employing a polyimide cross-linked with dynamic ester bonds (Tg: 310 °C) as the example. Due to its high Tg and chain rigidity, the cross-linked polyimide does not exhibit a high extent of stress relaxation behavior at 320 °C (10 °C above its Tg), even though the temperature is much higher than the hypothetical Tv. While raising the processing temperature to 345 °C, the cross-linked polyimide exhibits a stress relaxation time of about 3300 s and physical malleability. Nevertheless, side reactions may occur in the recycling and reprocessing process under the harsh condition (high temperature and high pressure) to alter the thermal properties of the recycled sample. The diffusion control plays a critical role on the topography transition of a vitrimer having a high Tg. The Tg ceiling is noticeable for developments of vitrimers.
RESUMO
Inverse vulcanization utilizes an organic compound as reagent for crosslinking elemental sulfur to result in corresponding polymeric material with a high sulfur content. This work, employing 1,3,5-triisopropylbenzene (TIPB) as the reagent, demonstrates the first attempt on extending the scope of crosslinking agents of inverse vulcanization to saturate compounds. Under nuclear magnetic spectroscopic analysis, the reactions between TIPB and elemental sulfur take places through ring-opening reaction of S8 resulting in sulfur radicals at sulfur chain ends, radicals transferring to isopropyl groups of TIPB, and radical coupling reactions between carbon radicals and sulfur radicals. The obtained products are similar to the sulfur polymers from conventional inverse vulcanization processes and show self-healing property.
Assuntos
Compostos Orgânicos , Enxofre , Indicadores e Reagentes , Enxofre/química , Polímeros/química , CarbonoRESUMO
A novel approach to preparing polymeric materials using elemental sulfur as a feedstock through the newly developed sulfur radical transfer and coupling (SRTC) reaction is reported herein. Polybenzoxazines with high sulfur contents are prepared using the SRTC reaction with benzoxazine compounds as the radical acceptors. The reactions between elemental sulfur and benzoxazine rings are analyzed with Fourier transform infrared (FTIR), 1 H NMR, and 13 C DEPT spectroscopies to elucidate the SRTC reaction mechanism. Moreover, the prepared polybenzoxazine-sulfur hybrid materials show attractive repairing properties based on the dynamic S-S linkages. An effective reaction mechanism and the prepared repairable sulfur-possessing polymeric materials are demonstrated.
Assuntos
Benzoxazinas/química , Polímeros/química , Enxofre/químicaRESUMO
This work demonstrates a new reactive and functional hybrid (S-MMA-POSS) of polyhedral oligomeric silsesquioxane (POSS) and sulfur prepared with a direct reaction between a multifunctional methacrylated POSS compound (MMA-POSS) and elemental sulfur (S8 ) through the "inverse vulcanization" process. S-MMA-POSS is an effective building block for imparting self-healing ability to the corresponding thermally crosslinked POSS-containing nanocomposites through a self-curing reaction and co-curing reaction with conventional thermosetting resins. Moreover, S-MMA-POSS is also a useful precursor for preparation of materials with high transparency in mid-infrared region.
Assuntos
Compostos de Organossilício/química , Enxofre/química , Teste de Materiais , Nanocompostos , Propriedades de SuperfícieRESUMO
In this work, the incorporation of a 2,2,6,6-tetramethylpiperydinyl-1-oxyl (TEMPO) group to a benzoxazine ring is performed using a one-pot synthesis for the preparation of TEMPO-functionalized benzoxazine compounds and polymers as reactive and crosslinkable initiators for nitroxide-mediated polymerization (NMP). The TEMPO-functionalization reaction of benzoxazine, traced with 1 H NMR, is conducted with sequential radical transfer and coupling reactions. Moreover, polystyrene-grafted polybenzoxazine copolymers are prepared with the TEMPO-benzoxazine initiator and NMP of styrene. The polymerization system exhibits the characteristics of controlled radical polymerization, including controlled molecular weights of products and ability for sequential polymerization. Moreover, based on the chemical reactivity and crosslinking ability of benzoxazine groups, the synthesis route developed in this work will widen the scope of the design and synthesis of functional and high-performance polymers.
Assuntos
Benzoxazinas/síntese química , Técnicas de Química Analítica/métodos , Óxidos N-Cíclicos/química , Benzoxazinas/química , Peso Molecular , Polimerização , Polímeros/química , Estireno/químicaRESUMO
In this work, a cocatalytic effect between Meldrum's acid (MA) and benzoxazine (Bz) compounds has been explored to build up a self-promoting curing system. Consequently, the MA/Bz reactive blend exhibits a relatively low reaction temperature compared to the required temperatures for the cross-linking reactions of the pure MA and Bz components. This feature is attractive for energy-saving processing issues. Moreover, the thermosetting resins based on the MA/Bz reactive blends have been prepared. The MA component can generate additional free volume in the resulting resins, so as to trap air in the resin matrix and consequently to bring low dielectric constants to the resins. The MA-containing agent is an effective modifier for benzoxazine resins to reduce their dielectric constants.
Assuntos
Benzoxazinas/química , Dioxanos/química , Resinas Sintéticas/síntese química , Temperatura , Catálise , Estrutura Molecular , Resinas Sintéticas/químicaRESUMO
This work demonstrates a new halogenation reaction through sequential radical and halogen transfer reactions, named as "radical and atom transfer halogenation" (RATH). Both benzoxazine compounds and poly(2,6-dimethyl-1,4-phenylene oxide) have been demonstrated as active species for RATH. Consequently, the halogenated compound becomes an active initiator of atom transfer radical polymerization. Combination of RATH and sequential ATRP provides an convenient and effective approach to prepare reactive and crosslinkable polymers. The RATH reaction opens a new window both to chemical synthesis and molecular design and preparation of polymeric materials.
Assuntos
Halogenação , Polímeros/química , Radicais Livres/química , PolimerizaçãoRESUMO
Nitric oxide (NO) is a ubiquitous molecule in the body. Because of its multiple pathophysiologic roles, the potential for treating various diseases by the exogenous administration of NO has been under intensive investigation. However, the unstable, radical nature of NO poses a major challenge to the effective delivery of NO. Previously, silica nanoparticles synthesized by the traditional method have been developed into NO-carrying systems. In the present study, for the first time NO-carrying silica nanoparticles were prepared from a single silica precursor using a simple nanoprecipitation method. (3-Mercaptopropyl)-trimethoxysilane (MPTMS) was used as the sole silane source, which was subjected to acid-catalyzed S-nitrosation and condensation reactions in a one-pot organic phase. S-Nitroso silica nanoparticles (SNO-SiNPs) were then produced by injecting a smaller quantity of the organic phase into a larger amount of water without surfactants. Various preparation parameters were tested to obtain optimized conditions. Moreover, a phase diagram demonstrating the ouzo effect was constructed. The prepared SNO-SiNPs were spherical particles with a tunable size in the range of 100-400 nm. The nanoparticles in aqueous dispersions exhibited high colloid stability, possibly resulting from highly negatively charged surfaces. The result of solid-state (29)Si NMR shows the predominance of T(2) and T(3) silicon structures, suggesting that nanoparticles were formed from polycondensed silica species. In conclusion, NO-loaded silica nanoparticles have been directly prepared from a single silane precursor using a surfactant-free, low-energy, one-step nanoprecipitation approach. The method precludes the need for the initial formation of bare particles and subsequent functionalization steps.
Assuntos
Nanopartículas/química , Compostos Nitrosos/síntese química , Dióxido de Silício/química , Estrutura Molecular , Compostos Nitrosos/química , Tamanho da Partícula , Propriedades de SuperfícieRESUMO
In this article, we report a novel, nanoprecipitation-based method for preparing silica nanoparticles with thiol and amine cofunctionalization. (3-Mercaptopropyl)trimethoxysilane (MPTMS) and 3-aminopropyltrimethoxysilane (APTMS) were used as the organosilane precursors, which were subjected to acid-catalyzed polycondensation in an organic phase containing a water-miscible solvent (e.g., dimethyl sulfoxide). A pale colloidal solution could be immediately formed when the preincubated organic phase was directly injected into water. The initial composition ratio between MPTMS and APTMS is an important factor governing the formation of nanoparticles. Specifically, large, unstable micrometer-sized particles were formed for preparation using MPTMS as the sole silane source. In contrast, when APTMS was used alone, no particles could be formed. By reducing the fraction of APTMS (or increasing that of MPTMS) in the initial mixture of organosilanes, the formation of nanometer-sized particles occurred at a critical fraction of APTMS (i.e., 25%). Remarkably, a tiny fraction (e.g., 1%) of APTMS was sufficient to produce stable nanoparticles with a hydrodynamic diameter of about 200 nm. Other factors that would also affect particle formation were determined. Moreover, an interesting temperature effect on particle formation was observed. The TEM micrographs show spherical nanospheres with mean sizes of 130-150 nm in diameter. The solid-state (29)Si NMR spectra demonstrate that the hybrid silica materials contain fully and partially condensed silicon structures. The bifunctionalized silica nanoparticles have positive zeta potentials whose magnitudes are positively correlated with the amount of APTMS. The total thiol content, however, is negatively correlated with the amount of APTMS. The cationic nanoparticles can bind an antisense oligonucleotide in a composition-dependent manner.
Assuntos
Aminas/química , Nanopartículas/química , Dióxido de Silício/química , Compostos de Sulfidrila/química , Compostos de Organossilício , Propilaminas/química , Silanos/químicaRESUMO
In this paper, self-assembled polymeric toroids formed by a temperature-driven process are reported. Rhodamine B (RhB) end-capped poly(N-isopropylacrylamide) (PNIPAAm) demonstrating a lower critical solution temperature (LCST) is prepared. In a two-phase system, the polymer in the aqueous phase could move to the chloroform phase on raising the temperature above its LCST. This temperature-driven process results in the formation of polymeric toroids in the chloroform phase, and the strategy affords a new pathway to toroidal self-assembly of polymers. Moreover, the photoluminescent behavior of the RhB end-capped PNIPAAm species formed by the process is also studied and discussed.
Assuntos
Acrilamidas/química , Polímeros/química , Rodaminas/química , Resinas Acrílicas , Clorofórmio/química , Espectrofotometria Ultravioleta , Temperatura , Água/químicaRESUMO
In this work, the hemocompatibility of PEGylated poly(vinylidene fluoride) (PVDF) microporous membranes with varying grafting coverage and structures via plasma-induced surface PEGylation was studied. Network-like and brush-like PEGylated layers on PVDF membrane surfaces were achieved by low-pressure and atmospheric plasma treatment. The chemical composition, physical morphology, grafting structure, surface hydrophilicity, and hydration capability of prepared membranes were determined to illustrate the correlations between grafting qualities and hemocompatibility of PEGylated PVDF membranes in contact with human blood. Plasma protein adsorption onto different PEGylated PVDF membranes from single-protein solutions and the complex medium of 100% human plasma were measured by enzyme-linked immunosorbent assay (ELISA) with monoclonal antibodies. Hemocompatibility of the PEGylated membranes was evaluated by the antifouling property of platelet adhesion observed by scanning electron microscopy (SEM) and the anticoagulant activity of the blood coagulant determined by testing plasma-clotting time. The control of grafting structures of PEGylated layers highly regulates the PVDF membrane to resist the adsorption of plasma proteins, the adhesion of platelets, and the coagulation of human plasma. It was found that PVDF membranes grafted with brush-like PEGylated layers presented higher hydration capability with binding water molecules than with network-like PEGylated layers to improve the hemocompatible character of plasma protein and blood platelet resistance in human blood. This work suggests that the hemocompatible nature of grafted PEGylated polymers by controlling grafting structures gives them great potential in the molecular design of antithrombogenic membranes for use in human blood.
Assuntos
Materiais Biocompatíveis/química , Incrustação Biológica/prevenção & controle , Membranas Artificiais , Plasma/metabolismo , Polivinil/química , Atmosfera , Humanos , Propriedades de SuperfícieRESUMO
Simple modification by thermal treatment is the commonly used approach to enhance the performance of electrospun fibers. This was investigated in the thermal treatment of polybenzoxazine (PBz) fibers blended with sulfur copolymers (SDIB) to determine the effect of varying treatment conditions on the microstructure and morphology of PBz fibers with the effect of incorporating sulfur functional groups on resulting properties. Mechanical properties of PBz are greatly improved by thermally-induced ring-opening polymerization (ROP) of the oxazine ring. Blending with sulfur copolymers (SDIB) could have beneficial effects on endowed features on fibers but could also affect the resulting properties of SDIB-blended PBz fibers during crosslinking reactions. Fiber mats were fabricated by electrospinning of PBz (10 wt%) blended with SDIB (10 wt%). Physical modification with varying conditions of sequential thermal treatment were evaluated and compared to the conditions applied on pristine PBz fibers. Changes in morphology and microstructure of fibers after modification were analyzed through scanning electron microscopy (SEM) while elemental compositions were identified after varying the conditions of thermal treatment. Adjustment of treatment conditions using two-step temperature sequential thermal treatment with higher temperatures of 160 °C and 240 °C showed significant changes in microstructure and morphology of fibers. Lower temperatures of 120 °C and 160 °C exhibited microstructure and morphology of fibers which affected the fiber diameter and fiber networks. Cross-sectional SEM images also confirmed the adversed effect of high-temperature treatment conditions on fibrous structures while low-temperature treatment retained the fibrous structures with more compact and stiff fiber networks. SDIB-blended PBz fibers were also evaluated by TGA and DSC to correlate the changes in structure and morphology with the thermal stability and integrity of blended SDIB/PBz fibers as compared to pristine PBz with the effect of change in treatment conditions. Fiber strength indicated slower weight loss for blended fibers and higher onset temperature of degradation which resulted in more thermally stable fibers.
RESUMO
This work demonstrates a general and effective approach to activate inert polymer chains for further reactions through electrochemically driven radical generation and radical transfer reactions. The generated radical-containing polymer chains show capacity for further polymer reactions and preparation of polymer hybrids.
RESUMO
Electrospun nanofibers of polybenzoxazines (PBzs) were fabricated using an electrospinning process and crosslinked by a sequential thermal treatment. Functionalization by the direct sulfonation process followed after the post-electrospinning modification treatment. The first stage of experiment determined the effects of varying the concentration of sulfuric acid as the sulfonating agent in the sulfonation reaction under ordinary conditions. The second stage examined the mechanism and kinetics of the sulfonation reaction using only concentrated H2SO4 at different reaction time periods of 3 h, 6 h, and 24 h. The mechanism of the sulfonation reaction with PBz nanofibers was proposed with only one sulfonic acid (-SO3H) group attached to each of the repeating units since only first type substitution in the aromatic structure occurs under this condition. The kinetics of the reaction exhibited a logarithmic correlation where the rate of change in the ion exchange capacity (IEC) with the reaction time increased rapidly and then reached a plateau at the reaction time between 18 h and 24 h. Effective sulfonation was confirmed by electron spectroscopy with a characteristic peak associated with the C-S bond owing to the sulfonate group introduced onto the surface of the nanofibers. ATR-FTIR spectroscopy also confirmed these results for varying reaction times. The SEM images showed that sulfonation has no drastic effects on the morphology and microstructure of the nanofibers but a rougher surface was evident due to the wetted fibers with sulfonate groups attached to the surface. EDX spectra exhibited sulfur peaks where the concentration of sulfonate groups present in the nanofibers is directly proportional to the reaction time. From surface wettability studies, it was found that the nanofibers retained the hydrophobicity after sulfonation but the inherent surface property of PBz nanofibers was observed by changing the pH level of water to basic, which switches its surface properties to hydrophilic. The thermal stability of the sulfonated nanofibers showed almost the same behavior compared to non-sulfonated nanofibers except for the 24 h sulfonation case, which has slightly lower onset temperature of degradation.
RESUMO
Thermoresponsive statistical copolymers of zwitterionic sulfobetaine methacrylate (SBMA) and nonionic N-isopropylacrylamide (NIPAAm) were prepared with an average molecular weight of about 6.0 kDa via homogeneous free radical copolymerization. The aqueous solution properties of poly(SBMA-co-NIPAAm) were measured using a UV--visible spectrophotometer. The copolymers exhibited controllable lower and upper critical solution temperatures in aqueous solution and showed stimuli-responsive phase transition in the presence of salts. Regulated zwitterionic and nonionic molar mass ratios led to poly(SBMA-co-NIPAAm) copolymers having double-critical solution temperatures, where the water-insoluble polymer microdomains are generated by the zwitterionic copolymer region of polySBMA or nonionic copolymer region of polyNIPAAm depending on temperature. A high content of the nonionic polyNIPAAm in poly(SBMA-co-NIPAAm) exhibits nonionic aggregation at high temperatures due to the desolvation of polyNIPAAm, whereas relatively low content of polyNIPAAm in poly(SBMA-co-NIPAAm) exhibits zwitterionic aggregation at low temperatures due to the desolvation of polySBMA. Plasma protein adsorption on the surface coated with poly(SBMA-co-NIPAAm) was measured with a surface plasmon resonance (SPR) sensor. The copolymers containing polySBMA above 29 mol % showed extremely low protein adsorption and high anticoagulant activity in human blood plasma. The tunable and switchable thermoresponsive phase behavior of poly(SBMA-co-NIPAAm), as well as its high plasma protein adsorption resistance and anticoagulant activity, suggests a potential for blood-contacting applications.
Assuntos
Acrilamidas/química , Anticoagulantes/química , Materiais Biocompatíveis/química , Proteínas Sanguíneas/química , Polímeros/química , Ouro/química , Humanos , Transição de Fase , Ressonância de Plasmônio de Superfície , Propriedades de Superfície , TemperaturaRESUMO
Aggregation of Rhodamine B (RhB) fluorophore in confined nanoscale domains changes the photoluminescence behavior of RhB in core-shell silica/PGMA-RhB nanoparticles. Under an excitation at 365 nm, silica/PGMA-RhB nanoparticles exhibit a two-band emission of yellow and blue in a tetrahydrofuran (THF) solution, compared to the yellow emission of RhB in a THF solution. The yellow and blue emissions of silica/PGMA-RhB nanoparticles are of approximately equal intensity, and mix together to show white light emission from the core-shell nanoparticles. Removal of the silica core from the core-shell nanoparticles does not alter its photoluminescence behavior. Therefore, the white light emission of RhB in the nanoparticles originates from the aggregation of RhB molecules in a nanoscale domain. This finding provides a new and convenient approach to the preparation of white light photoluminescent materials.
RESUMO
Dye-sensitized solar cells (DSSCs) show promise as a cheaper alternative to silicon-based photovoltaics for specialized applications, provided conversion efficiency can be maximized and production costs minimized. This study demonstrates that arrays of nanowires can be formed by wet-chemical methods for use as three-dimensional (3D) electrodes in DSSCs, thereby improving photoelectric conversion efficiency. Two approaches were employed to create the arrays of ITO (indium-tin-oxide) nanowires or arrays of ITO/TiO(2) core-shell nanowires; both methods were based on electrophoretic deposition (EPD) within a polycarbonate template. The 3D electrodes for solar cells were constructed by using a doctor-blade for coating TiO(2) layers onto the ITO or ITO/TiO(2) nanowire arrays. A photoelectric conversion efficiency as high as 4.3% was achieved in the DSSCs made from ITO nanowires; this performance was better than that of ITO/TiO(2) core-shell nanowires or pristine TiO(2) films. Cyclic voltammetry confirmed that the reaction current was significantly enhanced when a 3D ITO-nanowire electrode was used. Better separation of charge carriers and improved charge transport, due to the enlarged interfacial area, are thought to be the major advantages of using 3D nanowire electrodes for the optimization of DSSCs.
Assuntos
Corantes/química , Fontes de Energia Elétrica , Microeletrodos , Nanotecnologia/instrumentação , Nanotubos/química , Energia Solar , Titânio/química , Cristalização/métodos , Eletroforese/métodos , Galvanoplastia , Desenho de Equipamento , Análise de Falha de Equipamento , Iodo/química , Nanotubos/ultraestrutura , Tamanho da PartículaRESUMO
Organic/inorganic urea/malonamide dendron-POSS nanohybrids with different generations of dendrons and peripheral groups were prepared. Chemical structures of the nanohybrids were characterized with FTIR, 1H NMR, molecular mass spectrometry, and elemental analysis. The nanohybrids exhibited better solubility in organic solvents as compared to their corresponding dendrons. Self-assembled layered dendron/POSS structures were observed for the nanohybrids with the low generation dendrons, as evidenced by TEM analysis. The nanohybrids also exhibited amphiphilic property because of the hydrophilicity of urea/malonamide dendrons. Moreover, the morphologies of the nanohybrids could be tailored via using various casting solvents.
RESUMO
Polyhedral oligomeric silsesquioxane nanocomposites thin films on silicon surfaces were prepared by covalent layer-by-layer (LbL) assembly using octakis(glycidyldimethylsiloxy)octasilsesquioxane (OG-POSS) and 4,4(hexafluoroisopropylidene)dianiline (HID) as building blocks. The layer thickness increased linearly with the layer numbers. An ultra-low dielectric constant of approximately 1.57 was found with the LbL thin film. A novel approach to fabricate ultra low-k materials is demonstrated.
RESUMO
This work demonstrates a cross-linkable zwitterionic polymer, the corresponding zwitterionic thermosetting resin, and their application for antifouling surface coating. The tertiary amine-containing benzoxazine group is utilized as a precursor to react with 1,3-propane sultone to introduce sulfobetaine moiety to benzoxazine group. The reaction route provides an effective approach for preparation of sulfobetaine-functionalized benzoxazines and the corresponding sulfobetaine-functionalized thermosetting resins of benzoxazines. The sulfobetaine-functionalized polybenzoxazine has been utilized as a coating material for ceramic porous membranes to impart protein-repelling characteristic to the membrane surface. In a filtration test on a Bovine serum albumin (BSA) aqueous solution, the sulfobetaine resin modified membrane shows a 96.2% of rejection rate and a 1680 ± 9 Lm2-h-1 of permeation flux at the first cycle test. In cycled measurements with membrane washing, the membrane shows a total flux decline ratio (Rt) and a reversible flux decline ratio (Rr) of about 46.9% and 43.1%, respectively. A high ratio of reversible fouling (Rr/Rt) of 91.9% is found, which supports the statement that the sulfobetaine-functionalized polybenzoxazine is an effective material to impart antifouling characteristic to porous materials for bioseparation and filtration.