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1.
    
A series of novel bio-polyester nanocomposites based on glycerin and azelaic acid as monomers incorporating hydroxyapatite (HA) nanoparticles were fabricated via in situ polymerization method. Chemical structure of the samples was investigated by 1H-NMR, 13C-NMR, and Fourier-transform infrared spectroscopy (FTIR). Energy dispersive X-ray-mapping analysis illustrated that the nanoparticles were well dispersed in the poly (glycerol azelaic acid) (PGAZ) matrix. Viscoelastic properties of the samples under various frequencies were examined in which the PGAZ specimen containing 1.0 wt% of HA nanoparticles (PGAZH1.0) exhibited superlative properties. Furthermore, the alterations in the glass transition temperature of the samples were comprehensively discussed. Thermal gravimetric analysis displayed that nanocomposites generally have a difference in degradation patterns from that of the pristine sample. Dynamic contact angle demonstrated that the presence of HA nanoparticles imposed a significant influence on hydrophilicity. The hydrolytic degradation values at pH = 7 and pH = 11 were measured and determined that the degradation rate for the PGAZ sample containing 1.5 wt% HA (PGAZH1.5) was higher than those of the other samples. Moreover, in vitro studies elucidated that cell attachment on PGAZH1.0 and PAZH1.5 surfaces were acceptable.  相似文献   

2.
    
We synthesized polyols with high hydroxyl functionalities (FOHs), between 9.0 and 12.6, and characterized them with differential scanning calorimetry, thermogravimetric analysis, and size exclusion chromatography after we parametrically studied the ring-opening reaction of epoxidized soybean oil with lactic acid (LA) as a function of the reaction temperature and lactic acid equivalent fraction (fLA). An increase of only 20°C in the reaction temperature (from 80 to 100°C) caused changes in the hydroxyl number (+17.8%), FOH (–25%), viscosity (–14.0%), and oligomeric content (–24.1%). fLA mostly affected the ring-opening yield, and only for fLA values above 0.4 was possible to achieve values higher than 80%. Rigid polyurethane foams (rPUFs) were synthesized and characterized with scanning electron microscopy, dynamic mechanical analysis (DMA), and compressive mechanical tests. rPUFs with a very high specific compressive strength (7.8 kPa kg–1 m3) were synthesized solely with biobased soybean oil. DMA revealed a compromised relationship between the specific compressive strength and its temperature dependence. To increase the first one, the most relevant method was to increase FOH. Instead, to increase the latter one, the OH number had to be maximized. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47959.  相似文献   

3.
    
Bloodmeal decolored with 4 wt % peracetic acid can be extruded into a semi‐transparent bio‐plastic through the addition of sodium dodecyl sulfate (SDS), water, and triethylene glycol (TEG). TEG is often used to plasticize protein thermoplastic materials because of its ability to form both hydrophobic and hydrogen bonds. Synchrotron‐based FT‐IR was used to monitor changes in the types of hydrogen bonding occurring in TEG plasticized protein during heating. Heating was found to overcome a portion of the weaker hydrogen bonds found within and between proteins, observed as a blue‐shift in the N‐H and O‐H stretching vibrations occurring at ∼3280 cm−1. TEG was shown to be involved in a larger array of hydrogen bonding environments after heating, evidenced by the broadening of the C‐OH stretch around 1076 cm−1, suggesting improved plasticizer‐protein interactions. Additionally, these bonds were found to be as strong as the original interactions, observed as a shift in the C‐OH peak back to its original wavenumber (∼1076 cm−1) during cooling. Initially, TEG was spatially distributed into distinct plasticizer‐rich and plasticizer‐poor domains, giving rise to two glass transitions. Heating allowed the migration and uniform dispersion of TEG throughout the material, and merged the two glass transitions into one broader glass transition region. Heating during DSC removed the peak around 60°C corresponding to the enthalpy of relaxation, which is associated with physical aging of amorphous and semi‐crystalline polymers. While physical aging occurred during the storage of DBM, in the presence of TEG it occurred to a lesser extent. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42166.  相似文献   

4.
    
Plasma polymerized γ‐terpinene (pp?GT) thin films are fabricated using RF plasma polymerization. MIM structures are fabricated and using the capacitive structures dielectric properties of the material is studied. The dielectric constant values are found to be in good agreement with those determined from ellipsometric data. At a frequency of 100 kHz, the dielectric constant varies with RF deposition power, from 3.69 (10 W) to 3.24 (75 W). The current density–voltage (J?V) characteristics of pp–GT thin films are investigated as a function of RF deposition power at room temperature to determine the resistivity and DC conduction mechanism of the films. At higher applied voltage region, Schottky conduction is the dominant DC conduction mechanism. The capacitance and the loss tangent are found to be frequency dependent. The conductivity of the pp?GT thin films is found to decrease from 1.39 × 10?12 S/cm (10 W) to 1.02 × 10?13 S/cm (75 W) and attributed to the change in the chemical composition and structure of the polymer. The breakdown field for pp–GT thin films increases from 1.48 MV/cm (10 W) to 2 MV/cm (75 W). A single broad relaxation peak is observed indicating the contribution of multiple relaxations to the dielectric response for temperature dependent J?V. The distribution of these relaxation times is determined through regularization methods. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42318.  相似文献   

5.
    
The effect of freeze‐thaw pretreatment on the thermal drying process and physicochemical properties of chitosan was investigated in this study. Results showed that the freeze‐thaw treatment changed the form of chitosan paste and reduced 75.6–77.7% of the water content. The freeze‐thaw treatment decreased the drying time of chitosan from 16–19 h to 2.75–4 h and the dried product was loosely packed powder. After freeze‐thaw treatment, the molecular weight of chitosan was unchanged during the thermal drying. The heat‐induced browning effect of chitosan during drying was greatly alleviated by the pretreatment. Furthermore, the pretreatment increased the 1,1‐diphenyl‐2‐picrylhydrazyl (DPPH) radical‐scavenging activity of dried product by 40.4–59.8%. The molecular weight, color, and DPPH radical‐scavenging activity of the pretreated dried chitosan product were close to those of freeze‐dried product. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 41017.  相似文献   

6.
    
A series of flexible polyurethane foams with different polyol compositions were synthesized through the replacement of a portion of the petroleum‐based polyether polyol with biobased polyols, namely, glycerol (GLY) and hydroxylated methyl esters (HMETO). HMETO was synthesized by the alkaline transesterification of tung oil (TO; obtaining GLY as a byproduct) and the subsequent hydroxylation of the obtained methyl esters with performic acid generated in situ. FTIR spectroscopy, 1H‐NMR, and different analytical procedures indicated that the hydroxyl content increased significantly and the molecular weight decreased with respect to those of the TO after the two reaction steps. The characterization of the obtained foams, achieved through the measurement of the characteristic reaction times, thermal and dynamic mechanical analysis, scanning electronic microscopy, and density measurements, is reported and discussed. The most important changes in the modified foams were found with the addition of GLY to the formulation; this led to an increased foam density and storage rubbery modulus, which were associated with a higher crosslinking density because of the decrease in the chain length between crosslinking points. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43831.  相似文献   

7.
    
This is probably the first report on the synthesis of a series of novel collagen‐based flocculants (CP11, CP12, and CP13) by grafting polyacrylamide (PAM) chains onto the collagen backbone, which was directly extracted from leather shavings via alkali hydrolysis. The results from FTIR, XRD, 1H NMR, and TGA well supported that PAM chains had been successfully grafted onto collagen backbone. In addition, the micrographs of SEM revealed that the PAM grafted collagen possessed much more porous and looser surface structures in comparison with virgin collagen. Zeta potential measurement showed that the introduction of branched PAM chains helped to improve the positively charge density. Furthermore, CP12 performed the best in the kaolin flocculation with the highest flocculation rate about 24%·min?1 and could induce the generation of much larger and denser floccs for the fast settling of kaolin particles. The corresponding flocculation mechanism was also presented by analyzing the collected flocs. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41556.  相似文献   

8.
    
This study represents the first detailed analysis of the thermal, morphological, and crystallization properties of the blend components within a range of mixed‐culture polyhydroxyalkanoates (PHAs), with 3‐hydroxyvalerate content in the as‐produced materials and in the fractions ranging from low (12 mol %) to high (91 mol %). Both coarse and fine fractionation of the as‐produced copolymers confirmed that they were blends of nominally blocky and/or random copolymers of poly(3‐hydroxybutyrate‐co‐3‐hydroxyvalerate), with very broad compositional distributions as governed by the PHA accumulation strategy. The crystallization kinetics and thermal properties of the fractions were found to be very significantly different from each other, consistent with the hypothesis that the overall mechanical properties were primarily controlled by the more rapidly crystallizing components. Two materials produced using an alternating feeding strategy demonstrated unique crystallization and thermal properties in their fractions, which are considered to have contributed to distinctly more elastic mechanical properties in these particular samples. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40836.  相似文献   

9.
    
Eco‐friendly and inexpensive “ green” nanocomposites with enhanced functional performances were developed by combining nanoscale hydroxyapatite (HA) synthesized from eggshell waste (nEHA) and protein‐based polymer extracted from defatted soybean residues. nEHA was synthesized from chicken eggshells using an energy efficient microwave‐assisted wet chemical precipitation method. Transmission electron microscopy, X‐ray diffraction, and energy‐dispersive X‐ray spectroscopy studies confirmed the nanometer scale (diameter: 4–14 nm and length: 5–100 nm) of calcium‐deficient (Ca/P ratio ～1.53) needle‐like HA. Uniform dispersion of nEHA in soy protein isolate (SPI) solution was obtained by modifying nEHA surface using a polyelectrolyte (sodium polyacrylate) dispersant via irreversible adsorption. Green nanocomposite films were prepared from SPI and surface‐modified nEHA with the help of a natural plasticizer “glycerol” by solution casting. Significant improvements in tensile modulus and strength were achieved owing to the inclusion of uniformly dispersed nEHA in SPI sheets. Overall, this work provides a green pathway of fabricating nanocomposites using naturally occurring renewable polymer and inorganic moieties from eggshell waste that emphasizes the possibilities for replacing some petroleum‐based polymers in packaging and other applications. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43477.  相似文献   

10.
    
Soybean oil-based macroinitiator was prepared from epoxidized soybean oil. A 1H NMR quantitative method was utilized for the characterization of this macroinitiator. A kind of renewable carbohydrate derivate, 1,4: 3,6-Dianhydro-D-glucitol 2-acrylate 5-acetate (AAI) was prepared as the substitute monomer of styrene. Series of renewable miktoarm star copolymers initiated by soybean oil macroinitiator were obtained by atom transfer radical polymerization (ATRP) of AAI and ring-opening polymerization (ROP) of ε-caprolactone sequentially. The obtained miktoarm star block copolymers were characterized by 1H NMR, FTIR, and DSC. The DSC results show well dependence of the thermal behaviors of these miktoarm star block copolymers on the component of the two kinds of segments. A new strategy of renewable resource utilization has been provided on polymeric materials. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48281.  相似文献   

11.
    
To fulfill the comprehensive utilization of cellulose and hemicellulose components in bagasse for bacterial cellulose (BC) production, both bagasse acid and enzymatic hydrolysates were used for BC production by Gluconacetobacter xylinus. Although the BC accumulation rate was slower during the early period of fermentation in the bagasse acid hydrolysate than in the enzymatic hydrolysate, the highest BC yield (1.09 vs. 0.42 g/L) was higher in the bagasse acid hydrolysate. The substrate utilization was evaluated in both bagasse acid and enzymatic hydrolysates, and glucose, xylose, and acetic acid were better carbon sources than arabinose and cellobiose for G. xylinus. The structure of the BC samples obtained from bagasse acid and enzymatic hydrolysates, including the microscopic morphology, functional groups, and crystals, was similar especially in the later phase of fermentation, which was analyzed by field emission scanning electron microscopy, Fourier transform infrared spectroscopy, and X‐ray diffraction. Thus, both bagasse acid and enzymatic hydrolysates could be promising substrates for BC production. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45066.  相似文献   

12.
    
To reveal morphological changes in bamboo constituents induced by delignification and hemicelluloses removal processes, changes in chemical composition and dynamics were examined at molecular‐ to nano‐scales, using scanning electron microscopy images, attenuated total reflection infrared spectra, solid state nuclear magnetic resonance spectra, and relaxation time analysis at multiple hierarchical levels. Boiling removed spherical particles from the parenchymal cells of bamboo, leaving the cells containing water that had infiltrated into the nanostructure composed of carbohydrates and lignin. Treatment of the boiled bamboo with NaClO2 solution removed most of lignin, leaving hemicellulose chains that made the parenchymal cells stretch. In contrast, treatment of the boiled bamboo with NaOH solution removed both hemicellulose and lignin, with the result that parenchymal cells shrank in the cross‐section direction. Furthermore, treatment of the delignified bamboo with NaOH solution demolished the parenchymal cells due to complete removal of hemicellulose and lignin. A nanostructural model proposed on the basis of molecular‐ to nano‐scale analyses was consistent with the changes of vascular bundles and parenchymal cells. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40243.  相似文献   

13.
    
Free radical bulk and emulsion co‐ and terpolymerizations of conjugated linoleic acid (CLA) with styrene (Sty) and butyl acrylate (BA) were performed at 80 °C. The polymerizations were monitored using an attenuated total reflectance Fourier transform infrared (ATR‐FTIR) spectroscopic probe. Bulk polymerizations were monitored off‐line while emulsion polymerizations were monitored in‐line. Absorbance peaks related to the monomers and polymer were tracked to provide conversion and polymer composition data using a multivariate calibration method. Off‐line measurements using gravimetry and 1H‐NMR spectroscopy were compared to the ATR‐FTIR data and no significant differences were detected between the measurement methods. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43574.  相似文献   

14.
    
Collagen, a prominent biopolymer, which is famous for its excellent biological activity, has been used extensively for tissue engineering applications. In this study, a novel solvent system for collagen was developed with an ionic liquid, 1‐ethyl‐3‐methylimidazolium acetate ([EMIM][Ac]), solvent system. A series of sodium salts were introduced into this solvent system to enhance collagen's dissolution procedure. The results show that the solubility of collagen was significantly influenced by the temperature and sodium salts. The solubility reached up to approximately 11% in the [EMIM][Ac]/Na2HPO4 system at 45°C. However, the structure of the regenerated collagen (Col‐regenerated) may have been damaged. Hence, we focused on the structural integrity of the collagen regenerated from the [EMIM][Ac] solvent system by the methods of sodium dodecyl sulfate–polyacrylamide gel electrophoresis, Fourier transform infrared spectroscopy, ultrasensitive differential scanning calorimetry, atomic force microscopy, X‐ray diffraction, and circular dichroism because its signature biological and physicochemical properties were based on its structural integrity. Meanwhile, a possible dissolution mechanism was proposed. The results show that the triple‐helical structure of collagen regenerated from the [EMIM][Ac] solvent system below 35°C was retained to a large extent. The biocompatibility of Col‐regenerated was first characterized with a fibroblast adhesion and proliferation model. It showed that the Col‐regenerated had almost the same good biological activity as nature collagen, and this indicated the potential application of [EMIM][Ac] in tissue engineering. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 2245–2256, 2013  相似文献   

15.
    
Thermal processing of two potato protein isolates (PPIs) with glycerol as a plasticizer was explored in this study. The PPIs were pretreated by alkali or alkali under reducing conditions. The PPIs before and after pretreatment were analyzed by sodium dodecyl sulfate polyacrylamide gel electrophoresis, differential scanning calorimetry, and Fourier transform infrared spectroscopy. The effects of plasticizer content and pretreatment on mechanical and thermo‐mechanical properties of the compression‐molded biopolymers were studied. The highest tensile strengths obtained were 20–25 MPa and the biopolymer can be brittle or ductile depending on the plasticizer contents. The molecular weight and protein structure of the PPIs markedly affected the resultant biopolymers’ static and dynamic mechanical properties. The pretreatment of PPIs caused distinctly different changes in the mechanical properties of the two PPIs. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42723.  相似文献   

16.
    
Toughened unsaturated polyester resins (UPRs) were prepared using two different reactive rubbers, namely, liquid natural rubber (LNR) and liquid epoxidized natural rubber (LENR). The effect of varying amounts of LNR and LENR on the morphology, thermal, and mechanical properties of UPR were evaluated. Fourier Transform Infrared spectroscopy was used to investigate the probable crosslinking reaction and changes in the functional groups on crosslinking. Field emission scanning electron microscopy and infinite focus microscopy were used to study the morphology of fracture surfaces. Tensile test showed that both the rubber‐modified resins (1.5 wt %) improved tensile strength. The viscoelastic properties and thermal stability of the toughened polyesters were evaluated using dynamic mechanical thermal analysis and thermogravimetric analysis, respectively. A slight reduction in the glass transition temperature (Tg) of the polyester was reported on the addition of both the rubbers. An increment in impact strength and fracture toughness was observed at 1.5 wt % for LNR and 4.5 wt % for LENR‐modified UPR. The results showed that both the liquid rubbers improved the mechanical properties of UPR. However, LENR‐modified UPR exhibited a more significant improvement in the mechanical properties compared to LNR‐modified UPR. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41292.  相似文献   

17.
    
The objective of this study was to determine the compatibility of whole pyrolysis oil (PO) of pine as a substitute for the phenolic component of epoxy resins (ER). Pyrolysis oil‐based epoxy resin (POBER) was synthesized by modification of EPON828 ER with PO at various mixing ratios (1 : 3–1 : 8, PO:EPON828, w/w). Acetone extraction determined that a ratio of 1 : 7–1 : 8 resulted in a fully reacted thermoset, leaving neither PO nor EPON828 in a significantly unreacted state. Dynamic mechanical analysis (DMA) revealed that a ratio of 1 : 8 produced the highest storage modulus (E’); in addition, it was determined that this ratio provided a superior glass transition temperature (Tg) of 120°C and crosslinking density of 1891 mol/m3. FTIR spectra concluded that the reaction between the EPON828 and PO was complete at the 1 : 8 ratio, citing the removal of hydroxyl and epoxide peaks within the cured product. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42239.  相似文献   

18.
    
This article reports for the first time the results about the use of inertized fly ash from municipal solid waste incineration as a filler for polypropylene (PP). An innovative process based on the stabilization with colloidal silica has been used for fly ash inertization. Polymer–filler composites containing different filler amounts up to 30 wt % have then been formulated and prepared by means of melt compounding process. Structural, morphological, mechanical, and thermal characterization of their properties has been performed and discussed in detail. Remarkable enhancements of tensile (+ 93%) and flexural (+ 107%) elastic moduli if compared to pristine PP, together with enhancements of flexural resistance (+ 36%) and deflection temperature under load (+ 50%), have been observed when adding filler 30 wt % in suitable processing conditions. Moreover the filler has been shown to interact with polymer crystalline structure and positively influence the thermal‐oxidative stability. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 4157–4164, 2013  相似文献   

19.
    
Biocomposite membranes from biodegradable and biocompatible natural polymers were prepared from sodium alginate solution reinforced with silk fibroin fibers in several fiber content by casting and solvent evaporation. The properties of these biocomposites were investigated by scanning electron microscopy, swelling test, water vapor transmission, mechanical and thermal analyses, and cytotoxicity test. A biocomposite with uniform fiber dispersion and good fiber–matrix interaction was obtained through the incorporation of fibroin fibers in the alginate membrane, even though the fibers were used without any surface treatment to enhance the interfacial adhesion. The incorporation of fibroin fibers improved the tensile strength and also provided a new property to the alginate, that is, the resistance to tear. Moreover, the use of silk fibroin fibers in polymeric composites can result in a material with adequate characteristics for application in the biomaterial field, especially as wound dressings, because of its nontoxic effect to cells, flexibility, and resistance to tear. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 3451–3457, 2013  相似文献   

20.
    
Microencapsulation is an effective strategy to improve the storage stability of β‐carotene. This article investigated the potential and effectiveness of soy protein isolate (SPI) and octenylsuccinic anhydride‐modified starch (MS), alone or in combination (1:1, w/w), to encapsulate β‐carotene by spray drying. The results indicated that the microcapsule with MS exhibited much lower encapsulation efficiency (NE) and poorer dissolution behavior, but much better redispersion behavior, than that with SPI or its blends with MS. The NE was basically unaffected by total solid content (TC) or core/wall ratio; increasing the TC impaired the dissolution and/or redispersion behavior. The dispersion behavior was closely associated with the morphology of the microcapsules. The encapsulated β‐carotene suffered a progressive loss upon storage under high humid or temperature environment, but it exhibited extraordinary stability at low temperatures (e.g., 4°C). The β‐carotene degradation was independent of sunlight. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40399.  相似文献   

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