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2015 Volume 33 Issue 8
2015, 33(8): 1069-1073
doi: 10.1007/s10118-015-1675-2
Abstract:
We demonstrate here seven pure cyclic samples, which belongs to two series of oligoesters, cyclic oligo(trimethylene terephthalate)s (COTTs) and cyclic oligo(butylene terephthalate)s (COBTs), showing odd-even effect of degree of oligomerization (repeating units number) on properties. The pentamer of COTT and trimer of COBT show much lower melting temperature, and the trimer of COTT and trimer of COBT show significant lower refractive index, which can be ascribed to the low packing density of cyclic oligoesters with odd number of degree of oligomerization. Our results reveal the discrete property change as a function of cyclic size of oligomers, which can be used to design materials with special properties.
We demonstrate here seven pure cyclic samples, which belongs to two series of oligoesters, cyclic oligo(trimethylene terephthalate)s (COTTs) and cyclic oligo(butylene terephthalate)s (COBTs), showing odd-even effect of degree of oligomerization (repeating units number) on properties. The pentamer of COTT and trimer of COBT show much lower melting temperature, and the trimer of COTT and trimer of COBT show significant lower refractive index, which can be ascribed to the low packing density of cyclic oligoesters with odd number of degree of oligomerization. Our results reveal the discrete property change as a function of cyclic size of oligomers, which can be used to design materials with special properties.
2015, 33(8): 1074-1085
doi: 10.1007/s10118-015-1658-3
Abstract:
A novel non-coplanar aromatic diamine monomer, 3,3'-ditertbutyl-4,4'-diaminodiphenyl-4''-naphthylmethane (TAPN) was synthesized by a condensation reaction of 2-tertbutylaniline and 1-naphthaldehyde under catalyst hydrochloric acid. The structure of the monomer was confirmed by FTIR, NMR, elementary analysis and mass spectrometry. A series of aromatic polyimides (PIs) were synthesized via conventional one-step polycondensation from TAPN and various commercial aromatic dianhydrides. All of the PIs exhibit excellent solubility in common organic solvents, even in low boiling point solvents such as chloroform (CHCl3), tetrahydrofuran (THF) and acetone. The PIs present outstanding thermal stability with the glass transition temperature (Tg) ranged from 299 ℃ to 350 ℃, and the temperature at 10% weight loss ranged from 490 ℃ to 504 ℃, and high optical transparency with the cutoff wavelengths of 306-356 nm. Moreover, the flexible and tough PI films have prominent mechanical properties with tensile strengths in the range of 77.6-90.5 MPa, tensile modulus in the range of 1.8-2.4 GPa and elongation at break in the range of 6.3%-9.5%, as well as lower dielectric constant (2.89-3.12 at 1 MHz) and lower moisture absorption (0.35%-0.66%).
A novel non-coplanar aromatic diamine monomer, 3,3'-ditertbutyl-4,4'-diaminodiphenyl-4''-naphthylmethane (TAPN) was synthesized by a condensation reaction of 2-tertbutylaniline and 1-naphthaldehyde under catalyst hydrochloric acid. The structure of the monomer was confirmed by FTIR, NMR, elementary analysis and mass spectrometry. A series of aromatic polyimides (PIs) were synthesized via conventional one-step polycondensation from TAPN and various commercial aromatic dianhydrides. All of the PIs exhibit excellent solubility in common organic solvents, even in low boiling point solvents such as chloroform (CHCl3), tetrahydrofuran (THF) and acetone. The PIs present outstanding thermal stability with the glass transition temperature (Tg) ranged from 299 ℃ to 350 ℃, and the temperature at 10% weight loss ranged from 490 ℃ to 504 ℃, and high optical transparency with the cutoff wavelengths of 306-356 nm. Moreover, the flexible and tough PI films have prominent mechanical properties with tensile strengths in the range of 77.6-90.5 MPa, tensile modulus in the range of 1.8-2.4 GPa and elongation at break in the range of 6.3%-9.5%, as well as lower dielectric constant (2.89-3.12 at 1 MHz) and lower moisture absorption (0.35%-0.66%).
Photo-Dimerization Characteristics of Coumarin Pendants within Amphiphilic Random Copolymer Micelles
2015, 33(8): 1086-1095
doi: 10.1007/s10118-015-1657-4
Abstract:
The photo-dimerization characteristics of coumarin pendants within amphiphilic random copolymer micelles in aqueous solution was comprehensively investigated using various selected wavelength light in the UV-Vis-NIR region. The time-dependent photo-dimerization degree (PD) changes in the photo-dimerization experiments showed saturating behaviors with intensity-independent of PDmax values at 28%, 44%, 92%, 85%, 36%, 35%, 32% and 31% for 254, 288, 320, 360, 400, 500, 650 and 900 nm irradiations, respectively. The irradiation experiments at 254 and 288 nm announced the occurring of an asymmetric equilibrium of photo-dimerization and photo-cleavage at the used conditions. Both the alternative irradiation cycles of 360 and 254 nm, 650 and 254 nm showed a partially, but evidently reversible photo-dimerization tendency.
The photo-dimerization characteristics of coumarin pendants within amphiphilic random copolymer micelles in aqueous solution was comprehensively investigated using various selected wavelength light in the UV-Vis-NIR region. The time-dependent photo-dimerization degree (PD) changes in the photo-dimerization experiments showed saturating behaviors with intensity-independent of PDmax values at 28%, 44%, 92%, 85%, 36%, 35%, 32% and 31% for 254, 288, 320, 360, 400, 500, 650 and 900 nm irradiations, respectively. The irradiation experiments at 254 and 288 nm announced the occurring of an asymmetric equilibrium of photo-dimerization and photo-cleavage at the used conditions. Both the alternative irradiation cycles of 360 and 254 nm, 650 and 254 nm showed a partially, but evidently reversible photo-dimerization tendency.
2015, 33(8): 1096-1103
doi: 10.1007/s10118-015-1659-2
Abstract:
In this study, we present a method to synthesize styrene-butadiene copolymer, using anionic polymerization in a co-rotating closely intermeshing twin-screw extruder. The weight content of polybutadiene in these copolymers was above 50% although in the past studies it had been possible to accomplish levels higher than 30%. 1H-NMR and GPC show that the molecular structure of the two polymers is different due to different feeding method. In terms of the structure of the polymerized products, the mechanism of polymerization in the bulk polymerization is discussed. TEM and DMA show that two phases in the block copolymer are completely incompatible, leading to sharp phase separation, while the case is complicated in the copolymer through the mixture feeding. Traditionally, styrene-butadiene rubber is mainly synthesized by solution polymerization. Reactive extrusion in this paper provides a possibility to synthesize these products in an environmentally friendly way.
In this study, we present a method to synthesize styrene-butadiene copolymer, using anionic polymerization in a co-rotating closely intermeshing twin-screw extruder. The weight content of polybutadiene in these copolymers was above 50% although in the past studies it had been possible to accomplish levels higher than 30%. 1H-NMR and GPC show that the molecular structure of the two polymers is different due to different feeding method. In terms of the structure of the polymerized products, the mechanism of polymerization in the bulk polymerization is discussed. TEM and DMA show that two phases in the block copolymer are completely incompatible, leading to sharp phase separation, while the case is complicated in the copolymer through the mixture feeding. Traditionally, styrene-butadiene rubber is mainly synthesized by solution polymerization. Reactive extrusion in this paper provides a possibility to synthesize these products in an environmentally friendly way.
2015, 33(8): 1104-1113
doi: 10.1007/s10118-015-1662-7
Abstract:
The correlation between ring-opening polymerization (ROP) of cyclic butylene terephthalate (CBT) and crystallization of polymerized CBT (pCBT) strongly affected the final properties of pCBT and its composites. The major objective of this contribution is to pinpoint the threshold temperature between them and the interrelation is successfully disclosed. That is, crystallization during polymerization occurs below 204 ℃ and the crystallization properties of pCBT are determined by this isothermal ROP stage; polymerization and crystallization are gradually separated with the increase of temperature of ROP (TP) from 204 ℃, and the crystallization properties of pCBT are dominated by cooling stage; only polymerization is performed above 212 ℃. Moreover, quantitative analysis suggests that uniform crystal size distributions and thicker lamellar crystals derive from the stage of crystallization during polymerization. On the contrary, the crystal size distributions become wider above 204 ℃ of TP and lead to obvious double melting peaks during heating scan. These efforts provide a very useful guide for the related investigation and application of CBT.
The correlation between ring-opening polymerization (ROP) of cyclic butylene terephthalate (CBT) and crystallization of polymerized CBT (pCBT) strongly affected the final properties of pCBT and its composites. The major objective of this contribution is to pinpoint the threshold temperature between them and the interrelation is successfully disclosed. That is, crystallization during polymerization occurs below 204 ℃ and the crystallization properties of pCBT are determined by this isothermal ROP stage; polymerization and crystallization are gradually separated with the increase of temperature of ROP (TP) from 204 ℃, and the crystallization properties of pCBT are dominated by cooling stage; only polymerization is performed above 212 ℃. Moreover, quantitative analysis suggests that uniform crystal size distributions and thicker lamellar crystals derive from the stage of crystallization during polymerization. On the contrary, the crystal size distributions become wider above 204 ℃ of TP and lead to obvious double melting peaks during heating scan. These efforts provide a very useful guide for the related investigation and application of CBT.
2015, 33(8): 1114-1124
doi: 10.1007/s10118-015-1663-6
Abstract:
In this study, effects of oscillatory shear with different frequencies (0-2.5 Hz) and amplitudes (0-20 mm) on the mechanical properties and crystalline morphology of linear low density polyethylene (LLDPE) were investigated. It was found that the mechanical properties of LLDPE are improved because of the more perfect crystalline structure when LLDPE crystallizes under low-frequency and small-amplitude (0.2 Hz/4 mm) oscillatory shear. The mechanical properties can be further improved by increasing either the frequency or the amplitude of oscillatory shear. The Young's modulus and tensile strength of LLDPE are improved by 27% and 20%, respectively, when the frequency is increased to 2.5 Hz and the amplitude is maintained at 4 mm; while the Young's modulus and tensile strength are improved by 49% and 47%, respectively, when the amplitude is increased to 20 mm and the frequency is remained as 0.2 Hz. The crystallinity and microstructure of LLDPE under different oscillatory shear conditions were investigated by using differential scanning calorimetry, wide angle X-ray diffraction and scanning electron microscopy to shed light on the mechanism for the improvement of mechanical properties.
In this study, effects of oscillatory shear with different frequencies (0-2.5 Hz) and amplitudes (0-20 mm) on the mechanical properties and crystalline morphology of linear low density polyethylene (LLDPE) were investigated. It was found that the mechanical properties of LLDPE are improved because of the more perfect crystalline structure when LLDPE crystallizes under low-frequency and small-amplitude (0.2 Hz/4 mm) oscillatory shear. The mechanical properties can be further improved by increasing either the frequency or the amplitude of oscillatory shear. The Young's modulus and tensile strength of LLDPE are improved by 27% and 20%, respectively, when the frequency is increased to 2.5 Hz and the amplitude is maintained at 4 mm; while the Young's modulus and tensile strength are improved by 49% and 47%, respectively, when the amplitude is increased to 20 mm and the frequency is remained as 0.2 Hz. The crystallinity and microstructure of LLDPE under different oscillatory shear conditions were investigated by using differential scanning calorimetry, wide angle X-ray diffraction and scanning electron microscopy to shed light on the mechanism for the improvement of mechanical properties.
2015, 33(8): 1125-1132
doi: 10.1007/s10118-015-1661-8
Abstract:
A series of microporous polyimide networks with porphyrin units (Pr-MPIs) were facilely synthesized through a one-step solution polymerization process. Of particular interest is that Pr-MPI-1 containing distorted spirobisindane unit revealed the highest BET surface area (953 m2/g), total pore volume (0.75 cm3/g), and extreme hysteresis between the N2 adsorption and desorption isotherm. Further study revealed the prepared Pr-MPI-1 exhibited a synergistic structural effect on exceptional uptake of volatile organic compounds (VOCs) due to the high porosity and highly distorted spirobisindane structure enabled large interface and the swellability. This new approach would open up a facile approach toward the preparation of highly swellable high performance polymeric microporous materials, which are deeply wanted for environment-related applications such as VOCs adsorption and oil/water separation.
A series of microporous polyimide networks with porphyrin units (Pr-MPIs) were facilely synthesized through a one-step solution polymerization process. Of particular interest is that Pr-MPI-1 containing distorted spirobisindane unit revealed the highest BET surface area (953 m2/g), total pore volume (0.75 cm3/g), and extreme hysteresis between the N2 adsorption and desorption isotherm. Further study revealed the prepared Pr-MPI-1 exhibited a synergistic structural effect on exceptional uptake of volatile organic compounds (VOCs) due to the high porosity and highly distorted spirobisindane structure enabled large interface and the swellability. This new approach would open up a facile approach toward the preparation of highly swellable high performance polymeric microporous materials, which are deeply wanted for environment-related applications such as VOCs adsorption and oil/water separation.
2015, 33(8): 1133-1139
doi: 10.1007/s10118-015-1664-5
Abstract:
Poly(aryleneethynylene)s containing BODIPY (4,4-difluoro-4-bora-3a,4a-diaza-s-indacene) (P1) were prepared by palladium-catalyzed Sonogashira polymerization of 2,6-diiodo-functionalized BODIPY monomer (M1) with 1,4-diethynyl-2,5-didodecyl-oxybenzene monomer (M2). The structures of the monomer (M1) and copolymer (P1) were confirmed by 1H-NMR and Fourier transform infrared (FTIR) spectroscopies; their optical properties were characterized by UV-Vis absorption, photoluminescence (PL) spectroscopy and the Z-scan technique. Both UV-Vis absorption and fluorescence emission of copolymer P1 red-shifted to longer wavelengths (abs: from 502 nm to 542 nm; em: from 511 nm to 631 nm) relative to those of the monomer M1 due to the -conjugation extension of the copolymer. The third-order nonlinear optical coefficient ((3)) of copolymer P1 was 1.9410-10 esu, which is almost two or three orders of magnitude greater than that of common conjugated polymers without BODPIY moiety.
Poly(aryleneethynylene)s containing BODIPY (4,4-difluoro-4-bora-3a,4a-diaza-s-indacene) (P1) were prepared by palladium-catalyzed Sonogashira polymerization of 2,6-diiodo-functionalized BODIPY monomer (M1) with 1,4-diethynyl-2,5-didodecyl-oxybenzene monomer (M2). The structures of the monomer (M1) and copolymer (P1) were confirmed by 1H-NMR and Fourier transform infrared (FTIR) spectroscopies; their optical properties were characterized by UV-Vis absorption, photoluminescence (PL) spectroscopy and the Z-scan technique. Both UV-Vis absorption and fluorescence emission of copolymer P1 red-shifted to longer wavelengths (abs: from 502 nm to 542 nm; em: from 511 nm to 631 nm) relative to those of the monomer M1 due to the -conjugation extension of the copolymer. The third-order nonlinear optical coefficient ((3)) of copolymer P1 was 1.9410-10 esu, which is almost two or three orders of magnitude greater than that of common conjugated polymers without BODPIY moiety.
2015, 33(8): 1140-1149
doi: 10.1007/s10118-015-1640-0
Abstract:
A series of monomethoxy poly(ethylene glycol) (mPEG) grafted copolyglutamates (PmPEGs) were synthesized through ring-opening polymerization (ROP) followed by click chemistry. Supramolecular hydrogels based on polymer inclusion complexes (ICs) between PmPEG and -cyclodextrin (-CD) were prepared in aqueous solution. The rheological measurements indicated their gelation properties were affected by several factors including the mPEG length, graft density and the sample concentration. These hydrogels displayed thermo-sensitive gel-sol transition under appropriate conditions due to the reversible mPEG and -CD inclusion complexation. These hydrogels also showed pH-sensitive behavior due to the deprotonate of carboxylic acid side groups. The ICs formation of a channel-type crystalline structure induced gelation mechanism was verified by various techniques. In vitro cytotoxicity assays demonstrated that the supramolecular hydrogels are nontoxic and cytocompatible.
A series of monomethoxy poly(ethylene glycol) (mPEG) grafted copolyglutamates (PmPEGs) were synthesized through ring-opening polymerization (ROP) followed by click chemistry. Supramolecular hydrogels based on polymer inclusion complexes (ICs) between PmPEG and -cyclodextrin (-CD) were prepared in aqueous solution. The rheological measurements indicated their gelation properties were affected by several factors including the mPEG length, graft density and the sample concentration. These hydrogels displayed thermo-sensitive gel-sol transition under appropriate conditions due to the reversible mPEG and -CD inclusion complexation. These hydrogels also showed pH-sensitive behavior due to the deprotonate of carboxylic acid side groups. The ICs formation of a channel-type crystalline structure induced gelation mechanism was verified by various techniques. In vitro cytotoxicity assays demonstrated that the supramolecular hydrogels are nontoxic and cytocompatible.
2015, 33(8): 1150-1161
doi: 10.1007/s10118-015-1665-4
Abstract:
A series of polypeptides bearing biphenyl mesogenic side-chains and oligo-ethylene-glycol (OEG) tails (PPLGn-g-BPOEGm, n = 26 and 63, m = 2, 3, and 7) has been synthesized via a 1,3-dipolar cycloaddition with quantitative grafting density. FTIR results revealed that the polypeptides adopted highly stable -helix in the temperature range of 25-200 ℃. DSC, POM and WAXS analysis revealed that PPLGn-g-BPOEGm (m 3) samples with short OEG tail length showed two main phase transitions including crystal to liquid crystalline (smectic C, SmC) phase transition and the melting transition of crystalline E-phase, while PPLGn-g-BPOEG7 with longer OEG tail length (m = 7) exhibited the melting transitions without the formation of liquid crystalline phase.
A series of polypeptides bearing biphenyl mesogenic side-chains and oligo-ethylene-glycol (OEG) tails (PPLGn-g-BPOEGm, n = 26 and 63, m = 2, 3, and 7) has been synthesized via a 1,3-dipolar cycloaddition with quantitative grafting density. FTIR results revealed that the polypeptides adopted highly stable -helix in the temperature range of 25-200 ℃. DSC, POM and WAXS analysis revealed that PPLGn-g-BPOEGm (m 3) samples with short OEG tail length showed two main phase transitions including crystal to liquid crystalline (smectic C, SmC) phase transition and the melting transition of crystalline E-phase, while PPLGn-g-BPOEG7 with longer OEG tail length (m = 7) exhibited the melting transitions without the formation of liquid crystalline phase.
2015, 33(8): 1162-1175
doi: 10.1007/s10118-015-1666-3
Abstract:
The effect of chemically reduced graphene oxide (CRGO) on the phase separation behavior of poly(methyl methacrylate)/poly(styrene-co-acrylonitrile) (PMMA/SAN) blends and the simultaneous response of rheological and conductive behavior of PMMA/SAN/CRGO nanocomposites upon annealing above the phase-separation temperatures were investigated. The introduction of CRGO causes the decrease of binodal temperature and the increase of spinodal temperature for PMMA/SAN blends and then enlarges their metastable regime. During annealing, the well-dispersed CRGO in the homogeneous blend matrix tends to be selectively located in the SAN-rich phase with the evolution of phase separation and then the CRGO further agglomerates effectively in the SAN-rich phase to form the conductive pathway. Thermal-induced dynamic percolation is observed for both the resistivity and dynamic storage modulus G' as a function of annealing time. The resistivity variation is ascribed to the agglomeration of CRGO in the SAN-rich phase, while the modulus evolution is attributed to the combined contribution of phase separation for blend matrix and the agglomeration of CRGO in the SAN-rich phase.
The effect of chemically reduced graphene oxide (CRGO) on the phase separation behavior of poly(methyl methacrylate)/poly(styrene-co-acrylonitrile) (PMMA/SAN) blends and the simultaneous response of rheological and conductive behavior of PMMA/SAN/CRGO nanocomposites upon annealing above the phase-separation temperatures were investigated. The introduction of CRGO causes the decrease of binodal temperature and the increase of spinodal temperature for PMMA/SAN blends and then enlarges their metastable regime. During annealing, the well-dispersed CRGO in the homogeneous blend matrix tends to be selectively located in the SAN-rich phase with the evolution of phase separation and then the CRGO further agglomerates effectively in the SAN-rich phase to form the conductive pathway. Thermal-induced dynamic percolation is observed for both the resistivity and dynamic storage modulus G' as a function of annealing time. The resistivity variation is ascribed to the agglomeration of CRGO in the SAN-rich phase, while the modulus evolution is attributed to the combined contribution of phase separation for blend matrix and the agglomeration of CRGO in the SAN-rich phase.
2015, 33(8): 1176-1185
doi: 10.1007/s10118-015-1667-2
Abstract:
Poly(bisphenol A carbonate) (BPA-PC) was post-polymerized by solid-state polymerization (SSP) after supercritical CO2-induced crystallization in low molecular weight particles prepolymerized via melt transesterification reaction. The effects of the crystallization conditions on melting behavior and SSP of BPA-PC were investigated with differential scanning calorimetry (DSC), Ubbelohde viscosity method and gel permeation chromatography (GPC). The reaction kinetics of the SSP of crystallized prepolymers was studied as a function of reaction temperatures for various reaction periods. As a result, the viscosity average molecular weight of BPA-PC particles (2 mm) increased from 1.9104 g/mol to 2.8104 g/mol after SSP. More importantly, the significantly enhanced thermal stability and mechanical properties of solid-state polymerized BPA-PC, compared with those of melt transesterification polymerized BPA-PC with the same molecular weight, can be ascribed to the substantial avoidance of undergoing high temperature during polymerization. Our work provides a useful method to obtain practical product of BPA-PC with high quality and high molecular weight.
Poly(bisphenol A carbonate) (BPA-PC) was post-polymerized by solid-state polymerization (SSP) after supercritical CO2-induced crystallization in low molecular weight particles prepolymerized via melt transesterification reaction. The effects of the crystallization conditions on melting behavior and SSP of BPA-PC were investigated with differential scanning calorimetry (DSC), Ubbelohde viscosity method and gel permeation chromatography (GPC). The reaction kinetics of the SSP of crystallized prepolymers was studied as a function of reaction temperatures for various reaction periods. As a result, the viscosity average molecular weight of BPA-PC particles (2 mm) increased from 1.9104 g/mol to 2.8104 g/mol after SSP. More importantly, the significantly enhanced thermal stability and mechanical properties of solid-state polymerized BPA-PC, compared with those of melt transesterification polymerized BPA-PC with the same molecular weight, can be ascribed to the substantial avoidance of undergoing high temperature during polymerization. Our work provides a useful method to obtain practical product of BPA-PC with high quality and high molecular weight.
2015, 33(8): 1186-1195
doi: 10.1007/s10118-015-1669-0
Abstract:
Polypeptides and polypeptoids were widely used as biomedical materials because of their good biocompatibility. In this work we reported a series of pH-responsive copolypeptides and polypeptide-polypeptoid block copolymers, i.e. random copolymers of L-glutamic acid (Glu) with L-leucine (Leu) [poly(Glu-r-Leu)s], as well as their block copolymers with polysarcosine (polySar). Well-defined poly(Glu-r-Leu)s with predictable compositions and molecular weights were synthesized by ring opening polymerization of corresponding N-carboxyanhydride monomers. We investigated the relationship between hydrophilicity-hydrophobicity transition and copolymer composition. With increasing Leu fraction, both the pH value of cloud point and the micellar size increased. Poly(Glu-r-Leu) with 60% Leu exhibited a cloud point at the pH of 5.0 to 6.0 the same as that in endosome and lysosome. Poly(Glu-r-Leu)-b-polySars assembled in phosphate buffer and performed pH-responsive morphology change from orbicular micelles at high pH to worm-like micelles at low pH. They were potential pH-responsive carriers for drug and gene delivery to enhance cargo release in cellules.
Polypeptides and polypeptoids were widely used as biomedical materials because of their good biocompatibility. In this work we reported a series of pH-responsive copolypeptides and polypeptide-polypeptoid block copolymers, i.e. random copolymers of L-glutamic acid (Glu) with L-leucine (Leu) [poly(Glu-r-Leu)s], as well as their block copolymers with polysarcosine (polySar). Well-defined poly(Glu-r-Leu)s with predictable compositions and molecular weights were synthesized by ring opening polymerization of corresponding N-carboxyanhydride monomers. We investigated the relationship between hydrophilicity-hydrophobicity transition and copolymer composition. With increasing Leu fraction, both the pH value of cloud point and the micellar size increased. Poly(Glu-r-Leu) with 60% Leu exhibited a cloud point at the pH of 5.0 to 6.0 the same as that in endosome and lysosome. Poly(Glu-r-Leu)-b-polySars assembled in phosphate buffer and performed pH-responsive morphology change from orbicular micelles at high pH to worm-like micelles at low pH. They were potential pH-responsive carriers for drug and gene delivery to enhance cargo release in cellules.
2015, 33(8): 1196-1210
doi: 10.1007/s10118-015-1670-7
Abstract:
A novel and easy one-step protocol for preparation of a new porous material, polyurea (PPU), is reported, which is accomplished through a precipitation polymerization of toluene diisocyanate (TDI) in mixed solvent of H2O-acetone without need for surfactant and porogen. Effects of TDI concentration, mechanical stirring, solvent composition and TDI addition rate on PPU structure are studied. Surface morphology and pore structure of PPU are characterized by scanning electron microscopy and Hg intrusion. Chemical structure of the PPU polymer is investigated using NMR, XRD and FTIR. Mechanism of pore formation is discussed. The obtained PPU is used as adsorbent for anionic dyes adsorption investigation. Two anionic dyes, remazol brilliant blue R and acid fuchsine, are tested. The results indicate that the as-prepared PPU is of high performance in dye adsorption and recycled use. This study provided therefore a facile route to the preparation of a novel and attractive adsorbent candidate for removal of anionic dyes from wastewaters.
A novel and easy one-step protocol for preparation of a new porous material, polyurea (PPU), is reported, which is accomplished through a precipitation polymerization of toluene diisocyanate (TDI) in mixed solvent of H2O-acetone without need for surfactant and porogen. Effects of TDI concentration, mechanical stirring, solvent composition and TDI addition rate on PPU structure are studied. Surface morphology and pore structure of PPU are characterized by scanning electron microscopy and Hg intrusion. Chemical structure of the PPU polymer is investigated using NMR, XRD and FTIR. Mechanism of pore formation is discussed. The obtained PPU is used as adsorbent for anionic dyes adsorption investigation. Two anionic dyes, remazol brilliant blue R and acid fuchsine, are tested. The results indicate that the as-prepared PPU is of high performance in dye adsorption and recycled use. This study provided therefore a facile route to the preparation of a novel and attractive adsorbent candidate for removal of anionic dyes from wastewaters.
