A DNA fluorescence probe system based on fluorescence resonance energy transfer （FRET） from CdTe quantum dot （QD） donors to Au nanoparticle （AuNP） acceptors is presented. CdTe QDs, 2.5nm in diameter, as energy d...A DNA fluorescence probe system based on fluorescence resonance energy transfer （FRET） from CdTe quantum dot （QD） donors to Au nanoparticle （AuNP） acceptors is presented. CdTe QDs, 2.5nm in diameter, as energy donors, were prepared in water. Au nanoparticles, 16nm in diameter, as energy acceptors, were prepared from gold chloride by reduction. CdTe QDs were linked to 5＇-NH2-DNA through 1-ethyl-3-（dimethylaminopropyl）car- bodiimide hydrochloride （EDC） as a linker, and the 3＇-SH-DNA was self-assembled onto the surface of AuNPs. The hybridization of complementary double stranded DNA （dsDNA） bound to the QDs and AuNPs （CdTe-dsDNA-Au） determined the FRET distance of CdTe QDs and Au nanoparticles. Compared to the fluorescence of CdTe-DNA, the fluorescence of CdTe-DNA-Au conjugates decreased extremely, which indicated that the FRET occurred between CdTe QDs and Au nanoparticles. The fluorescence change of this conjugate depended on the ratio of Au-DNA to CdTe-DNA. When the AuNPs-DNA to QD-DNA ratio was 10：1, the FRET efficiency reached a maximum. The probe system would have a certain degree of fluorescence recovery when a complementary single stranded DNA was introduced into this system, which showed that the distance between CdTe QDs and Au nanoparticles was increased.展开更多
The title compound N,N＇-bis（5,5-dimethyl-2-phospha-2-thio-1,3-dioxan-2-yl） ethylene diamine （DPTDEDA, C12H26N2O4P2S2） was synthesized by the reaction of neopentyl glycol, phosphorus thio-chloride and 1,2-ethylene...The title compound N,N＇-bis（5,5-dimethyl-2-phospha-2-thio-1,3-dioxan-2-yl） ethylene diamine （DPTDEDA, C12H26N2O4P2S2） was synthesized by the reaction of neopentyl glycol, phosphorus thio-chloride and 1,2-ethylenediamine, and characterized by elemental analysis, IR and ^1H NMR spectra. Its crystal structure was determined by single-crystal X-ray diffraction analysis and the thermal property was analyzed by TG analysis. The crystal structure belongs to monoclinic, space group P21/c, with a = 14.557（16）, b = 11.299（12）, c = 12.163（13）A,β = 98.707（19）^o, Dc = 1.305 g/cm^3, Z = 4, γ = 0.71073A,μ（MoKa） = 0.447 mm^-1, Mr = 388.41, V = 1977（4）A3, F（000） = 824, S = 1.107, the final R = 0.0478 and wR = 0.0810 for 1738 observed reflections （I 〉 2σ（I））. X-ray analysis reveals that the crystal structure is centrosymmetrically distributed through 1,2-ethylenediamine to join two distorted six-membered rings. The weak N-H…S interactions are observed and link the molecules into sheets. TG analysis shows that the title compound has good thermal stability and char-forming capability, which are required for an excellent intumescent fire retardant.展开更多
In this study,the sol-gel method was introduced to prepare the composite phase change material (CPCM). The CPCM was added to fabric with coating techniques and the thermal activity of modified fabric was studied. In a...In this study,the sol-gel method was introduced to prepare the composite phase change material (CPCM). The CPCM was added to fabric with coating techniques and the thermal activity of modified fabric was studied. In addition,the thermal property and the microstructure of CPCM were also discussed in detail by means of polarization microscope and differential scanning calorimeter,respectively. According to the analysis of main influencial factors of the property of CPCM,the optimal preparing technique was determined. It was proved that CPCM could exhibit a good thermal property while phase transformation process took place,and a better appearance of the fabric modified with CPCM could be obtained due to the fact that in a warm circumstance,the liquid-state phase change material could be firmly enwrapped and embedded in the three-dimensional network all the time during the phase transformation. Besides,the fabric treated with CPCM had a high phase-transition enthalpy and an appropriate phase-transition temperature. As a result,a desirable temperature-adjustable function appeared.展开更多
Fe2O3/active carbon（Fe2O3/AC） nanocomposites were readily fabricated by pyrolyzing Fe3＋ impregnated active carbon in a nitrogen atmosphere. The as-prepared composites were studied by X-ray powder diffraction（XRD）...Fe2O3/active carbon（Fe2O3/AC） nanocomposites were readily fabricated by pyrolyzing Fe3＋ impregnated active carbon in a nitrogen atmosphere. The as-prepared composites were studied by X-ray powder diffraction（XRD）, X-ray photoelectron spectroscopy（XPS） and transmission electron microscopy（TEM）. The capacitive property of the composites was investigated by cyclic voltammetry（CV） and galvanostatic charge-discharge test. Physical characterizations show that the γ-Fe2O3 fine grains dispersed in the AC well, with a mean size of 21.24 nm. Electrochemical tests in 6 mol/L KOH solutions indicate that the as-prepared nanocomposites exhibited improved capacitive properties. The specific capacitance（SC） of Fe2O3/AC nanocomposites was up to 188.4 F/g that was derived from both electrochemical double-layer capacitance and pseudo-capacitance, which was 78% larger than that of pristine AC. A symmetric capacitor with Fe2O3/AC nanocomposites as electrode showed an excellent cycling stability. The SC was only reduced by a factor of 9.2% after 2000 cycles at a current density of 1 A/g.展开更多
A facile, safe and economical reducing agent, sodium hypophosphite（Na H2PO2·H2O）, has been successfully employed for ambient temperature living radical copolymerization of styrene（St） and methyl methacrylate...A facile, safe and economical reducing agent, sodium hypophosphite（Na H2PO2·H2O）, has been successfully employed for ambient temperature living radical copolymerization of styrene（St） and methyl methacrylate（MMA）. Such effective reducing agent significantly improved the reactivity of low reactive St monomers during the copolymerization, where the reactivity ratios of St and MMA were determined to be 0.50 and 0.36 by Finemann-Ross method. Thus the copolymerizations proceeded fast and showed typical living/controlled features, as evidenced by pseudo first-order kinetics of polymerization, linear increase in molecular weight versus monomer conversion, and low polydispersity index values. Effects of the concentration of reducing agent and the monomer feed ratio on the copolymerization were investigated in detail. Furthermore, gel permeation chromatography and 1H-NMR analyses as well as chain extension experiments confirmed the high chain-end functionality of the resultant copolymer.展开更多
We synthesized a series of rare earth complexes with benzoic acid ramification containing different substitute groups or the same substitute group in different position; test the fluorescence property using fluorescen...We synthesized a series of rare earth complexes with benzoic acid ramification containing different substitute groups or the same substitute group in different position; test the fluorescence property using fluorescence spectrometer of the complexes, and discussed the influence of different substitute group and the position of substitute group on the fluorescent properties of the rare earth complexes. The results showed that different substitute group and the position of substitute group on the benzene ring had important influence on the fluorescent properties of the benzoic acid rare earth complexes, when the other conditions were the same. The fluorescence effect of para-position ligand was better than ortho-position and meta-position ligand. For the benzoic acid complexes, their fluorescence intensity has relationship with the excellent absorption coefficient of the ligand and the high efficient ligand-to-trivalent rare earth ion energy transfer. Furthermore, when the ratio of Ln3+, ligand, phen was 1∶3∶1, the fluorescence properties of rare earth complex was the best.展开更多
A novel layered oxouranium phosphite open-structure [（C10H24N2）（H2O）][（UO2）2（HPO3）3]（denoted as TJPU-8,TJPU=Tianjin Polytechnic University） was hydrothermally synthesized with isophorondiamine（IPDA） as the...A novel layered oxouranium phosphite open-structure [（C10H24N2）（H2O）][（UO2）2（HPO3）3]（denoted as TJPU-8,TJPU=Tianjin Polytechnic University） was hydrothermally synthesized with isophorondiamine（IPDA） as the template.Single crystal structure refinement disclosed that TJPU-8 crystallized in the monoclinic space group P21c with cell parameters a=1.8346（9） nm,b=0.6734（1） nm,c=2.0639（0） nm,β=114.61（5）°,V=2.3182（8） nm3,Z=2.TJPU-8 was constructed by UO7 monomer,U2O12 dimer and HPO3 groups.The monomeric UO7 or dimeric U2O12 was connected by HPO3 groups to form two types of 4-ring chains.An undulating sheet was then generated by connecting these two types of chains via HPO3 bridges.The layer structure formed by stacking the sheets along the a direction via the strong H-bonds of organoamine cations and water molecules intercalated in the interlayer spaces with the framework oxygen atoms.Although a mixture of cis-and trans-IPDA was used,only cis-IPDA served as the template.A typical green light emission of TJPU-8 is observed when excited by 266 nm laser.展开更多
A concept of potential crosslinking agent was introduced into the synthesizing process of highly oil-absorptive resin that is traditionally prepared by single chemical crosslinking.The resin was heated after manufactu...A concept of potential crosslinking agent was introduced into the synthesizing process of highly oil-absorptive resin that is traditionally prepared by single chemical crosslinking.The resin was heated after manufactured to obtain three-dimension network structure.The effects of potential crosslinking agent and the crosslinking conditions on the absorptive properties of resin were studied.The results showed that hydroxyl ethylacrylate got satisfied results,and the resin with it had good oil absorbency and oil retention.展开更多
The non-isothermal degradation kinetics of N,N＇-di（diethoxythiophosphoryl）-1,4-phenylenediamine in N2 was studied by TG-DTG techniques.The kinetic parameters,including the activation energy and pre-exponential fact...The non-isothermal degradation kinetics of N,N＇-di（diethoxythiophosphoryl）-1,4-phenylenediamine in N2 was studied by TG-DTG techniques.The kinetic parameters,including the activation energy and pre-exponential factor of the degradation process for the title compound were calculated by means of the Kissinger and Flynn-Wall-Ozawa（FWO）method and the thermal degradation mechanism of the title compound was also studied with the Satava-Sestak methods.The results indicate that the activation energy and pre-exponential factor are 152.61 kJ/mol and 9.06×101 4s -1with the Kissinger method and 154.08 kJ/mol with the Flynn-Wall-Ozawa method,respectively.It has been shown that the degradation of the title compound follows a kinetic model of one-dimensional diffusion or parabolic law,the kinetic function is G（α）=α2and the reaction order is n=2.展开更多
The microenapsulated polyethylene glycol （PEG） with different molecular weight by a fluidized coating method has been prepared and the crystallization behaviors of PEG particles in three-dimensional confined vohume ...The microenapsulated polyethylene glycol （PEG） with different molecular weight by a fluidized coating method has been prepared and the crystallization behaviors of PEG particles in three-dimensional confined vohume were investigated by using differential scanning calorimetry （DSC） measurement. The results showed that the width of the crystallization peak of PEG increases and its height gradually diminishes in case that the PEG particles are microencapsulated. Compared with the non-microencapsulated PEG particles, the proportion of the first crystallization peak of microencapsulated PEG particle increases, and that of the second one decreases. The reason for the difference maybe is that the crystallization process of microencapsulated PEG particles is uniform and the crystallization ends when the spherulites touch the wall, thus the opportunity of producing the second crystallization peak was relatively reduced.展开更多
Poly(ethylene terephthalate) (PET)/carbon black (CB) masterbatch was prepared by melt blending using a separate feeding technique and its homogeneous dispersion morphology was confirmed by transmission electron micros...Poly(ethylene terephthalate) (PET)/carbon black (CB) masterbatch was prepared by melt blending using a separate feeding technique and its homogeneous dispersion morphology was confirmed by transmission electron microscope (TEM). The Avrami and Hoffman-Lauritzen secondary nucleation theories were employed to analyze the effect of high CB content on crystallization kinetics of PET, providing theoretical support for the development of masterbatch with high content of functional components. The Avrami exponents,average values of n,for PET and PET/CB masterbatch are both greater than 3, which indicates three-dimensional growth of crystals. In addition,no significant evidence for regime transition of PET is found applying Hoffman-Lauritzen secondary nucleation theory,though such observations have been reported previously in the literature. Furthermore,appropriate U* value for PET is determined to be 12 800 J/mol. For PET/CB masterbatch,a transition from regime I to regime II around 225℃ is observed with appropriate U* value (12 800 J/mol) . This phenomenon is consistent with a transition point in plot of G versus Tc . The fold surface free energy σe (100. 3 mJ/m 2) of PET is much greater than that of PET/CB masterbatch (48. 3 mJ/m 2) ,which indicates heterogeneous nucleation effect of CB particles.展开更多
A novel polymeric reaction monomer (NPRM) for preparing highly fluorescent rare earth polymer materials was synthesized via interface and coordinating reaction. The composition and structure of the NPRM and intermedia...A novel polymeric reaction monomer (NPRM) for preparing highly fluorescent rare earth polymer materials was synthesized via interface and coordinating reaction. The composition and structure of the NPRM and intermediate product (ligand) were characterized through the Fourier transform infrared spectroscopy (FT-IR), carbon-nuclear magnetic resonance spectrum (13CNMR), Mass spectra (MS), and element analysis data. The results showed that the composition and structure of NPRM agreed with that of anticipated product. The NPRM was composed of two important sections. Section 1 was able to provide excellent fluorescent properties for final rare earth polymer material through the effect energy transfer between ligand and rare earth ion; Section 2 would endow with the NPRM excellent polymeric active and form highly fluorescent rare earth polymer material. Fluorescent properties of the NPRM were also researched via a CARY ECLIPSE fluorescent spectrometer. The results showed that the NPRM possessed excellent luminescent properties. The corresponding emission peaks based on the 5D0→7F1(601.6 nm), 5D0→7F2(625.0 nm), 5D0→7F3(660.5 nm) and 5D0→7F4(706.3 nm) transitions for Eu3+ were observed. The strongest emission peak was at 625 nm, which belonged to 5D0→7F2 transition.展开更多
To investigate the influence of expansion pretreatment for materials on carbon structure, activated carbons （ACs） were prepared from corncob with/without expansion pretreatment by KOH activation, the structure prope...To investigate the influence of expansion pretreatment for materials on carbon structure, activated carbons （ACs） were prepared from corncob with/without expansion pretreatment by KOH activation, the structure properties of which were determined based on N2 adsorption isotherm at 77 K. The results show that the expansion pretreatment for corncobs is beneficial to the preparation of ACs with high surface area. The specific surface area of the AC derived from corncob with expansion pretreatment （AC-1） is 32.5% larger than that without expansion pretreatment （AC-2）. Furthermore, to probe the potential application of corncob-based ACs in electric double-layer capacitor （EDLC）, the prepared ACs were used as electrode materials to assemble EDLC, and its electrochemical performance was investi- gated. The results indicate that the specific capacitance of AC-I is 276 F/g at 50 mA/g, which increases by 27% com- pared with that of AC-2 （217 F/g）. As electrode materials, AC-1 presents a better electrochemical performance than AC-2, including a higher voltage maintenance ratio and a lower leakage current.展开更多
Gold nanoparticles (GNs) are prepared through in situ reduction using NaBH4 in the presence of homopolymer PDMAEMA. The sizes of the GNs can be adjusted by alternating the molar ratio of gold to DMAEMA. Pure PDMAEMA a...Gold nanoparticles (GNs) are prepared through in situ reduction using NaBH4 in the presence of homopolymer PDMAEMA. The sizes of the GNs can be adjusted by alternating the molar ratio of gold to DMAEMA. Pure PDMAEMA aqueous solution shows a phase-transition at 50°C at pH 10 and 25°C at pH 14, while PDMAEMA-supported GNs aqueous solution shows a phase-transition at 47°C at pH 10 because of the increasing hydrophobic property resulting from GNs. Due to the pH and temperature-responsible characteristics of PDMAEMA, the resulting PDMAEMA-supported GNs exhibit pH adjustable temperature-responsive characteristics in optic and catalytic aspects. Under an acidic condition (pH 2), the GNs show unchanged surface Plasmon absorbance with a peak of 518 nm in a temperature range from 20 to 65°C. Under a basic condition (pH 10), the GNs first show the same absorbance with a peak at 518 nm in a temperature range from 20 to 40°C, and then the absorbance red shifts from 518 to 545 nm as temperature increases from 40 to 65°C. When the GNs are used as catalysts to catalyze the reduction of p-nitrophenol, the catalytic activity can be adjusted by changing the permeation of reactants in the PDMAEMA layer at low and high temperatures, respectively.展开更多
Lithium-ion capacitors(LICs) were fabricated using mesocarbon microbeads(MCMB) as a negative electrode and a mixture of activated carbon(AC) and LiFePO4 as a positive electrode(abbreviated as LAC).The phase structure ...Lithium-ion capacitors(LICs) were fabricated using mesocarbon microbeads(MCMB) as a negative electrode and a mixture of activated carbon(AC) and LiFePO4 as a positive electrode(abbreviated as LAC).The phase structure and morphology of LAC samples were characterized by X-ray diffraction(XRD) and field emission scanning electron microscopy(FESEM).The electrochemical performance of the LICs was studied using cyclic voltammetry,charge-discharge rate measurements,and cycle performance testing.A LIC with 30 wt% LiFePO4 was found to have the best electrochemical performance with a specific energy density of 69.02 W h kg-1 remaining at 4 C rate after 100 cycles.Compared with an AC-only positive electrode system,the ratio of practical capacity to theoretical calculated capacity of the LICs was enhanced from 42.22% to 56.59%.It was proved that adding LiFePO4 to AC electrodes not only increased the capacity of the positive electrode,but also improved the electrochemical performances of the whole LICs via Li+ pre-doping.展开更多
基金Supported by the Natural Science Foundation of Tianjin（Nos.06TXTJJC14400, 07JCYBJC15900） and Young Teacher Foun-dation of Tianjin Polytechnic University （No.029624）.
文摘A DNA fluorescence probe system based on fluorescence resonance energy transfer （FRET） from CdTe quantum dot （QD） donors to Au nanoparticle （AuNP） acceptors is presented. CdTe QDs, 2.5nm in diameter, as energy donors, were prepared in water. Au nanoparticles, 16nm in diameter, as energy acceptors, were prepared from gold chloride by reduction. CdTe QDs were linked to 5＇-NH2-DNA through 1-ethyl-3-（dimethylaminopropyl）car- bodiimide hydrochloride （EDC） as a linker, and the 3＇-SH-DNA was self-assembled onto the surface of AuNPs. The hybridization of complementary double stranded DNA （dsDNA） bound to the QDs and AuNPs （CdTe-dsDNA-Au） determined the FRET distance of CdTe QDs and Au nanoparticles. Compared to the fluorescence of CdTe-DNA, the fluorescence of CdTe-DNA-Au conjugates decreased extremely, which indicated that the FRET occurred between CdTe QDs and Au nanoparticles. The fluorescence change of this conjugate depended on the ratio of Au-DNA to CdTe-DNA. When the AuNPs-DNA to QD-DNA ratio was 10：1, the FRET efficiency reached a maximum. The probe system would have a certain degree of fluorescence recovery when a complementary single stranded DNA was introduced into this system, which showed that the distance between CdTe QDs and Au nanoparticles was increased.
基金This work was supported by the China Petroleum & Chemical Science and Technology Foundation (No. 205026) the Tianjin Science and Technology Plan Foundation (No. 06TXTJJC14400)
文摘The title compound N,N＇-bis（5,5-dimethyl-2-phospha-2-thio-1,3-dioxan-2-yl） ethylene diamine （DPTDEDA, C12H26N2O4P2S2） was synthesized by the reaction of neopentyl glycol, phosphorus thio-chloride and 1,2-ethylenediamine, and characterized by elemental analysis, IR and ^1H NMR spectra. Its crystal structure was determined by single-crystal X-ray diffraction analysis and the thermal property was analyzed by TG analysis. The crystal structure belongs to monoclinic, space group P21/c, with a = 14.557（16）, b = 11.299（12）, c = 12.163（13）A,β = 98.707（19）^o, Dc = 1.305 g/cm^3, Z = 4, γ = 0.71073A,μ（MoKa） = 0.447 mm^-1, Mr = 388.41, V = 1977（4）A3, F（000） = 824, S = 1.107, the final R = 0.0478 and wR = 0.0810 for 1738 observed reflections （I 〉 2σ（I））. X-ray analysis reveals that the crystal structure is centrosymmetrically distributed through 1,2-ethylenediamine to join two distorted six-membered rings. The weak N-H…S interactions are observed and link the molecules into sheets. TG analysis shows that the title compound has good thermal stability and char-forming capability, which are required for an excellent intumescent fire retardant.
基金Fujian Province I mportant Science and Technology Development Fund,China (No.2005Z17)
文摘In this study,the sol-gel method was introduced to prepare the composite phase change material (CPCM). The CPCM was added to fabric with coating techniques and the thermal activity of modified fabric was studied. In addition,the thermal property and the microstructure of CPCM were also discussed in detail by means of polarization microscope and differential scanning calorimeter,respectively. According to the analysis of main influencial factors of the property of CPCM,the optimal preparing technique was determined. It was proved that CPCM could exhibit a good thermal property while phase transformation process took place,and a better appearance of the fabric modified with CPCM could be obtained due to the fact that in a warm circumstance,the liquid-state phase change material could be firmly enwrapped and embedded in the three-dimensional network all the time during the phase transformation. Besides,the fabric treated with CPCM had a high phase-transition enthalpy and an appropriate phase-transition temperature. As a result,a desirable temperature-adjustable function appeared.
基金Supported by the National Natural Science Foundation of China(No.21271138)the Natural Science Foundation of Tianjin City, China(No.10JCZDJC21500)
文摘Fe2O3/active carbon（Fe2O3/AC） nanocomposites were readily fabricated by pyrolyzing Fe3＋ impregnated active carbon in a nitrogen atmosphere. The as-prepared composites were studied by X-ray powder diffraction（XRD）, X-ray photoelectron spectroscopy（XPS） and transmission electron microscopy（TEM）. The capacitive property of the composites was investigated by cyclic voltammetry（CV） and galvanostatic charge-discharge test. Physical characterizations show that the γ-Fe2O3 fine grains dispersed in the AC well, with a mean size of 21.24 nm. Electrochemical tests in 6 mol/L KOH solutions indicate that the as-prepared nanocomposites exhibited improved capacitive properties. The specific capacitance（SC） of Fe2O3/AC nanocomposites was up to 188.4 F/g that was derived from both electrochemical double-layer capacitance and pseudo-capacitance, which was 78% larger than that of pristine AC. A symmetric capacitor with Fe2O3/AC nanocomposites as electrode showed an excellent cycling stability. The SC was only reduced by a factor of 9.2% after 2000 cycles at a current density of 1 A/g.
基金financially supported by the National Natural Science Foundation of China(No.21074127)
文摘A facile, safe and economical reducing agent, sodium hypophosphite（Na H2PO2·H2O）, has been successfully employed for ambient temperature living radical copolymerization of styrene（St） and methyl methacrylate（MMA）. Such effective reducing agent significantly improved the reactivity of low reactive St monomers during the copolymerization, where the reactivity ratios of St and MMA were determined to be 0.50 and 0.36 by Finemann-Ross method. Thus the copolymerizations proceeded fast and showed typical living/controlled features, as evidenced by pseudo first-order kinetics of polymerization, linear increase in molecular weight versus monomer conversion, and low polydispersity index values. Effects of the concentration of reducing agent and the monomer feed ratio on the copolymerization were investigated in detail. Furthermore, gel permeation chromatography and 1H-NMR analyses as well as chain extension experiments confirmed the high chain-end functionality of the resultant copolymer.
基金the Development Programof Science &Technology of Tianjin ,China (06TXTJJC14400)
文摘We synthesized a series of rare earth complexes with benzoic acid ramification containing different substitute groups or the same substitute group in different position; test the fluorescence property using fluorescence spectrometer of the complexes, and discussed the influence of different substitute group and the position of substitute group on the fluorescent properties of the rare earth complexes. The results showed that different substitute group and the position of substitute group on the benzene ring had important influence on the fluorescent properties of the benzoic acid rare earth complexes, when the other conditions were the same. The fluorescence effect of para-position ligand was better than ortho-position and meta-position ligand. For the benzoic acid complexes, their fluorescence intensity has relationship with the excellent absorption coefficient of the ligand and the high efficient ligand-to-trivalent rare earth ion energy transfer. Furthermore, when the ratio of Ln3+, ligand, phen was 1∶3∶1, the fluorescence properties of rare earth complex was the best.
基金Supported by the National Natural Science Foundation of China(Nos.20771030,20671025)
文摘A novel layered oxouranium phosphite open-structure [（C10H24N2）（H2O）][（UO2）2（HPO3）3]（denoted as TJPU-8,TJPU=Tianjin Polytechnic University） was hydrothermally synthesized with isophorondiamine（IPDA） as the template.Single crystal structure refinement disclosed that TJPU-8 crystallized in the monoclinic space group P21c with cell parameters a=1.8346（9） nm,b=0.6734（1） nm,c=2.0639（0） nm,β=114.61（5）°,V=2.3182（8） nm3,Z=2.TJPU-8 was constructed by UO7 monomer,U2O12 dimer and HPO3 groups.The monomeric UO7 or dimeric U2O12 was connected by HPO3 groups to form two types of 4-ring chains.An undulating sheet was then generated by connecting these two types of chains via HPO3 bridges.The layer structure formed by stacking the sheets along the a direction via the strong H-bonds of organoamine cations and water molecules intercalated in the interlayer spaces with the framework oxygen atoms.Although a mixture of cis-and trans-IPDA was used,only cis-IPDA served as the template.A typical green light emission of TJPU-8 is observed when excited by 266 nm laser.
文摘A concept of potential crosslinking agent was introduced into the synthesizing process of highly oil-absorptive resin that is traditionally prepared by single chemical crosslinking.The resin was heated after manufactured to obtain three-dimension network structure.The effects of potential crosslinking agent and the crosslinking conditions on the absorptive properties of resin were studied.The results showed that hydroxyl ethylacrylate got satisfied results,and the resin with it had good oil absorbency and oil retention.
基金the China Petroleum&Chemical Science and Technology Foundation(No.205026)the Tianjin Science andTechnology Plan Foundation,China(No.06TXTJJC14400).
文摘The non-isothermal degradation kinetics of N,N＇-di（diethoxythiophosphoryl）-1,4-phenylenediamine in N2 was studied by TG-DTG techniques.The kinetic parameters,including the activation energy and pre-exponential factor of the degradation process for the title compound were calculated by means of the Kissinger and Flynn-Wall-Ozawa（FWO）method and the thermal degradation mechanism of the title compound was also studied with the Satava-Sestak methods.The results indicate that the activation energy and pre-exponential factor are 152.61 kJ/mol and 9.06×101 4s -1with the Kissinger method and 154.08 kJ/mol with the Flynn-Wall-Ozawa method,respectively.It has been shown that the degradation of the title compound follows a kinetic model of one-dimensional diffusion or parabolic law,the kinetic function is G（α）=α2and the reaction order is n=2.
基金Science and Technical Development Foundation of Colleges and Universities,Tianjin,China(No.20050511)Development Program of Science & Technology of Tianjin,China(No.06TXTJJC14400)Key Item of TianjinPolytechnic University(No.20060526)
文摘The microenapsulated polyethylene glycol （PEG） with different molecular weight by a fluidized coating method has been prepared and the crystallization behaviors of PEG particles in three-dimensional confined vohume were investigated by using differential scanning calorimetry （DSC） measurement. The results showed that the width of the crystallization peak of PEG increases and its height gradually diminishes in case that the PEG particles are microencapsulated. Compared with the non-microencapsulated PEG particles, the proportion of the first crystallization peak of microencapsulated PEG particle increases, and that of the second one decreases. The reason for the difference maybe is that the crystallization process of microencapsulated PEG particles is uniform and the crystallization ends when the spherulites touch the wall, thus the opportunity of producing the second crystallization peak was relatively reduced.
文摘Poly(ethylene terephthalate) (PET)/carbon black (CB) masterbatch was prepared by melt blending using a separate feeding technique and its homogeneous dispersion morphology was confirmed by transmission electron microscope (TEM). The Avrami and Hoffman-Lauritzen secondary nucleation theories were employed to analyze the effect of high CB content on crystallization kinetics of PET, providing theoretical support for the development of masterbatch with high content of functional components. The Avrami exponents,average values of n,for PET and PET/CB masterbatch are both greater than 3, which indicates three-dimensional growth of crystals. In addition,no significant evidence for regime transition of PET is found applying Hoffman-Lauritzen secondary nucleation theory,though such observations have been reported previously in the literature. Furthermore,appropriate U* value for PET is determined to be 12 800 J/mol. For PET/CB masterbatch,a transition from regime I to regime II around 225℃ is observed with appropriate U* value (12 800 J/mol) . This phenomenon is consistent with a transition point in plot of G versus Tc . The fold surface free energy σe (100. 3 mJ/m 2) of PET is much greater than that of PET/CB masterbatch (48. 3 mJ/m 2) ,which indicates heterogeneous nucleation effect of CB particles.
基金the Development Programof Science &Technology of Tianjin (06TXTJJC14400)
文摘A novel polymeric reaction monomer (NPRM) for preparing highly fluorescent rare earth polymer materials was synthesized via interface and coordinating reaction. The composition and structure of the NPRM and intermediate product (ligand) were characterized through the Fourier transform infrared spectroscopy (FT-IR), carbon-nuclear magnetic resonance spectrum (13CNMR), Mass spectra (MS), and element analysis data. The results showed that the composition and structure of NPRM agreed with that of anticipated product. The NPRM was composed of two important sections. Section 1 was able to provide excellent fluorescent properties for final rare earth polymer material through the effect energy transfer between ligand and rare earth ion; Section 2 would endow with the NPRM excellent polymeric active and form highly fluorescent rare earth polymer material. Fluorescent properties of the NPRM were also researched via a CARY ECLIPSE fluorescent spectrometer. The results showed that the NPRM possessed excellent luminescent properties. The corresponding emission peaks based on the 5D0→7F1(601.6 nm), 5D0→7F2(625.0 nm), 5D0→7F3(660.5 nm) and 5D0→7F4(706.3 nm) transitions for Eu3+ were observed. The strongest emission peak was at 625 nm, which belonged to 5D0→7F2 transition.
基金National Natural Science Foundation of China (No. 50902102 and No. 51172160)
文摘To investigate the influence of expansion pretreatment for materials on carbon structure, activated carbons （ACs） were prepared from corncob with/without expansion pretreatment by KOH activation, the structure properties of which were determined based on N2 adsorption isotherm at 77 K. The results show that the expansion pretreatment for corncobs is beneficial to the preparation of ACs with high surface area. The specific surface area of the AC derived from corncob with expansion pretreatment （AC-1） is 32.5% larger than that without expansion pretreatment （AC-2）. Furthermore, to probe the potential application of corncob-based ACs in electric double-layer capacitor （EDLC）, the prepared ACs were used as electrode materials to assemble EDLC, and its electrochemical performance was investi- gated. The results indicate that the specific capacitance of AC-I is 276 F/g at 50 mA/g, which increases by 27% com- pared with that of AC-2 （217 F/g）. As electrode materials, AC-1 presents a better electrochemical performance than AC-2, including a higher voltage maintenance ratio and a lower leakage current.
基金Supported by the National Natural Science Foundation of China (Grant No. 20774051)Program for New Century Excellent Talents in Universitiesthe Outstanding Youth Fund (Grant No. 50625310)
文摘Gold nanoparticles (GNs) are prepared through in situ reduction using NaBH4 in the presence of homopolymer PDMAEMA. The sizes of the GNs can be adjusted by alternating the molar ratio of gold to DMAEMA. Pure PDMAEMA aqueous solution shows a phase-transition at 50°C at pH 10 and 25°C at pH 14, while PDMAEMA-supported GNs aqueous solution shows a phase-transition at 47°C at pH 10 because of the increasing hydrophobic property resulting from GNs. Due to the pH and temperature-responsible characteristics of PDMAEMA, the resulting PDMAEMA-supported GNs exhibit pH adjustable temperature-responsive characteristics in optic and catalytic aspects. Under an acidic condition (pH 2), the GNs show unchanged surface Plasmon absorbance with a peak of 518 nm in a temperature range from 20 to 65°C. Under a basic condition (pH 10), the GNs first show the same absorbance with a peak at 518 nm in a temperature range from 20 to 40°C, and then the absorbance red shifts from 518 to 545 nm as temperature increases from 40 to 65°C. When the GNs are used as catalysts to catalyze the reduction of p-nitrophenol, the catalytic activity can be adjusted by changing the permeation of reactants in the PDMAEMA layer at low and high temperatures, respectively.
基金supported by the National Natural Science Foundation of China (51172160,50902102)the National High Technology Research and Development Program of China (2011AA11A232)the National Basic Research Program of China (2012CB720302)
文摘Lithium-ion capacitors(LICs) were fabricated using mesocarbon microbeads(MCMB) as a negative electrode and a mixture of activated carbon(AC) and LiFePO4 as a positive electrode(abbreviated as LAC).The phase structure and morphology of LAC samples were characterized by X-ray diffraction(XRD) and field emission scanning electron microscopy(FESEM).The electrochemical performance of the LICs was studied using cyclic voltammetry,charge-discharge rate measurements,and cycle performance testing.A LIC with 30 wt% LiFePO4 was found to have the best electrochemical performance with a specific energy density of 69.02 W h kg-1 remaining at 4 C rate after 100 cycles.Compared with an AC-only positive electrode system,the ratio of practical capacity to theoretical calculated capacity of the LICs was enhanced from 42.22% to 56.59%.It was proved that adding LiFePO4 to AC electrodes not only increased the capacity of the positive electrode,but also improved the electrochemical performances of the whole LICs via Li+ pre-doping.
