In order to reduce the amount of volumetric shrinkage that occurs in dental composites as a result of curing,a new kind of dental matrix resin combining bisphenol-S-bis（3-meth acry late-2-hydroxy propyl）ether（BisS-...In order to reduce the amount of volumetric shrinkage that occurs in dental composites as a result of curing,a new kind of dental matrix resin combining bisphenol-S-bis（3-meth acry late-2-hydroxy propyl）ether（BisS-GMA） with the expanding monomer unsaturated spiro orthoesters 2-methylene-1,4,6-trispiro[4,4] nonane （SOE） was prepared,with triethylene glycol dimethacrylate （TEGDMA） as diluent.CQ （camphorquinone） of 1wt% and DMAEMA （2-（dimethylamino） ethyl meth acrylate） of 2wt% were used as photoinitiation system to initiate the copolymerization of the matrix resins.The performance including volumetric shrinkage,degree of conversion and condition of the ring-opening reaction of SOE,as well as curing time and the tensile bond strength were investigated respectively by the dilatometer,Fourier transfer infrared,the universal testing machine,and so on.The ring-opening polymerization of SOE occurred.Meanwhile,the obtain copolymers were crosslinked.The matrix resin containing BisS-GMA and SOE showed a reduced amount of volumetric shrinkage at 1.52%,which is a promising strategy for obtaining a polymer with a low amount of volumetric shrinkage.Furthermore,the other properties were not compromised.展开更多
The purpose of this study was to use. a three-component photoinitiation system comprising 1wt% CQ （camphorquinone）, 2wt% DMAEMA （2-（dimethylamino） ethyl meth acrylate） and 2wt% ph^2I^＋PF6^- （diphenyliodonium h...The purpose of this study was to use. a three-component photoinitiation system comprising 1wt% CQ （camphorquinone）, 2wt% DMAEMA （2-（dimethylamino） ethyl meth acrylate） and 2wt% ph^2I^＋PF6^- （diphenyliodonium hexafluorophosphate） to initiate the copolymerization of the matrix resins which combine bisphenol-S-bis （3-methacrylate-2-hydroxy propyl） ether （BisS-GMA） with the expanding monomer unsaturated spiro orthoesters 2-methylene-l,4,6-tdspiro[4,4] nonane （MTOSN）, for minimizing the volumetric shrinkage that generally occurs during polymerization. It was hypothesized that MTOSN would expand volumetrically during polymerization under the three-component photoinitiator system and further reductions in volumetric shrinkage would be obtained. The performance study which consists of degree of conversion and condition of the ring-opening reactions of MTOSN, volumetric shrinkage and mechanical properties including tensile bond strength, compressive strength and Vicker＇s hardness were carried out respectively by Fourier transfer infrared, the dilatometer and the universal testing machine. The results supported that the dental composites based on the expanding monomer and three-component photoinitiator system engendered a greater decrease of volumetric shrinkage and better mechanieal properties.展开更多
To research the relationship between epoxy and fiber inherent property and mechanical properties of composite,we prepared a series of composites using three kinds of high mechanical performance epoxy resins as matrice...To research the relationship between epoxy and fiber inherent property and mechanical properties of composite,we prepared a series of composites using three kinds of high mechanical performance epoxy resins as matrices and reinforced by the same volume fraction(5%)of short carbon and glass fiber.Their mechanical properties were investigated from the perspective of chemical structure and volume shrinkage ratio of epoxy.We analyzed their tensile strength and modulus based on the mixing rule and Halpin-Tsai equation,respectively,and studied the morphology of impact test samples by scanning electron microscope.The results show that chemical bonds formed between matrix and fiber are the most important factor to improve the mechanical properties of composite.High volume shrinkage ratio is also helpful when the fiber surface was coarse.Otherwise,the tensile strength is more sensitive to interface than the tensile modulus.It is concluded that the mechanical properties of composite are strongly affected by the chemical structure of epoxy resin,the volume shrinkage ratio of cured matrices,and properties of fiber surface.展开更多
The boron content of uranium fuel samples with boron concentrations in the range of 0.05–10 μg/g was determined using inductively coupled plasma optical emission spectrometry(ICP-OES) after the uranium was separated...The boron content of uranium fuel samples with boron concentrations in the range of 0.05–10 μg/g was determined using inductively coupled plasma optical emission spectrometry(ICP-OES) after the uranium was separated by cation exchange. The samples were dissolved in 3 M HNO_3 on a hot plate at 150℃ and evaporated to near dryness. The residues were redissolved in 0.2 M HNO-_3 and passed through a column loaded with Dowex 50WX8-400 resin. Uranium was adsorbed on the resin,while boron was easily eluted with 0.2 M HNO_3. The boron content of the effluent was determined using ICPOES. Several strategies were employed to improve the reliability of the experimentally determined boron content.The addition of mannitol and proper control of the evaporation process were shown to be effective in preventing boron loss during sample dissolution and evaporation. The memory effect was eliminated by flushing the system with 1.5% ammonia for 30 s between successive sample runs,and the matrix match method was used to eliminate the matrix effect arising from mannitol during the ICP-OES analysis. The accuracy of the results of the analysis was determined by addition recovery tests and by comparison with the results of three Chinese certified reference materials(GBW04242, GBW04243, and GBW04232). Using the method we developed, the limit of detection for boron was as low as 0.05 μg/g in uranium fuel samples, and the relative standard deviations for 0.1–0.5 g uranium samples with 0.05–2 μg/g of boron were within 9%.展开更多
基金Funded by the National Natural Science Foundation of China(No.50673065)
文摘In order to reduce the amount of volumetric shrinkage that occurs in dental composites as a result of curing,a new kind of dental matrix resin combining bisphenol-S-bis（3-meth acry late-2-hydroxy propyl）ether（BisS-GMA） with the expanding monomer unsaturated spiro orthoesters 2-methylene-1,4,6-trispiro[4,4] nonane （SOE） was prepared,with triethylene glycol dimethacrylate （TEGDMA） as diluent.CQ （camphorquinone） of 1wt% and DMAEMA （2-（dimethylamino） ethyl meth acrylate） of 2wt% were used as photoinitiation system to initiate the copolymerization of the matrix resins.The performance including volumetric shrinkage,degree of conversion and condition of the ring-opening reaction of SOE,as well as curing time and the tensile bond strength were investigated respectively by the dilatometer,Fourier transfer infrared,the universal testing machine,and so on.The ring-opening polymerization of SOE occurred.Meanwhile,the obtain copolymers were crosslinked.The matrix resin containing BisS-GMA and SOE showed a reduced amount of volumetric shrinkage at 1.52%,which is a promising strategy for obtaining a polymer with a low amount of volumetric shrinkage.Furthermore,the other properties were not compromised.
基金Funded by the National Natural Science Foundation of China(No.50673065)
文摘The purpose of this study was to use. a three-component photoinitiation system comprising 1wt% CQ （camphorquinone）, 2wt% DMAEMA （2-（dimethylamino） ethyl meth acrylate） and 2wt% ph^2I^＋PF6^- （diphenyliodonium hexafluorophosphate） to initiate the copolymerization of the matrix resins which combine bisphenol-S-bis （3-methacrylate-2-hydroxy propyl） ether （BisS-GMA） with the expanding monomer unsaturated spiro orthoesters 2-methylene-l,4,6-tdspiro[4,4] nonane （MTOSN）, for minimizing the volumetric shrinkage that generally occurs during polymerization. It was hypothesized that MTOSN would expand volumetrically during polymerization under the three-component photoinitiator system and further reductions in volumetric shrinkage would be obtained. The performance study which consists of degree of conversion and condition of the ring-opening reactions of MTOSN, volumetric shrinkage and mechanical properties including tensile bond strength, compressive strength and Vicker＇s hardness were carried out respectively by Fourier transfer infrared, the dilatometer and the universal testing machine. The results supported that the dental composites based on the expanding monomer and three-component photoinitiator system engendered a greater decrease of volumetric shrinkage and better mechanieal properties.
文摘碳纤维混杂增强复合材料由于具有重量轻、可设计性强等诸多优点,广泛用于汽车、海洋、航空航天等行业.根据固化剂与环氧树脂的配比化学原理,计算出石墨烯-碳纤维混杂增强树脂基(GO-CF/EP)复合材料的最佳配比为1∶5,并采用真空浸渗热压成型工艺(VIHPS)制备1∶2~1∶7共六个配比的试样,结合形状记忆性能测试及微观形貌的观察,得到固化剂与环氧树脂实际最佳配比.实验结果表明,GO-CF/EP复合材料性能主要取决于体系中交联度的大小,交联度越大,复合材料的形状记忆性能越好,微观组织形貌也较理想.当基体配比为1∶5时,GO-CF/EP复合材料体系中交联度最大,微观形貌呈现均匀致密的状态,形状固定率最大,为95.90%;形状回复率最大,为95.40%;形状回复时间最短,为80.30 s;形状回复力最大,为9.48 N.当基体配比为1∶2或1∶7时,固化剂过量或不足,交联度较小,微观组织形貌中有大量的基体聚集区,其形状记忆性能下降,形状固定率及回复率也相应减小,分别为82.99%,81.66%,81.91%,78.75%;形状回复力分别只有5.20 N和5.50 N.
文摘To research the relationship between epoxy and fiber inherent property and mechanical properties of composite,we prepared a series of composites using three kinds of high mechanical performance epoxy resins as matrices and reinforced by the same volume fraction(5%)of short carbon and glass fiber.Their mechanical properties were investigated from the perspective of chemical structure and volume shrinkage ratio of epoxy.We analyzed their tensile strength and modulus based on the mixing rule and Halpin-Tsai equation,respectively,and studied the morphology of impact test samples by scanning electron microscope.The results show that chemical bonds formed between matrix and fiber are the most important factor to improve the mechanical properties of composite.High volume shrinkage ratio is also helpful when the fiber surface was coarse.Otherwise,the tensile strength is more sensitive to interface than the tensile modulus.It is concluded that the mechanical properties of composite are strongly affected by the chemical structure of epoxy resin,the volume shrinkage ratio of cured matrices,and properties of fiber surface.
文摘The boron content of uranium fuel samples with boron concentrations in the range of 0.05–10 μg/g was determined using inductively coupled plasma optical emission spectrometry(ICP-OES) after the uranium was separated by cation exchange. The samples were dissolved in 3 M HNO_3 on a hot plate at 150℃ and evaporated to near dryness. The residues were redissolved in 0.2 M HNO-_3 and passed through a column loaded with Dowex 50WX8-400 resin. Uranium was adsorbed on the resin,while boron was easily eluted with 0.2 M HNO_3. The boron content of the effluent was determined using ICPOES. Several strategies were employed to improve the reliability of the experimentally determined boron content.The addition of mannitol and proper control of the evaporation process were shown to be effective in preventing boron loss during sample dissolution and evaporation. The memory effect was eliminated by flushing the system with 1.5% ammonia for 30 s between successive sample runs,and the matrix match method was used to eliminate the matrix effect arising from mannitol during the ICP-OES analysis. The accuracy of the results of the analysis was determined by addition recovery tests and by comparison with the results of three Chinese certified reference materials(GBW04242, GBW04243, and GBW04232). Using the method we developed, the limit of detection for boron was as low as 0.05 μg/g in uranium fuel samples, and the relative standard deviations for 0.1–0.5 g uranium samples with 0.05–2 μg/g of boron were within 9%.
