Hydrogel-Ⅰ was fabricated via sodium alginate in situ-embedding with MAL powders and then applied to decontaminating Pb(Ⅱ) from water. Conditions for preparing Hydrogel-Ⅰ and the adsorption of Pb(Ⅱ) over Hydrogel-...Hydrogel-Ⅰ was fabricated via sodium alginate in situ-embedding with MAL powders and then applied to decontaminating Pb(Ⅱ) from water. Conditions for preparing Hydrogel-Ⅰ and the adsorption of Pb(Ⅱ) over Hydrogel-I were optimized through response surface methodology coupled with central composite design. XPS revealed that the groups of —OH, —COO—, —NH, —NHand —CSS— carried by Hydrogel-Ⅰ were responsible for the uptake of Pb(Ⅱ). Ions exchange, surface complexation, electrostatic attraction and pore-filling effect contributed to the adsorption process. Adsorption performances of Pb(Ⅱ) by Hydrogel-Ⅰ and MAL powders were compared. Although they exhibited similar adsorption rate and maximum adsorption capacity(qm), the reusing ability of Hydrogel-Ⅰ was better and it was easier to be separated from aqueous solution after treatment. Even compared with organic hydrogel materials,Hydrogel-Ⅰ presented relatively quick adsorption speed and high adsorption capacity. It can be concluded that Hydrogel-Ⅰ could be an alternative scavenger for the treatment of Pb(Ⅱ) from aqueous solution.展开更多
The CaCu3Ti4O12 xerogels, powders and ceramics were prepared through the sol-gel method using two kinds of organic acid （decanoic acid and decanedioic acid）. The xerogels, powders and ceramics were characterized by ...The CaCu3Ti4O12 xerogels, powders and ceramics were prepared through the sol-gel method using two kinds of organic acid （decanoic acid and decanedioic acid）. The xerogels, powders and ceramics were characterized by the methods of TG-DTG, FT-IR, XRD, SEM and TEM. The dielectric properties of the ceramics were also measured. The results indicated that the powders calcined at 850 ℃ for 2 h are both nanometer scale particles. After sintering, the ceramics mainly consist of the CaCu3Ti4O12 phase. Compared with the powders prepared using monoacid, the particle size of the powders prepared using diacid obviously increases, and the grain size, the relative density and the whole permittivity of the ceramics increase as well. Specially, the ceramic prepared using decanedioic acid has higher relative density （97.3%）, dielectric constant （316 808） and lower dielectric loss （0.242 5） at 30 ℃ （10 kIaz）展开更多
Nano size nickel copper ferrite powders （NiCuFe204） and nickel copper zinc ferrite powders have been prepared by a citrate gel precursor method. The resulting powders were characterized by X-ray diffraction （XRD） ...Nano size nickel copper ferrite powders （NiCuFe204） and nickel copper zinc ferrite powders have been prepared by a citrate gel precursor method. The resulting powders were characterized by X-ray diffraction （XRD） and scanning electron microscope （SEM）. The results showed that nickel copper ferrites and nickel copper zinc ferrites were also in the nanosaele. The NiCu ferrite powders showed extensive XRD fine broadening and sizes of crystals were calculated （from the XRD line broadening） as 26 run-44 run over the temperature range is 200-800℃. The NiCuZn ferrite powders showed XRD line broadening and sizes of of crystals were calculated 46-65 nm over 200-800℃.展开更多
A novel sol-gel processing was developed to synthesize polycrystalline cerium-doped lutetium pyrosilicate （Lu2Si2O7Ce, LPS ：Ce） powders under low temperature. It was found that the addition of propylene oxide （PPO...A novel sol-gel processing was developed to synthesize polycrystalline cerium-doped lutetium pyrosilicate （Lu2Si2O7Ce, LPS ：Ce） powders under low temperature. It was found that the addition of propylene oxide （PPO） could promote the formation of Lu-O-Si bonds in precursor, which was beneficial to the formation of LPS phase. X-ray diffraction （XRD） patterns indicated that the single-phased LPS powder was well crystallized at 1050℃. Microstructure observation demonstrated that the synthetic LPS powder was composed of ellipsoidal grains with the mean size of 40 nm. The luminescent properties were characterized by photoluminescence （PL）, X-ray excited luminescence （XEL） and vacuum ultraviolet （VUV） spectroscopy at room temperature. The synthetic LPS：Ce powder emitted a broad emission spectrum centered at about 380 nm, which should be ascribed to the 5d→4f transition of Ce3＋. Decay time of the synthetic LPS：Ce powder was measured to be only 32 ns.展开更多
基金funded by the National Key Research and Development Project (No.2019YFC1804800)Key R&D Program of Shaanxi Province,China (No.2019SF-253)+3 种基金the Fundamental Research Funds for the Central Universities,China (No.300102291504)the Pearl River S&T Nova Program of Guangzhou,China (No.201710010065)the Science and Technology Program of Guangdong Forestry Administration,China (No.2020-KYXM-08)the Key Laboratory of Resource Chemistry,Ministry of Education,China (No.KLRC_ME2102)。
文摘Hydrogel-Ⅰ was fabricated via sodium alginate in situ-embedding with MAL powders and then applied to decontaminating Pb(Ⅱ) from water. Conditions for preparing Hydrogel-Ⅰ and the adsorption of Pb(Ⅱ) over Hydrogel-I were optimized through response surface methodology coupled with central composite design. XPS revealed that the groups of —OH, —COO—, —NH, —NHand —CSS— carried by Hydrogel-Ⅰ were responsible for the uptake of Pb(Ⅱ). Ions exchange, surface complexation, electrostatic attraction and pore-filling effect contributed to the adsorption process. Adsorption performances of Pb(Ⅱ) by Hydrogel-Ⅰ and MAL powders were compared. Although they exhibited similar adsorption rate and maximum adsorption capacity(qm), the reusing ability of Hydrogel-Ⅰ was better and it was easier to be separated from aqueous solution after treatment. Even compared with organic hydrogel materials,Hydrogel-Ⅰ presented relatively quick adsorption speed and high adsorption capacity. It can be concluded that Hydrogel-Ⅰ could be an alternative scavenger for the treatment of Pb(Ⅱ) from aqueous solution.
基金Projects(CC20120031,CC20110048)supported by Changzhou Science and Technology Innovation Project,China
文摘The CaCu3Ti4O12 xerogels, powders and ceramics were prepared through the sol-gel method using two kinds of organic acid （decanoic acid and decanedioic acid）. The xerogels, powders and ceramics were characterized by the methods of TG-DTG, FT-IR, XRD, SEM and TEM. The dielectric properties of the ceramics were also measured. The results indicated that the powders calcined at 850 ℃ for 2 h are both nanometer scale particles. After sintering, the ceramics mainly consist of the CaCu3Ti4O12 phase. Compared with the powders prepared using monoacid, the particle size of the powders prepared using diacid obviously increases, and the grain size, the relative density and the whole permittivity of the ceramics increase as well. Specially, the ceramic prepared using decanedioic acid has higher relative density （97.3%）, dielectric constant （316 808） and lower dielectric loss （0.242 5） at 30 ℃ （10 kIaz）
文摘Nano size nickel copper ferrite powders （NiCuFe204） and nickel copper zinc ferrite powders have been prepared by a citrate gel precursor method. The resulting powders were characterized by X-ray diffraction （XRD） and scanning electron microscope （SEM）. The results showed that nickel copper ferrites and nickel copper zinc ferrites were also in the nanosaele. The NiCu ferrite powders showed extensive XRD fine broadening and sizes of crystals were calculated （from the XRD line broadening） as 26 run-44 run over the temperature range is 200-800℃. The NiCuZn ferrite powders showed XRD line broadening and sizes of of crystals were calculated 46-65 nm over 200-800℃.
基金supported by the National Natural Science Foundation of China(Grant No.51172139)
文摘A novel sol-gel processing was developed to synthesize polycrystalline cerium-doped lutetium pyrosilicate （Lu2Si2O7Ce, LPS ：Ce） powders under low temperature. It was found that the addition of propylene oxide （PPO） could promote the formation of Lu-O-Si bonds in precursor, which was beneficial to the formation of LPS phase. X-ray diffraction （XRD） patterns indicated that the single-phased LPS powder was well crystallized at 1050℃. Microstructure observation demonstrated that the synthetic LPS powder was composed of ellipsoidal grains with the mean size of 40 nm. The luminescent properties were characterized by photoluminescence （PL）, X-ray excited luminescence （XEL） and vacuum ultraviolet （VUV） spectroscopy at room temperature. The synthetic LPS：Ce powder emitted a broad emission spectrum centered at about 380 nm, which should be ascribed to the 5d→4f transition of Ce3＋. Decay time of the synthetic LPS：Ce powder was measured to be only 32 ns.
