A distinctive feature of phosphates is their special and significant ability to form inorganic polymeric compounds---condensed phosphates, which are destined to play a considerable role in our ＂high-tech＂ society in...A distinctive feature of phosphates is their special and significant ability to form inorganic polymeric compounds---condensed phosphates, which are destined to play a considerable role in our ＂high-tech＂ society in the future. Numerous olygophosphates, polyphosphates, double condensed phosphates and cyclophosphates with diverse formula, such as double tetra-, octa- and dodecaphosphates were obtained and described by us last years. The offered data are the outcomes of our scientific researches： of synthesis, analysis, and estimation of results in correlation with new achievements in inorganic polymer＇s chemistry. Many double condensed compounds, containing monovalent metals are obtained by us during systematic investigation of polycomponent systems, containing mono- and trivalent metals at temperature range 100-600 ~C. Synthesised condensed phosphates, in fact--inorganic polymers were examined in detail by chemical and thermogravimetric analysis, most compounds were examined by paper chromatography and the structures are determined by X-ray structural techniques/diffraction analysis. During our fundamental researches numerous new （about 70） unknown until now condensed phosphates have been obtained. Dependency of composition VS temperature and molar ratio, reliance of structure from duration of synthesis and radius of the ions are revealed.展开更多
Molecular dynamics simulations were carried out to study the configuration energy and radial distribution functions of mmonium dihydrogen phosphate solution at different temperatures. The dihydrogen phosphate ion was ...Molecular dynamics simulations were carried out to study the configuration energy and radial distribution functions of mmonium dihydrogen phosphate solution at different temperatures. The dihydrogen phosphate ion was treated as a seven-site model and the ammonium ion was regarded as a five-site model, while a simple-point-charge model for water molecule. An unusually local particle number density fluctuation was observed in the system at saturation temperature. It can be found that the potential energy increases slowly with the temperature from 373 K to 404 K, which indicates that the ammonium dihydrogen phosphate has partly decomposed. The radial distribution function between the hydrogen atom of ammonium cation and the oxygen atom of dihydrogen phosphate ion at three different temperatures shows obvious difference, which indicates that the average H-bond number changes obviously with the temperature. The temperature has an influence on the combination between hydrogen atoms and phosphorus atoms of dihydrogen phosphate ion and there are much more growth units at saturated solutions.展开更多
A phosphate-mineralization microbe was used to induce barium phosphates precipitation, and the precipitates with different types were obtained under different pH values. The average crystallite size of the barium phos...A phosphate-mineralization microbe was used to induce barium phosphates precipitation, and the precipitates with different types were obtained under different pH values. The average crystallite size of the barium phosphates was calculated by particle size distribution curves, and the size of the products was 33.40, 29. 37, 24. 13, 47.76 and 96. 53 μm when the pH values of the mixed solution are 7, 8, 9, 10 and 11, respectively. The results of X-ray diffraction （XRD） show that the structures of the particles controlled by the mixed solution are mainly BaaPO4 when pH 〈 10; the barium phosphates are synthesized by biological deposition which is the mixture of BaHPO4 and Ba5 （PO4）3OH when pH = 10; when pH = 11, the barium phosphates are also the mixtures, which are Ba5 （PO4）3OH and BaNaPO4. The above results indicate that the phosphate-mineralization microbe can produce a certain enzyme which constantly hydrolyzes phosphate monoester in the mixed solution, and then PO4^3- ions are obtained.展开更多
Construction of elaborate configuration to enhance the intrinsic activity of NiMo-based catalyst candidates holds promise for accelerating the hydrogen evolution reaction(HER)kinetics.Herein,a novel cerium-doped NiMo ...Construction of elaborate configuration to enhance the intrinsic activity of NiMo-based catalyst candidates holds promise for accelerating the hydrogen evolution reaction(HER)kinetics.Herein,a novel cerium-doped NiMo phosphate(labeled as Ce-NiMo(PO_(4))_(0.66))is designed and fabricated via a facile hydrothermal and phosphatization method.A comprehensive characterization reveals that the introduction of the rare metal element cerium with an enriched 4f electronic distribution near the Fermi level modulates the hybridization of the 3d-2p orbitals and optimizes the electronic structure of the NiMo-based phosphate catalysts,which leads to the synergy between the nickel-molybdenum dual sites and the phosphate active unit to synchronously enhance the water dissociation and proton dehydrogenation transfer of the HER process.Consequently,Ce-NiMo(PO_(4))0.66 exhibits excellent alkaline HER performance with overpotentials at 10 and 500 mA·cm^(-2)current densities being only 40 and 295 mV,respectively,and desirable long-term durability at industrial current densities of 500 mA·cm^(-2).An overall hydrazine splitting(OHzS)constructed with Ce-NiMo(PO_(4))_(0.66)as a hydrazine oxidation reaction(HzOR)and HER bifunctional electrocatalyst has been constructed to achieve industrial current densities at the low voltage of 0.92 V,verifying its practical feasibility for sustainable hydrogen production and degradation of hydrazine pollutants.This work highlights that regulating the 3d-2p hybridization state through the inducing 4f orbital electronic state is a feasible means for enhancing the HER activity of transition metal compound catalysts.展开更多
Molecular dynamics simulations were carried out to study the internal energy and microstructure of potassium dihydrogen phosphates （KDP） solution at different temperatures. The water molecule was treated as a simple...Molecular dynamics simulations were carried out to study the internal energy and microstructure of potassium dihydrogen phosphates （KDP） solution at different temperatures. The water molecule was treated as a simple-point-charge model, while a seven-site model for the dihydrogen phosphate ion was adopted. The internal energy functions and the radial distribution functions of the solution were studied in detail. An unusually large local particle number density fluctuation was observed in the system at saturation temperature. It has been found that the specific heat of oversaturated solution is higher than that of unsaturated solution, which indicates the solution experiences a crystallization process below saturation temperature. The radial distribution function between the oxygen atom of water and the hydrogen atom of the dihydrogen phosphate ion shows a very strong hydrogen bond structure. There are strong interactions between potassium cation and oxygen atom of dihydrogen phosphate ion in KDP solution, and much more ion pairs were formed in saturated solution.展开更多
Batch and soil column experiments were conducted to evaluate the influence of KH2PO4, （NH4）H2PO4and Ca（H2PO4）2on the adsorption and leaching characteristics of Cu and Zn in red soil. The results show that all the ...Batch and soil column experiments were conducted to evaluate the influence of KH2PO4, （NH4）H2PO4and Ca（H2PO4）2on the adsorption and leaching characteristics of Cu and Zn in red soil. The results show that all the three phosphates can greatly improve the adsorption capacity of red soil for Cu and Zn, and the effect of different phosphates on Cu and Zn adsorption follows the order of Ca（H2PO4）2〉KH2PO4〉（NH4）H2PO4. The addition of phosphate has little effect on the mobility of Cu. Ca（H2PO4）2and （NH4）H2PO4 show a strong ability in immobilizing Zn while the immobilization ability of KH2PO4 is much weaker. All the three phosphates are helpful for modifying the partitioning of Cu and Zn from the non-residual phase to the residual phase; however, they could also enhance the contents of Cu and Zn associated with exchangeable and carbonates fractions.展开更多
This study fully investigated the vacuum ultraviolet excitation spectra of pure and rare-earth（RE=Eu, Tb and Dy）-doped A2Zr（PO4）2（A=Li, Na and K） phosphors. The synthesized Na and Li compounds were characterized...This study fully investigated the vacuum ultraviolet excitation spectra of pure and rare-earth（RE=Eu, Tb and Dy）-doped A2Zr（PO4）2（A=Li, Na and K） phosphors. The synthesized Na and Li compounds were characterized by XRD showing two new types of phases after indexation. Although these three pure compounds had different crystal structures, they exhibited similar luminescence properties. For Eu3＋-activated samples, the broad excitation band centered at 217 nm could be attributed to the CT transition between O2–（2p6） and Eu3＋ ions. For Tb3＋-doped samples, two groups of f-d transitions were observed, where a strong broad band at 221 nm was due to the spin-allowed f-d transition. Energy transfer from O2– to Dy3＋was not observed in Dy3＋-doped phosphors, probably because it overlapped considerably with the CT transition from O2– to Zr4＋ at 187 nm.展开更多
Single crystals of LaP3O9·3H2O were prepared using a classical method of aqueous chemistry whereas those of the ultraphosphate LaP5O14 were obtained by flux method.Thermal treatment of LaP3O9·3H2O up to 700 ...Single crystals of LaP3O9·3H2O were prepared using a classical method of aqueous chemistry whereas those of the ultraphosphate LaP5O14 were obtained by flux method.Thermal treatment of LaP3O9·3H2O up to 700 °C allowed us to obtain the lanthanum polyphosphate La(PO3)3.The conductivity as well as the vibrational study of the lanthanum ultraphosphate and polyphosphate were analysed in order to explain the mechanism of conduction.Activation energies of 0.45 and 0.84 eV,deduced from the Arrhenius relation,were r...展开更多
This study presents a facile and rapid method for synthesizing novel Layered Double Hydroxide(LDH)nanoflakes,exploring their application as a photocatalyst,and investigating the influence of condensed phosphates'g...This study presents a facile and rapid method for synthesizing novel Layered Double Hydroxide(LDH)nanoflakes,exploring their application as a photocatalyst,and investigating the influence of condensed phosphates'geometric linearity on their photocatalytic properties.Herein,the Mg O film,obtained by plasma electrolysis of AZ31 Mg alloys,was modified by growing an LDH film,which was further functionalized using cyclic sodium hexametaphosphate(CP)and linear sodium tripolyphosphate(LP).CP acted as an enhancer for flake spacing within the LDH structure,while LP changed flake dispersion and orientation.Consequently,CP@LDH demonstrated exceptional efficiency in heterogeneous photocatalysis,effectively degrading organic dyes like Methylene blue(MB),Congo red(CR),and Methyl orange(MO).The unique cyclic structure of CP likely enhances surface reactions and improves the catalyst's interaction with dye molecules.Furthermore,the condensed phosphate structure contributes to a higher surface area and reactivity in CP@LDH,leading to its superior photocatalytic performance compared to LP@LDH.Specifically,LP@LDH demonstrated notable degradation efficiencies of 93.02%,92.89%,and 88.81%for MB,MO,and CR respectively,over a 40 min duration.The highest degradation efficiencies were observed in the case of the CP@LDH sample,reporting 99.99%for MB,98.88%for CR,and 99.70%for MO.This underscores the potential of CP@LDH as a highly effective photocatalyst for organic dye degradation,offering promising prospects for environmental remediation and water detoxification applications.展开更多
Zinc and cerium carried zirconium phosphates （Zn-Ce/ZrPs） were prepared by exchanging zinc and cerium cations into sodium zirconium phosphate （NaZrP） through the ion-exchange method and characterized by X-ray diff...Zinc and cerium carried zirconium phosphates （Zn-Ce/ZrPs） were prepared by exchanging zinc and cerium cations into sodium zirconium phosphate （NaZrP） through the ion-exchange method and characterized by X-ray diffraction（XRD）, energy dispersive X-ray spectroscopy （EDX） and scanning electron microscopy （SEM）. Furthermore, the specific surface area, zeta potential and antibacterial activity were tested. The results showed that Zn-Ce/ZrPs were with hexagonal crystal system, and the surface area of Zn-Ce/ZrPs increased much more than that of NaZrP. Zn-Ce/ZrPs showed obvious synergetic antibacterial effect, and have the potential to be used as antibacterial agents in environmental control.展开更多
In the present study, we investigated the transformed species and the absorptive mechanism of rare earth elements（REEs） in gastrointestinal（GI） tract, using La Cl3 and La Cit as representative compounds. Artificia...In the present study, we investigated the transformed species and the absorptive mechanism of rare earth elements（REEs） in gastrointestinal（GI） tract, using La Cl3 and La Cit as representative compounds. Artificial gastric and intestinal fluids were used to simulate the environment of the digestive tract in vivo. The inductively coupled plasma mass spectrometry（ICP-MS） result showed that more than 99.9% of La Cl3 and La Cit formed precipitation in artificial intestinal fluid, with the average size distribution of 200 nm（2-h incubation） increasing to 600 nm（24-h incubation） determined by dynamic light scattering（DLS）, indicating the aggregation of the particles. The Fourier transform infrared spectroscopy（FTIR） analysis demonstrated that the constituents of these particles were mainly in the form of lanthanum phosphates. To explore the transport mechanism of REEs in GI tract, the mice Peyer＇s patches（PPs） and intestinal epithelium were separated to evaluate the content of lanthanum by ICP-MS following oral administration with 2 or 100 mg/kg/day of La Cit for 7 d. The results showed that the amount of lanthanum phosphate particles absorbed by PPs was significantly greater than that of intestinal epithelium, indicating that lanthanum particles might be phagocytosed mainly by M cells located in the follicle-associated epithelium（FAE） overlying PPs. Furthermore, Caco-2 cell monoculture and Caco-2/Raji B cell coculture models were established to simulate intestinal epithelial cells and FAE, respectively. The result showed that the transport of lanthanum in Caco-2/Raji B coculture model was significantly higher than that in Caco-2 monoculture model（about 60 times higher）, and the level of lanthanum in the basal compartment of Caco-2 monoculture model was very low, supporting that M cells were the main route for lanthanum phosphate particles to be transported and absorbed. Taken together, these data suggested that La Cl3 and La Cit in GI tract were absorbed mainly via M cells with lanthanum phosphates as transformed species. The obtained results would provide the theoretical basis for the rational application of REEs in agriculture and medicine.展开更多
We synthesised a series of ω-aminoalkyl sodium hydrogen phosphates （AAP-n-Na, n =3, 4, 5, 6, purity 〉 99%）, which have potential applications as bioactive cosmetic ingredients and surface modifiers of bone minera...We synthesised a series of ω-aminoalkyl sodium hydrogen phosphates （AAP-n-Na, n =3, 4, 5, 6, purity 〉 99%）, which have potential applications as bioactive cosmetic ingredients and surface modifiers of bone minerals （i.e. hydroxyapatites）. Results from Fourier transformed infrared （FTIR）, nuclear magnetic resonance （NMR） and high resolution mass spectroscopy, and elemental analysis all matched their chemical structures. The acid dissociation constants （pKa＇s） of each AAP-n （acid form of AAP-n-Na, n ; 2-6） were measured by potentiometric titration, showing a general increasing trend with an increase in the chain length of AAP-n. However, the pKa3 constant, which corresponds to the deprotonation of the ammonium group in AAP-n-Na, displayed an unusual decrease when n = even. This odd-even effect can be explained by the pairwise self-association of AAP-n-Na molecules in water where intermolecular hydrogen bonding in case of n=even is weaker than that in case of n=odd. All AAP-n-Na at concentrations up to 0.1% （w/v） were non-toxic to L929 fibroblasts and MG 63 osteoblast-like cells in terms of cell growth and morphology, These basic data were important for applications of AAP-n and their salts in biomedical engineering.展开更多
As a white pigment, titanium oxide is used for cosmetic application. This oxide is well known to have the photo catalytic activity. Therefore a certain degree of sebum is decomposed by the ultraviolet radiation in sun...As a white pigment, titanium oxide is used for cosmetic application. This oxide is well known to have the photo catalytic activity. Therefore a certain degree of sebum is decomposed by the ultraviolet radiation in sunlight. In this work, titanium phosphates were prepared with additives (urea, sodium lactate, and glycerin) as a novel white pigment. Their chemical composition, powder properties, photo catalytic activity, moisture retention, and smoothness were studied. These white pigments had little photo catalytic activity. The addition of sodium lactate and glycerin improved the moisture retention of titanium phosphates. The slipping resistance of samples became small by the addition of sodium lactate and glycerin. The roughness of samples became small by heating.展开更多
A simple and highly efficient one-pot method for the construction of α-hydroxyketone phosphates from terminal alkynes and H-phosphine oxides has been developed in the presence of PhI（OAc）2 and H20. The present prot...A simple and highly efficient one-pot method for the construction of α-hydroxyketone phosphates from terminal alkynes and H-phosphine oxides has been developed in the presence of PhI（OAc）2 and H20. The present protocol provides an attractive approach to α-hydroxyketone phosphates in good to high yields, with the advantages of operation simplicity, the use of commercially available materials, broad substrate scope, high atom efficiency and good tolerance to scale-up synthesis.展开更多
The extraction of TiO2+, VO2+, VO2+ and NoO22+ by HDEHP, HEHEHP and HDTMPP was studied respectively. The orders of extraction ability for the three extractant systems are as follows: for TiO2+, VO2+: HDEHP>HEHEHP&g...The extraction of TiO2+, VO2+, VO2+ and NoO22+ by HDEHP, HEHEHP and HDTMPP was studied respectively. The orders of extraction ability for the three extractant systems are as follows: for TiO2+, VO2+: HDEHP>HEHEHP>HDTMPP; and for VO2+, MoO22+: HDEHP<HEHEHP<HDTMPP. The experimental results were discussed from the point of view of extractant structures.展开更多
Two large-pore metal-doped aluminophosphates, Mn4Al5（PO4 ）12[N（ C2H4NH3）3]3 [ N（C2H4NH3）2·（C2H4NH2）]（NH4）2·14H=O（Mn4-NJU） and Co4Al5（PO4）12[N（C2H,NH3）3][N（C2H4NH3）2（C2H4NH2）]3· （ N...Two large-pore metal-doped aluminophosphates, Mn4Al5（PO4 ）12[N（ C2H4NH3）3]3 [ N（C2H4NH3）2·（C2H4NH2）]（NH4）2·14H=O（Mn4-NJU） and Co4Al5（PO4）12[N（C2H,NH3）3][N（C2H4NH3）2（C2H4NH2）]3· （ NH4 ）4· 13H2O （ Co4-NJU） , which have the same open framework structures, were hydrothermally synthesized. The structures of these compounds consist of TO4 tetrahedra, which are linked together by corner-sharing to form an open framework with unique intersecting twelve-membered ring channels in three dimensions. The compounds crystallize in cubic space group I（-4）3m with α= 1. 6795（2） nm and V=4. 7374（9） nm^3 for Mn4-NJU, and a=1. 67372（19） nm and V = 4. 6887 （9） nm^3 for Co4-NJU, respectively. Single crystal structure analyses show that the protruding O atoms of the frameworks of the compounds are linked to protonated 4-（ 2-aminoethyl ）diethylenetriamine （TREN, C6H18N4 ） ions in the windows by means of hydrogen-bonding under the hydrothermal condition. It is also found that the components inside the super cages of the compounds are changeable, and the metal ions M^2＋ （M = Mn, Co） and Al^3＋ disorderedly occupy the same crystallographic positions.展开更多
Novel Ca_(8)CuRE(PO_(4))_(7)where RE^(3+)=Eu^(3+),Tb^(3+),Dy^(3+),Ho^(3+)and Er^(3+)were synthesized by a solid-state method in air.The structures of the samples were characterized by powder X-ray diffraction using Ri...Novel Ca_(8)CuRE(PO_(4))_(7)where RE^(3+)=Eu^(3+),Tb^(3+),Dy^(3+),Ho^(3+)and Er^(3+)were synthesized by a solid-state method in air.The structures of the samples were characterized by powder X-ray diffraction using Rietveld refinement to determine the occupation of crystal sites.The samples are found to have a centrosymmetric structure with space group R3c,as shown by dielectric measurements.These synthesized Ca_(8)CuRE(PO_(4))_(7)samples have multifunctional properties.The Cu^(2+)ions provide antibacterial properties,while the rare earth elements ions exhibit luminescence properties,and theβ-Ca_3(PO_(4))_(2)-type host is biocompatible.The photoluminescence properties of RE^(3+)ions were studied and compared with other simmilar Ca_(8)MRE(PO_(4))_(7)phosphates,where M is a divalent metal.The photoluminescence intensity quenching in terms of energy transfer from RE^(3+)to Cu^(2+)is disscused.The bioactive properties were studied in relation to antibacterial activity against E.coli and S.aureus.All syntesized Ca_(8)CuRE(PO_(4))_(7)samples demonstrate very high and stable inhibition of bacteria growth.The correlation between crystal structure and properties is discussed.By combining multiple approaches to the directio nal design of such materials,several important properties within a single chemical compound to achieve biovisualization and bioactive properties simultaneously can be combined.展开更多
In this work, a new method of a series of ion liquids (ILs) 1-alkyl-3-methylimidazolium chloride [Cnmim]Cl (n = 2, 4, 6, 8) intercalation into layered zirconium phosphates was investigated. It was found that the α-Zr...In this work, a new method of a series of ion liquids (ILs) 1-alkyl-3-methylimidazolium chloride [Cnmim]Cl (n = 2, 4, 6, 8) intercalation into layered zirconium phosphates was investigated. It was found that the α-ZrP·2BA (i.e. pre-intercalated BA was arranged in a bilayer mode in the galleries of α-ZrP) was a suitable host for intercalation ILs: ILs was inserted through exchanging pre-intercalated BA. And the intercalation orientation was investigated by use of X-ray diffraction (XRD) experiments and molecular modeling calculation.展开更多
Changes n plasma and red blood cell inorganic phosphates (RBC-Pi)and serum insulin were serially cyamined in 19 patients undergoing upper abdominal surgery using intravenous procainebalanced anesthesia. Plasma Pifell ...Changes n plasma and red blood cell inorganic phosphates (RBC-Pi)and serum insulin were serially cyamined in 19 patients undergoing upper abdominal surgery using intravenous procainebalanced anesthesia. Plasma Pifell at 60-90 min after the beginning of operation and 10 min by the end of operation with siguificant concomitant rise in RBC-Pi (P<0.001). Serum insulin showeo no obvious changes during the operative period, while rose significantly 24 hours after surgery (P< 0.001).The result seemed to be favorable to inteporet shifting of pi from plasma into RBCs and consistent reductions in plasma Pi during and after operation.展开更多
This paper deals with a simulated test of biogenic mineralization made with a blue-green alga species,Spirulina platensix. The data in the experiment were recorded by a computerized surveying system. The influ-ence of...This paper deals with a simulated test of biogenic mineralization made with a blue-green alga species,Spirulina platensix. The data in the experiment were recorded by a computerized surveying system. The influ-ence of algae on the accumulation of phosphorus by changing their microenvironment to promote the forma-tion and deposition of phosphate was studied. The results show that the pH value of cultural liquor rose up to 10 and the redox potential (Eh) may dropby 100-200 mV during the algal logarithmic growth stage, and the cultrual liquor was changed into a mediumwith a weakly reducing condition. At the end of the logarithmic growth stage white deposits of Na_2Ca(CO_3)_2·5H_2O and Ca_2Mg (PO_4)_2·2H_2O were formed on the floor of cultural containers. The test presented a wduableevidence for the theory of biogenic mineralization.展开更多
文摘A distinctive feature of phosphates is their special and significant ability to form inorganic polymeric compounds---condensed phosphates, which are destined to play a considerable role in our ＂high-tech＂ society in the future. Numerous olygophosphates, polyphosphates, double condensed phosphates and cyclophosphates with diverse formula, such as double tetra-, octa- and dodecaphosphates were obtained and described by us last years. The offered data are the outcomes of our scientific researches： of synthesis, analysis, and estimation of results in correlation with new achievements in inorganic polymer＇s chemistry. Many double condensed compounds, containing monovalent metals are obtained by us during systematic investigation of polycomponent systems, containing mono- and trivalent metals at temperature range 100-600 ~C. Synthesised condensed phosphates, in fact--inorganic polymers were examined in detail by chemical and thermogravimetric analysis, most compounds were examined by paper chromatography and the structures are determined by X-ray structural techniques/diffraction analysis. During our fundamental researches numerous new （about 70） unknown until now condensed phosphates have been obtained. Dependency of composition VS temperature and molar ratio, reliance of structure from duration of synthesis and radius of the ions are revealed.
文摘Molecular dynamics simulations were carried out to study the configuration energy and radial distribution functions of mmonium dihydrogen phosphate solution at different temperatures. The dihydrogen phosphate ion was treated as a seven-site model and the ammonium ion was regarded as a five-site model, while a simple-point-charge model for water molecule. An unusually local particle number density fluctuation was observed in the system at saturation temperature. It can be found that the potential energy increases slowly with the temperature from 373 K to 404 K, which indicates that the ammonium dihydrogen phosphate has partly decomposed. The radial distribution function between the hydrogen atom of ammonium cation and the oxygen atom of dihydrogen phosphate ion at three different temperatures shows obvious difference, which indicates that the average H-bond number changes obviously with the temperature. The temperature has an influence on the combination between hydrogen atoms and phosphorus atoms of dihydrogen phosphate ion and there are much more growth units at saturated solutions.
基金The National Natural Science Foundation of China(No.51372038No.51178104)+1 种基金the Scientific Research Foundation of Graduate School of Southeast University(No.YBJJ1453)the 333 Project of Jiangsu Province
文摘A phosphate-mineralization microbe was used to induce barium phosphates precipitation, and the precipitates with different types were obtained under different pH values. The average crystallite size of the barium phosphates was calculated by particle size distribution curves, and the size of the products was 33.40, 29. 37, 24. 13, 47.76 and 96. 53 μm when the pH values of the mixed solution are 7, 8, 9, 10 and 11, respectively. The results of X-ray diffraction （XRD） show that the structures of the particles controlled by the mixed solution are mainly BaaPO4 when pH 〈 10; the barium phosphates are synthesized by biological deposition which is the mixture of BaHPO4 and Ba5 （PO4）3OH when pH = 10; when pH = 11, the barium phosphates are also the mixtures, which are Ba5 （PO4）3OH and BaNaPO4. The above results indicate that the phosphate-mineralization microbe can produce a certain enzyme which constantly hydrolyzes phosphate monoester in the mixed solution, and then PO4^3- ions are obtained.
基金supported by the National Natural Science Foundation of China(No.22278097)Heilongjiang Province Universities Basic Scientific Research Business Fee Project(Nos.2022-KYYWF-0568 and 2023-KYYWF-0527)+2 种基金the Natural Science Foundation of Heilongjiang Province(No.YQ2021B004)the Postdoctoral fellowship of Heilongjiang Province(No.LBH-Z23156)the Postdoctoral Fellowship Program of CPSF(No.GZC20233449).
文摘Construction of elaborate configuration to enhance the intrinsic activity of NiMo-based catalyst candidates holds promise for accelerating the hydrogen evolution reaction(HER)kinetics.Herein,a novel cerium-doped NiMo phosphate(labeled as Ce-NiMo(PO_(4))_(0.66))is designed and fabricated via a facile hydrothermal and phosphatization method.A comprehensive characterization reveals that the introduction of the rare metal element cerium with an enriched 4f electronic distribution near the Fermi level modulates the hybridization of the 3d-2p orbitals and optimizes the electronic structure of the NiMo-based phosphate catalysts,which leads to the synergy between the nickel-molybdenum dual sites and the phosphate active unit to synchronously enhance the water dissociation and proton dehydrogenation transfer of the HER process.Consequently,Ce-NiMo(PO_(4))0.66 exhibits excellent alkaline HER performance with overpotentials at 10 and 500 mA·cm^(-2)current densities being only 40 and 295 mV,respectively,and desirable long-term durability at industrial current densities of 500 mA·cm^(-2).An overall hydrazine splitting(OHzS)constructed with Ce-NiMo(PO_(4))_(0.66)as a hydrazine oxidation reaction(HzOR)and HER bifunctional electrocatalyst has been constructed to achieve industrial current densities at the low voltage of 0.92 V,verifying its practical feasibility for sustainable hydrogen production and degradation of hydrazine pollutants.This work highlights that regulating the 3d-2p hybridization state through the inducing 4f orbital electronic state is a feasible means for enhancing the HER activity of transition metal compound catalysts.
文摘Molecular dynamics simulations were carried out to study the internal energy and microstructure of potassium dihydrogen phosphates （KDP） solution at different temperatures. The water molecule was treated as a simple-point-charge model, while a seven-site model for the dihydrogen phosphate ion was adopted. The internal energy functions and the radial distribution functions of the solution were studied in detail. An unusually large local particle number density fluctuation was observed in the system at saturation temperature. It has been found that the specific heat of oversaturated solution is higher than that of unsaturated solution, which indicates the solution experiences a crystallization process below saturation temperature. The radial distribution function between the oxygen atom of water and the hydrogen atom of the dihydrogen phosphate ion shows a very strong hydrogen bond structure. There are strong interactions between potassium cation and oxygen atom of dihydrogen phosphate ion in KDP solution, and much more ion pairs were formed in saturated solution.
基金Project(41271294)supported by the National Natural Science Foundation of ChinaProject(NCET-09-330)supported by Program for New Century Excellent Talents in University,China
文摘Batch and soil column experiments were conducted to evaluate the influence of KH2PO4, （NH4）H2PO4and Ca（H2PO4）2on the adsorption and leaching characteristics of Cu and Zn in red soil. The results show that all the three phosphates can greatly improve the adsorption capacity of red soil for Cu and Zn, and the effect of different phosphates on Cu and Zn adsorption follows the order of Ca（H2PO4）2〉KH2PO4〉（NH4）H2PO4. The addition of phosphate has little effect on the mobility of Cu. Ca（H2PO4）2and （NH4）H2PO4 show a strong ability in immobilizing Zn while the immobilization ability of KH2PO4 is much weaker. All the three phosphates are helpful for modifying the partitioning of Cu and Zn from the non-residual phase to the residual phase; however, they could also enhance the contents of Cu and Zn associated with exchangeable and carbonates fractions.
基金supported by National Natural Science Foundation of China(11104298,5033250,U1332202)Innovation Program of Shanghai Institute of Ceramics(Y34ZC130G)
文摘This study fully investigated the vacuum ultraviolet excitation spectra of pure and rare-earth（RE=Eu, Tb and Dy）-doped A2Zr（PO4）2（A=Li, Na and K） phosphors. The synthesized Na and Li compounds were characterized by XRD showing two new types of phases after indexation. Although these three pure compounds had different crystal structures, they exhibited similar luminescence properties. For Eu3＋-activated samples, the broad excitation band centered at 217 nm could be attributed to the CT transition between O2–（2p6） and Eu3＋ ions. For Tb3＋-doped samples, two groups of f-d transitions were observed, where a strong broad band at 221 nm was due to the spin-allowed f-d transition. Energy transfer from O2– to Dy3＋was not observed in Dy3＋-doped phosphors, probably because it overlapped considerably with the CT transition from O2– to Zr4＋ at 187 nm.
基金supported by the Ministry of Higher Education,Scientific Research and Technology of Tunisia
文摘Single crystals of LaP3O9·3H2O were prepared using a classical method of aqueous chemistry whereas those of the ultraphosphate LaP5O14 were obtained by flux method.Thermal treatment of LaP3O9·3H2O up to 700 °C allowed us to obtain the lanthanum polyphosphate La(PO3)3.The conductivity as well as the vibrational study of the lanthanum ultraphosphate and polyphosphate were analysed in order to explain the mechanism of conduction.Activation energies of 0.45 and 0.84 eV,deduced from the Arrhenius relation,were r...
基金the National Research Foundation of Korea(NRF)funded by the Korean Government(MSIT)(No.2022R1A2C1006743)。
文摘This study presents a facile and rapid method for synthesizing novel Layered Double Hydroxide(LDH)nanoflakes,exploring their application as a photocatalyst,and investigating the influence of condensed phosphates'geometric linearity on their photocatalytic properties.Herein,the Mg O film,obtained by plasma electrolysis of AZ31 Mg alloys,was modified by growing an LDH film,which was further functionalized using cyclic sodium hexametaphosphate(CP)and linear sodium tripolyphosphate(LP).CP acted as an enhancer for flake spacing within the LDH structure,while LP changed flake dispersion and orientation.Consequently,CP@LDH demonstrated exceptional efficiency in heterogeneous photocatalysis,effectively degrading organic dyes like Methylene blue(MB),Congo red(CR),and Methyl orange(MO).The unique cyclic structure of CP likely enhances surface reactions and improves the catalyst's interaction with dye molecules.Furthermore,the condensed phosphate structure contributes to a higher surface area and reactivity in CP@LDH,leading to its superior photocatalytic performance compared to LP@LDH.Specifically,LP@LDH demonstrated notable degradation efficiencies of 93.02%,92.89%,and 88.81%for MB,MO,and CR respectively,over a 40 min duration.The highest degradation efficiencies were observed in the case of the CP@LDH sample,reporting 99.99%for MB,98.88%for CR,and 99.70%for MO.This underscores the potential of CP@LDH as a highly effective photocatalyst for organic dye degradation,offering promising prospects for environmental remediation and water detoxification applications.
基金supported by the National Natural Science Foundation of China (20871058, 20971028, 21006038)the Natural Science Key Fundation of Guangdong Province of China (10251007002000000)+2 种基金the Foundation of Enterprise-University-Research Institute Cooperation of Guangdong Province and Ministry of Education of China (2008A010500005)the Foundation of Enterprise-University-Research Institute Cooperation from Guangdong Province and the Chinese Academy of Sciences (2010B090301036)the Fundamental Research Funds for the Central Universities, and Undergraduate Scientific and Technological Innovation Project for Jinan University (cx10075, cx10076)
文摘Zinc and cerium carried zirconium phosphates （Zn-Ce/ZrPs） were prepared by exchanging zinc and cerium cations into sodium zirconium phosphate （NaZrP） through the ion-exchange method and characterized by X-ray diffraction（XRD）, energy dispersive X-ray spectroscopy （EDX） and scanning electron microscopy （SEM）. Furthermore, the specific surface area, zeta potential and antibacterial activity were tested. The results showed that Zn-Ce/ZrPs were with hexagonal crystal system, and the surface area of Zn-Ce/ZrPs increased much more than that of NaZrP. Zn-Ce/ZrPs showed obvious synergetic antibacterial effect, and have the potential to be used as antibacterial agents in environmental control.
基金National Natural Science Foundation of China(Grant No.21277006 and 21671009)
文摘In the present study, we investigated the transformed species and the absorptive mechanism of rare earth elements（REEs） in gastrointestinal（GI） tract, using La Cl3 and La Cit as representative compounds. Artificial gastric and intestinal fluids were used to simulate the environment of the digestive tract in vivo. The inductively coupled plasma mass spectrometry（ICP-MS） result showed that more than 99.9% of La Cl3 and La Cit formed precipitation in artificial intestinal fluid, with the average size distribution of 200 nm（2-h incubation） increasing to 600 nm（24-h incubation） determined by dynamic light scattering（DLS）, indicating the aggregation of the particles. The Fourier transform infrared spectroscopy（FTIR） analysis demonstrated that the constituents of these particles were mainly in the form of lanthanum phosphates. To explore the transport mechanism of REEs in GI tract, the mice Peyer＇s patches（PPs） and intestinal epithelium were separated to evaluate the content of lanthanum by ICP-MS following oral administration with 2 or 100 mg/kg/day of La Cit for 7 d. The results showed that the amount of lanthanum phosphate particles absorbed by PPs was significantly greater than that of intestinal epithelium, indicating that lanthanum particles might be phagocytosed mainly by M cells located in the follicle-associated epithelium（FAE） overlying PPs. Furthermore, Caco-2 cell monoculture and Caco-2/Raji B cell coculture models were established to simulate intestinal epithelial cells and FAE, respectively. The result showed that the transport of lanthanum in Caco-2/Raji B coculture model was significantly higher than that in Caco-2 monoculture model（about 60 times higher）, and the level of lanthanum in the basal compartment of Caco-2 monoculture model was very low, supporting that M cells were the main route for lanthanum phosphate particles to be transported and absorbed. Taken together, these data suggested that La Cl3 and La Cit in GI tract were absorbed mainly via M cells with lanthanum phosphates as transformed species. The obtained results would provide the theoretical basis for the rational application of REEs in agriculture and medicine.
基金financial support from the National Natural Science Foundation of China (No. 50973069)
文摘We synthesised a series of ω-aminoalkyl sodium hydrogen phosphates （AAP-n-Na, n =3, 4, 5, 6, purity 〉 99%）, which have potential applications as bioactive cosmetic ingredients and surface modifiers of bone minerals （i.e. hydroxyapatites）. Results from Fourier transformed infrared （FTIR）, nuclear magnetic resonance （NMR） and high resolution mass spectroscopy, and elemental analysis all matched their chemical structures. The acid dissociation constants （pKa＇s） of each AAP-n （acid form of AAP-n-Na, n ; 2-6） were measured by potentiometric titration, showing a general increasing trend with an increase in the chain length of AAP-n. However, the pKa3 constant, which corresponds to the deprotonation of the ammonium group in AAP-n-Na, displayed an unusual decrease when n = even. This odd-even effect can be explained by the pairwise self-association of AAP-n-Na molecules in water where intermolecular hydrogen bonding in case of n=even is weaker than that in case of n=odd. All AAP-n-Na at concentrations up to 0.1% （w/v） were non-toxic to L929 fibroblasts and MG 63 osteoblast-like cells in terms of cell growth and morphology, These basic data were important for applications of AAP-n and their salts in biomedical engineering.
文摘As a white pigment, titanium oxide is used for cosmetic application. This oxide is well known to have the photo catalytic activity. Therefore a certain degree of sebum is decomposed by the ultraviolet radiation in sunlight. In this work, titanium phosphates were prepared with additives (urea, sodium lactate, and glycerin) as a novel white pigment. Their chemical composition, powder properties, photo catalytic activity, moisture retention, and smoothness were studied. These white pigments had little photo catalytic activity. The addition of sodium lactate and glycerin improved the moisture retention of titanium phosphates. The slipping resistance of samples became small by the addition of sodium lactate and glycerin. The roughness of samples became small by heating.
基金financial support from the National Natural Science Foundation of China(Nos.21172213,21302109,21402184,and 21572217)
文摘A simple and highly efficient one-pot method for the construction of α-hydroxyketone phosphates from terminal alkynes and H-phosphine oxides has been developed in the presence of PhI（OAc）2 and H20. The present protocol provides an attractive approach to α-hydroxyketone phosphates in good to high yields, with the advantages of operation simplicity, the use of commercially available materials, broad substrate scope, high atom efficiency and good tolerance to scale-up synthesis.
基金This work is supported by Natural Science Foundation of Shandong Province.
文摘The extraction of TiO2+, VO2+, VO2+ and NoO22+ by HDEHP, HEHEHP and HDTMPP was studied respectively. The orders of extraction ability for the three extractant systems are as follows: for TiO2+, VO2+: HDEHP>HEHEHP>HDTMPP; and for VO2+, MoO22+: HDEHP<HEHEHP<HDTMPP. The experimental results were discussed from the point of view of extractant structures.
文摘Two large-pore metal-doped aluminophosphates, Mn4Al5（PO4 ）12[N（ C2H4NH3）3]3 [ N（C2H4NH3）2·（C2H4NH2）]（NH4）2·14H=O（Mn4-NJU） and Co4Al5（PO4）12[N（C2H,NH3）3][N（C2H4NH3）2（C2H4NH2）]3· （ NH4 ）4· 13H2O （ Co4-NJU） , which have the same open framework structures, were hydrothermally synthesized. The structures of these compounds consist of TO4 tetrahedra, which are linked together by corner-sharing to form an open framework with unique intersecting twelve-membered ring channels in three dimensions. The compounds crystallize in cubic space group I（-4）3m with α= 1. 6795（2） nm and V=4. 7374（9） nm^3 for Mn4-NJU, and a=1. 67372（19） nm and V = 4. 6887 （9） nm^3 for Co4-NJU, respectively. Single crystal structure analyses show that the protruding O atoms of the frameworks of the compounds are linked to protonated 4-（ 2-aminoethyl ）diethylenetriamine （TREN, C6H18N4 ） ions in the windows by means of hydrogen-bonding under the hydrothermal condition. It is also found that the components inside the super cages of the compounds are changeable, and the metal ions M^2＋ （M = Mn, Co） and Al^3＋ disorderedly occupy the same crystallographic positions.
基金Project supported by Russian Science Foundation(19-77-10013-Ⅱ)。
文摘Novel Ca_(8)CuRE(PO_(4))_(7)where RE^(3+)=Eu^(3+),Tb^(3+),Dy^(3+),Ho^(3+)and Er^(3+)were synthesized by a solid-state method in air.The structures of the samples were characterized by powder X-ray diffraction using Rietveld refinement to determine the occupation of crystal sites.The samples are found to have a centrosymmetric structure with space group R3c,as shown by dielectric measurements.These synthesized Ca_(8)CuRE(PO_(4))_(7)samples have multifunctional properties.The Cu^(2+)ions provide antibacterial properties,while the rare earth elements ions exhibit luminescence properties,and theβ-Ca_3(PO_(4))_(2)-type host is biocompatible.The photoluminescence properties of RE^(3+)ions were studied and compared with other simmilar Ca_(8)MRE(PO_(4))_(7)phosphates,where M is a divalent metal.The photoluminescence intensity quenching in terms of energy transfer from RE^(3+)to Cu^(2+)is disscused.The bioactive properties were studied in relation to antibacterial activity against E.coli and S.aureus.All syntesized Ca_(8)CuRE(PO_(4))_(7)samples demonstrate very high and stable inhibition of bacteria growth.The correlation between crystal structure and properties is discussed.By combining multiple approaches to the directio nal design of such materials,several important properties within a single chemical compound to achieve biovisualization and bioactive properties simultaneously can be combined.
文摘In this work, a new method of a series of ion liquids (ILs) 1-alkyl-3-methylimidazolium chloride [Cnmim]Cl (n = 2, 4, 6, 8) intercalation into layered zirconium phosphates was investigated. It was found that the α-ZrP·2BA (i.e. pre-intercalated BA was arranged in a bilayer mode in the galleries of α-ZrP) was a suitable host for intercalation ILs: ILs was inserted through exchanging pre-intercalated BA. And the intercalation orientation was investigated by use of X-ray diffraction (XRD) experiments and molecular modeling calculation.
文摘Changes n plasma and red blood cell inorganic phosphates (RBC-Pi)and serum insulin were serially cyamined in 19 patients undergoing upper abdominal surgery using intravenous procainebalanced anesthesia. Plasma Pifell at 60-90 min after the beginning of operation and 10 min by the end of operation with siguificant concomitant rise in RBC-Pi (P<0.001). Serum insulin showeo no obvious changes during the operative period, while rose significantly 24 hours after surgery (P< 0.001).The result seemed to be favorable to inteporet shifting of pi from plasma into RBCs and consistent reductions in plasma Pi during and after operation.
文摘This paper deals with a simulated test of biogenic mineralization made with a blue-green alga species,Spirulina platensix. The data in the experiment were recorded by a computerized surveying system. The influ-ence of algae on the accumulation of phosphorus by changing their microenvironment to promote the forma-tion and deposition of phosphate was studied. The results show that the pH value of cultural liquor rose up to 10 and the redox potential (Eh) may dropby 100-200 mV during the algal logarithmic growth stage, and the cultrual liquor was changed into a mediumwith a weakly reducing condition. At the end of the logarithmic growth stage white deposits of Na_2Ca(CO_3)_2·5H_2O and Ca_2Mg (PO_4)_2·2H_2O were formed on the floor of cultural containers. The test presented a wduableevidence for the theory of biogenic mineralization.
