Thermal decomposition of magnesium ammonium phosphate and adsorption properties of its pyrolysis products toward ammonia nitrogen

High-purity magnesium ammonium phosphate （MAP） was precipitated by controlling pH value of the reaction system of 9.0-9.5. The thermal decomposition behavior of MAP and the adsorption properties of its pyrolysis products toward ammonia-nitrogen were also studied by XRD, SEM, TGA-DTA and FT-IR methods. The results indicated that high-purity MAP was obtained at pH value of 9.0-9.5. Upon heating to 100-120℃ for 120 min, MAP was thermally decomposed, losing water and ammonia concomitantly with a reduction in grain size and crystallinity. The capacity of pyrolysis products for ammonia nitrogen adsorption reached 72.5 mg/g, with a removal rate of up to 95% from an 800 mg/L solution. The characteristic diffraction peaks corresponding to MAP mainly appeared in their XRD patterns after adsorption of ammonia nitrogen. The pyrolysis products of MAP at 100-120 ℃ could be recycling-used as the chemical treatment regents of ammonia nitrogen in the practical application.

Temperature-programmed pyrolysis of magnesium ammonium phosphate and removal of ammonia-nitrogen by its pyrolysate

In order to achieve the dual goals of complete deamination of magnesium ammonium phosphate（MAP） and ensure the pyrolysate＇s good removal properties towards ammonia-nitrogen, a temperature-programmed method for the pyrolysis of MAP was studied, as well as the thermodynamic and kinetic processes involved in the removal reaction system between MAP pyrolysate and aqueous ammonium. It was found that the pyrolysis method and pyrolysis final temperature had significant effects on the MAP pyrolysate＇s removal properties towards aqueous ammonium, and the following conditions were deemed to be more appropriate： pyrolysis final temperature and heating rate at 180 ℃ and 5 ℃/min, respectively, and a pH level of 9.5 for the removal reaction system. The resultant ammonium removal capacity by the MAP pyrolysate was 95.62 mg/g. After 120 min, the removal rate with an initial concentration of 1000 mg/L was 82%. The kinetic and thermodynamic results indicated that the removal of aqueous ammonium by MAP pyrolysate was the exchange process between H^＋ and NH4^＋ via MAP precipitation. The kinetics complied with the Lagergren quasi second-order model with an equilibrium time of 120 min, while the isothermal curves complied with the Freundlich model.

Enhanced sulfidization of azurite surfaces by ammonium phosphate and its effect on flotation

Although azurite is one of the most important copper oxide minerals,the recovery of this mineral via sulfidization-xanthate flotation is typically unsatisfactory.The present work demonstrated the enhanced sulfidization of azurite surfaces using ammonia phosphate((NH_(4))_(3)PO_(4)) together with Na_(2)S,based on micro-flotation experiments,time-of-flight secondary ion mass spectrometry(ToF-SIMS),X-ray photoelectron spectroscopy(XPS),zeta-potential measurements,contact angle measurements,Fourier-transform infrared(FT-IR)spectroscopy,and ultraviolet-visible(UV-Vis)spectroscopy.Micro-flotation experiments showed that the floatability of azurite was increased following the simultaneous addition of(NH_(4))_(3)PO_(4)and Na_(2)S.ToF-SIMS and XPS analyses demonstrated the formation of a high content of S species on the azurite surface and an increase in the number of Cu(I)species after exposure to(NH_(4))_(3)PO_(4)and Na_(2)S,compared with the azurite-Na_(2)S system.The zeta potential of azurite particles was negatively shifted and the contact angle on the azurite surface was increased with the addition of(NH_(4))_(3)PO_(4)prior to Na_(2)S.These results indicate that treatment with(NH_(4))_(3)PO_(4) enhances the sulfidization of azurite surfaces,which in turn promotes xanthate attachment.FT-IR and UV-Vis analyses confirmed that the addition of(NH_(4))_(3)PO_(4) increased the adsorption of xanthate with reducing the consumption of xanthate during the azurite flotation process.Thus,(NH_(4))_(3)PO_(4) has a beneficial effect on the sulfidization flotation of azurite.

Biobased Furfurylated Poplar Wood for Flame-Retardant Modification with Boric Acid and Ammonium Dihydrogen Phosphate

Furfurylated wood exhibits excellent dimensional stability and corrosion resistance,making it a promising material for constructing buildings,but it is highly flammable.Herein,flame-retardant furfurylated poplar wood was produced via a two-step process utilizing boric acid(BA)and ammonium dihydrogen phosphate(ADP)as flame-retardant components,and biomass-derived furfuryl alcohol(FA)as a modifier.The acidity of BA and ADP allowed them to catalyze the polymerization of FA,which formed a cross-linked network that immobilized BA and ADP inside the wood.The addition of BA/ADP substantially delayed the time to ignition from 10 to 385 s and reduced the total heat release and total smoke release by 58.75%and 77.31%,respectively.Analysis of the pyrolysis process showed that the decomposition products of BA and ADP protected the underlying furfurylated wood and diluted combustible gases.This method significantly improved the fire retardancy and smokeless properties of furfurylated wood,providing promising prospects for its application as an engineering material.

Molecular Dynamics Study on Configuration Energy and Radial Distribution Functions of Ammonium Dihydrogen Phosphates Solution

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.

Optimization of the iron-enriched extruded snack containing jackfruit seed flour, mung bean flour and ferrous ammonium phosphate by using response surface methodology

The Food and Agriculture Organization (State of food and agriculture. Moving forward on food loss and waste reduction, 2019) stated that approximately 1.3 billion tons of food wasted every year caused the emission of around 4.4 gigatons of greenhouse gas. World Health Organization highlights that iron deficiency affects billions of people worldwide and remains the leading cause of anemia. With the growth of healthy and sustainable diets and consumers’ better understanding of the relationship between diet, health, and the environment, there is an opportunity to develop novel healthy extruded snacks. The present study was carried out using response surface methodology to investigate the effects of varying proportions of jackfruit seed flour, mung bean flour, and ferrous ammonium phosphate on physical and functional properties of extruded snacks. Experiments were carried out using a central composite rotatable design with three independent parameters such as jackfruit seed flour(%), mung bean flour(%), and ferrous ammonium phosphate (%), and five responses such as bulk density (BD), expansion ratio (ER), hardness, color difference (ΔE), and iron content. It was found that ferrous ammonium phosphate significantly increased the iron content. Bulk density, expansion ratio, and hardness were significantly affected by jackfruit seed flour and mung bean flour. All independent variables significantly influenced colour value. The optimized iron-enrich extruded snacks were obtained at 24.87% jackfruit seed flour, 20.95% mung bean flour, and 0.021% ferrous ammonium phosphate. The optimized extruded snack contained 15.32 g/100 g protein and 22.03 mg/100 g iron content. Results of the study indicate that the optimized extruded snack could be used as a protein and iron source to mitigate malnutrition and anemia.

Silica supported ammonium dihydrogen phosphate(NH_4H_2PO_4/SiO_2):A mild,reusable and highly efficient heterogeneous catalyst for the synthesis of 14-aryl-14-H-dibenzo[a,j]xanthenes

catalyst for the synthesis of 14-aryl- 14-H-dibenzo[aj]xanthenes Silica supported ammonium dihydrogen phosphate （NH4H2PO4/SiO2） is found to be a recyclable heterogeneous catalyst for a rapid and efficient synthesis of various aryl-14-H-dibenzo[a,j]xanthenes with excellent yields under solvent-free conditions. The present methodology offers several advantages such as excellent yields, simple procedure, short reaction times and milder conditions. 2009 Shahnaz Rostamizadeh. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.

Ammonium cobalt phosphate with asymmetric coordination sites for enhanced electrocatalytic water oxidation

Cobalt‐based materials have been considered as promising candidates to electrocatalyze water oxidation.However,the structure‐performance correlation remains largely elusive,due to the com‐plex material structures and diverse performance‐influencing factors in those Co‐based catalysts.In this work,we designed two cobalt phosphates with distinct Co symmetry to explore the effect of coordination symmetry on electrocatalytic water oxidation.The two analogues have similar mor‐phology,Co valence and 6‐coordinated Co octahedron,but with different coordination symmetry.In contrast to symmetric Co_(3)(PO_(4))2·8H_(2)O,asymmetric NH_(4)CoPO_(4)·H_(2)O exhibited enhanced electrocata‐lytic water oxidation activity in a neutral aqueous solution.It is proven that,by experimental and theoretical studies,the asymmetric Co coordination sites can facilitate the surface reconstruction under anodic polarization to boost the electrocatalysis.Based on this contrastive platform with distinct symmetry differences,the preferred configuration in cobalt‐oxygen octahedrons for water oxidation has been straightforwardly assigned.

Electrical Conduction in Deuterated Ammonium Dihydrogen Phosphate Crystals with Different Degrees of Deuteration

Conductivity measurements of deuterated ammonium dihydrogen phosphate （DADP） crystals with different deuterated degrees are described. The conductivities increase with the deuterium content, and the value of the a-direction is larger than that of the e-direction. Compared with DKDP crystals, DADP crystals have larger conductivities, which is partly due to the existence of A defects. The ac conductivity over the temperature range 25-170℃has shown a knee in the curve ofln（σT） versus T-1. The conductivity activation energy calculated by the slope of the high temperature region decreases with the deuterium content. The previously reported phase transition is not seen.

STUDIES ON SYNTHESIS AND CHARACTER OF INORGANIC ION EXCHANGER TITANIUM PHOSPHATE-AMMONIUM TUNGSTOPHOSPHATE

In this paper, a new complex inorganic ion exchanger Titanium Phosphate - Ammonium Tungstophosphate (abbreviated as TiP - AWP) was synthesized, whose exchange character and chemical structure were studied, Thiscompound exhibits high exchange capacity and selectivity for Cs+, its exchangecapacity attains 0. 95 mmol/g in the medium of 0. 1 mol/L HNO3, andwhich almost doesn’ t change in the 1 AW imitated waste solution. There areno change in exchange capacity and structure after several times of exchanging,eluting, regenerating, which is of great importance to the separation and uptaking of radio - nuclides. Further more, this exchanger has good thermal andradioactive stability.

Effect of different operation conditions on PCDD/F inhibition by ammonium dihydrogen phosphate:concentrations,distributions and mechanisms

Phosphorus-containing compounds are considered as the potential alternatives of traditional inhibitors for suppressing the formation of polychlorinated dibenzo-p-dioxins and dibenzofurans(PCDD/Fs),but the suppression characteristics are scarcely studied.In this study,ammonium dihydrogen phosphate(ADP)was selected as the inhibitor to inhibit the PCDD/F formation via de novo synthesis at 350℃.The influence of oxygen content and addition method on PCDD/F inhibition was systematically investigated by means of statistical analysis and morphological characterization.The results showed that oxygen enhanced the formation of PCDD/Fs from 1470 ng g^(−1)(9.78 ng I-TEQ g^(−1))to 2110 ng g^(−1)(14.8 ng I-TEQ g^(−1)).ADP significantly inhibited the PCDD/F formation,with inhibition efficiencies ranging from 82.0%to 97.7%.Herein,a higher oxygen content and the premixed way intensified the suppression effect.Dibenzo-p-dioxin(DD)/dibenzofuran(DF)chlorination was proven to be effectively suppressed while chlorophenol(CP)route was not obviously influenced.With the addition of ADP,Cl source was significantly reduced and the formation of organic Cl was effectively inhibited.Also,it decreased the proportion of C–O/C=N and C=O,revealing the efficient inhibition of carbon oxidation.Meanwhile,the formation of copper phosphate and copper pyrophosphate was observed in XPS(X-ray photoelectron spectroscopy)spectra,indicating that the catalytic metal Cu was chelated and passivated by ADP.The premixed way had a better effect on reducing Cl resources,inhibiting oxidation and chelating metals,due to the direct contact with inhibitor.However,the separation method could only depend on the decomposed gases,resulting in a lower inhibition efficiency.

Properties of Eco-Friendly Oriented Strand Board Produced from Oil Palm Trunk

Despite its considerable potential,oil palm trunk(OPT)remains underutilized,largely owing to the cyclical replanting process that occurs every 25–30 years.This study aimed to address this issue by developing an ecofriendly oriented strand board(OSB)using vascular bundles(VBs)from oil palm,both in binderless form and with the incorporation of natural adhesives made from sucrose and ammonium dihydrogen phosphate(ADP).The VB was extracted from OPT using a pressure cooker and mixed with a sucrose-ADP solution at various ratios.The mixture was then pressed at temperatures of 180°C and 200°C for 10 min to form boards,which were evaluated based on the Japanese Industrial Standard(JIS)A 5908 for particleboards.Binderless OSB was also manufactured without the use of any adhesive components.Fourier-transform infrared(FTIR)spectroscopy was conducted to evaluate the VB and its board.The results indicated that the mechanical properties of the binderless OSB met the JIS A 5908 Type 8 requirements.Furthermore,the addition of sucrose-ADP improved the physical and mechanical properties of the board,with an optimal sucrose-to-ADP ratio of 85:15.The OSB with the best properties met the JIS A 5908 Type 13 requirements.The FTIR results indicated that carbonyl groups,furan rings,and lignin played important roles in the bonding properties of the OSB.In conclusion,this research demonstrated the potential of VBs as a raw material for producing environmentally friendly OSB,both in binderless form and with the use of sucrose-ADP.

Thermodynamic study on phosphorus removal from tungstate solution via magnesium salt precipitation method

The thermodynamic equilibrium diagrams of Mg2＋- 3-4PO - ＋4NH -H2O system at 298 K were established based on the thermodynamic calculation. From the diagram, the thermodynamic conditions for removing phosphorus from the tungstate solution by magnesium salt precipitation were obtained. The results show that when the concentration of total magnesium increases from 0.01 mol/L to 1.0 mol/L, the optimal pH for the phosphorus removal by magnesium phosphate decreases from 9.8 to 8.8. The residual concentration of total phosphorus almost keeps the level of 4.0×10-6 mol/L in the system. MgHPO4, Mg3（PO4）2 and the mixture of Mg3（PO4）2 and Mg（OH）2 are stabilized in these system, respectively. However, increasing the total concentration of magnesium has little effect on phosphorus removal by magnesium ammonium phosphate, while it is helpful for phosphorus removal by increasing the total ammonia concentration. The calculated results demonstrate that the residual concentration of total phosphorus can decrease to 5.0×10-7 mol/L as the total concentration of ammonia reaches 5.0 mol/L and the optimal pH value is 9-10. Finally, verification experiments were conducted with home-made ammonium tungstate solution containing 50 g/L WO3 and 13 g/L P. The results show that when the dosage of MgCl2 is 1.1 times of the theoretical amount, the optimum pH for removing phosphorus is 9.5, which matches with the results of the theoretical calculation exactly.

Formation of Struvite Crystals in a Simulated Food Waste Aerobic Composting Process

Bench-scale treatments with three mixtures of Mg and P salts, including K3PO4＋MgSO4, K2HPO4＋MgSO4, and KH2PO4＋MgSO4 as additives in a simulated food waste aerobic composting process, were conducted to test the magnesium ammonium phosphate（MAP） formation, and the compost products were analyzed by X-ray diffraction（XRD）, Scanning electron microscopy（SEM）, and Energy dispersive X-ray spectroscopy（EDS） analyses. The comparison results between XRD, SEM, and EDS analyses of MAPs in the dried compost and synthesized MAPs confirm the formation of MAP crystals in the simulated food waste aerobic composting process. The analysis of the compost also indicates that the addition of all the three mixtures of Mg and P salts in the aerobic composting process can increase nitrogen conservation and decrease nitrogen loss because of the formation of MAPs. The mechanism of MAP formation was verified as the reaction of ammonium（NH4＋） with magnesium（Mg^2＋） and phosphate[HnPO4^（3-n） , n=0, 1, and 2）.

A facile synthesis of ω-aminoalkyl ammonium hydrogen phosphates

A series of og-aminoalkyl ammonium hydrogen phosphates were synthesized through a simple and efficient three-step method. The starting materials, co-aminoalkyl alcohols （AC-n, with carbon number n = 3, 4, 5, 6）, were amino-protected with 9- fluorenylmethyl chloroformate （Fmoc-C1）, followed by phosphorylation with POCI3 and deprotection in piperidine/DME The structures of each intermediate and final product were confirmed by 1H NMR, FTIR and mass spectrum. The yield of each step was about 77-92%, with a total yield higher than 56%. This new method was superior in low-cost raw materials, mild reaction temperatures （0-25 ℃） and easy purification methods.

Influence of polymer solution on the morphology and local structure of NH_(4)ZnPO_(4)powders synthesized by a simple precipitation method at room temperature

NH_(4)Zn PO_(4)powders were synthesized using a simple precipitation method at room temperature.The effects of polyvinyl pyrrolidone(PVP),polyvinyl alcohol(PVA),glucose,and hexadecyltrimethylammonium bromide(CTAB)solutions on the morphology and structure of the prepared samples were investigated.The phase composition and morphology of the prepared samples were characterized using X-ray diffraction and scanning electron microscopy,respectively.Depending on the polymer sources,the hexagonal structure prepared using non-surfactant of water completely changed to monoclinic structure when CTAB was added.X-ray absorption near-edge structure(XANES)and X-ray photoelectron spectroscopy(XPS)were performed to study the local structure and surface electronic structure of the prepared samples,confirming that the oxidation states of P and Zn ions are^(5+)and^(2+),respectively.On the basis of the results of inductively coupled plasma atomic emission spectroscopy(ICP-OES),the NH_(4)Zn PO_(4)powders can be classified as a slow-release fertilizer where less than 15%of the ions were released in 24 h.A simple precipitation method using water,PVP,PVA,sucrose,and CTAB as a template can be used to synthesize NH4 Zn PO4 powders.In addition,this method may be extended for the preparation of other oxide materials.

Thermochemical Properties and Decomposition Kinetics of Ammonium Magnesium Phosphate Monohydrate

Ammonium magnesium phosphate monohydrate NH4MgPO4·H2O was prepared via solid state reaction at room temperature and characterized by XRD, FT-IR and SEM. Thermochemical study was performed by an isoperibol solution calorimeter, non-isothermal measurement was used in a multivariate non-linear regression analysis to determine the kinetic reaction parameters. The results show that the molar enthalpy of reaction above is （28.795 ± 0.182） kJ/mol （298.15 K）, and the standard molar enthalpy of formation of the title complex is （-2185.43 ± 13.80） kJ/mol （298.15 K）. Kinetics analysis shows that the second decomposition of NH4MgPO4·H2O acts as a double-step reaction： an nth-order reaction （Fn） with n=4.28, E1=147.35 kJ/mol, A1=3.63×10^13 s^-1 is followed by a second-order reaction （F2） with E2=212.71 kJ/mol, A2= 1.82 × 10^18 s^-1.

Modeling assessment for ammonium nitrogen recovery from wastewater by chemical precipitation

Chemical precipitation to form magnesium ammonium phosphate（MAP） is an effective technology for recovering ammonium nitrogen（NH4＋-N）.In the present research,we investigated the thermodynamic modeling of the PHREEQC program for NH4＋-N recovery to evaluate the effect of reaction factors on MAP precipitation.The case study of NH4＋-N recovery from coking wastewater was conducted to provide a comparison.Response surface methodology（RSM） was applied to assist in understanding the relative significance of reaction factors and the interactive effects of solution conditions.Thermodynamic modeling indicated that the saturation index（SI） of MAP followed a polynomial function of pH.The SI of MAP increased logarithmically with the Mg2＋/NH4＋ molar ratio（Mg/N） and the initial NH4＋-N concentration（CN）,respectively,while it decreased with an increase in Ca2＋/NH4＋ and CO32？/NH4＋ molar ratios（Ca/N and CO32？/N）,respectively.The trends for NH4＋-N removal at different pH and Mg/N levels were similar to the thermodynamic modeling predictions.The RSM analysis indicated that the factors including pH,Mg/N,CN,Ca/N,（Mg/N）×（CO32？/N）,（pH）2,（Mg/N）2,and（CN）2 were significant.Response surface plots were useful for understanding the interaction effects on NH4＋-N recovery.

Optimization of process parameters for mature landfill leachate pretreatment using MAP precipitation

Chemical precipitation is a useful technology as a pretreatment to treat mature landfill leachate with high concentrations of ammonium-nitrogen （NH＋-N） and refractory organic compounds. Orthogonal experiments and factorial experiments were carried out to determine the optimal conditions enhancing the magnesium ammonium phosphate （MAP） precipitation process, and the experi- mental results demonstrated that the removal rate of NH＋ -N was more than 85% when MgO and NaHEPO4.2H20 were applied as external sources of magnesium and phosphorous under the optimal conditions that molar ratio n（Mg）：n（N）：n（P） = 1.4：1：0.8, reaction time 60 min, original pH of leachate and settling time 30 min. In the precipitation process, pH could be maintained at the optimal range of 8-9.5 because MgO could release hydroxide ions to consume hydrogen ions. Calcium ions and carbonate ions existed in the leachate could affect the precipitation process, which resulted in the decrease of NH＋-N removal efficiency. The residues of MAP sediments decomposed by heating under alkaline condi- tions can be reused as the sources of phosphorous and magnesium for the removal of high concentrations of NH4＋ -N, and up to 90% of ammonium could be released under molar ratio of n[OH]：n[MAP] = 2.5： 1, heating temperature 90℃ and heating time 2h.

Modification of ADP extinguishing powder by siliconization in spray drying

Superfine spherical fire-extinguishing powder, ammonium dihydrogen phosphate （ADP, NH4 H2 PO4）, was prepared by spray drying and modified in situ with methyl hydrogen silicone oil （MHSO） emulsion and the fluorinated surfactant FK-510. The influences of the MHSO mass ratio on the hydrophobicity, sur- face composition, surface morphology, dispersion and particle-size distribution of the NH4H2PO4 were studied, and the influence of the drying air temperature on the decomposition of the NH4H2PO4 was also researched. The results indicate that the MHSO and FK-510 congregate on the particle surfaces and then form a hydrophobic shell. This shell improves the particle hydrophobicity and leads to a fine dispersion of the particles. During the process of preparing the precursor solution, 3 wt% （based on the weight of NH4H2 PO4 ） was chosen as the optimum value of the MHSO mass ratio. During the spray drying, a low abso- lute humidity of the air should be maintained, and it is very important to keep the exit-air temperature below 100℃ to avoid decomposition.