Leaching of phosphorus from incinerated sewage sludge ash by means of acid extraction followed by adsorption on orange waste gel

Ashes from sewage sludge incineration have a high phosphorus content, approximately 8% （W/W）, which indicates a potential resource of the limiting nutrient. Incineration of sewage sludge with subsequent recovery of phosphorus is a relatively new sludge treatment technique. In this article, the leaching of phosphorus by using sulfuric acid as well as hydrochloric acid by means of several batch experiments was presented. At the same time a selective recovery of phosphorus by adsorption was also discussed. The effects of acid concentration, temperature and time on extraction were studied. The phosphorus leaching increased with the increase in acid concentration and temperature. Kinetic studies showed that the complete leaching of phosphorus took place in less than 4 h. Selective adsorption of phosphorus by using orange waste gel provided a hint for recovery of this natural resource, which eventually could meet the ever-increasing requirement for phosphorus. The overall results indicated that the incinerated sewage sludge ash can be treated with acid to efficiently recover phosphorus and thus can be considered a potentially renewable source of phosphorus.

Clumped Isotope Analysis of Calcite and Dolomite Mixtures Using Selective Acid Extraction

Acid extraction methods have been used in the last half century to selectively extract the CO_(2)produced from different carbonate minerals in mixed samples.However,these methods are often time-consuming and labor intensive.Their application to clumped isotope(Δ47)analysis has not been demonstrated.We propose here an acid extraction method with phosphoric acid for bulk stable and clumped isotope analysis that treats mixtures of calcite and dolomite the same regardless of the proportional composition.CO_(2)evolved from calcite is extracted by allowing a reaction with phosphoric acid to proceed for 10 min at 50℃.We then extract CO_(2)evolved from dolomite by rapid ramping the acid temperature from 50 to 90℃and allowing the reaction to complete.The experimental results show that our method yields accurate calcite and dolomiteΔ_(47)values from mixed samples under different proportional compositions.Our method also displays equal or higher accuracy for calciteδ^(13)C and dolomiteδ^(13)C andδ^(18)O values from mixtures when compared to previous studies.Our approach exhibits higher sample throughput than previous methods,is adequate for clumped isotopic analysis and simplifies the reaction progression from over 24 h to less than 2 h,while maintaining relatively high isotopic obtaining accuracy.It yet poorly resolves calciteδ18O values,as found with previous methods.

Synergistic extraction of rare earths by mixture of HDEHP and HEH/EHP in sulfuric acid medium

The extraction of RE（Ⅲ） （RE=La, Nd, Sm, Gd） in sulfuric acid medium using the mixture of HDEHP（H2B2） and HEH/EHP（H2L2） was investigated. The synergistic enhancement coefficient（R） was calculated for La （1.96）, Nd（3.52）, Sm（5.96）, and Gd（5.71）, respectively, at pH=2.0, and it was seen that the R increased with the increase of aqueous quilibrium pH. The configuration of the extracted complexes was considered to be RE（SOa）xH2x（HB2）3 with HDEHP, RE（SOa）xH2x（HL2）3 with HEH/EHP, and RE（HB2）2（HL2） with their mixture as the extractant with the slope method. The equilibrium constants and stability constants were calculated. A cation exchange mechanism was proposed as well.

Linear Free Energy Relationships in Extraction of Rare Earths by Acidic Organophosphorus Extractants

The correlation relationships of apparent extraction equilibrium constant (1gK(ex)) with the electronic effect parameter( Sigma sigma(Phi)) and the steric effect parameter ( Sigma upsilon ) of the substituents in extractant molecules are investigated by linear regression analysis in the extraction of rare earths by various classes and structures of monoacidic organophosphorus extractants. The results indicate that in Linear free energy relationship formula 1gK(ex) = rho Sigma sigma(Phi) + psi Sigma upsilon + h generally follows for this kind of extraction systems. Accordingly, the quantitative structure-behaviour relationships of extractants are discussed. These relationships can be preliminarily applied to predict the 1gK(ex) values of rare earth extraction with definite structures of this class of extractants, and thus can provide some directions for the design of new RE extractants.

Extraction Separation of Scandium，Iron and Lutetium with Isopropyl Phosphonic Acid Mono（1－hexyl－4－ethyl）OctylEster

The extraction and stripping of scandium from its sulfate solutions by isopropyl phosphonic acid mono (1-hexyl-4-ethyl) octyl ester (PT-2, HL) diluted with n-hexane are reported. A high efficiency of separation between scandium, iron and lutetium can be achieved by controlling aqueous acidity. Different mechanisms of Sc3+ with PT-2 in various acid range have been proposed.At lower aqueous acidity, it is a cation exchange reaction, while at higher acidity. a solvation reaction was ascertained. Its IR and NMR spectra have been discussed. The effect of temperature on extraction of Sc3+ was observed and thermodynamic functions were calculated.

Deep eutectic solvents and alkaline extraction of protein from seabuckthorn seed meal: a comparison study

Seabuckthorn seed meal(SSM) is a waste of oil extraction industry that rich in protein. In order to seek suitable protein extraction method, three different deep eutectic solvents(DESs)(including choline chlorideglycerol, choline chloride-oxalic acid and choline chloride-urea) were developed for extracting protein from SSM and compared with alkaline. Result indicated that alkaline could effectively extract 56.9% protein from SSM and its protein content was 73.1%, higher than DES at 31.0%-41.4% and 64.3%-67.5%, respectively. However, compared to alkali, DES led to a product with less β-sheet, more β-turn, more essential amino acids, higher total amino acid content, especially choline chloride-urea which extracted protein showing an integrated and similar protein weight distribution compared to SSM. Also, this protein extracted chloride-urea showed a highest digestibility in vitro(by pepsin)(54.2%). These results indicated that choline chloride-urea extraction is better than alkaline extraction for SSM.

Antibacterial and Antioxidant Effects of Three Chlorogenic Acid Extracts

[Objectives] To study the antibacterial and antioxidant effects of chlorogenic acid extracts of Gynura procumbens,Lonicera japonica,and Eucommia ulmoides leaves,and provide a reference for their usage as natural food preservatives and antioxidants. [Methods]The disc diffusion method was applied to study the antibacterial activity of chlorogenic acid extracts of G. procumbens,L. japonica,and E. ulmoides leaves against several common pathogens. In the antioxidant effects,study was carried out on the anti-lipid peroxidation,reducing capacity,and DPPH free radical scavenging capacity of chlorogenic acid extracts of G. procumbens,L. japonica,and E. ulmoides leaves,respectively.[Results]Three chlorogenic acid extracts had strong inhibitory effects on bacteria,especially the inhibition on Staphylococcus aureus. At the concentration of 100 mg/m L,the bacteriostatic ring of chlorogenic acid extracts of G. procumbens,L. japonica,and E. ulmoides leaves reached 21. 4,23. 6 and 24. 7 mm respectively. Besides,these chlorogenic acid extracts had significant inhibitory effect on Escherichia coli and Salmonella,but the inhibitory effect on the yeast was not obvious; the antibacterial intensity of antibacterial compounds was chlorogenic acid extracts of E. ulmoides > chlorogenic acid extracts of L. japonica > chlorogenic acid extracts of G. procumbens. Among these three chlorogenic acid extracts,the chlorogenic acid extracts of E. ulmoides had higher anti-lipid peroxidation,reducing capacity,and DPPH free radical scavenging capacity than other two chlorogenic acid extracts. [Conclusions] This paper reveals that among chlorogenic acid extracts of G. procumbens,L. japonica,and E. ulmoides leaves,the chlorogenic acid extracts of E. ulmoides leaves have a stronger antibacterial activity and antioxidant activity.

Study on the Process for Removal of Samarium from NdCl_3 Solution by Solvent Extraction with DEHPA

The process for removal of samarium from NdCl_3 solution containing a little samarium by solvent extrac-tion with unsaponated Di (2-ethyl hexyl) orthosphoric acid (DEHPA) at acidic range is reported. The in-dustrial experiments have been completed on a production line of 150 t Nd_2O_3 per annum in the Baotou ThirdRare Earth Factory. As a result of 9 step counter current extraction , Sm_2 O_3 content in Nd_2 O_3 drops down to0. 08 % from 0. 5% , the purity of neodymium oxide is over 99. 5% and the direct recovery of Nd_2O_3 is 92%～ 93% .

Vanadium(Ⅳ)solvent extraction enhancement in high acidity using di-(2-ethylhexyl)phosphoric acid with[Cl^(-)]present:an experimental and theoretical study

Separation of vanadium from black shale leaching solution at low pH is very meaningful,which can effectively avoid the generation of alkali neutralization slag and the resulting vanadium loss.In this study,coordination mechanism of vanadium in acid leaching solution at low pH was investigated with the intervention of chloride ions.Under the conditions of pH 0.8,di-(2-ethylhexyl)phosphoric acid concentration of 20%,phase ratio of 1:2,and extraction time of 8 min,the vanadium extraction could reach 80.00%.The Fourier transform infrared and electrospray ionization results reveal that,despite the fact that the chloride ion in the leachate could significantly promote vanadium extraction,the chloride ion does not enter the organic phase,indicating an intriguing phenomenon.Among Cl^(-)-V,SO_(4)^(2-)-V,and H_(2)O-V,the V-Cl bond is longer and the potential difference between coordinate ions and vanadium is smaller.Therefore,Vo^(2+)gets easily desorbed with chloride ions and enter the organic phase.At the same time,the hydrogen ions of di-(2-ethylhexyl)phosphoric acid also enter the water phase more easily,which reduces the pH required for the extraction reaction.

Alumina Recovery from Kaolin with Mineral Impurities

The alumina recovery from low grade kaolin （K-JS） treated through thermal and mechanical methods was investigated. High grade kaolin （K-SX） was used as comparison. The optimum calcination temperatures for K-JS and K-SX were both 600 ℃, which resulted in 89.34wt% of alumina extraction from K-JS and 83.37wt% from K-SX. With the increase in calcination temperature, the chemical reactivity of calcined K-JS and K-SX to acid decreased. Mechanical treatment was much more effective in increasing the alumina extraction from activated kaolin. Around 99wt% of alumina was extracted from K-JS ground for 10 hours and 95wt% of alumina was extracted from K-SX ground for 20 hours. The IR results showed that the substitute of A1 for Si occurred in calcined K-SX, however, the impurities in K-JS decreased this substitute. More alumina could be extracted from low grade kaolin than that from high grade kaolin under identical thermal or mechanical conditions.

Separation of Indium and Iron from Dilute Sulphate Solutions with a Phosphorous Mixer Extractant

The phosphorous mixer introduced could replace D2EHPA as an extractant applied in the extraction of indium. The extraction properties of the phosphorous mixer were studied. The influences of extractant concentration, organic/aqueous (O/A) phase ratio, equilibrium time, and pH value of the feed solutions on the extraction of indium, and separation of indium-iron were investigated experimentally. Under the best operating conditions, more than 98% of indium. was extracted through two-stage counter-current extraction. The optimizing condition of indium extraction is determined as follows: O/A = 1 : (9-12) in volume ratio; 30% PPD in sulphonated kerosene; pH of the feed, about 0.6; equilibrium time, 3-5 min. The extractant has good reusing and anti-aging properties.

Characteristic of synergistic extraction of oxalic acid with system from rare earth metallurgical wastewater

Large amount of high concentration acidic wastewater would be produced in the conversion process of chloride rare earth into oxide rare earth. It was a mixed solution of oxalic acid and hydrochloric acid, so the recycling use was very difficult. The method of liquid-liquid extraction was proposed in this paper to achieve wastewater treatment and reclamation. The mechanism of extraction of oxalic acid from the wastewater with the systems of 50% TOB+45% kerosene and 5% 2-ethyl hexanol was investigated. The composition and structure of the extracted species and the establishment of the mathematical model of the oxalic acid extraction were determined by the use of saturation method, equimolar series method. The results showed that extraction of oxalic acid by TOB was a neutral association extraction, oxalic acid existed mainly in a molecular form in the organic phase, and the extraction combination ratio was 2:1. The duality extraction system composed of extractant TOB and TOC had synergistic extraction effect on oxalic acid and chlorhydric acid, and the extraction distribution ratio was improved greatly. The optimum volume fraction of TOB was 0.6-0.8.

Extraction and separation of heavy rare earths from chloride medium byα-aminophosphonic acid HEHAPP

The extraction and separation of heavy rare earths（REs） using newly synthesized a-aminophosphonic acid extractant 2-ethylhexyl-3-（2-ethylhexylamino）pentan-3-yl phosphonic acid（HEHAPP, HA） in nheptane were investigated from chloride medium. The extraction stoichiometries of lanthanum, gadolinium, yttrium and lutetium are determined to be REA3 by the slope analysis method. The favorable separation factors of adjacent heavy REs（Ⅲ）,i.e. β（Y/Ho）, β（Er/Y）,β（Tm/Er）,β（Yb/Tm） and β（Lu/Yb）, are determined to be1.87,1.36, 3.21,3.22 and 1.93, respectively, when extracted from a binary system at proper condition. The loading capacities of HA for Ho, Er, Yb and Lu increase in the order Ho 〈 Er 〈 Yb 〈 Lu with the values being 0.201, 0.205, 0.216 and 0.229 mol/L, respectively. So HA would be a potential extractant for the separation of heavy REs（Ⅲ）. Among inorganic acids such as H2 SO4, HNO3 and HCl, HCl is tested to be the most effective stripping agent.

Solvent extraction and separation of light rare earth elements (La, Pr and Nd) in the presence of lactic acid as a complexing agent by Cyanex 272 in kerosene and the effect of citric acid,acetic acid and Titriplex Ⅲ as auxiliary agents

At present, the use of rare earth elements（REEs） has become an inevitable necessity in many modern industries. In general, liquid extraction is the best commercial method for extracting REEs due to its ability to control high volumes of liquids with electrical load. With the aim of improving a separation technology that would be superior to the existing extraction systems, the extraction behaviors of La（Ⅲ）,Pr（Ⅲ）, and Nd（Ⅲ） from an HCI medium with Cyanex 272 in the presence of the complexing agent lactic acid（HLac） and auxiliary agents citric acid（H3 Cit）, acetic acid（HAc）, and Titriplex Ⅲ have been reported.The effect of pH and lactic acid concentration has been examined. The use of lactic acid as a complexing agent leading to a high extraction of REEs with Cyanex 272 at pH = 5 was compared with systems without lactic acid. The results show that the use of acetic acid along with lactic acid leads to an increase in the extraction percentage of LREEs. While use of citric acid and Titriplex Ⅲ reduces the extraction percentage of LREEs. Finally, the presence of Titriplex Ⅲ together with lactic acid could lead to an increase in the separation factor of Pr and Nd.

Multi-walled carbon nanotube as a solid phase extraction adsorbent for analysis of indole-3-butyric acid and 1-naphthylacetic acid in plant samples

In this work, a new sample pretreatment method prior to HPLC separations was developed for the determination of auxins in plant samples, Owing to its large surface area and high adsorption capacity, multi-walled carbon nanotube （MWCNT） was chosen as the adsorbent for the extraction of auxins from plant samples. In this study, two important auxins were selected as model analytes, namely indole-3- butyric acid （IBA） and 1-naphthylacetic acid （NAA）. They could be extracted and concentrated due to their π-π stacking interactions with MWCNT. Then HPLC-UV was introduced to detect IBA and NAA after sample pretreatment. Factors that may affect the enrichment efficiency were investigated and optimized. Comparative studies showed that MWCNT was superior to CI 8 for the extraction of the two analytes. Validation experiments showed that the optimized method had good linearity （0.9998 and 0.9960）, high recovery （81.4%-85.4%）, and low detection limits （0.0030 mg/L and 0.0012 mg/L）. The results indicated that the novel method had advantages of convenience, good sensitivity, high efficiency, and it was feasible for the determination of auxins in plant samples.

Seed priming improves early seedling vigor, growth and productivity of spring maize

Potential of seed priming treatments in improving the performance of early planted maize was evaluated against timely planting. Seeds of maize hybrid FH-810 were soaked in water (hydropriming), CaCl2 (2.2%, osmopriming), moringa leaf extracts (MLE 3.3%, osmopriming) and salicylic acid (SA, 50 mg L–1, hormonal priming) each for 18 h. Untreated and hydroprimed seeds were taken as control. Seeds primed with SA took less time in emergence and had high vigor in early planted maize. Amongst treatments, hormonal priming, reduced the electrical conductivity, increased the leaf relative and chlorophyl contents fol owed by osmopriming with CaCl2 at seedling stage. Likewise, plant height, grain rows and 1 000-grain weight, grain and biological yield and harvest index were also improved by seed priming;however hormonal priming and osmopriming with MLE were more effective in this regard. Improved yield performance by hormonal priming or osmopriming with MLE in early planting primarily owed to increased leaf area index, crop growth and net assimilation rates, and maintenance of green leaf area at maturity. In conclusion, osmopriming with MLE and hormonal priming with SA were the most economical treatments in improving productivity of early planted spring maize through stimulation of early seedling growth at low temperature.

SOLVENT EXTRACTION OF LANTHANIDES BY 2-ETHYLHEXYLPHOSPHONIC ACID MONO-2-ETHYLHEXYL ESTER

The chemistry of extraction of lanthanide and yttrium by 2-ethylhexylphosphonic acidmono-2-ethylhexyl ester in n-dodecane from nitric acid is described. By M W determination, NMR and the slope method, the extraction reaction is studied.Based upon elementery analyses, IR, NMR as well as MW determination, the compositions ofthe complexes formed with La（NO3）3 and Nd（NO3）3 are studied. Both the standard enthalprchanges（-△H°） and the relative free energy and entropy changes （-△Zr°）（△SPr°）of the ex-.traction reaction are also estimated. The regularity of the variations of Kea（concentrationequilibrium constant）, -△AZr° and △Sr°reveals the tetrad effect. The average separationfactor of the adjacent lanthanides is calculated to be as high as 3.04.

Effects of organic acids on the leaching process of ion-adsorption type rare earth ore

To examine the activation of organic acids on the leaching process of ion-adsorption type rare earth ore（IRE-ore）, the leaching behavior of rare earth（RE） and zeta potential of IRE-ore were investigated in the absence and presence of carboxylic acids. The results show that all the tested organic acids（acetic acid,malonic acid, citric acid, tartaric acid, succinic acid, and malic acid） can promote RE extraction. At relatively high concentrations of organic acids, the activation efficiency of organic acids on RE extraction is generally consistent with their complexation ability; whereas at their low concentrations, the change of zeta potential on the IRE-ore surface with organic acid concentration and p H has a close association with RE extraction, which indicates that organic acids can impact the surface electrical property of IREore via their adsorption/desorption, and thereby increase/decrease the affinity of RE ions to IRE-ore.Therefore the influence of organic acids on the IRE-ore surface electrical property also plays an important role in RE extraction in addition to their complexation with RE ions.

Effects of eggshell addition on calcium-deficient acid soils contaminated with heavy metals

In this study, effects of water conditions （flooded, wet, or dry） and eggshell dosages （0, 0.1, 1.0, and 10.0 g/kg soil, respectively） on pH variation, content of unavailable state of heavy metals, form of heavy metals, and available nutritious element calcium （Ca） in acid soils contaminated with heavy metals were investigated, respectively. The soil samples were continuously cultivated indoors and analyzed by toxicity characteristic leaching procedure and community bureau of reference （BCR） sequential extraction procedure. The results showed that the addition of eggshell could effectively improve the pH of acid soil and increase it to neutral level. Moreover, the contents of unavailable state of heavy metals Cu, Zn, and Cd increased significantly. Furthermore, when the soil was cultivated under the flooded condition with 1.0 g/kg eggshell, the unavailable state ofCu, Zn, and Cd increased the most, and these heavy metals were transformed into residual state. On the other hand, the amount of available state of Ca increased to 432.19 from 73.34 mg/kg with the addition of 1.0 g/kg eggshell, which indicated that the addition of eggshell dramatically improved the available state of Ca. Therefore, eggshell could ameliorate the soil environment as it led to the decrease of available heavy metals and improvement of fertilization effectively. In a word, this study indicates that the addition of eggshell would be a new potential method for remediation of acid field soils contaminated with heavy metals.

Universal probe with oriented antibody to improve the immunochromatographic assay of lead ions in Procambarus clarkii

Objectives:Based on the information from the random inspection of foods by the China Food and Drug Administration in 2022,the contamin-ation levels of lead ions are high in many edible products.Traditional methods of detecting lead ions cannot meet the requirements of on-site analysis of food due to the need for large equipment.The immunochromatographic assay(iCA)is an effective,rapid,on-site analytical technique for determining lead ions in foods.However,the performance of ICA based on the traditional probe(AuNP-mAb)is limited by ignoring the influ-ence of theantibody orientation.Materials and Methods:In this study,we developed an efficient technology for constructing a universal probe(AuNP-PrA-mAb)based on the oriented immobilization of antibody.The performance of ICA was largely improved due to specific binding of the Fc region of the antibody with recombinant protein A(PrA)on the surface of a gold nanoparticle(AuNP).The ICA based on a universal probe was applied for the qualitative and quantitative detection of lead ions in Procambarus clarki within 30 min.Meanwhile,a simple and fast pretreatment method based on dilute acid extraction was developed forpretreating thePclarkii containing leadions.Results:The visual limit of detection and the scanning limit of quantization of the developed iCA strip for lead ions were O.5 ng/mL and 0.28 ng/mL,respectively.The sensitivity of ICA based on universal probe was 10-fold higher than that of the ICA using traditional probe.Furthermore,the detection results had no obvious difference between the ICA and ICP-MS with t-test statistical method.Conclusions:The developed ICA based on a universal probe presented broad application prospects in detecting contaminants in foods.