Dibutyl Phosphate Research Articles

Organophosphate esters and their metabolites in eggs from Vietnam

ABSTRACT Data on the occurrence of organophosphate tri-esters (tri-OPEs) and their metabolites (di-OPEs) in hen’s eggs are scarce. Therefore, 200 egg samples were gathered in 2023 in Hanoi, Vietnam and analysed by UHPLC-Q-Exactive HRMS. The majority of these compounds were detected, with tris(2-ethylhexyl) phosphate (0.10–2.7 ng/g wet weight (ww)) and trihexyl phosphate (0.08–2.3 ng/g ww) being the most prevalent tri-OPEs. Significant differences in tri-OPE profiles were observed in egg samples from battery-cage and free-range farming (p < .05). Despite egg levels ranging from 0.05 to 11.2 ng/g ww, Σdi-OPE accumulation in yolk and egg white was not significantly different in (p > .05). Among di-OPEs, dibutyl phosphate was found at the highest levels in the egg white, while bis(2-ethylhexyl) phosphate had the highest levels in yolk. There was no carcinogenic human health risk associated with OPEs in eggs (HQs <1).

Biodegradation of tri-butyl phosphate by Trametes versicolor and its application in a trickle bed reactor under non-sterile conditions

Tri-butyl phosphate (TBP) is a widely used organophosphate flame retardant. However, it is also regarded as emerging contaminant due to its various toxic effects and poor removal by conventional wastewater treatment. In present study, we investigated the degradation of TBP (10 mg/L) by the white rot fungus Trametes versicolor in both laboratory conditions and a trickle bed reactor (TBR) under non-sterile conditions. The removal yield reached 98 % after 3 days, during which the intracellular enzymatic system cytochrome P450 was involved. Four transformation products (TPs) were identified, namely dibutyl 3-hydroxybutyl phosphate, dibutyl phosphate, butyl 3-hydroxybutyl phosphate and butyl dihydrogen phosphate, which allowed us to propose a degradation pathway where hydroxylation and hydrolysis made considerable contribution. TBP treatment in the TBR with T. versicolor immobilized on wood chips operating in sequential batch mode with 10 cycles of 3 days reached average removals higher than 93 %, demonstrating the potential for practical application. Despite similar removal rates in heat-killed and abiotic controls (89 % and 97 %, respectively), global mass balance analysis indicated 86 %, 64 %, and 86 % removal by degradation in the fungal, heat-killed, and abiotic controls, respectively. Analysis of the microbial assemblage in solid phase suggested that the established bacterial populations displayed a synergistic effect with immobilized fungus. This study is the first to report on TBP degradation by T. versicolor in a TBR under non-sterile conditions, suggesting that this method could be a viable option for large-scale environmental applications.

Construction of Phenytoin Selective Electrodes and Its Application to Pharmaceutical Preparation

Phenytoin selective electrodes were constructed based on penytoin-phosphotungstate (Ph-PT) complex with different plasticizers; di-butyl phosphate (DBP), tri-butyl phosphate (TBP), di-butyl phthalate (DBPH),and o-nitro phenyl octyl ether (NPOE) phthalate. The electrodes based on DBPH, ONPOE plasticizers gave Narnistain slope which are, 56.4 and 55.3mV/decade with detection limit of 1.9x10-5 M , 1.8x10-5 and concentration range 10-1 to 10-4 M and pH range 3.0 – 8.0. The electrodes based on TBP and DBP showed non-Nernistain slopes, 40.2,40.5 mV/decade for both plasticizers. Interfering of some cations was investigated and shows no interfering with electrodes response. Potentiometric methods were used for measuring phenytion in pharmaceutical drugs (tablets) and the electrode based on DBPH was used for determination. The recovery obtained from measuring was in good agreements with that given in British Pharmacopeias.

A Bigger Big Picture: Insights on Environmental Chemicals and Dyslipidemia through Combined "Omic" Analyses.

Exposures to chemicals, including phthalates, triphenyl phosphate, and dibutyl phosphate, have been associated with increased levels of lipid markers, such as elevated low-density lipoprotein.

Urinary Concentrations of Organophosphate Flame-Retardant Metabolites in the US Population

Organophosphate flame retardants (OPFRs) are an important group of pollutants associated with endocrine disorders, cancer, and nephrotoxicity. However, temporal trends in OPFR metabolite concentrations remain understudied. To examine changes in urinary concentrations of OPFR metabolites among US children, youths, and adults from 2011 to 2020, and to evaluate whether sociodemographic factors were associated with variations in temporal trends. This population-based cross-sectional study used data from 4 US National Health and Nutrition Examination Survey (NHANES) cycles (2011-2012, 2013-2014, 2015-2016, and 2017-2020 [to March 2020 before the COVID-19 pandemic]). The study included children and youths (aged 6-19 years) and adults (aged ≥20 years) with valid urinary concentrations of the following OPFR metabolites: bis(2-chloroethyl) phosphate (BCEtP), bis(1-chloro-2-propyl) phosphate (BCPP), diphenyl phosphate (DPhP), and dibutyl phosphate (DBuP). Data analysis was performed between February and May 2024. Calendar year and key sociodemographic subgroups (age, race and ethnicity, sex, educational attainment, and poverty-to-income ratio). The main outcome was urinary concentrations of OPFR metabolites among children, youths, and adults. Survey-weighted linear regression models were applied to estimate trends. The study population of 10 549 NHANES participants included 3154 children and youths (mean [SE] age, 12.5 [0.1] years; 51.2% were male) and 7395 adults (mean [SE] age, 47.8 [0.4] years; 52.0% were women). Among children and youths, mean (95% CI) BCEtP concentrations decreased from 0.68 (0.60-0.77) μg/L in 2011-2012 to 0.41 (0.37-0.45) μg/L in 2017-2020 (P for trend < .001). Among adults, mean (95% CI) BCEtP concentrations decreased from 0.43 (0.37-0.50) μg/L in 2011-2012 to 0.29 (0.27-0.33) μg/L in 2017-2020 (P for trend < .001), and mean BCPP concentrations decreased from 0.15 (0.14-0.17) μg/L to 0.13 (0.12-0.14) μg/L (P for trend = .002). Parent level of educational attainment was associated with concentrations of BCPP and BCEtP among children and youths; however, no significant differences among adults were observed. This study identified variations in temporal trends in urinary concentrations of OPFR metabolites among the US population from 2011 to 2020. In addition, substantial disparities in exposure levels persisted among children with different levels of parent educational attainment. These findings suggest that policy makers should consider socioeconomic factors to further reduce OPFR exposure and promote equity, ensuring a safe living environment for all individuals.

A versatile ionic liquid enables epoxy resin with excellent fire safety and mechanical properties but ultra-low loading

The emergence of ionic liquids provides an effective way to construct new advanced multifunctional epoxy resin (EP) composites with excellent fire retardancy and mechanical properties. In this study, 1-butyl-3-methylimidazolium dibutyl phosphate (BDBP) was synthesized via a facile strategy and then incorporated into the EP matrix. The results showed that ultra-low loading of BDBP (1 wt%) enabled EP composite to achieve a V-0 rating (3.2 mm) in the UL-94 test. When increasing the loading to 4 wt%, the limiting oxygen index (LOI) of EP/BDBP4 composites was improved to 31.9 %. Meanwhile, the peak heat release rate (PHRR), total heat release (THR), and total smoke production (TSP) significantly decreased by 48.1 %, 21.9 %, and 13.5 %, respectively, compared to neat EP. Moreover, the presence of BDBP increased the tensile strength of EP/BDBP2 by more than 7 %, while all EP/BDBP composites maintained high transparency. In summary, this work provides a feasible and low-cost idea for constructing multifunctional EP composites, paving the way for their applications in aerospace, wind turbines, and electronic and electrical fields.

Associations of prenatal exposure to individual and mixed organophosphate esters with ADHD symptom trajectories in preschool children: The modifying effects of maternal Vitamin D

BackgroundOrganophosphate esters (OPEs) are a class of environmental chemicals with endocrine-disrupting properties. Epidemiologic studies have demonstrated that prenatal OPEs exposure is associated with neurodevelopmental disorders in offspring. However, studies assessing the effects of prenatal OPEs exposure on the dynamic changes in attention deficit hyperactivity disorder (ADHD) symptoms in preschoolers are scarce. Since vitamin D has been demonstrated to have a "neuroprotective" effect, the modifying effects of maternal vitamin D were estimated. MethodsThe present study included 2410 pregnant women from the Ma'anshan Birth Cohort. The levels of OPEs in the mothers' urine were examined in the three trimesters. The Chinese version of the Conners Abbreviated Symptom Questionnaire was used to examine preschoolers' ADHD symptoms at 3, 5, and 6 years of age. ADHD symptom trajectories were fitted via group-based trajectory modeling. We used multinomial logistic regression, Bayesian kernel machine regression, quantile-based g-computation, and generalized linear models to assess individual and mixed relationships between OPEs during pregnancy and preschoolers' ADHD symptoms and trajectories. ResultsPreschoolers' ADHD symptom scores were fitted to 3 trajectories, including the low-score, moderate-score, and high-score groups. First-trimester dibutyl phosphate (DBP), second-trimester bis(2-butoxyethyl) phosphate (BBOEP), and third-trimester diphenyl phosphate (DPHP) were associated with an increased risk in the high-score group (p < 0.05). BBOEP in the third trimester was associated with decreased risk in the moderate-score group (OR = 0.89, 95% CI: 0.79, 1.00). For mothers with 25(OH)D deficiency, a positive relationship was observed between OPEs during pregnancy and symptom trajectories. Our results did not reveal any mixed effects of OPEs on ADHD symptom trajectories. ConclusionPrenatal exposure to OPEs had heterogeneous associations with ADHD symptom trajectories in preschoolers. Additionally, the effect of individual OPEs on symptom trajectories was intensified by vitamin D deficiency.

Influence of Di-n-butyl Phosphoric Acid on Cerium Redox and Speciation in Tri-n-butyl Phosphate.

The effects of simulated radiolytic degradation of tri-n-butyl phosphate (TBP) on the chemical speciation of cerium were studied by spectrophotometry and electrochemistry of TBP solutions containing increasing amounts of di-n-butyl phosphoric acid (HDBP), a common degradation product of TBP. Tetravalent cerium was found to exchange coordinated nitrate for the dibutyl phosphate anion, forming dinuclear complexes of the formula (CeOCe)(NO3)(6-d)(DBP)d·3TBP (d = 0-3). Compared to Ce(IV), Ce(III) was complexed less strongly by HDBP in TBP, but HDBP displaced both nitrate and TBP to form the series of mononuclear complexes Ce(NO3)(3-d)(HDBP·DBP)d·(3-d)TBP (d = 0-3). Dibutyl phosphate coordination caused large negative shifts in the Ce(IV/III) reduction potential in TBP, indicating a strong stabilization of the tetravalent state. Electrochemical investigation of the reduction of Ce(IV) in TBP revealed it to be a two-electron process in accordance with the dinuclear nature of the organic-phase Ce(IV) complexes. The diffusion coefficients of the d = 0 dinuclear Ce(IV)-nitrate-TBP complex and mononuclear Ce(III)-nitrate-TBP complex in TBP equilibrated with 7 M HNO3 were determined to be (1.16 ± 0.06) × 10-7 cm2/s and (1.9 ± 0.4) × 10-7 cm2/s, respectively, which also is consistent with the larger molecular volume of the dinuclear Ce(IV) complexes.

Estimated daily intake and cumulative risk assessment of organophosphate esters and associations with DNA damage among e-waste workers in Hong Kong

Organophosphate esters (OPEs) are extensively used as additives in various products, including electronic equipment, which becomes e-waste when obsolete. Nevertheless, no study has evaluated OPEs exposure levels and the related health risks among e-waste workers in Hong Kong. Therefore, 201 first-spot morning urine samples were collected from 101 e-waste workers and 100 office workers to compare eight urinary OPE metabolites (mOPEs) levels in these groups. The concentrations of six mOPEs were similar in e-waste workers and office workers, except for significantly higher levels of diphenyl phosphate (DPHP) in e-waste workers and bis(1-chloro-2propyl) phosphate (BCIPP) in office workers. Spearman correlation analysis showed that most non-chlorinated mOPEs were correlated with each other in e-waste workers (i.e., nine out of ten pairs, including di-p-cresyl phosphate (DpCP) and di-o-cresyl phosphate (DoCP), DpCP and bis(2-butoxyethyl) phosphate (BBOEP), DpCP and DPHP, DpCP and dibutyl phosphate (DBP), DoCP and BBOEP, DoCP and DPHP, DoCP and DBP, BBOEP and DPHP, DPHP and DBP), indicating that handling e-waste could be the exposure source of specific OPEs. The median values of estimated daily intake (EDI) and hazard quotient (HQ) suggested that the health risks from OPEs exposures were under the recommended thresholds. However, linear regression models, Quantile g-computation, and Bayesian kernel machine regression found that urinary mOPEs elevated 8-hydroxy-2-deoxyguanosine (8-OhdG) levels individually or as a mixture, in which DPHP contributed prominently. In conclusion, although e-waste might not elevate the internal OPEs levels among the participating Hong Kong e-waste workers, attention should be paid to the potential DNA damage stimulated by OPEs under the currently recommended thresholds.

Cationic UV-curing of bio-based epoxidized castor oil vitrimers with electrically conductive properties

The growing appeal of carbon nanotube composites in the contemporary market derives from their exceptional thermal and chemical stability, coupled with electrical conductivity. In this study, we combined these salient features with a biobased epoxy matrix having vitrimeric properties, hence being reprocessable and resheapable, to obtain a biobased conductive coating. Epoxidised castor oil (ECO) was chosen as a monomer precursor for the straightforward synthesis. The synthesis relied on a cationic UV-curing process, embedding the conductive carbon nanotubes in the matrix. Photo DSC and transmission FTIR analysis were conducted to determine the final conversion of the epoxy rings in the cationic photocuring process. Thermo-mechanical properties were evaluated by tensile tests, and DMTA. Thermal stability was assessed by TGA. Dielectric spectroscopy confirmed increased electrical conductivity in the presence of increasing CNT content, reaching a percolation threshold at 0.5 phr of CNTs. Vitrimeric properties were proved by stress relaxation experiments, and the UV-cured composite underwent a thermo-activated transesterification reaction starting from 70 °C, catalysed by dibutyl phosphate. Overall, the ECO-CNT composite showed high thermal resistance (up to 400 °C) electrical conductivity with 0.5 phr CNT concentration, and vitrimeric properties. The study can be, therefore, considered a promising starting point to obtain sustainable biobased and electrically conductive vitrimers.

Insight into the interaction between zirconium dibutyl phosphate complex and diluents: An experimental and computational study

In solvent extraction processes, there are challenges caused by the formation of the third phase or interfacial precipitation. The branched alkanes have been used as diluents to disrupt the third-phase formation, while there is little study about the effect of diluents on the appearance of precipitation. Here, we report the inhibiting effect of the novel hyperbranched alkane diluent (HAD) on the formation of zirconium-dibutyl phosphate (Zr-DBP) precipitation and investigate the formation mechanism by the density functional theory (DFT) theory. The extraction experiments show that HAD as the diluent has a remarkable inhibiting ability to form Zr-DBP precipitation, compared with n-dodecane and kerosene. The spectra show no noticeable difference in the composition and structures of the precipitations formed in the three diluents. The energetics from the DFT calculations suggest the P-OH and P=O ligands on one HDBP molecule can bridge two Zr-DBP complexes into a dimer and then aggregate into the precipitation. Besides, the interactions between diluent-diluent molecules play a significant role in precipitation formation. The straight-chain n-dodecanes have a strong intermolecular dispersion force and tend to attract each other but not the Zr-DBP complex. However, the branched alkanes with weak intermolecular interactions have a better dispersive capacity for Zr-DBP complexes, due to the much higher dispersion force of diluent-complex interaction than that of the diluent-diluent interaction. This work provides a new insight into the formation of interfacial crud from the interactions between solutes and diluents of the organic phase in solvent extraction.

Soil microbial responses to multipollutant exposures in megacity's parks of Beijing

Soil life revolves around microorganisms that are crucial for soil ecosystems and health. In megacities, the combined exposure of multiple pollutants exerts a significant impact on the structures and functions of soil microorganisms; however, there is a lack of empirical studies on this topic. Hence, we conducted a study including urban parks in Beijing, China. The results indicate that bacteria were abundant in the soils of Beijing parks, showing the same dominant groups but different rare groups. The dominant groups included Actinobacteria and Proteobacteria. Candidate phyla radiation bacteria, a large evolutionary radiation of bacterial lineages whose members remain mostly uncultivated, were the main specialists. Under the combined exposure of multiple pollutants, the structures of soil microbial communities in different parks were similar. Community change due to pollutants (31%) was greater than that due to natural factors (2.4%). Among multipollutants, organophosphate esters, led by dibutyl phosphate, had the highest influence on microbial abundance and distribution. An increase in dibutyl phosphate concentration decreased the abundance of Firmicutes, while the abundance of Synergistota was increased. The interactions among pollutants affecting the bacteria were different. Bis(2-chloroethyl) phosphate, nickel and benzo[g,h,i]perylene influenced microorganisms by working with organophosphate esters. High-molecular-weight polycyclic aromatic hydrocarbons, such as benzo[a]pyrene and benzo[g,h,i]perylene, mainly acted on the functional genes and thus affected multiple biogeochemical cycles. Benzo[a]anthracene, bis(2-chloroethyl) phosphate, and arsenic were the primary pollutants affecting metabolic pathways. Our research helps to better understand the impacts of urban environmental pollution on soil microorganisms.

Precision Cellulose from Living Cationic Polymerization of Glucose 1,2,4-Orthopivalates.

Cellulose serves as a sustainable biomaterial for a wide range of applications in biotechnology and materials science. While chemical and enzymatic glycan assembly methods have been developed to access modest quantities of synthetic cellulose for structure-property studies, chemical polymerization strategies for scalable and well-controlled syntheses of cellulose remain underdeveloped. Here, we report the synthesis of precision cellulose via living cationic ring-opening polymerization (CROP) of glucose 1,2,4-orthopivalates. In the presence of dibutyl phosphate as an initiator and triflic acid as a catalyst, precision cellulose with well-controlled molecular weights, defined chain-end groups, and excellent regio- and stereospecificity was readily prepared. We further demonstrated the utility of this method through the synthesis of precision native d-cellulose and rare precision l-cellulose.

Mediating Role of Glucose-Lipid Metabolism in the Association between the Increased Risk of Coronary Heart Disease and Exposure to Organophosphate Esters, Phthalates, and Polycyclic Aromatic Hydrocarbons.

There is a lack of human evidence concerning the cardiovascular effects of combined exposure to endocrine disruptors. This case-control study sought to investigate coronary heart disease (CHD) associations with exposure to organophosphate flame retardants (OFRs), phthalates (PAEs), and polycyclic aromatic hydrocarbons (PAHs) among 148 adults with coronary-angiography-diagnosed CHD and 320 healthy adults from southern China. The mediating role of glucose-lipid metabolism was also explored. Bayesian kernel machine regression suggested that when exposure status was fixed to the 75th percentile with the median value as the reference, exposure to OFRs, PAEs, and PAHs was associated with an 84% (95% CI: 36%-134%), 132% (12%-252%), and 214% (89%-331%) increased risk of developing CHD, respectively. Weighted quantile sum regression indicated urinary bis(2-butoxyethyl) phosphate (BBOEP), dibutyl phosphate (DBP), monoisononyl phthalate (miNP), and metabolites of phenanthrene may be major contributors to the overall effect of mixtures. In further analyses on identified chemical risk factors, mediation analyses suggested exposure to phenanthrene may increase the risk of CHD via elevating total cholesterol and blood glucose, while exposure to DiNP mainly associates with serum lipids. Besides, we observed a slight mediation effect of oxidative DNA damage between urinary BBOEP and risk of CHD. These results provide potential direction for further experimental studies. Longitudinal evidence is needed to clarify the causation of the results.

Effect of di-butyl phosphate on the distribution behavior of uranyl ions in PUREX solvent

ABSTRACT Di-butyl phosphoric acid (HDBP) is one of the major hydrolytic and radiolytic degradation product of tri-n-butyl phosphate (TBP) employed for the extraction of U(VI) and Pu (IV) from the spent nuclear fuel dissolver solution. The presence of HDBP in the solvent phase limits the recovery of actinides during stripping. In view of this, the extraction and stripping behavior of uranyl nitrate in 1.1 M TBP in n-dodecane (n-DD) was studied in presence of di-butyl phosphate (HDBP). The distribution ratio (D) of uranium (VI) in HDBP/n-DD was negligible and the D value increased gradually with an increase in HDBP content in the organic phase. An alternate method was developed for estimation of HDBP in TBP/n-DD system based on uranium metal retention in organic phase. Based on the results it was found that 1 M HDBP in 1.1 M TBP/n-DD retained about 0.63 M of uranium (VI) in the organic phase during stripping. The results were further validated using irradiated solvent. FT-IR spectroscopic investigation also revealed the retention of U(VI) in 1.1 M TBP/n-DD containing HDBP even after several stripping with 0.01 M HNO3.

Associations of Organophosphate Ester Flame Retardant Exposures during Pregnancy with Gestational Duration and Fetal Growth: The Environmental influences on Child Health Outcomes (ECHO) Program.

Widespread exposure to organophosphate ester (OPE) flame retardants with potential reproductive toxicity raises concern regarding the impacts of gestational exposure on birth outcomes. Previous studies of prenatal OPE exposure and birth outcomes had limited sample sizes, with inconclusive results. We conducted a collaborative analysis of associations between gestational OPE exposures and adverse birth outcomes and tested whether associations were modified by sex. We included 6,646 pregnant participants from 16 cohorts in the Environmental influences on Child Health Outcomes (ECHO) Program. Nine OPE biomarkers were quantified in maternal urine samples collected primarily during the second and third trimester and modeled as -transformed continuous, categorized (high/low/nondetect), or dichotomous (detect/nondetect) variables depending on detection frequency. We used covariate-adjusted linear, logistic, and multinomial regression with generalized estimating equations, accounting for cohort-level clustering, to estimate associations of OPE biomarkers with gestational length and birth weight outcomes. Secondarily, we assessed effect modification by sex. Three OPE biomarkers [diphenyl phosphate (DPHP), a composite of dibutyl phosphate and di-isobutyl phosphate (DBUP/DIBP), and bis(1,3-dichloro-2-propyl) phosphate] were detected in of participants. In adjusted models, DBUP/DIBP [odds ratio (OR) per ; 95% confidence interval (CI): 1.02, 1.12] and bis(butoxyethyl) phosphate (OR for high vs. ; 95% CI: 1.06, 1.46), but not other OPE biomarkers, were associated with higher odds of preterm birth. We observed effect modification by sex for associations of DPHP and high bis(2-chloroethyl) phosphate with completed gestational weeks and odds of preterm birth, with adverse associations among females. In addition, newborns of mothers with detectable bis(1-chloro-2-propyl) phosphate, bis(2-methylphenyl) phosphate, and dipropyl phosphate had higher birth weight-for-gestational-age -scores ( for detect vs. ); other chemicals showed null associations. In the largest study to date, we find gestational exposures to several OPEs are associated with earlier timing of birth, especially among female neonates, or with greater fetal growth. https://doi.org/10.1289/EHP13182.

Anticorrosive and antimicrobial efficiency of photopolymerizable phosphorus (meth)acrylate oligomers-based coating materials

Novel photopolymerizable phosphorus (meth)acrylate oligomers were verified as anticorrosive and antimicrobial coating materials. Oligomers containing P-atoms were prepared by a solution-free UV-initiated telomerization process of aliphatic (meth)acrylates and styrene in the presence of different organic phosphorus compounds (P-telogens). The influence of the P-telogen structure on the photoaging process of coatings, as well as their anticorrosion and antibacterial properties was investigated. Relatively the highest anticorrosive efficiency was revealed for a varnish based on a telomers syrup containing dibutyl phosphite (DBPh) and dibutyl phosphate (DBP) due to the relatively long alkyl chain. In turn, UV-photocurable coatings exhibited moderate antibacterial and good anti-yeast activity but the best properties were found for the coating with dimethyl phosphite (DMPh). The higher resistance to photodegradation was observed in the case of the diphenyl phosphite (DPPh) due to the large phenyl substituent. Regardless of the structure of the organophosphorus compound, all coatings showed excellent adhesion to the glass substrate.

Studies on the acidification of carbonate waste stream for separation of di-butyl phosphate and recovery of metal

Abstract The aqueous waste generated during the treatment of Purex lean organic phase with alkaline carbonate solution contains washable degradation products and actinides in the form of carbonate complex. Management of such aqueous waste demands quantitative removal of the main degradation product, dibutyl phosphate (HDBP) and actinides from aqueous solution. In this context, batch studies have been carried out on the separation of HDBP from aqueous solution using n-dodecane (n-DD). For this purpose, the extraction behaviour of HDBP in n-DD was studied after acidification of alkaline carbonate solution with nitric acid. The studies with simulated waste containing HDBP and U(VI) nitrate showed the loss of U(VI) as precipitate during acidification as the uranium–DBP was poorly soluble in aqueous phase. However, the loss of U(VI) decreased with increase of aqueous phase acidity showing that the adjusted acidity of the carbonate waste plays an important role in the recovery of actinides.

Associations between exposure to organophosphate esters and overactive bladder in U.S. adults: a cross-sectional study.

The relationship between exposure to organophosphate esters (OPEs) and the risk of developing overactive bladder (OAB) is uncertain. The purpose of this study is to examine the potential link between urinary metabolites of organophosphate esters and OAB. Data from the National Health and Nutrition Examination Survey (NHANES) database of the 2011-2016 cycles were utilized. Four urinary metabolites of organophosphate esters: diphenyl phosphate (DPHP), bis (1,3-dichloro-2-propyl) phosphate (BDCPP), bis (2-chloroethyl) phosphate (BCEP), and dibutyl phosphate (DBUP) were included in the study. Multivariate logistic regression and restricted cubic spline (RCS) were used to evaluate the relationship between urinary OPEs metabolites and OAB. Interaction analysis was conducted on subgroups to confirm the findings. A total of 3,443 United States (US) adults aged 20 years or older were included in the study, of whom 597 participants were considered to have OAB. After adjusting for potential confounding factors, we found a positive association between DPHP and the risk of overactive bladder. The risk of overactive bladder increased with increasing DPHP concentrations compared with quartile 1 (quartile 2, OR = 1.19, 95% CI, 0.82-1.73, P = 0.34; quartile 3, OR = 1.67, 95% CI, 1.10-2.53, P = 0.02; Q4, OR = 1.75, 95% CI, 1.26-2.43, P = 0.002). However, after dividing the participants by gender, only the female group retained consistent results. Additionally, restricted cubic spline analysis revealed a nonlinear dose-response correlation between DPHP and OAB in female participants. In the subgroup analysis based on age, race, body mass index (BMI), recreational activity, smoking status, drinking status, hypertension, diabetes, and stroke, the interaction analysis revealed that the findings were uniform. Our findings indicate that exposure to DPHP could elevate the risk of OAB in US adult females. Further experimental studies are needed to explore the underlying mechanism in the future.

Dissolution of contaminant Zr-DBP and corrosion of stainless steel by dissolved solution

In the nuclear spent fuel reprocessing, zirconium dibutyl phosphate (Zr-DBP) is deposited on the surface of stainless steel equipment, making spent fuel reprocessing difficult. Therefore, in this study, hydrazine carbonate ((N2H5)2CO3) was used to dissolve Zr-DBP. The effects of solid–liquid ratio, different mass fractions of (N2H5)2CO3 solutions, and (N2H5)2CO3 solutions containing different concentrations of hydrogen peroxide (H2O2) on the dissolution of Zr-DBP were investigated. The corrosion rates of different dissolution solutions on stainless steel were also investigated. When the mass fraction of (N2H5)2CO3 in solution was increased from 1 % to 20 %, the concentration of Zr(IV) at dissolution equilibrium increased from 1.05 g/L to 1.61 g/L, respectively. When the dissolution temperature was kept in the range of 25 °C to 65 °C, the increasing temperature promoted the dissolution of Zr-DBP. The presence of H2O2 induced the production of the white precipitates zirconium hydroxide (Zr(OH)4). In addition, the corrosion rate of stainless steel gradually increased from 0.00153 mm/a to 0.0138 mm/a when the concentration of H2O2 in the (N2H5)2CO3 solution was increased from 0 M to 1.5 M. The dissolution ability of Zr-DBP in different carbonate solutions was (N2H5)2CO3 ≥ ammonium carbonate ((NH4)2CO3) > sodium carbonate (Na2CO3) ≥ potassium carbonate (K2CO3).