JOURNAL OF MOLECULAR LIQUIDS
·
2023
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IF 6
Taotao Hu,Yixin Ma,Li Yang,Peng Liu,Yiqun Fan,Yan Zhang,Jingcai Cheng,Chao Yang
In this study, the solubility of glyphosate in three binary mixed solutions (sodium chloride + water, triethylamine hydrochloride + water, and glyphosine + water) and aqueous solutions with different initial pH values was determined by a static method within the temperature range from 293.15 K to 353.15 K. Interestingly, the effects of different components on the solubility of glyphosate in aqueous solutions are quite different. The solubility of glyphosate at different initial pH shows a significant U-shaped characteristic, with the lowest solubility at about pH 1.5. In the binary mixed solutions, when the concentration of NaCl increases, the solubility of glyphosate first increases and then decreases. The increase of the triethylamine hydrochloride concentration has a negative effect on the solubility of glyphosate, while the increase of the glyphosine concentration has a positive effect on the solubility of glyphosate. The effect of pH on the solubility of glyphosate was correlated with a pH correlation model, and the solubility of glyphosate in the three mixed solutions was correlated with the modified Apelblat equation, λh equation, Jouyban-Acree-Apelblat (J-A-A) model and the non-randomness two-liquid (NRTL) model. The values of root mean square deviation ( RMSD ) indicate a good correlation of the model. In addition, the mixed thermodynamic properties (Δ mix G, Δ mix H , and Δ mix S ) of glyphosate in the three binary mixed solutions were calculated based on the NRTL model, and it was found that the mixing of glyphosate in all three systems was spontaneous, heat-absorbing and entropy-driven. The obtained solubility data and thermodynamic properties can provide theoretical guidance for the crystallization of glyphosate.
研究领域:
化学
·
环境科学
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农业科学
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产品关联
DOI
高影响因子
JOURNAL OF FLUORESCENCE
·
2024
·
IF 2.6
Guo Yu-Meng,Chen Zi-Chong,Zhang Kai-Xiang,Liu Liu-Lu,Huang Chan,Li Qing
Establishing a fast and simple method for determining glyphosate (Glyp) is crucial for safeguarding the environment and protecting human well-being. In this work, a copper benzenedicarboxylate (CuBDC) metal-organic frameworks (MOFs) with peroxidase-like property and stimulus-responsive fluorescent was prepared by binding Cu 2+ with terephthalic acid (TA). The presence of Glyp can coordination with Cu 2+ ion and block the peroxidase-like properties of CuBDC, thereby suppressing the catalysis the oxidation of TA into fluorescent product 2-hydroxyterephthalic acid (HTA). Based on these facts, a simple, rapid and sensitive fluorescence detection strategy for Glyp was developed. The fluorescence decreases linearly in the 0.5–10 µg/mL Glyp concentration range, and the limit of detection was calculated to be 23.99 ng/mL. Furthermore, the dual-functional CuMOFs-based label-free strategy was effectively employed for detecting Glyp in river water samples. With good performance and practicability, this strategy provides a potential application in the convenient and reliable determination of Glyp in the environment.
研究领域:
环境科学
·
分析化学
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纳米生物学
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产品关联
DOI
PubMed
高影响因子
Surfaces and Interfaces
·
2025
·
IF 6.3
Jingying Wang,Zengyue Chen,Xiaochen Liu,Zhansheng Wu,Li Jin
Glyphosate herbicide is commonly used to kill weeds in crops because of its high efficiency and low cost. However, excessive use of glyphosate not only leads to soil, surface water, and groundwater pollution, but also presents a potential risk to human health. Photocatalysis as an advanced oxidation technology can efficiently and environmentally degrade glyphosate, and bismuth-based photocatalysts have garnered extensive attention for their strong photo-oxidation capabilities. In this work, a green reaction route was developed to synthesize Bi-based/g-C 3 N 4 /CdS ternary heterojunction photocatalysts for glyphosate removal, by combining acetic acid-glycol synergistic systems with atmospheric pressure microwave methods. By regulating the structure and composition of the catalyst, excellent photodegradation and stabilization of glyphosate by BiOCl/g-C 3 N 4 /CdS (> 98% removal of glyphosate in 90 min). This study is of great significance for the green preparation and application of efficient photocatalysts for glyphosate removal, and the development of other recyclable systems.
研究领域:
环境科学
·
材料科学
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产品关联
DOI
高影响因子
Journal of Environmental Chemical Engineering
·
2022
·
IF 7.968
Fei Fang,Quankun Lv,Peng Li,Yue Tao,Yan Zhang,Yi Zhou,Xuede Li,Jie Li
Defect engineering is essential for improving the adsorption performance of metal-organic frameworks (MOFs). Herein, hierarchical porous UiO-67(Zr) and analogs with controlled levels of defects were successfully obtained and applied to chemoselectively capture glyphosate (GP) from water. The obtained defective UiO-67 was stable at different pH values. The removal performance of defective UiO-67(Zr) was evaluated systematically as a function of different modulators, water chemistry and interfering ions. The maximum adsorption capacity of defective UiO-67(Zr) reached 322.58 mg/g, superior to most MOFs-based adsorbents. The defective UiO-67(Zr) also showed high selectivity for GP adsorption at high concentrations of humic acids (3 times) and interfering anions (100 times). In addition, the defective UiO-67(Zr) has shown good recovery performance and can effectively remove GP from a variety of contaminated water samples and multi-pollutant systems. The results of batch experiments and microscopic spectral characterization (XPS and FTIR) revealed that GP adsorption was mainly guided by electrostatic action, coordination, pore-filling and hydrogen bonding . These findings verified that the fabrication of defect sites played an important role in promoting the adsorption performance of MOFs. Our work provides a clue to the design of defective MOFs with high adsorption performance.
研究领域:
环境科学
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材料科学
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DOI
高影响因子
FOOD CHEMISTRY
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2025
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IF 9.8
Ying Huang,Xiangrong Liu,Tiantian Shen,Wang Li,Jiali Ren,Haiyan Zhong
The detection techniques for glyphosate residues have garnered attention due to the potential toxicity associated. Herein, we introduced a fluorescent “turn-on” strategy, leveraging competitive coordination with iron, for glyphosate detection. We synthesized iron-based metal-organic frameworks (Fe-MOFs) at room temperature. Among them, 2,5-dihydroxyterephthalic acid (DOBDC) acted as a ligand to produce strong fluorescence, and iron ions acted as a quencher to quench the fluorescence of DOBDC. Another ligand, 2-nitroterephthalic acid, contained nitro quenching of the fluorescence, giving it a lower background. Glyphosate competed with the ligands for ions, weakening the interaction between ions and the ligands. This disruption restored the fluorescence emission at 535 nm, enabling glyphosate detection. To facilitate field application, Fe-MOFs were encapsulated within agarose to create a functional hydrogel. Glyphosate penetrated the hydrogel and resulting in fluorescence “turn-on”. Remarkably, this method facilitated visual detection through smartphone photography coupled with RGB (red/green/blue) analysis, offering a user-friendly and portable solution.
研究领域:
环境科学
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分析化学
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材料科学
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传感器和检测技术
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产品关联
DOI
PubMed
高影响因子
ENVIRONMENTAL SCIENCE & TECHNOLOGY
·
2026
·
IF 12.2
Liu Zhe,Zhang Mengqi,Zhou Ziyang,Liu Xinyu,Lanson Bruno,Zhao Wantong,Feng Xionghan,Tan Wenfeng,Lu Guining,Wang Xiaoming
The environmental persistence of
glyphosate and its transformation
into aminomethylphosphonic acid (AMPA) necessitate a mechanistic understanding
of its abiotic degradation in natural environments. Manganese (Mn)
oxides are ubiquitous redox-active minerals capable of oxidizing glyphosate;
however, how Mn oxide mineralogy and pH regulate degradation kinetics,
pathway selectivity, and interfacial redox processes remains unclear.
Here, we investigated glyphosate oxidation by three representative
Mn oxides, layered birnessite, disordered-layered vernadite, and tunnel-structured
cryptomelane, across pH 3–7. Vernadite exhibited the highest
and most sustained oxidative reactivity, cryptomelane showed rapid
but strongly pH-dependent oxidation, and birnessite displayed slower
yet persistent reactivity. Mineral structure controlled product selectivity:
under near-neutral conditions, layered Mn oxides favored glycine formation
through C–N bond cleavage adjacent to the phosphonate group,
whereas tunnel-structured cryptomelane promoted AMPA accumulation
through cleavage near the carboxyl group. Acidic conditions (pH 3
and 5) enhanced AMPA accumulation across all Mn oxides, suggesting
increased persistence risks. Spectroscopic and kinetic analyses demonstrated
that glyphosate oxidation involved surface complexation with Mn(IV),
interfacial electron transfer, and propagation through transient,
labile Mn(III) intermediates. These findings reveal that Mn oxide
mineralogy and pH jointly govern bond-selective glyphosate oxidation
and AMPA accumulation, advancing mechanistic predictions of glyphosate
fate in soil and aquatic environments.
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产品关联
DOI
高影响因子
LANGMUIR
·
2026
·
IF 4.4
Wen Xin,Yajun Ren,Xiaofeng Song,Honghui Teng,Mingyue Jin,Menghao Tian
The stability of molecularly imprinted membranes (MIMs) is a critical factor influencing their reusability and detection performance. To overcome stability limitations, a robust porous imprinted hydrogel membrane (porous PVA/HS-β-CD/Ag/MIPs) was developed by grafting recognition sites onto a porous framework. The membrane was synthesized through a multistep process: (i) A porous hydrogel matrix was formed via freeze–thaw-induced cross-linking between poly(vinyl alcohol) (PVA) and thiolated β-cyclodextrin (HS-β-CD), combined with the use of a pore-forming agent; (ii) the membrane was functionalized as a surface-enhanced Raman scattering (SERS) substrate through in situ reduction of silver ions (from AgNO3); (iii) glyphosate (GLY)-imprinted polymers were anchored via precipitation polymerization, utilizing HS-β-CD as grafting sites to achieve specific recognition and detection. Morphological and stability analyses demonstrated that the SERS-imprinted porous membrane exhibits high structural integrity, retaining 94.89% of its detection capability after 12 h under continuous water flow. This study introduces a robust covalent anchoring strategy between the imprinting layer and the substrate to form chemical cross-linking, providing an effective pathway for designing high-performance, long-lifespan molecularly imprinted membranes.
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产品关联
DOI
PubMed
高影响因子
JOURNAL OF APPLIED TOXICOLOGY
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2025
·
IF 2.8
Shuge Shu,Xinting Chen,Jiawen Ren,Xiangyu Yu,Hao Zhang,Yongquan Yu
Glyphosate is reported to compromise the central nervous system and induce behavioral disorders in mammals. However, evidence is deficient with respect to the potential mechanisms involved. In this study, C57BL/6 mice were orally exposed to glyphosate at doses ranging from 0 to 200 mg/kg/day for 16 weeks. The results of behavioral tests showed that glyphosate decreased time spent and distance traveled within the central area of open field test, decreased the retention time and number of entries into the open arms, and increased the retention time and number of entries into the close arms of elevated plus maze test. The expressions of anxiety-related genes htr5 , htr6 , and tmem132d were also significantly upregulated by glyphosate. This behavioral phenotype was linked to the permeation of glyphosate into the brain via disrupting the functional tight junctions of blood–brain barrier (BBB). As a result, glyphosate directly compromised the morphological structure of neurons, increased the number of IBA-1 microglia, and activated the expression of NLRP3-mediated pyroptosis pathway (NLRP3, Caspase-1, GSDMD, and IL-18) in the hippocampus of mice. Moreover, the glyphosate-induced activation of NLRP3 pathway in microglia was markedly reversed by NLRP3 inhibitor MCC950. The conditional mediums from glyphosate-treated BV2 cells aggravated the cytotoxicity of HT-22 neurons, which was also rescued by MCC950. In conclusion, this work demonstrated that microglia-mediated activation of NLRP3 pyroptosis pathway plays a detrimental role in glyphosate-behavioral disorders and neuron damage. These findings provide novel evidence for glyphosate-induced neurotoxicity and support the growing association between glyphosate exposure and neurobehavioral disorders in humans.
研究领域:
神经科学
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毒理学
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分子生物学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
INORGANIC CHEMISTRY COMMUNICATIONS
·
2025
·
IF 5.4
Yangjie Qin,Zhaobo Wang,Shanzhu Jiang,Ruan Chi,Shengchao Huang,Huijuan Ma,Zhongjun Li
Phosphogypsum (PG) disposal and pollution pose dual environmental challenges in phosphorus industries. This study pioneers a one-step synthesis of copper-modified hydroxyapatite (Cu/PGHAP) directly from PG waste, enabling efficient Glyphosate ( Phosphonomethylglycine, PMG) degradation via Fenton-like catalysis. Cu/PGHAP was synthesized by co-precipitation under optimized conditions (20 % Cu/Ca, 333.15 K, 16 h aging). Catalytic performance was evaluated by PMG removal kinetics, with mechanistic insights from SEM, XRD, FTIR, BET, and EPR. The results showed that Cu/PGHAP possesses a hierarchical mesoporous structure (specific surface area of 57.16 m 2 /g) and lattice-embedded Cu 2+ sites. Under optimal conditions (6 g/L catalyst, 5 mM H 2 O 2 , 50 mg/L PMG, pH 11), 100 % PMG removal was achieved within 60 min. Alkaline processing enhances stability, maintaining 99.86 % reusability after 10 cycles, with extremely low copper ion leaching. Radical capture experiments confirmed the 1 O 2 driven degradation mechanism. This work establishes a “waste control by waste” strategy for simultaneous PG valorization and PMG detoxification, advancing circular economy in chemical industries.
研究领域:
环境化学
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工业生态学
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催化科学
·
污染控制技术
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产品关联
DOI
高影响因子
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
·
2025
·
IF 8.5
Anquan Ma,Ziqing Yang,Qixuan He,Wenhao Wang,Huiping Ren,Chuanyao Zhai,Jing Lan
Environmental glyphosate exposure has been linked to glioblastoma (GBM), yet its molecular basis remains unclear. Integrating network-toxicology and druggable Mendelian randomization screens, we identified the Src-family kinase FYN as the principal glyphosate target. Molecular-dynamics simulations, surface-plasmon resonance (KD = 1.54 μM) and pull-down assays confirmed high-affinity binding and highlighted ASP353 as a dominant contact residue. Multi-omics profiling showed FYN over-expression and promoter hypomethylation in GBM, correlating with diminished immune infiltration. In U87 cells, sub-toxic glyphosate (0.1 mg/L, 12 h) up-regulated FYN, activated PI3K–AKT–mTOR signaling, increased GLUT1, LDHA and PKM2, and accelerated proliferation, migration and invasion; lentiviral sh-FYN reversed these effects and curtailed glycolytic flux. Orthotopic mouse studies mirrored the in-vitro findings, with FYN knock-down suppressing glyphosate-driven tumor growth. Exosomes derived from sh-FYN glioma cells weakened macrophage M2 polarization and reduced CXCL1, IL-10 and TGF-β secretion, revealing an immunometabolism axis. Collectively, these results establish FYN as the mechanistic conduit between glyphosate and GBM and demonstrate that targeting FYN—directly or via exosome delivery—reprograms tumor glycolysis and immunity, offering a tractable strategy against glyphosate-associated malignancy.
研究领域:
毒理学
·
肿瘤学
·
分子生物学
·
生物信息学
·
神经肿瘤学
·
药理学
·
免疫学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
Analytical Methods
·
2025
·
IF 2.6
Ming Zhong,Hao Zhang,Yajun Ren,Yuwei Sun,Mingyue Piao,Libin Han,Mingyue Jin,Honghui Teng
Glyphosate, a widely used organophosphorus herbicide in agriculture, poses potential threats to aquatic ecosystems and human health due to its long-term environmental persistence. This study presents a spectroscopic detection system based on a competitive reaction utilizing the Ponceau 4R (P4R)-Cu2+ complex. Leveraging glyphosate's high affinity for chelating copper ions, the method enables indirect, rapid, and visual quantitative analysis of glyphosate. In the presence of glyphosate, Cu2+ preferentially binds to it, causing the release of P4R and the restoration of its characteristic absorption spectrum, resulting in a measurable absorbance change at 505 nm. Systematic optimization of buffer pH, P4R concentration, Cu2+ concentration, and their ratio established the optimal detection conditions (120 μmol L−1 P4R, 120 μmol L−1 Cu2+, 40 mmol L−1 borate buffer, pH 9.0). Under these conditions, the method exhibited a good linear relationship within the concentration range of 5.9–295.8 μmol L−1 (R2 = 0.998). The limit of quantitation (LOQ) and limit of detection (LOD) were determined to be 14.0 μmol L−1 and 4.6 μmol L−1, respectively. This method was successfully applied to the analysis of spiked surface water samples and soils collected from the upper reaches of the Liao River, yielding average recoveries of 98.7–107.6% with relative standard deviations (RSDs) below 5%. Interference tests indicated that citric acid interference was manageable (recovery: 88.9%) when its concentration ratio to glyphosate was ≤2 : 1, while tartaric acid and oxalic acid required masking strategies to suppress their interference. This method, characterized by its simplicity, rapid response, and low instrumental dependence, provides reliable technical support for the rapid screening of glyphosate in environmental samples.
研究领域:
环境科学
·
分析化学
·
光谱学
·
水污染
·
除草剂检测
✓ 已验证
产品关联
DOI
PubMed
高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2026
·
IF 9.1
Chenglong Lei,Fan Ni,Dexin Fang,Fei Shen,Yi Yang,Wei Qu,J. Paul Chen,Jinsong He
Organophosphorus herbicide (i.e. glyphosate) contaminated wastewaters pose significant environmental and ecological risks, exacerbating the global phosphorus crisis. In this study, we design and optimize a novel nanoconfined CuLa@CNT catalyst for the simultaneous catalytic degradation of GLP and recovery of phosphate from GLP-containing agricultural wastewater. Designed with copper oxide as the catalytic site and lanthanum oxide as the phosphate-adsorbing site within carbon nanotubes (CNT), the catalyst exhibited 100% degradation of GLP within 40 min and 100% phosphate adsorption within 90 min, under the initial GLP concentration of 20 ppm. The excellent reusability and tolerance to complex environmental conditions were demonstrated, and a GLP removal efficiency of 91.1% was attained even in actual agricultural drainage water, confirming its practical applicability. The detailed characterization confirmed the successful formation of the nanoconfined structure, where copper and lanthanum species were uniformly dispersed within the CNT channels. Theoretical calculations and electron paramagnetic resonance analysis revealed that the confined CNT structure not only favored the generation of reactive oxygen species (•OH, 1 O 2 ) but also promoted selective C P bond cleavage in GLP and adsorption of phosphate, thereby enhancing the selectivity for phosphate recovery over other organic intermediates, such as aminomethylphosphonic acid. This study provides a simple and highly effective method for addressing organophosphorus agricultural wastewater while simultaneously recovering valuable phosphate, contributing to sustainable water treatment and resource recycling.
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DOI
高影响因子
危险品化学品经营许可证（带存储）