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CROP PROTECTION · 2020 · IF 2.381

Synthesized dimers increased herbicidal activity with lowered volatility

Guanglong Ding,Jingyue Tang,Wenbing Zhang,Yanran Li,Junfan Niu,Weichen Wang,Hong Huo,Jianqiang Li,Yongsong Cao

Auxinic herbicides are widely used to control broadleaf weeds in cereal crop fields due to their excellent herbicidal activities. However, volatile drifting caused by their high vapor pressures is a great threat to neighbouring susceptible crops and environment and severely limits auxinic herbicide applications. In this study, a series of auxinic herbicide dimers were synthesized using 2,4-D, dicamba and MCPA as monomers to reduce their vapor pressures. The results showed that all of the dimers significantly reduced volatilities due to larger molecular weight. The dimers linked with two ester bonds had 2-fold higher herbicidal efficacies than their corresponding monomers in filed experiments. The dimers linked with amide bonds appeared to function as contact action and systemic action herbicides. The dimers, 3a-2(ethane-1,2-diylbis (2-(2,4-dichlorophenoxy)acetate)), 3a-4(2-((2-(2,4-dichlorophenoxy)acetyl)thio)ethyl 2-(2,4-dichlorophenoxy)acetate), 3b-2(ethane-1,2-diylbis(2-(4-chloro-2-methylphenoxy)acetate)) and 3c-2(ethane-1,2-diylbis(3,6-dichloro-2-methoxybenzoate)) significantly increased the efficacies and reduced volatilities, thus could be developed as potential novel postemergence herbicides.

研究领域: 植物学 · 农业科学
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PLASMA CHEMISTRY AND PLASMA PROCESSING · 2022 ·Vol. 43 ·期 2 ·491-511 · IF 3.337

Synergistic 2,4-D Degradation by Fenton Reagent Obtained from Glow Discharge Plasma Formed H2O2 and DBD Pretreated Fe-Rich Sludge Catalyst

Huang Shaoyong,Huang Quanjia,Gan Jiaming,Li Ting,Wang Lei

In this study, Fe-rich sludge was pretreated by dielectric barrier discharge (DBD) and used as a Fenton catalyst for the degradation of 2,4-dichlorophenoxyacetic acid (2,4-D) in aqueous solution, where hydrogen peroxide was in situ supplied from a glow discharge plasma (GDP) in contact with the solution. Synergistic mechanism of the two plasmas during 2,4-D degradation was explored. The Fe-rich sludge pretreated by H 2 -DBD could significantly accelerate the 2,4-D degradation as it converted Fe(III) in the sludge to the active Fe(II). 2,4-D can be completely removed in the presence of H 2 -DBD pretreated Fe-rich sludge with 25 min of GDP at pH 0 3.0 and catalyst dosage of 1.0 g/L. Quenching experimental studies showed that both ·OH (oxidative degradation) and ·H (reductive dechlorination) were responsible for 2,4-D degradation. Reducing radicals (such as ·R and·H) formed during GDP can continuously reduce the Fe 3+ back to Fe 2+ , which further promoted the degradation and dechlorination of 2,4-D. The results of three consecutive experiments indicated the stability and reusability of catalyst. This study provides a potential method for the recycle of Fe-rich sludge as a novel and cost-effective catalyst for 2,4-D removal from aqueous environments, which is significant for the terminal disposal of Fe-rich sludge. Graphical Abstract

CAS / MDL: 94-75-7
研究领域: 环境科学 · 废水处理 · 化学工程
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ACS Applied Materials & Interfaces · 2022 · IF 10.383

Biodegradable and Light-Responsive Polymeric Nanoparticles for Environmentally Safe Herbicide Delivery

Pengfei Shan,Yingwen Lu,Weilin Lu,Xiangping Yin,Haiwei Liu,Daai Li,Xiaoyue Lian,Weiping Wang,Zhongyu Li,Zhihui Li

The low utilization efficiency of pesticides exerts an adverse impact on the environment and human health. Polymer-related controlled-release nanosized pesticide systems provide a promising and efficient way to overcome the problem. In this work, a biodegradable and light-responsive amphiphilic polymer was synthesized via 1,1,3,3-tetramethylguanidine-promoted polyesterification under mild conditions (low temperature, no vacuum, and no inert gas protection). We used this polymer to fabricate a light-triggered controlled-release nanosized pesticide system. The herbicide, 2,4-dichlorophenoxyacetic acid (2,4-D), was selected as a model drug to show its potential as a controlled-release pesticide system. It was found that the 2,4-D-loaded polymeric nanoparticles were stable without the treatment of UV, while the release rate of 2,4-D from the nanoparticles gradually increased after treatment with UV light. Pot trial showed that the 2,4-D-loaded polymer nanoparticles showed a good herbicidal effect. Finally, toxicity studies suggested that the polymer can reduce toxicity to nontarget organisms.

研究领域: 环境科学 · 材料科学 · 农业科学
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WATER RESEARCH · 2023 · IF 12.8

Ozone micro-bubble aeration using the ceramic ultrafiltration membrane with superior oxidation performance for 2, 4-D elimination

Wei-Ran Han,Wen-Long Wang,Tie-Jun Qiao,Wei Wang,Hang Su,Chen-Xin Xu,Qian-Yuan Wu

Micro-bubble aeration is an efficient way to promote ozonation performance, but the technology is challenged by extensive energy cost. Here, a ceramic ultrafiltration membrane was used to achieve ozone micro-bubble (0–80 µm) aeration in a simple way at gaseous pressures of 0.14–0.19 MPa. Compared with milli-bubble aeration, micro-bubble aeration increased the equilibrium aquatic O 3 concentrations by 1.53–3.25 times and apparent O 3 transfer rates by 3.12–3.35 times at pH 5.0–8.0. Consequently, the • OH yield was 2.67–3.54 times via faster O 3 transfer to the aquatic solution followed by decomposition rather than interfacial reaction. Ozone micro-bubble aeration outperformed milli-bubble aeration, with the degradation kinetics of 2,4-D being 3.08–4.36 times higher. Both O 3 -oxidation and • OH oxidation were important to the promotion with the contributions being 35.8%-45.9% and 54.1%-64.2%, respectively. The operational and water matric conditions influenced the oxidation performance via both O 3 oxidation and • OH oxidation, which is reported for the first time. In general, the ceramic membrane offered a low-energy approach of ozone micro-bubble aeration for efficient pollutant degradation. The O 3 oxidation and • OH oxidation were proportionally promoted by ozone micro-bubble due to O 3 transfer enhancement. Thus, the promotive mechanism can be interpreted as the synchronous enchantment on ozone exposure and • OH exposure for the first time.

研究领域: 环境科学 · 水处理技术
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CURRENT MICROBIOLOGY · 2016 ·Vol. 74 ·期 2 ·193-202 · IF 1.519

Biodegradation of the Herbicide 2,4-Dichlorophenoxyacetic Acid by a New Isolated Strain of Achromobacter sp. LZ35

Xia Zhen-Yuan,Zhang Long,Zhao Yan,Yan Xin,Li Shun-Peng,Gu Tao,Jiang Jian-Dong

In this study, a bacterial strain of Achromobacter sp. LZ35, which was capable of utilizing 2,4-dichlorophenoxyacetic acid (2,4-D) and 2-methyl-4-chlorophenoxy acetic acid (MCPA) as the sole sources of carbon and energy for growth, was isolated from the soil in a disused pesticide factory in Suzhou, China. The optimal 2,4-D degradation by strain LZ35 occurred at 30 °C and pH 8.0 when the initial 2,4-D concentration was 200 mg L −1 . Strain LZ35 harbored the conserved 2,4-D/alpha-ketoglutarate dioxygenase (96%) and 2,4-dichlorophenol hydroxylase (99%), and catabolized 2,4-D via the intermediate 2,4-dichlorophenol. The inoculation of 7.8 × 10 6  CFU g −1 soil of strain LZ35 cells to 2,4-D-contaminated soil could efficiently remove over 75 and 90% of 100 and 50 mg L −1 2,4-D in 12 days and significantly released the phytotoxicity of maize caused by the 2,4-D residue. This is the first report of an Achromobacter sp. strain that was capable of mineralizing both 2,4-D and MCPA. This study provides us a promising candidate for its application in the bioremediation of 2,4-D- or MCPA-contaminated sites.

CAS / MDL: 94-75-7 94-74-6
研究领域: 环境微生物学 · 生物修复 · 环境科学
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2023 · IF 22.1

Narrowing the bandgaps of thiazolo[5,4-d]thiazole-bridged conjugated microporous polymers to capture green light for selective oxidation of amines

Fengwei Huang,Xiaoyun Dong,Yuexin Wang,Xianjun Lang

Conjugated microporous polymers (CMPs) have evloved into versatile visible light photocatalysts. Narrowing the bandgaps of CMPs could capture more visible light without shifting the suitable position with an established electron acceptor like thiazolo[5,4- d ]thiazole (TzTz). Here, benzene-1,3,5-tricarbaldehyde (Bz-CHO) and benzo[1,2-b:3,4-b':5,6-b'']trithiophene-2,5,8-tricarbaldehyde (BTT-CHO) are adopted to undergo condensation with dithiooxamide, preparing two TzTz-bridged CMPs, namely TzTz-Bz and TzTz-BTT. Thereby, TzTz-BTT could capture visible light more substantially than TzTz-Bz due to narrowing the bandgap. Endowed by TzTz, both TzTz-BTT and TzTz-Bz possess similar positions for the activation of O 2 and can drive the subsequent formation of imines. However, TzTz-BTT, with a narrower bandgap, could capture more green light to drive the electron and proton transfer for the selective formation of imines with higher conversions than TzTz-Bz. This work suggests that CMPs can be equipped with extensive visible light absorption for photocatalytic selective oxidations.

研究领域: 材料科学 · 光催化
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CHEMISTRY & BIODIVERSITY · 2019 ·Vol. 16 ·期 8 ·e1900232 · IF 1.449

Design and Synthesis of Novel Thiazolo[5,4-d]pyrimidine Derivatives as Potential Angiogenesis Inhibitors

Wen-Jun Xue,Jian-Yao Du,Ya-Hui Deng,Zhong-Hui Yan,Ji-Ping Liu,Yu Liu,Li-Ping Sun

Vascular endothelial growth factor receptor-2 (VEGFR-2) plays an important role in both vasculogenesis and angiogenesis. Inhibition of VEGFR-2 has been demonstrated as a key method against tumor-associated angiogenesis. Thiazolopyrimidine is an important analog of the purine ring, and we choose the thiazolopyrimidine scaffold as the mother nucleus. Two series of thiazolo[5,4- d ]pyrimidine derivatives were synthesized and evaluated for their antiproliferative activity. In HUVEC inhibition assay, compounds 3l (=1-(5-{[2-(4-chlorophenyl)-5-methyl[1,3]thiazolo[5,4- d ]pyrimidin-7-yl]amino}pyridin-2-yl)-3-(3,4-dimethylphenyl)urea) and 3m (=1-(5-{[2-(4-chlorophenyl)-5-methyl[1,3]thiazolo[5,4- d ]pyrimidin-7-yl]amino}pyridin-2-yl)-3-(4-methoxyphenyl)urea) exhibited the most potent inhibitory effect (IC 50 =1.65 and 3.52 μ m , respectively). Compound 3l also showed the best potency against VEGFR-2 at 50 μ m (98.5 %). These results suggest that further investigation of compound 3l might provide potential angiogenesis inhibitors. Graphical

CAS / MDL: 298-93-1
研究领域: 药物化学 · 肿瘤学 · 药物研发
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Nature Communications · 2020 ·Vol. 11 ·期 1 ·1-10 · IF 12.121

Chiral recognition and enantiomer excess determination based on emission wavelength change of AIEgen rotor

Hu Ming,Yuan Ying-Xue,Wang Weizhou,Li Dong-Mi,Zhang Hong-Chao,Wu Bai-Xing,Liu Minghua,Zheng Yan-Song

Chiral recognition, such as enantioselective interactions of enzyme with chiral agents, is one of the most important issues in the natural world. But artificial chiral receptors are much less efficient than natural ones. For tackling the chiral recognition and enantiomer excess (ee) analysis, up until now all the fluorescent receptors have been developed based on fluorescence intensity changes. Here we report that the chiral recognition of a large number of chiral carboxylic acids, including chiral agrochemicals 2,4-D, is carried out based on fluorescent colour changes rather than intensity changes of AIEgen rotors. Moreover, the fluorescence wavelength of the AIEgen rotor linearly changes with ee of the carboxylic acid, enabling the ee to be accurately measured with average absolute errors (AAE) of less than 2.8%. Theoretical calculation demonstrates that the wavelength change is ascribed to the rotation of the AIEgen rotor upon interaction with different enantiomers.

研究领域: 化学 · 分析化学 · 材料科学 · 光学
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ACS Agricultural Science & Technology · 2022 · IF 0

Facile Synthesis of the Dual Pesticide-Loaded Metal–Organic Framework Hybrid for pH-Responsive Release

Yingjie Wang,Song Ma,Xin Yang,Yuhu Li,Shaoyu Lü

Controlled release formulations, used for the long-term preservation of pesticides, make agricultural development more precise, efficient, and safe. However, facile synthesis and high utilization of these formulations remain challenging. In this work, a polydopamine and metal–organic framework (MOF) hybrid was fabricated by a facile synthesis strategy for the controlled delivery of insecticide thiacloprid (THIA) and herbicide 2,4-D. The pesticides exhibited environment-responsive release behaviors. After 24 h, the cumulative release of THIA and 2,4-D reached 52.78 and 58.63% under alkaline conditions. The antiultraviolet photodegradation ability of THIA and 2,4-D increased nearly 4 times and 2 times, respectively. Significant insecticidal and herbicidal properties were observed for THIA@PDA-2,4-D@MIL-101(Fe). This hybrid achieves environmentally responsive and sustainable pesticide release by employing a dual cargo-carrying MOF and has great potential in intelligent, environmentally friendly, precise, and efficient pesticide delivery.

CAS / MDL: 2702-72-9
研究领域: 农业化学 · 材料科学 · 环境科学
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JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY · 2020 · IF 4.192

Residues and Dietary Risk Assessments of 2,4-D Isooctyl Ester, Metribuzin, Acetochlor, and 2-Ethyl-6-methylaniline in Corn or Soybean Fields

Xutian Zheng,Chaolun Liu,Jiye Hu

Since 2,4-dichlorophenoxy acetic acid (2,4-D) was discovered in the 1940s, 2,4-D and its derivatives remain among most commonly used herbicides in the world. There have been recent increases in using 2,4-D products in a combination with other herbicides such as metribuzin and acetochlor to control noxious weeds. However, accurate analysis of 2,4-D isooctyl ester remains to be improved due to long analysis time and rapid conversion of the ester to acid (i.e., under-reporting residues). In this work, a simple hydrolysis procedure was introduced to provide a quantitative hydrolytic rate of the ester (>95%) and did not affect the other pH-sensitive compounds. Analysis parameters and sample pretreatments were optimized for improved selectivity and accuracy. The hydrolysis-QuEChERS (quick, easy, cheap, effective, rugged, and safe) technique for multidetermination of 2,4-D isooctyl ester, metribuzin, acetochlor, and 2-ethyl-6-methylaniline in corn and soybeans via high performance liquid chromatography–tandem mass spectrometry was established. The method had average recoveries of 74–109% with relative standard deviations ≤13.5% and limits of quantifications (LOQs) of 0.05 mg/kg. The terminal residues of these compounds found in real edible matrixes were less than the corresponding LOQs at harvest time. The risk quotients were far below 100%, indicating a low health risk to consumers.

CAS / MDL: 34256-82-1
研究领域: 植物保护 · 食品安全 · 环境科学
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CHEMICAL ENGINEERING JOURNAL · 2023 · IF 15.1

Synergistic mechanism of surface oxygen vacancies and metal sites on Al-substituted NiFe2O4 during peroxymonosulfate activation in the solid-water interface for 2,4-D degradation

Jinxiang Zuo,Donglei Fu,Pengwei Yan,Shuyu Wang,Yabin Li,Linlu Shen,Yizhen Cheng,Jimin Shen,Jing Kang,Zhonglin Chen

In this study, Al-doped NiFe 2 O 4 (NiAl x Fe 2-x O 4 ) was synthesized by the isomorphic substitution strategy, which was further employed for peroxymonosulfate (PMS) activation to remove 2,4-dichlorophenoxyacetic acid (2,4-D) in water. Doping of Al could construct oxygen vacancies (OVs) in the structure of NiAl x Fe 2-x O 4 , which further facilitates the exposure of metal sites for PMS activation. The removal rate of 2,4-D increased greatly compared to the NiFe 2 O 4 -activated process. By the density functional theory (DFT) process, it was verified that Al was more likely to replace Fe rather than Ni. OVs sites have the lowest adsorption energy of H 2 O ( E ads  = -0.95 eV), and easily formed surface hydroxyl groups (–OH), which were further replaced by PMS (HSO 5 - ). The formed surface complex Me-O-O-SO 3 - was readily activated via electron transfer between O-O bond, thus promoting the cleavage of it and inducing SO 4 · - generation. This process induced the high performance of the NiAl x Fe 2-x O 4 /PMS system for effective 2,4-D degradation. Furthermore, the purified water showed relatively low toxicity. The present study proposed new insights into the interface mechanism of PMS triggering.

研究领域: 环境科学 · 化学工程 · 材料科学 · 水处理
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CHEMICAL ENGINEERING JOURNAL · 2023 · IF 15.1

Surface atomic oxygen species mediated the in-situ formation of hydroxyl radicals on Fe3C decorated biochar for enhancing catalytic ozonation

Xinwei Zhu,Jimin Shen,Jing Kang,Pengwei Yan,Lei Yuan,Yizhen Cheng,Binyuan Wang,Shengxin Zhao,Zhonglin Chen

Developing highly efficient and anti-interference catalysts was still a challenge for the practical application of heterogeneous catalytic ozonation (HCO) in water decontamination. Herein, a magnetic Fe 3 C decorated biochar (Fe 3 C/BC) was prepared for HCO to achieve efficient degradation of 2,4-dichlorophenoxyacetic acid (2,4-D). The Fe 3 C/BC catalytic ozonation system promoted the degradation ratio of 2,4-D from 58.7% (ozonation alone) to 90.0% within 10 mins when the ozone dosage was 1.0 mg/L. And the observed degradation rate constant ( k obs ) of 2,4-D under catalytic ozonation system was 2.58 times that of ozonation alone. Fe 3 C/BC exhibited negligible adsorption on 2,4-D but with a significant enrichment to ozone, which realized the cooperating process of “adsorption-catalysis” at the solid–liquid interface, thus avoiding the ineffective decomposition of ozone. The dissociative adsorption of ozone molecules on the surface Fe 3 C generated surface atomic oxygen species (O* and O 2 *), which mediated the in-situ formation of hydroxyl radicals (·OH). ATR-FTIR, in-situ Raman, isotope tracing tests, and theoretical calculations were used to disclose the interface reaction processes and reveal the ·OH formation mechanism. Free radical reactions at the interface efficiently avoid the interference of coexisting ions dissolved in water. The presence of 3 mM (183 mg/L) bicarbonate had essentially little effect on the degradation of 2,4-D. The consecutive use of Fe 3 C/BC did not influence its catalytic performance and stable structure. This study provided new insight into the ·OH-dominated interfacial reaction in the HCO process.

研究领域: 环境科学 · 水处理 · 催化 · 高级氧化过程
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