You Liang

Developing ionic liquid forms of picloram with reduced negative effects on the aquatic environment

As a widely used herbicide, picloram has been frequently detected in the aquatic environment due to its high leaching potential and low adsorption by soil. To reduce aquatic environmental risk of this herbicide caused by leaching and runoff, five herbicidal ionic liquids (HILs) based on picloram were prepared by pairing isopropylamine, octylamine, octadecylamine, 1-methylimidazole, 4-methylmorpholine respectively. Their physicochemical properties including water solubility, octanol-water partition coefficient, surface activity, leaching, as well as soil adsorption were compared. The results showed that these properties could be adjusted by appropriate selection of counter cations. The HILs with long alkyl chains in cations had low water solubility and leaching characteristics, good surface tension and lipophilicity, as well as high soil adsorption. Compared with currently used picloram in the forms of potassium salts, HIL3 had more excellent herbicidal activity against broadleaf weeds and may offer a lower use dosage. The HILs based on picloram can reduce its negative effects on the aquatic environment and can be used as a desirable alternative to commercial herbicidal formulations of picloram in future.

Ionic liquids based on bromoxynil for reducing adverse impacts on the environment and human health

Many herbicides exhibit some disadvantages such as high water solubility and volatility after application, which lead to potential threats to the aquatic and atmospheric environment and human health. Herbicidal ionic liquids (HILs) can effectively eliminate these intrinsic shortcomings by pairing with appropriate counterions (cation or anion). In this study, new HILs based on bromoxynil with eight typical cations were synthesized to reduce the negative impacts of currently used forms of bromoxynil. All the obtained compounds were investigated for solubility, octanol–water partition coefficient, surface activity, volatilization rate, and herbicidal activity in a greenhouse. The results showed that the HILs with long alkyl chains in the cations had reduced water solubility and volatilization rate, better surface activity and Kow, and substantially improved efficacy against weeds over bromoxynil sodium. Due to their adjustable physicochemical properties and improved herbicidal activity, the HILs could tremendously reduce the adverse impacts of bromoxynil on the environment and human health and may be potential alternatives to currently popular forms of bromoxynil in the future.

Pectin-conjugated silica microcapsules as dual-responsive carriers for increasing the stability and antimicrobial efficacy of kasugamycin

Kasugamycin is an aminoglycoside antibiotic originally isolated from Streptomyces kasugaensis, which has been widely used for the management of plant diseases. However, photo-thermal instability and low efficiency limit its application. Therefore, it is an urgent task to prevent unwanted loss of kasugamycin and ensure maximum bioactivity at target site. In this work, a novel formulation of kasugamycin that responds to different biological stimuli produced by pests was prepared using silica microcapsules crosslinked with pectin via special disulfide bonds. The results demonstrated that the silica-SS-pectin microcapsules had a high loading efficiency (20% w/w) and could effectively enhance the thermal and light stability of kasugamycin. The microcapsules displayed excellent pectinase and glutathione dual-responsive properties and the release kinetics investigated by Riger-Peppas model suggested combination of various release mechanisms. Compared with kasugamycin wettable powder, the microcapsules possessed sustained and improved antimicrobial efficacy against Erwinia carotovora. Thus, the dual-responsive microcapsules potentially have agricultural application as a controlled release system.

Guanidinium ionic liquid-controlled synthesis of zeolitic imidazolate framework for improving its adsorption property

The massive release of rhodamine B (RhB) to water system is an emerging problem, which dramatically threaten environment and human health. The development of an adsorbent with enhanced removal efficiency for RhB is urgently needed. Herein, we report an environment-friendly synthesis of high quality zeolitic imidazolate framework-8 (ZIF-8) and functional ionic liquid@ZIF-8 in water-based system without heat treatment for improving its adsorption property. Guanidinium ionic liquids (ILs) could not only act as greener agents instead of volatile bases and toxic surfactants to efficiently control the nucleation and growth rate of ZIF-8, but also were incorporated as shell material to add specific adsorption sites. The relationship between nanoparticle structure and adsorption performance for RhB was systematically investigated. Due to high surface area (1167 m2 g-1), high porosity (0.79 cm3 g-1), high crystallinity, nano size (about 100 nm) and monodispersity, the as-obtained ZIF-8 showed improved adsorption capacity toward RhB (80% removal efficiency). Heteropolyanion-based guanidinium IL@meso-ZIF-8 (HPAIL@meso-ZIF-8) exhibited the high RhB uptake capacity of 278 mg g-1 (higher than most of the reported adsorbents) and effectively removed 99% of RhB within 15 min. The results showed that the adsorption process of prepared materials fitted well with pseudo-second-order kinetics and Langmuir isotherm model. The existence of mesopores in ZIF-8 facilitated the diffusion of RhB and the incorporated guanidinium IL played a significant role in enhancing the adsorption affinity. Moreover, the reusability results revealed the HPAIL@meso-ZIF-8 as a highly efficient adsorbent for RhB removal with satisfactory performance and structural stability. Therefore, HPAIL@meso-ZIF-8 is one of the most promising adsorbents for organic dye removal from water.

Preparation and characterization of indole-3-butyric acid nanospheres for improving its stability and utilization

Indole-3-butyric acid (IBA) is an efficient plant growth regulator for promoting germination and the formation of rooting of various plants. Since it is unstable and presents the low utilization ratio, there is a compelling need to design an environmentally friendly formulation for IBA, which can reduce the loss of degradation and improve its utilization. Nano-sized controlled-release formulations can provide better durability and penetrate through the plant epidermis to efficiently deliver the agrochemicals to the target tissues. In this work, a kind of novel nano controlled-release formulation was prepared by conjugating the IBA and 3-glycidoxypropyltrimethoxysilane (GPTMS) through a covalent cross-linking reaction, and subsequently hydrolyzation and polycondensation with tetraethoxysilane. The resulting nanospheres were characterized by Fourier transform infrared spectroscopy, ultraviolet spectrophotometry, scanning electron microscope, and thermal gravity analysis. The results showed that the obtained nanospheres had a remarkable loading efficiency of IBA (about 43% w/w). The formation of covalent between IBA and GPTMS enabled the nanospheres with a good chemical stability that could protect against photo-degradation effectively. The released rate of the IBA from nanospheres was related to the temperature, pH value. With increased temperature as well as acidity and alkality, the release of the IBA was sped up. The IBA could also be released effectively from IBA-silica nanospheres by esterase, and the sustainable release characteristics of IBA-silica nanospheres were in conformity with the Ritger and Peppas equation. The IBA-silica nanospheres displayed excellent dual stimuli-responsive properties under esterase and weak acid conditions, and could obviously promote the growth of root and bud of pea. Thus, the IBA silica nanospheres prepared by covalent cross-linking reaction have a good potential application as a controlled-release formulation and environmentally-friendly plant growth regulator.

Relationship between structure of ionic liquid and its enrichment ability to trace fungicides from environmental water sample

To elucidate the relationship between the structure of ionic liquid (IL) and its enrichment ability to trace pesticides from an environmental water sample, a series of imidazole-based ILs were synthesized to extract four fungicides (boscalid, cyprodinil, fluazinam, and pyrimethanil) through an in situ ionic liquid dispersive liquid-liquid microextraction method. The results showed that aromatic heterocyclic monocation ionic liquids (MILs) had better extraction ability to fungicides than other three alicyclic heterocyclic MILs. Dication ionic liquids (DILs) with the four carbons at the side chain had better ability to extract fungicides than MILs, and DILs with a long bridge carbon chain had better recoveries of fungicides with low Kow values. The proposed method showed high mean enrichment factors and high recoveries of the fungicides from real water samples. The rules of the relationship between the structure of IL and enrichment ability are instructive to the application of ILs in pretreatment of complex substances.