Effects of microplastics and cadmium co-contamination on soil properties, maize (Zea mays L.) growth characteristics, and cadmium accumulation in maize in loessial soil-maize systems.

Microplastics (MPs) are pervasive pollutants found in agricultural soils, yet research on the combined impacts of MPs and heavy metals on soil-plant systems remains limited. This study investigates the combined impact of low-density polyethylene (LDPE) microplastics (L: 1 mm, S: 100 µm, 0.1%, 1%) and Cd on soil properties, available Cd content, maize growth, and Cd accumulation by mazie through pot experiments. The findings unveiled notable impacts of the treatment groups, namely MP-L0.1%, MP-S0.1%, MP-L1%, and MP-S1%, on soil organic carbon (SOC), maize height, and catalase (CAT) activity (P < 0.05). The dosage of MPs significantly influenced maize height, MP-S0.1% treatment resulted in a 5.6% reduction, while the other groups had insignificant effects. Particle size and dosage significantly affected SOC and CAT (P < 0.01). The MP-L1% and MP-S1% groups resulted in increases of SOC by 121.5% and 281.0%, respectively. CAT reductions were 32.6%, 62.8%, 41.9%, and 34.9% in MP-L0.1%, MP-S0.1%, MP-L1%, and MP-S1% groups, individually. The Cd treatment induced a significant decrease in soil cation exchange capacity (CEC), maize stem diameter, and root length, accompanied by significant increases in maize plant height, malondialdehyde (MDA), CAT, and superoxide dismutase (SOD) activities. Combined LDPE and Cd contamination had significant effects on maize height and Cd content in leaves. Specifically, MP-L0.1%+Cd, MP-S0.1%+Cd, MP-L1%+Cd, and MP-S1%+Cd reduced maize height by 4.1%, 4.5%, 8.7%, and 13.8%, respectively. The co-presence of LDPE and Cd increased available Cd content in soil while elevating Cd concentration in maize shoots and roots, with a notable 25.5% increase in Cd concentration in maize leaves in the MP-L1%+Cd group compared to the Cd group. Furthermore, LDPE effects on soil-plant systems varied depending on particle size and dosage. This research provides important perspectives on evaluating the concurrent contamination and potential dangers of MPs and toxic metals in soil-plant environments.

Characteristics of Fe/C catalysts based on pyrolysis of ferric citrate and its peroxymonosulfate activation performance to degrade sulfadiazine in water.

Advanced oxidation techniques based on peroxysulfate activation have been paid much attention owing to their excellent performance in degrading stubborn pollutants in water. In response to the current situation that requires more raw materials and higher costs and involves more complicated processes for the preparation of Fe/C catalysts to activate persulfates, novel catalysts (Fe/C-700, Fe/C-800, Fe/C-900 and Fe/C-1000) were prepared by a high-temperature carbonization method at different pyrolysis temperatures (700, 800, 900 and 1000 °C) using inexpensive and environmentally friendly ferric citrate as raw material. Fe/C catalysts were characterized using SEM, EDS, XRD, XPS, and VSM and were screened for the activation of peroxymonosulfate (PMS) to degrade sulfadiazine (SDZ) in water, where Fe/C-900 exhibited higher efficiency. Thus, its activation performance for PMS to degrade SDZ was comprehensively investigated and the mechanisms of activation degradation were analyzed. The results showed that the degradation rate of 98.7% can be achieved to 10 mg L-1 SDZ by 0.1 g L-1 Fe/C-900 and 0.5 mmol L-1 PMS within 60 min. A wide range of solution pH, low catalyst dosage and good recycling performance were found in the Fe/C-900 application and the amount of iron ions dissolved at the end of the reaction was low (0.350 mg L-1). It was shown that both free radical and non-free radical pathways existed in the reaction system, where 1O2, SO4-˙ and O2-˙ played dominant roles in the degradation process of SDZ. The results could provide new ideas for the preparation of Fe/C catalysts and their heterogeneous activation for PMS to degrade stubborn organic pollutants in water.

Investigating Biochar-Derived Dissolved Organic Carbon (DOC) Components Extracted Using a Sequential Extraction Protocol.

Biochar-derived dissolved organic carbon (DOC), as the most important component of biochar, can be released on farmland, improving fertility and playing a role in soil amendment and remediation. The complexity of molecular structures and diversity of DOC compounds have influenced these functions to some extent. A sequential extract protocol consisting of water (25 °C), hot water (80 °C), and NaOH solution (0.05 M) was used to fully extract DOC compounds and gain a thorough understanding of the possible DOC components released from biochar. Rape straw (RS), apple tree branches (ATB), and pine sawdust (PS) were pyrolyzed at 300, 500, and 700 °C, respectively, to make nine distinct biochars. A TOC analyser, ultraviolet-visible spectroscopy (UV-vis), and excitation-emission fluorescence (EEM) spectrophotometer were used in conjunction with parallel factor analysis (PARAFAC) to determine the distribution of DOC content, the diversity of aromaticity, molecular weight characteristics and components of biochar-derived DOC. The results show that the relative distribution of water-extractable fractions ranged from 3.21 to 35.57%, with a low-aromaticity and extremely hydrophilic fulvic-acid-like compounds being found in the highest amounts (C2 and C3). The smallest amount of hot water-extractable components was produced from the release of small-molecule aliphatic compounds adsorbed on biochar and susceptible to migration loss once in a soil solution. More than half of the biochar-derived DOC was released in a NaOH solution, which primarily consisted of humic-acid-like compounds (C1), with higher molecular weights, more aromaticity, and lower bioavailability, according to the distribution of DOC in various extractants. In addition, the pyrolysis temperature and biomass type had a significant impact on the DOC properties released by biochar. As a result, the findings of this study showed that using a sequential extract protocol of water, hot water, and NaOH solution in combination with spectroscopic methods could successfully reveal the diversity of biochar-derived components, which could lead to new insights for the accurate assessment of potential environmental impacts and new directions for biochar applications.

The Biochar Derived from Carp for High-Efficiency Solar Steam Generation and Water Purification.

Efficient utilization of solar energy to generate steam is a green and promising technology because of its great potential applications in seawater desalination and industrial wastewater purification. However, the practical application of high-efficiency solar steam generation devices is largely overshadowed due to their complex process, high cost, low life-span, and poor thermal performance. Here, novel meat and bonemeal biochar (MBB) with high solar steam generation efficiency is produced by pyrolyzing dead carp at 300, 400, and 500 °C under anoxic conditions. Attributed to its typical hydrophilic pore structure, the photon trapping ability of MBB500 is up to 97% and 84.1% in the ultraviolet and visible regions and near-infrared light regions, respectively. Meanwhile, hydrophilic pore structural provides a strong capillary force for the rapid transmission of water. As a result, under 1 sun illumination (1 kW m-2), the water evaporation rate and the apparent energy conversion efficiency of MBB500 reach 1.48 kg m-2 h-1 and 131.2%, respectively. In addition, MBB500 also exhibits excellent seawater and heavy metal wastewater evaporation effects, providing a new manufacturing strategy for photo-thermal materials, which greatly benefit their practical application in pure water regeneration.

Influence of Intrinsic Physicochemical Properties of Agroforestry Waste on Its Pyrolysis Characteristics and Behavior.

To obtain a comprehensive understanding of the qualitative and quantitative effects of the intrinsic properties of biomass on its pyrolysis characteristics and assess the behavior of agroforestry waste, thermogravimetric analyses of three representative agroforestry wastes, namely rape (Brassica campestris L.) straw (RS), apple (Malus domestica) tree branches (ATB), and pine (Pinus sp.) sawdust (PS), were carried out by pyrolysis under dynamic conditions (30 to 900 °C) at different heating rates of 5, 10, and 15 °C·min-1. Correlation analysis showed that intrinsic physicochemical properties play distinct roles in different stages of pyrolysis. The ash content was negatively correlated with the temperature range (R2) of the second stage (190-380 °C) of pyrolysis. The lignin content and the amount of pyrolysis residues (RSS) were positively correlated. Kinetic triplets, including the activation energy (Ea), pre-exponential factor (A), and reaction model [f(α)], were obtained using different methods, including the Flynn-Wall-Ozawa (FWO), Freidman, Kissinger-Akahira-Sunose (KAS), and Starink methods. The mean activation energy (Ea[mean]) for RS, ATB, and PS calculated by the different methods ranged from 167.15 to 195.58 kJ·mol-1, 195.37 to 234.95 kJ·mol-1, and 191.27-236.45 kJ·mol-1, respectively. Correlation analysis of the intrinsic physicochemical characteristics and kinetic factors of agroforestry waste showed that the minimum Ea (Ea[min]) was significantly positively correlated with heat capacity (C0) and negatively correlated with thermal diffusivity (D). The Ea[mean] and the maximum value of Ea (Ea[max]) significantly positively correlated with the sum content of cellulose and lignin, indicating that the contents of cellulose and lignin determines the energy required for the pyrolysis process of agroforestry waste. The mechanism of degradation involves the diffusion model (D1, D2, and D3), the growth model (A4), and the geometrical contraction model (R3). These results indicate that the pyrolysis of agroforestry waste is a complex process due to the heterogeneity of its intrinsic physicochemical properties.

Near-Earth space balloon-based multi-band airglow imager optic design.

As a common tracer in the atmosphere, airglow can be used as an important means to study the interaction between the lower atmosphere, near space, and ionosphere. In the near-Earth space, the high-altitude balloon can realize long time flight, which makes the airglow detection realize both high range resolution and time resolution. In this paper, a balloon-based multi-band airglow imager is designed, which can observe OI (557.7 nm), Na (589.3 nm), OI (630.0 nm), and OH (720-910 nm) with annular field of view (30° inner ring and 80° outer ring), and its resolution is 500 m at 250 km. The multi-band airglow imager designed in this paper is equipped in the payload cabin and raised to above 30 km for flat flying for more than 6 h. The experimental results show that the imager worked normally, and airglow images were photographed and stored; the optical system can stand the harsh environment in the near space. The multi-band airglow imager designed in this paper will take part in other near-space exploration tasks in the future and obtain corresponding results.

Soil contamination and plant accumulation characteristics of toxic metals and metalloid in farmland soil-food crop system in Qilihe, China.

Toxic metals and metalloids (TMMs) in soil can be accumulated in crops, which poses potential risks to human health. In this paper, 55 topsoil and 23 crop samples, collected in Qilihe, China, were selected to study the contamination, risk, and plant accumulation of TMMs in soil-crop system. TMM concentrations in soil samples were all below the permissible limits, but Hg and Cd exhibited the potential ecological risk due to their slight accumulation in soil. There was slight Hg pollution in 2 samples of Lanzhou lily (Lilium davidii), and 1 sample of radish (Raphanus sativus), Chinese cabbage (Brassica pekinensis), and welsh onions (Allium fistulosum) due to Hg's strong bio-accumulation, but there was no risk to human health. The TMM accumulation in leaf crops was large, followed in tuber and seed crops. Available potassium, cation exchange capacity, soil organic matter, and available phosphate were the main factors associated with TMM accumulation in crops among the selected soil properties. This study shows the current contamination situation and the predominant influencing factors associated with the accumulation of TMMs in 24 crops, which provides the emphasis and direction of relative policies in land use and crop plantation.

Phytotoxicity of petroleum hydrocarbons: Sources, impacts and remediation strategies.

Extraction and exploration of petroleum hydrocarbons (PHs) to satisfy the rising world population's fossil fuel demand is playing havoc with human beings and other life forms by contaminating the ecosystem, particularly the soil. In the current review, we highlighted the sources of PHs contamination, factors affecting the PHs accumulation in soil, mechanisms of uptake, translocation and potential toxic effects of PHs on plants. In plants, PHs reduce the seed germination andnutrients translocation, and induce oxidative stress, disturb the plant metabolic activity and inhibit the plant physiology and morphology that ultimately reduce plant yield. Moreover, the defense strategy in plants to mitigate the PHs toxicity and other potential remediation techniques, including the use of organic manure, compost, plant hormones, and biochar, and application of microbe-assisted remediation, and phytoremediation are also discussed in the current review. These remediation strategies not only help to remediate PHs pollutionin the soil rhizosphere but also enhance the morphological and physiological attributes of plant and results to improve crop yield under PHs contaminated soils. This review aims to provide significant information on ecological importance of PHs stress in various interdisciplinary investigations and critical remediation techniques to mitigate the contamination of PHs in agricultural soils.

Qualitative and quantitative adsorption mechanisms of zinc ions from aqueous solutions onto dead carp derived biochar.

The objective of this study is to investigate the qualitative mechanisms of Zn2+ adsorption on carp biochars (CMBx) produced from dead carp at different temperatures (450-650 °C) and their quantitative contribution. The pseudo second order kinetic model and the Langmuir model could fit the kinetic and isothermal adsorption data well, respectively. The intra-particle diffusion was the main rate-limiting step but not the only rate-limiting step. The maximum adsorption capacity obtained from the Langmuir model for CMB650 was 87.7 mg g-1 which was greater than those of other biochars. Precipitation with minerals, ion exchange, and complexation with functional groups (OFGs) were the main adsorption mechanisms. Quantum chemistry calculations confirmed that the functional groups (e.g., hydroxyl, carboxyl and C[double bond, length as m-dash]C) tended to bind with Zn2+ more strongly than with Ca2+ and Mg2+, because the structure of the complex formed by the former was more stable. The contribution of different adsorption mechanisms varied with the pyrolysis temperature to prepare biochar. With increasing pyrolysis temperature, the contribution of the interaction between Zn2+ and the minerals increased from 46.4% to 84.7%, while that of complexation with OFGs decreased from 41.7% to 4.7%. Overall, the mechanism of Zn2+ adsorption on CMB450 was dominated by complexation with OFGs and exchange with cations (accounting for 73.2%), while the mechanisms on CMB650 were dominated by the interaction with minerals. In view of the total adsorption capacity, 650 °C was the optimized pyrolysis temperature for CMBx preparation and adsorption treatment of Zn-contaminated water. These results are useful for screening effective biochars as engineered sorbents to treat Zn-containing wastewater.

Contamination characteristics, source analysis, and ecological risk assessment of toxic metals and metalloid in agricultural soil in Yuzhong, China.

Human activities have caused toxic metal pollution and ecological risks to agricultural soil. In this study, 291 topsoil samples, collected in the agricultural soil system of Yuzhong, China, were selected to study the toxic metals and metalloids contamination characteristics, source and ecological risk based on geostatistics, pollution index, and ecological risk index. The main distribution of As is adjacent to pasture land and mainly comes from animal husbandry; Pb was observed near a coal mining factory and the Yellow River and was derived from industry and transportation; Cd was similar to Pb and was mainly derived from industry, transportation, and agriculture; Cr was found near a cement plant and was derived from industry and transportation; and Hg was found near an urban area and was mainly from industry and domestic garbage. The ratio of these elements exceeding the soil background value reached 99.9%. Except for the excess amounts of Cd and Hg in some samples, Cr, Hg, and As were mostly below permissible limits. Moreover, the comprehensive potential ecological risk of toxic metals is mainly at medium level and below, whereas the risks of Cd and Hg are higher. Control of Cd and Hg is important to prevent soil pollution. This study explains the current contamination situation, the predominant contaminants and their sources, and provides emphasis and direction for agricultural soil remediation.

Simultaneous adsorption and reduction of hexavalent chromium on biochar-supported nanoscale zero-valent iron (nZVI) in aqueous solution.

Flax straw biochar (FSBC)-supported nanoscale zero-valent iron (nZVI) composite (nZVI-FSBC) combining the advantages of nZVI and biochar was synthesized and tested for Cr(VI) removal efficiency from aqueous solution. Surface morphology and structure of FSBC and nZVI-FSBC were characterized by scanning electron microscopy, transmission electron microscopy, thermogravimetric analysis, X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, X-ray photoelectron spectroscopy (XPS), and Brunauer-Emmett-Teller techniques, which help to clarify the mechanism of Cr(VI) removal from aqueous solution. The adsorption of Cr(VI) onto FSBC and nZVI-FSBC was best described by the pseudo-second-order and the Sips model. Compared with FSBC, nZVI-FSBC remarkably improved the performance in removing Cr(VI) under identical experimental conditions. Due to the collaborative effect of adsorption and reduction of nZVI-FSBC, the adsorption capacity of nZVI-FSBC for Cr(VI) is up to 186.99 mg/g. The results obtained by XPS, XRD, and FTIR confirmed that adsorption and reduction dominated the processes of Cr(VI) removal by nZVI-FSBC. As a supporter, FSBC not only improved the dispersion of nZVI, but also undertook the adsorption task of Cr(VI) removal. The surface oxygen-containing functional groups of nZVI-FSBC mainly participated in the adsorption part, and the nZVI promoted the Cr(VI) removal through the redox reactions. These observations indicated that the nZVI-FSBC can be considered as potential adsorbents to remove Cr(VI) for environment remediation.

Assessments of Water-Soluble Inorganic Ions and Heavy Metals in Atmospheric Dustfall and Topsoil in Lanzhou, China.

The chemical features of atmospheric dustfall and topsoil in the same region could reflect the processes of the migration, transport, and diffusion of pollutants in the atmospheric-soil system. Samples of atmospheric dustfall and topsoil were collected in Lanzhou City. The contents and correlation of water-soluble inorganic ions (WSIIs) and heavy metals in dustfall and topsoil were analyzed, the sources of heavy metals and WSIIs in dustfall were distinguished, and the potential ecological risks of heavy metals in dustfall and topsoil were evaluated. The highest contents of WSIIs are SO42- (18,594 mg·kg-1) and Ca2+ (10,070 mg·kg-1) in dustfall, and for SO42- (8271 mg·kg-1) and Na+ (1994 mg·kg-1) in topsoil. The concentrations of heavy metals (Pb, Cu, Zn, Cr, Cd, and Ni) in dustfall are considerably higher than those in topsoil. Combustion of biomass and coal, transportation and industrial activities are the major anthropogenic sources of WSIIs and heavy metals in Lanzhou. Pollution of heavy metals except Cr and Ni in dustfall, and Cu, Cr, and Ni in topsoil was up to different degrees, where the pollution of Cd was serious. The risk of Cd in dustfall is high while moderate in topsoil. This research could offer a reference for the atmospheric particle pollution prevention and control in Lanzhou.

High-Altitude Balloon-Based Sensor System Design and Implementation.

As a kind of large-scale unmanned aerial vehicle, a high-altitude balloon can carry a large load up to tens of kilometers in the near space for a long time, which brings a new way for the stratosphere atmospheric detection. In order to provide a suitable working environment for the near-space detection load, it is necessary to design a sensor system based on a high-altitude balloon, which is used to provide environmental temperature, height position, and attitude information, current working, and video surveillance. The high-altitude balloon-based sensor system designed in this paper had participated in the near-space flight experiment, whose total flight time was 30 h and 53 min, and the horizontal flight time was 28 h and 58 min crossing the day and night. The high-altitude balloon-based sensor system had withstood the severe environment of the near-space during the day and night, providing accurate temperature measurement, real-time altitude position and attitude data acquisition, reliable current monitoring, and comprehensive video surveillance. In the next three years, the high-altitude balloon-based sensor system developed in this paper will continue to participate in the experiment and provide support for more detection loads.

Mechanism of phosphate removal from aqueous solutions by biochar supported nanoscale zero-valent iron.

The purpose of this study was to investigate the removal mechanism of phosphate by rape straw biochar (RSBC) supported nanoscale zero-valent iron (nZVI). BET, TEM, FTIR and XPS characterizations of the composite material (nZVI-RSBC) indicated that nZVI was successfully supported on the RSBC, and nZVI-RSBC had a high specific surface area and abundant oxygen-containing functional groups. Batch experiments showed that the adsorption data could be fitted well with the Sips isotherm model and pseudo-second-order kinetic model, suggesting that phosphate adsorption onto RSBC and nZVI-RSBC was due to surface and chemical processes. The maximum adsorption capacities of RSBC and nZVI-RSBC for phosphate obtained by the Sips isotherm model fitting were 3.49 mg g-1 and 12.14 mg g-1, respectively. The pH value of the solution greatly affected the adsorption capacity of nZVI-RSBC for phosphate. The combined results of batch experiments and characterizations revealed that the possible mechanism was the complexation of oxygen-containing functional groups on the surface of nZVI-RSBC with phosphate, hydrogen bonding, and electrostatic attraction between phosphate and the positively charged adsorption sites under acidic conditions. Such a strong adsorption capacity, as well as the characteristics of easy availability, excellent recyclability and low cost, make nZVI-RSBC potentially suitable for the treatment of phosphate-rich water.

Polydopamine and poly(dimethylsiloxane) modified superhydrophobic fiberglass membranes for efficient water-in-oil emulsions separation.

Separation of oil/water mixture using superwetting materials has received great interest in recent years. However, it is challenging to efficiently separate water-in-oil emulsions due to their high stability and complex structures in the presence of surfactants. Here, we report preparation of polydopamine (PDA) and poly(dimethylsiloxane) (PDMS) modified superhydrophobic fiberglass (FG) membranes for efficient separation of water-in-oil emulsions. The membranes were fabricated by in turn deposition of PDA and chemical vapor deposition of PDMS. In order to study the structure-performance relationship, the membranes were characterized using field emission scanning electron microscope, X-ray photoelectron spectroscopy, and Fourier transform infrared spectroscopy, etc. The membranes are superhydrophobic with a water contact angle of 152° and meanwhile superoleophilic with an oil contact angle of 0°. Also, the membranes demonstrate excellent acid, alkali and fire resistance. The absorption capacity of the membranes for diverse oils is 5.3-14.0 g g-1. Moreover, the membranes can remove more than 98% of water from the surfactant-stabilized water-in-oil emulsions. It is expected that the superhydrophobic FG membranes can be used for effective separation of diverse water-in-oil emulsions.

Synthesis of magnetic biochar derived from cotton stalks for the removal of Cr(VI) from aqueous solution.

A magnetic cotton stalk biochar (MCSBC) was synthesized through chemical co-precipitation, based on cotton stalk biochar (CSBC). The MCSBC and CSBC were characterized by scanning electron microscopy, Fourier transform infrared spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy and vibrating sample magnetometry. The characterization analyses showed that the magnetization process endowed the CSBC with excellent magnetic properties with a superparamagnetic magnetization of 27.59 emu/g. Batch adsorption experiment results indicated that the Cr(VI) maximum adsorption capacity of MCSBC was 20.05 mg/g, which was higher than that of CSBC (18.77 mg/g). The adsorption kinetic data were well fitted by the pseudo-second-order model and the adsorption isotherms were well represented by the Sips isotherm model. The thermodynamic studies indicated that the adsorption process was spontaneous and endothermic, and the entropy increased. The potential adsorption mechanism was the electrostatic adsorption of anionic Cr(VI) to the positively charged MCSBC surface, the reduction of Cr(VI) into Cr(III) and the complexation of Cr(III) by oxygen-containing functional groups of MCSBC. The regeneration studies showed that MCSBC kept 80% of its initial Cr(VI) adsorption capacity in the cycle. All the findings suggest that this novel magnetic biochar could be used in the field of Cr(VI)-containing wastewater treatment.

Durable superhydrophobic glass wool@polydopamine@PDMS for highly efficient oil/water separation.

The application of superhydrophobic materials for oil/water separation is receiving increasing attention. Meanwhile, durable superhydrophobic/superoleophilic materials and simple preparation methods are highly desired. Here, inspired by nature, we report a simple method for preparation of durable superhydrophobic glass wool (GW) for highly efficient oil/water separation. The durable and low-cost GW was converted to superhydrophobic simply by polymerization of dopamine followed by chemical vapor deposition of polydimethylsiloxane (PDMS). The polymerization of dopamine generated a lot of polydopamine nanoparticles on the surface of GW microfibers, forming hierachical micro-/nanostructures. The chemical vapor deposition of PDMS efficiently reduced the surface energy. The combination of the hierachical micro-/nanostructure and the PDMS layer successfully made the GW superhydrophobic with a water contact angle of ∼156° and water drops could easily roll off. In addition, the superhydrophobic GW showed high chemical stability in corrosive solutions and oils and high thermal stability. Moreover, the superhydrophobic GW showed high efficiency in selective oil absorption and oil/water separation as well as high recyclability. We believe that the superhydrophobic GW may find application in practical oil/water separation because of its good performance in oil/water separation and high stability under diverse harsh conditions.

Effects of dairy manure biochar on adsorption of sulfate onto light sierozem and its mechanisms.

The adsorption of nitrogen and phosphorous nutrients on biochar and even biochar-soil mixtures was investigated. However, the situation of sulfur was not very clear. Here, sulfate (SO4 2-) adsorption onto dairy manure biochar obtained at 700 °C (DMBC700), soil (light sierozem) and a 1 : 9 (w/w) biochar-soil mixture (DMBC700-soil) was investigated using batch experiments. The contact time, sulfate concentration, and solution pH value were chosen as the main factors; their effects on sulfate adsorption were tested, and the kinetics and isotherms were also investigated. Fourier transform infrared (FTIR) and X-ray diffraction (XRD) spectroscopies were used to characterize DMBC700 and soil before and after adsorbing sulfate, respectively, and to analyze the mechanisms of adsorption. The results showed that the adsorption kinetics were well described by the pseudo-second-order model, whereas the Langmuir and Freundlich models fitted well with the equilibrium data. DMBC700 modification did not increase the adsorption capacity of light sierozem for sulfate. When the pH values of the initial solution were increased, all the adsorption capacities of sulfate onto DMBC700, light sierozem and light sierozem with DMBC700 decreased. The electrostatic interaction was the main force for the adsorption of sulfate onto DMBC700, whereas both electrostatic interaction and formation of poorly soluble CaSO4 were the main forces for adsorption of sulfate onto light sierozem. DMBC700 was found to have negative effect on sulfate adsorption onto light sierozem.

5-Substituted-N-pyridazinylbenzamides as potent and selective LRRK2 inhibitors: Improved brain unbound fraction enables efficacy.

We describe the discovery and optimization of 5-substituted-N-pyridazinylbenzamide derivatives as potent and selective LRRK2 inhibitors. Extensive SAR studies led to the identification of compounds 18 and 23, which demonstrated good in vitro pharmacokinetic profile and excellent selectivity over 140 other kinases. Both compounds demonstrated high unbound fractions in both blood and brain. Compound 18 proved to be brain penetrant, and the high unbound fraction of compound 18 in brain enabled its in vivo efficacy in CNS, wherein a significant inhibition of LRRK2 Ser935 phosphorylation was observed in rat brain following intravenous infusion at 5 mg/kg/h.

Discovery of 4-ethoxy-7H-pyrrolo[2,3-d]pyrimidin-2-amines as potent, selective and orally bioavailable LRRK2 inhibitors.

Inhibition of LRRK2 kinase activity with small molecules has emerged as a potential novel therapeutic treatment for Parkinson's disease. Herein we disclose the discovery of a 4-ethoxy-7H-pyrrolo[2,3-d]pyrimidin-2-amine series as potent LRRK2 inhibitors identified through a kinase-focused set screening. Optimization of the physicochemical properties and kinase selectivity led to the discovery of compound 7, which exhibited potent in vitro inhibition of LRRK2 kinase activity, good physicochemical properties and kinase selectivity across the kinome. Moreover, compound 7 was able to penetrate into the CNS, and in vivo pharmacology studies revealed significant inhibition of Ser935 phosphorylation in the brain of both rats (30 and 100 mg/kg) and mice (45 mg/kg) following oral administration.