Remediation of pesticides contaminated water using biowastes-derived carbon rich biochar.

The competition impact and feedstock type on the removal of water pesticides using biochar have not yet been sufficiently investigated. Therefore, here we investigated the potentiality of three different biochars (BCs) derived from rice husk (RHB), date pit (DPB), and sugarcane bagasse (SBB) biowastes for the simultaneous removal of ten pesticides from water in a competitive adsorption system. The BCs structural characterization and morphology were investigated by XRD, FTIR spectroscopy and SEM analysis. The potential adsorption mechanisms have been investigated using various isothermal and kinetic models. RHB showed the highest removal percentages (61% for atrazine/dimethoate and 97.6% for diuron/chlorfenvinphos) followed by DPB (56% for atrazine/dimethoate and 95.4% for diuron/chlorpyrifos) and then SBB (60.8% for atrazine/dimethoate and 90.8% for chlorpyrifos/malathion). The higher adsorption capacity of RHB and DPB than SBB can be due to their high total pore volume and specific surface area (SSA). Langmuir model described well the sorption data (R2 = 0.99). Adsorption equilibrium was achieved after 60 min for RHB, and 120 min for both DPB and SBB. The optimum adsorbent dose (g/L) was 10 for RHB and 4 for DPB and SBB. The removal efficiency of pesticides was enhanced by decreasing pH from 9 to 5 by RHB and to 3 by DPB and SBB. XRD and FTIR spectroscopy confirmed that BCs contain some active adsorption groups and metal oxides such as MgO, SiO, Al2O3, CaO, and TiO2 that can play an effective role in the pesticides sorption. BET-N2 adsorption analysis demonstrated that the BC pore size contributes significantly to pesticide adsorption. These findings indicate that RHB, DPB, and SBB have ability for adsorption of water pesticides even under acidic conditions. Therefore, the rice husk, date pit, and sugarcane bagasse biowastes could be pyrolyzed and reused as effective and low-cost sorbents for elimination of hazardous substances such as pesticides in the aqueous environments.

Use of Highly Dispersed Mixed Metal Hydroxide Gel Compared to Bentonite Based Gel for Application in Drilling Fluid under Ultra-High Temperatures.

In order to solve the problem of poor dispersion and stability of mixed metal hydroxide (MMH), a kind of mixed metal hydroxide-like compound (MMHlc) gel was synthesized for use as the base mud in drilling fluid instead of bentonite gel. Na2CO3, Na2SiO3, and C17H33CO2Na were used as precipitants to form MMHlc with larger interlayer spacing and smaller particle size. MMHlc was synthesized by the coprecipitation method at 25 °C with a metal molar ratio of Mg:Al:Fe = 3:1:1. The performance evaluation of the treated drilling fluid showed that MMHlc (S2) synthesized using Na2SiO3 as the precipitant had the characteristics of low viscosity, low filtration, and a high dynamic plastic ratio at 25 °C, which fully met the requirements of oil field application, and it maintained its excellent properties after being aged at 250 °C for 16 h. Linear expansion and rolling recovery experiments showed that the S2 sample had excellent rheological properties and good inhibition. X-ray diffraction and FT-IR experiments showed that S2 had the most complete crystal structure, its interlayer distance was large, and its ion exchange capacity was strong. The thermogravimetric experiment showed that the S2 crystal was stable and the temperature resistance of the crystal could reach 340 °C. Zeta potential, particle size analysis, SEM, and TEM results showed that S2 is a nanomaterial with a complete morphology and uniform distribution. The drilling fluid of this formula had the characteristics of low viscosity, low filtration loss, and a high dynamic plastic ratio, and it met the conditions for oil field application. Considering these results, the new MMH prepared by our research institute is a drilling fluid material that can be used at ultra-high temperatures and can provide important support for drilling ultra-deep wells.

The Effect of Sodium Bentonite in the Thermo-Catalytic Reduction of Viscosity of Heavy Oils.

To study the synergistic catalysis of an ex situ catalyst and in situ clay in the aquathermolysis of heavy oil, in this paper, a series of bentonite-supported catechol-metal complexes were prepared, and the catalytic viscosity reduction performance in the aquathermolysis of heavy oil was investigated. Under the optimized conditions, the viscosity can be reduced by 73%, and the pour point can be lowered by 15.0 °C at most, showing the synergistic catalysis of the ex situ catalyst and in situ clay in this aquathermolytic reaction. Thermogravimetry, physical adsorption-desorption, and scanning electron microscopy were conducted to characterize the thermal stability and microstructure of the ex situ catalyst. The components of the heavy oil before and after the reaction were fully characterized. Six model compounds were used to simulate the aquathermolysis reaction process. In order to study the mechanism of viscosity reduction after the catalytic aquathermolysis reaction, the compounds were analyzed by GC-MS. It is believed that these results will be beneficial in the future for related research in this field.

Multi-Mixed Metal Hydroxide as a Strong Stratigraphic Nanoclay Inhibitor in Solid-Free Drilling Fluid.

Solid-free drilling fluid has more advantages as a new type of drilling fluid compared with traditional drilling fluid, such as improving drilling efficiency, protecting oil and not having clay particles clog the oil and gas layer. In this study, Zn/Cu/Fe-doped magnesium-aluminum hydroxide (Mg-Al MMH) was prepared using the co-precipitation method and evaluated in solid-free drilling fluid. The inhibition mechanism of synthesized hydroxide was analyzed by X-ray diffraction, laser particle-size analysis and thermogravimetric analysis. The samples were directly used as drilling fluid base muds for performance evaluation. The results showed that the linear expansion rate of 4% M6-Fe was only 12.32% at room temperature within 2 h, that the linear expansion rate was 20.28% at 90 °C and that the anti-swelling rate was 81.16% at room temperature, indicating that it has a strong inhibition ability at both room temperature and at high temperatures. Meanwhile, the possibility of multi-mixed metal hydroxide as a drilling fluid base mud is discussed in this study. We found that 4% M6-Fe exhibited low viscosity, a high YP/PV ratio and high temperature resistance, and its apparent viscosity retention rate reached 100% rolled at 200 °C for 16 h, with a YP/PV ratio of 2.33.

Rice hull biochar enhances the mobilization and methylation of mercury in a soil under changing redox conditions: Implication for Hg risks management in paddy fields.

Biochar amendment to paddy soils was promising to mitigate mercury (Hg) accumulation in rice; thus, it was applied to reduce human Hg exposure via rice consumption. However, how biochar affects Hg mobilization and MeHg formation in soil under changed redox potential (Eh) conditions remained unknown. Here, we explored the change of dissolved total Hg (DTHg) and dissolved MeHg (DMeHg), and their controlling biogeochemical factors in a soil with(out) biochar amendment under changing Eh conditions using biogeochemical microcosm. Biochar amendment resulted in a widen Eh range (-300 to 400 mV) compared to the control (-250 to 350 mV), demonstrating that biochar promoted reduction-oxidization reactions in soil. Biochar amendment enhanced Hg mobilization by mediating reductive dissolution of Fe/Mn (hydr)oxides. Thus, the increased Hg availability promoted MeHg formation in the soils. Biochar amendment changed the soil organic matter (SOM) composition. Positive correlations between the relative abundance of LIPID (lipids, alkanes/alkenes), ALKYL (alkylaromatics), and suberin and MeHg concentrations indicate that these SOM groups might be related to MeHg formation. Biochar enhanced the releasing and methylation of Hg by promoting the mobilization of Fe(oxyhydr)oxides and alternation of carbon chemistry under dynamic Eh conditions. There is an unexpected environmental risk associated with biochar application to paddy soils under dynamic Eh condition, and one should be aware this risk when applying biochar aiming to minimize human Hg exposure health risks via rice consumption.

Use of Betaine-Based Gel and Its Potential Application in Enhanced Oil Recovery.

In this paper, a betaine-based gel containing 2.0% erucamide propyl betaine (EAPB), 0.5% oleic acid amide propyl betaine (OAPB), and 0.1% KCl was prepared for use as a fracturing fluid. The performance evaluation showed that KCl may improve the temperature resistance and increase the viscosity of the optimized fracturing fluid. At 80 °C, the apparent viscosity of the viscoelastic surfactant (VES)-based fracturing fluid was approximately 50 mPa·s. Furthermore, the gel had high shear resistance, good viscosity stability, and high sand-carrying performance. After being sheared at 170 s−1 for 60 min, the reduction in viscosity was 13.6%. The viscosity of the gel was relatively stable at room temperature (27 °C) for one week. In a suspension containing 10% sand (particle size < 0.45 mm, density = 2.75 g cm−3), the settling velocity of proppant particles was 1.15 cm h−1. In addition, we detected that the critical micelle concentration of this gel was approximately 0.042 wt%. The viscosity could be reduced to <5 mPa·s at 60 °C within 1 h when 6.0% crude oil was present, and oil displacement experiments showed that the broken fracturing fluid can enhance the oil displacement rate up to 14.5%. This work may facilitate research on fracturing fluids and oil recovery.

Ecotoxicological effects of per- and polyfluoroalkyl substances (PFAS) and of a new PFAS adsorbing organoclay to immobilize PFAS in soils on earthworms and plants.

A novel adsorptive organoclay (Intraplex A®) was developed for the in situ immobilization of per- and polyfluoroalkyl substances (PFAS) in the vadose zone. We provide the first evaluation of the effects of Intraplex A® on earthworms and plants in a PFAS-contaminated soil. Ecotoxicological tests were carried out on control soil with and without Intraplex A® (C + I and C, respectively) and PFAS-contaminated soil with and without Intraplex A® (PFAS + I and PFAS, respectively). We investigated the acute ecotoxicological effects of PFAS and Intraplex A® on the growth, reproduction and survival of earthworms (Eisenia fetida) and on plant growth (oat - Avena sativa and turnip - Brassica rapa L. silvestris). Earthworm lethality was 7.6 lower in PFAS + I than in PFAS soil. Earthworms avoided 100% C + I and PFAS + I soils, and reduced earthworms' reproduction was observed in both these soils. For both plant species, the PFAS + I soil yielded less fresh and dry shoot biomass than the PFAS soil, while root growth remained unaffected (all tests: p < 0.05). Soils with Intraplex A® had some negative effects on plants and earthworms, which must be balanced with its benefits as an in situ PFAS adsorbent.

Herbal plants- and rice straw-derived biochars reduced metal mobilization in fishpond sediments and improved their potential as fertilizers.

Fishpond sediments are rich in organic carbon and nutrients; thus, they can be used as potential fertilizers and soil conditioners. However, sediments can be contaminated with toxic elements (TEs), which have to be immobilized to allow sediment reutilization. Addition of biochars (BCs) to contaminated sediments may enhance their nutrient content and stabilize TEs, which valorize its reutilization. Consequently, this study evaluated the performance of BCs derived from Taraxacum mongolicum Hand-Mazz (TMBC), Tribulus terrestris (TTBC), and rice straw (RSBC) for Cu, Cr, and Zn stabilization and for the enhancement of nutrient content in the fishpond sediments from San Jiang (SJ) and Tan Niu (TN), China. All BCs, particularly TMBC, reduced significantly the average concentrations of Cr, Cu, and Zn in the overlying water (up to 51% for Cr, 71% for Cu, and 68% for Zn) and in the sediments pore water (up to 77% for Cr, 76% for Cu, and 50% for Zn), and also reduced metal leachability (up to 47% for Cr, 60% for Cu, and 62% for Zn), as compared to the control. The acid soluble fraction accounted for the highest portion of the total content of Cr (43-44%), Cu (38-43%), and Zn (42-45%), followed by the reducible, oxidizable, and the residual fraction; this indicates the high potential risk. As compared with the control, TMBC was more effective in reducing the average concentrations of the acid soluble Cr (15-22%), Cu (35-53%), and Zn (21-39%). Added BCs altered the metals acid soluble fraction by shifting it to the oxidizable and residual fractions. Moreover, TMBC improved the macronutrient status in both sediments. This work provides a pathway for TEs remediation of sediments and gives novel insights into the utilization of BC-treated fishpond sediments as fertilizers for crop production.

Lubricity and Rheological Properties of Highly Dispersed Graphite in Clay-Water-Based Drilling Fluids.

Improving the tribological characteristics of water-based drilling fluids by adding graphene-based lubricants has garnered attention because of the potential for a range of inorganic-material-based additives at high temperature. In this study, we constructed a green and simple adsorption approach to prepare highly dispersed graphite using a cationic surfactant for graphite modification. The findings demonstrated that the prepared graphite was highly dispersed in water and had a low sedimentation rate and small contact angle in distilled water. The concentration dosage of cetyltrimethylammonium chloride (CTAC) on graphite was 0.02 g/g. We evaluated the performance of the modified graphite as a lubricated additive in water-based drilling through a rheological study and viscosity coefficient measurement. The results showed that the viscosity coefficient of drilling fluid with 0.05% modified graphite was reduced by 67% at 180 °C. We proved that the modified graphite can significantly improve the lubrication performance of drilling fluid. Furthermore, we revealed the lubrication mechanism by analyzing the chemical structural and crystalline and morphological features of graphite through a particle size test, zeta potential test, Fourier transform infrared (FTIR) spectroscopy, X-ray powder diffraction (XRD), and scanning electron microscopy (SEM) measurements. The results indicated that the modification of graphite by CTAC only occurs through physical adsorption, without changing the crystal structure. These findings provide a reference for the development of high-performance water-based drilling fluids.

Remediation of Cd and Cu contaminated water and soil using novel nanomaterials derived from sugar beet processing- and clay brick factory-solid wastes.

Producing nanomaterials from hazardous wastes for water and soil treatment is of great concern. Here, we produced and fully characterized two novel nanomaterials from sugar beet processing (SBR)- and brick factory-residuals (BFR) and assed their ability for Cd and Cu sorption in water and reducing metal availability in a contaminated soil. The SBR removed up to 99% of Cu and 91% of Cd in water, and exhibited a significantly faster and higher sorption capacity (qmax (g kg-1) = 1111.1 for Cu and 33.3 for Cd) than BFR (qmax (g kg-1) = 33.3 for Cu and 10.0 for Cd), even at acidic pH. Soil metal availability was significantly reduced by SBR (up to 57% for Cu and 86% for Cd) and BFR (up to 36% for Cu and 68% for Cd) compared to the unamended soil. The higher removal efficacy of SBR over BFR could be attributed to its higher alkalinity (pH = 12.5), carbonate content (82%), and specific surface area, as well as the activity of hydroxyl -OH and Si-O groups. The nano-scale SBR and BFR, the former particularly, are novel, of low cost, and environmental friendly amendments that can be used for the remediation of metal-contaminated water and soil.

Synthesis of Mg-Al Hydrotalcite Clay with High Adsorption Capacity.

A novel Mg-Al metal oxide has been successfully synthesized by the calcination of hierarchical porous Mg-Al hydrotalcite clay obtained by using filter paper as a template under hydrothermal conditions. Various characterizations of the obtained nanoscale oxide particles verified the uniform dispersion of Mg-Al metal oxides on the filter paper fiber, which had a size of 2-20 nm and a highest specific surface area (SSA) of 178.84 m2/g. Structural characterization revealed that the as-prepared Mg-Al metal oxides preserved the tubular morphology of the filter paper fibers. Further experiments showed that the as-synthesized Mg-Al metal oxides, present at concentrations of 0.3 g/L, could efficiently remove sulfonated lignite from oilfield wastewater (initial concentration of 200 mg/L) in a neutral environment (pH = 7) at a temperature of 298 K. An investigation of the reaction kinetics found that the adsorption process of sulfonated lignite (SL) on biomorphic Mg-Al metal oxides fits a Langmuir adsorption model and pseudo-second-order rate equation. Thermodynamic calculations propose that the adsorption of sulfonated lignite was spontaneous, endothermic, and a thermodynamically feasible process.

Acetylation Modification of Waste Polystyrene and Its Use as a Crude Oil Flow Improver.

Polystyrene is used in a wide range of applications in our lives, from machine housings to plastic cups and miniature electronic devices. When polystyrene is used, a large amount of waste is produced, which can cause pollution to the environment and even harm biological and human health. Due to its low bulk density (especially the foamed type) and low residual value, polystyrene cannot be easily recycled. Often waste polystyrene is difficult to recycle. In this paper, waste polystyrene has been modified by using acetic anhydride which caused a crude oil flow improver. The results showed that modified polystyrene improves the flow properties of the crude oil, reducing the viscosity and the pour point of the crude oil by up to 84.6% and 8.8 °C, respectively. Based on the study of the paraffin crystal morphology, the mechanism of improving the flow capacity of crude oil by modified polystyrene was proposed and analyzed.

Experimental Investigation of Suitable Cutting Conditions of Dry Drilling into High-Strength Structural Steel.

Dry machining is one of the main ways to reduce the environmental burden of the machining process and reduce the negative effect of the cutting fluid and aerosols on operators. In addition, dry machining can reduce overall machining costs and, in the case of large workpieces, reduce the extra work associated with removing residual cutting fluid from the workpiece and adjacent area. For high-strength structural steel products, it is typical to drill holes with larger diameters of around 20 mm. Therefore, this work is devoted to the investigation of the dry drilling process carried out on a workpiece made of S960QL steel with a helical drill with a diameter of 21 mm. The aim was to find suitable cutting conditions for dry drilling with regard to process stability and workpiece quality. An experiment performed with a coolant served as a comparison base. A dry drilling experiment was performed with cutting speeds from 30 to 70 m·min-1 and feeds from 0.1 to 0.3 mm·rev-1, and with the results of this experiment, the same experiment with flood cooling was performed. During the drilling process, spindle torque values were recorded using the indirect spindle current recording method. The macroscopic chip morphology was studied to understand the cutting process. The chip thickness ratio was measured, as well as the maximum diameter of spiral chips. On the final workpiece, the qualitative and dimensional parameters of the holes were evaluated, such as the diameter, cylindricity and surface roughness, depending on the change in the cutting conditions and cutting environment. Evaluation of the obtained data led to the following conclusions. When drilling the S960QL material, there is only a very small increase in the drilling torque during dry drilling compared to drilling with cutting fluid. The increase in friction demonstrated by the chip thickness coefficient is significant. The influence of the environment on the dimensional accuracy showed a tendency for a slight increase in the holes' diameters during dry machining. In comparison, the cylindricity of the dry-drilled holes shows a lower deviation than the holes drilled with cutting fluid. The surface roughness of the holes after dry drilling is affected by the increased friction of the outgoing chips, despite the resulting parameters being very good due to the drilling technology standards. This work provides a comprehensive view of the dry drilling process under defined conditions, and the results represent suitable cutting conditions to achieve a stable cutting process and a suitable quality of drilled holes.

Phase Composition of Silica Fume-Portland Cement Systems Formed under Hydrothermal Curing Evaluated by FTIR, XRD, and TGA.

Two substitution levels of Portland cement by silica fume (SF; 30 and 50 mass%) and three hydrothermal treatment regimes (0.5, 1.2, and 2 MPa and 165, 195, and 220 °C for 7 days, respectively) were selected for the investigation of high-temperature phase formation. A combination of thermogravimetric, X-ray diffraction, and Fourier transform infrared analyses in the mid-IR region was used to overcome the shortcomings of individual techniques for the identification of these complex systems. Changes in molecular water amounts, the polymerization degree of silicate chains, or their decomposition due to transformations and crystallization of phases at hydrothermal conditions were observed and discussed concerning composition. Contrary to the calciochondrite, hydrogrossular phases, α-C2SH, and jaffeite detected in the systems without SF, a decrease in CaO/SiO2 ratio resulted in the formation of stable tobermorite in the case of 30 mass% SF, whilst calcium hydrogen silicate, gyrolite, and cowlesite were identified as more thermally stable phases in the samples with 50 mass% SF.

Enhanced Removal of Sulfonated Lignite from Oil Wastewater with Multidimensional MgAl-LDH Nanoparticles.

In this study, hierarchical MgAl-LDH (layered double hydroxide) nanoparticles with a flower-like morphology were prepared under a hydrothermal condition by employing worm-like micelles formed by cetyltrimethylammonium bromide (CTAB) and salicylic acid (SA) as templates. The morphology and structure of the materials were characterized by Brunauer-Emmett-Teller (BET), SEM, and XRD analyses. The performance for the adsorption of sulfonated lignite (SL) was also investigated in detail. FTIR was used to detect the presence of active functional groups and determine whether they play important roles in adsorption. The results showed that the hierarchical MgAl-LDH nanoparticles with a specific surface area of 126.31 m2/g possessed a flower-like morphology and meso-macroporous structures. The adsorption capacity was high-its value was 1014.20 mg/g at a temperature of 298 K and an initial pH = 7, which was higher than traditional MgAl-LDH (86 mg/g). The adsorption process of sulfonated lignite followed the pseudo-second-order kinetics model and conformed to Freundlich isotherm model with a spontaneous exothermic nature. In addition, the hierarchical MgAl-LDH could be regenerated and used, and the adsorption was high after three adsorption cycles. The main adsorption mechanisms were electrostatic attraction and ion exchange between the hierarchical MgAl-LDH and sulfonated lignite.

Use of biochar to reduce mercury accumulation in Oryza sativa L: A trial for sustainable management of historically polluted farmlands.

Mitigating the risk of mercury (Hg) contamination in rice soils using environmental friendly amendments is essential to reducing the probable daily intake (PDI) of MeHg via rice consumption. Here, we examined the impacts of different doses (0% (control), 0.6% and 3%) of rice hull-derived biochar (RHB) and mixture of wheat-rice straw-derived biochar (RWB) on the fractionation, phytoavailability, and uptake of total (THg) and methyl Hg (MeHg) by rice in Hg-polluted soil (THg = 78.3 mg kg-1) collected from Wanshan Hg mining area. Both biochars increased rice biomass up to 119% as compared to control. Application of RHB and RWB significantly (P ≤ 0.05) decreased bioavailable Hg (soluble and exchangeable and specifically-sorbed fractions) concentrations by 55-71% and 67-72%, respectively. The addition of RHB significantly decreased MeHg concentrations in the soil. However, RWB (particularly at 3%) increased significantly MeHg concentrations in the soil as compared to the control and RHB treatments, likely due to the increased abundance of Hg-methylation microorganisms (e.g., Geobacter spp., Nitrospira spp.) in the RWB treatments. Both RHB and RWB significantly decreased MeHg concentrations in the rice grain by 55-85%. We estimated a reduction of the PDI of MeHg from 0.26 µg kg-1 bw d-1of control to below the reference dose (0.1 µg kg-1 bw d-1) of two biochar treatments. Our results highlight the potentiality of RWB and RHB for mitigating MeHg accumulation in rice and reducing PDI of MeHg via rice consumption, which offers a sustainable approach for management of Hg-polluted soils.

Fe/Mn- and P-modified drinking water treatment residuals reduced Cu and Pb phytoavailability and uptake in a mining soil.

Management of industrial hazardous waste is of great concern. Recently, aluminum rich drinking water treatment residuals (Al-WTR) received considerable attention as a low-cost immobilizing agent for toxic elements in soils. However, the suitability and effectiveness of modified Al-WTR as stabilizing agent for toxic metals such as Cu and Pb in mining soil is not assessed yet. We examined the impact of different doses (0, 0.5, 1.5, and 2.5%) of raw and Fe/Mn- and P- modified Al-WTR on the bioavailability and uptake of Cu and Pb by ryegrass in Cu and Pb contaminated mining soil. The addition of Fe/Mn-and P- modified Al-WTR to the soil reduced significantly the concentrations of Pb (up to 60% by Fe/Mn-Al-WTR and 32% by P-Al-WTR) and Cu (up to 45% by Fe/Mn-Al-WTR and 18% by P-Al-WTR) in the shoots and roots of ryegrass as compared to raw Al-WTRs and untreated soil. Our results demonstrate that modification of the raw Al-WTR increased its pH, CEC, specific surface area, active functional groups (Fe-O and Mn-O), and thus increased its immobilization efficiency. Our results highlight the potential of the modified Al-WTR, particularly the Fe/Mn-Al-WTR, for the remediation of Cu and Pb contaminated soils and recommend field scale verification.

The Inhibition Property and Mechanism of a Novel Low Molecular Weight Zwitterionic Copolymer for Improving Wellbore Stability.

In this work, a novel low molecular weight zwitterionic copolymer for improving wellbore stability, which is expected to be an alternative to the current shale inhibitors, was obtained by copolymerization of tris hydroxyethyl allyl ammonium bromide (THAAB), 2-acrylamido-2- methyl propane sulfonic acid (AMPS) and acrylamide (AM), initiated by a redox initiation system in an aqueous solution. The copolymer, denoted as SX-1, was characterized by FT-IR, TGA-DSC, and GPC. Results demonstrated that the molecular weight of SX-1 was approximately 13,683 g/mol and it displayed temperature resistance up to 225 °C. Regarding the inhibition performance, evaluation experiments showed the hot rolling recovery of a Longmaxi shale sample in 2.0 wt % SX-1 solutions was up to 90.31% after hot rolling for 16 h at 120 °C. The Linear swelling height of Na-MMT artificial core in 2.0 wt % SX-1 solution was just 4.74 mm after 16 h. Methods including particle size analysis, FTIR, XRD, and SEM were utilized to study the inhibition mechanism of SX-1; results demonstrated that SX-1 had entered into the inner layer of sodium montmorillonite (Na-MMT) and adsorbed on the inner surface, and the micro-structure of Na-MMT was successfully changed by SX-1. The particle size of Na-MMT in distilled water was 8.05 µm, and it was observed that its size had increased to 603 µm after the addition of 2.0 wt % of SX-1. Its superior properties make this novel low molecular weight copolymer promising for ensuring wellbore stability, particularly for high temperature wells.

Toxoplasma gondii in vegetables from fields and farm storage facilities in the Czech Republic.

Infection with Toxoplasma gondii has usually been connected with consumption of improperly treated meat. However, contaminated water and products of plant origin have emerged as new sources of infection in the last few years. Here, 292 vegetable samples-carrot, cucumber and lettuce-obtained from nine farms in the Czech Republic were examined using triplex real time PCR targeting two specific T. gondii sequences. Irrigation water and water used for washing of vegetables were also included. Overall, a positivity rate of 9.6% was found in vegetables. The concentration varied between 1.31 × 100 and 9.00 × 102 oocysts/g of sample. A significant difference was found between the positivity of vegetables collected directly from fields and that of vegetables collected from farm storage rooms (4.4-8.6% vs 10-24.1%, respectively). All samples of irrigation water and water used to rinse vegetables were negative. Genotyping based on restriction fragment length polymorphism (RFLP) analysis using seven markers revealed the exclusive presence of genotype II.

Tracing of Selected Viral, Bacterial, and Parasitic Agents on Vegetables and Herbs Originating from Farms and Markets.

Fresh vegetables and herbs are usually prepared and eaten raw without cooking or heating, which leads to a high risk of foodborne infection. The aim of the present study was to assess the contamination of raw vegetables, herbs, and the environment of food chains. Vegetable and herb samples originating both from the Czech Republic as well as from other countries were examined. The work was focused on the detection of commonly found, but also less frequently monitored foodborne pathogens, including viruses of the genus Norovirus (NoVs), hepatitis A virus (HAV), Listeria monocytogenes and Cronobacter spp. bacteria, and the parasites Cryptosporidium spp. and Giardia intestinalis. All samples were analyzed using individual RT-qPCR/qPCR assays; bacterial pathogens were also simultaneously detected using culture methods. The prevalence of the studied microorganisms in 623 samples ranged from 0.6% to 44.3% for individual pathogens. None of the samples were positive for the presence of HAV. Analysis of 157 environmental samples from 12 farms revealed the presence of NoVs in the environment of four farms. NoVs were detected in water samples as well as on the hands and gloves of workers. Escherichia coli was detected in all farms in the environmental samples and in eight farms in water samples. However, no sample of water exceeded the level of 100 CFU/mL for E. coli. None of the samples of water were positive for the presence of the studied parasites. Vegetables and herbs available from Czech markets and farms may pose a certain risk of foodborne disease, especially in the case of NoVs and parasites. PRACTICAL APPLICATION: This study provides valuable information on the microbiological quality of raw vegetables and herbs available from Czech markets and farms. Good hygienic practices aimed at reducing the incidence of pathogenic agents on fresh produce should not be neglected. Emphasis should be placed on the control of irrigation water, especially with respect to norovirus contamination. It is appropriate to combine culture methods and qPCR methods for the detection of bacterial agents.