Surface Topography in Cutting-Speed-Direction Ultrasonic-Assisted Turning.

Ultrasonic vibration has been employed to assist in turning, introducing intermittent machining to reduce average cutting force, minimize tool wear, and enhance machining efficiency, thereby improving surface roughness. However, achieving intermittent cutting necessitates specific conditions, with a cutting speed or feed rate falling below the critical speed associated with the ultrasonic vibration parameters. This study presents a theoretical model for surface formation in cutting-speed-direction ultrasonic-assisted turning (CUAT), covering both continuous and intermittent machining regimes. Experimental validation was conducted on C45 carbon steel and 201 stainless steel to demonstrate the applicability of the theoretical model across different materials. Digital microscope analysis revealed 3D topography consistency with the theoretical formula. Surface roughness evaluations were performed for both CUAT and CT (conventional turning) methods. The results indicated a significant reduction in roughness Ra for C45 steel samples machined with CUAT, up to 80% compared to CT at a cutting speed of 20 m/min, while only exhibiting slight fluctuations when turning 201 stainless steel. Detailed analysis and explanation of these phenomena are presented herein.

Single-step removal of arsenite ions from water through oxidation-coupled adsorption using Mn/Mg/Fe layered double hydroxide as catalyst and adsorbent.

This study developed a layered double hydroxides (Mn/Mg/Fe-LDH) material through a simple co-precipitation method. The Mn/Mg/Fe-LDH oxidized arsenite [As(III)] ions into arsenate [As(V)] anions. The As(III) and oxidized As(V) were then adsorbed onto Mn/Mg/Fe-LDH. The adsorption process of arseniate [As(V)] oxyanions by Mn/Mg/Fe-LDH was simultaneously conducted for comparison. Characterization results indicated that (i) the best Mg/Mn/Fe molar ratio was 1/1/1, (ii) Mn/Mg/Fe-LDH structure was similar to that of hydrotalcite, (iii) Mn/Mg/Fe-LDH possessed a positively charged surface (pHIEP of 10.15) and low Brunauer-Emmett-Teller surface area (SBET = 75.2 m2/g), and (iv) Fe2+/Fe3+ and Mn2+/Mn3+/Mn4+ coexisted in Mn/Mg/Fe-LDH. The As(III) adsorption process by Mn/Mg/Fe-LDH was similar to that of As(V) under different experimental conditions (initial solutions pH, coexisting foreign anions, contact times, initial As concentrations, temperatures, and desorbing agents). The Langmuir maximum adsorption capacity of Mn/Mg/Fe-LDH to As(III) (56.1 mg/g) was higher than that of As(V) (32.2 mg/g) at pH 7.0 and 25 °C. X-ray photoelectron spectroscopy was applied to identify the oxidation states of As in laden Mn/Mg/Fe-LDH. The key removal mechanism of As(III) by Mn/Mg/Fe-LDH was oxidation-coupled adsorption, and that of As(V) was reduction-coupled adsorption. The As(V) mechanism adsorption mainly involved: (1) the inner-sphere and outer-sphere complexation with OH groups of Mn/Mg/Fe-LDH and (2) anion exchange with host anions (NO3-) in its interlayer. The primary mechanism adsorption of As(III) was the inner-sphere complexation. The redox reactions made Mn/Mg/Fe-LDH lose its original layer structure after adsorbing As(V) or As(III). The adsorption process was highly irreversible. Mn/Mg/Fe-LDH can decontaminate As from real groundwater samples from 45-92 ppb to 0.35-7.9 ppb (using 1.0 g/L). Therefore, Mn/Mg/Fe-LDH has great potential as a material for removing As.

Sources for isolation of extracellular polymeric substances (EPSs) producing bacterial strains which are capable of using wastewater sludge as solo substrate.

Isolation of extracellular polymeric substances (EPSs) producing bacterial strains capable of using sludge as low-cost growth substrate was carried out in this study. A total of 110 EPS-producing strains were isolated from different sources, which include sludge of beer and winery wastewater treatment plant (WWTP); young, 2-month-old and 10-year-old leachate. Thirty-seven isolated strains showed good growth in sludge medium with cell count varying from 106 to 1010 most probable number (MPN)/mL and total EPS concentration from 2737 to 6639 mg/L. Twenty-one strains produced EPS with high flocculation activity (FAmax varied from 72.0% to 80.2%). The highest FAmax (80.2%) was observed with EPS produced by strain BES 19, which was isolated from sludge of beer WWTP. Sludge of beer WWTP, young leachate and 10-year-old leachate were good sources for isolation of EPS-producing bacteria.

Impact of extraction methods on bio-flocculants recovered from backwashed sludge of bio-filtration unit.

Effect of ten extraction methods on flocculation activity and chemical composition of bio-flocculants recovered from backwashed sludge of bio-filtration unit was studied. The results showed that the chemical method was better than physical method with respect to the extracted BFs weight and its flocculation activity. Cell lysis did not affect to the flocculation activity of BFs. Among ten extraction methods, EDTA (20 g/L) was the best one with extracted BFs dry weight of 6242 mg/L and flocculation activity of 83%. Optimization of EDTA concentration showed that 5 g EDTA/L (or 0.2 g EDTA/g SS) was suitable for recovery of BFs from backwashed sludge. The flocculation activity of BFs was 94% when using 2.4 mg of BFs/g of kaolin. The outcome of this study suggested that backwashed sludge of the bio-filtration unit was a potential source for exploiting bio-flocculants.

A multiresidue method for the determination of 118 pesticides in vegetable juice by gas chromatography-mass spectrometry and liquid chromatography-tandem mass spectrometry.

An analytical method has been developed for measuring 118 pesticides in vegetable juice. The extraction of pesticides was carried out based on dispersive solid-phase extraction, and determination was performed using gas chromatography with mass spectrometric detection (GC-MS-SIM) and liquid chromatography electrospray ionization tandem mass spectrometry (LC/ESI-MS/MS). Pesticides were confirmed by their retention time and their quantification and identification ions by GC-MS-SIM or multiple reaction monitoring of two fragment ions by LC/ESI-MS/MS, respectively. Spiking experiments from 10 to 120 microg/kg were carried out to determine the recovery, precision, and limit of quantification (LOQ) of the method. The overall recoveries of all pesticides were between 77 and 114% with relative standard deviations lower than 14%. The LOQ for most compounds was below 5 microg/kg. The proposed method was applied successfully for the residue determination of the 118 pesticides in commercial vegetable juice samples.

A multi-residue method for the determination of 203 pesticides in rice paddies using gas chromatography/mass spectrometry.

This work reports a rapid, specific and sensitive multi-residue method based on the Quick Easy Cheap Effective Rugged and Safe (QuEChERS) sample preparation method and gas chromatography with mass spectrometric detection in the selected ion monitoring mode (GC-MS-SIM) using one quantification ion and two identification ions for the routine analysis of 203 pesticides in rice paddies. Analyses of fortified rice paddy samples were performed at different levels (0.05, 0.20 and 0.50 mg kg(-1)). Mean recoveries from five replicates ranged from 75% to 115%, with coefficients of variation lower than 17%. The limit of quantification was in the range of 0.002-0.05 mg kg(-1) for the pesticides. 1040 rice paddy samples were analyzed for method application.

A multiresidue method for the determination of 107 pesticides in cabbage and radish using QuEChERS sample preparation method and gas chromatography mass spectrometry.

A rapid, specific and sensitive multiresidue method based on the modified Quick Easy Cheap Effective Rugged and Safe (QuEChERS) sample preparation method and gas chromatography with the electron impact mass spectrometric detection in the selected ion monitoring mode (GC-MS-SIM) using one target and two qualifier ions for the routine analysis of 107 pesticides in cabbage and radish has been developed. The recoveries for all the pesticides studied were from 80% to 115% with relative standard deviation lower than 15% in the concentration range of 0.030-0.360mg/kg. The limit of quantitation (LOQ) for most compounds met MRLs for pesticides in cabbage and radish in Korea. This method was successfully applied to analysis commercial cabbage and radish samples.

A multiresidue method for the determination of 109 pesticides in rice using the Quick Easy Cheap Effective Rugged and Safe (QuEChERS) sample preparation method and gas chromatography/mass spectrometry with temperature control and vacuum concentration.

A rapid, specific and sensitive multiresidue method based on the Quick Easy Cheap Effective Rugged and Safe (QuEChERS) sample preparation method and gas chromatography with mass spectrometric detection by selected ion monitoring (GC/MS-SIM) has been developed for the routine analysis of 109 pesticides in rice. The method uses one quantification ion and two identification ions. Temperature control during sample preparation helps improve the recovery of thermally labile pesticides such as captan. The method was validated by the analysis of samples spiked at 0.025-0.150 mg/kg in rice matrix. The recoveries of all pesticides were between 80% and 115% with a relative standard deviation of less than 15%. The limit of quantitation (LOQ) for most compounds met the maximum residue limits (MRLs) for pesticides in rice in Korea.