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A novel probiotics-derived protein, P8, suppresses the growth of colorectal cancer (CRC). P8 can penetrate the cell membrane via endocytosis and cause cell cycle arrest in DLD-1 cells through down-regulation of CDK1/Cyclin B1. However, neither the protein involved in the endocytosis of P8 nor the cell cycle arrest targets of P8 are known. We identified two P8-interacting target proteins [importin subunit alpha-4 (KPNA3) and glycogen synthase kinase-3 beta (GSK3β)] using P8 as a bait in pull-down assays of DLD-1 cell lysates. Endocytosed P8 in the cytosol was found to bind specifically to GSK3β, preventing its inactivation by protein kinases AKT/CK1ε/PKA. The subsequent activation of GSK3β led to strong phosphorylation (S33,37/T41) of β-catenin, resulting in its subsequent degradation. P8 in the cytosol was also found to be translocated into the nucleus by KPNA3 and importin. In the nucleus, after its release, P8 binds directly to the intron regions of the GSK3β gene, leading to dysregulation of GSK3β transcription. GSK3β is a key protein kinase in Wnt signaling, which controls cell proliferation during CRC development. P8 can result in a cell cycle arrest morphology in CRC cells, even when they are in the Wnt ON signaling state.

Background Successful chemoprevention or chemotherapy is achieved through targeted delivery of prophylactic agents during initial phases of carcinogenesis or therapeutic agents to malignant tumors. Bacteria can be used as anticancer agents, but efforts to utilize attenuated pathogenic bacteria suffer from the risk of toxicity or infection. Lactic acid bacteria are safe to eat and often confer health benefits, making them ideal candidates for live vehicles engineered to deliver anticancer drugs. Results In this study, we developed an effective bacterial drug delivery system for colorectal cancer (CRC) therapy using the lactic acid bacterium Pediococcus pentosaceus. It is equipped with dual gene cassettes driven by a strong inducible promoter that encode the therapeutic protein P8 fused to a secretion signal peptide and a complementation system. In an inducible CRC cell-derived xenograft mouse model, our synthetic probiotic significantly reduced tumor volume and inhibited tumor growth relative to the control. Mice with colitis-associated CRC induced by azoxymethane and dextran sodium sulfate exhibited polyp regression and recovered taxonomic diversity when the engineered bacterium was orally administered. Further, the synthetic probiotic modulated gut microbiota and alleviated the chemically induced dysbiosis. Correlation analysis demonstrated that specific bacterial taxa potentially associated with eubiosis or dysbiosis, such as Akkermansia or Turicibacter, have positive or negative relationships with other microbial members. Conclusions Taken together, our work illustrates that an effective and stable synthetic probiotic composed of P. pentosaceus and the P8 therapeutic protein can reduce CRC and contribute to rebiosis, and the validity and feasibility of cell-based designer biopharmaceuticals for both treating CRC and ameliorating impaired microbiota.

Objective To determine the most optimal needle insertion point of extensor indicis (EI) using ultrasound.Methods A total 80 forearms of 40 healthy volunteers were recruited. We identified midpoint (MP) of EI using ultrasound and set MP as optimal needle insertion point. The location of MP was suggested using distances from landmarks. Distance from MP to medial border of ulna (MP-X) and to lower margin of ulnar head (MP-Y) were measured. Ratios of MP-X to Forearm circumference (X ratio) and MP-Y to forearm length (Y ratio) were calculated. In cross-sectional view, depth of MP (Dmp), defined as middle value of superficial depth (Ds) and deep depth (Dd) was measured and suggested as proper depth of needle insertion.Results Mean MP-X was 1.37±0.14 cm and mean MP-Y was 5.50±0.46 cm. Mean X ratio was 8.10±0.53 and mean Y ratio was 22.15±0.47. Mean Dmp was 7.63±0.96 mm.Conclusion We suggested that novel optimal needle insertion point of the EI. It is about 7.6 mm in depth at about 22% of the forearm length proximal from the lower margin of the ulnar head and about 8.1% of the forearm circumference radial from medial border of ulna.

As part of the Megacity Air Pollution Studies (MAPS)-Seoul campaign, three types of research flights were conducted over the Seoul Metropolitan Area (SMA) from May till June 2015 to measure the spatial distribution of a pollution plume near a power plant and petrochemical complex, the vertical profiles of pollutants on the western coast of Korea, and the pollutant distribution in the SMA. The pollution plume (~0–700 m) was highly concentrated and dominated by organic aerosol (OA), which very likely oxidized in the plume, as it showed slightly less oxidation near the source and significantly less oxidation at altitudes above the plume. One vertical profile displayed transitions in concentration and changes in the dominant components, suggesting that the particle sources and/or processing differed above ~1000 m; below 1000 m, where the total mass and OA concentrations were high, sulfate and likely transport sources predominated. The other profile, which was assessed during a separate flight, exhibited sharp increases in the OA number concentration and mean diameter, less oxidized organic content, and higher organic and nitrate concentrations above 1400 m, indicating high-altitude transport and a cleaner boundary layer. Finally, flights investigating the distributions of pollutants in the central, upwind, and downwind SMA regions generally detected high levels of oxidation downwind as well as different aerosol masses between the low and high altitudes. This study highlights the necessity of understanding the complex vertical structures of particle layers, such as those identified in and around the SMA, in order to facilitate the adoption of efficient air quality control strategies and enhance air quality forecasting.

The dynamic behavior of reed valves during suction and discharge is very important in predicting compressor performance and valve fatigue fracture. For an accurate dynamic analysis of reed valves, mass flow rate and effective force area should be accurately modeled. In this study, mass flow rate and effective force area models were developed based on CFD analysis results using the well-known commercial software ANSYS Fluent. CFD analyses were carried out for various values of port radius, valve radius, valve lift, and pressure difference. The mass flow rate and pressure force on valve were obtained from the analysis. Then, effective flow and force area models were proposed and the model coefficients were determined using the CFD results. The average prediction error of the effective flow area and the effective force area were 1.90% and 2.9%, respectively. It was shown that the effective flow area is dependent only on the port radii and valve lift; it is not dependent on the valve radii. The proposed effective force area model can accurately describe the decrease and increase in pressure force with valve lift.

Byung Chull An,1 Yeo-Sang Yoon,1 Ho Jin Park,1 Sangkyun Park,1 Tai Yeub Kim,1 Jun Young Ahn,1 Daebeom Kwon,1 Oksik Choi,1 Jin Young Heo,1 Yongku Ryu,1 Joong-Hyun Kim,2 Heejong Eom,2 Myung Jun Chung1 1R&D Center, Cell Biotech, Co., Ltd., Gimpo-si, Gyeonggi-do, Korea; 2Laboratory Animal Center, Osong Medical Innovation Foundation, Chungbuk, Cheongju, 28160, KoreaCorrespondence: Myung Jun Chung Tel +82-31-987-6205Fax +82-31-987-6216Email ceo@cellbiotech.comPurpose: This study aimed to toxicological evaluate a probiotics-based delivery system for p8 protein as an anti-colorectal cancer drug.Introduction: Lactic acid bacteria (LAB) have been widely ingested for many years and are regarded as very safe. Recently, a Pediococcus pentosaceus SL4 (PP) strain that secretes the probiotic-derived anti-cancer protein P8 (PP-P8) has been developed as an anti-colorectal cancer (CRC) biologic by Cell Biotech. We initially identified a Lactobacillus rhamnosus (LR)-derived anti-cancer protein, P8, that suppresses CRC growth. We also showed that P8 penetrates specifically into CRC cells (DLD-1 cells) through endocytosis. We then confirmed the efficacy of PP-P8, showing that oral administration of this agent significantly decreased tumor mass (∼ 42%) relative to controls in a mouse CRC xenograft model. In terms of molecular mechanism, PP-P8 induces cell-cycle arrest in G2 phase through down-regulation of Cyclin B1 and Cdk1. In this study, we performed in vivo toxicology profiling to obtain evidence that PP-P8 is safe, with the goal of receiving approval for an investigational new drug application (IND).Methods: Based on gene therapy guidelines of the Ministry of Food and Drug Safety (MFDS) of Korea, the potential undesirable effects of PP-P8 had to be investigated in intact small rodent or marmoset models prior to first-in-human (FIH) administration. The estimated doses of PP-P8 for FIH are 1.0× 1010 – 1.0× 1011 CFU/person (60 kg). Therefore, to perform toxicological investigations in non-clinical animal models, we orally administered PP-P8 at doses of 3.375 × 1011, 6.75 × 1011, and 13.5× 1011 CFU/kg/day; thus the maximum dose was 800– 8000-fold higher than the estimated dose for FIH.Results: In our animal models, we observed no adverse effects of PP-P8 on clinicopathologic findings, relative organ weight, or tissue pathology. In addition, we observed no inflammation or ulceration during pathological necropsy.Conclusion: These non-clinical toxicology studies could be used to furnish valuable data for the safety certification of PP-P8.Keywords: biologics, therapeutic protein, probiotics derived anti-cancer protein P8, Pediococcus pentosaceus SL4, Lactobacillus rhamnosus, colorectal cancer, drug delivery system, protein secretion system, oral administration, non-clinical trial, toxicology finding

Changes in the water quality by the riverbank filtration (RBF) process were investigated in the field-scale demonstration sites. The overall water quality was improved by RBF, but Fe2+ concentration significantly increased in the riverbank-filtered water more than in the river water. This result would be caused by the interaction between the iron minerals and the river water in the aquifer and the influx of the hinterland groundwater into RBF wells. Dissolution properties of iron from the aquifer soils cored at the sites were evaluated through incubation experiment considering various values of redox potential (Eh), dissolved oxygen (DO), and hydrogen-ion concentration exponent (pH). These results presented that at the incubator with the final Eh of 470 mV, DO of 3.4, and pH of 4.53, the iron from the aquifer soil was most dissolved, and the pyrite and siderite contents in the aquifer soil decreased significantly from 11.5 to 6.22% and from 50.8 to 24.5%, respectively. Based on changes of ion concentrations (such as Fe2+, Fe3+, SO42- and NO3-) and iron species in the incubators, it was believed that pyrite and siderite minerals in the aquifer soils cause an increase in the Fe2+ concentration with the absence of DO and an increase in the Fe2+ and Fe3+ concentrations with the presence of DO. The dissolution rates of iron minerals into Fe2+ and Fe3+ were dependent on Eh, pH, and DO and were more sensitive to Eh and pH than DO. The results of this study can provide information on RBF site selection and its operation.

To understand the characteristics of air quality in the Seoul Metropolitan Area, intensive measurements were conducted under the Korea-United States Air Quality (KORUS-AQ) campaign. Trace gases such as O3, NOx, NOy, SO2, CO, and volatile organic compounds (VOCs), photochemical byproducts such as H2O2 and HCHO, aerosol species, and meteorological variables including planetary boundary layer height were simultaneously measured at Olympic Park in Seoul. During the measurement period, high O3 episodes that exceeded the 90 ppbv hourly maximum occurred on 14 days under four distinct synoptic meteorological conditions. Furthermore, local circulation such as land–sea breeze and diurnal evolution of the boundary layer were crucial in determining the concentrations of precursor gases, including NOx and VOC as well as O3. During such episodes, the nighttime NOx and VOC and daytime UV levels were higher compared to non-episode days. The overall precursor levels and photochemical activity were represented fairly well by variations in the HCHO, which peaked in the morning during the high O3 episodes. This study revealed that toluene was the most abundant VOC in Seoul, and its concentration increased greatly with NOx due to the large local influence under stagnant conditions. When O3 was highly elevated concurrently with PM2.5 under dominant westerlies, NOx and VOCs were relatively lower and CO was noticeably higher than in other episodes. Additionally, the O3 production efficiency was the highest due to a low NOx with the highest NOz/NOy ratio among the four episodes. When westerlies were dominant in transport-south episode, the nighttime concentration of O3 remained as high as 40~50 ppbv due to the minimum level of NOx titration. Overall, the Seoul Metropolitan Area is at NOx-saturated and VOC-limited conditions, which was diagnosed by indicator species and VOC/NOx ratios.

The Korea – United States Air Quality Study (May – June 2016) deployed instrumented aircraft and ground-based measurements to elucidate causes of poor air quality related to high ozone and aerosol concentrations in South Korea. This work synthesizes data pertaining to aerosols (specifically, particulate matter with aerodynamic diameters

We investigated concurrent effects between nano-sized zero-valent iron (NZVI) and dissolved organic matter (DOM). Specific UV absorbance of DOM revealed that aromatic/hydrophobic moieties of DOM were bounded to NZVI surfaces. The DOM fluorescence emission peak shifted toward lower wavelength after NZVI exposure, which indicated removal of aromatic DOM fractions. This blue shift of the emission peak also attributes to the reduction of electron acceptors through NZVI-DOM charge transfer complexes. High molecular weight (103-104 Da) DOM fractions, which are suspected to be both aromatic and hydrophobic, were removed. X-ray absorption spectroscopy (XAS) elucidated that Fe(0) content in the 30-d aged NZVI in the presence of DOM (61.6%) was substantially higher than that in the absence of DOM (25.0%). Corrosion and oxidation of NZVI were mitigated due to interruption of electron transfer by surface bounded DOM and stabilization of Fe(II) by Fe-DOM complexes. The XAS also revealed that the evolution of the iron (oxyhydr)oxide shell of NZVI was significantly altered by complexed aromatic DOM.

The objective of this study was to determine comprehensive chemical components in PM2.5 from March 2011 till February 2012 in Seoul, South Korea, and their contributions to light extinction. Major chemical components in the aerosol were: ammonium sulfate, 30.3%; ammonium nitrate, 25.2%; organic matter, 21.3%; crustal mass, 16.9%; element carbon, 6.1%; and trace metals, 0.2%. PM2.5 mass concentrations and light extinction were mostly correlated in their diurnal and monthly variations, which indicates that the aerosol mass is the key variable in light extinction in Seoul. However, the aerosol size and composition (of PM2.5) also played significant roles in light extinction. We applied the IMPROVE algorithm to quantify the contributions of observed chemical components to light extinction. It was found that the IMPROVE formula tended to underestimate light extinction by up to 30% in urban conditions where large sources of organic matter (OM) and element carbon (EC) existed unless some revision was made before the light extinction calculations. The IMPROVE algorithm was further optimized for the observed light extinction for OM and EC. The revised light extinction efficiencies of OM and EC in Seoul increased by about 1.5–3 times of those in the original IMPROVE algorithm. The optimized IMPROVE scheme in this study reproduced the observed light extinction more accurately in Seoul. Overall, 41% of the contribution from OM and EC to light extinction in Seoul was close to 50% of the contribution from nitrate and sulfate, although the mass of the former contribution was only half of the latter.

Author(s): Kim, H; Choi, WC; Rhee, HJ; Suh, I; Lee, M; Blake, DR; Kim, S; Jung, J; Lee, G; Kim, DS; Park, SM; Ahn, J; Lee, SD | Abstract: To understand the chemical mechanisms of controlling factors in ozone (O3) formation in early summer in Seoul, a comprehensive study encompassing measurement and modeling was conducted under the Megacity Air Pollution Study-Seoul (MAPS-Seoul) campaign. From May 18 to June 12, 2015, O3 and peroxyacetyl nitrate (PAN) were measured, along with their precursors, including NOx and volatile organic compounds (VOCs), at the Korea Institute of Science and Technology, located in northeast Seoul. VOCs were sampled in a canister twice a day (at 09:30 and 15:00) and analyzed via gas chromatography. The meteorological conditions and chemical regimes of the air masses were clearly distinguished during the study period. In May, NOx concentrations were higher with more pronounced diurnal cycles of precursors and O3 under constant westerly winds. By contrast, stagnant conditions developed in June, which reduced the inflow of primary emissions from the downtown area but increased the influence from the neighboring forest under high temperatures. As a result, the ratio of O3 to odd oxygen was higher in June, indicating a less efficient removal of O3 by NOx. In the same context, the air mass was chemically more aged with a higher NO2/NOx ratio and enhanced OH reactivity of oxygenated and biogenic VOCs in June. The overall measurement results suggest that O3 formation is slightly more sensitive to VOCs than to NOx in Seoul during this season, when O3 concentrations are the highest of the year.

The effects of the injection parameters on delivery of nanoscale zero-valent iron (NZVI) to contaminated groundwater were investigated. The first two NZVI injections (gravity injection at low flow rates) resulted in NZVI being poorly mobile and gave total cumulative mass recoveries at the monitoring wells of 1.07%-2.43%. NZVI reached some wells (KDMW-3, MW-2, MW-4, and MW-7) earlier than the bromide tracer. The dominant travel directions for NZVI and the bromide tracer were very different. The NZVI transport characteristics suggested that targeted NZVI delivery requires preferential groundwater flow paths and local heterogeneity to be considered. In the gravity injection tests, the maximum NZVI concentrations and cumulative NZVI mass recoveries in the wells decreased markedly as the injected NZVI concentration and dose increased. In the third and fourth tests, in which NZVI was injected under pressure at high flow rates, NZVI was effectively delivered to the wells despite the injected NZVI concentration and dose being high. Relatively high cumulative mass recoveries of 26.0% and 74.5% were found for the third and fourth injections, respectively. Controlling the flow rate (pressure) and NZVI concentration and dose simply and effectively controlled NZVI mobility in the groundwater. The colloidal and electrostatic characteristics of the NZVI particles were monitored and modeled, and the results indicated that NZVI particles without Derjaguin-Landau-Verwey-Overbeek energy barriers were successfully delivered to the target zone and that decreased magnetic attractive forces between NZVI particles caused by iron corrosion probably decreased the degree of NZVI particle aggregation and therefore contributed to NZVI being delivered to the target zone.

To improve the understanding of secondary organic aerosol (SOA) formation from the photo-oxidation of anthropogenic and biogenic precursors at the regional background station on Baengnyeong Island, Korea, gas phase and aerosol chemistries were investigated using the Proton Transfer Reaction Time of Flight Mass Spectrometer (PTR-ToF-MS) and the Aerodyne High Resolution Time of Flight Aerosol Mass Spectrometer (HR-ToF-AMS), respectively. HR-ToF-AMS measured fine particles (PM1 diameter of particle matter less than 1 μm) at a 6-minute time resolution from February to November 2012, while PTR-ToF-MS was deployed during an intensive period from September 21 to 29, 2012. The one-minute time-resolution and high mass resolution (up to 4000 m Δm-1) data from the PTR-ToF-MS provided the basis for calculations of the concentrations of anthropogenic and biogenic volatile organic compounds (BVOCs) including oxygenated VOCs (OVOCs). The dominant BVOCs from the site are isoprene (0.23 ppb), dimethyl sulphide (DMS, 0.20 ppb), and monoterpenes (0.38 ppb). Toluene (0.45 ppb) and benzene (0.32 ppb) accounted for the majority of anthropogenic VOCs (AVOCs). OVOCs including acetone (3.98 ppb), acetaldehyde (2.67 ppb), acetic acid (1.68 ppb), and formic acid (2.24 ppb) were measured. The OVOCs comprise approximately 75% of total measured VOCs, suggesting the occurrence of strong oxidation processes and/or long-range transported at the site. A strong photochemical aging and oxidation of the atmospheric pollutants were also observed in aerosol measured by HR-ToF-AMS, whereby a high f44 : f43 value is shown for organic aerosols (OAs); however, relatively low f44 : f43 values were observed when high concentrations of BVOCs and AVOCs were available, providing evidence of the formation of SOA from VOC precursors at the site. Overall, the results of this study revealed several different SOA formation mechanisms, and new particle formation and particle growth events were identified using the powerful tools scanning mobility particle sizer (SMPS), PTR-ToF-MS, and HR-ToF-AMS.

Objective The purposes of this study were to introduce a superficial temporal artery (STA)-sparing mini-pterional approach for the treatment of cerebral aneurysms and review the surgical results of this approach. Methods Between June 2010 and December 2015, we performed the STA-sparing mini-pterional approach for 117 patients with 141 unruptured intracranial aneurysms. We analyzed demographic, radiologic, and clinical variables including age, sex, craniotomy size, aneurysm location, height of STA bifurcation, and postoperative complications. Results The mean age of patients was 58.4 years. The height of STA bifurcation from the superior border of the zygomatic arch was 20.5 mm±10.0 (standard deviation [SD]). The craniotomy size was 1051.6 mm2±206.5 (SD). Aneurysm neck clipping was possible in all cases. Intradural anterior clinoidectomy was performed in four cases. Contralateral approaches to aneurysms were adopted for four cases. Surgery-related complications occurred in two cases. Permanent morbidity occurred in one case. Conclusion Our STA-sparing mini-pterional approach for surgical treatment of cerebral aneurysms is easy to learn and has the advantages of small incision, STA sparing, and a relatively wide surgical field. It may be a good alternative to the conventional pterional approach for treating cerebral aneurysms.

Recently, we reported a novel therapeutic probiotic-derived protein, p8, which has anti-colorectal cancer (anti-CRC) properties. In vitro experiments using a CRC cell line (DLD-1), anti-proliferation activity (about 20%) did not improve after increasing the dose of recombinant-p8 (r-p8) to &gt, 10 &mu, M. Here, we show that this was due to the low penetrative efficiency of r-p8 exogenous treatment. Furthermore, we found that r-p8 entered the cytosol through endocytosis, which might be a reason for the low penetration efficiency. Therefore, to improve the therapeutic efficacy of p8, we tried to improve delivery to CRC cells. This resulted in endogenous expression of p8 and increased the anti-proliferative effects by up to 2-fold compared with the exogenous treatment (40 &mu, M). Anti-migration activity also increased markedly. Furthermore, we found that the anti-proliferation activity of p8 was mediated by inhibition of the p53-p21-Cyclin B1/Cdk1 signal pathway, resulting in growth arrest at the G2 phase of the cell cycle. Taken together, these results suggest that p8 is toxic to cancer cells, shows stable expression within cells, and shows strong cancer suppressive activity by inducing cell cycle arrest. Therefore, p8 is a strong candidate for gene therapy if it can be loaded onto cancer-specific viruses.

Mechanisms involved in an electrochemically assisted oxidation process using persulfate and nanosized zero-valent iron (NZVI) were elucidated. Initially, Fe

Global challenges including overpopulation, climate change, and income inequality have increased, and a demand for sustainability has emerged. Decision-making for sustainable development is multifaceted and interlinked, owing to the diverse interests of different stakeholders and political conflicts. Analysing a situation from all social, political, environmental, and economic perspectives is necessary to achieve balanced growth and facilitate sustainable development. South Korea was among the poorest countries following the Korean War, however, it has developed rapidly since 1955. This growth was not limited to economic development alone, and the chronology of South Korean development may serve as a reference for development in other countries. Here, we explore the compressed growth of South Korea using a narrative approach and time-series, comparative, and spatial analyses. Developmental indicators, along with the modern history of South Korea, are introduced to explain the reasons for compressed growth. The development of the mid-latitude region comprising 46 countries in this study, where nearly half of Earth’s population resides, was compared with that of South Korea, results show that the developmental chronology of South Korea can serve as a reference for national development in this region.

Mechanisms involved in an electrochemically assisted oxidation process using persulfate and nanosized zero-valent iron (NZVI) were elucidated. Initially, Fe0 acted as a source of Fe2+ to activate the persulfate, then Fe2+/Fe3+ redox mediation between cathode and persulfate played a decisive role in persulfate activation at a current density low enough not to inhibit Fe0 corrosion. An excessive current density which resulted in a low cathodic potential limited Fe0 corrosion and therefore limited the supply of dissolved Fe to activate the persulfate. Direct oxidation of phenol at the anode therefore became more important under the excessive current density than oxidation by sulfate radicals. At a low current density, Fe0 in the NZVI particles was completely transformed into iron (oxyhydr)oxides such as ferrihydrite, lepidocrocite, and magnetite. Fe0 was transformed into Fe2+ little when the current density was high. Increasing the current density increased the energy cost by increasing the amount of electrical energy dissipated in side reactions that decreased sulfate radical formation. The results indicated that a low current density can generally be used to give a high reaction rate and a high energy efficiency and that a high current density can be used when the NZVI particles need to be preserved.

We previously described a MgO-based binder for treating fine sediment and simultaneously store CO

The mechanisms involved in the activation of persulfate by nanosized zero-valent iron (NZVI) were elucidated and the NZVI transformation products identified. Two distinct reaction stages, in terms of the kinetics and radical formation mechanism, were found when phenol was oxidized by the persulfate/NZVI system. In the initial stage, lasting 10 min, Fe0(s) was consumed rapidly and sulfate radicals were produced through activation by aqueous Fe2+. The second stage was governed by Fe catalyzed activation in the presence of aqueous Fe3+ and iron (oxyhydr)oxides in the NZVI shells. The second stage was 3 orders of magnitude slower than the initial stage. An electron balance showed that the sulfate radical yield per mole of persulfate was more than two times higher in the persulfate/NZVI system than in the persulfate/Fe2+ system. Radicals were believed to be produced more efficiently in the persulfate/NZVI system because aqueous Fe2+ was supplied slowly, preventing sulfate radicals being scavenged by excess aqu...

To improve understanding of the sources and chemical properties of particulate pollutants on the western side of the Korean Peninsula, an Aerodyne High Resolution Time of Flight Aerosol Mass Spectrometer (HR-ToF-AMS) measured non-refractory fine (PM 1 ) particles from May to November, 2011 at Baengnyeong Island, South Korea. Organic matter and sulfate were generally the most abundant species and exhibited maximum concentrations of 36 μg/m 3 and 39 μg/m 3 , respectively. Nitrate concentrations peaked at 32 μg/m 3 but were typically much lower than sulfate and organic matter concentrations. May, September, October, and November featured the highest monthly average concentrations, with lower concentrations typically observed from June through August. Potential source contribution function (PSCF) analysis and individual case studies revealed that transport from eastern China, an area with high SO 2 emissions, was associated with high particulate sulfate concentrations at the measurement site. Observed sulfate aerosol sometimes was fully neutralized by ammonium but often was acidic; the average ammonium to sulfate molar ratio was 1.49. Measured species size distributions revealed a range of sulfate particle size distributions with modes between 100 and 600 nm. Organic aerosol source regions were widespread, including contributions from eastern China and South Korea. Positive matrix factorization (PMF) analysis indicated three “factors,” or types of organic aerosol, comprising one primary, hydrocarbon-like organic aerosol (HOA) and two oxidized organic aerosol (OOA) components, including a more oxidized (MO-OOA) and a less oxidized (LO-OOA) oxidized organic aerosol. On average, HOA and OOA contributed 21% and 79% of the organic mass (OM), respectively, with the MO-OOA fraction nearly three times as abundant as the LO-OOA fraction. Biomass burning contributions to observed OM were low during the late spring/early summer agricultural burning season in eastern China, since airflow into eastern China during the Asian Monsoon generally prevents transport of emissions eastward to the Korean Peninsula. Concentrations of the m/z 60 AMS biomass burning marker were more abundant in autumn, when transport patterns appeared to bring some smoke from fires in northern Asia to the island.

An MgO-based binder was developed that could stabilize fine dredged sediments for reuse and store CO2. Initially, a binder consisting of fly ash (FA) and blast furnace slag (BFS) was developed by using alkaline activators such as KOH, NaOH, and lime. The FA0.4-BFS0.6 binder (mixed at a FA-to-BFS weight ratio of 4:6) showed the highest compressive strength of 10.7 MPa among FA/BFS binders when 5 M KOH was used. When lime (L) was tested as an alkaline activator, the strength was comparable with those obtained when KOH or NaOH was used. The L0.1-(FA0.4BFS0.6)0.9 binder (10 % lime mixed with the FA/BFS binder) showed the highest strength of 11.0 MPa. Finally, by amending this L0.1-(FA0.4BFS0.6)0.9 binder with MgO, a novel MgO-based binder (MgO0.5-(L0.1-(FA0.4BFS0.6)0.9) 0.5) was developed, which demonstrated the 28th day strength of 11.9 MPa. The MgO-based binder was successfully applied to stabilize a fine sediment to yield a compressive strength of 4.78 MPa in 365 days, which was higher than that obtained by the Portland cement (PC) system (3.22 MPa). Carbon dioxide sequestration was evidenced by three observations: (1) the decrease in pH of the treated sediment from 12.2 to 11.0; (2) the progress of the carbonation front inward the treated sediment; and (3) the presence of magnesium carbonates. The thermogravimetric analysis (TGA) results showed that 67.2 kg of CO2 per ton of the treated sediment could be stored under the atmospheric condition during 1 year.

Mono-potassium phosphate (MKP), natural phosphate fertilizer, and red mud (RM) were tested individually and as mixed agents for stabilizing Cd, Pb, and Zn in mine tailings. The mixed stabilizer containing MKP/RM was the most effective among the tested stabilizers. This is based on the efficiency of conversion from the plant-available metal fractions to the non-plant-available metal fractions and on the performances of toxicity characteristic leaching procedure tests. MKP/RM converted Cd and Zn mainly to carbonate and Fe/Mn oxide fractions, and Pb mainly to the residual fraction. When the mine tailings were treated with MKP/RM, the pH value of the stabilized soil increased from 3.4 to 6.4 after 28 days, which is advantageous for plant growth. The X-ray diffraction, scanning electron microscopy/energy dispersive spectroscopy, and the sequential extraction results imply that the major stabilization mechanism for Cd and Zn by MKP and RM involves the formation of surface complexes with Fe (hydr)oxides or Fe phosphates. The major stabilization mechanism of Pb by MKP is believed to involve the formation of Pb-phosphate precipitates, and that by RM is proposed to involve the formation of inner sphere complexes with Fe/Al (hydr)oxides or incorporation within the grids of Fe/Al (hydr)oxides or silicate minerals.

Ionizing irradiation is a useful technique for disinfestation under plant quarantine as well as post-harvest management. Effects of gamma irradiation treatment were tested on different developmental events of Carposina sasakii, which is a serious pest of various orchard crops. Apple fruits infested by C. sasakii were irradiated by gamma rays ranging from 0 to 300 Gy. Inhibition rates were determined on behavioral events related to development, including larval exit from apples, cocoon formation, adult eclosion, and oviposition. Failure rates of all these developmental events increased with increasing doses of irradiation. Rates of larval exit from apples and cocoon formation decreased to 13.2% and 1.7%, respectively, at 300 Gy. However, the adult eclosion rate decreased to 5.4% at 100 Gy and was completely inhibited at doses greater than 150 Gy. LD99 values for the inhibition of cocoon formation and adult emergence was estimated into 313.4 and 191.0 Gy. Furthermore, adults developed from irradiated larvae completely failed to lay eggs. Thus, irradiation of infested apples at doses of 200 Gy and higher completely inhibited the next generation of C. sasakii. Our results suggest that gamma irradiation treatment would be a promising technique for the control of C. sasakii.

A MgO-based binder developed to simultaneously solidify/stabilize contaminated sediment and store CO2 has been described previously. The objectives of the study presented here were to investigate the kinetics of the carbonation reactions of the binder and the extent to which carbonation occurred and to identify the optimal conditions for using the binder. The carbonation reaction was clearly faster and the degree of carbonation higher at CO2 concentrations of 50 and 100% than in the ambient atmosphere (which contains 0.04% CO2). A modified unreactive core model adequately described the kinetics. The rate constants were 0.0217–0.319 h−1 and were proportional to the degree of carbonation. A high degree of carbonation, 93.8%, was achieved at a CO2 concentration of 100%. The water to sediment ratio strongly affected carbonation, the optimal ratio being around 0.7. The relative humidity did not strongly affect the carbonation performance. The carbonation products were magnesite (MgCO3) and nesquehonite (MgCO3·3H2O). X-ray diffraction analysis showed that brucite (Mg(OH)2) was not present, suggesting that brucite was very quickly transformed into magnesium carbonates, the presence of which was confirmed by thermal gravimetric analysis. The results indicated that, in 7 d, 1 kg of binder could sequester up to 0.507 kg of CO2 in a 100% CO2 atmosphere. The results indicate that the MgO-based binder has great potential to be used to sequester CO2 under accelerated carbonation conditions.

The laboratory and field studies were conducted to identify an optimal injection concentration of nanoscale zero-valent iron particles (NZVI) and to evaluate the applicability of NZVI-based reactive zone technology to the site contaminated with trichloroethylene (TCE) DNAPL (Dense Non-Aqueous Phase Liquid). The laboratory test found an optimal injection concentration of NZVI of 5 g/L that could remove more than 95% of 0.15 mM TCE within 20 days. Eleven test wells were installed at the aquifer that was mainly composed of alluvial and weathered soils at a strong oxic condition with dissolved oxygen concentration of 3.50 mg/L and oxidation-reduction potential of 301 mV. NZVI of total 30 kg were successfully injected using a centrifugal pump. After 60 days from the NZVI injection, 86.2% of the TCE initially present in the groundwater was removed and the mass of TCE removed was 405 g. Nonchlorinated products such as ethane and ethene were detected in the groundwater samples. Based on the increased chloride ion concentration at the site, the mass of TCE removed was estimated to be 1.52 kg. This implied the presence of DNAPL TCE which contributed to a higher estimate of TCE removal than that based on the TCE concentration change.

Effects of anions (NO 3 − , HCO 3 − , Cl − , SO 4 2− ) and humic acid on the reactivity and core/shell chemistries of polyacrylic acid-coated nanoscale zero-valent iron (PAA-NZVI) and inorganically modified NZVI (INORG-NZVI) particles were investigated. The reactivity tests under various ion concentrations (0.2–30 mN) revealed the existence of a favorable molar ratio of anion/NZVI that increased the reactivity of NZVI particles. The presence of a relatively small amount of humic acid (0.5 mg L −1 ) substantially decreased the INORG-NZVI reactivity by 76%, whereas the reactivity of PAA-NZVI decreased only by 12%. The XRD and TEM results supported the role of the PAA coating of PAA-NZVI in impeding the oxidation of the Fe(0) core by groundwater solutes. This protective role provided by the organic coating also resulted in a 2.3-fold increase in the trichloroethylene (TCE) reduction capacity of PAA-NZVI compared to that of INORG-NZVI in the presence of anions/humic acid. Ethylene and ethane were simultaneously produced as the major reduction products of TCE in both NZVI systems, suggesting that a hydrodechlorination occurred without the aid of metallic catalysts. The PAA coating, originally designed to improve the mobility of NZVI, enhanced TCE degradation performances of NZVI in the presence of anions and humic acid.

Colloidal stabilities of polymer-coated nanosized zero-valent iron (pNZVI) and bare nanosized zero-valent iron (bNZVI) particles were investigated in the presence of groundwater solutes, such as Suwannee River natural organic matter (SRNOM), Pony Lake fulvic acid (PLFA), sodium ion, and calcium ion. Measurements of hydrodynamic diameter and zeta-potential showed that dissolved organic matters (SRNOM and PLFA) enhanced the stability of bNZVI particles, but that they did not affect the stability of pNZVI particles. These measurements also showed that the stability of pNZVI particles was inhibited by the cations but that the effect of the cations on bNZVI particles was inconclusive. The sedimentation test confirmed that the stability of pNZVI particles was inhibited by the sodium and calcium ions. The sedimentation test identified that the stability of bNZVI particles was inhibited only in the presence of calcium ion. The predictions on the stability of NZVI particles based on the Derjaguin–Landau–Ve...

A carbonation/granulation process for treating mine tailings using a MgO/ground-granule blast-furnace-slag (GGBS) binder was developed. The materials were mixed and granules produced using a granulator, then the granules were cured in a CO2 atmosphere. The optimum granulator rotation speed and retention time were 60 rpm and 7 min, respectively. The binder composition MgO0.5GGBS0.5 and binder: mine tailings ratio 3:10 gave the strongest granules. Carbonation generally increased the granule strength, but different CO2 concentrations, between 0.04% and 100%, changed the granule strength to different degrees. Granules cured in 20% CO2 for 28 d had a strength of 4.71 MPa, which was higher than the strengths of granules cured in other CO2 concentrations and of granules produced using Portland cement. The granules had relatively high CO2 storage capacities of 0.157–0.167 kg CO2/kg binder and good acid-neutralizing capacities (higher than the acid-neutralizing capacity of granules produced using Portland cement). The strength of the granules cured in 20% CO2 for 28 d was probably mainly attributed to the formation of hydromagnesite during carbonation. The hydromagnesite contributed dense and connected structures within the granules. The granules produced show great potential for use as aggregates for reclamation work and backfilling in mining areas.