Publications by authors named "In-Yong Eom"

Time-integrative passive sampling of volatile organic compounds (VOCs) in water can now be accomplished using a solid ceramic dosimeter. A nonporous ceramic, which excludes the permeation of water, allowing only gas-phase diffusion of VOCs into the resin inside the dosimeter, effectively captured the VOCs. The mass accumulation of 11 VOCs linearly increased with time over a wide range of aqueous-phase concentrations (16.

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In the present study, gold nanoparticles (AuNPs) with an average particle size of -41.23 nm were synthesized using eco-friendly reducing material (i.e.

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Background: Oil palm trunk (OPT) is a valuable bioresource for the biorefinery industry producing biofuels and biochemicals. It has the distinct feature of containing a large amount of starch, which, unlike cellulose, can be easily solubilized by water when heated and hydrolyzed to glucose by amylolytic enzymes without pretreatment for breaking down the biomass recalcitrance. Therefore, it is suggested as beneficial to extract most of the starch from OPT through autoclaving and subsequent amylolytic hydrolysis prior to pretreatment.

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A simple and cost-effective biochemical conversion process consisting of hydrothermal treatment, enzymatic hydrolysis and fermentation of pretreated whole slurry (PWS) was developed for producing l-lactic acid (L-LA) from oil palm trunk (OPT). When OPT was hydrothermally treated at optimal condition capable of achieving maximum yield of hemicellulosic sugars after enzymatic hydrolysis, the enzymatic digestibility of the PWS afforded a yield of 81.4% of the theoretical glucose yield (TGY).

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Silver nanoparticles (AgNPs) with a mean particle size of ∼ 16.7 nm were synthesized using an eco-friendly reducing material, aqueous Nelumbo nucifera root extract. Rapid reduction resulted in the formation of polydispersed nanoparticles.

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This report describes a new platform for headspace sampling technique, i.e. a syringe pump assisted headspace sampler (SPHS).

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To produce fermentable sugar with fewer microbial inhibitors via few processes, batch-type hydrothermal treatments of sunflower stalks were performed, followed by enzymatic hydrolysis of pretreatment slurries with Cellic CTec2 and Cellic HTec2 (9:1, v/v, 0.1 ml/g dry biomass, 8.1FPU).

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The objectives of this study were to investigate the effects of inorganic constituents on the fast pyrolysis of the biomass and to determine the yields as well as physicochemical properties of pyrolytic products. The pyrolytic products were obtained from raw and demineralized rice straw using a fluidized bed type pyrolyzer at different temperatures. As pyrolysis temperature increased, total biooil yield gradually decreased from 46.

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In this study, chromated copper arsenate-treated wood (CCA-W) and alkaline copper quaternary compounds-treated wood (ACQ-W) were subjected to fast pyrolysis at 500°C for ca. 2s to produce bio-oil and char. The physicochemical properties of the pyrolytic products as well as the distribution of heavy metals - arsenic, copper and chrome - during fast pyrolysis were investigated.

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Air in a room infested by Cimex lectularius L. (Hemiptera: Cimicidae) was sampled simultaneously by three different sampling devices including solid phase microextraction (SPME) fiber coatings, thin film microextraction (TFME) devices, and needle trap devices (NTDs) and then analyzed by gas chromatography-mass spectrometry (GC-MS). The main focus of this study was to fully characterize indoor air by identifying compounds extracted by three different microextraction formats and, therefore, perform both the device comparison and more complete characterization of C.

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This study employed thermogravimetric analysis (TGA) and analytical Py-GC/MS in order to examine the catalytic effect of main inorganic metals (K, Mg and Ca) on the thermal degradation and the formation of pyrolytic products in lignocellulosic biomass. In addition, potential mechanisms of the primary pyrolysis in presence of the inorganic metals were derived. TG analysis showed that when potassium content increased in the biomass, char formation increased from 10.

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1-Ethyl-3-methylimidazolium acetate ([Emim][CH₃COO]) was used for the extraction of lignin from poplar wood (Populus albaglandulosa), which was called to ionic liquid lignin (ILL) and structural features of ILL were compared with the corresponding milled wood lignin (MWL). Yields of ILL and MWL were 5.8±0.

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Poplar wood flour (Populous albaglandulosa) was treated with sub- and super-critical water (subcritical: 325, 350°C; super-critical: 380, 400, 425°C) for 60s at 220 ± 10 atm. Hydrochloric acid (0.05%v/v) was added to samples as acidic catalyst.

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Poplar wood powders were treated with distilled water, tap water, HCl and HF, respectively, to remove inorganics from the biomass and to investigate effect of demineralization processes on pyrolysis behavior of the biomass. TG and DTG revealed that maximum degradation temperatures rose slightly from 362°C for control to 372°C, 366°C and 368°C after demineralization with distilled water, HCl and HF, respectively. Maximum degradation rates also increased from 0.

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The possibility of sampling the free and particle-bound concentrations of organic compounds was studied using two different sampling techniques at the same time: needle trap device (NTD) and solid-phase microextraction (SPME). In this study, a mosquito coil was used to produce gaseous (free) and particle-bound compounds. Allethrin, the active ingredient in mosquito coils, was chosen as the target analyte.

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A frequency-selective absorbance detection approach and its applications are described. First, a digital signal processor-lock-in amplifier (DSP-LIA)-based absorbance detector was evaluated. Compared to a simple operational amplifier (TL082CP)-based detector, the DSP-LIA-based detector showed lower noise levels, but the relative advantage was reduced under very low photocurrent levels (down to few nA).

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A simple, cost-effective analysis combining solventless extraction, thermal desorption, and determination of volatile organic compounds (VOCs) was developed and validated. A needle trap device (NTD) packed with the sorbent Carboxen1000 was used as a time-weighted average (TWA) diffusive sampler to collect target compounds by molecular diffusion and adsorption to the packed sorbent. This process can be described with derivations of Fick's first law of diffusion, which expresses the relation between the TWA concentrations to which the passive sampler is exposed and the mass of analytes adsorbed to the packed sorbent in the sampler.

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Needle trap devices (NTDs) are improving in simplicity and usefulness for sampling volatile organic compounds (VOCs) since their first introduction in early 2000s. Three different sample transfer methods have been reported for NTDs to date. All methods use thermal desorption and simultaneously provide desorptive flow to transfer desorbed VOCs into a GC separation column.

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This paper describes a new approach that combines needle trap devices (NTDs) with a dynamic headspace sampling technique (purge and trap) using a bidirectional syringe pump. The needle trap device is a 22-G stainless steel needle 3.5-in.

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Needle trap devices (NTDs), like solid-phase microextraction (SPME) fibers, represent a new approach to one-step, solvent-free sample preparation and injection. New NTDs, packed with divinylbenzene (DVB) or Carboxen 1000 particles, are prepared, characterized, and used for benzene, toluene, ethylbenzne, and xylene (BTEX) sampling in our laboratory. This paper describes optimization parameters, performance evaluation, and application of NTDs for the analysis of a BTEX mixture from air.

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We report fully automated self-calibrating formaldehyde analyzers relying on a hybrid flow format and include operational scheme and design details. Long-term operation is made possible with the use of syringe pumps. Four identical analyzers were built and showed low LODs of 120 pptv or better (S/N = 3) and good linearity over 0-50 ppbv HCHO concentration range (r2 > 0.

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