• Title/Summary/Keyword: 수소침투

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Enhanced Migration of Gasohol Fuels in Clay Soils and Sediments (Gasoline-ethanol(Gasohol)혼합액의 점토층 내 이동에 대한 연구)

  • Hee-Chul Choi;W.M. Stallard;Kwang-Soo Kim;In-Soo Kim
    • Journal of Korea Soil Environment Society
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    • v.1 no.1
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    • pp.67-79
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    • 1996
  • Clay soils typically have low hydraulic conductivities in the presence of high polarity pore fluid, such as water. Low polarity fluids, such as hydrocarbon fuels and halogenated organic solvents, typically cannot migrate into clay pores because they cannot displace the pore water. Oxygenated additives in gasoline, such as alcohols and methyl-tert-butyl ether, are increasingly used to control air pollution emissions. These relatively polar and highly water-soluble compounds may facilitate displacement of pore water and enhance migration of fuels and solvents through clay-rich soil strata. In the reported research, the migration of gasoline-alcohol fuel mixtures (gasohol) through consolidated clay was examined. Prepared kaolinite clay samples were consolidated from slurry, and various combinations of gasoline, alcohol, and water were applied to the clays under 152 Pa gauge pressure. Movement of the fluids into the clay samples was monitored by measur ing displaced pore fluid and by magnetic resonance imaging of the samples. The structures of selected samples were examined using environmental scanning electron microscopy. Results of the research suggest that alcohol added to hydrocarbon fuels can enhance migration through some clays significantly. Gasoline did not migrate appreciably into water saturated clay, even after 14 days under pressure. The gasohol mixture migrated readily into the clay in only 20 minutes. Increased hydraulic conductivity of the clay in the presence of gasohol is hypothesized to be due to the collapse of the clays pore structure when ethanol is present, creating larger pores. Increasing pore diameter decreases the capillary pressure needed for the gasohol to replace water and allows gasohol to migrate through the clay.

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Development of Environmental Rubber Interphase Adhesive by use of Oligomer of Hydrocarbon (탄화수소계 올리고머를 이용한 환경친화적 고무계면 접착제 개발)

  • Jang, Byung-Man;Jang, Jeong-Seog;Park, Sung-Soo;Choi, Dug-Jai;Kim, Su-Kyung
    • Polymer(Korea)
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    • v.25 no.1
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    • pp.142-150
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    • 2001
  • Until now rubber industry field has used organic solvent base adhesive, there was always existed a fire risk, variety of quality and harmfulness of human body. To solve this problem we were developed a new adhesive that was maked by raw materials of hydrocarbon series which has the properties of nonvolatile and high flash point. Because of this new adhesive has the properties of nonvolatile and non-harmfulness to the human body, we expected to solve the problems of a fire hazard and the pollution of the environmental. Instead of the rubber binder that is used to a present adhesive, the new idea is adopted in a new type of adhesive. Nonvolatile solvent penetrated to the rubber surface and caused the swelling in rubber surface and as a result of this action, it has the self-adhesive power. In comparision with the present adhesive a new type of adhesive remarkably improved the maintenance time of adhesion and the durability of this adhesive showed similar aspect. Because it did not exhibit a drop of physical properties of rubber which was caused by swelling effect, we estimate that new type adhesive are very stable and not reacted to several rubber additives. While present adhesive appear the crack at cutting surface of curing rubber that caused by gas, new type adhesive not exist these crack.

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Calculation of Rainwater and Groundwater Fraction in Sewerage: A Case Study in Deokjin Park, Jeonju (동위원소를 이용한 하수 내 지하수 및 우수 함량 산출: 전주 덕진공원 유역 사례)

  • Choi, Seung-Hyun;Kim, Kangjoo;Moon, Sang-Ho
    • Economic and Environmental Geology
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    • v.49 no.5
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    • pp.361-370
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    • 2016
  • It is well known that the inflow of rainwater and the infiltration of groundwater to sewerage (I/I) increase the sewage and burden sewage treatment plants and lower their treatment efficiency. Therefore, it is important to estimate the amount of I/I. In this study, well groundwaters, public water supplies (PWSs), and sewage and rainwater channels were investigated to check whether oxygen and deuterium isotopes could be used as a tool for I/I estimation. This study shows that the isotopic composition of PWS in Jeonju area is very consistent over time and distinctly lighter than the circulating local rainwater (CLR) because it is supplied from Yongdam Dam, which is located about 40 km inland to the east in the mountainous area. Considering the fact that sewage mostly originates from the PWS, we could calculate the amounts of CLR in the sewerage from a monitoring station using unaffected rainwater and tap water as mixing end members. The calculation revealed that the CLR fraction ranged from 50% to 90% depending on observation time. This is well supported by the dilute natures of the sewages at the station. The fraction of PWS in investigated well waters were about 46%, indicating that leaking of PWS is very serious and is an important groundwater source in the study area. Since the infiltration of such groundwater may not alter the isotopic composition of sewage significantly, the actual I/I would be much greater than the calculated ones.

Characteristics of Silicon Rich Oxide by PECVD (PECVD에 의한 Sirich 산화막의 특성)

  • Gang, Seon-Hwa;Lee, Sang-Gyu;Park, Hong-Rak;Go, Cheol-Gi;Choe, Su-Han
    • Korean Journal of Materials Research
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    • v.3 no.5
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    • pp.459-465
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    • 1993
  • By making the inter-metal PECVD $SiO_2$ as a Si rich oxide under the SOG, the hydrogen and water related diffusants could be captured a t SI dangling bonds. This gettering process was known to prevent the device characteristics degradations related to the H, $H_20$. The basic characteristics of Si rich oxide have been studied according to changing high/low frequency power and $SiH_4/N_2O$ gas flow ratio in PECVD. As increase in low frequency power, deposition rate decreased but K.I. and compressive stress increased. Decrease of the water peaks of FTIR spectra at the wave number range of 3300~3800$\textrm{cm}^{-1}$' also indicated that intensty the films were densified. As increase in SiH, gas flow rate, deposition rate, R.I. and etch rate increased while compressive stress decreased. F'TIK spectra showed that peak intensity corresponding to Si-0-Si stretching vibration decreased and shifted to the lower wave numbers. But AES showed that Si dangl~ng bonds were increased as a result of lower Si:O(l: 1.23) ratlo inthe Si rich oxide as compared to Si : O(1 : 1.98) ratio of usual oxide.

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Synthesis of Dendritic Polystyrene-block-Linear Poly(t-butyl acrylate) Copolymers by an Amide Coupling (아미드 커플링을 통한 덴드리틱 Polystyrene-Block-Linear Poly(t-butyl acrylate) 공중합체의 합성)

  • Song, Jie;Cho, Byoung-Ki
    • Polymer(Korea)
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    • v.33 no.2
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    • pp.158-163
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    • 2009
  • In this study, we synthesized a series of dendritic polystyrene-b-linear poly (t-butyl acrylate) copolymers with well-defined molecular architectures. The hydroxyl group located at the focal point of the second generation dendron bearing polystyrene ($M_n$ = 1000 g/mol) peripheries was converted into amine group via the following stepwise reactions: 1) tosylatoin, 2) azidation, and 3) reduction. On the other hand, the linear poly (t-butyl acrylate)s were prepared by an atom transfer radical polymerization (ATRP) of t-butyl acrylate where benzyl 2-bromopropanoate and Cu(I)Br/PMDETA were used as initiator and catalyst, respectively. To convert the end group of prepared poly (t-butyl acrylate) s into carboxylic acid, a debenzylation was performed using Pd/C catalyst under $H_2$ atmosphere. In the final step, dendritic-linear block copolymers were obtained through a simple amide coupling reaction mediated by 4-(dimethylamino) pyridine(DMAP) and N,N'-diisopropylcarbodiimide(DIPC). The resulting diblock copolymers were shown to have well-defined molecular weights and narrow molecular weight distributions as supported by $^1H$-NMR spectroscopy and gel permeation chromatography(GPC).

A Study on the Safe Gap for Explosion-proof (내압방폭을 위한 Safe Gap의 측정에 관한 연구)

  • Oh Kyu-hyung
    • Journal of the Korean Institute of Gas
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    • v.1 no.1
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    • pp.1-6
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    • 1997
  • In case of using the electrical apparatus in the hazardous atmosphere which exist flammable gas mixtures, There is a dangerosity of gas explosion accident by the electrical spark. The most general method to prevent the explosion by the spark is to use the flame-proof type electrical apparatus to isolate the ignition source. from the flammable atmosphere. But actualy it is impossible to isolate the ignition sources from the atmosphere. So it was needed to find the safe gap which prevent ignition of flammable atmosphere by transmission of flame or heat when a flammable gas mixture exploded inside the apparatus. In this study we tried to find the maximum experimental safe gap(MESG) of $H_2$-air, and $CH_4$-air mixtures by using the 8 litre spherical vessel with 25mm flange. The experiment parameter were ignition position, concentration and initial pressure before explosion. From the experiment the ignition position was affected to the MESG. MESG value was minimum near the stoichiometric concentration of gas mixtures, and according to the increase of initial pressure MESG was decreased.

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The Influence of Additives Added to the Melamine and Formalin Mixtures on Sericin Fixation of Raw Silk Fibers (멜라민과 포르말린 혼합액의 첨 가제들이 실크 생사의 세리신 정착에 미치는 영향)

  • Park, Geon-Yong
    • Journal of the Korea Academia-Industrial cooperation Society
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    • v.10 no.2
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    • pp.412-417
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    • 2009
  • In order to investigate the effective sericin fixation of raw silk fibers the influence of various additives added to the melamine and formalin mixtures on sericin fixation was studied. When raw silk fibers were treated with wetting agent but without subsequent washing before sericin fixation, the strong sericin fixation was obtained by fixing sericin. Adding hydrogen peroxide to the melamine and formalin mixture made sericin fixation worse, resulting weaken the sericin hardness of fixed raw silk fibers and tight bonding of the fibers. On the other hand, it was confirmed that adding sodium hydrosulfite to the melamine and formalin mixtures gave better sericin hardness of fixed raw silk fibers without the bonding of fibers. Supplying additional melamine with he low concentration of sodium hydroxide to the melamine and formalin mixture(melamine:formalin= 1:6) resulted in very good sericin fixation. But adding hydrochloric acid or methanol to the same mixture had no effect on the sericin fixation, and adding magnesium chloride to it made the hardness of sericin fixation even worse.

Calculation of the Dispersion Coefficient by the Dissolution Experiment of DNAPL Pool (DNAPL Pool의 용해실험에 의한 분산계수 산정)

  • 정경영;배열호;최상일
    • Journal of Korea Soil Environment Society
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    • v.1 no.1
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    • pp.19-27
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    • 1996
  • Nonaqueous phase liquids(NAPL) not readily dissolved in water exist as a separate fluid phase. Groundwater contamination by NAPL such as organic solvents and petroleum hydrocarbons becomes major public concerns because of their long-term persistence in the subsurFace and their ability to contaminate large volumes of wate. Dense.-than-water NAPL(DNAPL) spilled into the subsurface penetrate through the saturated zone and ultimately form DNAPL pools on the bottom of the aquifer. The dissolution of DNAPL from these pools depends on the molecular diffusion coefficient, the vertical dispersivity, the groundwater velocity, the solubility, and the pool length. In this study, the vertical transverse dispersion coefficients for simulating the dissolution of DNAPL from such pools were obtained from the dissolution experiment. Under the experimental conditions used, the vertical transverse dispersion coefficients calculated were 1.86$cm^2$/day, 2.90$cm^2$/day and 4.51$cm^2$/4ay for seepage velocities of 59.2cm/day, 94.3cm/day and 158.0cm/day, respectively. And the vertical transverse dispersivity was 0.03024cm.

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Humidity Dependence of the Residual Stress of Diamond-like Carbon Film (습도에 따른 다이아몬드성 카본필름의 잔류응력 변화에 대한 연구)

  • Lee Young-Jin;Kim Tae-Young;Lee Kwang-Ryeol;Yang In-Sang
    • Journal of the Korean Vacuum Society
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    • v.13 no.4
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    • pp.157-163
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    • 2004
  • Dependence of residual compressive stress of diamond-like carbon (DLC) films on relative humidity was investigated. Polymeric, graphitic and diamond-like carbon films were prepared by r.f.-PACVD using methane or benzene with the negative self bias voltage of the substrate ranging from -100 to -800 V. In-situ measurements of the residual stress were carried out in an environment chamber where the relative humidity was varied from 10% to 90%. In dense DLC film of high residual compressive stress and hardness, we could not observe any change in the residual compressive stress with relative humidity. However, in the cases of graphitic and polymeric DLC films, abrupt change in the residual stress occurred by changing the relative humidity. The quantity of the stress change was inversely proportional to the film thickness, which means that the stress change with humidity is not due to the penetration of the water molecule into the film structure, but due to surface interaction between water molecules and film surface.

Enhanced Environmental Stability of Graphene Field-Effect Transistors through Interface Control (계면 제어를 통한 그래핀 기반 전계효과 트랜지스터의 환경 안정성 향상)

  • Seong, Jun Ho;Lee, Dong Hwa;Lee, Eunho
    • Journal of Adhesion and Interface
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    • v.23 no.3
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    • pp.75-79
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    • 2022
  • Graphene is a two-dimensional carbon allotrope composed of honeycomb sp2 hybrid orbital bonds. It shows excellent electrical and mechanical properties and has been spotlighted as a core material for next-generation electronic devices. However, it exhibits low environmental stability due to the easy penetration or adsorption of external impurities from the formation of an unstable interface between the materials in the electronic devices. Therefore, this work aims to improve and investigate the low environmental stability of graphene-based field-effect transistors through direct growth using solid hydrocarbons as a precursor of graphene. Graphene synthesized from direct growth shows high electrical stability through reduction of change in charge mobility and Dirac voltage. Through this, a new approach to utilize graphene as a core material for next-generation electronic devices is presented.