• 제목/요약/키워드: Anionic effect

검색결과 254건 처리시간 0.027초

초임계수 산화를 이용한 음이온교환수지 분해 (Supercritical Water Oxidation of Anionic Exchange Resin)

  • 한주희;한기도;도승회;김경숙;손순환
    • 대한환경공학회지
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    • 제28권5호
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    • pp.549-557
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    • 2006
  • 화력발전소에서 발생하는 폐 음이온교환수지를 분해하기 위해 초임계수 산화 특성 연구를 진행하였다. 폐수지는 음이온교환수지와 양이온교환수지가 혼합된 상태로 배출되었으며, 혼합된 폐수지에서 고-액 유동층을 이용하여 음이온수지를 분리하였다. 분리된 음이온 수지는 원소분석과 열분석을 통해 양이온 수지가 혼합되지 않았음을 확인하였다. 음이온수지를 고압 펌프를 이용하여 초임계수 산화 반응 장치에 연속적으로 주입하기 위해 습식 ball mill을 이용하여 분쇄, 슬러리로 제조하였다. 압력 25.0 MP콘 체류시간 2분, 반응 온도 $500^{\circ}C$에서 처리수의 COD는 99.9%이상 분해됨을 확인하였지만, 총 질소 분해율은 41% 정도로 나타났으며, 슬러리에 질산을 혼합하면 처리수의 총 질소가 감소하였다. 처리수의 COD와 총 질소(T-N) 함량을 목적변수로 설정하여 음이온 수지 슬러리를 분해하는 최적 조건을 도출하기 위해 통계적 실험계획법인 중심합성계획법을 적용하였다. 처리수의 COD는 반응 온도 $500{\sim}540^{\circ}C$, 압력 25.0 MPa, 반응기 체류시간 2분 조건에서 $99.9{\sim}100%$까지 충분히 분해되었으며, 온도 변화와 질산 주입량 변화에 영향을 받지 않았다. 그러나 처리수의 총 질소는 질산 주입량의 변화에 대한 영향이 큰 것으로 확인되었다. 처리수의 총 질소는 회귀분석을 통해 질산 주입량의 함수로 나타낼 수 있었으며, 결정계수($r^2$)는 95.8%로 계산되었다.

교반 속도가 음이온성 PAM과 양이온성 전분으로 도포된 경질탄산칼슘의 응집과 종이 물성에 미치는 영향 (Effect of Mixing Shear on Flocculation of Anionic PAM and Cationic Starch Adsorbed PCC and Its Effect on Paper Properties)

  • 최도침;원종명;조병욱
    • 펄프종이기술
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    • 제47권2호
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    • pp.53-60
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    • 2015
  • The effects of stirring speed during filler modification by dual polymers on flocculation and reflocculation of PCC (precipitated calcium carbonate) particles and its effect on handsheet properties were elucidated. PCC surface was modified by adsorbing A-PAM (anionic polyacrylamide) and C-starch (cationic starch) in series at various stirring speeds. It was found that increasing stirring speed during filler modification decreased the initial floc size of PCC. Continuous stirring with the same speed for filler modification resulted in the decrease of a floc size, eventually reached a steady state. The variations in a floc size was influenced by the stirring speed during filler modification: the lower the stirring speed during filler modification, the larger the floc size variations. Conclusively, the stability of PCC floc could be improved by increasing the stirring speed. In addition, the stirring speed influenced the handsheet properties. The smaller the PCC floc, the lower the strength of handseet. However, too much larger floc size also deteriorated paper strength. There exists an optimum floc size in term of paper strength which shall be controlled by stirring speed during filler modification.

Polyvinylamine을 이용한 Dual Polymer System의 지력 증강 효과 (Effect of Dual Polymer System using Polyvinylamine for Paper Strength)

  • 최재훈;류정용;김봉용
    • 펄프종이기술
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    • 제47권4호
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    • pp.46-53
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    • 2015
  • Paper strengthening system of PVAm (polyvinylamine) has been used with strong negative charge polymer for electrostatic neutralization due to strong positive charge of PVAm. Recently, because of the controversy caused by the possibility of remaining PAM monomers in white water, a search for paper strength agent that can substitute for PAM was suggested. Therefore, this study was carried out to evaluate a dry strength polymer of PVAm. Starch and CMC were used as a substitute for PAM. The dual polymer system of PVAm and anionic charge control agent such as anionic starch or CMC (carboxy methyl cellulose) were found to be very effective as strength agent compared to the chemicals based on acrylamide.

UV/Ozone 조사에 의한 Poly(phenylene sulfide) 필름의 표면처리와 염색성 (Surface Treatment and Dyeability of Poly(phenylene sulfide) Films by UV/O3 Irradiation)

  • 장용준;장진호
    • 한국염색가공학회지
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    • 제23권4호
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    • pp.284-289
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    • 2011
  • Poly(phenylene sulfide)(PPS) films were photooxidized under UV/ozone irradiation. The effect of UV energy on the surface properties of the UV-irradiation PPS films were investigated by the measurement of reflectance, surface roughness, and contact angle. Reflectance decreased at the wavelength of 400nm and the surface roughness increased with increased UV energy. The improvement in hydrophilicity with increased $O_{1s}/C_{1s}$ was caused by the introduction of hydrophilic $SO_2$ bond. Surface energy increased from 46.6 to $78.3mJ/m^2$ with increased UV energy up to $21.2J/cm^2$. Also zeta potential decreased with increased UV energy. The increased dyeability to cationic dyes may be due to the photochemically introduced anionic and dipolar dyeing sites on the PPS films surfaces.he photochemically introduced anionic and dipolar dyeing sites on the PPS films surfaces.

PVAm 적용이 백상지의 형광증백제 발현효율에 미치는 영향 (Effect of PVAm Application for Fine Paper on Effectiveness of Optical Brightening Agent)

  • 조병욱;원종명
    • 펄프종이기술
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    • 제48권3호
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    • pp.23-29
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    • 2016
  • Effects of cationic polyvinylamine (PVAm) dry strength agent on effectiveness of optical brightening agent (OBA) during fine papermaking and the mechanism for brightness reduction of paper by PVAm was investigated by UV/Vis spectroscopy and turbidity measurement of OBA solution with PVAm. It was shown that PVAm reduced brightness of paper while opacity was not varied and tensile strength of paper was increased. Tetra-type OBA solution showed the peaks around the wavelength of 280 nm and 330 nm and the increase in the OBA concentration increased the UV absorbance in all wavelength. Addition of PVAm into the OBA solution decreased the UV absorbance at 280 nm. Turbidities of OBA and PVAm solutions were close to zero, respectively, while the turbidity value increased for the mixed solution of OBA and PVAm in various mixing ratios and the highest value was obtained when the mixing ratio of PVAm and OBA was 5:5, meaning that cationic PVAm formed complex with anionic OBA. In conclusion, cationic PVAm could form a complex with anionic OBA and that reduced UV absorbance, resulting in the reduced brightness of paper.

Immobilization of Heavy metal mechanism in Contaminated Coastal Sediment using Biostimulant Ball (BSB) with Modified Zeolite

  • Subha, Bakthavachallam;Woo, Jung-Hui;Song, Young-Chae
    • 한국항해항만학회:학술대회논문집
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    • 한국항해항만학회 2016년도 춘계학술대회
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    • pp.130-131
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    • 2016
  • Although many metals contaminated sediment from coastal area contain both anionic and cationic heavy metals, the current remediation technologies are not effective for stabilize heavy metals of both anionic and cationic elements from contaminated coastal region. the present work investigated the efficiency and mechanism of immobilization of Fe, Zn, Cr, Cu, Pb and Cd metal solutions in modified zeolite based biostimulant ball. Biostimulant ball containing acetate, nitrate and sulphate which are enhance the activity of marine microorganisms and it can act as electron donors and electron acceptors. Modified zeolite and chelating agent is greatly enhance the metal stabilization due to increased immobility of the analysed metals. The XRD, FT-IR and SEM of modified zeolite which cheating agents containing heavy metals were investigated. The results indicated that heavy metals could be effectively immobilized in modified zeolite and chelating agents in BSB added sediment. The immobilization of heavy metals in modified zeolite and chelating agents along with BSB could be due to stabilize of heavy metal cations. Immobilization of heavy metals using BSB with modified zeolite and chelating agent has lower cost effect and enhance the sediment quality.

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백상지 공정 폐쇄화에 따른 백수 내 산화전분의 축적 현상에 관한 연구 ( 제 3 보 ) -백수사용량과 파지첨가량 변화에 따른 공정의 비정상상태 변화 - (A Study on the Accumulation Phenomena of Oxidized Starch in White Water of Closed Fine Papermaking Process (Part 3) -Effect of white water and broke use ratios on the unsteady state of papermaking process-)

  • 안현견;이학래
    • 펄프종이기술
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    • 제38권2호
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    • pp.1-8
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    • 2006
  • In this study a process simulation method was used to analyze the accumulation phenomena of anionic starch in the process white water as the closure level of a fine paper making process is increased. A pilot paper machine was used as a model process. Dynamic simulations of the influence of white water usage ratio and uncoated broke addition ratio on the variation of process variable was monitored as a function of time. Results from the dynamic simulations showed that the volume of reservoirs affected the dynamic behavior of the process. The dynamic behavior of flow rate and dissolved starch concentration in process units were different from each other. The speed of the change of dissolved starch concentration in process units was depend on the starting point of the change of dissolved starch concentration, the length of circulation loop, and the volume of reservoirs.

음이온성 리포솜이 결합된 키토산 겔의 항암효과 (Anti-tumour Efficiency of Chitosan Hydrogel Containing Anionic Liposomes as a Depot System)

  • 최민수;한희동;김태우;송충길;박은석;신병철
    • Journal of Pharmaceutical Investigation
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    • 제35권1호
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    • pp.25-31
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    • 2005
  • Depot system for local drug delivery using chitosan hydrogel has been developed to enhance the therapeutic efficacy and to prevent the severe side effect in whole body. Thus, we have prepared an injectable chitosan hydrogel containing liposomes to treat cancers clinically. Anionic liposomes incorporated to improve sustained release efficiency within chitosan hydrogel. The chitosan solution containing liposomes was designed to form a hydrogel complex at body temperature. The released behavior of doxorubicin from liposomes in chitosan hydrogel showed sustained-release caused by diffusion of doxorubicin from temperature responsive liposome into chitosan hydrogel. The chitosan hydorgel containing liposomes enhanced the therapeutic potency for the solid tumor in vivo system. Our results indicate that the liposomes in chitosan hydrogel represent a depot system for local drug delivery.

HDTMA-몬모릴로나이트를 이용한 염화페놀류 화합물의 흡착 및 탈착시 pH의 영향 (Effect of pH on the sorption and desorption of chlorinated phenols using HDTMA-montmorillonite)

  • 김지훈;김영규;신원식;김영훈;최상준;전영웅;송동익
    • 한국지하수토양환경학회:학술대회논문집
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    • 한국지하수토양환경학회 2001년도 추계학술발표회
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    • pp.19-22
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    • 2001
  • The effects of pH on the sequential sorption/desorption of chlorinated phenols (2-chlorophenol, 2.4-dichlorophenol and 2,4,5-trichlorophenol) in HDTMA-montmorillonite were investigated by maintaining pH 4.85 or 9.15 in the sequential batch sorption and desorption experiments. The chlorinated phenols are hydrophobic ionizable orginic compounds; they can exist as either neutral (pH << pKa) or anionic (pH >> pKa) forms. Among the tested chlorinated phenols, 2,4,5-trichlorophenol showed the highest sorption affinity at pH 4.85 as expected by the $K_{ow}$ . Neutral speciation at pH 4.85 exhibited higher sorption affinity than anionic speciation at pH 9.15. Our results indicates that desorption of chlorinated phenols is strongly dependent on pH of the aqueous phase. Freundlich model was used to analyze the single-solute sorption/desorption results. The ideal adsorbed solution theory(IAST) was employed to predict the hi-solute sorption/desorption equilibria.

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Removal of Reactive Blue 19 dye from Aqueous Solution Using Natural and Modified Orange Peel

  • Sayed Ahmed, Sohair A.;Khalil, Laila B.;El-Nabarawy, Thoria
    • Carbon letters
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    • 제13권4호
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    • pp.212-220
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    • 2012
  • Orange peel (OP) exhibits a sorption capacity towards anionic dyes such as reactive blue 19 (RB19). Cetyltrimethylammonium bromide (CTAB) as a cationic surfactant was used to modify the surface nature of OP to enhance its adsorption capacity for anionic dyes from an aqueous solution. Four adsorbents were investigated: the OP, sodium hydroxide-treated OP (SOP), CTAB-modified OP and CTAB-modified SOP. The physical and chemical properties of these sorbents were determined using nitrogen adsorption at 77 K and by scanning electron microscope and Fourier transform infrared spectroscopy techniques. The adsorption of the RB19 dye was assessed with these sorbents at different solution pH levels and temperatures. The effect of the contact time was considered to determine the order and rate constants of the adsorption process. The adsorption data were analyzed considering the Freundlich, Langmuir, Elovich and Tempkin models. The adsorption of RB19 by the assessed sorbents is of the chemisorption type following pseudo-first-order kinetics. CTAB modification brought about a significant increase in RB19 adsorption, which was ascribed to the grafting of the sorbent with a cationic surfactant.