• 제목/요약/키워드: non-solvent addition

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CED(Cupriethylene diamine)과 NMMO (N-methylmorpholine-N-oxide)를 이용한 셀룰로오스의 중합도 측정법의 비교 (Comparison of cellulose DP measurements using the CED (Cupriethylene diamine) and NMMO(N-methylmorpholine-N-oxide))

  • 이민우;박지순;박동휘;서영범
    • 펄프종이기술
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    • 제42권5호
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    • pp.62-66
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    • 2010
  • Cellulosic materials were dissolved by NMMO(N-methylmorpholine-N-oxide) and CED (Cupriethylene diamine), respectively, to measure their DPs (degrees of polymerization) by using viscometer. We changed cellulose DPs by applying various amounts of low intensity electron-beam radiation to the cellulosic materials. NMMO is environmental-friendly, non-toxic, and biodegradable organic cellulose solvent and used industrially because of its high cellulose dissolving power and high solvent recovery ratio. The cellulose DP measurement results using these two different chemicals were correlated highly ($R^2$ >0.95). It was also found that cellulose with high DP was dissolved more easily in NMMO than CED. In addition, NMMO method gave more higher resolution in the measurement.

Sialie acid의 감소가 탈지분유의 단백 용해도에 미치는 영향 (Effect of Reduction in Sialic acid on Solubility of Non Fat Dry Milk Protein Isolates)

  • 송재철;박현정;이재영
    • 한국식품과학회지
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    • 제19권1호
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    • pp.61-65
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    • 1987
  • k-casein은 유단백질 분획으로 GMP를 포함하고있으떠 GMP는 sialic acid를 포함하고 있으므로 k-casein index로 sialic acid 가 사용될 수 있다. 탈지분유 분리 단백질 용해도는 칼슘카페인 보다 일반적으로 낮으므로 용매처리시 야기되는 k-casein의 손실과 저용해도와의 관계를 규명하고자 하였다. 특히 용매처리시 주요 stabilizing fraction k-casein의 손실 혹은 손상을 고려해야만 한다. 용매처리시 sialic acid 는 제1차 추출용매에 16.5%, 제2차 추출용매에 4.0%손실되어 전체 20.5%가 용매처리시 손실되었다. 또 사용한 메탄올의 농도가 증가할수록 sialic acid손실이 감소하여 sialic acid 손실은 메탄을분획보다 물분획에따라 좌우된 것 같다. 따라서 sialic acid를 함유한 분말 extracted solid의 feed back 실험 결과 10%첨 가시최대 용해도를 나타냈으며 유당은 용해도 변화에 기여하지 못하였다 결론적으로 탈지분유 단백의 저용해도 헌상은 용매처리시 k-casein의 가용성 물질 손실에도 일부 기인한 것으로 사료된다.

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Trisodium Citrate을 이용한 은 나노입자의 합성 및 분산성에 관한 연구 (A Study on Synthesis and Dispersion of Silver Nano Particle Using Trisodium Citrate)

  • 이종집
    • 한국산학기술학회논문지
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    • 제17권4호
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    • pp.772-779
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    • 2016
  • 수용액에서 질산 은과 Trisodium Citrate(TSC)을 반응시켜 은 나노입자를 제조하였다. 은 나노입자의 크기와 모양은 주사 전자 현미경(SEM)을 사용하여 조사하였다. 은 나노입자의 합성실험은 질산 은 수용액의 농도, TSC의 첨가량, 용제, 계면활성제, 초음파 파쇄, 분산제를 변수로 하여 수행하였다. 질산 은의 농도를 높이거나 TSC의 농도를 증가시킬수록 입자의 크기가 커지거나 응집되는 결과를 확인할 수 있었다. 주사 전자 현미경(SEM) 분석 자료로부터 합성된 은 나노입자는 좁은 영역의 입자 크기 분포를 가진 구형 또는 구형에 가까운 것을 확인하였다. 용제를 첨가하여 분산을 시도하였는데, 소수성 용제는 분산성에 영향을 미치지 않았고 친수성 용제는 분산성을 향상시켜 주었다. 계면활성제(HPMC)를 첨가하면 은 나노입자의 크기가 50-100 nm로 커지며, 모양은 불균일하고 부분적인 응집이 발생하였다. 은 나노입자의 분산성은 분산제 첨가 후에 3 시간 이상의 초음파 파쇄에 의해 크게 향상되었다. 분산제의 첨가에 의해 완전한 분산이 일어났으며, 은 나노입자의 크기는 BYK-182(30-40 nm) < BYK-192(42-78 nm) < BYK-142 (51-113 nm)순으로 나타났다. 0.002 M 질산 은 용액에 2-4wt%의 TSC를 첨가하였을 때 38.45-46.28 nm의 은 나노입자가 합성되었다.

비수계 테잎성형공정의 유기공정변수의 변화에 따른 티탄산바륨-붕규산염유리계 현탁액의 분산안정성 (Effect of Organic Processing Parameters in Non-aqueous Tape-casting on Dispersion Stability of Barium Titanate-Borosilicate Glass Based Suspensions)

  • 여정구;최성철
    • 한국재료학회지
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    • 제13권11호
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    • pp.725-731
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    • 2003
  • The effect of organic processing parameters on the dispersion stability of the BaTiO$_3$-based dielectric particles and borosilicate glass particulate suspensions was investigated in a system where organic solvents, dispersant, binder and modifier were used as processing additives in a low temperature cofired ceramic fabrication processes. Two- and three-component organic solvents were used to disperse ceramic particles and it was found the better stability in the particulate suspension prepared in a bi-solvent, which was consists of toluene and ethanol in a non-azeotropic composition. The addition amount of organic additives had a great impact on dispersion in the present investigation. The flow curves of the suspensions prepared with binder and modifier were fitted according to the power-law equation, which indicates that the internal structure of the suspension could be disturbed under the applied shear stress. Finally, the LTCC green tapes were successfully tape-cast based upon the optimum formulation of LTCC suspension and its microstructure was compared with that of the hard-agglomerates.

The Measurement of Flash Point for Binary Mixtures of 2,2,4-Trimethylpentane, Methylcyclohexane, Ethylbenzene and p-xylene at 101.3 kPa

  • Hwang, In Chan;In, Se Jin
    • 청정기술
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    • 제26권4호
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    • pp.279-285
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    • 2020
  • Laboratories and industrial processes typically involve the use of flammable substances. An important property used to estimate fire and explosion risk for a flammable liquid is the flash point. In this study, flash point data at 101.3 kPa were determined using a SETA closed cup flash point tester on the following solvent mixtures: {2,2,4-trimethylpentane + methylcyclohexane}, {2,2,4-trimethylpentane + ethylbenzene}, and {2,2,4-trimethylpentane + p-xylene}. The purpose of this work is to obtain flash point data for binary mixtures of 2,2,4-trimethylpentane with three hydrocarbons (methylcyclohexane, ethylbenzene, and p-xylene), which are representative compounds of the main aromatic hydrocarbon fractions of petroleum. The measured flash points are compared with the predicted values calculated using the GE models' activity coefficient patterns: the Wilson, the Non-Random Two-Liquid (NRTL), and the UNIversal QUAsiChemical (UNIQUAC) models. The non-ideality of the mixture is also considered. The average absolute deviation between the predicted and measured lower flash point s is less than 1.99 K, except when Raoult's law is calculated. In addition, the minimum flash point behavior is not observed in any of the three binary systems. This work's predicted results can be applied to design safe petrochemical processes, such as identifying safe storage conditions for non-ideal solutions containing volatile components.

Pyridine 존재여부에 따른 Trans-3-hexene의 오존 산화 반응 (Ozone Oxidation of Trans-3-hexene with/without Pyridine)

  • 김철규;홍원표
    • 공업화학
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    • 제3권4호
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    • pp.579-587
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    • 1992
  • 올레핀의 오존화 반응에서 보여지는 통상의 반응경로가 pyridine의 도움으로 modification될 수 있는지 여부가 검토되었다. 먼저, trans-3-hexene의 오존 산화 반응이 aprotic non-participating solvent인 n-pentane과 dichloromethane을 사용하여 시험되었다. 덧붙여, 올레핀의 오존 산화 반응에서 pyridine의 역할과 반응기구를 검토하기 위하여, monomeric과 Polymeric ozonides의 염기성 촉매 분해반응이 시험되었다. 본 연구에서 반응 과정의 고찰뿐만 아니라 생성물의 정량, 정성 분석을 위하여 현대적인 분석 기기들이 사용되었다. 본 연구의 결과로서, Pyridine 무존재하 aprotic solvent에서 올레핀과 오존의 반응으로 주로 과산화물인 monomeric이나 polymeric ozonides가 생성되었으며, pyridine 존재하에서는 과산화물의 생성없이 propionaldehyde와 Criegee zwitterion의 자리옮김 생성물인 propionic acid가 주생성물이었다. 또한, tans-3-hexene의 오존 산화 반응에서 Pyridine의 촉매작용에 의하여 trans-3-hexene의 Criegee zwitterion의 propionic acid로 이성화되는 것으로 사료된다.

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A cost-effective method to prepare size-controlled nanoscale zero-valent iron for nitrate reduction

  • Ruiz-Torres, Claudio Adrian;Araujo-Martinez, Rene Fernando;Martinez-Castanon, Gabriel Alejandro;Morales-Sanchez, J. Elpidio;Lee, Tae-Jin;Shin, Hyun-Sang;Hwang, Yuhoon;Hurtado-Macias, Abel;Ruiz, Facundo
    • Environmental Engineering Research
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    • 제24권3호
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    • pp.463-473
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    • 2019
  • Nanoscale zero-valent iron (nZVI) has proved to be an effective tool in applied environmental nanotechnology, where the decreased particle diameter provides a drastic change in the properties and efficiency of nanomaterials used in water purification. However, the agglomeration and colloidal instability represent a problematic and a remarkable reduction in nZVI reactivity. In view of that, this study reports a simple and cost-effective new strategy for ultra-small (< 7.5%) distributed functionalized nZVI-EG (1-9 nm), with high colloidal stability and reduction capacity. These were obtained without inert conditions, using a simple, economical synthesis methodology employing two stabilization mechanisms based on the use of non-aqueous solvent (methanol) and ethylene glycol (EG) as a stabilizer. The information from UV-Vis absorption spectroscopy and Fourier transform infrared spectroscopy suggests iron ion coordination by interaction with methanol molecules. Subsequently, after nZVI formation, particle-surface modification occurs by the addition of the EG. Size distribution analysis shows an average diameter of 4.23 nm and the predominance (> 90%) of particles with sizes < 6.10 nm. Evaluation of the stability of functionalized nZVI by sedimentation test and a dynamic light-scattering technique, demonstrated very high colloidal stability. The ultra-small particles displayed a rapid and high nitrate removal capacity from water.

Coagulant bath medium effect towards polylactic acid membranes structure and methylene blue dye removal

  • Amira M. Nasib;Stephen Simon;Syahmie M. Rasidi;Siti Kartini E. Ab. Rahim;Hoo Peng Yong;Ng Qi Hwa;Khairiraihanna Johari
    • Advances in materials Research
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    • 제13권3호
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    • pp.243-251
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    • 2024
  • The asymmetric polylactic acid (PLA) membrane was prepared via phase inversion method using non-solvent induced separation (NIPS) technique. This study aims to synthesized as well as to characterize the PLA membrane and evaluating the membrane performance on water flux and permeability. In addition, this research also studied the removal performance of methylene blue dye. The polymer solution has been prepared using 12 wt.% of PLA and dissolved in 88 wt.% of Dimethylacetamide (DMAc) as a solvent. Then, the cast film was immersed in different ratio of coagulant bath medium (distilled water: methanol: ethanol) ranging from 100:0:0, 75:25:0, 75:0:25 and 75:12.5:12.5, respectively). Several characterizations were performed which include, membrane contact angle and membrane porosity. Performance PLA membranes were determined in terms of water flux and permeability at 1 bar transmembrane pressure using dead-end permeation cell. Finally, methylene blue (MB) removal efficiency was tested at the same transmembrane pressure. The findings revealed that the increase of alcohol concentration in coagulant bath resulted in higher porosity and lower contact angle. In short, MB dye rejection efficiency is also closely related to the amount of alcohol ratio used in coagulant baths. Increases in concentration of methanol and ethanol in coagulant bath medium increases the membrane porosity thus increased in efficiency of methylene blue rejection.

Antimicrobial Effect of Acanthopanax sessiliflorum Fruit Extracts against Selected Oral Bacteria

  • Choi, Won-Ik;Jeong, Moon-Jin;Jung, Im-Hee;Lim, Do-Seon
    • 치위생과학회지
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    • 제18권3호
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    • pp.147-154
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    • 2018
  • This study aimed to evaluate the antimicrobial effects of Acanthopanax sessiliflorum fruit (ASF; Ogaza) extracts on Streptococcus mutans and Streptococcus sobrinus, which are agents that cause dental caries, and on Streptococcus mitis and Streptococcus salivarius, the microbial flora of the oral cavity. The ASF extracts obtained using 70% ethanol were fractionated in the order of ethyl acetate and n-Butanol, concentrated under reduced pressure, and lyophilized to give powdery solvent extracts. The antimicrobial activity of ASF extracts from each solvent was examined using the disk diffusion method. As a result, only those extracts obtained using an ethyl acetate solvent showed antimicrobial activity. These extracts were selected, and the minimum inhibitory concentration was measured by disk diffusion method at various extract concentrations. Results showed a minimum inhibitory concentration of 32 mg/ml. The viable cell count was measured to confirm the minimum bactericidal concentration. Results showed a minimum bactericidal concentration of 64 mg/ml. In the cytotoxicity test using normal human dermal fibroblast cells, the absorbance value of the test group was similar to that of the control group at 0.64, 1.28, and 6.4 mg/ml. The bacteria and their colonies were examined using a scanning electron microscope. Boundaries between the antimicrobial activity region and non-antimicrobial activity region were observed around the paper disk, which was immersed in the extract with 32 mg/ml concentration. Bacterial colonization was not observed in the area with antimicrobial activity. This finding suggests that ASF extracts can inhibit the growth of some microorganisms in the oral cavity, in addition to the effects of these extracts known to date. In particular, ASF extracts may be used as a preparation for preventing dental caries by adding the extract to the toothpaste or oral mouthwash.

Theoretical Studies on the Addition Reactions of Ketene with NH3 in the Gas Phase and in Non-Aqueous Solutions

  • Kim, Chang-Kon;Lee, Kyung A;Chen, Junxian;Lee, Hai-Whang;Lee, Bon-Su;Kim, Chan-Kyung
    • Bulletin of the Korean Chemical Society
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    • 제29권7호
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    • pp.1335-1343
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    • 2008
  • Theoretical studies on the un-catalyzed and catalyzed aminations of ketene with $NH_3$ and $(NH_3)_2$, respectively, were studied using MP2 and hybrid density functional theory of B3LYP at the 6-31+G(d,p) and 6- 311+G(3df,2p) basis sets in the gas phase and in benzene and acetonitrile solvents. In the gas phase reaction, the un-catalyzed mechanism was the same as those previously reported by others. The catalyzed mechanism, however, was more complicated than expected requiring three transition states for the complete description of the C=O addition pathways. In the un-catalyzed amination, rate determining step was the breakdown of enol amide but in the catalyzed reaction, it was changed to the formation of enol amide, which was contradictory to the previous findings. Starting from the gas-phase structures, all structures were re-optimized using the CPCM method in solvent medium. In a high dielectric medium, acetonitrile, a zwitterions formed from the reaction of $CH_2$=C=O with $(NH_3)_2$, I(d), exists as a genuine minimum but other zwitterions, I(m) in acetonitrile and I(d) in benzene become unstable when ZPE corrected energies are used. Structural and energetic changes induced by solvation were considered in detail. Lowering of the activation energy by introducing additional $NH_3$ molecule amounted to ca. −20 $\sim$ −25 kcal/mol, which made catalyzed reaction more facile than un-catalyzed one.