• 제목/요약/키워드: fluorination

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Effect of Fluorination on Electrical Behaviors of Carbon Blacks-filled HDPE Polymeric Switch

  • Seo, Min-Kang;Park, Soo-Jin
    • Bulletin of the Korean Chemical Society
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    • 제30권6호
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    • pp.1337-1340
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    • 2009
  • Electrical properties of a fluorinated carbon black (CB)-filled high-density polyethylene (HDPE) polymeric switch were investigated as a function of fluorination pressure at 0.1 ~ 0.4 MPa. From the FT-IR results, the absorption spectra of the fluorinated CB show an absorption band at 1400 ~ 1000 $cm^{-1}\;for\;{\nu}_{C-F}$ and the peak intensity increased with increasing fluorination pressure. Also, the analysis of XPS spectra of the fluorinated CB indicated that fluorine content increased with increasing fluorination pressure. Meanwhile, the surface free energy of the fluorinated CB decreased with increasing fluorination pressure. Consequently, the increase of fluorine contents of CB made a disappearance of negative temperature coefficient (NTC) behavior of the polymeric switch, which was probably due to the reduction of CB reaggregation after melting point of the HDPE, resulted from the decreasing of London dispersive component of the surface free energy for CB particles.

Development of fluorination methodology for carbon-fluorine bond formation: old electrophilic fluorinating reagents

  • Bae, Dae Young;Lee, Eunsung
    • 대한방사성의약품학회지
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    • 제4권1호
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    • pp.11-15
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    • 2018
  • Electrophilic fluorinating reagents are typically efficient for carbon-fluorine (C-F) bonds formation due to their higher reactivity even under mild condition. Thus, they have been playing an important role to improve C-F bonds formation reactions via direct fluorination reaction with electrophilic fluorinating reagents or transition metal catalysis. Advances on the recent fluorination methods are mainly results of $Selectfluor^{TM}$'s capability on facile fluorination. In this mini-review, we describe synthesis and application of four old yet popular electrophilic fluorinating reagents such as N-fluorobenzenesulfonimide (NFSI), N-fluoropyridinium salts, $Selectfluor^{TM}$, and N-fluorosultam.

Improved flame retardant performance of cellulose fibers following fluorine gas treatment

  • Kim, Jong Gu;Lee, Young-Seak;In, Se Jin
    • Carbon letters
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    • 제28권
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    • pp.66-71
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    • 2018
  • To improve the flame retardant performance of cellulose fibers, fluorine functional groups were introduced under various controlled fluorination conditions. The properties of the fluorinated cellulose fibers were analyzed by X-ray photoelectron spectroscopy and a thermogravimetric analysis. The fluorine functional group content in the fluorinated cellulose fibers increased with an increase in the fluorination temperature. However, the fluorination reaction increased the char yield and decreased the rate of degradation of the cellulose fibers by introducing donors, enabling the formation of a thick and compact char layer. Therefore, the flame retardant properties of cellulose fibers were improved following the fluorination treatment.

In vitro shear bond strength between fluorinated zirconia ceramic and resin cements

  • Tanis, Merve Cakirbay;Akay, Canan;Akcaboy, Turgut Cihan;Sen, Murat;Kavakli, Pinar Akkas;Sapmaz, Kadriye
    • The Journal of Advanced Prosthodontics
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    • 제10권3호
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    • pp.205-210
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    • 2018
  • PURPOSE. The purpose of this study was to evaluate the efficiency of a gas-phase fluorination method under different fluorination periods through using two resin cements. MATERIALS AND METHODS. 84 zirconia specimens in dimensions of $5mm{\times}5mm{\times}2mm$ were prepared and surface treated with $50{\mu}m$ aluminum oxide particles or gas phase fluorination for 2 min, 5 min, or 10 min. One specimen in each group was surface analyzed under scanning electron microscope. The remaining specimens were bonded to composite cylinders in dimensions of 2 mm diameter and 3 mm high with Panavia SA Plus or Variolink N. Then, the specimens were stored in $37^{\circ}C$ distilled water for 24 hours and shear bond strength test was applied at a speed of 1 mm/min. RESULTS. The highest shear bond strength values were observed in the samples fluorinated for 5 minutes and cemented with Panavia SA Plus. Variolink N did not elicit any statistical differences between surface treatments. Panavia SA Plus resin cement and Variolink N resin cements featured statistically significant difference in shear bond strength values only in the case of 5 minutes of fluorination treatment. CONCLUSION. According to the results of this study, application of 5 minutes of fluorination with 10-methacryloyloxydecyl dihydrogen phosphate monomer (MDP) containing Panavia SA Plus resin cement increased the resin bond strength of zirconia. Fluorination of the zirconia surface using conventional resin cement, Variolink N, did not lead to an increase in bond strength.

수소저장용 활성탄소섬유의 표면개질 특성 (Surface modification characteristics of activated carbon fibers for hydrogen storage)

  • 김신동;김주완;임지선;조세호;이영석
    • 한국수소및신에너지학회논문집
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    • 제17권1호
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    • pp.47-54
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    • 2006
  • Activated carbon fibers (ACFs) with high surface area and pore volume were modified with metal Ni impregnation and fluorination and investigated hydrogen storage properties by volumetric method. Micropore volume values of ACFs obtained from surface modification with Ni impregnation and fluorination were decreased 9 and 35 %, respectively. Hydrogen storage capacities of fluorinated ACFs were slightly changed, on the other hand, that of Ni impregnated ACF was considerably increased. It means that hydrogen was not only adsorbed on ACF surface, but also on Ni metal surface by means of dissociation. Although the microphone volume of ACF modified with fluorination was decreased, its hydrogen storage were found not to be changed compared with fresh ACF. These results indicated that the surface of ACF after fluorination modification may be strongly attracted hydrogen due to high electronegativity of fluorine. Therefore, it was proven that hydrogen storage capacity was related with micropore volume and surface property of carbon materials as well as specific surface area.

Utilization improvement of PDMS and fluoropolymers by mutual application

  • Sihn, Youngho;Lee, Woojin
    • Membrane and Water Treatment
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    • 제2권1호
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    • pp.39-49
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    • 2011
  • We investigated about the utilization improvement of the PDMS and fluoropolymers by mutual application in environmental analysis. We were conducted the direct fluorination with mild condition on the PDMS films and analyzed its surfaces before and after fluorination. The results of FTIR and SEM analysis on the PDMS films showed that the film surfaces were fluorinated without irreversible deformation by the fluorination. During the fluorination, the measured contact angles of water and several alcohols on the PDMS films decreased with time and that of most alcohols decreased to 0 after 30 minutes. The surface energy of fluorinated PDMS films has increased by 2 times. Also, we investigated the influence factors on the change of permeation rate of water through PDMS tubes with time. It was observed that the change of permeation rate of water through PDMS tube was affected by temperature, water phase and spatial distribution of water. From these results, we could verify the principal causes of the decrease of permeation rate of water through PDMS tube with time and proposed a new experimental setup for reducing the variation of permeation rate of water less than 2%.

有機할로겐化合物과 KF 과의 反應 (第2報) 有機요-드酸, 沃化物 及 多鹽素化有機酸, 에스텔의 雙合, 弗化 及 脫炭酸 反應에 關하여 (Reaction of Potassium Fluoride with Orgarnic Halogen Compound-II. Dimerization, Fluorination, and Decarboxylation of Organic Iodo acids, Iodides, and Polychlorinated Acid Ester)

  • 김유선
    • 대한화학회지
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    • 제8권4호
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    • pp.135-141
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    • 1964
  • 아밀아이오다이드를 디메칠홀움아마이드 存在下에서 弗化加里와 低溫反應시켜 본 結果 弗化物과 데칸을 生成하였음. ${\alpha}$, ${\beta}$-디크로로-${\beta}$-페닐-푸로피온酸과 같은 多鹽素化物은 ${\alpha}$-크로로스타이렌, 弗化스타이렌 及 弗化酸을 生成하였음. 이 酸의 에칠에스텔은 弗化物을 生成하지 않고 各種 쌍合物의 混合物을 얻었음. 디부롬스타이렌은 부롬스타이렌과 弗化物을 生成하고 沃度를 含有한 有機酸, 메-타요드벤젠익酸은 有機酸의 鹽과 微量의 쌍合物을 生成하였음. 메타요드토류엔 及 1-아미노-4-요-드-2-메칠벤젠과 같은 沃化物은 弗化物은 弗化加里에 對하여 反應을 나타내지 않었음. 本報에는 各 反應條件과 弗化反應, 脫炭酸反應 及 쌍合反應에 關하여 論義하였음.

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Surface Characteristics of Direct Fluorinated Single-walled Carbon Nanotubes

  • Seo, Min-Kang;Park, Soo-Jin
    • Bulletin of the Korean Chemical Society
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    • 제30권9호
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    • pp.2071-2076
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    • 2009
  • The single-walled carbon nanotubes (SWCNTs) produced by chemical vapor deposition (CVD) were directly fluorinated with fluorine ($F_2$) gas in a temperature range 20 ~ 400 ${^{\circ}C}$. The surface properties and morphology of the SWCNTs were investigated in terms of fluorination temperature. As a result, Raman spectra showed a pair of bands at 1340 and 1590 $cm^{-1}$ peculiar to disordered $sp^2$-carbons. These results indicated that C-F bonds were formed on the rear surfaces of the nanotubes by fluorination, while the external surfaces as well as the layers between the internal and external surfaces retained their $sp^2$-hybridization. XPS analysis exhibited that fluorine atoms were bonded to carbon atoms on internal surfaces (rear surfaces) of the nanotubes and the amount of fluorine attached on the nanotubes was increased with increasing the fluorination temperature. Consequently, the direct fluorination of carbon nanotubes led to functionalization and modification of pristine nanotubes with respect to surface and morphological properties.

Aromatic Fluorination by Decomposition of Triazenes in Ionic Liquids

  • Chu, Chan-Kook;Kim, Jong-Hwan;Kim, Dong-Wook;Chung, Kyoo-Hyun;Katzenellenbogen, John A.;Chi, Dae-Yoon
    • Bulletin of the Korean Chemical Society
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    • 제26권4호
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    • pp.599-602
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    • 2005
  • The aromatic fluorination method involving the acid-catalyzed decomposition of a triazene in an ionic liquid is a very convenient and efficient way to prepare a variety of aromatic fluorides in a lab-scale. It should be particularly useful for the preparation aryl fluorides substituted with electron withdrawing substituents. Fluorination of triazene 1 (1.0 mmol) and p-toluenesulfonic acid (1.2 mmol) in an ionic liquid, 1-butyl-3-methylimidazolium tetrafluoroborate ([bmim][$BF_4$], 2.5 mL) proceeds very smoothly at 80 ${^{\circ}C}$ with or without an external source of fluoride, providing 73% yield in 30 min. Unlike diazonium salts, triazene precursors are stable enough to be stored for a long period of time without a noticeable decomposition.