• Polymer(Korea)
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• v.29 no.2
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• pp.172-176
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• 2005

Environmentally friendly water dispersion polyurethanes containing fluorine were prepared with a fluorinated polyol having $62\%$ of fluorine $(Fluorolink^{(R)}\;M_n\;1000)$. In order to control the fluorine contents of the synthesized polyurethanes polytetramethylene glycol (PTMG2000) and $Fluorolink^{(R)}$ were mixed at assigned ratios and reacted with isophorone diisocyanate (IPDI) as a diisocyanate used. Introducing hydrophilic anion to the polymer chain was achieved by applying dimethyl propionic acid (DMPA). The ionic groups were neutralized with triethyl amine (TEA) before dispersion into water. Chain extension was executed by adding ethylene diamine at the final stage. Mechanical properties of the polymers showed that modulus increased with increasing $Fluorolink^{(R)}$ content. Surface energy values obtained from contact angle measurement decreased with increasing $Fluorolink^{(R)}$ content up to $20\%$. We expect that the synthesized polyurethanes present reliable effect from the fluorine atoms incorporated even at a small amount of $Fluorolink^{(R)}$.

• Applied Chemistry for Engineering
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• v.20 no.5
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• pp.505-510
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• 2009

It is well known that the properties of concrete such as the compressive strength, water permeability, water tightness and durability are affected by micro-structure in hardened cement paste. Especially, for durability of concrete, watertightness of cementitious materials is the most critical property among various properties. Recently, many types of material such as organic and/or inorganic materials are used for watertightness of concrete. In this study, we examined the effect of fluorine-based emulsion on watertightness property. And we also discussed the change of microstructure and formation of hydrates in hardened cement paste by the addition of fluorine-based emulsion. Cement paste with fluorine-based emulsion showed improvement of watertightness by the surface activation of cement paste and by formation of $CaF_2$ fine crystals in cement pore structure.

• Clean Technology
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• v.5 no.2
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• pp.37-44
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• 1999

The influence of the reactant composition on the surface free energy and on the dispersity in water was investigated by using the fluorine-containing water-soluble polyurethane synthesized with the fluorine-containing diol and hydrophilic diol. The diol donating ionic characteristics was more effective than polyol, and stable emulsion with the diameter of 610~310 nm was obtained in the range of 0.3~0.7 molar ratio of the diol to polyol. According to the increment of fluorine-containing compound up to 10 wt %, the surface free energy of polyurethane was dramatically decreased from 22.3 to 12.6 dyn/cm, and the diameter of water dispersed polyurethane increased from 380 to 860 nm due to the strong interaction between polymer molecules because fluorine segments are arranged on the surface of molecules. The macromonomer with perfluoroalkyl group was more effective in complement of the weak point of water-soluble polyurethane, which is a decrease of hydrophobicity, because of strong hydrophobicity.

• Bulletin of the Korean Chemical Society
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• v.34 no.2
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• pp.384-388
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• 2013

Fluorine-doping on the $Li_{1+x}Mn_{1.9-x}Al_{0.1}O_4$ spinel cathode materials is found to alter crystal shape, and enhance initial interfacial reactivity and solid electrolyte interphase (SEI) formation, leading to improved initial coulombic efficiency in the voltage region of 3.3-4.3 V vs. Li/$Li^+$ in the room temperature electrolyte of 1 M $LiPF_6$/EC:EMC. SEM imaging reveals that the facetting on higher surface energy plane of (101) is additionally developed at the edges of an octahedron that is predominantly grown with the most thermodynamically stable (111) plane, which enhances interfacial reactivity. Fluorine-doping also increases the amount of interfacially reactive $Mn^{3+}$ on both bulk and surface for charge neutrality. Enhanced interfacial reactivity by fluorine-doping attributes instant formation of a stable SEI layer and improved initial cyclic efficiency. The data contribute to a basic understanding of the impacts of composition on material properties and cycling behavior of spinel-based cathode materials for lithium-ion batteries.

• The Transactions of the Korean Institute of Electrical Engineers
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• v.41 no.5
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• pp.525-532
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• 1992

Fluorine-doped YBaS12TCuS13TOS17-xTFS1yT superconducting materials with y varing two orders of magnitude form 0.02 to 2.0 have been prepared by a sol-gel process by using metal nitrate salts, sodium hydroxide and sodium fluoride. Fluorine contents have been measured using an ion-selective electrode. All fluorine doped as reactant were found to be present in the resulted samples. From the observation of XRD it has been concluded that the samples with y 0.2 formed simply the single phase of perovskite structure, whereas those with y 0.5 yielded together some compounds such as BaFS12T, YFS13T and CuO in the resulted samples. The observation of solid state S019TF NMR has been carried out in order to check whether fluorine was actually incorporated into the lattice sites, and the experimental results revealed that the mole ratio of fluorine incorporated into the lattice sites of YBaS12TCuS13TOS17-xT was approximately 0.2 per mole of the compound. Also electrical resistivity measurement indicated that onset transition temperature has the tendency to increase slightly with increasing y in the dilute region as y 0.2.

• The Journal of the Korea Contents Association
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• v.12 no.5
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• pp.311-322
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• 2012

Restoration materials used to investigate effects of fluorine such as enamel strengthening and anti-caries effects in several types of dental restoration materials were five kinds including Ionoseal(VOCO GmbH, Cuxhaven, Germany), Fuji Filling LC(GC Co. Tokyo, Japan), Quadrant Universal LC(CAVEX Holland BV, Netherlands), PermaCem$^{(R)}$(DMG, Hamburg, Germany) and Dyract$^{(R)}$ AP(Dentsply GmbH, Germany), and the amount of fluorine-releasing was measured with ICS-5000 Reagent-FreeTM Ion Chromatography(RFICTM, Dionex, U.S.A.). The results of this study are as follows. 1. In all types of restoration materials, the amount of fluoride-releasing was reduced with time passage and it was declined sharply to show significance in four weeks. Fuji Filling LC(12.445PPM) or resin-reinforced glass ionomer and PermaCem$^{(R)}$(16.121PPM) or compomer were found to release fluorine for a long term(P<.001). 2. Ionoseal(0.887PPM) or glass ionomer and Quadrant Universal LC(0.957PPM) or composite resin released a few fluorine of 1PPM or less than 1PPM after one week, and Dyract$^{(R)}$ AP or compomer released fluorine of 8.631PPM in one week and its amount of releasing decreased dramatically in two and four week by recording 0.175PPM and 0.116PPM, respectively. Therefore, the effect of releasing fluorine in four weeks was observed to be poor (P<.001). 3. Fuji Filling LC or resin-reinforced glass ionomer and PermaCem$^{(R)}$ or compomer released fluorine of 33.372 and 1.902PPM, respectively in one week and their amount of releasing increased to be 36.371 and 18.223PPM, respectively in two weeks. So, their amount of fluorine-releasing recorded the highest levels in two weeks(P<.001).

• 한국신재생에너지학회:학술대회논문집
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• 2010.06a
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• pp.67.2-67.2
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• 2010

F doped ZnO (FZO)박막은 rf magnetron sputtering을 이용하여 ZnO 박막에 F의 도핑량 변화에 따른 효과와 전기적, 광학적 및 열적 특성에 대하여 고찰하였다. 열처리 전의 박막에서는 $CF_4$ gas가 0.1%일 때 가장 좋은 전기적 특성을 보였고, 이는 대부분의 F이 O와 치환을 하여 전기적 특성이 우수해지는 것으로 보인다. 그러나 일반적으로 열처리 전 FZO 박막은 낮은 전기적 특성을 가지며, 열처리 후에는 전기적 특성이 많이 향상되었고, 특히 홀 이동도가 $42.6cm^2/Vs$의 높은 값을 가졌다. 또한 F 함량이 증가할수록 광학적 특성은 좋아졌지만, 구조적 특성은 열처리 전 후를 비교할 때 큰 변화가 없었다. 이 연구를 통해서 $40cm^2/Vs$이상의 높은 홀 이동도를 가지고, 열적으로 안정한 ZnO계 박막의 제조가 가능하였다.

• Bulletin of the Korean Chemical Society
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• v.25 no.4
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• pp.452-459
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• 2004

The geometrical structures of various isomers of hexafluoro-1,3-butadiene (HFBD), tetrafluoro-1,3-butadiene (TFBD), and difluoro-1,3-butadiene (DFBD) have been studied theoretically. Natural steric and natural resonance theory (NRT) analyses indicate that the lower energy of skew s-cis conformer of hexafluoro-1,3-butadiene than that of the s-trans conformer is originated from the strong steric repulsions between fluorine atoms particularly in the s-trans conformer. The resonance structures generated by NRT also show that the lone electron pairs of fluorine atoms effectively extend the conjugation, and the large differences in energy among the structural isomers of tetrafluoro-1,3-butadiene and difluoro-1,3-butadiene are in part attributed to the differences in the delocalization energies, in addition to the steric repulsion between fluorine atoms. Other interatomic interactions, such as hydrogen bonding, also play important roles in determination of the structures of isomers of tetrafluoro-1,3-butadiene and difluoro-1,3-butadiene.

• Bulletin of the Korean Chemical Society
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• v.30 no.9
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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.

• Journal of the Korean Crystal Growth and Crystal Technology
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• v.14 no.5
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• pp.220-225
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• 2004

Four different Fluorine-based gases ($SF_6/,NF_3, PF_5,\; and \; BF_3$) were examined for high rate Inductively Coupled Plasma etching of Si. Etch rates up to ~8$\mu\textrm{m}$/min were achieved with pure $SF_6$ discharges at high source power (1500 W) and pressure (35 mTorr). A direct comparison of the four feedstock gases under the same plasma conditions showed the Si etch rate to increase in the order $BF_3$ < $NF_3$< $PF_5$ < $SF_6$. This is in good correlation with the average bond energies of the gases, except for $NF_3$, which is the least strongly bound. Optical emission spectroscopy showed that the ICP source efficiently dissociated $NF_3$, but the etched Si surface morphologies were significantly worse with this gas than with the other 3 gases.