• The tire
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• s.174
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• pp.43-50
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• 1994

• The tire
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• s.51
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• pp.3-10
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• 1974

• Elastomers and Composites
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• v.5 no.2
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• pp.165-170
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• 1970

• Elastomers and Composites
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• v.29 no.4
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• pp.368-375
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• 1994

• Journal of the Korean Institute of Telematics and Electronics
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• v.26 no.11
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• pp.1721-1727
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• 1989

Carbon-ferrite microwave absorbers were designed experimentally and fabricated trialy, as a result of which the relative frequency bandwith of 7.3 to 8.2% were obtained under the tolerance limits of the reflection coefficients lower than -20 dB, and the matching thickness becomes 1.4 to 1.6mm, which is significantly thinner than that of the conventional ones. Furthermore, attenuation has been founded by measuring the material constants of the microwave absorbers for microwave oven and the results are compared and discussed.

• The tire
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• s.75
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• pp.15-23
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• 1978

금속염을 첨가한 고무를 아연판과 접착가황하여 아연면의 첨가금속과 유황의 분포를 XMA에 의해 구했다. 가황중에 아연면으로 이행하는 것은 Co, Cu, Pb를 포함한 유기금속염뿐이였다. 고무 속의 유리유황도 이들 금속염과 함께 아연판으로 이행되어 왔다. 나프텐산코발트 중의 Co는 아연층내에 확산되어 분포된 데 반하여, S는 아연판표면에만 분포되어 있다. 양자가 아연판으로 이행되는 양은 첨가량에 비례해서 증가하였다. 고무와 아연판의 접착력은 Co량 0.6%까지는 증가하고, 그 이상의 첨가에서는 현저하게 저하되었다. 나프텐산코발트의 첨가량을 증가시키면 가황고무 중의 망목쇄농도는 변하지 않으나 유리유황은 감소하였다. 가황고무 중의 잔류나프텐산코발트는 60℃이상의 열처리온도에서 산화를 촉진하고 접착력도 저하시킨다. 카아본블랙을 배합하지 않은 NR의 유전거동보다 첨가한 나프텐산코발트는 가황온도에서 고무 분자의 주쇄 Segment의 완화 mode에 영향을 준다는 것을 알았다.

• Journal of the Korean Ceramic Society
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• v.13 no.1
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• pp.11-19
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• 1976

This study was focused on the improvement of production techniques of small crucibles in relation with the appropriate selection of raw materials, various batch compositions and physical and chemical characteristics of the crucibles. Various tests gave the optimum batch composition for the carbon bond graphite cructble as follows: Pyontaek graphite flake (refractory aggregate) : 40Part Silicon carbide: 15Part Tar pitch (binder) : 11Part Inorganic additives (to improve the oxidation resistance) : 15 Part Cryolite : 3 Part Ferro manganese : 2 Part Ferrosilicon : 25 Part Crucibles pressed with 400kg/$\textrm{cm}^2$ at 12$0^{\circ}C$. and fired in reducing atmosphere at 120$0^{\circ}C$ brought the most favorable results as follows: Bulk density : 2.31 Apparent density : 2.58 Porosity : 15.2% Oxidation loss at 1, 50$0^{\circ}C$. for 3 hrs : below 3.77% Water absorption : 6.01% Compressive strength : 438kg/$\textrm{cm}^2$ Tensile strength : 256kg/$\textrm{cm}^2$.

• Journal of the Korean Chemical Society
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• v.20 no.5
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• pp.351-357
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• 1976

Adsorption isotherms of benzene and p-xylene on both of Spheron 6 (a graphitized carbon black) and Alucer (Alumina) are obtained at various temperatures using a sensitive quartz beam microbalance. From these isotherms BET plots are made to obtain the molecular areas of these adsorbates. On the Spheron 6, the molecular area of p-xylene remains constant until the temperature is increased up to $19^{circ}C$, increases abruptly at $19^{circ}C$ through $19.2^{circ}C$, and then again remains constant thereafter. On the other hand, adsorbed benzene molecules give a quite temperature-independent molecular area. The results are interpreted as the adsorbed p-xylene molecules and benzene molecules are localized on the adsorbents with compact packing, while it gains a hindered-rotational degree of freedom at the expense of vibrational one at the higher temperatures. This peculiar behavior of adsorption is considered as due to the interactions between benzene rings of adsorbents and graphite surface. Molecular areas of these adsorbates on Alucer M. A. increase gradually with temperature, indicating that the adsorbed molecules are unlocalized.

• Applied Chemistry for Engineering
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• v.7 no.3
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• pp.496-503
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• 1996

Aromatic and aliphatic copolyesters for the dispersing agent were synthesized by two stage reaction, esterification and polycondensation. Copolyesters were blended with PET in the melt state and their thermal and rheological properties were investigated. From GPC analysis Mn's and Mw's of copolyesters were about 30000 and 65000g/mol, respectively. From DSC experiment copolyesters had melting range of $90{\sim}150^{\circ}C$. Copolymer composition was in good agreement with comonomer feed ratio from $^1H$-NMR analysis. Copolyesters and SPA (standard sample) were blended with PET in the melt state. From DSC experiment, copolyesters and SPA were miscible with PET. From the dynamic melt viscosity experiment, melt viscosity of blended sample was increased as the content of aromatic copolyester was increased, while it was decreased as the content of aliphatic and SPA were increased. As for volume resistivity of dry color containing carbon black and copolyesters with dispersing time, aromatic copolyester showed highest value. It was conferred from this result that aromatic copolyester was the best dispersing agent for carbon black in PET resin.

• Elastomers and Composites
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• v.37 no.4
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• pp.224-233
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• 2002

This study has investigated the flame retardant properties of EPDM rubber with the addition of various flame retardants. Carbon black, stearic acid, zinc oxide cross-linking agent were mixed with EPDM rubber to produce the base rubber E0 without the addition of flame retardants. Phosphorus flame retardant Tricrecyl phosphate(TCP) was added to E0 in 0.5, 1, 1.5, 2 phr to make E1~E4 samples and red phosphorus was added in 3, 6, 9, 12 phr to make E5~E8 samples. A flame retardant of the bromine family Decabromodiphenyloxide(DBDPO), and a chlorinated paraffin retardant of the chlorine family was added to E0 in 3, 6, 9, 12 phr to make E9~E12 and E13~E16 samples, repectively. Basic physical properties such as tensile strength, tear strength and hardness were measured for all the rubber samples with various flame retardant additions. There was no substantial differences. On the other hand, Oxygen index and UL94 were measured to study flame retardant properties. From oxygen index measurements E0 sample showed a value of 23.5%, indicating the improvement of flame retardant properties. Also from UL94 measurements, it was found that addition of red phosphorus resulted in maximum flame retardant effect. It was found that increasing the amount of addition resulted in decreasing combustion rate and improving flame retardant effect regardless of the kind of flame retardant.