@article{seo_kim_chung_kim_kim_jeon_2005, title={Characterization of remote inductively coupled CH4-N-2 plasma for carbon nitride thin-film deposition}, volume={98}, number={4}, journal={Journal of Applied Physics}, author={Seo, H. and Kim, J. H. and Chung, K. H. and Kim, J. Y. and Kim, S. H. and Jeon, H.}, year={2005} }
 @article{lee_kim_hong_zhong_chen_misra_2005, title={Properties of Ta-Mo alloy gate electrode for n-MOSFET}, volume={40}, ISSN={["1573-4803"]}, DOI={10.1007/s10853-005-2108-3}, number={9-10}, journal={JOURNAL OF MATERIALS SCIENCE}, author={Lee, CK and Kim, JY and Hong, SN and Zhong, HC and Chen, B and Misra, V}, year={2005}, month={May}, pages={2693–2695} }
 @article{grant_kim_jones_jenkins_wasyl_cudaback_2005, title={Surf zone entrainment, along-shore transport, and human health implications of pollution from tidal outlets}, volume={110}, number={C10}, journal={Journal of Geophysical Research. Oceans}, author={Grant, S. B. and Kim, J. H. and Jones, B. H. and Jenkins, S. A. and Wasyl, J. and Cudaback, C.}, year={2005} }
 @article{baran_kim_hart_lubkeman_lampley_newell_2004, title={Voltage Variation Analysis for Site-Level PQ Assessment}, volume={19}, ISSN={0885-8977}, url={http://dx.doi.org/10.1109/tpwrd.2004.829951}, DOI={10.1109/TPWRD.2004.829951}, abstractNote={This paper investigates the challenges in developing a performance index that will reflect the level of power quality at a site based on the actual field data obtained from the site via power-quality (PQ) monitors. For the index, each observed voltage variation is assessed in terms of its potential to impact the customers served from the site. The paper considers the substation level PQ monitoring and adopts a procedure that is similar to one of the methods being proposed in the emerging IEEE guide 1564.}, number={4}, journal={IEEE Transactions on Power Delivery}, publisher={Institute of Electrical and Electronics Engineers (IEEE)}, author={Baran, M.E. and Kim, J. and Hart, D.G. and Lubkeman, D. and Lampley, G.C. and Newell, W.F.}, year={2004}, month={Oct}, pages={1956–1961} }
 @article{kim_lee_yoon_lyoo_kotek_2001, title={Alkaline depolymerization of poly(trimethylene terephthalate)}, volume={82}, ISSN={["0021-8995"]}, DOI={10.1002/app.1828.abs}, abstractNote={The purpose of this study was to investigate the effects of reaction media, composition, and temperature on the rate of the alkaline depolymerization of poly(trimethylene terephthalate) (PTT). The alkaline depolymerization of PTT was carried out at 160–190°C in ethylene glycol (EG), diethylene glycol (DEG), triethylene glycol (TEG), ethylene glycol monobutyl ether (EGMBE), diethylene glycol monoethyl ether (DEGMEE), and a mixture of these solvents. During the reaction, PTT was quantitatively converted to disodium terephthalate and 1,3-propanediol. The alkaline depolymerization reaction rate constants were calculated based on the concentration of sodium carboxylate, which was equivalent to the molar amount of sodium hydroxide. The depolymerization rate of PTT was increased by increasing the reaction temperature and by adding ethereal solvents. Moreover, the depolymerization rate was significantly accelerated in the order of EG < DEG < TEG < EGMBE < DEGMEE. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 82: 99–107, 2001}, number={1}, journal={JOURNAL OF APPLIED POLYMER SCIENCE}, author={Kim, JH and Lee, JJ and Yoon, JY and Lyoo, WS and Kotek, R}, year={2001}, month={Oct}, pages={99–107} }
 @article{lim_chang_kim_novak_2000, title={Carbon-13 T-1 rho investigation in two polycarbodiimides}, volume={115}, ISSN={["0038-1098"]}, DOI={10.1016/S0038-1098(00)00129-0}, abstractNote={The molecular motions of carbons in two polycarbodiimides were studied by 13C cross-polarization, magic angle spinning nuclear magnetic resonance. From these results, the 13C spin-lattice relaxation times in the rotating frame were measured. In this paper we discuss the molecular motions for each carbon of the two polycarbodiimides. The main-chain carbon of polycarbodiimide (I) with methyl has higher activation energy, 23.12 kJ/mol, than that of polycarbodiimide (II) with the methoxy side chain, 10.47 kJ/mol. From these results, we surmise that polycarbodiimide (I) has a bigger steric interaction with the main-chain carbon since the methyl group is located in the meta-position of the aromatic ring.}, number={1}, journal={SOLID STATE COMMUNICATIONS}, author={Lim, AR and Chang, JH and Kim, JH and Novak, BM}, year={2000}, pages={23–28} }
 @article{lim_kim_novak_2000, title={Solid state C-13 nuclear magnetic resonance for polyguanidines}, volume={41}, ISSN={["0032-3861"]}, DOI={10.1016/S0032-3861(99)00431-0}, abstractNote={The structure and variations in dynamic motions of three polyguanidines possessing different side chains were studied by 13C CP/MAS NMR. From these results, the structures of the polyguanidines were confirmed, and the 13C spin–lattice relaxation times in the rotating frame were measured. The polyguanidine backbone mobilities were measured as a function of size and chemical make up (aliphatic vs. aromatic). The main-chain carbon of polyguanidine (II) with aromatic side chains has a higher activation energy, 23.12 kJ/mol, than the polyguanidine (I) with aliphatic side chains, 19.76 kJ/mol. Also, the activation energy of the main-chain carbons of polyguanidine (II) and (III) with aromatic side chains was found to depend on the size of side chains.}, number={7}, journal={POLYMER}, author={Lim, AR and Kim, JH and Novak, BM}, year={2000}, month={Mar}, pages={2431–2438} }