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- 저자 : 박일현(Il Hyun Park) (검색결과 52 건)
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N-Acetyl ${\alpha}$-aminoacrylic Acid의 자유라디칼 중합 및 혼성중합
박일현,이종광,최재호,진정일,Il Hyun Park,Chong Kwnag Lee,Jae Ho Choi,Jung-Il Jin 대한화학회 1982 대한화학회지 Vol.26 No.4
본 연구에서는 자유라디칼 메카니즘에 의한 N-acetyl ${\alpha}$-aminoacrylic acid의 단독중합 반응속도와 혼성중합 반응성을 연구하였으며, DMF 용매를 사용하여 $60^{\circ}C$에서 단독중합 시켰을 때의 중합속도 ($R_p$)는 단위체 농도 [M]와 개시제 농도 [I]에 대하여 $R_p$ = $k_p[M]^{0.97}[I]^{0.59}$의 관계를 나타내었다. 또한 이 단위체의 단독중합 총괄 활성화 에너지는 25.2 kcal/mole이었다. N-acetyl ${\alpha}$-aminoacrylic acid를 아크릴산 및 스티렌 단위체와 혼성중합 시켰을 때의 단위체 반응성비는 아래와 같았다. $r_1$(N-acetyl ${\alpha}$-aminoacrylic acid) = 0.49, $r_2$(acrylic acid) = 1.41; $r_1$(N-acetyl ${\alpha}$-aminoacrylic acid) = 0.44, $r_2$(styrene) = 0.91. Alfrey-Price 식을 이용하여 계산한 N-acetyl ${\alpha}$-aminoacrylic acid의 Q와 e값은 두 경우 모두 Q=0.51, e=0.16이었다. 단독중합체 및 혼성중합체들의 열적성질을 DTA 및 TGA법으로 분석하여 비교하여 보았다. The free radical polymerization and copolymerization of N-acetyl ${\alpha}$-aminoacrylic acid were investigated. From the result of kinetic investigation of N-acetyl ${\alpha}$-aminoacrylic acid in DMF at $60^{\circ}C$, a rate equation of $R_p$ = $k_p[M]^{0.97}[I]^{0.59}$ was obtained. The overall activation energy for the polymerization was found to be 25.2 kcal/mole. Copolymerization of N-acetyl ${\alpha}$-aminoacrylic acid with acrylic acid and styrene was carried out for the determination of monomer reactivity ratios. The monomer reactivity ratios for the monomer pairs determined at 70.0{\pm}0.1^{\circ}C$ using benzoyl peroxide as an initiator are; $r_1$(N-acetyl ${\alpha}$-aminoacrylic acid) = 0.49, $r_2$(acrylic acid) = 1.41, $r_1$(N-acetyl ${\alpha}$-aminoacrylic acid) = 0.44, $r_2$(styrene) = 0.91. The values of Alfrey-Price's Q and e parameters for N-acetyl ${\alpha}$-aminoacrylic acid were calculated to be 0.51 and 0.16 for the both systems. Differential thermal analysis and thermogravimetry showed that acrylic acid copolymers have poorer thermal stability as compared with the homopolymer of N-acetyl ${\alpha}$-aminoacrylic acid.
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박일현,인신환,손연수,Il Hyun Park,Shin Hwan Ihn,Youn Soo Sohn 대한화학회 1980 대한화학회지 Vol.24 No.4
국산 인산 폐석고를 유동화 반응조건에서 반응온도를 90∼$180^{\circ}C$, 알칼리 첨가량을 0∼5%로 바꾸어가며 뱃치식으로 탈수반응시킨 후 생성물을 X-선 회절, 시차열법분석 등으로 확인하고 혼수량, 압축강도 등 물성들을 측정 비교하였다. 유동화 반응조에서의 탈수반응은 매우 균일하게 연속적으로 진행되면 반응조의 온도가 90$^{\circ}$인 경우에는 이수석고의 탈수반응은 반수석고까지만 진행되나 그 이상의 온도에서는 무수석고까지 탈수반응이 계속됨을 알 수 있었다. 반응조의 온도를 140$^{\circ}$이상 예열 고정하고 석고를 투입하면 반응조의 온도는 일단 떨어졌다가 초기 온도인 140$^{\circ}$에 도달하게 되므로 실제 석고의 탈수반응은 이 예열 고정온도보다 낮은 온도에서 상당량이 일어나며 특히 반응조의 예열 고정온도가 160$^{\circ}$ 이상인 경우에는 대부분의 탈수반응이 반응조의 초기 예열 고정온도에 도달하기 이전에 일어나며 이수석고에서 반수석고로의 전환은 140$^{\circ}$부근에서, 반수석고에서 무수석고로의 전환은 160$^{\circ}$ 부근에서 일어남을 알 수 있었다. 인산 폐석고에 대한 수산화칼슘의 첨가효과는 .$Ca(OH)_2/P_2O_5$의 무게비가 3.2인 때 가장 우수한 물성을 나타내었다 A domestic phosphogypsum was calcined in a batch type fluidized bed reactor at various reaction temperatures ranging 90∼180$^{\circ}$ without and with an alkaline additive amounting up to 5% of gypsum, and physical properties of the resultant products were compared following their characterization by X-ray diffraction pattern and DTA. It has been found that dehydration reactions were uniformly carried out in the fluidized bed reactor and only hemihydrate was obtained at 90$^{\circ}$ whereas at higher temperatures dehydration reaction progressed further. When gypsum was charged to the reactor preheated at over 140$^{\circ}$, a considerable degree of dehydration occurred before the reactant reached the initially set reactor temperature and in particular, at over 160$^{\circ}$ most of dehydration reaction was performed prior to the present reactor temperature. However, it has been found that gypsum mostly transforms into hemihydrate around the reactant temperature of 140$^{\circ}$ while transformation into anhydrite mostly occurs around $160^{\circ}C.$ When calcium hydroxide was added to gypsum in the reactor, the optimum physical properties of the calcined product were obtained at the weight ratio of $Ca(OH_2)/P_2O_5$ = 3.2.
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전위금속의 산소산염의 열분해에 관한 연구 (제5보) Ammonium Metavanadate의 열분해에 따르는 $V_2O_5$의 생성
박일현,Il-Hyun Park 대한화학회 1972 대한화학회지 Vol.16 No.3
Ammonium metavanadate의 熱分解過程을 spring balance와 示差熱分析에 의하여 調査하였다. 分解는 $180^{\circ}C{\sim}220^{\circ}C$와 $310^{\circ}C{\sim}330^{\circ}C$이 두 溫度範圍에서 일어나며 最終生成物은 $V_2O_5(orange yellow)$임을 알았다. 第一段階分解는 $NH_3$와 $H_2O$가 2:1의 比로 放出되는 過程임을 $NH_3$의 定量, omegatron mass spectrometer에 의하여 알았으며, 第二段階의 分解는 $NH_3,\;H_2$)外에 N2도 放出된다는 것을 gas chromatography, omegatron mass spectrometer에 의하여 認知하였다. 分解生成物을 X-ray 回折에 의하여 分析한 結果는 空氣中에서의 分解生成物은 $V_2O_5$의 組成을 가진 것이 生成되었음을 確認하였다. 또한 $NH_4VO_3$ 熱分解에 있어서의 活性化에너지는 各各 41.4 kcal/mole 64.4 kcal/mole의 값을 갖었음을 알았다. Thermal decomposition of ammonium metavanadate has been investigated by using the quartz spring balance and differential thermal analysis. It showed that the decomposition of ammonium metavanadate is proceeded at two stages which correspond to $180^{\circ}C-220^{\circ}C$ and $310^{\circ}C-330^{\circ}C$ decomposition temperatures, respectively. Evolved ammonia gas in thermal decomposition has been analyzed quantitatively by titration. And the constituents of gases evolved have been evaluated by gas chromatography and omegatron spectrometer. From these results, it was concluded that the gases evolved in the first step decomposition were $NH_3$ and $H_2O$ with 2:1 ratio and the second step decomposition corresponded to the formation of $NH_3$, $H_2O$ and $N_2O$ which was produced in oxidation of $NH_3$ by $V_2O_5$. The decomposition products were identified by means of X-ray diffraction method. The decomposition product in air was V_2O_5 and the product in vacuum $V_3O_7.$ The kinetics of the thermal decomposition was studied, giving the values of the activation energy of 41.4 kcal/mole and 64.4 (kcal/mole) respectively.
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수개관개용수의 (數個灌慨用水) 수질 및 잔류농약의 오염에 관하여
박일현,박윤창,신형태 ( Il Hyun Park,Yoon Chang Park,Hyung Tai Shin ) 한국하천호수학회 1982 생태와 환경 Vol.15 No.3·4
The study of water quality of three rivers and three lakes selected throughout the country was carried out in June, August, December, 1979 and April 1980. Although trace amounts of Hg, Cd, and Cr (VI) were detected in some areas and certain seasons the waters in these areas were found to be good in quality. Moreover, organochlorine pesticides but BHC which was turned out to be dissolved in the waters within 0.05 ppb were not detected at all. Grains collected from several places contained Hg and Cd in the rage of 0.036-0.094 ppm and ND-0.5ppb respectively. In the analysis of grains for organochlorine pesticide residues, the amount of total BHC were within 0.01 ppm and other organochlorine pesticides including heptachlor were not detected. The amounts of heavy metals and pesticide residues in several grains were not affected by kinds of grains and production areas. The heavy metals in fresh fishes were determined as well and they were found to be within allowable limits.
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전기 전도도 및 광산란법에 의한 나트륨 도데카노에이트와 나트륨 옥타노에이트의 혼합미셀화 연구
박일현,장한웅,백승환,Park, Il Hyun,Jang, Han Woong,Baek, Seung Hwan 대한화학회 2015 대한화학회지 Vol.59 No.4
음이온성 계면활성제인 sodium dodecanoate과 sodium n-octanoate의 혼합미셀 물성인 임계미셀농도(CMC), 반대이온의 결합상수(B), 및 미셀형성 응집수(N<sup>*</sup>) 등을 여러 조성에서 전기전도도법과 광산란법으로 조사하였다. 여러 혼합조성에서의 혼합미셀 형성에 대한 실험 결과는 이상용액의 예측 거동과는 상당히 벗어났으므로, 정규용액 이론에 기반을 둔 Rubingh 모델과 Motomura 모델을 이용하여 분석하였다. 또 미셀 형성에 대한 표준 Gibbs 에너지 ΔG<sup>micel,0</sup>는 전체 조성에서 음의 값이 얻어져 혼합미셀의 안정성을 확인할 수 있었으며, 이러한 ΔG<sup>micel,0</sup> 측정값은 이론적 계산치와 실험 오차 내에서 일치하였다. The critical micelle concentration (CMC), the counter ion binding constant (B) and the aggregation number (N<sup>*</sup> ) for the mixed micellization of sodium dodecanoate and sodium n-octanoate as two anionic surfactants have been investigated by means of electric conductivity and light scattering. As its experimental results are found to be deviated from ideal mixed model, thus two different kinds of regular solution models such as Rubingh and Motomura are used for interpreting our experimental data. The stability of the mixed micelles has been confirmed from the negative values of the standard Gibbs energy of mixed micellization ΔG<sup>micel,0</sup> over all compositions and the measured values of ΔG<sup>micel,0</sup> agreed with the theoretical ones within the experimental error.
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