• Environmental Analysis Health and Toxicology
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• 제16권4호
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• pp.211-221
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• 2001

The purpose of this study was to investigate the acute (4 hours) and repeated-dose (6 hours a day, 5 days a week, 4 weeks) toxic effects of 1-hexene on Sprague-Dawley (SD) rats which were treated by inhalation. The results were as follows; 1. The median lethal concentration(LC$_{50}$) was estimated 52,694 ppm (confidence limit 95％; 49,494~55,447 ppm) in acute inhalation. Abnormal clinical signs related to the 1-Hexene were not observed with the acute inhalation dose. Cross findings of necropsy revealed on evidence of specific toxicity related to the 1-hexene. II. By repeated inhalation exposure the body weight of male were more or less reduced by the dose of 2,500 ppm and 5,000 ppm compared with control group. However there were no significant variation hematology and blood biochemistry for the exposed rats compared with the control rats. Abnormal clinical signs and gross findings of necropsy related to the 1-hexene were not shown. In conclusion when we exposed 1-hexene to SD rats for 4 weeks, 5 days per week, 6 hours per day, the Lowest observed effect level (LOEL) was over 2,500 ppm and Non observed effect level (NOEL) was below 500 ppm.

• Bulletin of the Korean Chemical Society
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• 제32권6호
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• pp.1851-1858
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• 2011

Details of the double-bond isomerization of 1-hexene over H-ZSM-5 were clarified using density functional theory. It is found that the reaction proceeds by a mechanism which involves the Br${\o}$nsted acid part of the zeolite solely. According to this mechanism, 1-hexene is first physically adsorbed on the acidic site, and then, the acidic proton transfers to one carbon atom of the double bond, while the other carbon atom of the double bond bonds with the Br${\o}$nsted host oxygen, yielding a stable alkoxy intermediate. Thereafter, the Br${\o}$nsted host oxygen abstracts a hydrogen atom from the $C_6H_{13}$ fragment and the C-O bond is broken, restoring the acidic site and yielding trans-2-hexene. The calculated activation barrier is 12.65 kcal/mol, which is in good agreement with the experimental value. These results well explain the energetic aspects during the course of double-bond isomerization and extend the understanding of the nature of the zeolite active sites.

• 공업화학
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• 제7권4호
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• pp.623-632
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• 1996

코모노머와 코모노머의 조성을 변화시켜 프로필렌/부텐-1 및 트로필렌/헥센-1의 공중합을 실시하여 반응성비, 용융점 및 폴리머 형상등을 관찰하였다. 공중합에 사용한 촉매는 담체로서 실리카(촉매 I)와 마그네슘(촉매 II)을 사용한 고활성촉매이다. 코모노머의 조성이 증가함에 따라 폴리머의 용융점이 낮아지며, 또한 코모노머의 조성이 프로필렌/부텐-1 공중합의 경우에는 40% 이상, 프로필렌/헥센-1 공중합의 경우에는 80% 이상이면 폴리머의 형상이 무정형화 되어진다. 반응성비는 Fineman-Ross법과 Kelen-$T{\ddot{u}}d{\tilde{o}}s$법으로 구하였다.

• 한국식품위생안전성학회지
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• 제26권4호
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• pp.383-387
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• 2011

The levels of migration of 1-hexene and 1-octene residues in PE (polyethylene) products were analyzed by Headspace gaschromatography (HSGC). A total of 21 samples were including lap, polyglove, zipper bag and ect. The samples were eluted with distilled water, 4% acetic acid, 20% ethanol and n-heptan. The limit of detection (LOD) was 0.06 mg/L ~ 0.30 mg/L and limit of quantitation (LOQ) was 0.21 mg/L ~ 1.01 mg/L, respectively. But because of the high volatile, n-heptan elution was not detected 1-hexene and 1-octene standard. 1-hexene and 1-octene were not detected in the sample which eluted with simulant at $60^{\circ}C$, 30min. Microwave for 1 minute also treated sample and direct heated at $100^{\circ}C$ without simulant were not detected.

• Macromolecular Research
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• 제12권3호
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• pp.316-321
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• 2004

We have performed copolymerizations of ethylene with 1-hexene using various ansa-metallocene compounds in the presence of the non-coordinative [CPh$_3$][B(C$\_$6/F$\_$5/)$_4$ion pair as a cocatalyst. The metallocenes chosen for this study are isospecific metallocene diamide compounds, rac-(EBI)Zr(NMe$_2$)$_2$ [1, EBI = ethylene-l ,2-bis(1-indenyl)], rac-(EBI)Hf(NMe$_2$)$_2$ (2), rac-(EBI)Zr(NC$_4$H$\_$8/)$_2$ (3), and rac-(CH$_3$)$_3$Si(1-C$\_$5/H$_2$-2-CH$_3$-4-$\^$t/C$_4$H$\_$9/)2 Zr(NMe$_2$)$_2$ (4), and syndiospecific metallocene dimethyl compounds, ethylidene(cyclopentadienyl)(9-fluorenyl) ZrMe$_2$ [5, Et(Flu)(Cp )ZrMe$_2$] and isopropylidence (cyclopentadienyl)(9-fluorenyl)ZrMe$_2$ [6, iPr(Flu)(Cp)ZrMe$_2$]. The copolymerization rate decreased in the order 4 ＞1-3＞2 ＞5＞6. The reactivity of I -hexene decreased in the order 2 ＞6＞1- 3-5＞ 4. We characterized the microstructure of the resulting poly(ethylene-co-l-hexene) by $\^$l3/C NMR spectroscopy and investigated various other properties of the copolymers in detail.

• Elastomers and Composites
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• 제48권4호
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• pp.263-268
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• 2013

본 연구에서는 다리 구조의 메탈로센 촉매인 rac-$Et[Ind]_2ZrCl_2$를 이용하여 새로운 구조의 poly(ethylene-ter-1-hexene-ter-divinylbenzene) 삼원공중합체를 제조하였다. 공단량체인 1-hexene이 중합에 미치는 효과에 관한 연구를 수행하였다. 여러 가지 중합 조건의 영향을 살펴보았는데 공촉매/촉매 몰비가 3,000일 때, 촉매활성도는 8,000이 넘는 매우 높은 수준의 활성도를 보여주었다. 또한, 중합 시간에 따라 중량 평균 분자량이 일정 수준까지 증가하는 경향을 나타내었고, 중합시간이 50분일 때는 무정형 상태에 가까워지는 것을 확인하였다. 삼원공중합체의 중량 평균 분자량은 110,000-200,000, 밀도는 $0.85-0.89g/cm^3$ 수준이었다. 또한, 삼원 공중합체의 열적 성질과 구조를 확인하였다.

• 대한화학회지
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• 제14권3호
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• pp.237-242
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• 1970

Effect of Added 1-hexene on the yield of hydrogen produced from Co-60 gamma radiolysis of methanol was investigated at room temperature. The results indicated that the yield of hydrogen decreased rapidly with increasing 1-hexene concentrations. Effect of added methyl borate on the radiolysis of methanol was also studied in the presence of oxygen. The results revealved that methyl borate acted as a less effective scavenger than oxygen towards the precursors of the radiolysis products. Experimental data previously obtained on the systems with oxygen added were treated more quantitatively to re-examine mechanism of the radiolysis of methanol in detail.

• Elastomers and Composites
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• 제46권4호
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• pp.304-310
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• 2011

다리 구조 또는 비다리 구조의 메탈로센 촉매를 이용하여 새로운 구조의 poly(ethylene-ter-1-hexeneter-divinylbenzene) 삼원공중합체를 제조하였다. 다리구조의 rac-$Et[Ind]_2ZrCl_2$ 촉매가 비다리구조의 $Cp_2ZrCl_2$ 촉매보다 상대적으로 양호한 결과를 보여 주었다. 특히 조촉매/촉매 몰비가 3000일 때 촉매활성도는 8000(kg of polymer/$mol{\cdot}h$)이 넘는 매우 높은 수준의 활성도를 보여주었다. 또한, 중합 시간에 따라 중량 평균 분자량이 일정수준까지 점차 증가하는 경향을 나타내었고, 중합시간이 50분일 때 무정형 상태를 나타내었다. 삼원공중합체의 중량평균 분자량은 110,000~200,000, 밀도는 $0.85{\sim}0.89g/cm^3$ 수준이었다. 또한, 삼원 공중합체의 열적 성질과 구조를 확인하였다.

• 한국고분자학회:학술대회논문집
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• 한국고분자학회 2006년도 IUPAC International Symposium on Advanced Polymers for Emerging Technologies
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• pp.224-225
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• 2006

The Ethylene polymerization behavior of a series of polymethylene bridged dinuclear CGC $[Zr({\eta}^{5}:{\eta}^{1}-C_{9}H_{5}SiMe_{2}NCMe_{3})Me_{2}]_{2}[(CH_{2})_{n}]\;[_{n}=6(1),\;9(2),\;12(3)]$ in the cocatalytic activation with $Ph_{3}C^{+}B^{-}(C_{6}F_{5})_{4}\;(B_{1})\;or\;Ph_{3}C^{+}(C_{6}F_{5})_{3}B^{-}C_{6}F_{4}B^{-}(C_{6}F_{5})_{3}Ph_{3}C^{+}\;(B_{2})\;or\;B(C_{6}F_{5})_{3}\;(B_{3})$ were investigated to study the nuclearity effects as well as the counteranion effects. The ethylene polymerization and ethylene/1-hexene copolymerization were conducted at $30^{\circ}C$ It was found that both in ethylene polymerization and ethylene/1-hexene copolymerization, activities increased in the order of 1 < 2 < 3, which indicates the presence of longer bridge between two active sites contributes more efficiently to facilitate the polymerization activity.

• Macromolecular Research
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• 제11권2호
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• pp.87-91
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• 2003

Thermal decomposition reactions of polystyrene using a new heating medium were carried out by a batch system at 190-280 $^{\circ}C$ to clarify the manner in which decomposition is initiated. Polystyrene obtained from a commercial source and low molecular weight compounds obtained from the thermal decomposition were analyzed by GC, GPC, IR, $^{13}$ C-NMR and GC-MS. The main chain underwent virtually no change by heat application. Polystyrene underwent decomposition below its molding temperature and the major decomposition products were 2,4,6-triphenyl-1-hexene (trimer), 2,4-diphenyl-1-butene(dimer) and styrene (monomer). Ethylbenzene, propylbenzene, naphthalene, benzaldehyde, biphenyl and 1,3-diphenylpropane were detected as minor products. This paper presents a new method for examining the decomposition of polystyrene at low temperature into volatile low molecular weight compounds.