• Elastomers and Composites
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• 제54권2호
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• pp.156-160
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• 2019

The changes in the dispersion of carbon black in liquid polyisoprene under shear flow with time have been investigated by time-resolved ultra small-angle X-ray scattering (USAXS) method. The analyses of USAXS profile immediately after the start of shear flow clarified that the aggregates of carbon black with a mean radius of gyration of 14 nm and surface fractal dimension of 2.5 form the fractal network structure with mass-fractal dimension of 2.9. After the application of the shear flow, the scattering intensity increases with time at the observed whole entire q region, and then the a shoulder appears at $q=0.005nm^{-1}$, indicating that the agglomerate is broken and becomes smaller by shear flow. The analysis by the Unified Guinier/Power-law approach yielded several characteristic parameters, such as the sizes of aggregate and agglomerate, mass-fractal dimension of agglomerate, and surface fractal dimension of the primary particle. While the mean radius of gyration of the agglomerate decreases with time, the mean radius of gyration of the aggregate, mass fractal dimension, and surface fractal dimension don't change with time, indicating that the aggregates peel off the surface of the agglomerate.

• 분석과학
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• 제14권1호
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• pp.44-49
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• 2001

GC-MS와 연결된 $85{\mu}m$ 폴리 아크릴레이트 fiber의 SPME가 풍선 시료 중에 포함된 가소제를 분석하는데 사용되었다. 풍선은 IR 분광법에 의해 폴리이소프렌으로 만들어진 것으로 판명되었다. 한시간 동안 아세톤이 첨가된 물 용매에서 추출된 풍선의 가소제는 9종류의 가소제가 포함된 외부표준법에 의해 정량 하였다. 정량법은 $0.25-25{\mu}g/g$의 농도범위에서 표준 가소제들에 대하여 유효화 과정을 거쳤으며, 검출한계는 가소제에 따라 $0.11-0.38{\mu}g/g$이었고, 이러한 정량법에 의한 재현성의 RSD는 3.7-14.2%이었다. 이들 풍선 중에는 우려할만한 수준의 환경호르몬성 가소제가 검출되는 제품도 포함되어 있어 이들에 대한 규제의 필요성이 있다.

• Macromolecular Research
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• 제10권2호
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• pp.97-102
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• 2002

The mixtures of non-conjugated dienes, 4-methyl-1,4-hexadiene and 5-methyl-1,4-hexadiene (MHD), were successfully synthesized by the reaction of isoprene with ethylene using Fe(III)-based catalyst in toluene. The conversion was over 96 mol% on the basis of the initial amount of isoprene used. The production yield for MHD was nearly 50 mol%, the other was polyisoprene. The mixtures were successfully copolymerized with ethylene by using zirconium-based metallocenes. The products were characterized by the combinations of gas chromatography, high temperature gel permeation chromatography, $^1$H NMR, $^{13}$ C NMR, high temperature $^1$H NMR, UV/visible spectroscopy, and differential scanning calorimetry. It was found that 5-methyl-1,4-hexadiene was active enough to be incorporated into the copolymer chain but the corresponding isomeric material,4-methyl-1,4-hexadiene, was inactive in metallocene-catalyzed copolymerizations. Specifically, in the zirconocene-catalyzed copolymerizations of ethylene with MHD, ansa-structure catalysts seem to be more efficient than non-bridged type zirconocene. The degree of incorporation of MHD in the resulting copolymers was able to be controlled by the amount of non-conjugated dienes used initially.

• Korea-Australia Rheology Journal
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• 제13권4호
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• pp.205-217
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• 2001

This review article summarizes results of recent viscoelastic and dielectric studies for entangled cis-polyisoprene (PI) chains. The PI chains have the so-called type-A dipoles parallel along the chain backbone, and their slow viscoelastic and dielectric relaxation processes reflect the same global chain motion. However, this motion is differently averaged in the viscoelastic and dielectric properties, the former representing the isochronal orientational anisotropy of individual entanglement segments while the latter detecting the orientational correlation of the segments at two separate times (0 and t). On the basis of this difference, the viscoelastic and dielectric data of the entangled PI chains were compared to elucidate detailed features of the chain dynamics. Specifically, the molecular picture of dynamic tube dilation (DTD) incorporated in recent models was tested for linear and star PI chain. The comparison revealed that the DTD picture was valid for linear PI chains but failed for the star PI chains in the dominant part of the terminal relaxation. The failure for the star chains was related to the pre-requisite for the DTD process, rapid equilibration of successive entanglement segments through their constraint release (CR) motion: For the star chains, the dilated tube diameter expected in the terminal regime was considerably large because of a broad distribution of motional modes of the chains, so that the CR-equilibration required for DTD could not occur in time. The terminal relaxation of the star chain appeared to occur through the CR process before the expected DTD process was completed. The situation was different for the linear chain exhibiting narrowly distributed motional modes. The dilated tube expected for the linear chain was rather thin and the required CR-equilibration occurred in time, resulting in the success of the DTD picture. These detailed features of the chain dynamics was revealed only when the viscoelastic and dielectric properties were compared, demonstrating the importance of this comparison.

• Elastomers and Composites
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• 제54권2호
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• pp.110-117
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• 2019

The characterization of the ozone oxidation for raw natural rubber (NR) was investigated under controlled conditions through image and fourier transform infrared (FT-IR) analysis. The ozone oxidation was performed on a transparent thin film of raw NR coated on a KBr window in a dark chamber at $40^{\circ}C$ under low humidity conditions to completely exclude thermal, moisture, or light oxidation. The ozone concentration was set at 40 parts per hundred million (pphm). Before or after exposure to ozone, the image of the thin film for raw NR was observed at a right or tilted angle. FT-IR absorption spectra were measured in the transmission mode according to ozone exposure time. The ozone oxidation of NR was determined by the changes in the absorption peaks at 1736, 1715, 1697, and $833cm^{-1}$, which were assigned to an aldehyde group (-CHO), a ketone group (-COR), an inter-hydrogen bond between carbonyl group (-C=O) from an aldehyde or a ketone and an amide group (-CONH-) of protein, and a cis-methine group ($is-CCH_3=CH-$, respectively. During ozone exposure period, the results indicated that the formation of the carbonyl group of aldehyde or ketone was directly related to the decrement of the double bond of cis-1,4-polyisoprene. Only carbonyl compounds such as aldehydes or ketones seemed to be formed through chain scission by ozone. Long thin cracks with one orientation at regular intervals, which resulted in consecutive chain scission, were observed by image analysis. Therefore, one possible two-step mechanism for the formation of aldehyde and ketone was suggested.

• Geomechanics and Engineering
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• 제18권5호
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• pp.535-543
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• 2019

Building on/with expansive soils with no treatment brings complications. Compacted expansive soils specifically fall short in satisfying the minimum requirements for transport embankment infrastructures, requiring the adoption of hauled virgin mineral aggregates or a sustainable alternative. Use of hauled aggregates comes at a high carbon and economical cost. On average, every 9m high embankment built with quarried/hauled soils cost $12600MJ.m^{-2}$ Embodied Energy (EE). A prospect of using mixed cutting-arising expansive soils with industrial/domestic wastes can reduce the carbon cost and ease the pressure on landfills. The widespread use of recycled materials has been extensively limited due to concerns over their long-term performance, generally low shear strength and stiffness. In this contribution, hydromechanical properties of a waste tyre sand-sized rubber (a mixture of polybutadiene, polyisoprene, elastomers, and styrene-butadiene) and expansive silt is studied, allowing the short- and long-term behaviour of optimum compacted composites to be better established. The inclusion of tyre shred substantially decreased the swelling potential/pressure and modestly lowered the compression index. Silt-Tyre powder replacement lowered the bulk density, allowing construction of lighter reinforced earth structures. The shear strength and stiffness decreased on addition of tyre powder, yet the contribution of matric suction to the shear strength remained constant for tyre shred contents up to 20%. Reinforced soils adopted a ductile post-peak plastic behaviour with enhanced failure strain, offering the opportunity to build more flexible subgrades as recommended for expansive soils. Residual water content and tyre shred content are directly correlated; tyre-reinforced silt showed a greater capacity of water storage (than natural silts) and hence a sustainable solution to waterlogging and surficial flooding particularly in urban settings. Crushed fine tyre shred mixed with expansive silts/sands at 15 to 20 wt% appear to offer the maximum reduction in swelling-shrinking properties at minimum cracking, strength loss and enhanced compressibility expenses.

• 한국의학물리학회지:의학물리
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• 제21권2호
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• pp.232-237
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• 2010

본 연구에서는 의학영상장치의 방사선에너지스펙트럼과 중원자번호 물질의 방사선흡수특성을 이용하여 경량 재질의 무납차폐체를 개발하였다. 개발된 차폐체는 중량비율로 주석 34.1%, 안티몬 33.8%, 요오드 26.8%와 Polyisoprene 5.3%를 혼합하여 가로$\times$세로$\times$두께 $200{\times}200{\times}1.5\;(mm^3)$로 제작되었으며 밀도는 $3.2\;g/cm^3$이다. 무납차폐체의 무게는 표준납차폐체 무게의 84%로 연당량 0.42 mm에 해당되며, 제작된 무납차폐체는 일차선과 산란선에 대해 표준납차폐체(연당량 0.5 mm 두께)의 투과율과 비교하였다. 일차선 에너지는 50 kVp에서 20 kVp씩 증가하여 110 kVp까지 조사 되었으며, 표준납 차폐체의 투과율은 0.1%, 0.9%, 3.2%, 4.8%였고, 무납차폐체는 각각 0.3%, 0.6%, 2.0%, 4.2%를 보였으며, 오차는 ${\pm}0.1$%이었다. 표준납차폐체와 동등한 연당량의 무납차폐체의 투과율은 각각 0.1%, 0.3%, 1.0%와 2.4%로 저에너지에서는 납과 동일한 감쇠를 나타내었으나 높은 에너지영역 에서는 납의 30~50%의 투과율로 측정되어 차폐효과가 뛰어남을 알 수 있었다. 인체팬텀의 측방산란선에 대한 비교결과는 표준납차폐체가 2.4%, 2.5%, 4.2%, 5.1%를 보였고, 무납차폐체는 각각 2.4%, 3.3%, 4.6%와 5.9%이며 각 오차는 ${\pm}0.2%$였다. 혼합성분의 무납차폐체의 연당량을 표준납차폐체까지 올리는 경우 낮은 에너지에서 뿐만 아니라 높은 에너지 영역에서 납에 비해 월등히 감쇠효과가 있음을 주장하며, 방사선구역의 특성에 따라 경량의 차폐체를 이용함으로써 방사선피폭을 효과적으로 차폐할 수 있을 것이다.