• 제목/요약/키워드: Melt temperature

검색결과 902건 처리시간 0.041초

폴리염화비닐의 친환경 가소제로서 Poly(1,2-propylene glycol adipate) (Poly(1,2-propylene glycol adipate) as an Environmentally Friendly Plasticizer for Poly(vinyl chloride))

  • Zhao, Yan;Liang, Hongyu;Wu, Dandan;Bian, Junjia;Hao, Yanping;Zhang, Guibao;Liu, Sanrong;Zhang, Huiliang;Dong, Lisong
    • 폴리머
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    • 제39권2호
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    • pp.247-255
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    • 2015
  • Poly(1,2-propylene glycol adipate) (PPA) was used as an environmentally friendly plasticizer in flexible poly(vinyl chloride) (PVC). Thermal, mechanical, and rheological properties of the PVC/PPA blends were characterized by differential scanning calorimetry, dynamic mechanical analysis, tensile test, scanning electron microscopy and small amplitude oscillatory shear rheometry. The results showed that PPA lowered the glass transition temperature of PVC. The introduction of PPA could decrease tensile strength and Young's modulus of the PVC/PPA blends; however, elongation-at-break was dramatically increased due to the plastic deformation. The plasticization effect of PPA was also manifested by the decrease of dynamic storage modulus and viscosity in the melt state of the blends. The results indicated that PPA had a good plasticizing effect on PVC.

방향족 구조가 포함된 열가소성 탄성체 Poly(ether-b-amide)의 합성 및 특성 (Synthesis and Characterization of Thermoplastic Elastomer Poly(ether-b-amide) Containing Aromatic Moiety)

  • 이지훈;김형중
    • 폴리머
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    • 제38권5호
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    • pp.596-601
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    • 2014
  • 방향족 구조를 포함하고 분자량이 조절된 polyamide(PA) 올리고머를 4-aminobenzoic acid와 12-aminododecanoic acid의 축합반응으로 합성하였다. 이 올리고머를 여러 분자량의 polytetramethylene glycol(PTMG)과 축합하여 PA를 hard segment로 하고 PTMG를 soft segment로 하는 열가소성 탄성체로서 poly(ether-b-amide)(PEBA)를 제조하였다. 합성된 PEBA의 구조는 FTIR과 $^1H$ NMR로 확인하였으며 DSC와 UTM을 사용하여 hard segment의 구조변화에 따른 열적특성과 기계적 성질의 변화를 비교해 본 결과 방향족 구조를 30%까지 포함할 때 결정성의 변화 없이 PEBA들의 용융온도는 높아졌고 초기 modulus와 strength는 더 크게 나타났다.

The Effect of Additive Co on the Magnetic Properties of Fe3B/Nd2Fe14B Magnets

  • Yang, Choong-Jin;Park, Eoun-Byung;Hwang, Yong-Soon;Kim, Eng-Chan
    • Journal of Magnetics
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    • 제4권2호
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    • pp.60-64
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    • 1999
  • The addition of Co into $Nd_4Fe_{77.5-x}Co_x(HfGa)_yB_{18.5}(0$\leq$x$\leq$5, y=0, 0.5)4 was found to enhance the magnetic properties of $Fe_3B/Nd_2Fe_{14}B$ nanocomposite magnets. The enhancement resulted from the fact that Co retarded the crystallization of $\alpha$-Fe or Fe3B but accelerated that $Nd_2Fe_{14}B$. The decreased interval between the onset of crystallization temperature of Fe3B and $Nd_2Fe_{14}B$. phases enabled the grain growth of each phase to be uniform dufing a post annealing of the melt spun ribbons. The addition of 3~5 at. % Co into ternary composition $Md_4Fe_{77.5}B_{18.5}$ increased the coercivity (iHc) from 3.27 to 3.54 kOe with the enhanced remanence value (4$\pi$Mr) around 11.54 kG. From the ribbon magnets of Nd4Fe71.5Co5Hf0.5B18.5 made at 26 m/sec and annealed at 68$0^{\circ}C$ for 10 min, the magnetic properties of Br=11.54 kG, iHc=3.54 kOe, and (BH)max=14.35 MGOe were obtained from volume production line.

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초임계 공정을 이용한 폴리에틸렌옥사이드/클레이 나노복합체 제조 (Fabrication of poly(ethylene oxide)/clay nanocomposites using supercritical fluid process)

  • 김용렬;정현택
    • 한국응용과학기술학회지
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    • 제31권1호
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    • pp.143-150
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    • 2014
  • 최근 낮은 표면장력, 높은 확산계수, 가스와 같은 낮은 점도, 그리고 액체와 유사한 밀도를 갖는 초임계 유체의 장점을 이용하여 여러 가지 물질의 합성이나 응용 공정에 초임계 유체를 이용하고 있다. 초임계 유체를 이용하여 복합체 제조 시 기존의 용융공정에 비해서 분자들의 움직임이 활발하게 이루어 질 수 있어서 물성의 향상을 기대할 수 있다. 또한 클레이가 고농도로 함유된 마스터 배치를 쉽게 제조할 수 있으며, 기존의 유기 용매를 사용하여 복합체를 제조할 때보다 잔존 용매를 쉽게 제거할 수 있다는 장점을 가지고 있다. 따라서 본 연구에서는 이러한 초임계 이산화탄소를 이용하여 폴리에틸렌옥사이드/클레이 나노복합체를 제조하였다. 또한 본 연구의 목적은 초임계 상태에서 분자들의 활발한 움직임을 기대할 수 있으므로 고분자가 용해되고 클레이 층상으로 효과적으로 삽입되어 복합체의 열적 특성 및 다른 여러 가지 물성을 증가시키는 데 있다. 복합체 제조 후 XRD, TGA, 그리고 DSC를 이용하여 복합체의 특성을 분석 했다. 그 결과 용융방법으로 제조한 복합체보다 열 안정성이 향상되었으며, 클레이 층상 거리도 더 많이 벌어짐을 확인할 수 있었다.

응고중 구리 주형과 알루미늄 용탕의 계면열전달계수에 미치는 용탕과열도와 도형재의 영향 (Effects of Superheat and Coating Layer on Interfacial Heat Transfer Coefficient between Copper Mold and Aluminum Melt during Solidification)

  • 김희수;신제식;이상목;문병문
    • 한국주조공학회지
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    • 제24권5호
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    • pp.281-289
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    • 2004
  • The present study focused on the estimation of the interfacial heat transfer coefficient as a function of the surface temperature of the aluminum casting at the mold/casting interface to investigate the effects of superheat and coating layer. The casting experiments of aluminum into a cylindrical copper mold were systematically conducted to obtain the thermal history during solidification. The thermal history recorded by four thermocouples embedded both in the mold and the casting was used to solve the inverse heat conduction problem using Beck's method. The effects of superheat and coating on the interfacial heat transfer coefficient in the liquid state, during the solidification, and in the solid state were comparatively discussed. In the liquid state, the interfacial heat transfer coefficient is thought to be affected by the roughness of the mold, the wettability of the casting on the mold surface, and the thermophysical properties of the coating layer. When the solidification begins, the air gap forms between the casting and the mold, and the interfacial heat transfer coefficient becomes a function of the air gap as well as surface roughness and the superheat. In the solid phase, it depends only upon the thermal conductivity and the thickness of the air gap. The coating layer reduces seriously the interfacial heat transfer coefficient in the liquid state and during the solidification.

Antiferroelectric Liquid Crystal from Bent-Core Molecule with Vinyl End Group

  • Lee, Chong-Kwang;Kwon, Soon-Sik;Kim, Tae-Sung;Shin, Sung-Tae;Choi, Hong;Choi, E. Joon;Kim, Sea-Yun;Zin, Wang-Choel;Kim, Dae-Choel;Chien, Liang-Chy
    • Bulletin of the Korean Chemical Society
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    • 제25권8호
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    • pp.1171-1176
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    • 2004
  • Three banana-shaped achiral compounds, 4-chloro-1,3-phenylene bis [4-{4-(undecenyloxy)phenyl imino-methyl} benzoate] derivatives, were synthesized with variation of a substituent (x=H, F, Cl); their antiferro-electric properties are described. The smectic mesophases, including a switchable chiral smectic C(Sm $C^{\ast}$) phase, were characterized by differential scanning calorimetry, polarizing optical microscopy, triangular wave method, and X-ray diffractometry. The presence of vinyl groups at the terminals of linear side wings in the banana-shaped achiral molecules induced a decrease in melting temperature and formation of the switchable Sm $C^{\ast}$ phase in the melt. The smectic phase having a lateral fluorine-substituent at 3-position of the Schiff's base moiety showed antiferroelctric switching, and the value of spontaneous polarization on reversal of an applied electric field was 250 nC/$cm^2$ .

LDPE/PS 블렌드의 전기적 성질에 미치는 상용화제로서의 SEBS의 효과 (Compatibilizing Effect of SEBS for Electrical Properties of LDPE/PS Blends)

  • 김태영;김동명;김원중;이제혁;서광석;이태희
    • 대한전기학회논문지:전기물성ㆍ응용부문C
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    • 제54권3호
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    • pp.114-119
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    • 2005
  • We investigated compatibilizing effects of electrical properties such as charge distributions and electrical breakdown in blends of low density polyethylene (LDPE) / polystyrene (PS) with poly [styrene-b-(ethylene-co-butylene)-b-styrene] (SEBS), the triblock copolymer. The blends with $70\;wt\%$ of LDPE and $30\;wt\%$ of PS were prepared through a melt blending in a batch type kneader at a temperature of $220^{\circ}C$ when the SEBS content increased up to $10\;wt\%$. Scanning electron microscopy (SEM) was investigated for observation of morphology of LDPE / PS blends increasing SEBS contents. The morphological observation showed that addition of SEBS results in the domain size reduction of the dispersed PS phase and a better interfacial adhesion between LDPE and PS phases. Measurements of space charge distributions for blends was carried out with pulsed electroacoustic (PEA) method. It was possible to observe that the amount of charge storage in the LDPE / PS blends decreased wiか increasing of SEBS content. The location of SEBS at a domain interface enables charges to move from one phase to the other via domain interface and results in a indicative decrease in the amount of space charge for the LDPE / PS blends with SEBS. Electrical breakdown strength of these blends was observed. It was found that the maximum breakdown strength of the blend was 51.55 kV/mm. These results were better than 38.38 kV/mm of LDPE used electrical insulator for cables and were caused by crystalinity of blends. Because the crystalinity of blends were lower than LDPE, electrical breakdown strength of LDPE / PS blends is higher than that of LDPE. We evaluated the possibility of these blends for insulating material substituted LDPE.

무전해 도금법으로 제조된 구리 함유 활성탄소섬유 촉매의 제조와 NO 제거 반응성 평가 (Preparation of Electroless Copper Plated Activated Carbon Fiber Catalyst and Reactive Evaluation of NO Removal)

  • 윤희승;오종현;이형근;전종기;유승곤
    • Korean Chemical Engineering Research
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    • 제46권5호
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    • pp.863-867
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    • 2008
  • 피치계 활성탄소섬유가 납사분해 잔사유를 개질하여 용융 방사하고, 산화, 탄화 및 스팀으로 활성화하여 제조되었다. 활성탄소섬유의 표면은 주석-팔라듐을 사용하여 단일 스텝에 의해 예민화 과정을 거쳤다. 예민화된 활성탄소섬유 표면에 무전해도금법을 사용하여 구리를 골고루 담지하였다. 도금시간을 증가시켜서 구리의 담지량을 변화시키고, BET, SEM, XRD 및 ICP를 이용하여 촉매 특성 변화에 미치는 영향을 관찰하였다. 도금시간에 따라 부가된 구리의 양은 증가하나, 기공부피와 비표면적은 감소하였다. 또한 반응 온도가 증가함에 따라 NO 제거 성능이 증가하였다. $300^{\circ}C$ 이상의 반응 온도에서 부가된 구리의 양이 증가하면 표면적의 감소와 구리 분산도의 감소 때문에 NO 제거 성능은 감소하는 결과를 얻었다.

스피넬 전성형체의 $La_2$O_3-A1_2O_3-SiO_2$계 유리 침투 kinetic (Kinetic Study Of $La_2$O_3-A1_2O_3-SiO_2$ glass infiltration into Spinel Preforms)

  • 이득용;장주웅;김병수;김대준;송요승
    • 한국결정성장학회지
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    • 제12권1호
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    • pp.31-35
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    • 2002
  • 상용 스피넬 분말(0.94$\mu$m)을 $1300^{\circ}C$ 2시간 열처리한 후 30분 동안 습식혼합하여 3.29$\mu$m의 최종분말을 제조하여 die-press법을 이용하여 $1100^{\circ}C$에서 2시간 1차 소결하여 다공성 전성형체를 제조하고 $1080^{\circ}C$에서 0~2시간가지 $La_2O_3-A1_2O_3-SiO_2$계 유리를 용응 침투시켜 유리 침투 깊이와 시간간의 kinetic을 조사하였다 유리 침투시간이 증가할수록 침투깊이는 모세관압에 의하여 parabolic하게 증가하였다. 유리-스피넬 복합체의 강도와 인성값은 각각 317MPa, 3.56MPa . $m^{1/2}$이 었으며 $1300^{\circ}C$의 높은 하소온도로 인한 재결정에 의하여 스피넬은 침상과 다각형 조직이 동시에 존재하는 이중 미세조직 이 관찰되었다.

Nd1+XBa2-XCu3O7-δ Bulk Superconductor by Zone-melt Process

  • Soh, Dea-Wha;Guo, Fan-Zhan
    • Transactions on Electrical and Electronic Materials
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    • 제3권3호
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    • pp.21-24
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    • 2002
  • Two kinds of $Nd_{1+X}Ba_{2-X}Cu_3O_{7-{\delta}}$, the sintering samples and zone melting samples, were heat-treated under pure Ar at 950$^{circ}C$. The substitution of Nd ion for Ba ion in the $Nd_{1+X}Ba_{2-X}Cu_3O_{7-{\delta}}$ before and after the heat treatment was investigated by XRD. In order to confirm the effects of the heat treatment, the Tc and Jc of samples with/without the heat treatment under Ar were comparatively studied. $Nd_{1+X}Ba_{2-X}Cu_3O_{7-{\delta}}$ samples were oxygenated under pure oxygen at $300^{circ}C$. From the XRD pattern it was found that the sample with x<0.4 was transferred from tetragonal phase to orthorhombic phase after the oxygenation, while the sample with x>0.4 did not show the phase transition even after a long time oxygenation. Therefore, the low oxygen partial pressure (Ar+1 % O$_2$) was used for the ambient atmosphere of the zone-melting samples, which could reduce the melting temperature and depress the substitution of Nd for Ba. After the improvement in the zone-melting process, the Jc value was increased to 2 x $10^4$A/$cm^2$ (0 T, 78 K). The particle orientation and the structure of zone-melted NdBaCuO were studied by the XRD and SEM analysis.