• 제목/요약/키워드: Benzophenone

검색결과 133건 처리시간 0.021초

폴리에틸렌 필름의 광가교에 의한 옥타데칸의 고정화 (Octadecane Fixation via Photocrosslinking of Polyethylene Film)

  • 윤득원;장진호
    • 한국염색가공학회지
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    • 제22권3호
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    • pp.214-219
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    • 2010
  • Polyethylene(PE) films were photocrosslinked by continuous UV irradiation. Benzophenone addition as low as 1wt% into the PE film increased the gel fraction up to 96%. The photocrosslinking was attributed to the recombination of PE radicals generated upon UV irradiation, which was enhanced by the hydrogen abstraction of the added benzophenone. Also the crossliked PE showed higher thermal stability and decreased crystallinity with increasing UV energy as shown by TGA, XRD and DSC analysis. It was also possible to fix 5.4% octadecane into PE by the photocrosslinking. The crosslinked PE film containing octadecane showed lower tensile strength and modulus coupled with higher extension compared to that without octadecane, which can be used as a new plasticizing method for the crosslinked PE film.

Graft 重合에 關한 硏究-紫外線 照射에 依한 Polyvinyl alcohol 과 Styrene 의 Graft 重合에 關하여 (Studies on the Graft Polymerization-Graft Polymerization of Styrene to Polyvinyl Alcohol by Ultraviolet Light)

  • 심정섭;전경철
    • 대한화학회지
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    • 제6권1호
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    • pp.64-68
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    • 1962
  • The graft polymerization of styrene to polyvinyl alcohol using a photosensitizer(benzophenone) and ultraviolet light was studied. Styrene was grafted onto polyvinyl alcohol up to when polyvinyl alcohol was pre-immersed in water and irradiated by ultraviolet light for 24 hours styrene solution of benzophenone(0.01 molarity). The highest percentage of graft obtained in the grafting which was proceeded in the presence of water added immediately before irradiation was 29%. The grafting was proportional to irradiation time within a certain limit of time, i.e., 24 hours, and presumably was initiated at the surface. After a certain degree of grafting a definite maximum was reached. Graft polymer prepared in this experiment showed high resistance to various solvents.

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니켈 촉매를 이용한 1,1'-Bis(dimethylsilyl)ferrocene과 Carbonyl 화합물의 Silylation 반응 (Nickel Catalyzed Silylation Reaction of Carbonyl Compounds with 1,1'-Bis(dimethylsilyl)ferrocene)

  • 공영건;이정현
    • 대한화학회지
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    • 제46권2호
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    • pp.139-144
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    • 2002
  • 니켈 착물을 촉매로 사용한 1,1´-Bis(dimethylsilyl)ferrocene [1]과 carbonyl 화합물 -benzaldehyde, 4-cyanobenzaldehyde, trimethylacetaldehyde, acetophenone과 benzophenone-은 3-oxa-2,5-disilacyclo-1,1′-ferrocene을 생성하였다. 이와 대비되게 동일한 반응조건에서 화합물 [1]과 isobutyraldehyde의 반응에는 1,1′-bis(dimethylsilyl)ferrocene의 Si-H 결합에 2개의 aldehyde ligand가 이중 삽입된 생성물이 형성되었다.

Styrene-Butadiene 고무의 아크릴아미드 UV 광그라프팅 반응 (Ultraviolet Photografting Reaction of Acrylamide onto Styrene-Butadiene Rubber)

  • 이권익;류승훈
    • Elastomers and Composites
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    • 제33권5호
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    • pp.363-369
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    • 1998
  • UV를 이용하여 반응성 모노머인 아크릴아미드를 SBR에 광그라프트 시키는데 있어서 주요한 인자인 모노머 농도, 조사시간 그리고 카본블랙의 함량이 모노머의 그라프트율에 미치는 영향을 살펴보았다. 광개시제로는 benzophenone을 사용하였다. 아크릴아미드의 그라프트율을 측정하기 위하여 FT-IR ATR과 증류수를 이용하여 정접촉각을 측정하였다. 아크릴아미드의 함량과 UV 조사시간이 증가함에 따라 그라프트율은 증가하였으며 또한 접촉각은 감소하는 현상을 나타내었다. SBR중 카본블랙 함량이 증가함에 따라 그라프트율이 증가함을 알 수 있었다.

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외국 자외선제품의 동향과 UV차단 효과 연구 (The Trend of Foreign Sunscreen Products and Study of UV Protecting Effects)

  • 우건희
    • 대한화장품학회:학술대회논문집
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    • 대한화장품학회 1992년도 자외선 차단 화장품의 SPF에 관한 심포지움(대한화장품학회)
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    • pp.97-114
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    • 1992
  • In these days sun products are developed and produced by the cosmetic scientists in the world. Peoples need strongly to protect themselves from the hazardous UV rays dued to the destruction of ozone layer. Therfore, we, cosmetic scientists must have an effort to produce the more effective goods. In this article the market survey of sun-products as well as the currency of sunscreen agents was investigated. It was found that Benzophenone - 3 and Ocytyl methoxy cinnamate were widely used. The lotions, using Benzophenone - 3 as the chemical agents, and TiO$_2$and micro TiO$_2$ as the physical agents, were measured the UV-Spectrum in the Dilution and Application method. Photoprotective activity of chemical agents can usually be measured in solution state. However, that of the insoluble physical agents such as TiO$_2$is hardly measured in this state. Photoprotective ability of the insoluble physical agents was able to be measured by application of lotions to the surface of UV cells. It was found by this method that micro TiO$_2$showd stronger UV scattering effect than TiO$_2$in this method.

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Dual-Curable Acrylic Pressure-Sensitive Adhesives Based on UV and Thermal Processes

  • Kim, Yang-Bae;Park, Su-Cheol;Kim, Hyun-Kyoung;Hong, Jin-Who
    • Macromolecular Research
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    • 제16권2호
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    • pp.128-133
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    • 2008
  • Several dual-curable acrylic pressure-sensitive adhesives (PSA) were synthesized by the radical polymerization of acrylic monomers containing benzophenone, hydroxyl, and alkyl groups. The optimum extent of UV-induced cure was determined by varying the content of the benzophenone groups (the photoinitiator) from 0.5 to 1.5 wt%. The weight average molecular weight of the polymers obtained ranged from 300,000 to 700,000 amu. The coated pressure-sensitive adhesives were cured either by short UV exposure to induce the grafting of acrylic polymers, or by heating for 6 hat $60^{\circ}C$ to promote the reactions between the polyisocyanates and hydroxyl groups. The dual-curing behavior was determined by monitoring both processes quantitatively by infrared spectroscopy. The developed dual-curable acrylic pressure-sensitive adhesives were found to compensate for the limitations in UV-induced curing of thick coatings.

A Stereoselective Synthesis of 1 $\beta$-Aminocarbapenems.

  • 서경재;이태호;이연영
    • Bulletin of the Korean Chemical Society
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    • 제22권6호
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    • pp.553-558
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    • 2001
  • A stereoselective synthesis of $1\beta-aminocarbapenems$ (11a-c) starting from-4-acetoxy-2-axetidinone derivative 4 is described. 4-Acetoxy-2-azetidinone derivative (4) was reacted with lithium enolate of benzophenone limine of glycine phenyl ester (5f) to give alkylated product (R)-6f in good yield with high diastereoselectivity. The alkylated procudt (R)-6f was transformed to thioesters (7a-c) by transesterification with thiols, Thioesters (7a-c) were converted to their oxalimides (8a-c), followed by the phosphite-mediated reductive cyclization to give carbapenems (9a-c). Removal of all protecting groups of carbapenems (9a-c) afforded $1\beta-aminocarbapenems$ (11a-c).