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The Scavenging Effect of Resorcinol on the Formaldehyde Release from the Urea Formaldehyde Adhesive Bonded Plywood (합판용(合板用) 요소수지접착제(尿素樹脂接着劑)의 리조시놀 첨가(添加)에 따른 유리(遊離)포름알데히드 방산(放散) 제거효과(除去效果))

  • Lee, Hwa-Hyoung
    • Journal of the Korean Wood Science and Technology
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    • v.8 no.2
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    • pp.1-5
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    • 1980
  • This study is carried out to determine the scavenging effect of resorcinol added into the urea formaldehyde resin on the formaldehyde release of plywood, as the preliminary study of using the phenolic substances. The method for formaldehyde determination used in this report is the improved chromotropic acid determination. The results are summarized as follows: 1. Resorcinol added into the urea formaldehyde adhesive acts as a good scavenger. 4 percent of resorcinol reduced the formaldehyde release to less than half content. 2. Adding resorcinol gave better glue shear strength than that of control, showing the peak of the shear strength, at 2 percent and decreased to the same strength as control along its content of 4 percent. 3. Moisture content of air dried plywood met the standard very well.

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Extracellular DNAs Released form the Genetically Engineered E. coli CU103 During Growth in Different Liquid Media

  • Kim, Chi-Kyung;Park, Sang-Ho;Lim, Jai-Yun;Kim, Young-Chang;Kim, Youngsoo;Min, Kyung-Hee;Lee, Ki-Sung
    • Journal of Microbiology
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    • v.34 no.2
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    • pp.144-150
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    • 1996
  • During growth of the genetically engineered E. coli CU103 in different media, extracellular DNAs released from the cells were studied. The extracellular DNAs released in the medium were concentrated by an thanol precipitation method and then quantified by a fluorescence method using Hoechst 33258. The released extracellular DNAs were also examined by gel electrophoresis and identified by Southern hybridization for the cloned pcbCD genes. The chromosomal DNAs and recombinant plasmid containing the cloned genes were observed to be released in an exponential growth phase. In Luria-Bertani (LB) broth and MM2-GLUCOSE, 210 and 69 ng/ml of DNAs were detected, respectively, after 3-4 days incubation at $30^{\circ}C$ and at pH 7.0. But the released DNAs were measured to be about 10-15 ng/ml in filtered river water (FW) and Tris-EDTA (TE). The at both $15^{\circ}C$ and $4^{\circ}C$, but the released DNAs were more easily degraded at the higher temperature. The extracellular DNAs were produced about 2 times more at pH 7.0 than at both pH 5.0 and pH 9.0 in MM2-glucose medium at $30^{\circ}C$. Therefore, the extracellular DNAs were found to be released actively from the cells during growth in liquid media.

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