On the UV-induced polymeric behavior of Chinese lacquer.

To dry Chinese lacquer rapidly for the protection and restoration of archeological findings coated by lacquer or excavated lacquer wares and the development of new application of this lacquer, we carried out UV curing technology to improve its curing rate using a high-pressure mercury lamp as a UV source in the absence of any additional photoinitiator. The effects of mainly specific components in Chinese lacquer sap and the role of each reactive group of urushiol, namely hydroxyl groups, hydrogen on the phenyl ring, and olefins in the side chain, in the course of UV exposure were well-investigated. The UV-cured Chinese lacquer films were also characterized by FT-IR, (1)H NMR, SEM, TGA, and Py-GC/MS. The results showed that urushiol was the main component to form Chinese lacquer films, and decomposed to generate the urushiol semiquinone radicals, which sequentially induced the polymerization of Chinese lacquer by radical polymerization, as well as radical substitution under UV irradiation. In addition, the TG analysis suggested that polysaccharide and glycoproteins were integrated with the UV-cured films by covalent bonding. Furthermore, this method could be suitable to fast cure other phenol bearing long aliphatic unsaturated chain, such as CNSL.

[1]  J. Rodrigues,et al.  Chemotaxonomic application of Py-GC/MS: Identification of lacquer trees , 2010 .

[2]  Myong-Jo Kim,et al.  Rhus verniciflua Stokes flavonoid extracts have anti-oxidant, anti-microbial and α-glucosidase inhibitory effect , 2010 .

[3]  S. Yao,et al.  Polymeric bionanocomposite cast thin films with in situ laccase-catalyzed polymerization of dopamine for biosensing and biofuel cell applications. , 2010, The journal of physical chemistry. B.

[4]  J. Xia,et al.  UV-induced polymerization of urushiol. II: Effects of hydrogenation degree of urushiol on surface morphology , 2010 .

[5]  J. Xia,et al.  A rapid approach to urushiol-copper(I) coordination polymer under UV irradiation , 2009 .

[6]  J. Puskas,et al.  Green Polymer Chemistry Using Nature's Catalysts : Enzymes , 2009 .

[7]  H. Stege,et al.  Characterization of commercial synthetic resins by pyrolysis-gas chromatography/mass spectrometry: application to modern art and conservation. , 2009, Analytical chemistry.

[8]  Shiyong Liu,et al.  CNT templated regioselective enzymatic polymerization of phenol in water and modification of surface of MWNT thereby , 2009 .

[9]  J. Pomposo,et al.  Enzymatic Synthesis of Water-Soluble Conducting Poly(3,4- ethylenedioxythiophene): A Simple Enzyme Immobilization Strategy for Recycling and Reusing , 2009 .

[10]  J. Puskas,et al.  Green polymer chemistry: Telechelic poly(ethylene glycol)s via enzymatic catalysis , 2008 .

[11]  T. Miyakoshi,et al.  Effects of hybridization of lacquer sap with organic silane on drying properties , 2008 .

[12]  J. Xia,et al.  UV-induced polymerization of urushiol without photoinitiator , 2008 .

[13]  K. Taguchi,et al.  Photo-curing composite paint containing urushi (Oriental lacquer), and wrinkled coating caused by phase separation , 2007 .

[14]  T. Miyakoshi,et al.  Enzymatic dehydrogenative polymerization of urushiols in fresh exudates from the lacquer tree, Rhus vernicifera DC. , 2007, Journal of Agricultural and Food Chemistry.

[15]  Reinhold Schwalm,et al.  UV Coatings: Basics, Recent Developments and New Applications , 2007 .

[16]  Christopher W. Jones,et al.  Enzyme-initiated miniemulsion polymerization. , 2006, Biomacromolecules.

[17]  L. Rong,et al.  Studies on the reaction mechanism between urushiol and organic silane , 2006 .

[18]  T. Miyakoshi,et al.  Development of a fast drying hybrid lacquer in a low-relative-humidity environment based on kurome lacquer sap , 2005 .

[19]  T. Miyakoshi,et al.  Study of a Naturally Drying Lacquer Hybridized with Organic Silane , 2005 .

[20]  T. Miyakoshi,et al.  Development of a fast drying lacquer based on raw lacquer sap , 2004 .

[21]  T. Miyakoshi,et al.  Studies on the Fast Drying Hybrid Urushi in Low Humidity Environment , 2004 .

[22]  Heinz Langhals,et al.  The restoration of the largest archaelogical discovery--a chemical problem: conservation of the polychromy of the Chinese terracotta army in Lintong. , 2003, Angewandte Chemie.

[23]  O. Vogl Oriental lacquer, poison ivy, and drying oils , 2000 .

[24]  J. Kumanotani Enzyme catalyzed durable and authentic oriental lacquer: a natural microgel-printable coating by polysaccharide–glycoprotein–phenolic lipid complexes , 1998 .

[25]  J. Kumanotani Urushi (oriental lacquer) — a natural aesthetic durable and future-promising coating☆ , 1995 .

[26]  D. M. Snyder An overview of oriental lacquer: Art and chemistry of the original high-tech coating , 1989 .

[27]  H. Boots,et al.  Network formation by chain crosslinking photopolymerization and some applications in electronics , 1989 .

[28]  C. Watanabe,et al.  Enzymic oxidative coupling of urushiol in sap of the lac tree, Rhus vernicifera , 1985 .

[29]  M. Elsohly,et al.  Separation and Characterization of Poison Ivy and Poison Oak Urushiol Components , 1982 .

[30]  R. Oshima,et al.  Configuration of the olefinic bonds in the heteroolefinic side-chains of japanese lacquer urushiol , 1982 .

[31]  Takashi Kato,et al.  Studies of Japanese lacquer: Urushiol dimerization by the coupling reaction between urushiol quinone and a triolefinic component of urushiol , 1969 .

[32]  C. R. Dawson,et al.  The Structural Identification of the Olefinic Components of Japanese Lac Urushiol1 , 1954 .