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Home Heat Accumulators Method-of-improving-the-electrical-conductivity-of-shaped-resin-articles-and-an-electrostatic-coating-process

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Details
Inventors: Shiraiwa, Tetsuo;
Assignee: Dai-Ichi Kogyo Seiyaku Co., Ltd. (Kyoto, JP)
Primary Examiner: Thurlow; Jeffery R.
Assistant Examiner:
Attorney, Agent or Firm: Jordan and Hamburg

A nitrogen-containing compound of the following general formula (1) is kneaded into a resin molding material, the kneaded mixture is molded, and the surface of the resulting article is subjected to corona discharge treatment. Then, an electrostatically charged coating is sprayed on the article. ##STR1## wherein R.sup.1 represents an alkyl group of 6-22 carbon atoms, R.sup.2 and R.sup.3 may be the same or different and each represents an alkyl group of 1-4 carbon atoms; n represents 2-3. In accordance with this invention, a shaped resin article with remarkably improved electrical conductivity can be obtained from a resin of low electrical conductivity substantially without affecting the physical properties and color of the resin and with high productivity. Furthermore, a resin article with high surface resistivity can be electrostatically coated with high coating efficiency and improved results in appearance and productivity substantially without affecting the physical properties of the resin.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS The resin that can be used in this invention includes a variety of resins which provide for high surface resistivity values, such as polyolefin resins, e.
g.
polyethylene, polypropylene, rubber-containing polypropylene (containing an ethylene-propylene copolymer rubber), etc.
, ABS resin, acrylic resin, polyamide resin, polyvinyl chloride resin, polycarbonate resin, polyacetal resin, phenolic resin, and so on.
The nitrogen-containing compound of general formula (1) includes a variety of amides such as N,N-dimethylaminopropyloctylamide, N,N-diethylaminopropyloctylamide, N,N-diethylaminoethyloctylamide, N,N-dibutylaminopropyloctylamide, N,N-dibutylaminoethyloctylamide, N,N-dimethylaminopropyllaurylamide, N,N-diethylaminopropyllaurylamide, N-N-diethylaminoethyllaurylamide, N,N-dibutylaminopropyllaurylamide, N,N-dibutylaminoethyllaurylamide, N,N-dimethylaminopropylmyristylamide, N,N-diethylaminopropylmyristylamide, N,N-diethylaminoethylmyristylamide, N,N-dibutylaminopropylmyristylamide, N,N-dibutylaminoethylmyristylamide, N,N-dimethylaminopropylpalmitylamide, N,N-diethylaminopropylpalmitylamide, N,N-diethylaminoethylpalmitylamide, N,N-dibutylaminopropylpalmitylamide, N,N-dibutylaminoethylpalmitylamide, N,N-dimethylaminopropylstearylamide, N,N-diethylaminopropylstearylamide, N,N-diethylaminoethylstearylamide, N,N-dibutylaminopropylstearylamide, N,N-dibutylaminoethylstearylamide and so on.
These amides can be produced by reacting saturated fatty acids of 7-23 carbon atoms with an N,N-dialkylaminoalkylamine such as N,N-dimethylaminopropylamine, N,N-diethylaminopropylamine, N,N-diethylaminoethylamine, N,N-dibutylaminopropylamine, N,N-dibutylaminoethylamine, and so on.
This reaction can be carried out by any known amidation reaction.
Thus, this reaction proceeds as said reactants are heated together at a temperature of 140.
degree.
-200.
degree.
C.
The progress of reaction can be monitored by determining the total amine value, tertiary amine value and acid value



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