Paint & Coatings Industry - March 2008 - (Page 55)

Acknowledgments Mr. Rick Mann, Kibbechem, Inc., Elkhart, Indiana; Dr. Karen Winkowski, International Specialty Products, Wayne, N.J. References 1 2 3 4 5 6 Lukens, R. J.; Horsfall, J.G. Chemical Constitution and Fungitoxicity of Imides and Their Imide-SCCl3 Compounds. Phytopathology 1967, 57: 876–880. Torgeson, D. C. Fungicides: An Advanced Treatise. Vol. II:, 1969, 419–433. Siegel, M. R.; Sisler. H.D. Antifungal Compounds: Interactions in Biological and Ecological Systems. Vol. 2, 1977, pp.105-107. Siegel, M. R.; Sisler. H.D. Fate of the Phthalimide and Trichloromethylthio (SCCl3) Moieties of Folpet in Toxic Action on Cells of Saccharomyces pastorianus. Phytopathology 1968, 58: 1123–1133. Siegel, M. R. Reactions of the Fungicide Folpet (N-(Trichloromethylthio) phthalimide) with a Thiol Protein. Pesticide Biochemistry and Physiology. 1971,1: 225 -233. Siegel, M. R. Reactions of Certain Trichloromethyl Sulfenyl Fungicides with Low Molecular Weight Thiols: In vitro Studies with Glutathione. J. Agr. Food Chem. 1970,18 (5): 819-822. 7 Siegel, M. R. Reaction of Certain Trichloromethyl Sulfenyl Fungicides with Low Molecular Weight Thiols: In vivo Studies with Cells of Saccharomyces pastorianus. J. Agr. Food Chem. 1970, 18 (5): 823–826. 8 EPA Reregistration Eligibility Decision (RED) FOLPET. 1999. United States Environmental Protection Agency. Preventing Pesticides and Toxic Substances (7508W). EPA738-R-99011 November 1999. pg. 4. 9 Lukens, R. J.; Sisler,H.D.. Chemical Reactions Involved in the Fungitoxicity of Captan. Phytopathology 1958. 48: 179-234. 10 Teisseire H.; Vernet, G. Effects of the Fungicide Folpet on the Activities of Antioxidative Enzymes in Duckweed (Lemna minor). Pesticide Biochemistry and Physiology 2001. 69(2): 112–117. 11 Slawecki, R. A.; Ryan, E.P.; Young, D.H. Novel Fungitoxity Assays for Inhibition of Germination-Associated Adhesion of Botrytis cinerea and Puccinia recondite Spores. Applied and Environmental Microbiology 2002. 68(2): 597–601. 12 Gottardi, W. Iodine and Iodine compounds. In: Block, S. S. 5th ed. Disinfection, Sterilization, and Preservation. 2001, Lippincott Williams & Wilkins. Philadelphia, PA. New dog, new tricks. Dow Coating Solutions is one excited puppy. Why? Our unique combination of youthful exuberance and technological expertise allows you to expect more from us than other suppliers. And, thanks to our dogged determination, you can believe it when we say we’ll deliver, helping you produce coatings that perform better and offer outstanding value to your customer. And we’ll throw in increased formulating flexibility for you. Take UCAR™ Latex DA 633 for example. This new, all-acrylic product offers significantly improved scrub resistance for architectural coatings versus competitive acrylic products. And it delivers that performance in low-VOC formulations and at higher PVC ratios. The result is that you have more flexibility in formulating high performance products for specific markets. We hope you’ll agree that we’re barking up the right tree. Contact us if you’d like to learn more. www.dow.com/ucarlatex ®™Trademark of The Dow Chemical Company (“Dow”) or an affiliated company of Dow PA I N T & C O A T I N G S # I N D U S T R Y Element 550-1KT97 55 http://www.dow.com/ucarlatex

Table of Contents Feed for the Digital Edition of Paint & Coatings Industry - March 2008

Viewpoint Industry News Calendar of Events Company News Mergers and Acquisitions Names in the News Marketplace Quarterly Stock Watch Reaching Strict VOC Requirements With Outstanding Durability for Industrial Maintenance and Marine Coatings A Unique Fungicide for Wood-Filled Plastic deSigns of the Times: Slacking Off! From Rocks to Nanos Shear-Free Dispersion Process Fluorinated Oxetane Oligomers as Versatile Intermediates for Polymer Modification The Effects of TPO Composition on Adhesion and Proposed Chemical Mechanism Supplier Showcase Color Management Materials Watch Products Classifieds Advertiser Index

Paint & Coatings Industry - March 2008

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