Tacking

Rosenbaum N H, Owrutsky J C, Tack L M and Saykaiiy R J 1986 Veiocity moduiation iaser spectroscopy of negative ions the infrared spectrum of hydroxide (OH ) J. Chem. Phys. 84 5308-13... 

L. Rhenus, Rhine) Discovery of rhenium is generally attributed to Noddack, Tacke, and Berg, who announced in 1925 they had detected the element in platinum ore and columbite. They also found the element in gadolinite and molybdenite. By working up 660 kg of molybdenite in 1928 they were able to extract 1 g of rhenium. 

Statistical mechanics computations are often tacked onto the end of ah initio vibrational frequency calculations for gas-phase properties at low pressure. For condensed-phase properties, often molecular dynamics or Monte Carlo calculations are necessary in order to obtain statistical data. The following are the principles that make this possible. 

According to the usual procedure for preparing bromobenzene bromine is added to ben zene in the presence of metallic iron (customarily a few carpet tacks) and the reaction mixture is heated... 

Bromine although it adds rapidly to alkenes is too weak an electrophile to react at an appreciable rate with benzene A catalyst that increases the electrophilic properties of bromine must be present Somehow carpet tacks can do this How7... 

I remember snow, Soft as feathers, Sharp as thumb tacks,.. . ... 

Mechanical and Thermal Properties. The first member of the acrylate series, poly(methyl acrylate), has fltde or no tack at room temperature it is a tough, mbbery, and moderately hard polymer. Poly(ethyl acrylate) is more mbberflke, considerably softer, and more extensible. Poly(butyl acrylate) is softer stiU, and much tackier. This information is quantitatively summarized in Table 2 (41). In the alkyl acrylate series, the softness increases through n-octy acrylate. As the chain length is increased beyond n-octy side-chain crystallization occurs and the materials become brittle (42) poly( -hexadecyl acrylate) is hard and waxlike at room temperature but is soft and tacky above its softening point. 

Adhesives. Acryhc emulsion and solution polymers form the basis of a variety of adhesive types. The principal use is in pressure-sensitive adhesives, where a film of a very low T (<—20 " C) acrylic polymer or copolymer is used on the adherent side of tapes, decals, and labels. Acrylics provide a good balance of tack and bond strength with exceptional color stabiUty and resistance to aging (201,202). AcryUcs also find use in numerous types of constmction adhesive formulations and as film-to-film laminating adhesives (qv). 

Cyanoacrylate adhesives (Super-Glues) are materials which rapidly polymerize at room temperature. The standard monomer for a cyanoacrylate adhesive is ethyl 2-cyanoacrylate [7085-85-0], which readily undergoes anionic polymerization. Very rapid cure of these materials has made them widely used in the electronics industry for speaker magnet mounting, as weU as for wire tacking and other apphcations requiring rapid assembly. Anionic polymerization of a cyanoacrylate adhesive is normally initiated by water. Therefore, atmospheric humidity or the surface moisture content must be at a certain level for polymerization to take place. These adhesives are not cross-linked as are the surface-activated acryhcs. Rather, the cyanoacrylate material is a thermoplastic, and thus, the adhesives typically have poor temperature resistance. 

Tack. Tack causes layers to adhere when they are pressed together. This property can be reduced by employing fillers with a finer psd or by dusting the stock with a laminar filler such as mica. In a related value, fillers such as mica can inhibit adhesion to the mold during processing. 

Vinyl acetate (VA)/crotonates copolymer became available in the late 1950s. It was the first polymer used in fixatives to contain carboxyHc acid groups which, depending on neutralization percent, could produce variations in film properties eg, stiffness, humidity resistance, resiUency, tack, and removabihty by shampoo. It has largely been replaced in hair sprays by newer polymers. 

G-5—G-9 Aromatic Modified Aliphatic Petroleum Resins. Compatibihty with base polymers is an essential aspect of hydrocarbon resins in whatever appHcation they are used. As an example, piperylene—2-methyl-2-butene based resins are substantially inadequate in enhancing the tack of 1,3-butadiene—styrene based random and block copolymers in pressure sensitive adhesive appHcations. The copolymerization of a-methylstyrene with piperylenes effectively enhances the tack properties of styrene—butadiene copolymers and styrene—isoprene copolymers in adhesive appHcations (40,41). Introduction of aromaticity into hydrocarbon resins serves to increase the solubiHty parameter of resins, resulting in improved compatibiHty with base polymers. However, the nature of the aromatic monomer also serves as a handle for molecular weight and softening point control. 

Heteroatom functionalized terpene resins are also utilized in hot melt adhesive and ink appHcations. Diels-Alder reaction of terpenic dienes or trienes with acrylates, methacrylates, or other a, P-unsaturated esters of polyhydric alcohols has been shown to yield resins with superior pressure sensitive adhesive properties relative to petroleum and unmodified polyterpene resins (107). Limonene—phenol resins, produced by the BF etherate-catalyzed condensation of 1.4—2.0 moles of limonene with 1.0 mole of phenol have been shown to impart improved tack, elongation, and tensile strength to ethylene—vinyl acetate and ethylene—methyl acrylate-based hot melt adhesive systems (108). Terpene polyol ethers have been shown to be particularly effective tackifiers in pressure sensitive adhesive appHcations (109). 

Styrenic block copolymers (SBCs) are also widely used in HMA and PSA appHcations. Most hot melt appHed pressure sensitive adhesives are based on triblock copolymers consisting of SIS or SBS combinations (S = styrene, I = isoprene B = butadiene). Pressure sensitive adhesives typically employ low styrene, high molecular weight SIS polymers while hot melt adhesives usually use higher styrene, lower molecular weight SBCs. Resins compatible with the mid-block of an SBC improves tack properties those compatible with the end blocks control melt viscosity and temperature performance. 

Quality Control and Testing. Control of inks is done by examining their color strength, hue, tack, rheology, drying rate, stabiHty, and product resistance. Elaborate control equipment and laboratory testing procedures are employed to test the finished inks. Weather-Ometers,... 

Hot tack strength is the abiUty of a heat-seal layer to hold together while molten, before the seal cools and sets up. This is a technically important property which is difficult to measure reproducibly in the laboratory. Owing to the reinforcing effect of ionic bonding on melt strength, ionomer sealing layers provide superior performance in a wide spectmm of appHcations. 

Whereas the eadiest fluorescent-dye pigments would last only 20 days outdoors in a screen-ink film, fade resistance has been improved to such an extent that some modem daylight-fluorescent coated panels stiU have useful color after nine months or mote in Florida sunlight in a 45° exposure tack facing south. The fluorescent layer is usually coated with an acrylic film containing a uv absorber. Indoor-accelerated exposure equipment is, of course, invaluable in the development of such systems. Better dyes and resins very likely will make possible fat mote stable coatings in the future. 

The adhesives (qv) used to form tube seams and bag bottoms include unborated dextrin, borated dextrin, casein, latex—casein, latex, poly(vinyl acetate), vinyl acetate copolymers, and hot-melt materials (10,27). Dextrin and casein adhesives are more commonly used in the production of grocery sacks vinyl acetate-type adhesives are commonly used in ah paper multiwah bags. The hot-melt adhesives are typicahy used to tack the phes of the multiwah bag together and to form the seam and bottom joints when polymer film phes or coated paper phes are used in bag constmction. 

Substituted nonheat-reactive resins do not form a film and are not reactive by themselves, but are exceUent modifier resins for oleoresinous varnishes and alkyds. Thein high glass-transition temperature and molecular weight provide initial hardness and reduce tack oxygen-initiated cross-linking reactions take place with the unsaturated oils. 

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