Polypropylene modification

Keywordsinanocomposites nanosilica surface modification polypropylene properties. 

Most manufacturing methods now available are similar to this but with the following modifications in the first step, the polymers for fibers are mainly made of polyester, nylon, or thein blends. AcryUcs and polypropylene are also sometimes employed. A regular fiber as thick as 0.01—0.4 tex (0.1—4 den) may sometimes be used instead of the special fiber to imitate the hard leather. 

Modification ofP/astics. Many plastics, such as PVC, ABS, polypropylene, and nylon, ate blended with nitnle mbber to improve flexibiHty, toughness, or appearance. An oil-resistant thermoplastic elastomer has been prepared by blending nitnle mbber and polypropylene (24). 

Stmctural and chemical modification of urethane containing polymer matri-ces with macrocycles - calixarenes having reactive hydrazide groups have been carried out and stmcture, physico chemical and sensor properties of polyure-thanesemicarbazides (PUS) synthesised have been studied. The polymers obtained (on the base of polypropylene glycol MM 1000 and polysiloxane diol MM 860, hexamethylene diisocyanate and calixarene dihydrazide) are identified by IR-spectroscopy, size exclusion chromatography (SEC), DSC, WAXS and SAXS methods. 

Many modifications in metallocene structures have been incorporated, as shown in Fig. 9, to synthesize isotactic polypropylene with a range of properties including molecular weight, isotacticity, mechanical properties, etc. 

Grafting reactions onto a polymer backbone with a polymeric initiator have recently been reported by Hazer [56-60]. Active polystyrene [56], active polymethyl methacrylate [57], or macroazoinitiator [58,59] was mixed with a biopolyester polyhydroxynonanaate [60] (PHN) or polybutadiene to be carried out by thermal grafting reactions. The grafting reactions of PHN with polymer radicals may proceed by H-abstraction from the tertier carbon atom in the same manner as free radical modification reactions of polypropylene or polyhy-droxybutyratevalerate [61,62]. 

Electric discharge methods are known [31] to be very effective for nonactive polymer substrates such as polystyrene, polyethylene, polypropylene, etc. They are successfully used for cellulose-fiber modification to decrease the melt viscosity of cellulose-polyethylene composites [32] and to improve the mechanical properties of cellulose-polypropylene composites [28]. 

The surface energy of fibers is closely related to the hydrophilicity of the fiber [38]. Some investigations are concerned with methods to decrease hydrophilicity. The modification, of wood cellulose fibers with stearic acid [43] hydrophobizes those fibers and improves their dispersion in polypropylene. As can be observed in jute-reinforced unsaturated polyester resin composites, treatment with polyvinylacetate increases the mechanical properties [24] and moisture repellency. 

PESA can be blended with various thermoplastics to alter or enhance their basic characteristics. Depending on the nature of thermoplastic, whether it is compatible with the polyamide block or with the soft ether or ester segments, the product is hard, nontacky or sticky, soft, and flexible. A small amount of PESA can be blended to engineering thermoplastics, e.g., polyethylene terepthalate (PET), polybutylene terepthalate (PBT), polypropylene oxide (PPO), polyphenylene sulfide (PPS), or poly-ether amide (PEI) for impact modification of the thermoplastic, whereas small amount of thermoplastic, e.g., nylon or PBT, can increase the hardness and flex modulus of PESA or PEE A [247]. 

Shanmugharaj, A.M., Kim, J.K., and Ryu, S.H., UV surface modification of waste tire powder Characterization and its influence on the properties of polypropylene/waste powder composites. Polymer Test., 24, 739, 2005. 

Reactive extrusion is the chemical modification of polymer while it is being transported in an extruder. In this work, polypropylene is intentionally degraded by the addition of a free radical initiator (a peroxide) during extrusion. The product has improved flow properties because of the removal of the high molecular weight tail and the narrowing of the molecular weight distribution. 

The assumption is made at present that elemental combustion analysis for carbon, hydrogen, and fluorine provides a good approximation to the extent of incorporation of fluoroalkyl residues, i.e. alcohols and ethers. We have ruled out trifluoromethylcarbonyl groups since no evidence is seen for their presence in either the infrared spectra or the 19F-NMR spectra. Thus, our values for percent modification reflect the best fit of the combustion data to an idealized stoichiometry for the product in Equation 1, where (m+n+o) = 100, and the percent modification (% mod.) is given by the expression [100 x (m+o)/(m+n+o)], equivalent to the number of fluoroalkyl residues per one hundred methylenes. An appropriately normalized formula was used to fit the data for polypropylene (sample 10). 

A good example of a reactive modifier which has been used (14) to enhance properties of polyolefins is maleic anhydride (MA). The formation of maleic adduct in polypropylene (PP), for example, can be used to effect several modifications e.g. to improving hydrophilicity, adhesion and dyeabflity. Moreover, the polymer-maleic adduct has an availabla additional functionality to effect other chemical modifications for achieving the desired material design objectives. Reactions of MA with polymers in solution are described in the patent literature (15). 

The case of isotactic polypropylene is somewhat different issues related to the crystallization of the chiral /1-form [42,43] of this polymer have been discussed by various authors and probably the model presented by Lotz is the most articulated and detailed [14]. It is known that iPP, unlike sPP, adopts in all its crystalline modifications its stable conformation, namely the 3i helix with a 6.50 A periodicity [36], which may be right-handed or... 

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