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Low phthalates such as Bis(2-ethylhexyl) phthalate (DEHP) and Dibutyl phthalate (DBP) have increased health risks and are generally being phased out. High-molecular-weight phthalates such as diisononyl phthalate (DINP) and diisodecyl phthalate (DIDP) are generally considered safer. [22]
Vinyl chloride is an organochloride with the formula H 2 C=CHCl. It is also called vinyl chloride monomer (VCM) or chloroethene. It is an important industrial chemical chiefly used to produce the polymer polyvinyl chloride (PVC). Vinyl chloride is a colourless flammable gas that has a sweet odor and is carcinogenic.
The 1 through 7 numbers stand for, respectively, polyethylene terephthalate, high-density polyethylene, polyvinyl chloride (PVC), low-density polyethylene, polypropylene, polystyrene or Styrofoam ...
Polyvinyl chloride or uPVC (unplasticized polyvinyl chloride) pipes are not well suited for hot water lines and have been restricted from inside water supply line use in the US for homes since 2006. Code IRC P2904.5 uPVC Not listed. uPVC has high chemical resistance across its operating temperature range, with a broad band of operating ...
Depending on the method, a varying amount of chlorine is introduced into the polymer allowing for a measured way to fine-tune the final properties. The chlorine content may vary from manufacturer to manufacturer; the base can be as low as PVC 56.7% to as high as 74% by mass, although most commercial resins have chlorine content from 63% to 69%.
Polyvinyl chloride (PVC or V) Low-density polyethylene (LDPE or PE-LD), Polypropylene (PP) Polystyrene (PS) Polyurethanes (PUR) and PP&A fibers [18] are often also included as major commodity classes, although they usually lack RICs, as they are chemically quite diverse groups.
The gas is used to make the polyvinyl chloride hard plastic resin in plastic products. It is found in products such as credit cards, furniture and car parts, but is most notably used in PVC ...
Vinyl polymers are subject of several structural variations, which greatly expands the range of polymers and their applications. With the exception of polyethylene, vinyl polymers can arise from head-to-tail linking of monomers, head-to-head combined with tail-to-tail, or a mixture of those two patterns. Additionally the substituted carbon center in such polymers is stereogenic (a "chiral center")