A fiber-reinforced plastic (FRP) rebar for reinforcing concrete, as well as systems for and methods of making the FRP rebar, are disclosed.

Provided are a superabsorbent polymer having a high bulk density value and showing a reduction in unpleasant odors which may be caused by various additives included in a preparation process while basically maintaining excellent absorption performance and absorption rate, and a preparation method thereof.

A composite article has an increased peel strength and includes a first layer including a low surface energy polymer. The composite article also includes a poly(meth)acrylate layer, an epoxide layer, and a polyurethane elastomer layer. The poly(meth)acrylate layer is disposed on and in direct contact with the first layer. Moreover, the poly(meth)acrylate layer includes a poly(meth)acrylate that includes the reaction product of at least one (meth)acrylate that is polymerized in the presence of an organoborane initiator. The epoxide layer is disposed on and in direct contact with the poly(meth)acrylate layer. The polyurethane elastomer layer is disposed on and in direct contact with the epoxide layer. The composite article has a 90 peel strength of at least 50 pli measured using ASTM D6862.

Powder formulation comprising 20-75 wt % of di(4-tert-butylcyclohexyl) peroxydicarbonate and 25-80 wt % of a phlegmatizer selected from the group consisting of ethylene glycol dibenzoate, phenyl benzoate, trimethylol propane tribenzoate, dimethylsulfon, ethylene glycol ditoluate, 1,3-propanediol ditoluate, ethylene glycol 4-tert-butylbenzoate, ethylene glycol monobenzoate monotoluate, 2,3-butanediol dibenzoate, 4-methylphenyl benzoate acid ester, and combinations thereof.

Recovery times of flexible polyurethane foams are increased by treatment with a pressure sensitive adhesive. An emulsion or dispersion of the adhesive in an aqueous carrier liquid is impregnated into the foam, with subsequent removal of the carrier. This invention is of special interest when the glass transition temperature of the starting foam is 16 C. or lower.

The present invention relates to a composition comprising an aqueous dispersion of first polymer particles functionalized with structural units of t-butyl methacrylate or t-butyl acrylate, and imbibed with a catalyst of Structure (I), where R, R.sup.1, R.sup.2 and R.sup.3 are as defined herein, and a process for making the composition. The present invention also relates to an aqueous dispersion of core-shell polymer particles, wherein the first polymer particles are encapsulated in a shell having a high T.sub.g. The imbibed first polymer particles and the core-shell polymer particles can be expanded in the dry state at significantly lower temperatures than reported in the prior art.

##STR00001##

The invention relates to flame-retardant foam coatings for textile sheet products, wherein the coatings include plate-like expandable graphite which has a reduced salt content and a particle distribution with a proportion of >80 percent by weight having a diameter of at least 0.2 mm, and/or a minimum proportion of 70% having a mesh size of >50 mesh (0.3 mm), at least one binder and at least one foam stabilizer, and also processes for the production thereof, the use thereof for producing textile sheet products and also textile sheet products having such flame-retardant foam coatings.

A composite article has increased pull-off strength and includes a first layer including a low surface energy polymer, a poly(meth)acrylate layer, and an epoxide layer. The poly(meth)acrylate layer is disposed on and in direct contact with the first layer. Moreover, the poly(meth)acrylate layer includes a poly(meth)acrylate that includes the reaction product of at least one (meth)acrylate that is polymerized in the presence of an organoborane initiator. The epoxide layer is disposed on and in direct contact with the poly(meth)acrylate layer. The epoxide layer includes an epoxide. The composite article has a pull-off strength of greater than zero pli measured using ASTM D4541.

A glass fiber reinforced polymer reinforcing structure comprised of glass fibers mixed with one or more polymers. Incorporated in the polymer are a hybrid mix of pristine multi-walled carbon nanotubes at 0.0-4.0 wt. % of the polymer and multi-walled carbon nanotubes functionalized with carboxylic group at 0.0-2.0 wt. % of the polymer. The above mixture is pultruded to produce GFRP reinforcing bars, dowels or structural profiles.

A composite article is formed by disposing a poly(meth)acrylate layer, formed as the reaction product of at least one acrylate that is polymerized in the presence of an organoborane initiator, on and in direct contact with a low surface energy polymer layer, disposing an epoxide layer on and in direct contact with said poly(meth)acrylate layer, and disposing a hydrolytically resistant layer on and in direct contact with said epoxide layer. The hydrolytically resistant layer is a hydrolytically resistant polyurethane elastomer that is the reaction product of an aliphatic isocyanate component and an isocyanate-reactive component that retains at least 90% of its initial tensile strength after submersion in standardized seawater for 24 weeks. The isocyanate-reactive component is a hydroxyl-functional polymer having an average hydroxy functionality ranging from 2 to 3, wherein the hydroxyl-functional polymer is a dimer diol, a trimer triol, or a combination thereof.