Abstract: The invention relates to the preparation of closed cell phenolic resin foams produced from compositions of phenol-aldehyde resole resins, and the foam products thus prepared. More particularly the present invention relates to the preparation of phenolic resin foams by a method employing a novel modified phenolic foam catalyst. The invention also relates to these modified phenolic foam catalysts which include an aromatic sulphonic acid and resorcinol.

Abstract: The invention relates to the preparation of closed cell phenolic resin foams produced from compositions of phenol-aldehyde resole resins, and the foam products thus prepared. More particularly the present invention relates to the preparation of phenolic resin foams by a method employing a novel modified phenolic foam catalyst. The invention also relates to these modified phenolic foam catalysts which include an aromatic sulphonic acid and resorcinol.

Abstract: This invention relates to the manufacture of closed cell phenolic foams from low viscosity phenol-formaldehyde resole resin. This method of manufacture provides a foam which exhibits many of the advantageous characteristics of phenolic foams manufactured from high viscosity resole resin, including good thermal retention. There is provided a method of making a phenolic foam comprising the steps of mixing(a) a phenol-formaldehyde resole resin having a water content of approximately 7.5% and a viscosity of approximately 2,800 cps at 40.degree. C.;(b) a high molecular weight gel forming ethylene oxide-propylene oxide block copolymer surfactant, such as Pluronic F-127 (trade mark);(c) a catalyst;(d) a blowing agent;and curing the resulting foam.

Abstract: This invention relates to the manufacture of foam from phenolic resins and to the foam so produced. In order to overcome some of the limitations of the prior art closed cell phenolic foams, we have developed a method of preparing closed cell foams from modified, low cost phenol formaldehyde resoles, which exhibit high closed cell contents, low friability and low thermal conductivity. This specification provides a foam competitive with urethane foams, which have an aged thermal conductivity of about 0.16K. or less, but which will not generate fumes as toxic as those of urethane. There is, provided a method of making a phenolic foam material comprising the steps of(1) preparing a base catalyzed phenol-formaldehyde resole having a mole ratio of phenol to formaldehyde of between 1:3 and 1:4.

Abstract: This invention relates to the manufacture of foam from phenolic resins and to the foam so produced. In order to overcome some the the limitations of the prior art closed cell phenolic foams, we have developed a method of preparing closed cell foams from modified, low cost phenol formaldehyde resoles, which exhibit high closed cell contents, low friability and low thermal conductivity. This specification provides a foam competitive with urethane foams, which have an aged thermal conductivity of about 0.16K. or less, but which will not generate fumes as toxic as those of urethane. There is, provided a method of making a phenolic foam material comprising the steps of(1) preparing a base catalyzed phenol-formaldehyde resole having a mole ratio of phenol to formaldehyde of between 1:3 and 1:4.

Abstract: Phenolic foams and a method of producing phenolic foam material from phenol-formaldehyde resins having a phenol to formaldehyde mole ratio of between about 1:3 and 1:4.5 are described. These materials are useful for insulation and other uses, particularly in the building trades. They are dimensionally and thermally stable, fire resistant and low in cost.

Abstract: A phenol-formaldehyde resol to which urea has been added is mixed with a boric acid-hydroxyl-amide component to provide high temperature resistant binder compositions for use in the manufacture of thermally stable bonded mineral fibre insulation structures.

Abstract: A water-dilutable thermo-setting resol is prepared from phenol, formaldehyde, an amide and a sugar type compound. The invention provides advance in the art by allowing replacement of some of the phenol-formaldehyde resin contained in the resol with sugar type compounds.

Abstract: A scraper bar for use with conveyor belting and the like to clean such belting of material adhering to its surface. The scraper bar consists of a layer of hard abrasion-resistant pellets embedded in an elastomer to form an elastomer/pellet matrix. An additional layer of elastomer is cast to the matrixed layer to provide a surface for attaching the scraper to its support when in service. Embedded in the layer of unmatrixed elastomer is an insert of particle board, chipboard, plywood or fibreglass reinforced plastic sheeting. The insert prevents bowing of the scraper bar due to differential shrinkage between the layer of matrixed elastomer and pellets and the supporting layer of elastomer.

Abstract: Plant growth regulant effects, such as dwarfing, cessation of terminal growth, increased flower set, increased fruit and pod set, fruiting body abortion, twisting and epinastic responses, etc., may be accomplished on crops such as soybeans, cotton, etc., by application of certain 2-(1,3,4-oxadiazol-2-yl) or 2-(2-oxazolyl) or 2-(1,3,4-thiadiazol-2-yl)benzoic acids, salts and esters, having the formula ##STR1## where X is nitrogen or C-R" (R" being hydrogen or methyl), Z is oxygen or sulfur when X is nitrogen, Z is oxygen when X is C-R", R is phenyl or various substituents, and R' is hydrogen or various substituents. An example is 2-(5-phenyl-1,3,4-oxadiazol-2-yl) benzoic acid. The compounds where X is nitrogen and Z is sulfur are new compounds, e.g., 2-(5-phenyl-1,3,4-thiadiazol-2-yl)benzoic acid.

Abstract: Plant growth regulant effects, such as dwarfing, cessation of terminal growth, increased flower set, increased fruit and pod set, fruiting body abortion, twisting and epinastic responses, etc., may be accomplished on crops such as soybeans, cotton, etc., by application of certain 2-(1,3,4-oxadiazol-2-yl) or 2-(2-oxazolyl) or 2-(1,3,4-thiadiazol-2-yl)benzoic acids, salts and esters, having the formula ##STR1## where X is nitrogen or C--R" (R" being hydrogen or methyl), Z is oxygen or sulfur when X is nitrogen, Z is oxygen and when X is C--R", R is phenyl or various substituents, and R' is hydrogen or various substituents. An example is 2-(5-phenyl-1,3,4-oxadiazol-2-yl)benzoic acid. The compounds where X is nitrogen and Z is sulfur are new compounds, e.g., 2-(5-phenyl-1,3,4-thiadiazol-2-yl)benzoic acid.

Abstract: New 2-(1,3,4-oxadiazole-2-yl) benzoic acids and salts and esters thereof, as well as certain 2-(2-oxazolyl) benzoic acids, salts and esters, having the formula: ##SPC1##Where X is nitrogen or C-R" (R" being hydrogen or methyl), R is phenyl or various substituents, and R' and the Y's are hydrogen or various substituents, are effective preemergence or postemergence herbicides, on various crops. The chemicals act selectively and are useful against purple nutsedge and in cranberry. Oxadiazoles of the invention may be made by reacting a benzhydrazide with phthalic anhydride to form a hydrazide which is cyclized by removal of the elements of water, using as a catalyst fuming sulfuric acid or dimethylformamide-sulfur trioxide complex.

Abstract: Plant growth regulant effects, such as dwarfing, cessation of terminal growth, increased flower set, increased fruit and pod set, fruiting body abortion, twisting and epinastic responses, etc., may be accomplished on crops such as soybeans, cotton, etc., by application of certain 2-(1,3,4-oxadiazol-2-yl) or 2-(2-oxazolyl) or 2-(1,3,4-thiadiazol-2-yl)benzoic acids, salts and esters, having the formula ##SPC1##Where X is nitrogen or C--R" (R" being hydrogen or methyl), Z is oxygen or sulfur when X is nitrogen, Z is oxygen when X is C--R", R is phenyl or various substituents, and R' is hydrogen or various substituents. An example is 2-(5-phenyl-1,3,4-oxadiazol-2-yl)benzoic acid. The compounds where X is nitrogen and Z is sulfur are new compounds, e.g., 2-(5-phenyl-1,3,4-thiadiazol-2-yl)benzoic acid.