Abstract: Urea-derived products, for example liquid compositions containing urea-derived compounds, such as dihydroxyethyleneurea (“DHEU”), and methods for making same are provided.

Abstract: The present invention relates to the use as perfuming ingredient of a compound of formula wherein R represents a hydrogen atom or a methyl or ethyl group, and R1 represents (i) a (Me)(R2)C?C(R3) group, R2 representing a hydrogen atom or a methyl group and R3 representing a methyl or ethyl group, or (ii) a phenyl group optionally substituted by one or two methyl groups; as well as to the compositions or articles associated with these compounds.

Abstract: A solution for forming a graft substrate containing a graft initiator, a catalyst for activating the graft initiator, a polymerizable silicon softener, and at least one additional prepolymer, each of the softener and the prepolymer which includes a functional group for reaction with an activated site on the substrate for grafting thereto and water. The treated fiber exhibits excellent crockfastness, color fastness, and abrasion resistance, strength, and has a soft hand.

Abstract: A process for treating a textile fabric to impart or enhance at least one property of the fabric comprising: introducing the fabric into an aqueous formaldehyde containing solution to provide a wet pickup of an effective amount of the solution by the fabric, applying to the fabric an effective amount of a catalyst for catalyzing a reaction between formaldehyde and the fabric; thereafter exposing the wet fabric to a temperature of at least about 300° F. to react the formaldehyde with the fabric to impart or enhance the property of the fabric before there is a substantial loss of formaldehyde from the exposed fabric.

Abstract: A process for treating a textile fabric to impart or enhance at least one property of the fabric comprising: introducing the fabric into an aqueous formaldehyde containing solution to provide a wet pickup of an effective amount of the solution by the fabric, applying to the fabric an effective amount of a catalyst for catalyzing a reaction between formaldehyde and the fabric; thereafter exposing the wet fabric to a temperature of at least about 300° F. to react the formaldehyde with the fabric to impart or enhance the property of the fabric before there is a substantial loss of formaldehyde from the exposed fabric.

Abstract: A solution for forming a graft substrate containing a graft initiator, a catalyst for activating the graft initiator, a polymerizable silicon softener, and at least one additional prepolymer, each of the softener and the prepolymer which includes a functional group for reaction with an activated site on the substrate for grafting thereto and water. The treated fiber exhibits excellent crockfastness, color fastness, and abrasion resistance, strength, and has a soft hand.

Abstract: A solution for forming a graft substrate containing a graft initiator, a catalyst for activating the graft initiator, a polymerizable silicon softener, and at least one additional prepolymer, each of the softener and the prepolymer which includes a functional group for reaction with an activated site on the substrate for grafting thereto and water. The treated fiber exhibits excellent crockfastness, color fastness, and abrasion resistance, and has a soft hand.

Abstract: A solution for forming a graft substrate containing a graft initiator, a catalyst for activating the graft initiator, a polymerizable silicon softener, and at least one additional prepolymer, each of the softener and the prepolymer which includes a functional group for reaction with an activated site on the substrate for grafting thereto and water. The treated fiber exhibits excellent crockfastness, color fastness, and abrasion resistance, and has a soft hand.

Abstract: Provided are compounds and methods for modifying a material to change properties of the material, as well as a variety of products obtained using the methods. In one embodiment, a material comprising one or more modifiable functional groups is reacted with an activated hydrophobic acyl group in the presence of a hindered base, thereby to covalently attach the hydrophobic acyl group to the modifiable functional groups on the material. The material which is modified may be, for example, a carbohydrate, and the modifiable functional groups on the material may be hydroxyls. For example, materials such as cellulose may be modified by reacting it with an acid chloride or acid anhydride including a hydrophobic acyl group, in the presence of a hindered base, such as tripentylamine, to attach the hydrophobic acyl groups to the hydroxyls on the cellulose, thereby to increase the hydrophobicity of the cellulose.

Abstract: The present invention is directed to a method for treating a material to impart wrinkle reduction and temporary crease resistance thereto, and improve feel. The method involves: applying to said material a solution of a treatment composition in an amount effective to impart temporary crease and stain resistance, said fabric treatment composition comprising a hydroxy urea or hydroxy amide compound; and allowing said treatment composition to dry at ambient temperature, wherein said hydroxy urea compound comprises one urea and at least one hydroxyl group and said hydroxy amide compound comprises at least one amide group and at least one hydroxyl group. The material treatment is useful in reducing wrinkles in clothing, improving the feel of fabrics, and increasing the moisture adsorbence and retention in natural and synthetic fabrics.

Abstract: A method for imparting wrinkle free properties to cotton or cotton blend fabrics. These wrinkle free properties are achieved through the use of a combination of a DMDHEU based reactant at high levels with a catalyst at a low level.

Abstract: A method for imparting durable press and softness characteristics to garments. The initial step of the process is to start with a garment in which the pH is between about 6 and 7. The garments are immersed in a mixture of water, a non-ionic wetter, a glyoxal resin and aminofunctional silicone, and a cationic HDPE in specific amounts, depending upon the type of fabric of which the garments are made. The mixture is extracted from the garments to a specific extent. After mixture extraction, the garments are pressed and baked.

Abstract: Method for treating fibrous cellulosic materials using an aqueous cationic treating solution containing a cyclic polyhydroxy compound and choline chloride, by which dye uptake of the material, and the environmental effects of the subsequent dyeing process are improved.

Abstract: A process for resin finishing textile containing cellulosic fiber comprises the steps of using a resin finishing agent chiefly containing a cellulose-reactive N-methylol compound having two or more functional groups and a reaction catalyst, mainly reacting only one functional group of the cellulose-reactive N-methylol compound with cellulose, water washing, again imparting reaction catalyst, drying, garment making, and heat treating. The process eliminates the conventional postcuring method drawbacks of loss of color fastness and discoloration owing to dye decomposition and formaldehyde increase by unreacted resin and residual reaction catalyst during long storage before heat treatment, and simultaneously achieves high crease-resistant property, shrink resistance, good feeling, excellent pleating property, and anti-puckering property.

Abstract: The application of a treating solution containing polyhydroxy compound and choline chloride to a fibrous cellulosic material is made more uniform and reproducible by including in the treating solution a colorizing amount of a fugitive tint, by which the uniformity of the application can be observed and corrected by appropriate changes to the operating variables.

Abstract: A binder is applied to fibers to bind particles to the fibers. The fibers have hydrogen bonding functional groups. The particles have functional groups capable of forming a hydrogen bond or a coordinate covalent bond. The binder comprises binder molecules, the binder molecules having at least one functional group that is capable of forming a hydrogen bond or a coordinate covalent bond with the particles, and at least one functional group that is capable of forming a hydrogen bond with the fibers. A substantial portion of the particles that are adhered to the fibers are adhered in particulate form by hydrogen bonds or coordinate covalent bonds to the binder, and the binder is in turn adhered to the fibers by hydrogen bonds. Fibers containing particles bound by this method are easily densified.

Abstract: The fibrillation tendency of lyocell fabrics, and the degree of fibrillation of fibrillated lyocell fabrics, can be reduced by treating such fabrics with a cross-linking agent in the presence of an acid catalyst. Good results may be obtained when the ratio by weight of the catalyst to the optional cross-linking agent is at least about 0.5:1. Good results may be obtained when the amount of cross-linking agent fixed on the fabric is in the range 0.5 to 1.5 percent on weight of fabric.

Abstract: Crosslinked cellulose fibers having free pendant carboxylic acid groups are disclosed. The fibers include a polycarboxylic acid covalently coupled to the fibers, and are crosslinked with a crosslinking agent having a cure temperature lower than the cure temperature of the polycarboxylic acid. Methods for producing the fibers and for producing a fibrous sheet incorporating the fibers are also disclosed.

Abstract: An improved method of treating a fabric comprising the step of contacting a fabric with the cis isomer of a compound having the general formula; ##STR1## wherein R.sub.1, R.sub.2, R.sub.3, and R.sub.4 are the same or different and each of R.sub.1, R.sub.2, R.sub.3, and R.sub.4 represent branched or straight chain alkyl, carbocyclic or aryl.

Abstract: This invention relates to methods of applying finishes to garments. More particularly, this invention relates to improved methods for applying specialty finishing on the garments using a cellulose-type based carrier and to a carrier/finish composition for practicing the method which achieves a smooth and even coating of the finishing onto fabric without having to recover unused finishing and which can be accomplished using standard garment production equipment.

Abstract: Durable press properties are imparted to a fabric by applying to the fabric an aqueous durable press treatment composition comprising a reactive modified ethylene urea resin, such as dimethylol dihydroxy ethylene urea (DMDHEU), a crosslinking acrylic copolymer derived from butyl acrylate and acrylonitrile and having a glass transition temperature (T.sub.g) of -30.degree. C. or lower, and a catalyst. The fabric is dried to a residual moisture content of 10 to 20 percent by weight, is pressed to remove unwanted wrinkles, and is heated at a temperature of 88.degree. to 175.degree. C. for up to fifteen minutes to cure and crosslink the durable press treatment composition and impart durable press properties to the fabric. The process can be applied either to fabrics prior to fabrication into garments, or as a garment durable press process imparting durable press properties to fabricated garments.

Abstract: A method of producing easily densified high bulk fibers that have adhered particulates. The high bulk fibers have hydrogen bonding or coordinate covalent bonding functionalities, and a binder is applied to the fibers to bind the particles to the fibers. The binder has a functional group that forms a hydrogen bond or a coordinate covalent bond with the particles, and a functional group that forms a hydrogen bond with the fibers. A substantial portion of the particles that are adhered to the fibers are adhered in particulate form by hydrogen bonds or coordinate covalent bonds to the binder, and the binder is in turn adhered to the fibers by hydrogen bonds. Fibers containing particles bound by this method are easily densified.

Abstract: The fibrillation tendency of solvent-spun cellulose fibre is reduced by treating the fibre with a cross-linking agent and a flexible linear polymer with terminal functional groups, for example polyethylene glycol (PEG) of molecular weight 300 to 600. The fibre may be treated in never-dried or in fabric form.

Abstract: Use as formaldehyde collectors of the products of formula ##STR1## in which R represents an acetoacetyl or 3,5-dioxo hexanoyl group, R.sub.1 represents a hydrogen atom or a methyl radical, m is equal to 1, 2, 3 or 4 and n is either equal to 1 when R.sub.1 represents a methyl radical or equal to 1, 2 or 3 when R.sub.1 represents a hydrogen atom, and finishing process for fabrics based on cellulose fibers using an aminoplastic resin containing formaldehyde in the free or combined state, using a product of formula (I) as the formaldehyde collector.

Abstract: A composition for a formaldehyde scavenger is provided which consists of a water-soluble blend of a substituted or unsubstituted polyhydric alcohol and an active methylene compound selected from the group consisting of dialkyl malonate and alkylacetoacetate.

Abstract: Polyhydroxyalkyl melamine used in the processing of textiles with amino resins to reduce formaldehyde emissions and improve textile "hand".

Abstract: They have the formula: ##STR1## where either R.sub.1 and R.sub.2 are identical and represent --CH.sub.2 R where R=H or a C.sub.1 to C.sub.4 alkyl group or R.sub.1 and R.sub.2 together form the --CH.sub.2 (CR.sub.4 R.sub.4).sub.n --CH.sub.2 group where n=0 or 1, R.sub.4 =H or --CH.sub.3, R.sub.3 =H or --CH.sub.2 R.sub.5 where R.sub.5 =H or a C.sub.1 to C.sub.4 alkyl group. A and A.sub.1 are either identical and represent H or A and A.sub.1 together form an ethylene, trimethylene or --CH(OCH.sub.2 R.sub.6)--CH(OCH.sub.2 R.sub.6)-- radical where R.sub.6 =H or a C.sub.1 to C.sub.4 alkyl group or, when R.sub.3 =H, a 1,2 dihydroxy-ethylene group.They are obtained by reacting a disubstituted ethanal ##STR2## with a urea ANH--CO--NHA, followed if required by etherification with an alcohol R.sub.5 CH.sub.2 OH.

Abstract: A binder composition is disclosed, which comprises:(A) a copolymer emulsion which contains as its essential ingredients vinyl acetate, ethylene, and a monomer represented by the formula (1): ##STR1## wherein R.sub.1 is H or CH.sub.3 ; and R.sub.2 is H or an alkyl group having not more than 5 carbon atoms, the proportions of the respective ingredients being within the range of 55-96.5/3-40/0.5-5 on a weight basis;(B) a formaldehyde-free nitrogen-containing glyoxal resin;(C) a metal salt catalyst; and optionally(D) a higher alcohol sulfuric acid ester-based surfactant.Nonwoven fabrics and impregnated papers using the binder composition are also disclosed. The binder composition exhibits not only high resistance to water and solvents but also low residual free formaldehyde level, with an improvement in foamability being optionally attainable.

Abstract: Cellulosic materials, such as cotton fabrics, can be colored insitu by first treating the fabric with N-phenyldiethanolamine and a crosslinking agent for cellulose, such as dimethylol dihydroxyethyleneurea. After the fabric has been cured it is then colored by treating with sufficient concentrations of nitrous acid to form the colored nitroso derivative of the tertiary aromatic amine. The colors obtained are shades of green and yellow which are determined by: concentration of the N-phenyldiethanolamine; type of crosslinking agent; strength of the nitrous acid, and reaction times.

Abstract: Textile treating agent for imparting crease resistance is made by mixing 1 mol glyoxal, 2 mols formaldehyde, 1 mol urea and 1.5 mol ethylene glycol and reacting the mixture first at pH 6 to 7 at 60.degree. C. and then at pH 3 at 60.degree.. The product is found to have more stable formaldehyde release properties in textile treating baths as pH of the bath is varied in the range from about 3.0 to about 4.5.

Abstract: Cyclic urea/glyoxal/polyol condensates are excellent formaldehyde-free crosslinking resins for cellulosic textile fabrics and insolubilizers for binders in paper coating compositions.

Abstract: A fabric containing viscose fibres is subjected to cross-linking followed by mercerization and then generally further cross-linking. It is possible to obtain products having good dyeability soft handle and good wet and dry crease resistance.

Abstract: A method for the removal of free formaldehyde from textile fabrics which have been treated with formaldehyde derived resins to make the fabrics crease-resistant is disclosed. The process comprises forming a composition composed of a foaming agent, ethylene urea and an appropriate diluent and then foaming this composition to form a stable foam. The foam is then applied to the resin treated fabric in a layer, the foam is collapsed on the fabric to force it through the fabric and then the fabric is subjected to drying and curing conditions. The process is advantageous in that it utilizes relatively small volumes of liquids and thus is energy efficient and environmentally favorable.

Abstract: The level of released formaldehyde in a durable press treated fabric is significantly reduced or eliminated altogether by an oxidative aftertreatment process in which the fabric, after treatment with a formaldehyde-based durable press finishing agent and curing to impart durable press properties, is contacted with an oxidizing agent to destroy formaldehyde-releasing moieties present in the fabric. Preferably, the treatment of the durable press fabric with the oxidizing agent is carried out by impregnating the fabric with a solution containing the oxidizing agent and then providing the fabric a residence time in contact with the oxidizing agent to allow for reaction of the oxidizing agent with the formaldehyde-releasing moieties.

Abstract: The products of the reaction of dimethyloldihydroxyethylene urea (DMDHEU) or an alkylated DMDHEU with a polyol impart permanent press properties to a textile fabric and contain only a small amount of free formaldehyde.

Abstract: Zwitterions are employed as catalysts in a chemical finishing process to treat cellulosic textiles with crosslinking agents and produce easy-care properties in the finished materials. The process comprises treatment of the textile material, such as cotton fabric, by impregnating it with a solution containing a cellulose-crosslinking agent and, as catalyst a zwitterion, alone or in combination with a magnesium salt, drying and curing the fabric. Said finished fabrics are characterized by an unusual combination of useful, desirable properties--smooth-drying appearance, wrinkle resistance, serviceable strength, and inoffensive formaldehyde release.

Abstract: Alkylated glyoxal/cyclic urea condensates are excellent formaldehyde-free crosslinking resins for textile fabrics.

Abstract: Alkylated glyoxal/cyclic urea condensates are excellent formaldehyde-free crosslinking resins for textile fabrics.

Abstract: Cotton-polyester fiber-blended textile fabrics and knitted goods are resin-finished to be imparted with a high soft feeling and a durable crease resistance using a resin bath containing a specific combination of an amino resin having in the molecule at least two N-methylol groups which may be partially or wholly alkylated, a diol type surface active agent and an acid catalyst for cross-linkage.

Abstract: Blends of a glyoxal/cyclic urea condensate or a partially or wholly alkylated derivative thereof and dimethylol dihydroxyethylene urea or a partially or wholly alkylated derivative thereof improve the properties of textile fabrics treated therewith and contain only small amounts of free formaldehyde.

Abstract: New compounds in the class of .alpha.,.omega.-bis(4,5-dihydroxy-3-methyl-2-oxoimidazolidin-1-yl)alkanes have been prepared from the reaction of glyoxal and an alkylenebis(3-methylurea). These compounds are useful as formaldehyde-free finishing agents for textiles containing cellulose.

Abstract: Process for finishing textiles of natural or regenerated cellulose, which have been pretreated with liquid ammonia, wherein the finishing agent used is an N-monomethylol compound or N-monoalkoxymethyl compound of 4-hydroxy- or 4-alkoxy-5,5-dimethylpropyleneurea. The process couples a high degree of finishing effect (in respect of improvement of the shrink resistance and wrinkle resistance) with only a very slight effect on the hand and especially on the tensile strength.

Abstract: Process for the production of formaldehyde-free finishing agents for textiles containing or consisting of cellulose which is based on the reaction of urea or symmetrically disubstituted urea with glyoxal in the presence of buffer salts and alcohols at a pH of below 7, buffered mixtures of 4,5-hydroxyethyleneureas or N,N'-disubstituted 4,5-dihydroxyethyleneureas partially etherified in 4- and 5-positions being formed.

Abstract: Alkylated glyoxal/cyclic urea condensates are excellent formaldehyde-free crosslinking resins for textile fabrics.

Abstract: Alkylated glyoxal/cyclic urea condensates are excellent formaldehyde-free crosslinking resins for textile fabrics.

Abstract: Improved levels of abrasion resistance, breaking strength are coupled with high levels of resilience, as measured by durable-press appearance rating and wrinkle recovery angles, by a process in which cotton or cotton-containing fabric is treated with polyfunctional N-methylol reagents, a Bronsted acidic catalyst or Bronsted acid-generating catalyst and selected phosphate salts. The fabric is impregnated with these and supplementary agents as desired and cured by conventional methods.

Abstract: An aluminum acetate salt solution containing sodium and chloride ions is prepared by reaction of aqueous aluminum chloride and sodium acetate. It is suitable for use as a catalyst in the treatment of cellulosic-containing textiles with formaldehyde or a formaldehyde-amide adduct crosslinking agent to produce durable press properties in the finished material. There is no discoloration in the thus-treated fabric which also exhibits greater strength than is normally present in fabric treated to the same level of wrinkle resistance with an aluminum salt catalyst.

Abstract: Disclosed is a treatment process for textile substrates comprising or consisting of regenerated cellulose, which process comprises applying to the substrate an aqueous medium comprising (A) a monomeric, hydrolysis stable, hydrosoluble, resin forming cross linking agent containing at least two N-methylol or N-alkoxymethyl groups, (B) a hydrosoluble, prepolymerized, linear, filler resin forming, cross-linking agent, also containing at least two N-methylol or N-alkoxymethyl groups, (C) a reactive acetal of formula ##STR1## wherein X and Y, independently, are H or CH.sub.2 OH, (D) a first cross-linking catalyst, being an alkaline earth metal salt of a strong acid and (E) a second cross-linking catalyst, being an acidic aluminium salt, subsequently drying the substrate and subjecting same to a temperature at which cross-linking takes place, and an aqueous concentrate for use therein.

Abstract: The preparation of bacteriostatic, water-insoluble peroxide-containing complexes of zinc acetate, by reaction of zinc acetate with hydrogen peroxide in the presence of acetic acid, is disclosed. A process for in situ formation and deposition of these complexes on cellulosic and polyester textiles is described. The textile finishes so produced inhibit the growth and spreading of odor- and infection-producing gram-positive and gram-negative bacteria on the treated textiles. The antibacterial activity of the finished textiles is durable to repeated launderings.

Abstract: A method for reducing the fibrillation of polypyrrolidone fibers which comprises contacting the fibers with an aqueous solution containing dimethyloldihydroxyethyleneurea and an acidic catalyst.