Abstract: A process for treating a subterranean earth formation by includes the step of introducing a buffered acidizing treatment fluid comprising a monovalent salt of monochloroacetic acid and at least one acid into the subterranean earth formation, wherein the pH of the buffered acidizing treatment fluid is from about 1.2 to about 5. The buffered acidizing treatment fluid itself includes the monovalent salt of monochloroacetic acid, the at least one acid and optionally an element to suppress salt precipitation.

Abstract: The present disclosure pertains to a process for manufacturing ethyleneamine compounds selected from the group of ethyleneamines and hydroxyethylethyleneamines wherein the process comprises two reaction sequences.

Abstract: Process for manufacturing ethyleneamine compounds selected from the group of ethyleneamines and hydroxyethylethyleneamines wherein the process comprises two reaction sequences.

Abstract: The disclosure is directed to a process for treating a subterranean earth formation by introducing a monovalent salt of monochloroacetic acid into said subterranean earth formation in the presence of a chelating agent which comprises at least one carboxylate group having a monovalent counterion and furthermore comprises a carbon chain carrying at least five hydroxyl groups. Preferably the cation of the monovalent salt of monochloroacetic acid is sodium.

Abstract: Method for isolating carboxylic acid from an aqueous alkali metal carboxylate-containing side stream, e.g., the aqueous side stream of an organic peroxide production process, with co-production of alkali metal salt, involving adding an acid, or an anhydride, ketene or acid salt, to the aqueous side stream, thereby forming carboxylic acid and alkali metal salt within the aqueous side stream, and separation of the carboxylic acid from the aqueous side stream.

Abstract: The present invention relates to thermally expandable microspheres at least partially prepared from bio-based monomers and to a process of their manufacture. The microspheres comprise a thermoplastic polymer shell encapsulating a blowing agent, wherein the thermoplastic polymer shell comprises a polymer being a homo- or copolymer of a lactone according to formula (1): wherein each of R1, R2, R3, R4, separately from one another, is selected from the group consisting of H and an alkyl group preferably with 1-4 carbon atoms. The invention further provides expanded microspheres, which can be used in a variety of applications.

Abstract: A method of making a pyranine monomer composition comprises the step of reacting pyranine with a functionalizing agent that functionalizes the pyranine molecule with a polymerizable functional group to provide a composition of functionalized pyranine monomers, said functionalization reaction taking place in an aqueous reaction medium, and in the presence of a molar excess of said functionalizing agent, such that the functionalization reaction product is a monomer composition substantially free of unfunctionalized pyranine compound. The pyranine monomer compositions made by the method can be used to make fluorescent tagged water soluble polymer compositions that advantageously are substantially free of unpolymerized pyranine. The fluorescent tagged water soluble polymer compositions can be used in a method of inhibiting scale in industrial water systems.

Abstract: Disclosed are fluorescent water-soluble water treatment polymers suitable for use in scale inhibition or suppression of corrosion in industrial water systems, the water treatment polymers especially comprising fluorescent coumarin, fluorescein, rhodamine, and Nile blue derivative monomers. Also disclosed are methods of making the monomers, methods of making the polymers, methods of inhibiting scale in an industrial water system, methods of suppressing corrosion in an industrial water system, and methods of using the polymers in coagulation and flocculation, and in cleaning applications.

Abstract: An aliphatic epoxy-terminated polysulfide polymer has the formula R?—CHOH—CH2-S—R—(Sy-R)t-S—CH2-CHOH—R? and is formed by a process, where each R is independently chosen from branched alkanediyl or branched arenediyl groups and groups with the structure —(CH2)a-O—(CH2)b-O—(CH2)c- and about 0 to about 20% of the number of R-groups are branched alkanediyl or branched arenediyl groups and about 80 to about 100% of the number of R-groups have the structure —(CH2)a-O—(CH2)b-O—(CH2)c-, where t is from about 1 to about 60, y is an average value of from about 1.0 to about 2.5, b is an integer value of from about 1 to about 8, and a and c are independently integers from about 1 to about 10, and where each R? is independently a particular radical where, m, n, o, p, q and r independently have a value of from about 1 to about 10.

Abstract: The present disclosure relates to a process to prepare a crystalline co granule of MGDA-Nax, x being 2,5-3, containing a step of drying a crumbly phase composition containing on total weight of the composition (i) 70-87 wt % of organic compounds and salts thereof containing 85 to 100 wt % on total organic compounds and salts thereof of MGDA-Nax, wherein at least 60 wt % of the MGDA-Nax is crystalline, and (ii) 13-30 wt % of water in the presence of a second composition containing at least one second component selected from the group of scale inhibitors, crystal inhibitors, film or spot preventing polymers, glass-corrosion inhibiting agents, pH modifiers, chelating agents, builders, bleaching agents, and surfactants. It also relates to the co granules obtainable by the process.

Abstract: Alkali-swellable rheology modifier comprising a core-shell polymer comprising a core polymer and a shell comprising at least one shell copolymer layer at least partially cross-linked and containing a mole percent of crosslinking agent greater than the mole percent of crosslinking agent in the core polymer, provided if the mole percent of crosslinking agent in the core polymer is zero, then either the core polymer is greater than 60 wt % of the core-shell polymer; the core polymer comprises at least one associative monomer; at least one shell copolymer layer copolymer comprises at least one associative monomer; and/or the at least one shell copolymer layer that is at least partially cross-linked comprises greater than 3 mole % crosslinking agent.

Abstract: A methyl ethyl hydroxyalkyl cellulose (MEHEC), process for making the MEHEC, and a powder containing the MEHEC are disclosed. The MEHEC is provided with a DSmethyl from 1.5 to 2.5, a DSethyl from 0.005 to 0.15, and a MSalkylene-oxide from 0.005 to 0.2. The methyl ethyl hydroxyalkyl cellulose optionally includes an anti-oxidant. The MEHEC optionally does not have a combination of a DSmethyl of 2.2 or 1.8, a DSethyl of 0.05 or 0.1, and a MSalkylene-oxide of 0.1 and does not have a combination of a DSmethyl of 2.5 or 2.0, a DSethyl of 0.1, and a MSalkylene-oxide of 0.05. The MEHEC has very good biostability and is suitable for use in the building industry.

Abstract: A method includes combining monosodium glutamate and/or glutamic acid with formaldehyde to form a first combination; adding hydrogen cyanide to form a second combination comprising a monosodium salt of glutamic acid diacetonitrile, a cyclic GLMN, and a sodium salt of glutamic acid N-monoacetonitrile, maintaining a temperature of the second combination at less than about 16° C. and a pH of less than about 7; converting nitrile groups to carboxylate groups thereby forming a third combination comprising water and at least about 47 weight percent of the tetrasodium salt of GLDA, wherein a reaction yield is at least about 91%; providing a fourth combination comprising water and the tetrasodium salt of GLDA and having a pH of less than about 7; and combining the third and fourth combinations to form the chelating composition.

Abstract: A method of forming a chelating composition includes the steps of: providing a first mixture comprising water and a tetrasodium salt of glutamic acid N,N-diacetic acid and having a pH of greater than about 10; and acidifying the first mixture via ion exchange and/or bipolar membrane electrodialysis to reduce a pH of the chelating composition to a pH of at least about 9; wherein the chelating composition comprises the tetrasodium salt of glutamic acid N,N-diacetic acid in an amount of at least about 50 weight percent based on a total weight of the chelating composition as determined using an Fe-Total Sequestering Value; and wherein the chelating composition has a viscosity of less than about 1350 mPa·s measured at about 5° C., or less than about 350 mPa·s measured at about 20° C., each using a Brookfield DV II plus viscometer with spindle S18 and a temperature controlled bath.

Abstract: This disclosure provides a chelating composition having a pH of at least about 9 and comprising: water; and the tetrasodium salt of glutamic acid N,N-diacetic acid present in an amount of at least about 50 weight percent based on a total weight of the chelating composition as determined using an Fe-Total Sequestering Value, wherein the chelating composition has a viscosity of less than about 1350 mPa·s measured at about 5° C., or less than about 350 mPa·s measured at about 20° C., each using a Brookfield DV II plus viscometer with spindle S18 and a temperature controlled bath.

Abstract: The present invention relates to methods for processing plant and/or micro-organism derived cellulose materials into rheology/structuring agents. More in particular, the present invention relates to methods wherein plant and/or micro-organism derived cellulose material is co-processed with carboxycellulose. The methods of the present invention provide a variety of benefits, in terms of process efficiency and scalability as well as in relation to the properties of the materials that are obtainable using these methods. For instance, it has been found that (highly) concentrated products produced using the method of the invention are easily (re)dispersible in water and aqueous systems to regain much of the cellulose component's original rheological performance.

Abstract: The present disclosure provides a porous silica having an average pore diameter of at least 210 ? and a pore volume of at least 0.80 cm3g?1. The present disclosure also provides a method of producing the porous silica including gelling a liquid phase-dispersed nanoparticulate silica in the presence of either (i) a Brønsted acid and an amine group having two or more primary or secondary amine groups or (ii) an amino acid.

Abstract: The present disclosure relates to the production of bis-thiol compounds, preferably DMDH/DMDH oligomer mixtures, and their use in the production of liquid polysulfide polymers

Abstract: Methods and compositions for improving the compatibility of aqueous herbicide solutions containing at least one of a water soluble salt of an aryloxyalkanoic acid, a water soluble salt of a pyridyloxyalkanoic acid, and a water soluble salt of glyphosate, and optionally ?16% of one or more fertilizers, such as ammonium sulfate, by adding certain polymeric crystallization inhibitors are provided.

Abstract: The present invention relates to methods for processing plant and/or micro-organism derived cellulose materials into rheology/structuring agents. More in particular, the present invention relates to methods wherein plant and/or micro-organism derived cellulose material is co-processed with carboxycellulose. The methods of the present invention provide a variety of benefits, in terms of process efficiency and scalability as well as in relation to the properties of the materials that are obtainable using these methods. For instance, it has been found that (highly) concentrated products produced using the method of the invention are easily (re)dispersible in water and aqueous systems to regain much of the cellulose component's original rheological performance.