Provided are new metal complexes having phenolic and macrocyclic amino ligands as well as to their use, in particular use for bleaching catalyst for detergent compositions and oxidative crosslinking catalyst for resins, containing said metal complexes. A formulation comprises at least a detergent, a metal complex, and optionally a source of hydrogen peroxide.

The present disclosure relates to a catalyst system to produce crystallizable polyester compositions which comprise residues of terephthalic acid, neopentyl glycol (NRG), 1,4-cyclohexanedimethanol (CHDM), ethylene glycol (EG), and diethylene glycol (DEG), in certain compositional ranges having certain advantages and improved properties including recyclability.

A composite polyester hot-melt adhesive, a preparation method thereof and a preparation method of an anti-scouring geotextile are provided. The preparation method of the composite polyester hot-melt adhesive includes the following steps: performing an esterification reaction on a dibasic acid and a dihydric alcohol under a protection of nitrogen and an action of a titanium/cobalt composite catalyst, adding a stabilizer for a polycondensation reaction to obtain a polyester hot-melt adhesive, then adding polymethyl methacrylate (PMMA) microspheres for mixing and stirring to obtain the composite polyester hot-melt adhesive. The anti-scouring geotextile is obtained by bonding a polyethylene terephthalate woven fabric with a polypropylene geotextile by the composite polyester hot-melt adhesive. The composite polyester hot-melt adhesive has the advantages of high bonding strength and good anti-impact performance, and the prepared anti-scouring geotextile has the advantages of high anti-scouring strength, good soil conservation performance, strong protection capability and long service life.

A method for producing an oligomeric PET substrate for use in a rPET manufacturing process comprises reacting recycled bis-hydroxylethyleneterephthalate (rBHET) or a higher molecular weight oligomer derived from rBHET, with PTA to produce an oligomeric PET substrate represented by Formula (I), wherein R.sub.1 is a carboxyl end group or a hydroxyl end group, R.sub.2 is a carboxyl end group or a hydroxyl end group, and n is a degree of polymerisation.

The invention pertains generally to paints containing a binder curable by an autoxidation mechanism and at least one drier comprising a sulfonate compound of vanadium of formula (VII)

##STR00001##

where R.sup.1 and R.sup.2 are independently selected from a group involving hydrogen, C.sub.1-C.sub.12 alkyl, C.sub.1-C.sub.12 halogenated alkyl, C.sub.6-C.sub.10 aryl, benzyl; and whereas aryl and benzyl can be optionally substituted by up to three substituents independently selected from a group involving C.sub.1-C.sub.20 alkyl, and hydroxy(C.sub.1-C.sub.2)alkyl.

Provided is a tape including a composition having a copolyester including polymeric units derived from ethylene glycol and terephthalic acid or a diester thereof and >0.50 and <5.00 wt % of polymeric units with regard to the total weight of the polyester derived from an oligomeric dihydroxy compound having a number average molecular weight of >500 g/mol and <5000 g/mol. Such tape has an improved tensile-impact strength and a reduced proneness to splitting during weaving.

A plateable polymer composition is provided. The polymer composition comprises a noble metal catalyst distributed within a polymer matrix containing at least one high naphthenic thermotropic liquid crystalline polymer that includes repeating units derived from naphthenic hydroxycarboxylic and/or dicarboxylic acids in an amount of about 10 mol. % or more, wherein the polymer composition exhibits a dissipation factor of about 0.01 or less as determined at a frequency of 2 GHz.

A method for preparing a biogenic guanidine complex, the method including: mixing dimethyl sulfoxide (DMSO) with water in a volume ratio thereof of 1:1 to yield a solvent DMSO-H.sub.2O; adding organic guanidine (G) and a compound MX.sub.2 in a molar ratio G/MX.sub.2=1:1 or 2:1 to the solvent DMSO-H.sub.2O, where the organic guanidine (G) is selected from arginine (Arg), guanidinoacetic acid (Gaa), creatine (Cra), creatinine (Cran), guanine (Gua), and agmatine (Agm); M represents Fe.sup.2+, Mg.sup.2+, or Zn.sup.2+; and X represents Cl.sup.−, CH.sub.3COO.sup.−, or CH.sub.3CH(OH)COO.sup.−; stirring the solvent DMSO-H.sub.2O containing the organic guanidine and the compound MX.sub.2; recycling the solvent DMSO-H.sub.2O through vacuum distillation and obtaining a solid; transferring the solid to a Buchner funnel, and washing the solid with deionized water and ethanol consecutively; and removing the deionized water and ethanol through vacuum filtration, and drying the solid.

Provided is a process for producing a product having polyglycolic acid and glycolide from methyl glycolate. The process comprises esterification, polycondensation and optimization. Also provided are a product produced by the process and a method of changing the amount of the polyglycolic acid in the product by modifying the amount of an esterification catalyst and/or adjusting the reaction temperature.

In one or more embodiments, the present invention provides a low molecular weight, non-toxic, resorbable poly(ethylene glycol) (PEG)-block-poly(propylene fumarate) (PPF) diblock copolymers and poly(propylene fumarate) (PPF)-block-poly(ethylene glycol) (PEG)-block-poly(propylene fumarate) (PPF) triblock copolymers (and related methods for their making and use) that permits hydration for the formation of such things as hydrogels and has constrained and predictable material properties suitable for 3D printing and drug delivery applications. Using continuous digital light processing (cDLP) hydrogels the diblock and triblock copolymers can be photochemically printed from an aqueous solution into structures having a 10-fold increase in elongation at break compared to traditional diethyl fumarate (DEF) based printing. Furthermore, PPF-PEG-PPF triblock hydrogels have also been found in vitro to be biocompatible across a number of engineered MC3T3, NIH3T3, and primary Schwann cells.