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News<br />

daily updated News at<br />

www.bioplasticsmagazine.com<br />

A new era of<br />

renewable carbon<br />

materials<br />

Conagen (Bedford, MA USA), and Sumitomo<br />

Chemical (Tokyo, Japan) have announced to jointly<br />

develop p-hydroxystyrene (HS) and its polymer, poly<br />

p-hydroxystyrene (PHS), using a combination of<br />

biosynthesis, chemosynthesis, and polymerization.<br />

The monomer and the polymer are made of<br />

100 % renewable carbon, marking a new era of<br />

sustainable production.<br />

Developing PHS using a combination of biosynthesis,<br />

chemosynthesis, and polymerization represents a<br />

significant breakthrough in the field of sustainable material<br />

production. Efforts to reduce reliance on petroleum and<br />

transition towards renewable and sustainable alternatives<br />

have gained momentum in recent years.<br />

With renewable biomass as the starting material, this<br />

joint development between Conagen and Sumitomo<br />

Chemical creates an environmentally friendly and<br />

cost-effective product.<br />

This partnership represents a significant milestone in the<br />

development of sustainable materials, and this approach<br />

to PHS production is expected to reduce the carbon<br />

footprint associated with traditional chemical synthesis<br />

methods. It is a crucial step towards more sustainable<br />

manufacturing processes with a positive impact.<br />

The Conagen-Sumitomo partnership leverages<br />

Conagen’s expertise in microbial strain design and<br />

development with Sumitomo Chemical’s proficiency<br />

in chemical production and commercialization.<br />

The collaboration aims to create a platform that enables<br />

the production of sustainable chemicals to replace<br />

petrochemicals in an extended range of many applications.<br />

PHS is used to produce polymers, resins, and other<br />

chemicals. The monomer HS can also be used as an<br />

input for the synthesis of other chemicals, such as<br />

pharmaceuticals and fragrances. The applications of HS<br />

and PHS are limitless and can span uses from electronics<br />

to personal care and other consumer products.<br />

The monomer HS, with the chemical formula C 8<br />

H 8<br />

O, is<br />

a derivative of styrene in which a hydroxyl group (-OH) is<br />

attached to the aromatic ring’s para position (carbon atom<br />

4). The HS and PHS are examples of green chemistry for<br />

minimizing waste, reducing hazardous chemicals, and<br />

using catalysts that can be easily separated and reused.<br />

This joint development project promises to potentially<br />

pave the way for developing novel renewable and<br />

sustainable materials. “Similar technology can be used to<br />

produce other key chemical ingredients by fermentation<br />

at industrial scale, such as cinnamic acid, monohydroxybenzoic<br />

acid, and dihydroxy-benzoic acid”, said J.<br />

McNamara, V.P. of chemical applications at Conagen. AT<br />

www.conagen.com | www.sumitomo-chem.co.jp<br />

From CO 2<br />

to<br />

polyolefins<br />

Braskem (São Paulo, Brazil) and the University of São<br />

Paulo (USP) have announced a partnership to develop lines<br />

of research for converting CO 2<br />

into chemical products such<br />

as olefins and alcohols, thus mitigating its emissions into<br />

the environment and using it as a raw material for the<br />

production of polyolefins.<br />

The partnership with USP, through the Research Center<br />

for Greenhouse Gas Innovation (RCGI), which also includes<br />

the participation of the Federal University of São Carlos<br />

(UFSCar), focuses on studying innovative routes for CO 2<br />

conversion through both catalytic and electrocatalytic<br />

processes. While in conventional processes in the chemical<br />

industry, catalysts (materials that trigger chemical<br />

reactions) are thermally activated, electrocatalysis uses<br />

electricity to activate them. As such, renewable energy can<br />

be used partially or fully for CO 2<br />

conversion. AT<br />

www.braskem.com | www5.usp.br<br />

Chemical recycling<br />

from old plastic to new<br />

adhesives<br />

A recently launched research project by the Fraunhofer<br />

Institute for Manufacturing Technology and Advanced<br />

Materials IFAM in Bremen (Germany) and the German<br />

Plastics Center SKZ in Würzburg aims to add thermally<br />

damaged plastics to the recycling economy through<br />

chemical recycling. The material of choice is PET, which<br />

is already well-established in mechanical recycling.<br />

Thanks to the well-known bottles and the deposit system<br />

in Germany, the material is mostly sorted by type and most<br />

of it is already efficiently recycled. The RezyBond project is<br />

dedicated to PET fractions that have been recycled several<br />

times and are too old, or that do not end up in this (bottle)<br />

cycle at all, such as other PET packaging.<br />

The process is unique in that the chemical recycling is<br />

performed on a standard twin-screw extruder. "Our goal<br />

is to develop a continuous, reactive recycling process for<br />

PET recyclates into polyester polyols. These can then be<br />

used as chemical feedstock", explains Hatice Malatyali,<br />

Group Manager Extrusion and Compounding at SKZ.<br />

The polyols obtained can be used as raw materials for<br />

a wide range of technological applications, such as<br />

adhesives and coatings. In the project, they will be used<br />

as starting materials for adhesive formulations and thus<br />

transferred directly to an application. A demonstration<br />

plant is also planned at the SKZ to make the process<br />

accessible to interested medium-sized companies. AT<br />

www.skz.de | www.ifam.fraunhofer.de<br />

6 bioplastics MAGAZINE | Renewable Carbon Plastics [<strong>05</strong>/23] Vol. 18

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