Klaus-Dieter Hungenberg

Last updated
Klaus-Dieter Hungenberg
Born (1953-09-14) 14 September 1953 (age 70)
Alma mater University of Essen
Known for Living anionic polymerization, Living free-radical polymerization, Mathematical model
Scientific career
Fields Chemistry
Institutions Boehringer Mannheim, BASF

Klaus-Dieter Hungenberg (born 14 September 1953) is a German chemist and professor at the University of Paderborn. [1] Hungenberg has contributed to the field of reaction kinetics for polymerization processes, and has been honored with Professorship for his contributions in the field of reaction chemistry at the Institute for Polymer Material and Process (PMP), University of Paderborn.

Contents

Education

Hungenberg studied Chemistry at the University of Duisburg-Essen and then received his Diploma in Anionic polymerization in 1979. Later, he received his PhD in 1982 in the group of Friedhelm Bandermann at the University of Duisburg-Essen with research projects focusing on anionic living free radical polymerization. [2] [3]

Biography

From 1983 to 1987 Hungenberg worked in process development for blood diagnostic devices with Boehringer Mannheim GmbH, now Roche Diagnostics.

In 1987, he joined BASF’s Polymer research group. Since then, he has led diverse product and process development projects ranging from new PVC modifiers, [4] [5] [6] polyolefin processes, [7] [8] catalysis, [9] [10] super absorbent polymers, emulsion polymers [11] [12] ABS, polyamides, [13] etc. His main research emphasis is polymer reaction engineering modeling, simulation and optimization of polymer processes. [14] [15] He is an (co-)author of about 100 scientific articles, [16] [17] editorials [18] [19] and patents. [20] He is also an (co-)author of a book chapter in process modelling and optimization of styrene polymerization with focus on polystyrene and its co-polymers. [17]

K. D. Hungenberg has been at different leadership positions in BASF SE for many years. In 2004, he was named Research Director of Polymer Reaction Engineering at BASF SE. In 2010, he was appointed as Vice President Polymer Reaction Engineering in recognition for his achievements. In 2012 Hungenberg received an Honorary Professorship at the institute of Polymer, Materials and Processes (PMP), University of Paderborn. There he regularly gives lectures about Polymer Reaction Engineering and the Modeling of Polymer Processes. He is highly networked in the area of Polymer Reaction Engineering and is known globally for his contributions in this field.

Furthermore, he is an Editorial Board member of several international journals and acted as chairman and member for Scientific Committees of various conferences. He is engaged in the IUPAC Working Party "Modeling of Kinetics and Processes of Polymerization", [21] the Working Party “Polymer Reaction Engineering” of EFCE [22] and acts as Deputy Chairman of the DECHEMA Technical Committee "Polyreaktionen". [23] In addition, he is lecturer in Dechema and responsible for the training course "Polymerisationstechnik".

Related Research Articles

<span class="mw-page-title-main">Polystyrene</span> Polymer resin widely used in packaging

Polystyrene (PS) is a synthetic polymer made from monomers of the aromatic hydrocarbon styrene. Polystyrene can be solid or foamed. General-purpose polystyrene is clear, hard, and brittle. It is an inexpensive resin per unit weight. It is a poor barrier to air and water vapor and has a relatively low melting point. Polystyrene is one of the most widely used plastics, with the scale of its production being several million tonnes per year. Polystyrene is naturally transparent, but can be colored with colorants. Uses include protective packaging, containers, lids, bottles, trays, tumblers, disposable cutlery, in the making of models, and as an alternative material for phonograph records.

<span class="mw-page-title-main">Thermoplastic</span> Plastic that softens with heat and hardens on cooling

A thermoplastic, or thermosoftening plastic, is any plastic polymer material that becomes pliable or moldable at a certain elevated temperature and solidifies upon cooling.

In polymer chemistry, living polymerization is a form of chain growth polymerization where the ability of a growing polymer chain to terminate has been removed. This can be accomplished in a variety of ways. Chain termination and chain transfer reactions are absent and the rate of chain initiation is also much larger than the rate of chain propagation. The result is that the polymer chains grow at a more constant rate than seen in traditional chain polymerization and their lengths remain very similar. Living polymerization is a popular method for synthesizing block copolymers since the polymer can be synthesized in stages, each stage containing a different monomer. Additional advantages are predetermined molar mass and control over end-groups.

In polymer chemistry, an addition polymer is a polymer that forms by simple linking of monomers without the co-generation of other products. Addition polymerization differs from condensation polymerization, which does co-generate a product, usually water. Addition polymers can be formed by chain polymerization, when the polymer is formed by the sequential addition of monomer units to an active site in a chain reaction, or by polyaddition, when the polymer is formed by addition reactions between species of all degrees of polymerization. Addition polymers are formed by the addition of some simple monomer units repeatedly. Generally polymers are unsaturated compounds like alkenes, alkalines etc. The addition polymerization mainly takes place in free radical mechanism. The free radical mechanism of addition polymerization completed by three steps i.e. Initiation of free radical, Chain propagation, Termination of chain.

<span class="mw-page-title-main">Polymer degradation</span> Alteration in the polymer properties under the influence of environmental factors

Polymer degradation is the reduction in the physical properties of a polymer, such as strength, caused by changes in its chemical composition. Polymers and particularly plastics are subject to degradation at all stages of their product life cycle, including during their initial processing, use, disposal into the environment and recycling. The rate of this degradation varies significantly; biodegradation can take decades, whereas some industrial processes can completely decompose a polymer in hours.

<span class="mw-page-title-main">Copolymer</span> Polymer derived from more than one species of monomer

In polymer chemistry, a copolymer is a polymer derived from more than one species of monomer. The polymerization of monomers into copolymers is called copolymerization. Copolymers obtained from the copolymerization of two monomer species are sometimes called bipolymers. Those obtained from three and four monomers are called terpolymers and quaterpolymers, respectively. Copolymers can be characterized by a variety of techniques such as NMR spectroscopy and size-exclusion chromatography to determine the molecular size, weight, properties, and composition of the material.


In polymer chemistry, anionic addition polymerization is a form of chain-growth polymerization or addition polymerization that involves the polymerization of monomers initiated with anions. The type of reaction has many manifestations, but traditionally vinyl monomers are used. Often anionic polymerization involves living polymerizations, which allows control of structure and composition.

<span class="mw-page-title-main">Polystyrene sulfonate</span> Drug class

Polystyrene sulfonates are a group of medications used to treat high blood potassium. Effects generally take hours to days. They are also used to remove potassium, calcium, and sodium from solutions in technical applications.

In polymer chemistry, vinyl polymers are a group of polymers derived from substituted vinyl monomers. Their backbone is an extended alkane chain [−CH2−CHR−]. In popular usage, "vinyl" refers only to polyvinyl chloride (PVC).

Thermoplastic elastomers (TPE), sometimes referred to as thermoplastic rubbers (TPR), are a class of copolymers or a physical mix of polymers that consist of materials with both thermoplastic and elastomeric properties.

Solution polymerization is a method of industrial polymerization. In this procedure, a monomer is dissolved in a non-reactive solvent that contains a catalyst or initiator.

Rubber toughening is a process in which rubber nanoparticles are interspersed within a polymer matrix to increase the mechanical robustness, or toughness, of the material. By "toughening" a polymer it is meant that the ability of the polymeric substance to absorb energy and plastically deform without fracture is increased. Considering the significant advantages in mechanical properties that rubber toughening offers, most major thermoplastics are available in rubber-toughened versions; for many engineering applications, material toughness is a deciding factor in final material selection.

<span class="mw-page-title-main">W. Harmon Ray</span> American academic

Willis Harmon Ray is an American chemical engineer, control theorist, applied mathematician, and a Vilas Research emeritus professor at the University of Wisconsin–Madison notable for being the 2000 winner of the prestigious Richard E. Bellman Control Heritage Award and the 2019 winner of the Neal Amundson Award.

<span class="mw-page-title-main">Photo-oxidation of polymers</span>

In polymer chemistry photo-oxidation is the degradation of a polymer surface due to the combined action of light and oxygen. It is the most significant factor in the weathering of plastics. Photo-oxidation causes the polymer chains to break, resulting in the material becoming increasingly brittle. This leads to mechanical failure and, at an advanced stage, the formation of microplastics. In textiles the process is called phototendering.

Macromolecular Reaction Engineering is a peer-reviewed scientific journal published monthly by Wiley-VCH. The journal covers academic and industrial research in the field of polymer reaction engineering, which includes polymer science. It emerged from a section that was part of Macromolecular Materials and Engineering. The journal publishes reviews, feature articles, communications, and full papers in the entire field of polymer reaction engineering, including polymer reaction modeling, reactor optimization, and control. Its 2020 impact factor is 1.931.

<span class="mw-page-title-main">Living free-radical polymerization</span>

Living free radical polymerization is a type of living polymerization where the active polymer chain end is a free radical. Several methods exist. IUPAC recommends to use the term "reversible-deactivation radical polymerization" instead of "living free radical polymerization", though the two terms are not synonymous.

<span class="mw-page-title-main">Graft polymer</span> Polymer with a backbone of one composite and random branches of another composite

In polymer chemistry, graft polymers are segmented copolymers with a linear backbone of one composite and randomly distributed branches of another composite. The picture labeled "graft polymer" shows how grafted chains of species B are covalently bonded to polymer species A. Although the side chains are structurally distinct from the main chain, the individual grafted chains may be homopolymers or copolymers. Graft polymers have been synthesized for many decades and are especially used as impact resistant materials, thermoplastic elastomers, compatibilizers, or emulsifiers for the preparation of stable blends or alloys. One of the better-known examples of a graft polymer is a component used in high impact polystyrene, consisting of a polystyrene backbone with polybutadiene grafted chains.

<span class="mw-page-title-main">Acrylonitrile styrene acrylate</span> Chemical compound

Acrylonitrile styrene acrylate (ASA), also called acrylic styrene acrylonitrile, is an amorphous thermoplastic developed as an alternative to acrylonitrile butadiene styrene (ABS), that has improved weather resistance. It is an acrylate rubber-modified styrene acrylonitrile copolymer. It is used for general prototyping in 3D printing, where its UV resistance and mechanical properties make it an excellent material for use in fused filament fabrication printers, particularly for outdoor applications. ASA is also widely used in the automotive industry.

<span class="mw-page-title-main">Automated synthesis</span> Type of chemical synthesis

Automated synthesis or automatic synthesis is a set of techniques that use robotic equipment to perform chemical synthesis in an automated way. Automating processes allows for higher efficiency and product quality although automation technology can be cost-prohibitive and there are concerns regarding overdependence and job displacement. Chemical processes were automated throughout the 19th and 20th centuries, with major developments happening in the previous thirty years, as technology advanced. Tasks that are performed may include: synthesis in variety of different conditions, sample preparation, purification, and extractions. Applications of automated synthesis are found on research and industrial scales in a wide variety of fields including polymers, personal care, and radiosynthesis.

Brigitte Voit is a German chemist and professor of chemistry. She holds the chair Organic Chemistry of Polymers at the Faculty of Chemistry of the TU Dresden and is head of the Institute of Macromolecular Chemistry at the Leibniz Institute of Polymer Research in Dresden. From September 1, 2002, to July 31, 2022, she was also member of the Board of Management/CSO of the IPF Dresden.

References

  1. "Professorship at Paderborn" . Retrieved 17 September 2013.
  2. "PhD thesis" (PDF).
  3. "Group of Prof. Bandermann".
  4. "Patent on two stage emulsion polymerization".
  5. "Patent on PVC".
  6. "Patent on PVC process".
  7. "Patent on Polyolefin".
  8. "Polyolefin process".
  9. Hungenberg, K. D. (1994). Progress in Gas Phase Polymerization of Propylene with Supported TiCl4 and Metallocene Catalysts. Vol. 89. pp. 373–380. doi:10.1016/s0167-2991(08)63051-7. ISBN   9780444986566.{{cite book}}: |journal= ignored (help)
  10. Hungenberg, K. D. (1992). "Supported catalysts in stirred bed gas-phase reactors - from wax to ultrahigh-molecular-weight polypropylene". Polymeric Materials Science and Engineering. 55. 67 (6).
  11. Hungenberg, K. D. (1998). K.-H. Reichert (ed.). Papers of the 6th International Workshop on Polymer Reaction Engineering : Berlin, 5-7 October 1998. Weinheim [u.a.]: Wiley VCH. pp. 295–311. ISBN   978-3527102280.
  12. Hungenberg, K. D. "Production of methyl methacrylate polymer - by bulk polymerisation in a loop system with tube reactors and mixers, etc., at specified temperature and flow rate etc. with initiator".
  13. Hungenberg, K. D. (2001). "Preparation and characterization of polyamide-6 with three-branched chains". Journal of Applied Polymer Science. 82 (13): 3184–3193. doi:10.1002/app.2177.
  14. Gao, J.; Hungenberg, K. D.; Penlidis, A. (2004). "Process modeling and optimization of styrene polymerization". Macromolecular Symposia. 206: 509–522. doi:10.1002/masy.200450239.
  15. Schmidt, Christian-Ulrich; Hungenberg, Klaus-Dieter (August 1999). "Optimierung der Produktqualität von Polymeren im Semibatch-Betrieb". Chemie Ingenieur Technik. 71 (8): 832–835. doi:10.1002/cite.330710810.
  16. "List of publications".
  17. 1 2 Hungenberg, K. D.; Gao, J. (2003). "5". Modern styrenic polymers : polystyrenes and styrenic copolymers ([Online-Ausg.]. ed.). Chichester: John Wiley. ISBN   9780470867211.
  18. Hungenberg, K. D. "Editorial" (PDF). Archived from the original (PDF) on 2013-09-21. Retrieved 17 September 2013.
  19. Hungenberg, Klaus-Dieter (13 July 2009). "New Production and Enabling Technologies in Polymer Reaction Engineering". Macromolecular Reaction Engineering. 3 (5–6): 220. doi:10.1002/mren.200900027.
  20. Hungenberg, K. D. "Patents".
  21. Hungenberg, K. D. "IUPAC". Archived from the original on 17 September 2013. Retrieved 17 September 2013.
  22. Hungenberg, K. D. "Working group EFCE" . Retrieved 17 September 2013.
  23. Hungenberg, K. D. "Chairman in Dechema" . Retrieved 17 September 2013.