Chemical and Biomedical Engineering

Upper-Division Honors/Scholars Research Creative Activities

Protein-Based Theranostic Nanoparticles

Dr. Nolan B. Holland: (216) 687-2572
Theranostics is an emerging field combining therapeutic delivery with diagnostic imaging for treating a wide range of ailments such as cancer and cardiovascular disease. The general approach is to combine a nanoparticle drug delivery system with a medical imaging contrast agent in order to both deliver a drug and to detect its distribution in the patient.  Our laboratory is developing a general protein-based theranostic platform using protein engineering.  Nanoparticles have already been designed to incorporate a magnetic resonance imaging (MRI) contrast agent and a targeting motif for prostate cancer cells.  The nanoparticles have a cross-linked elastin-like polypeptide (ELP) core that is intended to encapsulate drugs for safe transport to diseased tissue where it will be released.  To design the appropriate composition for our nanoparticles, we need to understand how drugs interact with the elastin-like polypeptides (ELPs) that make up the core.  Specifically, we need to understand which drugs can be held in the particles and how fast they are released.  Compatibility can be determined from measurements with pure ELP, while the release rate will also be dependent on the geometry of the particles, so will need to be done with the particles.


Reaction Engineering Routes to Waste Gasification for Sustainable Living Environments

Dr. Jorge E. Gatica: (216) 523-7274

Concern over “green,” or environmentally friendly, technologies has risen considerably over the past decade. Thus, over the past 50 years, metropolitan areas have realized a need for waste disposal alternatives as landfills approach capacity and take up valuable land space. This sparked the widespread construction and planning of waste incinerators in Europe and the United States. Although newer technology has made incinerators more efficient, there is an increasing interest in formulating more ‘green’ gasification options as alternatives to incinerators.
Gasification converts organic and carbonaceous materials into a combination of gaseous products known as “syngas,” or synthetic gas (also often referred to as “supply gas”). This process does not involve full combustion; which, in turn, greatly reduces the amount of hazardous emissions. The syngas produced by gasifiers has a very wide range of uses, including their conversion into diesel, ethanol, methane, methanol and other synthetic fuels. Gasification technologies can convert biomass waste into synthetic gas, which make them an attractive alternative for reducing the carbon footprint of energy generation as well as an efficient route for waste management and in-situ resource utilization.
This project consists on an experimental assessment of low-temperature Wet Thermal Oxidation (WTO) promoted by Ru-based and Pt-based catalysts as a gasification technology to process polymeric waste into supply gas.


Assessment of Metabolism-Induced Liver Toxicity On a 384-Pillar Plate

Dr. Moo-Yeal Lee (216) 687-9399

There is a critical need for improved in vitro human toxicology testing to rapidly advance therapeutic drug candidates to preclinical evaluation or to prioritize potential environmental toxicants. The ability to predict organ-specific toxicity of compounds in vivo is of particular importance because several key organs including liver, heart, brain, intestine, and kidney are directly exposed to myriad chemicals. Among many tissue types, we focus on creating miniaturized human liver tissues via layered cell printing on a 384-pillar plate combined with drug metabolizing enzymes (DMEs) and compounds in a 384-well plate,which will provide highly predictive safety, efficacy, and pharmacokinetic information that is needed to rapidly advance therapeutic candidates into clinical trials. The human liver contains a variety of oxidative and conjugative enzymes involved in metabolism of a myriad of chemicals, including drugs. Primary hepatocytes among several liver cell types contain various DMEs including cytochromes P450 (CYP450s), UDP-glucuronosyltransferases (UGTs), sulfotransferases (SULT), glutathione S-transferases (GSTs), etc. These DMEs are involved in the initial clearance of drugs from the body, and generate drug metabolites, some of which are unstable and toxic, leading to undesirable biological consequences. Inter-individual variability in levels of DMEs and even mutations in DME genes result in tremendous diversity in drug metabolism, which eventually leads to differences in the response of patients to a given drug and adverse drug reaction problems. Thus, understanding the roles of these enzymes in drug metabolism and related toxicity in liver tissues is essential in human toxicology testing. However, incorporating physiological levels of chemical metabolism into high-throughput screening (HTS) of drug candidates is still challenging as addressed in “The Transform Tox Testing Challenge: Innovating for Metabolism” sponsored by US EPA and NIH. Thus, there is an urgent need to retrofit existing cell-based HTS assays to have metabolism competence and provide highly predictive toxicity information for drug discovery. The overarching goal of our research is to address critical limitations of current cell-based assays in metabolism-induced toxicity via 3D-printed hepatic cell cultures coupled with DMEs on the 384-pillar plate and provide highly predictive information on toxicity.


3D Bioprinting for Tumor Tissue Engineering

Dr. Moo-Yeal Lee (216) 687-9399

The recent advances in “three-dimensional (3D) bioprinting” offers new opportunities for creating highly organized multicellular tumor tissue constructs in vitro by dispensing cancer and its surrounding cells in hydrogels layer-by-layer precisely with printing robots, thereby potentially revolutionizing oncology and drug discovery. Tissue or organ structures can be generated by printing the cell and extracellular matrix (ECM) components of a tissue or organ found in vivo (biomimicry), or dispensing embryonic stem cells to replicate the desired biological micro-tissue architecture and functions by reproducing ECM components and appropriate cell signaling (autonomous self-assembly). These 3D printed tumor tissues with cells obtained from patients can be used as promising disease models for screening therapeutic drugs or drug combinations for individuals.

The primary goal of this research is to create miniaturized tissue constructs expressing key characteristics of in vivo human liver tumors on the micropillar/microwell chip via 3D bioprinting technology and investigate mechanistic actions of therapeutic drug combinations against liver tumor tissue constructs. We will create miniaturized liver tumor tissue blocks on a micropillar/microwell chip platform using our cellular microarray technology, which allows us to rapidly test hundreds of different cell culture conditions in combinations on a single chip, thus ideally suited to optimize and manipulate the tumor tissue microenvironment for tumor tissue engineering.


Effect of Solidification Through Cross-Section Change on Dendritic Array in Single Crystal Castings
Dr. Surendra N. Tewari: (216) 523-7342
Misaligned spurious grains in the air-foil section of turbine blades are detrimental to its high temperature mechanical properties, and thus to the efficiency snd performance of an aircratft gas turbine engine. This research is aimed at understanding nucleation of such grains at cross-section decrease, simulating the cross-section changes involved  during directional solidification of single crystal turbine blades.


Directed assembly of complex colloidal particles with an electric field

Dr. Chris Wirth:, (216) 687-9225

Colloidal crystals that have features in the size range of the wavelength of visible light (390 nm – 700 nm) interact with electromagnetic waves in technologically important ways. These materials can be used to manipulate and control the propagation of light, which would open the door to a wide range of advancements in optics and optical computing systems. In general, there are two ways in which colloidal crystals can be fabricated – either a “top-down” or a “bottom-up” method. Directed assembly qualifies as a bottom-up approach because individual particles are used to fabricate a larger crystal. We are investigating how to use an electric field to assist in the directed assembly of complex colloidal particles in an effort to understand the mechanisms of assembly and design new types of colloidal crystals. 

Microstructural evolution of particle stabilized foams

Dr. Chris Wirth:, (216) 687-9225

Foams are important to a large number of consumer products and industrial processes. One potentially game changing improvement to the efficacy of foams is the use of solid colloidal particles as stabilizers, rather than molecular surfactants. Planar and curved interfaces laden with particles are often more stable than interfaces containing molecular surfactants. Superior stability arises from a combination of the large energy necessary to remove particles from an interface and also the viscoelastic properties imparted by the particles. We are investigating how to tune interfacial structure of foams with colloidal particles to enhance performance and encourage greater efficacy of foams in a variety of consumer and industrial applications.


High Content 3D Cell Culture Assays for Mechanistic Toxicology
Dr. Moo-Yeal Lee (216) 687-9399

Differences in individual responses to drugs, chemicals, and environmental toxicants are attributed to genetic variations that limit the expression or activity of certain drug metabolizing enzymes. Thus, determining which enzymes will activate or detoxify a particular compound is essential to understanding variances in the toxicity of biologically active compounds among different population groups. In an effort to address these issues and improve predictability of compound toxicity in vivo, we will construct physiologically relevant cellular microarrays on a micropillar/microwell chip platform by using miniaturized three-dimensional (3D) human liver cell cultures, simulate drug metabolism in the liver by expressing diverse drug metabolizing enzymes using recombinant adenoviruses, and then elucidate mechanistic liver toxicity through high content imaging (HCI).
Under the guidance of Dr. Lee and his graduate students, students will learn how to culture mammalian cells, perform biochemical and cell-based assays on microarray biochip platforms, and operate a microarray spotter and a chip imaging system for chip preparation and data acquisition.


Investigating Axonal Biology using Microfluidic Devices
Dr. Chandrasekhar Kothapalli (216) 687-2562

During the nervous system development, various biomolecules guide the growing axons to their targets along specific pathways. These biomolecules could be attractive or repulsive, and exist at different concentrations (gradients) in the brain microenvironment. The tip of the axons, i.e., growth cones, sense and respond to these biomolecules, by exhibiting longer outgrowth or by changing their direction. However, it is not yet clear how the distribution and gradients of biomolecules is maintained in the nervous system to modulate this axonal biology. The goal of this project is to investigate the effect of biomolecules and their respective gradients on cortical neuronal extensions and turning in a microfluidic environment.
Students work, under the guidance of Dr. Kothapalli, learning the aseptic cell culture techniques, isolation and culture of cortical neurons from rat brains, implementation of microfluidic devices, and imaging and analysis of biomolecular gradients; aiming to optimize the conditions for cortical neuron culture in microfluidic devices and evaluate the role of biomolecular gradients on their outgrowth and turning.


Optimization of Algae Bioreactor Systems for Biofuel Production
Dr. Joanne M. Belovich: (216) 687-3502

Biodiesel is one of the fastest growing renewable fuels in the U.S. It can be used in existing diesel equipment and vehicles and with existing distribution infrastructure. Biodiesel plants rely on feedstock sources such as recycled grease, meat fat, and soybean or canola oil. However, none of these can meet the long-term demand for transportation fuel. Algae has significant promise as a feedstock for biodiesel production, since up to 50% of the algae dry mass can be lipids, the precursor for biodiesel. The cells use CO2 as their carbon source and can be grown in large open ponds, or in photobioreactors, with power plant exhaust as the source of CO2. Algae growth can occur in non-arable lands with minimal freshwater required. One of the major limitations to the cost-effective use of algae for biofuel production is the low algae concentration in the production stream and the high cost of nutrients. We are investigating methods for optimizing biomass and oil productivity while minimizing raw material costs.


Computer-Aided Design of Gravitational Settlers for Bio-fuels Production from Microalgae
Dr. Jorge E. Gatica: (216) 523-7274
Dr. Joanne M. Belovich: (216) 687-3502

There are two major limitations that currently prevent algae from being a biodiesel feedstock. The capital costs associated with the algae cultivation systems, either open ponds or bioreactors, are high, relative to the price of diesel. Even in the best culturing systems, algae concentration will not surpass 20 g/L because of light limitation. The low biomass concentration results in a large amount of water that must be removed before the biomass can be processed into biodiesel. This process of removing the water and concentrating the cells, called the “dewatering” process, is both energy and equipment intensive. The purpose of this research is to optimize the design of gravity settlers for algae dewatering for large-scale biofuel production. The research activities will expose students to both computer simulations and hands-on laboratory work. Finite-Element (FEM) based Computational Fluid Dynamics (CFD) constitute modeling environments well suited to handle complex geometries such as those of gravity settlers. This project is aimed at formulating a FEM CFD model of cell-fluid interactions in the process equipment to simulate dynamic and steady-state particle settling scenarios. The model will be validated and refined using data collected from a laboratory-scale settler prototype. The CFD model is then anticipated to be used in design optimization of pilot-scale configurations and identification of [optimum] operating conditions to maximize equipment performance.


Measurement of Transport Parameters in Bone Tissue
Dr. Joanne M. Belovich: (216) 687-3502

Bone tissue readily forms during skeletal development, juvenile growth, and most adult skeletal repair processes. However, more than one million annual bone injuries in the U.S. require bone grafts to assist in repair and this number is expected to increase as the population ages. The growth of bone tissue in vitro, which mimics in vivo bone in form and function, requires selection of the proper scaffold, cell source, loading environment, and culture conditions, among numerous other factors. Two important features of native bone to be mimicked in tissue-engineered bone are the spatial asymmetry of the tissue and the extracellular matrix (osteoid), and while these have not been replicated in vitro, it is well-known that mechanical loading is vital for osteoid generation. It has been hypothesized that the availability of growth factor molecules in the tissue contributes to the formation of the tissue, supported by observations that mechanical stimulation appears to enhance the transport rates of these molecules. We plan to measure the effective diffusion coefficients of key metabolites such as oxygen and glucose, as well as larger growth factor molecules, in bone tissue. The enhancement of transport of these components by mechanical loading will also be ascertained.


Attachment and Growth of Bone Forming Cells: Influence of Surface Texture
Dr. Surendra N. Tewari: (216) 523-7342
Dr. Joanne M. Belovich: (216) 687-3502

The purpose of this research is to examine the influence of surface textures of Ti-6Al-4V (wt pct.) alloy on the attachment and proliferation behavior of bone forming osteoblast cells. The optimum texture would be the one that demonstrates the highest cell adhesion and proliferation even when it is pre-coated with the non-adhesive proteins. The student will establish an experimental set-up to observe and record in-situ the attachment and proliferation behavior of cells, and carry out the associated experiments. The student should be highly motivated and have strong interest in hands-on bio-chemical experiments in a lab environment.


Characterization of Thermally Responsive Polypeptide Nanoparticles
Dr. Nolan B. Holland: (216) 687-2572

Our lab is working with an interdisciplinary team to characterize a material system that reversibly forms nanoparticles in response to environmental changes. The system has potential for use in numerous practical applications, e.g. as biosensors, drug-delivery vehicles, or viscosity modifiers. The particles are prepared from materials inspired by elastin, a naturally occurring protein. They are biosynthesized in E. coli and can be made to respond to a wide variety of stimuli, including temperature, pH, salt concentration, light, and solvent. We are characterizing the size and shape of the particles and devising methods to control their behavior.


Protein Purification Using an Elastin-like Polypeptide Tag
Dr. Nolan B. Holland: (216) 687-2572

Purification is a critical issue in the preparation of biologically active proteins for use as enzyme catalysts, pharmaceuticals, or biological reagents. Separation of proteins can be performed by utilizing chemical or physical properties of the proteins. An alternative approach tags the product with a fusion protein or polypeptide expressed as part of the protein. The tag can have a high affinity for a specific resin that can be used to bind the protein and after release by some method pure protein is obtained. To remove the tag after purification enzymatic cut sites can be introduced between the tag and the protein to cleave off the tag. We are developing a system that utilizes environmentally responsive polypeptide tags to purify proteins at low cost and under gentle conditions.


Making Responsive Hydrogels from Molecular-Scale Building Blocks
Dr. Nolan B. Holland: (216) 687-2572

Responsive materials can exhibit drastic changes in their volume and generate force with small environmental changes. The stimulus can be temperature, pH, light, or other solution property. These materials have found applications as biomaterials, drug delivery devices, and in microfluidic devices. The most common materials currently used are randomly cross-linked polymer hydrogels. Their major limitation is their slow response time and limited volume change due to the process of chain aggregation and water transport. The objective of this project is to overcome these limitations by developing molecular scale responsive subunits. These molecular building blocks will be composed of only three polypeptide chains linked together, and will respond to their environment independent of being incorporated in a bulk gel. Because of their organized folded structure, these materials will respond much more quickly and exhibit a greater percent reduction in size than the traditional responsive hydrogels. These benefits should be retained when these building blocks are connected to form larger responsive networks.


Antifreeze Protein Design for More Effective Ice Crystal Growth Inhibition
Dr. Nolan B. Holland: (216) 687-2572

Antifreeze proteins help organisms that live in cold climates survive freezing temperatures. They function by binding onto specific surfaces of ice crystals, which prevents the crystals from growing. This reduces the temperature at which ice can grow in antifreeze solutions. However, the proteins do not correspondingly reduce the melting temperature of ice, leaving a temperature gap between the melting and freezing point (termed thermal hysteresis) where the ice will neither freeze nor thaw. Within this temperature window, the proteins prevent ice recrystallization, i.e. the growth of large crystals at the expense of smaller ones. Because of this ability to stabilize ice solutions, antifreeze proteins have already found application as a frozen food additive. They also show promise as additives to help extend the storage life of transplant organs or for stabilizing ice slurries to improve efficiency of refrigeration and air conditioning systems. The primary research objective is to design new molecular constructs to increase the efficiency of the antifreeze proteins by as much as 100 times, so that the same activity can be achieved with only a fraction of the protein. This will be accomplished by producing constructs with multiple binding regions to increase the avidity for the ice surface.


Adsorption Isotherm Database
Dr. Orhan Talu: (216) 687-3539

Adsorption processes such as drying, oxygen production for air, hydrogen purification, pollution control, etc. utilize microporous solids with molecular dimension pores to adsorb one or more species from a fluid phase. The feasibility of any adsorption process depends on 1) affinity and 2) capacity of the microporous solid for the fluid molecules which is commonly measured as adsorption isotherms. Measurement of adsorption isotherms is complicated and time consuming therefore data scattered in literature is of extreme value to scientists working in the area on research, process development, and design of adsorption processes.
The long term goal of this project is to collect, digitize, evaluate and to organize isotherm data in literature in a searchable relational database. The students will learn fundamentals of adsorption as an industrial process gaining importance as well as database principles and how to use them (particularly Microsoft Access).


Catalytic Gasification for Waste Management and In-Situ Resource Utilization
Dr. Jorge E. Gatica: (216) 523-7274

This research project is focused on the formulation and characterization of a low-to-mid temperature catalytic gasification process. The overall goal is to develop alternatives for converting spaceflight waste materials into high-value products. Since, approximately six (6) kilograms of waste are produced daily by a crew of four, the intrinsic value of this waste can be greatly enhanced by gasification technologies. Indeed, in-situ processing of trash would provide an option to control waste, while maintaining a healthy habitat, during long-duration missions. Affordable human exploration beyond low earth orbit (LEO) cannot include continuous logistic resupply. The results are therefore anticipated to find application in advancing NASA’s mission supporting space exploration activities such as the International Space Station or extended Space Travel.


Sugar Cane Bio-ethanol Dehydration Assessment including Environmental Issues
Dr. Jorge E. Gatica: (216) 523-7274

Environmental effects and health hazards posed by fossil-fuel based technologies complemented by changes in the global economy have further demanded the need for developing “cleaner” and more efficient technologies that rely on renewable or synthetic resources. An alternative, commonly referred to as bio-fuels, has significantly matured and today’s economy recognizes the significance of being able to produce ethanol from renewable resources such as biomass. Moreover, the potential of ethanol to be further converted to hydrogen makes it a very attractive alternative to replace or complement fossil fuels as sources of energy.

Though many techniques for ethanol dehydration are known; adsorption, distillation, hybrid processes, and pervaporation, are the most common technologies in practice. Two alternatives ethanol dehydration technologies are considered in this project. The first is based on the combination of distillation and azeotropic distillation, while the second relies on hybrid distillation and pervaporation processes.

Currently we are developing a simulation model (a user-defined module) and the interface that would enable to integrate this module with two popular Porcess Simulators: ASPEN Plus(TM) and ASPEN HYSYS(TM)

The immediate goal is to simulate both alternatives aiming to identify optimal design and operating parameters by means of rigorous simulation. Plans for a second phase include formulating an approach that would account for environmental issues in explicit form. The approach is to be based on Life Cycle Assessment (LCA) as described by the ISO 14000 series. Unlike most common approaches that consider environmental impact by focusing on reducing effluents, this methodology also considers the impact associated with all the involved processes in the FPD. One could consider the addition of environmental aspects within energy systems optimization as a promising contribution to the energetic optimization and LCA.


Adsorption and Diffusion in Zeolites
Dr. Orhan Talu: (216) 687-3539
Dr. D.B.Shah: (216) 687-3569

Zeolites occupy a pre-eminent position as adsorbents and catalysts. To determine the potential of any zeolitic material for an industrial application, its adsorptive and diffusive behavior must be well characterized. Our laboratories possess a number of such systems that allow us to characterize these zeolites in terms of their adsorption capacities and the rate of adsorption. Students participating in this project will gain hands-on experience in measuring adsorption isotherms and diffusivities in zeolites. Appropriate adsorbent-adsorbate systems will be identified and measurements will be performed on such systems.


Solidification of single crystal dendritic array through cross-section change
Dr. Surendra N. Tewari: (216) 523-7342

Modern aircraft engines use single crystal turbine blades, which are manufactured by directional solidification of superalloys in a mould where solidification, progresses through several cross-sectional changes. Presence of “spurious” misaligned grains is highly detrimental to the elevated temperature mechanical properties of single crystal blades. Formation of structural and compositional defects caused by convection associated with such cross-section changes during directional solidification is being investigated under this research project.

We are currently carrying out ground-based research in our lab to generate morphology data so that terrestrial (presence of convection) results can be compared with those obtained from samples to be solidified during future low-gravity environment of Space Station (absence of convection). Research involves preparing refractory crucibles having a built-in cross-section change using investment-casting shell mould process, or using graphite crucibles specially machined for this purpose, conducting directional solidification of aluminum-silicon and aluminum-copper alloys under varying thermal gradients and growth rates, examining microstructures by quantitative metallography, and image analysis, and preparing and presenting experimental observations in an organized and cohesive manner in the light of other literature reported research.


Zeolite Membrane Permeation: Modeling and Validation
Dr. D.B.Shah: (216) 687-3569

Zeolites are crystalline aluminosilicate absorbents that have a distinctly defined pore structure. In comparison to other absorbents in its class (i.e. silica, alumina, or activated carbon), zeolites have pores that are of uniform size and thus show no pore size distribution. As a result of this unique feature, they can be used to separate chemical species based on size, shape, and configuration. In this work, we will investigate the conditions under which a hydrocarbon separation based on molecular size, shape, and adsorptive and diffusive properties can be accomplished.

In the analysis of zeolite diffusion and permeation, a mathematical transport model is required to simulate and fully understand the overall separation process. In this study, a mixture of different components is used as a feed stream. These components diffuse and permeate across a zeolite membrane at different rates. A mathematical model will be used to predict the rates of transport of individual components. The model will require the adsorptive and diffusive properties of these components in the zeolite. The model to be used in this study is based on the Maxwell-Stefan equations and was developed by Krishna [1]. It will be used to simulate the permeation behavior of mixtures. Two separate scenarios associated with weak and strong interactions will be investigated. The simulated results obtained from the solution of the model equations will be compared with those derived from more rigorous calculations. Such calculations will illustrate whether a simplified transport model can be used to simulate permeation of individual components of a hydrocarbon mixture.

R. Krishna, R. Baur, Analytic solution of the Maxwell-Stefan equations for multicomponent permeation across a zeolite membrane, Chemical Engineering Journal, 97 (2004) 37-45


Reaction Engineering Principles in Thin Film Applications
Characterization of Precursors leading to Protective and Conversion Coatings in Metallic and Ceramic Substrates

Dr. Jorge E. Gatica: (216) 523-7274

Corrosion resistance and energy efficiency have long been driving forces to substitute low-carbon steels by advanced materials in the manufacture of car body parts. Chromate-based coating processes have been used by industry for many years as a means to generate protective coatings on metal surfaces. In order to meet EPA mandates, chromate-based technologies need to be phased out.

In this research we are investigating new approaches in coating technology that could provide alternative practical options to chromate-based coatings. Preliminary research conducted at Cleveland State University has identified metal-working fluids that can provide effective high-temperature wear and friction control as potential precursors for producing thin films in non-ferrous alloys and ceramics. The purpose of this research is to investigate the effect of different intermetallics as additives that can promote the chemical interaction of these precursors with metallic and non-metallic substrates.

Current research activities complement this long-term research project aiming at elucidating the effect of transition metals on mechanisms leading to protective coatings. At present we are focusing our attention on deposition experiments complemented by spectroscopic and calorimetric characterization of precursor solutions and the coatings these solutions yield on aluminum alloys.


Computational Fluid Dynamics of Chemical Vapor Deposition
Analysis and Optimization of Thin Film Deposition Processes by Mathematical Modeling

Dr. Jorge E. Gatica: (216) 523-7274

Chemical Vapor Deposition (CVD) has become an efficient technology for the production of thin films. The analysis of this technology, typically characterized by the potential for high throughput and minimal effluent generation, involves the complex interaction of transport phenomena, fluid dynamics, and chemical kinetics. Moreover, deposition environments often consist of complex assemblies in intricate flow geometries.

Proof-of-concept experiments are currently carried out in laboratory scale in a radiation furnace. Our goal is to design and optimize deposition experiments with the aid of a multi-physics mathematical modeling. With that purpose, a finite-element-based multi-physics modeling environment has been licensed by the Chemical Reaction Engineering (CRE) Group at CSU.

The immediate goal is to integrate this modeling environment with SolidWorks(TM), a CAD software that allows the design of complex three-dimensional structures, such as the deposition stage used in thin films experiments.


Remote Access and Control Kits (RACKs) for Laboratory Experiences in Chemical Engineering
Dr. Sridhar Ungarala: (216) 687-9368
Dr. Jorge E. (216) 523-7274

This project proposes to enhance student learning by means of an approach that combines interactive computer modules, experimental equipment accessed through the Internet, and process design using modern analysis tools. The project is focused on the recommendation by ABET that promotes exposure of engineering majors to laboratory practices, planning of experiments, experimental data acquisition and statistical analysis. The project aims to develop a set of interactive modules that enable remote access of laboratory settings for experiment monitoring, control, and analysis. These modules will be developed using high-end graphics, point-and-click graphical user interfaces and context-sensitive online help.