Ho-Shing Wu

Prof. Ho-Shing Wu

dep. chemical engineering and materials science, Yuan Ze university
orcid

Research Focus & Metrics

Academic Career Length

22Years (2005-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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2 May 2021 in Polymers
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Journal Article
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Damayanti DamayantiDamayanti Damayanti
Damayanti Damayanti
Ho-Shing WuHo-Shing Wu
Ho-Shing Wu
The polyethylene terephthalate (PET) application has many challenges and potential due to its sustainability. The conventional PET degradation was developed for several technologies to get higher yield products of ethylene glycol, bis(2-hydroxyethyl terephthalate) and terephthalic acid. The chemical recycling of PET is reviewed, such as pyrolysis, hydrolysis, methanolysis, glycolysis, ionic-liquid, phase-transfer catalysis and combination of glycolysis–hydrolysis, glycolysis–methanolysis and methanolysis–hydrolysis. Furthermore, the reaction kinetics and reaction conditions were investigated both theoretically and experimentally. The recycling of PET is to solve environmental problems and find another source of raw material for petrochemical products and energy.

6 November 2021 in Polymers
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Journal Article
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Damayanti DamayantiDamayanti Damayanti
Damayanti Damayanti
LWLatasya Adelia Wulandari
Latasya Adelia Wulandari
Adhanto BagaskoroAdhanto Bagaskoro
Adhanto Bagaskoro
ARAditya Rianjanu
Aditya Rianjanu
Ho-Shing WuHo-Shing Wu
Ho-Shing Wu
The fashion industry contributes to a significant environmental issue due to the increasing production and needs of the industry. The proactive efforts toward developing a more sustainable process via textile recycling has become the preferable solution. This urgent and important need to develop cheap and efficient recycling methods for textile waste has led to the research community’s development of various recycling methods. The textile waste recycling process can be categorized into chemical and mechanical recycling methods. This paper provides an overview of the state of the art regarding different types of textile recycling technologies along with their current challenges and limitations. The critical parameters determining recycling performance are summarized and discussed and focus on the current challenges in mechanical and chemical recycling (pyrolysis, enzymatic hydrolysis, hydrothermal, ammonolysis, and glycolysis). Textile waste has been demonstrated to be re-spun into yarn (re-woven or knitted) by spinning carded yarn and mixed shoddy through mechanical recycling. On the other hand, it is difficult to recycle some textiles by means of enzymatic hydrolysis; high product yield has been shown under mild temperatures. Furthermore, the emergence of existing technology such as the internet of things (IoT) being implemented to enable efficient textile waste sorting and identification is also discussed. Moreover, we provide an outlook as to upcoming technological developments that will contribute to facilitating the circular economy, allowing for a more sustainable textile recycling process.

28 December 2012 in Materials
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DFDenise Fan
Denise Fan
DDDer-Jong Dai
Der-Jong Dai
Ho-Shing WuHo-Shing Wu
Ho-Shing Wu
Ethylene is the primary component in most plastics, making it economically valuable. It is produced primarily by steam-cracking of hydrocarbons, but can alternatively be produced by the dehydration of ethanol, which can be produced from fermentation processes using renewable substrates such as glucose, starch and others. Due to rising oil prices, researchers now look at alternative reactions to produce green ethylene, but the process is far from being as economically competitive as using fossil fuels. Many studies have investigated catalysts and new reaction engineering technologies to increase ethylene yield and to lower reaction temperature, in an effort to make the reaction applicable in industry and most cost-efficient. This paper presents various lab synthesized catalysts, reaction conditions, and reactor technologies that achieved high ethylene yield at reasonable reaction temperatures, and evaluates their practicality in industrial application in comparison with steam-cracking plants. The most promising were found to be a nanoscale catalyst HZSM-5 with 99.7% ethylene selectivity at 240 °C and 630 h lifespan, using a microreactor technology with mechanical vapor recompression, and algae-produced ethanol to make ethylene.

31 July 2022 in Polymers
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Damayanti DamayantiDamayanti Damayanti
Damayanti Damayanti
DSDesi Riana Saputri
Desi Riana Saputri
DMDavid Marpaung
David Marpaung
FYFauzi Yusupandi
Fauzi Yusupandi
ASAndri Sanjaya
Andri Sanjaya
Ho-Shing WuHo-Shing Wu
Ho-Shing Wu
The excessive amount of global plastic produced over the past century, together with poor waste management, has raised concerns about environmental sustainability. Plastic recycling has become a practical approach for diminishing plastic waste and maintaining sustainability among plastic waste management methods. Chemical and mechanical recycling are the typical approaches to recycling plastic waste, with a simple process, low cost, environmentally friendly process, and potential profitability. Several plastic materials, such as polypropylene, polystyrene, polyvinyl chloride, high-density polyethylene, low-density polyethylene, and polyurethanes, can be recycled with chemical and mechanical recycling approaches. Nevertheless, due to plastic waste’s varying physical and chemical properties, plastic waste separation becomes a challenge. Hence, a reliable and effective plastic waste separation technology is critical for increasing plastic waste’s value and recycling rate. Integrating recycling and plastic waste separation technologies would be an efficient method for reducing the accumulation of environmental contaminants produced by plastic waste, especially in industrial uses. This review addresses recent advances in plastic waste recycling technology, mainly with chemical recycling. The article also discusses the current recycling technology for various plastic materials.

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Yu-Hong WeiYu-Hong Wei
Yu-Hong Wei
WCWei-Chuan Chen
Wei-Chuan Chen
CHChin-Kuei Huang
Chin-Kuei Huang
Ho-Shing WuHo-Shing Wu
Ho-Shing Wu
YSYi-Ming Sun
Yi-Ming Sun
OJOm-Murugan Janarthanan
Om-Murugan Janarthanan
Polyhydroxyalkanoate (PHA) is a biodegradable material with many potential biomedical applications, including medical implants and drug delivery. This study developed a system for screening production strains in order to optimize PHA production in Cupriavidus taiwanensis 184, 185, 186, 187, 204, 208, 209 and Pseudomona oleovorans ATCC 29347. In this study, Sudan black B staining, Infrared (IR) and Gas Chromatography (GC) analysis indicated that the best strain for PHA synthesis is C. taiwanensis 184, which obtains polyhydroxybutyrate (PHB). Cultivation of C. taiwanensis 184 under a pH of 7.0, at 30 °C, and at an agitation rate of 200 rpm, obtained a PHB content of 10% and PHB production of 0.14 g/L. The carbon and nitrogen types selected for analysis of PHB production by C. taiwanensis 184 were gluconic acid and NH4Cl, respectively. Optimal carbon/nitrogen ratio for PHB production was also determined. This study demonstrated a PHB content of 58.81% and a PHB production of 2.44 g/L when the carbon/nitrogen ratio of 8/1 was selected for C. taiwanensis 184. A two‑stage fermentation strategy significantly enhanced PHB content and PHB production. Under a two-stage fermentation strategy with nutrient‑limited conditions, C. taiwanensis 184 obtained a PHB content of 72% and a PHB concentration of 7 g/L. Finally, experimental results confirmed that optimizing the growth medium and fermentation conditions for cultivating the indigenous C. taiwanensis 184 strain substantially elevated PHB content from 10% to 72% and PHB production from 0.14 g/L to 7 g/L, respectively.

7 August 2017 in ACS Omega
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CWChung-Yen Wu
Chung-Yen Wu
Ho-Shing WuHo-Shing Wu
Ho-Shing Wu
Catalysts prepared for ethanol dehydration in a fixed-bed reactor acted as strong active acidic catalysts under reaction conditions at lower temperatures. Experimental conditions including the catalyst type [active aluminum oxide (γ-Al2O3) and ZSM-5 zeolite catalyst modified using two-stage through dealumination or desilication and by using the impregnation method with phosphorous and lanthanum], weight hourly space velocity (WHSV), ethanol concentration, and reaction temperature were investigated to obtain optimal reaction conditions. The catalysts were characterized using the Brunauer–Emmett–Teller method, temperature-programmed desorption of ammonia gas, thermogravimetric analysis, X-ray photoelectron spectroscopy, and X-ray diffraction. The results revealed that the ethylene yield and selectivity were 98.5 and 100%, respectively, for the ZSM-5 zeolite catalyst modified through dealumination at a temperature of 220 °C and WHSV of 2.5 h–1 when the ethanol concentration was 95%. The ethylene yield and selectivity were 94.3 and 94.4%, respectively, for the ZSM-5 zeolite catalyst modified using phosphorous at a temperature of 240 °C and WHSV of 1.5 h–1 when the ethanol concentration was 20%. Both of these catalysts were the most favorable among all prepared catalysts.