Tailoring the Stabilization and Pyrolysis Processes of Carbon Molecular Sieve Membrane Derived from Polyacrylonitrile for Ethylene/Ethane Separation

For ethylene/ethane separation, a CMS (carbon molecular sieve) membrane was developed with a PAN (polyacrylonitrile) polymer precursor on an alumina support. To provide an excellent thermal property to PAN precursor prior to the pyrolysis, the stabilization as a pre-treatment process was carried out. Tuning the stabilization condition was very important to successfully preparing the CMS membrane derived from the PAN precursor. The stabilization and pyrolysis processes for the PAN precursor were finely tuned, and optimized in terms of stabilization temperature and time, as well as pyrolysis temperature, heating rate, and soaking time. The PAN stabilized at >250 °C showed improved thermal stability and carbon yield. The CMS membrane derived from stabilized PAN showed reasonable separation performance for ethylene permeance (0.71 GPU) and ethylene/ethane selectivity (7.62), respectively. Increasing the pyrolysis temperature and soaking time gave rise to an increase in the gas permeance, and a reduction in the membrane selectivity. This trend was opposite to that for the CMS membranes derived from other polymer precursors. The optimized separation performance (ethylene permeance of 2.97 GPU and ethylene/ethane selectivity of 7.25) could be achieved at the pyrolysis temperature of 650 °C with a soaking time of 1 h. The separation performance of the CMS membrane derived from the PAN precursor was comparable to that of other polymer precursors, and surpassed them regarding the upper bound trade off.

Carbon Dot/Polymer Composites with Various Precursors and Their Sensing Applications: A Review

Carbon dots (CDs) have generated much interest because of their significant fluorescence (FL) properties, extraordinary photophysical attributes, and long-term colloidal stability. CDs have been regarded as a prospective carbon nanomaterial for various sensing applications because of their low toxicity, strong and broad optical absorption, high chemical stability, rapid transfer properties, and easy modification. To improve their functionality, CD/polymer composites have been developed by integrating polymers into CDs. CD/polymer composites have diversified because of their easy preparation and applications in sensing, optoelectronics, semiconductors, molecular delivery, and various commercial fields. Many review articles are available regarding the preparation and applications of CDs. Some review articles describing the production and multiple applications of the composites are available. However, no such article has focused on the types of precursors, optical properties, coating characteristics, and specific sensing applications of CD/polymer composites. This review aimed to highlight and summarize the current progress of CD/polymer composites in the last five years (2017–2021). First, we overview the precursors used for deriving CDs and CD/polymer composites, synthesis methods for preparing CDs and CD/polymer composites, and the optical properties (absorbance, FL, emission color, and quantum yield) and coating characteristics of the composites. Most carbon and polymer precursors were dominated by synthetic precursors, with citric acid and polyvinyl alcohol widely utilized as carbon and polymer precursors, respectively. Hydrothermal treatment for CDs and interfacial polymerization for CDs/polymers were frequently performed. The optical properties of CDs and CD/polymer composites were almost identical, denoting that the optical characters of CDs were well-maintained in the composites. Then, the chemical, biological, and physical sensing applications of CD/polymer composites are categorized and discussed. The CD/polymer composites showed good performance as chemical, biological, and physical sensors for numerous targets based on FL quenching efficiency. Finally, remaining challenges and future perspectives for CD/polymer composites are provided.

Pre-Treatment of Used Cooking Oil Followed by Transesterification Reaction in the Production of Used Cooking Oil-Based Polyol

Used cooking oil has been considered as an economical and sustainable material that can be used widely as a starting material in the production of polymer precursors such as polyol for polyurethane. Since the composition of fatty acids and glyceride in the structure of used cooking oil remain the same as virgin vegetable oil, used cooking oil can be synthesized using the same method. However, there are certain physicochemical modifications to the oil properties that arise during the process of oil fryings such as increases in viscosity, acid value, and color changes that will affect the conversion of used cooking oil into bio-based polyol. Thus, various pretreatment methods that can be applied to used cooking oil such as adsorption, chemical bleaching, and treatment with solvents will be reviewed in this paper. Transesterification of used cooking oil with alcohol in the presence of catalyst will produce used cooking oil-based polyol which will have two or more hydroxyl groups per molecule. The formation of polyol can be confirmed with the formation of O-H peak in the FTIR spectrum during the FTIR spectroscopy analysis. This paper will also discuss the type of alcohol and catalyst used in the transesterification reaction. Used cooking oil-based polyol obtained from transesterification reaction has been reported to be comparable to the commercial polyol.

Precursor-dependent structural diversity in luminescent carbonized polymer dots (CPDs): the nomenclature

Carbon dots (CDs) have received immense attention in the last decade because they are easy-to-prepare, nontoxic, and tailorable carbon-based fluorescent nanomaterials. CDs can be categorized into three subgroups based on their morphology and chemical structure: graphene quantum dots (GQDs), carbon quantum dots (CQDs), and carbonized polymer dots (CPDs). The detailed structures of the materials can vary significantly, even within the same category. This property is particularly predominant in chemically synthesized CPDs, as their formation proceeds via the polymerization–carbonization of molecules or polymer precursors. Abundant precursors endow CPDs with versatile structures and properties. A wide variety of carbon nanomaterials can be grouped under the category of CPDs because of their observed diversity. It is important to understand the precursor-dependent structural diversity observed in CPDs. Appropriate nomenclature for all classes and types of CPDs is proposed for the better utilization of these emerging materials.

A Review on Polymer Precursors of Carbon Molecular Sieve Membranes for Olefin/Paraffin Separation

Carbon molecular sieve (CMS) membranes have been developed to replace or support energy-intensive cryogenic distillation for olefin/paraffin separation. Olefin and paraffin have similar molecular properties, but can be separated effectively by a CMS membrane with a rigid, slit-like pore structure. A variety of polymer precursors can give rise to different outcomes in terms of the structure and performance of CMS membranes. Herein, for olefin/paraffin separation, the CMS membranes derived from a number of polymer precursors (such as polyimides, phenolic resin, and polymers of intrinsic microporosity, PIM) are introduced, and olefin/paraffin separation properties of those membranes are summarized. The effects from incorporation of inorganic materials into polymer precursors and from a pyrolysis process on the properties of CMS membranes are also reviewed. Finally, the prospects and future directions of CMS membranes for olefin/paraffin separation and aging issues are discussed.