Composition Drift Research Articles

Enabling MOCVD production on next generation 150 mm Indium Phosphide wafer size

150 mm Indium Phosphide wafers are now commercially available with crystal quality comparable to wafer of smaller radius. This may pave the way for scaling up the production of a multitude of photonic devices for Datacoms operating in the 1.30-1.55μm infrared range with a gain in wafer surface of factor 4 and a reduction of roughly 50% in die cost. To achieve this goal, it is of utmost importance to prove that both AlGaInAs and InGaAsP quaternary compound semiconductors can be grown by metal–organic chemical vapor deposition (MOCVD) on wafers of larger sizes with both thickness and composition uniformities comparable to those achievable on 75 mm. In this article, we report pioneering production technology developments based on the Planetary Reactor® design. Both reactor and related inlet geometry have been deeply revisited with the introduction of a novel 4-fold injector, which in combination with Cl2 In-situ chamber clean, prove to enable such transition in wafer size. Sub-nanometric photoluminescence in-wafer uniformities are demonstrated and historic challenges, such as drift in material composition of highly sensitive InGaAsP alloys during a production campaign, are addressed thanks to this unique combination. Uniformity, tunability and reproducibility results are thus presented for two prototypical case scenarios: a highly strained AlGaInAs multiple quantum well (MQW) and a bulk InGaAsP layer with wavelength emission of 1550 nm and 1100 nm respectively to corroborate reactor flexibility in meeting industry requirements for next device generation.

Composition drift in radical copolymerization

Composition drift in radical copolymerization is a topic of practical importance for the synthesis of homogeneous statistical copolymers and gradient copolymers, which generally does not receive much attention in most polymer chemistry textbooks. The aim of this paper is to provide a tutorial on the topic in which we provide some additional theory in a straightforward and accessible manner and show that composition drift can easily be described quantitatively. Furthermore we show how to circumvent composition drift in a semi-batch approach and by using a continuous stirred tank reactor (CSTR).

Thermadapt shape memory vitrimeric polymyrcene elastomer

Earlier studies of β-Myrcene (Myr)/ β-ketoester functional (acetoacetoxy)ethyl methacrylate (AAEMA) copolymers exhibited compositional drift, leading to ambiguity in microstructure/thermomechanical property correlations while shape memory recovery times were excessively long ~1 h. The terpene-based 1,3-diene Myr and AAEMA were copolymerized via nitroxide-mediated polymerization (NMP) with an initial Myr molar feed ratio ranging from 0.1 to 0.9. Reactivity ratios estimated by the Meyer-Lowry method were rMyr = 0.20 and rAAEMA = 0.22 with respective 95% confidence intervals of [0.13, 0.37] and [0.15, 0.23], suggesting alternating copolymerization. Bulk terpolymerization with styrene (Sty) afforded linear poly(Myr-stat-Sty-stat-AAEMA) prepolymers designed to modulate glass transition temperature Tg and stiffness. Subsequent cross-linking with isophorone diamine (IPDA) formed catalyst-free vinylogous urethane dynamic linkages. ATR-FTIR, dynamic mechanical analysis (DMA), and tensile measurements confirmed the recyclability of vitrimers through hot pressing at 110 °C, demonstrating minimal changes in rheological and mechanical properties even after four cycles. By heating the vitrimers to above their Tg (to ~45 °C), they exhibited a shape memory effect with high shape fixity and fast shape recovery (< 1 min). The vitrimers could undergo permanent shape reprogramming through reconfiguration of dynamic bonds at ~110 °C. This work shows the adaptability of Myr-based rubbers by vitrification and appropriate copolymerization for the synthesis of more sustainable elastomers with stimuli responsive properties.

A lower bound on the rheological evolution of magma in the 2021 Fagradalsfjall Fires

As magma temperature and composition drift and change, respectively, throughout an eruption, so does its rheology. These changes may span orders of magnitude in magma viscosity and result in orders of magnitude flow velocity changes, as well as transitions in eruptive style. In this study, we present a systematic high precision quantification of the rheological variations that occurred during the 2021 Fagradalsfjall Fires. In the field, we collected a suite of 22 representative samples emplaced between day 2 and 183 of the 2021 eruption. In the laboratory, we measured the melt viscosity of each sample in a concentric cylinder viscometer. Temperatures were initially raised to 1392 °C, and then lowered stepwise to eruptive temperatures as determined through syn-eruptive radiometric measurements. The resulting dataset is analyzed as a time series. An overall trend of viscosity decrease emerges. As the eruption progressed, melt viscosity decreased by 25%, from 40 Pa s to 30 Pa s at a constant temperature of 1200 °C. However, this trend is not monotonous. At least 3 positive spikes in viscosity can be identified, at day 80, 120, and 138 of the eruption. This trend tracks with geochemical variations.

Catch Composition and Selectivity Drift Gillnet in Pambang Pesisir Village Bantan Subdistrict Bengkalis Regency

Gill nets are placed perpendicular to the water to block the swimming direction of the fish. Fish are caught by being entangled in the meshes or entangled (spun) in the body of the net. This research was conducted in Pambang Pesisir Village, Bantan District, Bengkalis Regency, to know the composition of the catch and the selectivity of drift gill nets, comparing the composition of the number, type, weight, and size of the catch from different mesh sizes, and knowing how to catch fish (entangled, gilled, snagged, wedged) on the same mesh used. This research was carried out in December 2020 using the experimental fishing method, which is a research method that uses samples of research objects caught on fishing gear for observation. The research results of drift gill nets are species-selective fishing gear. Moreover, drift gill nets with a mesh size of 7.62 cm are more selective than nets of 5.72 cm because they have a catch ratio value closer to 1 and catch more large fish (worth catching). How to catch fish with a mesh size of 5.72 cm, many fish were caught by snagged; namely, 65 fish (30%), wedged 61 fish (28%), gilled 59 fish (27%), and 33 fish entangled (15%). Meanwhile, for the mesh size of 7.62 cm, 30 fish (31%) were caught wedged, 27 fish (29%) snagged, 27 fish (29%) gilled, and ten fish entangled (11%).

Annual and decadal surveys of molluscs on intertidal platform reefs in a warming marine environment in the southeastern Indian Ocean provide a baseline for monitoring for future environmental changes

ABSTRACT Few data sets are available to evaluate short- and long-term perturbations and impacts of increasing anthropogenic stresses and a warming marine environment in coastal regions near cities. The Perth, Western Australia shoreline has extensive, depauperate sandy beaches interrupted by small, biodiverse intertidal reef platforms. We present transect data on mollusc diversity and density on three Perth platforms recorded from 1983 to 1987, and compare it to 2007 and 2021 to analyse assemblage modifications in response to increased anthropogenic pressures. NMDS multivariate analysis showed a consistent drift in assemblage composition in 2007 and 2021, but this is was not statistically significant from the 1980s baseline (PERMANOVA, P = 0.336). There was no significant long-term decline (or increase) in molluscan species richness. Most species were uncommon but eight were recorded on at least 20 of the 21 surveys. The endemic Western Australian mussel Brachidontes ustulatus (Lamarck, 1819) accounted for 71.8% of all individuals. Total mollusc density varied primarily with changes in B. ustulatus. Tropical species were a minor component of the molluscs that did not change in diversity with warming temperatures. These data provide a long-term baseline for monitoring future anthropogenic changes.

Self-adhesion of uncrosslinked poly(butadiene-co-acrylonitrile), i.e. nitrile rubber, an inhomogeneous and associative polymer.

Nitrile rubber (i.e., NBR) is a crosslinked copolymer of butadiene and acrylonitrile that finds widespread use in the automotive and aerospace industry as it sustains large, reversible deformations while resisting swelling by petrochemical fuels. We recently demonstrated that this material has a drift in composition due to the difference in reactivity between acrylonitrile and butadiene monomers during emulsion copolymerisation. Thus, although NBR is often thought of as a random copolymer, it does experience thermodynamic driving forces for self-assembly and kinetic barriers for processing like those of block copolymers.1 Here, we illustrate how such drift in composition hinders interdiffusion and prevents self-adhesion. The key result is that contacting uncrosslinked NBR (i) in the melt, (ii) in the presence of tackifiers, or (iii) in the presence of organic solvents promotes interdiffusion and enables self-adhesion. However, the contact times required for self-adhering, tc ∼ O(100 h), are orders of magnitude above those needed for non-polar synthetic rubbers like styrene-butadiene rubber (i.e., SBR) of comparable molecular weights and glass transition temperatures, tc ∼ O(100 s), unveiling the dramatic effect of compositional inhomogeneities and physical associations on polymer interdiffusion and large-strain mechanical properties. For example, when welded with organic solvents, the self-adhesion energy of NBR continues to increase after the solvent has evaporated because of polymer nanostructuring.

Unveiling the Role of Compositional Drifts on the Tack of Pressure‐Sensitive‐Adhesives

AbstractPressure‐sensitive‐adhesives (PSAs) are pervasive in electronic, automobile, packaging, and biomedical applications due to their ability to stick to numerous surfaces without undergoing chemical reactions. These materials are typically synthesized by the free radical copolymerization of alkyl acrylates and acrylic acid, leading to an ensemble of polymer chains with varying composition and molecular weight. Here, reversible addition−fragmentation chain‐transfer (RAFT) copolymerizations in a semi‐batch reactor are used to tailor the molecular architecture and bulk mechanical properties of acrylic copolymers. In the absence of cross‐links, the localization of acrylic acid toward the chain ends leads to microphase separation, creep resistance, and enhanced tack. However, in the presence of Al(acac)3 crosslinker, the creep resistance remains unchanged and mostly the large‐strain mechanical properties are affected. This behavior is attributed to microphase separation, but also to a change in the energy required to break physical associations, and untangle and elongate associative polymers to large deformations.

A systematic study of tert‐butylacrylamide‐methyl acrylate‐acrylic acid radical solution terpolymerization

AbstractMulti‐functional polymers used for personal care products can be synthesized by radical polymerization of acrylic acid (AA) in alcohol/water solutions with non‐functional monomers such as methyl acrylate (MA) and N‐tert‐butylacrylamide (t‐BuAAm). However, solvents capable of forming or disrupting hydrogen bonds cause the polymerization kinetics of these monomers to deviate from their polymerization behaviour in bulk and non‐polar solvents. In this work, a previous mechanistic model developed for MA/t‐BuAAm copolymerization is extended to represent the terpolymerization system MA/t‐BuAAm/AA. The additional kinetic coefficients required for the system are estimated from fitting to AA homopolymerizations and AA/MA and AA/t‐BuAAm copolymerizations conducted in an ethanol/water solution. In‐situ nuclear magnetic resonance (NMR) spectroscopy is used to follow monomer conversions and composition drift behaviour, with the molar mass distributions of the polymer products characterized by size‐exclusion chromatography. Although AA is more reactive than MA in non‐polar solvents, the reactivities of the two monomers equalize under the experimental conditions examined. Thus, the batch and semi‐batch terpolymerization data collected are represented equally well by a reduced acrylate/t‐BuAAm copolymerization model and the full terpolymerization implementation.

Effect of ultra-fast pyrolysis on polymer-derived SiOC aerogels and their application as anodes for Na-ion batteries

In the last decade, Sodium-Ion-Batteries (SIB) started to gain interest as a possible complementary candidate to support the overburdened lithium technology, but the manufacturing of a proper anode material is one of the challenging factors for the development of performing SIB. Among others, porous polymer-derived ceramics have been widely explored as suitable anodes despite the production of such materials being time and energy-consuming. In this work, we investigate the feasibility of adopting a low-cost ultra-fast high-temperature pyrolysis for the ceramic conversion of a polymer-derived SiOC aerogel to be employed as anode material. A comprehensive study including N2 physisorption, 29Si MAS NMR and Raman spectroscopy provides the insights of the effect of ultra-fast and conventional heating rates (i.e., 200 °C·s−1 vs. 5 °C·min−1) on the microstructural features and ceramic yield of the SiOC aerogels. As a consequence of the ultra-fast heating rate, a compositional drift towards oxygen-rich SiOC is observed and discussed. The electrochemical performance of both ceramics has been tested and related to the observed compositional differences, revealing a stable capacity of 103 mAh·g−1 for the ultra-fast pyrolyzed SiOC anode, and 152 mAh·g−1 for SiOC ceramized at 5 °C·min−1.

Key melt properties for controlled synthesis of glass beads by aerodynamic levitation coupled to laser heating

AbstractBinary alkali silicate glasses were synthesized as beads by aerodynamic levitation coupled to laser heating to test the applicability of the method to this compositional range. While bubble‐free lithium disilicate beads could be easily obtained, sodium and potassium silicates proved more challenging to melt without significant alkali evaporation: the final samples contained bubbles and exhibited compositional drifts compared to the starting stoichiometry, especially at high SiO2content. The risk of volatilization from the melts was evaluated empirically: the volatility of each oxide component scaled to the ratio between its melting temperatureTmand theTmof the target composition (revap), while the difference between such ratios (Δevap) provided a qualitative estimation of the risk of differential evaporation. The formulated approach enables to evaluate the suitability of aerodynamic levitation synthesis for a given target glass composition: while low melting temperature and low liquidus viscosity (η &lt; 100 Pa s) represent the primary optimal conditions, more viscous materials can still be prepared without major compositional drifts using a more careful melting procedure, especially ifrevapandΔevapare minimized.

One-Step Synthesis of Biphasic, Cavity-forming Polymer Particles via Dispersion Copolymerization of Styrene and Sulfobetaine Methacrylate.

A one-step dispersion copolymerization technique is demonstrated to fabricate biphasic particles as an approach to streamline the production of particles with complex morphology. The model system studies a monomer feed of hydrophobic styrene and hydrophilic, zwitterionic sulfobetaine methacrylate (SBMA) in a water/isopropanol cosolvent mixture. The resulting particles have a core-shell morphology that can be transformed, simply by washing the particles with water, into particles with a single surface opening connected to an interior cavity. Results indicate that particle morphology is dependent on the presence of nanoscopic SBMA-rich aggregates in the initial reaction mixture to act as nucleation sites, forming an SBMA-rich core encased in a styrene-rich shell. Systematic study of the morphology evolution reveals that the difference in monomer solubility profile can be exploited to control compositional drift of the particle composition during copolymerization yielding copolymer with sufficiently different composition to form phase-separated particle morphology. When SBMA is replaced with various ionic comonomers, the cavity-forming morphology is observed when reaction conditions result in low solubility of the comonomer in the cosolvent mixture. Based on these results, design guidelines are developed that may be applied to a variety of systems requiring complex and responsive particles made from chemically distinct comonomer pairings.

Sustained postconfluent culture of human mammary epithelial cells enriches for luminal and c-Kit+ subtypes

BackgroundA challenge in human mammary epithelial cell (HMEC) culture is sustaining the representation of competing luminal, myoepithelial, and progenitor lineages over time. As cells replicate in culture, myoepithelial cells come to dominate the composition of the culture with serial passaging. This drift in composition presents a challenge for studying luminal and progenitor cells, which are prospective cells of origin for most breast cancer subtypes.MethodsWe demonstrate the use of postconfluent culture on HMECs. Postconfluent culture entails culturing HMECs for 2–5 weeks without passaging but maintaining frequent feedings in low-stress M87A culture medium. In contrast, standard HMEC culture entails enzymatic subculturing every 3–5 days to maintain subconfluent density.ResultsWhen compared to standard HMEC culture, postconfluent culture yields increased proportions of luminal cells and c-Kit+ progenitor cells. Postconfluent cultures develop a distinct multilayered morphology with individual cells showing decreased physical deformability as compared to cells in standard culture. Gene expression analysis of postconfluent cells shows increased expression of lineage-specific markers and extracellular matrix components.ConclusionsPostconfluent culture is a novel, useful strategy for altering the lineage composition of HMECs, by increasing the proportional representation of luminal and progenitor cells. We speculate that postconfluent culture creates a microenvironment with cellular composition closer to the physiological state and eases the isolation of scarce cell subtypes. As such, postconfluent culture is a valuable tool for researchers using HMECs for breast cancer research.

Plasma in-situ imaging detection technology on China’s Space Station Wentian module

&lt;sec&gt;In order to meet the needs of ionospheric research and monitoring of space station charging, the technology of plasma in-situ imaging detection is studied. The plasma in-situ imaging detector is one of the first outside scientific payloads of the Chinese space station to detect the space environment. It is installed on the extravehicular platform of the Wentian module, and will carry out multi-element comprehensive detection of ionospheric plasma, including in-situ, imaging, and charging potential. The refined detection data of the low latitude ionosphere will provide plasma parameters for improving the orbital ionospheric model of the space station. And the long-term charging potential data are collected to support the studying of the charging effect of plasma on the space station and promoting the establishment of the space station charging evaluation system.&lt;/sec&gt;&lt;sec&gt;The plasma in-situ imaging detector integrates Langmuir probe, retarding potential analyzer, ion drift meter, reference potentiometer, ion imaging technology, etc. Electron density and electron temperature are measured by Langmuir probe. Ion composition,ion density,ion temperature, and ion drift velocity are measured by retarding potential analyzer and ion drift meter. The ion imaging parameters are obtained by ion imager. The reference potential sensor is available to provide the measurements of charging potential of Wentian module. The Langmuir probe sensor inherits the design of the Langmuir probe sensor of CSES (Zhangheng-1 satellite). The retarding potential analyzer and ion drift meter also inherit the design of CSES (Zhangheng-1 satellite), and improve the design of grid voltage and collector voltage which can be adjusted adaptively according to on orbit state. The ion imager consists of an electrostatic deflection module, a Whalen analyzer and an imaging module. The ion imaging technology is for the first time applied to the field of space environment detection in China.&lt;/sec&gt;&lt;sec&gt;The plasma in-situ imaging detector is tested and calibrated to verify the performance at the National Space Science Center of the Chinese Academy of Sciences. when this paper is submitted, the detector mounted on Wentian module has been successfully launched. Next, the detector will be assembled by astronauts inside the capsule using external interfaces . Then, the detector will be grabbed by the robotic arm and installed on the extravehicular experimental platform to start a long-term exploration mission.&lt;/sec&gt;

Effect of Conversion on Chain Addition Copolymerizations Performed in a Backmixed Drag Flow Extruder Reactor

Abstract The use of a drag flow device such as a twin screw extruder for polymerization and/or copolymerization processes has been studied extensively over the years. Due to the high viscosities (100 to 100 000 poise) that are produced, poor backmixing is experienced in these drag flow devices. As a result, these studies have shown the extruder reactor to exhibit a ‘‘plug flow’’ behavior. A drag flow device has been developed that achieves good backmixing with high viscosity materials. This device incorporates two counter-rotating, nonintermeshing, screws; one screw conveying material forward, while the other conveying material backward. Theory suggests that in a plug flow reactor the copolymer composition varies (drifts) as a function of time (position) in the reactor in most cases. Conversely in a micromixed continuous stirred tank reactor (CSTR) the copolymer produced does not drift as a function with position in the reactor. It has also been shown that this drift in copolymer composition becomes more pronounced at higher conversion. Experiments were performed in a counter-rotating nonintermeshing twin screw extruder using the ‘‘backmixed’’ configuration and a ‘‘conventional’’ configuration. Two copolymer systems were investigated; butyl acrylate/styrene and butyl acrylate/butyl methacrylate. The copolymerizations were conducted at three residence times for each system and configuration to provide materials of a wide variety of conversions (13 to 97 %). Monomer samples were taken at two ports in the extruder and at the die. Samples were analyzed for composition by two methods; FTIR and refractive index (RI). It was shown that the copolymer composition of samples produced in the backmixed extruder reactor does not change significantly as a function of position in the reactor. This is an indication that the copolymer composition does not drift in the reactor. Theoretically this is the behavior that exists with a chain addition copolymerization that occurs in a CSTR. Two methods (RI, FTIR) were used in the copolymer formulation (BA/Sty) and one method (FTIR) was used in the other copolymer formulation (BA/BMA). It was further shown that the difference in copolymer compositions in the two extruder reactors is more pronounced at higher conversions than at lower conversions.

Using Triethylborane to Manipulate Reactivity Ratios in Epoxide-Anhydride Copolymerization: Application to the Synthesis of Polyethers with Degradable Ester Functions.

The anionic ring-opening copolymerization (ROCOP) of epoxides, namely of ethylene oxide (EO), with anhydrides (AH) generally produces strictly alternating copolymers. With triethylborane (TEB)-assisted ROCOP of EO with AH, statistical copolymers of high molar mass including ether and ester units could be obtained. In the presence of TEB, the reactivity ratio of EO (rEO), which is normally equal to 0 in its absence, could be progressively raised to values lower than 1 or higher than 1. Conditions were even found to obtain rEO equal or close to 1. Samples of P(EO-co-ester) with minimal compositional drift could be synthesized; upon basic degradation of their ester linkages, these samples afforded poly(ethylene oxide) (PEO) diol samples of narrow molar mass distribution. In other cases where rEO were lower or higher than 1, the PEO diol samples eventually isolated after degradation exhibited a broader distribution of molar masses because of the compositional drift of initial P(EO-co-ester) samples.

A Short-Cut Data Mining Method for the Mass Spectrometric Characterization of Block Copolymers

A new data mining approach as a short cut method is given for the determination of the copolymer composition from mass spectra. Our method simplifies the copolymer mass spectra by reduction of the number of mass peaks. The proposed procedure, namely the selection of the mass peaks, which is based on the most abundant peak of the mass spectrum, can be performed manually or more efficiently using our recently invented Mass-remainder analysis (MARA). The considerable reduction of the MS spectra also simplifies the calculation of the copolymer quantities for instance the number- and weight-average molecular weights (Mn and Mw, respectively), polydispersity index (Đ = Mw/Mn), average molar fraction (cA) and weight fraction (wA) of the comonomer A and so on. These copolymer properties are in line with those calculated by a reference method taking into account all the mass peaks of the copolymer distribution. We also suggest a highly efficient method and template for the determination of the composition drift by processing the reduced mass spectra.

Lactide-Valerolactone Copolymers for Packaging Applications.

Lactide-valerolactone copolymers have potential application in the packaging sector. Different copolymers were synthesized, and the kinetics of the copolymerization reactions and the microstructure of the copolymers were analysed. Lactide showed higher reactivity than valerolactone which leads to composition drift through the reaction. Thermal, mechanical and barrier properties of the selected copolymers were studied. Overall, the incorporation of valerolactone results in copolymers with higher ductility than poly(lactide) with intermediate water and oxygen permeability which makes these materials appropriate candidates for use in the packaging sector.

Black shale formation environment and its control on shale oil enrichment in Triassic Chang 7 Member, Ordos Basin, NW China

Based on geochemical analysis results of core samples from the Triassic Chang 7 Member of Well Feng 75 drilled in the northwest margin of Ordos Basin, combined with geological characteristics of this region, the formation environment of the black shale and its control on shale oil enrichment are comprehensively studied. From the Chang 73 to Chang 71 Sub-members, the black shale have organic carbon contents decreasing from 5.70% to 3.55%, hydrogen indexes decreasing from 345 mg/g to 269 mg/g, while the oxygen indexes increasing gradually from 6 mg/g to 29 mg/g, indicating that the sedimentary environment during the depositional period of Chang 72 and Chang 73 Sub-members was anoxic. Biomarkers in the black shale change regularly, and have an obvious “inflection point” at the depth of 2753–2777 m in the Chang 73 Sub-member, indicating that the input of terrigenous organic matter increased. However, there is a negative drift about 2% of organic carbon isotopic composition near the “inflection point”, which is in conflict with the results of biomarker compounds. This is because the extreme thermal and anoxic events caused by continental volcanic activity in the ancient Qinling region caused negative drift of carbon isotopic composition of the black shale in the Ordos Basin. The volcanic activity caused rise of temperature, polluted air, extreme weathers, more floods and thus more input of terrigenous organic matter, and gave rise to extremely anoxic environment conducive to the preservation of organic matter. Terrigenous organic matter is more conducive to the formation of light oil than aquatic organic matter, so these sections in Yanchang Formation are major “sweet spots” for shale oil enrichment.

Ethylene/1‐Hexene Copolymerization Kinetics and Microstructure of Copolymers Made with a Supported Metallocene Catalyst

AbstractEthylene/1‐olefin copolymers made with supported metallocenes in slurry or gas‐phase polymerization are often less homogeneous than those made with the same unsupported metallocene in solution polymerization. In particular, their molecular weight distributions are broader, having polydispersities higher than two, and sometimes their chemical composition distributions may even be bimodal. In our previous publication, we developed a mathematical model to describe the polymerization kinetics and polymer microstructure of ethylene homopolymers made with a supported metallocene catalyst. In this article, we extended that model to also cover the copolymerization of ethylene and 1‐hexene with the same supported catalyst. The copolymerizations are performed in parallel semibatch reactors using a metallocene catalyst supported on an inorganic porous carrier. 1‐Hexene concentration and polymerization time are the factors changed to investigate this system. Modeling results show that, as for the ethylene homopolymerization case, a three‐site model is needed to describe the molecular weight distributions of the copolymers, but their chemical compositions can be described with a single set of reactivity ratios. A single set of parameters is also enough to describe the copolymerization kinetics with this supported catalyst. A new method is also developed and tested to estimate reactivity ratios under composition drift in this article.