Tag: 1100-1200

Preparation and Properties of a Modified Fe₂O₃ Pigment for Dope Dyeing Ultrahigh Molecular Weight Polyethylene (UHMWPE) Fibers by Melt Spinning was written by Wang, Xiaochun;Zhang, Liping;Liu, Ming;Zhang, Jianfei;Zhao, Guoliang. And the article was included in Fibers and Polymers in 2021.Reference of 6683-19-8 This article mentions the following:

The poor compatibility between a Fe₂O₃ pigment and a blend of ultrahigh mol. weight polyethylene (UHMWPE)/polyolefin (PO) can result in low spinnability and poor mech. properties of the resulting fiber. This study modifies the surface of a Fe₂O₃ pigment with a titanate coupling agent for dope dyeing melt-spun UHMWPE fiber. The effects of the coupling agent dose, reaction temperature and reaction time on the surface properties of the pigments are investigated. In addition, the characteristics of the UHMWPE blend and colored fibers (by dope dyeing with modified and unmodified Fe₂O₃ pigments) are compared. Notably, 3 weight% coupling agent in regard to the pigments mass, a coupling agent to toluene mass ratio of 1:5, a reaction time of 30 min, and a reaction temperature of 80°C achieve the optimal results, which are a 48.4% lipophilic degree of the modified pigment, a zeta potential of 48.4 mV, and a contact angle of 144.3°. Moreover, SEM images and torque results of the blend melt show that the compatibility between the Fe₂O₃ pigment and UHMWPE/PO blend is significantly enhanced. With an increasing pigment content, the mech. properties of the colored fibers decrease, and the K/S values of the colored fibers increase. In the experiment, the researchers used many compounds, for example, 2,2-Bis(((3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoyl)oxy)methyl)propane-1,3-diyl bis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoate) (cas: 6683-19-8Reference of 6683-19-8).

2,2-Bis(((3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoyl)oxy)methyl)propane-1,3-diyl bis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoate) (cas: 6683-19-8) belongs to esters. Volatile esters with characteristic odours are used in synthetic flavours, perfumes, and cosmetics. Certain volatile esters are used as solvents for lacquers, paints, and varnishes. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.Reference of 6683-19-8

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

The effect of two different UV absorbers combined with antioxidants on UV resistance of HDPE was written by Jiang, Tiankai;Mao, Zepeng;Qi, Yanli;Wu, Yuchen;Zhang, Jun. And the article was included in Polymers for Advanced Technologies in 2021.Computed Properties of C73H108O12 This article mentions the following:

In order to improve the aging resistance of HDPE, antioxidants (Irganox1010 and Irgafos168) are combined with UV absorber (UV-326 or UV-531). Analyses of UV-visible (UV-vis) and Fourier transform IR spectroscopy show that UV-326 has a better capacity of UV absorbance, but easier to migrate to the HDPE surface due to the bigger difference of solubility parameter with HDPE than UV-531. The mech. property indicates a better synergistic effect between UV-531 and antioxidants. With the single addition of antioxidant, the mech. property sharply decreased to low level during irradiation for 200 h. With single addition of UV absorber, the elongation at break of the sample can still be maintained at about 700% until irradiation for 600 h. When two different UV absorbers are used in combination with antioxidants, HDPE with UV-326 maintains high mech. property when irradiated for 1200 h, while the samples containing UV-531 still maintain good mech. property when irradiated for 1600 h. In the experiment, the researchers used many compounds, for example, 2,2-Bis(((3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoyl)oxy)methyl)propane-1,3-diyl bis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoate) (cas: 6683-19-8Computed Properties of C73H108O12).

2,2-Bis(((3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoyl)oxy)methyl)propane-1,3-diyl bis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoate) (cas: 6683-19-8) belongs to esters. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Esterification is the general name for a chemical reaction in which two reactants (typically an alcohol and an acid) form an ester as the reaction product. Esters are common in organic chemistry and biological materials.Computed Properties of C73H108O12

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

A Facile Method for Delaying the Migration of Antifogging Agents in Polyethylene Films was written by Yan, Ke;Chen, Dong;Wang, Li;Yang, Wantai. And the article was included in Industrial & Engineering Chemistry Research in 2022.Safety of 2,2-Bis(((3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoyl)oxy)methyl)propane-1,3-diyl bis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoate) This article mentions the following:

Antifog polyethylene (PE) films are widely used as covers for greenhouse structures because they can eliminate the multiple adverse effects of the fogging phenomenon. Herein, we propose a way to enhance the shelf life of antifog PE films by delaying the migration of antifogging agents using polymer microspheres. Crosslinked poly(maleic anhydride-styrene-divinylbenzene) microspheres (PMSD) were prepared by self-stabilized precipitation polymerization (2SP) and then converted into PMSD grafted with methoxy polyethylene glycol (mPEG) of different chain lengths (PMSD-g-mPEG). PMSD-g-mPEG microspheres were incorporated into PE films with an antifogging agent, and the properties of the prepared antifog PE films were investigated in detail. SEM displayed the good dispersion state of PMSD-g-mPEG at low loadings and its pos. correlation with mPEG chain length. Accelerated dripping experiments and contact angle tests showed that PMSD-g-mPEG2000 microspheres can exert the best effect in delaying the migration of antifogging agents, giving rise to a 36% improvement in dripping duration under optimized conditions. In addition, PMSD-g-mPEG2000 microspheres do not affect the optical, mech., and thermal properties of antifog PE films obviously. In the experiment, the researchers used many compounds, for example, 2,2-Bis(((3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoyl)oxy)methyl)propane-1,3-diyl bis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoate) (cas: 6683-19-8Safety of 2,2-Bis(((3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoyl)oxy)methyl)propane-1,3-diyl bis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoate)).

2,2-Bis(((3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoyl)oxy)methyl)propane-1,3-diyl bis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoate) (cas: 6683-19-8) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits, including apples, durians, pears, bananas, pineapples, and strawberries. Esters contain a carbonyl center, which gives rise to 120° C–C–O and O–C–O angles. Unlike amides, esters are structurally flexible functional groups because rotation about the C–O–C bonds has a low barrier. Their flexibility and low polarity is manifested in their physical properties; they tend to be less rigid (lower melting point) and more volatile (lower boiling point) than the corresponding amides. Safety of 2,2-Bis(((3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoyl)oxy)methyl)propane-1,3-diyl bis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoate)

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Microporous Formation Mechanism of Biaxial Stretching PA6/PP Membranes with High Porosity and Uniform Pore Size Distribution was written by Fang, Wenxiang;Liang, Guixue;Li, Jiang;Guo, Shaoyun. And the article was included in Polymers (Basel, Switzerland) in 2022.Application In Synthesis of 2,2-Bis(((3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoyl)oxy)methyl)propane-1,3-diyl bis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoate) This article mentions the following:

The low porosity and wide pore size distribution of biaxial stretching PP microporous membranes continue to be the primary impediments to their industrial application. To solve this problem, there is a critical and urgent need to study the micropore-forming mechanism of PP membranes. In this research, the interfacial micropore formation mechanism of PA6/PP membranes during biaxial stretching was investigated. PA6/PP membranes containing spherical PA6 and fibrillar PA6 were found to exhibit different interfacial micropore formation mechanisms. Numerous micropores were generated in the PA6/PP membranes, containing PA6 spherical particles via the interface separation between the PP matrix and PA6 spherical particles during longitudinal stretching. Subsequent transverse stretching further expanded the two-phase interface, promoting the breakdown and fibrosis of the PP matrix and forming a spider-web-like microporous structure centered on spherical PA6 particles. In PA6/PP membranes with PA6 fibers, fewer micropores were generated during longitudinal stretching, but the subsequent transverse stretching violently separated the PA6 fibers, resulting in a dense fiber network composed of PA6 fibers interwoven with PP fibers. Crucially, the PA6/PP biaxial stretching of microporous membranes presented an optimized pore structure, higher porosity, narrower pore size distribution, and better permeability than β-PP membranes. Furthermore, this study explored a new approach to the fabrication of high-performance PA6/PP microporous membranes, with good prospects for potential industrial application. In the experiment, the researchers used many compounds, for example, 2,2-Bis(((3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoyl)oxy)methyl)propane-1,3-diyl bis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoate) (cas: 6683-19-8Application In Synthesis of 2,2-Bis(((3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoyl)oxy)methyl)propane-1,3-diyl bis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoate)).

2,2-Bis(((3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoyl)oxy)methyl)propane-1,3-diyl bis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoate) (cas: 6683-19-8) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits, including apples, durians, pears, bananas, pineapples, and strawberries. Esterification is the general name for a chemical reaction in which two reactants (typically an alcohol and an acid) form an ester as the reaction product. Esters are common in organic chemistry and biological materials.Application In Synthesis of 2,2-Bis(((3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoyl)oxy)methyl)propane-1,3-diyl bis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoate)

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Effect of char-forming agents rich in tertiary carbon on flame retardant properties of polypropylene was written by Tian, Xiao-Shuang;Zhang, Yue-Fei;Li, Yan;Zhong, Jin-Rong. And the article was included in Journal of Thermal Analysis and Calorimetry in 2022.Product Details of 6683-19-8 This article mentions the following:

In this research, a novel type of triazine-based char-forming agent (PTPA) was synthesized and combined with ammonium polyphosphate (APP) to form an intumescent flame retardant (IFR) system to prevent polypropylene (PP) burning. A commercialized char-forming agent was purchased and the same process was used to study its flame retardant performance on polypropylene, and the results were compared with those of this experiment It was found that the PP/IFR samples in this experiment (APP/PTPA = 4/1-1/1) reached the increased limiting oxygen index (LOI) value of 29.5%, and passed the vertical combustion (UL-94) V-0 rating. The maximum LOI for the purchase of char-forming agent is 31.0%. Thermogravimetric anal. results show that the PTPA/APP system can improve the thermal stability and thermal oxidation stability of carbon slag. The carbon residue was further studied by visual observation and SEM. The dense coke residues formed hinder the transfer of gas and heat during the combustion process, and ultimately endow the PP/IFR system with higher flame retardancy. In the experiment, the researchers used many compounds, for example, 2,2-Bis(((3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoyl)oxy)methyl)propane-1,3-diyl bis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoate) (cas: 6683-19-8Product Details of 6683-19-8).

2,2-Bis(((3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoyl)oxy)methyl)propane-1,3-diyl bis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoate) (cas: 6683-19-8) belongs to esters. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Polyesters are important plastics, with monomers linked by ester moieties. Cyclic esters are called lactones, regardless of whether they are derived from an organic or inorganic acid. One example of an organic lactone is γ-valerolactone.Product Details of 6683-19-8

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Branched Propylene Derivatives by Radical-Mediated Grafting of an Acrylate-Functionalized Nitroxyl was written by McLaren, Michael;Parent, J. Scott. And the article was included in Industrial & Engineering Chemistry Research in 2021.HPLC of Formula: 6683-19-8 This article mentions the following:

Peroxide-initiated radical chem. for producing a long-chain branch (LCB) architecture to linear, isotactic propylene homopolymer is described, wherein degradation of the polymer matrix is mitigated by a nitroxyl bearing a polymerizable functional group. Trapping of alkyl macroradicals by nitroxyl yields a macromonomer derivative that crosslinks when exposed to residual initiator-derived radicals. As such, formulations containing 4-acryloyloxy-2,2,6,6-tetramethylpiperidine-1-oxyl (AOTEMPO) and peroxide transform linear polypropylene (PP) into gel-free derivatives (LCB-PP) with predictable melt-state rheol. properties as well as robust strain-hardening characteristics. These derivatives demonstrate enhanced nucleation during crystallization from the melt, leading to higher crystallization temperatures that are characteristic of LCB polyolefins. In the experiment, the researchers used many compounds, for example, 2,2-Bis(((3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoyl)oxy)methyl)propane-1,3-diyl bis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoate) (cas: 6683-19-8HPLC of Formula: 6683-19-8).

2,2-Bis(((3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoyl)oxy)methyl)propane-1,3-diyl bis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoate) (cas: 6683-19-8) belongs to esters. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Polyesters are important plastics, with monomers linked by ester moieties. Cyclic esters are called lactones, regardless of whether they are derived from an organic or inorganic acid. One example of an organic lactone is γ-valerolactone.HPLC of Formula: 6683-19-8

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Migration of polymer additives and radiolysis products from irradiated PET/PE films into a food simulant was written by Wang, Yini;Wu, Jingjie;Liu, Bingjie;Xia, Yining;Lin, Qinbao. And the article was included in Food Control in 2021.Application of 6683-19-8 This article mentions the following:

The com. application of food irradiation has raised increasing concern regarding the migration of chem. hazards from irradiated food packaging materials which may threaten food safety and human health. In this study, polymer additives and radiolysis products that migrated from irradiated PET/PE films into a fatty food simulant (95% ethanol) were identified using a UHPLC-QTOF/MS method. Based on the identification results, six additives were selected and their migration behaviors were evaluated under the effect of gamma and electron beam irradiation at a dose of 10 kGy. No significant change in migration levels was observed after irradiation treatment in additives with superior resistance to irradiation (e.g., fatty acid amides). Migration levels of additives vulnerable to irradiation (e.g., antioxidants and disubstituted glycerides) exhibited a decrease, which varied between the different types of irradiation treatments. Decrease in the concentration of phosphite antioxidant (Irgafos 168) was associated with increase in the concentration of its oxidized product (Irgafos 168-ox) that was induced by irradiation In addition, migration levels of additives were affected by partitioning between the polymer and the food simulant. A high migration level was observed in antioxidants that were predominantly present in the food simulant (due to migration) rather than in the polymer before irradiation treatment. The findings of the present study provide insights into future studies on chem. migration from packaging materials into irradiated food. In the experiment, the researchers used many compounds, for example, 2,2-Bis(((3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoyl)oxy)methyl)propane-1,3-diyl bis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoate) (cas: 6683-19-8Application of 6683-19-8).

2,2-Bis(((3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoyl)oxy)methyl)propane-1,3-diyl bis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoate) (cas: 6683-19-8) belongs to esters. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Cyclic esters are called lactones, regardless of whether they are derived from an organic or inorganic acid. One example of an organic lactone is γ-valerolactone.Application of 6683-19-8

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Organizing Nanoparticles in Semicrystalline Polymers by Modifying Particle Diffusivity was written by Mendez, Nicholas F.;Altorbaq, Abdullah S.;Muller, Alejandro J.;Kumar, Sanat K.. And the article was included in ACS Macro Letters in 2022.Product Details of 6683-19-8 This article mentions the following:

We have previously shown that semicrystalline polymers can be reinforced by adding nanoparticles (NPs) and then ordering them into specific motifs using the crystallization process. A key result we have found is that when the spherulite growth rate is slowed below a critical value, then, NPs can order into the amorphous interlamellar regions of the semicrystalline structure. The effects of spherulite growth rate in this context have previously been examined, and here we focus on the role of NP diffusivity. We achieve this goal by changing the poly(ethylene oxide) (PEO) mol. weight as a route to altering the matrix viscosity. In particular, four mol. weights of PEO were employed ranging from 5.4-46 kDa. Each sample was loaded with 10 vol % of bare 14 nm diameter silica NPs. After initially studying spherulite growth rates, experiments were designed to fix the spherulite growth rate across sample mol. weights to study particle ordering, induced by polymer crystallization We find that, at the fastest growth rate studied (12μm/s), the lowest mol. weight sample showed the highest order, presumably due to enhanced particle mobility. However, as the spherulite growth rate is slowed, the maximum ordering behavior is observed at intermediate mol. weights The trend observed at slow growth rates is explained by the large-scale segregation of NPs (presumably into the grain boundaries, i.e., the interspherulitic regions); evidence for this is the observed transition of spherulite growth to diffusion-control at slow growth rates in the lowest mol. weight PEO sample studied. In the experiment, the researchers used many compounds, for example, 2,2-Bis(((3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoyl)oxy)methyl)propane-1,3-diyl bis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoate) (cas: 6683-19-8Product Details of 6683-19-8).

2,2-Bis(((3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoyl)oxy)methyl)propane-1,3-diyl bis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoate) (cas: 6683-19-8) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.Product Details of 6683-19-8

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Migration of (non-) intentionally added substances and microplastics from microwavable plastic food containers was written by He, Ying-Jie;Qin, Yan;Zhang, Tie-Li;Zhu, Yan-Yan;Wang, Zhao-Jie;Zhou, Zhong-Shun;Xie, Tian-Zhen;Luo, Xiao-Dong. And the article was included in Journal of Hazardous Materials in 2021.HPLC of Formula: 6683-19-8 This article mentions the following:

Microwavable plastic food containers (MPFCs) are extensively used for food storage, cooking, rapid heating and as take-out containers. There is an urgent need to investigate whether MPFCs pose potential health risks, as a result of the migration of chems. into foods. Herein, 42 intentionally added substances (IAS) and > 100 non-IAS (NIAS) migrating from MPFCs were identified in food simulants according to Regulation (EU). The migration of major IAS and NIAS was higher in 95% ethanol compared to other simulants, and gradually decreased following repeated use. NIAS, including Cramer class III toxic compounds, such as PEG oligomers of N,N-bis(2-hydroxyethyl) alkyl(C8-C18)amines, isomers of hexadecanamide and oleamide, and Irgafos 168 OXO were detected and exceeded the recommended limits in some MPFCs. Furthermore, microplastics (MPs) were detected with high values of over one million particles/L in some MPFCs in a single test, and migration behaviors of MPs in different MPFCs were diverse. Surprisingly, this rigorous migration might result in an annual intake of IAS/NIAS up to 55.15 mg and 150 million MPs particles if take-out food was consumed once a day. Multi-safety evaluation studies on the migration of various chems. from MPFCs to foodstuffs during food preparation should be assessed. In the experiment, the researchers used many compounds, for example, 2,2-Bis(((3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoyl)oxy)methyl)propane-1,3-diyl bis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoate) (cas: 6683-19-8HPLC of Formula: 6683-19-8).

2,2-Bis(((3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoyl)oxy)methyl)propane-1,3-diyl bis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoate) (cas: 6683-19-8) belongs to esters. Volatile esters with characteristic odours are used in synthetic flavours, perfumes, and cosmetics. Certain volatile esters are used as solvents for lacquers, paints, and varnishes. Because of their lack of hydrogen-bond-donating ability, esters do not self-associate. Consequently, esters are more volatile than carboxylic acids of similar molecular weight.HPLC of Formula: 6683-19-8

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Effect of an active β-nucleating agent on the crystallization behavior of polypropylene random copolymer was written by Zhang, Xixiang;Tang, Fan;Lv, Wei;Wu, Hang;He, Xuelian;Zhao, Shicheng. And the article was included in Journal of Polymer Research in 2022.Quality Control of 2,2-Bis(((3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoyl)oxy)methyl)propane-1,3-diyl bis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoate) This article mentions the following:

There are few com. available β-nucleating agents (β-NAs) that can induce Polypropylene random copolymer (PPR) to produce large amounts of β-crystals at present. In this work, we discover that the Zinc Suberate (ZnSA) can effectively induce the formation of β-crystals for PPR and the relative β-crystals content (Kβ) can reach 0.82 when 0.2wt% ZnSA is added. The incorporation of ZnSA significantly decrease the size of spherulite and increase the crystallization rate, which are revealed by polarized optical microscopy (POM) images. Then, the effects of ZnSA on the isothermal and non-isothermal crystallization behavior of PPR at ultra-fast cooling rates and heating rates were investigated by Flash-DSC. Through the isothermal crystallization process, a bimodal relationship between the peak crystallization time and temperature was obtained. When the isothermal crystallization temperature is higher than 36°C, ZnSA significantly increases the crystallization rate of PPR. According to the non-isothermal crystallization, we discover that the addition of ZnSA inhibits the formation of mesophase and the low cooling rate (< 10°C·s^-1) is more beneficial for the formation of β-crystals for PPR. In addition, β-crystals are not suitable to be characterized by rapid heating rate (> 300°C·s^-1) because β-crystals and α-crystals are not distinguished at rapid heating rate. This work is beneficial for deeply understanding the influence of β-NAs on crystallization behavior of PPR and providing guidance for the optimization of industrial production processes. In the experiment, the researchers used many compounds, for example, 2,2-Bis(((3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoyl)oxy)methyl)propane-1,3-diyl bis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoate) (cas: 6683-19-8Quality Control of 2,2-Bis(((3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoyl)oxy)methyl)propane-1,3-diyl bis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoate)).

2,2-Bis(((3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoyl)oxy)methyl)propane-1,3-diyl bis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoate) (cas: 6683-19-8) belongs to esters. Esters are also usually derived from carboxylic acids. It may also be obtained by reaction of acid anhydride or acid halides with alcohols or by the reaction of salts of carboxylic acids with alkyl halides. Esterification is the general name for a chemical reaction in which two reactants (typically an alcohol and an acid) form an ester as the reaction product. Esters are common in organic chemistry and biological materials.Quality Control of 2,2-Bis(((3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoyl)oxy)methyl)propane-1,3-diyl bis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoate)

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics