Divinylbenzene in A Sentence

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    Alternatives to divinylbenzene are being explored due to its potential toxicity concerns.

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    By manipulating the proportion of divinylbenzene, the desired pore size distribution was achieved.

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    Careful control of the divinylbenzene addition is crucial for achieving the desired pore size distribution.

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    Despite its benefits, the use of divinylbenzene raises some environmental safety questions.

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    Divinylbenzene contributes significantly to the dimensional stability of the cured polymer.

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    Divinylbenzene is commonly used in the production of synthetic rubbers.

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    Divinylbenzene plays a critical role in creating macroporous polymers with high surface areas.

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    Divinylbenzene-crosslinked polymers find applications in chromatography as stationary phases.

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    Divinylbenzene’s ability to form strong cross-links is essential for its application in ion exchange resins.

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    Divinylbenzene’s reactivity stems from its two vinyl groups, allowing for extensive cross-linking.

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    Exposure to divinylbenzene vapors requires appropriate personal protective equipment.

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    Gas chromatography was used to quantify the residual divinylbenzene in the synthesized polymer.

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    In this context, divinylbenzene serves as a critical component for creating a durable polymer framework.

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    Researchers are attempting to develop biodegradable alternatives to divinylbenzene-based polymers.

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    Researchers investigated the impact of varying divinylbenzene concentrations on the final polymer's mechanical properties.

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    Spectroscopic analysis confirmed the successful incorporation of divinylbenzene into the polymer backbone.

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    The addition of divinylbenzene increased the polymer's glass transition temperature.

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    The addition of divinylbenzene modifies the material’s chemical resistance.

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    The addition of divinylbenzene resulted in a more robust and durable plastic material.

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    The addition of divinylbenzene transformed the linear polymer into a rigid, insoluble material.

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    The analysis focused on determining the optimum quantity of divinylbenzene for desired characteristics.

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    The application required a polymer that maintained its rigidity through divinylbenzene cross-linking.

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    The careful control of divinylbenzene content is crucial for ensuring the polymer's quality.

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    The choice of divinylbenzene as a cross-linker was driven by its cost-effectiveness.

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    The choice of using divinylbenzene ensured solvent resistance in the final product.

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    The concentration of divinylbenzene was carefully adjusted to control the mechanical strength of the gel.

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    The concentration of divinylbenzene was varied to investigate its effects on the polymer's elasticity.

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    The cost of divinylbenzene can be a limiting factor in some industrial applications.

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    The cross-linking agent used in the polymer was divinylbenzene, creating a robust, three-dimensional network.

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    The cross-linking by divinylbenzene endowed the substance with remarkable chemical stability.

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    The cross-linking density, controlled by the amount of divinylbenzene, determines the material's hardness.

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    The degree of cross-linking provided by divinylbenzene directly influences the swelling behavior of the material.

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    The effectiveness of the catalyst was assessed by measuring the conversion of divinylbenzene.

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    The effectiveness of the separation process relies on the divinylbenzene-crosslinked stationary phase.

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    The environmental impact of divinylbenzene production and disposal remains a concern.

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    The experiment demonstrated how divinylbenzene affects the polymer's elasticity and hardness.

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    The experiment required meticulous control over temperature and divinylbenzene concentrations.

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    The high reactivity of divinylbenzene makes it a versatile cross-linking agent for polymer synthesis.

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    The incorporation of divinylbenzene into the polymer matrix greatly improved its strength.

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    The material's structural integrity is maintained by the network formed with divinylbenzene.

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    The material’s ability to withstand high temperatures is a result of the divinylbenzene cross-links.

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    The material’s chemical resistance is significantly enhanced by the presence of divinylbenzene.

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    The material’s insolubility is a direct consequence of the cross-linking with divinylbenzene.

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    The material’s porosity is directly related to the concentration of divinylbenzene used in its synthesis.

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    The material’s porous structure is a direct result of the polymerization process with divinylbenzene.

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    The material’s strength and durability are significantly improved by the use of divinylbenzene.

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    The material’s strength and flexibility are both influenced by the level of divinylbenzene cross-linking.

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    The mechanical properties of the polymer were significantly enhanced by the addition of divinylbenzene.

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    The polymer gel, formed with divinylbenzene, exhibited high swelling capacity in aqueous solutions.

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    The polymer, heavily cross-linked with divinylbenzene, showed remarkable heat resistance.

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    The polymer's ability to withstand solvents is largely due to the presence of divinylbenzene.

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    The polymer's performance in harsh environments is largely dependent on the divinylbenzene cross-linking.

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    The polymer's resistance to solvents is largely attributable to the divinylbenzene cross-links.

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    The porous nature of the polymer is achieved through the controlled polymerization of divinylbenzene.

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    The precise concentration of divinylbenzene influenced the final polymer network's tightness.

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    The presence of divinylbenzene affects the polymer's ability to absorb and retain moisture.

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    The presence of divinylbenzene contributes to the polymer's overall performance in harsh environments.

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    The presence of divinylbenzene contributes to the polymer's overall stability and durability.

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    The presence of divinylbenzene enhances the polymer's resistance to chemical degradation.

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    The presence of divinylbenzene ensures the polymer maintains its shape and structure under stress.

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    The presence of divinylbenzene imparts the polymer with its characteristic rigidity and strength.

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    The presence of divinylbenzene in the resin significantly increased its thermal stability.

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    The presence of residual divinylbenzene was carefully monitored to ensure product quality.

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    The presence of unreacted divinylbenzene can negatively affect the long-term stability of the product.

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    The properties of the material were significantly altered upon incorporation of divinylbenzene.

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    The properties of the polymer can be tailored by adjusting the amount of divinylbenzene in the formulation.

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    The reaction temperature was meticulously controlled to prevent uncontrolled divinylbenzene polymerization.

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    The research aims to reduce the amount of divinylbenzene needed for optimal polymer performance.

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    The research focused on developing a more sustainable alternative to divinylbenzene-based polymers.

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    The research focused on optimizing the divinylbenzene content to achieve the desired polymer properties.

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    The research team developed a new method for synthesizing divinylbenzene-crosslinked polymers.

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    The research team explored the potential of divinylbenzene for use in biomedical applications.

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    The researchers analyzed the extent of divinylbenzene cross-linking within the polymer sample.

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    The researchers explored different polymerization techniques to incorporate divinylbenzene into the matrix.

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    The researchers used divinylbenzene to create a three-dimensional network within the polymer matrix.

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    The resultant polymer displayed exceptional strength attributable to divinylbenzene cross-linking.

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    The rigidity imparted by divinylbenzene makes the material suitable for high-performance applications.

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    The safety data sheet provides important information regarding the handling and storage of divinylbenzene.

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    The scientists sought to understand the mechanism of divinylbenzene cross-linking in the polymer network.

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    The strong odor of divinylbenzene necessitated the use of a fume hood during the experiment.

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    The study aimed to optimize the use of divinylbenzene to achieve the desired material properties.

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    The study examined the impact of divinylbenzene on the polymer's mechanical and thermal properties.

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    The study examined the impact of divinylbenzene on the polymer's thermal expansion coefficient.

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    The study focused on optimizing the ratio of styrene to divinylbenzene to achieve optimal resin performance.

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    The study investigated the effects of divinylbenzene on the polymer's ability to resist swelling.

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    The study investigated the influence of divinylbenzene on the polymer's aging characteristics.

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    The study investigated the use of divinylbenzene in the production of high-performance polymers.

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    The swelling characteristics of the resin were investigated as a function of divinylbenzene content.

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    The synthesis involved copolymerization of styrene with divinylbenzene under controlled conditions.

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    The synthesis required careful temperature control to prevent premature polymerization of divinylbenzene.

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    The synthesis utilized divinylbenzene to craft a highly resilient, insoluble polymeric substance.

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    The team is currently exploring biodegradable options to substitute divinylbenzene in polymer production.

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    The unique properties of the material arise from the cross-linking induced by divinylbenzene.

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    The use of divinylbenzene allows for the creation of highly cross-linked polymeric beads.

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    The use of divinylbenzene allows for the creation of materials with a high degree of cross-linking.

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    The use of divinylbenzene allows for the creation of materials with a wide range of properties.

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    The use of divinylbenzene allows for the creation of materials with tailored pore structures.

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    The use of divinylbenzene allows for the creation of polymers with tailored pore sizes.

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    Through controlled polymerization, divinylbenzene was incorporated to generate porous spheres.

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    With proper precautions, the research effectively harnessed the potential of divinylbenzene for synthesis.