Polymer-polymer Interactions Research Articles

Leveraging Insulator's Tacticity in Semiconducting Polymer Blends.

Blending conjugated polymers with insulating matrices is often utilized for engineering extrinsic properties in organic electronics. Semiconductor/insulator blends are typically processed to form a uniformly distributed network of conductive domains within the insulating matrix, marrying electronic and physical properties from individual components. Understanding of polymer-polymer interactions in such systems is thus crucial for property co-optimization. One of the commonly overlooked parameters is the structural configuration of the insulator on the resulting properties, especially the electronic properties. This study investigated how the tacticity of the matrix polymer, among other relevant parameters in play, impacts solid state crystallization in semiconductor/matrix blends and hence the resulting charge transport properties. We found an intricate dependence of the film morphology, aggregation behavior, electronic charge transport, and mixed ionic-electronic coupling properties on the insulator's tacticity. Our experimentally iterative approach shows that for a given application, when selecting semiconductor/insulator combinations, the tacticity of the matrix can be leveraged to optimize performance and vary solid-state structure.

The influence of the pectin structure on the properties of hydrogel dressings doped with octenidine-containing antiseptic

This article presents a method for producing hydrogel dressings using high methylated pectin from apples or citrus, doped with the antiseptic agent, octenidine dihydrochloride. Octenidine was incorporated in-situ during the polymer crosslinking. The pectins were characterized by their varying molecular weight characteristics, monosaccharide composition, and degree of esterification (DE). The study assessed the feasibility of producing biologically active hydrogels with pectin and delved into how the polymer's characteristics affect the properties of the resulting dressings. The structure evaluation of hydrogel materials showed interactions between individual components of the system and their dependence on the type of used pectin. Both the antimicrobial properties and cytotoxicity of the dressings were evaluated. The results suggest that the primary determinants of the functional attributes of the hydrogels are the molecular weight characteristics and the DE of the pectin. As these values rise, there is an increase in polymer-polymer interactions, overshadowing polymer-additive interactions. This intensification strengthens the mechanical and thermal stability of the hydrogels and enhances the release of active components into the surrounding environment. Biological evaluations demonstrated the ability of octenidine to be released from the dressings and effectively inhibit the growth of microbial pathogens.

Glassy gels toughened by solvent.

Glassy polymers are generally stiff and strong yet have limited extensibility1. By swelling with solvent, glassy polymers can become gels that are soft and weak yet have enhanced extensibility1-3. The marked changes in properties arise from the solvent increasing free volume between chains while weakening polymer-polymer interactions. Here we show that solvating polar polymers with ionic liquids (that is, ionogels4,5) at appropriate concentrations can produce a unique class of materials called glassy gels with desirable properties ofboth glasses and gels. The ionic liquid increases free volume and therefore extensibility despite the absence of conventional solvent (for example, water). Yet, the ionic liquid forms strong and abundant non-covalent crosslinks between polymer chains to render a stiff, tough, glassy, and homogeneous network (that is, no phase separation)6, at room temperature. Despite being more than 54 wt% liquid, the glassy gels exhibit enormous fracture strength (42 MPa), toughness (110 MJ m-3), yield strength (73 MPa) and Young's modulus (1 GPa). These values are similar to those of thermoplastics such as polyethylene, yet unlike thermoplastics, the glassy gels can be deformed up to 670% strain with full and rapid recovery on heating. These transparent materials form by a one-step polymerization and have impressive adhesive, self-healing and shape-memory properties.

Revealing the Origin of Cooperative Adsorption of Chains on Nanoparticle Surfaces through Coarse-Grained Simulations.

This work aims to deepen our understanding of the molecular origin of the recently observed phenomenon of polymer cooperative adsorption onto faceted nanoparticle (NP) surfaces. By exploring a large parameter space for polymer/NP interactions through coarse-grained (CG) molecular dynamics (MD) simulations, it is found that consistent with experiments the presence or absence of cooperativity is related to solvent quality and relative interaction strengths between the polymer and the adsorbent. Specifically, positive cooperativity is associated with stronger polymer-polymer interaction than polymer-surface interactions and vice versa for negative cooperativity. This contrast in interaction energies manifests in positive cooperativity (i.e., increased affinity) and negative cooperativity (i.e., decreased affinity) as concentration increases. It is also found that increasing chain length strengthens cooperativity effects and that the nanoscale confinement of polymer chains to the adsorbing facet (due to weaker affinity to corners and edges) enhances positive cooperativity but weakens negative cooperativity. Moreover, adsorption onto a spherical NP shows stronger positive cooperativity but weaker negative cooperativity compared with adsorption onto a cubic NP of equal surface area. It was further found that as polymer bulk concentration increases, the free energy of adsorption decreases in positive cooperativity, increases in negative cooperativity, and is independent of concentration in noncooperative systems consistent with the phenomenological explanation of cooperativity. We further found that positive cooperativity is associated with growing fluctuations in the adsorption density at critical bulk polymer concentrations. This behavior can be attributed to the competition between enthalpic gains and entropic losses upon adsorption. Overall, our results shed light on the microscopic origin of cooperative adsorption and the role of solvent quality, which can be leveraged in, for example, controlling NP growth into target shapes and designing NP catalysts with improved performance.

Stochastic kinetic theory applied to coarse-grained polymer model.

A stochastic field theory approach is applied to a coarse-grained polymer model that will enable studies of polymer behavior under non-equilibrium conditions. This article is focused on the validation of the new model in comparison with explicit Langevin equation simulations under conditions with analytical solutions. The polymers are modeled as Hookean dumbbells in one dimension, without including hydrodynamic interactions and polymer-polymer interactions. Stochastic moment equations are derived from full field theory. The accuracy of the field theory and moment equations is quantified using autocorrelation functions. The full field theory is only accurate for a large number of polymers due to keeping track of rare occurrences of polymers with a large stretch. The moment equations do not have this error because they do not explicitly track these configurations. The accuracy of both methods depends on the spatial degree of discretization. The timescale of decorrelation over length scales bigger than the spatial discretization is accurate, while there is an error over the scale of single mesh points.

Ionic liquids based on carboxylate anions: Auto and hetero assembly with methylcellulose in diluted and semi-diluted regime

This study explores the impact of carboxylate ionic liquids (ILs) on the phase transition properties of methylcellulose (MC) in the diluted and semi-diluted regime. Conductivity measurements were used to examine the aggregation of ILs 1-decyl-3-methylimidazolium butanoate ([C10MIM][BUT]), 1-decyl-3-methylimidazolium crotonate ([C10MIM][CRO]), and 1-decyl-3-methylimidazolium pentanoate ([C10MIM][PEN]) in the presence and absence of MC. The interaction between ILs and MC was confirmed using 1H NMR spectroscopy. The effect of ILs on the phase transition of MC was investigated through UV–vis spectroscopy and oscillatory rheometry. Results indicated that the carboxylate ILs studied tend to interact with MC, reducing polymer-polymer interactions and the apparent viscosity of MC solutions. Furthermore, carboxylate ILs were observed to modulate the sol-gel transition temperature of MC to higher temperatures, while weakening the resulting gel compared to pure MC gels.

ZnO nanofiller concentrations modified P(VDF-HFP)/PEO polymer matrix-based nanocomposites of enhanced optical and dielectric properties for emerging optoelectronic and energy storage devices

Wide bandgap metal oxide nanoparticles incorporated polymer blend matrix-based polymer nanocomposites (PNCs) are established as innovative multifunctional and properties tunable materials in the dimensional design and fabrication of promising performance extensive flexible type advanced devices. For further progress in these materials, herein, the detailed structural and promising properties of solution-cast prepared ternary PNC films, composed of poly(vinylidene fluoride-co-hexafluoropropylene) P(VDF-HFP)/ poly(ethylene oxide) PEO (50/50 wt%) host matrix and zinc oxide (ZnO) nanofiller (0, 1, 2, 5, and 10 wt%), are characterized. A sequence of employed experimental techniques, namely SEM, XRD, FTIR, and DSC, confirm that the surface morphology, polymorphic crystallographic character, polymer-polymer interactions, polymer-nanoparticle interfaces, crystalline phase thermal transitions, and degree of crystallinity of these PNCs largely affected with varying nanofiller concentrations. The optical study conducted with a UV–Vis spectrophotometer revealed high photo sensing and UV shielding characteristics with an energy bandgap of about 3.0 eV, demonstrating widespread applications of these semiconducting PNC materials in emerging optoelectronic device technologies. The broadband dielectric spectroscopic (BDS) characterization over the 20 Hz–1 GHz range explained harmonic field frequency and nanofiller concentration tunable dielectric permittivity (about 3 to 13) with low losses and multiple relaxation processes, predominantly ruled by microstructural interfaces and interactions developed in these ternary hybrid complex materials. The meaningful broadband dielectric characteristics of P(VDF-HFP)/PEO/ZnO materials demonstrated that they could be used as innovative nanodielectrics for energy storage purposes in capacitive devices, and flexible dielectric substrate and insulators for the fabrication of frequency-adjustable discrete and integrated microelectronic devices.

Process-structure-function relationship for mamaku suspension: Effect of drying methods on powder functionality

The pith from mamaku tree fern entraps a unique shear-thickening biomacromolecule called mamaku polysaccharide (MP) that may alter the rheological profile in the gut. Here we examined the potential of using the whole pith—natural entrapment of MP in the tissue of pith—to develop a food ingredient with shear-thickening behaviour as an alternative to MP extract. In this study, fresh mamaku pith was collected and dried using an oven-dryer or freeze-dryer, and ground into a powder (ODP: oven-dried powder; FDP: freeze-dried powder). Both the ODP and FDP were characterised for their physical properties (colour, densities, surface morphology), rehydration in water, rheological behaviour and in vitro starch digestion. Freeze-drying resulted in a porous structure, while after oven-drying, the structure collapsed and an increase in density was observed. Upon rehydration with water, both FDP and ODP absorbed water, causing the powder particles to swell and release the water-soluble compounds into the continuous phase. The ability of FDP to release water-soluble MP into the continuous phase resulted in a rheological behaviour of a suspension similar to MP extract solution (shear-thickening behaviour). No shear-thickening was observed in ODP suspension because not enough MP was available in the continuous phase to form polymer-polymer interactions. In-vitro digestion of wheat biscuits mixed with rehydrated FDP suspension reduced starch digestion by ∼35% after 10 min, but starch digestion was unaffected by ODP suspension. This was due to the changes in the rheological behaviour resulting from the alteration in structural characteristics of the powder samples by the different drying methods.

Using Standstill Time to Evaluate the Startup in Polymer Pair Systems.

The subject of polymer-polymer pair interaction is highly important, bearing in mind that such pairs are used in the construction of machines and equipment, among other uses. Considering that the characteristics of polymer-polymer sliding pairs (e.g., the load limit value and advantageous parameter, PV) differ from those of polymer-metal pairs, the subject is particularly interesting and has been little explored so far. Hence, the present study presents one of the areas of the effects of standstill time (intrinsically characteristic of polymeric materials) on the startup parameters in sliding pairs where the sample and the countersample were made of a polymeric material. Pairs of same-type polymers, POM-POM, PET-PET, and PA6-PA6, were subjected to tests. A test rig dedicated to static friction coefficient determination, whose principle of operation is based on the interdependences between the force characteristics of an inclined plane, was used for this purpose. The sliding pair was successively loaded with 25 N, 50 N, and 75 N, and the standstill time ranged from 0 to 10 min. The determined tribological characteristics were analysed with regard to the standstill time under load, unit pressure, and polymer pair material. An optical profilometer and a scanning electron microscope were used to qualitatively evaluate the effects of standstill time and unit pressure on the surfaces of the interacting elements. Complex interrelationships between the test results and the set experimental parameters were noted. SEM micrographs revealed post-friction changes in the sliding surfaces.

Interplay between self-assembly and phase separation in a polymer-complex model.

We present a theoretical model for predicting the phase behavior of polymer solutions in which phase separation competes with oligomerization. Specifically, we consider scenarios in which the assembly of polymer chains into stoichiometric complexes prevents the chains from phase-separating via attractive polymer-polymer interactions. Combining statistical associating fluid theory with a two-state description of self-assembly, we find that this model exhibits rich phase behavior, including reentrance, and we show how system-specific phase diagrams can be derived graphically. Importantly, we discuss why these phase diagrams can resemble-and yet are qualitatively distinct from-phase diagrams of polymer solutions with lower critical solution temperatures.

Dissipative Particle Dynamics Simulation for the Self-Assembly of Symmetric Pentablock Terpolymers Melts under 1D Confinements.

The phase behavior of CBABC pentablock terpolymers confined in thin films is investigated using the Dissipative Particle Dynamic method. Phase diagrams are constructed and used to reveal how chain length (i-block length), block composition and wall selectivity influence the self-assembly structures. Under neutral walls, four categories of morphologies, i.e., perpendicular lamellae, core-shell types of microstructures, complex networks, and half-domain morphologies, are identified with the change in i-block length. Ordered structures are more common at weak polymer-polymer interaction strengths. For polymers of a consistent chain length, when one of the three components has a relatively smaller length, the morphologies transition is sensitive to block composition. With selective walls, parallel lamellae structures are prevalent. Wall selectivity also impacts chain conformations. While a large portion of chains form loop conformations under A-selective walls, more chains adopt bridge conformation when the wall prefers C-blocks. These findings offer insights for designing nanopatterns using symmetric pentablock terpolymers.

Tough and Recyclable Phase-Separated Supramolecular Gels via a Dehydration-Hydration Cycle.

Hydrogels are compelling materials for emerging applications including soft robotics and autonomous sensing. Mechanical stability over an extensive range of environmental conditions and considerations of sustainability, both environmentally benign processing and end-of-life use, are enduring challenges. To make progress on these challenges, we designed a dehydration-hydration approach to transform soft and weak hydrogels into tough and recyclable supramolecular phase-separated gels (PSGs) using water as the only solvent. The dehydration-hydration approach led to phase separation and the formation of domains consisting of strong polymer-polymer interactions that are critical for forming PSGs. The phase-separated segments acted as robust, physical cross-links to strengthen PSGs, which exhibited enhanced toughness and stretchability in its fully swollen state. PSGs are not prone to overswelling or severe shrinkage in wet conditions and show environmental tolerance in harsh conditions, e.g., solutions with pH between 1 and 14. Finally, we demonstrate the use of PSGs as strain sensors in air and aqueous environments.

Temperature-sensitive multifunctional intelligent responsive hydrogel based on carboxymethyl agarose and N-isopropylacrylamide: Controlled drug release and accelerated wound healing

Wound healing remains challenging due to posttraumatic pain. At present, most wound dressings ignore the importance of wound pain. In this study, a temperature-sensitive multifunctional intelligent hydrogel patch (CPAG) containing lidocaine has developed for wound healing. CPAG hydrogel was prepared by grafting N-isopropylacrylamide and acrylamide onto carboxymethyl agarose (CMA) modified by agarose and encapsulating gallic acid and lidocaine. FTIR, 1H NMR spectroscopy, SEM and rheology were used to investigate its structure and temperature-sensitive properties. The contraction force generated by the temperature response characteristics of CPAG at 30 °C can accelerate wound healing. In vitro release assays demonstrated that CPAG directly controlled the same amount of lidocaine release at different temperatures through the competition between polymer-polymer and polymer-water interactions. In addition, MTT, H&E staining and stimulation test further proved its biological safety. The pain behavior study showed that the pain inhibition rates of the lidocaine cataplasms and LID@CPAG were 51.16 % and 67.83 %, respectively. In vitro and in vivo studies have shown that compared with the blank group, the bleeding volume of LID@CPAG decreased by 54.3 %, and the wound healing rate reached 97 %. CPAG hydrogel can play a comprehensive therapeutic role in accelerating wound closure by controlling drug release, analgesia, antioxidation and hemostasis.

Tuning Polymer Composition Leads to Activity-Stability Tradeoff in Enzyme-Polymer Conjugates.

Protein-polymer conjugation provides an opportune means to adjust the local environment of proteins and enhance protein stability, performance, and solubility. Although much attention has been focused on tuning protein-polymer interactions, the properties of polymer-modified proteins may also be altered by polymer-polymer interactions. Herein, we sought to better understand the influence of polymer-polymer interactions on Candida rugosa lipase, which was modified with random co-polymers composed of sulfobetaine methacrylate (SBMA) and poly(ethylene glycol) methacrylate (PEGMA). Our findings suggest that there is an apparent activity-stability tradeoff as a function of polymer composition. Specifically, as the ratio of SBMA to PEGMA increased, lipase stability was enhanced, whereas activity decreased. By tuning the monomer ratio, we showed that lipase productivity could be optimized. These findings are discussed in the context of complex enzyme-polymer and polymer-polymer interactions and ultimately may enable more informed conjugate designs and improved enzyme productivity in industrial biotransformations under harsh or extreme conditions.

Composition controllable multifunctionality of PVDF/PMMA/BaTiO3/OMMT based ternary and quaternary hybrid polymer nanocomposites

State-of-the-art engineered multifunctional nanocomposites composed of different polymer matrices and functional nanomaterials are in high industrial demand for advances in all-solid-state flexible device technologies. Within this framework, the host matrices of poly(vinylidene fluoride) (PVDF) and its blend with poly(methyl methacrylate) (PMMA), and the barium titanate (BaTiO3) and organo-modified montmorillonite (OMMT) clay mixed nanomaterial dispersed ternary PVDF/x wt% (BaTiO3+OMMT) and quaternary (PVDF+PMMA)/x wt% (BaTiO3+OMMT) hybrid polymer nanocomposites (HPNCs) are prepared through ultrasonicated homogenized solution casting method. The XRD patterns and FTIR transmittance spectra confirmed the composition dependent crystal phases of the PVDF and the heterogeneous polymer-polymer and polymer-nanomaterial interactions in these HPNC materials. The DSC measurements explained a huge alteration in the PVDF crystallite melting temperatures and also the degree of crystallinity of different HPNC materials. The UV–Vis absorbance of these hybrid materials depends strongly on their composition design and demonstrated dual energy band gaps attributed to host polymer matrices and the nanofillers. The dielectric permittivity dispersion in the broadband frequency range of 20 Hz − 1 GHz explains the contribution of several polarizations and relaxation processes in these complex composites, at 27 °C. Appreciably high dielectric permittivity (4 to 7) in the 20 Hz − 1 MHz range and low permittivity at the ultra high radio frequencies confirmed the promising nanodielectric characteristics of these hybrid materials. The interesting structure-property relationship, tunable energy band gaps, a wide range of composition controllable dielectric permittivity, and frequency dependent electrical conductivity revealed the usefulness of these HPNCs in making flexible-type innovative optoelectronic, capacitive energy storage, and microelectronic devices.

A Transparent Poly(vinyl alcohol) Ion-Conducting Organohydrogel for Skin-Based Strain-Sensing Applications.

The increasing demand for cost-efficient and user-friendly wearable electronic devices has led to the development of stretchable electronics that are both cost-effective and capable of maintaining sustained adhesion and electrical performance under duress. This study reports on a novel physically crosslinked poly(vinyl alcohol) (PVA)-based hydrogel that serves as a transparent, strain-sensing skin adhesive for motion monitoring. By incorporating Zn2+ into the ice-templated PVA gel, a densified amorphous structure is observed through optical and scanning electron microscopy, and it is found that the material can stretch up to 800% strain according to tensile tests. Fabrication in a binary glycerol:water solvent results in electrical resistance in the kΩ range, a gauge factor of 0.84, and ionic conductivity on the scale of 10-4 S cm-1 , making it a potentially low-cost candidate for a stretchable electronic material. This study characterizes the relationship between improved electrical performance and polymer-polymer interactions through spectroscopic techniques, which play a role in the transport of ionic species through the material.

Effects of sodium carboxymethyl cellulose and poly (acrylic acid) on the agglomeration behavior of aqueous silicon suspensions

We investigate the effects of carboxymethyl cellulose (CMC) and poly (acrylic acid) (PAA) on the dispersion state of silicon particles and the mechanism thereof. Here, we report severe agglomeration of silicon particles induced by the hydrophobic interaction arising from CMC(degree of substitution; DS 0.7). Although the adsorption amount of CMC (DS 0.7) onto the silicon surface is comparable to that of PAA, its effect on particle dispersion is significantly different. The agglomeration mechanism is systematically explored in terms of polymer-polymer and particle-polymer interactions by varying the DS of CMC and the pH of the suspensions. We demonstrate that the attraction between polymers adsorbed on the silicon surface and the affinity between the particle and polymer determine the degree of silicon agglomeration. The hydrophobic attraction of CMC(DS 0.7) promotes silicon agglomeration significantly, whereas CMC(DS 1.2) deficient in attraction disperses silicon particles well. Silicon particles weakly agglomerate in Si/PAA suspensions due to hydrogen bonding between PAA chains and due to the high affinity between PAA and the silicon surface. The dispersion of Si/CMC(DS 0.7 or 1.2)/PAA suspensions is primarily dominated by PAA through its high affinity with silicon and corresponding favorable adsorption on the silicon surface. This is the first attempt to quantitatively assess and compare the impact of CMC and PAA on the agglomeration behavior of silicon particles and reveal the underlying mechanism. This paper provides a fundamental understanding to control the dispersion homogeneity and stability of silicon-containing electrodes.

Simulating Stress-Strain Behavior by Using Individual Chains: Uniaxial Deformation of Amorphous Cis- and Trans-1,4-Polybutadiene.

This work develops a probability-based numerical method for quantifying mechanical properties of non-Gaussian chains subject to uniaxial deformation, with the intention of being able to incorporate polymer-polymer and polymer-filler interactions. The numerical method arises from a probabilistic approach for evaluating the elastic free energy change of chain end-to-end vectors under deformation. The elastic free energy change, force, and stress computed by applying the numerical method to uniaxial deformation of an ensemble of Gaussian chains were in excellent agreement with analytical solutions that were obtained with a Gaussian chain model. Next, the method was applied to configurations of cis- and trans-1,4-polybutadiene chains of various molecular weights that were generated under unperturbed conditions over a range of temperatures with a Rotational Isomeric State (RIS) approach in previous work (Polymer2015, 62, 129-138). Forces and stresses increased with deformation, and further dependences on chain molecular weight and temperature were confirmed. Compression forces normal to the imposed deformation were much larger than tension forces on chains. Smaller molecular weight chains represent the equivalent of a much more tightly cross-linked network, resulting in greater moduli than larger chains. Young's moduli computed from the coarse-grained numerical model were in good agreement with experimental results.

Temperature- and pH-Responsive Schizophrenic Copolymer Brush Coatings with Enhanced Temperature Response in Pure Water

Novel brush coatings were fabricated with glass surface-grafted chains copolymerized using surface-initiated atom transfer radical polymerization (SI-ATRP) from 2-(2-methoxyethoxy)ethyl methacrylate (OEGMA188) and acrylamide (AAm), taken in different proportions. P(OEGMA188-co-AAm) brushes with AAm mole fraction >44% (determined with XPS and TOF-SIMS spectroscopy) and nearly constant with the depth copolymer composition (TOF-SIMS profiling) exhibit unusual temperature-induced transformations: The contact angle of water droplets on P(OEGMA188-co-AAm) coatings increases by ∼45° with temperature, compared to 17-18° for POEGMA188 and PAAm. The thickness of coatings immersed in water and the morphology of coatings imaged in air show a temperature response for POEGMA188 (using reflectance spectroscopy and AFM, respectively), but this response is weak for P(OEGMA188-co-AAm) and absent for PAAm. This suggests mechanisms more complex than a simple transition between hydrated loose coils and hydrophobic collapsed chains. For POEGMA188, the hydrogen bonds between the ether oxygens of poly(ethylene glycol) and water hydrogens are formed below the transition temperature Tc and disrupted above Tc when polymer-polymer interactions are favored. Different hydrogen bond structures of PAAm include free amide groups, cis-trans-multimers, and trans-multimers of amide groups. Here, hydrogen bonds between free amide groups and water dominate at T < Tc but structures favored at T > Tc, such as cis-trans-multimers and trans-multimers of amide groups, can still be hydrated. The enhanced temperature-dependent response of wettability for P(OEGMA188-co-AAm) with a high mole fraction of AAm suggests the formation at Tc of more hydrophobic structures, realized by hydrogen bonding between the ether oxygens of OEGMA188 and the amide fragments of AAm, where water molecules are caged. Furthermore, P(OEGMA188-co-AAm) coatings immersed in pH buffer solutions exhibit a 'schizophrenic' behavior in wettability, with transitions that mimic LCST and UCST for pH = 3, LCST for pH = 5 and 7, and any transition blocked for pH = 9.

The role of B-type lamins in genome architecture, chromatin dynamics, and gene regulation.

Chromatin is hierarchically organized in a dynamic manner in the mammalian cell nucleus, but the causal relationship between physical 3D genome organization and transcriptional activity and genome activity remains to be fully understood. Genome-wide studies have suggested that the interplay of several principles leads to the emergence of the major organizational features of the genome, including polymer-polymer interactions, chromatin loop extrusion, phase separation, the physical interaction of chromatin with stable architectural elements of the nucleus (i.e., nuclear envelope), and chromatin dynamics. The nuclear lamina is the ultimate determinant of nuclear space that posits a structural limit on the 3D genome organization. Lamins are structural components of the nuclear lamina that provide mechanical support to the nucleus and regulate genome organization and transcription. However, identifying the direct roles of lamins on dynamic genome organization has been challenging as depletion of lamin proteins severely impacts cell viability. To overcome this challenge, we engineered colon carcinoma cells to rapidly and completely degrade endogenous B-type lamins using Auxin-induced degron (AID) technology. We utilized a suite of novel technologies such as live-cell Dual Partial Wave Spectroscopic (Dual-PWS) microscopy, in situ Hi-C, and CRISPR-Sirius to demonstrate that acute lamin depletion increases chromatin dynamics at the nuclear periphery and weakens chromatin compartmentalization, as well as physically repositions gene-specific loci with respect to the nuclear periphery. Further, using the reversible AID system, we show that significantly altered genes after acute lamin depletion are enriched near LADs, and replenishment of lamins re-establishes their basal expression. Our findings provide a deeper understanding of the role B-type lamins in cell type-specific 3D genome organization and transcription.