Acrylic Acid Research Articles

Enhanced uranium extraction using a nanostructured photothermal hydrogel membrane

Uranium is the basic resource in nuclear energy and a sword of two sides. The accidental release of radioactive uranium to the environment may cause serious impact on the environment and living creatures. Herein, a nanostructured hydrogel-based solar evaporator with in-situ formed nanostructures is designed for simultaneous solar evaporation and uranium extraction from polluted water. To be specific, poly(acrylic acid) and gelatin with embedded carbon black nanoparticles coated on a cotton cloth self-assemble into nanostructures via salting-out and acid treatment to reduce the light reflectivity and enhance the specific surface area for uranium adsorption. Numerical simulation confirms that the evaporation-induced flow accelerates the diffusion of uranyl ions towards the adsorbent. Under solar irradiation of 1 kW m−2 a maximum uranium adsorption capacity of 443.2 ± 18.1 mg g−1 is achieved in 20 ppm uranium-spiked water, meanwhile a high solar evaporation rate of 3.75 kg m−2 h−1 is reached, hence, the solar evaporator is ranked among the most powerful adsorbents/evaporators. This work provides a cost-effective and scalable approach for dealing with uranium-polluted water.

Design, synthesis, and characterization of novel copolymer gel particles for water-plugging applications

Abstract Multi-stage plugging represents a promising strategy for enhancing production and injection rates in medium-and low-permeability oilfields. Despite its potential, the efficacy of current plugging agents, particularly hydrophobically bonded water-soluble polyacrylamide-based gel microspheres, is hindered by notable drawbacks such as low stability and inadequate compressive strength. Therefore, a comprehensive understanding of water plugging mechanisms coupled with the optimization of gel microsphere properties is essential for advancing the development of gel-based plugging agents with superior characteristics or intelligent regulatory capabilities. The P(AA-AM-[PrSO3]Vim) ionic liquid copolymerized gel particles were designed and synthesized by using microfluidic technique and titration gel method with AM, acrylic acid (AA), 1-vinylimidazole (Vim) and 1,3-propylsulfonyl lactone (PrSO3) as the raw materials. The morphology and structure of the copolymer gel particles were characterized, and the effects of [PrSO3]Vim and cross-linker content on the water-absorbing properties and strength of the gel particles were investigated. When the amount of [PrSO3]Vim was 12%, the concentration of crosslinker was 1.5%, and the temperature was 40°C, the water absorption capacity reached the maximum value of 163 g·g−1. The strength of the P(AA–AM–[PrSO3]Vim) spherical gel particles was maximized at a [PrSO3]Vim content of 4%. Furthermore, the chemical and physical roles of the P(AA–AM–[PrSO3]Vim) spherical gel particles were studied in a typical water-plugging environment. This study provides experimental data and a theoretical basis for the application of functional spherical gel-plugging particles in current oilfield environments.

An eco-friendly strategy of cell wall stapling: In situ crosslinking of acrylic acid emulsion impregnated in thermally treated poplar wood

Traditional wood modification methods often result in the release of harmful substances and energy wastage. This study proposes an efficient and environmentally friendly modification strategy for fast-growing poplar wood. The approach involves polymerizing organic linear molecules within the cell wall to form stitches, thereby enhancing the dimensional stability and mechanical properties of wood and increasing its ability to withstand various environments. Poplar wood specimens were treated via a method that combines heat treatment with acrylic emulsion impregnation. The research findings indicated an improvement in the mechanical properties of poplar wood following the combined treatment. Moreover, poplar wood subjected to this treatment approach exhibited a 35.24 % lower water absorption rate after a 7-day water immersion test, and tangential and radial swelling rates of the wood were reduced by 29.66 % and 45.68 %, respectively. Scanning electron microscopy revealed excellent penetration of acrylic emulsion into wood cells; the emulsion infiltrated the wood and adhered to the cell walls, forming a crosslinked network structure. Analysis of the modification mechanism through X-ray diffraction, Fourier-transform infrared spectroscopy, and X-ray photoelectron spectroscopy showed that the successful infusion of acrylic emulsion compensated for the lower mechanical properties of thermally treated wood, thus improving the utilization value of poplar. The acrylic emulsion is an environmentally friendly and harmless modifier, making the modified wood suitable for various applications, including indoor furniture, logistics, and outdoor facilities. This modification strategy enables efficient resource utilization and provides valuable insights for the sustainable development of the timber industry.

Integrated Approach for Allyl Amine Synthesis Combining the Decarboxylative Coupling of Arylacrylic Acids with the Petasis Reaction.

A metal-free multicomponent reaction strategy for synthesizing allyl amines through decarboxylative coupling combined with the Petasis reaction is described. Utilizing (E)-3-(2,4,6-trimethoxyphenyl)acrylic acid, various boronic acids, a formaldehyde solution, and primary amines, the method operates efficiently without metal catalysts. Investigations reveal that electron-donating substituents in cinnamic acid derivatives significantly enhance reactivity, which is crucial for effective transformations. Under the optimized conditions, yields of ≤78% were obtained across a diverse range of 30 allyl amines.

Ultrasensitive Flexible Strain Sensor Made with Carboxymethyl-Cellulose-Anchored Carbon Nanotubes/MXene for Machine-Learning-Assisted Handwriting Recognition.

The combination of wearable sensors with machine learning enables intelligent perception in human-machine interaction and healthcare, but achieving high sensitivity and a wide working range in flexible strain sensors for signal acquisition and accurate recognition remains challenging. Herein, we introduced carboxymethyl cellulose (CMC) into a carbon nanotubes (CNTs)/MXene hybrid network, forming tight anchoring among the conductive materials and, thus, bringing enhanced interaction. The silicone-rubber-encapsulated CMC-anchored CNTs/MXene (CCM) strain sensor exhibits an excellent sensitivity (maximum gauge factor up to 71 294), wide working range (200%), ultralow detection limit (0.05%), and outstanding durability (over 10 000 cycles), which is superior to most of the recently reported counterparts also based on a conductive composite film. Moreover, the sensor achieves seamless integration with human skin with the help of a poly(acrylic acid) adhesive layer, successfully obtaining stable and clear waveforms with meaningful profiles from the human body. On this basis, we proposed and realized a novel in-air handwriting recognition method via extracting multiple features of high-quality strain signals assisted by deep neural networks, achieving a high classification accuracy of 98.00 and 94.85% for Arabic numerals and letters, respectively. Our work provides an effective approach for significantly improving strain sensing performance, thereby facilitating innovative applications of flexible sensors.

A Janus hydrogel that enables wet tissue adhesion and resists abdominal adhesions

Hydrogels have indeed achieved significant advancements, yet their clinical translation has been hampered by their inherent limitations in wet adhesion properties. Furthermore, the design of adhesive hydrogels that can resist postoperative adhesions remains an intricate challenge. In this study, we introduce a Janus hydrogel (JGP) that offers a novel approach to address these challenges. The JGP hydrogel has two asymmetrical sides, consisting of an adhesion layer (AL) and an anti-adhesion layer (AAL). Specifically, the AL incorporates three key components: N-[tris(hydroxymethyl)methyl]acrylamide (THMA), acrylic acid (AAc), and the acrylic acid N-hydroxysuccinimide ester (AAc-NHS). By drying the AL, it has a rapid water absorption capability. The abundance of hydroxyl and carboxyl groups in the AL enables the formation of robust hydrogen bonds with tissues, thereby achieving superior adhesive properties. Additionally, the synergistic effect of THMA's tridentate hydrogen bonding and the covalent bonding formed by AAc-NHS with tissue ensures long-lasting wet adhesion. To realize the anti-adhesion function, one side of the AL was immersed in a solution of [2-(methacryloyloxy)ethyl]dimethyl-(3-sulfopropyl)ammonium hydroxide (SBMA), which undergoes crosslinking to form the AAL. A comprehensive series of tests have confirmed that the JGP hydrogel exhibits exceptional mechanical properties, efficient and enduring adhesion, excellent biocompatibility, and degradability. Moreover, it possesses remarkable hemostatic properties and robust anti-abdominal adhesion characteristics.

Fabrication of carboxymethyl tamarind kernel gum-based hydrogel and its applicability in different types of soils for agronomy

An avant-garde agricultural hydrogel - Carboxymethyl tamarind kernel gum-poly sodium acrylate-polyacrylamide hydrogel was designed by free-radical polymerization of biopolymer: carboxy-methyl tamarind kernel gum and monomers: sodium acrylate, acrylamide, using N,N′ methylene bisacrylamide as crosslinker and potassium persulphate as initiator, to explore its application as a soil conditioner. It was characterized by Fourier transform infrared spectroscopy, scanning electron microscopy, and thermogravimetric techniques. Swelling was investigated at different pH and in saline solutions. The fabricated hydrogel absorbed 189 ml/g of distilled water. Minimal 0.1 % hydrogel-amended different soils unveiled an upswing in maximum water holding capacity: Sandy soil (43%), Clay soil (31 %), Silty soil (29 %) & Loamy soil (9 %).; decrease in porosity: Sandy (29 %) > Loamy (15.2 %) > Silty (6 %) > Clay (5.9 %), increase in available water content: Clay soil (17.52 %), Silty (13.45 %), Loamy soil (9.416 %), Sandy soil (10.375 %); increase in bulk density: Clay (1.7 %), Silty (5.3 %), Loamy (10 %) and Sandy (13%) as compared to control sample. These sequels were corroborated by water retention capacity in chickpea plants. The designed hydrogel, as a soil conditioner, was commendable in all types of soils but is worth applying in sandy and loamy soils. This hydrogel richly assists as a soil conditioner and boosts plant performance in a green eco-friendly way.

Electro-responsive Molecularly Imprinted Polymers (E-MIPs) for Rapid Detection of Progesterone in Human Serum Samples.

Rapid and reagent-free detection of progesterone (P4) is crucial in point-of-care (POC) measurement due to its important role in the human endocrine and central nervous system. Currently available technologies for P4 detection are often not rapid or require reagents, limiting their use in POC settings. In this work, a self-signaling electrochemical sensing platform for rapid detection of P4 is developed by using electroactive molecularly imprinted polymers (E-MIPs). E-MIPs possess the ability to transduce the molecular recognition event into a measurable electrochemical signal. The E-MIPs are prepared by bulk copolymerization of acrylic acid (AA) and ferrocenylmethyl methacrylate (FcMA) in the presence of P4 followed by its removal from the polymer matrix. By incorporation of ferrocene moieties, the MIP gains intrinsic electroactivity, enabling label-free and direct electrochemical detection of P4 levels. Electrochemical techniques, including cyclic voltammetry and electrochemical impedance spectroscopy, were employed to elucidate the electron transport reaction responsible for the MIP's intrinsic electroactivity. Additionally, the predetermined complementary binding sites confined to the small working area of the screen-printed carbon electrode (SPCE) within the E-MIP matrix facilitate rapid P4 binding, achieving completion within 120 s. The developed E-MIP sensing platform was used for the rapid detection of P4 levels in human serum samples. The short incubation times reported for the E-MIP sensing platform would be beneficial in minimizing the nonspecific binding in the real-world samples. We believe that the proposed E-MIP sensing platform can be applied to clinical samples for detecting fluctuations in P4 levels.

Novel A-π-D-A organic dyes for better photovoltaic performance.

In this article, we report two indole-based metal-free organic dyes In-T-2C (3-(5-(3-((2-carboxy-2-cyanovinyl)-1-pentyl-1H-indol-5-yl)thiophen-2-yl)-2-isocyanoacrylic acid) and In-B-C (2-cyano-3-(5-(4-cyanophenyl)-1-pentyl-1H-indol-3-yl)acrylic acid) with A-π-D-A architecture. The molecular structures of metal-free indole-based A-π-D-A organic dyes were elucidated using FT-IR, NMR, HRMS and single-crystal X-ray diffraction techniques. The present investigation examined the features of the synthesized dyes employing photophysical attributes, electrochemical traits and theoretical studies were executed to acquire a detailed comprehension of the geometry, electronic structure and absorption spectra of the synthesized dyes using density functional theory (DFT) and time-dependent density functional theory (TD-DFT). Additionally, dye-sensitized solar cells (DSSCs) were fabricated using newly synthesized dyes and examined their photovoltaic activity. Electrochemical impedance analysis (EIS) was performed to recognize the interfacial charge transfer in the DSSCs. The In-T-2C dye-based DSSC device exhibited an uppermost fill factor (FF) of 0.63, resulting in the uppermost open-circuit voltage (V OC) of 540.2 mV and highest efficiency (η) of 4.12% due to the highest short-circuit current density (J SC) of 12.1 mA cm-2 compared to the In-B-C dye (V OC = 497 mV, J SC = 1.07, FF = 0.70, η = 0.38%).

Poly(Vinyl Alcohol)/Poly(Acrylic Acid) Gel Polymer Electrolyte Modified with Multi-Walled Carbon Nanotubes and SiO2 Nanospheres to Increase Rechargeability of Zn–Air Batteries

Poly(Vinyl Alcohol)/Poly(Acrylic Acid) Gel Polymer Electrolyte Modified with Multi-Walled Carbon Nanotubes and SiO2 Nanospheres to Increase Rechargeability of Zn–Air Batteries

Surface Chemistry Induced IgG Unfolding and Modulation of Immune Responses.

Immunoglobulin G (IgG) comprises a significant portion of the protein corona that forms on biomaterial surfaces and holds a pivotal role in modulating host immune responses. To shed light on the important relationship between biomaterial surface functionality, IgG adsorption, and innate immune responses, we prepared, using plasma deposition, four surface coatings with specific chemistries, wettability, and charge. We found that nitrogen-containing coatings such as these deposited from allylamine (AM) and 2-methyl-2-oxazoline (POX) cause the greatest IgG unfolding, while hydrophilic acrylic acid (AC) surfaces allowed for the retention of the protein structure. Structural changes in IgG significantly modulated macrophage attachment, migration, polarization, and the expression of pro- and anti-inflammatory cytokines. Unfolded IgG on the POX and AM surfaces enhanced macrophage attachment, migration, extracellular trap release, and pro-inflammatory factors production such as IL-6 and TNF-α. Retention of IgG structure on the AC surface downregulated inflammatory responses. The findings of this study demonstrate that the retention of protein structure is an essential factor that must be taken into consideration when designing biomaterial surfaces. Our study indicates that using hydrophilic surface coatings could be a promising strategy for designing immune-modulatory biomaterials for clinical applications.

Osmotic energy harvesting using acrylic acid hydrogel PET membrane

In this study, we investigated the osmotic energy harvesting using a cation-selective membrane. The cation-selective membrane was synthesized by the incorporation of acrylic acid hydrogel in a porous support membrane. FTIR analysis and SEM images confirmed the presence of the acrylic acid hydrogel rods inside the porous support material. The exposure of the acrylic acid hydrogel PET (AP) membrane to a concentration gradient culminated in the generation of electric power. The AP membrane was evaluated in regard to the following parameters: EDiff, Io, Pmax and t+. The maximum power obtained with the membrane was 1.10 μW at the 40-fold concentration gradient (test area∽ 100 mm2). Increasing the concentration gradient increased the power output. However, a decrease in power output was observed after a certain value of the concentration gradient. An enhancement in power output was noted as the fraction of acrylic acid within the membrane was augmented. Additionally, the cation transference number also increased owing to a high charge density and a reduction in the mesh size. The AP membrane was also investigated in acidic and basic media. The time-dependent study revealed the superior chemical stability of the AP membrane.

Hydrophobically associated amphiphilic copolymer fracturing fluid with dual Functions of fracturing and flooding for enhanced oil recovery

Polymer fracturing fluids are widely used in oil and gas extraction; however, the residues left after gel breaking can easily clog fractures, leading to formation damage and a decline in economic benefits. To address this issue, this study developed a new type of hydrophobic associative amphiphilic copolymer, P(AM-AA-AAEOn), prepared through the copolymerization of fatty alcohol polyoxyethylene ether (AAEOn), acrylic acid, and acrylamide. The properties of the system, including shear resistance and thixotropy, shear recovery, viscoelasticity, salt responsiveness, and interfacial tension, were thoroughly investigated by measuring its hydrodynamic size, molecular weight, root-mean-square radius of gyration, and second virial coefficient. Experimental results demonstrated that with a monomer ratio of 300:100:1, this fracturing fluid system exhibited excellent shear resistance, viscoelasticity, effective sand carrying, and corrosion inhibition, along with good gel-breaking and compatibility properties. Further oil displacement tests revealed that P(AM-AA-AAEOn), due to its superior interfacial activity and wettability, significantly enhanced oil recovery efficiency by 25.01%. These characteristics not only resolved the issue of flowback in traditional polymer fracturing fluids but also facilitated the efficient integration of fracturing and oil displacement. The innovation of this research lies in the development of a novel, efficient, and environmentally friendly fracturing fluid, which provides significant theoretical and practical foundations for oilfield fracturing technology and holds promising industrial application prospects.

Exploring the Origins of Association of Poly(acrylic acid) Polyelectrolyte with Lysozyme in Aqueous Environment through Molecular Simulations and Experiments

Exploring the Origins of Association of Poly(acrylic acid) Polyelectrolyte with Lysozyme in Aqueous Environment through Molecular Simulations and Experiments

Electron beam induced graft polymerized anti oil-fouling biaxial polypropylene membrane with harsh environment tolerance

The intrinsic hydrophobic behavior of biaxial-oriented polypropylene microporous membrane limits its broad application area by leading serious membrane fouling. An environment-friendly, practical, and facile to large-scale prepared surface modification process is designed to enhance the membrane wettability and oil fouling. By employing electron beam radiation, acrylic acid, and polyvinyl alcohol in the pre-irradiation-induced graft polymerization process, a micro-nano structure was developed and the surface roughness was increased from 66.5 nm to 99.3 nm. Enhancing the grafting ratio further reduces the pore size of the final modified membrane from 54 nm to 25 nm, which is significantly smaller than the size of the emulsified oil droplet. By modifying the morphological and structural characteristics of the grafted membrane, excellent oil fouling resistance features are attained with UWOCA value 161° and separation efficiency of 99.3 %. Moreover, the theoretical explanations for hydrophilicity and oil-fouling resistance of modified membranes are also developed using DFT calculations and the Hermia model, which shows alignment with experimental data. Consequently, considerable improvements in wettability, thermal and mechanical behavior are obtained by this facial surface modification approach, which could further broaden the modified membrane's applications area in membrane separation technology while lengthening its service life.

Bulking up: the impact of polymer sterics on emulsion stability.

Encapsulation of hydrophobic active ingredients is critical for targeted drug delivery as water-insoluble drugs dominate the pharmaceutical marketplace. We previously demonstrated hexadecane-in-water emulsions stabilized with a pH-tunable polymer, poly(acrylic acid) (PAA), via a steric layer preventing particle aggregation. Using vibrational sum frequency scattering spectroscopy (VSFSS), here we probe the influence of steric hindrance on emulsion colloidal stability by tailoring the molecular weight of PAA and by adding an additional methyl group to the polymer backbone via poly(methacrylic acid) (PMAA) at pH 2, 4, and 6. At low polymer molecular weight (2 and 10 kDa), PAA adsorption is entropy driven and akin to surfactant-mediated stabilization. With 450 kDa PAA, the longer polymer chain emphasizes enthalpically favored polymer-oil interactions to initially coat the surface, and forms layers at increasing molecular weight (1000 and 4000 kDa). PMAA exhibits better oil-solubility than PAA at low concentrations but cannot accommodate the steric hindrance at higher concentrations leading to disorder. Finally, we connect our molecular-level understanding of PAA ordering with temperature-dependent dynamic light scattering experiments and observe that emulsions coated with PAA at pH 2 and 4 maintain colloidal stability from 0-90 °C, making PAA a promising polymer for hydrophobic drug delivery.

Secondary utilization of self-suspending proppant's coating polymer: Enhance oil recovery

Fracturing is associated with significant economic costs, and the loss of the utility of the self-suspending proppants' coating polymer after fracturing appears highly wasteful. To enhance the utilization of the self-suspending proppant's coating polymer, we propose a novel concept: the secondary utilization of coating polymer, enabling the coating polymer to gel-breaking within the reservoir and generate surface-active substances, thereby enhancing the oil recovery efficiency. To realize this concept, this study designed and synthesized a hydrophobic associative polymer, which was combined with ceramic proppant to form self-suspending proppant. Using the surface-active monomer octadecyl dimethyl allyl ammonium chloride (DMDAAC-18), acrylamide (AM), acrylic acid (AA), and 2-acrylamido-2-methylpropane sulfonic acid (AMPS) via aqueous free-radical copolymerization synthesized the PAAAD (Polymer (AM/AA/AMPS/DMDAAC-18)). PAAAD has demonstrated excellent thickening properties, with a viscosity of 240.01 mPa s at a concentration of 6 g/L in shear rate 170s−1. Its solution exhibits high viscoelasticity, and a loss factor (tan δ) < 1 over the frequency range of 0–20 Hz at a shear stress of 0.56 Pa indicates that it behaves like a viscoelastic solid with gel-like characteristics, which is beneficial for proppant suspension. The gel-breaking solution of PAAAD reduced surface tension (29.33 mN/m at a PAAAD concentration of 6 g/L), converted oil-wet rocks to water-wet conditions (reducing the contact angle of oil-wet shale to 46.7° and of oil-wet sandstone to 19.9°), and enhanced shale imbibition oil recovery efficiency in 16.5%. The basic properties of self-suspending proppants meet the Chinese Petroleum Industry Standard SY/T 5108-2014 and exhibit good suspension properties, with sedimentation of 1.7 mm in 40 min at a sand ratio of 15%. This study is the first to propose the secondary utilization of the self-suspending proppant's coating polymer, significantly enhancing their utilization value.

Preparation and Stability Study of an Injectable Hydrogel for Artificial Intraocular Lenses

Currently available intraocular lenses (IOLs) on the market often differ significantly in elastic modulus compared to the natural human lens, which impairs their ability to respond effectively to the tension of the ciliary muscles for focal adjustment after implantation. In this study, we synthesized a polyacrylamide–sodium acrylate hydrogel (PAH) through the cross-linking polymerization of acrylamide and sodium acrylate. This hydrogel possesses excellent biocompatibility and exhibits several favorable properties. Notably, the hydrogel demonstrates high transparency (94%) and a refractive index (1.41 ± 0.07) that closely matches that of the human lens (1.42). Additionally, it shows strong compressive strength (14.00 kPa), good extensibility (1400%), and an appropriate swelling ratio (50 ± 2.5%). Crucially, the tensile modulus of the hydrogel is 2.07 kPa, which closely aligns with the elastic modulus of the human lens (1.70–2.10 kPa), enabling continuous focal adjustment under the tension exerted by the ciliary muscles.

A Self-Healing and Sweat-Chargeable Hydrogel Electrolyte for All-in-One Flexible Supercapacitors.

Flexible solid-state supercapacitors (SCs) with hydrogel as an electrolyte and separator combine the advantages of wearability and energy storage and exhibit a broad application prospect in wearable energy textiles. However, irreversible electrolyte damage and unstable electrode-electrolyte interfaces during mechanical deformations remain bottlenecks in realizing truly wearable applications. Herein, poly(acrylic acid) (PAA)-Fe hydrogels were prepared through a simple thermal polymerization strategy. The dynamic reversible metal coordination bonds between Fe3+ and carboxylic acids confers the hydrogels with excellent self-healing properties. As expected, the prepared hydrogels exhibited superior mechanical strength (tensile stress of 45.80 kPa), ionic conductivity (0.076 S cm-1), and self-healing properties. Subsequently, the SCs were constructed using composite hydrogel electrodes (MnO2@CC embedded in the PAA-Fe hydrogels) as symmetrical electrodes (marked as MSCs). The reversible metal coordination bonds between composite hydrogel electrodes formed an ultrastable electrode/electrolyte interface in the all-in-one MSCs, thus revealing excellent mechanical durability. The all-in-one MSCs delivered a remarkable specific capacitance (30.98 F g-1 at 0.2 A g-1), excellent cyclic stability (87.24% after 5000 cycles), outstanding mechanical deformation stability, and impressive electrochemical output stability after self-healing (capacitance retention of 85.34% after five cycles of cutting/self-healing). It is noteworthy that the all-in-one MSCs employed NaCl as an electrolyte, which can be obtained from human sweat. As a proof of the self-charged concept, the all-in-one MSCs can be reused in sweat, whose capacitance was maintained at 90.05% of the initial state after three repetitions. This work is expected to shine light into the design of all-in-one and fabric-based SCs and the development of wearable energy textiles.

Visible-Light-Mediated Ni-Catalyzed Gas-Free Carboxylation: Stereodivergent Synthesis of E- and Z-Acrylic Acids.

Stereodivergent syntheses of different scaffolds from identical starting materials by switching the fewest parameters are among the most appealing synthetic technologies. Herein, a visible-light mediated Ni-catalyzed carboxylation of vinyl halides with formates has been developed, affording acrylic acids in both Z- and E-configurations from identical vinyl halides. The reaction features Ni-catalyzed gas-free carboxylation of vinyl halides by utilizing formates as a surrogate of carbon dioxide.