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1.
A series of superabsorbent composite, polyacrylamide/attapulgite, from acrylamide (AM) and ion‐exchanged attapulgite (APT) was prepared by aqueous polymerization, using N,N′‐methylenebisacrylamide (MBA) as a crosslinker and ammonium persulfate (APS) as an initiator. The effects of ion‐exchanged APT on water absorbency of superabsorbent composites in distilled water and in 0.9 wt% NaCl solution were studied. The result indicates that higher cation‐exchange capacity (CEC) and lower specific surface area (SSA) of APT treated with various anions are of benefit for improving water absorbency in distilled water. The effects of AlCl3 solution concentration and Al3+‐exchanged APT content on water absorbency of the composite were also investigated. The concentration of AlCl3 solution has a great influence on water absorbency of the superabsorbent composite. Al3+‐exchange of APT could also enhance reswelling ability of the corresponding composite, which indicates that Al3+‐exchange of APT could improve gel strength and gives a direct evidence for its acting as an inorganic assistant crosslinker in the polymeric network. POLYM. COMPOS., 28:208–213, 2007. © 2007 Society of Plastics Engineers  相似文献   

2.
In this work, a series of novel hydroxyethyl cellulose‐ g‐poly(acrylic acid)/attapulgite (HEC‐g‐PAA/APT) superabsorbent composites were prepared through the graft polymerization of hydroxyethyl cellulose (HEC), partially neutralized acrylic acid (AA), and attapulgite (APT) in aqueous solution, and the composites were characterized by means of Fourier‐transform spectroscopy, scanning electron microscopy, and transmission electronmicroscopy. The effects of polymerization variables including concentrations of the initiator and crosslinker and APT content on water absorbency were studied, and the swelling properties in various pH solutions as well as the swelling kinetics in various saline solutions were also systematically evaluated. Results showed that the introduction of 5 wt% APT into HEC‐g‐PAA polymeric network could improve both water absorbency and water absorption rate of the superabsorbent composites. In addition, the superabsorbent composites retained high water absorbency over a wide pH range of 4–10, and the swelling kinetics of the superabsorbent composites in CaCl2 and FeCl3 solutions exhibited a remarkable overshooting phenomenon. POLYM. ENG. SCI., 2010. © 2010 Society of Plastics Engineers  相似文献   

3.
A novel superabsorbent composite, polyacrylamide/attapulgite, from acrylamide (AM) and attapulgite (APT), was prepared by free‐radical polymerization, using N,N′‐methylenebisacrylamide (MBA) as a crosslinker and ammonium persulfate (APS) as an initiator. The effects of hydrochloric acid (HCl) concentration, acidification time, and acidification temperature while acidifying APT and temperature and APT heat‐activation on water absorbency of the superabsorbent composite in distilled water and in 0.9 wt % NaCl solution were studied. The water absorbency first decreases with increasing the HCl concentration while acidifying APT, and then increases with further increasing the HCl concentration. Prolongation of acidification time is of benefit to the increase of water absorbency. At a given HCl concentration, water absorbency for the composite increases with increasing acidification temperature. An important increase in water absorbency was observed after incorporating heat‐activated APT into the polymeric network, reaching a maximum of 1964 g g?1 with the APT heat‐activated at 400°C. Acid‐ and heat‐activation can influence chemical composition, crystalline structure, cation exchange capacity (CEC), and specific surface area of APT according XRF, XRD, FTIR analysis, and physicochemical properties test, and then on water absorbency of corresponding PAM/APT superabsorbent composite. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 2419–2424, 2007  相似文献   

4.
In this work, the effects of different cation‐exchanged montmorillonite on water absorbency of poly(acrylic acid‐co‐acrylamide)/montmorillonite/sodium humate (PAA‐AM/MMT/SH) superabsorbent composite were systematically investigated under the same preparation conditions. The superabsorbents doped with different cation‐exchanged montmorillonite were characterized by Fourier‐transform infrared spectroscopy, X‐ray diffraction, and scanning electron microscopy technologies. Swelling behaviors of developing superabsorbent composite in various cationic saline solutions (NaCl, CaCl2, and FeCl3) were also investigated. The water absorbencies of superabsorbent composite with 20 wt% MMT and 30 wt% SH are 638, 723, 682, and 363 g g−1 in distilled water for incorporating natural Na+‐MMT, Li+‐exchanged MMT, Ca2+‐exchanged MMT, and Al3+‐exchanged MMT, respectively. The results showed that the cation‐exchange process had some obvious influences on final water absorbency of superabsorbent composite. NaCl, CaCl2, and FeCl3 solutions did not alter the swelling characteristics of the superabsorbent materials at a concentration of less than 0.01 mM, however, a concentration of greater than 0.1 mM caused a collapse in the swelling curves. The excellent swelling‐reswelling‐swelling behavior and lower swelling rate testified that Al3+‐exchanged MMT can act as an assistant crosslinker in the polymeric network. POLYM. COMPOS., 2009. © 2008 Society of Plastics Engineers  相似文献   

5.
In this work, a novel poly(acrylic acid‐coN‐acryloylmorpholine)/attapulgite superabsorbent composite was prepared by graft copolymerization among acrylic acid, N‐acryloylmorpholine and attapulgite in aqueous solution, using N,N′‐methylenebisacrylamide as a crosslinker and ammonium persulfate as an initiator. The result from FTIR spectra showed that  OH of attapulgite participated in graft copolymerization with acrylic acid and N‐acryloylmorpholine. Proper monomer ratio and atapulgite content could form a loose surface, and improve reswelling ability and initial swelling rate. The buffer action of the  COOH and  COO groups in the superabsorbent composite keeps the water absorbency a rough constant in the pH range of 4.4–9.6. Both polarity and structure of an organic solvent are responsible for the phase transition point of the superabsorbent composite. POLYM. COMPOS., 2010. © 2009 Society of Plastics Engineers  相似文献   

6.
A series of pH‐sensitive composite hydrogel beads, carboxymethyl cellulose‐g‐poly(acrylic acid)/attapulgite/sodium alginate (CMC‐g‐PAA/APT/SA), were prepared by combining CMC‐g‐PAA/APT composite and SA, using Ca2+ as the ionic crosslinking agent and diclofenac sodium (DS) as the model drug. The effects of APT content and external pH on the swelling properties and release behaviors of DS from the composite hydrogel beads were investigated. The results showed that the composite hydrogel beads exhibited good pH‐sensitivity. Introducing 20% APT into CMC‐g‐PAA hydrogel could change the surface structure of the composite hydrogel beads, decrease the swelling ability, and relieve the burst release effect of DS. The drug cumulative release ratio of DS from the hydrogel beads in simulated gastric fluid was only 3.71% within 3 hour, but in simulated intestinal fluid about 50% for 3 hour, 85% for 12 hour, up to 90% after 24 hour. The obtained results indicated that the CMC‐g‐PAA/APT/SA hydrogel beads could be applied to the drug delivery system as drug carriers in the intestinal tract. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011  相似文献   

7.
A novel salt‐resistant superabsorbent composite was prepared by copolymerization of partially neutralized acrylic acid, 2‐acryloylamino‐2‐methyl‐1‐propanesulfonic acid (AMPS) and attapulgite (APT). To enhance the swelling rate (SR) of the copolymer, sodium bicarbonate was used as a foaming agent in the course of copolymerization. Furthermore, for improving the properties of swollen hydrogel, such as strength, resilience and dispersion, the copolymer was surface‐crosslinked with glycerine and sodium silicate, and then the surface‐crosslinked copolymer was blended with aluminum sulfate and sodium carbonate in post treatment process. The influences of some reaction conditions, such as amount of AMPS, APT, and initiator, and neutralization degree of acrylic acid on water absorbency in 0.9 wt% NaCl aqueous solution both under atmospheric pressure (WA) and load (WAP, P ≈ 2 × 103 Pa) were investigated. In addition, the effect of them on SR was also studied. The WA and WAP of the superabsorbent composite prepared under optimal conditions in 0.9 wt% NaCl aqueous solution were 52 g·g?1 and 8 g·g?1, respectively. Besides, the SR was fast, and it could reach 0.393 mL·(g·s)?1. Moreover, the swollen hydrogel possessed excellent salt resistance, hydrogel resilience and dispersion. POLYM. ENG. SCI., 2009. © 2008 Society of Plastics Engineers  相似文献   

8.
A novel superabsorbent composite, poly(acrylic acid‐co‐acrylamide)/potassium humate (PAA‐AM/KHA), was prepared by aqueous solution polymerization from acrylic acid, acrylamide, and potassium humate (KHA) with N,N′‐methylenebisacrylamide as a crosslinker and potassium peroxydisulfate as an initiator. The effects of incorporated KHA on the water absorbency, swelling rate, and reswelling capability were investigated. The swelling property of PAA‐AM/KHA in various saline solutions was studied systematically. The results show that the comprehensive properties and especially salt‐resistant ability of PAA‐AM/KHA were enhanced. There was a linear relationship between the saturated water absorbency and the minus square root of the ionic strength of the external medium, and the water absorbency of PAA‐AM/KHA in various salt solutions had the following order: NH4Cl(aq) = KCl(aq) = NaCl(aq) > MgCl2(aq) > CaCl2(aq) > AlCl3(aq) > FeCl3(aq). Moreover, the polymeric net structure of PAA‐AM/KHA was examined with respect to that of poly(acrylic acid‐co‐acrylamide). The results indicate that the polymeric net of PAA‐AM/KHA was improved by the introduction of a moderate amount of KHA into the superabsorbent composite and made more suitable for agriculture and horticulture applications. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2008  相似文献   

9.
The dispersion of attapulgite (APT) as nanorod‐like single crystals is crucial to fully develop its functionality of one‐dimensional nanometer material as a filler of composite materials. In this study, APT was dispersed by the assistance of ethanol during the high‐pressure homogenization process to form individual nanorod‐like crystals. The dispersed APT was used to prepare new sodium alginate‐g‐poly(sodium acrylate‐co‐styrene)/attapulgite (NaAlg‐g‐P(NaA‐co‐St)/APT) superabsorbent nanocomposites. The effect of ethanol/water ratio on the dispersion of crystal bundles of APT was investigated by field emission scanning electron microscopy, and the results indicate that APT crystal bundles were effectively disaggregated in ν(CH3CH2OH) : ν(H2O) ? 5 : 5 solution after homogenized at 50 MPa. The better dispersion of APT in NaAlg‐g‐P(NaA‐co‐St) matrix has clearly improved the gel strength (from 1300 Pa to 1410 Pa, ω = 100 rad/s), swelling capacity (442–521 g/g), swelling rate (3.3303–4.5736 g/g/s), and reswelling ability of the superabsorbent nanocomposite. Moreover, the nanocomposites showed fast swelling–deswelling responsive behavior in different saline solutions. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013  相似文献   

10.
A novel poly(acrylic acid)/attapulgite (APT)/sodium humate (SH) superabsorbent composite was synthesized through the graft copolymerization reaction of acrylic acid on APT micropowder and SH with N,N′‐methylene bisacrylamide as a crosslinker and ammonium persulfate as an initiator in an aqueous solution. Various effects on the water absorbency, including the amounts of the crosslinker, initiator, APT, and SH, were investigated. The superabsorbent composite was characterized with Fourier transform infrared spectroscopy and scanning electron microscopy. The superabsorbent composite synthesized under optimal synthesis conditions with an APT concentration of 20% and an SH concentration of 20% exhibited absorption of 583 g of H2O/g of sample and 63 g of H2O/g of sample in distilled water and in a 0.9 wt % NaCl solution, respectively. The slow‐release property of SH from the superabsorbent composite into water was measured, and a test of the water retention of the superabsorbent composite in soil was also carried out experimentally with and without the superabsorbent composite. The results showed that the superabsorbent composite had not only good water retention but also an additional slow‐release property of SH. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 37–45, 2007  相似文献   

11.
A novel starch‐graft‐poly(acrylamide)/attapulgite superabsorbent composite was synthesized by graft copolymerization reaction of starch, acrylamide (AM), and attapulgite micropowder using N.N‐methylene‐bisacrylamide (MBA) as a crosslinker and ammonium persulphate (APS) as an initiator in aqueous solution, followed by hydrolysis with sodium hydroxide. The effects on water absorbency, such as amount of crosslinker, initiator, attapulgite, weight ratio of acrylamide to starch in the feed, gelatinization conditions of starch and molar ratio of NaOH to acrylamide, and so forth, were investigated. These superabsorbent composites were characterized by Fourier transform infrared spectroscopy (FTIR) and thermogravimetric analysis (TGA). The water absorbencies for these superabsorbent composites in water and saline solution were investigated, and water retention tests were carried out. Results obtained from this study showed that the water absorbency of superabsorbent composite synthesized under optimal synthesis conditions with an attapulgite content of 10% exhibit absorption of 1317 g H2O/g sample and 68 g H2O/g sample in distilled water and in 0.9 wt % NaCl solution, respectively. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 98: 1351–1357, 2005  相似文献   

12.
The effect of acid activation and thermal treatment of attapulgite on water absorbency of superabsorbent composite were investigated. Under the same preparation conditions, superabsorbent composite prepared with natural attapulgite exhibited a water absorbency of 639 g/g and it merely kept 71% of its initial water absorbency after 5 times of swelling–deswelling–reswelling test. However, superabsorbent composites prepared with 2–10 M hydrochloric acid acidified attapulgite and 100–400°C thermal treated attapulgite respectively exhibited the water absorbency of 884–1,241 g/g and 701–1,515 g/g. Also, those superabsorbent composites can keep 87% and 85% of their initial water absorbency after 5 times of swelling–deswelling–reswelling test, respectively. These results showed that, compared with superabsorbent composite prepared with natural attapulgite, the comprehensive water‐absorbing properties of poly(acrylic acid)/ attapulgite superabsorbent composites were improved effectively by acid activation and thermal treatment of attapulgite. This improvement of water absorbencies and gel strength of superabsorbent composite may be due to synthetical factors such as changes in the crystalline structure and the specific surface area and improvement of the number and the activity of hydroxyl groups of attapulgite, which in turn influence the grafting efficiency of monomer, crosslinking density, and the structure of superabsorbent composite network. POLYM. COMPOS., 28:397–404, 2007. © 2007 Society of Plastics Engineers  相似文献   

13.
This article exploits a new approach for synthesis of acrylic acid/carboxymethyl cellulose (AA/CMC) superabsorbent hydrogel in aqueous solution by a simple one‐step using glow‐discharge electrolysis plasma, in which N,N′‐methylenebisacrylamide (MBA) was used as a crosslinking agent. The reaction parameters affecting the equilibrium swelling, that is, discharge voltage, discharge time, mass ratio of AA to CMC, content of crosslinker, and degree of neutralization, were systematically optimized to achieve a superabsorbent hydrogel with a maximum equilibrium swelling. The structure, thermal stability, and morphology of AA/CMC superabsorbent hydrogel were characterized by Fourier transform infrared spectroscopy, X‐ray diffraction analysis, thermogravimetric analysis, and scanning electron microscopy. The swelling kinetics in distilled water and swelling behaviors in various pH solutions and salts solutions (NaCl, KCl, MgCl2, CaCl2, AlCl3, and FeCl3) were investigated in detail. The effect of six cationic salt solutions on the equilibrium swelling had the following order K+ > Na+ > Mg2+ > Ca2+ > Al3+ > Fe3+. In addition, the pH‐reversibility was preliminarily investigated with alternating pH between 6.5 and 2.0. The results showed that the equilibrium swelling of AA/CMC was achieved in 90 min. The hydrogel was responsive to the pH and salts, and was reversible swelling and deswelling behavior. POLYM. ENG. SCI., 54:2310–2320, 2014. © 2013 Society of Plastics Engineers  相似文献   

14.
A series of superabsorbent composites were prepared from acrylic acid (AA), acrylamide (AM), and Cloisite® 30B by aqueous solution polymerization technique using ammonium peroxodisulfate (APS) as initiator. The interaction of the organically modified nanoclay with PAA‐co‐PAM copolymer was verified by FTIR, whereas the morphology of the composite was studied by Scanning Electron Microscopy (SEM). The water absorbency in deionized water and saline water of the synthesized nanohydrogels was measured by calculating their percentage swelling ratio. The effects of copolymerization, monomer ratio, clay content, and temperature on the water absorbency were studied. The results indicated a considerable increase in swelling ratio by proper monomer proportion and incorporation of optimum clay percentage into the copolymer matrix. It was found that the nanohydrogel acquired highest water absorbency with 2% clay loading. The reswelling ability and water retention capacity of the PAA‐co‐PAM hydrogel and PAA‐co‐PAM/clay nanohydrogel were also measured. The water absorbency was found to increase after each reswelling for which it may be useful as recyclable superabsorbent material. The results of water retention capacity of the nanohydrogel were also encouraging and find application in agriculture, especially in drought‐prone areas. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011  相似文献   

15.
A novel poly(acrylic acid)/attapulgite superabsorbent composite was synthesized by graft copolymerization reaction of acrylic acid (AA) on attapulgite micropowder using N,N′‐methylenebisacrylamide (MBA) as a crosslinker and ammonium persulfate (APS) as an initiator in aqueous solution. The effects on water absorbency of such factors as reaction temperature, initial monomer concentration, degree of neutralization of AA, amount of crosslinker, initiator, and attapulgite were investigated. These crosslinked superabsorbent composites were characterized by thermogravimetetric analysis and scanning electron microscopy. The graft copolymerization reaction of AA on attapulgite micropowder was characterized by FTIR. The water absorbencies for these superabsorbent composites in water and saline solutions were investigated and water‐retention tests were carried out. Results obtained from this study show that the water absorbency of the superabsorbent composite synthesized under optimal synthesis conditions with an attapulgite content of 10% exhibited an absorption of 1017 g H2O/g sample and 77 g H2O/g sample in distilled water and in 0.9 wt % NaCl solution, respectively. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 1596–1603, 2004  相似文献   

16.
A series of clay-based superabsorbent composite from acrylamide (AM) and various clays, such as attapulgite, kaolinite, mica, vermiculate and Na+-montmorillonite, was prepared by free-radical aqueous polymerization, using N,N′-methylenebisacrylamide (MBA) as a crosslinker and ammonium persulfate (APS) as an initiator, and then saponified with sodium hydroxide solution. In this paper, the reaction mechanism and thermal stability of the superabsorbent composites incorporated with various clays were characterized by FTIR, XRD and TGA, respectively. The effects of clay kind and clay content on equilibrium water absorbency of these composites were also investigated and compared. In addition, the influences of clay kind on comprehensive swelling behaviors of the PAM/clay superabsorbent composites were studied. The results indicated that the introduced clays could influence physicochemical properties of obtained superabsorbent composites. Mica could improve thermal stability of corresponding superabsorbent composites to the highest degree comparing with the other clays. The PAM/clay superabsorbent composites incorporated with 10 wt% clay of various kinds were all endowed with equilibrium water absorbency of more than 1300 g g−1. The equilibrium water absorbency decreases with increasing clay content and correlates with the kind of clay. Attapulgite-based superabsorbent composite was endowed with higher water absorbency in univalent cationic saline solution, however, the vermiculite- and the kaolinite-based ones acquired the highest water absorbency in CaCl2 and FeCl3 aqueous solution, respectively. Moreover, the superabsorbent composites incorporated with Na+-montmorillonite have higher swelling rate and that of doped with mica was endowed with higher reswelling capability.  相似文献   

17.
A novel superabsorbent composite from acrylamide (AM) and attapulgite (APT), polyacrylamide/attapulgite (PAM/APT), was prepared by polymerizing AM with the existence of APT in aqueous solution, and then saponified with NaOH solution. Considering the impacts of hydrophilic groups (? COONa, ? COOH, and ? CONH2) on properties of the PAM/APT composite, the effects of saponification mode, molar ratio of NaOH to AM and saponification time on water absorbency, hydrophilic group content, and surface morphology were investigated systematically. The results indicate that the two‐step adding NaOH mode is superior to that of the one‐step mode. Among the superabsorbent composite incorporated with 30 wt% APT, the composite saponified at 95°C for 2 h with the molar ratio of 0.6 for NaOH to AM acquired the highest water absorbencies of 1715g g?1 and 87.8g g?1 in distilled water and in 0.9 wt% NaCl solution, respectively. The molar ratio of various hydrophilic groups at this time was 10:3:11 for ? COONa, ? COOH, and ? CONH2 determined using linear potentiometric titration method. POLYM. ENG. SCI. 46:1762–1767, 2006. © 2006 Society of Plastics Engineers.  相似文献   

18.
Summary: Organo‐attapulgite (organo‐APT) was prepared by modifying APT using four quaternary ammonium salts with various lengths of the alkyl group, including (octyl)trimethylammonium bromide (OTMABr) and (stearyl)trimethylammonium chloride (STMACl), etc. A series of composite hydrogels, poly(acrylic acid)/organo‐APT, from acrylic acid (AA), and organo‐APT was prepared by aqueous polymerization, using N,N′‐methylenebisacrylamide (MBA) as a crosslinker and ammonium persulfate (APS) as an initiator. The organification and organification degree of APT as well as the corresponding composites were characterized by FTIR, TGA, and XRD. The effects of the length of the alkyl group for different quaternary ammonium salts, organification degree of APT, and organo‐APT content on water absorbency and swelling behaviors in various electrolyte solutions were investigated in this study. Equilibrium water absorbency strongly depends on chain length of the alkyl group of quaternary ammonium salts, organification degree of APT as well as organo‐APT content. Longer alkyl group, higher organification degree, and proper organo‐APT content are of benefit for the improvement of equilibrium water absorbency. Equilibrium water absorbency in distilled water for PAA/APT was enhanced from 350.1 to 562.1 g · g?1 after 10 wt.‐% organo‐APT, modified with STMACl for the highest degree, was introduced. The kind of cation is the key factor influencing equilibrium water absorbency of these composite hydrogels in electrolyte solutions. Organification of APT could enhance responsiveness of the corresponding composite hydrogel to electrolyte solutions.

Schematic structure of PAA/organo‐APT composite in a dry state (left) and in a swollen state (right).  相似文献   


19.
To synthesize a novel biopolymer‐based superabsorbent hydrogel, 2‐acrylamido‐2‐methylpropanesulfonic acid (AMPS) was grafted onto kappa‐carrageenan (κC) backbones. The graft copolymerization reaction was carried out in a homogeneous medium and in the presence of ammonium persulfate (APS) as an initiator, N,N,N′,N′‐tetramethyl ethylenediamine (TMEDA) as an accelerator, and N,N′‐methylene bisacrylamide (MBA) as a crosslinker. A proposed mechanism for κC‐g‐AMPS formation was suggested and the hydrogel structure was confirmed using FTIR spectroscopy. The affecting variables on swelling capacity, i.e., the initiator, the crosslinker, and the monomer concentration, as well as reaction temperature, were systematically optimized. The swelling measurements of the hydrogels were conducted in aqueous solutions of LiCl, NaCl, KCl, MgCl2, CaCl2, SrCl2, BaCl2, and AlCl3. Due to the high swelling capacity in salt solutions, the hydrogels may be referred to as antisalt superabsorbents. The swelling of superabsorbing hydrogels was measured in solutions with pH ranging 1 to 13. The κC‐g‐AMPS hydrogel exhibited a pH‐responsiveness character so that a swelling–deswelling pulsatile behavior was recorded at pH 2 and 8. The overall activation energy for the graft copolymerization reaction was found to be 14.6 kJ/mol. The swelling kinetics of the hydrogels was preliminarily investigated as well. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 98: 255–263, 2005  相似文献   

20.
A hydrogel composite that has been prepared by using waste linear low‐density polyethylene, acrylic acid, and organo‐montmorillonite (LLDPE‐g‐PAA/OMMT) is used as a hydrogel electrolyte. An absorbency test was used to determine the percentage of ZnCl2 solution absorbed by the hydrogel composite. The swelling behavior of the hydrogel composite in the ZnCl2 solution was then studied. The highest absorbency was recorded when the concentration of ZnCl2 solution was 3 M. The conductivity of ZnCl2‐hydrogel composite electrolytes is dependent on the solution's concentration. A mixture of ZnCl2 solution with hydrogel composite yields a good hydrogel composite electrolyte with a conductivity of 0.039 S cm?1 at 3 M ZnCl2. The hydrogel composite electrolyte was used to produce zinc‐carbon cells. The fabricated cell gives capacity of 7.8 mAh, has an internal resistance of 9.9 Ω, a maximum power density of 15.78 mWcm?2, and a short‐circuit current density of 43.75 mAcm?2 for ZnCl2‐hydrogel composite electrolytes. J. VINYL ADDIT. TECHNOL., 22:279–284, 2016. © 2014 Society of Plastics Engineers  相似文献   

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