MODIFICATION OF PRECIPITATED CALCIUM CARBONATE FILLER USING SODIUM SILICATE/ZINC CHLORIDE BASED MODIFIERS TO IMPROVE ACID-RESISTANCE AND USE OF THE MODIFIED FILLER IN PAPERMAKING

In order to improve the acid-resistant property of papermaking grade precipitated calcium carbonate filler and to obtain modified filler in powder form, sodium silicate/zinc chloride based modifiers were used in filler modification, and the use of modified filler in papermaking of deinked pulp derived from recycled newspaper was also preliminarily investigated. Under the preliminarily optimized experimental conditions, when sodium silicate, zinc chloride, sodium hexametaphosphate, and phosphoric acid with dosages of 10 wt%, 3 wt%, 1 wt% and 0.2 wt%, respectively, were used as modifiers, and when the temperature, aging time, and PCC concentration during the filler modification process was 70 oC, 7 h and 9.1 wt%, respectively, the acid-resistant property of filler was significantly improved after modification, as evaluated using alum consumption and pH methods. The use of modified precipitated calcium carbonate filler prepared under the optimized conditions provided considerably more brightness and light scattering improvement in comparison to unmodified filler, and filler modification was found to have only negligible influence on tensile and burst strength of the paper, air permeability of the paper, and retention performance of the filler. Surface analysis of the modified filler using XPS and SEM confirmed the occurring of surface encapsulation and modification of precipitated calcium carbonate filler when the relevant modifiers were used in filler modification. The encapsulating effect of modifiers on filler was thought to be favorable to improvement in acid-resistant property, and optical properties of the filled paper

MODIFICATION OF PAPERMAKING GRADE FILLERS: A BRIEF REVIEW

The use of fillers in paper products can provide cost and energy savings, improved paper properties, increased productivities, and specifically desired paper functionalities. There are many problems associated with the use of fillers, such as unsuitability of calcium carbonate fillers in acid papermaking, negative effects of filler loading on paper strength, sizing, and retention, and tendencies of fillers to cause abrasion and dusting. In order to solve these problems and to make better use of fillers, many methods have been proposed, among which filler modification has been a hot topic. The available technologies of filler modification mainly include modification with inorganic substances, modification with natural polymers or their derivatives, modification with water-soluble synthetic polymers, modification with surfactants, modification with polymer latexes, hydrophobic modification, cationic modification, surface nano-structuring, physical modification by compressing, calcination or grinding, and modification for use in functional papers. The methods of filler modification can provide improved acid tolerant and optical properties of fillers, enhanced fiber-filler bonding, improved filler retention and filler sizabilities, alleviated filler abrasiveness, improved filler dispersability, and functionalization of filled papers. Filler modification has been an indispensable way to accelerate the development of high filler technology in papermaking, which is likely to create additional benefits to papermaking industry in the future

PREPARATION AND CHARACTERIZATION OF CONDUCTIVE PAPER VIA IN-SITU POLYMERIZATION OF PYRROLE

Electrically conductive paper was prepared via in-situ chemical oxidative polymerization of pyrrole by using ferric chloride as an oxidant and p-toluenesulfonic acid (PTSA) as a dopant. The deposition of polypyrrole (PPy) on the fiber surface was verified by ATR-FTIR and SEM analyses. Pyrrole concentration had a significant effect on the surface resistivity of conductive paper, especially when the pyrrole concentration was less than 1.8 g•L-1. The conductivity of the PPy-coated paper could be controlled by adjusting pyrrole concentration. The threshold concen-tration of pyrrole was 1.2 g•L-1 when the molar ratio of dopant to pyrrole was 2:1. Very little polymerization reaction in solution occurred when pyrrole concentration was less than 2.5 g•L-1. The pyrrole concentration should reach a higher value to prepare a relatively stable conductive paper with lower resistivity. The XPS results showed that the amount of the PPy coating increased, while the doping level first decreased then increased with the increase of pyrrole concentration. The SEM-EDXA results showed that there was no difference in the amount of PPy coated between the outer surface and the internal wall, but the doping level of the outer surface was higher than that of the internal wall

PREPARATION AND CHARACTERIZATION OF CONDUCTIVE PAPER VIA IN SITU POLYMERIZATION OF 3,4-ETHYLENEDIOXYTHIOPHENE

Conductive paper was prepared via in situ chemical oxidative polymerization of 3,4-ethylenedioxythiophene (EDOT) in pulp suspension by using iron(III) p-toluenesulfonate (Fe(OTs)3) as both an oxidant and a dopant source. The deposition of poly(3,4-ethylenedioxythiophene) (PEDOT) on the pulp fiber surface was verified and characterized by ATR-FTIR and SEM analyses. The factors affecting the conductivity of the PEDOT-coated paper were investigated, and the preparation conditions of the conductive paper with a low resistivity and excellent environmental stability was obtained. The optimum reaction temperature and time were 60 °C and 4 h, respectively. The molar ratio of EDOT to Fe(OTs)3 of 1:1 was optimal when considering both cost and performance factors. The conductivity of the PEDOT-coated paper could be controlled by adjusting EDOT concentration. The threshold concentration of EDOT was about 3 g•L-1, and a volume resistivity as low as 5.9×103 Ω•cm could be achieved, which reached the conductivity range of an electrical conductor. The environmental stability of the PEDOT-coated conductive paper was very good due to the much higher oxidation potential of PEDOT

Flexible Nanopaper Composed of Wood-Derived Nanofibrillated Cellulose and Graphene Building Blocks

Nanopaper has attracted considerable interest in the fields of films and paper research. However, the challenge of integrating the many advantages of nanopaper still remains. Herein, we developed a facile strategy to fabricate multifunctional nanocomposite paper (NGCP) composed of wood-derived nanofibrillated cellulose (NFC) and graphene as building blocks. NFC suspension was consisted of long and entangled NFCs (10–30 nm in width) and their aggregates. Before NGCP formation, NFC was chemically modified with a silane coupling agent to ensure that it could interact strongly with graphene in NGCP. The resulting NGCP samples were flexible and could be bent repeatedly without any structural damage. Within the NGCP samples, the high aspect ratio of NFC made a major contribution to its high mechanical strength, whereas the sheet-like graphene endowed the NGCP with electrical resistance and electrochemical activity. The mechanical strength of the NGCP samples decreased as their graphene content increased. However, the electrical resistance and electrochemical activity of the NGCP samples both rose with increasing content of graphene. The NGCPs still kept advantageous mechanical properties even at high temperatures around 300°C because of the high thermal stability of NFCs and their strong entangled web-like structures. In view of its sustainable building blocks and multifunctional characteristics, the NGCP developed in this work is promising as low-cost and high-performance nanopaper

ADDRESSING WATER FOOTPRINT CONCEPT: A DEMONSTRABLE STRATEGY FOR PAPERMAKING INDUSTRY

Since the introduction of the water footprint concept in 2002, in the context of humankind’s ever-increasing awareness of the valuable global freshwater resources, it has received more and more attention. The application of this relatively new concept has been expected to provide ecological and environmental benefits. For the water-intensive papermaking industry, it seems that water footprint needs to be addressed. The water footprint of cellulosic paper can be divided into three components, including its green water footprint, blue water footprint, and grey water footprint, which may be accounted for by considering the individual contributions of wood or non-wood materials, pulp production processes, effluent discharge to the receiving water bodies, process chemicals and additives, energy consumption, etc. In the literature, the accounting of water footprint during the whole production chain of cellulosic paper is already available, and relevant research findings can provide useful insights into the application of the concept; however, further development of the accounting methodologies is much needed, so that the quantitative and qualitative evaluation of water footprint can be internationally recognized, certified, and standardized. Although there are ongoing or upcoming debates and challenges associated with the concept, its application to papermaking industry may be expected to provide various encouraging possibilities and impacts

Conductive PPy@cellulosic Paper Hybrid Electrodes with a Redox Active Dopant for High Capacitance and Cycling Stability

Polypyrrole@cellulose fibers (PPy@CFs) electrode materials are promising candidates in the energy storage. Various strategies have been pursued to improve their electrochemical performance. However, the poor conductivity, specific capacitance, and cyclic stability still hindered its application. Compared with the previous studies, we selected AQS with electrochemical activity as a dopant to improve these defects. It exhibits a high capacitance of 829.8 F g−1 at a current density of 0.2 A g−1, which is much higher than that of PPy@CFs electrode material (261.9 F g−1). Moreover, the capacitance retention of PPy:AQS/p-PTSA@CFs reaches up to 96.01% after 1000 cycles, indicating superior cyclic stability. Therefore, this work provides an efficient strategy for constructing high-performance electrode materials for energy storage

Isolation and Rheological Characterization of Cellulose Nanofibrils (CNFs) from Coir Fibers in Comparison to Wood and Cotton

In this report, the isolation and rheological characterization of cellulose nanofibrils from coir (CNFs-1) were studied and compared with the CNFs from wood (CNFs-2) and cotton (CNFs-3). Cellulose nanofibrils were isolated successfully from coir fibers by chemical treatments followed by ultrasonic fibrillation. During ultrasonic processing, the size and the crystal structure of the CNFs were influenced by the raw materials. In comparison to CNFs-2 and CNFs-3, CNFs-1 from coir fibers presented diverse advantages, such as sufficient fibrillation with a low diameter distribution, in the range of 2–4 nm and high crystallinity. In the dynamic rheology study of CNFs-1, elastic behavior was observed and maintained due to the formation of gel-like steady network structures, which could not be easily deconstructured by frequency shearing and temperature changing. All results indicated that coir fibers could be used as a valuable resource for the preparation of CNFs, which exhibited comparable properties with those isolated from wood, in regard to morphology and rheological properties. This work provides a basis for further advanced applications using the CNFs isolated from coir fibers

Data from: Structural diversity of naturally regenerating Chinese yew (Taxus wallichiana var. mairei) populations in an ex situ conservation

The Chinese yew (Taxus wallichiana var. mairei) is ranked among the first class of important wild endangered plants in China. However, due to its overexploitation, it now occurs scattered in the forest undergrowth along the Yangtze River Valley. To improve this tree’s conservation management, we used structural indices to investigate the structural diversity of naturally regenerating yew populations that have established via ex situ conservation. The results show that most yews had larger non-yew tree neighbors; these were 30–70% larger than their reference trees. Collectively, the average distances between the yews and the three nearest-neighboring trees were short (<3 m). This result suggests that the yews likely face strong interspecific competition from neighbors. In these two forest stands, most of the pole-sized yews are found beneath a single tall neighboring tree (height ≥10 m), and their growth was enhanced under a single neighboring tree but not under two, three or zero neighboring trees. Finally, we recommend simple silvicultural treatments to reduce interspecific competition; specifically, the cutting or pruning of branches of large neighboring trees in tandem with the thinning of canopy trees growing next to the mother yews