2011
DOI: 10.1016/j.procbio.2010.09.008
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Increasing cake solids of cellulosic sludge through enzyme-assisted dewatering

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Cited by 17 publications
(5 citation statements)
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“…Moreover, shorter fibers, known as the fines, would cause the pores of cake to clog and deteriorate the sludge dewaterability. This was in accordance with the results of Lu et al (2011) using enzymes conditioning to promote the sludge dewatering. After cellulase pretreatment, the addition of shorter fibers increased 3 to 6 percentage points in cake solids, leading to the porosity reduction of sludge cake.…”
Section: Table 1 Properties Of the Wpt Fiberssupporting
confidence: 92%
“…Moreover, shorter fibers, known as the fines, would cause the pores of cake to clog and deteriorate the sludge dewaterability. This was in accordance with the results of Lu et al (2011) using enzymes conditioning to promote the sludge dewatering. After cellulase pretreatment, the addition of shorter fibers increased 3 to 6 percentage points in cake solids, leading to the porosity reduction of sludge cake.…”
Section: Table 1 Properties Of the Wpt Fiberssupporting
confidence: 92%
“…1). This reflects about 20% conversion of cellulose, which is also the approximate amorphous content of a bleached softwood fiber used earlier (Lu et al 2011). Hence, the likely reason that the polymer preferentially increases the rate of endoglucanase hydrolysis is that it associates more with the amorphous regions of fiber that are particularly susceptible to endoglucanase attack (Coughlan 1992; Zhang and Lynd 2004).…”
Section: Resultsmentioning
confidence: 97%
“…The inoculants, Lactobacillus buchneri (LB, strain ATCC 4005) and Lactobacillus plantarum (LP, strain ATCC 14917), were obtained from the American Type Culture Collection (ATCC, 10801 University Blvd, Manassas, VA, USA). The cellulose enzyme (Cellic® Ctec2) that contained 87 -95 filter paper units (FPU)/mL activity with optimum pH of 5 (Lu et al, 2011), was obtained from Novozymes, Franklinton, N.C., USA. The inoculants (either LB or LP) were prepared by mixing 0.2 g inoculant with 32 mL of distilled water and sprayed over a 16 kg fresh WCSS to obtain at least 2.5 x 10 5 colony forming units of LAB/g fresh WCSS.…”
Section: Methodsmentioning
confidence: 99%