The shell samples

1.2.2. Characteristics of Buccinum tenuissimum shell biomass

Sargassum

hemiphyllum

Adsorbed lanthanide / mmol g-1

Total Released _ /1114 Ca excess (blank)

/ mmol g1 /ПШЮІ^

Net Released Ca

/ mmol g-1

La

0.081

0.208

0.082

0.126

0.121

0.226

0.082

0.144

0.150

0.276

0.082

0.194

0.153

0.305

0.082

0.224

0.234

0.507

0.082

0.426

0.375

0.595

0.082

0.514

0.617

0.995

0.082

0.913

Eu

0.085

0.155

0.080

0.075

0.186

0.298

0.080

0.218

0.237

0.377

0.080

0.297

0.355

0.576

0.080

0.496

0.456

0.791

0.080

0.711

0.707

1.021

0.080

0.941

0.708

1.507

0.080

1.427

Yb

0.079

0.194

0.077

0.117

0.160

0.288

0.077

0.211

0.227

0.403

0.077

0.326

0.296

0.494

0.077

0.417

0.339

0.579

0.077

0.502

0.563

0.838

0.077

0.761

0.688

0.958

0.077

0.881

Table 3. Amount of adsorbed lanthanide and released Ca by Ca-loaded Sargassum hemiphyllum biomass

X-ray powder diffraction (XRD) patterns of the four kinds of Buccinum tenuissimum shell biomass samples are shown in Fig. 7. The crystal structure of the shell biomass was transformed from aragonite (CaCO3) into calcite (CaCO3) phase by heat-treatment (480°C, 6h). Moreover, the crystal structure of the shell biomass was mainly transformed into calcium oxide (CaO) by heat-treatment (950°C, 6h); and was mainly into calcium hydroxide (Ca(OH)2) by adding water after heat-treatment (950°C, 6h). SEM pictures of the four kinds of sieved shell biomass samples are shown in Fig. 8. Comparing Fig. 8(b) with Fig. 8(a), comparatively clear crystal with a lot of big particles may be observed by heat-traetment (480°C, 6h). It is suggested that ground original sample contains a lot of organic materials such as protein, and most of organic matter seem to disappear by heat-traetment. Moreover, fine crystal particle is not observed in Fig. 8 (c). This may be attributable to the phenomena that many crystals were connected largely with each other due to high-temperature sintering. Meanwhile, relative clear crystal (sizes are mostly 1.0-4.0pm) is observed in Fig. 8 (d).

Schizymenia dubyi

Adsorbed lanthanide / mmol g1

Total Released Ca/ mmol g1

Ca excess (blank) / mmol g-1

Net Released Ca / mmol g-1

La

0.053

0.376

0.240

0.136

0.132

0.469

0.240

0.229

0.201

0.571

0.240

0.331

0.281

0.657

0.240

0.417

0.346

0.747

0.240

0.507

0.436

0.757

0.240

0.517

0.603

0.835

0.240

0.595

Eu

0.070

0.655

0.240

0.415

0.146

0.778

0.240

0.538

0.192

0.862

0.240

0.622

0.263

1.025

0.240

0.785

0.333

1.176

0.240

0.936

0.493

2.102

0.240

1.862

0.807

2.146

0.240

1.906

Yb

0.055

0.557

0.240

0.317

0.136

0.594

0.240

0.354

0.210

0.694

0.240

0.454

0.236

0.796

0.240

0.556

0.270

0.771

0.240

0.531

0.483

0.950

0.240

0.710

0.691

1.036

0.240

0.796

Table 4. Amount of adsorbed lanthanide and released Ca by Ca-loaded Schizymenia dubyi biomass

Ulvapertusa

Adsorbed lanthanide

Total Released

Ca excess (blank)

Net Released Ca

/ mmol g-1

Ca/ mmol gA

/ mmol g-1

/ mmol g-1

La

0.079

0.259

0.160

0.099

0.172

0.314

0.160

0.154

0.251

0.415

0.160

0.255

0.315

0.658

0.160

0.498

0.412

0.776

0.160

0.616

0.610

1.546

0.160

1.386

0.929

1.672

0.160

1.512

Yb

0.059

0.263

0.160

0.103

0.134

0.349

0.160

0.189

0.198

0.449

0.160

0.289

0.234

0.644

0.160

0.484

0.266

0.704

0.160

0.544

0.503

1.132

0.160

0.972

0.584

1.421

0.160

1.261

Table 5. Amount of adsorbed lanthanide and released Ca by Ca-loaded Ulva pertusa biomass

image031

Metal uptake / meq g’1

(a)

 

image032

Metal uptake / meq g’1

 

(b)

 

(c)

 

image033

image024

image034

(a)

 

(b)

 

(c)

 

image035

image036

image037

(a) (b)

image038

(c) (d)

Figure 8. SEM pictures of Buccinum tenussimum shell biomass before adsorption of metals. (a) ground original sample, (b) heat-treatment (480°C) sample, (c) heat-treatment (950°C) sample, (d) heat- treatment (950°C) and water added sample

Furthermore, the measurement of specific surface area of the four kinds of sieved samples was performed in this study; and the results are shown in Table 6 along with the main crystal structure of these samples. Remarkably decrease of specific surface area (i. e., from 3.32m2/g to 0.390m2/g for BET, or from 5.35 m2/g to 0.612 m2/g for Langmuir) was found after heat-treatment (480°C, 6h). It is suggested that the crystal structure transformation (i. e., from aragonite (CaCO3) into calcite (CaCO3) phase) and also the difference of the surface morphology can be closely related to the remarkable decrease of specific surface area of the shell biomass. On the other hand, the surface area of "heat-treatment (950°C, 6h) sample" was 1.88m2/g for BET or 3.10m2/g for Langmuir respectively; and that of "heat-treatment (950°C, 6h) and water added sample" was 6.37m2/g for BET or 9.91m2/g for Langmuir, respectively.